CN104202986A - 杀虫组合物及与其相关的方法 - Google Patents
杀虫组合物及与其相关的方法 Download PDFInfo
- Publication number
- CN104202986A CN104202986A CN201380018750.5A CN201380018750A CN104202986A CN 104202986 A CN104202986 A CN 104202986A CN 201380018750 A CN201380018750 A CN 201380018750A CN 104202986 A CN104202986 A CN 104202986A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- haloalkyl
- cycloalkyl
- phenyl
- thiazolinyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims description 112
- 238000000034 method Methods 0.000 title claims description 38
- 230000008569 process Effects 0.000 title description 10
- 230000000361 pesticidal effect Effects 0.000 title description 2
- -1 halogenophenyl Chemical group 0.000 claims description 156
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 145
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 114
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 105
- 150000001875 compounds Chemical class 0.000 claims description 94
- 229910052799 carbon Inorganic materials 0.000 claims description 78
- 229910052731 fluorine Inorganic materials 0.000 claims description 63
- 239000002917 insecticide Substances 0.000 claims description 60
- 229910052739 hydrogen Inorganic materials 0.000 claims description 51
- 229910052801 chlorine Inorganic materials 0.000 claims description 47
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 46
- 125000003545 alkoxy group Chemical group 0.000 claims description 43
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 41
- 241000238631 Hexapoda Species 0.000 claims description 38
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 35
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 33
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 32
- 229910052794 bromium Inorganic materials 0.000 claims description 31
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 31
- 150000002148 esters Chemical class 0.000 claims description 30
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 29
- 229910052740 iodine Inorganic materials 0.000 claims description 29
- 239000005864 Sulphur Substances 0.000 claims description 28
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 26
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 125000002769 thiazolinyl group Chemical group 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000002541 furyl group Chemical group 0.000 claims description 21
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 21
- 125000001544 thienyl group Chemical group 0.000 claims description 21
- 241000196324 Embryophyta Species 0.000 claims description 20
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 19
- 239000004009 herbicide Substances 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 17
- 239000001301 oxygen Substances 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 241000607479 Yersinia pestis Species 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 125000000304 alkynyl group Chemical group 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 13
- 125000000623 heterocyclic group Chemical group 0.000 claims description 12
- 239000000417 fungicide Substances 0.000 claims description 11
- 230000002363 herbicidal effect Effects 0.000 claims description 11
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 11
- 229920006395 saturated elastomer Polymers 0.000 claims description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 11
- 230000001069 nematicidal effect Effects 0.000 claims description 10
- 239000005645 nematicide Substances 0.000 claims description 10
- 125000001425 triazolyl group Chemical group 0.000 claims description 10
- 125000002971 oxazolyl group Chemical group 0.000 claims description 9
- 230000000855 fungicidal effect Effects 0.000 claims description 8
- CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical compound C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 claims description 7
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 claims description 7
- MCGBIXXDQFWVDW-UHFFFAOYSA-N 4,5-dihydro-1h-pyrazole Chemical compound C1CC=NN1 MCGBIXXDQFWVDW-UHFFFAOYSA-N 0.000 claims description 7
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 7
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 7
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 7
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 7
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 7
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 7
- 125000000259 cinnolinyl group Chemical class N1=NC(=CC2=CC=CC=C12)* 0.000 claims description 7
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 7
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 7
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 7
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 7
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 7
- 125000002757 morpholinyl group Chemical group 0.000 claims description 7
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 7
- 125000005968 oxazolinyl group Chemical group 0.000 claims description 7
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims description 7
- 125000004193 piperazinyl group Chemical group 0.000 claims description 7
- 125000005936 piperidyl group Chemical group 0.000 claims description 7
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 7
- 125000002755 pyrazolinyl group Chemical group 0.000 claims description 7
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 7
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 7
- 125000005493 quinolyl group Chemical group 0.000 claims description 7
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 7
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 claims description 7
- 125000000335 thiazolyl group Chemical group 0.000 claims description 7
- 125000004306 triazinyl group Chemical group 0.000 claims description 7
- 244000061456 Solanum tuberosum Species 0.000 claims description 6
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 6
- 240000008042 Zea mays Species 0.000 claims description 6
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 235000005822 corn Nutrition 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 5
- 235000021307 Triticum Nutrition 0.000 claims description 5
- 229960003692 gamma aminobutyric acid Drugs 0.000 claims description 5
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims description 5
- 235000016068 Berberis vulgaris Nutrition 0.000 claims description 4
- 241000335053 Beta vulgaris Species 0.000 claims description 4
- 235000002566 Capsicum Nutrition 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 4
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 4
- 239000006002 Pepper Substances 0.000 claims description 4
- 235000016761 Piper aduncum Nutrition 0.000 claims description 4
- 235000017804 Piper guineense Nutrition 0.000 claims description 4
- 235000008184 Piper nigrum Nutrition 0.000 claims description 4
- 240000003768 Solanum lycopersicum Species 0.000 claims description 4
- OBISXEJSEGNNKL-UHFFFAOYSA-N dinitrogen-n-sulfide Chemical compound [N-]=[N+]=S OBISXEJSEGNNKL-UHFFFAOYSA-N 0.000 claims description 4
- 229940121819 ATPase inhibitor Drugs 0.000 claims description 3
- 229920002101 Chitin Polymers 0.000 claims description 3
- 229940118183 Chloride channel agonist Drugs 0.000 claims description 3
- 229940123715 Chloride channel antagonist Drugs 0.000 claims description 3
- 235000010469 Glycine max Nutrition 0.000 claims description 3
- 244000068988 Glycine max Species 0.000 claims description 3
- 235000003228 Lactuca sativa Nutrition 0.000 claims description 3
- 240000008415 Lactuca sativa Species 0.000 claims description 3
- 241001597008 Nomeidae Species 0.000 claims description 3
- 239000000362 adenosine triphosphatase inhibitor Substances 0.000 claims description 3
- 239000003467 chloride channel stimulating agent Substances 0.000 claims description 3
- 238000012239 gene modification Methods 0.000 claims description 3
- 230000005017 genetic modification Effects 0.000 claims description 3
- 235000013617 genetically modified food Nutrition 0.000 claims description 3
- 230000010627 oxidative phosphorylation Effects 0.000 claims description 3
- 239000012453 solvate Substances 0.000 claims description 3
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims description 2
- 108010009685 Cholinergic Receptors Proteins 0.000 claims description 2
- 241000675108 Citrus tangerina Species 0.000 claims description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 2
- 244000061176 Nicotiana tabacum Species 0.000 claims description 2
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 claims description 2
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims description 2
- 241000220324 Pyrus Species 0.000 claims description 2
- 229930001406 Ryanodine Natural products 0.000 claims description 2
- 108010052164 Sodium Channels Proteins 0.000 claims description 2
- 102000018674 Sodium Channels Human genes 0.000 claims description 2
- 241000219793 Trifolium Species 0.000 claims description 2
- 102000034337 acetylcholine receptors Human genes 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 239000000544 cholinesterase inhibitor Substances 0.000 claims description 2
- 238000005336 cracking Methods 0.000 claims description 2
- 239000004220 glutamic acid Substances 0.000 claims description 2
- 235000013922 glutamic acid Nutrition 0.000 claims description 2
- 230000012010 growth Effects 0.000 claims description 2
- 235000021017 pears Nutrition 0.000 claims description 2
- 239000000018 receptor agonist Substances 0.000 claims description 2
- 229940044601 receptor agonist Drugs 0.000 claims description 2
- JJSYXNQGLHBRRK-SFEDZAPPSA-N ryanodine Chemical compound O([C@@H]1[C@]([C@@]2([C@]3(O)[C@]45O[C@@]2(O)C[C@]([C@]4(CC[C@H](C)[C@H]5O)O)(C)[C@@]31O)C)(O)C(C)C)C(=O)C1=CC=CN1 JJSYXNQGLHBRRK-SFEDZAPPSA-N 0.000 claims description 2
- 244000075850 Avena orientalis Species 0.000 claims 1
- 235000007319 Avena orientalis Nutrition 0.000 claims 1
- 235000007558 Avena sp Nutrition 0.000 claims 1
- 235000016623 Fragaria vesca Nutrition 0.000 claims 1
- 240000009088 Fragaria x ananassa Species 0.000 claims 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 claims 1
- 241000219146 Gossypium Species 0.000 claims 1
- 240000005979 Hordeum vulgare Species 0.000 claims 1
- 235000007340 Hordeum vulgare Nutrition 0.000 claims 1
- 241000220225 Malus Species 0.000 claims 1
- 244000203593 Piper nigrum Species 0.000 claims 1
- 244000018633 Prunus armeniaca Species 0.000 claims 1
- 235000009827 Prunus armeniaca Nutrition 0.000 claims 1
- 244000046109 Sorghum vulgare var. nervosum Species 0.000 claims 1
- 244000098338 Triticum aestivum Species 0.000 claims 1
- 244000078703 ectoparasite Species 0.000 claims 1
- 244000079386 endoparasite Species 0.000 claims 1
- 229960002989 glutamic acid Drugs 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 244000025254 Cannabis sativa Species 0.000 description 51
- 239000002585 base Substances 0.000 description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 49
- 238000002360 preparation method Methods 0.000 description 46
- 239000007787 solid Substances 0.000 description 45
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 39
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 38
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 37
- 239000000460 chlorine Substances 0.000 description 33
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 32
- 239000000243 solution Substances 0.000 description 32
- 239000002904 solvent Substances 0.000 description 31
- 238000005481 NMR spectroscopy Methods 0.000 description 29
- 239000000376 reactant Substances 0.000 description 28
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 27
- 239000011737 fluorine Substances 0.000 description 27
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 26
- 239000011734 sodium Substances 0.000 description 26
- 229910052708 sodium Inorganic materials 0.000 description 26
- 241000894006 Bacteria Species 0.000 description 24
- 150000001412 amines Chemical class 0.000 description 24
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 23
- 239000004094 surface-active agent Substances 0.000 description 23
- 239000002253 acid Substances 0.000 description 22
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 20
- 239000012141 concentrate Substances 0.000 description 20
- 238000010189 synthetic method Methods 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 17
- 239000000543 intermediate Substances 0.000 description 17
- 239000002245 particle Substances 0.000 description 17
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- 239000012071 phase Substances 0.000 description 16
- 238000003756 stirring Methods 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- GWJYYOWGLLHNRJ-UHFFFAOYSA-N n-hydrazinylmethanethioamide Chemical compound NNNC=S GWJYYOWGLLHNRJ-UHFFFAOYSA-N 0.000 description 15
- 239000003921 oil Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 150000003851 azoles Chemical class 0.000 description 14
- 239000007788 liquid Substances 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 241001124076 Aphididae Species 0.000 description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 12
- 238000003818 flash chromatography Methods 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 12
- 239000011591 potassium Substances 0.000 description 12
- 229910052700 potassium Inorganic materials 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 239000003513 alkali Substances 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 10
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 10
- 235000013305 food Nutrition 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052698 phosphorus Inorganic materials 0.000 description 10
- 239000011574 phosphorus Substances 0.000 description 10
- 239000004563 wettable powder Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 241000866584 Cryptotermes Species 0.000 description 9
- 241000256602 Isoptera Species 0.000 description 9
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 9
- 239000000284 extract Substances 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000007857 hydrazones Chemical class 0.000 description 9
- 239000012044 organic layer Substances 0.000 description 9
- NOLHRFLIXVQPSZ-UHFFFAOYSA-N 1,3-thiazolidin-4-one Chemical compound O=C1CSCN1 NOLHRFLIXVQPSZ-UHFFFAOYSA-N 0.000 description 8
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 8
- 241001509967 Reticulitermes flavipes Species 0.000 description 8
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 238000010790 dilution Methods 0.000 description 8
- 239000012895 dilution Substances 0.000 description 8
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 8
- 239000002270 dispersing agent Substances 0.000 description 8
- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 8
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 8
- 229940072033 potash Drugs 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 235000015320 potassium carbonate Nutrition 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229940124530 sulfonamide Drugs 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 235000007516 Chrysanthemum Nutrition 0.000 description 7
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 7
- 241000254173 Coleoptera Species 0.000 description 7
- 241000254099 Melolontha melolontha Species 0.000 description 7
- 239000002169 Metam Substances 0.000 description 7
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 7
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 7
- 229940043237 diethanolamine Drugs 0.000 description 7
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 7
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 7
- 238000001291 vacuum drying Methods 0.000 description 7
- 238000003828 vacuum filtration Methods 0.000 description 7
- 235000015112 vegetable and seed oil Nutrition 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 241001600407 Aphis <genus> Species 0.000 description 6
- 241001674044 Blattodea Species 0.000 description 6
- 235000006008 Brassica napus var napus Nutrition 0.000 description 6
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 6
- 241001674939 Caulanthus Species 0.000 description 6
- 239000005644 Dazomet Substances 0.000 description 6
- HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 description 6
- 241000255925 Diptera Species 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 241000244206 Nematoda Species 0.000 description 6
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 6
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229960000583 acetic acid Drugs 0.000 description 6
- 239000000443 aerosol Substances 0.000 description 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N aminothiocarboxamide Natural products NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 6
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 6
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 6
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 235000019439 ethyl acetate Nutrition 0.000 description 6
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 6
- 239000002316 fumigant Substances 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 6
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 5
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 5
- BIHPYCDDPGNWQO-UHFFFAOYSA-N 5-iai Chemical compound C1=C(I)C=C2CC(N)CC2=C1 BIHPYCDDPGNWQO-UHFFFAOYSA-N 0.000 description 5
- 239000005711 Benzoic acid Substances 0.000 description 5
- 241001414720 Cicadellidae Species 0.000 description 5
- 241001414830 Diaspididae Species 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 241000233866 Fungi Species 0.000 description 5
- RMFGNMMNUZWCRZ-UHFFFAOYSA-N Humulone Natural products CC(C)CC(=O)C1=C(O)C(O)(CC=C(C)C)C(O)=C(CC=C(C)C)C1=O RMFGNMMNUZWCRZ-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 5
- 241001674048 Phthiraptera Species 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 5
- 241000270708 Testudinidae Species 0.000 description 5
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 235000010233 benzoic acid Nutrition 0.000 description 5
- 230000003115 biocidal effect Effects 0.000 description 5
- 239000003139 biocide Substances 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 5
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- NDYULEPTCXJCJM-UHFFFAOYSA-N dazomet, sodium salt Chemical compound [Na+].CN1CN(C)C(=S)S[CH-]1 NDYULEPTCXJCJM-UHFFFAOYSA-N 0.000 description 5
- 239000003480 eluent Substances 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 229960002125 enilconazole Drugs 0.000 description 5
- VMSLCPKYRPDHLN-NRFANRHFSA-N humulone Chemical compound CC(C)CC(=O)C1=C(O)C(CC=C(C)C)=C(O)[C@@](O)(CC=C(C)C)C1=O VMSLCPKYRPDHLN-NRFANRHFSA-N 0.000 description 5
- 150000002576 ketones Chemical class 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- CSJDCSCTVDEHRN-UHFFFAOYSA-N methane;molecular oxygen Chemical compound C.O=O CSJDCSCTVDEHRN-UHFFFAOYSA-N 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 5
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- TZLVRPLSVNESQC-UHFFFAOYSA-N potassium azide Chemical compound [K+].[N-]=[N+]=[N-] TZLVRPLSVNESQC-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 235000015424 sodium Nutrition 0.000 description 5
- 239000001632 sodium acetate Substances 0.000 description 5
- 235000017281 sodium acetate Nutrition 0.000 description 5
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 5
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 5
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 4
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 4
- QQHRSBLQLJPBPJ-UHFFFAOYSA-N (2,4-dinitro-6-pentan-2-ylphenyl) propan-2-yl carbonate Chemical compound CCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C QQHRSBLQLJPBPJ-UHFFFAOYSA-N 0.000 description 4
- IXNUTQCZWAHNPN-UHFFFAOYSA-N (2-tert-butyl-4,6-dinitrophenyl) ethyl carbonate Chemical compound CCOC(=O)OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1C(C)(C)C IXNUTQCZWAHNPN-UHFFFAOYSA-N 0.000 description 4
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 4
- OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 description 4
- PSOZMUMWCXLRKX-UHFFFAOYSA-N 2,4-dinitro-6-pentan-2-ylphenol Chemical compound CCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O PSOZMUMWCXLRKX-UHFFFAOYSA-N 0.000 description 4
- IRCMYGHHKLLGHV-UHFFFAOYSA-N 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl methanesulfonate Chemical compound C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 IRCMYGHHKLLGHV-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 4
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 4
- 241001143309 Acanthoscelides obtectus Species 0.000 description 4
- 241001136523 Anastrepha Species 0.000 description 4
- 244000003416 Asparagus officinalis Species 0.000 description 4
- 235000005340 Asparagus officinalis Nutrition 0.000 description 4
- FMTFEIJHMMQUJI-UHFFFAOYSA-N Cinerin I Natural products C1C(=O)C(CC=CC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C FMTFEIJHMMQUJI-UHFFFAOYSA-N 0.000 description 4
- 241001465977 Coccoidea Species 0.000 description 4
- OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 4
- 239000005630 Diquat Substances 0.000 description 4
- 239000005512 Ethofumesate Substances 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 239000005795 Imazalil Substances 0.000 description 4
- XRHGWAGWAHHFLF-UHFFFAOYSA-N Isazofos Chemical compound CCOP(=S)(OCC)OC=1N=C(Cl)N(C(C)C)N=1 XRHGWAGWAHHFLF-UHFFFAOYSA-N 0.000 description 4
- QVJMXSGZTCGLHZ-VWADHSNXSA-N Juvenile hormone III Natural products O=C(OC)/C=C(\CC/C=C(\CC[C@H]1C(C)(C)O1)/C)/C QVJMXSGZTCGLHZ-VWADHSNXSA-N 0.000 description 4
- 241000255777 Lepidoptera Species 0.000 description 4
- 241000270322 Lepidosauria Species 0.000 description 4
- 239000005805 Mepanipyrim Substances 0.000 description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
- UDSJPFPDKCMYBD-UHFFFAOYSA-N Metsulfovax Chemical compound S1C(C)=NC(C)=C1C(=O)NC1=CC=CC=C1 UDSJPFPDKCMYBD-UHFFFAOYSA-N 0.000 description 4
- LVPGGWVHPIAEMC-UHFFFAOYSA-L Morfamquat Chemical compound [Cl-].[Cl-].CC1COCC(C)N1C(=O)C[N+]1=CC=C(C=2C=C[N+](CC(=O)N3C(COCC3C)C)=CC=2)C=C1 LVPGGWVHPIAEMC-UHFFFAOYSA-L 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- CVRALZAYCYJELZ-UHFFFAOYSA-N O-(4-bromo-2,5-dichlorophenyl) O-methyl phenylphosphonothioate Chemical compound C=1C=CC=CC=1P(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl CVRALZAYCYJELZ-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 241000676810 Phytocoris Species 0.000 description 4
- ITVQAKZNYJEWKS-UHFFFAOYSA-N Profluralin Chemical compound [O-][N+](=O)C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1N(CCC)CC1CC1 ITVQAKZNYJEWKS-UHFFFAOYSA-N 0.000 description 4
- 239000005869 Pyraclostrobin Substances 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 241001492664 Solenopsis <angiosperm> Species 0.000 description 4
- PNRAZZZISDRWMV-UHFFFAOYSA-N Terbucarb Chemical compound CNC(=O)OC1=C(C(C)(C)C)C=C(C)C=C1C(C)(C)C PNRAZZZISDRWMV-UHFFFAOYSA-N 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 241000700605 Viruses Species 0.000 description 4
- YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 description 4
- 239000003905 agrochemical Substances 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 230000002152 alkylating effect Effects 0.000 description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
- QLULGSLAHXLKSR-UHFFFAOYSA-N azane;phosphane Chemical compound N.P QLULGSLAHXLKSR-UHFFFAOYSA-N 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 4
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 4
- 229910021538 borax Inorganic materials 0.000 description 4
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 4
- VAIZTNZGPYBOGF-UHFFFAOYSA-N butyl 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OCCCC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 VAIZTNZGPYBOGF-UHFFFAOYSA-N 0.000 description 4
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 description 4
- 229930193529 cinerin Natural products 0.000 description 4
- FMTFEIJHMMQUJI-DFKXKMKHSA-N cinerin I Chemical compound C1C(=O)C(C\C=C/C)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1C=C(C)C FMTFEIJHMMQUJI-DFKXKMKHSA-N 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229940120693 copper naphthenate Drugs 0.000 description 4
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 description 4
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 4
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 4
- 239000013530 defoamer Substances 0.000 description 4
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 description 4
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical compound Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- 229960002563 disulfiram Drugs 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 4
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- 125000001841 imino group Chemical group [H]N=* 0.000 description 4
- 230000009545 invasion Effects 0.000 description 4
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 4
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 4
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 description 4
- AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 150000002923 oximes Chemical class 0.000 description 4
- XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 229940097322 potassium arsenite Drugs 0.000 description 4
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 4
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 4
- HEQWEGCSZXMIJQ-UHFFFAOYSA-M potassium;oxoarsinite Chemical compound [K+].[O-][As]=O HEQWEGCSZXMIJQ-UHFFFAOYSA-M 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- CPTJXGLQLVPIGP-UHFFFAOYSA-N precocene I Chemical compound C1=CC(C)(C)OC2=CC(OC)=CC=C21 CPTJXGLQLVPIGP-UHFFFAOYSA-N 0.000 description 4
- PTIDGSWTMLSGAH-UHFFFAOYSA-N precocene II Chemical compound O1C(C)(C)C=CC2=C1C=C(OC)C(OC)=C2 PTIDGSWTMLSGAH-UHFFFAOYSA-N 0.000 description 4
- 235000019260 propionic acid Nutrition 0.000 description 4
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 4
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 4
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 4
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 239000004328 sodium tetraborate Substances 0.000 description 4
- 235000010339 sodium tetraborate Nutrition 0.000 description 4
- 239000001593 sorbitan monooleate Substances 0.000 description 4
- 235000011069 sorbitan monooleate Nutrition 0.000 description 4
- 229940035049 sorbitan monooleate Drugs 0.000 description 4
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 4
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 3
- OTKXWJHPGBRXCR-UHFFFAOYSA-N (2-chloro-4-nitrophenoxy)-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1Cl OTKXWJHPGBRXCR-UHFFFAOYSA-N 0.000 description 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 3
- RLLPVAHGXHCWKJ-MJGOQNOKSA-N (3-phenoxyphenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-MJGOQNOKSA-N 0.000 description 3
- MTXSIJUGVMTTMU-JTQLQIEISA-N (S)-anabasine Chemical compound N1CCCC[C@H]1C1=CC=CN=C1 MTXSIJUGVMTTMU-JTQLQIEISA-N 0.000 description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- WBEJYOJJBDISQU-UHFFFAOYSA-N 1,2-Dibromo-3-chloropropane Chemical compound ClCC(Br)CBr WBEJYOJJBDISQU-UHFFFAOYSA-N 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical class ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 3
- OWEGWHBOCFMBLP-UHFFFAOYSA-N 1-(4-chlorophenoxy)-1-(1H-imidazol-1-yl)-3,3-dimethylbutan-2-one Chemical compound C1=CN=CN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 OWEGWHBOCFMBLP-UHFFFAOYSA-N 0.000 description 3
- OZOMQRBLCMDCEG-VIZOYTHASA-N 1-[(e)-[5-(4-nitrophenyl)furan-2-yl]methylideneamino]imidazolidine-2,4-dione Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(O1)=CC=C1\C=N\N1C(=O)NC(=O)C1 OZOMQRBLCMDCEG-VIZOYTHASA-N 0.000 description 3
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 3
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical compound C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 3
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 description 3
- JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 description 3
- LUBCBEANYIETCW-UHFFFAOYSA-N 2-diethoxyphosphorylsulfanyl-n,n-diethylethanamine;oxalic acid Chemical compound OC(=O)C(O)=O.CCOP(=O)(OCC)SCCN(CC)CC LUBCBEANYIETCW-UHFFFAOYSA-N 0.000 description 3
- MLDVVJZNWASRQL-UHFFFAOYSA-N 4-diethoxyphosphinothioyloxy-n,n,6-trimethylpyrimidin-2-amine Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(N(C)C)=N1 MLDVVJZNWASRQL-UHFFFAOYSA-N 0.000 description 3
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 description 3
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 description 3
- 241001427556 Anoplura Species 0.000 description 3
- 235000000832 Ayote Nutrition 0.000 description 3
- 239000005739 Bordeaux mixture Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 240000007124 Brassica oleracea Species 0.000 description 3
- 239000005945 Chlorpyrifos-methyl Substances 0.000 description 3
- 244000241257 Cucumis melo Species 0.000 description 3
- 240000004244 Cucurbita moschata Species 0.000 description 3
- 235000009854 Cucurbita moschata Nutrition 0.000 description 3
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 3
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 3
- 241001124144 Dermaptera Species 0.000 description 3
- IIPZYDQGBIWLBU-UHFFFAOYSA-N Dinoterb Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O IIPZYDQGBIWLBU-UHFFFAOYSA-N 0.000 description 3
- 229920005682 EO-PO block copolymer Polymers 0.000 description 3
- 208000035126 Facies Diseases 0.000 description 3
- JHJOOSLFWRRSGU-UHFFFAOYSA-N Fenchlorphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Cl)C=C1Cl JHJOOSLFWRRSGU-UHFFFAOYSA-N 0.000 description 3
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 description 3
- MNFMIVVPXOGUMX-UHFFFAOYSA-N Fluchloralin Chemical compound CCCN(CCCl)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O MNFMIVVPXOGUMX-UHFFFAOYSA-N 0.000 description 3
- 239000005784 Fluoxastrobin Substances 0.000 description 3
- 239000005785 Fluquinconazole Substances 0.000 description 3
- 239000005562 Glyphosate Substances 0.000 description 3
- PMAAYIYCDXGUAP-UHFFFAOYSA-N Indanofan Chemical compound O=C1C2=CC=CC=C2C(=O)C1(CC)CC1(C=2C=C(Cl)C=CC=2)CO1 PMAAYIYCDXGUAP-UHFFFAOYSA-N 0.000 description 3
- 241000661345 Leptocorisa Species 0.000 description 3
- 241001414823 Lygus hesperus Species 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000005580 Metazachlor Substances 0.000 description 3
- 239000005916 Methomyl Substances 0.000 description 3
- 241000721621 Myzus persicae Species 0.000 description 3
- 241000131101 Oryzaephilus surinamensis Species 0.000 description 3
- 241001494479 Pecora Species 0.000 description 3
- 240000003889 Piper guineense Species 0.000 description 3
- 241000219843 Pisum Species 0.000 description 3
- 235000010582 Pisum sativum Nutrition 0.000 description 3
- 229930182764 Polyoxin Natural products 0.000 description 3
- 239000005821 Propamocarb Substances 0.000 description 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 3
- 241000180219 Sitobion avenae Species 0.000 description 3
- 241000736128 Solenopsis invicta Species 0.000 description 3
- 241000883295 Symphyla Species 0.000 description 3
- 239000005623 Thifensulfuron-methyl Substances 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- MYPKGPZHHQEODQ-UHFFFAOYSA-N [3-(dimethylaminomethylideneamino)phenoxy]carbonyl-methylazanium;chloride Chemical compound Cl.CNC(=O)OC1=CC=CC(N=CN(C)C)=C1 MYPKGPZHHQEODQ-UHFFFAOYSA-N 0.000 description 3
- 229940100198 alkylating agent Drugs 0.000 description 3
- 239000002168 alkylating agent Substances 0.000 description 3
- 238000005804 alkylation reaction Methods 0.000 description 3
- 125000005133 alkynyloxy group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 229960002587 amitraz Drugs 0.000 description 3
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 229930014345 anabasine Natural products 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- 239000003849 aromatic solvent Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- MXZACTZQSGYANA-UHFFFAOYSA-N chembl545463 Chemical compound Cl.C1=CC(OC)=CC=C1C(N=C1)=CN2C1=NC(C)=C2O MXZACTZQSGYANA-UHFFFAOYSA-N 0.000 description 3
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 3
- QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229960003344 climbazole Drugs 0.000 description 3
- WEBQKRLKWNIYKK-UHFFFAOYSA-N demeton-S-methyl Chemical compound CCSCCSP(=O)(OC)OC WEBQKRLKWNIYKK-UHFFFAOYSA-N 0.000 description 3
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 3
- OGGXGZAMXPVRFZ-UHFFFAOYSA-N dimethylarsinic acid Chemical compound C[As](C)(O)=O OGGXGZAMXPVRFZ-UHFFFAOYSA-N 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 description 3
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 3
- ZXQYGBMAQZUVMI-GCMPRSNUSA-N gamma-cyhalothrin Chemical compound CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-GCMPRSNUSA-N 0.000 description 3
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 3
- 239000003349 gelling agent Substances 0.000 description 3
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 3
- 150000002460 imidazoles Chemical class 0.000 description 3
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 3
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 description 3
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 description 3
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 3
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 3
- 229940102396 methyl bromide Drugs 0.000 description 3
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 3
- BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 3
- BVPSSZAVUQHOML-UHFFFAOYSA-N n-chloropyridin-2-amine Chemical compound ClNC1=CC=CC=N1 BVPSSZAVUQHOML-UHFFFAOYSA-N 0.000 description 3
- 229960002715 nicotine Drugs 0.000 description 3
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 3
- YCIMNLLNPGFGHC-UHFFFAOYSA-N o-dihydroxy-benzene Natural products OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 3
- 235000006408 oxalic acid Nutrition 0.000 description 3
- 229940116315 oxalic acid Drugs 0.000 description 3
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 3
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 3
- 230000001717 pathogenic effect Effects 0.000 description 3
- 229960000490 permethrin Drugs 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 231100000614 poison Toxicity 0.000 description 3
- 239000002574 poison Substances 0.000 description 3
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 3
- 229920001021 polysulfide Polymers 0.000 description 3
- 239000005077 polysulfide Substances 0.000 description 3
- 150000008117 polysulfides Polymers 0.000 description 3
- SMKRKQBMYOFFMU-UHFFFAOYSA-N prallethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC#C)C(=O)C1 SMKRKQBMYOFFMU-UHFFFAOYSA-N 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 3
- YRRBXJLFCBCKNW-UHFFFAOYSA-N prothiocarb Chemical compound CCSC(=O)NCCCN(C)C YRRBXJLFCBCKNW-UHFFFAOYSA-N 0.000 description 3
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 3
- 235000015136 pumpkin Nutrition 0.000 description 3
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 3
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- 230000012865 response to insecticide Effects 0.000 description 3
- 239000003128 rodenticide Substances 0.000 description 3
- 229940080817 rotenone Drugs 0.000 description 3
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 3
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000005936 tau-Fluvalinate Substances 0.000 description 3
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 3
- 229930192474 thiophene Natural products 0.000 description 3
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 3
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 3
- YNWVFADWVLCOPU-MAUPQMMJSA-N uniconazole P Chemical compound C1=NC=NN1/C([C@@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MAUPQMMJSA-N 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 2
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 2
- KAATUXNTWXVJKI-GGPKGHCWSA-N (1R)-trans-(alphaS)-cypermethrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-GGPKGHCWSA-N 0.000 description 2
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 2
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 2
- FUZORIOHZSVKAW-WINLOITPSA-N (1R,4S)-1,2,3,4,7,7-hexachloro-5,6-bis(chloromethyl)bicyclo[2.2.1]hept-2-ene Chemical compound ClCC1C(CCl)[C@@]2(Cl)C(Cl)=C(Cl)[C@]1(Cl)C2(Cl)Cl FUZORIOHZSVKAW-WINLOITPSA-N 0.000 description 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 description 2
- YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 description 2
- MYUPFXPCYUISAG-UHFFFAOYSA-N (2,4-dichlorophenyl)(phenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC(Cl)=CC=1)Cl)(O)C1=CC=CC=C1 MYUPFXPCYUISAG-UHFFFAOYSA-N 0.000 description 2
- FHNKBSDJERHDHZ-UHFFFAOYSA-N (2,4-dimethylphenyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(C)C=C1C FHNKBSDJERHDHZ-UHFFFAOYSA-N 0.000 description 2
- PTKVPQXEKZOPNA-UHFFFAOYSA-N (2,4-dinitro-6-octan-2-ylphenyl) methylsulfanylformate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)SC PTKVPQXEKZOPNA-UHFFFAOYSA-N 0.000 description 2
- YHVJMJFNSRLYIC-WEVVVXLNSA-N (2,6-dinitro-4-octan-2-ylphenyl) (e)-but-2-enoate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=C(OC(=O)\C=C\C)C([N+]([O-])=O)=C1 YHVJMJFNSRLYIC-WEVVVXLNSA-N 0.000 description 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 2
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 description 2
- MIZYPRIEDMSCAC-UHFFFAOYSA-N (2-methyl-4-oxo-3-prop-2-enylcyclopent-2-en-1-yl) 2,2,3,3-tetramethylcyclopropane-1-carboxylate Chemical compound CC1=C(CC=C)C(=O)CC1OC(=O)C1C(C)(C)C1(C)C MIZYPRIEDMSCAC-UHFFFAOYSA-N 0.000 description 2
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 description 2
- OTLLEIBWKHEHGU-TUNUFRSWSA-N (2R,3S,4S,5S)-2-[(2R,3R,4R,5S,6R)-5-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy]-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxyhexanedioic acid Chemical compound C([C@H]1O[C@H]([C@@H]([C@@H]1O)O)N1C=2N=CN=C(C=2N=C1)N)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]([C@H](O)[C@H](OP(O)(O)=O)[C@H](O)C(O)=O)C(O)=O)[C@H](O)[C@H]1O OTLLEIBWKHEHGU-TUNUFRSWSA-N 0.000 description 2
- LZTIMERBDGGAJD-SNAWJCMRSA-N (2e)-2-(nitromethylidene)-1,3-thiazinane Chemical compound [O-][N+](=O)\C=C1/NCCCS1 LZTIMERBDGGAJD-SNAWJCMRSA-N 0.000 description 2
- URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 description 2
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 2
- XJPOOEMIUDHWSO-PHIMTYICSA-N (2s,5r)-2,5-dimethyl-n-phenylpyrrolidine-1-carboxamide Chemical compound C[C@H]1CC[C@@H](C)N1C(=O)NC1=CC=CC=C1 XJPOOEMIUDHWSO-PHIMTYICSA-N 0.000 description 2
- DSVOTYIOPGIVPP-UHFFFAOYSA-N (3,4-dichlorophenyl)methyl n-methylcarbamate Chemical compound CNC(=O)OCC1=CC=C(Cl)C(Cl)=C1 DSVOTYIOPGIVPP-UHFFFAOYSA-N 0.000 description 2
- YJXNJQHBVKTWCC-UHFFFAOYSA-N (3-cyclopent-2-en-1-yl-2-methyl-4-oxocyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(C2C=CCC2)C(=O)C1 YJXNJQHBVKTWCC-UHFFFAOYSA-N 0.000 description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 2
- OZJCQBUSEOVJOW-UHFFFAOYSA-N (4-ethylsulfanylphenyl) n-methylcarbamate Chemical compound CCSC1=CC=C(OC(=O)NC)C=C1 OZJCQBUSEOVJOW-UHFFFAOYSA-N 0.000 description 2
- KEZAYQGUTKCBLO-UHFFFAOYSA-N (5,7-dichloro-1,3-benzoxazol-2-yl)methylsulfanyl-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound ClC1=CC(Cl)=C2OC(CSP(=S)(OCC)OCC)=NC2=C1 KEZAYQGUTKCBLO-UHFFFAOYSA-N 0.000 description 2
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 2
- KPMWGGRSOPMANK-UHFFFAOYSA-N (6-chloro-1,3-benzodioxol-5-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC(C(=C1)Cl)=CC2=C1OCO2 KPMWGGRSOPMANK-UHFFFAOYSA-N 0.000 description 2
- GFMMMCXLNNLCPJ-NSCUHMNNSA-N (E)-2,3-dinitrobut-2-enoic acid Chemical compound [N+](=O)([O-])\C(=C(/C(=O)O)\[N+](=O)[O-])\C GFMMMCXLNNLCPJ-NSCUHMNNSA-N 0.000 description 2
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 description 2
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 description 2
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 description 2
- NWWZPOKUUAIXIW-DHZHZOJOSA-N (E)-thiamethoxam Chemical compound [O-][N+](=O)/N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-DHZHZOJOSA-N 0.000 description 2
- IQVNEKKDSLOHHK-FNCQTZNRSA-N (E,E)-hydramethylnon Chemical compound N1CC(C)(C)CNC1=NN=C(/C=C/C=1C=CC(=CC=1)C(F)(F)F)\C=C\C1=CC=C(C(F)(F)F)C=C1 IQVNEKKDSLOHHK-FNCQTZNRSA-N 0.000 description 2
- ADDQHLREJDZPMT-AWEZNQCLSA-N (S)-metamifop Chemical compound O=C([C@@H](OC=1C=CC(OC=2OC3=CC(Cl)=CC=C3N=2)=CC=1)C)N(C)C1=CC=CC=C1F ADDQHLREJDZPMT-AWEZNQCLSA-N 0.000 description 2
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 description 2
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 description 2
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 description 2
- PCKNFPQPGUWFHO-SXBRIOAWSA-N (Z)-flucycloxuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1)=CC=C1CO\N=C(C=1C=CC(Cl)=CC=1)\C1CC1 PCKNFPQPGUWFHO-SXBRIOAWSA-N 0.000 description 2
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 description 2
- UNQDVBLGFWIFGX-UHFFFAOYSA-M (carbamoylamino)-phenylmercury Chemical compound NC(=O)N[Hg]C1=CC=CC=C1 UNQDVBLGFWIFGX-UHFFFAOYSA-M 0.000 description 2
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 description 2
- QQVNWNVUGXNUJN-BENRWUELSA-N (e)-n-dimethoxyphosphinothioyloxybenzenecarboximidoyl cyanide Chemical compound COP(=S)(OC)O\N=C(\C#N)C1=CC=CC=C1 QQVNWNVUGXNUJN-BENRWUELSA-N 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- YGLMVCVJLXREAK-MTVMDMGHSA-N 1,1-dimethyl-3-[(1S,2R,6R,7S,8R)-8-tricyclo[5.2.1.02,6]decanyl]urea Chemical compound C([C@H]12)CC[C@@H]1[C@@H]1C[C@@H](NC(=O)N(C)C)[C@H]2C1 YGLMVCVJLXREAK-MTVMDMGHSA-N 0.000 description 2
- JCIIKRHCWVHVFF-UHFFFAOYSA-N 1,2,4-thiadiazol-5-amine;hydrochloride Chemical compound Cl.NC1=NC=NS1 JCIIKRHCWVHVFF-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical class ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- MVHWKYHDYCGNQN-UHFFFAOYSA-N 1,5-dichloro-3-fluoro-2-(4-nitrophenoxy)benzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=C(F)C=C(Cl)C=C1Cl MVHWKYHDYCGNQN-UHFFFAOYSA-N 0.000 description 2
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 2
- VQHHIQJPQOLZGF-UHFFFAOYSA-N 1-(2-iodophenyl)sulfonyl-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)I)=N1 VQHHIQJPQOLZGF-UHFFFAOYSA-N 0.000 description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 2
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 2
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 2
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 2
- ULCWZQJLFZEXCS-UHFFFAOYSA-N 1-[[2-(2,4-dichlorophenyl)-5-(2,2,2-trifluoroethoxy)oxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1C(OCC(F)(F)F)CCC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-UHFFFAOYSA-N 0.000 description 2
- IBYHHJPAARCAIE-UHFFFAOYSA-N 1-bromo-2-chloroethane Chemical class ClCCBr IBYHHJPAARCAIE-UHFFFAOYSA-N 0.000 description 2
- KPNPDRFFWQBXGT-UHFFFAOYSA-N 1-dimethoxyphosphorylsulfanyl-2-ethylsulfanylethane;2-ethylsulfanylethoxy-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSCCOP(=S)(OC)OC.CCSCCSP(=O)(OC)OC KPNPDRFFWQBXGT-UHFFFAOYSA-N 0.000 description 2
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 2
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 2
- QZEKHJXYZSJVCL-UHFFFAOYSA-N 2,2,3-trichloropropanoic acid Chemical compound OC(=O)C(Cl)(Cl)CCl QZEKHJXYZSJVCL-UHFFFAOYSA-N 0.000 description 2
- KNGWEAQJZJKFLI-UHFFFAOYSA-N 2,2-dimethyl-4h-1,3-benzodioxine-6-carbaldehyde Chemical compound O=CC1=CC=C2OC(C)(C)OCC2=C1 KNGWEAQJZJKFLI-UHFFFAOYSA-N 0.000 description 2
- XTVIFVALDYTCLL-UHFFFAOYSA-N 2,3,5-trichloro-1h-pyridin-4-one Chemical compound ClC1=CNC(Cl)=C(Cl)C1=O XTVIFVALDYTCLL-UHFFFAOYSA-N 0.000 description 2
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 description 2
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 2
- UXPRZZZNGFVXRR-UHFFFAOYSA-N 2,3-difluoro-1h-pyrrole Chemical compound FC=1C=CNC=1F UXPRZZZNGFVXRR-UHFFFAOYSA-N 0.000 description 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 2
- PTWBGBDKDZWGCL-UHFFFAOYSA-N 2,4-dinitro-1-pentylsulfonylbenzene Chemical compound CCCCCS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O PTWBGBDKDZWGCL-UHFFFAOYSA-N 0.000 description 2
- JLPUISACQXFVRC-UHFFFAOYSA-N 2,5-dihydro-1,3-thiazole Chemical compound C1SCN=C1 JLPUISACQXFVRC-UHFFFAOYSA-N 0.000 description 2
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 2
- JTHMHWAHAKLCKT-UHFFFAOYSA-N 2,6-difluoro-n-[[4-(trifluoromethyl)phenyl]carbamoyl]benzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(C(F)(F)F)C=C1 JTHMHWAHAKLCKT-UHFFFAOYSA-N 0.000 description 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 2
- BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 0.000 description 2
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 description 2
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 2
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 2
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 2
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 description 2
- DSABESMCWFGGNQ-UHFFFAOYSA-N 2-(ethoxymethyl)-4,6-dinitrophenol Chemical compound CCOCC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O DSABESMCWFGGNQ-UHFFFAOYSA-N 0.000 description 2
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 description 2
- KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 description 2
- OTWBGXPTCSGQEJ-UHFFFAOYSA-N 2-[(dimethylcarbamothioyldisulfanyl)carbothioylamino]ethylcarbamothioylsulfanyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SSC(=S)NCCNC(=S)SSC(=S)N(C)C OTWBGXPTCSGQEJ-UHFFFAOYSA-N 0.000 description 2
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 description 2
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 description 2
- KQUYPOJCTWSLSE-UHFFFAOYSA-N 2-[4-[1-[2-(diethylamino)-2-oxoethyl]pyridin-1-ium-4-yl]pyridin-1-ium-1-yl]-n,n-diethylacetamide Chemical compound C1=C[N+](CC(=O)N(CC)CC)=CC=C1C1=CC=[N+](CC(=O)N(CC)CC)C=C1 KQUYPOJCTWSLSE-UHFFFAOYSA-N 0.000 description 2
- WDRGQGLIUAMOOC-UHFFFAOYSA-N 2-benzamidooxyacetic acid Chemical compound OC(=O)CONC(=O)C1=CC=CC=C1 WDRGQGLIUAMOOC-UHFFFAOYSA-N 0.000 description 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 description 2
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 description 2
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 description 2
- UDRNNGBAXFCBLJ-UHFFFAOYSA-N 2-chloro-n-(2,3-dimethylphenyl)-n-propan-2-ylacetamide Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC(C)=C1C UDRNNGBAXFCBLJ-UHFFFAOYSA-N 0.000 description 2
- KZNDFYDURHAESM-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(propan-2-yloxymethyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(COC(C)C)C(=O)CCl KZNDFYDURHAESM-UHFFFAOYSA-N 0.000 description 2
- NTHGWXIWFHGPLK-UHFFFAOYSA-N 2-dimethoxyphosphinothioylsulfanyl-1-morpholin-4-ylethanone Chemical compound COP(=S)(OC)SCC(=O)N1CCOCC1 NTHGWXIWFHGPLK-UHFFFAOYSA-N 0.000 description 2
- FCUBTKFQDYNIIC-UHFFFAOYSA-N 2-dimethoxyphosphinothioylsulfanyl-n-(methoxymethyl)acetamide Chemical compound COCNC(=O)CSP(=S)(OC)OC FCUBTKFQDYNIIC-UHFFFAOYSA-N 0.000 description 2
- ZVZQKNVMDKSGGF-UHFFFAOYSA-N 2-ethylsulfanylethoxy-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSCCOP(=S)(OC)OC ZVZQKNVMDKSGGF-UHFFFAOYSA-N 0.000 description 2
- AWSZRJQNBMEZOI-UHFFFAOYSA-N 2-methoxyethyl 2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-[2-(trifluoromethyl)phenyl]propanoate Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(C#N)(C(=O)OCCOC)C(=O)C1=CC=CC=C1C(F)(F)F AWSZRJQNBMEZOI-UHFFFAOYSA-N 0.000 description 2
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 2
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 2
- AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 description 2
- NKDFYOWSKOHCCO-YPVLXUMRSA-N 20-hydroxyecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@](C)(O)[C@H](O)CCC(C)(O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 NKDFYOWSKOHCCO-YPVLXUMRSA-N 0.000 description 2
- HXWZQRICWSADMH-SEHXZECUSA-N 20-hydroxyecdysone Natural products CC(C)(C)CC[C@@H](O)[C@@](C)(O)[C@H]1CC[C@@]2(O)C3=CC(=O)[C@@H]4C[C@@H](O)[C@@H](O)C[C@]4(C)[C@H]3CC[C@]12C HXWZQRICWSADMH-SEHXZECUSA-N 0.000 description 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 2
- QOBMKVRRANLSMZ-WJZAEVBBSA-N 3(1+2)-(3a,4,5,6,7,7a-hexahydro-4,7-methanoindanyl)-1,1-dimethylurea Chemical compound C1C[C@H]2C3C(NC(=O)N(C)C)CCC3[C@@H]1C2 QOBMKVRRANLSMZ-WJZAEVBBSA-N 0.000 description 2
- YRSSHOVRSMQULE-UHFFFAOYSA-N 3,5-dichloro-4-hydroxybenzonitrile Chemical compound OC1=C(Cl)C=C(C#N)C=C1Cl YRSSHOVRSMQULE-UHFFFAOYSA-N 0.000 description 2
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 description 2
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 2
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 description 2
- LQHMZSQJOYPNND-UHFFFAOYSA-N 3-(diethoxyphosphinothioylsulfanylmethyl)-5-propan-2-yloxy-1,3,4-thiadiazol-2-one Chemical compound CCOP(=S)(OCC)SCN1N=C(OC(C)C)SC1=O LQHMZSQJOYPNND-UHFFFAOYSA-N 0.000 description 2
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 description 2
- AMVYOVYGIJXTQB-UHFFFAOYSA-N 3-[4-(4-methoxyphenoxy)phenyl]-1,1-dimethylurea Chemical compound C1=CC(OC)=CC=C1OC1=CC=C(NC(=O)N(C)C)C=C1 AMVYOVYGIJXTQB-UHFFFAOYSA-N 0.000 description 2
- SOPHXJOERHTMIL-UHFFFAOYSA-N 3-methyl-4,6-dinitro-2-propan-2-ylphenol Chemical compound CC(C)C1=C(C)C([N+]([O-])=O)=CC([N+]([O-])=O)=C1O SOPHXJOERHTMIL-UHFFFAOYSA-N 0.000 description 2
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 description 2
- RBTXNWWNDUZLDU-UHFFFAOYSA-N 4-[1-[4-(trifluoromethoxy)phenyl]-1,2,4-triazol-3-yl]benzaldehyde Chemical compound C1=CC(OC(F)(F)F)=CC=C1N1N=C(C=2C=CC(C=O)=CC=2)N=C1 RBTXNWWNDUZLDU-UHFFFAOYSA-N 0.000 description 2
- ZOMKCDYJHAQMCU-UHFFFAOYSA-N 4-butyl-1,2,4-triazole Chemical compound CCCCN1C=NN=C1 ZOMKCDYJHAQMCU-UHFFFAOYSA-N 0.000 description 2
- RRCWSLBKLVBFQD-UHFFFAOYSA-N 4-chloro-1-(2-methylpropyl)imidazo[4,5-c]quinoline Chemical compound C1=CC=CC2=C3N(CC(C)C)C=NC3=C(Cl)N=C21 RRCWSLBKLVBFQD-UHFFFAOYSA-N 0.000 description 2
- NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 description 2
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 description 2
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 2
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 description 2
- QHXDTLYEHWXDSO-UHFFFAOYSA-N 6-chloro-2-n,2-n,4-n,4-n-tetraethyl-1,3,5-triazine-2,4-diamine Chemical compound CCN(CC)C1=NC(Cl)=NC(N(CC)CC)=N1 QHXDTLYEHWXDSO-UHFFFAOYSA-N 0.000 description 2
- OOHIAOSLOGDBCE-UHFFFAOYSA-N 6-chloro-4-n-cyclopropyl-2-n-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound CC(C)NC1=NC(Cl)=NC(NC2CC2)=N1 OOHIAOSLOGDBCE-UHFFFAOYSA-N 0.000 description 2
- MZTLOILRKLUURT-QPEQYQDCSA-N 6-tert-butyl-4-[(z)-2-methylpropylideneamino]-3-methylsulfanyl-1,2,4-triazin-5-one Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1\N=C/C(C)C MZTLOILRKLUURT-QPEQYQDCSA-N 0.000 description 2
- 239000005651 Acequinocyl Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000002890 Aclonifen Substances 0.000 description 2
- 241000254032 Acrididae Species 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- 241001014341 Acrosternum hilare Species 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 241001672675 Adoxophyes Species 0.000 description 2
- 241000256111 Aedes <genus> Species 0.000 description 2
- 241001136265 Agriotes Species 0.000 description 2
- 241000108079 Aleyrodes Species 0.000 description 2
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 description 2
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 description 2
- FBEHFRAORPEGFH-UHFFFAOYSA-N Allyxycarb Chemical compound CNC(=O)OC1=CC(C)=C(N(CC=C)CC=C)C(C)=C1 FBEHFRAORPEGFH-UHFFFAOYSA-N 0.000 description 2
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 2
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 description 2
- 241000256186 Anopheles <genus> Species 0.000 description 2
- 241001609695 Anoplophora glabripennis Species 0.000 description 2
- 241001435074 Anthomyia Species 0.000 description 2
- 241001414828 Aonidiella aurantii Species 0.000 description 2
- 241000273311 Aphis spiraecola Species 0.000 description 2
- 241000239223 Arachnida Species 0.000 description 2
- 241000238421 Arthropoda Species 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 241001174347 Atomaria Species 0.000 description 2
- 241000193388 Bacillus thuringiensis Species 0.000 description 2
- 241001124183 Bactrocera <genus> Species 0.000 description 2
- 241001124181 Bactrocera dorsalis Species 0.000 description 2
- 239000005470 Beflubutamid Substances 0.000 description 2
- 241000254123 Bemisia Species 0.000 description 2
- 241001302798 Bemisia argentifolii Species 0.000 description 2
- 241000254127 Bemisia tabaci Species 0.000 description 2
- 239000005471 Benfluralin Substances 0.000 description 2
- QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 description 2
- MQIVNMHALJNFMG-ILYHAJGMSA-N Benquinox Chemical compound O/N=C(\C=C1)/C=C/C\1=N\NC(C1=CC=CC=C1)=O MQIVNMHALJNFMG-ILYHAJGMSA-N 0.000 description 2
- RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 description 2
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 description 2
- DTCJYIIKPVRVDD-UHFFFAOYSA-N Benzthiazuron Chemical compound C1=CC=C2SC(NC(=O)NC)=NC2=C1 DTCJYIIKPVRVDD-UHFFFAOYSA-N 0.000 description 2
- 239000005653 Bifenazate Substances 0.000 description 2
- 239000005484 Bifenox Substances 0.000 description 2
- 241000238662 Blatta orientalis Species 0.000 description 2
- 241001629132 Blissus leucopterus Species 0.000 description 2
- 241000219198 Brassica Species 0.000 description 2
- 235000003351 Brassica cretica Nutrition 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 240000003259 Brassica oleracea var. botrytis Species 0.000 description 2
- 235000003343 Brassica rupestris Nutrition 0.000 description 2
- 241001444260 Brassicogethes aeneus Species 0.000 description 2
- 241000982105 Brevicoryne brassicae Species 0.000 description 2
- XTFNPKDYCLFGPV-OMCISZLKSA-N Bromofenoxim Chemical compound C1=C(Br)C(O)=C(Br)C=C1\C=N\OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-OMCISZLKSA-N 0.000 description 2
- NYQDCVLCJXRDSK-UHFFFAOYSA-N Bromofos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl NYQDCVLCJXRDSK-UHFFFAOYSA-N 0.000 description 2
- 239000005741 Bromuconazole Substances 0.000 description 2
- 235000004936 Bromus mango Nutrition 0.000 description 2
- 239000005742 Bupirimate Substances 0.000 description 2
- 239000005885 Buprofezin Substances 0.000 description 2
- SLZWBCGZQRRUNG-UHFFFAOYSA-N Butacarb Chemical compound CNC(=O)OC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1 SLZWBCGZQRRUNG-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- ZZVVDIVWGXTDRQ-BSYVCWPDSA-N Buthiobate Chemical compound C=1C=CN=CC=1\N=C(/SCCCC)SCC1=CC=C(C(C)(C)C)C=C1 ZZVVDIVWGXTDRQ-BSYVCWPDSA-N 0.000 description 2
- BKAQXYNWONVOAX-UHFFFAOYSA-N Butonate Chemical compound CCCC(=O)OC(C(Cl)(Cl)Cl)P(=O)(OC)OC BKAQXYNWONVOAX-UHFFFAOYSA-N 0.000 description 2
- ZOGDSYNXUXQGHF-XIEYBQDHSA-N Butroxydim Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(\C(CC)=N\OCC)=C(O)C2)=C1C ZOGDSYNXUXQGHF-XIEYBQDHSA-N 0.000 description 2
- BYYMILHAKOURNM-UHFFFAOYSA-N Buturon Chemical compound C#CC(C)N(C)C(=O)NC1=CC=C(Cl)C=C1 BYYMILHAKOURNM-UHFFFAOYSA-N 0.000 description 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RMBBSOLAGVEUSI-UHFFFAOYSA-H Calcium arsenate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-][As]([O-])([O-])=O.[O-][As]([O-])([O-])=O RMBBSOLAGVEUSI-UHFFFAOYSA-H 0.000 description 2
- 241000907862 Callosobruchus maculatus Species 0.000 description 2
- 239000005745 Captan Substances 0.000 description 2
- MPKTWNYCNKUVKZ-UHFFFAOYSA-N Carbamorph Chemical compound CN(C)C(=S)SCN1CCOCC1 MPKTWNYCNKUVKZ-UHFFFAOYSA-N 0.000 description 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
- 239000005490 Carbetamide Substances 0.000 description 2
- VEDTXTNSFWUXGQ-UHFFFAOYSA-N Carbophenothion Chemical compound CCOP(=S)(OCC)SCSC1=CC=C(Cl)C=C1 VEDTXTNSFWUXGQ-UHFFFAOYSA-N 0.000 description 2
- 239000005746 Carboxin Substances 0.000 description 2
- 241001450756 Ceroplastes rubens Species 0.000 description 2
- 241001124145 Cerotoma Species 0.000 description 2
- 241000604356 Chamaepsila rosae Species 0.000 description 2
- DXXVCXKMSWHGTF-UHFFFAOYSA-N Chlomethoxyfen Chemical compound C1=C([N+]([O-])=O)C(OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 DXXVCXKMSWHGTF-UHFFFAOYSA-N 0.000 description 2
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 2
- VCBRBUKGTWLJOB-UHFFFAOYSA-N Chloranocryl Chemical compound CC(=C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 VCBRBUKGTWLJOB-UHFFFAOYSA-N 0.000 description 2
- 239000005886 Chlorantraniliprole Substances 0.000 description 2
- ULBXWWGWDPVHAO-UHFFFAOYSA-N Chlorbufam Chemical compound C#CC(C)OC(=O)NC1=CC=CC(Cl)=C1 ULBXWWGWDPVHAO-UHFFFAOYSA-N 0.000 description 2
- URYAFVKLYSEINW-UHFFFAOYSA-N Chlorfenethol Chemical compound C=1C=C(Cl)C=CC=1C(O)(C)C1=CC=C(Cl)C=C1 URYAFVKLYSEINW-UHFFFAOYSA-N 0.000 description 2
- 239000005493 Chloridazon (aka pyrazone) Substances 0.000 description 2
- ZHLKXBJTJHRTTE-UHFFFAOYSA-N Chlorobenside Chemical compound C1=CC(Cl)=CC=C1CSC1=CC=C(Cl)C=C1 ZHLKXBJTJHRTTE-UHFFFAOYSA-N 0.000 description 2
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 description 2
- GQKRUMZWUHSLJF-NTCAYCPXSA-N Chlorphoxim Chemical compound CCOP(=S)(OCC)O\N=C(/C#N)C1=CC=CC=C1Cl GQKRUMZWUHSLJF-NTCAYCPXSA-N 0.000 description 2
- 239000005647 Chlorpropham Substances 0.000 description 2
- 241001124179 Chrysops Species 0.000 description 2
