JP2011102303A - 4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1及びアベルメクチンb1単糖誘導体 - Google Patents
4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1及びアベルメクチンb1単糖誘導体 Download PDFInfo
- Publication number
- JP2011102303A JP2011102303A JP2010286151A JP2010286151A JP2011102303A JP 2011102303 A JP2011102303 A JP 2011102303A JP 2010286151 A JP2010286151 A JP 2010286151A JP 2010286151 A JP2010286151 A JP 2010286151A JP 2011102303 A JP2011102303 A JP 2011102303A
- Authority
- JP
- Japan
- Prior art keywords
- spp
- alkyl
- heterocyclyl
- aryl
- compound
- 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
- 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 title claims description 7
- NJTGMYOUKBELLQ-NVQQORPBSA-N avermectin b1 monosaccharide Chemical class O1C(C)C(O)C(OC)CC1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(C3)C=C[C@H](C)[C@@H](C(C)C)O2)C[C@@H]3OC(=O)[C@@H]([C@]23O)C=C(C)[C@@H](O)[C@H]3OC\C2=C/C=C/[C@@H]1C NJTGMYOUKBELLQ-NVQQORPBSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 295
- 125000001424 substituent group Chemical group 0.000 claims description 138
- -1 methylenedioxy Chemical group 0.000 claims description 105
- 239000000203 mixture Substances 0.000 claims description 78
- 125000003118 aryl group Chemical group 0.000 claims description 53
- 125000000623 heterocyclic group Chemical group 0.000 claims description 49
- 229910052736 halogen Inorganic materials 0.000 claims description 32
- 150000002367 halogens Chemical class 0.000 claims description 32
- 241000607479 Yersinia pestis Species 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 20
- 150000003839 salts Chemical group 0.000 claims description 18
- 125000004104 aryloxy group Chemical group 0.000 claims description 17
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- 125000005110 aryl thio group Chemical group 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 11
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 11
- 229910052717 sulfur Inorganic materials 0.000 claims description 11
- 125000004643 (C1-C12) haloalkoxy group Chemical group 0.000 claims description 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 5
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 4
- 229910005965 SO 2 Inorganic materials 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 3
- 125000006711 (C2-C12) alkynyl group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 1
- 239000003905 agrochemical Substances 0.000 claims 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 abstract description 11
- 241000238876 Acari Species 0.000 abstract description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 105
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 49
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 43
- 239000011734 sodium Substances 0.000 description 43
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 42
- 239000000243 solution Substances 0.000 description 36
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 32
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 28
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 28
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 27
- 230000000694 effects Effects 0.000 description 27
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 26
- 241000196324 Embryophyta Species 0.000 description 26
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 22
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 22
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 20
- 238000003818 flash chromatography Methods 0.000 description 20
- 238000001819 mass spectrum Methods 0.000 description 20
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 17
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 16
- 238000012360 testing method Methods 0.000 description 16
- 241001465754 Metazoa Species 0.000 description 15
- 239000002253 acid Substances 0.000 description 15
- 239000004480 active ingredient Substances 0.000 description 15
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 15
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- 239000000460 chlorine Substances 0.000 description 13
- 239000000741 silica gel Substances 0.000 description 13
- 229910002027 silica gel Inorganic materials 0.000 description 13
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 229910052794 bromium Inorganic materials 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 238000004128 high performance liquid chromatography Methods 0.000 description 10
- 230000014759 maintenance of location Effects 0.000 description 10
- 239000007858 starting material Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethyl sulfoxide Natural products CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- 239000011737 fluorine Substances 0.000 description 9
- 229910052731 fluorine Inorganic materials 0.000 description 9
- GRJJQCWNZGRKAU-UHFFFAOYSA-N pyridin-1-ium;fluoride Chemical compound F.C1=CC=NC=C1 GRJJQCWNZGRKAU-UHFFFAOYSA-N 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 238000006467 substitution reaction Methods 0.000 description 8
- 125000004187 tetrahydropyran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 7
- 240000001307 Myosotis scorpioides Species 0.000 description 7
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 7
- 208000027418 Wounds and injury Diseases 0.000 description 7
- 230000006378 damage Effects 0.000 description 7
- 208000014674 injury Diseases 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 241000256248 Spodoptera Species 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- 229940098779 methanesulfonic acid Drugs 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000005660 Abamectin Substances 0.000 description 5
- 244000068988 Glycine max Species 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
- 239000002671 adjuvant Substances 0.000 description 5
- RRZXIRBKKLTSOM-XPNPUAGNSA-N avermectin B1a Chemical class 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 RRZXIRBKKLTSOM-XPNPUAGNSA-N 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
- 238000004587 chromatography analysis Methods 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 244000144972 livestock Species 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- URUUZIAJVSGYRC-UHFFFAOYSA-N oxan-3-one Chemical compound O=C1CCCOC1 URUUZIAJVSGYRC-UHFFFAOYSA-N 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 238000002953 preparative HPLC Methods 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 240000007124 Brassica oleracea Species 0.000 description 3
- 241000668561 Chrysomphalus Species 0.000 description 3
- 240000008067 Cucumis sativus Species 0.000 description 3
- 241001480224 Heterodera Species 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Chemical compound IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 3
- 241000500437 Plutella xylostella Species 0.000 description 3
- 241000220324 Pyrus Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000004450 alkenylene group Chemical group 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound 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 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 235000021017 pears Nutrition 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 3
- 125000000335 thiazolyl group Chemical group 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- 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 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-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
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 241001506414 Aculus Species 0.000 description 2
- 241001368048 Agrochola Species 0.000 description 2
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 2
- 241000625753 Anticarsia Species 0.000 description 2
- 241001174347 Atomaria Species 0.000 description 2
- 241000193388 Bacillus thuringiensis Species 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 241001347512 Carposina Species 0.000 description 2
- 241000255945 Choristoneura Species 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 239000005946 Cypermethrin Substances 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
- 241000489975 Diabrotica Species 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- 241000255925 Diptera Species 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241001203900 Eudonia Species 0.000 description 2
- 241000060469 Eupoecilia ambiguella Species 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 241000257303 Hymenoptera Species 0.000 description 2
- 241000255777 Lepidoptera Species 0.000 description 2
- 241000500881 Lepisma Species 0.000 description 2
- 241000243786 Meloidogyne incognita Species 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 241000168038 Orthosia <moth> Species 0.000 description 2
- 241000721452 Pectinophora Species 0.000 description 2
- 241000562493 Pegomya Species 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- 241000531582 Pulvinaria <Pelagophyceae> Species 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 241001338644 Retinia Species 0.000 description 2
- 241001481703 Rhipicephalus <genus> Species 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 241001468227 Streptomyces avermitilis Species 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
- 230000000895 acaricidal effect Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000012872 agrochemical composition Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- RRZXIRBKKLTSOM-UHFFFAOYSA-N avermectin B1a Natural products C1=CC(C)C(C(C)CC)OC11OC(CC=C(C)C(OC2OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C2)C(C)C=CC=C2C3(C(C(=O)O4)C=C(C)C(O)C3OC2)O)CC4C1 RRZXIRBKKLTSOM-UHFFFAOYSA-N 0.000 description 2
- ZFUKERYTFURFGA-PVVXTEPVSA-N avermectin B1b Chemical class 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 ZFUKERYTFURFGA-PVVXTEPVSA-N 0.000 description 2
- 229940097012 bacillus thuringiensis Drugs 0.000 description 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 235000008504 concentrate Nutrition 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
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 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
- 238000005516 engineering process Methods 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000004995 haloalkylthio group Chemical group 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001041 indolyl group Chemical group 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000012669 liquid formulation Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000001630 malic acid Substances 0.000 description 2
- 235000011090 malic acid Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- RMIODHQZRUFFFF-UHFFFAOYSA-M methoxyacetate Chemical compound COCC([O-])=O RMIODHQZRUFFFF-UHFFFAOYSA-M 0.000 description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 150000002772 monosaccharides Chemical class 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000008262 pumice Substances 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 238000009331 sowing Methods 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 125000004665 trialkylsilyl group Chemical group 0.000 description 2
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000006886 vinylation reaction Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 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
- LZTIMERBDGGAJD-SNAWJCMRSA-N (2e)-2-(nitromethylidene)-1,3-thiazinane Chemical compound [O-][N+](=O)\C=C1/NCCCS1 LZTIMERBDGGAJD-SNAWJCMRSA-N 0.000 description 1
- VEMKTZHHVJILDY-WOJBJXKFSA-N (5-benzylfuran-3-yl)methyl (1s,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)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-WOJBJXKFSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-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
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- 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 1