- 241001635683 Cimex hemipterus Species 0.000 description 2
- 241001327638 Cimex lectularius Species 0.000 description 2
- WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 description 2
- 241001498622 Cixius wagneri Species 0.000 description 2
- 239000005497 Clethodim Substances 0.000 description 2
- PITWUHDDNUVBPT-UHFFFAOYSA-N Cloethocarb Chemical compound CNC(=O)OC1=CC=CC=C1OC(CCl)OC PITWUHDDNUVBPT-UHFFFAOYSA-N 0.000 description 2
- 239000005654 Clofentezine Substances 0.000 description 2
- 239000005499 Clomazone Substances 0.000 description 2
- 239000005500 Clopyralid Substances 0.000 description 2
- 239000005888 Clothianidin Substances 0.000 description 2
- 241000683561 Conoderus Species 0.000 description 2
- 241001509964 Coptotermes Species 0.000 description 2
- 241001509962 Coptotermes formosanus Species 0.000 description 2
- 241001340508 Crambus Species 0.000 description 2
- DNPSYFHJYIRREW-UHFFFAOYSA-N Credazine Chemical compound CC1=CC=CC=C1OC1=CC=CN=N1 DNPSYFHJYIRREW-UHFFFAOYSA-N 0.000 description 2
- XXXSILNSXNPGKG-ZHACJKMWSA-N Crotoxyphos Chemical compound COP(=O)(OC)O\C(C)=C\C(=O)OC(C)C1=CC=CC=C1 XXXSILNSXNPGKG-ZHACJKMWSA-N 0.000 description 2
- 241000592377 Cryptolestes ferrugineus Species 0.000 description 2
- 235000009847 Cucumis melo var cantalupensis Nutrition 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
- 241000256054 Culex <genus> Species 0.000 description 2
- VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 description 2
- 241000721021 Curculio Species 0.000 description 2
- 241000254171 Curculionidae Species 0.000 description 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 2
- LRNJHZNPJSPMGK-UHFFFAOYSA-N Cyanofenphos Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C(C#N)C=C1 LRNJHZNPJSPMGK-UHFFFAOYSA-N 0.000 description 2
- TWDJIKFUVRYBJF-UHFFFAOYSA-N Cyanthoate Chemical compound CCOP(=O)(OCC)SCC(=O)NC(C)(C)C#N TWDJIKFUVRYBJF-UHFFFAOYSA-N 0.000 description 2
- 239000005754 Cyazofamid Substances 0.000 description 2
- DFCAFRGABIXSDS-UHFFFAOYSA-N Cycloate Chemical compound CCSC(=O)N(CC)C1CCCCC1 DFCAFRGABIXSDS-UHFFFAOYSA-N 0.000 description 2
- 239000005501 Cycloxydim Substances 0.000 description 2
- 241001135545 Cydia pomonella granulovirus Species 0.000 description 2
- 239000005655 Cyflumetofen Substances 0.000 description 2
- MKZGVGOBXZJKGV-UHFFFAOYSA-N Cypendazole Chemical compound C1=CC=C2N(C(=O)NCCCCCC#N)C(NC(=O)OC)=NC2=C1 MKZGVGOBXZJKGV-UHFFFAOYSA-N 0.000 description 2
- 239000005946 Cypermethrin Substances 0.000 description 2
- 239000005758 Cyprodinil Substances 0.000 description 2
- PLQDLOBGKJCDSZ-UHFFFAOYSA-N Cypromid Chemical compound C1=C(Cl)C(Cl)=CC=C1NC(=O)C1CC1 PLQDLOBGKJCDSZ-UHFFFAOYSA-N 0.000 description 2
- 239000005891 Cyromazine Substances 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 description 2
- 241000969022 Dasineura Species 0.000 description 2
- 241001414890 Delia Species 0.000 description 2
- 241001609607 Delia platura Species 0.000 description 2
- IATBEFPCSHFQJS-UHFFFAOYSA-N Demephion-O Chemical compound COP(=S)(OC)OCCSC IATBEFPCSHFQJS-UHFFFAOYSA-N 0.000 description 2
- PSTWJANBJOHFQJ-UHFFFAOYSA-N Demephion-S Chemical compound COP(=O)(OC)SCCSC PSTWJANBJOHFQJ-UHFFFAOYSA-N 0.000 description 2
- DGLIBALSRMUQDD-UHFFFAOYSA-N Demeton-O Chemical compound CCOP(=S)(OCC)OCCSCC DGLIBALSRMUQDD-UHFFFAOYSA-N 0.000 description 2
- GRPRVIYRYGLIJU-UHFFFAOYSA-N Demeton-S Chemical compound CCOP(=O)(OCC)SCCSCC GRPRVIYRYGLIJU-UHFFFAOYSA-N 0.000 description 2
- 241001641896 Dermestes lardarius Species 0.000 description 2
- 241001513837 Dermestes maculatus Species 0.000 description 2
- 239000005503 Desmedipham Substances 0.000 description 2
- HCRWJJJUKUVORR-UHFFFAOYSA-N Desmetryn Chemical compound CNC1=NC(NC(C)C)=NC(SC)=N1 HCRWJJJUKUVORR-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- MUMQYXACQUZOFP-UHFFFAOYSA-N Dialifor Chemical compound C1=CC=C2C(=O)N(C(CCl)SP(=S)(OCC)OCC)C(=O)C2=C1 MUMQYXACQUZOFP-UHFFFAOYSA-N 0.000 description 2
- SPANOECCGNXGNR-UITAMQMPSA-N Diallat Chemical compound CC(C)N(C(C)C)C(=O)SC\C(Cl)=C\Cl SPANOECCGNXGNR-UITAMQMPSA-N 0.000 description 2
- 241000832201 Diaphania Species 0.000 description 2
- WGOWCPGHOCIHBW-UHFFFAOYSA-N Dichlofenthion Chemical compound CCOP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl WGOWCPGHOCIHBW-UHFFFAOYSA-N 0.000 description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
- JDZSMXLTQNHBRF-UHFFFAOYSA-N Dichlozoline Chemical compound O=C1C(C)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 JDZSMXLTQNHBRF-UHFFFAOYSA-N 0.000 description 2
- LWLJUMBEZJHXHV-UHFFFAOYSA-N Dienochlor Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C1(Cl)C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LWLJUMBEZJHXHV-UHFFFAOYSA-N 0.000 description 2
- 239000005760 Difenoconazole Substances 0.000 description 2
- 239000005507 Diflufenican Substances 0.000 description 2
- IIUZTXTZRGLYTI-UHFFFAOYSA-N Dihydrogriseofulvin Natural products COC1CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 IIUZTXTZRGLYTI-UHFFFAOYSA-N 0.000 description 2
- PGJBQBDNXAZHBP-UHFFFAOYSA-N Dimefox Chemical compound CN(C)P(F)(=O)N(C)C PGJBQBDNXAZHBP-UHFFFAOYSA-N 0.000 description 2
- 239000005761 Dimethomorph Substances 0.000 description 2
- 239000005762 Dimoxystrobin Substances 0.000 description 2
- QJYHUJAGJUHXJN-UHFFFAOYSA-N Dinex Chemical compound C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1C1CCCCC1 QJYHUJAGJUHXJN-UHFFFAOYSA-N 0.000 description 2
- OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 description 2
- ODOSVAWLEGXOPB-UHFFFAOYSA-N Dinocton 6 Chemical compound COC(=O)OC1=C(CCCCCC(C)C)C=C([N+]([O-])=O)C=C1[N+]([O-])=O ODOSVAWLEGXOPB-UHFFFAOYSA-N 0.000 description 2
- RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 description 2
- VBKKVDGJXVOLNE-UHFFFAOYSA-N Dioxation Chemical compound CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC VBKKVDGJXVOLNE-UHFFFAOYSA-N 0.000 description 2
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 description 2
- 241000511318 Diprion Species 0.000 description 2
- NPWMZOGDXOFZIN-UHFFFAOYSA-N Dipropetryn Chemical compound CCSC1=NC(NC(C)C)=NC(NC(C)C)=N1 NPWMZOGDXOFZIN-UHFFFAOYSA-N 0.000 description 2
- MTBZIGHNGSTDJV-UHFFFAOYSA-N Ditalimfos Chemical compound C1=CC=C2C(=O)N(P(=S)(OCC)OCC)C(=O)C2=C1 MTBZIGHNGSTDJV-UHFFFAOYSA-N 0.000 description 2
- 239000005764 Dithianon Substances 0.000 description 2
- YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 description 2
- 239000005510 Diuron Substances 0.000 description 2
- 239000005765 Dodemorph Substances 0.000 description 2
- 239000005766 Dodine Substances 0.000 description 2
- OOTHTARUZHONSW-LCYFTJDESA-N Drazoxolon Chemical compound CC1=NOC(=O)\C1=N/NC1=CC=CC=C1Cl OOTHTARUZHONSW-LCYFTJDESA-N 0.000 description 2
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 2
- 241000241133 Earias Species 0.000 description 2
- DCEFCUHVANGEOE-UHFFFAOYSA-N Ecdysterone Natural products CC(CC(C)(C)O)C(O)C(C)(O)C1CCC2(O)C3=CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C DCEFCUHVANGEOE-UHFFFAOYSA-N 0.000 description 2
- YCAGGFXSFQFVQL-UHFFFAOYSA-N Endothion Chemical compound COC1=COC(CSP(=O)(OC)OC)=CC1=O YCAGGFXSFQFVQL-UHFFFAOYSA-N 0.000 description 2
- 239000005767 Epoxiconazole Substances 0.000 description 2
- KMHZPJNVPCAUMN-UHFFFAOYSA-N Erbon Chemical compound CC(Cl)(Cl)C(=O)OCCOC1=CC(Cl)=C(Cl)C=C1Cl KMHZPJNVPCAUMN-UHFFFAOYSA-N 0.000 description 2
- 241000510928 Erysiphe necator Species 0.000 description 2
- 239000005895 Esfenvalerate Substances 0.000 description 2
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 description 2
- WARIWGPBHKPYON-UHFFFAOYSA-N Ethiolate Chemical compound CCSC(=O)N(CC)CC WARIWGPBHKPYON-UHFFFAOYSA-N 0.000 description 2
- 239000004258 Ethoxyquin Substances 0.000 description 2
- UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- FGIWFCGDPUIBEZ-UHFFFAOYSA-N Etrimfos Chemical compound CCOC1=CC(OP(=S)(OC)OC)=NC(CC)=N1 FGIWFCGDPUIBEZ-UHFFFAOYSA-N 0.000 description 2
- RIBGOMBPPVSIHP-UHFFFAOYSA-N FNC1=C(C=CC=C1)C(C)C Chemical compound FNC1=C(C=CC=C1)C(C)C RIBGOMBPPVSIHP-UHFFFAOYSA-N 0.000 description 2
- 239000005772 Famoxadone Substances 0.000 description 2
- 241000371383 Fannia Species 0.000 description 2
- 239000005774 Fenamidone Substances 0.000 description 2
- IWDQPCIQCXRBQP-UHFFFAOYSA-M Fenaminosulf Chemical compound [Na+].CN(C)C1=CC=C(N=NS([O-])(=O)=O)C=C1 IWDQPCIQCXRBQP-UHFFFAOYSA-M 0.000 description 2
- OQOULEWDDRNBSG-UHFFFAOYSA-N Fenapanil Chemical compound C=1C=CC=CC=1C(CCCC)(C#N)CN1C=CN=C1 OQOULEWDDRNBSG-UHFFFAOYSA-N 0.000 description 2
- ISVQSVPUDBVFFU-UHFFFAOYSA-N Fenazaflor Chemical compound FC(F)(F)C1=NC2=CC(Cl)=C(Cl)C=C2N1C(=O)OC1=CC=CC=C1 ISVQSVPUDBVFFU-UHFFFAOYSA-N 0.000 description 2
- 239000005656 Fenazaquin Substances 0.000 description 2
- 239000005776 Fenhexamid Substances 0.000 description 2
- HMIBKHHNXANVHR-UHFFFAOYSA-N Fenothiocarb Chemical compound CN(C)C(=O)SCCCCOC1=CC=CC=C1 HMIBKHHNXANVHR-UHFFFAOYSA-N 0.000 description 2
- 239000005777 Fenpropidin Substances 0.000 description 2
- 239000005657 Fenpyroximate Substances 0.000 description 2
- SPJOZZSIXXJYBT-UHFFFAOYSA-N Fenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=CC=C1 SPJOZZSIXXJYBT-UHFFFAOYSA-N 0.000 description 2
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 2
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 description 2
- 239000005514 Flazasulfuron Substances 0.000 description 2
- HWATZEJQIXKWQS-UHFFFAOYSA-N Flazasulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(F)(F)F)=N1 HWATZEJQIXKWQS-UHFFFAOYSA-N 0.000 description 2
- 239000005900 Flonicamid Substances 0.000 description 2
- 239000005529 Florasulam Substances 0.000 description 2
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 description 2
- 239000005780 Fluazinam Substances 0.000 description 2
- 239000005901 Flubendiamide Substances 0.000 description 2
- FICWGWVVIRLNRB-UHFFFAOYSA-N Flucetosulfuron Chemical compound COCC(=O)OC(C(C)F)C1=NC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 FICWGWVVIRLNRB-UHFFFAOYSA-N 0.000 description 2
- 239000005781 Fludioxonil Substances 0.000 description 2
- XAERLJMOUYEBAB-UHFFFAOYSA-N Fluenetil Chemical group C1=CC(CC(=O)OCCF)=CC=C1C1=CC=CC=C1 XAERLJMOUYEBAB-UHFFFAOYSA-N 0.000 description 2
- 239000005531 Flufenacet Substances 0.000 description 2
- RXCPQSJAVKGONC-UHFFFAOYSA-N Flumetsulam Chemical compound N1=C2N=C(C)C=CN2N=C1S(=O)(=O)NC1=C(F)C=CC=C1F RXCPQSJAVKGONC-UHFFFAOYSA-N 0.000 description 2
- 239000005533 Fluometuron Substances 0.000 description 2
- 239000005782 Fluopicolide Substances 0.000 description 2
- HHMCAJWVGYGUEF-UHFFFAOYSA-N Fluorodifen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O HHMCAJWVGYGUEF-UHFFFAOYSA-N 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- LXMQMMSGERCRSU-UHFFFAOYSA-N Fluotrimazole Chemical compound FC(F)(F)C1=CC=CC(C(C=2C=CC=CC=2)(C=2C=CC=CC=2)N2N=CN=C2)=C1 LXMQMMSGERCRSU-UHFFFAOYSA-N 0.000 description 2
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 description 2
- PXRROZVNOOEPPZ-UHFFFAOYSA-N Flupropanate Chemical compound OC(=O)C(F)(F)C(F)F PXRROZVNOOEPPZ-UHFFFAOYSA-N 0.000 description 2
- 239000005558 Fluroxypyr Substances 0.000 description 2
- 239000005559 Flurtamone Substances 0.000 description 2
- 239000005786 Flutolanil Substances 0.000 description 2
- 239000005787 Flutriafol Substances 0.000 description 2
- 239000005789 Folpet Substances 0.000 description 2
- 239000005560 Foramsulfuron Substances 0.000 description 2
- MVBGKYGTNGPFHT-UHFFFAOYSA-N Fosmethilan Chemical compound COP(=S)(OC)SCN(C(=O)CCC)C1=CC=CC=C1Cl MVBGKYGTNGPFHT-UHFFFAOYSA-N 0.000 description 2
- RHJOIOVESMTJEK-UHFFFAOYSA-N Fosthietan Chemical compound CCOP(=O)(OCC)N=C1SCS1 RHJOIOVESMTJEK-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- ULCWZQJLFZEXCS-KGLIPLIRSA-N Furconazole-cis Chemical compound O1[C@@H](OCC(F)(F)F)CC[C@@]1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-KGLIPLIRSA-N 0.000 description 2
- 239000005903 Gamma-cyhalothrin Substances 0.000 description 2
- 241001660201 Gasterophilus intestinalis Species 0.000 description 2
- 244000299507 Gossypium hirsutum Species 0.000 description 2
- 241000578422 Graphosoma lineatum Species 0.000 description 2
- UXWOXTQWVMFRSE-UHFFFAOYSA-N Griseoviridin Natural products O=C1OC(C)CC=C(C(NCC=CC=CC(O)CC(O)C2)=O)SCC1NC(=O)C1=COC2=N1 UXWOXTQWVMFRSE-UHFFFAOYSA-N 0.000 description 2
- 241000257232 Haematobia irritans Species 0.000 description 2
- 241000790933 Haematopinus Species 0.000 description 2
- 241000670091 Haematopinus suis Species 0.000 description 2
- YDNLKBDXQCHOTH-UHFFFAOYSA-N Halacrinate Chemical compound C1=CC=C2C(Cl)=CC(Br)=C(OC(=O)C=C)C2=N1 YDNLKBDXQCHOTH-UHFFFAOYSA-N 0.000 description 2
- 241000258937 Hemiptera Species 0.000 description 2
- RWNKSTSCBHKHTB-UHFFFAOYSA-N Hexachloro-1,3-butadiene Chemical compound ClC(Cl)=C(Cl)C(Cl)=C(Cl)Cl RWNKSTSCBHKHTB-UHFFFAOYSA-N 0.000 description 2
- DOJXGHGHTWFZHK-UHFFFAOYSA-N Hexachloroacetone Chemical compound ClC(Cl)(Cl)C(=O)C(Cl)(Cl)Cl DOJXGHGHTWFZHK-UHFFFAOYSA-N 0.000 description 2
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 description 2
- 239000005661 Hexythiazox Substances 0.000 description 2
- 241000322682 Hoplopleura Species 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 241000577496 Hypothenemus hampei Species 0.000 description 2
- 239000005566 Imazamox Substances 0.000 description 2
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 description 2
- 239000005906 Imidacloprid Substances 0.000 description 2
- 239000005907 Indoxacarb Substances 0.000 description 2
- 241000500891 Insecta Species 0.000 description 2
- LFVLUOAHQIVABZ-UHFFFAOYSA-N Iodofenphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(I)C=C1Cl LFVLUOAHQIVABZ-UHFFFAOYSA-N 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- 244000017020 Ipomoea batatas Species 0.000 description 2
- 235000002678 Ipomoea batatas Nutrition 0.000 description 2
- 239000005867 Iprodione Substances 0.000 description 2
- 239000005797 Iprovalicarb Substances 0.000 description 2
- LRWHHSXTGZSMSN-UHFFFAOYSA-N Isobenzan Chemical compound ClC1=C(Cl)C2(Cl)C3C(Cl)OC(Cl)C3C1(Cl)C2(Cl)Cl LRWHHSXTGZSMSN-UHFFFAOYSA-N 0.000 description 2
- PSYBGEADHLUXCS-UHFFFAOYSA-N Isocil Chemical compound CC(C)N1C(=O)NC(C)=C(Br)C1=O PSYBGEADHLUXCS-UHFFFAOYSA-N 0.000 description 2
- QBYJBZPUGVGKQQ-KCHUEWMZSA-N Isodrin Chemical compound C1[C@H]2C=C[C@H]1[C@H]1[C@](C3(Cl)Cl)(Cl)C(Cl)=C(Cl)[C@@]3(Cl)[C@H]12 QBYJBZPUGVGKQQ-KCHUEWMZSA-N 0.000 description 2
- NEKOXWSIMFDGMA-UHFFFAOYSA-N Isopropalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(C)C)C=C1[N+]([O-])=O NEKOXWSIMFDGMA-UHFFFAOYSA-N 0.000 description 2
- 239000005799 Isopyrazam Substances 0.000 description 2
- JLLJHQLUZAKJFH-UHFFFAOYSA-N Isouron Chemical compound CN(C)C(=O)NC=1C=C(C(C)(C)C)ON=1 JLLJHQLUZAKJFH-UHFFFAOYSA-N 0.000 description 2
- NZKIRHFOLVYKFT-UHFFFAOYSA-N Jasmolin I Natural products C1C(=O)C(CC=CCC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C NZKIRHFOLVYKFT-UHFFFAOYSA-N 0.000 description 2
- CPVQJXZBSGXTGJ-UHFFFAOYSA-N Juvenile hormone II Natural products CCC1(C)OC1CCC(C)=CCCC(C)=CC(=O)OC CPVQJXZBSGXTGJ-UHFFFAOYSA-N 0.000 description 2
- UQVYUTAMNICZNI-UHFFFAOYSA-N Karbutilate Chemical compound CN(C)C(=O)NC1=CC=CC(NC(=O)OC(C)(C)C)=C1 UQVYUTAMNICZNI-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 description 2
- 241001177117 Lasioderma serricorne Species 0.000 description 2
- 239000005572 Lenacil Substances 0.000 description 2
- 241000669027 Lepidosaphes Species 0.000 description 2
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 2
- 241000661348 Leptocorisa acuta Species 0.000 description 2
- 241001646976 Linepithema humile Species 0.000 description 2
- 241001113970 Linognathus Species 0.000 description 2
- 239000005573 Linuron Substances 0.000 description 2
- 241000403259 Liogenys Species 0.000 description 2
- 241000594036 Liriomyza Species 0.000 description 2
- 241000966204 Lissorhoptrus oryzophilus Species 0.000 description 2
- 229920000161 Locust bean gum Polymers 0.000 description 2
- FPMIAGPUNXEUCZ-UHFFFAOYSA-N Lythidathion Chemical compound CCOC1=NN(CSP(=S)(OC)OC)C(=O)S1 FPMIAGPUNXEUCZ-UHFFFAOYSA-N 0.000 description 2
- 241000623906 Lytta vesicatoria Species 0.000 description 2
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 description 2
- 241000721715 Macrosiphum Species 0.000 description 2
- 241000180172 Macrosiphum rosae Species 0.000 description 2
- 241000203984 Macrotermes Species 0.000 description 2
- 241001598997 Maecolaspis Species 0.000 description 2
- 239000005949 Malathion Substances 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 239000005802 Mancozeb Substances 0.000 description 2
- 239000005804 Mandipropamid Substances 0.000 description 2
- 235000014826 Mangifera indica Nutrition 0.000 description 2
- 240000007228 Mangifera indica Species 0.000 description 2
- PUTUPQVEMBRCAG-UHFFFAOYSA-N Mecarphon Chemical compound COC(=O)N(C)C(=O)CSP(C)(=S)OC PUTUPQVEMBRCAG-UHFFFAOYSA-N 0.000 description 2
- 240000004658 Medicago sativa Species 0.000 description 2
- OKIBNKKYNPBDRS-UHFFFAOYSA-N Mefluidide Chemical compound CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C OKIBNKKYNPBDRS-UHFFFAOYSA-N 0.000 description 2
- SUYHYHLFUHHVJQ-UHFFFAOYSA-N Menazon Chemical compound COP(=S)(OC)SCC1=NC(N)=NC(N)=N1 SUYHYHLFUHHVJQ-UHFFFAOYSA-N 0.000 description 2
- LTQSAUHRSCMPLD-CMDGGOBGSA-N Mephosfolan Chemical compound CCOP(=O)(OCC)\N=C1/SCC(C)S1 LTQSAUHRSCMPLD-CMDGGOBGSA-N 0.000 description 2
- 239000005577 Mesosulfuron Substances 0.000 description 2
- 239000005578 Mesotrione Substances 0.000 description 2
- 239000005914 Metaflumizone Substances 0.000 description 2
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 description 2
- 239000005807 Metalaxyl Substances 0.000 description 2
- 239000005808 Metalaxyl-M Substances 0.000 description 2
- 239000005579 Metamitron Substances 0.000 description 2
- 239000005868 Metconazole Substances 0.000 description 2
- RRVIAQKBTUQODI-UHFFFAOYSA-N Methabenzthiazuron Chemical compound C1=CC=C2SC(N(C)C(=O)NC)=NC2=C1 RRVIAQKBTUQODI-UHFFFAOYSA-N 0.000 description 2
- NTAHCMPOMKHKEU-AATRIKPKSA-N Methacrifos Chemical compound COC(=O)C(\C)=C\OP(=S)(OC)OC NTAHCMPOMKHKEU-AATRIKPKSA-N 0.000 description 2
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 2
- LRUUNMYPIBZBQH-UHFFFAOYSA-N Methazole Chemical compound O=C1N(C)C(=O)ON1C1=CC=C(Cl)C(Cl)=C1 LRUUNMYPIBZBQH-UHFFFAOYSA-N 0.000 description 2
- 239000005951 Methiocarb Substances 0.000 description 2
- MMCJEAKINANSOL-UHFFFAOYSA-N Methiuron Chemical compound CN(C)C(=S)NC1=CC=CC(C)=C1 MMCJEAKINANSOL-UHFFFAOYSA-N 0.000 description 2
- DDUIUBPJPOKOMV-UHFFFAOYSA-N Methoprotryne Chemical compound COCCCNC1=NC(NC(C)C)=NC(SC)=N1 DDUIUBPJPOKOMV-UHFFFAOYSA-N 0.000 description 2
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical group CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 239000005810 Metrafenone Substances 0.000 description 2
- 239000005583 Metribuzin Substances 0.000 description 2
- YNEVBPNZHBAYOA-UHFFFAOYSA-N Mexacarbate Chemical compound CNC(=O)OC1=CC(C)=C(N(C)C)C(C)=C1 YNEVBPNZHBAYOA-UHFFFAOYSA-N 0.000 description 2
- UOSHUBFBCPGQAY-UHFFFAOYSA-N Mipafox Chemical compound CC(C)NP(F)(=O)NC(C)C UOSHUBFBCPGQAY-UHFFFAOYSA-N 0.000 description 2
- KXGYBSNVFXBPNO-UHFFFAOYSA-N Monalide Chemical compound CCCC(C)(C)C(=O)NC1=CC=C(Cl)C=C1 KXGYBSNVFXBPNO-UHFFFAOYSA-N 0.000 description 2
- LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 2
- 241000555285 Monomorium Species 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 241000238745 Musca autumnalis Species 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- FTCOKXNKPOUEFH-UHFFFAOYSA-N Myclozolin Chemical compound O=C1C(COC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FTCOKXNKPOUEFH-UHFFFAOYSA-N 0.000 description 2
- WXZVAROIGSFCFJ-UHFFFAOYSA-N N,N-diethyl-2-(naphthalen-1-yloxy)propanamide Chemical compound C1=CC=C2C(OC(C)C(=O)N(CC)CC)=CC=CC2=C1 WXZVAROIGSFCFJ-UHFFFAOYSA-N 0.000 description 2
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 description 2
- ZJMZZNVGNSWOOM-UHFFFAOYSA-N N-(butan-2-yl)-N'-ethyl-6-methoxy-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NC(C)CC)=NC(OC)=N1 ZJMZZNVGNSWOOM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IUFUITYPUYMIHI-UHFFFAOYSA-N N-[1-(3,5-dimethylphenoxy)propan-2-yl]-6-(2-fluoropropan-2-yl)-1,3,5-triazine-2,4-diamine Chemical compound N=1C(N)=NC(C(C)(C)F)=NC=1NC(C)COC1=CC(C)=CC(C)=C1 IUFUITYPUYMIHI-UHFFFAOYSA-N 0.000 description 2
- FFQPZWRNXKPNPX-UHFFFAOYSA-N N-benzyl-2-[4-fluoro-3-(trifluoromethyl)phenoxy]butanamide Chemical compound C=1C=CC=CC=1CNC(=O)C(CC)OC1=CC=C(F)C(C(F)(F)F)=C1 FFQPZWRNXKPNPX-UHFFFAOYSA-N 0.000 description 2
- JMPFSEBWVLAJKM-UHFFFAOYSA-N N-{5-chloro-4-[(4-chlorophenyl)(cyano)methyl]-2-methylphenyl}-2-hydroxy-3,5-diiodobenzamide Chemical compound ClC=1C=C(NC(=O)C=2C(=C(I)C=C(I)C=2)O)C(C)=CC=1C(C#N)C1=CC=C(Cl)C=C1 JMPFSEBWVLAJKM-UHFFFAOYSA-N 0.000 description 2
- LVKTWOXHRYGDMM-UHFFFAOYSA-N Naproanilide Chemical compound C=1C=C2C=CC=CC2=CC=1OC(C)C(=O)NC1=CC=CC=C1 LVKTWOXHRYGDMM-UHFFFAOYSA-N 0.000 description 2
- 239000005585 Napropamide Substances 0.000 description 2
- CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 description 2
- DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 description 2
- 241000406465 Neodiprion Species 0.000 description 2
- 241000359016 Nephotettix Species 0.000 description 2
- 241000615716 Nephotettix nigropictus Species 0.000 description 2
- 239000005586 Nicosulfuron Substances 0.000 description 2
- 229930184499 Nikkomycin Natural products 0.000 description 2
- 241001556089 Nilaparvata lugens Species 0.000 description 2
- UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 description 2
- 241001585712 Noctua Species 0.000 description 2
- 241000256259 Noctuidae Species 0.000 description 2
- AJOYWWOYZZEDNE-UHFFFAOYSA-N O-(4-chlorobutyl) carbamothioate Chemical compound C(N)(OCCCCCl)=S AJOYWWOYZZEDNE-UHFFFAOYSA-N 0.000 description 2
- 241000238814 Orthoptera Species 0.000 description 2
- 239000005587 Oryzalin Substances 0.000 description 2
- 241001570894 Oulema oryzae Species 0.000 description 2
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 2
- JAYZFNIOOYPIAH-UHFFFAOYSA-N Oxydeprofos Chemical compound CCS(=O)CC(C)SP(=O)(OC)OC JAYZFNIOOYPIAH-UHFFFAOYSA-N 0.000 description 2
- 239000005590 Oxyfluorfen Substances 0.000 description 2
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 description 2
- SGEJQUSYQTVSIU-UHFFFAOYSA-N Pebulate Chemical compound CCCCN(CC)C(=O)SCCC SGEJQUSYQTVSIU-UHFFFAOYSA-N 0.000 description 2
- 241000517307 Pediculus humanus Species 0.000 description 2
- 241000517306 Pediculus humanus corporis Species 0.000 description 2
- 239000005813 Penconazole Substances 0.000 description 2
- 239000005814 Pencycuron Substances 0.000 description 2
- 239000005591 Pendimethalin Substances 0.000 description 2
- WGVWLKXZBUVUAM-UHFFFAOYSA-N Pentanochlor Chemical compound CCCC(C)C(=O)NC1=CC=C(C)C(Cl)=C1 WGVWLKXZBUVUAM-UHFFFAOYSA-N 0.000 description 2
- WHTBVLXUSXVMEV-UHFFFAOYSA-N Perfluidone Chemical compound C1=C(NS(=O)(=O)C(F)(F)F)C(C)=CC(S(=O)(=O)C=2C=CC=CC=2)=C1 WHTBVLXUSXVMEV-UHFFFAOYSA-N 0.000 description 2
- 241000238675 Periplaneta americana Species 0.000 description 2
- 241001510004 Periplaneta australasiae Species 0.000 description 2
- 241001510001 Periplaneta brunnea Species 0.000 description 2
- 239000005593 Pethoxamid Substances 0.000 description 2
- PWEOEHNGYFXZLI-UHFFFAOYSA-N Phenisopham Chemical compound C=1C=CC=CC=1N(CC)C(=O)OC1=CC=CC(NC(=O)OC(C)C)=C1 PWEOEHNGYFXZLI-UHFFFAOYSA-N 0.000 description 2
- GGNLTHFTYNDYNK-UHFFFAOYSA-N Phenkapton Chemical compound CCOP(=S)(OCC)SCSC1=CC(Cl)=CC=C1Cl GGNLTHFTYNDYNK-UHFFFAOYSA-N 0.000 description 2
- 239000005594 Phenmedipham Substances 0.000 description 2
- QQXXYTVEGCOZRF-UHFFFAOYSA-N Phenobenzuron Chemical compound C=1C=C(Cl)C(Cl)=CC=1N(C(=O)N(C)C)C(=O)C1=CC=CC=C1 QQXXYTVEGCOZRF-UHFFFAOYSA-N 0.000 description 2
- HEMINMLPKZELPP-UHFFFAOYSA-N Phosdiphen Chemical compound C=1C=C(Cl)C=C(Cl)C=1OP(=O)(OCC)OC1=CC=C(Cl)C=C1Cl HEMINMLPKZELPP-UHFFFAOYSA-N 0.000 description 2
- ILBONRFSLATCRE-UHFFFAOYSA-N Phosfolan Chemical compound CCOP(=O)(OCC)N=C1SCCS1 ILBONRFSLATCRE-UHFFFAOYSA-N 0.000 description 2
- 239000005921 Phosmet Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241001640279 Phyllophaga Species 0.000 description 2
- 241000275067 Phyllotreta Species 0.000 description 2
- 241000941941 Physokermes Species 0.000 description 2
- 239000005595 Picloram Substances 0.000 description 2
- UNLYSVIDNRIVFJ-UHFFFAOYSA-N Piperophos Chemical compound CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C UNLYSVIDNRIVFJ-UHFFFAOYSA-N 0.000 description 2
- TZBPRYIIJAJUOY-UHFFFAOYSA-N Pirimiphos-ethyl Chemical group CCOP(=S)(OCC)OC1=CC(C)=NC(N(CC)CC)=N1 TZBPRYIIJAJUOY-UHFFFAOYSA-N 0.000 description 2
- 241001289556 Pogonomyrmex Species 0.000 description 2
- 241001447361 Polyplax Species 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000005820 Prochloraz Substances 0.000 description 2
- RSVPPPHXAASNOL-UHFFFAOYSA-N Prodiamine Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O RSVPPPHXAASNOL-UHFFFAOYSA-N 0.000 description 2
- GGRLUNQHANDPSC-UHFFFAOYSA-N Promacyl Chemical compound CCCC(=O)CNC(=O)OC1=CC(C)=CC(C(C)C)=C1 GGRLUNQHANDPSC-UHFFFAOYSA-N 0.000 description 2
- DTAPQAJKAFRNJB-UHFFFAOYSA-N Promecarb Chemical compound CNC(=O)OC1=CC(C)=CC(C(C)C)=C1 DTAPQAJKAFRNJB-UHFFFAOYSA-N 0.000 description 2
- 239000005600 Propaquizafop Substances 0.000 description 2
- 239000005822 Propiconazole Substances 0.000 description 2
- 239000005823 Propineb Substances 0.000 description 2
- UEKQGZQLUMSLNW-UHFFFAOYSA-N Propyl isome Chemical compound C1=C2C(C(=O)OCCC)C(C(=O)OCCC)C(C)CC2=CC2=C1OCO2 UEKQGZQLUMSLNW-UHFFFAOYSA-N 0.000 description 2
- 239000005602 Propyzamide Substances 0.000 description 2
- 239000005603 Prosulfocarb Substances 0.000 description 2
- 235000005805 Prunus cerasus Nutrition 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- 241000517304 Pthirus pubis Species 0.000 description 2
- 239000005925 Pymetrozine Substances 0.000 description 2
- IHHMUBRVTJMLQO-UHFFFAOYSA-N Pyraclonil Chemical compound C#CCN(C)C1=C(C#N)C=NN1C1=NN(CCCC2)C2=C1Cl IHHMUBRVTJMLQO-UHFFFAOYSA-N 0.000 description 2
- VXMNDQDDWDDKOQ-UHFFFAOYSA-N Pyrazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C(O)=O)C)=N1 VXMNDQDDWDDKOQ-UHFFFAOYSA-N 0.000 description 2
- 239000005663 Pyridaben Substances 0.000 description 2
- 239000005926 Pyridalyl Substances 0.000 description 2
- 239000005606 Pyridate Substances 0.000 description 2
- JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 description 2
- OVZITGHGWBXFEA-UHFFFAOYSA-N Pyridinitril Chemical compound ClC1=NC(Cl)=C(C#N)C(C=2C=CC=CC=2)=C1C#N OVZITGHGWBXFEA-UHFFFAOYSA-N 0.000 description 2
- RRKHIAYNPVQKEF-UHFFFAOYSA-N Pyriftalid Chemical compound COC1=CC(OC)=NC(SC=2C=3C(=O)OC(C)C=3C=CC=2)=N1 RRKHIAYNPVQKEF-UHFFFAOYSA-N 0.000 description 2
- 239000005927 Pyriproxyfen Substances 0.000 description 2
- CNILNQMBAHKMFS-UHFFFAOYSA-M Pyrithiobac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(SC=2C(=C(Cl)C=CC=2)C([O-])=O)=N1 CNILNQMBAHKMFS-UHFFFAOYSA-M 0.000 description 2
- 239000005607 Pyroxsulam Substances 0.000 description 2
- 240000003085 Quassia amara Species 0.000 description 2
- 235000009694 Quassia amara Nutrition 0.000 description 2
- CDEWHBGYSWJUFP-UHFFFAOYSA-N Quinacetol sulfate Chemical compound OS(O)(=O)=O.C1=CC=C2C(C(=O)C)=CC=C(O)C2=N1.C1=CC=C2C(C(=O)C)=CC=C(O)C2=N1 CDEWHBGYSWJUFP-UHFFFAOYSA-N 0.000 description 2
- 239000005608 Quinmerac Substances 0.000 description 2
- OBLNWSCLAYSJJR-UHFFFAOYSA-N Quinoclamin Chemical compound C1=CC=C2C(=O)C(N)=C(Cl)C(=O)C2=C1 OBLNWSCLAYSJJR-UHFFFAOYSA-N 0.000 description 2
- 239000002167 Quinoclamine Substances 0.000 description 2
- 239000005615 Quizalofop-P-tefuryl Substances 0.000 description 2
- 241001509970 Reticulitermes <genus> Species 0.000 description 2
- 241001136903 Rhagoletis pomonella Species 0.000 description 2
- 241000282806 Rhinoceros Species 0.000 description 2
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 2
- 241000167882 Rhopalosiphum maidis Species 0.000 description 2
- 241000318997 Rhyzopertha dominica Species 0.000 description 2
- 239000005616 Rimsulfuron Substances 0.000 description 2
- 241000220317 Rosa Species 0.000 description 2
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 2
- WOZQBERUBLYCEG-UHFFFAOYSA-N SWEP Chemical compound COC(=O)NC1=CC=C(Cl)C(Cl)=C1 WOZQBERUBLYCEG-UHFFFAOYSA-N 0.000 description 2
- OUNSASXJZHBGAI-UHFFFAOYSA-N Salithion Chemical compound C1=CC=C2OP(OC)(=S)OCC2=C1 OUNSASXJZHBGAI-UHFFFAOYSA-N 0.000 description 2
- 241000722027 Schizaphis graminum Species 0.000 description 2
- SZKKRCSOSQAJDE-UHFFFAOYSA-N Schradan Chemical compound CN(C)P(=O)(N(C)C)OP(=O)(N(C)C)N(C)C SZKKRCSOSQAJDE-UHFFFAOYSA-N 0.000 description 2
- 241000545593 Scolytinae Species 0.000 description 2
- WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 description 2
- ZZMNWJVJUKMZJY-AFHBHXEDSA-N Sesamolin Chemical compound C1=C2OCOC2=CC([C@H]2OC[C@H]3[C@@H]2CO[C@@H]3OC2=CC=C3OCOC3=C2)=C1 ZZMNWJVJUKMZJY-AFHBHXEDSA-N 0.000 description 2
- ZZMNWJVJUKMZJY-UHFFFAOYSA-N Sesamolin Natural products C1=C2OCOC2=CC(C2OCC3C2COC3OC2=CC=C3OCOC3=C2)=C1 ZZMNWJVJUKMZJY-UHFFFAOYSA-N 0.000 description 2
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 2
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 description 2
- JXVIIQLNUPXOII-UHFFFAOYSA-N Siduron Chemical compound CC1CCCCC1NC(=O)NC1=CC=CC=C1 JXVIIQLNUPXOII-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 241001168723 Sitona lineatus Species 0.000 description 2
- 241000254181 Sitophilus Species 0.000 description 2
- 241000254179 Sitophilus granarius Species 0.000 description 2
- 241000254152 Sitophilus oryzae Species 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- KSQXVLVXUFHGJQ-UHFFFAOYSA-M Sodium ortho-phenylphenate Chemical compound [Na+].[O-]C1=CC=CC=C1C1=CC=CC=C1 KSQXVLVXUFHGJQ-UHFFFAOYSA-M 0.000 description 2
- 241000176086 Sogatella furcifera Species 0.000 description 2
- 235000002597 Solanum melongena Nutrition 0.000 description 2
- 244000061458 Solanum melongena Species 0.000 description 2
- 239000005665 Spiromesifen Substances 0.000 description 2
- 241000256247 Spodoptera exigua Species 0.000 description 2
- 235000009184 Spondias indica Nutrition 0.000 description 2
- 241001177161 Stegobium paniceum Species 0.000 description 2
- XJCLWVXTCRQIDI-UHFFFAOYSA-N Sulfallate Chemical compound CCN(CC)C(=S)SCC(Cl)=C XJCLWVXTCRQIDI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 239000005839 Tebuconazole Substances 0.000 description 2
- 239000005937 Tebufenozide Substances 0.000 description 2
- 239000005658 Tebufenpyrad Substances 0.000 description 2
- HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 description 2
- 239000005938 Teflubenzuron Substances 0.000 description 2
- 239000005939 Tefluthrin Substances 0.000 description 2
- IOYNQIMAUDJVEI-BMVIKAAMSA-N Tepraloxydim Chemical compound C1C(=O)C(C(=N/OC\C=C\Cl)/CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-BMVIKAAMSA-N 0.000 description 2
- NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 description 2
- 239000005840 Tetraconazole Substances 0.000 description 2
- 239000005940 Thiacloprid Substances 0.000 description 2
- JZFICWYCTCCINF-UHFFFAOYSA-N Thiadiazin Chemical compound S=C1SC(C)NC(C)N1CCN1C(=S)SC(C)NC1C JZFICWYCTCCINF-UHFFFAOYSA-N 0.000 description 2
- YIJZJEYQBAAWRJ-UHFFFAOYSA-N Thiazopyr Chemical compound N1=C(C(F)F)C(C(=O)OC)=C(CC(C)C)C(C=2SCCN=2)=C1C(F)(F)F YIJZJEYQBAAWRJ-UHFFFAOYSA-N 0.000 description 2
- GNOOAFGERMHQJE-UHFFFAOYSA-N Thicyofen Chemical compound CCS(=O)C=1SC(C#N)=C(Cl)C=1C#N GNOOAFGERMHQJE-UHFFFAOYSA-N 0.000 description 2
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 description 2
- IRVDMKJLOCGUBJ-UHFFFAOYSA-N Thionazin Chemical compound CCOP(=S)(OCC)OC1=CN=CC=N1 IRVDMKJLOCGUBJ-UHFFFAOYSA-N 0.000 description 2
- 239000005842 Thiophanate-methyl Substances 0.000 description 2
- 239000005843 Thiram Substances 0.000 description 2
- OTLLEIBWKHEHGU-UHFFFAOYSA-N Thuringiensin Natural products C1=NC=2C(N)=NC=NC=2N1C(C(C1O)O)OC1COC1C(CO)OC(OC(C(O)C(OP(O)(O)=O)C(O)C(O)=O)C(O)=O)C(O)C1O OTLLEIBWKHEHGU-UHFFFAOYSA-N 0.000 description 2
- 241001414989 Thysanoptera Species 0.000 description 2
- 239000005625 Tri-allate Substances 0.000 description 2
- MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 description 2
- 239000005846 Triadimenol Substances 0.000 description 2
- 241000018135 Trialeurodes Species 0.000 description 2
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 2
- BABJTMNVJXLAEX-UHFFFAOYSA-N Triamiphos Chemical compound N1=C(N)N(P(=O)(N(C)C)N(C)C)N=C1C1=CC=CC=C1 BABJTMNVJXLAEX-UHFFFAOYSA-N 0.000 description 2
- 241001414833 Triatoma Species 0.000 description 2
- 239000005847 Triazoxide Substances 0.000 description 2
- 241000254086 Tribolium <beetle> Species 0.000 description 2
- 241000254113 Tribolium castaneum Species 0.000 description 2
- 241000254112 Tribolium confusum Species 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- NHTFLYKPEGXOAN-UHFFFAOYSA-N Trichlamide Chemical compound CCCCOC(C(Cl)(Cl)Cl)NC(=O)C1=CC=CC=C1O NHTFLYKPEGXOAN-UHFFFAOYSA-N 0.000 description 2
- ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 description 2
- IBZHOAONZVJLOB-UHFFFAOYSA-N Tridiphane Chemical compound ClC1=CC(Cl)=CC(C2(CC(Cl)(Cl)Cl)OC2)=C1 IBZHOAONZVJLOB-UHFFFAOYSA-N 0.000 description 2
- HFBWPRKWDIRYNX-UHFFFAOYSA-N Trietazine Chemical compound CCNC1=NC(Cl)=NC(N(CC)CC)=N1 HFBWPRKWDIRYNX-UHFFFAOYSA-N 0.000 description 2
- 239000005859 Triticonazole Substances 0.000 description 2
- 239000005629 Tritosulfuron Substances 0.000 description 2
- 241000778089 Trogoderma variabile Species 0.000 description 2
- 241001630065 Unaspis yanonensis Species 0.000 description 2
- 241000256838 Vespula Species 0.000 description 2
- CVQODEWAPZVVBU-UHFFFAOYSA-N XMC Chemical compound CNC(=O)OC1=CC(C)=CC(C)=C1 CVQODEWAPZVVBU-UHFFFAOYSA-N 0.000 description 2
- 241000256654 Xylocopa <genus> Species 0.000 description 2
- 239000005870 Ziram Substances 0.000 description 2
- 241001247821 Ziziphus Species 0.000 description 2
- 239000005863 Zoxamide Substances 0.000 description 2
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 2
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 description 2
- NPYQHCFKDKPILU-UHFFFAOYSA-N [(3,5,5-trimethyl-4-oxo-1,3-thiazolidin-2-ylidene)amino] n-methylcarbamate Chemical compound CNC(=O)ON=C1SC(C)(C)C(=O)N1C NPYQHCFKDKPILU-UHFFFAOYSA-N 0.000 description 2
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 description 2
- QSGNQELHULIMSJ-POHAHGRESA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] dimethyl phosphate Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl QSGNQELHULIMSJ-POHAHGRESA-N 0.000 description 2
- OOWCJRMYMAMSOH-UHFFFAOYSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1C=C(C)C OOWCJRMYMAMSOH-UHFFFAOYSA-N 0.000 description 2
- GQNBIMLHUAWKHJ-UHFFFAOYSA-N [4-(methoxymethyl)phenyl]methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound C1=CC(COC)=CC=C1COC(=O)C1C(C)(C)C1C=C(C)C GQNBIMLHUAWKHJ-UHFFFAOYSA-N 0.000 description 2
- JNVCSEDACVAATK-UHFFFAOYSA-L [Ca+2].[S-]SSS[S-] Chemical compound [Ca+2].[S-]SSS[S-] JNVCSEDACVAATK-UHFFFAOYSA-L 0.000 description 2
- VQSUKBFBVMSNES-UHFFFAOYSA-K [Cl-].[Cl-].[Cu+].[Cu+].[Cu+].CN(C)C([S-])=S Chemical compound [Cl-].[Cl-].[Cu+].[Cu+].[Cu+].CN(C)C([S-])=S VQSUKBFBVMSNES-UHFFFAOYSA-K 0.000 description 2
- OYVABZRZDZPVQD-UHFFFAOYSA-N [F].C=1C=CSC=1 Chemical compound [F].C=1C=CSC=1 OYVABZRZDZPVQD-UHFFFAOYSA-N 0.000 description 2
- WHDHEVMINMZADQ-UHFFFAOYSA-N [F].N1C=CC=C1 Chemical class [F].N1C=CC=C1 WHDHEVMINMZADQ-UHFFFAOYSA-N 0.000 description 2
- HXELGNKCCDGMMN-UHFFFAOYSA-N [F].[Cl] Chemical compound [F].[Cl] HXELGNKCCDGMMN-UHFFFAOYSA-N 0.000 description 2
- XWMXGQDVMVZKPD-UHFFFAOYSA-N [S].N1=CC=CC=C1.[F] Chemical compound [S].N1=CC=CC=C1.[F] XWMXGQDVMVZKPD-UHFFFAOYSA-N 0.000 description 2
- GDKICXLWRDALGC-UHFFFAOYSA-N [S].[Cl].N1C=CC=C1 Chemical compound [S].[Cl].N1C=CC=C1 GDKICXLWRDALGC-UHFFFAOYSA-N 0.000 description 2
- IHVPAVRHNZFQKC-UHFFFAOYSA-N [cyano-(6-phenoxypyridin-2-yl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=N1 IHVPAVRHNZFQKC-UHFFFAOYSA-N 0.000 description 2
- QDRXWCAVUNHOGA-UHFFFAOYSA-N acequinocyl Chemical group C1=CC=C2C(=O)C(CCCCCCCCCCCC)=C(OC(C)=O)C(=O)C2=C1 QDRXWCAVUNHOGA-UHFFFAOYSA-N 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- YLJLLELGHSWIDU-OKZTUQRJSA-N acetic acid;(2s,6r)-4-cyclododecyl-2,6-dimethylmorpholine Chemical compound CC(O)=O.C1[C@@H](C)O[C@@H](C)CN1C1CCCCCCCCCCC1 YLJLLELGHSWIDU-OKZTUQRJSA-N 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- CGIHPACLZJDCBQ-UHFFFAOYSA-N acibenzolar Chemical compound SC(=O)C1=CC=CC2=C1SN=N2 CGIHPACLZJDCBQ-UHFFFAOYSA-N 0.000 description 2
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 description 2
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 2
- GMAUQNJOSOMMHI-JXAWBTAJSA-N alanycarb Chemical compound CSC(\C)=N/OC(=O)N(C)SN(CCC(=O)OCC)CC1=CC=CC=C1 GMAUQNJOSOMMHI-JXAWBTAJSA-N 0.000 description 2
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 description 2
- 239000003619 algicide Substances 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 239000011717 all-trans-retinol Substances 0.000 description 2
- 235000019169 all-trans-retinol Nutrition 0.000 description 2
- ZCVAOQKBXKSDMS-UHFFFAOYSA-N allethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-UHFFFAOYSA-N 0.000 description 2
- 229940024113 allethrin Drugs 0.000 description 2
- UPEZCKBFRMILAV-UHFFFAOYSA-N alpha-Ecdysone Natural products C1C(O)C(O)CC2(C)C(CCC3(C(C(C(O)CCC(C)(C)O)C)CCC33O)C)C3=CC(=O)C21 UPEZCKBFRMILAV-UHFFFAOYSA-N 0.000 description 2
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 2
- ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 description 2
- IMIDOCRTMDIQIJ-UHFFFAOYSA-N aminocarb Chemical compound CNC(=O)OC1=CC=C(N(C)C)C(C)=C1 IMIDOCRTMDIQIJ-UHFFFAOYSA-N 0.000 description 2
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000008365 aqueous carrier Substances 0.000 description 2
- PXWUKZGIHQRDHL-UHFFFAOYSA-N atraton Chemical compound CCNC1=NC(NC(C)C)=NC(OC)=N1 PXWUKZGIHQRDHL-UHFFFAOYSA-N 0.000 description 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 239000005667 attractant Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 description 2
- 229950000294 azaconazole Drugs 0.000 description 2
- LVYAMPSKHSIFNV-UHFFFAOYSA-N azane;methylcarbamodithioic acid Chemical compound [NH4+].CNC([S-])=S LVYAMPSKHSIFNV-UHFFFAOYSA-N 0.000 description 2
- CYOOVEAWXNAHJA-UHFFFAOYSA-N azane;phosphane Chemical compound N.N.P CYOOVEAWXNAHJA-UHFFFAOYSA-N 0.000 description 2
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 2
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 2
- RQVGAIADHNPSME-UHFFFAOYSA-N azinphos-ethyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OCC)OCC)N=NC2=C1 RQVGAIADHNPSME-UHFFFAOYSA-N 0.000 description 2
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 description 2
- DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 description 2
- 229940097012 bacillus thuringiensis Drugs 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 210000003323 beak Anatomy 0.000 description 2
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 description 2
- LJOZMWRYMKECFF-UHFFFAOYSA-N benodanil Chemical compound IC1=CC=CC=C1C(=O)NC1=CC=CC=C1 LJOZMWRYMKECFF-UHFFFAOYSA-N 0.000 description 2
- 229950006402 benoxafos Drugs 0.000 description 2
- YFXPPSKYMBTNAV-UHFFFAOYSA-N bensultap Chemical compound C=1C=CC=CC=1S(=O)(=O)SCC(N(C)C)CSS(=O)(=O)C1=CC=CC=C1 YFXPPSKYMBTNAV-UHFFFAOYSA-N 0.000 description 2
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 2
- 229960000686 benzalkonium chloride Drugs 0.000 description 2
- YVGQISQVTCHQJD-UHFFFAOYSA-N benzoic acid;4-cyclododecyl-2,6-dimethylmorpholine Chemical compound OC(=O)C1=CC=CC=C1.C1C(C)OC(C)CN1C1CCCCCCCCCCC1 YVGQISQVTCHQJD-UHFFFAOYSA-N 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 2
- NKDFYOWSKOHCCO-UHFFFAOYSA-N beta-ecdysone Natural products C1C(O)C(O)CC2(C)C(CCC3(C(C(C)(O)C(O)CCC(C)(O)C)CCC33O)C)C3=CC(=O)C21 NKDFYOWSKOHCCO-UHFFFAOYSA-N 0.000 description 2
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 description 2
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 2
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 description 2
- 229960001901 bioallethrin Drugs 0.000 description 2
- 239000012681 biocontrol agent Substances 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 2
- JFIOVJDNOJYLKP-UHFFFAOYSA-N bithionol Chemical compound OC1=C(Cl)C=C(Cl)C=C1SC1=CC(Cl)=CC(Cl)=C1O JFIOVJDNOJYLKP-UHFFFAOYSA-N 0.000 description 2
- 229960002326 bithionol Drugs 0.000 description 2
- CXNPLSGKWMLZPZ-UHFFFAOYSA-N blasticidin-S Natural products O1C(C(O)=O)C(NC(=O)CC(N)CCN(C)C(N)=N)C=CC1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-UHFFFAOYSA-N 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 description 2
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 2
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 description 2
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 description 2
- VIHAEDVKXSOUAT-UHFFFAOYSA-N but-2-en-4-olide Chemical class O=C1OCC=C1 VIHAEDVKXSOUAT-UHFFFAOYSA-N 0.000 description 2
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 2
- JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 description 2
- CURLHBZYTFVCRG-UHFFFAOYSA-N butan-2-yl n-(3-chlorophenyl)carbamate Chemical compound CCC(C)OC(=O)NC1=CC=CC(Cl)=C1 CURLHBZYTFVCRG-UHFFFAOYSA-N 0.000 description 2
- 229950010691 butonate Drugs 0.000 description 2
- KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229940103357 calcium arsenate Drugs 0.000 description 2
- YALMXYPQBUJUME-UHFFFAOYSA-L calcium chlorate Chemical compound [Ca+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O YALMXYPQBUJUME-UHFFFAOYSA-L 0.000 description 2
- 229940117949 captan Drugs 0.000 description 2
- 229960005286 carbaryl Drugs 0.000 description 2
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 2
- 239000006013 carbendazim Substances 0.000 description 2
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 2
- JLQUFIHWVLZVTJ-UHFFFAOYSA-N carbosulfan Chemical compound CCCCN(CCCC)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 JLQUFIHWVLZVTJ-UHFFFAOYSA-N 0.000 description 2
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- SILSDTWXNBZOGF-KUZBFYBWSA-N chembl111058 Chemical compound CCSC(C)CC1CC(O)=C(\C(CC)=N\OC\C=C\Cl)C(=O)C1 SILSDTWXNBZOGF-KUZBFYBWSA-N 0.000 description 2
- PNCNFDRSHBFIDM-WOJGMQOQSA-N chembl111617 Chemical compound C=CCO\N=C(/CCC)C1=C(O)C(C(=O)OC)C(C)(C)CC1=O PNCNFDRSHBFIDM-WOJGMQOQSA-N 0.000 description 2
- GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 description 2
- 230000031902 chemoattractant activity Effects 0.000 description 2
- 230000003559 chemosterilizing effect Effects 0.000 description 2
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 description 2
- LHHGDZSESBACKH-UHFFFAOYSA-N chlordecone Chemical compound ClC12C3(Cl)C(Cl)(Cl)C4(Cl)C2(Cl)C2(Cl)C4(Cl)C3(Cl)C1(Cl)C2=O LHHGDZSESBACKH-UHFFFAOYSA-N 0.000 description 2
- QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 description 2
- UISUNVFOGSJSKD-UHFFFAOYSA-N chlorfluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1Cl)=CC(Cl)=C1OC1=NC=C(C(F)(F)F)C=C1Cl UISUNVFOGSJSKD-UHFFFAOYSA-N 0.000 description 2
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 2
- AWGTVRDHKJQFAX-UHFFFAOYSA-M chloro(phenyl)mercury Chemical compound Cl[Hg]C1=CC=CC=C1 AWGTVRDHKJQFAX-UHFFFAOYSA-M 0.000 description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
- PFIADAMVCJPXSF-UHFFFAOYSA-N chloroneb Chemical compound COC1=CC(Cl)=C(OC)C=C1Cl PFIADAMVCJPXSF-UHFFFAOYSA-N 0.000 description 2
- AXGUBXVWZBFQGA-UHFFFAOYSA-N chloropropylate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Cl)C=C1 AXGUBXVWZBFQGA-UHFFFAOYSA-N 0.000 description 2
- CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 2
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 description 2
- FRCCEHPWNOQAEU-LDSHLKOWSA-N cis-heptachlordane Chemical compound ClC1=C(Cl)[C@@]2(Cl)[C@H]3C=C[C@H](Cl)[C@H]3[C@]1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-LDSHLKOWSA-N 0.000 description 2
- 235000020971 citrus fruits Nutrition 0.000 description 2
- UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 description 2
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 description 2
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 2
- 229950004178 closantel Drugs 0.000 description 2
- VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 description 2
- 229960004022 clotrimazole Drugs 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229940030341 copper arsenate Drugs 0.000 description 2
- 229940116318 copper carbonate Drugs 0.000 description 2
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 2
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 2
- RKYSWCFUYJGIQA-UHFFFAOYSA-H copper(ii) arsenate Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-][As]([O-])([O-])=O.[O-][As]([O-])([O-])=O RKYSWCFUYJGIQA-UHFFFAOYSA-H 0.000 description 2
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 2
- ZZBBCSFCMKWYQR-UHFFFAOYSA-N copper;dioxido(oxo)silane Chemical compound [Cu+2].[O-][Si]([O-])=O ZZBBCSFCMKWYQR-UHFFFAOYSA-N 0.000 description 2
- JOXAXMBQVHFGQT-UHFFFAOYSA-J copper;manganese(2+);n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[Cu+2].[S-]C(=S)NCCNC([S-])=S.[S-]C(=S)NCCNC([S-])=S JOXAXMBQVHFGQT-UHFFFAOYSA-J 0.000 description 2
- 239000006184 cosolvent Substances 0.000 description 2
- BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 150000001896 cresols Chemical class 0.000 description 2
- DNTGGZPQPQTDQF-XBXARRHUSA-N crotamiton Chemical compound C/C=C/C(=O)N(CC)C1=CC=CC=C1C DNTGGZPQPQTDQF-XBXARRHUSA-N 0.000 description 2
- 229960003338 crotamiton Drugs 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 229910001610 cryolite Inorganic materials 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 229940112669 cuprous oxide Drugs 0.000 description 2
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 2
- YXKMMRDKEKCERS-UHFFFAOYSA-N cyazofamid Chemical compound CN(C)S(=O)(=O)N1C(C#N)=NC(Cl)=C1C1=CC=C(C)C=C1 YXKMMRDKEKCERS-UHFFFAOYSA-N 0.000 description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 description 2
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 description 2
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 2
- 229960005424 cypermethrin Drugs 0.000 description 2
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 2
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 2
- 229950000775 cyromazine Drugs 0.000 description 2
- BSBSDQUZDZXGFN-UHFFFAOYSA-N cythioate Chemical compound COP(=S)(OC)OC1=CC=C(S(N)(=O)=O)C=C1 BSBSDQUZDZXGFN-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 2
- WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 2
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
- PPJXIHLNYDVTDI-UHFFFAOYSA-N dicloralurea Chemical compound ClC(Cl)(Cl)C(O)NC(=O)NC(O)C(Cl)(Cl)Cl PPJXIHLNYDVTDI-UHFFFAOYSA-N 0.000 description 2
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 description 2
- VEENJGZXVHKXNB-VOTSOKGWSA-N dicrotophos Chemical compound COP(=O)(OC)O\C(C)=C\C(=O)N(C)C VEENJGZXVHKXNB-VOTSOKGWSA-N 0.000 description 2
- FAXIJTUDSBIMHY-UHFFFAOYSA-N diethoxy-(2-ethylsulfanylethoxy)-sulfanylidene-$l^{5}-phosphane;1-diethoxyphosphorylsulfanyl-2-ethylsulfanylethane Chemical compound CCOP(=O)(OCC)SCCSCC.CCOP(=S)(OCC)OCCSCC FAXIJTUDSBIMHY-UHFFFAOYSA-N 0.000 description 2
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
- FFYPMLJYZAEMQB-UHFFFAOYSA-N diethyl pyrocarbonate Chemical compound CCOC(=O)OC(=O)OCC FFYPMLJYZAEMQB-UHFFFAOYSA-N 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 description 2
- BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 description 2
- CJHXCRMKMMBYJQ-UHFFFAOYSA-N dimethirimol Chemical compound CCCCC1=C(C)NC(N(C)C)=NC1=O CJHXCRMKMMBYJQ-UHFFFAOYSA-N 0.000 description 2
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 2
- ZIBCESDMUREVIU-UHFFFAOYSA-N dimethoxy-(2-methylsulfanylethoxy)-sulfanylidene-$l^{5}-phosphane;1-dimethoxyphosphorylsulfanyl-2-methylsulfanylethane Chemical compound COP(=O)(OC)SCCSC.COP(=S)(OC)OCCSC ZIBCESDMUREVIU-UHFFFAOYSA-N 0.000 description 2
- SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 2
- ZHIKKPYAYGUYPV-UHFFFAOYSA-N dimethylaminocarbamothioylsulfanyl n-(dimethylamino)carbamodithioate Chemical compound CN(C)NC(=S)SSC(=S)NN(C)C ZHIKKPYAYGUYPV-UHFFFAOYSA-N 0.000 description 2
- RDBIYWSVMRVKSG-UHFFFAOYSA-N dimetilan Chemical compound CN(C)C(=O)OC=1C=C(C)N(C(=O)N(C)C)N=1 RDBIYWSVMRVKSG-UHFFFAOYSA-N 0.000 description 2
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 description 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical group [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 2
- DOFZAZXDOSGAJZ-UHFFFAOYSA-N disulfoton Chemical compound CCOP(=S)(OCC)SCCSCC DOFZAZXDOSGAJZ-UHFFFAOYSA-N 0.000 description 2
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 description 2
- JMXKCYUTURMERF-UHFFFAOYSA-N dodemorph Chemical compound C1C(C)OC(C)CN1C1CCCCCCCCCCC1 JMXKCYUTURMERF-UHFFFAOYSA-N 0.000 description 2
- QLFZZSKTJWDQOS-YDBLARSUSA-N doramectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C3CCCCC3)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C QLFZZSKTJWDQOS-YDBLARSUSA-N 0.000 description 2
- 229960003997 doramectin Drugs 0.000 description 2
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- UPEZCKBFRMILAV-JMZLNJERSA-N ecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@H]([C@H](O)CCC(C)(C)O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 UPEZCKBFRMILAV-JMZLNJERSA-N 0.000 description 2
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 2
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- DFBKLUNHFCTMDC-GKRDHZSOSA-N endrin Chemical compound C([C@@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@@H]2[C@H]2[C@@H]1O2 DFBKLUNHFCTMDC-GKRDHZSOSA-N 0.000 description 2
- 230000000967 entomopathogenic effect Effects 0.000 description 2
- WPNHOHPRXXCPRA-TVXIRPTOSA-N eprinomectin Chemical compound O1[C@@H](C)[C@@H](NC(C)=O)[C@H](OC)C[C@@H]1O[C@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C\C=C/[C@@H]2C)\C)O[C@H]1C WPNHOHPRXXCPRA-TVXIRPTOSA-N 0.000 description 2
- 229960002346 eprinomectin Drugs 0.000 description 2
- NYPJDWWKZLNGGM-RPWUZVMVSA-N esfenvalerate Chemical compound C=1C([C@@H](C#N)OC(=O)[C@@H](C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-RPWUZVMVSA-N 0.000 description 2
- DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 description 2
- IRLGCAJYYKDTCG-UHFFFAOYSA-N ethametsulfuron Chemical compound CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 IRLGCAJYYKDTCG-UHFFFAOYSA-N 0.000 description 2
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 2
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 2
- 229940093500 ethoxyquin Drugs 0.000 description 2
- 235000019285 ethoxyquin Nutrition 0.000 description 2
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 2
- OSUHJPCHFDQAIT-UHFFFAOYSA-N ethyl 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoate Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 OSUHJPCHFDQAIT-UHFFFAOYSA-N 0.000 description 2
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 description 2
- ZHCJUZJGMJDUKJ-UHFFFAOYSA-M ethyl(phosphonatooxy)mercury;hydron Chemical compound CC[Hg+].OP(O)([O-])=O ZHCJUZJGMJDUKJ-UHFFFAOYSA-M 0.000 description 2
- QWUGXIXRFGEYBD-UHFFFAOYSA-M ethylmercuric chloride Chemical compound CC[Hg]Cl QWUGXIXRFGEYBD-UHFFFAOYSA-M 0.000 description 2
- QMTNOLKHSWIQBE-FGTMMUONSA-N exo-(+)-cinmethylin Chemical compound O([C@H]1[C@]2(C)CC[C@@](O2)(C1)C(C)C)CC1=CC=CC=C1C QMTNOLKHSWIQBE-FGTMMUONSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- JISACBWYRJHSMG-UHFFFAOYSA-N famphur Chemical compound COP(=S)(OC)OC1=CC=C(S(=O)(=O)N(C)C)C=C1 JISACBWYRJHSMG-UHFFFAOYSA-N 0.000 description 2
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 description 2
- ZCJPOPBZHLUFHF-UHFFFAOYSA-N fenamiphos Chemical compound CCOP(=O)(NC(C)C)OC1=CC=C(SC)C(C)=C1 ZCJPOPBZHLUFHF-UHFFFAOYSA-N 0.000 description 2
- DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 description 2
- 229950006668 fenfluthrin Drugs 0.000 description 2
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 description 2
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 description 2
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 2
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 2
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 description 2
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 2
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 2
- XDNBJTQLKCIJBV-UHFFFAOYSA-N fensulfothion Chemical compound CCOP(=S)(OCC)OC1=CC=C(S(C)=O)C=C1 XDNBJTQLKCIJBV-UHFFFAOYSA-N 0.000 description 2
- NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 2
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 description 2
- 239000011790 ferrous sulphate Substances 0.000 description 2
- 235000003891 ferrous sulphate Nutrition 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 description 2
- MXWAGQASUDSFBG-RVDMUPIBSA-N fluacrypyrim Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C(F)(F)F)=NC(OC(C)C)=N1 MXWAGQASUDSFBG-RVDMUPIBSA-N 0.000 description 2
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 description 2
- YOWNVPAUWYHLQX-UHFFFAOYSA-N fluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C(OC=2C(=CC(=CN=2)C(F)(F)F)Cl)=C1 YOWNVPAUWYHLQX-UHFFFAOYSA-N 0.000 description 2
- 229950006719 fluazuron Drugs 0.000 description 2
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 2
- GBIHOLCMZGAKNG-CGAIIQECSA-N flucythrinate Chemical compound O=C([C@@H](C(C)C)C=1C=CC(OC(F)F)=CC=1)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-CGAIIQECSA-N 0.000 description 2
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 2
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 2
- RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 description 2
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 2
- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 description 2
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 description 2
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 description 2
- OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical compound FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 description 2
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 2
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 2
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 description 2
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 2
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 2
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 description 2
- KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 2
- PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 description 2
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- HAWJXYBZNNRMNO-UHFFFAOYSA-N furathiocarb Chemical compound CCCCOC(=O)N(C)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 HAWJXYBZNNRMNO-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229940097068 glyphosate Drugs 0.000 description 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
- 244000304962 green bristle grass Species 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 description 2
- 229960002867 griseofulvin Drugs 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 2
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 description 2
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 229940056881 imidacloprid Drugs 0.000 description 2
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 2
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- 239000002418 insect attractant Substances 0.000 description 2
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- YFVOXLJXJBQDEF-UHFFFAOYSA-N isocarbophos Chemical compound COP(N)(=S)OC1=CC=CC=C1C(=O)OC(C)C YFVOXLJXJBQDEF-UHFFFAOYSA-N 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 2
- WLPCAERCXQSYLQ-UHFFFAOYSA-N isotianil Chemical compound ClC1=NSC(C(=O)NC=2C(=CC=CC=2)C#N)=C1Cl WLPCAERCXQSYLQ-UHFFFAOYSA-N 0.000 description 2
- NZKIRHFOLVYKFT-VUMXUWRFSA-N jasmolin I Chemical compound C1C(=O)C(C\C=C/CC)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1C=C(C)C NZKIRHFOLVYKFT-VUMXUWRFSA-N 0.000 description 2
- WKNSDDMJXANVMK-XIGJTORUSA-N jasmolin II Chemical compound C1C(=O)C(C\C=C/CC)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1\C=C(/C)C(=O)OC WKNSDDMJXANVMK-XIGJTORUSA-N 0.000 description 2
- WKNSDDMJXANVMK-UHFFFAOYSA-N jasmolin II Natural products C1C(=O)C(CC=CCC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C(=O)OC WKNSDDMJXANVMK-UHFFFAOYSA-N 0.000 description 2
- RQIDGZHMTWSMMC-TZNPKLQUSA-N juvenile hormone I Chemical compound COC(=O)/C=C(C)/CC\C=C(/CC)CC[C@H]1O[C@@]1(C)CC RQIDGZHMTWSMMC-TZNPKLQUSA-N 0.000 description 2
- CPVQJXZBSGXTGJ-TZDLBHCHSA-N juvenile hormone II Chemical compound CC[C@]1(C)O[C@@H]1CC\C(C)=C\CC\C(C)=C\C(=O)OC CPVQJXZBSGXTGJ-TZDLBHCHSA-N 0.000 description 2
- QVJMXSGZTCGLHZ-HONBPKQLSA-N juvenile hormone III Chemical compound COC(=O)\C=C(/C)CC\C=C(/C)CC[C@H]1OC1(C)C QVJMXSGZTCGLHZ-HONBPKQLSA-N 0.000 description 2
- 229930000024 juvenile hormones I Natural products 0.000 description 2
- 229930002340 juvenile hormones II Natural products 0.000 description 2
- 229930000772 juvenile hormones III Natural products 0.000 description 2
- PWAJCNITSBZRBL-UHFFFAOYSA-N ketazolam Chemical compound O1C(C)=CC(=O)N2CC(=O)N(C)C3=CC=C(Cl)C=C3C21C1=CC=CC=C1 PWAJCNITSBZRBL-UHFFFAOYSA-N 0.000 description 2
- 229960004423 ketazolam Drugs 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-UHFFFAOYSA-N 0.000 description 2
- 239000005910 lambda-Cyhalothrin Substances 0.000 description 2
- UWRBYRMOUPAKLM-UHFFFAOYSA-L lead arsenate Chemical compound [Pb+2].O[As]([O-])([O-])=O UWRBYRMOUPAKLM-UHFFFAOYSA-L 0.000 description 2