- RVHSTXJKKZWWDQ-UHFFFAOYSA-N 1,1,1,2-tetrabromoethane Chemical compound BrCC(Br)(Br)Br RVHSTXJKKZWWDQ-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- 125000004530 1,2,4-triazinyl group Chemical group N1=NC(=NC=C1)* 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-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
- NEFNOUUWYACOKP-UHFFFAOYSA-N 1-(chloromethoxy)butane Chemical compound CCCCOCCl NEFNOUUWYACOKP-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- QZEDXQFZACVDJE-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 QZEDXQFZACVDJE-UHFFFAOYSA-N 0.000 description 1
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 description 1
- PAHCSXMDRKCMGY-UHFFFAOYSA-N 2-(chloromethoxy)ethyl acetate Chemical compound CC(=O)OCCOCCl PAHCSXMDRKCMGY-UHFFFAOYSA-N 0.000 description 1
- 125000003821 2-(trimethylsilyl)ethoxymethyl group Chemical group [H]C([H])([H])[Si](C([H])([H])[H])(C([H])([H])[H])C([H])([H])C(OC([H])([H])[*])([H])[H] 0.000 description 1
- JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical group CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- ZKHJRFIWLBHZLV-UHFFFAOYSA-N 2-phenyl-1,4-dioxane-2-thiol Chemical compound C=1C=CC=CC=1C1(S)COCCO1 ZKHJRFIWLBHZLV-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- UUIMDJFBHNDZOW-UHFFFAOYSA-N 2-tert-butylpyridine Chemical compound CC(C)(C)C1=CC=CC=N1 UUIMDJFBHNDZOW-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-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
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000863245 Abraxas Species 0.000 description 1
- 241000934067 Acarus Species 0.000 description 1
- 241000934064 Acarus siro Species 0.000 description 1
- 241001558864 Aceria Species 0.000 description 1
- 239000005875 Acetamiprid Substances 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000511823 Acompsia Species 0.000 description 1
- 241001579828 Acria Species 0.000 description 1
- 239000005652 Acrinathrin Substances 0.000 description 1
- 241001340513 Acrobasis Species 0.000 description 1
- 241000539113 Acrolepia Species 0.000 description 1
- 241001212435 Acropolitis Species 0.000 description 1
- 241000495221 Actebia Species 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- 241001203928 Aethes Species 0.000 description 1
- 241001362583 Agapeta Species 0.000 description 1
- 241000050078 Agonopterix Species 0.000 description 1
- 241001491686 Agriopis Species 0.000 description 1
- 241001136265 Agriotes Species 0.000 description 1
- 241000218473 Agrotis Species 0.000 description 1
- 241000885978 Albuna Species 0.000 description 1
- 241000733426 Alcis Species 0.000 description 1
- 241000108079 Aleyrodes 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
- 241001491659 Alsophila <moth> Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000019114 Amata Species 0.000 description 1
- 241001340548 Amblyptilia Species 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241001420350 Amorbia Species 0.000 description 1
- 241001044369 Amphion Species 0.000 description 1
- 241000566546 Amphipyra Species 0.000 description 1
- 241001259788 Amyelois Species 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 241000566548 Anagrapha Species 0.000 description 1
- 241001198492 Anarsia Species 0.000 description 1
- 241001657809 Anhimella Species 0.000 description 1
- 241000254177 Anthonomus Species 0.000 description 1
- 241001414827 Aonidiella Species 0.000 description 1
- 241000368734 Apamea Species 0.000 description 1
- 241001166274 Aphelia <angiosperm> Species 0.000 description 1
- 241001600407 Aphis <genus> Species 0.000 description 1
- 241001203925 Apotomis Species 0.000 description 1
- 241000511861 Aproaerema Species 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241001002469 Archips Species 0.000 description 1
- 241000856916 Arctia Species 0.000 description 1
- 241001480748 Argas Species 0.000 description 1
- 241000032400 Argolamprotes Species 0.000 description 1
- 241001163967 Argyrogramma Species 0.000 description 1
- 241001579822 Arotrophora Species 0.000 description 1
- 241001002589 Ascotis Species 0.000 description 1
- 244000003416 Asparagus officinalis Species 0.000 description 1
- 235000005340 Asparagus officinalis Nutrition 0.000 description 1
- 241000387313 Aspidiotus Species 0.000 description 1
- 241000032402 Aspilapteryx Species 0.000 description 1
- 241001574899 Aterpia Species 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
- 241000486721 Atypha Species 0.000 description 1
- 241001367049 Autographa Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- ZFUKERYTFURFGA-UHFFFAOYSA-N Avermectin B1b Chemical class O1C(C)C(O)C(OC)CC1OC1C(OC)CC(OC2C(=CCC3CC(CC4(O3)C=CC(C)C(C(C)C)O4)OC(=O)C3C=C(C)C(O)C4OCC(C34O)=CC=CC2C)C)OC1C ZFUKERYTFURFGA-UHFFFAOYSA-N 0.000 description 1
- 241000486626 Axylia Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 241001574381 Bactra Species 0.000 description 1
- 241001367512 Battaristis Species 0.000 description 1
- 241000868184 Bembecia Species 0.000 description 1
- 241000254123 Bemisia Species 0.000 description 1
- 241000254127 Bemisia tabaci Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 239000005884 Beta-Cyfluthrin Substances 0.000 description 1
- 241001142392 Bibio Species 0.000 description 1
- 239000005653 Bifenazate Substances 0.000 description 1
- 241001362549 Bisigna Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000238659 Blatta Species 0.000 description 1
- 241001351998 Bleptina Species 0.000 description 1
- 241000255791 Bombyx Species 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- 241001573600 Bradina Species 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 241001643374 Brevipalpus Species 0.000 description 1
- NYQDCVLCJXRDSK-UHFFFAOYSA-N Bromofos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl NYQDCVLCJXRDSK-UHFFFAOYSA-N 0.000 description 1
- 241000488564 Bryobia Species 0.000 description 1
- 241000398201 Bryobia praetiosa Species 0.000 description 1
- 241001201735 Bryotropha 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
- 241001491664 Bupalus Species 0.000 description 1
- 241000661267 Busseola Species 0.000 description 1
- 241000661305 Busseola fusca Species 0.000 description 1
- UHSWTWIKWIEADG-DXLNZPLUSA-N CCC(C)[C@H]([C@@H](C)C=C1)OC1(C[C@H](C1)OC([C@]2C=C(C)[C@H]([C@H]3OC4)O)=O)O[C@@H]1C/C=C(\C)/[C@@H](C(C[C@@H]1OC)O[C@@H](C)[C@@H]1OCOCCN)[C@@H](C)/C=C/C=C4/[C@@]23O Chemical compound CCC(C)[C@H]([C@@H](C)C=C1)OC1(C[C@H](C1)OC([C@]2C=C(C)[C@H]([C@H]3OC4)O)=O)O[C@@H]1C/C=C(\C)/[C@@H](C(C[C@@H]1OC)O[C@@H](C)[C@@H]1OCOCCN)[C@@H](C)/C=C/C=C4/[C@@]23O UHSWTWIKWIEADG-DXLNZPLUSA-N 0.000 description 1
- 0 CCC(CC1)C(*C(*)OC)C(C)C1=C Chemical compound CCC(CC1)C(*C(*)OC)C(C)C1=C 0.000 description 1
- JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-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
- 241000863292 Cabera Species 0.000 description 1
- 241000842516 Cacoecimorpha Species 0.000 description 1
- 241000726763 Cadra Species 0.000 description 1
- 241000726760 Cadra cautella Species 0.000 description 1
- 241000368766 Caenurgina Species 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000486625 Callierges Species 0.000 description 1
- 241001584935 Calophasia Species 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
- 241001350371 Capua Species 0.000 description 1
- 241001605401 Caradrina Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEDTXTNSFWUXGQ-UHFFFAOYSA-N Carbophenothion Chemical compound CCOP(=S)(OCC)SCSC1=CC=C(Cl)C=C1 VEDTXTNSFWUXGQ-UHFFFAOYSA-N 0.000 description 1
- 241001584923 Caripeta Species 0.000 description 1
- 241000885985 Carmenta Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 241000486623 Celaena Species 0.000 description 1
- 241001574880 Celypha Species 0.000 description 1
- 241000486661 Ceramica Species 0.000 description 1
- 241000403238 Cerapteryx Species 0.000 description 1
- 241000255580 Ceratitis <genus> Species 0.000 description 1
- 241001098608 Ceratophyllus Species 0.000 description 1
- 241000902406 Chaetocnema Species 0.000 description 1
- 241001087583 Chaetocnema tibialis Species 0.000 description 1
- 241000769697 Chiasmia Species 0.000 description 1
- 241000426499 Chilo Species 0.000 description 1
- 241001391664 Chionodes Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
- 239000005944 Chlorpyrifos Substances 0.000 description 1
- 241001364932 Chrysodeixis Species 0.000 description 1
- 241000191839 Chrysomya Species 0.000 description 1
- 241001201730 Chrysoteuchia Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 241001672694 Citrus reticulata Species 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- 241001231789 Clepsis Species 0.000 description 1
- 239000005888 Clothianidin Substances 0.000 description 1
- 241000098277 Cnaphalocrocis Species 0.000 description 1
- 241001350387 Cnephasia Species 0.000 description 1
- 241001478240 Coccus Species 0.000 description 1
- 241001479447 Coccus hesperidum Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- 241001605779 Conistra Species 0.000 description 1
- 241001476526 Conopomorpha Species 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241000063688 Cornutiplusia Species 0.000 description 1
- 241000220362 Cosmia Species 0.000 description 1
- 241001212536 Cosmopolites Species 0.000 description 1
- 241000661276 Cosmopterix Species 0.000 description 1
- 241001579853 Cossus Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241001340508 Crambus Species 0.000 description 1
- 241001362570 Croesia Species 0.000 description 1
- 241001574944 Cryptaspasma Species 0.000 description 1
- 241001352386 Cryptocala Species 0.000 description 1
- 241000918681 Ctenopseustis Species 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000721021 Curculio Species 0.000 description 1
- 241000692095 Cuterebra Species 0.000 description 1
- 241001634817 Cydia Species 0.000 description 1
- 241001635274 Cydia pomonella Species 0.000 description 1
- 241000024163 Cymbalophora Species 0.000 description 1
- 239000005891 Cyromazine Substances 0.000 description 1
- 206010011732 Cyst Diseases 0.000 description 1
- 241000157278 Dacus <genus> Species 0.000 description 1
- 241000567472 Dasychira Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 241000794667 Deilephila Species 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- 241001631715 Dendrolimus Species 0.000 description 1
- 241000592368 Depressaria Species 0.000 description 1
- 241001641895 Dermestes Species 0.000 description 1
- 241001529600 Diabrotica balteata Species 0.000 description 1
- 241000789085 Diachrysia Species 0.000 description 1
- 241001605650 Diarsia Species 0.000 description 1
- 241000122105 Diatraea Species 0.000 description 1
- 241000497893 Dichagyris Species 0.000 description 1
- WGOWCPGHOCIHBW-UHFFFAOYSA-N Dichlofenthion Chemical compound CCOP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl WGOWCPGHOCIHBW-UHFFFAOYSA-N 0.000 description 1
- 241001063554 Dicycla Species 0.000 description 1
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- VBKKVDGJXVOLNE-UHFFFAOYSA-N Dioxation Chemical compound CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC VBKKVDGJXVOLNE-UHFFFAOYSA-N 0.000 description 1
- 241000511318 Diprion Species 0.000 description 1
- 241000511320 Diprionidae Species 0.000 description 1
- 241001201717 Ditula Species 0.000 description 1
- 241000399934 Ditylenchus Species 0.000 description 1
- 241001580309 Diurnea Species 0.000 description 1
- 241001491944 Drepana Species 0.000 description 1
- 241000255601 Drosophila melanogaster Species 0.000 description 1
- 241000019115 Dysauxes Species 0.000 description 1
- 241001425477 Dysdercus Species 0.000 description 1
- 241000863176 Dysstroma Species 0.000 description 1
- 241001362576 Eana Species 0.000 description 1
- 241000241133 Earias Species 0.000 description 1
- 241001575036 Ecdytolopha Species 0.000 description 1
- 241001590640 Ecpyrrhorrhoe Species 0.000 description 1
- 241000959081 Ectomyelois Species 0.000 description 1
- 239000005894 Emamectin Substances 0.000 description 1
- 241001369063 Enargia Species 0.000 description 1
- 241001574086 Enarmonia Species 0.000 description 1
- 241001574067 Endothenia Species 0.000 description 1
- 241000661281 Eoreuma Species 0.000 description 1
- 241001350128 Epagoge Species 0.000 description 1
- 241001420426 Epelis Species 0.000 description 1
- 241000630736 Ephestia Species 0.000 description 1
- 241000760915 Epiblema <orchid> Species 0.000 description 1
- 241001147395 Epinotia Species 0.000 description 1
- 241000776776 Epiplema Species 0.000 description 1
- 241001408614 Epirrhoe Species 0.000 description 1
- 241001574718 Episimus Species 0.000 description 1
- 241001491718 Erannis Species 0.000 description 1
- 241000917109 Eriosoma Species 0.000 description 1
- 241001515686 Erythroneura Species 0.000 description 1
- 239000005895 Esfenvalerate Substances 0.000 description 1
- 241000567413 Estigmene Species 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical class CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- 241001486247 Etiella Species 0.000 description 1
- 241001573987 Eucosma Species 0.000 description 1
- 241001574084 Eucosmomorpha Species 0.000 description 1
- 241001369089 Eufidonia Species 0.000 description 1
- 241000064199 Euhyponomeutoides Species 0.000 description 1
- 241001201696 Eulia Species 0.000 description 1
- 241001585065 Eulithis Species 0.000 description 1
- 241000421096 Euplesia Species 0.000 description 1
- 241001362584 Eupoecilia Species 0.000 description 1
- 241001331999 Euproctis Species 0.000 description 1
- 241001322248 Eurois Species 0.000 description 1
- 241000515838 Eurygaster Species 0.000 description 1
- 241000364046 Eurythmia Species 0.000 description 1
- 241001585293 Euxoa Species 0.000 description 1
- 241001200555 Euzophera Species 0.000 description 1
- 241001340524 Evergestis Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 241000233488 Feltia Species 0.000 description 1
- HMIBKHHNXANVHR-UHFFFAOYSA-N Fenothiocarb Chemical compound CN(C)C(=O)SCCCCOC1=CC=CC=C1 HMIBKHHNXANVHR-UHFFFAOYSA-N 0.000 description 1
- 239000005657 Fenpyroximate Substances 0.000 description 1
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 1
- 241000753086 Filatima Species 0.000 description 1
- 239000005899 Fipronil Substances 0.000 description 1
- 239000005900 Flonicamid Substances 0.000 description 1
- 239000005780 Fluazinam Substances 0.000 description 1
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical class NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 241000189565 Frankliniella Species 0.000 description 1
- 241001590634 Fumibotys Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241001660203 Gasterophilus Species 0.000 description 1
- 241000258727 Gilpinia Species 0.000 description 1
- 241000291751 Gilpinia polytoma Species 0.000 description 1
- 241001442498 Globodera Species 0.000 description 1
- 241001442497 Globodera rostochiensis Species 0.000 description 1
- 241001338515 Glyphipterix Species 0.000 description 1
- 241001421572 Glyphodes Species 0.000 description 1
- 241001421122 Gonodonta Species 0.000 description 1
- 244000299507 Gossypium hirsutum Species 0.000 description 1
- 241000206581 Gracilaria Species 0.000 description 1
- 241001150406 Grapholita Species 0.000 description 1
- 241000659076 Grapholitha Species 0.000 description 1
- 241001574136 Gravitarmata Species 0.000 description 1
- 241001574137 Gretchena Species 0.000 description 1
- 241001243091 Gryllotalpa Species 0.000 description 1
- 241001574138 Gypsonoma Species 0.000 description 1
- 241000630665 Hada Species 0.000 description 1
- 241000790933 Haematopinus Species 0.000 description 1
- 241001352379 Harrisina Species 0.000 description 1
- 241001201681 Hedya Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000255990 Helicoverpa Species 0.000 description 1
- 241000256257 Heliothis Species 0.000 description 1
- 241001635236 Hemaris Species 0.000 description 1
- 241001269005 Herculia Species 0.000 description 1
- 241000444781 Hermonassa Species 0.000 description 1
- 241000498254 Heterodera glycines Species 0.000 description 1
- 241001611147 Heterogenea Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241000771999 Hippobosca Species 0.000 description 1
- 241000526466 Homoeosoma Species 0.000 description 1
- 241001637851 Homoglaea Species 0.000 description 1
- 241000497901 Homohadena Species 0.000 description 1
- 241000679711 Homona Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- 244000025221 Humulus lupulus Species 0.000 description 1
- 241001585249 Hydraecia Species 0.000 description 1
- 241001491886 Hydriomena Species 0.000 description 1
- 241001488334 Hyles Species 0.000 description 1
- 241000776609 Hypatima Species 0.000 description 1
- 241001531333 Hyphantria Species 0.000 description 1
- 241001531327 Hyphantria cunea Species 0.000 description 1
- 241000022822 Hypocala Species 0.000 description 1
- 241001657635 Hypocoena Species 0.000 description 1
- 241000114623 Hypomecis Species 0.000 description 1
- 241001060790 Hypsipyla Species 0.000 description 1
- 241000278585 Hyssia Species 0.000 description 1
- 208000004356 Hysteria Diseases 0.000 description 1
- 241001491815 Idaea Species 0.000 description 1
- 241000370541 Idia Species 0.000 description 1
- 239000005907 Indoxacarb Substances 0.000 description 1
- 241001369153 Ipimorpha Species 0.000 description 1
- 241001201644 Iridopsis Species 0.000 description 1
- 241001495069 Ischnocera Species 0.000 description 1
- 241000023813 Isia Species 0.000 description 1
- 241000256602 Isoptera Species 0.000 description 1
- 241000278583 Isotrias Species 0.000 description 1
- 241001585244 Itame Species 0.000 description 1
- 241000238681 Ixodes Species 0.000 description 1
- 241000063963 Jodia Species 0.000 description 1
- 241001491869 Jodis Species 0.000 description 1
- 241000400434 Keiferia Species 0.000 description 1
- 241000400431 Keiferia lycopersicella Species 0.000 description 1
- 241001193010 Labdia Species 0.000 description 1
- 241000566532 Lacinipolia Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 241001658021 Lambdina Species 0.000 description 1
- 241000256686 Lasius <genus> Species 0.000 description 1
- 241001268491 Laspeyresia Species 0.000 description 1
- 240000004322 Lens culinaris Species 0.000 description 1
- 235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
- 241000669027 Lepidosaphes Species 0.000 description 1
- 241000258915 Leptinotarsa Species 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- 241000661345 Leptocorisa Species 0.000 description 1
- 241000109232 Leptostales Species 0.000 description 1
- 241000022851 Lesmone Species 0.000 description 1
- 241000931974 Leucania Species 0.000 description 1
- 241001573244 Leucinodes Species 0.000 description 1
- 241000828880 Leucoptera <angiosperm> Species 0.000 description 1
- 241001578972 Leucoptera malifoliella Species 0.000 description 1
- 241001113970 Linognathus Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 241001367846 Lithomoia Species 0.000 description 1
- 241000566529 Lithophane Species 0.000 description 1
- 241001585383 Lobophora <moth> Species 0.000 description 1
- 241000254023 Locusta Species 0.000 description 1
- 241001585369 Lomographa Species 0.000 description 1
- 241000257162 Lucilia <blowfly> Species 0.000 description 1
- 239000005912 Lufenuron Substances 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241000721696 Lymantria Species 0.000 description 1
- 241001190211 Lyonetia Species 0.000 description 1
- 241000255676 Malacosoma Species 0.000 description 1
- 239000005949 Malathion Substances 0.000 description 1
- 244000070406 Malus silvestris Species 0.000 description 1
- 240000000982 Malva neglecta Species 0.000 description 1
- 235000000060 Malva neglecta Nutrition 0.000 description 1
- 241000555300 Mamestra Species 0.000 description 1
- 241000555303 Mamestra brassicae Species 0.000 description 1
- 241000256010 Manduca Species 0.000 description 1
- 241001575018 Matsumuraeses Species 0.000 description 1
- 241000824682 Melanagromyza Species 0.000 description 1
- JCYZMTMYPZHVBF-UHFFFAOYSA-N Melarsoprol Chemical compound NC1=NC(N)=NC(NC=2C=CC(=CC=2)[As]2SC(CO)CS2)=N1 JCYZMTMYPZHVBF-UHFFFAOYSA-N 0.000 description 1
- 241001556396 Melipotes Species 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 241000243785 Meloidogyne javanica Species 0.000 description 1
- 241001268447 Meritastis Species 0.000 description 1
- 241001268438 Merophyas Species 0.000 description 1
- 241000486479 Mesapamea Species 0.000 description 1
- 241000486426 Mesogona Species 0.000 description 1
- 241001637853 Mesoleuca Species 0.000 description 1
- 241001585497 Metanema Species 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 241001340883 Metzneria Species 0.000 description 1
- 241001531279 Mnesictena Species 0.000 description 1
- 241000237852 Mollusca Species 0.000 description 1
- 241000555285 Monomorium Species 0.000 description 1
- 241000197310 Monopsis Species 0.000 description 1
- 241001585490 Morrisonia Species 0.000 description 1
- 240000005561 Musa balbisiana Species 0.000 description 1
- 241000257229 Musca <genus> Species 0.000 description 1
- 241000063939 Myelois Species 0.000 description 1
- 241001477928 Mythimna Species 0.000 description 1
- 241000721623 Myzus Species 0.000 description 1
- 241000566515 Nedra Species 0.000 description 1
- 241001340913 Nemapogon Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- 241000406465 Neodiprion Species 0.000 description 1
- 241001605621 Nephelodes Species 0.000 description 1
- 241001671714 Nezara Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 241001556090 Nilaparvata Species 0.000 description 1
- 241000270882 Niphonympha Species 0.000 description 1
- 241001585712 Noctua Species 0.000 description 1
- 241001585714 Nola Species 0.000 description 1
- 241000150800 Nudaurelia Species 0.000 description 1
- 241001585701 Ochropleura Species 0.000 description 1
- 241000207836 Olea <angiosperm> Species 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 241000566511 Oncocnemis Species 0.000 description 1
- 241001440153 Ophisma Species 0.000 description 1
- 241000661265 Opogona Species 0.000 description 1
- 241001440151 Oraesia Species 0.000 description 1
- 241001465800 Orgyia Species 0.000 description 1
- 241001465829 Orseolia Species 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 241000131102 Oryzaephilus Species 0.000 description 1
- 241001157806 Oscinella Species 0.000 description 1
- 241000975417 Oscinella frit Species 0.000 description 1
- 241001147397 Ostrinia Species 0.000 description 1
- 241000131737 Otiorhynchus Species 0.000 description 1
- 241000863932 Ourapteryx Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000840198 Pachetra Species 0.000 description 1
- 241001585670 Paleacrita Species 0.000 description 1
- 241001575015 Pammene Species 0.000 description 1
- 241001441428 Pandemis Species 0.000 description 1
- 241000318678 Panemeria Species 0.000 description 1
- 241000486437 Panolis Species 0.000 description 1
- 241000488585 Panonychus Species 0.000 description 1
- 240000001090 Papaver somniferum Species 0.000 description 1
- 235000008753 Papaver somniferum Nutrition 0.000 description 1
- 241000486435 Paradiarsia Species 0.000 description 1
- 241000885974 Paranthrene Species 0.000 description 1
- 241001351428 Parapediasia Species 0.000 description 1
- 241000517325 Pediculus Species 0.000 description 1
- 241000721454 Pemphigus Species 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 241001408683 Peribatodes Species 0.000 description 1
- 241001013845 Peridroma Species 0.000 description 1
- 241000238661 Periplaneta Species 0.000 description 1
- 241000011421 Perizoma Species 0.000 description 1
- 244000025272 Persea americana Species 0.000 description 1
- 235000008673 Persea americana Nutrition 0.000 description 1
- 241001579274 Pexicopia Species 0.000 description 1