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 2
- 229960002809 lindane Drugs 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- VIMSQXDDXJYTLW-UHFFFAOYSA-M lithium;5-bromo-3-butan-2-yl-6-methylpyrimidin-1-ide-2,4-dione Chemical compound [Li+].CCC(C)N1C(=O)[N-]C(C)=C(Br)C1=O VIMSQXDDXJYTLW-UHFFFAOYSA-M 0.000 description 2
- 235000010420 locust bean gum Nutrition 0.000 description 2
- 239000000711 locust bean gum Substances 0.000 description 2
- 229960000453 malathion Drugs 0.000 description 2
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 2
- 229920000940 maneb Polymers 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 2
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 description 2
- VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 2
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 2
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- IXJOSTZEBSTPAG-UHFFFAOYSA-N methasulfocarb Chemical compound CNC(=O)SC1=CC=C(OS(C)(=O)=O)C=C1 IXJOSTZEBSTPAG-UHFFFAOYSA-N 0.000 description 2
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 2
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 description 2
- FWJLFUVWQAXWLE-UHFFFAOYSA-N methometon Chemical compound COCCCNC1=NC(NCCCOC)=NC(OC)=N1 FWJLFUVWQAXWLE-UHFFFAOYSA-N 0.000 description 2
- GEPDYQSQVLXLEU-AATRIKPKSA-N methyl (e)-3-dimethoxyphosphoryloxybut-2-enoate Chemical compound COC(=O)\C=C(/C)OP(=O)(OC)OC GEPDYQSQVLXLEU-AATRIKPKSA-N 0.000 description 2
- RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 description 2
- JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 description 2
- LYPWWQLKWQNQKV-UHFFFAOYSA-N methyl 2-[5-ethyl-2-[[4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]phenoxy]methyl]phenoxy]propanoate Chemical compound COC(=O)C(C)OC1=CC(CC)=CC=C1COC1=CC=C(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)C=C1 LYPWWQLKWQNQKV-UHFFFAOYSA-N 0.000 description 2
- AHGMXAFUHVRQAD-UHFFFAOYSA-N methyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 AHGMXAFUHVRQAD-UHFFFAOYSA-N 0.000 description 2
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 2
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 2
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
- MYURAHUSYDVWQA-UHFFFAOYSA-N methyl n'-(4-chlorophenyl)-n,n-dimethylcarbamimidate Chemical compound COC(N(C)C)=NC1=CC=C(Cl)C=C1 MYURAHUSYDVWQA-UHFFFAOYSA-N 0.000 description 2
- 229940073769 methyl oleate Drugs 0.000 description 2
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 description 2
- JVJUWCMBRUMDDQ-UHFFFAOYSA-N methylmercuric dicyanamide Chemical compound C[Hg]N=C(N)NC#N JVJUWCMBRUMDDQ-UHFFFAOYSA-N 0.000 description 2
- 229960002939 metizoline Drugs 0.000 description 2
- VOEYXMAFNDNNED-UHFFFAOYSA-N metolcarb Chemical compound CNC(=O)OC1=CC=CC(C)=C1 VOEYXMAFNDNNED-UHFFFAOYSA-N 0.000 description 2
- DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 description 2
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 description 2
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 2
- 229960001952 metrifonate Drugs 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- CKVMAPHTVCTEMM-ALPQRHTBSA-N milbemycin oxime Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\2)O)C[C@H]4C1.C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\1)O)C[C@H]4C2 CKVMAPHTVCTEMM-ALPQRHTBSA-N 0.000 description 2
- 229940099245 milbemycin oxime Drugs 0.000 description 2
- GVYLCNUFSHDAAW-UHFFFAOYSA-N mirex Chemical compound ClC12C(Cl)(Cl)C3(Cl)C4(Cl)C1(Cl)C1(Cl)C2(Cl)C3(Cl)C4(Cl)C1(Cl)Cl GVYLCNUFSHDAAW-UHFFFAOYSA-N 0.000 description 2
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 2
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 2
- 235000010460 mustard Nutrition 0.000 description 2
- AIMMSOZBPYFASU-UHFFFAOYSA-N n-(4,6-dimethoxypyrimidin-2-yl)-n'-[3-(2,2,2-trifluoroethoxy)pyridin-1-ium-2-yl]sulfonylcarbamimidate Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)OCC(F)(F)F)=N1 AIMMSOZBPYFASU-UHFFFAOYSA-N 0.000 description 2
- GLBLPMUBLHYFCW-UHFFFAOYSA-N n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1NS(=O)(=O)C1=C(OC)N=CC=C1C(F)(F)F GLBLPMUBLHYFCW-UHFFFAOYSA-N 0.000 description 2
- YUANPWFOQAEKNA-UHFFFAOYSA-N n-[2-amino-3-nitro-5-(trifluoromethyl)phenyl]-2,2,3,3-tetrafluoropropanamide Chemical compound NC1=C(NC(=O)C(F)(F)C(F)F)C=C(C(F)(F)F)C=C1[N+]([O-])=O YUANPWFOQAEKNA-UHFFFAOYSA-N 0.000 description 2
- CHEDHKBPPDKBQF-UPONEAKYSA-N n-[5-[(6s,7ar)-6-fluoro-1,3-dioxo-5,6,7,7a-tetrahydropyrrolo[1,2-c]imidazol-2-yl]-2-chloro-4-fluorophenyl]-1-chloromethanesulfonamide Chemical compound N1([C@@H](C2=O)C[C@@H](C1)F)C(=O)N2C1=CC(NS(=O)(=O)CCl)=C(Cl)C=C1F CHEDHKBPPDKBQF-UPONEAKYSA-N 0.000 description 2
- HZDIJTXDRLNTIS-DAXSKMNVSA-N n-[[(z)-but-2-enoxy]methyl]-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(COC\C=C/C)C(=O)CCl HZDIJTXDRLNTIS-DAXSKMNVSA-N 0.000 description 2
- UCFRFUMJIKZSBD-UHFFFAOYSA-N n-[azido(dimethylamino)phosphoryl]-n-methylmethanamine Chemical compound CN(C)P(=O)(N(C)C)N=[N+]=[N-] UCFRFUMJIKZSBD-UHFFFAOYSA-N 0.000 description 2
- VHEWQRWLIDWRMR-UHFFFAOYSA-N n-[methoxy-(4-methyl-2-nitrophenoxy)phosphinothioyl]propan-2-amine Chemical group CC(C)NP(=S)(OC)OC1=CC=C(C)C=C1[N+]([O-])=O VHEWQRWLIDWRMR-UHFFFAOYSA-N 0.000 description 2
- DGPBHERUGBOSFZ-UHFFFAOYSA-N n-but-3-yn-2-yl-2-chloro-n-phenylacetamide Chemical compound C#CC(C)N(C(=O)CCl)C1=CC=CC=C1 DGPBHERUGBOSFZ-UHFFFAOYSA-N 0.000 description 2
- SKSVCKGZZUFGGC-UHFFFAOYSA-N n-methylmethanamine;propanoic acid Chemical compound C[NH2+]C.CCC([O-])=O SKSVCKGZZUFGGC-UHFFFAOYSA-N 0.000 description 2
- QNSIFYWAPWSAIJ-UHFFFAOYSA-N naftalofos Chemical compound C1=CC(C(N(OP(=O)(OCC)OCC)C2=O)=O)=C3C2=CC=CC3=C1 QNSIFYWAPWSAIJ-UHFFFAOYSA-N 0.000 description 2
- 229950011528 naftalofos Drugs 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 2
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 2
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 2
- 229940079888 nitenpyram Drugs 0.000 description 2
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 2
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 description 2
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 2
- YTYGAJLZOJPJGH-UHFFFAOYSA-N noviflumuron Chemical compound FC1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F YTYGAJLZOJPJGH-UHFFFAOYSA-N 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- PZXOQEXFMJCDPG-UHFFFAOYSA-N omethoate Chemical compound CNC(=O)CSP(=O)(OC)OC PZXOQEXFMJCDPG-UHFFFAOYSA-N 0.000 description 2
- LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 description 2
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 description 2
- UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 description 2
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 2
- PMCVMORKVPSKHZ-UHFFFAOYSA-N oxydemeton-methyl Chemical group CCS(=O)CCSP(=O)(OC)OC PMCVMORKVPSKHZ-UHFFFAOYSA-N 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical group COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 2
- HTSABAUNNZLCMN-UHFFFAOYSA-F paris green Chemical compound [Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-][As]=O.[O-][As]=O.[O-][As]=O.[O-][As]=O.[O-][As]=O.[O-][As]=O.CC([O-])=O.CC([O-])=O HTSABAUNNZLCMN-UHFFFAOYSA-F 0.000 description 2
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 2
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 2
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 description 2
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 2
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 2
- CSWIKHNSBZVWNQ-UHFFFAOYSA-N pethoxamide Chemical compound CCOCCN(C(=O)CCl)C(=C(C)C)C1=CC=CC=C1 CSWIKHNSBZVWNQ-UHFFFAOYSA-N 0.000 description 2
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 2
- 229960003536 phenothrin Drugs 0.000 description 2
- KDNVJBRRDKAHDA-UHFFFAOYSA-L phenyl-[3-[[3-(phenylmercuriooxysulfonyl)naphthalen-2-yl]methyl]naphthalen-2-yl]sulfonyloxymercury Chemical compound C=1C2=CC=CC=C2C=C(CC=2C(=CC3=CC=CC=C3C=2)S(=O)(=O)O[Hg]C=2C=CC=CC=2)C=1S(=O)(=O)O[Hg]C1=CC=CC=C1 KDNVJBRRDKAHDA-UHFFFAOYSA-L 0.000 description 2
- 229940096826 phenylmercuric acetate Drugs 0.000 description 2
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 2
- IOUNQDKNJZEDEP-UHFFFAOYSA-N phosalone Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=S)(OCC)OCC)C2=C1 IOUNQDKNJZEDEP-UHFFFAOYSA-N 0.000 description 2
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 description 2
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 2
- 229950001664 phoxim Drugs 0.000 description 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 2
- PEUGKEHLRUVPAN-UHFFFAOYSA-N piperidin-3-amine Chemical compound NC1CCCNC1 PEUGKEHLRUVPAN-UHFFFAOYSA-N 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 229920000867 polyelectrolyte Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 229940016373 potassium polysulfide Drugs 0.000 description 2
- 229940116357 potassium thiocyanate Drugs 0.000 description 2
- DQRQIQZHRCRSDB-UHFFFAOYSA-M potassium;n-methylcarbamodithioate Chemical compound [K+].CNC([S-])=S DQRQIQZHRCRSDB-UHFFFAOYSA-M 0.000 description 2
- WEQIKOGPPFEIPX-UHFFFAOYSA-N potassium;propanoic acid Chemical compound [K].CCC(O)=O WEQIKOGPPFEIPX-UHFFFAOYSA-N 0.000 description 2
- RFJPSAYWKBGVAW-UHFFFAOYSA-N precocene III Chemical compound O1C(C)(C)C=CC2=C1C=C(OCC)C(OC)=C2 RFJPSAYWKBGVAW-UHFFFAOYSA-N 0.000 description 2
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 2
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 2
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 2
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 2
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 2
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 2
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 2
- IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 description 2
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 description 2
- PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 2
- FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 description 2
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 2
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 2
- BZNDWPRGXNILMS-VQHVLOKHSA-N propetamphos Chemical compound CCNP(=S)(OC)O\C(C)=C\C(=O)OC(C)C BZNDWPRGXNILMS-VQHVLOKHSA-N 0.000 description 2
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 2
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 2
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 description 2
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 2
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 2
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 2
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 2
- 229940070846 pyrethrins Drugs 0.000 description 2
- 239000002728 pyrethroid Substances 0.000 description 2
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 description 2
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 2
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 description 2
- 229950010685 pyrimitate Drugs 0.000 description 2
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 2
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 2
- 229940013788 quassia Drugs 0.000 description 2
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 2
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 2
- BBKDWPHJZANJGB-IKJXHCRLSA-N quizalofop-P-tefuryl Chemical group O=C([C@H](OC=1C=CC(OC=2N=C3C=CC(Cl)=CC3=NC=2)=CC=1)C)OCC1CCCO1 BBKDWPHJZANJGB-IKJXHCRLSA-N 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229940108410 resmethrin Drugs 0.000 description 2
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 2
- 238000004007 reversed phase HPLC Methods 0.000 description 2
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 2
- 238000006798 ring closing metathesis reaction Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- AFJYYKSVHJGXSN-KAJWKRCWSA-N selamectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(O[C@@H]([C@@H](C)CC2)C2CCCCC2)C2)C[C@@H]2OC(=O)[C@@H]([C@]23O)C=C(C)C(=N\O)/[C@H]3OC\C2=C/C=C/[C@@H]1C AFJYYKSVHJGXSN-KAJWKRCWSA-N 0.000 description 2
- 229960002245 selamectin Drugs 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 2
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 2
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 2
- 210000004894 snout Anatomy 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- HYHCSLBZRBJJCH-UHFFFAOYSA-N sodium polysulfide Chemical compound [Na+].S HYHCSLBZRBJJCH-UHFFFAOYSA-N 0.000 description 2
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 2
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 2
- TURJLPVZRPWSJO-UHFFFAOYSA-N sodium;2-(2,2-diphenylacetyl)inden-2-ide-1,3-dione Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)[C-]1C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 TURJLPVZRPWSJO-UHFFFAOYSA-N 0.000 description 2
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 2
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000003206 sterilizing agent Substances 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- NMGNJWORLGLLHQ-UHFFFAOYSA-M sulcofuron-sodium Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 NMGNJWORLGLLHQ-UHFFFAOYSA-M 0.000 description 2
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 2
- CTPKSRZFJSJGML-UHFFFAOYSA-N sulfiram Chemical compound CCN(CC)C(=S)SC(=S)N(CC)CC CTPKSRZFJSJGML-UHFFFAOYSA-N 0.000 description 2
- 229950008316 sulfiram Drugs 0.000 description 2
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical compound CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 2
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 2
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 2
- 150000003462 sulfoxides Chemical class 0.000 description 2
- 239000004548 suspo-emulsion Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 229960001367 tartaric acid Drugs 0.000 description 2
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 2
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 2
- LWLJEQHTPVPKSJ-UHFFFAOYSA-N tebufloquin Chemical compound C1=C(C(C)(C)C)C=C2C(OC(=O)C)=C(C)C(C)=NC2=C1F LWLJEQHTPVPKSJ-UHFFFAOYSA-N 0.000 description 2
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 0.000 description 2
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 2
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 2
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 2
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 2
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 2
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 2
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 2
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 2
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 2
- 229960005199 tetramethrin Drugs 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 2
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 2
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 2
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 2
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 2
- GYICYQJEVCIYJY-UHFFFAOYSA-N thiophen-1-ylidenemethanone Chemical compound O=C=S1C=CC=C1 GYICYQJEVCIYJY-UHFFFAOYSA-N 0.000 description 2
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229940074152 thuringiensin Drugs 0.000 description 2
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 description 2
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 2
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 2
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 2
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 2
- JWXZLCFGVKMEEK-UHFFFAOYSA-N triarathene Chemical compound C1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)S1 JWXZLCFGVKMEEK-UHFFFAOYSA-N 0.000 description 2
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 2
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 2
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 2
- ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-UHFFFAOYSA-N 0.000 description 2
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 2
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 2
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 2
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 2
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 2
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 2
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 2
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000012873 virucide Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 238000009333 weeding Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 239000005943 zeta-Cypermethrin Substances 0.000 description 2
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 2
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 1
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- WRGKWWRFSUGDPX-HUUCEWRRSA-N (1R,2R)-1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)cycloheptan-1-ol Chemical compound N1([C@@H]2CCCCC[C@@]2(O)C=2C=CC(Cl)=CC=2)C=NC=N1 WRGKWWRFSUGDPX-HUUCEWRRSA-N 0.000 description 1
- DAASOABUJRMZAD-NRYKZSQYSA-N (1R,4S,5S)-5-(bromomethyl)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene Chemical compound BrC[C@H]1C[C@@]2(Cl)C(Cl)=C(Cl)[C@]1(Cl)C2(Cl)Cl DAASOABUJRMZAD-NRYKZSQYSA-N 0.000 description 1
- VIXCLRUCUMWJFF-KGLIPLIRSA-N (1R,5S)-benzobicyclon Chemical compound CS(=O)(=O)c1ccc(C(=O)C2=C(Sc3ccccc3)[C@H]3CC[C@H](C3)C2=O)c(Cl)c1 VIXCLRUCUMWJFF-KGLIPLIRSA-N 0.000 description 1
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 description 1
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 description 1
- AIAYSXFWIUNXRC-PHIMTYICSA-N (1r,5s)-3-[hydroxy-[2-(2-methoxyethoxymethyl)-6-(trifluoromethyl)pyridin-3-yl]methylidene]bicyclo[3.2.1]octane-2,4-dione Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(O)=C1C(=O)[C@@H](C2)CC[C@@H]2C1=O AIAYSXFWIUNXRC-PHIMTYICSA-N 0.000 description 1
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 description 1
- SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 1
- PGMZYNZXIYOOHJ-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) butanoate Chemical compound CCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br PGMZYNZXIYOOHJ-UHFFFAOYSA-N 0.000 description 1
- BHZWBQPHPLFZSV-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) heptanoate Chemical compound CCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br BHZWBQPHPLFZSV-UHFFFAOYSA-N 0.000 description 1
- DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 1
- ZBCPHFKSIUPISV-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) oxolan-2-ylmethyl carbonate Chemical compound BrC1=CC(C#N)=CC(Br)=C1OC(=O)OCC1OCCC1 ZBCPHFKSIUPISV-UHFFFAOYSA-N 0.000 description 1
- HEJVROKEIMJTIN-UHFFFAOYSA-N (2-butan-2-yl-4,6-dinitrophenyl) (2,4-dinitrophenyl) carbonate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HEJVROKEIMJTIN-UHFFFAOYSA-N 0.000 description 1
- QWZIGUJYMLBQCY-UHFFFAOYSA-N (2-chloro-3,5-diiodopyridin-4-yl) acetate Chemical compound CC(=O)OC1=C(I)C=NC(Cl)=C1I QWZIGUJYMLBQCY-UHFFFAOYSA-N 0.000 description 1
- IPPAUTOBDWNELX-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group C1=C([N+]([O-])=O)C(C(=O)OCC(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 IPPAUTOBDWNELX-UHFFFAOYSA-N 0.000 description 1
- YQRBOMYQIMHOLM-UHFFFAOYSA-M (2-hydroxybenzoyl)oxy-phenylmercury Chemical compound OC1=CC=CC=C1C(=O)O[Hg]C1=CC=CC=C1 YQRBOMYQIMHOLM-UHFFFAOYSA-M 0.000 description 1
- JTBBRGSSVACAJM-UHFFFAOYSA-N (2-methyl-2,3-dihydro-1-benzofuran-7-yl) n-methylcarbamate Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)C2 JTBBRGSSVACAJM-UHFFFAOYSA-N 0.000 description 1
- UGDSMVBQVGFJGW-UHFFFAOYSA-N (2-methyl-5,6,7,8-tetrahydroquinolin-4-yl) n,n-dimethylcarbamate Chemical compound C1CCCC2=C1N=C(C)C=C2OC(=O)N(C)C UGDSMVBQVGFJGW-UHFFFAOYSA-N 0.000 description 1
- BMJYKXALMDAIEG-UHFFFAOYSA-N (2-tert-butyl-4,6-dinitrophenyl) acetate Chemical compound CC(=O)OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1C(C)(C)C BMJYKXALMDAIEG-UHFFFAOYSA-N 0.000 description 1
- YMTQHWMPGDSBOD-UHFFFAOYSA-N (2-tert-butylpyrimidin-5-yl)oxy-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CN=C(C(C)(C)C)N=C1 YMTQHWMPGDSBOD-UHFFFAOYSA-N 0.000 description 1
- WWJFFVUVFNBJTN-UIBIZFFUSA-N (2S)-2-[[(2S,3S,4S)-2-amino-4-hydroxy-4-(5-hydroxypyridin-2-yl)-3-methylbutanoyl]amino]-2-[(2R,3S,4S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]acetic acid Chemical class C[C@@H]([C@H](N)C(=O)N[C@@H]([C@H]1O[C@H]([C@@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O)C(O)=O)[C@H](O)c1ccc(O)cn1 WWJFFVUVFNBJTN-UIBIZFFUSA-N 0.000 description 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
- ROBSGBGTWRRYSK-SNVBAGLBSA-N (2r)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CC=C(C#N)C=C1F ROBSGBGTWRRYSK-SNVBAGLBSA-N 0.000 description 1
- MPPOHAUSNPTFAJ-SECBINFHSA-N (2r)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-SECBINFHSA-N 0.000 description 1
- NYHLMHAKWBUZDY-QMMMGPOBSA-N (2s)-2-[2-chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl]oxypropanoic acid Chemical compound C1=C(Cl)C(C(=O)O[C@@H](C)C(O)=O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NYHLMHAKWBUZDY-QMMMGPOBSA-N 0.000 description 1
- HUNDISMVCBSIKO-UHFFFAOYSA-N (3,5-diethylphenyl) n-methylcarbamate Chemical compound CCC1=CC(CC)=CC(OC(=O)NC)=C1 HUNDISMVCBSIKO-UHFFFAOYSA-N 0.000 description 1
- ZCMOTOWEBLMCEO-UHFFFAOYSA-N (3-chloro-7-methylpyrazolo[1,5-a]pyrimidin-2-yl)oxy-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CC1=CC=NC2=C(Cl)C(OP(=S)(OCC)OCC)=NN21 ZCMOTOWEBLMCEO-UHFFFAOYSA-N 0.000 description 1
- LNGRZPZKVUBWQV-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanone Chemical compound CS(=O)(=O)C1=CC(Cl)=CC=C1C(=O)C1=C(C2CC2)ON=C1 LNGRZPZKVUBWQV-UHFFFAOYSA-N 0.000 description 1
- SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 description 1
- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 1
- JKVBWACRUUUEAR-UHFFFAOYSA-N (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene Chemical compound C1=CC(Cl)=CC=C1SN=NC1=CC(Cl)=C(Cl)C=C1Cl JKVBWACRUUUEAR-UHFFFAOYSA-N 0.000 description 1
- GGQDJKYTNRIKQS-UHFFFAOYSA-N (4-cyano-2,6-diiodophenyl) prop-2-enyl carbonate Chemical compound IC1=CC(C#N)=CC(I)=C1OC(=O)OCC=C GGQDJKYTNRIKQS-UHFFFAOYSA-N 0.000 description 1
- UGJQNSILMBYITH-UHFFFAOYSA-N (4-hydroxyphenyl)iminourea Chemical compound NC(=O)N=Nc1ccc(O)cc1 UGJQNSILMBYITH-UHFFFAOYSA-N 0.000 description 1
- MGRRXBWTLBJEMS-YADHBBJMSA-N (5-benzylfuran-3-yl)methyl (1r,3r)-3-(cyclopentylidenemethyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C([C@H]1C([C@@H]1C(=O)OCC=1C=C(CC=2C=CC=CC=2)OC=1)(C)C)=C1CCCC1 MGRRXBWTLBJEMS-YADHBBJMSA-N 0.000 description 1
- YSEUOPNOQRVVDY-OGEJUEGTSA-N (5-benzylfuran-3-yl)methyl (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 YSEUOPNOQRVVDY-OGEJUEGTSA-N 0.000 description 1
- VEMKTZHHVJILDY-PMACEKPBSA-N (5-benzylfuran-3-yl)methyl (1r,3s)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-PMACEKPBSA-N 0.000 description 1
- QNZZKGBRJAVCIQ-UHFFFAOYSA-N (6-chloro-3,4-dihydro-2h-thiochromen-4-yl)sulfanyl-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound C1=C(Cl)C=C2C(SP(=S)(OCC)OCC)CCSC2=C1 QNZZKGBRJAVCIQ-UHFFFAOYSA-N 0.000 description 1
- IIJPGEXICYPSKQ-UHFFFAOYSA-N (6-ethoxy-2-propan-2-ylpyrimidin-4-yl)oxy-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOC1=CC(OP(=S)(OC)OC)=NC(C(C)C)=N1 IIJPGEXICYPSKQ-UHFFFAOYSA-N 0.000 description 1
- CQRUIYKYVFQBRT-UHFFFAOYSA-N (6-methyl-2-propylpyrimidin-4-yl) n,n-dimethylcarbamate Chemical compound CCCC1=NC(C)=CC(OC(=O)N(C)C)=N1 CQRUIYKYVFQBRT-UHFFFAOYSA-N 0.000 description 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 description 1
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 description 1
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 description 1
- ULDHMXUKGWMISQ-VIFPVBQESA-N (S)-(+)-Carvone Natural products CC(=C)[C@H]1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-VIFPVBQESA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 description 1
- OVXMBIVWNJDDSM-UHFFFAOYSA-N (benzhydrylideneamino) 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(=O)ON=C(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 OVXMBIVWNJDDSM-UHFFFAOYSA-N 0.000 description 1
- ZJXKMHFMOPXCOJ-BIIKFXOESA-N (e)-4-[4-[4-(trifluoromethyl)phenoxy]phenoxy]pent-2-enoic acid Chemical compound C1=CC(OC(C)\C=C\C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 ZJXKMHFMOPXCOJ-BIIKFXOESA-N 0.000 description 1
- FHTHQERUYXJRSJ-LSFURLLWSA-N (e)-[4-[1-[4-(trifluoromethoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]methylidenehydrazine Chemical compound C1=CC(/C=N/N)=CC=C1C1=NN(C=2C=CC(OC(F)(F)F)=CC=2)C=N1 FHTHQERUYXJRSJ-LSFURLLWSA-N 0.000 description 1
- SZOLUXDHHKCYKT-ONEGZZNKSA-N (e)-but-1-en-1-amine Chemical compound CC\C=C\N SZOLUXDHHKCYKT-ONEGZZNKSA-N 0.000 description 1
- IKNXXTIMVROREQ-WXXKFALUSA-N (e)-but-2-enedioic acid;[2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl]-imidazol-1-ylmethanone Chemical compound OC(=O)\C=C\C(O)=O.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 IKNXXTIMVROREQ-WXXKFALUSA-N 0.000 description 1
- DQXKOHDUMJLXKH-PHEQNACWSA-N (e)-n-[2-[2-[[(e)-oct-2-enoyl]amino]ethyldisulfanyl]ethyl]oct-2-enamide Chemical compound CCCCC\C=C\C(=O)NCCSSCCNC(=O)\C=C\CCCCC DQXKOHDUMJLXKH-PHEQNACWSA-N 0.000 description 1
- IBHCSFXTRODDNR-CYBMUJFWSA-N (propan-2-ylideneamino) (2r)-2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate Chemical compound C1=CC(O[C@H](C)C(=O)ON=C(C)C)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 IBHCSFXTRODDNR-CYBMUJFWSA-N 0.000 description 1
- RRLHZVASKJLNFJ-UPHRSURJSA-N (z)-2,3,5,5,5-pentachloro-4-oxopent-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(\Cl)C(=O)C(Cl)(Cl)Cl RRLHZVASKJLNFJ-UPHRSURJSA-N 0.000 description 1
- QVLAWKAXOMEXPM-UHFFFAOYSA-N 1,1,1,2-tetrachloroethane Chemical class ClCC(Cl)(Cl)Cl QVLAWKAXOMEXPM-UHFFFAOYSA-N 0.000 description 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 description 1
- DQCMWCVJSOFDSA-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl.CC(Cl)(Cl)Cl DQCMWCVJSOFDSA-UHFFFAOYSA-N 0.000 description 1
- FCAKZZMVXCLLHM-UHFFFAOYSA-N 1,1-dimethyl-3-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]urea Chemical compound CN(C)C(=O)NC1=CC=CC(OC(F)(F)C(F)F)=C1 FCAKZZMVXCLLHM-UHFFFAOYSA-N 0.000 description 1
- IKAACYWAXDLDPM-UHFFFAOYSA-N 1,2,3,4,4a,5-hexahydronaphthalene Chemical compound C1=CCC2CCCCC2=C1 IKAACYWAXDLDPM-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- XFNJYAKDBJUJAJ-UHFFFAOYSA-N 1,2-dibromopropane Chemical compound CC(Br)CBr XFNJYAKDBJUJAJ-UHFFFAOYSA-N 0.000 description 1
- HWUQTXJBKRUEII-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl.CC(Cl)CCl HWUQTXJBKRUEII-UHFFFAOYSA-N 0.000 description 1
- JJSBMWMYKICVIZ-UHFFFAOYSA-N 1,3,5-trichloro-2-[ethoxy(propylsulfanyl)phosphoryl]oxybenzene Chemical compound CCCSP(=O)(OCC)OC1=C(Cl)C=C(Cl)C=C1Cl JJSBMWMYKICVIZ-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- YVPVBTOOGFLALI-UHFFFAOYSA-N 1,3-dichloroprop-1-ene Chemical compound ClCC=CCl.ClCC=CCl YVPVBTOOGFLALI-UHFFFAOYSA-N 0.000 description 1
- MYMALJRSNVUBAI-UHFFFAOYSA-N 1,3-thiazol-4-imine Chemical compound N=C1CSC=N1 MYMALJRSNVUBAI-UHFFFAOYSA-N 0.000 description 1
- IHDKBHLTKNUCCW-UHFFFAOYSA-N 1,3-thiazole 1-oxide Chemical compound O=S1C=CN=C1 IHDKBHLTKNUCCW-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical class ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- HJTAZXHBEBIQQX-UHFFFAOYSA-N 1,5-bis(chloromethyl)naphthalene Chemical compound C1=CC=C2C(CCl)=CC=CC2=C1CCl HJTAZXHBEBIQQX-UHFFFAOYSA-N 0.000 description 1
- AALBAFHYFNQXNT-UHFFFAOYSA-N 1-$l^{1}-oxidanylcyclobutene Chemical compound O=C1[CH]CC1 AALBAFHYFNQXNT-UHFFFAOYSA-N 0.000 description 1
- KTPQMGCGSZEAEJ-UHFFFAOYSA-N 1-$l^{1}-oxidanylcyclopentene Chemical compound O=C1[CH]CCC1 KTPQMGCGSZEAEJ-UHFFFAOYSA-N 0.000 description 1
- IHSBKMBNDURWAT-UHFFFAOYSA-N 1-(1,1,4-trimethyl-6-propan-2-yl-2,3-dihydroinden-5-yl)propan-1-one Chemical compound C1=C(C(C)C)C(C(=O)CC)=C(C)C2=C1C(C)(C)CC2 IHSBKMBNDURWAT-UHFFFAOYSA-N 0.000 description 1
- NCJRWSQYSLEKEI-UHFFFAOYSA-N 1-(1,3-benzothiazol-2-yl)-3-propan-2-ylurea Chemical compound C1=CC=C2SC(NC(=O)NC(C)C)=NC2=C1 NCJRWSQYSLEKEI-UHFFFAOYSA-N 0.000 description 1
- DHYXNIKICPUXJI-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-n-(2,4-difluorophenyl)-5-oxo-n-propan-2-yl-1,2,4-triazole-4-carboxamide Chemical compound C=1C=C(F)C=C(F)C=1N(C(C)C)C(=O)N(C1=O)C=NN1C1=CC=C(Cl)C=C1Cl DHYXNIKICPUXJI-UHFFFAOYSA-N 0.000 description 1
- PYCINWWWERDNKE-UHFFFAOYSA-N 1-(2-chloro-6-propylimidazo[1,2-b]pyridazin-3-yl)sulfonyl-3-(4,6-dimethoxypyrimidin-2-yl)urea Chemical compound N12N=C(CCC)C=CC2=NC(Cl)=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 PYCINWWWERDNKE-UHFFFAOYSA-N 0.000 description 1
- WPRAXAOJIODQJR-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)ethanone Chemical compound CC(=O)C1=CC=C(C)C(C)=C1 WPRAXAOJIODQJR-UHFFFAOYSA-N 0.000 description 1
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 description 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- RURQAJURNPMSSK-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3-{[2-(4-ethoxyphenyl)-3,3,3-trifluoropropoxy]methyl}benzene Chemical compound C1=CC(OCC)=CC=C1C(C(F)(F)F)COCC1=CC=CC(OC=2C=CC(Cl)=CC=2)=C1 RURQAJURNPMSSK-UHFFFAOYSA-N 0.000 description 1
- JIGPTDXPKKMNCN-UHFFFAOYSA-N 1-(5-butylsulfonyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Chemical compound CCCCS(=O)(=O)C1=NN=C(N(C)C(=O)NC)S1 JIGPTDXPKKMNCN-UHFFFAOYSA-N 0.000 description 1
- GUGLRTKPJBGNAF-UHFFFAOYSA-N 1-(5-tert-butyl-1,2-oxazol-3-yl)-3-methylurea Chemical compound CNC(=O)NC=1C=C(C(C)(C)C)ON=1 GUGLRTKPJBGNAF-UHFFFAOYSA-N 0.000 description 1
- HVQHXBNMBZJPLK-UHFFFAOYSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[(2-methylprop-2-en-1-yl)amino]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound CC(=C)CNC1=C([S+]([O-])C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl HVQHXBNMBZJPLK-UHFFFAOYSA-N 0.000 description 1
- LWWDYSLFWMWORA-BEJOPBHTSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[(E)-(4-hydroxy-3-methoxyphenyl)methylideneamino]-4-(trifluoromethylsulfanyl)pyrazole-3-carbonitrile Chemical compound c1cc(O)c(OC)cc1\C=N\c1c(SC(F)(F)F)c(C#N)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl LWWDYSLFWMWORA-BEJOPBHTSA-N 0.000 description 1
- IXWKBUKANTXHJH-UHFFFAOYSA-N 1-[5-chloro-2-methyl-4-(5-methyl-5,6-dihydro-1,4,2-dioxazin-3-yl)pyrazol-3-yl]sulfonyl-3-(4,6-dimethoxypyrimidin-2-yl)urea Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C=2OC(C)CON=2)C)=N1 IXWKBUKANTXHJH-UHFFFAOYSA-N 0.000 description 1
- KOKBUARVIJVMMM-UHFFFAOYSA-N 1-amino-3-(2,2-dimethylpropyl)-6-ethylsulfanyl-1,3,5-triazine-2,4-dione Chemical compound CCSC1=NC(=O)N(CC(C)(C)C)C(=O)N1N KOKBUARVIJVMMM-UHFFFAOYSA-N 0.000 description 1
- DELJNDWGTWHHFA-UHFFFAOYSA-N 1-azaniumylpropyl(hydroxy)phosphinate Chemical compound CCC(N)P(O)(O)=O DELJNDWGTWHHFA-UHFFFAOYSA-N 0.000 description 1
- ORPVVAKYSXQCJI-UHFFFAOYSA-N 1-bromo-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1Br ORPVVAKYSXQCJI-UHFFFAOYSA-N 0.000 description 1
- ZKDOQFPDSUOLGF-UHFFFAOYSA-N 1-bromo-3-chloro-2-methylpropane Chemical compound ClCC(C)CBr ZKDOQFPDSUOLGF-UHFFFAOYSA-N 0.000 description 1
- YPWDDFGPYBIPBG-UHFFFAOYSA-N 1-bromo-4-[1-(4-bromophenyl)-2,2,2-trichloroethyl]benzene Chemical compound C=1C=C(Br)C=CC=1C(C(Cl)(Cl)Cl)C1=CC=C(Br)C=C1 YPWDDFGPYBIPBG-UHFFFAOYSA-N 0.000 description 1
- NIDSRGCVYOEDFW-UHFFFAOYSA-N 1-bromo-4-chlorobutane Chemical compound ClCCCCBr NIDSRGCVYOEDFW-UHFFFAOYSA-N 0.000 description 1
- HDVSGSCCJZSVQP-UHFFFAOYSA-N 1-butoxypropan-2-yl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CCCCOCC(C)OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl HDVSGSCCJZSVQP-UHFFFAOYSA-N 0.000 description 1
- ZKFARSBUEBZZJT-UHFFFAOYSA-N 1-butoxypropan-2-yl 2-(4-amino-3,5-dichloro-6-fluoropyridin-2-yl)oxyacetate Chemical group CCCCOCC(C)OC(=O)COC1=NC(F)=C(Cl)C(N)=C1Cl ZKFARSBUEBZZJT-UHFFFAOYSA-N 0.000 description 1
- VVFYQBFGXTYSMW-UHFFFAOYSA-N 1-chloro-1-phenoxyethanol Chemical compound CC(O)(Cl)OC1=CC=CC=C1 VVFYQBFGXTYSMW-UHFFFAOYSA-N 0.000 description 1
- SKKUAUZTZZRYPW-UHFFFAOYSA-N 1-chloro-2,4-dinitronaphthalene Chemical compound C1=CC=CC2=C(Cl)C([N+](=O)[O-])=CC([N+]([O-])=O)=C21 SKKUAUZTZZRYPW-UHFFFAOYSA-N 0.000 description 1
- GBZXOIUBLKUSJR-UHFFFAOYSA-N 1-chloro-4-[(4-fluorophenyl)sulfanylmethyl]benzene Chemical compound C1=CC(F)=CC=C1SCC1=CC=C(Cl)C=C1 GBZXOIUBLKUSJR-UHFFFAOYSA-N 0.000 description 1
- WLKSPGHQGFFKGE-UHFFFAOYSA-N 1-chloropropan-2-yl n-(3-chlorophenyl)carbamate Chemical compound ClCC(C)OC(=O)NC1=CC=CC(Cl)=C1 WLKSPGHQGFFKGE-UHFFFAOYSA-N 0.000 description 1
- PWKNBLFSJAVFAB-UHFFFAOYSA-N 1-fluoro-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1F PWKNBLFSJAVFAB-UHFFFAOYSA-N 0.000 description 1
- BXKKQFGRMSOANI-UHFFFAOYSA-N 1-methoxy-3-[4-[(2-methoxy-2,4,4-trimethyl-3h-chromen-7-yl)oxy]phenyl]-1-methylurea Chemical compound C1=CC(NC(=O)N(C)OC)=CC=C1OC1=CC=C2C(C)(C)CC(C)(OC)OC2=C1 BXKKQFGRMSOANI-UHFFFAOYSA-N 0.000 description 1
- WXJYKXOIFICRPR-UHFFFAOYSA-L 1-methyl-4-(1-methylpyridin-1-ium-4-yl)pyridin-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.COS([O-])(=O)=O.C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 WXJYKXOIFICRPR-UHFFFAOYSA-L 0.000 description 1
- LMGBDZJLZIPJPZ-UHFFFAOYSA-M 1-methyl-4-phenylpyridin-1-ium;chloride Chemical compound [Cl-].C1=C[N+](C)=CC=C1C1=CC=CC=C1 LMGBDZJLZIPJPZ-UHFFFAOYSA-M 0.000 description 1
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 description 1
- PNXGNYJXJBKFRG-UHFFFAOYSA-N 1-pent-4-ynoxy-4-phenoxybenzene Chemical compound C1=CC(OCCCC#C)=CC=C1OC1=CC=CC=C1 PNXGNYJXJBKFRG-UHFFFAOYSA-N 0.000 description 1
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
- YRBRVMGXTWJLBZ-UHFFFAOYSA-N 1h-imidazole;1h-pyrrole Chemical class C=1C=CNC=1.C1=CNC=N1 YRBRVMGXTWJLBZ-UHFFFAOYSA-N 0.000 description 1
- YNEKMCSWRMRXIR-UHFFFAOYSA-N 2,3,5,5-tetrachloro-4,7-bis(chloromethyl)-7-(dichloromethyl)bicyclo[2.2.1]heptane Chemical compound C1C(Cl)(Cl)C2(CCl)C(Cl)C(Cl)C1C2(C(Cl)Cl)CCl YNEKMCSWRMRXIR-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- KVJOLVBEUYUHLD-UHFFFAOYSA-M 2,3-dihydroxypropylsulfanyl(ethyl)mercury Chemical compound CC[Hg]SCC(O)CO KVJOLVBEUYUHLD-UHFFFAOYSA-M 0.000 description 1
- 239000002794 2,4-DB Substances 0.000 description 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 1
- ZGPVUVBRTCPAPZ-UHFFFAOYSA-N 2,4-dichloro-1-[ethoxy(propylsulfanyl)phosphoryl]oxybenzene Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Cl)C=C1Cl ZGPVUVBRTCPAPZ-UHFFFAOYSA-N 0.000 description 1
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- NIOPZPCMRQGZCE-WEVVVXLNSA-N 2,4-dinitro-6-(octan-2-yl)phenyl (E)-but-2-enoate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)\C=C\C NIOPZPCMRQGZCE-WEVVVXLNSA-N 0.000 description 1
- XEPBBUCQCXXTGR-UHFFFAOYSA-N 2,5-dimethyl-n-phenylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC=2C=CC=CC=2)=C1C XEPBBUCQCXXTGR-UHFFFAOYSA-N 0.000 description 1
- CCBICDLNWJRFPO-UHFFFAOYSA-N 2,6-dichloroindophenol Chemical compound C1=CC(O)=CC=C1N=C1C=C(Cl)C(=O)C(Cl)=C1 CCBICDLNWJRFPO-UHFFFAOYSA-N 0.000 description 1
- KGKGSIUWJCAFPX-UHFFFAOYSA-N 2,6-dichlorothiobenzamide Chemical compound NC(=S)C1=C(Cl)C=CC=C1Cl KGKGSIUWJCAFPX-UHFFFAOYSA-N 0.000 description 1
- QZKXBNCXPQMZLF-UHFFFAOYSA-N 2-(2,4,5-trichlorophenoxy)acetate;triethylazanium Chemical compound CCN(CC)CC.OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl QZKXBNCXPQMZLF-UHFFFAOYSA-N 0.000 description 1
- ATKFMEGWDYLXBP-UHFFFAOYSA-N 2-(2,4,5-trichlorophenoxy)ethanol Chemical compound OCCOC1=CC(Cl)=C(Cl)C=C1Cl ATKFMEGWDYLXBP-UHFFFAOYSA-N 0.000 description 1
- VQRSXYVRBBWVSQ-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;diethylazanium Chemical compound CCNCC.OC(=O)COC1=CC=C(Cl)C=C1Cl VQRSXYVRBBWVSQ-UHFFFAOYSA-N 0.000 description 1
- IUQJDHJVPLLKFL-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;dimethylazanium Chemical compound CNC.OC(=O)COC1=CC=C(Cl)C=C1Cl IUQJDHJVPLLKFL-UHFFFAOYSA-N 0.000 description 1
- DLDBIAPNKRBPRS-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;tetradecylazanium Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl.CCCCCCCCCCCCCCN DLDBIAPNKRBPRS-UHFFFAOYSA-N 0.000 description 1
- GDOSCZDDZQGBAJ-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetic acid;dodecan-1-amine Chemical compound CCCCCCCCCCCCN.OC(=O)COC1=CC=C(Cl)C=C1Cl GDOSCZDDZQGBAJ-UHFFFAOYSA-N 0.000 description 1
- UTILIQPPRUUSFN-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetic acid;heptan-1-amine Chemical compound CCCCCCCN.OC(=O)COC1=CC=C(Cl)C=C1Cl UTILIQPPRUUSFN-UHFFFAOYSA-N 0.000 description 1
- FEGJYGNUIXVOOQ-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetic acid;n,n-diethylethanamine Chemical compound CCN(CC)CC.OC(=O)COC1=CC=C(Cl)C=C1Cl FEGJYGNUIXVOOQ-UHFFFAOYSA-N 0.000 description 1
- HXMBBZAHRWCZOX-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetic acid;propan-2-amine Chemical compound CC(C)[NH3+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl HXMBBZAHRWCZOX-UHFFFAOYSA-N 0.000 description 1
- LGURYBCSJPXHTF-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)ethyl benzoate Chemical compound ClC1=CC(Cl)=CC=C1OCCOC(=O)C1=CC=CC=C1 LGURYBCSJPXHTF-UHFFFAOYSA-N 0.000 description 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 description 1
- JVGPVVUTUMQJKL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl thiocyanate Chemical compound CCCCOCCOCCSC#N JVGPVVUTUMQJKL-UHFFFAOYSA-N 0.000 description 1
- OILIYWFQRJOPAI-UHFFFAOYSA-N 2-(2-chlorophenyl)-1h-benzimidazole Chemical compound ClC1=CC=CC=C1C1=NC2=CC=CC=C2N1 OILIYWFQRJOPAI-UHFFFAOYSA-N 0.000 description 1
- BIPAGODSEBNAJR-UHFFFAOYSA-N 2-(3,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C(Cl)=C1 BIPAGODSEBNAJR-UHFFFAOYSA-N 0.000 description 1
- ROKVVMOXSZIDEG-UHFFFAOYSA-N 2-(3,5,6-trichloropyridin-2-yl)oxyacetate;triethylazanium Chemical compound CCN(CC)CC.OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl ROKVVMOXSZIDEG-UHFFFAOYSA-N 0.000 description 1
- RUGYNGIMTAFTLP-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-1h-benzimidazole Chemical compound N1=C(C)C=C(C)N1C1=NC2=CC=CC=C2N1 RUGYNGIMTAFTLP-UHFFFAOYSA-N 0.000 description 1
- YNTJKQDWYXUTLZ-UHFFFAOYSA-N 2-(3-chlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=CC(Cl)=C1 YNTJKQDWYXUTLZ-UHFFFAOYSA-N 0.000 description 1
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 description 1
- CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 description 1
- GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 description 1
- VTGXDWHWZQHAPU-UHFFFAOYSA-N 2-(aminomethyl)phenol iodo hypoiodite Chemical compound C(C=1C(O)=CC=CC1)N.IOI VTGXDWHWZQHAPU-UHFFFAOYSA-N 0.000 description 1
- ISERORSDFSDMDV-UHFFFAOYSA-N 2-(n-(2-chloroacetyl)-2,6-diethylanilino)acetic acid Chemical compound CCC1=CC=CC(CC)=C1N(CC(O)=O)C(=O)CCl ISERORSDFSDMDV-UHFFFAOYSA-N 0.000 description 1
- WZZRJCUYSKKFHO-UHFFFAOYSA-N 2-(n-benzoyl-3,4-dichloroanilino)propanoic acid Chemical compound C=1C=C(Cl)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 WZZRJCUYSKKFHO-UHFFFAOYSA-N 0.000 description 1
- FHCUXGCMUASJQQ-UHFFFAOYSA-N 2-[(2-chlorophenyl)methylsulfanyl]-5-propyl-1,3,4-oxadiazole Chemical compound O1C(CCC)=NN=C1SCC1=CC=CC=C1Cl FHCUXGCMUASJQQ-UHFFFAOYSA-N 0.000 description 1
- HCNBYBFTNHEQQJ-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(N=2)C(F)(F)F)C(O)=O)=N1 HCNBYBFTNHEQQJ-UHFFFAOYSA-N 0.000 description 1
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 description 1
- ZAIWHXZLOUBQCG-UHFFFAOYSA-N 2-[(5-bromo-6-oxo-1-phenylpyridazin-4-yl)amino]-2-oxoacetic acid;2-(dimethylamino)ethanol Chemical compound CN(C)CCO.O=C1C(Br)=C(NC(=O)C(=O)O)C=NN1C1=CC=CC=C1 ZAIWHXZLOUBQCG-UHFFFAOYSA-N 0.000 description 1
- YXBDMGSFNUJTBR-NFSGWXFISA-N 2-[(E)-N-[(E)-3-chloroprop-2-enoxy]-C-propylcarbonimidoyl]-5-(2-ethylsulfanylpropyl)-3-hydroxycyclohex-2-en-1-one Chemical compound Cl/C=C/CO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O YXBDMGSFNUJTBR-NFSGWXFISA-N 0.000 description 1
- IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 description 1
- OVQJTYOXWVHPTA-UHFFFAOYSA-N 2-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-nitropyrazol-3-amine Chemical compound NC1=C([N+]([O-])=O)C=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl OVQJTYOXWVHPTA-UHFFFAOYSA-N 0.000 description 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 description 1
- FSKNXCHJIFBRBT-UHFFFAOYSA-N 2-[2-[2-(dodecylamino)ethylamino]ethylamino]acetic acid Chemical compound CCCCCCCCCCCCNCCNCCNCC(O)=O FSKNXCHJIFBRBT-UHFFFAOYSA-N 0.000 description 1
- GQQIAHNFBAFBCS-UHFFFAOYSA-N 2-[2-chloro-5-(1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)-4-fluorophenoxy]acetic acid Chemical compound C1=C(Cl)C(OCC(=O)O)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F GQQIAHNFBAFBCS-UHFFFAOYSA-N 0.000 description 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 description 1
- SVGBNTOHFITEDI-UHFFFAOYSA-N 2-[4-(3,5-dichloropyridin-2-yl)oxyphenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1Cl SVGBNTOHFITEDI-UHFFFAOYSA-N 0.000 description 1
- BSFAVVHPEZCASB-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1 BSFAVVHPEZCASB-UHFFFAOYSA-N 0.000 description 1
- VAZKTDRSMMSAQB-UHFFFAOYSA-N 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 VAZKTDRSMMSAQB-UHFFFAOYSA-N 0.000 description 1
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
- ONNQFZOZHDEENE-UHFFFAOYSA-N 2-[5-(but-3-yn-2-yloxy)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione Chemical compound C1=C(Cl)C(OC(C)C#C)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F ONNQFZOZHDEENE-UHFFFAOYSA-N 0.000 description 1
- XAYMVFWOJIOUTA-UHFFFAOYSA-N 2-[8-[8-(diaminomethylideneamino)octylamino]octyl]guanidine;2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O.NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N XAYMVFWOJIOUTA-UHFFFAOYSA-N 0.000 description 1
- WUZNHSBFPPFULJ-UHFFFAOYSA-N 2-[[4-chloro-6-(cyclopropylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile Chemical compound N#CC(C)(C)NC1=NC(Cl)=NC(NC2CC2)=N1 WUZNHSBFPPFULJ-UHFFFAOYSA-N 0.000 description 1
- WZMRBCPVLHJXNQ-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]-2-chloroethanol Chemical compound ClC(N(CCO)CCO)CO WZMRBCPVLHJXNQ-UHFFFAOYSA-N 0.000 description 1
- ULNWEXDKQHEUSK-UHFFFAOYSA-N 2-[ethoxy-(propan-2-ylamino)phosphoryl]sulfanyl-n-methyl-n-phenylacetamide Chemical compound CCOP(=O)(NC(C)C)SCC(=O)N(C)C1=CC=CC=C1 ULNWEXDKQHEUSK-UHFFFAOYSA-N 0.000 description 1
- RCOHXZITQFQFRZ-UHFFFAOYSA-N 2-[n-[2-(3,5-dichloro-2-methoxybenzoyl)oxyethyl]anilino]ethyl 3,6-dichloro-2-methoxybenzoate Chemical compound COC1=C(Cl)C=C(Cl)C=C1C(=O)OCCN(C=1C=CC=CC=1)CCOC(=O)C1=C(Cl)C=CC(Cl)=C1OC RCOHXZITQFQFRZ-UHFFFAOYSA-N 0.000 description 1
- AHZYHYXTZOYUEV-UHFFFAOYSA-N 2-amino-1-chloroethanol Chemical compound NCC(O)Cl AHZYHYXTZOYUEV-UHFFFAOYSA-N 0.000 description 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
- NQQBTWVFKDDVIB-UHFFFAOYSA-N 2-aminoethanol;3,6-dichloropyridine-2-carboxylic acid Chemical compound NCCO.OC(=O)C1=NC(Cl)=CC=C1Cl NQQBTWVFKDDVIB-UHFFFAOYSA-N 0.000 description 1
- ODFHXXQVNHHDDG-UHFFFAOYSA-N 2-benzylpropanedinitrile Chemical compound N#CC(C#N)CC1=CC=CC=C1 ODFHXXQVNHHDDG-UHFFFAOYSA-N 0.000 description 1
- ALTMCDJIFXTEPV-UHFFFAOYSA-N 2-bromo-1-[4-(diethylamino)phenyl]ethanone Chemical compound CCN(CC)C1=CC=C(C(=O)CBr)C=C1 ALTMCDJIFXTEPV-UHFFFAOYSA-N 0.000 description 1
- LSTRKXWIZZZYAS-UHFFFAOYSA-N 2-bromoacetyl bromide Chemical compound BrCC(Br)=O LSTRKXWIZZZYAS-UHFFFAOYSA-N 0.000 description 1
- MONMFXREYOKQTI-UHFFFAOYSA-N 2-bromopropanoic acid Chemical compound CC(Br)C(O)=O MONMFXREYOKQTI-UHFFFAOYSA-N 0.000 description 1
- ZMWGIGHRZQTQRE-UHFFFAOYSA-N 2-butoxyethyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCOCCOC(=O)COC1=CC=C(Cl)C=C1Cl ZMWGIGHRZQTQRE-UHFFFAOYSA-N 0.000 description 1
- IVDRCZNHVGQBHZ-UHFFFAOYSA-N 2-butoxyethyl 2-(3,5,6-trichloropyridin-2-yl)oxyacetate Chemical group CCCCOCCOC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl IVDRCZNHVGQBHZ-UHFFFAOYSA-N 0.000 description 1
- OFYUBGDUYQVZHD-UHFFFAOYSA-N 2-butoxypropyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CCCCOC(C)COC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl OFYUBGDUYQVZHD-UHFFFAOYSA-N 0.000 description 1
- LRWRQXJLRYTGCK-UHFFFAOYSA-N 2-butoxypropyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCOC(C)COC(=O)COC1=CC=C(Cl)C=C1Cl LRWRQXJLRYTGCK-UHFFFAOYSA-N 0.000 description 1
- ZGGSVBWJVIXBHV-UHFFFAOYSA-N 2-chloro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1Cl ZGGSVBWJVIXBHV-UHFFFAOYSA-N 0.000 description 1
- QCTALYCTVMUWPT-UHFFFAOYSA-N 2-chloro-3-(4-chlorophenyl)propanoic acid Chemical compound OC(=O)C(Cl)CC1=CC=C(Cl)C=C1 QCTALYCTVMUWPT-UHFFFAOYSA-N 0.000 description 1
- QEGVVEOAVNHRAA-UHFFFAOYSA-N 2-chloro-6-(4,6-dimethoxypyrimidin-2-yl)sulfanylbenzoic acid Chemical compound COC1=CC(OC)=NC(SC=2C(=C(Cl)C=CC=2)C(O)=O)=N1 QEGVVEOAVNHRAA-UHFFFAOYSA-N 0.000 description 1
- OGBSAJWRIPNIER-UHFFFAOYSA-N 2-chloro-6-(furan-2-ylmethoxy)-4-(trichloromethyl)pyridine Chemical compound ClC1=CC(C(Cl)(Cl)Cl)=CC(OCC=2OC=CC=2)=N1 OGBSAJWRIPNIER-UHFFFAOYSA-N 0.000 description 1
- RPCKKUFLSMORHB-UHFFFAOYSA-N 2-chloro-6-methoxy-4-(trichloromethyl)pyridine Chemical compound COC1=CC(C(Cl)(Cl)Cl)=CC(Cl)=N1 RPCKKUFLSMORHB-UHFFFAOYSA-N 0.000 description 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
- CQQUWTMMFMJEFE-UHFFFAOYSA-N 2-chloro-n,n-diethylacetamide Chemical compound CCN(CC)C(=O)CCl CQQUWTMMFMJEFE-UHFFFAOYSA-N 0.000 description 1
- CPKUDYUJOXRCAJ-UHFFFAOYSA-N 2-chloroacetic acid Chemical compound OC(=O)CCl.OC(=O)CCl CPKUDYUJOXRCAJ-UHFFFAOYSA-N 0.000 description 1
- GYJQWEIGUGMFMU-UHFFFAOYSA-N 2-chloroethyl n-(3-chlorophenyl)carbamate Chemical compound ClCCOC(=O)NC1=CC=CC(Cl)=C1 GYJQWEIGUGMFMU-UHFFFAOYSA-N 0.000 description 1
- IWRFWZPCCDGEFJ-UXBLZVDNSA-N 2-cyanoethyl (1e)-n-(methylcarbamoyloxy)ethanimidothioate Chemical compound CNC(=O)O\N=C(/C)SCCC#N IWRFWZPCCDGEFJ-UXBLZVDNSA-N 0.000 description 1
- PJISLFCKHOHLLP-UHFFFAOYSA-N 2-diethoxyphosphorylsulfanyl-n,n-diethylethanamine Chemical compound CCOP(=O)(OCC)SCCN(CC)CC PJISLFCKHOHLLP-UHFFFAOYSA-N 0.000 description 1
- YHDXOFFTMOZZPE-UHFFFAOYSA-N 2-ethyl-3-[3-ethyl-5-(4-ethylphenoxy)pentyl]-2-methyloxirane Chemical compound O1C(CC)(C)C1CCC(CC)CCOC1=CC=C(CC)C=C1 YHDXOFFTMOZZPE-UHFFFAOYSA-N 0.000 description 1
- ZDOOQPFIGYHZFV-UHFFFAOYSA-N 2-ethyl-4-[(4-phenoxyphenoxy)methyl]-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C=C1)=CC=C1OC1=CC=CC=C1 ZDOOQPFIGYHZFV-UHFFFAOYSA-N 0.000 description 1
- MNELUOHPQMJXGU-UHFFFAOYSA-N 2-ethylhexyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CCCCC(CC)COC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl MNELUOHPQMJXGU-UHFFFAOYSA-N 0.000 description 1
- QZSFJRIWRPJUOH-UHFFFAOYSA-N 2-ethylhexyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCC(CC)COC(=O)COC1=CC=C(Cl)C=C1Cl QZSFJRIWRPJUOH-UHFFFAOYSA-N 0.000 description 1
- RPDJBUSVCYFTRU-UHFFFAOYSA-N 2-ethylhexyl 4-amino-3,5,6-trichloropyridine-2-carboxylate Chemical group CCCCC(CC)COC(=O)C1=NC(Cl)=C(Cl)C(N)=C1Cl RPDJBUSVCYFTRU-UHFFFAOYSA-N 0.000 description 1
- ADRPZEYTIFWCBC-UHFFFAOYSA-N 2-fluoro-n-methyl-n-naphthalen-1-ylacetamide Chemical compound C1=CC=C2C(N(C(=O)CF)C)=CC=CC2=C1 ADRPZEYTIFWCBC-UHFFFAOYSA-N 0.000 description 1
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 1
- FYEWDLAVQKIKQE-UHFFFAOYSA-N 2-methyl-4-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazinane-3,5-dione Chemical compound O=C1N(C)OCC(=O)N1C1=CC=CC(C(F)(F)F)=C1 FYEWDLAVQKIKQE-UHFFFAOYSA-N 0.000 description 1
- ZRNSSRODJSSVEJ-UHFFFAOYSA-N 2-methylpentacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(C)C ZRNSSRODJSSVEJ-UHFFFAOYSA-N 0.000 description 1
- KIIVFWSIMRWBKW-UHFFFAOYSA-N 2-methylpropyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CC(C)COC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl KIIVFWSIMRWBKW-UHFFFAOYSA-N 0.000 description 1
- GPSGZZSRFJXXBA-UHFFFAOYSA-N 2-methylpropyl 2-(2,4-dichlorophenoxy)acetate Chemical group CC(C)COC(=O)COC1=CC=C(Cl)C=C1Cl GPSGZZSRFJXXBA-UHFFFAOYSA-N 0.000 description 1
- NDAWJMAYLOFILH-UHFFFAOYSA-N 2-methylpropyl 3-[benzyl(methyl)amino]-2-cyanoprop-2-enoate Chemical compound CC(C)COC(=O)C(C#N)=CN(C)CC1=CC=CC=C1 NDAWJMAYLOFILH-UHFFFAOYSA-N 0.000 description 1
- PIAOLBVUVDXHHL-UHFFFAOYSA-N 2-nitroethenylbenzene Chemical compound [O-][N+](=O)C=CC1=CC=CC=C1 PIAOLBVUVDXHHL-UHFFFAOYSA-N 0.000 description 1
- IDPWXVBDDIYDKT-UHFFFAOYSA-N 2-phenoxyquinoline Chemical compound C=1C=C2C=CC=CC2=NC=1OC1=CC=CC=C1 IDPWXVBDDIYDKT-UHFFFAOYSA-N 0.000 description 1
- 229940061334 2-phenylphenol Drugs 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- UFAPVJDEYHLLBG-UHFFFAOYSA-N 2-{2-chloro-4-(methylsulfonyl)-3-[(tetrahydrofuran-2-ylmethoxy)methyl]benzoyl}cyclohexane-1,3-dione Chemical compound ClC1=C(COCC2OCCC2)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O UFAPVJDEYHLLBG-UHFFFAOYSA-N 0.000 description 1
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 description 1
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 description 1
- AUQAUAIUNJIIEP-UHFFFAOYSA-N 3,4,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(C)C(C)=C1 AUQAUAIUNJIIEP-UHFFFAOYSA-N 0.000 description 1
- NRAYWXLNSHEHQO-UHFFFAOYSA-N 3-(1-benzothiophen-2-yl)-5,6-dihydro-1,4,2-oxathiazine 4-oxide Chemical compound O=S1CCON=C1C1=CC2=CC=CC=C2S1 NRAYWXLNSHEHQO-UHFFFAOYSA-N 0.000 description 1
- OVFHHJZHXHZIHT-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)quinazolin-4-one Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C2=CC=CC=C2N=C1N1N=CN=C1 OVFHHJZHXHZIHT-UHFFFAOYSA-N 0.000 description 1
- SWBHWUYHHJCADA-UHFFFAOYSA-N 3-(2-chlorophenyl)-6-(2,6-difluorophenyl)-1,2,4,5-tetrazine Chemical compound FC1=CC=CC(F)=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 SWBHWUYHHJCADA-UHFFFAOYSA-N 0.000 description 1
- BZGLBXYQOMFXAU-UHFFFAOYSA-N 3-(2-methylpiperidin-1-yl)propyl 3,4-dichlorobenzoate Chemical compound CC1CCCCN1CCCOC(=O)C1=CC=C(Cl)C(Cl)=C1 BZGLBXYQOMFXAU-UHFFFAOYSA-N 0.000 description 1
- GPUHJQHXIFJPGN-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-1-(3-methylbutanoyl)imidazolidine-2,4-dione Chemical compound O=C1N(C(=O)CC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 GPUHJQHXIFJPGN-UHFFFAOYSA-N 0.000 description 1
- YKYGJHGXTSEGDB-UHFFFAOYSA-N 3-(3-chloro-4-ethoxyphenyl)-1,1-dimethylurea Chemical compound CCOC1=CC=C(NC(=O)N(C)C)C=C1Cl YKYGJHGXTSEGDB-UHFFFAOYSA-N 0.000 description 1
- HBLSGPQATABNRY-UHFFFAOYSA-N 3-(4-chlorophenyl)-2-n-methyl-4-n,5-n-bis(trifluoromethyl)-1,3-thiazolidine-2,4,5-triimine Chemical compound CN=C1SC(=NC(F)(F)F)C(=NC(F)(F)F)N1C1=CC=C(Cl)C=C1 HBLSGPQATABNRY-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- YFEUKKUPOVGUIW-UHFFFAOYSA-N 3-[3-chloro-4-[chloro(difluoro)methyl]sulfanylphenyl]-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC=C(SC(F)(F)Cl)C(Cl)=C1 YFEUKKUPOVGUIW-UHFFFAOYSA-N 0.000 description 1
- WYJOEQHHWHAJRB-UHFFFAOYSA-N 3-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]oxolane Chemical compound C1=C(OC2COCC2)C([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1Cl WYJOEQHHWHAJRB-UHFFFAOYSA-N 0.000 description 1
- CASLETQIYIQFTQ-UHFFFAOYSA-N 3-[[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)pyrazol-4-yl]methylsulfonyl]-5,5-dimethyl-4h-1,2-oxazole Chemical compound CN1N=C(C(F)(F)F)C(CS(=O)(=O)C=2CC(C)(C)ON=2)=C1OC(F)F CASLETQIYIQFTQ-UHFFFAOYSA-N 0.000 description 1
- LCOWUMNPNWEMAZ-UHFFFAOYSA-N 3-[benzyl(methyl)amino]-2-cyanoprop-2-enoic acid Chemical compound N#CC(C(O)=O)=CN(C)CC1=CC=CC=C1 LCOWUMNPNWEMAZ-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- ISEZZVFHNHWUQW-UHFFFAOYSA-N 3-butoxypropyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CCCCOCCCOC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl ISEZZVFHNHWUQW-UHFFFAOYSA-N 0.000 description 1
- KZWPFFFDRDASOU-UHFFFAOYSA-N 3-butoxypropyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCOCCCOC(=O)COC1=CC=C(Cl)C=C1Cl KZWPFFFDRDASOU-UHFFFAOYSA-N 0.000 description 1
- NSMRHYDOKZAMKJ-UHFFFAOYSA-N 3-diethoxyphosphinothioyloxy-7,8,9,10-tetrahydrobenzo[c]chromen-6-one Chemical compound C1CCCC2=C1C1=CC=C(OP(=S)(OCC)OCC)C=C1OC2=O NSMRHYDOKZAMKJ-UHFFFAOYSA-N 0.000 description 1
- HHSBHVJQXZLIRW-UHFFFAOYSA-N 3-n,3-n-dimethylbenzene-1,3-diamine Chemical class CN(C)C1=CC=CC(N)=C1 HHSBHVJQXZLIRW-UHFFFAOYSA-N 0.000 description 1
- NMWKWBPNKPGATC-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2-benzofuran-1(3H)-one Chemical compound ClC1=C(Cl)C(Cl)=C2COC(=O)C2=C1Cl NMWKWBPNKPGATC-UHFFFAOYSA-N 0.000 description 1
- KSROTSBULDYPKA-UHFFFAOYSA-N 4,5-dichloro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound ClC1=CC=C2NC(C(F)(F)F)=NC2=C1Cl KSROTSBULDYPKA-UHFFFAOYSA-N 0.000 description 1
- NEFZKJCNHBXWLP-UHFFFAOYSA-N 4,5-dimethoxy-2-phenylpyridazin-3-one Chemical compound O=C1C(OC)=C(OC)C=NN1C1=CC=CC=C1 NEFZKJCNHBXWLP-UHFFFAOYSA-N 0.000 description 1
- PKTIFYGCWCQRSX-UHFFFAOYSA-N 4,6-diamino-2-(cyclopropylamino)pyrimidine-5-carbonitrile Chemical compound NC1=C(C#N)C(N)=NC(NC2CC2)=N1 PKTIFYGCWCQRSX-UHFFFAOYSA-N 0.000 description 1
- HTXMJCHSFOPGME-UHFFFAOYSA-N 4,7-dimethoxy-1,3-benzodioxole Chemical compound COC1=CC=C(OC)C2=C1OCO2 HTXMJCHSFOPGME-UHFFFAOYSA-N 0.000 description 1
- RTWCZQFXFMXXKP-UHFFFAOYSA-N 4-(2,4,5-trichlorophenoxy)butanoic acid Chemical compound OC(=O)CCCOC1=CC(Cl)=C(Cl)C=C1Cl RTWCZQFXFMXXKP-UHFFFAOYSA-N 0.000 description 1
- KEIXJOCOXNOKHI-UHFFFAOYSA-N 4-(2,4-dichlorophenoxy)butanoate;dimethylazanium Chemical compound CNC.OC(=O)CCCOC1=CC=C(Cl)C=C1Cl KEIXJOCOXNOKHI-UHFFFAOYSA-N 0.000 description 1
- SIYAHZSHQIPQLY-UHFFFAOYSA-N 4-(4-chlorophenoxy)butanoic acid Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1 SIYAHZSHQIPQLY-UHFFFAOYSA-N 0.000 description 1
- UJVMVEZTSSMXAC-UHFFFAOYSA-N 4-[(3-chlorophenyl)diazenyl]-3-methyl-2H-1,2-oxazol-5-one Chemical compound ClC=1C=C(C=CC=1)N=NC1=C(NOC1=O)C UJVMVEZTSSMXAC-UHFFFAOYSA-N 0.000 description 1
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 description 1
- QDFVXXBCJYNKKC-UHFFFAOYSA-N 4-[4-(4-chlorophenyl)-4-cyclopropylbutyl]-1-fluoro-2-phenoxybenzene Chemical compound C1=C(OC=2C=CC=CC=2)C(F)=CC=C1CCCC(C=1C=CC(Cl)=CC=1)C1CC1 QDFVXXBCJYNKKC-UHFFFAOYSA-N 0.000 description 1
- WFMULRZXIUQYFV-UHFFFAOYSA-N 4-amino-3,5,6-trichloropyridine-2-carboxylic acid;n,n-diethylethanamine Chemical compound CCN(CC)CC.NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl WFMULRZXIUQYFV-UHFFFAOYSA-N 0.000 description 1
- VUTBELPREDJDDH-UHFFFAOYSA-N 4-amino-5-hydroxymethyl-2-methylpyrimidine Chemical compound CC1=NC=C(CO)C(N)=N1 VUTBELPREDJDDH-UHFFFAOYSA-N 0.000 description 1
- QCPASDYEQAVIJF-UHFFFAOYSA-N 4-chloro-3-methyl-1,3-benzothiazol-2-one Chemical compound C1=CC=C2SC(=O)N(C)C2=C1Cl QCPASDYEQAVIJF-UHFFFAOYSA-N 0.000 description 1
- CYQMVKQKBFFDOO-UHFFFAOYSA-N 4-chloro-5-(dimethylamino)-2-[3-(trifluoromethyl)phenyl]pyridazin-3-one Chemical compound O=C1C(Cl)=C(N(C)C)C=NN1C1=CC=CC(C(F)(F)F)=C1 CYQMVKQKBFFDOO-UHFFFAOYSA-N 0.000 description 1
- NNPRCLUGHFXSOU-UHFFFAOYSA-N 4-chloro-n-[cyano(ethoxy)methyl]benzamide Chemical compound CCOC(C#N)NC(=O)C1=CC=C(Cl)C=C1 NNPRCLUGHFXSOU-UHFFFAOYSA-N 0.000 description 1
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 description 1
- MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 description 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 description 1
- BFTGQIQVUVTBJU-UHFFFAOYSA-N 5,6-dihydroimidazo[2,1-c][1,2,4]dithiazole-3-thione Chemical compound C1CN2C(=S)SSC2=N1 BFTGQIQVUVTBJU-UHFFFAOYSA-N 0.000 description 1
- OPEJGICLTMWFNQ-UHFFFAOYSA-N 5-[(2,6-difluorophenyl)methoxymethyl]-5-methyl-3-(3-methylthiophen-2-yl)-4h-1,2-oxazole Chemical compound C1=CSC(C=2CC(C)(COCC=3C(=CC=CC=3F)F)ON=2)=C1C OPEJGICLTMWFNQ-UHFFFAOYSA-N 0.000 description 1
- QQOGZMUZAZWLJH-UHFFFAOYSA-N 5-[2-chloro-6-fluoro-4-(trifluoromethyl)phenoxy]-n-ethylsulfonyl-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)CC)=CC(OC=2C(=CC(=CC=2F)C(F)(F)F)Cl)=C1 QQOGZMUZAZWLJH-UHFFFAOYSA-N 0.000 description 1
- UIQAVIOOENLZRU-UHFFFAOYSA-N 5-[[ethoxy(propylsulfanyl)phosphoryl]sulfanylmethyl]-3-methyl-1,2-oxazole Chemical compound CCCSP(=O)(OCC)SCC1=CC(C)=NO1 UIQAVIOOENLZRU-UHFFFAOYSA-N 0.000 description 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 description 1
- ODNZLRLWXRXPOH-UHFFFAOYSA-N 5-amino-4-bromo-2-phenylpyridazin-3-one Chemical compound O=C1C(Br)=C(N)C=NN1C1=CC=CC=C1 ODNZLRLWXRXPOH-UHFFFAOYSA-N 0.000 description 1
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 description 1
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 description 1
- SJDGOKGRYGWNTC-UHFFFAOYSA-N 5-isothiocyanato-2-methoxy-n,n,3-trimethylbenzamide Chemical compound COC1=C(C)C=C(N=C=S)C=C1C(=O)N(C)C SJDGOKGRYGWNTC-UHFFFAOYSA-N 0.000 description 1
- WZXQWLWGLWIQGK-UHFFFAOYSA-N 5-methoxy-4,6,6-trimethyl-2-(2-methylpropanoyl)cyclohex-4-ene-1,3-dione Chemical compound COC1=C(C)C(=O)C(C(=O)C(C)C)C(=O)C1(C)C WZXQWLWGLWIQGK-UHFFFAOYSA-N 0.000 description 1
- DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 description 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 description 1
- HZKBYBNLTLVSPX-UHFFFAOYSA-N 6-[(6,6-dimethyl-5,7-dihydropyrrolo[2,1-c][1,2,4]thiadiazol-3-ylidene)amino]-7-fluoro-4-prop-2-ynyl-1,4-benzoxazin-3-one Chemical compound C#CCN1C(=O)COC(C=C2F)=C1C=C2N=C1SN=C2CC(C)(C)CN21 HZKBYBNLTLVSPX-UHFFFAOYSA-N 0.000 description 1
- ZUSHSDOEVHPTCU-UHFFFAOYSA-N 6-chloro-3-phenyl-1h-pyridazin-4-one Chemical compound N1C(Cl)=CC(=O)C(C=2C=CC=CC=2)=N1 ZUSHSDOEVHPTCU-UHFFFAOYSA-N 0.000 description 1
- VIRFVCLSHYKKRP-UHFFFAOYSA-N 6-chloro-4-diethoxyphosphorylsulfanyl-3,4-dihydro-2h-thiochromene Chemical compound C1=C(Cl)C=C2C(SP(=O)(OCC)OCC)CCSC2=C1 VIRFVCLSHYKKRP-UHFFFAOYSA-N 0.000 description 1
- PMYBBBROJPQQQV-UHFFFAOYSA-N 6-chloro-4-n-(3-methoxypropyl)-2-n-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound COCCCNC1=NC(Cl)=NC(NC(C)C)=N1 PMYBBBROJPQQQV-UHFFFAOYSA-N 0.000 description 1