- 241000256497 Phalonia Species 0.000 description 1
- 241001338668 Phalonidia Species 0.000 description 1
- 241001575054 Phaneta Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241001582372 Phragmatobia Species 0.000 description 1
- 241001439020 Phthorimaea Species 0.000 description 1
- 241001525543 Phyllocnistis Species 0.000 description 1
- 241000497193 Phyllocoptruta Species 0.000 description 1
- 241000497192 Phyllocoptruta oleivora Species 0.000 description 1
- 241000255972 Pieris <butterfly> Species 0.000 description 1
- 241000907661 Pieris rapae Species 0.000 description 1
- 241000690748 Piesma Species 0.000 description 1
- 235000016761 Piper aduncum Nutrition 0.000 description 1
- 240000003889 Piper guineense Species 0.000 description 1
- 235000017804 Piper guineense Nutrition 0.000 description 1
- 235000008184 Piper nigrum Nutrition 0.000 description 1
- 241000193804 Planococcus <bacterium> Species 0.000 description 1
- 241000918702 Planotortrix Species 0.000 description 1
- 241000278587 Platyedra Species 0.000 description 1
- 241001608845 Platynota Species 0.000 description 1
- 241001105494 Platyptilia Species 0.000 description 1
- 241000595626 Plodia Species 0.000 description 1
- 241001363501 Plusia Species 0.000 description 1
- 241000500439 Plutella Species 0.000 description 1
- 241000885673 Podosesia Species 0.000 description 1
- 241001582367 Polia Species 0.000 description 1
- 208000000474 Poliomyelitis Diseases 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000486397 Polymixis Species 0.000 description 1
- 241000952080 Polyphagotarsonemus Species 0.000 description 1
- 241000952063 Polyphagotarsonemus latus Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000193943 Pratylenchus Species 0.000 description 1
- DTAPQAJKAFRNJB-UHFFFAOYSA-N Promecarb Chemical compound CNC(=O)OC1=CC(C)=CC(C(C)C)=C1 DTAPQAJKAFRNJB-UHFFFAOYSA-N 0.000 description 1
- 241001257035 Proselena Species 0.000 description 1
- 241000912702 Proserpinus Species 0.000 description 1
- 235000005805 Prunus cerasus Nutrition 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 241001573780 Pseudohermenias Species 0.000 description 1
- 241001415024 Psocoptera Species 0.000 description 1
- 241001649229 Psoroptes Species 0.000 description 1
- 241000526145 Psylla Species 0.000 description 1
- 241001256461 Pterophorus Species 0.000 description 1
- 241000220302 Ptycholoma Species 0.000 description 1
- 241001340896 Pyralis Species 0.000 description 1
- 241001590455 Pyrausta Species 0.000 description 1
- 239000005663 Pyridaben Substances 0.000 description 1
- 239000005926 Pyridalyl Substances 0.000 description 1
- 239000005927 Pyriproxyfen Substances 0.000 description 1
- 241000345276 Raphia <palm> Species 0.000 description 1
- 241000722251 Rhodnius Species 0.000 description 1
- 241001201821 Rhopobota Species 0.000 description 1
- 241001322324 Rhyacia Species 0.000 description 1
- 241001575051 Rhyacionia Species 0.000 description 1
- 241001510241 Rhyparobia Species 0.000 description 1
- 241001510236 Rhyparobia maderae Species 0.000 description 1
- 241001667664 Rondotia Species 0.000 description 1
- 240000007651 Rubus glaucus Species 0.000 description 1
- 241000004261 Sabulodes Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000902402 Sahlbergella Species 0.000 description 1
- 241000256008 Samia Species 0.000 description 1
- 241000669155 Sannina Species 0.000 description 1
- 241000509416 Sarcoptes Species 0.000 description 1
- 241001515838 Schinia Species 0.000 description 1
- 241000722272 Schizaphis Species 0.000 description 1
- 241001486234 Sciota Species 0.000 description 1
- 241001529553 Scoparia <angiosperm> Species 0.000 description 1
- 241001491813 Scopula Species 0.000 description 1
- 241001400584 Scotogramma Species 0.000 description 1
- 241001341012 Scrobipalpa Species 0.000 description 1
- 241000713246 Scrobipalpopsis Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 241001574948 Sereda Species 0.000 description 1
- 241000931987 Sesamia Species 0.000 description 1
- 241000842763 Sesia Species 0.000 description 1
- 241001369138 Sicya Species 0.000 description 1
- 241001369140 Sideridis Species 0.000 description 1
- 241000258242 Siphonaptera Species 0.000 description 1
- 241000252792 Smerinthus Species 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical group [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 241001492664 Solenopsis <angiosperm> Species 0.000 description 1
- 241000511902 Sophronia Species 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- 240000003829 Sorghum propinquum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 241001601122 Spaelotis Species 0.000 description 1
- 241001362569 Spatalistis Species 0.000 description 1
- 241000252794 Sphinx Species 0.000 description 1
- 235000009337 Spinacia oleracea Nutrition 0.000 description 1
- 244000300264 Spinacia oleracea Species 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- 241000256250 Spodoptera littoralis Species 0.000 description 1
- 241000063068 Stagmatophora Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 241001494139 Stomoxys Species 0.000 description 1
- 241001574946 Strophedra Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241001256523 Syllomatia Species 0.000 description 1
- 241000004263 Synaxis Species 0.000 description 1
- 241001338738 Syncopacma Species 0.000 description 1
- 241001341020 Syndemis Species 0.000 description 1
- 241001363660 Syngrapha Species 0.000 description 1
- 241000255626 Tabanus <genus> Species 0.000 description 1
- 241001256535 Taeniarchis Species 0.000 description 1
- 239000005937 Tebufenozide Substances 0.000 description 1
- 239000005658 Tebufenpyrad Substances 0.000 description 1
- 239000005939 Tefluthrin Substances 0.000 description 1
- 241000003955 Tehama Species 0.000 description 1
- 241001198495 Teleiodes Species 0.000 description 1
- 241000254105 Tenebrio Species 0.000 description 1
- 241000452415 Tethea Species 0.000 description 1
- 241001454294 Tetranychus Species 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 240000006474 Theobroma bicolor Species 0.000 description 1
- 241001575048 Thiodia Species 0.000 description 1
- 241000333694 Thyridopteryx Species 0.000 description 1
- 241000863814 Thyris Species 0.000 description 1
- 241000333689 Tineola Species 0.000 description 1
- 241000131345 Tipula <genus> Species 0.000 description 1
- 241001369313 Tortricidia Species 0.000 description 1
- 241000242541 Trematoda Species 0.000 description 1
- 241000018135 Trialeurodes Species 0.000 description 1
- 241001414833 Triatoma Species 0.000 description 1
- 241000214545 Triaxomera Species 0.000 description 1
- 241000254086 Tribolium <beetle> Species 0.000 description 1
- 241001220308 Trichodorus Species 0.000 description 1
- 241000255985 Trichoplusia Species 0.000 description 1
- 241001255746 Trichoptilus Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000005942 Triflumuron Substances 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 1
- 241001414858 Trioza Species 0.000 description 1
- 241000462092 Trioza erytreae Species 0.000 description 1
- 241000284460 Triphosa Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000267823 Trogoderma Species 0.000 description 1
- 241000789056 Tyria Species 0.000 description 1
- 241001201507 Udea Species 0.000 description 1
- 241000669245 Unaspis Species 0.000 description 1
- 241000368303 Unaspis citri Species 0.000 description 1
- 244000078534 Vaccinium myrtillus Species 0.000 description 1
- 241000360034 Virbia Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 241000885980 Vitacea Species 0.000 description 1
- 241001201488 Vitula Species 0.000 description 1
- 241001408667 Xanthorhoe Species 0.000 description 1
- 240000001781 Xanthosoma sagittifolium Species 0.000 description 1
- 241001582681 Xanthotype Species 0.000 description 1
- 241001605585 Xestia Species 0.000 description 1
- 241001582722 Xylena Species 0.000 description 1
- 241001466337 Yponomeuta Species 0.000 description 1
- 241001340997 Ypsolopha Species 0.000 description 1
- 241001523432 Zale Species 0.000 description 1
- 241001078316 Zeiraphera Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 241000842515 Zygaena Species 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-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
- 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 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
- 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 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
- 229950008167 abamectin Drugs 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 description 1
- 229940022663 acetate Drugs 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- WRYNUJYAXVDTCB-UHFFFAOYSA-M acetyloxymercury Chemical compound CC(=O)O[Hg] WRYNUJYAXVDTCB-UHFFFAOYSA-M 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
- 239000013543 active substance Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005910 alkyl carbonate group Chemical group 0.000 description 1
- 125000005011 alkyl ether group Chemical group 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960002587 amitraz Drugs 0.000 description 1
- 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 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 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
- ONHBDDJJTDTLIR-UHFFFAOYSA-N azocyclotin Chemical compound C1CCCCC1[Sn](N1N=CN=C1)(C1CCCCC1)C1CCCCC1 ONHBDDJJTDTLIR-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000021015 bananas Nutrition 0.000 description 1
- 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 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
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- BCOZLGOHQFNXBI-UHFFFAOYSA-M benzyl-bis(2-chloroethyl)-ethylazanium;bromide Chemical compound [Br-].ClCC[N+](CC)(CCCl)CC1=CC=CC=C1 BCOZLGOHQFNXBI-UHFFFAOYSA-M 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 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 1
- 239000011230 binding agent Substances 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- ACBQROXDOHKANW-UHFFFAOYSA-N bis(4-nitrophenyl) carbonate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC(=O)OC1=CC=C([N+]([O-])=O)C=C1 ACBQROXDOHKANW-UHFFFAOYSA-N 0.000 description 1
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 description 1
- 235000021029 blackberry Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 239000001511 capsicum annuum Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 229960005286 carbaryl Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000012876 carrier material Substances 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
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000005056 cell body Anatomy 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019693 cherries Nutrition 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
- 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 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 1
- 229940089960 chloroacetate Drugs 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 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
- 235000017803 cinnamon Nutrition 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 208000012839 conversion disease Diseases 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 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
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 1
- 229950000775 cyromazine Drugs 0.000 description 1
- 208000031513 cyst Diseases 0.000 description 1
- 238000004163 cytometry Methods 0.000 description 1
- 229960002483 decamethrin Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 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 1
- WEBQKRLKWNIYKK-UHFFFAOYSA-N demeton-S-methyl Chemical compound CCSCCSP(=O)(OC)OC WEBQKRLKWNIYKK-UHFFFAOYSA-N 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
- 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 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 229940120124 dichloroacetate Drugs 0.000 description 1
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
- 229950001327 dichlorvos Drugs 0.000 description 1
- VEENJGZXVHKXNB-VOTSOKGWSA-N dicrotophos Chemical compound COP(=O)(OC)O\C(C)=C\C(=O)N(C)C VEENJGZXVHKXNB-VOTSOKGWSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 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 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-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
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 244000079386 endoparasite Species 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
- 230000002255 enzymatic effect Effects 0.000 description 1
- 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 1
- 230000012173 estrus Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 125000005313 fatty acid group Chemical group 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
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229940013764 fipronil Drugs 0.000 description 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 description 1
- 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 1
- FGIVSGPRGVABAB-UHFFFAOYSA-N fluoren-9-ylmethyl hydrogen carbonate Chemical compound C1=CC=C2C(COC(=O)O)C3=CC=CC=C3C2=C1 FGIVSGPRGVABAB-UHFFFAOYSA-N 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical class O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 229940044170 formate Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 1
- 125000005347 halocycloalkyl group Chemical group 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 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 1
- 238000011141 high resolution liquid chromatography Methods 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 210000003000 inclusion body Anatomy 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 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
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000005910 lambda-Cyhalothrin Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 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
- 239000003120 macrolide antibiotic agent Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229960000453 malathion Drugs 0.000 description 1
- 240000004308 marijuana Species 0.000 description 1
- 238000004949 mass spectrometry Methods 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 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
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical class COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-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
- 235000010460 mustard Nutrition 0.000 description 1
- ZUHZZVMEUAUWHY-UHFFFAOYSA-N n,n-dimethylpropan-1-amine Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940079888 nitenpyram Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 125000005547 pivalate group Chemical group 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical class [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 1
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 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 1
- 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 1
- GWKKVWOEQGDUSY-UHFFFAOYSA-N pyridine;sodium Chemical compound [Na].C1=CC=NC=C1 GWKKVWOEQGDUSY-UHFFFAOYSA-N 0.000 description 1
- GGZRVXCSRWTOME-UHFFFAOYSA-N pyridine;toluene Chemical compound C1=CC=NC=C1.CC1=CC=CC=C1 GGZRVXCSRWTOME-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
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 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 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 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
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008117 stearic acid Chemical class 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 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 1
- 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 1
- 229950004921 temefos Drugs 0.000 description 1
- 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 1
- FGTJJHCZWOVVNH-UHFFFAOYSA-N tert-butyl-[tert-butyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)O[Si](C)(C)C(C)(C)C FGTJJHCZWOVVNH-UHFFFAOYSA-N 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- 229940066528 trichloroacetate Drugs 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical class OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-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
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Biotechnology (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
nは0又は1であり;
A−Bは−CH=CH−又は−CH2−CH2−であり;
R1はC1〜C12−アルキル、C3〜C8−シクロアルキル又はC2〜C12−アルケニルであり;
R2はC1〜C12−アルキル、C2〜C12−アルケニル、C2〜C12−アルキニルである;又はC1〜C12−アルキル、C2〜C12−アルケニルもしくはC2〜C12−アルキニルであり、それらは1〜5個の置換により置換されており、その置換基は、OH、ハロゲン、CN、−N3、−NO2、C3〜C8−シクロアルキル(任意に1〜3個のC1〜C6−アルキル基で置換されている)、C3〜C8−シクロアルケニル(任意に1〜3個のC1〜C6−アルキル基で置換されている)、ノルボルニレニル(norbornylenyl)、C3〜C8−ハロシクロアルキル、C1〜C12−アルコキシ、C1〜C6−アルコキシ−C1〜C6−アルコキシ、C3〜C8−シクロアルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C3〜C8−シクロアルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C12−アルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−ハロアルキルスルフィニル、C3〜C8−ハロシクロアルキルスルフィニル、C1〜C12−アルキルスルホニル、C3〜C8−シクロアルキルスルホニル、C1〜C12−ハロアルキルスルホニル、C3〜C8−ハロシクロアルキルスルホニル、−NR4R6、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、−P(=O)(OC1〜C6−アルキル)2、アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシからなる群から選択されており;ここで当該アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロサイクリルオキシ基は任意に、環上での置換の可能性に依存して、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、Si(C1〜C12−アルキル)3、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、アリール、アリールオキシ、ヘテロサイクリル及びヘテロシクリルオキシから選択された1〜5個の置換基により置換されている;又は
R2はアリール、ヘテロシクリルC3〜C8−シクロアルキル、C3〜C8−シクロアルケニルである;又はアリール、ヘテロシクリルC3〜C8−シクロアルキルもしくはC3〜C8−シクロアルケニルであり、それらは任意に環上での置換の可能性に依存して、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、ジメチルアミノ−C1〜C6−アルコキシ、C2〜C8−アルケニル、C2〜C8−アルキニル、メチレンジオキシ、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシから選択された1〜5個の置換基で置換されており;
R3はH、C1〜C12−アルキル又はC1〜C12−アルキル(OH、ハロゲン、CN、−N3、−NO2から選択された1〜5個の置換基で置換されている);C3〜C8−シクロアルキル(任意に1〜3個のC1〜C6−アルキル基で置換されている);ノルボルニレニル−;C3〜C8−シクロアルケニル(任意に1〜3個のメチル基で置換されている);C3〜C8−ハロシクロアルキル、C1〜C12−アルコキシ、C1〜C6−アルコキシ−C1〜C6−アルコキシ、C3〜C8−シクロアルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C3〜C8−シクロアルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C12−アルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−ハロアルキルスルフィニル、C3〜C8−ハロシクロアルキルスルフィニル、C1〜C12−アルキルスルホニル、C3〜C8−シクロアルキルスルホニル、C1〜C12−ハロアルキルスルホニル、C3〜C8−ハロシクロアルキルスルホニル、−NR4R6、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、−P(=O)(OC1〜C6−アルキル)2、アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシであり;ここで当該アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシ基は任意に、環上での置換の可能性に依存して、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、Si(C1〜C12−アルキル)3、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシからなる群から選択された1〜5個の置換基により任意に置換されており;又は
R2とR3は一緒になって3〜7員のアルキレン架橋又は4〜7員のアルケニレン架橋であり、ここで1又は2個のCH2−基は互いに独立して基−C(=O)−、−C(=S)−、O、S、−NR5−、−OC(=O)−O−、−OC(=O)S−、−OC(=O)N(R5)−、−C(=O)O−、−C(=O)S−、−C(=O)N(R5)−、−N(R5)C(=O)S−、−N(R5)C(=O)N(R5)−からなる群から選択された置換基によって置換されていてもよく、そしてここで当該アルキレン又はアルケニレン架橋は互いに独立してC1〜C4−アルキル(任意に、OH、ハロゲン、CN、NO2、−N3及びC1〜C4−アルコキシからなる群から選択された1〜5個の置換基で置換されてもよい)からなる群から選択された1又は2個の置換基で置換されていてもよく;
XはO、NR5又は結合であり;
YはO又はSであり;
ZはO、S又はNR5であり;
R4はH、C1〜C12−アルキル(ハロゲン、ヒドロキシ、C1〜C6−アルコキシ及びCNからなる群から選択された1〜5個の置換基で置換されている);C2〜C8−アルケニル、C2〜C8−アルキニル、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキル;又はアリール、ヘテロシクリル、アリール−C1〜C12−アルキル又はヘテロシクリル−C1〜C12−アルキルであり、それらは置換の可能性に依存して、環中、任意にハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキル及びC1〜C6−ハロアルコキシから選択される1〜5個の置換基で置換されており;
R5はH、C1〜C8−アルキル、C3〜C8−シクロアルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、ベンジル又は−C(=O)−C1〜C12−アルキルであり;
R6はH、C1〜C12−アルキル(任意にハロゲンで置換されている)、C1〜C6−アルコキシ、CN、C2〜C8−アルケニル、C2〜C8−ハロアルケニル、C2〜C8−アルキニル、C1〜C12−ハロアルケニル、−X−C(=Y)−R9、−X−C(=Y)−Z−R9、−SO2−R9、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキルである;又はアリール、ヘテロシクリル、アリール−C1〜C12−アルキル又はヘテロシクリル−C1〜C12−アルキルであり、それらは、環中での置換の可能性に依存して、任意にハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキルもしくはC1〜C6−ハロアルコキシから選択された1〜5個の置換基で置換されている;又は
R4とR6は一緒になって3〜5員のアルキレン架橋であり、ここでメチレン基の1つがO、S又はSO2によって置換されていてもよく;そして
R9はH、C1〜C12−アルキル(ハロゲン、ヒドロキシ、C1〜C6−アルコキシ及びCNからなる群から選択された1〜5個の置換基によって置換されている);C2〜C8−アルケニル、C2〜C8−アルキニル、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキルである;又はアリール、ヘテロシクリル、アリール−C1〜C12−アルキルもしくはヘテロシクリル−C1〜C12−アルキルであり、それらは、置換の可能性に依存して、環中、任意に、ハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキル及びC1〜C6−ハロアルコキシからなる群から選択された1〜5個の置換基で置換されている);
の化合物、及び、該当する場合には、E/Z異性体、E/Z異性体及び/又は互変異性体の混合物に関する。これらは何れも遊離形態でも塩形態でもよい。
R2は、1つの置換基で置換されたC1〜C8−アルキルであり、前記置換基は、C3〜C8−シクロアルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C12−アルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−ハロアルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−アルキルスルホニル、C3〜C8−シクロアルキルスルホニル、C1〜C12−ハロアルキルスルホニル、C3〜C8ハロシクロアルキルスルホニル、−NR4R6、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、−P(=O)(OC1〜C6アルキル)2からなる群から選択される、式(I)の群(1)〜(4)のいずれか1つの化合物。
(A)式:
の化合物(これは公知であるか、又は実質的に公知の方法で調製し得る)と、
式:
の化合物(これは公知であるか、又は実質的に公知の方法で調製し得る)を反応させ、
式:
の化合物を形成させ;
(B)得られた式(IV)の化合物の保護基Qを除去することを含んで成る。
(C)式(II)の化合物と、式:
の化合物を反応させることを含んで成る。
溶媒及び希釈剤としては:芳香族、脂肪族及び脂環式の炭化水素及び水素化された炭化水素の例えば、ベンゼン、トルエン、キシレン、メシチレン、テトラリン、クロロベンゼン、ジクロロベンゼン、ブロモベンゼン、石油エーテル、ヘキサン、シクロヘキサン、ジクロロメタン、トリクロロメタン、テトラクロロメタン、ジクロロエタン、トリクロロエタン又はテトラクロロエタン;エーテルの例えば、ジエチルエーテル、ジイソプロピルエーテル、ジイソプロピルエーテル、ジブチルエーテル、tert−ブチルメチルエーテル、エチレングリコールモノメチルエーテル、エチレングリコールモノメチルエーテル、エチレングリコールジメチルエーテル、ジメトキシジエチルエーテル、テトラヒドロフラン又はジオキサン;カルボン酸のエステルの例えば、酢酸エチル;アミドの例えばジメチルホルムアミド、ジメチルアセトアミド又は1−メチル−2−ピロリドン;ニトリルの例えばアセトニトリル;スルホキシドの例えばジメチルスルホキシド;又は例に挙げた溶媒の混合物が挙げられる。アミドの例えば、ジメチルホルムアミド及びジメチルアセトアミド、特にジメチルアセトアミドが好適である。
溶媒及び希釈剤の例は、変法Aで挙げたものと同じである。尚、アルコールの例えばメタノール、エタノール又は2−プロパノール、及び水が適切である。
溶媒及び希釈剤の例は、変法Aの下に挙げたものと同じである。
溶媒及び希釈剤の例は、変法Aの下に挙げたものと同じである。
ポモネラ(Cydiapomonella)、シンバラフォーラ(Cymbalophora)spp.、ダクチレトーラ(Dactylethra)spp.、ダクス(Dacus)spp.、ダヂカ(Dadica)spp.、ダマリネア(Damalinea)spp.、ダシキラ(Dasychira)spp.、デカダルキス(Decadarchia)spp.、デコデス(Decodes)spp.、デイレフィラ(Deilephila)spp.、デルトデス(Deltodes)spp.、デンドロリマス(Dendrolimus)spp.、デプレサリア(Depressaria)spp.、デルメステス(Dermestes)spp.、デルマニサス(Dermanyssus)spp.、デルマニサス・ガリナエ(Dermanyssusgallinae)、ジアブロチカ(Diabrotica)spp.、ジアクリシア(Diachrysia)spp.、ジアファニア(Diaphania)spp.、ジアルシア(Diarsia)spp.、ジアセミア(Diasemia)spp.、ジアトレアエア(Diatraea)spp.、ジクレラトウラ(Diceratura)spp.、ジクロメリス(Dichomeris)spp.、ジクロクロシス(Dichrocrocis)spp.、ジクロランファ(Dichrorampha)spp.、ジシクラ(Dicycla)spp.、ジオリクトリア(Dioryctria)spp.、ジパロプシス(Diparopsis)spp.、ジパロプシス・カスタネア(Diparopsiscastanea)、ジプレウリナ(Dipleurina)spp.、ジプリオン(Diprion)spp.、ジプリオニダエ(Diprionidae)、ジスセストリア(Discestra)spp.、ジスタンチエラ(Distantiella)spp.、ジスタンチエラ・テオブロマ(Distantiellatheobroma)、ジツラ(Ditula)spp.、ジウルネア(Diurnea)spp.、ドラトプテリクス(Doratopteryx)spp.、ドレパナ(Drepana)spp.、ドロスフィラ(Drosphila)spp.、ドロスフィラ・メラノガスター(Drosphilamelanogaster)、ジサウセス(Dysauxes)spp.、ジスデルカス(Dysdercus)spp.、ジストローマ(Dysstroma)spp.、エナ(Eana)spp.、エアリアス(Earias)spp.、エクリチカ(Ecclitica)spp.、エクジトローファ(Ecdytolopha)spp.、エクピルロルロエ(Ecpyrrhorrhoe)spp.、エクトミエロイス(Ectomyelois)spp.、イエトロピス(Eetropis)spp.、エジラ(Egira)spp.、エマスモパルパス(Elasmopalpus)spp.、エメリア(Emmelia)spp.、ムポアスカ(mpoasca)spp.、エンピレウマ(Empyreuma)spp.、エナルジア(Enargia)spp.、エナルモニア(Enarmonia)spp.、エンドピザ(Endopiza)spp.、エンドテニア(Endothenia)spp.、エンドトリキア(Endotricha)spp.、エオレウマ(Eoreuma)spp.、エオテトラニクス(Eotetranychus)spp.、エオテトラニクス・カルピニ(Eotetranychuscarpini)、エパゴゲ(Epagoge)spp.、エペリス(Epelis)spp.、エフェスチア(Ephestia)spp.、エフェスチオデス(Ephestiodes)spp.、エピブレマ(Epiblema)spp.、エピエホリストデス(Epiehoristodes)spp.、エピノチア(Epinotia)spp.、エピフィラス(Epiphyas)spp.、エピプレマ(Epiplema)spp.、エピプセスチス(Epipsestis)spp.、エピルロエ(Epirrhoe)spp.、エピシマス(Episimus)spp.、エピチムビア(Epitymbia)spp.、エプラキナ(Epllachna)spp.、エラニス(Erannis)spp.、エラストリア(Erastria)spp.、エレムナス(Eremnus)spp.、エレウネチス(Ereunetis)spp.、エリオフィエス(Eriophyes)spp.、エリオソーマ(Eriosoma)spp.、エリオソーマ・ラニゲラム(Eriosomalanigerum)、エリトロネウラ(Erythroneura)spp.、エスチグメン(Estigmene)spp.、エトミア(Ethmia)spp.、エチエラ(Etiella)spp.、エウアグロチス(Euagrotis)spp.、エウコスマ(Eucosma)spp.、エウヘラエナ(Euehlaena)spp.、エウエリジア(Euelidia)spp.、エウエノソーマ