- UCOIYRGMDBGBOU-UHFFFAOYSA-N 6-chloro-4-n-propan-2-ylpyrimidine-2,4-diamine Chemical compound CC(C)NC1=CC(Cl)=NC(N)=N1 UCOIYRGMDBGBOU-UHFFFAOYSA-N 0.000 description 1
- QQRJUWIHLNBDQF-UHFFFAOYSA-N 6-chloro-5-methylsulfanylpyrimidine-2,4-diamine Chemical compound CSC1=C(N)N=C(N)N=C1Cl QQRJUWIHLNBDQF-UHFFFAOYSA-N 0.000 description 1
- NGZWZIAGFHOSDS-UHFFFAOYSA-N 6-methylheptyl 4-amino-3,5,6-trichloropyridine-2-carboxylate Chemical group CC(C)CCCCCOC(=O)C1=NC(Cl)=C(Cl)C(N)=C1Cl NGZWZIAGFHOSDS-UHFFFAOYSA-N 0.000 description 1
- HVHHQHTXTGUMSR-UHFFFAOYSA-N 6-tert-butyl-3-(dimethylamino)-4-methyl-1,2,4-triazin-5-one Chemical compound CN(C)C1=NN=C(C(C)(C)C)C(=O)N1C HVHHQHTXTGUMSR-UHFFFAOYSA-N 0.000 description 1
- LJGZUMNXGLDTFF-UHFFFAOYSA-N 6-tert-butyl-3-methyl-2,4-dinitrophenol Chemical compound CC1=C([N+]([O-])=O)C=C(C(C)(C)C)C(O)=C1[N+]([O-])=O LJGZUMNXGLDTFF-UHFFFAOYSA-N 0.000 description 1
- VSVKOUBCDZYAQY-UHFFFAOYSA-N 7-chloro-1,2-benzothiazole Chemical compound ClC1=CC=CC2=C1SN=C2 VSVKOUBCDZYAQY-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 1
- 239000005660 Abamectin Substances 0.000 description 1
- 240000004507 Abelmoschus esculentus Species 0.000 description 1
- 235000003934 Abelmoschus esculentus Nutrition 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241001143308 Acanthoscelides Species 0.000 description 1
- 239000005875 Acetamiprid Substances 0.000 description 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 1
- 239000005652 Acrinathrin Substances 0.000 description 1
- 241000908424 Acromyrmex Species 0.000 description 1
- QRJMLIPXTTYRMQ-SYJWXDLUSA-N Actinamine Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](NC)[C@H]1O QRJMLIPXTTYRMQ-SYJWXDLUSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000253994 Acyrthosiphon pisum Species 0.000 description 1
- 241001516607 Adelges Species 0.000 description 1
- 241000275062 Agrilus planipennis Species 0.000 description 1
- 241000059559 Agriotes sordidus Species 0.000 description 1
- 241000993143 Agromyza Species 0.000 description 1
- 241001003964 Agromyza frontella Species 0.000 description 1
- 241000218473 Agrotis Species 0.000 description 1
- YRRKLBAKDXSTNC-UHFFFAOYSA-N Aldicarb sulfonyl Natural products CNC(=O)ON=CC(C)(C)S(C)(=O)=O YRRKLBAKDXSTNC-UHFFFAOYSA-N 0.000 description 1
- YRRKLBAKDXSTNC-WEVVVXLNSA-N Aldoxycarb Chemical compound CNC(=O)O\N=C\C(C)(C)S(C)(=O)=O YRRKLBAKDXSTNC-WEVVVXLNSA-N 0.000 description 1
- 241000108084 Aleurodicus dispersus Species 0.000 description 1
- 241000307865 Aleurothrixus floccosus Species 0.000 description 1
- 241000107983 Aleyrodes proletella Species 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- MDWNFWDBQGOKNZ-UHFFFAOYSA-N Allosamidin Natural products OCC1C2OC(N(C)C)=NC2C(O)C1OC(C(C1O)NC(C)=O)OC(CO)C1OC1OC(CO)C(O)C(O)C1NC(C)=O MDWNFWDBQGOKNZ-UHFFFAOYSA-N 0.000 description 1
- 239000005726 Ametoctradin Substances 0.000 description 1
- GDTZUQIYUMGJRT-UHFFFAOYSA-N Amidithion Chemical compound COCCNC(=O)CSP(=S)(OC)OC GDTZUQIYUMGJRT-UHFFFAOYSA-N 0.000 description 1
- 239000003666 Amidosulfuron Substances 0.000 description 1
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 description 1
- 239000005468 Aminopyralid Substances 0.000 description 1
- 239000005727 Amisulbrom Substances 0.000 description 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000501766 Ampelomyces quisqualis Species 0.000 description 1
- 241000318945 Amrasca biguttula biguttula Species 0.000 description 1
- 244000099147 Ananas comosus Species 0.000 description 1
- 235000007119 Ananas comosus Nutrition 0.000 description 1
- 241001136525 Anastrepha ludens Species 0.000 description 1
- 241001136527 Anastrepha suspensa Species 0.000 description 1
- 241000254177 Anthonomus Species 0.000 description 1
- 241000254175 Anthonomus grandis Species 0.000 description 1
- 241000952610 Aphis glycines Species 0.000 description 1
- 241001600408 Aphis gossypii Species 0.000 description 1
- 241001095118 Aphis pomi Species 0.000 description 1
- 241001164244 Aphrophora Species 0.000 description 1
- 241000533363 Apion Species 0.000 description 1
- 241001227591 Apogonia Species 0.000 description 1
- 101100477360 Arabidopsis thaliana IPSP gene Proteins 0.000 description 1
- 241001149932 Archaeognatha Species 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 241000384127 Argyrotaenia Species 0.000 description 1
- 235000010894 Artemisia argyi Nutrition 0.000 description 1
- 244000189799 Asimina triloba Species 0.000 description 1
- 235000006264 Asimina triloba Nutrition 0.000 description 1
- 241000387313 Aspidiotus Species 0.000 description 1
- 241001227734 Ataenius strigatus Species 0.000 description 1
- 241001503477 Athalia rosae Species 0.000 description 1
- QAOFKYGUSMPWNY-UHFFFAOYSA-N Athidathion Chemical compound CCOP(=S)(OCC)SCN1N=C(OC)SC1=O QAOFKYGUSMPWNY-UHFFFAOYSA-N 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
- 241000580299 Atta texana Species 0.000 description 1
- 241000668551 Aulacaspis Species 0.000 description 1
- 241000902805 Aulacophora Species 0.000 description 1
- 241001166626 Aulacorthum solani Species 0.000 description 1
- 239000005878 Azadirachtin Substances 0.000 description 1
- 239000005469 Azimsulfuron Substances 0.000 description 1
- AFIIBUOYKYSPKB-UHFFFAOYSA-N Aziprotryne Chemical compound CSC1=NC(NC(C)C)=NC(N=[N+]=[N-])=N1 AFIIBUOYKYSPKB-UHFFFAOYSA-N 0.000 description 1
- DCEAEHHJGXAROU-WUKNDPDISA-N Azothoate Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1\N=N\C1=CC=C(Cl)C=C1 DCEAEHHJGXAROU-WUKNDPDISA-N 0.000 description 1
- 239000005730 Azoxystrobin Substances 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 241000967809 Bactrocera zonata Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 239000005734 Benalaxyl Substances 0.000 description 1
- 239000005735 Benalaxyl-M Substances 0.000 description 1
- 239000005472 Bensulfuron methyl Substances 0.000 description 1
- 239000005476 Bentazone Substances 0.000 description 1
- NCLRGQCNIDLTDW-UHFFFAOYSA-M Bentazone-sodium Chemical compound [Na+].C1=CC=C2[N-]S(=O)(=O)N(C(C)C)C(=O)C2=C1 NCLRGQCNIDLTDW-UHFFFAOYSA-M 0.000 description 1
- 239000005736 Benthiavalicarb Substances 0.000 description 1
- 239000005884 Beta-Cyfluthrin Substances 0.000 description 1
- 239000005874 Bifenthrin Substances 0.000 description 1
- 239000005488 Bispyribac Substances 0.000 description 1
- 239000005738 Bixafen Substances 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 239000005740 Boscalid Substances 0.000 description 1
- 241000260909 Bothynoderes Species 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- 241000272639 Brachycaudus mimeuri Species 0.000 description 1
- 241001093996 Brachycorynella asparagi Species 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 1
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- KWGUFOITWDSNQY-UHFFFAOYSA-N Bromophos-ethyl Chemical group CCOP(=S)(OCC)OC1=CC(Cl)=C(Br)C=C1Cl KWGUFOITWDSNQY-UHFFFAOYSA-N 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- 241001325378 Bruchus Species 0.000 description 1
- 241001414201 Bruchus pisorum Species 0.000 description 1
- MYTVVMGUDBRCDJ-UHFFFAOYSA-N Bufencarb Chemical compound CCCC(C)C1=CC=CC(OC(=O)NC)=C1.CCC(CC)C1=CC=CC(OC(=O)NC)=C1 MYTVVMGUDBRCDJ-UHFFFAOYSA-N 0.000 description 1
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 description 1
- SWMGXKSQWDSBKV-UHFFFAOYSA-N Buthidazole Chemical compound O=C1N(C)CC(O)N1C1=NN=C(C(C)(C)C)S1 SWMGXKSQWDSBKV-UHFFFAOYSA-N 0.000 description 1
- SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 description 1
- GQBZOKZFJYNVPJ-UHFFFAOYSA-N C(=O)N.C(C1=CC=CC=C1)#N.[S] Chemical compound C(=O)N.C(C1=CC=CC=C1)#N.[S] GQBZOKZFJYNVPJ-UHFFFAOYSA-N 0.000 description 1
- ZQVYPVAEBSMDFW-UHFFFAOYSA-N C(C1=CC=CC=C1)#N.[S] Chemical compound C(C1=CC=CC=C1)#N.[S] ZQVYPVAEBSMDFW-UHFFFAOYSA-N 0.000 description 1
- DPKVMWZHBXODRF-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)NO.C(C1=CC=CC=C1)(=O)NO Chemical compound C(C1=CC=CC=C1)(=O)NO.C(C1=CC=CC=C1)(=O)NO DPKVMWZHBXODRF-UHFFFAOYSA-N 0.000 description 1
- XMIWZAAFHXNIJV-UHFFFAOYSA-N C(CC)P.N Chemical compound C(CC)P.N XMIWZAAFHXNIJV-UHFFFAOYSA-N 0.000 description 1
- FKYHEOWAJPETTA-UHFFFAOYSA-N CCCC#C[O] Chemical compound CCCC#C[O] FKYHEOWAJPETTA-UHFFFAOYSA-N 0.000 description 1
- SKUQUGGNMOLHMK-UHFFFAOYSA-N CCCC[CH]C=O Chemical compound CCCC[CH]C=O SKUQUGGNMOLHMK-UHFFFAOYSA-N 0.000 description 1
- BKKSKJXQHLKZJO-UHFFFAOYSA-N CCC[CH]C=O Chemical compound CCC[CH]C=O BKKSKJXQHLKZJO-UHFFFAOYSA-N 0.000 description 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 description 1
- DKHJWWRYTONYHB-UHFFFAOYSA-N CPP Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1 DKHJWWRYTONYHB-UHFFFAOYSA-N 0.000 description 1
- 241001212014 Cacoecia Species 0.000 description 1
- 241000906761 Calocoris Species 0.000 description 1
- 241001525574 Caloptilia Species 0.000 description 1
- 241000722666 Camponotus Species 0.000 description 1
- 241000131329 Carabidae Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000009467 Carica papaya Nutrition 0.000 description 1
- 241001183369 Carpophilus hemipterus Species 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- 241001130355 Cassida nebulosa Species 0.000 description 1
- 241000411507 Cassida vittata Species 0.000 description 1
- 241001481710 Cerambycidae Species 0.000 description 1
- 241000255580 Ceratitis <genus> Species 0.000 description 1
- 241000255579 Ceratitis capitata Species 0.000 description 1
- 241001414824 Cercopidae Species 0.000 description 1
- 241001450758 Ceroplastes Species 0.000 description 1
- 241001156313 Ceutorhynchus Species 0.000 description 1
- 241001180296 Ceutorhynchus assimilis Species 0.000 description 1
- 241001399348 Ceutorhynchus napi Species 0.000 description 1
- 241000902406 Chaetocnema Species 0.000 description 1
- 241000239202 Chelicerata Species 0.000 description 1
- 241000426499 Chilo Species 0.000 description 1
- 241000668556 Chionaspis Species 0.000 description 1
- REEFSLKDEDEWAO-UHFFFAOYSA-N Chloraniformethan Chemical compound ClC1=CC=C(NC(NC=O)C(Cl)(Cl)Cl)C=C1Cl REEFSLKDEDEWAO-UHFFFAOYSA-N 0.000 description 1
- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 1
- STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 description 1
- YJKIALIXRCSISK-UHFFFAOYSA-N Chlorfenprop-methyl Chemical compound COC(=O)C(Cl)CC1=CC=C(Cl)C=C1 YJKIALIXRCSISK-UHFFFAOYSA-N 0.000 description 1
- JKVBWACRUUUEAR-ISLYRVAYSA-N Chlorfensulphide Chemical compound C1=CC(Cl)=CC=C1S\N=N\C1=CC(Cl)=C(Cl)C=C1Cl JKVBWACRUUUEAR-ISLYRVAYSA-N 0.000 description 1
- OUDYXRYNDPEKLK-XNTDXEJSSA-N Chloromebuform Chemical compound CCCCN(C)\C=N\C1=CC=C(Cl)C=C1C OUDYXRYNDPEKLK-XNTDXEJSSA-N 0.000 description 1
- IBZZDPVVVSNQOY-UHFFFAOYSA-N Chloromethiuron Chemical compound CN(C)C(=S)NC1=CC=C(Cl)C=C1C IBZZDPVVVSNQOY-UHFFFAOYSA-N 0.000 description 1
- 239000005747 Chlorothalonil Substances 0.000 description 1
- 239000005494 Chlorotoluron Substances 0.000 description 1
- 239000005944 Chlorpyrifos Substances 0.000 description 1
- 239000005496 Chlorsulfuron Substances 0.000 description 1
- KZCBXHSWMMIEQU-UHFFFAOYSA-N Chlorthal Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(C(O)=O)C(Cl)=C1Cl KZCBXHSWMMIEQU-UHFFFAOYSA-N 0.000 description 1
- JAZJVWLGNLCNDD-UHFFFAOYSA-N Chlorthiophos Chemical compound CCOP(=S)(OCC)OC1=CC(Cl)=C(SC)C=C1Cl JAZJVWLGNLCNDD-UHFFFAOYSA-N 0.000 description 1
- 239000005887 Chromafenozide Substances 0.000 description 1
- 241001364932 Chrysodeixis Species 0.000 description 1
- 241000668561 Chrysomphalus Species 0.000 description 1
- LTNDZDRYUXNFCU-NEWSRXKRSA-N Cinerin II Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]2[C@@H](C=C(C)OC(=O)C)C2(C)C LTNDZDRYUXNFCU-NEWSRXKRSA-N 0.000 description 1
- 244000241235 Citrullus lanatus Species 0.000 description 1
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- LPXYXBZAXFTFKH-UHFFFAOYSA-N ClC=1C(=C(C(=NC1)C(=O)O)C(=O)O)Cl Chemical compound ClC=1C(=C(C(=NC1)C(=O)O)C(=O)O)Cl LPXYXBZAXFTFKH-UHFFFAOYSA-N 0.000 description 1
- ZLCMJEOAMHCVEV-UHFFFAOYSA-N ClCC(C(C(C(=O)O)=O)(Cl)Cl)(Cl)Cl Chemical compound ClCC(C(C(C(=O)O)=O)(Cl)Cl)(Cl)Cl ZLCMJEOAMHCVEV-UHFFFAOYSA-N 0.000 description 1
- 239000005498 Clodinafop Substances 0.000 description 1
- 241000255749 Coccinellidae Species 0.000 description 1
- 241001478240 Coccus Species 0.000 description 1
- 241000933851 Cochliomyia Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 241000720864 Coleophoridae Species 0.000 description 1
- 241000143940 Colias Species 0.000 description 1
- 241000532642 Conotrachelus nenuphar Species 0.000 description 1
- 241001663470 Contarinia <gall midge> Species 0.000 description 1
- 241001663467 Contarinia tritici Species 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- 241000405691 Coptotermes curvignathus Species 0.000 description 1
- 241000897297 Cornitermes Species 0.000 description 1
- 241000867174 Cotinis nitida Species 0.000 description 1
- 241000902369 Crioceris asparagi Species 0.000 description 1
- BOFHKBLZOYVHSI-UHFFFAOYSA-N Crufomate Chemical compound CNP(=O)(OC)OC1=CC=C(C(C)(C)C)C=C1Cl BOFHKBLZOYVHSI-UHFFFAOYSA-N 0.000 description 1
- 241000456565 Cryptolestes pusillus Species 0.000 description 1
- 241000456564 Cryptolestes turcicus Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000242268 Ctenicera Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 239000005889 Cyantraniliprole Substances 0.000 description 1
- 241001156075 Cyclocephala Species 0.000 description 1
- OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 0.000 description 1
- DQZCVNGCTZLGAQ-UHFFFAOYSA-N Cycluron Chemical compound CN(C)C(=O)NC1CCCCCCC1 DQZCVNGCTZLGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000005755 Cyflufenamid Substances 0.000 description 1
- 239000005502 Cyhalofop-butyl Substances 0.000 description 1
- TYIYMOAHACZAMQ-CQSZACIVSA-N Cyhalofop-butyl Chemical group C1=CC(O[C@H](C)C(=O)OCCCC)=CC=C1OC1=CC=C(C#N)C=C1F TYIYMOAHACZAMQ-CQSZACIVSA-N 0.000 description 1
- 241001183634 Cylindrocopturus Species 0.000 description 1
- 239000005756 Cymoxanil Substances 0.000 description 1
- 244000019459 Cynara cardunculus Species 0.000 description 1
- 235000019106 Cynara scolymus Nutrition 0.000 description 1
- FMGYKKMPNATWHP-UHFFFAOYSA-N Cyperquat Chemical compound C1=C[N+](C)=CC=C1C1=CC=CC=C1 FMGYKKMPNATWHP-UHFFFAOYSA-N 0.000 description 1
- 239000005757 Cyproconazole Substances 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 description 1
- 241000592374 Daktulosphaira vitifoliae Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 239000004287 Dehydroacetic acid Substances 0.000 description 1
- BIQOEDQVNIYWPQ-UHFFFAOYSA-N Delachlor Chemical compound CC(C)COCN(C(=O)CCl)C1=C(C)C=CC=C1C BIQOEDQVNIYWPQ-UHFFFAOYSA-N 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- PZIRJMYRYORVIT-UHFFFAOYSA-N Demeton-S-methylsulphon Chemical compound CCS(=O)(=O)CCSP(=O)(OC)OC PZIRJMYRYORVIT-UHFFFAOYSA-N 0.000 description 1
- 102100034289 Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 Human genes 0.000 description 1
- 241001564528 Deporaus marginatus Species 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- 241000489975 Diabrotica Species 0.000 description 1
- ZKIBFASDNPOJFP-UHFFFAOYSA-N Diamidafos Chemical compound CNP(=O)(NC)OC1=CC=CC=C1 ZKIBFASDNPOJFP-UHFFFAOYSA-N 0.000 description 1
- 235000009355 Dianthus caryophyllus Nutrition 0.000 description 1
- 240000006497 Dianthus caryophyllus Species 0.000 description 1
- 241000526125 Diaphorina citri Species 0.000 description 1
- 241000586568 Diaspidiotus perniciosus Species 0.000 description 1
- 241000122105 Diatraea Species 0.000 description 1
- 239000005504 Dicamba Substances 0.000 description 1
- 241001549096 Dichelops furcatus Species 0.000 description 1
- 239000005505 Dichlorprop-P Substances 0.000 description 1
- 239000005506 Diclofop Substances 0.000 description 1
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 description 1
- 239000005759 Diethofencarb Substances 0.000 description 1
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 description 1
- 239000005893 Diflubenzuron Substances 0.000 description 1
- DHWRNDJOGMTCPB-UHFFFAOYSA-N Dimefuron Chemical compound ClC1=CC(NC(=O)N(C)C)=CC=C1N1C(=O)OC(C(C)(C)C)=N1 DHWRNDJOGMTCPB-UHFFFAOYSA-N 0.000 description 1
- 239000005508 Dimethachlor Substances 0.000 description 1
- IKYICRRUVNIHPP-UHFFFAOYSA-N Dimethametryn Chemical compound CCNC1=NC(NC(C)C(C)C)=NC(SC)=N1 IKYICRRUVNIHPP-UHFFFAOYSA-N 0.000 description 1
- 239000005509 Dimethenamid-P Substances 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
- FVCPXLWAKNJIKK-UHFFFAOYSA-N Dimexano Chemical group COC(=S)SSC(=S)OC FVCPXLWAKNJIKK-UHFFFAOYSA-N 0.000 description 1
- 239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 description 1
- SDKQRNRRDYRQKY-UHFFFAOYSA-N Dioxacarb Chemical compound CNC(=O)OC1=CC=CC=C1C1OCCO1 SDKQRNRRDYRQKY-UHFFFAOYSA-N 0.000 description 1
- HJEINPVZRDJRBY-UHFFFAOYSA-N Disul Chemical compound OS(=O)(=O)OCCOC1=CC=C(Cl)C=C1Cl HJEINPVZRDJRBY-UHFFFAOYSA-N 0.000 description 1
- 241001279823 Diuraphis noxia Species 0.000 description 1
- 241001581006 Dysaphis plantaginea Species 0.000 description 1
- 241001425472 Dysdercus cingulatus Species 0.000 description 1
- 241001035625 Dysdercus suturellus Species 0.000 description 1
- 241001533565 Dysmicoccus brevipes Species 0.000 description 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
- 241000051720 Edessa meditabunda Species 0.000 description 1
- IAUFMJOLSFEAIJ-UHFFFAOYSA-N Eglinazine Chemical compound CCNC1=NC(Cl)=NC(NCC(O)=O)=N1 IAUFMJOLSFEAIJ-UHFFFAOYSA-N 0.000 description 1
- 239000005894 Emamectin Substances 0.000 description 1
- YUGWDVYLFSETPE-JLHYYAGUSA-N Empenthrin Chemical compound CC\C=C(/C)C(C#C)OC(=O)C1C(C=C(C)C)C1(C)C YUGWDVYLFSETPE-JLHYYAGUSA-N 0.000 description 1
- 241000995023 Empoasca Species 0.000 description 1
- 241000630736 Ephestia Species 0.000 description 1
- 241000462639 Epilachna varivestis Species 0.000 description 1
- 241001350892 Epimecis Species 0.000 description 1
- 241000917107 Eriosoma lanigerum Species 0.000 description 1
- PTFJIKYUEPWBMS-UHFFFAOYSA-N Ethalfluralin Chemical compound CC(=C)CN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O PTFJIKYUEPWBMS-UHFFFAOYSA-N 0.000 description 1
- KCOCSOWTADCKOL-UHFFFAOYSA-N Ethidimuron Chemical compound CCS(=O)(=O)C1=NN=C(N(C)C(=O)NC)S1 KCOCSOWTADCKOL-UHFFFAOYSA-N 0.000 description 1
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 description 1
- DICRHEJCQXFJBY-UHFFFAOYSA-N Ethoate-methyl Chemical group CCNC(=O)CSP(=S)(OC)OC DICRHEJCQXFJBY-UHFFFAOYSA-N 0.000 description 1
- 239000005961 Ethoprophos Substances 0.000 description 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 description 1
- 239000005896 Etofenprox Substances 0.000 description 1
- 239000005897 Etoxazole Substances 0.000 description 1
- 239000005769 Etridiazole Substances 0.000 description 1
- 241000221079 Euphorbia <genus> Species 0.000 description 1
- 240000002395 Euphorbia pulcherrima Species 0.000 description 1
- 241001181621 Eurygaster maura Species 0.000 description 1
- 241000098295 Euschistus heros Species 0.000 description 1
- 241001619920 Euschistus servus Species 0.000 description 1
- OAVWAYKTGUABMP-UHFFFAOYSA-N FC(OC(C(=O)O)(C)OC1=CC=CC=C1)(F)F Chemical compound FC(OC(C(=O)O)(C)OC1=CC=CC=C1)(F)F OAVWAYKTGUABMP-UHFFFAOYSA-N 0.000 description 1
- 241000953886 Fannia canicularis Species 0.000 description 1
- 241000958182 Fannia scalaris Species 0.000 description 1
- 241000233488 Feltia Species 0.000 description 1
- 239000005958 Fenamiphos (aka phenamiphos) Substances 0.000 description 1
- 239000005775 Fenbuconazole Substances 0.000 description 1
- AYBALPYBYZFKDS-OLZOCXBDSA-N Fenitropan Chemical compound CC(=O)OC[C@@H]([N+]([O-])=O)[C@@H](OC(C)=O)C1=CC=CC=C1 AYBALPYBYZFKDS-OLZOCXBDSA-N 0.000 description 1
- ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 description 1
- PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 description 1
- 239000005513 Fenoxaprop-P Substances 0.000 description 1
- 239000005898 Fenoxycarb Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- WHWHBAUZDPEHEM-UHFFFAOYSA-N Fenthiaprop Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2S1 WHWHBAUZDPEHEM-UHFFFAOYSA-N 0.000 description 1
- 239000005899 Fipronil Substances 0.000 description 1
- YQVMVCCFZCMYQB-SNVBAGLBSA-N Flamprop-M Chemical compound C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-SNVBAGLBSA-N 0.000 description 1
- 239000005530 Fluazifop-P Substances 0.000 description 1
- KVKHBPGBGOVMBN-PWLVHAGJSA-N Flubenzimine Chemical compound C=1C=CC=CC=1N/1C(=N/C(F)(F)F)/S\C(=N/C(F)(F)F)\C\1=N/C1=CC=CC=C1 KVKHBPGBGOVMBN-PWLVHAGJSA-N 0.000 description 1
- IRECWLYBCAZIJM-UHFFFAOYSA-N Flumiclorac pentyl Chemical group C1=C(Cl)C(OCC(=O)OCCCCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F IRECWLYBCAZIJM-UHFFFAOYSA-N 0.000 description 1
- 239000005783 Fluopyram Substances 0.000 description 1
- DHAHEVIQIYRFRG-UHFFFAOYSA-N Fluoroglycofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OCC(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 DHAHEVIQIYRFRG-UHFFFAOYSA-N 0.000 description 1
- QJYOCYOOZHULNN-UHFFFAOYSA-N Fluoromidine Chemical compound C1=C(Cl)C=C2NC(C(F)(F)F)=NC2=N1 QJYOCYOOZHULNN-UHFFFAOYSA-N 0.000 description 1
- 239000005902 Flupyradifurone Substances 0.000 description 1
- YWBVHLJPRPCRSD-UHFFFAOYSA-N Fluridone Chemical compound O=C1C(C=2C=C(C=CC=2)C(F)(F)F)=CN(C)C=C1C1=CC=CC=C1 YWBVHLJPRPCRSD-UHFFFAOYSA-N 0.000 description 1
- 239000005535 Flurochloridone Substances 0.000 description 1
- 239000005788 Fluxapyroxad Substances 0.000 description 1
- 239000005948 Formetanate Substances 0.000 description 1
- 241001251094 Formica Species 0.000 description 1
- AIKKULXCBHRFOS-UHFFFAOYSA-N Formothion Chemical compound COP(=S)(OC)SCC(=O)N(C)C=O AIKKULXCBHRFOS-UHFFFAOYSA-N 0.000 description 1
- 239000005790 Fosetyl Substances 0.000 description 1
- 239000005959 Fosthiazate Substances 0.000 description 1
- 239000005791 Fuberidazole Substances 0.000 description 1
- 229930184093 Furanether Natural products 0.000 description 1
- ILACEZQKVDMRMW-UHFFFAOYSA-N Furanether A Natural products C1C2=COC=C2C2C3CC(C)(C)CC3C1(C)O2 ILACEZQKVDMRMW-UHFFFAOYSA-N 0.000 description 1
- QTDRLOKFLJJHTG-UHFFFAOYSA-N Furmecyclox Chemical compound C1=C(C)OC(C)=C1C(=O)N(OC)C1CCCCC1 QTDRLOKFLJJHTG-UHFFFAOYSA-N 0.000 description 1
- 240000004859 Gamochaeta purpurea Species 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- 239000005561 Glufosinate Substances 0.000 description 1
- 108050006905 Glutamate-Gated Chloride Channel Proteins 0.000 description 1
- DYMNZCGFRHLNMT-UHFFFAOYSA-N Glyodin Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCC1=NCCN1 DYMNZCGFRHLNMT-UHFFFAOYSA-N 0.000 description 1
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical compound [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 241000875835 Haematopinus asini Species 0.000 description 1
- LXKOADMMGWXPJQ-UHFFFAOYSA-N Halosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C(O)=O)C)=N1 LXKOADMMGWXPJQ-UHFFFAOYSA-N 0.000 description 1
- 239000005564 Halosulfuron methyl Substances 0.000 description 1
- 239000005565 Haloxyfop-P Substances 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000255967 Helicoverpa zea Species 0.000 description 1
- 241000345510 Helopeltis antonii Species 0.000 description 1
- 241000877151 Helopeltis theivora Species 0.000 description 1
- 241001640034 Heteropterys Species 0.000 description 1
- 241000590466 Heterotermes Species 0.000 description 1
- 241001387517 Heterotermes aureus Species 0.000 description 1
- 235000018081 Hibiscus syriacus Nutrition 0.000 description 1
- 244000130592 Hibiscus syriacus Species 0.000 description 1
- 101000641031 Homo sapiens Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 Proteins 0.000 description 1
- 241001153229 Hylobius Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 239000005794 Hymexazol Substances 0.000 description 1
- 241001508558 Hypera Species 0.000 description 1
- 241001508566 Hypera postica Species 0.000 description 1
- 241000257174 Hypoderma lineatum Species 0.000 description 1
- MFESCIUQSIBMSM-UHFFFAOYSA-N I-BCP Chemical compound ClCCCBr MFESCIUQSIBMSM-UHFFFAOYSA-N 0.000 description 1
- KOTOUBGHZHWCCJ-UHFFFAOYSA-N IPSP Chemical compound CCS(=O)CSP(=S)(OC(C)C)OC(C)C KOTOUBGHZHWCCJ-UHFFFAOYSA-N 0.000 description 1
- 241001058150 Icerya purchasi Species 0.000 description 1
- 241000595926 Idioscopus nitidulus Species 0.000 description 1
- KJTYJTCKKSDSQF-UHFFFAOYSA-N Imazalil nitrate Chemical compound O[N+]([O-])=O.ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 KJTYJTCKKSDSQF-UHFFFAOYSA-N 0.000 description 1
- 239000005981 Imazaquin Substances 0.000 description 1
- 239000005567 Imazosulfuron Substances 0.000 description 1
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 description 1
- PPCUNNLZTNMXFO-ACCUITESSA-N Imicyafos Chemical compound CCCSP(=O)(OCC)N1CCN(CC)\C1=N/C#N PPCUNNLZTNMXFO-ACCUITESSA-N 0.000 description 1
- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 description 1
- 241000204026 Incisitermes Species 0.000 description 1
- 239000005568 Iodosulfuron Substances 0.000 description 1
- JUJFQMPKBJPSFZ-UHFFFAOYSA-M Iodosulfuron-methyl-sodium Chemical compound [Na+].COC(=O)C1=CC=C(I)C=C1S(=O)(=O)[N-]C(=O)NC1=NC(C)=NC(OC)=N1 JUJFQMPKBJPSFZ-UHFFFAOYSA-M 0.000 description 1
- QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 description 1
- 239000005796 Ipconazole Substances 0.000 description 1
- 241000764238 Isis Species 0.000 description 1
- SBYAVOHNDJTVPA-UHFFFAOYSA-N Isocarbamid Chemical compound CC(C)CNC(=O)N1CCNC1=O SBYAVOHNDJTVPA-UHFFFAOYSA-N 0.000 description 1
- 239000005570 Isoxaben Substances 0.000 description 1
- 239000005571 Isoxaflutole Substances 0.000 description 1
- ANFHKXSOSRDDRQ-UHFFFAOYSA-N Isoxapyrifop Chemical compound C1CCON1C(=O)C(C)OC(C=C1)=CC=C1OC1=NC=C(Cl)C=C1Cl ANFHKXSOSRDDRQ-UHFFFAOYSA-N 0.000 description 1
- 241001506109 Kalotermes Species 0.000 description 1
- POSKOXIJDWDKPH-UHFFFAOYSA-N Kelevan Chemical compound ClC1(Cl)C2(Cl)C3(Cl)C4(Cl)C(CC(=O)CCC(=O)OCC)(O)C5(Cl)C3(Cl)C1(Cl)C5(Cl)C42Cl POSKOXIJDWDKPH-UHFFFAOYSA-N 0.000 description 1
- 239000005800 Kresoxim-methyl Substances 0.000 description 1
- 241001470017 Laodelphax striatella Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241000670112 Linognathus ovillus Species 0.000 description 1
- 241000685571 Liriomyza brassicae Species 0.000 description 1
- 241000594033 Liriomyza bryoniae Species 0.000 description 1
- 239000005912 Lufenuron Substances 0.000 description 1
- 241001177134 Lyctus Species 0.000 description 1
- 241001414826 Lygus Species 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- AZFKQCNGMSSWDS-UHFFFAOYSA-N MCPA-thioethyl Chemical group CCSC(=O)COC1=CC=C(Cl)C=C1C AZFKQCNGMSSWDS-UHFFFAOYSA-N 0.000 description 1
- 239000005575 MCPB Substances 0.000 description 1
- 101150039283 MCPB gene Proteins 0.000 description 1
- 241000208467 Macadamia Species 0.000 description 1
- 241000766395 Maconellicoccus hirsutus Species 0.000 description 1
- 241000721714 Macrosiphum euphorbiae Species 0.000 description 1
- 241001259998 Macrosteles quadrilineatus Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001164204 Mahanarva Species 0.000 description 1
- MZOPWQKISXCCTP-UHFFFAOYSA-N Malonoben Chemical compound CC(C)(C)C1=CC(C=C(C#N)C#N)=CC(C(C)(C)C)=C1O MZOPWQKISXCCTP-UHFFFAOYSA-N 0.000 description 1
- 241000273029 Marginitermes Species 0.000 description 1
- ZCAHBOURBFRXOT-UHFFFAOYSA-N Mecarbinzid Chemical compound C1=CC=C2N(C(=O)NCCSC)C(NC(=O)OC)=NC2=C1 ZCAHBOURBFRXOT-UHFFFAOYSA-N 0.000 description 1
- 239000005576 Mecoprop-P Substances 0.000 description 1
- 235000010624 Medicago sativa Nutrition 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- GZJNBGYLANALSV-UHFFFAOYSA-N Medinoterb acetate Chemical compound CC(=O)OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C)=C1C(C)(C)C GZJNBGYLANALSV-UHFFFAOYSA-N 0.000 description 1
- 241000902265 Megascelis Species 0.000 description 1
- 241001394950 Melanotus communis (Gyllenhal, 1817) Species 0.000 description 1
- 240000000233 Melia azedarach Species 0.000 description 1
- 241000766511 Meligethes Species 0.000 description 1
- 241000771994 Melophagus ovinus Species 0.000 description 1
- 239000005806 Meptyldinocap Substances 0.000 description 1
- 241000223250 Metarhizium anisopliae Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000005917 Methoxyfenozide Substances 0.000 description 1
- BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 description 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 description 1
- 239000005809 Metiram Substances 0.000 description 1
- 241000168713 Metopolophium dirhodum Species 0.000 description 1
- 239000005582 Metosulam Substances 0.000 description 1
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 description 1
- LTMQQEMGRMBUSL-UHFFFAOYSA-N Metoxadiazone Chemical compound O=C1OC(OC)=NN1C1=CC=CC=C1OC LTMQQEMGRMBUSL-UHFFFAOYSA-N 0.000 description 1
- 239000005584 Metsulfuron-methyl Substances 0.000 description 1
- 231100000757 Microbial toxin Toxicity 0.000 description 1
- 241001002437 Microcerotermes Species 0.000 description 1
- 241000243190 Microsporidia Species 0.000 description 1
- 241000333575 Microtermes obesi Species 0.000 description 1
- 241001219549 Mictis Species 0.000 description 1
- 239000005918 Milbemectin Substances 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 241000399155 Monomorium minimum Species 0.000 description 1
- 241000952627 Monomorium pharaonis Species 0.000 description 1
- 241000257229 Musca <genus> Species 0.000 description 1
- 239000005811 Myclobutanil Substances 0.000 description 1
- 241000883290 Myriapoda Species 0.000 description 1
- 241001364991 Myrmecina Species 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 description 1
- BZRUVKZGXNSXMB-UHFFFAOYSA-N N-(butan-2-yl)-6-chloro-N'-ethyl-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(Cl)=NC(NC(C)CC)=N1 BZRUVKZGXNSXMB-UHFFFAOYSA-N 0.000 description 1
- XFOXDUJCOHBXRC-UHFFFAOYSA-N N-Ethyl-N-methyl-4-(trifluoromethyl)-2-(3,4-dimethoxyphenyl)benzamide Chemical compound CCN(C)C(=O)C1=CC=C(C(F)(F)F)C=C1C1=CC=C(OC)C(OC)=C1 XFOXDUJCOHBXRC-UHFFFAOYSA-N 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 description 1
- NTBVTCXMRYKRTB-UHFFFAOYSA-N N-{2-[(4,6-dimethoxypyrimidin-2-yl)(hydroxy)methyl]-6-(methoxymethyl)phenyl}-1,1-difluoromethanesulfonamide Chemical compound COCC1=CC=CC(C(O)C=2N=C(OC)C=C(OC)N=2)=C1NS(=O)(=O)C(F)F NTBVTCXMRYKRTB-UHFFFAOYSA-N 0.000 description 1
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 description 1
- GMPONCCQARMHBI-UHFFFAOYSA-N N.[Na+].P Chemical compound N.[Na+].P GMPONCCQARMHBI-UHFFFAOYSA-N 0.000 description 1
- AQGDXJQRVOCUQX-UHFFFAOYSA-N N.[S] Chemical compound N.[S] AQGDXJQRVOCUQX-UHFFFAOYSA-N 0.000 description 1
- CYUIZYSKRBPGNU-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.[O].C1=CC=CC=C1 Chemical compound N1=CC=CC2=CC=CC=C12.[O].C1=CC=CC=C1 CYUIZYSKRBPGNU-UHFFFAOYSA-N 0.000 description 1
- XQBGXQWWZCTBQH-UHFFFAOYSA-N N1C=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1 Chemical compound N1C=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1.C1=CC=CC=C1 XQBGXQWWZCTBQH-UHFFFAOYSA-N 0.000 description 1
- QSMTUAJDOTXEDZ-UHFFFAOYSA-N N1C=CC=C1.[Cl] Chemical compound N1C=CC=C1.[Cl] QSMTUAJDOTXEDZ-UHFFFAOYSA-N 0.000 description 1
- SCQCUWMFZHLVCO-UHFFFAOYSA-N N1N=CC=C1.[F] Chemical class N1N=CC=C1.[F] SCQCUWMFZHLVCO-UHFFFAOYSA-N 0.000 description 1
- JHXVRRJXCDAINK-UHFFFAOYSA-N NC(=O)N.N#CC#N Chemical compound NC(=O)N.N#CC#N JHXVRRJXCDAINK-UHFFFAOYSA-N 0.000 description 1
- 241001666408 Neurocolpus longirostris Species 0.000 description 1
- 241001671714 Nezara Species 0.000 description 1
- 241001671709 Nezara viridula Species 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- FWISWWONCDDGEX-KPKJPENVSA-N Nitrilacarb Chemical compound CNC(=O)O\N=C\C(C)(C)CCC#N FWISWWONCDDGEX-KPKJPENVSA-N 0.000 description 1
- VJAWBEFMCIINFU-UHFFFAOYSA-N Nitrothal-isopropyl Chemical compound CC(C)OC(=O)C1=CC(C(=O)OC(C)C)=CC([N+]([O-])=O)=C1 VJAWBEFMCIINFU-UHFFFAOYSA-N 0.000 description 1
- 241000819999 Nymphes Species 0.000 description 1
- GPSSJHKOZAOGIF-UHFFFAOYSA-N O1C=CC=C1.N1C=CC=C1.[Cl] Chemical compound O1C=CC=C1.N1C=CC=C1.[Cl] GPSSJHKOZAOGIF-UHFFFAOYSA-N 0.000 description 1
- FJJCLZXIWTUOED-UHFFFAOYSA-N O1C=CC=C1.[F] Chemical compound O1C=CC=C1.[F] FJJCLZXIWTUOED-UHFFFAOYSA-N 0.000 description 1
- 241001105104 Oberea Species 0.000 description 1
- 241001352334 Oberea linearis Species 0.000 description 1
- 241000543819 Oestrus ovis Species 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 241001250072 Oryctes rhinoceros Species 0.000 description 1
- 241001275917 Oryzaephilus mercator Species 0.000 description 1
- 241000975417 Oscinella frit Species 0.000 description 1
- 241000131737 Otiorhynchus Species 0.000 description 1
- 241001160353 Oulema melanopus Species 0.000 description 1
- 239000005588 Oxadiazon Substances 0.000 description 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 description 1
- 239000005950 Oxamyl Substances 0.000 description 1
- XRGQIRXQFSJBKJ-UHFFFAOYSA-N Oxapyrazon Chemical compound O=C1C(Br)=C(NC(=O)C(=O)O)C=NN1C1=CC=CC=C1 XRGQIRXQFSJBKJ-UHFFFAOYSA-N 0.000 description 1
- 239000005589 Oxasulfuron Substances 0.000 description 1
- FCOHEOSCARXMMS-UHFFFAOYSA-N Oxaziclomefone Chemical compound C1OC(C)=C(C=2C=CC=CC=2)C(=O)N1C(C)(C)C1=CC(Cl)=CC(Cl)=C1 FCOHEOSCARXMMS-UHFFFAOYSA-N 0.000 description 1
- UPUGLJYNCXXUQV-UHFFFAOYSA-N Oxydisulfoton Chemical compound CCOP(=S)(OCC)SCCS(=O)CC UPUGLJYNCXXUQV-UHFFFAOYSA-N 0.000 description 1
- 241000940835 Pales Species 0.000 description 1
- 206010033546 Pallor Diseases 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 241001204961 Pantomorus Species 0.000 description 1
- CDHBAZHPEVDWMO-UHFFFAOYSA-N Parafluron Chemical compound CN(C)C(=O)NC1=CC=C(C(F)(F)F)C=C1 CDHBAZHPEVDWMO-UHFFFAOYSA-N 0.000 description 1
- 241001523670 Parcoblatta pensylvanica Species 0.000 description 1
- 241001130603 Parlatoria <angiosperm> Species 0.000 description 1
- 241000669431 Parlatoria pergandii Species 0.000 description 1
- 241001630088 Parlatoria ziziphi Species 0.000 description 1
- 241001668545 Pascopyrum Species 0.000 description 1
- 241000517325 Pediculus Species 0.000 description 1
- 241000562493 Pegomya Species 0.000 description 1
- 239000005815 Penflufen Substances 0.000 description 1
- 239000005592 Penoxsulam Substances 0.000 description 1
- SYJGKVOENHZYMQ-UHFFFAOYSA-N Penoxsulam Chemical compound N1=C2C(OC)=CN=C(OC)N2N=C1NS(=O)(=O)C1=C(OCC(F)F)C=CC=C1C(F)(F)F SYJGKVOENHZYMQ-UHFFFAOYSA-N 0.000 description 1
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 description 1
- 239000005816 Penthiopyrad Substances 0.000 description 1
- 241000256682 Peregrinus maidis Species 0.000 description 1
- 241001510010 Periplaneta fuliginosa Species 0.000 description 1
- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropyl alcohol Natural products CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 description 1
- 241001414822 Philaenus Species 0.000 description 1
- 241000425347 Phyla <beetle> Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 241000437063 Phyllotreta striolata Species 0.000 description 1
- 239000005596 Picolinafen Substances 0.000 description 1
- 239000005818 Picoxystrobin Substances 0.000 description 1
- 241000940371 Piezodorus Species 0.000 description 1
- 241000098283 Piezodorus guildinii Species 0.000 description 1
- 239000005597 Pinoxaden Substances 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000005923 Pirimicarb Substances 0.000 description 1
- 239000005924 Pirimiphos-methyl Substances 0.000 description 1
- 241000193804 Planococcus <bacterium> Species 0.000 description 1
- 241001662912 Poecilocapsus lineatus Species 0.000 description 1
- 241000256835 Polistes Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000592274 Polypodium vulgare Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000181603 Popillia flavosellata Species 0.000 description 1
- 241000254101 Popillia japonica Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000710078 Potyvirus Species 0.000 description 1
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 description 1
- GPGLBXMQFQQXDV-UHFFFAOYSA-N Primisulfuron Chemical compound OC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC(F)F)=CC(OC(F)F)=N1 GPGLBXMQFQQXDV-UHFFFAOYSA-N 0.000 description 1
- 241001474791 Proboscis Species 0.000 description 1
- 241000181848 Procornitermes Species 0.000 description 1
- 239000005599 Profoxydim Substances 0.000 description 1
- XCXCBWSRDOSZRU-UHFFFAOYSA-N Proglinazine Chemical compound CC(C)NC1=NC(Cl)=NC(NCC(O)=O)=N1 XCXCBWSRDOSZRU-UHFFFAOYSA-N 0.000 description 1
- MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 description 1
- 239000005601 Propoxycarbazone Substances 0.000 description 1
- 239000005824 Proquinazid Substances 0.000 description 1
- 241001459657 Prostephanus Species 0.000 description 1
- 239000005604 Prosulfuron Substances 0.000 description 1
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 description 1
- 239000005825 Prothioconazole Substances 0.000 description 1
- QTXHFDHVLBDJIO-UHFFFAOYSA-N Prothoate Chemical compound CCOP(=S)(OCC)SCC(=O)NC(C)C QTXHFDHVLBDJIO-UHFFFAOYSA-N 0.000 description 1
- UOJYYXATTMQQNA-UHFFFAOYSA-N Proxan Chemical compound CC(C)OC(S)=S UOJYYXATTMQQNA-UHFFFAOYSA-N 0.000 description 1
- 241001274606 Pseudacysta perseae Species 0.000 description 1
- 241000722234 Pseudococcus Species 0.000 description 1
- 241001510228 Pycnoscelus surinamensis Species 0.000 description 1
- BKVRQJSQZDTXCG-UHFFFAOYSA-N Pydanon Chemical compound OC(=O)CC1(O)CC(=O)NNC1=O BKVRQJSQZDTXCG-UHFFFAOYSA-N 0.000 description 1
- 241000421343 Pygovepres vaccinicola Species 0.000 description 1
- YPCALTGLHFLNGA-UHFFFAOYSA-N Pyracarbolid Chemical compound C1CCOC(C)=C1C(=O)NC1=CC=CC=C1 YPCALTGLHFLNGA-UHFFFAOYSA-N 0.000 description 1
- 239000005605 Pyraflufen-ethyl Substances 0.000 description 1
- 241001340903 Pyralis farinalis Species 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical group C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- VMORCWYWLVLMDG-YZGWKJHDSA-N Pyrethrin-II Natural products CC(=O)OC(=C[C@@H]1[C@H](C(=O)O[C@H]2CC(=O)C(=C2C)CC=CC=C)C1(C)C)C VMORCWYWLVLMDG-YZGWKJHDSA-N 0.000 description 1
- 239000005828 Pyrimethanil Substances 0.000 description 1
- 239000005829 Pyriofenone Substances 0.000 description 1
- MWMQNVGAHVXSPE-UHFFFAOYSA-N Pyriprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SC(F)F)=C1NCC1=CC=CC=N1 MWMQNVGAHVXSPE-UHFFFAOYSA-N 0.000 description 1
- ZIEWAMOXCOLNSJ-UHFFFAOYSA-N Quinonamid Chemical compound C1=CC=C2C(=O)C(NC(=O)C(Cl)Cl)=C(Cl)C(=O)C2=C1 ZIEWAMOXCOLNSJ-UHFFFAOYSA-N 0.000 description 1
- 239000005831 Quinoxyfen Substances 0.000 description 1
- 239000005609 Quizalofop-P Substances 0.000 description 1
- 239000005614 Quizalofop-P-ethyl Substances 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 241001499681 Reticulitermes banyulensis Species 0.000 description 1
- 241000010212 Reticulitermes grassei Species 0.000 description 1
- 241000344466 Reticulitermes hageni Species 0.000 description 1
- 241001152954 Reticulitermes hesperus Species 0.000 description 1
- 241000590379 Reticulitermes santonensis Species 0.000 description 1
- 241000866500 Reticulitermes speratus Species 0.000 description 1
- 241001105413 Reticulitermes tibialis Species 0.000 description 1
- 241000577913 Reticulitermes virginicus Species 0.000 description 1
- 241000157279 Rhagoletis cerasi Species 0.000 description 1
- 241001465970 Rhagoletis mendax Species 0.000 description 1
- 241000125162 Rhopalosiphum Species 0.000 description 1
- 241000125167 Rhopalosiphum padi Species 0.000 description 1
- 241001168761 Rhynchites Species 0.000 description 1
- 241000344244 Rhynchophorus Species 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 241001253920 Ryania Species 0.000 description 1
- DICDYWOAKAGJLU-UHFFFAOYSA-N S(=O)(C1=CC=C(C=C1)N)(=O)N.[F] Chemical compound S(=O)(C1=CC=C(C=C1)N)(=O)N.[F] DICDYWOAKAGJLU-UHFFFAOYSA-N 0.000 description 1
- 239000005617 S-Metolachlor Substances 0.000 description 1
- CQPTWYFXAPBSKB-UHFFFAOYSA-N SCC(O)CO.C(C)[Hg] Chemical compound SCC(O)CO.C(C)[Hg] CQPTWYFXAPBSKB-UHFFFAOYSA-N 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241001450655 Saissetia Species 0.000 description 1
- 241000316887 Saissetia oleae Species 0.000 description 1
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
- 241000726725 Scaptocoris castanea Species 0.000 description 1
- 241000590404 Schedorhinotermes Species 0.000 description 1
- 241001163248 Schoenocaulon officinale Species 0.000 description 1
- 241000055238 Scolytus Species 0.000 description 1
- 239000005834 Sedaxane Substances 0.000 description 1
- 239000005835 Silthiofam Substances 0.000 description 1
- 241000068648 Sitodiplosis mosellana Species 0.000 description 1
- 241000254154 Sitophilus zeamais Species 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 241000208292 Solanaceae Species 0.000 description 1
- 241000958652 Solenopsis molesta Species 0.000 description 1
- 241001221807 Solenopsis xyloni Species 0.000 description 1
- 235000009337 Spinacia oleracea Nutrition 0.000 description 1
- 244000300264 Spinacia oleracea Species 0.000 description 1
- 239000005929 Spinetoram Substances 0.000 description 1
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- 239000005664 Spirodiclofen Substances 0.000 description 1
- 239000005931 Spirotetramat Substances 0.000 description 1
- 239000005837 Spiroxamine Substances 0.000 description 1
- 241000509371 Steinernema feltiae Species 0.000 description 1
- 241001494115 Stomoxys calcitrans Species 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000005618 Sulcotrione Substances 0.000 description 1
- 239000005619 Sulfosulfuron Substances 0.000 description 1
- 239000005934 Sulfoxaflor Substances 0.000 description 1
- 239000005935 Sulfuryl fluoride Substances 0.000 description 1
- 241001649248 Supella longipalpa Species 0.000 description 1
- SSDZRWBPFCFZGB-UHFFFAOYSA-N TCA-ethadyl Chemical group ClC(Cl)(Cl)C(=O)OCCOC(=O)C(Cl)(Cl)Cl SSDZRWBPFCFZGB-UHFFFAOYSA-N 0.000 description 1
- SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 1
- 241000255626 Tabanus <genus> Species 0.000 description 1
- 241001157793 Tapinoma sessile Species 0.000 description 1
- 239000005620 Tembotrione Substances 0.000 description 1
- 241000255588 Tephritidae Species 0.000 description 1
- 239000005621 Terbuthylazine Substances 0.000 description 1
- NKNPHSJWQZXWIX-DCVDGXQQSA-N Tetranactin Chemical compound C[C@H]([C@H]1CC[C@H](O1)C[C@@H](OC(=O)[C@@H](C)[C@@H]1CC[C@@H](O1)C[C@@H](CC)OC(=O)[C@H](C)[C@H]1CC[C@H](O1)C[C@H](CC)OC(=O)[C@H]1C)CC)C(=O)O[C@H](CC)C[C@H]2CC[C@@H]1O2 NKNPHSJWQZXWIX-DCVDGXQQSA-N 0.000 description 1
- NKNPHSJWQZXWIX-UHFFFAOYSA-N Tetranactin Natural products CC1C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(CC)CC2CCC1O2 NKNPHSJWQZXWIX-UHFFFAOYSA-N 0.000 description 1
- QUWSDLYBOVGOCW-UHFFFAOYSA-N Tetrasul Chemical compound C1=CC(Cl)=CC=C1SC1=CC(Cl)=C(Cl)C=C1Cl QUWSDLYBOVGOCW-UHFFFAOYSA-N 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- KDWQYMVPYJGPHS-UHFFFAOYSA-N Thenylchlor Chemical compound C1=CSC(CN(C(=O)CCl)C=2C(=CC=CC=2C)C)=C1OC KDWQYMVPYJGPHS-UHFFFAOYSA-N 0.000 description 1
- 241000530360 Therioaphis Species 0.000 description 1
- 239000005941 Thiamethoxam Substances 0.000 description 1
- BBJPZPLAZVZTGR-UHFFFAOYSA-N Thiazafluron Chemical compound CNC(=O)N(C)C1=NN=C(C(F)(F)F)S1 BBJPZPLAZVZTGR-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 description 1
- 239000005622 Thiencarbazone Substances 0.000 description 1
- FOCVUCIESVLUNU-UHFFFAOYSA-N Thiotepa Chemical compound C1CN1P(N1CC1)(=S)N1CC1 FOCVUCIESVLUNU-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- PHSUVQBHRAWOQD-UHFFFAOYSA-N Tiocarbazil Chemical compound CCC(C)N(C(C)CC)C(=O)SCC1=CC=CC=C1 PHSUVQBHRAWOQD-UHFFFAOYSA-N 0.000 description 1
- 241000131345 Tipula <genus> Species 0.000 description 1
- 239000005845 Tolclofos-methyl Substances 0.000 description 1
- 241001651212 Toumeyella Species 0.000 description 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N Toxaphene Natural products C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 1
- 241000271862 Toxoptera Species 0.000 description 1
- 239000005624 Tralkoxydim Substances 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 239000005626 Tribenuron Substances 0.000 description 1
- 241000223259 Trichoderma Species 0.000 description 1
- 239000005627 Triclopyr Substances 0.000 description 1
- 239000005857 Trifloxystrobin Substances 0.000 description 1
- 239000005858 Triflumizole Substances 0.000 description 1
- 239000005942 Triflumuron Substances 0.000 description 1
- 239000005628 Triflusulfuron Substances 0.000 description 1
- 240000000359 Triticum dicoccon Species 0.000 description 1
- 241000669245 Unaspis Species 0.000 description 1
- 241000993338 Uranotaenia <genus> Species 0.000 description 1
- 240000000851 Vaccinium corymbosum Species 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 229930195482 Validamycin Natural products 0.000 description 1
- 239000005860 Valifenalate Substances 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 244000263375 Vanilla tahitensis Species 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- FVECELJHCSPHKY-UHFFFAOYSA-N Veratridine Natural products C1=C(OC)C(OC)=CC=C1C(=O)OC1C2(O)OC34CC5(O)C(CN6C(CCC(C)C6)C6(C)O)C6(O)C(O)CC5(O)C4CCC2C3(C)CC1 FVECELJHCSPHKY-UHFFFAOYSA-N 0.000 description 1
- 241000256856 Vespidae Species 0.000 description 1
- 235000010726 Vigna sinensis Nutrition 0.000 description 1
- 244000042314 Vigna unguiculata Species 0.000 description 1
- 241001274788 Viteus vitifoliae Species 0.000 description 1
- 241000254234 Xyeloidea Species 0.000 description 1
- 241000424289 Zabrus tenebrioides Species 0.000 description 1
- 241000482268 Zea mays subsp. mays Species 0.000 description 1
- 241001136529 Zeugodacus cucurbitae Species 0.000 description 1
- 241000258237 Zootermopsis Species 0.000 description 1
- 241001164238 Zulia Species 0.000 description 1
- GBAWQJNHVWMTLU-RQJHMYQMSA-N [(1R,5S)-7-chloro-6-bicyclo[3.2.0]hepta-2,6-dienyl] dimethyl phosphate Chemical compound C1=CC[C@@H]2C(OP(=O)(OC)OC)=C(Cl)[C@@H]21 GBAWQJNHVWMTLU-RQJHMYQMSA-N 0.000 description 1
- LUZZPGJQJKMMDM-JTQLQIEISA-N [(2s)-1-ethoxy-1-oxopropan-2-yl] 2-chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoate Chemical group C1=C(Cl)C(C(=O)O[C@@H](C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 LUZZPGJQJKMMDM-JTQLQIEISA-N 0.000 description 1
- HOERQTQCTISLFR-UHFFFAOYSA-N [(3-chloro-2,6-dimethoxybenzoyl)-ethylamino] benzoate Chemical compound COC=1C=CC(Cl)=C(OC)C=1C(=O)N(CC)OC(=O)C1=CC=CC=C1 HOERQTQCTISLFR-UHFFFAOYSA-N 0.000 description 1
- QQODLKZGRKWIFG-RUTXASTPSA-N [(R)-cyano-(4-fluoro-3-phenoxyphenyl)methyl] (1S)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-RUTXASTPSA-N 0.000 description 1
- FZSVSABTBYGOQH-XFFZJAGNSA-N [(e)-(3,3-dimethyl-1-methylsulfanylbutan-2-ylidene)amino] n-methylcarbamate Chemical compound CNC(=O)O\N=C(C(C)(C)C)\CSC FZSVSABTBYGOQH-XFFZJAGNSA-N 0.000 description 1
- ORDKAVSHIKNMAN-XYOKQWHBSA-N [(e)-2-bromo-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C\Br)C1=CC=C(Cl)C=C1Cl ORDKAVSHIKNMAN-XYOKQWHBSA-N 0.000 description 1
- CTJBHIROCMPUKL-WEVVVXLNSA-N [(e)-3-methylsulfonylbutan-2-ylideneamino] n-methylcarbamate Chemical compound CNC(=O)O\N=C(/C)C(C)S(C)(=O)=O CTJBHIROCMPUKL-WEVVVXLNSA-N 0.000 description 1
- WEDGYOKZJHBCGP-VOTSOKGWSA-N [(e)-4-[methoxy(methyl)amino]-4-oxobut-2-en-2-yl] dimethyl phosphate Chemical compound CON(C)C(=O)\C=C(/C)OP(=O)(OC)OC WEDGYOKZJHBCGP-VOTSOKGWSA-N 0.000 description 1
- BZMIHNKNQJJVRO-LVZFUZTISA-N [(e)-c-(3-chloro-2,6-dimethoxyphenyl)-n-ethoxycarbonimidoyl] benzoate Chemical compound COC=1C=CC(Cl)=C(OC)C=1C(=N/OCC)\OC(=O)C1=CC=CC=C1 BZMIHNKNQJJVRO-LVZFUZTISA-N 0.000 description 1
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 1
- KVIZNNVXXNFLMU-AIIUZBJTSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3r)-2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1\C=C\C KVIZNNVXXNFLMU-AIIUZBJTSA-N 0.000 description 1
- MWFQAAWRPDRKDG-KOLCDFICSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1C=C(Cl)Cl MWFQAAWRPDRKDG-KOLCDFICSA-N 0.000 description 1
- APEPLROGLDYWBS-UHFFFAOYSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2,3,3-tetramethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1(C)C APEPLROGLDYWBS-UHFFFAOYSA-N 0.000 description 1
- OTSYOPHQYHLKTK-UHFFFAOYSA-N [2-(azepan-1-yl)-2-oxoethyl] n-methylsulfamate Chemical compound CNS(=O)(=O)OCC(=O)N1CCCCCC1 OTSYOPHQYHLKTK-UHFFFAOYSA-N 0.000 description 1
- CFGPESLNPCIKIX-UHFFFAOYSA-N [2-[ethoxy(propylsulfanyl)phosphoryl]oxyphenyl] n-methylcarbamate Chemical compound CCCSP(=O)(OCC)OC1=CC=CC=C1OC(=O)NC CFGPESLNPCIKIX-UHFFFAOYSA-N 0.000 description 1
- FMPFURNXXAKYNE-UHFFFAOYSA-N [2-ethyl-3,7-dimethyl-6-[4-(trifluoromethoxy)phenoxy]quinolin-4-yl] methyl carbonate Chemical compound C1=C2C(OC(=O)OC)=C(C)C(CC)=NC2=CC(C)=C1OC1=CC=C(OC(F)(F)F)C=C1 FMPFURNXXAKYNE-UHFFFAOYSA-N 0.000 description 1
- MVEFZZKZBYQFPP-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-(3-methylphenyl)carbamate Chemical group CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 MVEFZZKZBYQFPP-UHFFFAOYSA-N 0.000 description 1
- CYDCAYZRTPOUJJ-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] n-(1-chlorobutan-2-yl)carbamate Chemical compound CCC(CCl)NC(=O)OC1=CC=CC(NC(=O)OC)=C1 CYDCAYZRTPOUJJ-UHFFFAOYSA-N 0.000 description 1
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
- SDIUYIZASVDZKT-UHFFFAOYSA-N [4-(dimethylaminomethylideneamino)-3-methylphenyl] n-methylcarbamate;hydrochloride Chemical compound [Cl-].CNC(=O)OC1=CC=C(N=C[NH+](C)C)C(C)=C1 SDIUYIZASVDZKT-UHFFFAOYSA-N 0.000 description 1
- ZHAFUINZIZIXFC-UHFFFAOYSA-N [9-(dimethylamino)-10-methylbenzo[a]phenoxazin-5-ylidene]azanium;chloride Chemical compound [Cl-].O1C2=CC(=[NH2+])C3=CC=CC=C3C2=NC2=C1C=C(N(C)C)C(C)=C2 ZHAFUINZIZIXFC-UHFFFAOYSA-N 0.000 description 1
- QBQQMUDUVXZUOS-UHFFFAOYSA-N [Cl].[O].N1C=CC=C1 Chemical compound [Cl].[O].N1C=CC=C1 QBQQMUDUVXZUOS-UHFFFAOYSA-N 0.000 description 1
- BAOWVDHYZBLYMB-UHFFFAOYSA-N [F].C1=CC=NC=C1 Chemical compound [F].C1=CC=NC=C1 BAOWVDHYZBLYMB-UHFFFAOYSA-N 0.000 description 1
- CAWBOJFIANSPRE-UHFFFAOYSA-N [I].C(C(=O)O)(=O)O Chemical compound [I].C(C(=O)O)(=O)O CAWBOJFIANSPRE-UHFFFAOYSA-N 0.000 description 1
- HBKBJWNMSQXYOP-UHFFFAOYSA-N [N+](=O)([O-])C1=C(C2=CC=CC=C2C=C1)[N+](=O)[O-].[Cl] Chemical compound [N+](=O)([O-])C1=C(C2=CC=CC=C2C=C1)[N+](=O)[O-].[Cl] HBKBJWNMSQXYOP-UHFFFAOYSA-N 0.000 description 1
- BNOODXBBXFZASF-UHFFFAOYSA-N [Na].[S] Chemical compound [Na].[S] BNOODXBBXFZASF-UHFFFAOYSA-N 0.000 description 1
- JSOJVSBOEOWZJX-UHFFFAOYSA-N [O].N1=CC=CC2=CC=CC=C21 Chemical compound [O].N1=CC=CC2=CC=CC=C21 JSOJVSBOEOWZJX-UHFFFAOYSA-N 0.000 description 1
- OASZCUUPKKGVSG-UHFFFAOYSA-N [O].NC(O)=N Chemical compound [O].NC(O)=N OASZCUUPKKGVSG-UHFFFAOYSA-N 0.000 description 1
- UOBPHQJGWSVXFS-UHFFFAOYSA-N [O].[F] Chemical compound [O].[F] UOBPHQJGWSVXFS-UHFFFAOYSA-N 0.000 description 1
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical compound [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 description 1
- NRAINUFKKPBZQY-UHFFFAOYSA-N [O]C1CC1 Chemical compound [O]C1CC1 NRAINUFKKPBZQY-UHFFFAOYSA-N 0.000 description 1
- GYAPJISEIGCPQO-UHFFFAOYSA-N [O]C1CCC1 Chemical compound [O]C1CCC1 GYAPJISEIGCPQO-UHFFFAOYSA-N 0.000 description 1
- XHQNHTRJJRRYEP-UHFFFAOYSA-N [P].C(CC)N Chemical compound [P].C(CC)N XHQNHTRJJRRYEP-UHFFFAOYSA-N 0.000 description 1
- ZSUFBRGARNXNBX-UHFFFAOYSA-N [P].C1=CC=NC=C1 Chemical compound [P].C1=CC=NC=C1 ZSUFBRGARNXNBX-UHFFFAOYSA-N 0.000 description 1
- HGFGGVSJWPEDPT-UHFFFAOYSA-N [P].O1C=NC=C1 Chemical compound [P].O1C=NC=C1 HGFGGVSJWPEDPT-UHFFFAOYSA-N 0.000 description 1
- GJMMXPXHXFHBPK-UHFFFAOYSA-N [P].[Cl] Chemical compound [P].[Cl] GJMMXPXHXFHBPK-UHFFFAOYSA-N 0.000 description 1
- LQXIXEWBEPQTTN-UHFFFAOYSA-N [P].[Cl].S1C=CC=C1 Chemical compound [P].[Cl].S1C=CC=C1 LQXIXEWBEPQTTN-UHFFFAOYSA-N 0.000 description 1
- QCJQWJKKTGJDCM-UHFFFAOYSA-N [P].[S] Chemical compound [P].[S] QCJQWJKKTGJDCM-UHFFFAOYSA-N 0.000 description 1
- AHIBWURJLGCHAY-UHFFFAOYSA-N [S].C1=CC=CC=C1 Chemical compound [S].C1=CC=CC=C1 AHIBWURJLGCHAY-UHFFFAOYSA-N 0.000 description 1
- FSXPZSJEXMUNIU-UHFFFAOYSA-N [S].C=1C=CNC=1 Chemical class [S].C=1C=CNC=1 FSXPZSJEXMUNIU-UHFFFAOYSA-N 0.000 description 1
- GOIGHUHRYZUEOM-UHFFFAOYSA-N [S].[I] Chemical compound [S].[I] GOIGHUHRYZUEOM-UHFFFAOYSA-N 0.000 description 1
- XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 description 1
- INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 description 1
- ZJOCMGQZWCTWNX-UHFFFAOYSA-N [ethoxy(ethylsulfanyl)phosphoryl]oxycyclohexane Chemical compound CCOP(=O)(SCC)OC1CCCCC1 ZJOCMGQZWCTWNX-UHFFFAOYSA-N 0.000 description 1
- XRAFOYUFLGWMQB-UHFFFAOYSA-N [ethoxy(propylsulfanyl)phosphoryl]oxybenzene Chemical compound CCCSP(=O)(OCC)OC1=CC=CC=C1 XRAFOYUFLGWMQB-UHFFFAOYSA-N 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 229950008167 abamectin Drugs 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 description 1
- GDZNYEZGJAFIKA-UHFFFAOYSA-N acetoprole Chemical compound NC1=C(S(C)=O)C(C(=O)C)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl GDZNYEZGJAFIKA-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- UVCFFGYNJOPUSF-UHFFFAOYSA-M acetyloxy(ethyl)mercury Chemical compound CC[Hg+].CC([O-])=O UVCFFGYNJOPUSF-UHFFFAOYSA-M 0.000 description 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 description 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- MDWNFWDBQGOKNZ-XYUDZHFQSA-N allosamidin Chemical compound O([C@@H]1[C@@H](CO)O[C@H]([C@@H]([C@@H]1O)NC(C)=O)O[C@H]1[C@H](O)[C@H]2N=C(O[C@H]2[C@@H]1CO)N(C)C)[C@@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@H]1NC(C)=O MDWNFWDBQGOKNZ-XYUDZHFQSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical compound [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 0.000 description 1
- GGKQIOFASHYUJZ-UHFFFAOYSA-N ametoctradin Chemical compound NC1=C(CCCCCCCC)C(CC)=NC2=NC=NN21 GGKQIOFASHYUJZ-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- KWAIHLIXESXTJL-UHFFFAOYSA-N aminocyclopyrachlor Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 KWAIHLIXESXTJL-UHFFFAOYSA-N 0.000 description 1
- NIXXQNOQHKNPEJ-UHFFFAOYSA-N aminopyralid Chemical compound NC1=CC(Cl)=NC(C(O)=O)=C1Cl NIXXQNOQHKNPEJ-UHFFFAOYSA-N 0.000 description 1
- BREATYVWRHIPIY-UHFFFAOYSA-N amisulbrom Chemical compound CN(C)S(=O)(=O)N1C=NC(S(=O)(=O)N2C3=CC(F)=CC=C3C(Br)=C2C)=N1 BREATYVWRHIPIY-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000001887 anti-feedant effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- GOLCXWYRSKYTSP-UHFFFAOYSA-N arsenic trioxide Inorganic materials O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000016520 artichoke thistle Nutrition 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 description 1
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 description 1
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 description 1
- XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 description 1
- VNKBTWQZTQIWDV-UHFFFAOYSA-N azamethiphos Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=O)(OC)OC)C2=N1 VNKBTWQZTQIWDV-UHFFFAOYSA-N 0.000 description 1
- MHMUIIBVMBOAON-UHFFFAOYSA-N azane;2,2,2-trichloroacetic acid Chemical compound [NH4+].[O-]C(=O)C(Cl)(Cl)Cl MHMUIIBVMBOAON-UHFFFAOYSA-N 0.000 description 1
- AQKNQRMIGNOQQF-UHFFFAOYSA-N azane;2-(2,4-dichlorophenoxy)acetic acid Chemical compound [NH4+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl AQKNQRMIGNOQQF-UHFFFAOYSA-N 0.000 description 1
- ARRGVXFLPAQYKA-UHFFFAOYSA-N azane;2-benzamidooxyacetic acid Chemical compound [NH4+].[O-]C(=O)CONC(=O)C1=CC=CC=C1 ARRGVXFLPAQYKA-UHFFFAOYSA-N 0.000 description 1
- GNZZHGJSMCDMBU-UHFFFAOYSA-N azane;5-(methoxymethyl)-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)pyridine-3-carboxylic acid Chemical compound [NH4+].[O-]C(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 GNZZHGJSMCDMBU-UHFFFAOYSA-N 0.000 description 1
- QRSHQJLLXXEYPS-UHFFFAOYSA-N azane;5-ethyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)pyridine-3-carboxylic acid Chemical compound [NH4+].[O-]C(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 QRSHQJLLXXEYPS-UHFFFAOYSA-N 0.000 description 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 description 1
- MLWMZTRCXNCAPF-UHFFFAOYSA-N azane;methylarsonic acid Chemical compound [NH4+].C[As](O)([O-])=O MLWMZTRCXNCAPF-UHFFFAOYSA-N 0.000 description 1
- VJBCNMFKFZIXHC-UHFFFAOYSA-N azanium;2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)quinoline-3-carboxylate Chemical compound N.N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O VJBCNMFKFZIXHC-UHFFFAOYSA-N 0.000 description 1
- RVSKHYSPNBOJDL-UHFFFAOYSA-N azanium;2-butan-2-yl-4,6-dinitrophenolate Chemical compound [NH4+].CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1[O-] RVSKHYSPNBOJDL-UHFFFAOYSA-N 0.000 description 1
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 1
- ONHBDDJJTDTLIR-UHFFFAOYSA-N azocyclotin Chemical compound C1CCCCC1[Sn](N1N=CN=C1)(C1CCCCC1)C1CCCCC1 ONHBDDJJTDTLIR-UHFFFAOYSA-N 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 1
- KKTYYONKWVCNJI-UHFFFAOYSA-N benazolin-dimethylammonium Chemical compound CNC.C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl KKTYYONKWVCNJI-UHFFFAOYSA-N 0.000 description 1
- WQRCEBAZAUAUQC-UHFFFAOYSA-N benazolin-ethyl Chemical group C1=CC=C2SC(=O)N(CC(=O)OCC)C2=C1Cl WQRCEBAZAUAUQC-UHFFFAOYSA-N 0.000 description 1
- BVAQOPQXUNGRCM-UHFFFAOYSA-M benazolin-potassium Chemical compound [K+].C1=CC=C2SC(=O)N(CC(=O)[O-])C2=C1Cl BVAQOPQXUNGRCM-UHFFFAOYSA-M 0.000 description 1
- LVKBXDHACCFCTA-UHFFFAOYSA-N bencarbazone Chemical compound C1=C(C(N)=S)C(NS(=O)(=O)CC)=CC(N2C(N(C)C(=N2)C(F)(F)F)=O)=C1F LVKBXDHACCFCTA-UHFFFAOYSA-N 0.000 description 1
- XEGGRYVFLWGFHI-UHFFFAOYSA-N bendiocarb Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)O2 XEGGRYVFLWGFHI-UHFFFAOYSA-N 0.000 description 1