(Eueosma)spp.、エウキスタス(Euchistus)spp.、エウコスモモルファ(Eucosmomorpha)spp.、エウドニア(Eudonia)spp.、エウフィドニア(Eufidonia)spp.、エウフィポノメウトイデス(Euhyponomeutoides)spp.、エウレピトデス(Eulepitodes)spp.、エウリア(Eulia)spp.、エウリチス(Eulithis)spp.、エウピテシア(Eupithecia)spp.、エウプレシア(Euplexia)spp.、エウポエシリア(Eupoecilia)spp.、エウポエシリア・アンビグエア(Eupoeciliaambiguella)、エウプロクチス(Euproctis)spp.、エウプシリア(Eupsilia)spp.、エルホドープ(Eurhodope)spp.、エウロイス(Eurois)spp.、エウリガスター(Eurygaster)spp.、エウリトミア(Eurythmia)spp.、エウストロチア(Eustrotia)spp.、エウキソア(Euxoa)spp.、エウゾフィーラ(Euzophera)spp.、エベルゲスチス(Evergestis)spp.、エビペ(Evippe)spp.、エクサルテマ(Exartema)spp.、ファニア(Fannia)spp.、ファロンタ(Faronta)spp.、フェルチア(Feltia)spp.、フィラチマ(Filatima)spp.、フィシア(Fishia)spp.、フランクリニエラ(Frankliniella)spp.、フミボチス(Fumibotys)spp.、ガエサ(Gaesa)spp.、ガスガルシア(Gasgardia)spp.、ガストロフィルス(Gastrophilus)spp.、ゲレチア(Gelechia)spp.、ギルピニア(Gilpinia)spp.、ギルピニア・ポリトーマ(Gilpiniapolytoma)、グロシナ(Glossina)spp.、グリフィプテリクス(Glyphipterix)spp.、グリフォデス(Glyphodes)spp.、グノリモスケミニ(Gnorimoschemini)spp.、ゴノドンタ(Gonodonta)spp.、ゴルチナ(Gortyna)spp.、グラシラリア(Gracillaria)spp.、グラファニア(Graphania)spp.、グラフォリタ(Grapholita)spp.、グラフォリザ(Grapholitha)spp.、グラビタルメタ(Gravitarmata)spp.、グレトケナ(Gretchena)spp.、グリセルダ(Griselda)spp.、グリロタルパ(Gryllotalpa)spp.、ジナエフォーラ(Gynaephora)spp.、グリプソノーマ(Gypsonoma)spp.、ハダ(Hada)spp.、ハエマトビヌス(Haematopinus)spp.、ハリシドータ(Halisidota)spp.、ハルピプテリクス(Harpipteryx)spp.、ハリシナ(Harrisina)spp.、ヘヂア(Hedya)spp.、ヘリコベルパ(Helicoverpa)spp.、ヘリフォバス(Heliophobus)spp.、ヘリオチス(Heliothis)spp.、ヘルラ(Hellula)spp.、ヘロトロパ(Helotropa)spp.、ヘマリス(Hemaris)spp.、ヘルシノトリプス(Hercinothrips)spp.、ヘルクリア(Herculia)spp.、ヘルモナッサ(Hermonassa)spp.、ヘテロゲネア(Heterogenea)spp.、ホロメリナ(Holomelina)spp.、ホマダウラ(Homadaula)spp.、ホモエオソーマ(Homoeosoma)spp.、ホモグラエア(Homoglaea)spp.、ホモハデナ(Homohadena)spp.、ホモナ(Homona)spp.、ホモノプシス(Homonopsis)spp.、ホプロカンンパ(Hoplocampa)spp.、ホプロドリナ(Hoplodrina)spp.、ホシノア(Hoshinoa)spp.、ヒクサローマ(Hxalomma)spp.、ヒドラエシア(Hydraecia)spp.、ヒドリオメナ(Hydriomena)spp.、ヒレス(Hyles)spp.、ヒロイカス(Hyloicus)spp.、ピパジルチス(Hypagyrtis)spp.、ヒパチマ(Hypatima)spp.、ヒパントリア(Hyphantria)spp.、ヒパントリア・クネア(Hyphantriacunea)、ヒポカーラ(Hypocala)spp.、ヒポコエナ(Hypocoena)spp.、ヒポデマ(Hypodema)spp.、ヒポボスカ(Hyppobosca)spp.、ヒプシピラ(Hypsipyla)spp.、ヒシア(Hyssia)spp.、ヒステロシア(Hysterosia)spp.、イダエア(Idaea)spp.、イヂア(Idia)spp.、イピモルファ(Ipimorpha)spp.、イシア(Isia)spp.、イソコリスタ(Isochorista)spp.、イソフリクチス(Isophrictis)spp.、イソポリア(Isopolia)spp.、イソトリアス(Isotrias)spp.、イクソデス(Ixodes)spp.、イタメ(Itame)spp.、ジョジア(Jodia)spp.、ジョジス(Jodis)spp.、カワベア(Kawabea)spp.、ケイフェリア(Keiferia)spp.、ケイフェリア・リコペルシセラ(Keiferialycopersicella)、ラブジア(Labdia)spp.、ラシニポリア(Lacinipolia)spp.、ランブジナ(Lambdina)spp.、ランプロトリトパ(Lamprothritpa)spp.、ラオデルファクス(Laodelphax)spp.、ラシウス(Lasius)spp.、ラスペイレシア(Laspeyresia)spp.、レプチノタルサ(Leptinotarsa)spp.、レプチノタルサ・デセムリネアタ(Leptinotarsadecemlineata)、レプトコリサ(Leptocorisa)spp.、レプトスタレス(Leptostales)spp.、レカニウム(Lecanium)spp.、レカニウム・コミ(Lecaniumcomi)、レピドサフェス(Lepidosaphes)spp.、レピスマ(Lepisma)spp.、レピスマ・サッカリナ(Lepismasaccharina)、レスモン(Lesmone)spp.、ルーカニア(Leucania)spp.、ルーシノデス(Leucinodes)spp.、ルーコファエア(Leucophaea)spp.、ルーコファエア・マデラエ(Leucophaeamaderae)、ルーコプテラ(Leucoptera)spp.、ルーコプテラ・シテラ(Leucopterascitella)、リノグナタス(Linognathus)spp.、リポセリス(Liposcelis)spp.、リソルホプトラス(Lissorhoptrus)spp.、リタコジア(Lithacodia)spp.、リトコレチス(Lithocolletis)spp.、リトモイア(Lithomoia)spp.、リトファン(Lithophane)spp.、リキソデッサ(Lixodessa)spp.、ロベシア(Lobesia)spp.、ロベシア・ボトラナ(Lobesiabotrana)、ロボフォーラ(Lobophora)spp.、ロクスタ(Locusta)spp.、ロマナルテス(Lomanaltes)spp.、ロモグラファ(Lomographa)spp.、ロクサグロチス(Loxagrotis)spp.、ロクソステージ(Loxostege)spp.、ルシリア(Lucilia)spp.、リマントリア(Lymantria)spp.、リムナエシア(Lymnaecia)spp.、リオネチア(Lyonetia)spp.、リリオミザ(Lyriomyza)spp.、マクドンノウジア(Macdonnoughia)spp.、マクラウゼータ(Macrauzata)spp.、マクロノクタ(Macronoctua)spp.、マクロシファス(Macrosiphus)spp.、マラコスマ(Malacosoma)spp.、マリアルファ(Maliarpha)spp.、マメストラ(Mamestra)spp.、マメストラ・ブラシアエ(Mamestrabrassicae)、マンドウカ(Manduca)spp.、マンドウカ・セクスタ(Manducasexta)、マラズミア(Marasmia)spp.、マルガリチア(Margaritia)spp.、マトラチネア(Matratinea)spp.、マツマラエセス(Matsumuraeses)spp.、メラナグロミザ(Melanagromyza)spp.、メリポテス(Melipotes)spp.、メリソプス(Melissopus)spp.、メリチア(Melittia)spp.、メロロンタ(Melolontha)spp.、メリスチス(Meristis)spp.、メリタスチス(Meritastis)spp.、メロフィアス(Merophyas)spp.、メサパメア(Mesapamea)spp.、メソゴナ(Mesogona)spp.、メソレウカ(Mesoleuca)spp.、メタネマ(Metanema)spp.、メテンドテニア(Metendothenia)spp.、メトズネリア(Metzneria)spp.、メカルジア(Micardia)spp.、ミクロコルセス(Microcorses)spp.、ミクロレオン(Microleon)spp.、ムネシクテナ(Mnesictena)spp.、モシス(Mocis)spp.、モニマ(Monima)spp.、モノクロア(Monochroa)spp.、モノモリウム(Monomorium)spp.、モノモリウム・ファラノイス(Monomoriumpharaonis)、モノプシス(Monopsis)spp.、モリソニア(Morrisonia)spp.、ムスカ(Musca)spp.、ムトゥウライア(Mutuuraia)spp.、ミエロイス(Myelois)spp.、ミチムナ(Mythimna)spp.、ミザス(Myzus)spp.、ナランガ(Naranga)spp.、ネドラ(Nedra)spp.、ネマポゴン(Nemapogon)spp.、ネオジプリオン(Neodiprion)spp.、ネオスファレロプテラ(Neosphaleroptera)spp.、ネフェロデス(Nephelodes)spp.、ネフォテチクス(Nephotettix)spp.、ネザラ(Nezara)spp.、ニラパルバータ(Nilaparvata)spp.、ニフォニンファ(Niphonympha)spp.、ニッポプチリア(Nippoptilia)spp.、ノクツア(Noctua)spp.、ノーラ(Nola)spp.、ノトセリア(Notocelia)spp.、ノトドンタ(Notodonta)spp.、ノダウレリア(Nudaurelia)spp.、オクロプレウラ(Ochropleura)spp.、オクネロストーマ(Ocnerostoma)spp.、オエストルス(Oestrus)spp.、オレトレウテス(Olethreutes)spp.、オリジア(Oligia)spp.、オリニジア(Olindia)spp.、オリゴニクス(Olygonychus)spp.、オリゴニクス・ガリナエ(Olygonychusgallinae)、オンコクネミス(Oncocnemis)spp.、オペロプテラ(Operophtera)spp.、オフィズマ(Ophisma)spp.、オポゴナ(Opogona)spp.、オラエシア(Oraesia)spp.、オルニオドロス(Orniodoros)spp.、オルジア(Orgyia)spp.、オリア(Oria)spp.、オルセオリア(Orseolia)spp.、オルトデス(Or
thodes)spp.、オルトゴニア(Orthogonia)spp.、オルトシア(Orthosia)spp.、オリザエフィルス(Oryzaephilus)spp.、オスシネラ(Oscinella)spp.、オスシネラ・フリト(Oscinellafrit)、オスミナ(Osminia)spp.、オストリナ(Ostrinia)spp.、オストリナ・ヌビラリス(Ostrinianubilalis)、オチオリンカス(Otiorhynchus)spp.、オウラプテリクス(Ourapteryx)spp.、パケトラ(Pachetra)spp.、パキスフィニクス(Pachysphinx)spp.、パジダ(Pagyda)spp.、パレアクリタ(Paleacrita)spp.、パリガ(Paliga)spp.、パルチス(Palthis)spp.、パメンセ(Pammene)spp.、パンデミス(Pandemis)spp.、パネメリア(Panemeria)spp.、パノリス(Panolis)spp.、パメリス・フラメア(Panolisflammea)、パノニカス(Panonychus)spp.、パラルジレスチア(Parargyresthia)spp.、パラジアルシア(Paradiarsia)spp.、パラロベシア(Paralobesia)spp.、パラントレン(Paranthrene)spp.、パラパンデミス(Parapandemis)spp.、パラペジアシア(Parapediasia)spp.、パラスチクチス(Parastichtis)spp.、パラシンデミス(Parasyndemis)spp.、パラトリア(Paratoria)spp.、パレロメメ(Pareromeme)spp.、ペクチノフォーラ(Pectinophora)spp.、ペクチノフォーラ・ゴッシピエラ(Pectinophoragossypiella)、ペジクルス(Pediculus)spp.、ペゴミア(Pegomyia)spp.、ペゴミア・ヒオシアミ(Pegomyiahyoscyami)、ペロクリスタ(Pelochrista)spp.、ペニセチア(Pennisetia)spp.、ペンステモニア(Penstemonia)spp.、ペンフィガス(Pemphigus)spp.、ペリバトデス(Peribatodes)spp.、ペリドロマ(Peridroma)spp.、ペリルウコプテラ(Perileucoptera)spp.、ペリプラネタ(Periplaneta)spp.、ペリゾーマ(Perizoma)spp.、ペトローバ(Petrova)spp.、ペキシコピア(Pexicopia)spp.、ファロニア(Phalonia)spp.、ファロニジア(Phalonidia)spp.、ファネタ(Phaneta)spp.、フリクタエニア(Phlyctaenia)spp.、フリクチヌス(Phlyctinus)spp.、フォルビア(Phorbia)spp.、ファラグマトビア(Phragmatobia)spp.、フィリカンテス(Phricanthes)spp.、フトリマエア(Phthorimaea)spp.、フトリマエア・オペルクレラ(Phthorimaeaoperculella)、フィロクニスチス(Phyllocnistis)spp.、フィロコプトルタ(Phyllocoptruta)spp.、フィロコプトルタ・オレイボーラ(Phyllocoptrutaoleivora)、フィロノリクテル(Phyllonorycter)spp.、フィロフィラ(Phyllophila)spp.、フィロキセラ(Phylloxera)spp.、ピエリス(Pieris)spp.、ピエリス・ラパエ(Pierisrapae)、ピエスマ(Piesma)spp.、プラノコッカス(Planococus)spp.、プラノトルトリクス(Planotortrix)spp.、プラチエドラ(Platyedra)spp.、プラチノータ(Platynota)spp.、プラチプチラ(Platyptilia)spp.、プラチセンタ(Platysenta)spp.、プロジア(Plodia)spp.、プルシア(Plusia)spp.、プルテラ(Plutella)spp.、プルテラ・キシロステラ(Plutellaxylostella)、ポドセシア(Podosesia)spp.、ポリア(Polia)spp.、ポピリア(Popillia)spp.、ポリミクシス(Polymixis)spp.、ポリファゴタルソネムス(Polyphagotarsonemus)spp.、ポリファゴタルソネムス・ラタス(Polyphagotarsonemuslatus)、プレイス(Prays)spp.、プリオノキシスタス(Prionoxystus)spp.、プロボール(Probole)spp.、プロセラス(Proceras)spp.、プロケロデス(Prochoerodes)spp.、プロエウリア(Proeulia)spp.、プロスキスチス(Proschistis)spp.、プロセレナ(Proselena)spp.、プロセルピヌ
ス(Proserpinus)spp.、プロタグロチス(Protagrotis)spp.、プロテオテラス(Proteoteras)spp.、プロトバスラ(Protobathra)spp.、プロトスキニア(Protoschinia)spp.、セロノフォラス(Pselnophorus)spp.、スーダレチア(Pseudaletia)spp.、スーダントモノムス(Pseudanthonomus)spp.、スーダンテルニア(Pseudaternelia)spp.、スーダウルアカスピス(Pseudaulacaspis)spp.、スーデクスセンテラ(Pseudexentera)spp.、スードコッカス(Pseudococus)spp.、スードヘルメニアス(Pseudohermenias)spp.、スードプルシア(Pseudoplusia)spp.、プソロプテス(Psoroptes)spp.、プシラ(Psylla)spp.、プシリオデス(Psylliodes)spp.、プテロフォロス(Pterophorus)spp.、プチコローマ(Ptycholoma)spp.、プルビナリア(Pulvinaria)spp.、プルビナリア・アエチオピカ(Pulvinariaaethiopica)、ピラリス(Pyralis)spp.、ピラウスタ(Pyrausta)spp.、ピルゴチス(Pyrgotis)spp.、ピルレフェラ(Pyrreferra)spp.、ピルハルクチア(Pyrrharctia)spp.、クアドラスピジオタス(Quadraspidiotus)spp.、ランコーラ(Rancora)spp.、ラピア(Raphia)spp.、レチクルテルメス(Reticultermes)spp.、レチニア(Retinia)spp.、ラゴレチス(Rhagoletis)spp.、ラゴレチス・ポモネラ(Rhagoletispomonella)、リピセファルス(Rhipicephalus)spp.、リゾグリフス(Rhizoglyphus)spp.、リゾペルタ(Rhizopertha)spp.、ロドニウス(Rhodnius)spp.、ロファロシフム(Rhophalosiphum)spp.、ロポボータ(Rhopobota)spp.、リアシア(Rhyacia)spp.、リアシオニア(Rhyacionia)spp.、リンコパチヤ(Rhynchopacha)spp.、リゾステネス(Rhyzosthenes)spp.、リブラ(Rivula)spp.、ロンドチア(Rondotia)spp.、ルシドリナ(Rusidrina)spp.、リンカグラエア(Rynchaglaea)spp.、サブロデス(Sabulodes)spp.、サヒルベルゲラ(Sahlbergella)spp.、サヒルベルゲラ・シングラリス(Sahlbergellasingularis)、サイセッチア(Saissetia)spp.、サミア(Samia)spp.、サンニマ(Sannina)spp.、サンニノイデア(Sanninoidea)spp.、サフォイデウス(Saphoideus)spp.、サルコプテス(Sarcoptes)spp.、サトロブロタ(Sathrobrota)spp.、スカラベイダエ(Scarabeidae)、セリオデス(Sceliodes)spp.、シヒニア(Schinia)spp.、シストセルカ(Schistocerca)spp.、シザフィス(Schizaphis)spp.、シズラ(Schizura)spp.、シェレケンステニア(Schreckensteinia)spp.、シアラ(Sciara)spp.、シロポファーガ(Scirpophaga)spp.、シルトリプス・アウランチ(Scirthripsauranti)、スコパリア(Scoparia)spp.、スコプーラ(Scopula)spp.、スコチア(Scotia)spp.、スコチノファーラ(Scotinophara)spp.、スコトグランマ(Scotogramma)spp.、スクロビパルパ(Scrobipalpa)spp.、スクロビパルポプシス(Scrobipalpopsis)spp.、セミオチサ(Semiothisa)spp.、セレダ(Sereda)spp.、セサミア(Sesamia)spp.、セシア(Sesia)spp.、シクヤ(Sicya)spp.、シデリジス(Sideridis)spp.、シミラ(Simyra)spp.、シネウグラフェ(Sineugraphe)spp.、シトコーラ(Sitochroa)spp.、シトビオン(Sitobion)spp.、シトフィルス(Sitophilus)spp.、シトトロガ(Sitotroga)spp.、ソレノプシス(Solenopsis)spp.、スメリンザス(Smerinthus)spp.、ソフロニア(Sophronia)spp.、スパエロチス(Spaelotis)spp.、スパルガローマ(Spargaloma)spp.、スパルガノチス(Sparganothis)spp.、スパタリスチス(Spatalistis)spp.、スペルキア(Sperchia)spp.、スペシア(Sphecia)spp.、スフィンクス(Sphinx)spp.、スピロノタ(Spilonota)spp.、スポドプテラ(Spodoptera)spp.、スポドプテラ・リットラリス(Spodopteralittoralis)、スタグマトフォーラ(Stagmatophora)spp.、スタフィリノコロウス(Staphylinochrous)spp.、スタトモポダ(Stathmopoda)spp.、ステノデス(Stenodes)spp.、ステルハ(Sterrha)spp.、ストモキシス(Stomoxys)spp.、ストロフェドラ(Strophedra)spp.、スニラ(Sunira)spp.、スチナ(Sutyna)spp.、スワメルダミア(Swammerdamia)spp.、シロマチア(Syllomatia)spp.、シンピスチス(Sympistis)spp.、シナンテドン(Synanthedon)spp.、シナクシス(Synaxis)spp.、シンコパクマ(Syncopacma)spp.、シンデミス(Syndemis)spp.、シングラファ(Syngrapha)spp.、シントメイダ(Synthomeida)spp.、タバヌス(Tabanus)spp.、タエニアルキス(Taeniarchis)spp.、タエニオトリプス(Taeniothrips)spp.、タニア(Tannia)spp.、タルソネムス(Tarsonemus)spp.、テグリフェラ(Tegulifera)spp.、テハマ(Tehama)spp.、テレイオデス(Teleiodes)spp.、テロルタ(Telorta)spp.、テネブリオ(Tenebrio)spp.、テフリナ(Tephrina)spp.、テラトグラエア(Teratoglaea)spp.、テリクーラ(Terricula)spp.、テチア(Tethea)spp.、テトラニクス(Tetranychus)spp.、タルフォフィラ(Thalpopila)spp.、タウメトポエア(Thaumetopoea)spp.、チオジア(Thiodia)spp.、トリプス(Thrips)spp.、トリプス・パルミ(Thripspalmi)、トリプス・タバキ(Thripstabaci)、チリドプテリクス(Thyridopteryx)spp.、チリス(Thyris)spp.、チネオラ(Tineola)spp.、チプラ(Tipula)spp.、トルトリシジア(Tortricidia)spp.、トルトリクス(Tortrix)spp.、トラキエア(Trachea)spp.、トリアレウロデス(Trialeurodes)spp.、トリアロウロデス・バポラリオラム(Trialeurodesvaporariorum)、トリアトーマ(Triatoma)spp.、トリアキソメラ(Triaxomera)spp.、トリボリウム(Tribolium)spp.、トリコデクテス(Tricodectes)spp.、トリコプルシア(Trichoplusia)spp.、トリコプルシア・ニ(Trichoplusiani)、トリコプチルス(Trichoptilus)spp.、トリオザ(Trioza)spp.、トリオザ・エリトレアエ(Triozaerytreae)、トリファエニア(Triphaenia)spp.、トリフォサ(Triphosa)spp.、トロゴデルマ(Trogoderma)spp.、チリア(Tyria)spp.、ウデア(Udea)spp.、ウナスピス(Unaspis)spp.、ウナスピス・シトリ(Unaspiscitri)、ウテテシア(Utetheisa)spp.、バレリオデス(Valeriodes)spp.、ベスパ(Vespa)spp.、ベスパミナ(Vespamima)spp.、ビタセア(Vitacea)spp.、ビツラ(Vitula)spp.、ウィトレシア(Witlesia)spp.、キサンチア(Xanthia)spp.、キサントロエ(Xanthorhoe)spp.、キサントタイプ(Xanthotype)spp.、キセノミクタ(Xenomicta)spp.、キセノフシラ(Xenopsylla)spp.、キセノフシラ・ケオプシス(Xenopsyllacheopsis)、キセスチア(Xestia)spp.、キシレナ(Xylena)spp.、キシロマイゲス(Xylomyges)spp.、キシロサリス(Xyrosaris)spp.、イポノメウタ(Yponomeuta)spp.、イプソロファ(Ypsolopha)spp.、ザレ(Zale)spp.、ザンクログナタス(Zanclognathus)spp.、ゼイラフェラ(Zeiraphera)spp.、ゼノドキサス(Zenodoxus)spp.、ゼウゼラ(Zeuzera)spp.、ジガエナ(Zygaena)spp.。
以下の例では、アベルメクチンB1誘導体(アベルメクチンB1a及びB1b誘導体の混合物)の調製を記す。混合物に対するB1b誘導体の比率は、通常は僅か5〜10重量%程度である。このため、NMRスペクトルでは通常、B1a誘導体の結合のみが検出される。
s:一重項、MHz:メガヘルツ、brs:ブロード一重項;t:三重項;m:多重項;d:二重項;J:総合定数;bd:ブロード二重項;LCMS:液体クロマトグラフィーマススペクトロメトリー;tRT:保持時間(min);M+H:質量ピーク+H;M+Na:質量ピーク+Naである。TBDMSは例中で基−Si(CH3)2(tert−ブチル)を示す。溶媒の混合比を体積部で与えている。「エーテル」とはジエチルエーテルと解される。
第一のエピマー:B1aC46H66O13,MW:826.5.LCMS:tRT,11.69min,827.5(M+H);849.3(M+Na).
第二のエピマー:B1aC46H66O13,MW:826.5.LCMS:tRT,10.94min,849.4(M+Na);844.5(M+NH4).
R1がイソプロピルである誘導体に関するHPLC分析の保持時間:13.40min
例B1:スポドプテラ・リットラリスに対する活性
若いダイズ植物に、12.5ppmの試験化合物を含んで成る水性エマルションスプレー混合物をスプレーし、その後、当該スプレーコーティングが乾いた後、当該植物にスポドプテラ・リットラリスのイモムシを10匹、第一段階において住まわせ、そしてプラスチック容器に置いた。3日後、集団の%減少及び摂食傷害の減少(%活性)を、処理した植物と処理しなかった植物上での死んだイモムシの数と摂食傷害を比較することによって決定した。
ダイズ苗を試験溶液に配置した。6日後、葉を切除し、ペトリ皿中の湿ったろ紙上に配置し、そして12〜15匹のスポドプテラ・リットラリスの幼虫をL1段階において感染させた。4日後、集団の%減少及び摂食傷害の減少(%活性)を、処理した植物と処理しなかった植物上での死んだイモムシの数と摂食傷害を比較することによって決定した。
30〜35個のヘリオチス・ビレセンスの卵(0〜24時間齢)をペトリ皿中人工栄養の層上のろ紙上に配置した。次いで0.8mlの試験溶液をこのろ紙上にピペットで滴下した。6日後に評価を行った。集団の%減少(%活性)を、処理した植物と処理しなかった植物上での死んだ卵と幼虫の数を比較することによって決定した。特に化合物1.5、1.6及び4.8がこの試験において80%を超える活性を示した。
若いキャベツ植物に、12.5ppmの試験化合物及びを含んで成る水性スプレー混合物をスプレーした。当該スプレーコーティングスプレーが乾いた後、当該キャベツ植物にプルテラ・キシロステラのイモムシを10匹、第一段階において住まわせ、そしてプラスチック容器に置いた。3日後に評価をした。集団の%減少及び摂食傷害の減少(%活性)を、処理した植物と処理しなかった植物上での死んだイモムシの数と摂食傷害を比較することによって決定した。
ダイズ苗に、12.5ppmの試験化合物を含んで成る水性エマルションスプレー混合物をスプレーし、その後、当該スプレーコーティングスプレーが乾いた後、当該ダイスにジアブロチカ・バルテアータの幼虫を10匹、第二段階において住まわせ、そしてプラスチック容器に置いた。6日後、集団の%減少(%活性)を、処理した植物と処理しなかった植物上での死んだイモムシの数と摂食傷害を比較した。
若いマメ植物に、テトラニクス・ウルチカエの混合集団を住まわせ、そして1日後、12.5ppmの試験化合物を含んで成る水性エマルションスプレー混合物をスプレーした。この植物を25℃で6日に渡りインキュベートし、その後評価した。集団の減少(%活性)を処理した植物と処理しなかった植物上での死んだ卵、幼虫及び成獣の数を比較することによって決定した。
Claims (7)
- 式(I)
nは、0又は1であり;
A−Bは、−CH=CH−又は−CH2−CH2−であり;
R1は、C1〜C12−アルキル、C3〜C8−シクロアルキル又はC2〜C12−アルケニルであり;
R2は、C1〜C12−アルキル、C2〜C12−アルケニルもしくはC2〜C12−アルキニル、又は、1〜5個の置換基により置換されたC1〜C12−アルキル、C2〜C12−アルケニルもしくはC2〜C12−アルキニルであり、前記の置換基は、OH、ハロゲン、CN、−N3、−NO2、任意に1〜3個のC1〜C6−アルキル基で置換されていてもよいC3〜C8−シクロアルキル、任意に1〜3個のC1〜C6−アルキル基で置換されていてもよいC3〜C8−シクロアルケニル、ノルボルニレニル(norbornylenyl)、C3〜C8−ハロシクロアルキル、C1〜C12−アルコキシ、C1〜C6−アルコキシ−C1〜C6−アルコキシ、C3〜C8−シクロアルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C3〜C8−シクロアルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C12−アルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−ハロアルキルスルフィニル、C3〜C8−ハロシクロアルキルスルフィニル、C1〜C12−アルキルスルホニル、C3〜C8−シクロアルキルスルホニル、C1〜C12−ハロアルキルスルホニル、C3〜C8−ハロシクロアルキルスルホニル、−NR4R6、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、−P(=O)(OC1〜C6−アルキル)2、アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシからなる群から選択され、前記のアリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシ基は、環が置換され得る場合には、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、Si(C1〜C12−アルキル)3、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシから選択される1〜5個の置換基により任意に置換されてもよく;又は
R2は、アリール、ヘテロシクリルC3〜C8−シクロアルキルもしくはC3〜C8−シクロアルケニル、又は、1〜5個の置換基により置換されたアリール、ヘテロシクリルC3〜C8−シクロアルキルもしくはC3〜C8−シクロアルケニルであり、前記の置換基は、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、ジメチルアミノ−C1〜C6−アルコキシ、C2〜C8−アルケニル、C2〜C8−アルキニル、メチレンジオキシ、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシから選択され;
R3は、H、C1〜C12−アルキル、又は、1〜5個の置換基で置換されたC1〜C12−アルキルであり、前記置換基は、OH、ハロゲン、CN、−N3、−NO2、1〜3個のC1〜C6−アルキル基で任意に置換されていてもよいC3〜C8−シクロアルキル、ノルボルニレニル−、1〜3個のメチル基で任意に置換されていてもよいC3〜C8−シクロアルケニル;C3〜C8−ハロシクロアルキル、C1〜C12−アルコキシ、C1〜C6−アルコキシ−C1〜C6−アルコキシ、C3〜C8−シクロアルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C3〜C8−シクロアルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C12−アルキルスルフィニル、C3〜C8−シクロアルキルスルフィニル、C1〜C12−ハロアルキルスルフィニル、C3〜C8−ハロシクロアルキルスルフィニル、C1〜C12−アルキルスルホニル、C3〜C8−シクロアルキルスルホニル、C1〜C12−ハロアルキルスルホニル、C3〜C8−ハロシクロアルキルスルホニル、−NR4R6、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、−P(=O)(OC1〜C6−アルキル)2、アリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシからなる群より選択され、前記のアリール、ヘテロシクリル、アリールオキシ、アリールチオ及びヘテロシクリルオキシ基は、環が置換され得る場合には、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、Si(C1〜C12−アルキル)3、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシからなる群から選択された1〜5個の置換基により任意に置換されていてもよく;又は
R2とR3とが一緒になって、3〜7員のアルキレン架橋、又は、4〜7員のアルケニレン架橋を形成し、ここで1又は2個のCH2−基が互いに独立に、基−C(=O)−、−C(=S)−、O、S、−NR5−、−OC(=O)−O、−OC(=O)S−、−OC(=O)N(R5)−、−C(=O)O−、−C(=O)S−、−C(=O)N(R5)−、−N(R5)C(=O)S−、−N(R5)C(=O)N(R5)−によって置換されていてもよく、前記のアルキレン又はアルケニレン架橋は互いに独立に、C1〜C4−アルキル、C1〜C4−アルコキシ及びC1〜C4ハロゲンアルキルからなる群から選択された1又は2個の置換基で置換されていてもよく;
Xは、O、NR5又は単結合であり;
Yは、O又はSであり;
Zは、O、S又はNR5であり;
R4は、H、ハロゲン、ヒドロキシ、C1〜C6−アルコキシ及びCNからなる群から選択された1〜5個の置換基で置換されていてもよいC1〜C12−アルキル;C2〜C8−アルケニル、C2〜C8−アルキニル、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキル;又は、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル又はヘテロシクリル−C1〜C12−アルキルであり、前記のアリール、ヘテロシクリル、アリール−C1〜C12−アルキル又はヘテロシクリル−C1〜C12−アルキルは、環が置換され得る場合には、ハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキル及びC1〜C6−ハロアルコキシからなる群より選択された1〜5個の置換基で置換されており;
R5は、H、C1〜C8−アルキル、C3〜C8−シクロアルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、ベンジル又は−C(=O)−C1〜C12−アルキルであり;
R6は、H、任意にハロゲンで置換されていてもよいC1〜C12−アルキル、C1〜C6−アルコキシ、CN、C2〜C8−アルケニル、C2〜C8−ハロアルケニル、C2〜C8−アルキニル、C1〜C12−ハロアルケニル、−X−C(=Y)−R9、−X−C(=Y)−Z−R9、−SO2−R9、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキル;又は、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル又はヘテロシクリル−C1〜C12−アルキルであり、それらは、環が置換され得る場合には、ハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキルもしくはC1〜C6−ハロアルコキシから選択された1〜5個の置換基で任意に置換されていてもよく;又は
R4とR6とが一緒になって、3〜5員のアルキレン架橋を形成し、ここでメチレン基の1つが、O、S又はSO2によって置換されていてもよく;
R9は、H、ハロゲン、ヒドロキシ、C1〜C6−アルコキシ及びCNからなる群から選択された1〜5個の置換基によって置換されていてもよいC1〜C12−アルキル;C2〜C8−アルケニル、C2〜C8−アルキニル、アリール、ヘテロシクリル、アリール−C1〜C12−アルキル、ヘテロシクリル−C1〜C12−アルキル;又はアリール、ヘテロシクリル、アリール−C1〜C12−アルキルもしくはヘテロシクリル−C1〜C12−アルキルであり、それらは、環が置換され得る場合には、ハロゲン、C1〜C6−アルコキシ、C1〜C6−ハロアルキル及びC1〜C6−ハロアルコキシからなる群から選択された1〜5個の置換基で任意に置換されていてもよい)
の化合物、及び、該当する場合には、E/Z異性体、E/Z異性体及び/又は互変異性体の混合物の、遊離形態又は塩形態であって;
但し、nが1であり、R3がHであり、R2が−CH2−CH2−OCH3又は−CH2−CH2−O−フェニルである場合、当該化合物はアベルメクチンB1誘導体ではなく;nが2であり、R3がHであり、R2が−CH2−CH2−O−フェニルである場合、当該化合物はB1a又はB1b誘導体ではなく;nが1であり、R2とR3が一緒になって無置換の−CH2−CH2−CH3−を形成する場合、当該化合物はB1a又はB1b誘導体ではなく;nが1であり、R3がHであり、R2が−CH2−CH2−OCH3である場合、当該化合物はB2a又はB2b誘導体ではない、化合物。 - 遊離形態である請求項1に記載の式(I)の化合物。
- R3がメチルである請求項1又は2に記載の式(I)の化合物。
- R3がC3〜C8−アルキルである請求項1又は2に記載の式(I)の化合物。
- R3が、1〜5個の置換基で置換されたC1〜C8−アルキルであり、前記置換基が、OH、ハロゲン、CN、−N3、−NO2;任意に1〜3個のC1〜C6−アルキル基で置換されていてもよいC3〜C8−シクロアルキル;ノルボルニレニル−;任意に1〜3個のメチル基で置換されていてもよいC3〜C8−シクロアルケニル;C3〜C8−ハロシクロアルキル、C3〜C8−シクロアルコキシ;C1〜C12−ハロアルコキシ;C1〜C12−アルキルチオ;アリール;ヘテロシクリル;アリールチオ又はヘテロシクリルオキシからなる群より選択され;当該アリール、ヘテロシクリル、アリールチオ及びヘテロサイクリルオキシ基は、環が置換され得る場合には、OH、ハロゲン、CN、NO2、C1〜C12−アルキル、C3〜C8−シクロアルキル、C1〜C12−ハロアルキル、C1〜C12−アルコキシ、C1〜C12−ハロアルコキシ、C1〜C12−アルキルチオ、C1〜C12−ハロアルキルチオ、C1〜C6−アルコキシ−C1〜C6−アルキル、C2〜C8−アルケニル、C2〜C8−アルキニル、Si(C1〜C12−アルキル)3、−X−C(=Y)−R4、−X−C(=Y)−Z−R4、アリール、アリールオキシ、ヘテロシクリル及びヘテロシクリルオキシからなる群から選択された1〜5個の置換基で任意に置換されていてもよい、請求項1又は2に記載の式(I)の化合物。
- 請求項1に記載の式(I)の化合物を1種類以上、活性化合物として含有すると共に、1種類以上の助剤を含有する農薬。
- 請求項6に記載の組成物を害虫又はその生息部位に施用する、害虫を抑制する方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0229804.0 | 2002-12-20 | ||
GBGB0229804.0A GB0229804D0 (en) | 2002-12-20 | 2002-12-20 | Avermection b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"- or 4'-position |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004561378A Division JP4851094B2 (ja) | 2002-12-20 | 2003-12-19 | アベルメクチンb1及び4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1モノサッカライド誘導体 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2011102303A true JP2011102303A (ja) | 2011-05-26 |
JP5302297B2 JP5302297B2 (ja) | 2013-10-02 |
Family
ID=9950151
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004561378A Expired - Lifetime JP4851094B2 (ja) | 2002-12-20 | 2003-12-19 | アベルメクチンb1及び4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1モノサッカライド誘導体 |
JP2010286151A Expired - Fee Related JP5302297B2 (ja) | 2002-12-20 | 2010-12-22 | 4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1及びアベルメクチンb1単糖誘導体 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004561378A Expired - Lifetime JP4851094B2 (ja) | 2002-12-20 | 2003-12-19 | アベルメクチンb1及び4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1モノサッカライド誘導体 |
Country Status (22)
Country | Link |
---|---|
US (3) | US7737261B2 (ja) |
EP (1) | EP1581546B1 (ja) |
JP (2) | JP4851094B2 (ja) |
KR (1) | KR101109500B1 (ja) |
CN (1) | CN1738828B (ja) |
AR (1) | AR042533A1 (ja) |
AU (1) | AU2003302284B2 (ja) |
BR (1) | BR0317601A (ja) |
CA (1) | CA2507774C (ja) |
CO (1) | CO5690647A1 (ja) |