- FYZBOYWSHKHDMT-UHFFFAOYSA-N benfuracarb Chemical compound CCOC(=O)CCN(C(C)C)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 FYZBOYWSHKHDMT-UHFFFAOYSA-N 0.000 description 1
- PPWBRCCBKOWDNB-UHFFFAOYSA-N bensulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)CC=2C(=CC=CC=2)C(O)=O)=N1 PPWBRCCBKOWDNB-UHFFFAOYSA-N 0.000 description 1
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical group COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 description 1
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 description 1
- USRKFGIXLGKMKU-ABAIWWIYSA-N benthiavalicarb-isopropyl Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@H](C(C)C)NC(=O)OC(C)C)=NC2=C1 USRKFGIXLGKMKU-ABAIWWIYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- ZWIPGARCRSFMHK-UHFFFAOYSA-N benzene;1h-imidazole Chemical class C1=CNC=N1.C1=CC=CC=C1 ZWIPGARCRSFMHK-UHFFFAOYSA-N 0.000 description 1
- OXRBQAFZWZYMGH-UHFFFAOYSA-N benzene;mercury Chemical class [Hg].C1=CC=CC=C1 OXRBQAFZWZYMGH-UHFFFAOYSA-N 0.000 description 1
- JWEUEBNMCPTTMC-UHFFFAOYSA-N benzene;methyl hydrogen sulfate Chemical compound COS(O)(=O)=O.C1=CC=CC=C1 JWEUEBNMCPTTMC-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
- AWZBRJCPLJOIKQ-UHFFFAOYSA-N benzoic acid;methylmercury Chemical compound [Hg]C.OC(=O)C1=CC=CC=C1 AWZBRJCPLJOIKQ-UHFFFAOYSA-N 0.000 description 1
- WKDZZKIPDBZSRW-UHFFFAOYSA-M benzoyloxy(methyl)mercury Chemical compound C[Hg]OC(=O)C1=CC=CC=C1 WKDZZKIPDBZSRW-UHFFFAOYSA-M 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000000443 biocontrol Effects 0.000 description 1
- 230000000853 biopesticidal effect Effects 0.000 description 1
- 230000002051 biphasic effect Effects 0.000 description 1
- BKAYSPSVVJBHHK-UHFFFAOYSA-N bis(4-chlorophenyl)-cyclopropylmethanol Chemical compound C=1C=C(Cl)C=CC=1C(C=1C=CC(Cl)=CC=1)(O)C1CC1 BKAYSPSVVJBHHK-UHFFFAOYSA-N 0.000 description 1
- RYVIXQCRCQLFCM-UHFFFAOYSA-N bispyribac Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(O)=O)=N1 RYVIXQCRCQLFCM-UHFFFAOYSA-N 0.000 description 1
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GHXRKGHKMRZBJH-UHFFFAOYSA-N boric acid Chemical compound OB(O)O.OB(O)O GHXRKGHKMRZBJH-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229940118790 boscalid Drugs 0.000 description 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 description 1
- 229940069206 bromax Drugs 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- FOANIXZHAMJWOI-UHFFFAOYSA-N bromopropylate Chemical compound C=1C=C(Br)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Br)C=C1 FOANIXZHAMJWOI-UHFFFAOYSA-N 0.000 description 1
- 235000021329 brown rice Nutrition 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- RIMGDBZXWSGBQN-UHFFFAOYSA-N burimamide Chemical compound CNC(=S)NCCCCC1=CN=C[N]1 RIMGDBZXWSGBQN-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- SFNPDDSJBGRXLW-UITAMQMPSA-N butocarboxim Chemical compound CNC(=O)O\N=C(\C)C(C)SC SFNPDDSJBGRXLW-UITAMQMPSA-N 0.000 description 1
- 125000006226 butoxyethyl group Chemical group 0.000 description 1
- FNEXNZUHBCBQTI-UHFFFAOYSA-N butyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CCCCOC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl FNEXNZUHBCBQTI-UHFFFAOYSA-N 0.000 description 1
- UQMRAFJOBWOFNS-UHFFFAOYSA-N butyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCOC(=O)COC1=CC=C(Cl)C=C1Cl UQMRAFJOBWOFNS-UHFFFAOYSA-N 0.000 description 1
- IXXKVXJYFVAQBI-UHFFFAOYSA-N butyl 4-(2,4-dichlorophenoxy)butanoate Chemical group CCCCOC(=O)CCCOC1=CC=C(Cl)C=C1Cl IXXKVXJYFVAQBI-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical group CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 description 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 1
- 229950004243 cacodylic acid Drugs 0.000 description 1
- HFEJHAAIJZXXRE-UHFFFAOYSA-N cafenstrole Chemical compound CCN(CC)C(=O)N1C=NC(S(=O)(=O)C=2C(=CC(C)=CC=2C)C)=N1 HFEJHAAIJZXXRE-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- GNQSHICPZJOYDM-UHFFFAOYSA-N calcium;2,2,2-trichloroacetic acid Chemical compound [Ca].OC(=O)C(Cl)(Cl)Cl GNQSHICPZJOYDM-UHFFFAOYSA-N 0.000 description 1
- JBGIVEALFOAXPA-UHFFFAOYSA-L calcium;2,2-dichloropropanoate Chemical compound [Ca+2].CC(Cl)(Cl)C([O-])=O.CC(Cl)(Cl)C([O-])=O JBGIVEALFOAXPA-UHFFFAOYSA-L 0.000 description 1
- STRTXDFFNXSZQB-UHFFFAOYSA-N calcium;cyanamide Chemical compound [Ca+2].NC#N STRTXDFFNXSZQB-UHFFFAOYSA-N 0.000 description 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- FNAAOMSRAVKQGQ-UHFFFAOYSA-N carbanolate Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1Cl FNAAOMSRAVKQGQ-UHFFFAOYSA-N 0.000 description 1
- RXDMAYSSBPYBFW-UHFFFAOYSA-N carpropamid Chemical compound C=1C=C(Cl)C=CC=1C(C)NC(=O)C1(CC)C(C)C1(Cl)Cl RXDMAYSSBPYBFW-UHFFFAOYSA-N 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- IRUJZVNXZWPBMU-UHFFFAOYSA-N cartap Chemical compound NC(=O)SCC(N(C)C)CSC(N)=O IRUJZVNXZWPBMU-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 239000012174 chinese wax Substances 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- XFDJMIHUAHSGKG-UHFFFAOYSA-N chlorethoxyfos Chemical compound CCOP(=S)(OCC)OC(Cl)C(Cl)(Cl)Cl XFDJMIHUAHSGKG-UHFFFAOYSA-N 0.000 description 1
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 description 1
- RIUXZHMCCFLRBI-UHFFFAOYSA-N chlorimuron Chemical compound COC1=CC(Cl)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 RIUXZHMCCFLRBI-UHFFFAOYSA-N 0.000 description 1
- NSWAMPCUPHPTTC-UHFFFAOYSA-N chlorimuron-ethyl Chemical group CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(Cl)=CC(OC)=N1 NSWAMPCUPHPTTC-UHFFFAOYSA-N 0.000 description 1
- XQNAUQUKWRBODG-UHFFFAOYSA-N chlornitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=C(Cl)C=C(Cl)C=C1Cl XQNAUQUKWRBODG-UHFFFAOYSA-N 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- VJTAZCKMHINUKO-UHFFFAOYSA-M chloro(2-methoxyethyl)mercury Chemical compound [Cl-].COCC[Hg+] VJTAZCKMHINUKO-UHFFFAOYSA-M 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229940018556 chloropropylate Drugs 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
- IVUXTESCPZUGJC-UHFFFAOYSA-N chloroxuron Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1OC1=CC=C(Cl)C=C1 IVUXTESCPZUGJC-UHFFFAOYSA-N 0.000 description 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 1
- NHTGQOXRZFUGJX-UHFFFAOYSA-N chlorquinox Chemical compound N1=CC=NC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 NHTGQOXRZFUGJX-UHFFFAOYSA-N 0.000 description 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 1
- HPNSNYBUADCFDR-UHFFFAOYSA-N chromafenozide Chemical compound CC1=CC(C)=CC(C(=O)N(NC(=O)C=2C(=C3CCCOC3=CC=2)C)C(C)(C)C)=C1 HPNSNYBUADCFDR-UHFFFAOYSA-N 0.000 description 1
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- SHCRDCOTRILILT-WOBDGSLYSA-N cinerin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C)C(=O)C1 SHCRDCOTRILILT-WOBDGSLYSA-N 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 description 1
- JBDHZKLJNAIJNC-LLVKDONJSA-N clodinafop-propargyl Chemical group C1=CC(O[C@H](C)C(=O)OCC#C)=CC=C1OC1=NC=C(Cl)C=C1F JBDHZKLJNAIJNC-LLVKDONJSA-N 0.000 description 1
- YIANBKOBVRMNPR-UHFFFAOYSA-N cloransulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1C(O)=O YIANBKOBVRMNPR-UHFFFAOYSA-N 0.000 description 1
- BIKACRYIQSLICJ-UHFFFAOYSA-N cloransulam-methyl Chemical group N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1C(=O)OC BIKACRYIQSLICJ-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 1
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 description 1
- FHTUCVJPHHUQIS-UHFFFAOYSA-N copper;zinc;dioxido(dioxo)chromium Chemical compound [Cu+2].[Zn+2].[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O FHTUCVJPHHUQIS-UHFFFAOYSA-N 0.000 description 1
- 229950004222 coumafos Drugs 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000012272 crop production Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 229950002363 crufomate Drugs 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 1
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 description 1
- 125000004465 cycloalkenyloxy group Chemical group 0.000 description 1
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 1
- 125000006317 cyclopropyl amino group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- APJLTUBHYCOZJI-VZCXRCSSSA-N cyenopyrafen Chemical compound CC1=NN(C)C(\C(OC(=O)C(C)(C)C)=C(/C#N)C=2C=CC(=CC=2)C(C)(C)C)=C1C APJLTUBHYCOZJI-VZCXRCSSSA-N 0.000 description 1
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 description 1
- 229960001591 cyfluthrin Drugs 0.000 description 1
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 description 1
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 1
- 229960002483 decamethrin Drugs 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 235000019258 dehydroacetic acid Nutrition 0.000 description 1
- 229940061632 dehydroacetic acid Drugs 0.000 description 1
- JEQRBTDTEKWZBW-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1=C(O)OC(C)=CC1=O JEQRBTDTEKWZBW-UHFFFAOYSA-N 0.000 description 1
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Natural products CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 1
- 229960003887 dichlorophen Drugs 0.000 description 1
- 229950001327 dichlorvos Drugs 0.000 description 1
- YEJGPFZQLRMXOI-PKEIRNPWSA-N diclocymet Chemical compound N#CC(C(C)(C)C)C(=O)N[C@H](C)C1=CC=C(Cl)C=C1Cl YEJGPFZQLRMXOI-PKEIRNPWSA-N 0.000 description 1
- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 description 1
- 229940004812 dicloran Drugs 0.000 description 1
- PNKGIAQRMACYGQ-UHFFFAOYSA-N dicopper;dizinc;chromium(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Cr+3].[Cr+3].[Cu+2].[Cu+2].[Zn+2].[Zn+2] PNKGIAQRMACYGQ-UHFFFAOYSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LNJNFVJKDJYTEU-UHFFFAOYSA-N diethofencarb Chemical compound CCOC1=CC=C(NC(=O)OC(C)C)C=C1OCC LNJNFVJKDJYTEU-UHFFFAOYSA-N 0.000 description 1
- RVQMZGWUSHPUCC-UHFFFAOYSA-N diethoxy-(2-methylquinolin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical compound C1=CC=C2C(OP(=S)(OCC)OCC)=CC(C)=NC2=C1 RVQMZGWUSHPUCC-UHFFFAOYSA-N 0.000 description 1
- WGWJBWHBOKETRC-UHFFFAOYSA-N diethoxy-(3-methyl-4-methylsulfanylphenoxy)-sulfanylidene-$l^{5}-phosphane Chemical group CCOP(=S)(OCC)OC1=CC=C(SC)C(C)=C1 WGWJBWHBOKETRC-UHFFFAOYSA-N 0.000 description 1
- CDCTYRNLXFEDHC-UHFFFAOYSA-N diethyl (5-methyl-1h-pyrazol-3-yl) phosphate Chemical compound CCOP(=O)(OCC)OC=1C=C(C)NN=1 CDCTYRNLXFEDHC-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 description 1
- 229940019503 diflubenzuron Drugs 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- NZZFYRREKKOMAT-UHFFFAOYSA-N diiodomethane Chemical compound ICI NZZFYRREKKOMAT-UHFFFAOYSA-N 0.000 description 1
- SCCDDNKJYDZXMM-UHFFFAOYSA-N dimethachlor Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1C SCCDDNKJYDZXMM-UHFFFAOYSA-N 0.000 description 1
- JLYFCTQDENRSOL-VIFPVBQESA-N dimethenamid-P Chemical compound COC[C@H](C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-VIFPVBQESA-N 0.000 description 1
- DLAPIMGBBDILHJ-UHFFFAOYSA-N dimethoxy-(3-methyl-4-methylsulfinylphenoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)OC1=CC=C(S(C)=O)C(C)=C1 DLAPIMGBBDILHJ-UHFFFAOYSA-N 0.000 description 1
- RNGDKAQQWUYBAS-UHFFFAOYSA-N dimethoxy-quinoxalin-2-yloxy-sulfanylidene-$l^{5}-phosphane Chemical group C1=CC=CC2=NC(OP(=S)(OC)OC)=CN=C21 RNGDKAQQWUYBAS-UHFFFAOYSA-N 0.000 description 1
- XCBOKUAJQWDYNI-UHFFFAOYSA-N dimethyl (3,5,6-trichloropyridin-2-yl) phosphate Chemical compound COP(=O)(OC)OC1=NC(Cl)=C(Cl)C=C1Cl XCBOKUAJQWDYNI-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000004656 dimethylamines Chemical class 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 229950010151 dioxation Drugs 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- ZZUUAHLFRDBNIS-UHFFFAOYSA-N diphenylmethanone;1h-pyrrole Chemical class C=1C=CNC=1.C=1C=CC=CC=1C(=O)C1=CC=CC=C1 ZZUUAHLFRDBNIS-UHFFFAOYSA-N 0.000 description 1
- ZHDBTKPXEJDTTQ-UHFFFAOYSA-N dipyrithione Chemical compound [O-][N+]1=CC=CC=C1SSC1=CC=CC=[N+]1[O-] ZHDBTKPXEJDTTQ-UHFFFAOYSA-N 0.000 description 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 description 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 description 1
- XRHVZWWRFMCBAZ-PXYBLNDHSA-L disodium;(1s,2r,3s,4r)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylate Chemical compound [Na+].[Na+].C1C[C@@H]2[C@@H](C([O-])=O)[C@@H](C(=O)[O-])[C@H]1O2 XRHVZWWRFMCBAZ-PXYBLNDHSA-L 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940044165 dodicin Drugs 0.000 description 1
- KSCFJBIXMNOVSH-UHFFFAOYSA-N dyphylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1N(CC(O)CO)C=N2 KSCFJBIXMNOVSH-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000002451 electron ionisation mass spectrometry Methods 0.000 description 1
- 229910001254 electrum Inorganic materials 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- ZINJLDJMHCUBIP-UHFFFAOYSA-N ethametsulfuron-methyl Chemical group CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC)=N1 ZINJLDJMHCUBIP-UHFFFAOYSA-N 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- HEZNVIYQEUHLNI-UHFFFAOYSA-N ethiofencarb Chemical compound CCSCC1=CC=CC=C1OC(=O)NC HEZNVIYQEUHLNI-UHFFFAOYSA-N 0.000 description 1
- BBXXLROWFHWFQY-UHFFFAOYSA-N ethirimol Chemical compound CCCCC1=C(C)NC(NCC)=NC1=O BBXXLROWFHWFQY-UHFFFAOYSA-N 0.000 description 1
- HBKPGGUHRZPDIE-UHFFFAOYSA-N ethoxy-methoxy-sulfanylidene-(2,4,5-trichlorophenoxy)-$l^{5}-phosphane Chemical compound CCOP(=S)(OC)OC1=CC(Cl)=C(Cl)C=C1Cl HBKPGGUHRZPDIE-UHFFFAOYSA-N 0.000 description 1
- OYFLKNAULOKYRI-UHFFFAOYSA-N ethoxy-phenyl-quinolin-8-yloxy-sulfanylidene-$l^{5}-phosphane Chemical compound C=1C=CC2=CC=CN=C2C=1OP(=S)(OCC)C1=CC=CC=C1 OYFLKNAULOKYRI-UHFFFAOYSA-N 0.000 description 1
- JSLBZIVMVVHMDJ-UHFFFAOYSA-N ethyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCOC(=O)COC1=CC=C(Cl)C=C1Cl JSLBZIVMVVHMDJ-UHFFFAOYSA-N 0.000 description 1
- KXAVVWXJUDQGDA-UHFFFAOYSA-N ethyl 2-(3,5,6-trichloropyridin-2-yl)oxyacetate Chemical group CCOC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl KXAVVWXJUDQGDA-UHFFFAOYSA-N 0.000 description 1
- VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- HVHDXEBXZOWTMV-UHFFFAOYSA-N ethyl formate propanoic acid Chemical compound C(C)C(=O)O.C(=O)OCC HVHDXEBXZOWTMV-UHFFFAOYSA-N 0.000 description 1
- XAGAASDWSFGQEC-UHFFFAOYSA-N ethyl-(n-(4-methylphenyl)sulfonylanilino)mercury Chemical compound C=1C=C(C)C=CC=1S(=O)(=O)N([Hg]CC)C1=CC=CC=C1 XAGAASDWSFGQEC-UHFFFAOYSA-N 0.000 description 1
- WBBZUMDPZLYKIZ-UHFFFAOYSA-N ethylammonium propionate Chemical compound CC[NH3+].CCC([O-])=O WBBZUMDPZLYKIZ-UHFFFAOYSA-N 0.000 description 1
- UREACWLAXSOUKG-UHFFFAOYSA-M ethylmercury(1+);bromide Chemical compound CC[Hg]Br UREACWLAXSOUKG-UHFFFAOYSA-M 0.000 description 1
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 1
- 229950005085 etofenprox Drugs 0.000 description 1
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 description 1
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 1
- 210000003414 extremity Anatomy 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
- ACDZDIIWZVQMIX-UHFFFAOYSA-N fenoxasulfone Chemical compound C1=C(Cl)C(OCC)=CC(Cl)=C1CS(=O)(=O)C1=NOC(C)(C)C1 ACDZDIIWZVQMIX-UHFFFAOYSA-N 0.000 description 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 229940013764 fipronil Drugs 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- YUVKUEAFAVKILW-SECBINFHSA-N fluazifop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-SECBINFHSA-N 0.000 description 1
- GINFBXXYGUODAT-UHFFFAOYSA-N flucarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F GINFBXXYGUODAT-UHFFFAOYSA-N 0.000 description 1
- UOUXAYAIONPXDH-UHFFFAOYSA-M flucarbazone-sodium Chemical compound [Na+].O=C1N(C)C(OC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1OC(F)(F)F UOUXAYAIONPXDH-UHFFFAOYSA-M 0.000 description 1
- ABOVRDBEJDIBMZ-UHFFFAOYSA-N flucofuron Chemical compound C1=C(Cl)C(C(F)(F)F)=CC(NC(=O)NC=2C=C(C(Cl)=CC=2)C(F)(F)F)=C1 ABOVRDBEJDIBMZ-UHFFFAOYSA-N 0.000 description 1
- XSNMWAPKHUGZGQ-UHFFFAOYSA-N fluensulfone Chemical compound FC(F)=C(F)CCS(=O)(=O)C1=NC=C(Cl)S1 XSNMWAPKHUGZGQ-UHFFFAOYSA-N 0.000 description 1
- GJEREQYJIQASAW-UHFFFAOYSA-N flufenerim Chemical compound CC(F)C1=NC=NC(NCCC=2C=CC(OC(F)(F)F)=CC=2)=C1Cl GJEREQYJIQASAW-UHFFFAOYSA-N 0.000 description 1
- WFZSZAXUALBVNX-UHFFFAOYSA-N flufenpyr Chemical compound O=C1C(C)=C(C(F)(F)F)C=NN1C1=CC(OCC(O)=O)=C(Cl)C=C1F WFZSZAXUALBVNX-UHFFFAOYSA-N 0.000 description 1
- DNUAYCRATWAJQE-UHFFFAOYSA-N flufenpyr-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(N2C(C(C)=C(C=N2)C(F)(F)F)=O)=C1F DNUAYCRATWAJQE-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 description 1
- OMMCTJVFFKBTRG-UHFFFAOYSA-N fluorobenzene 1H-pyrrole Chemical compound N1C=CC=C1.FC1=CC=CC=C1 OMMCTJVFFKBTRG-UHFFFAOYSA-N 0.000 description 1
- QOIYTRGFOFZNKF-UHFFFAOYSA-N flupyradifurone Chemical compound C=1C(=O)OCC=1N(CC(F)F)CC1=CC=C(Cl)N=C1 QOIYTRGFOFZNKF-UHFFFAOYSA-N 0.000 description 1
- XWROTTLWMHCFEC-LGMDPLHJSA-N fluthiacet Chemical compound C1=C(Cl)C(SCC(=O)O)=CC(\N=C/2N3CCCCN3C(=O)S\2)=C1F XWROTTLWMHCFEC-LGMDPLHJSA-N 0.000 description 1
- KGXUEPOHGFWQKF-ZCXUNETKSA-N flutianil Chemical compound COC1=CC=CC=C1N(CCS\1)C/1=C(C#N)/SC1=CC(C(F)(F)F)=CC=C1F KGXUEPOHGFWQKF-ZCXUNETKSA-N 0.000 description 1
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- CRHGSCXKJPJNAB-UHFFFAOYSA-M fomesafen-sodium Chemical compound [Na+].C1=C([N+]([O-])=O)C(C(/[O-])=N/S(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CRHGSCXKJPJNAB-UHFFFAOYSA-M 0.000 description 1
- RMFNNCGOSPBBAD-MDWZMJQESA-N formetanate Chemical compound CNC(=O)OC1=CC=CC(\N=C\N(C)C)=C1 RMFNNCGOSPBBAD-MDWZMJQESA-N 0.000 description 1
- NPCUJHYOBSHUJJ-RIYZIHGNSA-N formparanate Chemical compound CNC(=O)OC1=CC=C(\N=C\N(C)C)C(C)=C1 NPCUJHYOBSHUJJ-RIYZIHGNSA-N 0.000 description 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 description 1
- 229950005302 fospirate Drugs 0.000 description 1
- DUFVKSUJRWYZQP-UHFFFAOYSA-N fosthiazate Chemical compound CCC(C)SP(=O)(OCC)N1CCSC1=O DUFVKSUJRWYZQP-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 description 1
- ZEYJIQLVKGBLEM-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2N=C3[CH]C=CC=C3N=2)=C1 ZEYJIQLVKGBLEM-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 229960002598 fumaric acid Drugs 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 238000003197 gene knockdown Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 229950006191 gluconic acid Drugs 0.000 description 1
- IAJOBQBIJHVGMQ-BYPYZUCNSA-N glufosinate-P Chemical compound CP(O)(=O)CC[C@H](N)C(O)=O IAJOBQBIJHVGMQ-BYPYZUCNSA-N 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000010940 green gold Substances 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- WIFXJBMOTMKRMM-UHFFFAOYSA-N halfenprox Chemical compound C=1C=C(OC(F)(F)Br)C=CC=1C(C)(C)COCC(C=1)=CC=CC=1OC1=CC=CC=C1 WIFXJBMOTMKRMM-UHFFFAOYSA-N 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- CNKHSLKYRMDDNQ-UHFFFAOYSA-N halofenozide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)NC(=O)C1=CC=C(Cl)C=C1 CNKHSLKYRMDDNQ-UHFFFAOYSA-N 0.000 description 1
- MJAWMRVEIWPJRW-UHFFFAOYSA-N haloxydine Chemical compound FC=1NC(F)=C(Cl)C(=O)C=1Cl MJAWMRVEIWPJRW-UHFFFAOYSA-N 0.000 description 1
- GOCUAJYOYBLQRH-MRVPVSSYSA-N haloxyfop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-MRVPVSSYSA-N 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- RBJAKRVCYLJDPZ-UHFFFAOYSA-N hexyl 2-[5-(4-bromophenoxy)-2-nitrophenoxy]propanoate Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(=O)OCCCCCC)=CC(OC=2C=CC(Br)=CC=2)=C1 RBJAKRVCYLJDPZ-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229950000858 hydrargaphen Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229930000073 hydroprene Natural products 0.000 description 1
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 description 1
- 230000001969 hypertrophic effect Effects 0.000 description 1
- HICUREFSAIZXFQ-JOWPUVSESA-N i9z29i000j Chemical compound C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\[C@H](OC(=O)C(=N/OC)\C=1C=CC=CC=1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 HICUREFSAIZXFQ-JOWPUVSESA-N 0.000 description 1
- 238000005417 image-selected in vivo spectroscopy Methods 0.000 description 1
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 description 1
- VPRAQYXPZIFIOH-UHFFFAOYSA-N imiprothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)N(CC#C)CC1=O VPRAQYXPZIFIOH-UHFFFAOYSA-N 0.000 description 1
- YFONKFDEZLYQDH-BOURZNODSA-N indaziflam Chemical compound CC(F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-BOURZNODSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000012739 integrated shape imaging system Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 description 1
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 description 1
- HOQADATXFBOEGG-UHFFFAOYSA-N isofenphos Chemical compound CCOP(=S)(NC(C)C)OC1=CC=CC=C1C(=O)OC(C)C HOQADATXFBOEGG-UHFFFAOYSA-N 0.000 description 1
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 description 1
- GRHBQAYDJPGGLF-UHFFFAOYSA-N isothiocyanic acid Chemical compound N=C=S GRHBQAYDJPGGLF-UHFFFAOYSA-N 0.000 description 1
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 description 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
- 229940088649 isoxaflutole Drugs 0.000 description 1
- SDMSCIWHRZJSRN-UHFFFAOYSA-N isoxathion Chemical compound O1N=C(OP(=S)(OCC)OCC)C=C1C1=CC=CC=C1 SDMSCIWHRZJSRN-UHFFFAOYSA-N 0.000 description 1
- 229960002418 ivermectin Drugs 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 229930001540 kinoprene Natural products 0.000 description 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- WBGFKUKWGNKHTN-UHFFFAOYSA-M lithium;2-(2,4-dichlorophenoxy)acetate Chemical compound [Li+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl WBGFKUKWGNKHTN-UHFFFAOYSA-M 0.000 description 1
- WMMYHMKUTCMAIJ-UHFFFAOYSA-M lithium;4-cyano-2,6-diiodophenolate Chemical compound [Li+].[O-]C1=C(I)C=C(C#N)C=C1I WMMYHMKUTCMAIJ-UHFFFAOYSA-M 0.000 description 1
- 229960000521 lufenuron Drugs 0.000 description 1
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WQAVEBBGHAIAQZ-UHFFFAOYSA-N magnesium;2,2,2-trichloroacetic acid Chemical compound [Mg].OC(=O)C(Cl)(Cl)Cl WQAVEBBGHAIAQZ-UHFFFAOYSA-N 0.000 description 1
- QPPXJFBMSFYKMM-UHFFFAOYSA-L magnesium;2,2-dichloropropanoate Chemical compound [Mg+2].CC(Cl)(Cl)C([O-])=O.CC(Cl)(Cl)C([O-])=O QPPXJFBMSFYKMM-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229940098895 maleic acid Drugs 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 229940099690 malic acid Drugs 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- OPXLLQIJSORQAM-UHFFFAOYSA-N mebendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1C(=O)C1=CC=CC=C1 OPXLLQIJSORQAM-UHFFFAOYSA-N 0.000 description 1
- KLGMSAOQDHLCOS-UHFFFAOYSA-N mecarbam Chemical compound CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC KLGMSAOQDHLCOS-UHFFFAOYSA-N 0.000 description 1
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 1
- 229960002523 mercuric chloride Drugs 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- NGYIMTKLQULBOO-UHFFFAOYSA-L mercury dibromide Chemical compound Br[Hg]Br NGYIMTKLQULBOO-UHFFFAOYSA-L 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 229910000474 mercury oxide Inorganic materials 0.000 description 1
- 229960005479 mesulfen Drugs 0.000 description 1
- AHXDSVSZEZHDLV-UHFFFAOYSA-N mesulfen Chemical compound CC1=CC=C2SC3=CC(C)=CC=C3SC2=C1 AHXDSVSZEZHDLV-UHFFFAOYSA-N 0.000 description 1
- ZWJNEYVWPYIKMB-UHFFFAOYSA-N methfuroxam Chemical compound CC1=C(C)OC(C)=C1C(=O)NC1=CC=CC=C1 ZWJNEYVWPYIKMB-UHFFFAOYSA-N 0.000 description 1
- 229930002897 methoprene Natural products 0.000 description 1
- 229950003442 methoprene Drugs 0.000 description 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 1
- JUCNGUOYQGHBJC-UHFFFAOYSA-N methyl 2-(2,4,5-trichlorophenoxy)acetate Chemical group COC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl JUCNGUOYQGHBJC-UHFFFAOYSA-N 0.000 description 1
- HWIGZMADSFQMOI-UHFFFAOYSA-N methyl 2-(2,4-dichlorophenoxy)acetate Chemical group COC(=O)COC1=CC=C(Cl)C=C1Cl HWIGZMADSFQMOI-UHFFFAOYSA-N 0.000 description 1
- NIFKBBMCXCMCAO-UHFFFAOYSA-N methyl 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoate Chemical group COC(=O)C1=CC=C(CNS(C)(=O)=O)C=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 NIFKBBMCXCMCAO-UHFFFAOYSA-N 0.000 description 1
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
- MDXGYOOITGBCBW-UHFFFAOYSA-N methyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 MDXGYOOITGBCBW-UHFFFAOYSA-N 0.000 description 1
- IAUMNRCGDHLAMJ-UHFFFAOYSA-N methyl 2-[4-[5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 IAUMNRCGDHLAMJ-UHFFFAOYSA-N 0.000 description 1
- ZTYVMAQSHCZXLF-UHFFFAOYSA-N methyl 2-[[4,6-bis(difluoromethoxy)pyrimidin-2-yl]carbamoylsulfamoyl]benzoate Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC(F)F)=CC(OC(F)F)=N1 ZTYVMAQSHCZXLF-UHFFFAOYSA-N 0.000 description 1
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 1
- LINPVWIEWJTEEJ-UHFFFAOYSA-N methyl 2-chloro-9-hydroxyfluorene-9-carboxylate Chemical group C1=C(Cl)C=C2C(C(=O)OC)(O)C3=CC=CC=C3C2=C1 LINPVWIEWJTEEJ-UHFFFAOYSA-N 0.000 description 1
- HQTUEAOWLVWJLF-UHFFFAOYSA-N methyl 3,6-dichloropyridine-2-carboxylate Chemical group COC(=O)C1=NC(Cl)=CC=C1Cl HQTUEAOWLVWJLF-UHFFFAOYSA-N 0.000 description 1
- WXUNXXKSYBUHMK-UHFFFAOYSA-N methyl 4-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate;methyl 5-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate Chemical compound COC(=O)C1=CC=C(C)C=C1C1=NC(C)(C(C)C)C(=O)N1.COC(=O)C1=CC(C)=CC=C1C1=NC(C)(C(C)C)C(=O)N1 WXUNXXKSYBUHMK-UHFFFAOYSA-N 0.000 description 1
- KBHDSWIXRODKSZ-UHFFFAOYSA-N methyl 5-chloro-2-(trifluoromethylsulfonylamino)benzoate Chemical compound COC(=O)C1=CC(Cl)=CC=C1NS(=O)(=O)C(F)(F)F KBHDSWIXRODKSZ-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- ZGUYPJJFHYFLBV-UHFFFAOYSA-N methyl n-(5-tert-butyl-1,2-oxazol-3-yl)carbamate Chemical compound COC(=O)NC=1C=C(C(C)(C)C)ON=1 ZGUYPJJFHYFLBV-UHFFFAOYSA-N 0.000 description 1
- ZTFLDKYLDUZSMN-UHFFFAOYSA-N methyl n-[4-(methoxycarbonylamino)phenyl]sulfonylcarbamate Chemical compound COC(=O)NC1=CC=C(S(=O)(=O)NC(=O)OC)C=C1 ZTFLDKYLDUZSMN-UHFFFAOYSA-N 0.000 description 1
- LFDDUUFFHPNIPZ-UHFFFAOYSA-N methyl n-[4-[[2-(4-chloro-2-methylphenoxy)acetyl]amino]phenyl]sulfonylcarbamate Chemical compound C1=CC(S(=O)(=O)NC(=O)OC)=CC=C1NC(=O)COC1=CC=C(Cl)C=C1C LFDDUUFFHPNIPZ-UHFFFAOYSA-N 0.000 description 1
- TZUAKKVHNFEFBG-UHFFFAOYSA-N methyl n-[[2-(furan-2-ylmethylideneamino)phenyl]carbamothioyl]carbamate Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1N=CC1=CC=CO1 TZUAKKVHNFEFBG-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- QFSGULCPPNDNPU-UHFFFAOYSA-M methyl-(2,3,4,5,6-pentachlorophenoxy)mercury Chemical compound C[Hg]OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl QFSGULCPPNDNPU-UHFFFAOYSA-M 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- QYPPRTNMGCREIM-UHFFFAOYSA-M methylarsonate(1-) Chemical compound C[As](O)([O-])=O QYPPRTNMGCREIM-UHFFFAOYSA-M 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- ACBJBUNIAHRWAN-UHFFFAOYSA-N methylmercury;2,3,4,5,6-pentachlorophenol Chemical compound [Hg]C.OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl ACBJBUNIAHRWAN-UHFFFAOYSA-N 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 229920000257 metiram Polymers 0.000 description 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 description 1
- RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- FXWHFKOXMBTCMP-WMEDONTMSA-N milbemycin Natural products COC1C2OCC3=C/C=C/C(C)CC(=CCC4CC(CC5(O4)OC(C)C(C)C(OC(=O)C(C)CC(C)C)C5O)OC(=O)C(C=C1C)C23O)C FXWHFKOXMBTCMP-WMEDONTMSA-N 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 description 1
- 229960004816 moxidectin Drugs 0.000 description 1
- WKQYAIDXQNGNIQ-UHFFFAOYSA-N n'-(3,4-dichlorophenyl)-n,n-dimethylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=C(Cl)C(Cl)=C1 WKQYAIDXQNGNIQ-UHFFFAOYSA-N 0.000 description 1
- WZFNZVJGDCKNME-UHFFFAOYSA-N n'-(4-chloro-2-methylphenyl)-n,n-dimethylmethanimidamide;hydrochloride Chemical compound [Cl-].C[NH+](C)C=NC1=CC=C(Cl)C=C1C WZFNZVJGDCKNME-UHFFFAOYSA-N 0.000 description 1
- TUCSJFNYZJYLHE-UHFFFAOYSA-N n'-tert-butyl-n'-(3,5-dimethylbenzoyl)-2,7-dimethyl-2,3-dihydro-1-benzofuran-6-carbohydrazide Chemical compound CC1=C2OC(C)CC2=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 TUCSJFNYZJYLHE-UHFFFAOYSA-N 0.000 description 1
- HEUHRGXVQSOSHP-UHFFFAOYSA-N n,n-diethyl-4-[methoxy(methylamino)phosphoryl]oxy-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(=O)(NC)OC)=N1 HEUHRGXVQSOSHP-UHFFFAOYSA-N 0.000 description 1
- DRWWMFAZIDKURY-UHFFFAOYSA-N n-(2-methylprop-2-enyl)-2,6-dinitro-n-propyl-4-(trifluoromethyl)aniline Chemical compound CCCN(CC(C)=C)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O DRWWMFAZIDKURY-UHFFFAOYSA-N 0.000 description 1
- JYNOTRFRRIKTHZ-UHFFFAOYSA-N n-(2-tert-butyl-6-methylphenyl)-2-chloroacetamide Chemical compound CC1=CC=CC(C(C)(C)C)=C1NC(=O)CCl JYNOTRFRRIKTHZ-UHFFFAOYSA-N 0.000 description 1
- COHTVILOUURPNC-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-4-hydroxy-1,3-dimethyl-2,6-dioxopyrimidine-5-carboxamide Chemical compound O=C1N(C)C(=O)N(C)C(O)=C1C(=O)NC1=CC=C(Cl)C(Cl)=C1 COHTVILOUURPNC-UHFFFAOYSA-N 0.000 description 1
- RGKLVVDHWRAWRO-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-n-(dimethylcarbamoyl)-4-methoxybenzamide Chemical compound C1=CC(OC)=CC=C1C(=O)N(C(=O)N(C)C)C1=CC=C(Cl)C(Cl)=C1 RGKLVVDHWRAWRO-UHFFFAOYSA-N 0.000 description 1
- FBFCWTCMDMUSDI-UHFFFAOYSA-N n-(4-diethoxyphosphinothioyloxy-6-methylpyrimidin-2-yl)-n-ethylacetamide Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(N(CC)C(C)=O)=N1 FBFCWTCMDMUSDI-UHFFFAOYSA-N 0.000 description 1
- KGMBZDZHRAFLBY-UHFFFAOYSA-N n-(butoxymethyl)-n-(2-tert-butyl-6-methylphenyl)-2-chloroacetamide Chemical compound CCCCOCN(C(=O)CCl)C1=C(C)C=CC=C1C(C)(C)C KGMBZDZHRAFLBY-UHFFFAOYSA-N 0.000 description 1
- LKVOXDJKFRBRQV-UHFFFAOYSA-N n-(dimethyl-$l^{4}-sulfanylidene)-4-(dipropylamino)-3,5-dinitrobenzenesulfonamide Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(=O)(=O)N=S(C)C)C=C1[N+]([O-])=O LKVOXDJKFRBRQV-UHFFFAOYSA-N 0.000 description 1
- FVJQBZVCJVMBIP-UHFFFAOYSA-N n-[2-chloro-5-(trifluoromethyl)phenyl]-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=CC(C(F)(F)F)=CC=C1Cl FVJQBZVCJVMBIP-UHFFFAOYSA-N 0.000 description 1
- IDFXUDGCYIGBDC-UHFFFAOYSA-N n-[4-ethylsulfanyl-2-(trifluoromethyl)phenyl]methanesulfonamide Chemical compound CCSC1=CC=C(NS(C)(=O)=O)C(C(F)(F)F)=C1 IDFXUDGCYIGBDC-UHFFFAOYSA-N 0.000 description 1
- KDOKZLSGPVBDLS-UHFFFAOYSA-N n-[5-(1-chloro-2-methylpropan-2-yl)-1,3,4-thiadiazol-2-yl]cyclopropanecarboxamide Chemical compound S1C(C(C)(CCl)C)=NN=C1NC(=O)C1CC1 KDOKZLSGPVBDLS-UHFFFAOYSA-N 0.000 description 1
- YNKFZRGTXAPYFD-UHFFFAOYSA-N n-[[2-chloro-3,5-bis(trifluoromethyl)phenyl]carbamoyl]-2,6-difluorobenzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1Cl YNKFZRGTXAPYFD-UHFFFAOYSA-N 0.000 description 1
- FVLVBVSILSHUAF-UHFFFAOYSA-N n-benzyl-3,5-dimethyl-n-propan-2-ylbenzamide Chemical compound C=1C(C)=CC(C)=CC=1C(=O)N(C(C)C)CC1=CC=CC=C1 FVLVBVSILSHUAF-UHFFFAOYSA-N 0.000 description 1
- MAGVJLLHDZWQFM-UHFFFAOYSA-N n-chloro-n-methylmethanamine Chemical compound CN(C)Cl MAGVJLLHDZWQFM-UHFFFAOYSA-N 0.000 description 1
- OYRIKLVYHTWHCZ-UHFFFAOYSA-N n-cyclohexyl-2,5-dimethylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC2CCCCC2)=C1C OYRIKLVYHTWHCZ-UHFFFAOYSA-N 0.000 description 1
- MZEVGJJYKJDFQA-UHFFFAOYSA-N n-cyclohexylcyclohexanamine;2-cyclohexyl-4,6-dinitrophenol Chemical compound C1CCCCC1NC1CCCCC1.C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1C1CCCCC1 MZEVGJJYKJDFQA-UHFFFAOYSA-N 0.000 description 1
- KCNUWLJAWRWKMO-UHFFFAOYSA-N n-ethyl-n-propyl-3-propylsulfonyl-1,2,4-triazole-1-carboxamide Chemical compound CCCN(CC)C(=O)N1C=NC(S(=O)(=O)CCC)=N1 KCNUWLJAWRWKMO-UHFFFAOYSA-N 0.000 description 1
- QSFRJEUITMJQCX-UHFFFAOYSA-N n-methylmethanamine;2,3,6-trichlorobenzoic acid Chemical compound C[NH2+]C.[O-]C(=O)C1=C(Cl)C=CC(Cl)=C1Cl QSFRJEUITMJQCX-UHFFFAOYSA-N 0.000 description 1
- VDCHTAFVUAPYGO-UHFFFAOYSA-N n-methylmethanamine;2-(phosphonomethylamino)acetic acid Chemical compound CNC.OC(=O)CNCP(O)(O)=O VDCHTAFVUAPYGO-UHFFFAOYSA-N 0.000 description 1
- VHLJOTFFKVPIAA-UHFFFAOYSA-N n-phenyl-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide Chemical compound FC(F)(F)C1=CC=CC(OC=2C(=CC=CN=2)C(=O)NC=2C=CC=CC=2)=C1 VHLJOTFFKVPIAA-UHFFFAOYSA-N 0.000 description 1
- UQJQVUOTMVCFHX-UHFFFAOYSA-L nabam Chemical compound [Na+].[Na+].[S-]C(=S)NCCNC([S-])=S UQJQVUOTMVCFHX-UHFFFAOYSA-L 0.000 description 1
- JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 description 1
- 235000010298 natamycin Nutrition 0.000 description 1
- 239000004311 natamycin Substances 0.000 description 1
- 229960003255 natamycin Drugs 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- WWJFFVUVFNBJTN-UHFFFAOYSA-N neopolyoxin C Natural products C=1C=C(O)C=NC=1C(O)C(C)C(N)C(=O)NC(C(O)=O)C(C(C1O)O)OC1N1C=CC(=O)NC1=O WWJFFVUVFNBJTN-UHFFFAOYSA-N 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- WWJFFVUVFNBJTN-VHDFTHOZSA-N nikkomycin Z Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@H]2O)O)[C@H](NC(=O)[C@@H](N)[C@H](C)[C@H](O)C=2N=CC(O)=CC=2)C(O)=O)C=CC(=O)NC1=O WWJFFVUVFNBJTN-VHDFTHOZSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000005181 nitrobenzenes Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- BMQNWLUEXNQIGL-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O.CCCCCCCCC(O)=O BMQNWLUEXNQIGL-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- JWEDKKSQRXHXJD-UHFFFAOYSA-N octyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCCCCCCOC(=O)COC1=CC=C(Cl)C=C1Cl JWEDKKSQRXHXJD-UHFFFAOYSA-N 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- UCDPMNSCCRBWIC-UHFFFAOYSA-N orthosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)N(C)C)=N1 UCDPMNSCCRBWIC-UHFFFAOYSA-N 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 1
- IOXAXYHXMLCCJJ-UHFFFAOYSA-N oxetan-3-yl 2-[(4,6-dimethylpyrimidin-2-yl)carbamoylsulfamoyl]benzoate Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC2COC2)=N1 IOXAXYHXMLCCJJ-UHFFFAOYSA-N 0.000 description 1
- 125000005188 oxoalkyl group Chemical group 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- JZPKLLLUDLHCEL-UHFFFAOYSA-N pentoxazone Chemical compound O=C1C(=C(C)C)OC(=O)N1C1=CC(OC2CCCC2)=C(Cl)C=C1F JZPKLLLUDLHCEL-UHFFFAOYSA-N 0.000 description 1
- 125000005981 pentynyl group Chemical group 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004477 pesticide formulation type Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
- FSRHNWZLCJXDBK-UHFFFAOYSA-M phenyl(quinolin-8-yloxy)mercury Chemical compound C=1C=CC2=CC=CN=C2C=1O[Hg]C1=CC=CC=C1 FSRHNWZLCJXDBK-UHFFFAOYSA-M 0.000 description 1
- PDTFCHSETJBPTR-UHFFFAOYSA-N phenylmercuric nitrate Chemical compound [O-][N+](=O)O[Hg]C1=CC=CC=C1 PDTFCHSETJBPTR-UHFFFAOYSA-N 0.000 description 1
- XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 description 1
- DCNLOVYDMCVNRZ-UHFFFAOYSA-N phenylmercury(.) Chemical class [Hg]C1=CC=CC=C1 DCNLOVYDMCVNRZ-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- RJQUHEYNLDNJLN-UHFFFAOYSA-N picloram-methyl Chemical group COC(=O)C1=NC(Cl)=C(Cl)C(N)=C1Cl RJQUHEYNLDNJLN-UHFFFAOYSA-N 0.000 description 1
- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 description 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
- MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 description 1
- QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 1
- 239000005962 plant activator Substances 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
- QTWDVSMYLOZQBZ-UHFFFAOYSA-N potassium;(5-acetamido-2,4-dimethylphenyl)-(trifluoromethylsulfonyl)azanide Chemical compound [K+].CC(=O)NC1=CC([N-]S(=O)(=O)C(F)(F)F)=C(C)C=C1C QTWDVSMYLOZQBZ-UHFFFAOYSA-N 0.000 description 1
- LIOPHZNMBKHGAV-UHFFFAOYSA-M potassium;2-(phosphonomethylamino)acetate Chemical compound [K+].OC(=O)CNCP(O)([O-])=O LIOPHZNMBKHGAV-UHFFFAOYSA-M 0.000 description 1
- RLQCYSVYYHHLIL-UHFFFAOYSA-M potassium;3,6-dichloropyridine-2-carboxylate Chemical compound [K+].[O-]C(=O)C1=NC(Cl)=CC=C1Cl RLQCYSVYYHHLIL-UHFFFAOYSA-M 0.000 description 1
- WRBJKRRJBCSNLE-UHFFFAOYSA-M potassium;4-(2,4-dichlorophenoxy)butanoate Chemical compound [K+].[O-]C(=O)CCCOC1=CC=C(Cl)C=C1Cl WRBJKRRJBCSNLE-UHFFFAOYSA-M 0.000 description 1
- ZRHANBBTXQZFSP-UHFFFAOYSA-M potassium;4-amino-3,5,6-trichloropyridine-2-carboxylate Chemical compound [K+].NC1=C(Cl)C(Cl)=NC(C([O-])=O)=C1Cl ZRHANBBTXQZFSP-UHFFFAOYSA-M 0.000 description 1
- 244000062645 predators Species 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229950005488 proclonol Drugs 0.000 description 1
- ASALLPQQHGTWEF-UHFFFAOYSA-N prop-2-ynyl 2-[4-(3,5-dichloropyridin-2-yl)oxyphenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OCC#C)=CC=C1OC1=NC=C(Cl)C=C1Cl ASALLPQQHGTWEF-UHFFFAOYSA-N 0.000 description 1
- SXHQLHGHMREHMX-UHFFFAOYSA-N propan-2-yl 2-(2,4,5-trichlorophenoxy)acetate Chemical group CC(C)OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SXHQLHGHMREHMX-UHFFFAOYSA-N 0.000 description 1
- WHOKDONDRZNCBC-UHFFFAOYSA-N propan-2-yl 2-(2,4-dichlorophenoxy)acetate Chemical group CC(C)OC(=O)COC1=CC=C(Cl)C=C1Cl WHOKDONDRZNCBC-UHFFFAOYSA-N 0.000 description 1
- IXTOWLKEARFCCP-UHFFFAOYSA-N propan-2-yl 2-[methoxy-(propan-2-ylamino)phosphinothioyl]oxybenzoate Chemical group CC(C)NP(=S)(OC)OC1=CC=CC=C1C(=O)OC(C)C IXTOWLKEARFCCP-UHFFFAOYSA-N 0.000 description 1
- OYJMHAFVOZPIOY-UHFFFAOYSA-N propan-2-yl 2-chloro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]benzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1 OYJMHAFVOZPIOY-UHFFFAOYSA-N 0.000 description 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- URELEWKDONECLX-UHFFFAOYSA-N propyl 2-(2,4-dichlorophenoxy)acetate Chemical group CCCOC(=O)COC1=CC=C(Cl)C=C1Cl URELEWKDONECLX-UHFFFAOYSA-N 0.000 description 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- YXIIPOGUBVYZIW-UHFFFAOYSA-N pyraflufen Chemical compound ClC1=C(OC(F)F)N(C)N=C1C1=CC(OCC(O)=O)=C(Cl)C=C1F YXIIPOGUBVYZIW-UHFFFAOYSA-N 0.000 description 1
- APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 description 1
- DDIQWGKUSJOETH-UHFFFAOYSA-N pyrafluprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SCF)=C1NCC1=CN=CC=N1 DDIQWGKUSJOETH-UHFFFAOYSA-N 0.000 description 1
- DWTVBEZBWMDXIY-UHFFFAOYSA-N pyrametostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=C(C)C(C=2C=CC=CC=2)=NN1C DWTVBEZBWMDXIY-UHFFFAOYSA-N 0.000 description 1
- URXNNPCNKVAQRA-XMHGGMMESA-N pyraoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C=2C=CC(Cl)=CC=2)=NN1C URXNNPCNKVAQRA-XMHGGMMESA-N 0.000 description 1
- DWSPRBSLSXQIEJ-UHFFFAOYSA-N pyrasulfotole Chemical compound CC1=NN(C)C(O)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1S(C)(=O)=O DWSPRBSLSXQIEJ-UHFFFAOYSA-N 0.000 description 1
- ROVGZAWFACYCSP-VUMXUWRFSA-N pyrethrin I Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-VUMXUWRFSA-N 0.000 description 1
- CRFYLQMIDWBKRT-LPYMAVHISA-N pyribencarb Chemical compound C1=C(Cl)C(CNC(=O)OC)=CC(C(\C)=N\OCC=2N=C(C)C=CC=2)=C1 CRFYLQMIDWBKRT-LPYMAVHISA-N 0.000 description 1
- CXJSOEPQXUCJSA-UHFFFAOYSA-N pyridaphenthion Chemical compound N1=C(OP(=S)(OCC)OCC)C=CC(=O)N1C1=CC=CC=C1 CXJSOEPQXUCJSA-UHFFFAOYSA-N 0.000 description 1
- MIOBBYRMXGNORL-UHFFFAOYSA-N pyrifluquinazon Chemical compound C1C2=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C2N(C(=O)C)C(=O)N1NCC1=CC=CN=C1 MIOBBYRMXGNORL-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- ITKAIUGKVKDENI-UHFFFAOYSA-N pyrimidifen Chemical compound CC1=C(C)C(CCOCC)=CC=C1OCCNC1=NC=NC(CC)=C1Cl ITKAIUGKVKDENI-UHFFFAOYSA-N 0.000 description 1
- DEIKMOQTJBGGAX-DJKKODMXSA-N pyriminobac Chemical compound CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(O)=O DEIKMOQTJBGGAX-DJKKODMXSA-N 0.000 description 1
- USSIUIGPBLPCDF-KEBDBYFISA-N pyriminobac-methyl Chemical group CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC USSIUIGPBLPCDF-KEBDBYFISA-N 0.000 description 1
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 description 1
- 229960003811 pyrithione disulfide Drugs 0.000 description 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- JTDPJYXDDYUJBS-UHFFFAOYSA-N quinoline-2-carbohydrazide Chemical compound C1=CC=CC2=NC(C(=O)NN)=CC=C21 JTDPJYXDDYUJBS-UHFFFAOYSA-N 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 229950010630 quintiofos Drugs 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
- OSUHJPCHFDQAIT-GFCCVEGCSA-N quizalofop-P-ethyl Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 OSUHJPCHFDQAIT-GFCCVEGCSA-N 0.000 description 1
- RDYMFSUJUZBWLH-AZVNHNRSSA-N qy5y9r7g0e Chemical compound C([C@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-AZVNHNRSSA-N 0.000 description 1
- NEMNPWINWMHUMR-UHFFFAOYSA-N rafoxanide Chemical compound OC1=C(I)C=C(I)C=C1C(=O)NC(C=C1Cl)=CC=C1OC1=CC=C(Cl)C=C1 NEMNPWINWMHUMR-UHFFFAOYSA-N 0.000 description 1
- 229950002980 rafoxanide Drugs 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 description 1
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 description 1
- BUHNESFUCHPWED-UHFFFAOYSA-N s-[(4-methoxyphenyl)methyl] n,n-diethylcarbamothioate Chemical compound CCN(CC)C(=O)SCC1=CC=C(OC)C=C1 BUHNESFUCHPWED-UHFFFAOYSA-N 0.000 description 1
- YGBMMMOLNODPBP-GWGZPXPZSA-N s-ethyl (2e,4e)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienethioate Chemical compound CCSC(=O)\C=C(/C)\C=C\CC(C)CCCC(C)(C)OC YGBMMMOLNODPBP-GWGZPXPZSA-N 0.000 description 1
- NMFAMPYSJHIYMR-UHFFFAOYSA-N s-ethyl n-[3-(dimethylamino)propyl]carbamothioate;hydrochloride Chemical compound [Cl-].CCSC(=O)NCCC[NH+](C)C NMFAMPYSJHIYMR-UHFFFAOYSA-N 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 description 1
- 229960000581 salicylamide Drugs 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- HKAMKLBXTLTVCN-UHFFFAOYSA-N simeton Chemical compound CCNC1=NC(NCC)=NC(OC)=N1 HKAMKLBXTLTVCN-UHFFFAOYSA-N 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- CBXWGGFGZDVPNV-UHFFFAOYSA-N so4-so4 Chemical compound OS(O)(=O)=O.OS(O)(=O)=O CBXWGGFGZDVPNV-UHFFFAOYSA-N 0.000 description 1
- RTWIRLHWLMNVCC-WQYNNSOESA-M sodium (2S)-2-[[(2S)-2-[[(2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoyl]amino]propanoyl]amino]propanoate Chemical compound [Na+].[O-]C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O RTWIRLHWLMNVCC-WQYNNSOESA-M 0.000 description 1
- ZLVSYODPTJZFMK-UHFFFAOYSA-M sodium 4-hydroxybenzoate Chemical compound [Na+].OC1=CC=C(C([O-])=O)C=C1 ZLVSYODPTJZFMK-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- PDEFQWNXOUGDJR-UHFFFAOYSA-M sodium;2,2-dichloropropanoate Chemical compound [Na+].CC(Cl)(Cl)C([O-])=O PDEFQWNXOUGDJR-UHFFFAOYSA-M 0.000 description 1
- DPMABEYFRYKAHD-UHFFFAOYSA-M sodium;2,3,6-trichlorobenzoate Chemical compound [Na+].[O-]C(=O)C1=C(Cl)C=CC(Cl)=C1Cl DPMABEYFRYKAHD-UHFFFAOYSA-M 0.000 description 1
- KXVMKVOQCMSZSZ-UHFFFAOYSA-M sodium;2-(2,4,5-trichlorophenoxy)acetate Chemical compound [Na+].[O-]C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl KXVMKVOQCMSZSZ-UHFFFAOYSA-M 0.000 description 1
- RFOHRSIAXQACDB-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)acetate Chemical compound [Na+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl RFOHRSIAXQACDB-UHFFFAOYSA-M 0.000 description 1
- KISFEBPWFCGRGN-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)ethyl sulfate Chemical compound [Na+].[O-]S(=O)(=O)OCCOC1=CC=C(Cl)C=C1Cl KISFEBPWFCGRGN-UHFFFAOYSA-M 0.000 description 1
- ZEVCJZRMCOYJSP-UHFFFAOYSA-N sodium;2-(dithiocarboxyamino)ethylcarbamodithioic acid Chemical compound [Na+].SC(=S)NCCNC(S)=S ZEVCJZRMCOYJSP-UHFFFAOYSA-N 0.000 description 1
- XKKTVIWAHIWFAN-UHFFFAOYSA-M sodium;2-[2-[2-(dodecylamino)ethylamino]ethylamino]acetate Chemical compound [Na+].CCCCCCCCCCCCNCCNCCNCC([O-])=O XKKTVIWAHIWFAN-UHFFFAOYSA-M 0.000 description 1
- LRWSMDCIWRLZIX-UHFFFAOYSA-M sodium;2-butan-2-yl-4,6-dinitrophenolate Chemical compound [Na+].CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1[O-] LRWSMDCIWRLZIX-UHFFFAOYSA-M 0.000 description 1
- PPKIJAQKBAYNNL-UHFFFAOYSA-M sodium;4-(2,4-dichlorophenoxy)butanoate Chemical compound [Na+].[O-]C(=O)CCCOC1=CC=C(Cl)C=C1Cl PPKIJAQKBAYNNL-UHFFFAOYSA-M 0.000 description 1
- QGKPUZOFTJQTHL-UHFFFAOYSA-M sodium;4-cyano-2,6-diiodophenolate Chemical compound [Na+].[O-]C1=C(I)C=C(C#N)C=C1I QGKPUZOFTJQTHL-UHFFFAOYSA-M 0.000 description 1
- JXIAOZNHSODSNJ-UHFFFAOYSA-M sodium;5-bromo-3-butan-2-yl-6-methylpyrimidin-1-ide-2,4-dione Chemical compound [Na+].CCC(C)N1C(=O)[N-]C(C)=C(Br)C1=O JXIAOZNHSODSNJ-UHFFFAOYSA-M 0.000 description 1
- HLPHHOLZSKWDAK-UHFFFAOYSA-M sodium;formaldehyde;naphthalene-1-sulfonate Chemical compound [Na+].O=C.C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HLPHHOLZSKWDAK-UHFFFAOYSA-M 0.000 description 1
- JRQGDDUXDKCWRF-UHFFFAOYSA-M sodium;n-(2-methoxycarbonylphenyl)sulfonyl-4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carboximidate Chemical compound [Na+].O=C1N(C)C(OCCC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1C(=O)OC JRQGDDUXDKCWRF-UHFFFAOYSA-M 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000010129 solution processing Methods 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 229930185156 spinosyn Natural products 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- SFZCNBIFKDRMGX-UHFFFAOYSA-N sulfur hexafluoride Chemical compound FS(F)(F)(F)(F)F SFZCNBIFKDRMGX-UHFFFAOYSA-N 0.000 description 1
- 229960000909 sulfur hexafluoride Drugs 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 239000006273 synthetic pesticide Substances 0.000 description 1
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- ICTQUFQQEYSGGJ-UHFFFAOYSA-N thiocyclam oxalate Chemical compound OC(=O)C(O)=O.CN(C)C1CSSSC1 ICTQUFQQEYSGGJ-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 229960004906 thiomersal Drugs 0.000 description 1
- PYNKFIVDSJSNGL-UHFFFAOYSA-N thiosultap Chemical compound OS(=O)(=O)SCC(N(C)C)CSS(O)(=O)=O PYNKFIVDSJSNGL-UHFFFAOYSA-N 0.000 description 1
- MBNMHBAJUNHZRE-UHFFFAOYSA-M thiosultap monosodium Chemical compound [Na+].OS(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O MBNMHBAJUNHZRE-UHFFFAOYSA-M 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- OEJNXTAZZBRGDN-UHFFFAOYSA-N toxaphene Chemical compound ClC1C(Cl)C2(Cl)C(CCl)(CCl)C(=C)C1(Cl)C2(Cl)Cl OEJNXTAZZBRGDN-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- PIHCREFCPDWIPY-UHFFFAOYSA-N tris[2-(2,4-dichlorophenoxy)ethyl] phosphite Chemical compound ClC1=CC(Cl)=CC=C1OCCOP(OCCOC=1C(=CC(Cl)=CC=1)Cl)OCCOC1=CC=C(Cl)C=C1Cl PIHCREFCPDWIPY-UHFFFAOYSA-N 0.000 description 1
- 210000005239 tubule Anatomy 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- FVECELJHCSPHKY-JLSHOZRYSA-N veratridine Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)O[C@@H]1[C@@]2(O)O[C@]34C[C@@]5(O)[C@H](CN6[C@@H](CC[C@H](C)C6)[C@@]6(C)O)[C@]6(O)[C@@H](O)C[C@@]5(O)[C@@H]4CC[C@H]2[C@]3(C)CC1 FVECELJHCSPHKY-JLSHOZRYSA-N 0.000 description 1
- VRNFXUOQGOAQBZ-DYXAMGHASA-N veratrin Chemical compound C1[C@@H](C)CC[C@H]2[C@](O)(C)[C@@]3(O)[C@@H](O)C[C@@]4(O)[C@@H]5CC[C@H]6[C@]7(C)CC[C@H](OC(=O)C(\C)=C/C)[C@@]6(O)O[C@@]75C[C@@]4(O)[C@@H]3CN21.C1=C(OC)C(OC)=CC=C1C(=O)O[C@@H]1[C@@]2(O)O[C@@]34C[C@@]5(O)[C@H](CN6[C@@H](CC[C@H](C)C6)[C@@]6(C)O)[C@]6(O)[C@@H](O)C[C@@]5(O)[C@@H]4CC[C@H]2[C@]3(C)CC1 VRNFXUOQGOAQBZ-DYXAMGHASA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/86—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
本申请公开了具有下式(“式1”和“式2”和“式3”)的分子。Ar1、Het、Ar2、R1、R2、R3、R4和R5在本申请中进一步描述。
Description
对相关申请的交叉参考
该申请要求2012年2月2日提交的美国临时申请61/594,054的优先权。将该临时申请的全部内容引入到本申请中作为参考。
技术领域
本申请公开的发明涉及的领域是生产可用作杀虫剂(例如杀螨虫剂、杀昆虫剂、杀软体动物剂和杀线虫剂)的分子的方法、所述分子和使用所述分子来防治害虫的方法。
背景技术
每年在世界各地害虫导致数百万人死亡。此外,存在一万种以上导致农业损失的害虫物种。这些全世界范围内的农业损失每年达到几十亿美元。
白蚁(termite)导致对各种私人和公共结构的破坏。这些全世界范围内的白蚁破坏损失每年达到几十亿美元。
贮存的食物(stored food)中的害虫吃掉贮存食物并掺杂到这些贮存食物中。这些全世界范围内的贮存食物损失每年达到几十亿美元,但更重要的是,这剥夺了人们所需要的食物。
人们急需新的杀虫剂。某些害虫对目前使用的杀虫剂形成耐药。数百种害虫对一种或多种杀虫剂耐药。对一些较老的杀虫剂(例如DDT、氨基甲酸酯类和有机磷类)形成耐药是公知的,但是对一些较新的杀虫剂也已经形成耐药。
因此,出于多种原因(包括上述原因)需要新的杀虫剂。
定义
在定义中给出的实例是通常非穷举性的且不能解释为对本申请公开的本发明进行限制。应当理解的是,取代基应当符合化学成键规则并就其与之相连的具体分子而言满足立体相容约束。
“杀螨虫剂组”在“杀螨虫剂”标题下定义。
“AI组”在“除草剂组”标题下定义。
“烯基”是指由碳和氢构成的非环状不饱和(至少一个碳-碳双键)支化或非支化取代基,例如乙烯基、烯丙基、丁烯基、戊烯基和己烯基。
“烯基氧基”是指还包含碳-氧单键的烯基,例如烯丙基氧基、丁烯基氧基、戊烯基氧基和己烯基氧基。
“烷氧基”是指还包含碳-氧单键的烷基,例如甲氧基、乙氧基、丙氧基、异丙氧基、丁氧基、异丁氧基和叔丁氧基。
“烷基”是指由碳和氢构成的非环状饱和支化或非支化取代基,例如甲基、乙基、丙基、异丙基、丁基和叔丁基。
“炔基”是指由碳和氢构成的非环状不饱和(至少一个碳-碳叁键)支化或非支化取代基,例如乙炔基、炔丙基、丁炔基和戊炔基。
“炔基氧基”是指还包含碳-氧单键的炔基,例如戊炔基氧基、己炔基氧基、庚炔基氧基和辛炔基氧基。
“芳基”是指由碳和氢构成的环状芳族取代基,例如苯基、萘基和联苯基。
“环烯基”是指由碳和氢构成的单环或多环不饱和(至少一个碳-碳双键)取代基,例如环丁烯基、环戊烯基、环己烯基、降冰片烯基、二环[2.2.2]辛烯基、四氢萘基、六氢萘基和八氢萘基。
“环烯基氧基”是指还包含碳-氧单键的环烯基,例如环丁烯基氧基、环戊烯基氧基、降冰片烯基氧基和二环[2.2.2]辛烯基氧基。
“环烷基”是指由碳和氢构成的单环或多环饱和取代基,例如环丙基、环丁基、环戊基、降冰片基、二环[2.2.2]辛基和十氢萘基。
“环烷氧基”是指还包含碳-氧单键的环烷基,例如环丙基氧基、环丁基氧基、环戊基氧基、降冰片基氧基和二环[2.2.2]辛基氧基。
“杀真菌剂组”在“杀真菌剂”标题下定义。
“卤素”是指氟、氯、溴和碘。
“卤代烷氧基”是指还包含一个至最大可能数目的相同或不同卤素的烷氧基,例如氟甲氧基、三氟甲氧基、2,2-二氟丙氧基、氯甲氧基、三氯甲氧基、1,1,2,2-四氟乙氧基和五氟乙氧基。
“卤代烷基”是指还包含一个至最大可能数目的相同或不同卤素的烷基,例如氟甲基、三氟甲基、2,2-二氟丙基、氯甲基、三氯甲基和1,1,2,2-四氟乙基。
“除草剂组”在“除草剂”标题下定义。
“杂环基”是指可为完全饱和、部分不饱和或完全不饱和的环状取代基,其中所述环状结构含有至少一个碳和至少一个杂原子,其中所述杂原子为氮、硫或氧。芳族杂环基的实例包括但不限于苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、三嗪基和三唑基。完全饱和杂环基的实例包括但不限于哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基和四氢吡喃基。部分不饱和杂环基的实例包括但不限于1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
“杀昆虫剂组”在“杀昆虫剂”标题下定义。
“杀线虫剂组”在“杀线虫剂”标题下定义。
“协同剂组”在“协同性混合物和协同剂”标题下定义。
发明内容
本申请公开了具有下式(“式1”、“式2”和“式3”)的分子(下式中的氮仅出于识别它们且能够在本申请通篇中清楚地指代它们的目的而被编号为1、2和3):
其中
(a)Ar1为
(1)呋喃基、苯基、哒嗪基、吡啶基、嘧啶基或噻吩基,或
(2)取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基或取代的噻吩基,
其中所述取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基和取代的噻吩基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(b)Het为含有一个或多个独立选自氮、硫或氧的杂原子的5或6元饱和或不饱和杂环,其中Ar1和Ar2彼此不处于邻位(但可为间位或对位例如就5元环而言它们为1,3位且就6元环而言它们为1,3位或1,4位)且其中所述杂环还可取代有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(c)Ar2为
(1)呋喃基、苯基、哒嗪基、吡啶基、嘧啶基或噻吩基,或
(2)取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基或取代的噻吩基,
其中所述取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基和取代的噻吩基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C1-C6卤代烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(d)R1选自H、CN、F、Cl、Br、I、C1-C6烷基、C3-C6环烷基、C3-C6环烷氧基、C1-C6烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、OSO2(C1-C6烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基或苯氧基,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基和苯氧基任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(e)R2为H、C1-C6烷基、C3-C6环烷基、C2-C6烯基、C2-C6炔基、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、C1-C6烷基苯基、C1-C6烷基-O-苯基、C(=O)Het-1、Het-1、C1-C6烷基Het-1或C1-C6烷基-O-Het-1,
其中每个烷基、环烷基、烯基、炔基、苯基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基和Het-1;
(f)R3为C1-C6烷基、C3-C6环烷基、C2-C6烯基、C2-C6炔基、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、C1-C6烷基苯基、C1-C6烷基-O-苯基、C(=O)Het-1、Het-1、C1-C6烷基Het-1、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6烷基-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6卤代烷基、C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-苯基、C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-C1-C6烷基苯基、C1-C6烷基C(=O)N(Rx)C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基Het-1C(=O)-O-C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基Het-1、C1-C6烷基C(=O)Het-1、C1-C6烷基C(=O)N(Rx)C1-C6烷基(N(Rx)(Ry))(C(=O)OH)、C1-C6烷基C(=O)N(Rx)C1-C6烷基N(Rx)(Ry)、C1-C6烷基C(=O)N(Rx)C1-C6烷基N(Rx)C(=O)-O-C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基(N(Rx)C(=O)-O-C1-C6烷基)(C(=O)OH)、C1-C6烷基C(=O)Het-1C(=O)-O-C1-C6烷基、C1-C6烷基-O-C(=O)-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基、C1-C6烷基-O-C(=O)C3-C6环烷基、C1-C6烷基-O-C(=O)Het-1、C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-C1-C6烷基、C1-C6烷基-NRxRy或C1-C6烷基-O-Het-1,
其中每个烷基、环烷基、烯基、炔基、苯基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、Si(C1-C6烷基)3、S(=O)nNRxRy和Het-1;
(g)R4为H、C1-C6烷基、C3-C6环烷基、C2-C6烯基、C2-C6炔基、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、C1-C6烷基苯基、C1-C6烷基-O-苯基、C(=O)Het-1、Het-1、C1-C6烷基Het-1或C1-C6烷基-O-Het-1,
其中每个烷基、环烷基、烯基、炔基、苯基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基和Het-1;
(h)R5为1元饱和或2-4元饱和或不饱和烃基连接物,其中所述连接物还可取代有F、Cl、Br、I、CN、NO2、氧代、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基和Het-1,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基、苯氧基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、卤代苯基、苯氧基和Het-1;
(i)n=0、1或2;
(j)Rx和Ry独立选自H、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)和苯基,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基、苯氧基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、卤代苯基、苯氧基和Het-1,
或Rx和Ry一起可任选形成可含有一个或多个选自氮、硫和氧的杂原子的5至7元饱和或不饱和环状基团且其中所述环状基团可含有>C=O或>C=S且其中所述环状基团可取代有F、Cl、Br、I、CN、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、取代的苯基、苯氧基和Het-1;和
(k)Het-1为含有一个或多个独立选自氮、硫或氧的杂原子的5或6元饱和或不饱和杂环。
应当理解的是,在式1中,当R2为H时,所述化合物可按不止一种互变异构形式或异构形式存在,其中所述氢连接于任意一个氮原子;进一步地,E和Z异构体都存在。本发明要求保护所述化合物的任意和所有异构形式。
在另一个实施方案中,Ar1为取代的苯基,其中所述取代的苯基具有一个或多个独立选自以下的取代基:C1-C6卤代烷基和C1-C6卤代烷氧基。
在另一个实施方案中,Ar1为取代的苯基,其中所述取代的苯基具有一个或多个独立选自以下的取代基:CF3、OCF3和OCF2CF3。
在另一个实施方案中,Het选自三唑基、咪唑基或吡唑基,所述基团可为取代或未取代的。
在另一个实施方案中,Het为1,2,4-三唑基:
在另一个实施方案中,Het为1,4-咪唑基:
在另一个实施方案中,Het为1,3-吡唑基:
在另一个实施方案中,Het为取代的1,3-吡唑基。
在另一个实施方案中,Het为1,4-吡唑基:
在另一个实施方案中,Ar2为苯基。
在另一个实施方案中,R1为H或C1-C6烷基。
在另一个实施方案中,R1为H或CH3。
在另一个实施方案中,R2为H。
在另一个实施方案中,R3选自C1-C6烷基、C2-C6烯基、C2-C6炔基、C1-C6烷基苯基、C1-C6烷基Het-1、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6烷基-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基-O-C1-C6卤代烷基、C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-苯基、C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-C1-C6烷基苯基、C1-C6烷基C(=O)N(Rx)C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基Het-1C(=O)-O-C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基Het-1、C1-C6烷基C(=O)Het-1、C1-C6烷基C(=O)N(Rx)C1-C6烷基(N(Rx)(Ry))(C(=O)OH)、C1-C6烷基C(=O)N(Rx)C1-C6烷基N(Rx)(Ry)、C1-C6烷基C(=O)N(Rx)C1-C6烷基N(Rx)C(=O)-O-C1-C6烷基、C1-C6烷基C(=O)N(Rx)C1-C6烷基(N(Rx)C(=O)-O-C1-C6烷基)(C(=O)OH)、C1-C6烷基C(=O)Het-1C(=O)-O-C1-C6烷基、C1-C6烷基-O-C(=O)-O-C1-C6烷基、C1-C6烷基-O-C(=O)C1-C6烷基、C1-C6烷基-O-C(=O)C3-C6环烷基、C1-C6烷基-O-C(=O)Het-1或C1-C6烷基-O-C(=O)C1-C6烷基-N(Rx)C(=O)-O-C1-C6烷基,其中每个烷基、烯基、炔基、苯基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、C1-C6烷基、C1-C6卤代烷基、C1-C6卤代烷氧基、S(=O)n(C1-C6烷基)、C(=O)OH、C(=O)O(C1-C6烷基)、苯基、Si(C1-C6烷基)3和S(=O)nNRxRy。
在另一个实施方案中,R4为苯基、C1-C6烷基苯基、Het-1或C1-C6烷基-O-苯基,其中每个烷基、Het-1和苯基任选取代有一个或多个独立选自以下的取代基:F、Cl、NRxRy、C1-C6烷基、C3-C6环烷基、C1-C6卤代烷氧基、C(=O)O C1-C6烷基或C1-C6烷氧基。
在另一个实施方案中,R5取代有氧代、C(=O)OH、苯基和Het-1,其中每个苯基和Het-1可任选取代有一个或多个独立选自以下的取代基:氧代、C1-C6卤代烷基、C1-C6卤代烷氧基、C(=O)OH和卤代苯基。
在另一个实施方案中,Rx和Ry独立选自H和苯基,其中所述苯基可任选取代有一个或多个独立选自以下的取代基:F和Cl。
在另一个实施方案中:
Ar1为取代的苯基其中所述取代的苯基具有一个或多个C1-C6卤代烷氧基;
Het为三唑基;
Ar2为苯基;
R1为H;
R2为H;
R3为C1-C6烷基Het-1,其中所述烷基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、C1-C6烷基、C1-C6卤代烷基、C1-C6卤代烷氧基、S(=O)n(C1-C6烷基)、C(=O)OH、C(=O)O(C1-C6烷基)、苯基、Si(C1-C6烷基)3和S(=O)nNRxRy;
R4为苯基,其中所述苯基任选取代有一个或多个独立选自以下的取代基:F、Cl、NRxRy、C1-C6烷基或C1-C6烷氧基;和
n=0、1或2;
Rx和Ry独立选自H和苯基,其中所述苯基可任选取代有一个或多个独立选自以下的取代基:F和Cl;和
Het-1为含有一个或多个独立选自氮、硫或氧的杂原子的5或6元饱和或不饱和杂环。
在另一个实施方案中,Het-1选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
在另一个实施方案中,Het选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
在另一个实施方案中,Het-1选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、苯并噻二唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、噻吩基、吡唑基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
在另一个实施方案中,Het-1选自苯并噻二唑基、呋喃基、噁唑基、噻吩基和吡唑基。
尽管已经详细描述了这些实施方案,但是这些详细描述的实施方案的其它实施方案和组合也是可能的。
式1、式2和式3分子通常会具有约100道尔顿至约1200道尔顿的分子量。然而,通常优选的是,所述分子质量为约120道尔顿至约900道尔顿且通常更优选的是,所述分子质量为约400道尔顿至约800道尔顿。
制备三芳基中间体
本发明化合物可通过制备三芳基中间体Ar1-Het-Ar2,然后将其与所期望的中间体连接形成所期望的化合物来制备。多种三芳基中间体可用于制备本发明化合物,条件是所述三芳基在Ar2上含有适当的官能团,所期望中间体的剩余部分可与所述官能团相连。适当的官能团包括氧代烷基或甲酰基。这些三芳基-中间体可通过之前在化学文献包括PCT国际申请公开文本WO2009/102736 A1(Crouse等人)中描述的方法来制备。
制备与腙连接的化合物
与腙连接的化合物可通过以下三种方法中的一种由相应的芳基醛或芳基酮来制备:(1)与肼反应,然后在四氢呋喃(THF)中在0至100℃的温度与芳基异硫氰酸酯反应(反应A);(2)与肼基二硫代羧酸甲酯反应,然后在极性非质子性溶剂例如N,N-二甲基甲酰胺(DMF)中在25至150℃的温度与苯胺反应(反应B);或(3)在极性质子性溶剂例如乙醇(EtOH)中在0至100℃的温度与芳基氨基硫代脲反应(反应C),所述芳基氨基硫代脲为商购的或可由本领域技术人员来制备。
制备与烷基化的腙连接的化合物
与烷基化的腙连接的化合物可通过以下两种方法中的一种由相应的与腙连接的化合物来制备:(1)在EtOH或丙酮中在0至100℃的温度与烷化剂反应1至24小时;或(2)在氯仿(CHCl3)、二氯甲烷(CH2Cl2)或其它卤代碳溶剂中在存在或不存在碱例如碳酸氢钠的情况下在20至60℃与烷化剂反应。
其中R5与N3形成环(参见以下方案)的式2化合物或其中R5与N2形成环的式3化合物可通过使用α-卤代酸、酰卤、酯或酮由适当的非环状前体来制备(F或G或H)。例如,在质子性溶剂例如EtOH或甲醇(CH3OH)中用稍过量的α-卤代酯处理硫代半卡巴腙,导致S-烷基化,随后专一性地在N3上环闭合(反应F;参见例如J.Indian Chemical Society 1966,43,275-276或J.Heterocycl.Chem.1978,15,335-336)。当在30℃至80℃的温度使用非质子性溶剂例如CH2Cl2或二氯乙烷(ClCH2CH2Cl)时,选择添加α-卤代酮也有利于在N3上闭合,随后脱水形成亚氨基噻唑啉(反应G)。当在卤代烃溶剂例如CH2Cl2或ClCH2CH2Cl中使用α-卤代酸或酰卤或酯时,观察到在N2(反应H)和N3上都发生环闭合。尽管这些反应经常在不添加碱的情况下进行,但是可加入碱例如碳酸氢钠、碳酸钠或乙酸钠或胺碱例如吡啶或三乙胺。
可选择地,如以下方案(I)中所示,可通过在乙酸中在30至70℃用3-氨基-2-(芳基亚氨基)噻唑烷-4-酮处理醛或酮来制备3-亚芳基亚氨基-2-芳基亚氨基噻唑啉-4-酮,其中R1如前所述。已描述了中间体1-氨基-2-芳基亚氨基噻唑啉-5-酮(其中R4为苯基)(参见例如J.Org.Chem.1962,27,2878);其通过在热EtOH中用2-氯乙酸乙酯和乙酸钠处理4-苯基氨基硫代脲来制备(收率为80%)。
可选择地,式2和式3化合物可如下形成:在丙酮或2-丁酮或其它适当的溶剂中在环境温度至100℃的温度将硫代半卡巴腙前体和二卤代化合物“Hal1-R5-Hal2”例如1-溴-2-氯乙烷加热1至72小时,其中使用碱例如碳酸钾或三乙胺。S-烷基化中间体在N2或N3处发生环化,得到式2或式3化合物(反应J)。在一些情况下,可需要加入KI以加速中间体S-烷基化衍生物环化成环闭合产物。
制备本发明化合物的可选择方法是用不饱和酯或酰氯处理硫代半卡巴腙前体(反应L)。
取代的肼基硫代甲酰胺中间体(例如在以上方法C中使用的那些)可通过化学文献中记载的多种方法来制备。可选择地,化合物(其中Ra、Rb和Rc不是源自商购的苯胺)可根据以下方案来制备。例如,取代有一个或多个Rc取代基的2-卤代硝基苯(其中Rc可为H、烷基、烷氧基或卤素(例如氟))(例如2-溴硝基苯)可在碱(例如碳酸钠)和钯催化剂(例如二(三苯基膦)二氯化钯(II))存在下在含水溶剂系统(例如4:1二噁烷/水)中在升高的温度(例如80℃)与硼酸或硼酸酯(例如取代的4,4,5,5-四甲基-1,3,2-二氧杂硼杂环戊烷(其中Ra和Rb为H))反应,得到取代有烯基的硝基苯化合物。可选择地,Ra和Rb可一起形成环例如环戊烯,得到相应的2-(环戊-1-烯-1-基)-4,4,5,5-四甲基-1,3,2-二氧杂硼杂环戊烷,其在上述条件下得到取代有环状烯基的硝基苯。在催化剂例如钯/炭(Pd/C)存在下用氢气处理烯基硝基苯于非质子性溶剂例如乙酸乙酯中的溶液,得到相应的取代有烷基或环烷基的苯胺,其中Ra、Rb和Rc如以上所定义。用碱例如碳酸氢钠处理所述苯胺在卤代溶剂和水的混合物例如2:1二氯甲烷/水中的双相溶液,然后用硫光气处理,得到中间体异硫氰酸基苯,其中Ra、Rb和Rc如本申请所定义。分离各相,然后干燥并蒸发有机溶剂,得到粗中间体,将所述粗中间体立即溶解在醇例如乙醇中且用水合肼处理,得到肼基硫代甲酰胺中间体,其中Ra、Rb和Rc如本申请所定义。
实施例
这些实施例用于说明目的,而不应解释为将本申请说明书所公开的发明仅限于在这些实施例中所公开的实施方案。
由商业来源获得的起始物质、试剂和溶剂未经进一步纯化就使用。购买无水溶剂(其为来自Aldrich的Sure/SealTM)并原样使用。在Thomas HooverUnimelt毛细管熔点仪上或来自Sanford Research Systems的OptiMelt自动化熔点系统上或获得熔点且未经校正。分子以它们已知的名称给出(根据MDLISISTM/Draw 2.5、ChemBioDraw Ultra 12.0或ACD Name Pro中的命名程序来命名)。如果所述程序不能命名分子,则用常规命名法则命名所述分子。除非另有说明,1H NMR光谱以ppm(δ)为单位且在300、400或600MHz记录,和13C NMR光谱数据以(δ)为单位且在75、100或150MHz记录。
实施例1:制备(E)-N-(4-二甲基氨基)苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(化合物I-1)[合成方法A].
步骤1.(E)-3-(4-(亚肼基甲基)苯基)-1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑.在80℃历时5分钟(min)向装有水合肼(64%水溶液(aq);7.27mL,15.0毫摩尔(mmol))/EtOH(100mL)的250毫升(mL)圆底烧瓶中逐份加入4-[1-(4-三氟甲氧基苯基)-1H-[1,2,4]三唑-3-基]苯甲醛(5.00克(g),1.50mmol)。将溶液再回流搅拌3小时(h),然后用水(H2O;300mL)稀释并冷却至0℃。真空过滤收集析出的产物,其为白色固体(4.89g,93%):mp 222-226℃;1H NMR(400MHz,DMSO-d6)δ8.59(s,1H),8.22(d,J=8.2Hz,2H),7.84-7.79(m,3H),7.66(d,J=8.3Hz,2H),7.41(d,J=8.2Hz,2H),7.29(s,1H),5.63(br s,2H);ESIMSm/z348(M+H).
步骤2.向装有(E)-3-(4-(亚肼基甲基)苯基)-1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑(250mg,0.720mmol)/THF(10mL)的25mL圆底烧瓶中加入4-异硫氰酸基-N,N-二甲基苯胺(385mg,2.16mmol)。将内容物在搅拌下在65℃加热2小时,然后减压除去溶剂。将残余物在CH2Cl2(10mL)中浆化,导致产物析出。真空过滤得到所需产物,其为黄色固体(350mg,93%):mp205-208℃;1H NMR(400MHz,DMSO-d6)δ11.78(s,1H),10.02(s,1H),9.42(s,1H),8.19-7.99(m,6H),7.64(d,J=8.3Hz,2H),7.28(d,J=8.3Hz,2H),7.73(d,J=8.3Hz,2H),2.92(s,6H);ESIMS m/z 526(M+H).
实施例2:制备N-(3-(二甲基氨基)苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(化合物I-2)[合成方法B].
步骤1.(E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基二硫代羧酸甲酯.向装有肼基二硫代羧酸甲酯(2.38g,1.95mmol)/EtOH(100mL)的250mL圆底烧瓶中加入4-[1-(4-三氟甲氧基苯基)-1H-[1,2,4]三唑-3-基]苯甲醛(5.00g,1.50mmol)。将容器在80℃加热3小时,然后用H2O(300mL)稀释并冷却至0℃。真空过滤收集析出的产物,其为灰白色固体(6.13g,93%):mp 204-206℃;1H NMR(400MHz,DMSO-d6)δ13.39(s,1H),9.43(s,1H),8.38(s,1H),8.21(d,J=8.3Hz,2H),8.09(d,J=8.4Hz,2H),7.88(d,J=8.4Hz,2H),7.62(d,J=8.3Hz,2H),2.57(s,3H);ESIMS m/z 438(M+H).
步骤2.向装有(E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基二硫代羧酸甲酯(250mg,0.571mmol)/DMF(3mL)的50mL圆底烧瓶中加入N1,N1-二甲基苯-1,3-二胺(195mg,1.43mmol)。将内容物在搅拌下在150℃加热5h,然后将溶液冷却过夜。过滤混合物且通过RP-HPLC纯化滤液,得到所需物质(235mg,78%),其为灰白色固体:mp 192-194℃;1HNMR(400MHz,DMSO-d6)δ11.82(s,1H),10.04(s,1H),9.41(s,1H),8.19(s,1H),8.16-7.99(m,6H),7.61(d,J=8.3Hz,2H),7.16(t,J=7.2Hz,1H),7.01(m,1H),6.87(m,1H),6.58(m,1H),2.88(s,6H);ESIMS m/z 526([M+H]+).
实施例3:制备N-苄基-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(化合物I-3)[合成方法C].
向装有4-[1-[4-(三氟甲氧基)苯基]-1,2,4-三唑-3-基]苯甲醛(500mg,1.5mmol)/EtOH(3mL)的50mL圆底烧瓶中加入4-苄基氨基硫代脲(650mg,3.6mmol)。将反应混合物在80℃加热过夜。反应结束后加入H2O且通过真空过滤分离出粗产物。通过RP-HPLC分离出标题化合物,其为白色固体(390mg,52%):mp 220-224℃;1H NMR(400MHz,CDCl3)δ9.29(s,1H),8.59(s,1H),8.21(d,J=8.4Hz,2H),7.85-7.79(m,3H),7.71(d,J=8.4Hz,2H),7.46-7.30(m,8H),5.01(d,J=5.8Hz,2H);ESIMS m/z 497.2(M+H).
表1中的化合物I-4至I-31根据以上实施例来合成。在制备本发明化合物中使用的其它中间体根据在Brown等人的WO 2011017504 A1中描述的操作或通过其它已知的路线来制备。
实施例4:制备N-(4-二甲基氨基苯基)-S-甲基-2-{4-[1-(4-三氟甲氧基苯基)-1H-[1,2,4]-三唑-3-基]-亚苄基}肼基硫代甲酰胺(化合物1C)(合成方法D)
将含有(E)-N-(4-(二甲基氨基)苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(150mg,0.285mmol)和碘甲烷(0.054mL,0.856mmol)/EtOH(5mL)的溶液在80℃加热3h,然后减压除去溶剂。残余物通过正相快速色谱法(用己烷/EtOAc梯度洗脱)来纯化,得到标题化合物,其为橙色泡沫状物(93毫克(mg),60%):1H NMR(400MHz,DMSO-d6)δ8.61(s,1H),8.48(s,1H),8.22(d,J=8.24Hz,2H),8.17(s,1H),7.89(d,J=8.24Hz,2H),7.80(d,J=8.28Hz,2H),7.41(d,J=8.28Hz,2H),7.19(d,J=8.24Hz,2H),6.71(d,J=8.24Hz,2H),2.99(s,6H),2.42(s,3H);EIMS m/z 540(M+).
实施例5:使三芳基硫代半卡巴腙发生S-烷基化的一般方法(合成方法E)
将搅拌的硫代半卡巴腙和烷化剂于CH2Cl2或氯仿(CHCl3)中的溶液在35至50℃加热10至24小时。将冷却的溶液减压浓缩。残余物通常通过色谱法(使用氯仿/甲醇(CHCl3/CH3OH)或EtOAc/己烷溶液作为洗脱剂)来纯化,得到S-烷基化的产物。
实施例6:制备(S)-3-((2-((Z)-(2,6-二甲基苯基亚氨基)-((E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基)甲基硫基)乙酰氨基)甲基)哌啶-1-甲酸叔丁酯(化合物56C)(合成方法E)
向溴乙酰溴(26微升(μL),0.299mmol)于二氯乙烷(3mL)中的溶液中滴加(S)-3-(氨基甲基)哌啶-1-甲酸叔丁酯(63.9mg,0.298mmol)于二氯甲烷(1mL)中的溶液,然后加入N-乙基-N-异丙基丙烷-2-胺(76mg,0.588mmol)。将混合物在室温搅拌30分钟,然后加入呈固体形式的(E)-N-(2,6-二甲基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(100mg,0.196mmol)且将混合物在40℃加热90分钟。然后冷却至室温并减压蒸发,得到浅黄色玻璃状物,将其溶解在乙腈(2mL)中并在室温静置。所得析出物通过离心和滗出来分离,用新鲜的乙腈洗涤。将固体在氮气流中干燥,然后高真空干燥。粗产物用丙酮-异丙醇重结晶。分离出标题化合物,其为白色固体(36.5mg,24%):mp 148-151℃;1H NMR(400MHz,甲醇-d4)δ9.18(s,1H),8.59(s,1H),8.30(d,J=8.1Hz,2H),8.12(m,2H),8.07-8.00(m,2H),7.58-7.43(m,2H),7.33(dd,J=8.6,6.5Hz,1H),7.25(d,J=7.6Hz,2H),4.02(m,2H),3.97-3.75(m,2H),3.21(d,J=6.9Hz,2H),2.90(m,1H),2.59(m,1H),2.35(s,6H),1.84(m,2H),1.78-1.63(m,2H),1.44(s,9H),1.29(m,3H);ESIMS m/z765(M+H).
实施例7:制备(1Z,2E)-N-(2,6-二甲基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基亚氨代硫代甲酸(2-氧代-2-(((R)-哌啶-3-基甲基)氨基)乙基)酯·三氟乙酸(化合物62C)(合成方法K)
将(S)-3-((2-((Z)-(2,6-二甲基苯基亚氨基)-((E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基)甲基硫基)乙酰氨基)甲基)哌啶-1-甲酸叔丁酯(32.0mg,0.042mmol)于TFA(250μL,3.24mmol)中的溶液在室温搅拌10min。然后加入Et2O(10mL),得到白色析出物,其通过离心和滗出来分离,然后用新鲜的Et2O(5mL)冲洗。将固体在氮气流中干燥,然后高真空干燥,得到标题化合物,其为白色固体(19.8mg,60%):mp 110-120℃;1HNMR(400MHz,甲醇-d4)δ9.18(s,1H),8.56(m,1H),8.26(m,2H),8.16-7.84(m,4H),7.52(m,2H),7.27(m,1H),7.22(m,2H),4.00(s,2H),3.28(m,3H),3.06-2.83(m,1H),2.75(t,J=12.2Hz,1H),2.34(s,6H),2.21-1.83(m,4H),1.72(m,1H),1.47-1.19(m,2H);ESIMS m/z 665(M+H).
实施例8:2-(((Z)-((4-甲氧基-2,6-二甲基苯基)亚氨基)((E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基)甲基)硫基)乙酸钠(化合物68C)
在室温向2-((Z)-(4-甲氧基-2,6-二甲基苯基亚氨基)((E)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基)甲基硫基)乙酸(77.7mg,0.130mmol)于THF(10mL)中的溶液中缓慢加入甲醇钠(0.5M于甲醇中;260μL,0.130mmol)。混合物立即变为深黄色,然后在室温真空蒸发,得到浅橙色固体。该物质用Et2O(2×)研磨且通过滗出使用离心来分离,在氮气流中干燥,然后高真空干燥。分离出标题化合物,其为浅橙色固体(32mg,39%).mp146-154℃;1H NMR(400MHz,甲醇-d4)δ9.11(s,1H),8.64-7.68(m,7H),7.51(m,2H),6.70(s,2H),3.85-3.70(m,4H),3.61(m,1H),2.29(s,6H);ESIMS m/z599(M+H).
实施例9:制备(Z)-3-(4-甲氧基-2,6-二甲基苯基)-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)噻唑烷-4-酮(化合物69C)(合成方法F)
向(E)-N-(4-甲氧基-2,6-二甲基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(250mg,0.462mmol)于EtOH(5mL)中的溶液中加入溴乙酸甲酯(100mg,0.65mmol),将混合物加热至70℃且保持4小时。将混合物冷却至室温且用水(1mL)稀释。真空过滤析出物,得到标题化合物,其为白色固体(204mg,76%):mp 188-190℃;1HNMR(400MHz,CDCl3)δ8.56(s,1H),8.33(s,1H),8.22(d,J=8.1Hz,2H),7.90-7.70(m,4H),7.39(d,J=8.7Hz,2H),6.72(s,2H),4.01(s,2H),3.87-3.73(s,3H),2.18(s,6H);ESIMS m/z 581(M+H).
实施例10:制备4-((2Z)-3-(2,6-二甲基苯基)-2-((4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-2,3-二氢噻唑-4-基)-N,N-二乙基苯胺(化合物74C)(合成方法G)
向(E)-N-(2,6-二甲基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(74.7mg,0.144mmol)于二氯乙烷(5mL)中的溶液中加入α-溴-4-(二乙基氨基)苯乙酮(53.9mg,0.199mmol)且将混合物加热至40℃且保持4小时。然后将混合物冷却至室温并真空蒸发。粗品用乙腈研磨并滗出(2×)。将所得固体在氮气流中干燥,得到标题化合物,其为浅黄色固体(25mg,25%):mp 190-193℃(dec);1H NMR(400MHz,甲醇-d4)δ9.20(s,1H),8.38(s,1H),8.31-8.24(m,2H),8.08-8.00(m,2H),7.95-7.88(m,2H),7.55-7.48(m,3H),7.48-7.36(m,5H),7.31(d,J=7.7Hz,2H),3.60(q,J=7.2Hz,4H),2.20(s,6H),1.07(t,J=7.2Hz,6H);ESIMS m/z 682(M+H).
实施例11:制备(Z)-2-(2,6-二甲基苯基亚氨基)-3-((E)-4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基氨基)噻唑烷-4-酮(化合物81C)(合成方法I)
向1-(2,6-二甲基苯基)硫脲(1.0g,5.55mmol)于EtOH(10mL)中的溶液中加入2-溴乙酸甲酯(1.0g,6.5mmol)和乙酸钠(1.0g,12.2mmol)。将溶液搅拌并回流加热1小时,然后冷却且将液体与少量固体物质滗离,然后液体用水(10mL)稀释。过滤分离出析出物,得到(Z)-3-氨基-2-(2,6-二甲基苯基亚氨基)噻唑烷-4-酮(1.1g,83%):mp 149-152℃;1H NMR(400MHz,CDCl3)δ7.06(d,J=7.2Hz,2H),6.98(m,1H),4.75(s,2H),3.80(s,2H),2.12(s,6H);ESIMS m/z 236(M+H).
将一部分该物质(0.07g,0.3mmol)溶解在冰醋酸(3mL)中且用4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)苯甲醛(0.10g,0.30mmol)处理,将溶液加热至60℃且保持2小时。然后将溶液冷却且用水(1mL)稀释,过滤所得固体并风干,得到标题化合物(0.12g,67%):mp 209-213℃;1H NMR(400MHz,CDCl3)δ9.42(s,1H),8.59(s,1H),8.28(d,J=8.4Hz,2H),8.01(d,J=8.3Hz,2H),7.80-7.77(m,2H),7.43-7.34(m,2H),7.07(d,J=7.5Hz,2H),6.98(dd,J=8.2,6.7Hz,1H),3.90(s,2H),2.17(s,6H);ESIMS m/z 551(M+H).
实施例12:制备(2Z,NE)-2-((2-异丙基苯基)亚氨基)-N-(4-(1-(4-(三氟甲基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)-1,3-硫杂氮杂环己烷-3-胺和(Z)-3-(2-异丙基苯基)-2-((E)-(4-(1-(4-(三氟甲基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环己烷(化合物87C和179C)(合成方法J)
在配备有搅拌子和Vigruex柱的25mL小瓶中向(E)-N-(2-异丙基苯基)-2-(4-(1-(4-(三氟甲基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(200mg,0.393mmol)和碳酸钾(217mg,1.57mmol)/丁酮(10ml)中加入1-溴-3-氯丙烷(0.047ml,0.472mmol)。将反应混合物加热至60℃且保持过夜。通过LCMS确定反应结束。反应混合物用DCM稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到两种化合物。将较少的化合物真空干燥过夜,得到标题化合物87C即(2Z,NE)-2-((2-异丙基苯基)亚氨基)-N-(4-(1-(4-(三氟甲基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)-1,3-硫杂氮杂环己烷-3-胺(28.5mg,13%),其为黄色固体:mp187-189℃;1H NMR(400MHz,CDCl3)δ8.81(s,1H),8.66(s,1H),8.21(d,J=8.3Hz,2H),7.92(d,J=8.4Hz,2H),7.81(t,J=10.2Hz,4H),7.30-7.26(m,2H),7.17-7.04(m,1H),6.83(d,J=6.4Hz,1H),3.96(t,J=6.1Hz,2H),3.13(七重峰,J=6.9Hz,1H),2.97-2.90(m,2H),2.47-2.38(m,2H),1.25(d,J=7.5Hz,6H);ESIMS m/z 550(M+H)。较多的化合物用MeOH重结晶。过滤固体,用MeOH洗涤并在50℃真空干燥。然后将固体与丙酮(3×)共沸且将所得固体在50℃真空干燥,得到标题化合物179C即(Z)-3-(2-异丙基苯基)-2-((E)-(4-(1-(4-(三氟甲基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环己烷,其为黄色固体(92.3mg,0.168mmol,43%):mp 212-213℃;1H NMR(400MHz,CDCl3)δ8.64(s,1H),8.15(d,J=8.4Hz,2H),8.06(s,1H),7.91(d,J=8.5Hz,2H),7.79(d,J=8.6Hz,2H),7.75(d,J=8.4Hz,2H),7.38(dd,J=7.8,1.6Hz,1H),7.33(td,J=7.5,1.4Hz,1H),7.29-7.23(m,1H),7.18(dd,J=7.8,1.4Hz,1H),3.78-3.72(m,1H),3.59-3.48(m,1H),3.18-3.04(m,3H),2.40-2.30(m,2H),1.26-1.20(m,6H);ESIMS m/z 550(M+H).
实施例13:制备(Z)-3-(2-环丙基苯基)-5-甲基-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)噻唑烷-4-酮(化合物127C)(合成方法F)
向(E)-N-(2-环丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(100mg,0.191mmol)和乙酸钠(63.0mg,0.765mmol)/EtOH(4mL)中加入2-溴丙酸甲酯(0.026mL,0.230mmol)。将反应混合物加热至60℃且保持过夜。然后将反应混合物加热至85℃且保持72小时。反应混合物用DCM稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到标题化合物,其为白色固体(32.5mg,0.056mmol,30%):mp 112-115℃;1H NMR(400MHz,CDCl3)δ8.58(s,1H),8.32(s,1H),8.22(d,J=8.3Hz,2H),7.87-7.75(m,4H),7.43-7.32(m,4H),7.26-7.24(m,2H),4.23(q,J=7.3Hz,1H),1.85-1.78(m,4H),0.90-0.78(m,2H),0.78-0.69(m,1H),0.65-0.55(m,1H);ESIMS m/z 578(M+H).
实施例14:制备(Z)-3-(2-异丙基苯基)-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)噻唑烷(化合物132C)(合成方法J)
向(E)-N-(2-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(214mg,0.407mmol)和碳酸钾(225mg,1.63mmol)/丁酮(4ml)中加入1-溴-2-氯乙烷(70.0mg,0.489mmol)。将反应混合物加热至90℃且保持过夜。通过LCMS确定反应结束。将反应混合物冷却,用DMC稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来分离并在55℃真空干燥所回收的固体,得到标题化合物,其为白色固体(137mg,0.249mmol,61%):mp 193-196℃;1H NMR(400MHz,CDCl3)δ8.56(s,1H),8.22(s,1H),8.17(d,J=8.4Hz,2H),7.80(ddd,J=9.5,6.9,4.9Hz,4H),7.43-7.33(m,4H),7.31-7.21(m,2H),4.05(td,J=9.4,7.1Hz,1H),3.97-3.87(m,1H),3.42-3.33(m,1H),3.33-3.24(m,1H),3.12(七重峰,J=6.8Hz,1H),1.27(d,J=6.8Hz,3H),1.22(d,J=6.9Hz,3H);ESIMS m/z 552(M+H).
实施例15:制备(Z)-3-(2-异丙基苯基)-4-甲基-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)噻唑烷(化合物155C)(合成方法J)
向(E)-N-(2-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(300mg,0.572mmol)和碳酸钾(316mg,2.29mmol)/丁酮(4ml)中加入1,2-二溴丙烷(0.072ml,0.686mmol)。将反应混合物加热至85℃且保持过夜。通过LCMS确定反应结束。反应混合物用DMC稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到黄色固体。固体用MeOH重结晶。过滤固体,用MeOH洗涤并干燥,得到标题化合物,其为黄色固体,将其溶解在丙酮中并浓缩(3×)。收集浅黄色固体并真空干燥,得到标题化合物,其为旋转非对映异构体的1:1混合物(75.1mg,0.133mmol,23%):mp 201-204℃;混合物的1HNMR(400MHz,CDCl3)δ8.56(s,2H),8.18(dd,J=10.8,7.4Hz,6H),7.84-7.73(m,8H),7.45-7.30(m,8H),7.30-7.23(m,2H),7.20(d,J=6.7Hz,1H),7.12(dd,J=7.8,1.2Hz,1H),4.43-4.33(m,1H),4.16(dd,J=12.6,6.3Hz,1H),3.48(dt,J=13.3,6.7Hz,1H),3.37(dd,J=10.8,6.2Hz,1H),3.24(dt,J=13.7,6.9Hz,1H),3.08-2.92(m,3H),1.33-1.16(m,18H);ESIMS m/z 566(M+H).
实施例16:制备(Z)-3-(2,6-二甲基苯基)-4-甲基-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-2,3-二氢噻唑(化合物173C)(合成方法G)
向(E)-N-(邻甲苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(257mg,0.520mmol)于丁酮(5mL)中的溶液中加入三乙胺(0.14mL,1.0mmol)和氯丙酮(0.06mL,0.73mmol)并在75℃回流15h。将混合物冷却至室温,然后转移到装有水(5mL)的分液漏斗中且用二氯甲烷萃取两次。用相分离器过滤有机层,吸附到硅胶上且通过快速柱色谱法来纯化,得到标题化合物,其为黄色固体(229mg,83%):mp 87℃(dec);1HNMR(400MHz,CDCl3)δ8.56(s,1H),8.19-8.15(m,3H),7.82-7.75(m,4H),7.43-7.30(m,5H),7.24(d,J=7.3Hz,1H),5.88(d,J=1.3Hz,1H),2.21(s,3H),1.80(d,J=1.2Hz,3H);ESIMS m/z 536(M+H).
实施例17:制备(Z)-3-(2-异丙基苯基)-5-甲基-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环己烷(化合物178C)(合成方法J)
向(E)-N-(2-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(100mg,0.191mmol)和碳酸钾(105mg,0.763mmol)/丁酮(4ml)中加入1-溴-3-氯-2-甲基丙烷(39.0mg,0.229mmol)。将反应混合物加热至80℃且保持过夜。然后反应混合物用DMC稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到标题化合物,其为浅黄色固体且为旋转非对映异构体的混合物:mp 186-190℃;1H NMR(400MHz,CDCl3)δ8.55(d,J=3.6Hz,1H),8.14(d,J=8.4Hz,2H),8.06(s,1H),7.84-7.77(m,2H),7.74(d,J=8.4Hz,2H),7.38(d,J=9.0Hz,3H),7.32(td,J=7.5,1.4Hz,1H),7.26(s,1H),7.17(t,J=7.1Hz,1H),3.69-3.26(m,1H),3.55-3.37(m,1H),3.18-2.98(m,2H),2.93-2.80(m,1H),2.47(d,J=35.9Hz,1H),1.31-1.12(m,9H);ESIMS m/z 580(M+H).
实施例18:制备(Z)-3-(2,6-二甲基苯基)-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环庚烷(化合物211C)(合成方法J)
向(E)-N-(2,6-二甲基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(500mg,0.979mmol)和碳酸钾(541mg,3.92mmol)/丙酮(4ml)中加入1-溴-4-氯丁烷(0.135ml,1.18mmol)。将反应混合物加热至60℃且保持过夜。通过超高效液相色谱法(“UPLC”)确定烷基化结束。反应混合物用DMC稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到(1Z,N’E)-N-(2,6-二甲基苯基)-N’-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼代硫代氨基甲酸(4-氯丁基)酯(427mg,0.710mmol,73%),其为黄色胶状物且不经进一步纯化即使用。向(1Z,N’E)-N-(2,6-二甲基苯基)-N’-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼代硫代氨基甲酸(4-氯丁基)酯(427mg,0.710mmol)、碘化钾(236mg,1.42mmol)和碳酸钾(393mg,2.84mmol)中加入丙酮(7ml)。将反应混合物加热至65℃且保持72小时。将反应混合物冷却至室温,用DMC稀释且用水洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到黄色油状物。黄色油状物用MeOH重结晶,过滤,用MeOH洗涤并干燥,得到标题化合物,其为黄色固体(100mg,0.177mmol,25%):mp 100-106℃;1H NMR(400MHz,CDCl3)δ8.55(s,1H),8.15(d,J=8.4Hz,2H),8.10(s,1H),7.79(dt,J=10.4,5.8Hz,4H),7.38(d,J=8.3Hz,2H),7.11(s,3H),3.85-3.78(m,2H),3.20-3.12(m,2H),2.30(s,6H),2.13-2.07(m,2H),1.87-1.82(m,2H);ESIMS m/z 566(M+H).
实施例19:制备(Z)-3-(2-异丙基苯基)-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环己烷-4-酮(化合物224C)(合成方法L)
向(E)-N-(2-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(500mg,0.953mmol)/丁酮(9.5ml)中加入丙烯酰氯(0.077ml,0.953mmol)。将反应混合物在环境温度搅拌10分钟,然后在50℃搅拌2h。将反应混合物冷却至40℃且保持过夜。通过LCMS确定反应结束。反应混合物用DCM稀释且用饱和碳酸氢钠洗涤。水层用DCM萃取。将有机层倒入且通过相分离器且浓缩。通过快速柱色谱法来纯化,得到黄色油状物。油状物用二乙基醚/己烷重结晶,得到标题化合物,其为浅黄色固体(125mg,0.217mmol,23%):mp 118℃(dec);1H NMR(400MHz,CDCl3)δ8.57(s,1H),8.21(d,J=8.4Hz,2H),8.16(s,1H),7.85-7.75(m,4H),7.46-7.36(m,4H),7.33-7.26(m,1H),7.10(d,J=7.6Hz,1H),3.26-3.14(m,4H),2.81(七重峰,J=6.9Hz,1H),1.21(t,J=7.2Hz,6H);ESIMS m/z 580(M+H).
实施例20:制备(Z)-3-(2,6-二氟苯基)-2-((E)-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)亚肼基)-1,3-硫杂氮杂环丁烷(化合物245C)(合成方法J)
在配备有磁力搅拌子的25mL小瓶中向(E)-N-(2,6-二氟苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(0.50g,0.96mmol)和碳酸钾(0.53g,3.9mmol)于丁酮(10mL)中的混合物中加入二碘甲烷(0.093ml,1.2mmol)。将反应混合物加热至55℃并搅拌两天。反应混合物用DCM稀释,用水洗涤并分离各相。水相用DCM萃取且合并的有机相通过流经相分离器柱来干燥,然后浓缩。通过快速柱色谱法来纯化,得到黄色油状物,其在静置后结晶。将固体在二乙基醚和己烷中浆化且真空过滤收集。固体用己烷洗涤并干燥,得到标题化合物(0.086g,0.16mmol,17%),其为浅黄色固体:mp 144-146℃;1H NMR(400MHz,CDCl3)δ8.58(s,1H),8.34(s,1H),8.20(d,J=8.3Hz,2H),7.81(d,J=8.8Hz,4H),7.40(d,J=8.3Hz,2H),7.31-7.23(m,1H),7.03-6.97(m,2H),5.05(s,2H);ESIMS m/z 532(M+H).
表3中所示的化合物240-244和246-261根据实施例20中描述的方法由表1中公开的经适当取代的中间体来制备。这些化合物的表征数据报道在表4中。
实施例21:从外消旋混合物中分离旋转稳定的阻转异构体
可使用以下手性HPLC方法中的一种从外消旋混合物中分离组成性异构体。
分离方法A:分离所使用的柱是Chiral Technologies INC Chiral Pak 1A5μm,4.6×250mm柱(Part编号为80325)。方法包括:在0-30分钟流速为1.0mL/min且在运行期间保持25%B的恒溶剂。A洗脱剂为正己烷,B洗脱剂为异丙醇。
分离方法B:分离所使用的柱为Chiral Technologies INC Chiral Pak 1B5μm,4.6×250mm柱(Part编号为81325)。方法包括:在0-30分钟流速为1.0mL/min且在运行期间保持15%B的恒溶剂。A洗脱剂为正戊烷,B洗脱剂为正丁醇。
实施例22:制备(E)-N-(2-氟-6-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(化合物I-40)(合成方法C)
步骤1:制备1-氟-2-硝基-3-(丙-1-烯-2-基)苯(I-37)(方法M).在配备有磁力搅拌子和氮气进气口的100mL圆底烧瓶中向1-溴-3-氟-2-硝基苯(0.953g,4.33mmol)的混合物中加入二噁烷(17.3mL)、碳酸钠(0.551g,5.20mmol)、水(4.33mL)和4,4,5,5-四甲基-2-(丙-1-烯-2-基)-1,3,2-二氧杂硼杂环戊烷(0.977mL,5.20mmol)。向该混合物中加入二(三苯基膦)二氯化钯(II)(0.243g,0.347mmol)。将烧瓶抽空且用氮气吹洗(3×),然后加热至80℃并搅拌过夜。将反应混合物冷却至室温,用过滤且垫用乙酸乙酯洗涤。分离各相并浓缩有机相。通过快速柱色谱法来纯化,得到标题化合物(0.590g,3.26mmol,75%收率),其为浅黄色油状物:1H NMR(400MHz,CDCl3)δ7.48-7.36(m,1H),7.21-7.06(m,2H),5.23(p,J=1.5Hz,1H),5.05(q,J=1.1Hz,1H),2.09(s,3H);13CNMR(101MHz,CDCl3)δ153.56(d,JCF=257.5Hz),139.62,139.60,138.83,131.48(d,JCF=8.6Hz),124.47(d,JCF=3.6Hz),117.60,115.51(d,JCF=19.1Hz),23.18.
步骤2:制备2-氟-6-异丙基苯胺(I-38)(方法M).在配备有磁力搅拌子和氮气进气口的250mL圆底烧瓶中向1-氟-2-硝基-3-(丙-1-烯-2-基)苯(0.590g,3.26mmol)于乙酸乙酯(32.6mL)中的溶液中加入钯/炭(5%Pd/C,0.693g,0.326mmol)。将反应烧瓶抽空且用氢气吹洗(2×),然后放置在1大气压(atm)氢气下并在室温搅拌过夜。反应混合物用过滤且垫用乙酸乙酯洗涤。浓缩滤液,得到标题化合物(0.423g,2.76mmol,85%收率),其为澄清无色油状物:IR(洁净的)3476(m),3392(m),2966(m),2872(m),1628(s),1474(s),1270(m)cm-1;1H NMR(400MHz,CDCl3)δ6.92(dt,J=7.7,1.2Hz,1H),6.86(ddd,J=10.8,8.1,1.4Hz,1H),6.69(td,J=8.0,5.6Hz,1H),3.71(bs,2H),2.92(七重峰,J=6.8Hz,1H),1.26(d,J=6.8Hz,6H);13C NMR(101MHz,CDCl3)δ151.91(d,J=237.6Hz),135.10(d,J=2.3Hz),131.60(d,J=11.8Hz),120.52(d,J=3.0Hz),117.99(d,J=8.0Hz),112.28(d,J=19.6Hz),27.77(d,J=2.9Hz),22.22.
步骤3:制备N-(2-氟-6-异丙基苯基)肼基硫代甲酰胺(I-39)(方法M).向配备有搅拌子和氮气进气口的100mL圆底烧瓶中加入2-氟-6-异丙基苯胺(0.415g,2.71mmol)、二氯甲烷(13.6mL)、水(6.78mL)和碳酸氢钠(0.683g,8.13mmol)。向该两相混合物中加入硫光气(0.199mL,2.60mmol)且将反应混合物剧烈搅拌2小时。混悬液用相分离器柱过滤且将有机相在100mL圆底烧瓶中浓缩。烧瓶配备有磁力搅拌子和氮气进气口且将残余物溶解在乙醇(6.78mL)中。向所得溶液中加入水合肼(0.131mL,2.71mmol)且将反应混合物在室温搅拌2天。将溶液浓缩且将所得残余物混悬在二乙基醚和己烷的混合物中并重新浓缩,得到固体。将固体混悬在最少量的二乙基醚中且混合物用己烷稀释。蒸发掉大部分二乙基醚并真空过滤收集所得固体,用己烷洗涤,然后真空干燥,得到标题化合物(0.518g,2.28mmol,84%收率),其为白色固体:mp 122-124℃;1H NMR(400MHz,CDCl3)δ8.56(bs,1H),7.52(bs,1H),7.32(td,J=8.1,5.6Hz,1H),7.17-7.12(m,1H),7.00(ddd,J=9.5,8.2,1.4Hz,1H),4.07(bs,2H),3.15(七重峰,J=7.0Hz,1H),1.24(d,J=6.9Hz,6H);ESIMS m/z229([M+H]+).
步骤4:制备(E)-N-(2-氟-6-异丙基苯基)-2-(4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)亚苄基)肼基硫代甲酰胺(I-40)(方法C).在配备有磁力搅拌子和回流冷凝器的100mL圆底烧瓶中向4-(1-(4-(三氟甲氧基)苯基)-1H-1,2,4-三唑-3-基)苯甲醛(0.760g,2.28mmol)于甲醇(22.8mL)中的溶液中加入N-(2-氟-6-异丙基苯基)肼基硫代甲酰胺(0.518g,2.28mmol),将反应混合物加热至65℃并搅拌6小时。将温度降至50℃且将反应混合物搅拌过夜。将反应混合物冷却至室温并过滤所得固体,用甲醇洗涤并在55℃真空干燥(25mmHg),得到标题化合物(0.907g,1.67mmol,73%收率),其为白色固体:mp210-212℃;1H NMR(400MHz,CDCl3)δ9.54(s,1H),8.60(s,1H),8.56(s,1H),8.30-8.22(m,2H),7.92(s,1H),7.86-7.76(m,4H),7.44-7.38(m,2H),7.35(dd,J=8.1,5.6Hz,1H),7.18(d,J=7.9Hz,1H),7.04(ddd,J=9.4,8.2,1.3Hz,1H),3.22(p,J=6.9Hz,1H),1.29(d,J=6.9Hz,6H);ESIMS m/z 544([M+H]+).
表1中所示的中间体化合物I-32至I-36和I-41至I-65根据实施例22步骤1-4中描述的方法来制备。这些中间体的表征数据显示在表2中。
实施例23:对甜菜夜蛾(“BAW”)和谷实夜蛾(“CEW”)进行的生物测定
BAW几乎没有有效的寄生虫、疾病或捕食者来降低BAW的种群。BAW侵袭多种杂草、树木、青草、豆科植物和田间作物。在不同地方,出于经济上的原因要考虑包括以下植物上的BAW:芦笋、棉花、玉米、大豆、烟草、苜蓿、甜菜、胡椒、番茄、马铃薯、洋葱、豌豆、向日葵和柑桔。已知CEW侵袭玉米和番茄,而且其侵袭的植物还包括朝鲜蓟、芦笋、甘蓝、香瓜、芥蓝、豇豆、黄瓜、茄子、莴苣、菜豆、甜瓜、秋葵、豌豆、胡椒、马铃薯、倭瓜、菜豆、菠菜、南瓜、甘薯和西瓜。还已知CEW对某些杀昆虫剂耐药。因此,由于上述因素,防治这些害虫是重要的。此外,防治这些害虫的分子可用于防治其它害虫。
用以下实施例中描述的操作对本申请公开的一些分子的抗BAW和CEW进行测试。在报道结果时使用“BAW和CEW评级表”(参见表格部分)。
对BAW(Spodoptera exigua)进行的生物测定
使用128孔饲料托盘测定对BAW进行生物测定。将1-5只第二龄期的BAW幼虫放置在饲料托盘的每个孔(3mL)中,所述每个孔已经预填充有1mL人工饲料,已向所述人工饲料中加入50μg/cm2试验化合物(溶解在丙酮-水混合物(90:10,50μL)中)(向八个孔中的每个孔中),然后干燥。托盘用透明自粘型盖子盖住并在25℃和14:10光照-黑暗条件下保持5-7天。记录每个孔中的幼虫死亡百分比;然后对八个孔中的活性进行平均。结果在标题为“表5:生物结果”(参见表格部分)的表格中示出。
对CEW(Helicoverpa zea)进行的生物测定
使用128孔饲料托盘测定对CEW进行生物测定。将1-5只第二龄期的CEW幼虫放置在饲料托盘的每个孔(3mL)中,所述每个孔已经预填充有1mL人工饲料,已向所述人工饲料中加入50μg/cm2试验化合物(溶解在丙酮-水混合物(90:10,50μL)中)(向八个孔中的每个孔中),然后干燥。托盘用透明自粘型盖子盖住并在25℃和14:10光照-黑暗条件下保持5-7天。记录每个孔中的幼虫死亡百分比;然后对八个孔中的活性进行平均。结果在标题为“表5:生物结果”(参见表格部分)的表格中示出。
实施例24:对绿色桃蚜(“GPA”)(Myzus persicae)进行的生物测定
GPA是桃树最重要的蚜虫类害虫,其导致生长缓慢、叶子枯萎和各种组织死亡。其也因用作植物病毒转运的载体而是有害的,所述植物病毒为例如危害葵/马铃薯科茄科成员的马铃薯病毒Y和马铃薯卷叶病毒和危害多种其它食用作物的各种花斑病病毒。GPA侵袭的植物包括诸如:绿花椰菜、牛蒡、甘蓝、胡萝卜、花椰菜、萝卜、茄子、青豆、莴苣、夏威夷果、木瓜、胡椒、甘薯、番茄、水芥和南瓜。GPA还侵袭多种观赏性作物例如康乃馨、菊花、白花甘蓝、猩猩木和玫瑰。GPA已发展成对多种杀虫剂耐药。
用以下实施例中描述的操作对本申请公开的一些分子的抗GPA进行测试。在报道结果时使用“GPA评级表”(参见表格部分)。
在3英寸盆中生长且具有2-3片小(3-5cm)真叶的甘蓝幼苗用作测试底物。在化学施用前一天,用20-50只GPA(无翅成虫和若虫阶段)侵害幼苗。每种处理使用四个具有单独幼苗的盆。将测试化合物(2mg)溶解在2mL丙酮/甲醇(1:1)溶剂中,形成浓度为1000ppm的测试化合物原液。原液用0.025%Tween 20/H2O稀释5倍,得到浓度为200ppm的测试化合物溶液。使用手持抽吸型喷雾器将溶液喷至甘蓝叶子的两面直到径流。用仅含有20体积%丙酮/甲醇(1:1)溶剂的稀释液对参照植物(溶剂对照)进行喷雾。将经处理的植物在贮存室中在约25℃和环境相对湿度(RH)的条件下放置3天,然后评级。通过在显微镜下计数每株植物上的活蚜虫数目来进行评价。通过使用以下Abbott’s校正公式(W.S.Abbott,“A Method of Computing theEffectiveness of an Insecticide”J.Econ.Entomol.18(1925),pp.265-267)来计算防治百分比:
经校正的防治%=100*(X-Y)/X
其中
X=溶剂对照植物上的活蚜虫数目
Y=经处理的植物上的活蚜虫数目
结果在标题为“表5:生物结果”(参见表格部分)的表格中示出。
杀虫用酸加成盐、盐衍生物、溶剂化物、酯衍生物、多晶型物、同位素和放射线核素
式1、2和3的分子可被制成杀虫用酸加成盐。非限定举例而言,胺官能团可与以下的酸形成盐:盐酸、氢溴酸、硫酸、磷酸、乙酸、苯甲酸、枸橼酸、丙二酸、水杨酸、苹果酸、富马酸、草酸、琥珀酸、酒石酸、乳酸、葡糖酸、抗坏血酸、马来酸、门冬氨酸、苯磺酸、甲磺酸、乙磺酸、羟基甲磺酸和羟基乙磺酸。此外,非限定举例而言,酸官能团可形成盐,包括衍生自碱金属或碱土金属的那些盐和衍生自氨和胺的那些盐。优选阳离子的实例包括钠、钾和镁。
可将式1、2和3的分子制成盐衍生物。非限定举例而言,可通过使游离碱与足量的所需酸接触以生产盐来制备盐衍生物。可通过用适当的碱的稀水溶液处理使游离碱再生,所述碱的稀水溶液为例如稀的氢氧化钠(NaOH)水溶液、稀的碳酸钾水溶液、稀氨水和稀的碳酸氢钠水溶液。作为实例,在多种情况下,通过将杀虫剂诸如2,4-D转变成其二甲基胺盐而使其为更可水溶的。
可将式1、2和3的分子与溶剂一起制成稳定的复合物,从而使所述复合物在除去溶剂后仍保持完整。这些复合物经常被称作"溶剂化物”。然而,特别期望的是与作为溶剂的水形成稳定的水合物。
可将式1、2和3的分子制成酯衍生物。然后可将这些酯衍生物按与本文件披露的发明相同的施用方式来施用。
可将式1、2和3的分子制成不同的结晶性多晶型物。多晶型现象在农业化学的发展中是重要的,因为同一分子的不同结晶性多晶型物或结构可具有截然不同的物理性质和生物性能。
式1、2和3的分子可经制备具有不同的同位素。特别重要的是用2H(也称作氘)代替1H的分子。
式1、2和3的分子可经制备具有不同的同位素。特别重要的是具有14C的分子。
立体异构体
式1、2和3的分子可按一种或多种立体异构体形式存在。因此,一些分子可按外消旋混合物形式生产。本领域技术人员应当理解的是,一种立体异构体可能比其它立体异构体更具活性。单独的立体异构体可通过已知的选择性合成方法获得、用经拆分的起始物质通过常规的合成操作获得或通过常规的拆分方法来获得。
杀昆虫剂
式1、2和3的分子也可与以下杀昆虫剂中的一种或多种联用(例如在组合性混合物中,或同时或顺序施用):1,2-二氯丙烷(1,2-dichloropropane)、阿维菌素(abamectin)、高灭磷(acephate)、吡虫清(acetamiprid)、家蝇磷(acethion)、乙酰虫腈(acetoprole)、氟酯菊酯(acrinathrin)、丙烯腈(acrylonitrile)、棉铃威(alanycarb)、涕灭威(aldicarb)、砜灭威(aldoxycarb)、艾氏剂(aldrin)、丙烯除虫菊(allethrin)、阿洛氨菌素(allosamidin)、除害威(allyxycarb)、α-氯氰菊酯(alpha-cypermethrin)、α-蜕皮素(alpha-ecdysone)、α-硫丹(alpha-endosulfan)、赛果(amidithion)、灭害威(aminocarb)、胺吸磷(amiton)、草酸胺吸磷(amitonoxalate)、虫螨脒(amitraz)、新烟碱(anabasine)、艾噻达松(athidathion)、艾扎丁(azadirachtin)、唑啶磷(azamethiphos)、益棉磷(azinphos-ethyl)、保棉磷(azinphos-methyl)、偶氮磷(azothoate)、六氟硅酸钡(barium hexafluorosilicate)、熏虫菊(barthrin)、唑虫威(bendiocarb)、丙硫克拜威(benfuracarb)、杀虫磺(bensultap)、β-氟氯氰菊酯(beta-cyfluthrin)、β-氯氰菊酯(beta-cypermethrin)、联苯菊酯(bifenthrin)、反式丙烯除虫菊(bioallethrin)、bioethanomethrin、生物氯菊酯(biopermethrin)、双二氟虫脲(bistrifluron)、硼砂(borax)、硼酸(boricacid)、溴苯烯磷(bromfenvinfos)、溴烯杀(bromocyclen)、溴-DDT、溴硫磷(bromophos)、乙基溴硫磷(bromophos-ethyl)、合杀威(bufencarb)、噻嗪酮(buprofezin)、畜虫威(butacarb)、特嘧硫磷(butathiofos)、丁叉威(butocarboxim)、丁酯磷(butonate)、氧丁叉威(butoxycarboxim)、硫线磷(cadusafos)、砷酸钙(calcium arsenate)、石硫合剂(calcium polysulfide)、毒杀芬(camphechlor)、氯灭杀威(carbanolate)、甲萘威(carbaryl)、虫螨威(carbofuran)、二硫化碳(carbondisulfide)、四氯化碳(carbon tetrachloride)、三硫磷(carbophenothion)、丁硫克百威(carbosulfan)、巴丹(cartap)、盐酸巴丹(cartap hydrochloride)、氯虫酰胺(chlorantraniliprole)、冰片丹(chlorbicyclen)、氯丹(chlordane)、开蓬(chlordecone)、氯苯脒(chlordimeform)、盐酸氯苯脒(chlordimeformhydrochloride)、壤土氯磷(chlorethoxyfos)、氟唑虫清(chlorfenapyr)、毒虫畏(chlorfenvinphos)、定虫隆(chlorfluazuron)、氯甲磷(chlormephos)、氯仿(chloroform)、氯化苦(chloropicrin)、氯腈肟磷(chlorphoxim)、氯吡唑磷(chlorprazophos)、毒死蜱(chlorpyrifos)、甲基毒死蜱(chlorpyrifos-methyl)、氯甲硫磷(chlorthiophos)、环虫酰胺(chromafenozide)、瓜菊酯I(cinerin I)、瓜菊酯I(cinerin II)、瓜菊酯(cinerins)、左旋反灭虫菊酯(cismethrin)、除线威(cloethocarb)、氯氰碘柳胺(closantel)、噻虫胺(clothianidin)、乙酰亚砷酸铜(copper acetoarsenite)、砷酸铜(copper arsenate)、环烷酸铜(copper naphthenate)、油酸铜(copper oleate)、库马磷(coumaphos)、畜虫磷(coumithoate)、克罗米通(crotamiton)、丁烯磷(crotoxyphos)、育畜磷(crufomate)、氟铝酸钠(cryolite)、苯腈磷(cyanofenphos)、杀螟磷(cyanophos)、果虫磷(cyanthoate)、氰虫酰胺(cyantraniliprole)、环戊烯菊酯(cyclethrin)、乙氰菊酯(cycloprothrin)、氟氯氰菊酯(cyfluthrin)、三氟氯氰菊酯(cyhalothrin)、氯氰菊酯(cypermethrin)、苯醚氰菊酯(cyphenothrin)、灭蝇胺(cyromazine)、赛灭磷(cythioate)、DDT、一甲呋喃丹(decarbofuran)、溴氰菊酯(deltamethrin)、田乐磷(demephion)、田乐磷-O(demephion-O)、田乐磷-S(demephion-S)、内吸磷(demeton)、甲基内吸磷(demeton-methyl)、内吸磷-O(demeton-O)、内吸磷-O-甲基(demeton-O-methyl)、内吸磷-S(demeton-S)、内吸磷-S-甲基(demeton-S-methyl)、内吸磷-S-甲基硫(demeton-S-methylsulphon)、杀螨硫隆(diafenthiuron)、氯亚磷(dialifos)、硅藻土(diatomaceous earth)、二嗪农(diazinon)、异氯硫磷(dicapthon)、除线磷(dichlofenthion)、敌敌畏(dichlorvos)、N-(3-甲基苯基)氨基甲酸甲酯(dicresyl)、百治磷(dicrotophos)、环虫腈(dicyclanil)、狄氏剂(dieldrin)、氟脲杀(diflubenzuron)、丙羟茶碱(dilor)、四氟甲醚菊酯(dimefluthrin)、甲氟磷(dimefox)、地麦威(dimetan)、乐果(dimethoate)、苄菊酯(dimethrin)、甲基毒虫畏(dimethylvinphos)、敌蝇威(dimetilan)、消螨酚(dinex)、dinex-diclexine、丙硝酚(dinoprop)、戊硝酚(dinosam)、呋虫胺(dinotefuran)、噁茂醚(diofenolan)、杀抗松(dioxabenzofos)、二氧威(dioxacarb)、敌噁磷(dioxathion)、乙拌磷(disulfoton)、噻喃磷(dithicrofos)、右旋柠檬烯(d-limonene)、二硝甲酚(DNOC)、二硝甲酚-铵、二硝甲酚-钾、二硝甲酚-钠、多拉克汀(doramectin)、促蜕皮甾酮(ecdysterone)、甲氨基阿维菌素(emamectin)、苯甲酸甲氨基阿维菌素(emamectin benzoate)、多杀威(EMPC)、烯炔菊酯(empenthrin)、硫丹(endosulfan)、因毒磷(endothion)、异狄氏剂(endrin)、苯硫磷(EPN)、保幼醚(epofenonane)、爱普瑞菌素(eprinomectin)、Es-生物烯丙菊酯(esdepalléthrine)、高氰戊菊酯(esfenvalerate)、etaphos、苯虫威(ethiofencarb)、乙硫磷(ethion)、乙虫腈(ethiprole)、益果(ethoate-methyl)、灭克磷(ethoprophos)、甲酸乙酯(ethylformate)、乙基-DDD、1,2-二溴乙烷(ethylene dibromide)、1,2-二氯乙烷(ethylenedichloride)、环氧乙烷(ethylene oxide)、醚菊酯(etofenprox)、乙嘧硫磷(etrimfos)、EXD、氨磺磷(famphur)、克线磷(fenamiphos)、抗螨唑(fenazaflor)、皮蝇磷(fenchlorphos)、乙苯威(fenethacarb)、五氟苯菊酯(fenfluthrin)、杀螟硫磷(fenitrothion)、丁苯威(fenobucarb)、fenoxacrim、双氧威(fenoxycarb)、吡氯氰菊酯(fenpirithrin)、甲氰菊酯(fenpropathrin)、丰索磷(fensulfothion)、倍硫磷(fenthion)、倍硫磷-乙基(fenthion-ethyl)、氰戊菊酯(fenvalerate)、锐劲特(fipronil)、flometoquin、氟啶虫酰胺(flonicamid)、氟虫酰胺(flubendiamide)(其额外拆分的异构体)、氟氯双苯隆(flucofuron)、氟螨脲(flucycloxuron)、氟氰菊酯(flucythrinate)、嘧虫胺(flufenerim)、氟虫脲(flufenoxuron)、氟丙苄醚(flufenprox)、flufiprole、flupyradifurone、氟胺氰菊酯(fluvalinate)、地虫磷(fonofos)、伐虫脒(formetanate)、盐酸伐虫脒(formetanate hydrochloride)、安果(formothion)、胺甲威(formparanate)、盐酸胺甲威(formparanatehydrochloride)、丁苯硫磷(fosmethilan)、甲基毒死蜱(fospirate)、伐线丹(fosthietan)、呋喃虫酰肼(fufenozide)、呋线威(furathiocarb)、糠醛菊酯(furethrin)、γ-三氟氯氰菊酯(gamma-cyhalothrin)、γ-HCH、卤醚菊酯(halfenprox)、特丁苯酰肼(halofenozide)、HCH、HEOD、七氯(heptachlor)、庚虫磷(heptenophos)、速杀硫磷(heterophos)、氟铃脲(hexaflumuron)、艾氏剂(HHDN)、灭蚁腙(hydramethylnon)、氰化氢(hydrogen cyanide)、蒙五一二(hydroprene)、喹啉威(hyquincarb)、吡虫啉(imidacloprid)、氯噻啉(imidaclothiz)、咪炔菊酯(imiprothrin)、茚虫威(indoxacarb)、碘甲烷(iodomethane)、丰丙磷(IPSP)、氯唑磷(isazofos)、碳氯灵(isobenzan)、水胺硫磷(isocarbophos)、异艾氏剂(isodrin)、丙胺磷(isofenphos)、丙胺磷-甲基(isofenphos-methyl)、异丙威(isoprocarb)、稻瘟灵(isoprothiolane)、叶蚜磷(isothioate)、噁唑磷(isoxathion)、齐墩螨素(ivermectin)、茉莉菊酯I(jasmolin I)、茉莉菊酯II(jasmolin II)、碘硫磷(jodfenphos)、保幼激素I(juvenile hormone I)、保幼激素II(juvenile hormone II)、保幼激素III(juvenile hormone III)、克来范(kelevan)、蒙七七七(kinoprene)、λ-三氟氯氰菊酯(lambda-cyhalothrin)、砷酸铅(lead arsenate)、lepimectin、溴苯磷(leptophos)、林丹(lindane)、啶虫磷(lirimfos)、氟丙氧脲(lufenuron)、噻唑磷(lythidathion)、马拉硫磷(malathion)、苄丙二腈(malonoben)、叠氮磷(mazidox)、ME-5343、MEB-5343、灭蚜磷(mecarbam)、甲基灭蚜磷(mecarphon)、灭蚜松(menazon)、氯氟醚菊酯(meperfluthrin)、二噻磷(mephosfolan)、氯化亚汞(mercurous chloride)、甲亚砜磷(mesulfenfos)、氰氟虫腙(metaflumizone)、虫螨畏(methacrifos)、甲胺磷(methamidophos)、杀扑磷(methidathion)、灭虫威(methiocarb)、丁烯胺磷(methocrotophos)、灭多虫(methomyl)、蒙五一五(methoprene)、甲醚菊酯(methothrin)、甲氧滴滴涕(emthoxychlor)、甲氧苯酰肼(methoxyfenozide)、溴甲烷(methyl bromide)、异硫氰酸甲酯、甲基氯仿(methyl chloroform)、二氯甲烷(methylene chloride)、氧卞氟菊酯(metofluthrin)、速灭威(metolcarb)、噁虫酮(metoxadiazone)、速灭磷(mevinphos)、自克威(mexacarbate)、米尔螨素(milbemectin)、米尔贝肟(milbemycin oxime)、丙胺氟磷(mipafox)、灭蚁灵(mirex)、molosultap、久效磷(monocrotophos)、杀虫单(monomehypo)、杀虫单(monosultap)、茂果(morphothion)、莫西克丁(moxidectin)、萘肽磷(naftalofos)、二溴磷(naled)、萘(naphthalene)、烟碱(nicotine)、氟蚁灵(nifluridide)、硝胺烯啶(nitenpyram)、硝虫噻嗪(nithiazine)、腈叉威(nitrilacarb)、双苯氟脲(novaluron)、多氟脲(noviflumuron)、氧乐果(omethoate)、甲氨叉威(oxamyl)、砜吸磷(oxydemeton-methyl)、异砜磷(oxydeprofos)、砜拌磷(oxydisulfoton)、对-二氯苯、对硫磷(parathion)、甲基对硫磷(parathion-methyl)、氟幼脲(penfluron)、五氯酚(pentachlorophenol)、苄氯菊脂(permethrin)、芬硫磷(phenkapton)、苯醚菊酯(phenothrin)、稻丰散(phenthoate)、甲拌磷(phorate)、伏杀磷(phosalone)、棉安磷(phosfolan)、亚胺硫磷(phosmet)、对氯硫磷(phosnichlor)、磷胺(phosphamidon)、磷化氢(phosphine)、肟硫磷(phoxim)、甲基肟硫磷(phoxim-methyl)、甲胺嘧磷(pirimetaphos)、抗蚜威(pirimicarb)、乙基虫螨磷(pirimiphos-ethyl)、甲基虫螨磷(pirimiphos-methyl)、亚砷酸钾(potassium arsenite)、硫氰酸钾(potassium thiocyanate)、pp’-DDT、炔酮菊酯(prallethrin)、早熟素I(precocene I)、早熟素II(precocene II)、早熟素III(precocene III)、酰胺嘧啶啉(primidophos)、丙溴磷(profenofos)、环丙氟灵(profluralin)、丙氟菊酯(profluthrin)、蜱虱威(promacyl)、猛杀威(promecarb)、丙虫磷(propaphos)、烯虫磷(propetamphos)、残杀威(propoxur)、乙噻唑磷(prothidathion)、丙硫磷(prothiofos)、发果(prothoate)、protrifenbute、拒嗪酮(pymetrozine)、吡唑硫磷(pyraclofos)、嘧啶威(pyrafluprole)、吡菌磷(pyrazophos)、反灭虫菊(pyresmethrin)、除虫菊酯I(pyrethrin I)、除虫菊酯II(pyrethrin II)、除虫菊(pyrethrins)、哒螨酮(pyridaben)、啶虫丙醚(pyridalyl)、打杀磷(pyridaphenthion)、pyrifluquinazon、嘧胺苯醚(pyrimidifen)、嘧啶磷(pyrimitate)、吡啶醇(pyriprole)、蚊蝇醚(pyriproxyfen)、苦木(quassia)、喹噁啉(quinalphos)、甲基喹噁啉(quinalphos-methyl)、喹塞昂(quinothion)、碘醚柳胺(rafoxanide)、苄呋菊酯(resmethrin)、鱼藤酮(rotenone)、鱼泥汀(ryania)、沙巴草(sabadilla)、八甲磷(schradan)、赛拉菌素(selamectin)、灭虫硅醚(silafluofen)、硅胶(silica gel)、亚砷酸钠(sodium arsenite)、氟化钠(sodiumfluoride)、六氟硅酸钠(sodium hexafluorosilicate)、硫氰酸钠(sodiumthiocyanate)、苏果(sophamide)、多虫菌素(spinetoram)、艾克敌(spinosad)、螺甲螨酯(spiromesifen)、螺虫乙酯(spirotetramat)、磺苯醚隆(sulcofuron)、磺苯醚隆钠(sulcofuron-sodium)、氟虫胺(sulfluramid)、硫特普(sulfotep)、氟啶虫胺腈(sulfoxaflor)、氟化硫(sulfuryl fluoride)、乙丙硫磷(sulprofos)、tasmanone、τ-氟胺氰菊酯(tau-fluvalinate)、噻螨威(tazimcarb)、滴滴滴(TDE)、双苯酰肼(tebufenozide)、吡螨胺(tebufenpyrad)、嘧丙磷(tebupirimfos)、伏虫隆(teflubenzuron)、七氟菊酯(tefluthrin)、双硫磷(temephos)、特普(TEPP)、环戊烯丙菊酯(terallethrin)、特丁磷(terbufos)、四氯乙烷(tetrachloroethane)、杀虫畏(tetrachlorvinphos)、胺菊酯(tetramethrin)、tetramethylfluthrin、θ-氯氰菊酯(theta-cypermethrin)、噻虫啉(thiacloprid)、噻虫嗪(thiamethoxam)、噻氯磷(thicrofos)、抗虫威(thiocarboxime)、硫环杀(thiocyclam)、草酸硫环杀(thiocyclam oxalate)、硫双灭多威(thiodicarb)、特氨叉威(thiofanox)、甲基乙拌磷(thiometon)、杀虫双(thiosultap)、杀虫双-二钠(thiosultap-disodium)、杀虫双-单钠(thiosultap-mono钠)、敌贝特(thuringiensin)、唑虫酰胺(tolfenpyrad)、四溴菊酯(tralomethrin)、四氟菊酯(transfluthrin)、反氯菊酯(transpermethrin)、苯螨噻(triarathene)、醚苯磺隆(triazamate)、三唑磷(triazophos)、敌百虫(trichlorfon)、异皮蝇磷(trichlormetaphos-3)、壤虫磷(trichloronat)、氯苯乙丙磷(trifenofos)、杀虫隆(triflumuron)、混杀威(trimethacarb)、硫烯酸酯(triprene)、蚜灭多(vamidothion)、氟吡唑虫(vaniliprole)、二甲威(XMC)、灭杀威(xylylcarb)、ζ-氯氰菊酯(zeta-cypermethrin)和zolaprofos(这些通常命名的杀昆虫剂被统一定义为“杀昆虫剂组”)。
杀螨虫剂
式1、2和3的分子也可与以下杀螨虫剂中的一种或多种联用(例如在组合性混合物中,或同时或顺序施用):灭螨醌(acequinocyl)、磺胺螨酯(amidoflumet)、三氧化二砷(arsenous oxide)、偶氮苯(azobenzene)、唑环锡(azocyclotin)、苯菌灵(benomyl)、苯噁磷(benoxafos)、苯螨特(benzoximate)、苯甲酸苄酯(benzyl benzoate)、联苯肼酯(bifenazate)、乐杀螨(binapacryl)、溴螨酯(bromopropylate)、灭螨猛(chinomethionat)、氯杀螨(chlorbenside)、杀螨醇(chlorfenethol)、杀螨酯(chlorfenson)、敌螨丹(chlorfensulphide)、乙酯杀螨醇(chlorobenzilate)、伊托明(chloromebuform)、螟铃畏(chloromethiuron)、丙酯杀螨醇(chloropropylate)、四螨嗪(clofentezine)、cyenopyrafen、丁氟螨酯(cyflumetofen)、三环锡(cyhexatin)、苯氟磺胺(dichlofluanid)、开乐散(dicofol)、除螨灵(dienochlor)、氟螨嗪(diflovidazin)、消螨通(dinobuton)、敌螨普(dinocap)、敌螨普-4(dinocap-4)、敌螨普-6(dinocap 6)、敌螨通(dinocton)、硝戊酯(dinopenton)、硝辛酯(dinosulfon)、硝丁酯(dinoterbon)、二苯砜(diphenylsulfone)、双硫仑(disulfiram)、苯氧炔螨(dofenapyn)、特苯噁唑(etoxazole)、喹螨醚(fenazaquin)、杀螨锡(fenbutatin oxide)、苯硫威(fenothiocarb)、唑螨酯(fenpyroximate)、除螨酯(fenson)、氟硝二苯胺(fentrifanil)、嘧螨酯(fluacrypyrim)、氟佐隆(fluazuron)、噻唑螨(flubenzimine)、联氟螨(fluenetil)、氟氯苯菊酯(flumethrin)、氟杀螨(fluorbenside)、噻螨酮(hexythiazox)、灭芥(mesulfen)、MNAF、华光霉素(nikkomycins)、灭螨醇(proclonol)、克螨特(propargite)、quintiofos、螺螨酯(spirodiclofen)、舒非仑(sulfiram)、硫黄(sulfur)、三氯杀螨砜(tetradifon)、杀螨霉素(tetranactin)、杀螨好(tetrasul)和克杀螨(thioquinox)(这些通常命名的杀螨虫剂被统一定义为“杀螨虫剂组”)。
杀线虫剂
式1、2和3的分子也可与以下杀线虫剂中的一种或多种联用(例如在组合性混合物中,或同时或顺序施用):1,3-二氯丙烯(1,3-dichloropropene)、benclothiaz、棉隆(dazomet)、棉隆钠(dazomet-sodium)、DBCP、DCIP、除线特(diamidafos)、fluensulfone、噻唑酮磷(fosthiazate)、糠醛(furfural)、新烟碱类(imicyafos)、isamidofos、氯唑磷(isazofos)、威百亩(metam)、安百亩(metam-ammonium)、metam-potassium、威百亩(metam-sodium)、乙丙磷威(phosphocarb)和硫磷嗪(thionazin)(这些通常命名的杀线虫剂被统一定义为“杀线虫剂组”)。
杀真菌剂
式1、2和3的分子也可与以下杀真菌剂中的一种或多种联用(例如在组合性混合物中,或同时或顺序施用):(3-乙氧基丙基)溴化汞、2-甲氧基乙基氯化汞、2-苯基苯酚、8-羟基喹啉硫酸盐、8-苯基汞基氧基喹啉(8-phenylmercurioxyquinoline)、acibenzolar、活化酯(acibenzolar-S-methyl)、acypetacs、acypetacs-copper、acypetacs-zinc、烯丙菊酯(aldimorph)、烯丙醇、辛唑嘧菌胺(ametoctradin)、双甲脒(amisulbrom)、氨丙膦酸(ampropylfos)、敌菌灵(anilazine)、aureofungin、阿扎康唑(azaconazole)、氧化福美双(azithiram)、腈嘧菌酯(azoxystrobin)、多硫化钡(barium polysulfide)、苯霜灵(benalaxyl)、精苯霜灵(benalaxyl-M)、麦锈灵(benodanil)、苯菌灵(benomyl)、醌肟腙(benquinox)、丙唑草隆(bentaluron)、苯噻菌胺(benthiavalicarb)、苯噻菌胺酯(benthiavalicarb-isopropyl)、苯扎氯铵(benzalkonium chloride)、苄烯酸(benzamacril)、苄烯酸异丁酯(benzamacril-isobutyl)、苯杂吗(benzamorf)、苯基异羟肟酸(benzohydroxamic acid)、bethoxazin、乐杀螨(binapacryl)、联苯(biphenyl)、联苯三唑醇(bitertanol)、硫双二氯酚(bithionol)、bixafen、灭瘟素(blasticidin-S)、波尔多液(Bordeaux Mixture)、烟酰胺(boscalid)、糠菌唑(bromuconazole)、乙嘧酚磺酸酯(bupirimate)、波尔多液(Burgundy mixture)、丁硫啶(buthiobate)、丁胺(butylamine)、石硫合剂(calcium polysulfide)、敌菌丹(captafol)、克菌丹(captan)、吗菌威(carbamorph)、多菌灵(carbendazim)、萎锈灵(carboxin)、环丙酰菌胺(carpropamid)、香芹酮(carvone)、切欣特液(Cheshunt mixture)、灭螨猛(chinomethionat)、灭瘟唑(chlobenthiazone)、双胺灵(chloraniformethan)、氯醌(chloranil)、苯咪唑菌(chlorfenazole)、氯二硝基萘(chlorodinitronaphthalene)、地茂散(chloroneb)、氯化苦(chloropicrin)、百菌清(chlorothalonil)、四氯喹噁啉(chlorquinox)、乙菌利(chlozolinate)、咪菌酮(climbazole)、克霉唑(clotrimazole)、乙酸铜(copper acetate)、碱式碳酸铜(coppercarbonate basic)、氢氧化铜(copper hydroxide)、环烷酸铜(copper naphthenate)、油酸铜(copper oleate)、碱式氯化铜(copper oxychloride)、硅酸铜(coppersilicate)、硫酸铜(copper sulfate)、铬酸铜锌(copper zinc chromate)、甲酚(cresol)、硫杂灵(cufraneb)、福美铜氯(cuprobam)、氧化亚铜(cuprous oxide)、氰霜唑(cyazofamid)、环糠酰胺(cyclafuramid)、放线菌胺(cycloheximide)、环氟苄酰胺(cyflufenamid)、霜脲氰(cymoxanil)、氰菌灵(cypendazole)、环菌唑(cyproconazole)、嘧菌环胺(cyprodinil)、棉隆(dazomet)、棉隆-钠(dazomet-sodium)、二溴氯丙烷(DBCP)、咪菌威(debacarb)、癸磷锡(decafentin)、脱氢乙酸(dehydroacetic acid)、苯氟磺胺(dichlofluanid)、二氯萘醌(dichlone)、双氯酚(dichlorophen)、菌核利(dichlozoline)、苄氯三唑醇(diclobutrazol)、双氯氰菌胺(diclocymet)、哒菌酮(diclomezine)、哒菌酮-钠(diclomezine-sodium)、dicloran、乙霉威(diethofencarb)、焦碳酸二乙酯(diethyl pyrocarbonate)、苯醚甲环唑(difenoconazole)、氟嘧菌胺(diflumetorim)、甲菌定(dimethirimol)、烯酰吗啉(dimethomorph)、醚菌胺(dimoxystrobin)、烯唑醇(diniconazole)、精烯唑醇(diniconazole-M)、消螨通(dinobuton)、二硝巴豆酸酯(dinocap)、二硝巴豆酸酯-4(dinocap-4)、二硝巴豆酸酯-6(dinocap-6)、敌螨通(dinocton)、硝戊酯(dinopenton)、硝辛酯(dinosulfon)、硝丁酯(dinoterbon)、二苯基胺(diphenylamine)、吡菌硫(dipyrithione)、双硫仑(disulfiram)、灭菌磷(ditalimfos)、二氰蒽醌(dithianon)、二硝甲酚、二硝甲酚-铵、二硝甲酚-钾、二硝甲酚-钠、十二环吗啉(dodemorph)、十二环吗啉乙酸盐(dodemorph acetate)、十二环吗啉苯甲酸盐(dodemorph benzoate)、多敌菌(dodicin)、多敌菌-钠(dodicin-钠)、多果定(dodine)、敌菌酮(drazoxolon)、敌瘟磷(edifenphos)、氟环唑(epoxiconazole)、乙环唑(etaconazole)、代森硫(etem)、噻唑菌胺(ethaboxam)、乙嘧酚(ethirimol)、乙氧喹啉(ethoxyquin)、2,3-二羟基丙基硫醇乙基汞(ethylmercury 2,3-dihydroxypropyl mercaptide)、乙酸乙基汞(ethylmercuryacetate)、溴乙基汞(ethylmercury bromide)、氯乙基汞(ethylmercury chloride)、磷酸乙基汞(ethylmercury phosphate)、土菌灵(etridiazole)、噁唑菌酮(famoxadone)、咪唑菌酮(fenamidone)、敌磺钠(fenaminosulf)、咪菌腈(fenapanil)、氯苯嘧啶醇(fenarimol)、腈苯唑(fenbuconazole)、甲呋酰胺(fenfuram)、环酰菌胺(fenhexamid)、种衣酯(fenitropan)、稻瘟酰胺(fenoxanil)、拌种咯(fenpiclonil)、苯锈啶(fenpropidin)、丁苯吗啉(fenpropimorph)、三苯锡(fentin)、三苯基氯化锡(fentin chloride)、三苯基氢氧化锡(fentin hydroxide)、福美铁(ferbam)、嘧菌腙(ferimzone)、氟啶胺(fluazinam)、咯菌腈(fludioxonil)、氟酰菌胺(flumetover)、氟吗啉(flumorph)、氟吡菌胺(fluopicolide)、氟吡菌酰胺(fluopyram)、氟氯菌核利(fluoroimide)、三氟苯唑(fluotrimazole)、氟嘧菌酯(fluoxastrobin)、氟喹唑(fluquinconazole)、氟硅唑(flusilazole)、磺菌胺(flusulfamide)、氟噻菌净(flutianil)、氟酰胺(flutolanil)、粉唑醇(flutriafol)、fluxapyroxad、灭菌丹(folpet)、甲醛(formaldehyde)、三乙膦酸(fosetyl)、三乙膦酸铝(fosetyl-aluminium)、麦穗宁(fuberidazole)、呋霜灵(furalaxyl)、呋吡菌胺(furametpyr)、灭菌胺(furcarbanil)、呋菌唑(furconazole)、顺式呋菌唑(furconazole-cis)、糠醛(furfural)、拌种胺(furmecyclox)、呋菌隆(furophanate)、果绿啶(glyodine)、灰黄霉素(griseofulvin)、双胍辛乙酸盐(guazatine)、丙烯酸喹啉酯(halacrinate)、六氯苯(hexachlorobenzene)、瘤氯丁二烯(hexachlorobutadiene)、己唑醇(hexaconazole)、环己硫磷(hexylthiofos)、萘磺汞(hydrargaphen)、噁霉灵(hymexazol)、抑霉唑(imazalil)、硝酸抑霉唑(imazalilnitrate)、硫酸抑霉唑(imazalil sulfate)、亚胺唑(imibenconazole)、双胍辛胺(iminoctadine)、三乙酸双胍辛胺(iminoctadine triacetate)、双胍辛胺三(对十二烷基苯磺酸盐)[iminoctadine tris(albesilate)]、碘甲烷(iodomethane)、种菌唑(ipconazole)、异稻瘟净(iprobenfos)、异菌脲(iprodione)、缬霉威(iprovalicarb)、稻瘟灵(isoprothiolane)、吡唑萘菌胺(isopyrazam)、异噻菌胺(isotianil)、氯苯咪菌酮(isovaledione)、春雷霉素(kasugamycin)、醚菌甲酯(kresoxim-methyl)、代森锰铜(mancopper)、代森锰锌(mancozeb)、双炔酰菌胺(mandipropamid)、代森锰(maneb)、邻酰胺(mebenil)、咪卡病西(mecarbinzid)、嘧菌胺(mepanipyrim)、灭锈胺(mepronil)、二硝巴豆酸酯(meptyldinocap)、氯化汞(mercuric chloride)、氧化汞(mercuric oxide)、氯化亚汞(mercurous chloride)、甲霜灵(metalaxyl)、精甲霜灵(metalaxyl-M)、威百亩(metam)、安百亩(metam-ammonium)、metam-potassium、威百亩(metam-sodium)、肼叉噁唑酮(metazoxolon)、叶菌唑(metconazole)、磺菌威(methasulfocarb)、呋菌胺(methfuroxam)、溴甲烷(methyl bromide)、异硫氰酸甲酯、苯甲酸甲基汞(methylmercury benzoate)、氰胍甲汞(methylmercury dicyandiamide)、五氯苯酚甲基汞(methylmercury pentachlorophenoxide)、代森联(metiram)、苯氧菌胺(metominostrobin)、苯菌酮(metrafenone)、噻菌胺(metsulfovax)、代森环(milneb)、腈菌唑(myclobutanil)、甲菌利(myclozolin)、N-(乙基汞基)-对-甲苯磺酰苯胺(N-(ethylmercury)-p-toluenesulphonanilide)、代森钠(nabam)、多马霉素(natamycin)、硫氰散(nitrostyrene)、酞菌异丙酯(nitrothal-isopropyl)、氟苯嘧啶醇(nuarimol)、八氯酮(OCH)、辛噻酮(octhilinone)、呋酰胺(ofurace)、肟醚菌胺(orysastrobin)、噁霜灵(oxadixyl)、喹啉铜(oxine-copper)、噁咪唑(oxpoconazole)、富马酸噁咪唑(oxpoconazole fumarate)、氧化萎锈灵(oxycarboxin)、稻瘟酯(pefurazoate)、戊菌唑(penconazole)、戊菌隆(pencycuron)、戊苯吡菌胺(penflufen)、五氯酚(pentachlorophenol)、吡噻菌胺(penthiopyrad)、苯基汞脲(phenylmercuriurea)、乙酸苯汞(phenyl mercuryacetate)、氯化苯汞(phenylmercury chloride)、儿茶酚的苯汞衍生物(phenylmercury derivative of pyrocatechol)、硝酸苯汞(phenylmercury nitrate)、水杨酸苯汞(phenylmercury salicylate)、氯瘟磷(phosdiphen)、四氯苯酞(phthalide)、啶氧菌酯(picoxystrobin)、病花灵(piperalin)、聚氨基甲酸酯(polycarbamate)、多抗霉素(polyoxin)、多氧霉素(polyoxorim)、多氧霉素-锌(polyoxorim-zinc)、叠氮化钾(potassium azide)、多硫化钾(potassiumpolysulfide)、硫氰酸钾(potassium thiocyanate)、烯丙苯噻唑(probenazole)、咪鲜胺(prochloraz)、腐霉利(procymidone)、霜霉威(propamocarb)、盐酸霜霉威(propamocarb hydrochloride)、丙环唑(propiconazole)、丙森锌(propineb)、丙氧喹啉(proquinazid)、硫菌威(prothiocarb)、盐酸硫菌威(prothiocarbhydrochloride)、丙硫菌唑(prothioconazole)、吡喃灵(pyracarbolid)、吡唑醚菌酯(pyraclostrobin)、吡唑醚菌酯(pyraclostrobin)、唑胺菌酯(pyrametostrobin)、唑菌酯(pyraoxystrobin)、定菌磷(pyrazophos)、pyribencarb、啶菌腈(pyridinitril)、啶斑肟(pyrifenox)、嘧霉胺(pyrimethanil)、pyriofenone、咯喹酮(pyroquilon)、吡氧氯(pyroxychlor)、氯吡呋醚(pyroxyfur)、5-乙酰基-8-羟基喹啉(quinacetol)、5-乙酰基-8-羟基喹啉硫酸盐(quinacetol sulfate)、酯菌腙(quinazamid)、喹唑菌酮(quinconazole)、苯氧喹啉(quinoxyfen)、五氯硝基苯(quintozene)、吡咪唑菌(rabenzazole)、水杨酰胺(salicylanilide)、环丙吡菌胺(sedaxane)、硅噻菌胺(silthiofam)、硅氟唑(simeconazole)、叠氮化钠(sodiumazide)、邻苯基苯酚钠(sodium orthophenylphenoxide)、五氯苯酚钠(sodiumpentachlorophenoxide)、多硫化钠(sodium polysulfide)、螺环菌胺(spiroxamine)、链霉素(streptomycin)、硫磺(sulfur)、戊苯砜(sultropen)、TCMTB、戊唑醇(tebuconazole)、异丁乙氧喹啉(tebufloquin)、叶枯酞(tecloftalam)、四氯硝基苯(tecnazene)、福代硫(tecoram)、四氟醚唑(tetraconazole)、噻菌灵(thiabendazole)、噻二氟(thiadifluor)、噻菌腈(thicyofen)、噻氟菌胺(thifluzamide)、苯菌胺(thiochlorfenphim)、硫柳汞(thiomersal)、硫菌灵(thiophanate)、甲基硫菌灵(thiophanate-methyl)、克杀螨(thioquinox)、福美双(thiram)、噻酰菌胺(tiadinil)、硫氰苯甲酰胺(tioxymid)、甲基立枯磷(tolclofos-methyl)、甲苯氟磺胺(tolylfluanid)、乙酸甲苯汞(tolylmercuryacetate)、三唑酮(triadimefon)、三唑醇(triadimenol)、三唑磷胺(triamiphos)、嘧菌醇(triarimol)、叶锈特(triazbutil)、咪唑嗪(triazoxide)、氧化三丁基锡(tributyltin oxide)、水杨菌胺(trichlamide)、三环唑(tricyclazole)、十三吗啉(tridemorph)、肟菌酯(trifloxystrobin)、氟菌唑(triflumizole)、嗪氨灵(triforine)、灭菌唑(triticonazole)、烯效唑(uniconazole)、精烯效唑(uniconazole-P)、井冈霉素(validamycin)、valifenalate、乙烯菌核利(vinclozolin)、灭杀威(zarilamid)、环烷酸锌(zinc naphthenate)、代森锌(zineb)、福美锌(ziram)、苯酰菌胺(zoxamide)(这些通常命名的杀真菌剂被统一定义为“杀真菌剂组”)。
除草剂
式1、2和3的分子也可与以下除草剂中的一种或多种联用(例如在组合性混合物中,或同时或顺序施用):草芽平(2,3,6-TBA)、2,3,6-TBA-二甲基铵、2,3,6-TBA-钠、2,4,5-T、2,4,5-T-2-丁氧基丙基、2,4,5-T-2-乙基己基、2,4,5-T-3-丁氧基丙基、2,4,5-TB、2,4,5-T-丁氧基异丙基(2,4,5-T-butometyl)、2,4,5-T-丁氧基乙基、2,4,5-T-丁基、2,4,5-T-异丁基、2,4,5-T-异辛基、2,4,5-T-异丙基、2,4,5-T-甲基、2,4,5-T-戊基、2,4,5-T-钠、2,4,5-T-三乙基铵、2,4,5-T-三乙醇胺、2,4-D、2,4-D-2-丁氧基丙基、2,4-D-2-乙基己基、2,4-D-3-丁氧基丙基、2,4-D-铵、2,4-DB、2,4-DB-丁基、2,4-DB-二甲基铵、2,4-DB-异辛基、2,4-DB-钾、2,4-DB-钠、2,4-D-丁氧基乙基、2,4-D-丁基、2,4-D-二乙基铵、2,4-D-二甲基铵、2,4-D-二乙醇胺、2,4-D-十二烷基铵、2,4-DEB、2,4-DEP、2,4-D-乙基、2,4-D-庚基铵、2,4-D-异丁基、2,4-D-异辛基、2,4-D-异丙基、2,4-D-异丙基铵、2,4-D-锂、2,4-D-甲基庚基、2,4-D-甲基、2,4-D-辛基、2,4-D-戊基、2,4-D-钾、2,4-D-丙基、2,4-D-钠、2,4-D-四氢呋喃基、2,4-D-四癸基铵、2,4-D-三乙基铵、2,4-D-三(2-羟基丙基)铵、2,4-D-三乙醇胺、3,4-DA、3,4-DB、3,4-DP、4-CPA、4-CPB、4-CPP、刈草胺(acetochlor)、三氟羧草醚(acifluorfen)、三氟羧草醚-甲基(acifluorfen-methyl)、三氟羧草醚-钠(acifluorfen-sodium)、苯草醚(aclonifen)、丙烯醛(acrolein)、甲草胺(alachlor)、草毒死(allidochlor)、禾草灭(alloxydim)、禾草灭-钠、烯丙醇、五氯戊酮酸(alorac)、特津酮(ametridione)、莠灭净(ametryn)、特草嗪酮(amibuzin)、氨唑草酮(amicarbazone)、磺氨磺隆(amidosulfuron)、环丙嘧啶酸(aminocyclopyrachlor)、环丙嘧啶酸-甲基、环丙嘧啶酸-钾、氯氨基吡啶酸(aminopyralid)、氯氨基吡啶酸-钾、氯氨基吡啶酸-三(2-羟基丙基)铵、甲基胺草磷(amiprofos-methyl)、杀草强(amitrole)、氨基磺酸铵(ammonium sulfamate)、莎稗磷(anilofos)、疏草隆(anisuron)、磺草灵(asulam)、磺草灵-钾、磺草灵-钠、莠去通(atraton)、莠去津(atrazine)、唑啶炔草(azafenidin)、四唑磺隆(azimsulfuron)、叠氮净(aziprotryne)、燕麦灵(barban)、BCPC、氟丁酰草胺(beflubutamid)、草除灵(benazolin)、草除灵-二甲基铵、草除灵-乙基、草除灵-钾、bencarbazone、氟草胺(benfluralin)、呋草磺(benfuresate)、苄嘧磺隆(bensulfuron)、苄嘧磺隆-甲基、地散磷(bensulide)、噻草平(bentazone)、噻草平-钠、胺酸杀(benzadox)、胺酸杀-铵、双苯嘧草酮(benzfendizone)、苄草胺(benzipram)、苯并双环酮(benzobicyclon)、吡草酮(benzofenap)、氟磺胺草(benzofluor)、新燕灵(benzoylprop)、新燕灵-乙基、噻草隆(benzthiazuron)、bicyclopyrone、治草醚(bifenox)、双丙氨酰膦(bilanafos)、双丙氨酰膦-钠、双嘧苯甲酸(bispyribac)、双嘧苯甲酸-钠、硼砂(borax)、除草定(bromacil)、除草定-锂(bromacil-lithium)、除草定-钠、糠草腈(bromobonil)、溴丁酰草胺(bromobutide)、杀草全(bromofenoxim)、溴苯腈(bromoxynil)、丁酸溴苯腈(bromoxynil butyrate)、庚酸溴苯腈(bromoxynilheptanoate)、辛酸溴苯腈(bromoxynil octanoate)、溴苯腈-钾、杀莠敏(brompyrazon)、丁草胺(butachlor)、氟丙嘧草酯(butafenacil)、抑草膦(butamifos)、丁烯草胺(butenachlor)、特咪唑草(buthidazole)、丁噻隆(buthiuron)、地乐胺(butralin)、丁苯草酮(butroxydim)、炔草隆(buturon)、苏达灭(butylate)、二甲胂酸(cacodylic acid)、苯酮唑(cafenstrole)、氯酸钙(calciumchlorate)、氰氨化钙(calcium cyanamide)、克草胺酯(cambendichlor)、卡巴草灵(carbasulam)、长杀草(carbetamide)、特噁唑威(carboxazole)、氟酮唑草(carfentrazone)、氟酮唑草-乙基、CDEA、CEPC、氯硝醚(chlomethoxyfen)、草灭平(chloramben)、草灭平-铵、草灭平-二乙醇胺、草灭平-甲基、草灭平-甲基铵、草灭平-钠、丁酰草胺(chloranocryl)、炔禾灵(chlorazifop)、炔禾灵-炔丙基(chlorazifop-propargyl)、可乐津(chlorazine)、氯溴隆(chlorbromuron)、氯炔灵(chlorbufam)、乙氧苯隆(chloreturon)、伐草克(chlorfenac)、伐草克-钠、燕麦酯(chlorfenprop)、燕麦酯-甲基、氟嘧杀(chlorflurazole)、氯甲丹(chlorflurenol)、氯甲丹-甲基、氯草敏(chloridazon)、氯嘧磺隆(chlorimuron)、氯嘧磺隆-乙基、草枯醚(chlornitrofen)、三氯丙酸(chloropon)、氯麦隆(chlorotoluron)、枯草隆(chloroxuron)、羟敌草腈(chloroxynil)、草败死(chlorprocarb)、氯苯胺灵(chlorpropham)、绿磺隆(chlorsulfuron)、氯酞酸(chlorthal)、氯酞酸-二甲基、氯酞酸-单甲基、草克乐(chlorthiamid)、吲哚酮草酯(cinidon-ethyl)、环庚草醚(cinmethylin)、醚磺隆(cinosulfuron)、咯草隆(cisanilide)、烯草酮(clethodim)、碘氯啶酯(cliodinate)、炔草酯(clodinafop)、炔草酯-炔丙基、氯丁草(clofop)、氯丁草-异丁基、异噁草酮(clomazone)、稗草胺(clomeprop)、调果酸(cloprop)、环丁烯草酮(cloproxydim)、二氯吡啶酸(clopyralid)、二氯吡啶酸-甲基、二氯吡啶酸-乙醇胺、二氯吡啶酸-钾、二氯吡啶酸-三(2-羟基丙基)铵、氯酯磺草胺(cloransulam)、氯酯磺草胺-甲基、CMA、硫酸铜、CPMF、CPPC、醚草敏(credazine)、甲酚(cresol)、苄草隆(cumyluron)、氨基氰(cyanamide)、氰草净(cyanatryn)、氰草津(cyanazine)、草灭特(cycloate)、环丙磺隆(cyclosulfamuron)、噻草酮(cycloxydim)、环莠隆(cycluron)、氰氟草酯(cyhalofop)、氰氟草酯-丁基、牧草快(cyperquat)、盐酸牧草快(cyperquat chloride)、环丙津(cyprazine)、三环塞草胺(cyprazole)、环酰草胺(cypromid)、香草隆(daimuron)、茅草枯(dalapon)、茅草枯-钙、茅草枯-镁、茅草枯-钠、棉隆(dazomet)、棉隆-钠、敌草乐(delachlor)、甜菜安(desmedipham)、敌草净(desmetryn)、燕麦敌(di-allate)、麦草畏(dicamba)、麦草畏-二甲基铵、麦草畏-二乙醇胺、麦草畏-异丙基铵、麦草畏-甲基、麦草畏-乙醇胺、麦草畏-钾、麦草畏-钠、麦草畏-三醇胺、敌草腈(dichlobenil)、氯全隆(dichloralurea)、苄胺灵(dichlormate)、2,4-滴丙酸(dichlorprop)、2,4-滴丙酸-2-乙基己基、2,4-滴丙酸-丁氧基乙基、2,4-滴丙酸-二甲基铵、2,4-滴丙酸-乙基铵、2,4-滴丙酸-异辛基、2,4-滴丙酸-甲基、精2,4-滴丙酸(dichlorprop-P)、精2,4-滴丙酸-二甲基铵、2,4-滴丙酸-钾、2,4-滴丙酸-钠、氯甲草(diclofop)、氯甲草-甲基、唑嘧磺胺(diclosulam)、二乙除草双(diethamquat)、二盐酸二乙除草双(diethamquat dichloride)、安塔(diethatyl)、安塔-乙基、氟苯戊烯酸(difenopenten)、氟苯戊烯酸-乙基、枯莠隆(difenoxuron)、苯敌快(difenzoquat)、甲硫酸苯敌快、吡氟酰草胺(diflufenican)、二氟吡隆(diflufenzopyr)、二氟吡隆-钠、噁唑隆(dimefuron)、哌草丹(dimepiperate)、克草胺(dimethachlor)、戊草津(dimethametryn)、二甲吩草胺(dimethenamid)、精二甲吩草胺(dimethenamid-P)、敌灭生(dimexano)、敌米达松(dimidazon)、敌乐胺(dinitramine)、地乐特(dinofenate)、丙硝酚(dinoprop)、戊硝酚(dinosam)、地乐酚(dinoseb)、乙酸地乐酚(dinoseb acetate)、地乐酚-铵、地乐酚-二乙醇胺、地乐酚-钠、地乐酚-三乙醇胺、特乐酚(dinoterb)、乙酸特乐酚(dinoterb acetate)、敌鼠-钠(diphacinone-sodium)、草乃敌(diphenamid)、杀草净(dipropetryn)、敌草快(diquat)、敌草快二溴化物(diquatdibromide)、2,4-滴硫酸(disul)、2,4-滴硫钠(disul-sodium)、氟硫草定(dithiopyr)、敌草隆(diuron)、DMPA、二硝甲酚、二硝甲酚-铵、二硝甲酚-钾、二硝甲酚-钠、DSMA、EBEP、甘草津(eglinazine)、甘草津-乙基、草藻灭(endothal)、草藻灭-二铵、草藻灭-二钾、草藻灭-二钠、磺唑草(epronaz)、EPTC、抑草蓬(erbon)、禾草畏(esprocarb)、丁氟消草(ethalfluralin)、胺苯磺隆(ethametsulfuron)、胺苯磺隆-甲基、噻二唑隆(ethidimuron)、抑草威(ethiolate)、乙呋草磺(ethofumesate)、氯氟草醚(ethoxyfen)、氯氟草醚-乙基、乙氧嘧磺隆(ethoxysulfuron)、硝草酚(etinofen)、乙胺草醚(etnipromid)、乙氧苯酰草(etobenzanid)、EXD、酰苯磺威(fenasulam)、2,4,5-涕丙酸(fenoprop)、2,4,5-涕丙酸-3-丁氧基丙基、2,4,5-涕丙酸-丁氧基异丙基、2,4,5-涕丙酸-丁氧基乙基、2,4,5-涕丙酸-丁基、2,4,5-涕丙酸-异辛基、2,4,5-涕丙酸-甲基、2,4,5-涕丙酸-钾、噁唑禾草灵(fenoxaprop)、噁唑禾草灵-乙基、精噁唑禾草灵(fenoxaprop-P)、精噁唑禾草灵-乙基、fenoxasulfone、氯苯氧乙醇(fenteracol)、噻唑禾草灵(fenthiaprop)、噻唑禾草灵-乙基、四唑草胺(fentrazamide)、非草隆(fenuron)、非草隆TCA、硫酸亚铁(ferrous sulfate)、氟燕灵(flamprop)、氟燕灵-异丙基、强氟燕灵(flamprop-M)、氟燕灵-甲基、强氟燕灵-异丙基、强氟燕灵-甲基、啶嘧磺隆(flazasulfuron)、双氟磺草胺(florasulam)、吡氟禾草灵(fluazifop)、吡氟禾草灵-丁基、吡氟禾草灵-甲基、精吡氟禾草灵(fluazifop-P)、精吡氟禾草灵-丁基、异丙吡草酯(fluazolate)、氟酮磺隆(flucarbazone)、氟酮磺隆-钠、氟吡磺隆(flucetosulfuron)、氟消草(fluchloralin)、氟噻草胺(flufenacet)、氟苯吡草(flufenican)、氟哒嗪草酯(flufenpyr)、氟哒嗪草酯-乙基、氟唑啶草(flumetsulam)、三氟噁嗪(flumezin)、氟烯草酸(flumiclorac)、氟烯草酸-戊基、丙炔氟草胺(flumioxazin)、炔草胺(flumipropyn)、伏草隆(fluometuron)、消草醚(fluorodifen)、乙羧氟草醚(fluoroglycofen)、乙羧氟草醚-乙基、唑啶草(fluoromidine)、氟除草醚(fluoronitrofen)、氟苯隆(fluothiuron)、氟胺草唑(flupoxam)、flupropacil、四氟丙酸(flupropanate)、四氟丙酸-钠、氟啶磺隆(flupyrsulfuron)、氟啶磺隆-甲基-钠、氟草同(fluridone)、氟咯草酮(flurochloridone)、氯氟吡氧乙酸(fluroxypyr)、氯氟吡氧乙酸-丁氧基异丙酯(fluroxypyr-butometyl)、氯氟吡氧乙酸-异辛酯、呋草酮(flurtamone)、达草氟(fluthiacet)、达草氟-甲基、氟磺胺草醚(fomesafen)、氟磺胺草醚-钠、甲酰胺磺隆(foramsulfuron)、膦铵素(fosamine)、膦铵素-铵、氟呋草醚(furyloxyfen)、草铵膦(glufosinate)、草铵膦-铵、精草铵膦(glufosinate-P)、精草铵膦-铵、精草铵膦-钠、草甘膦(glyphosate)、草甘膦-二铵、草甘膦-二甲基铵、草甘膦-异丙基铵、草甘膦-单铵、草甘膦-钾、草甘膦-一倍半钠、草甘膦-三甲基锍盐(glyphosate trimesium)、氟硝磺酰胺(halosafen)、吡氯磺隆(halosulfuron)、吡氯磺隆-甲基、卤草定(haloxydine)、氟吡禾灵(haloxyfop)、氟吡禾灵-乙氧基乙基、氟吡禾灵-甲基、精氟吡禾灵(haloxyfop-P)、精氟吡禾灵-乙氧基乙基、精氟吡禾灵-甲基、氟吡禾灵-钠、六氯丙酮(hexachloroacetone)、六氟胂酸盐(hexaflurate)、六嗪酮(hexazinone)、咪草酯(imazamethabenz)、咪草酯-甲基、咪草啶酸(imazamox)、咪草啶酸-铵、甲咪唑烟酸(imazapic)、甲咪唑烟酸-铵、灭草烟(imazapyr)、灭草烟-异丙基铵、灭草喹(imazaquin)、灭草喹-铵、灭草喹-甲基、灭草喹-钠、咪草烟(imazethapyr)、咪草烟-铵、啶咪磺隆(imazosulfuron)、茚草酮(indanofan)、indaziflam、碘草腈(iodobonil)、碘甲烷(iodomethane)、碘磺隆(iodosulfuron)、甲基碘磺隆钠盐、iofensulfuron、iofensulfuron、碘苯腈(ioxynil)、辛酸碘苯腈(ioxynil octanoate)、碘苯腈-锂、碘苯腈-钠、抑草津(ipazine)、ipfencarbazone、丙草定(iprymidam)、丁咪胺(isocarbamid)、异草定(isocil)、丁嗪草酮(isomethiozin)、异草完隆(isonoruron)、氮草(isopolinate)、异丙乐灵(isopropalin)、异丙隆(isoproturon)、异恶隆(isouron)、异噁酰草胺(isoxaben)、异噁氯草酮(isoxachlortole)、异噁氟草酮(isoxaflutole)、噁草醚(isoxapyrifop)、特胺灵(karbutilate)、ketospiradox、乳氟禾草灵(lactofen)、环草定(lenacil)、利谷隆(linuron)、甲基胂酸(MAA)、甲胂一铵(MAMA)、2甲4氯(MCPA)、2甲4氯-2-乙基己基、2甲4氯-丁氧基乙基、2甲4氯-丁基、2甲4氯-二甲基铵、2甲4氯-二乙醇胺、2甲4氯-乙基、2甲4氯-异丁基、2甲4氯-异辛基、2甲4氯-异丙基、2甲4氯-甲基、2甲4氯-乙醇胺、2甲4氯-钾、2甲4氯-钠、酚硫杀(MCPA-thioethyl)、2甲4氯-三乙醇胺、2甲4氯丁酸(MCPB)、2甲4氯丁酸-乙基、2甲4氯丁酸-甲基、2甲4氯丁酸-钠、2甲4氯丙酸(mecoprop)、2甲4氯丙酸-2-乙基己基、2甲4氯丙酸-二甲基铵、2甲4氯丙酸-二乙醇胺、2甲4氯丙酸-ethadyl、2甲4氯丙酸-异辛基、2甲4氯丙酸-甲基、精2甲4氯丙酸(mecoprop-P)、精2甲4氯丙酸-二甲基铵、精2甲4氯丙酸-异丁基、2甲4氯丙酸-钾、精2甲4氯丙酸-钾、2甲4氯丙酸-钠、2甲4氯丙酸-三乙醇胺、丁硝酚(medinoterb)、乙酸丁硝酚(medinoterb acetate)、苯噻酰草胺(mefenacet)、氟磺酰草胺(mefluidide)、氟磺酰草胺-二乙醇胺、氟磺酰草胺-钾、灭莠津(mesoprazine)、甲基二磺隆(mesosulfuron)、甲基二磺隆-甲基、甲基磺草酮(mesotrione)、威百亩(metam)、威百亩-铵、噁唑酰草胺(metamifop)、苯嗪草酮(metamitron)、威百亩-钾、威百亩-钠、吡草胺(metazachlor)、双醚氯吡嘧磺隆(metazosulfuron)、氟哒草(metflurazon)、噻唑隆(methabenzthiazuron)、氟烯硝草(methalpropalin)、灭草定(methazole)、甲硫苯威(methiobencarb)、methiozolin、灭草恒(methiuron)、醚草通(methometon)、盖草津(methoprotryne)、溴甲烷(methyl bromide)、异硫氰酸甲酯、苯丙隆(methyldymron)、色满隆(metobenzuron)、异丙甲草胺(metolachlor)、唑草磺胺(metosulam)、甲氧隆(metoxuron)、嗪草酮(metribuzin)、甲磺隆(metsulfuron)、甲磺隆-甲基、草达灭(molinate)、庚酰草胺(monalide)、特噁唑隆(monisouron)、单氯代乙酸(monochloroacetic acid)、绿谷隆(monolinuron)、灭草隆(monuron)、灭草隆TCA、伐草快(morfamquat)、伐草快二氯化物(morfamquat dichloride)、甲胂一钠(MSMA)、萘丙胺(naproanilide)、敌草胺(napropamide)、萘草胺(naptalam)、萘草胺-钠、草不隆(neburon)、烟嘧磺隆(nicosulfuron)、吡氯草胺(nipyraclofen)、甲磺乐灵(nitralin)、除草醚(nitrofen)、三氟甲草醚(nitrofluorfen)、达草灭(norflurazon)、草完隆(noruron)、八氯酮(OCH)、坪草丹(orbencarb)、邻-二氯苯(ortho-dichlorobenzene)、orthosulfamuron、黄草消(oryzalin)、炔丙噁唑草(oxadiargyl)、噁草灵(oxadiazon)、噁杀草敏(oxapyrazon)、噁杀草敏-二甲氨基乙醇(oxapyrazon-dimolamine)、噁杀草敏-钠、环丙氧磺隆(oxasulfuron)、氯噁嗪草(oxaziclomefone)、乙氧氟草醚(oxyfluorfen)、对伏隆(parafluron)、百草枯(paraquat)、百草枯二氯化物(paraquat dichloride)、二甲硫酸百草枯(paraquat dimetilsulfate)、克草猛(pebulate)、壬酸(pelargonic acid)、胺硝草(pendimethalin)、五氟磺草胺(penoxsulam)、五氯酚(pentachlorophenol)、甲氯酰草胺(pentanochlor)、戊噁唑草(pentoxazone)、氟草磺胺(perfluidone)、烯草胺(pethoxamid)、棉胺宁(phenisopham)、甜菜宁(phenmedipham)、甜菜宁-乙基、稀草隆(phenobenzuron)、乙酸苯汞、氨氯吡啶酸(picloram)、氨氯吡啶酸-2-乙基己基、氨氯吡啶酸-异辛基、氨氯吡啶酸-甲基、氨氯吡啶酸-乙醇胺、氨氯吡啶酸-钾、氨氯吡啶酸-三乙基铵、氨氯吡啶酸-三(2-羟基丙基)铵、氟吡草胺(picolinafen)、pinoxaden、哌草磷(piperophos)、亚砷酸钾(potassiumarsenite)、叠氮化钾(potassium azide)、氰酸钾(potassium azide)、冰草胺(pretilachlor)、氟嘧磺隆(primisulfuron)、氟嘧磺隆-甲基、环氰津(procyazine)、氨氟乐灵(prodiamine)、氟唑草胺(profluazol)、环丙氟灵(profluralin)、环苯草酮(profoxydim)、丙草止津(proglinazine)、丙草止津-乙基、扑灭通(prometon)、扑草净(prometryn)、毒草安(propachlor)、敌稗(propanil)、喔草酯(propaquizafop)、扑灭津(propazine)、苯胺灵(propham)、异丙草胺(propisochlor)、丙苯磺隆(propoxycarbazone)、丙苯磺隆钠、嗪咪唑嘧磺隆(propyrisulfuron)、炔苯酰草胺(propyzamide)、磺亚胺草(prosulfalin)、苄草丹(prosulfocarb)、氟丙磺隆(prosulfuron)、扑灭生(proxan)、扑灭生-钠、广草胺(prynachlor)、比达农(pydanon)、双唑草腈(pyraclonil)、氟唑草酯(pyraflufen)、吡草醚(pyraflufen-ethyl)、pyrasulfotole、吡唑特(pyrazolynate)、吡嘧磺隆(pyrazosulfuron)、乙基吡嘧磺隆(pyrazosulfuron-ethyl)、苄草唑(pyrazoxyfen)、嘧苯草肟(pyribenzoxim)、稗草丹(pyributicarb)、氯草定(pyriclor)、pyridafol、哒草特(pyridate)、环酯草醚(pyriftalid)、肟啶草(pyriminobac)、甲基肟啶草(pyriminobac-methyl)、pyrimisulfan、嘧硫草醚(pyrithiobac)、嘧硫草醚钠、pyroxasulfone、甲氧磺草胺(pyroxsulam)、二氯喹啉酸(quinclorac)、氯甲喹啉酸(quinmerac)、灭藻醌(quinoclamine)、氯藻胺(quinonamid)、喹禾灵(quizalofop)、乙基喹禾灵(quizalofop-ethyl)、精喹禾灵(quizalofop-P)、精乙基喹禾灵(quizalofop-P-ethyl)、喹禾糠酯(quizalofop-P-tefuryl)、硫氰苯乙胺(rhodethanil)、玉嘧磺隆(rimsulfuron)、苯嘧磺草胺(saflufenacil)、另丁津(sebuthylazine)、密草通(secbumeton)、稀禾定(sethoxydim)、环草隆(siduron)、西玛津(simazine)、西玛通(simeton)、西草净(simetryn)、氯乙酸(SMA)、S-异丙甲草胺(S-metolachlor)、亚砷酸钠(sodium arsenite)、叠氮化钠(sodiumazide)、氯酸钠(sodium chlorate)、磺草酮(sulcotrione)、草克死(sulfallate)、磺胺草唑(sulfentrazone)、嘧磺隆(sulfometuron)、甲基嘧磺隆(sulfometuron-methyl)、乙磺磺隆(sulfosulfuron)、硫酸(sulfuric acid)、吖庚磺酯(sulglycapin)、灭草灵(swep)、三氯醋酸(TCA)、三氯醋酸铵、三氯醋酸钙、乙二基三氯醋酸(TCA-ethadyl)、三氯醋酸镁、三氯醋酸钠、牧草胺(tebutam)、丁唑隆(tebuthiuron)、tefuryltrione、tembotrione、吡喃草酮(tepraloxydim)、特草定(terbacil)、特草灵(terbucarb)、猛杀草(terbuchlor)、甲氧去草净(terbumeton)、特丁津(terbuthylazine)、去草净(terbutryn)、氟氧隆(tetrafluron)、噻醚草胺(thenylchlor)、赛唑隆(thiazafluron)、噻草啶(thiazopyr)、噻二唑胺(thidiazimin)、赛二唑素(thidiazuron)、噻酮磺隆(thiencarbazone)、噻酮磺隆-甲基(thiencarbazone-methyl)、噻磺隆(thifensulfuron)、甲基噻磺隆(thifensulfuron-methyl)、禾草丹(thiobencarb)、丁草威(tiocarbazil)、嘧草胺(tioclorim)、topramezone、苯草酮(tralkoxydim)、野麦畏(tri-allate)、醚苯磺隆(triasulfuron)、三嗪氟草胺(triaziflam)、苯磺隆(tribenuron)、甲基苯磺隆(tribenuron-methyl)、杀草畏(tricamba)、三氯吡氧乙酸(triclopyr)、丁氧基乙基三氯吡氧乙酸(triclopyr-butotyl)、乙基三氯吡氧乙酸(triclopyr-ethyl)、三氯吡氧乙酸-三乙基铵(triclopyr-triethylammonium)、灭草环(tridiphane)、草达津(trietazine)、三氟啶磺隆(trifloxysulfuron)、三氟啶磺隆钠(trifloxysulfuron-sodium)、氟乐灵(trifluralin)、氟胺磺隆(triflusulfuron)、氟胺磺隆-甲基(triflusulfuron-methyl)、三氟苯氧丙酸(trifop)、三氟苯氧丙酸-甲基(trifop-methyl)、三氟禾草肟(trifopsime)、三羟基三嗪(trihydroxytriazine)、三甲隆(trimeturon)、茚草酮(tripropindan)、草达克(tritac)、三氟甲磺隆(tritosulfuron)、灭草猛(vernolate)、二甲苯草胺(xylachlor)(这些通常命名的杀真菌剂被统一定义为“除草剂组”)。
杀生物剂
式1、2和3的分子也可用于与一种或多种杀生物剂组合(例如在组合性混合物中,或同时或顺序施用)。术语“杀生物剂”用来指微生物害虫防治剂,按与化学杀虫剂相似的方式施用所述杀生物剂。通常,这些是细菌防治剂,但也有真菌防治剂的实例,包括木霉种(Trichoderma spp)和白粉寄生孢(Ampelomyces quisqualis)(用于葡萄白粉病(grape powdery mildew)的防治剂)。芽孢杆菌(Bacillus subtilis)用于防治植物病原。也可用微生物剂防治杂草和啮齿动物。一种公知的杀昆虫剂实例为苏芸金杆菌(Bacillusthuringiensis)(鳞翅目(Lepidoptera)、鞘蛾目(Coleoptera)和双翅目(Diptera)细菌疾病)。由于其对其它微生物具有很小的影响,因此认为其比合成杀虫剂更环保。生物杀昆虫剂包括基于以下的产物:
1.昆虫病原真菌(entomopathogenic fungi)(例如拜欧1020(Metarhiziumanisopliae));
2.昆虫病原线虫(例如芫菁夜蛾线虫(Steinernema feltiae));和
3.昆虫病原病毒(例如苹果蠢蛾颗粒体病毒(Cydia pomonellagranulovirus))。
昆虫病原有机体的其它实例包括但不限于杆状病毒、细菌和其它原核有机体、真菌、原生动物和微孢子虫(Microsproridia)。生物衍生的杀昆虫剂包括但不限于鱼藤酮、藜芦定以及微生物毒素;耐昆虫或抗昆虫的植物种类;和通过重组DNA技术修饰的有机体,其中所述有机体经所述修饰后产生杀昆虫剂或将抗昆虫性质转移到遗传修饰的有机体上。在一个实施方案中,式1、2和3的分子可与种子处理和土壤改良领域的一种或多种杀生物剂一起使用。《生物防治剂手册》(The Manual of Biocontrol Agents)给出了可用生物杀昆虫剂(和其它基于生物的防治)产物的综述。Copping L.G.(ed.)(2004).TheManual of Biocontrol Agents(formerly the Biopesticide Manual)3rd Edition.British Crop Production Council(BCPC),Farnham,Surrey UK。
其它活性化合物
式1、2和3的分子也可与以下一种或多种化合物组合使用(例如在组合性混合物中,或同时或顺序施用):
1.3-(4-氯-2,6-二甲基苯基)-4-羟基-8-氧杂-1-氮杂螺[4,5]癸-3-烯-2-酮;
2.3-(4’-氯-2,4-二甲基[1,1’-联苯]-3-基)-4-羟基-8-氧杂-1-氮杂螺[4,5]癸-3-烯-2-酮;
3.4-[[(6-氯-3-吡啶基)甲基]甲基氨基]-2(5H)-呋喃酮;
4.4-[[(6-氯-3-吡啶基)甲基]环丙基氨基]-2(5H)-呋喃酮;
5.3-氯-N2-[(1S)-1-甲基-2-(甲基磺酰基)乙基]-N1-[2-甲基-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基]-1,2-苯二甲酰胺;
6.2-氰基-N-乙基-4-氟-3-甲氧基-苯磺酰胺;
7.2-氰基-N-乙基-3-甲氧基-苯磺酰胺;
8.2-氰基-3-二氟甲氧基-N-乙基-4-氟-苯磺酰胺;
9.2-氰基-3-氟甲氧基-N-乙基-苯磺酰胺;
10.2-氰基-6-氟-3-甲氧基-N,N-二甲基-苯磺酰胺;
11.2-氰基-N-乙基-6-氟-3-甲氧基-N-甲基-苯磺酰胺;
12.2-氰基-3-二氟甲氧基-N,N-二甲基苯磺酰胺;
13.3-(二氟甲基)-N-[2-(3,3-二甲基丁基)苯基]-1-甲基-1H-吡唑-4-甲酰胺;
14.N-乙基-2,2-二甲基丙酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)腙;
15.烟碱N-乙基-2,2-二氯-1-甲基环丙烷-甲酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)腙;
16.O-{(E-)-[2-(4-氯-苯基)-2-氰基-1-(2-三氟甲基苯基)-乙烯基]}硫代碳酸S-甲基酯;
17.(E)-N1-[(2-氯-1,3-噻唑-5-基甲基)]-N2-氰基-N1-甲基乙脒;
18.1-(6-氯吡啶-3-基甲基)-7-甲基-8-硝基-1,2,3,5,6,7-六氢-咪唑并[1,2-a]吡啶-5-醇;
19.甲磺酸4-[4-氯苯基-(2-亚丁基-肼叉)甲基)]苯基酯;和
20.N-乙基-2,2-二氯-1-甲基环丙甲酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)腙。
式1、2和3的分子也可与下组中的一个或多个化合物组合使用(例如在组合性混合物中,或同时或顺序施用):灭藻剂、拒食剂、杀鸟剂(avicide)、杀菌剂、驱鸟剂(bird repellent)、化学绝育剂(chemosterilant)、除草剂安全剂(herbicide safener)、昆虫引诱剂(insect attractant)、驱虫剂(insect repellent)、驱哺乳动物剂(mammal repellent)、交配干扰剂(mating disrupter)、杀软体动物剂、植物激活剂(plant activator)、植物生长调节剂(plant growth regulator)、杀啮齿动物剂(rodenticide)和/或杀病毒剂(这些通常命名的杀真菌剂被统一定义为“AI组”)。应当注意的是,落入AI组、杀昆虫剂组、杀真菌剂组、除草剂组、杀螨虫剂组或杀线虫剂组的化合物可能在不止一组中,这是由于所述化合物具有多重活性。更多信息请参阅本文件提交日期之前的“Compendium ofPesticide Common Names”(位于http://www.alanwood.net/pesticides/index.html)。还请参阅“The PesticideManual”14th Edition,edited by C D S Tomlin,copyright 2006 by British CropProduction Council或其优先或更新版本。
协同性混合物和增效剂
式1、2和3的分子可用于与杀昆虫剂组一起使用以形成协同性混合物,其中所述杀昆虫剂组化合物的作用模式与式1、2和3的分子的作用模式是相同、相似或不同的。作用模式的实例包括但不限于:乙酰胆碱酯酶抑制剂;钠通道调节剂;壳多糖生物合成抑制剂(chitin biosynthesis inhibitor);GABA门控氯化物通道拮抗剂(GABA-gated chloride channel antagonist);GABA和谷氨酸门控氯化物通道激动剂(GABA and glutamate-gated chloride channelagonist);乙酰胆碱受体激动剂;MET I抑制剂;Mg刺激性ATP酶抑制剂(Mg-stimulated ATPase inhibitor);烟碱性乙酰胆碱受体;中肠膜破裂剂(midgutmembrane disrupter);和氧化磷酸化中断剂(oxidative phosphorylation disrupter)和利阿诺定受体(ryanodine receptor,RyRs)。此外,式1、2和3的分子可与杀真菌剂组、杀螨虫剂组、除草剂组或杀线虫剂组中的化合物一起使用以形成协同性混合物。此外,式1、2和3的分子可与其它活性化合物例如“其它活性化合物”标题下的化合物一起使用以形成协同性混合物,所述“其它活性化合物”标题下的化合物为灭藻剂、杀鸟剂、杀菌剂、杀软体动物剂、杀啮齿动物剂、杀病毒剂、除草剂安全剂、助剂和/或表面活性剂。大体上,在协同性混合物中,式1、2和3的分子与另一种化合物的重量比为约10:1至约1:10,优选从约5:1至约1:5且更优选为约3:1且甚至更优选为约1:1。此外,已知以下化合物为增效剂并可与式I披露的分子一起使用:胡椒基丁醚(piperonyl butoxide)、增效醛(piprotal)、增效酯(propyl isome)、增效菊(sesamex)、芝麻啉(sesamolin)、亚砜(sulfoxide)和脱叶磷(Tribufos)(总体上,这些增效剂如“增效剂组”中所定义)。
制剂
杀虫剂几乎不适于以其纯形式来施用。通常需要加入其它物质,从而使杀虫剂可按所需的浓度和适当的形式来使用,由此易于施用、处理、运输、贮存和使杀虫剂活性最大化。因此,将杀虫剂配制成例如诱饵(bait)、浓缩乳液、粉剂(dust)、乳油(emulsifiable concentrate)、熏蒸剂(fumigant)、凝胶、颗粒、微囊形式(microencapsulation)、种子处理形式(seed treatment)、混悬浓缩物、混悬乳液(suspoemulsion)、片剂、水溶性液体、水可分散颗粒或干燥可流动物(dry flowable)、可润湿粉末(wettable powder)和超低体积溶液(ultra lowvolume solution)。有关制剂类型的进一步信息请参阅“Catalogue of pesticideformulation types and international coding system”Technical Monograph n°2,5thEdition by CropLife International(2002)。
杀虫剂最常见的是以由所述杀虫剂的浓缩制剂制备的含水混悬液或乳液的形式来施用。这样的水溶性制剂、水可混悬制剂或可乳化制剂为固体(通常已知为可润湿粉末或水可分散颗粒)或液体(通常已知为乳油或含水混悬液)。可润湿粉末(其可以被压制以形成水可分散颗粒)包含杀虫剂、载体和表面活性剂的充分混合物(intimate mixture)。杀虫剂的浓度通常为约10wt%(重量百分比)至约90wt%。所述载体通常选自硅镁土(attapulgite clay)、蒙脱土(montmorillonite clay)、硅藻土(diatomaceous earth)或精制硅酸盐(purifiedsilicate)。有效的表面活性剂(占可润湿粉末的约0.5%至约10%)选自磺酸化的木质素、浓缩的萘磺酸盐、萘磺酸盐、烷基苯磺酸盐、烷基硫酸盐和非离子表面活性剂(例如烷基酚的氧化乙烯加成物)。
杀虫剂的乳油包含溶解在载体(所述载体为水可混合溶剂或水不可混合有机溶剂和乳化剂的混合物)中的合适浓度的杀虫剂(例如每升液体约50至约500克)。有用的有机溶剂包括芳香族溶剂(特别是二甲苯)和石油馏分(特别是石油的高沸点萘部分和烯烃部分例如重芳香族石脑油)。也可使用其它有机溶剂,例如萜类溶剂(包括松香衍生物)、脂肪族酮(例如环己酮)和复杂的醇(例如2-乙氧基乙醇)。用于乳油的合适乳化剂选自常见的阴离子表面活性剂和非离子表面活性剂。
含水混悬液包括水不溶性杀虫剂分散在含水载体中的混悬液,其浓度为约5wt%至约50wt%。混悬液如下制备:精细研磨所述杀虫剂且将其剧烈混合到载体中,所述载体包含水和表面活性剂。也可加入诸如无机盐和合成胶或天然胶那样的成分,以增加含水载体的密度和粘度。通常最有效的是通过在设备例如砂磨机(sand mill)、球磨机(ball mill)或活塞式匀化器(piston-typehomogenizer)中制备含水混合物并对其进行匀化来同时研磨和混合杀虫剂。
杀虫剂也可按颗粒组合物的形式来施用,所述颗粒组合物特别可用于施用到土壤中。颗粒组合物通常含有分散在载体中的约0.5wt%至约10wt%的所述杀虫剂,所述载体包含粘土(clay)或相似的物质。上述组合物通常如下制备:将所述杀虫剂溶解在合适的溶剂中且将其施用到颗粒载体上,所述颗粒载体已经被预先制成合适的粒度(范围为约0.5至3mm)。上述组合物也可如下制备:将所述载体和化合物制成面团状或糊状,然后压碎并干燥,从而得到所需颗粒粒度。
含有杀虫剂的粉剂如下制备:对粉末状的杀虫剂与合适的粉尘状农用载体(例如高岭粘土、研碎的火山石等)进行充分混合。粉剂可合适地含有约1%至约10%杀虫剂。它们可用于拌种(seed dressing)或与粉尘鼓风机一起用于叶面施用(foliage application)。
同样可行的是施用溶液形式的杀虫剂(在广泛用于农业化学的合适有机溶剂(通常为石油(petroleum oil)例如喷雾油)中)。
杀虫剂也可按气溶胶组合物的形式来施用。在这样的组合物中,将杀虫剂溶解或分散在载体中,所述载体为可产生压力的推进剂混合物。将所述气溶胶组合物包装在容器中,通过雾化阀使所述混合物从所述容器中分散出来。
当将杀虫剂与食物或引诱剂混合或与食物和引诱剂混合时,形成了杀虫剂诱饵。当害虫吃掉诱饵时,它们也消耗了杀虫剂。诱饵可呈颗粒、凝胶、可流动粉末、液体或固体的形式。它们用在害虫藏身处。
熏蒸剂是具有相对高蒸汽压的杀虫剂,因此可按气体形式存在,其以足够的浓度杀死土壤或密封空间中的害虫。熏蒸剂的毒性与其浓度和暴露时间成比例。它们的特征在于具有良好的扩散能力且通过渗透到害虫的呼吸系统中或通过害虫的表皮被吸收来发挥作用。施用熏蒸剂以便在气密房间或气密建筑物中或在专门腔室中对防气片(gas proof sheet)下的储藏产品害虫(storedproduct pest)进行防治。
可通过将杀虫剂粒子或小滴混悬在各种类型的塑料聚合物(plasticpolymer)中来对杀虫剂进行微囊化。通过改变聚合物的化学性质或通过改变处理中的因素,可形成各种大小、各种溶解度、各种壁厚度和各种渗透度的微囊。这些因素控制其中活性成分的释放速度,而释放速度又影响产品的残留性能、作用速度和气味。
通过将杀虫剂溶于使杀虫剂保持为溶液形式的溶剂中来制备油溶液浓缩物。杀虫剂的油溶液由于溶剂本身具有杀虫作用和体被(integument)蜡质覆盖物(waxy covering)的溶解增加了杀虫剂的摄取速度而通常提供比其它制剂更快的击倒及杀死害虫作用。油溶液的其它优点包括更好的贮藏稳定性、更好的裂缝渗透性和更好的油腻表面粘附性。
另一个实施方案是水包油型乳剂,其中所述乳剂包含油性小球(oilyglobule),所述油性小球各自提供有层状液晶包衣(lamellar liquid crystalcoating)并分散在水相中,其中每个油性小球包含至少一种具有农业活性的化合物并各自包衣有单层的层或几层的层,所述层包含(1)至少一种非离子性亲脂性表面活性剂、(2)至少一种非离子性亲水性表面活性剂和(3)至少一种离子性表面活性剂,其中所述小球具有小于800纳米的平均粒径。有关该实施方案的进一步信息披露在美国专利公开文本20070027034(公开日期为2007年2月1日且专利申请号为11/495,228)中。为了易于使用,将该实施方案称作“OIWE”。
进一步信息请参阅“Insect Pest Management”2nd Edition by D.Dent,copyright CAB International(2000)。此外,更多详细信息请参阅“Handbook ofPest Control-The Behavior,Life Histroy,and Control of Household Pests”byArnold Mallis,9th Edition,copyright 2004 by GIE Media Inc。
其它制剂组分
一般地,当式1、2和3的分子中披露的化合物在制剂中使用时,所述制剂也可含有其它组分。这些组分包括但不限于(这是非穷举性且非相互排斥性的列举)润湿剂、展布剂(spreader)、粘着剂、渗透剂、缓冲剂、隔离剂(sequestering agent)、防飘移剂(drift reduction agent)、相容剂(compatibilityagent)、消泡剂、清洁剂和乳化剂。接下来描述了几种组分。
润湿剂是这样的物质,当将其加到液体中时,所述物质通过降低液体和液体在其上展布的表面之间的界面张力来增加液体的展布或渗透能力。润湿剂在农用化学制剂中发挥两种主要功能:在处理和制造期间增加粉末在水中的润湿速率从而制备可溶性液体的浓缩物或混悬浓缩物;和在将产品与水在喷雾罐中混合期间降低可润湿粉末的润湿时间并改善水向水可分散颗粒中的渗透。用于可润湿粉末、混悬浓缩物和水可分散颗粒制剂中的润湿剂的实例有月桂基硫酸钠、二辛基磺基琥珀酸钠(sodium dioctyl sulphosuccinate)、烷基酚乙氧基化物和脂肪醇乙氧基化物。
分散剂是这样的物质,其吸附到粒子的表面上并有助于保持粒子的分散状态以及防止粒子重新聚集。将分散剂加到农用化学制剂中以有助于制造期间的分散和混悬且有助于确保粒子在喷雾罐中重新分散到水中。它们广泛用于可润湿粉末、混悬浓缩物和水可分散颗粒中。用作分散剂的表面活性剂具有牢固吸附到粒子表面上的能力并提供对抗粒子重新聚集的荷电屏障或立体屏障。最常用的表面活性剂是阴离子型表面活性剂、非离子型表面活性剂或这两种类型的混合物。对于可润湿粉末制剂而言,最常见的分散剂为木质素磺酸钠(sodium lignosulphonate)。对于混悬浓缩物而言,使用聚电解质(polyelectrolyte)如萘磺酸钠甲醛缩合物(sodium naphthalene sulphonateformaldehyde condensate)来得到非常好的吸附和稳定作用。也使用三苯乙烯基苯酚乙氧基化物磷酸酯(tristyrylphenol ethoxylate phosphate ester)。非离子型表面活性剂(如烷基芳基氧化乙烯缩合物(alkylarylethylene oxidecondensate)和EO-PO嵌段共聚物)有时与阴离子型表面活性剂组合起来作为用于混悬浓缩物的分散剂。近年来,已经开发了分子量非常高的聚合物表面活性剂的新类型作为分散剂。这些分散剂具有非常长的疏水性“骨架”和形成“梳”状表面活性剂的“齿”的很多个氧化乙烯链。这些高分子量聚合物可为混悬浓缩物提供非常好的长期稳定性,这是因为疏水性骨架具有固定到粒子表面上的多个锚点。用于农用化学制剂中的分散剂的实例有木质素磺酸钠、萘磺酸钠甲醛缩合物、三苯乙烯基苯酚乙氧基化物磷酸酯、脂肪醇乙氧基化物、烷基乙氧基化物、EO-PO嵌段共聚物和接枝共聚物。
乳化剂是使一种液相的小滴于另一种液相中的混悬液稳定的物质。在没有乳化剂的情况下,两种液体会分离成两个不可混合的液相。最常用的乳化剂共混物含有具有12个或更多个氧化乙烯单元的烷基酚或脂肪醇以及十二烷基苯磺酸的油溶性钙盐。范围为8至18的亲水亲油平衡(“HLB”)值通常将提供良好的稳定乳剂。乳剂稳定性有时可通过加入少量EO-PO嵌段共聚物表面活性剂来改善。
增溶剂是在浓度超过临界胶束浓度时在水中形成胶束的表面活性剂。然后胶束能够在胶束的疏水部分内溶解或增溶水不溶性物质。通常用于增溶的表面活性剂类型是非离子型表面活性剂:去水山梨糖醇单油酸酯(sorbitanmonooleate)、去水山梨糖醇单油酸酯乙氧基化物(sorbitan monooleateethoxylate)和油酸甲酯(methyl oleate ester)。
表面活性剂有时单独使用,或有时与其它添加剂(如作为喷雾罐混合物辅料的矿物油或植物油)一起使用以改善杀虫剂对靶标的生物性能。用于生物增强(bioenhancement)的表面活性剂类型通常取决于杀虫剂的性质和作用模式。然而,它们通常是非离子型的,如烷基乙氧基化物、线性脂肪醇乙氧基化物、脂肪族胺乙氧基化物。
农业制剂中的载体或稀释剂是加到杀虫剂中以得到所需强度产品的物质。载体通常是具有高吸收能力(absorptive capacity)的物质,而稀释剂通常是具有低吸收能力的物质。载体和稀释剂用在粉剂制剂、可润湿粉末制剂、颗粒制剂和水可分散颗粒制剂中。
有机溶剂主要用在乳油制剂、水包油乳液、混悬乳液(suspoemulsion)和超低体积制剂中以及以较小的程度用在颗粒制剂中。有时使用溶剂的混合物。第一主要组的溶剂有脂肪族石蜡基油(paraffinic oil),如煤油或精炼石蜡。第二主要组(且最常见的)溶剂包括芳香族溶剂,如二甲苯和分子量较高的馏分即C9和C10芳香族溶剂。氯代烃可用作共溶剂以当将制剂乳化到水中时防止杀虫剂的结晶。有时醇类用作共溶剂以增加溶剂能力(solvent power)。其它溶剂可包括植物油、籽油和植物油的酯和籽油的酯。
增稠剂或胶凝剂主要用在混悬浓缩物制剂、乳剂制剂和混悬乳剂制剂中以改变液体的流变学或流动性并防止经分散的颗粒或小滴发生分离或沉降。增稠剂、胶凝剂和抗沉降剂通常分为两类即水不溶性粒子和水溶性聚合物。使用粘土和硅石来产生混悬浓缩物制剂是可能的。这些类型的物质的实例包括但不限于蒙脱石、膨润土、硅酸镁铝和活性白土(attapulgite)。水溶性多糖已用作增稠-胶凝剂多年。最常用的多糖的类型为种子或海藻的天然提取物或为纤维素的合成衍生物。这些类型的物质的实例包括但不限于瓜尔胶、豆角胶(locust bean gum)、角叉菜胶(carrageenam)、藻酸盐、甲基纤维素、羧甲基纤维素钠(SCMC)、羟乙基纤维素(HEC)。其它类型的抗沉降剂基于变性淀粉、聚丙烯酸酯、聚乙烯醇和聚氧化乙烯。另一种良好的抗沉降剂为黄原胶。
微生物引起所配制产品的酸败(spoilage)。因此防腐剂用于消除或减小微生物的作用。这些试剂的实例包括但不限于丙酸及其钠盐、山梨酸及其钠盐或钾盐、苯甲酸及其钠盐、对羟基苯甲酸钠盐、对羟基苯甲酸甲酯和1,2-苯并异噻唑啉-3-酮(BIT)。
表面活性剂的存在通常导致水基制剂当生产和通过喷雾罐施用时在混合操作期间起泡。为了减小起泡倾向,通常在生产阶段或在装入瓶中前加入消泡剂。一般而言,有两种类型的消泡剂即硅氧烷和非硅氧烷。硅氧烷通常为聚二甲基硅氧烷的水性乳剂,而非硅氧烷消泡剂为水不溶性油(如辛醇和壬醇)和二氧化硅。在这两种情况下,消泡剂的功能都是从空气-水界面中置换表面活性剂。
“绿色”试剂(例如助剂、表面活性剂、溶剂)可减少作物保护制剂的整体环境足迹。绿色试剂为生物可降解的且一般衍生自天然和/或可持续资源例如植物和动物资源。具体的实例为:植物油、籽油及它们的酯,也包括烷氧基化烷基多葡萄糖苷。
进一步信息请参阅“Chemistry and Technology of AgrochemicalFormulations”edited by D.A.Knowles,copyright 1998 by Kluwer AcademicPublishers。还请参阅“Insecticides in Agriculture and Environment-Retrospectsand Prospects”by A.S.Perry,I.Yamamoto,I.Ishaaya,and R.Perry,copyright1998 by Springer-Verlag。
害虫
大体上,式1、2和3的分子可用于防治害虫例如甲虫(beetle)、蠷螋(earwig)、蟑螂(cockroach)、苍蝇(flies)、蚜虫(aphid)、蚧(scale)、粉虱(whiteflies)、叶蝉(leafhopper)、蚂蚁(ant)、黄蜂(wasp)、白蚁(termite)、蛾(moth)、蝶(butterfly)、虱(lice)、蚱蜢(grasshopper)、蝗虫(locust)、蟋蟀(cricket)、蚤(flea)、蓟马(thrip)、蠹虫(bristletail)、螨虫(mite)、蜱(tick)、线虫(nematode)和综合虫(symphylan)。
在另一个实施方案中,式1、2和3的分子可用于防治以下门(phyla)害虫:线虫门(Nematoda)和/或节肢动物门(Arthropoda)中的害虫。
在另一个实施方案中,式1、2和3的分子可用于防治以下亚门(subphyla)害虫:螯肢亚门(Chelicerata)、多足亚门(Myriapoda)和/或六足亚门(Hexapoda)中的害虫。
在另一个实施方案中,式1、2和3的分子可用于防治以下纲害虫:蛛形纲(Arachnida)、综合纲(Symphyla)和/或昆虫纲(Insecta)中的害虫。
在另一个实施方案中,在其文本中公开的本发明可用于防治虱目(Anoplura)害虫。非穷尽性列举的具体属包括但不限于吸血虱属(Haematopinus spp.)、甲胁虱属(hoplopleura spp.)、颚虱属(Linognathus spp.),虱子属(Pediculus spp.)和鳞虱属(Polyplax spp)。非穷举性列举的具体种包括但不限于驴血虱(Haematopinus asini),猪血虱(Haematopinus suis),棘颚虱(Linognathus setosus),绵羊颚虱(Linognathus ovillus),人头虱(Pediculushumanus capitis),人体虱(Pediculus humanus humanus)和阴虱(Pthirus pubis)。
在另一个实施方案中,在其文本中公开的本发明可用于防治吸允虱目(Order Coleoptera)害虫。非穷举性列举的具体属包括但不限于豆象属(Acanthoscelides spp.)、叩头虫属(Agriotes spp.)、花象属(Anthonomus spp.)、梨象属(Apion spp.)、金龟属(Apogonia spp.)、守瓜属(Aulacophora spp.)、豆象属(Bruchus spp.)、天牛属(Cerosterna spp)、叶甲属(Cerotoma spp.)、龟象属(Ceutorhynchus spp.)、跳甲属(Chaetocnema spp.)、肖叶甲属(Colaspis spp.)、Ctenicera spp.、象虫属(Curculio spp.)、圆头犀金龟属(Cyclocephala spp.)、叶甲属(Diabrotica spp.)、叶象属(Hypera spp.)、齿小蠹属(Ips spp.)、粉蠹属(Lyctusspp.)、Megascelis spp.、Meligethes spp.、鸟喙象属(Otiorhynchus spp.)、玫瑰短喙象属(Pantomorus spp.)、食叶鳃金龟属(Phyllophaga spp.)、黄条跳甲属(Phyllotreta spp.)、根鳃金龟属(Rhizotrogus spp.)、Rhynchites spp.、隐颏象属(Rhynchophorus spp.)、小蠹属(Scolytus spp.)、Shenophorus spp.、米象属(Sitophilus spp.)和拟谷盗属(Tribolium spp.)。非穷举性列举的具体种包括但不限于菜豆象(Acanthoscelides obtectus)、白蜡窄吉丁(Agrilus planipennis)、光肩星天牛(Anoplophora glabripennis)、棉铃象(Anthonomus grandis)、黑绒金龟(Ataenius spretulus)、甜菜隐食甲(Atomaria linearis)、甜菜象(Bothynoderespunctiventris)、豌豆象(Bruchus pisorum)、四纹豆象(Callosobruchusmaculatus)、酱曲露尾甲(Carpophilus hemipterus)、甜菜龟甲(Cassida vittata)、豆叶甲(Cerotoma trifurcate)、白菜籽龟象(Ceutorhynchus assimilis)、芫菁龟象(Ceutorhynchus napi)、Conoderus scalaris、Conoderus stigmosus、李象(Conotrachelus nenuphar)、绿金龟(Cotinis nitida)、石刁柏负泥虫(Criocerisasparagi)、锈赤扁谷盗(Cryptolestes ferrugineus)、长角扁谷盗(Cryptolestespusillus)、土耳其扁谷盗(Cryptolestes turcicus)、密点细枝象(Cylindrocopturusadspersus)、芒果剪叶象(Deporaus marginatus)、火腿皮蠹(Dermestes lardarius)、白腹皮蠹(Dermestes maculatus)、墨西哥豆瓢虫(Epilachna varivestis)、蛀茎象甲(Faustinus cubae)、苍白根颈象(Hylobius pales)、紫苜蓿叶象(Hyperapostica)、咖啡果小蠹(Hypothenemus hampei)、烟草甲(Lasioderma serricorne)、马铃薯甲虫(Leptinotarsa decemlineata)、Liogenys fuscus、Liogenys suturalis、稻水象甲(Lissorhoptrus oryzophilus)、Maecolaspis joliveti、玉米叩甲(Melanotus communis)、油菜花露尾甲(Meligethes aeneus)、五月金龟子(Melolontha melolontha)、Oberea brevis、线性筒天牛(Oberea linearis)、椰蛀犀金龟(Oryctes rhinoceros)、贸易锯谷盗(Oryzaephilus mercator)、锯谷盗(Oryzaephilus surinamensis)、黑角负泥虫(Oulema melanopus)、水稻负泥虫(Oulema oryzae)、Phyllophaga cuyabana、日本弧丽金龟(Popillia japonica)、大谷蠹(Prostephanus truncates)、谷蠧(Rhyzopertha dominica)、豌豆叶象(Sitonalineatus)、谷象(Sitophilus granarius)、米象(Sitophilus oryzae)、玉米象(Sitophiluszeamais)、药材甲(Stegobium paniceum)、赤拟谷盗(Tribolium castaneum)、杂拟谷盗(Tribolium confusum)、花斑皮蠹(Trogoderma variabile)和玉米距步甲(Zabrus tenebrioides)。
在另一个实施方案中,式1、2和3的分子可用于防治革翅目(OrderDermaptera)害虫。
在另一个实施方案中,式1、2和3的分子可用于防治蜚蠊目(OrderBlattaria)害虫。非穷尽性列举的具体种包括但不限于德国小蠊(Blattellagermanica)、东方蜚蠊(Blatta orientalis)、宾夕法尼亚木蠊(Parcoblattapennsylvanica)、美洲大蠊(Periplaneta americana)、澳洲大蠊(Periplanetaaustralasiae)、褐色大蠊(Periplaneta brunnea)、烟色大蠊(Periplaneta fuliginosa)、蔗绿蜚蠊(Pycnoscelus surinamensis)和长须蜚蠊(Supella longipalpa)。
在另一个实施方案中,式1、2和3的分子可用于防治双翅目(OrderDiptera)害虫。非穷尽性列举的具体属包括但不限于伊蚊属(Aedes spp.)、潜蝇属(Agromyza spp.)、按实蝇属(Anastrepha spp.)、疟蚊属(Anopheles spp.)、果实蝇属(Bactrocera spp.)、小条实蝇属(Ceratitis spp.)、斑虻属(Chrysops spp.)、锥蝇属(Cochliomyia spp.)、瘿蚊属(Contarinia spp.)、库蚊属(Culex spp.)、叶瘿蚊属(Dasineura spp.)、地种蝇属(Delia spp.)、果蝇属(Drosophila spp.)、厕蝇属(Fannia spp.)、黑蝇属(Hylemyia spp.)、斑潜蝇属(Liriomyza spp.)、蝇属(Musca spp.)、种蝇属(Phorbia spp.)、牛虻属(Tabanus spp.)和大蚊属(Tipulaspp.)。非穷尽性列举的具体种包括但不限于紫苜蓿潜蝇(Agromyza frontella)、加勒比按实蝇(Anastrepha suspensa)、墨西哥实蝇(Anastrepha ludens)、西印度实蝇(Anastrepha obliqa)、瓜实蝇(Bactrocera cucurbitae)、桔小实蝇(Bactroceradorsalis)、入侵实蝇(Bactrocera invadens)、桃实蝇(Bactrocera zonata)、地中海小条实蝇(Ceratitis capitata)、油菜叶瘿蚊(Dasineura brassicae)、灰地种蝇(Deliaplatura)、黄腹厕蝇(Fannia canicularis)、灰腹厕蝇(Fannia scalaris)、肠胃蝇(Gasterophilus intestinalis)、Gracillia perseae、扰血蝇(Haematobia irritans)、纹皮蝇(Hypoderma lineatum)、甘蓝斑潜蝇(Liriomyza brassicae)、绵羊虱蝇(Melophagus ovinus)、秋家蝇(Musca autumnalis)、家蝇(Musca domestica)、羊狂蝇(Oestrus ovis)、欧洲麦秆蝇(Oscinella frit)、甜菜泉蝇(Pegomya betae)、胡萝卜茎蝇(Psila rosae)、樱桃果蝇(Rhagoletis cerasi)、苹果实蝇(Rhagoletispomonella)、越桔绕实蝇(Rhagoletis mendax)、麦红吸浆虫(Sitodiplosismosellana)和厩螫蝇(Stomoxys calcitrans)。
在另一个实施方案中,式1、2和3的分子可用于防治半翅目(OrderHemiptera)害虫。非穷尽性列举的具体属包括但不限于球蚜属(Adelges spp.)、轮盾蚧属(Aulacaspis spp.)、Aphrophora spp.、蚜虫属(Aphis spp.)、粉虱属(Bemisia spp.)、蜡蚧属(Ceroplastes spp.)、雪盾蚧属(Chionaspis spp.)、圆盾蚧属(Chrysomphalus spp.)、软蜡蚧属(Coccus spp.)、绿小叶蝉属(Empoasca spp.)、蛎盾蚧属(Lepidosaphes spp.)、蝽属(Lagynotomus spp.)、草盲蝽属(Lygus spp.)、长管蚜属(Macrosiphum spp.)、黑尾叶蝉属(Nephotettix spp.)、绿蝽属(Nezaraspp.)、沫蝉属(Philaenus spp.)、植盲蝽属(Phytocoris spp.)、Piezodorus spp.、臀纹粉蚧属(Planococcus spp.)、粉蚧属(Pseudococcus spp.)、溢管蚜属(Rhopalosiphum spp.)、珠蜡蚧属(Saissetia spp.)、彩斑蚜属(Therioaphis spp.)、龟蚧属(Toumeyella spp.)、声蚜属(Toxoptera spp.)、结翅粉虱属(Trialeurodesspp.)、锥蝽属(Triatoma spp.)和尖盾蚧属(Unaspis spp.)。非穷尽性列举的具体种包括但不限于拟绿蝽(Acrosternum hilare)、豌豆蚜(Acyrthosiphon pisum)、甘蓝粉虱(Aleyrodes proletella)、螺旋粉虱(Aleurodicus dispersus)、丝绒粉虱(Aleurothrixus floccosus)、叶蝉(Amrasca biguttula biguttula)、红圆蚧(Aonidiellaaurantii)、棉蚜(Aphis gossypii)、大豆芽(Aphis glycines)、苹果蚜(Aphis pomi)、马铃薯长须蚜(Aulacorthum solani)、银叶粉虱(Bemisia argentifolii)、甘薯粉虱(Bemisia tabaci)、美洲谷长蝽(Blissus leucopterus)、天门冬小管蚜(Brachycorynella asparagi)、Brevennia rehi、甘蓝蚜(Brevicoryne brassicae)、马铃薯俊盲蝽(Calocoris norvegicus)、红蜡蚧(Ceroplastes rubens)、热带臭虫(Cimex hemipterus)、臭虫(Cimex lectularius)、Dagbertus fasciatus、Dichelopsfurcatus、麦双尾蚜(Diuraphis noxia)、桔木虱(Diaphorina citri)、车前圆尾蚜(Dysaphis plantaginea)、美棉红蝽(Dysdercus suturellus)、Edessa meditabunda、苹果棉蚜(Eriosoma lanigerum)、欧扁盾蝽(Eurygaster maura)、Euschistus heros、褐美洲蝽(Euschistus servus)、安氏角盲蝽(Helopeltis antonii)、茶角盲蝽(Helopeltis theivora)、吹棉蚧(Icerya purchasi)、芒果黄线叶蝉(Idioscopusnitidulus)、灰飞虱(Laodelphax striatellus)、大稻缘蝽(Leptocorisa oratorius)、异稻缘蝽(Leptocorisa varicornis)、豆荚草盲蝽(Lygus hesperus)、木槿曼粉蚧(Maconellicoccus hirsutus)、大戟长管蚜(Macrosiphum euphorbiae)、麦长管蚜(Macrosiphum granarium)、蔷薇长管蚜(Macrosiphum rosae)、Macrostelesquadrilineatus、Mahanarva frimbiolata、麦无网蚜(Metopolophium dirhodum)、Mictis longicornis、桃蚜(Myzus persicae)、黑尾叶蝉(Nephotettix cinctipes)、Neurocolpus longirostris、稻绿蝽(Nezara viridula)、褐飞虱(Nilaparvata lugens)、糠片盾蚧(Parlatoria pergandii)、黑片盾蚧(Parlatoria ziziphi)、玉米花翅飞虱(Peregrinus maidis)、葡萄根瘤蚜(Phylloxera vitifoliae)、去杉球蚧(Physokermespiceae)、Phytocoris californicus、Phytocoris relativus、Piezodorus guildinii、四蚊盲蝽(Poecilocapsus lineatus)、Psallus vaccinicola、Pseudacysta perseae、菠萝洁粉蚧(Pseudococcus brevipes)、梨园盾蚧(Quadraspidiotus perniciosus)、玉米蚜(Rhopalosiphum maidis)、禾谷溢管蚜(Rhopalosiphum padi)、榄珠蜡蚧(Saissetia oleae)、Scaptocoris castanea、麦二叉蚜(Schizaphis graminum)、麦长管蚜(Sitobion avenae)、白背飞虱(Sogatella furcifera)、温室粉虱(Trialeurodesvaporariorum)、结翅粉虱(Trialeurodes abutiloneus)、矢尖蚧(Unaspis yanonensis)和Zulia entrerriana。
在另一个实施方案中,式1、2和3的分子可用于防治膜翅目(OrderHymenoptera)害虫。非穷尽性列举的具体属包括但不限于切叶蚁属(Acromyrmex spp.)、叶蚁属(Atta spp.)、黑蚁属(Camponotus spp.)、松叶蜂属(Diprion spp.)、蚁属(Formica spp.)、厨蚁属(Monomorium spp.)新松叶蜂属(Neodiprion spp.)、收获蚁属(Pogonomyrmex spp.)、马蜂属(Polistes spp.)、火蚁属(Solenopsis spp.)、黄胡蜂属(Vespula spp.)和木蜂属(Xylocopa spp.)。非穷尽性列举的具体种包括但不限于新疆菜叶蜂(Athalia rosae)、Atta texana、阿根廷蚁(Iridomyrmex humilis)、小家蚁(Monomoriumminimum)、厨蚁(Monomorium pharaonis)、外来红火蚁(Solenopsis invicta)、热带红火蚁(Solenopsis geminate)、盗窃火蚁(Solenopsis molesta)、黑火蚁(Solenopsisrichtery)、Solenopsis xyloni和酸臭蚁(Tapinoma sessile)。
在另一个实施方案中,式1、2和3的分子可用于防治等翅目(OrderIsoptera)害虫。非穷尽性列举的具体属包括但不限于乳白蚁属(Coptotermesspp.)、角白蚁属(Cornitermes spp.)、砂白蚁属(Cryptotermes spp.)、异白蚁属(Heterotermes spp.)、木白蚁属(Kalotermes spp.)、楹白蚁属(Incisitermes spp.)、大白蚁属(Macrotermes spp.)、缘木白蚁属(Marginitermes spp.)、锯白蚁属(Microcerotermes spp.)、原角白蚁属(Procornitermes spp.)、散白蚁属(Reticulitermes spp.)、长鼻白蚁属(Schedorhinotermes spp.)和古白蚁属(Zootermopsis spp.)。非穷尽性列举的具体种包括但不限于曲颚白蚁(Coptotermes curvignathus)、新西兰乳白蚁(Coptotermes frenchii)、台湾乳白蚁(Coptotermes formosanus)、金黄异白蚁(Heterotermes aureus)、稻麦小白蚁(Microtermes obesi)、Reticulitermes banyulensis、Reticulitermes grassei、黄肢散白蚁(Reticulitermes flavipes)、美小黄散白蚁(Reticulitermes hageni)、西方散白蚁(Reticulitermes hesperus)、桑特散白蚁(Reticulitermes santonensis)、栖北散白蚁(Reticulitermes speratus)、美黑胫散白蚁(Reticulitermes tibialis)和美小黑散白蚁(Reticulitermes virginicus)。
在另一个实施方案中,式1、2和3的分子可用于防治鳞翅目(OrderLepidoptera)害虫。非穷尽性列举的具体属包括但不限于褐带卷蛾属(Adoxophyes spp.)、地虎属(Agrotis spp.)、卷蛾属(Argyrotaenia spp.)、Cacoeciaspp.、细蛾属(Caloptilia spp.)、禾草螟属(Chilo spp.)、夜蛾属(Chrysodeixis spp.)、豆粉蝶属(Colias spp.)、草螟属(Crambus spp.)、绢野螟属(Diaphania spp.)、螟属(Diatraea spp.)、金刚钻属(Earias spp.)、粉斑螟属(Ephestia spp.)、Epimecisspp.、Feltia spp.、角剑夜蛾属(Gortyna spp.)、青虫属(Helicoverpa spp.)、实夜蛾属(Heliothis spp.)、Indarbela spp.、细蛾属(Lithocolletis spp.)、Loxagrotis spp.、天幕毛虫属(Malacosoma spp.)、Peridroma spp.、细蛾属(Phyllonorycter spp.)、Pseudaletia spp.、蛀茎夜蛾属(Sesamia spp.)、灰翅夜蛾属(Spodoptera spp.)、兴透翅蛾属(Synanthedon spp.)和巢蛾属(Yponomeuta spp.)。非穷尽性列举的具体种包括但不限于飞扬阿夜蛾(Achaea janata)、棉褐带卷蛾(Adoxophyesorana)、小地蚕(Agrotis ipsilon)、棉叶波纹夜蛾(Alabama argillacea)、Amorbiacuneana、Amyelois transitella、Anacamptodes defectaria、桃条麦蛾(Anarsialineatella)、黄麻桥夜蛾(Anomis sabulifera)、黎豆夜蛾(Anticarsia gemmatalis)、果树卷叶蛾(Archips argyrospila)、玫瑰卷叶蛾(Archips rosana)、桔带卷蛾(Argyrotaenia citrana)、Autographa gamma、Bonagota cranaodes、籼弄蝶(Borbocinnara)、Bucculatrix thurberiella、Capua reticulana、桃蛀果蛾(Carposinaniponensis)、芒果横线尾夜蛾(Chlumetia transversa)、玫瑰色卷蛾(Choristoneurarosaceana)、稻纵卷叶野螟(Cnaphalocrocis medinalis)、荔枝爻纹细蛾(Conopomorpha cramerella)、芳香木蠹蛾(Cossus cossus)、Cydia caryana、李小食心虫(Cydia funebrana)、梨小食心虫(Cydia molesta)、Cydia nigricana、苹果小卷蛾(Cydia pomonella)、Darna diducta、小蔗螟(Diatraea saccharalis)、西南玉米杆草螟(Diatraea grandiosella)、埃及金刚钻(Earias insulana)、翠纹金刚钻(Earias vittella)、Ecdytolopha aurantianum、南美玉米苗斑螟(Elasmopalpuslignosellus)、粉斑螟(Ephestia cautella)、烟草粉斑螟(Ephestia elutella)、地中海粉螟(Ephestia kuehniella)、夜小卷蛾(Epinotia aporema)、Epiphyaspostvittana、香蕉弄蝶(Erionota thrax)、女贞细卷蛾(Eupoecilia ambiguella)、Euxoa auxiliaris、东方蛀果蛾(Grapholita molesta)、三纹螟蛾(Hedyleptaindicata)、棉铃虫(Helicoverpa armigera)、谷实夜蛾(Helicoverpa zea)、烟芽夜蛾(Heliothis virescens)、菜心野螟(Hellula undalis)、番茄蠹蛾(Keiferialycopersicella)、茄白翅野螟(Leucinodes orbonalis)、咖啡潜叶蛾(Perileucopteracoffeella)、旋纹潜蛾(Leucoptera malifoliella)、葡萄小卷叶蛾(Lobesia botrana)、Loxagrotis albicosta、舞毒蛾(Lymantria dispar)、桃潜蛾(Lyonetia clerkella)、Mahasena corbetti、甘蓝夜蛾(Mamestra brassicae)、豆荚野螟(Marucatestulalis)、袋蛾(Metisa plana)、Mythimna unipuncta、Neoleucinodes elegantalis、三点水螟(Nymphula depunctalis)、冬尺蠖(Operophtera brumata)、玉米螟(Ostrinia nubilalis)、Oxydia vesulia、Pandemis cerasana、苹褐卷蛾(Pandemisheparana)、非洲达摩凤蝶(Papilio demodocus)、红铃麦蛾(Pectinophoragossypiella)、杂色地老虎(Peridroma saucia)、咖啡潜叶蛾(Perileucopteracoffeella)、马铃薯块茎蛾(Phthorimaea operculella)、柑桔叶潜蛾(Phyllocnistiscitrella)、菜粉蝶(Pieris rapae)、苜蓿绿夜蛾(Plathypena scabra)、印度谷斑蛾(Plodia interpunctella)、菜蛾(Plutella xylostella)、Polychrosis viteana、桔果巢蛾(Prays endocarpa)、油橄榄巢蛾(Prays oleae)、Pseudaletia unipuncta、大豆夜蛾(Pseudoplusia includens)、尺蠖(Rachiplusia nu)、三化螟(Scirpophagaincertulas)、稻蛀茎夜蛾(Sesamia inferens)、粉茎螟(Sesamia nonagrioides)、铜斑褐刺蛾(Setora nitens)、麦蛾(Sitotroga cerealella)、葡萄长须卷蛾(Sparganothis pilleriana)、甜菜夜蛾(Spodoptera exigua)、草地贪夜蛾(Spodoptera frugiperda)、南部灰翅夜蛾(Spodoptera eridania)、Thecla basilides、衣蛾(Tineola bisselliella)、粉斑夜蛾(Trichoplusia ni)、番茄斑潜蝇(Tutaabsoluta)、咖啡豹蠹蛾(Zeuzera coffeae)和梨豹蠹蛾(Zeuzera pyrina)。
在另一个实施方案中,式1、2和3的分子可用于防治食毛目(OrderMallophaga)害虫。非穷尽性列举的具体属包括但不限于毛虱属(Anaticolaspp.)、Bovicola spp.、Chelopistes spp.、Goniodes spp.、Menacanthus spp.和Trichodectes spp.。非穷尽性列举的具体种包括但不限于牛毛虱(Bovicolabovis)、山羊虱(Bovicola caprae)、绵羊虱(Bovicola ovis)、Chelopistesmeleagridis、鸡角羽虱(Goniodes dissimilis)、大角羽虱(Goniodes gigas)、火鸡短角鸟虱(Menacanthus stramineus)、鸡羽虱(Menopon gallinea)和犬啮毛虱(Trichodectes canis)。
在另一个实施方案中,式1、2和3的分子可用于防治直翅目(OrderOrthoptera)害虫。非穷尽性列举的具体属包括但不限于蚱蜢属(Melanoplusspp.)和Pterophylla spp.。非穷尽性列举的具体种包括但不限于黑斑阿纳螽(Anabrus simplex)、非洲蝼蛄(Gryllotalpa africana)、Gryllotalpa australis、Gryllotalpa brachyptera、Gryllotalpa hexadactyla、东亚飞蝗(Locustamigratoria)、纲翅细刺螽(Microcentrum retinerve)、沙漠蝗(Schistocerca gregaria)和叉尾斯奎螽(Scudderia furcata)。
在另一个实施方案中,式1、2和3的分子可用于防治蚤目(OrderSiphonaptera)害虫。非穷尽性列举的具体种包括但不限于鸡蚤(Ceratophyllusgallinae)、Ceratophyllus niger、犬栉头蚤(Ctenocephalides canis)、猫栉头蚤(Ctenocephalides felis)和人蚤(Pulex irritans)。
在另一个实施方案中,式1、2和3的分子可用于防治缨翅目(OrderThysanoptera)害虫。非穷尽性列举的具体属包括但不限于巢蓟马属(Caliothrips spp.)、花蓟马属(Frankliniella spp.0、硬蓟马属(Scirtothrips spp.)和蓟马属(Thrips spp.)。非穷尽性列举的具体种包括但不限于烟褐蓟马(Frankliniella fusca)、苜蓿花蓟马(Frankliniella occidentalis)、Frankliniellaschultzei、Frankliniella williamsi、温室蓟马(Heliothrips haemorrhoidalis)、腹钩针蓟马(Rhipiphorothrips cruentatus)、桔硬蓟马(Scirtothrips citri)、茶黄蓟马(Scirtothrips dorsalis)和Taeniothrips rhopalantennalis、黄胸蓟马(Thripshawaiiensis)、茼蒿蓟马(Thrips nigropilosus)、东方蓟马(Thrips orientalis)、烟蓟马(Thrips tabaci)。
在另一个实施方案中,式1、2和3的分子可用于防治缨尾目(OrderThysanura)害虫。非穷尽性列举的具体属包括但不限于衣鱼属(Lepisma spp.)和小灶衣鱼属(Thermobia spp.)。
在另一个实施方案中,式1、2和3的分子可用于防治螨目(Order Acarina)害虫。非穷尽性列举的具体属包括但不限于粉螨属(Acarus spp.)、刺皮瘿螨属(Aculops spp.)、牛蜱属(Boophilus spp.)、脂螨属(Demodex spp.)、革蜱属(Dermacentor spp.)、上瘿螨属(Epitrimerus spp.)、瘿螨属(Eriophyes spp.)、硬蜱属(Ixodes spp.)、小爪螨属(Oligonychus spp.)、全爪螨属(Panonychus spp.)、根螨属(Rhizoglyphus spp.)和叶螨属(Tetranychus spp.)。非穷尽性列举的具体种包括但不限于Acarapis woodi、粗脚粉螨(Acarus siro)、Aceria mangiferae、番茄刺皮瘿螨(Aculops lycopersici)、桔刺皮瘿螨(Aculus pelekassi)、斯氏刺瘿螨(Aculus schlechtendali)、Amblyomma americanum、卵形短须螨(Brevipalpusobovatus)、紫红短须螨(Brevipalpus phoenicis)、美洲狗蜱(Dermacentorvariabilis)、屋尘螨(Dermatophagoides pteronyssinus)、鹅耳枥始叶螨(Eotetranychus carpini)、猫耳螨(Notoedres cati)、咖啡小爪螨(Oligonychuscoffeae)、冬青小爪螨(Oligonychus ilicis)、柑桔全爪螨(Panonychus citri)、苹果全爪螨(Panonychus ulmi)、桔皱叶刺瘿螨(Phyllocoptruta oleivora)、食跗线螨属(Polyphagotarsonemus latus)、血红扇头蜱(Rhipicephalus sanguineus)、疥螨(Sarcoptes scabiei)、鳄梨顶冠瘿螨(Tegolophus perseaflorae)、二点叶螨(Tetranychus urticae)和狄氏瓦螨(Varroa destructor)。
在另一个实施方案中,式1、2和3的分子可用于防治综合目(OrderSymphyla)害虫。非穷尽性列举的具体种包括但不限于白松虫(Scutigerellaimmaculata)。
在另一个实施方案中,式1、2和3的分子可用于防治线虫门(PhylumNematoda)害虫。非穷尽性列举的具体属包括但不限于滑刃线虫属(Aphelenchoides spp.)、刺线虫属(Belonolaimus spp.)、小环线虫属(Criconemella spp.)、茎线虫属(Ditylenchus spp.)、棘皮线虫属(Heteroderaspp.)、潜根线虫属(Hirschmanniella spp.)、纽带线虫属(Hoplolaimus spp.)、根结线虫属(Meloidogyne spp.)、短体线虫属(Pratylenchus spp.)和穿孔线虫属(Radopholus spp.)。非穷尽性列举的具体种包括但不限于犬恶丝虫(Dirofilariaimmitis)、玉米胞囊线虫(Heterodera zeae)、南方根结线虫(Meloidogyneincognita)、Meloidogyne javanica、旋盘尾丝虫(Onchocerca volvulus)、香蕉穿孔线虫(Radopholus similes)和香蕉肾状线虫(Rotylenchus reniformis)。
更多信息参考“Handbook of Pest Control-The Behavior,Life History,andControl of Household Pests”by Arnold Mallis,9th Edition,copyright 2004 byGIE Media Inc。
应用
通常使用约0.01克/公顷至约5000克/公顷量的式1、2和3的分子来提供防治。通常优选的量为约0.1克/公顷至约500克/公顷,通常更优选的量为约1克/公顷至约50克/公顷。
式1、2和3的分子施用到的位置可以是害虫占据(或可能被害虫占据或被害虫爬过)的任何位置,例如:作物、树木、水果、谷物、饲料类植物、藤本植物、草地和观赏植物的生长位置;家畜的居住地;建筑物的内或外表面(例如谷物贮存地)、建筑物中使用的建筑材料(例如浸渍木)和建筑物周围的土壤。使用式1、2和3的分子的具体作物位置包括苹果、玉米、向日葵、棉花、大豆、芸苔、小麦、稻谷、高粱、大麦、燕麦、马铃薯、柑橘、苜蓿、莴苣、草莓、番茄、胡椒、十字花科植物、梨、烟草、杏、甜菜、豆类和其它有价值作物的生长地或其种子的待种植位置。还有利的是当栽培各种植物时将硫酸铝与式1、2和3的分子一起使用。
防治害虫通常是指区域中的害虫数、害虫活性或两者都得到减少。当在以下情况下时可发生该防治:从区域驱逐害虫总体;使区域中或区域周围的害虫丧失能力;或区域中或区域周围的害虫整体或部分被灭绝。当然,可发生这些结果的组合。通常,害虫数、害虫活性或两者都被令人满意地减少多于50%,优选减少多于90%。大体上,所述区域不在人类体内或人体上;因此,所述区域通常为非人类区域。
式1、2和3的分子可用在同时或顺序施用的混合物中,所述化合物单独或与其它化合物一起增强植物活力(例如长出更好的根系、更好地经受应激生长条件)。所述其它化合物为例如调节植物乙烯受体的化合物,最著名的为1-甲基环丙烯(也称作1-MCP)。
可将式1、2和3的分子施用到植物的叶子和果实部分以防治害虫。所述分子与所述害虫直接接触或当所述害虫吃食含有所述杀虫剂的叶子、果实或吸食树液(extracting sap)时会摄入所述杀虫剂。也可将式1、2和3的分子施用到土壤且当以该方式施用时,可防治以根和茎为食的害虫。所述根可吸收分子,将其向上运送到植物的叶部分,从而防治地上咀嚼和以树液为食的害虫。
一般而言,就诱饵而言,将诱饵置于例如白蚁可与诱饵发生接触和/或白蚁可被吸引到所述诱饵的场所。也可将诱饵施用到例如蚂蚁、白蚁、蟑螂和苍蝇可与诱饵发生接触和/或蚂蚁、白蚁、蟑螂和苍蝇可被吸引到所述诱饵的场所的建筑物表面(水平表面、垂直表面或倾斜表面)。诱饵可包含式1、2和3的分子。
可将式1、2和3的分子包封在囊的内部或可将其放置在囊的表面上。所述囊的大小可在纳米级尺寸(直径为约100-900纳米)至微米级尺寸(直径为约10-900微米)范围内变化。
由于某些害虫的卵具有抗一些杀虫剂的独特能力,因此可能需要重复施用式1、2和3的分子以防治新出现的幼虫。
杀虫剂在植物中的系统移动可用于通过将式1、2和3的分子施用到所述植物的不同部位而对所述植物的另一个部位进行害虫防治。例如,防治食叶昆虫可以通过滴注灌溉施用或沟槽施用、通过用例如种植前或种植后土壤浇灌处理土壤、或通过种植前处理植物种子来防治。
种子处理可以应用于所有类型的种子,包括可生长成遗传修饰为表达特定属性的植物的那些种子。代表性的实例包括表达对无脊椎害虫有毒的蛋白质或其它杀虫毒素(例如苏芸金杆菌(Bacillus thuringiensis))的那些种子、表达除草剂抵抗性的那些种子(例如“Roundup Ready”种子)、或具有“叠加”外源基因的那些种子(所述“叠加”外源基因表达杀虫毒素、除草剂抵抗性、营养提高特性、抗旱或任何其它有益特性)。此外,用式1、2和3的分子进行的所述种子处理可进一步增强植物更好经受应激生长条件的能力。这导致更健康更旺盛的植物,由此可在收获时得到更高的产量。一般而言,每100,000粒种子约1克至约500克式1、2和3的分子预期提高良好益处,每100,000粒种子约10克至约100克量的式1、2和3的分子提供更好益处,每100,000粒种子25克至约75克式1、2和3的分子提供甚至更高的益处。
应该显而易见的是,式1、2和3的分子可用在遗传修饰为表达特定属性(specialized traits)例如苏芸金杆菌或其它杀虫毒素的植物上或用在所述植物中或用在所述植物周围,或用在表达除草剂抵抗性的那些植物上或用在所述植物中或用在所述植物周围,或用在具有“叠加”外源基因(所述“叠加”外源基因表达杀虫毒素、除草剂抵抗性、营养提高特性或任何其它有益特性)的植物上或用在所述植物中或用在所述植物周围。
式1、2和3的分子可用于在兽医学方面或在非人类动物饲养领域防治内寄生物(endoparasite)和外寄生物(ectoparasite)。式I的化合物按已知的方式来施用,如以例如片剂、胶囊剂、饮用剂、颗粒剂的形式来口服给药,以例如浸蘸、喷雾、倾倒、点样和撒粉的形式来进行皮肤施用,以及以例如注射剂的形式来进行肠胃外给药。
式1、2和3的分子也可有利地用于家畜(例如牛、羊、猪、鸡和鹅)饲养。它们也可有利地用在宠物(例如马、狗和猫)中。所防治的具体害虫是蚤和蜱和烦扰所述动物的蛰蝇。将合适的制剂与饮用水或饲料一起口服给予所述动物。合适的剂量和制剂取决于物种。
式1、2和3的分子也可用于在上面所列动物中防治寄生虫,特别是肠部寄生虫。
式1、2和3的分子也可用在用于人体保健的治疗方法中。所述方法包括但不限于以诸如片剂、胶囊剂、饮用剂、颗粒剂的形式口服给药和通过皮肤施用。
世界范围内的害虫已迁移到新的环境(对于所述害虫来说),之后在所述新的环境中变成新的入侵物种。式1、2和3的分子也可用在所述新的入侵物种上,从而在所述新的环境中对它们进行防治。
式1、2和3的分子也可用在植物例如作物的生长位置(例如种植前、种植中、收获前)中且所述位置存在可商业上破坏所述植物的低水平(甚至无实际存在)害虫。在所述位置使用所述分子是为了有益于在所述位置生长的所述植物。所述益处可包括但不限于提高植物的健康、提高植物的收率(例如增加有价值成分的生物量和/或增加有价值成分的含量)、增强植物活力(例如促进植物生长和/或使叶子更绿)、提高植物质量(例如提高一些成分的含量或组成)和增强所述植物对非生物应激和/或生物应激的耐受。
在杀虫剂可被使用或商业销售前,所述杀虫剂经历各种政府当局(当地、地区、州、国家、国际)的漫长评价过程。大量数据要求(voluminous datarequirement)由管理当局来规定且必须通过数据生成(data generation)来给出(address),以及由产品登记人或由代表产品登记人的第三方来提交(通常使用与万维网连接的计算机)。这些政府当局然后评价所述数据且若作出安全性的决定,则将产品登记许可(product registration approval)提供给潜在的使用者或销售者。之后,在产品登记被授权和支持的地方,所述使用者或销售者可使用或销售所述杀虫剂。
可对式1、2和3的分子进行试验以确定其抗害虫效力。此外,可进行作用模式研究以确定所述分子是否具有不同于其它杀虫剂的作用模式。之后,可将由此获得数据发放(例如通过互联网)给第三方。
本申请中的标题仅是为了方便,而决不是用于解释本申请中的任何部分。
表格部分
表1:化合物的结构
表2:表1中化合物的分析数据
除非另有说明,使用400MHz仪器得到NMR光谱数据。
P*:根据在Crouse等人的PCT国际申请公开文本WO 2009/102736 A1和Brown等人的WO 2011/017504 A1中描述的方法来制备。
表3:化合物的结构
表4:表3中化合物的分析数据
除非另有说明,使用400MHz仪器得到NMR光谱数据。
表4A:表3中光学活性化合物的分析数据
除非另有说明,使用400MHz仪器得到NMR光谱数据。
表5:生物结果
Claims (32)
1.一种组合物,其包含式2或式3分子:
其中:
(a)Ar1为
(1)呋喃基、苯基、哒嗪基、吡啶基、嘧啶基或噻吩基,或
(2)取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基或取代的噻吩基,
其中所述取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基和取代的噻吩基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(b)Het为含有一个或多个独立选自氮、硫或氧的杂原子的5或6元饱和或不饱和杂环,其中Ar1和Ar2彼此不处于邻位(但可为间位或对位例如就5元环而言它们为1,3位且就6元环而言它们为1,3位或1,4位)且其中所述杂环还可取代有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(c)Ar2为
(1)呋喃基、苯基、哒嗪基、吡啶基、嘧啶基或噻吩基,或
(2)取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基或取代的噻吩基,
其中所述取代的呋喃基、取代的苯基、取代的哒嗪基、取代的吡啶基、取代的嘧啶基和取代的噻吩基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基、取代的苯基和取代的苯氧基,
其中所述取代的苯基和取代的苯氧基具有一个或多个独立选自以下的取代基:H、F、Cl、Br、I、CN、NO2、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C1-C6卤代烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(d)R1选自H、CN、F、Cl、Br、I、C1-C6烷基、C3-C6环烷基、C3-C6环烷氧基、C1-C6烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、OSO2(C1-C6烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基或苯氧基,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基和苯氧基任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基和苯氧基;
(g)R4为H、C1-C6烷基、C3-C6环烷基、C2-C6烯基、C2-C6炔基、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、C1-C6烷基苯基、C1-C6烷基-O-苯基、C(=O)Het-1、Het-1、C1-C6烷基Het-1或C1-C6烷基-O-Het-1,
其中每个烷基、环烷基、烯基、炔基、苯基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基和Het-1;
(h)R5为1元饱和烃基连接物,其中所述连接物还可取代有F、Cl、Br、I、CN、NO2、氧代、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、苯氧基和Het-1,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基、苯氧基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、NRxRy、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)NRxRy、(C1-C6烷基)NRxRy、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、卤代苯基、苯氧基和Het-1;
(i)n=0、1或2;
(j)Rx和Ry独立选自H、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C2-C6烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)和苯基,
其中每个烷基、环烷基、环烷氧基、烷氧基、烯基、炔基、苯基、苯氧基和Het-1任选取代有一个或多个独立选自以下的取代基:F、Cl、Br、I、CN、NO2、氧代、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)H、C(=O)OH、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、卤代苯基、苯氧基和Het-1,
或Rx和Ry一起可任选形成可含有一个或多个选自氮、硫和氧的杂原子的5至7元饱和或不饱和环状基团且其中所述环状基团可含有>C=O或>C=S且其中所述环状基团可取代有F、Cl、Br、I、CN、C1-C6烷基、C1-C6卤代烷基、C3-C6环烷基、C3-C6卤代环烷基、C3-C6环烷氧基、C3-C6卤代环烷氧基、C1-C6烷氧基、C1-C6卤代烷氧基、C2-C6烯基、C3-C6环烯基、C2-C6炔基、S(=O)n(C1-C6烷基)、S(=O)n(C1-C6卤代烷基)、OSO2(C1-C6烷基)、OSO2(C1-C6卤代烷基)、C(=O)(C1-C6烷基)、C(=O)O(C1-C6烷基)、C(=O)(C1-C6卤代烷基)、C(=O)O(C1-C6卤代烷基)、C(=O)(C3-C6环烷基)、C(=O)O(C3-C6环烷基)、C(=O)(C2-C6烯基)、C(=O)O(C2-C6烯基)、(C1-C6烷基)O(C1-C6烷基)、(C1-C6烷基)S(C1-C6烷基)、C(=O)(C1-C6烷基)C(=O)O(C1-C6烷基)、苯基、取代的苯基、苯氧基和Het-1;和
(k)Het-1为含有一个或多个独立选自氮、硫或氧的杂原子的5或6元饱和或不饱和杂环。
2.权利要求1的分子,其中Ar1为取代的苯基,其中所述取代的苯基具有一个或多个独立选自以下的取代基:C1-C6卤代烷基和C1-C6卤代烷氧基。
3.权利要求1的分子,其中Ar1为取代的苯基,其中所述取代的苯基具有一个或多个独立选自以下的取代基:CF3、OCF3和OCF2CF3。
4.权利要求1的分子,其中Het选自三唑基、咪唑基或吡唑基,所述基团可为取代或未取代的。
5.权利要求1的分子,其中Het为1,2,4-三唑基:
6.权利要求1的分子,其中Het为1,4-咪唑基:
7.权利要求1的分子,其中Het为1,3-吡唑基:
8.权利要求1的分子,其中Het为取代的1,3-吡唑基。
9.权利要求1的分子,其中Het为1,4-吡唑基:
10.权利要求1的分子,其中Ar2为苯基。
11.权利要求1的分子,其中R1为H或C1-C6烷基。
12.权利要求1的分子,其中R1为H或CH3。
13.权利要求1的分子,其中R4为苯基、C1-C6烷基苯基或C1-C6烷基-O-苯基,其中每个烷基和苯基任选取代有一个或多个独立选自以下的取代基:F、Cl、NRxRy、C1-C6烷基或C1-C6烷氧基。
14.权利要求1的分子,其中R5为未取代的。
15.权利要求1的分子,其中Rx和Ry独立选自H和苯基,其中所述苯基可任选取代有一个或多个独立选自以下的取代基:F和Cl。
16.权利要求1的分子,其中Het-1选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
17.权利要求1的分子,其中Het选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
18.权利要求1的分子,其中Het-1选自苯并呋喃基、苯并异噻唑基、苯并异噁唑基、苯并噁唑基、苯并噻吩基、苯并噻唑基、苯并噻二唑基、噌啉基、呋喃基、吲唑基、吲哚基、咪唑基、异吲哚基、异喹啉基、异噻唑基、异噁唑基、噁二唑基、噁唑啉基、噁唑基、酞嗪基、吡嗪基、吡唑啉基、吡唑基、哒嗪基、吡啶基、嘧啶基、吡咯基、喹唑啉基、喹啉基、喹喔啉基、四唑基、噻唑啉基、噻唑基、噻吩基、噻吩基吡唑基、三嗪基、三唑基、哌嗪基、哌啶基、吗啉基、吡咯烷基、四氢呋喃基、四氢吡喃基、1,2,3,4-四氢-喹啉基、4,5-二氢-噁唑基、4,5-二氢-1H-吡唑基、4,5-二氢-异噁唑基和2,3-二氢-[1,3,4]-噁二唑基。
19.权利要求1的分子,其中Het-1选自苯并噻二唑基、呋喃基、噁唑基和噻吩基吡唑基。
20.权利要求1的分子,其中所述分子选自:
21.施用权利要求1的组合物的方法,所述方法包括为了防治害虫而向位置施用足以防治所述害虫量的权利要求1的组合物。
22.权利要求21的方法,其中所述分子选自:
且所述害虫为BAW、CEW或GPA。
23.权利要求21的方法,其中所述位置为苹果、玉米、棉花、大豆、芸苔、小麦、稻谷、高粱、大麦、燕麦、马铃薯、柑橘、苜蓿、莴苣、草莓、番茄、胡椒、十字花科植物、梨、烟草、杏、甜菜或豆类的生长位置或其种子的待种植位置。
24.权利要求1的组合物,其包含权利要求1的分子的杀虫用酸加成盐、盐衍生物、溶剂化物或酯衍生物。
25.权利要求1的组合物,其包含权利要求1的分子的多晶型。
26.权利要求1的组合物,其包含权利要求1的分子,其中至少一个H为2H或至少一个C为14C。
27.一种组合物,其包含权利要求1的分子和至少一种其它选自以下的化合物:杀昆虫剂组、杀螨虫剂组、杀线虫剂组、杀真菌剂组、除草剂组、AI组或协同剂组。
28.一种组合物,其包含权利要求1的组合物和种子。
29.权利要求28的组合物,其中所述种子已被遗传修饰为表达一种或多种特定属性。
30.权利要求1的组合物和至少一种具有选自以下作用模式的化合物:乙酰胆碱酯酶抑制剂、钠通道调节剂、壳多糖生物合成抑制剂、GABA门控氯化物通道拮抗剂、GABA和谷氨酸门控氯化物通道激动剂、乙酰胆碱受体激动剂、MET I抑制剂、Mg刺激性ATP酶抑制剂、烟碱性乙酰胆碱受体、中肠膜破裂剂、氧化磷酸化中断剂和利阿诺定受体(RyRs)。
31.一种方法,其包括向经遗传修饰的植物施用权利要求1的组合物,所述经遗传修饰的植物已被遗传修饰为表达一种或多种特定属性。
32.一种方法,其包括向非人类动物口服或局部施用权利要求1的组合物以防治内寄生物、外寄生物或这两者。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261594054P | 2012-02-02 | 2012-02-02 | |
US61/594,054 | 2012-02-02 | ||
PCT/US2013/022659 WO2013116052A1 (en) | 2012-02-02 | 2013-01-23 | Pesticidal compositions and processes related thereto |
Publications (2)
Publication Number | Publication Date |
---|---|
CN104202986A true CN104202986A (zh) | 2014-12-10 |
CN104202986B CN104202986B (zh) | 2016-08-24 |
Family
ID=48903407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201380018750.5A Expired - Fee Related CN104202986B (zh) | 2012-02-02 | 2013-01-23 | 杀虫组合物及与其相关的方法 |
Country Status (22)
Country | Link |
---|---|
US (2) | US20130203593A1 (zh) |
EP (1) | EP2809159A4 (zh) |
JP (1) | JP6117825B2 (zh) |
KR (1) | KR20140119789A (zh) |
CN (1) | CN104202986B (zh) |
AP (1) | AP2014007823A0 (zh) |
AR (1) | AR089875A1 (zh) |
AU (1) | AU2013215536B2 (zh) |
BR (1) | BR112014018943A8 (zh) |
CA (1) | CA2861353A1 (zh) |
CL (1) | CL2014002051A1 (zh) |
CO (1) | CO7020932A2 (zh) |
HK (1) | HK1204752A1 (zh) |
IL (1) | IL233704B (zh) |
MX (1) | MX338200B (zh) |
NZ (1) | NZ627331A (zh) |
PH (1) | PH12014501744B1 (zh) |
RU (1) | RU2616808C2 (zh) |
TW (1) | TWI571464B (zh) |
UA (1) | UA114313C2 (zh) |
WO (1) | WO2013116052A1 (zh) |
ZA (1) | ZA201405157B (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107935961A (zh) * | 2017-12-01 | 2018-04-20 | 赣南师范大学 | 一种2‑亚氨基噻唑烷‑4‑酮类化合物的制备方法 |
CN113166063A (zh) * | 2018-11-28 | 2021-07-23 | 巴斯夫欧洲公司 | 杀害虫化合物 |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112014018943A8 (pt) | 2012-02-02 | 2017-07-11 | Dow Agrosciences Llc | Composições pesticidas e processos relacionados as mesmas |
US8916183B2 (en) * | 2012-02-02 | 2014-12-23 | Dow Agrosciences, Llc. | Pesticidal compositions and processes related thereto |
BR112017015505B1 (pt) | 2015-01-23 | 2021-09-14 | Syngenta Participations Ag | Composto, composição pesticida, método para controle de pragas, método para a proteção de material de propagação de plantas do ataque por pragas e material de propagação revestido |
JP6807876B2 (ja) | 2015-06-05 | 2021-01-06 | シンジェンタ パーティシペーションズ アーゲー | 殺有害生物的に活性なオキシムおよびヒドラゾン誘導体 |
JP6970176B2 (ja) | 2016-07-22 | 2021-11-24 | シンジェンタ パーティシペーションズ アーゲー | 有害生物防除剤としての尿素およびチオ尿素置換二環式誘導体 |
CA3121202A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
WO2020229398A1 (de) | 2019-05-14 | 2020-11-19 | Bayer Aktiengesellschaft | (1-alkenyl)-substituierte pyrazole und triazole als schädlingsbekämpfungsmittel |
KR20220035939A (ko) | 2019-07-22 | 2022-03-22 | 바이엘 악티엔게젤샤프트 | 살충제로서의 5-아미노-치환된 피라졸 및 트리아졸 |
WO2021219513A1 (en) | 2020-04-28 | 2021-11-04 | Basf Se | Pesticidal compounds |
WO2022033991A1 (de) | 2020-08-13 | 2022-02-17 | Bayer Aktiengesellschaft | 5-amino substituierte triazole als schädlingsbekämpfungsmittel |
WO2022053453A1 (de) | 2020-09-09 | 2022-03-17 | Bayer Aktiengesellschaft | Azolcarboxamide als schädlingsbekämpfungsmittel |
EP3974414A1 (de) | 2020-09-25 | 2022-03-30 | Bayer AG | 5-amino substituierte pyrazole und triazole als schädlingsbekämpfungsmittel |
EP4036083A1 (de) | 2021-02-02 | 2022-08-03 | Bayer Aktiengesellschaft | 5-oxy substituierte hetereozyklen, als schädlingsbekämpfungsmittel |
EP4144739A1 (de) | 2021-09-02 | 2023-03-08 | Bayer Aktiengesellschaft | Anellierte pyrazole als schädlingsbekämpfungsmittel |
EP4198023A1 (en) | 2021-12-16 | 2023-06-21 | Basf Se | Pesticidally active thiosemicarbazone compounds |
WO2023156402A1 (en) | 2022-02-17 | 2023-08-24 | Basf Se | Pesticidally active thiosemicarbazone compounds |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1474694A (zh) * | 2000-10-27 | 2004-02-11 | �ݶ�ũ������˾ | 取代的4,5-二氢-1,2,4-三嗪-3-酮,1,2,4-三嗪-3-酮,以及它们作为杀真菌剂和杀虫剂的用途 |
US20090209476A1 (en) * | 2008-02-12 | 2009-08-20 | Dow Agrosciences Llc | Pesticidal compositions |
US20100010058A1 (en) * | 2006-06-22 | 2010-01-14 | Basf Se | Azoline Compounds for Combating Arthropod Pests |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4209561A1 (de) * | 1992-03-20 | 1993-09-23 | Univ Leipzig | 4-benzimino-3-phenyl-1,3-selenazetidin-2- thione, 4-benzimino-(ethoxycarbimino)-3-phenyl -1,3-thiazetidin-2-thione und verfahren zu ihrer herstellung |
AU1555797A (en) * | 1996-01-30 | 1997-08-22 | Takeda Chemical Industries Ltd. | Arylpyrazole insecticides |
US6413992B1 (en) * | 1998-10-23 | 2002-07-02 | Dow Agrosciences Llc | 3-(substituted pyridyl)-1,2,4-triazole compounds |
TWI412322B (zh) * | 2005-12-30 | 2013-10-21 | Du Pont | 控制無脊椎害蟲之異唑啉 |
EP2019095A1 (en) * | 2007-07-06 | 2009-01-28 | Bayer CropScience AG | Iminooxazole and iminothiazole compounds as pesticides |
UA108619C2 (xx) * | 2009-08-07 | 2015-05-25 | Пестицидні композиції | |
BR112012002677A2 (pt) * | 2009-08-07 | 2021-03-09 | Dow Agrosciences Llc | Moléculas de heteroaril-n-aril carbamatos, e composição pesticida |
EP2585443B1 (en) * | 2010-06-23 | 2015-02-18 | Basf Se | Process for producing imine compounds for combating invertebrate pests |
MX2013009129A (es) | 2011-02-07 | 2013-10-01 | Dow Agrosciences Llc | Composiciones pesticidas y procesos relacionados. |
BR112014018943A8 (pt) | 2012-02-02 | 2017-07-11 | Dow Agrosciences Llc | Composições pesticidas e processos relacionados as mesmas |
-
2013
- 2013-01-23 BR BR112014018943A patent/BR112014018943A8/pt not_active Application Discontinuation
- 2013-01-23 WO PCT/US2013/022659 patent/WO2013116052A1/en active Application Filing
- 2013-01-23 UA UAA201409615A patent/UA114313C2/uk unknown
- 2013-01-23 AP AP2014007823A patent/AP2014007823A0/xx unknown
- 2013-01-23 JP JP2014555581A patent/JP6117825B2/ja active Active
- 2013-01-23 RU RU2014135519A patent/RU2616808C2/ru not_active IP Right Cessation
- 2013-01-23 NZ NZ627331A patent/NZ627331A/en not_active IP Right Cessation
- 2013-01-23 KR KR1020147024119A patent/KR20140119789A/ko not_active Application Discontinuation
- 2013-01-23 CA CA2861353A patent/CA2861353A1/en not_active Abandoned
- 2013-01-23 AU AU2013215536A patent/AU2013215536B2/en not_active Ceased
- 2013-01-23 MX MX2014009346A patent/MX338200B/es active IP Right Grant
- 2013-01-23 CN CN201380018750.5A patent/CN104202986B/zh not_active Expired - Fee Related
- 2013-01-23 US US13/747,497 patent/US20130203593A1/en not_active Abandoned
- 2013-01-23 EP EP13742831.4A patent/EP2809159A4/en not_active Withdrawn
- 2013-02-01 AR ARP130100316A patent/AR089875A1/es active IP Right Grant
- 2013-02-01 TW TW102104027A patent/TWI571464B/zh not_active IP Right Cessation
-
2014
- 2014-03-24 US US14/223,314 patent/US9018388B2/en active Active
- 2014-07-15 ZA ZA2014/05157A patent/ZA201405157B/en unknown
- 2014-07-17 IL IL233704A patent/IL233704B/en not_active IP Right Cessation
- 2014-07-28 CO CO14163273A patent/CO7020932A2/es unknown
- 2014-07-31 CL CL2014002051A patent/CL2014002051A1/es unknown
- 2014-08-01 PH PH12014501744A patent/PH12014501744B1/en unknown
-
2015
- 2015-06-02 HK HK15105245.5A patent/HK1204752A1/zh not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1474694A (zh) * | 2000-10-27 | 2004-02-11 | �ݶ�ũ������˾ | 取代的4,5-二氢-1,2,4-三嗪-3-酮,1,2,4-三嗪-3-酮,以及它们作为杀真菌剂和杀虫剂的用途 |
US20100010058A1 (en) * | 2006-06-22 | 2010-01-14 | Basf Se | Azoline Compounds for Combating Arthropod Pests |
US20090209476A1 (en) * | 2008-02-12 | 2009-08-20 | Dow Agrosciences Llc | Pesticidal compositions |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107935961A (zh) * | 2017-12-01 | 2018-04-20 | 赣南师范大学 | 一种2‑亚氨基噻唑烷‑4‑酮类化合物的制备方法 |
CN107935961B (zh) * | 2017-12-01 | 2019-10-29 | 赣南师范大学 | 一种2-亚氨基噻唑烷-4-酮类化合物的制备方法 |
CN113166063A (zh) * | 2018-11-28 | 2021-07-23 | 巴斯夫欧洲公司 | 杀害虫化合物 |
Also Published As
Publication number | Publication date |
---|---|
AP2014007823A0 (en) | 2014-07-31 |
EP2809159A4 (en) | 2015-08-12 |
EP2809159A1 (en) | 2014-12-10 |
CL2014002051A1 (es) | 2014-11-21 |
US20140235440A1 (en) | 2014-08-21 |
IL233704B (en) | 2018-03-29 |
CA2861353A1 (en) | 2013-08-08 |
CN104202986B (zh) | 2016-08-24 |
PH12014501744A1 (en) | 2014-11-10 |
PH12014501744B1 (en) | 2014-11-10 |
BR112014018943A8 (pt) | 2017-07-11 |
ZA201405157B (en) | 2015-11-25 |
JP2015506959A (ja) | 2015-03-05 |
US20130203593A1 (en) | 2013-08-08 |
UA114313C2 (uk) | 2017-05-25 |
MX338200B (es) | 2016-04-07 |
KR20140119789A (ko) | 2014-10-10 |
WO2013116052A1 (en) | 2013-08-08 |
RU2616808C2 (ru) | 2017-04-18 |
AR089875A1 (es) | 2014-09-24 |
RU2014135519A (ru) | 2016-03-20 |
TW201336841A (zh) | 2013-09-16 |
CO7020932A2 (es) | 2014-08-11 |
AU2013215536A1 (en) | 2014-07-31 |
TWI571464B (zh) | 2017-02-21 |
US9018388B2 (en) | 2015-04-28 |
HK1204752A1 (zh) | 2015-12-04 |
NZ627331A (en) | 2016-03-31 |
AU2013215536B2 (en) | 2016-03-17 |
JP6117825B2 (ja) | 2017-04-19 |
MX2014009346A (es) | 2014-09-01 |
BR112014018943A2 (zh) | 2017-06-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2017228717B2 (en) | Pesticidal compositions and related methods | |
CN103458687B (zh) | 杀虫组合物及其相关方法 | |
CN104202986B (zh) | 杀虫组合物及与其相关的方法 | |
CN102458403B (zh) | 杀虫组合物 | |
US8551914B2 (en) | Pesticidal compositions | |
US9107410B2 (en) | Pesticidal compositions and processes related thereto | |
US20120220453A1 (en) | Pesticidal compostions and processes related thereto | |
CN104244715A (zh) | 杀虫组合物及与其相关的方法 | |
CN103188936A (zh) | 杀虫组合物 | |
CN107072206A (zh) | 杀虫组合物及相关方法 | |
CN105792651A (zh) | 杀虫组合物和与其相关的方法 | |
CN105682461B (zh) | 杀虫组合物和与其相关的方法 | |
OA16336A (en) | Pesticidal compositions. | |
OA16501A (en) | Pesticidal compositions and processes related thereto. | |
NZ613711B2 (en) | Pesticidal compositions and processes related thereto | |
OA16500A (en) | Pesticidal compositions and processes related thereto. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1204752 Country of ref document: HK |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: GR Ref document number: 1204752 Country of ref document: HK |
|
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160824 Termination date: 20190123 |
|
CF01 | Termination of patent right due to non-payment of annual fee |