ES (1) | ES2742899T3 (ja) |
GB (1) | GB0229804D0 (ja) |
IL (1) | IL169092A (ja) |
MA (1) | MA27646A1 (ja) |
MX (1) | MXPA05006036A (ja) |
PE (1) | PE20040713A1 (ja) |
PL (1) | PL211483B1 (ja) |
RU (1) | RU2330857C2 (ja) |
TW (1) | TW200512214A (ja) |
UA (1) | UA81281C2 (ja) |
WO (1) | WO2004056844A1 (ja) |
ZA (1) | ZA200504353B (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10518445B2 (en) | 2014-12-24 | 2019-12-31 | Ntn Corporation | Cage for rolling bearing, and rolling bearing |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0229804D0 (en) * | 2002-12-20 | 2003-01-29 | Syngenta Participations Ag | Avermection b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"- or 4'-position |
JP2010006703A (ja) * | 2006-11-07 | 2010-01-14 | Hokko Chem Ind Co Ltd | アベルメクチンモノ配糖体誘導体 |
RU2472801C1 (ru) * | 2011-05-11 | 2013-01-20 | Игорь Викторович Заварзин | 5-о-производные авермектина, способ их получения и антипаразитарные средства на их основе |
RU2453553C1 (ru) * | 2011-05-11 | 2012-06-20 | Игорь Викторович Заварзин | 5-о-сукциноилавермектин, способ его получения и антипаразитарное средство на его основе |
CN103613625B (zh) * | 2013-12-02 | 2016-03-02 | 兰州大学 | 一种阿维菌素类化合物及其制备方法和在农药中的用途 |
CN104402953B (zh) * | 2014-11-28 | 2017-07-28 | 大庆志飞生物化工有限公司 | 阿维菌素单糖化合物及其制备方法和用途 |
CN104402954A (zh) * | 2014-11-28 | 2015-03-11 | 大庆志飞生物化工有限公司 | 甲胺基阿维菌素单糖化合物及其制备方法和用途 |
CN107501368B (zh) * | 2017-09-30 | 2020-02-21 | 中国科学院成都生物研究所 | 一种多拉菌素衍生物的合成及其杀虫应用 |
CN113150053A (zh) * | 2020-01-22 | 2021-07-23 | 华东理工大学 | 偶氮苯类阿维菌素衍生物及其制备方法和应用 |
CN113817008B (zh) * | 2021-07-15 | 2023-05-23 | 湖州师范学院 | 新型琥珀酰基十六元大环内酯的制备方法及用途 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0570476A (ja) * | 1990-05-11 | 1993-03-23 | Merck & Co Inc | 3′−および3″−o−デスメチルアベルメクチン化合物の誘導体 |
JPH05255342A (ja) * | 1991-06-20 | 1993-10-05 | Merck & Co Inc | 4a−置換アベルメクチン誘導体 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US87519A (en) * | 1869-03-02 | Improvement in furnace-stoves and registers | ||
US148520A (en) * | 1874-03-10 | Improvement in faucets | ||
US18993A (en) * | 1857-12-29 | Cider-mill | ||
SE434277B (sv) | 1976-04-19 | 1984-07-16 | Merck & Co Inc | Sett att framstella nya antihelmintiskt verkande foreningar genom odling av streptomyces avermitilis |
GB8811037D0 (en) | 1988-05-10 | 1988-06-15 | Glaxo Group Ltd | Chemical compounds |
EP0353959A2 (en) | 1988-08-02 | 1990-02-07 | Beecham Group Plc | Antihelmintic macrolide antibiotics |
SE465605B (sv) * | 1990-02-26 | 1991-10-07 | Harry Nilsson | Skivfilter |
JP2622197B2 (ja) | 1990-03-01 | 1997-06-18 | 三共株式会社 | 13−エーテル置換ミルベマイシン誘導体 |
US5411737A (en) | 1991-10-15 | 1995-05-02 | Merck & Co., Inc. | Slow release syneresing polymeric drug delivery device |
PL174488B1 (pl) | 1993-05-10 | 1998-08-31 | Merck & Co Inc | Preparat do zwalczania pasożytów zwierząt oraz sposób wytwarzania preparatu do zwalczania pasożytów zwierząt |
US5602107A (en) | 1993-05-10 | 1997-02-11 | Merck & Co., Inc. | Pour-on formulations consisting of gylcols, glycerides and avermectin compounds |
US5436355A (en) | 1994-02-03 | 1995-07-25 | Merck & Co., Inc. | Process for making avermectin/zein compositions |
TW327125B (en) | 1994-02-07 | 1998-02-21 | Merck & Co Inc | Composition and method for protecting against pine exhausted |
CA2418975C (en) | 2000-08-09 | 2012-01-17 | Satoshi Omura | Avermectin derivatives |
JPWO2002012261A1 (ja) | 2000-08-09 | 2004-01-15 | 社団法人北里研究所 | エバーメクチン誘導体 |
WO2003075742A2 (en) * | 2002-03-05 | 2003-09-18 | Merck & Co., Inc. | Biomarker for efficacy of appetite suppressant drugs |
GB0229804D0 (en) * | 2002-12-20 | 2003-01-29 | Syngenta Participations Ag | Avermection b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"- or 4'-position |
-
2002
- 2002-12-20 GB GBGB0229804.0A patent/GB0229804D0/en not_active Ceased
-
2003
- 2003-12-12 PE PE2003001284A patent/PE20040713A1/es active IP Right Grant
- 2003-12-18 TW TW092135927A patent/TW200512214A/zh unknown
- 2003-12-18 AR ARP030104712A patent/AR042533A1/es active IP Right Grant
- 2003-12-19 JP JP2004561378A patent/JP4851094B2/ja not_active Expired - Lifetime
- 2003-12-19 BR BR0317601-0A patent/BR0317601A/pt not_active Application Discontinuation
- 2003-12-19 US US10/539,274 patent/US7737261B2/en active Active
- 2003-12-19 MX MXPA05006036A patent/MXPA05006036A/es active IP Right Grant
- 2003-12-19 EP EP03810843.7A patent/EP1581546B1/en not_active Expired - Lifetime
- 2003-12-19 PL PL377497A patent/PL211483B1/pl unknown
- 2003-12-19 CA CA2507774A patent/CA2507774C/en not_active Expired - Fee Related
- 2003-12-19 RU RU2005122943/04A patent/RU2330857C2/ru active
- 2003-12-19 WO PCT/EP2003/014613 patent/WO2004056844A1/en active Application Filing
- 2003-12-19 AU AU2003302284A patent/AU2003302284B2/en not_active Ceased
- 2003-12-19 UA UAA200507209A patent/UA81281C2/uk unknown
- 2003-12-19 ES ES03810843T patent/ES2742899T3/es not_active Expired - Lifetime
- 2003-12-19 KR KR1020057011622A patent/KR101109500B1/ko active IP Right Grant
- 2003-12-19 CN CN2003801088575A patent/CN1738828B/zh not_active Expired - Lifetime
-
2005
- 2005-06-09 IL IL169092A patent/IL169092A/en active IP Right Grant
- 2005-06-17 MA MA28349A patent/MA27646A1/fr unknown
- 2005-06-17 CO CO05059203A patent/CO5690647A1/es not_active Application Discontinuation
-
2006
- 2006-01-06 ZA ZA200504353A patent/ZA200504353B/en unknown
-
2010
- 2010-04-27 US US12/768,280 patent/US8017589B2/en not_active Expired - Fee Related
- 2010-12-22 JP JP2010286151A patent/JP5302297B2/ja not_active Expired - Fee Related
-
2011
- 2011-05-27 US US13/117,292 patent/US8263566B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0570476A (ja) * | 1990-05-11 | 1993-03-23 | Merck & Co Inc | 3′−および3″−o−デスメチルアベルメクチン化合物の誘導体 |
JPH05255342A (ja) * | 1991-06-20 | 1993-10-05 | Merck & Co Inc | 4a−置換アベルメクチン誘導体 |
Non-Patent Citations (3)
Title |
---|
JPN6010034182; BIOORGANIC & MEDICINAL CHEMISTRY VOL.8,NO.1, 2000, PP.19-26 * |
JPN6010034183; INTERNATIONAL JOURNAL FOR PARASITOLOGY VOL.26,NO.11, 1996, PP.1227-1235 * |
JPN6010034184; JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY VOL.42,NO.8, 1994, PP.1786-1790 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10518445B2 (en) | 2014-12-24 | 2019-12-31 | Ntn Corporation | Cage for rolling bearing, and rolling bearing |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5302297B2 (ja) | 4”位又は4’−位にアルコキシメチル置換基を有するアベルメクチンb1及びアベルメクチンb1単糖誘導体 | |
EP1594878B1 (en) | Avermectin monosaccharide derivatives having pesticidal properties | |
EP1613639B1 (en) | Avermectins substituted in the 4'' and 4´-positions having pesticidal properties | |
DE602004012840T2 (de) | 4''- bzw. 4'-substituierte avermectin- und avermectinmonosaccharidderivate mit pestiziden eigenschaften | |
JP2006509794A (ja) | 殺虫活性を有すジハロ−アリルオキシ−フェノール誘導体 | |
DE602004012874T2 (de) | Avermectine und avermectinmonosaccharide substituiert in der 4'- und 4''-stellung mit pestiziden eigenschaften | |
JP4750698B2 (ja) | アベルメクチンb1単糖誘導体 | |
JP2006517554A (ja) | アベルメクチンと殺菌作用を有する4”−および4’−位置で置換されたアベルメクチン単糖 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A711 Effective date: 20120621 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130115 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130410 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130521 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130620 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5302297 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
S631 | Written request for registration of reclamation of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313631 |
|
S634 | Written request for registration of reclamation of nationality |
Free format text: JAPANESE INTERMEDIATE CODE: R313634 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |