CN101287703B - 农药联苯脒衍生物 - Google Patents
农药联苯脒衍生物 Download PDFInfo
- Publication number
- CN101287703B CN101287703B CN2006800330715A CN200680033071A CN101287703B CN 101287703 B CN101287703 B CN 101287703B CN 2006800330715 A CN2006800330715 A CN 2006800330715A CN 200680033071 A CN200680033071 A CN 200680033071A CN 101287703 B CN101287703 B CN 101287703B
- Authority
- CN
- China
- Prior art keywords
- spp
- alkyl
- expression
- compound
- general formula
- 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.)
- Expired - Fee Related
Links
- 239000000575 pesticide Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 134
- 238000000034 method Methods 0.000 claims abstract description 106
- -1 benzene carbon amidine Chemical class 0.000 claims description 47
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 229910052731 fluorine Inorganic materials 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- 235000013399 edible fruits Nutrition 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical compound OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 244000000004 fungal plant pathogen Species 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 3
- 239000002689 soil Substances 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 239000003905 agrochemical Substances 0.000 claims description 2
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 claims description 2
- 125000005936 piperidyl group Chemical group 0.000 claims description 2
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 2
- 230000008635 plant growth Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 56
- 238000002360 preparation method Methods 0.000 abstract description 22
- 230000008569 process Effects 0.000 abstract description 12
- 230000000855 fungicidal effect Effects 0.000 abstract description 11
- 239000013543 active substance Substances 0.000 abstract description 9
- 241000233866 Fungi Species 0.000 abstract description 7
- 241000238631 Hexapoda Species 0.000 abstract description 6
- 239000000417 fungicide Substances 0.000 abstract description 5
- 239000002917 insecticide Substances 0.000 abstract 2
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 description 82
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 82
- 241000196324 Embryophyta Species 0.000 description 44
- 238000012360 testing method Methods 0.000 description 32
- 230000000857 drug effect Effects 0.000 description 31
- 239000002253 acid Substances 0.000 description 29
- 239000002585 base Substances 0.000 description 29
- 241000894006 Bacteria Species 0.000 description 28
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 28
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 24
- 239000002904 solvent Substances 0.000 description 21
- 230000000694 effects Effects 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 241001124076 Aphididae Species 0.000 description 16
- 150000001412 amines Chemical class 0.000 description 16
- 239000003995 emulsifying agent Substances 0.000 description 16
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 241000256259 Noctuidae Species 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- 241000256602 Isoptera Species 0.000 description 13
- 238000009472 formulation Methods 0.000 description 13
- 239000000843 powder Substances 0.000 description 13
- 241000244206 Nematoda Species 0.000 description 12
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 11
- 238000001035 drying Methods 0.000 description 11
- 125000000623 heterocyclic group Chemical group 0.000 description 11
- 241001414720 Cicadellidae Species 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 9
- 235000013339 cereals Nutrition 0.000 description 9
- 210000004209 hair Anatomy 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 238000005507 spraying Methods 0.000 description 9
- 241000258937 Hemiptera Species 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 125000002877 alkyl aryl group Chemical group 0.000 description 8
- 150000003851 azoles Chemical class 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 8
- 239000010695 polyglycol Substances 0.000 description 8
- 229920000151 polyglycol Polymers 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 241000123650 Botrytis cinerea Species 0.000 description 7
- 241000254171 Curculionidae Species 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000004305 biphenyl Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 238000011081 inoculation Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- 241000256118 Aedes aegypti Species 0.000 description 6
- 241001672694 Citrus reticulata Species 0.000 description 6
- 241000255925 Diptera Species 0.000 description 6
- 241000221785 Erysiphales Species 0.000 description 6
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 241001466030 Psylloidea Species 0.000 description 6
- 241001361634 Rhizoctonia Species 0.000 description 6
- 241001414989 Thysanoptera Species 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000003958 fumigation Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 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 6
- 0 *c1cc(S(O*)O*)c(*)cc1N Chemical compound *c1cc(S(O*)O*)c(*)cc1N 0.000 description 5
- 241000223600 Alternaria Species 0.000 description 5
- 241000213004 Alternaria solani Species 0.000 description 5
- 241000219193 Brassicaceae Species 0.000 description 5
- 241000254173 Coleoptera Species 0.000 description 5
- 241000223218 Fusarium Species 0.000 description 5
- 241000578422 Graphosoma lineatum Species 0.000 description 5
- 241000257303 Hymenoptera Species 0.000 description 5
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 5
- 244000046052 Phaseolus vulgaris Species 0.000 description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 5
- 241001674048 Phthiraptera Species 0.000 description 5
- 241000220324 Pyrus Species 0.000 description 5
- 241001122767 Theaceae Species 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 241000267822 Trogoderma granarium Species 0.000 description 5
- 241000221576 Uromyces Species 0.000 description 5
- 241000221566 Ustilago Species 0.000 description 5
- 240000006365 Vitis vinifera Species 0.000 description 5
- 235000014787 Vitis vinifera Nutrition 0.000 description 5
- 208000000260 Warts Diseases 0.000 description 5
- 241000429635 Xestobium rufovillosum Species 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 238000004440 column chromatography Methods 0.000 description 5
- 201000010153 skin papilloma Diseases 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000002023 wood Substances 0.000 description 5
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 4
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 4
- QDFXRVAOBHEBGJ-UHFFFAOYSA-N 3-(cyclononen-1-yl)-4,5,6,7,8,9-hexahydro-1h-diazonine Chemical compound C1CCCCCCC=C1C1=NNCCCCCC1 QDFXRVAOBHEBGJ-UHFFFAOYSA-N 0.000 description 4
- 241001143309 Acanthoscelides obtectus Species 0.000 description 4
- 241000238818 Acheta domesticus Species 0.000 description 4
- 241001427556 Anoplura Species 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 241000228212 Aspergillus Species 0.000 description 4
- 241001674044 Blattodea Species 0.000 description 4
- 241000257163 Calliphora vicina Species 0.000 description 4
- 241000871189 Chenopodiaceae Species 0.000 description 4
- 241001465977 Coccoidea Species 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 241001481695 Dermanyssus gallinae Species 0.000 description 4
- 241001124144 Dermaptera Species 0.000 description 4
- 241001414830 Diaspididae Species 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- 241000258963 Diplopoda Species 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 241000255896 Galleria mellonella Species 0.000 description 4
- 241000237858 Gastropoda Species 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 241001466007 Heteroptera Species 0.000 description 4
- 241000832180 Hylotrupes bajulus Species 0.000 description 4
- 241000221775 Hypocreales Species 0.000 description 4
- 241001149911 Isopoda Species 0.000 description 4
- 241000500881 Lepisma Species 0.000 description 4
- 241000555303 Mamestra brassicae Species 0.000 description 4
- 241000254099 Melolontha melolontha Species 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-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
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 4
- 241000168255 Opiliones Species 0.000 description 4
- 241000238814 Orthoptera Species 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- 241000721454 Pemphigus Species 0.000 description 4
- 241000238675 Periplaneta americana Species 0.000 description 4
- 241000233679 Peronosporaceae Species 0.000 description 4
- 241000233614 Phytophthora Species 0.000 description 4
- 241000589516 Pseudomonas Species 0.000 description 4
- 241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 4
- 241000233639 Pythium Species 0.000 description 4
- 241001510236 Rhyparobia maderae Species 0.000 description 4
- 241000318997 Rhyzopertha dominica Species 0.000 description 4
- 235000004789 Rosa xanthina Nutrition 0.000 description 4
- 241000220222 Rosaceae Species 0.000 description 4
- 241001533598 Septoria Species 0.000 description 4
- 241000258242 Siphonaptera Species 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- 241000208292 Solanaceae Species 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 241000243777 Trichinella spiralis Species 0.000 description 4
- 235000009754 Vitis X bourquina Nutrition 0.000 description 4
- 235000012333 Vitis X labruscana Nutrition 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000001409 amidines Chemical class 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 235000008504 concentrate Nutrition 0.000 description 4
- 239000012973 diazabicyclooctane Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 4
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 229940096911 trichinella spiralis Drugs 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- JUMBSPQABSHVMN-UHFFFAOYSA-N (4-tert-butylphenoxy)boronic acid Chemical compound CC(C)(C)C1=CC=C(OB(O)O)C=C1 JUMBSPQABSHVMN-UHFFFAOYSA-N 0.000 description 3
- NNPRCLUGHFXSOU-UHFFFAOYSA-N 4-chloro-n-[cyano(ethoxy)methyl]benzamide Chemical compound CCOC(C#N)NC(=O)C1=CC=C(Cl)C=C1 NNPRCLUGHFXSOU-UHFFFAOYSA-N 0.000 description 3
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 3
- 241000219495 Betulaceae Species 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 241001481710 Cerambycidae Species 0.000 description 3
- 241000258920 Chilopoda Species 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 241000931705 Cicada Species 0.000 description 3
- 241001327638 Cimex lectularius Species 0.000 description 3
- 241000222290 Cladosporium Species 0.000 description 3
- 241000228437 Cochliobolus Species 0.000 description 3
- 241000202828 Dermatobia hominis Species 0.000 description 3
- 102000002322 Egg Proteins Human genes 0.000 description 3
- 108010000912 Egg Proteins Proteins 0.000 description 3
- 241000283070 Equus zebra Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 241000720914 Forficula auricularia Species 0.000 description 3
- 206010018498 Goitre Diseases 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- 241001177134 Lyctus Species 0.000 description 3
- UDSJPFPDKCMYBD-UHFFFAOYSA-N Metsulfovax Chemical compound S1C(C)=NC(C)=C1C(=O)NC1=CC=CC=C1 UDSJPFPDKCMYBD-UHFFFAOYSA-N 0.000 description 3
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 3
- 208000031888 Mycoses Diseases 0.000 description 3
- 241000131448 Mycosphaerella Species 0.000 description 3
- 241000935974 Paralichthys dentatus Species 0.000 description 3
- 241000517307 Pediculus humanus Species 0.000 description 3
- 241001223281 Peronospora Species 0.000 description 3
- 229930182764 Polyoxin Natural products 0.000 description 3
- 241000813090 Rhizoctonia solani Species 0.000 description 3
- 240000000111 Saccharum officinarum Species 0.000 description 3
- 235000007201 Saccharum officinarum Nutrition 0.000 description 3
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 3
- 241000545593 Scolytinae Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 241000254152 Sitophilus oryzae Species 0.000 description 3
- 240000003768 Solanum lycopersicum Species 0.000 description 3
- 241000256248 Spodoptera Species 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 241000722133 Tilletia Species 0.000 description 3
- 241000130771 Tinea pellionella Species 0.000 description 3
- 241000333690 Tineola bisselliella Species 0.000 description 3
- 241000425037 Toona sinensis Species 0.000 description 3
- 241001251949 Xanthium sibiricum Species 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 241001414985 Zygentoma Species 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- 210000003323 beak Anatomy 0.000 description 3
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical group C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 3
- 230000001851 biosynthetic effect Effects 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 238000012239 gene modification Methods 0.000 description 3
- 230000005017 genetic modification Effects 0.000 description 3
- 235000013617 genetically modified food Nutrition 0.000 description 3
- 201000003872 goiter Diseases 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 229940031815 mycocide Drugs 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 210000004681 ovum Anatomy 0.000 description 3
- 235000021017 pears Nutrition 0.000 description 3
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000013049 sediment Substances 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000000375 suspending agent Substances 0.000 description 3
- 239000004308 thiabendazole Substances 0.000 description 3
- 235000010296 thiabendazole Nutrition 0.000 description 3
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 3
- 229960004546 thiabendazole Drugs 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 3
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 2
- 125000006711 (C2-C12) alkynyl group Chemical group 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 2
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 description 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- ZQZAHPFFZWEUCL-UHFFFAOYSA-N 2-chloropyridine-3-carboxamide Chemical class NC(=O)C1=CC=CN=C1Cl ZQZAHPFFZWEUCL-UHFFFAOYSA-N 0.000 description 2
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 2
- AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241000934064 Acarus siro Species 0.000 description 2
- 241001351288 Achroia grisella Species 0.000 description 2
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 2
- 241000256173 Aedes albopictus Species 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- 241000059559 Agriotes sordidus Species 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- 241000208223 Anacardiaceae Species 0.000 description 2
- 241000663922 Anasa tristis Species 0.000 description 2
- 241001147657 Ancylostoma Species 0.000 description 2
- 241000498253 Ancylostoma duodenale Species 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 241000411449 Anobium punctatum Species 0.000 description 2
- 241000256186 Anopheles <genus> Species 0.000 description 2
- 241001640910 Anthrenus Species 0.000 description 2
- 241000294569 Aphelenchoides Species 0.000 description 2
- 241000208173 Apiaceae Species 0.000 description 2
- 241000239223 Arachnida Species 0.000 description 2
- 241000239290 Araneae Species 0.000 description 2
- 241001480754 Argas reflexus Species 0.000 description 2
- 241000244186 Ascaris Species 0.000 description 2
- 201000002909 Aspergillosis Diseases 0.000 description 2
- 241000228197 Aspergillus flavus Species 0.000 description 2
- 241001225321 Aspergillus fumigatus Species 0.000 description 2
- 208000036641 Aspergillus infections Diseases 0.000 description 2
- 241001530056 Athelia rolfsii Species 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241001490249 Bactrocera oleae Species 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 229940123208 Biguanide Drugs 0.000 description 2
- 241001573716 Blaniulus guttulatus Species 0.000 description 2
- 241000238662 Blatta orientalis Species 0.000 description 2
- 241000238657 Blattella germanica Species 0.000 description 2
- 241001629132 Blissus leucopterus Species 0.000 description 2
- 241001480061 Blumeria graminis Species 0.000 description 2
- 239000005740 Boscalid Substances 0.000 description 2
- 241001465180 Botrytis Species 0.000 description 2
- 241000233684 Bremia Species 0.000 description 2
- 241000982105 Brevicoryne brassicae Species 0.000 description 2
- 241000143302 Brugia timori Species 0.000 description 2
- 241000398201 Bryobia praetiosa Species 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 241000282836 Camelus dromedarius Species 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 235000014653 Carica parviflora Nutrition 0.000 description 2
- 241000255579 Ceratitis capitata Species 0.000 description 2
- 241001365958 Ceroplastes cirripediformis Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241001635683 Cimex hemipterus Species 0.000 description 2
- 241000221760 Claviceps Species 0.000 description 2
- 241000098277 Cnaphalocrocis Species 0.000 description 2
- 241000243321 Cnidaria Species 0.000 description 2
- 241000255749 Coccinellidae Species 0.000 description 2
- 241001427559 Collembola Species 0.000 description 2
- 241000222199 Colletotrichum Species 0.000 description 2
- 241001133184 Colletotrichum agaves Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 241000304165 Cordylobia anthropophaga Species 0.000 description 2
- 241001529717 Corticium <basidiomycota> Species 0.000 description 2
- 241000490513 Ctenocephalides canis Species 0.000 description 2
- 241000258924 Ctenocephalides felis Species 0.000 description 2
- 241000256054 Culex <genus> Species 0.000 description 2
- 241000256061 Culex tarsalis Species 0.000 description 2
- 239000005755 Cyflufenamid Substances 0.000 description 2
- 201000003808 Cystic echinococcosis Diseases 0.000 description 2
- 241000238710 Dermatophagoides Species 0.000 description 2
- 241001641895 Dermestes Species 0.000 description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- 241001399709 Dinoderus minutus Species 0.000 description 2
- 244000281702 Dioscorea villosa Species 0.000 description 2
- 241000399949 Ditylenchus dipsaci Species 0.000 description 2
- 239000005766 Dodine Substances 0.000 description 2
- 241001319090 Dracunculus medinensis Species 0.000 description 2
- 241001595884 Drosicha Species 0.000 description 2
- 241000353522 Earias insulana Species 0.000 description 2
- 241000244170 Echinococcus granulosus Species 0.000 description 2
- 241000244163 Echinococcus multilocularis Species 0.000 description 2
- 241000223924 Eimeria Species 0.000 description 2
- 241001063191 Elops affinis Species 0.000 description 2
- 241000125117 Elsinoe Species 0.000 description 2
- 241000498255 Enterobius vermicularis Species 0.000 description 2
- 241000122098 Ephestia kuehniella Species 0.000 description 2
- 241000738498 Epitrix pubescens Species 0.000 description 2
- 235000002756 Erythrina berteroana Nutrition 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 241000490229 Eucephalus Species 0.000 description 2
- 241000219428 Fagaceae Species 0.000 description 2
- 239000005778 Fenpropimorph Substances 0.000 description 2
- 239000005784 Fluoxastrobin Substances 0.000 description 2
- 235000016623 Fragaria vesca Nutrition 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 2
- 206010017533 Fungal infection Diseases 0.000 description 2
- 241000223194 Fusarium culmorum Species 0.000 description 2
- 241000223195 Fusarium graminearum Species 0.000 description 2
- 241001149504 Gaeumannomyces Species 0.000 description 2
- 241000248126 Geophilus Species 0.000 description 2
- 241000555709 Guignardia Species 0.000 description 2
- 241000243976 Haemonchus Species 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241001508566 Hypera postica Species 0.000 description 2
- 241001058149 Icerya Species 0.000 description 2
- 241000758791 Juglandaceae Species 0.000 description 2
- 241001479676 Kakothrips pisivorus Species 0.000 description 2
- 241001506109 Kalotermes Species 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- 241000218195 Lauraceae Species 0.000 description 2
- 241000255777 Lepidoptera Species 0.000 description 2
- 241000661345 Leptocorisa Species 0.000 description 2
- 241000228456 Leptosphaeria Species 0.000 description 2
- 241000228457 Leptosphaeria maculans Species 0.000 description 2
- 241000234280 Liliaceae Species 0.000 description 2
- 241001113970 Linognathus Species 0.000 description 2
- 241000322701 Liposcelidae Species 0.000 description 2
- 241000966204 Lissorhoptrus oryzophilus Species 0.000 description 2
- 241000257162 Lucilia <blowfly> Species 0.000 description 2
- 241000255685 Malacosoma neustria Species 0.000 description 2
- 241001179564 Melanaphis sacchari Species 0.000 description 2
- 239000005805 Mepanipyrim Substances 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- 239000005810 Metrafenone Substances 0.000 description 2
- 241001459558 Monographella nivalis Species 0.000 description 2
- 241000952627 Monomorium pharaonis Species 0.000 description 2
- 241000218231 Moraceae Species 0.000 description 2
- 240000005561 Musa balbisiana Species 0.000 description 2
- 241000234615 Musaceae Species 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 241000409991 Mythimna separata Species 0.000 description 2
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241001226034 Nectria <echinoderm> Species 0.000 description 2
- 241001137882 Nematodirus Species 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 241001671714 Nezara Species 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 241001385056 Niptus hololeucus Species 0.000 description 2
- 241001036422 Nosopsyllus fasciatus Species 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 241000036147 Ochlerotatus taeniorhynchus Species 0.000 description 2
- 241000207834 Oleaceae Species 0.000 description 2
- 241000565675 Oncomelania Species 0.000 description 2
- 241000384103 Oniscus asellus Species 0.000 description 2
- 241000233654 Oomycetes Species 0.000 description 2
- 241000131101 Oryzaephilus surinamensis Species 0.000 description 2
- 241001147398 Ostrinia nubilalis Species 0.000 description 2
- 241001570894 Oulema oryzae Species 0.000 description 2
- 241001480233 Paragonimus Species 0.000 description 2
- 241000736122 Parastagonospora nodorum Species 0.000 description 2
- 241000721451 Pectinophora gossypiella Species 0.000 description 2
- 241000256682 Peregrinus maidis Species 0.000 description 2
- 241001510004 Periplaneta australasiae Species 0.000 description 2
- 241001510001 Periplaneta brunnea Species 0.000 description 2
- 241000440444 Phakopsora Species 0.000 description 2
- 241001058119 Phenacoccus Species 0.000 description 2
- 241001516577 Phylloxera Species 0.000 description 2
- 241001149949 Phytophthora cactorum Species 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 241000193804 Planococcus <bacterium> Species 0.000 description 2
- 241000233626 Plasmopara Species 0.000 description 2
- 241000595629 Plodia interpunctella Species 0.000 description 2
- 241000500437 Plutella xylostella Species 0.000 description 2
- 241000896242 Podosphaera Species 0.000 description 2
- 241000317981 Podosphaera fuliginea Species 0.000 description 2
- 241001337928 Podosphaera leucotricha Species 0.000 description 2
- 241000254101 Popillia japonica Species 0.000 description 2
- 241000908127 Porcellio scaber Species 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- 241000517304 Pthirus pubis Species 0.000 description 2
- 241000221300 Puccinia Species 0.000 description 2
- 241001123569 Puccinia recondita Species 0.000 description 2
- 241000718000 Pulex irritans Species 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 235000014443 Pyrus communis Nutrition 0.000 description 2
- 241000918584 Pythium ultimum Species 0.000 description 2
- 241000173767 Ramularia Species 0.000 description 2
- 206010037888 Rash pustular Diseases 0.000 description 2
- 241001509967 Reticulitermes flavipes Species 0.000 description 2
- 241001481696 Rhipicephalus sanguineus Species 0.000 description 2
- 241001515786 Rhynchosporium Species 0.000 description 2
- 241001107098 Rubiaceae Species 0.000 description 2
- 241001093501 Rutaceae Species 0.000 description 2
- 241000914334 Sahlbergella singularis Species 0.000 description 2
- 241000304160 Sarcophaga carnaria Species 0.000 description 2
- 241000509427 Sarcoptes scabiei Species 0.000 description 2
- 241000253973 Schistocerca gregaria Species 0.000 description 2
- 241000722272 Schizaphis Species 0.000 description 2
- 241000221662 Sclerotinia Species 0.000 description 2
- 241001597359 Septoria apiicola Species 0.000 description 2
- 241000256108 Simulium <genus> Species 0.000 description 2
- 241000254179 Sitophilus granarius Species 0.000 description 2
- 241000254154 Sitophilus zeamais Species 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 241000579741 Sphaerotheca <fungi> Species 0.000 description 2
- 241001674391 Sphaerulina musiva Species 0.000 description 2
- 241001161749 Stenchaetothrips biformis Species 0.000 description 2
- 241000180126 Strongyloides fuelleborni Species 0.000 description 2
- 241000883295 Symphyla Species 0.000 description 2
- 241000189578 Taeniothrips Species 0.000 description 2
- 241000254109 Tenebrio molitor Species 0.000 description 2
- 241001374808 Tetramorium caespitum Species 0.000 description 2
- 241000865903 Thielaviopsis Species 0.000 description 2
- 241000511627 Tipula paludosa Species 0.000 description 2
- 241000255901 Tortricidae Species 0.000 description 2
- 241000254086 Tribolium <beetle> Species 0.000 description 2
- 241001584775 Tunga penetrans Species 0.000 description 2
- 241001286670 Ulmus x hollandica Species 0.000 description 2
- 241000510929 Uncinula Species 0.000 description 2
- 241000254198 Urocerus gigas Species 0.000 description 2
- 241001154828 Urocystis <tapeworm> Species 0.000 description 2
- 241000221577 Uromyces appendiculatus Species 0.000 description 2
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 2
- 241000228452 Venturia inaequalis Species 0.000 description 2
- 241000244005 Wuchereria bancrofti Species 0.000 description 2
- 241000353223 Xenopsylla cheopis Species 0.000 description 2
- 210000001015 abdomen Anatomy 0.000 description 2
- 239000000642 acaricide Substances 0.000 description 2
- YLJLLELGHSWIDU-OKZTUQRJSA-N acetic acid;(2s,6r)-4-cyclododecyl-2,6-dimethylmorpholine Chemical compound CC(O)=O.C1[C@@H](C)O[C@@H](C)CN1C1CCCCCCCCCCC1 YLJLLELGHSWIDU-OKZTUQRJSA-N 0.000 description 2
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 2
- 235000010419 agar Nutrition 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 2
- 150000008046 alkali metal hydrides Chemical class 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 125000005133 alkynyloxy group Chemical group 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 229940091771 aspergillus fumigatus Drugs 0.000 description 2
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 2
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 2
- 150000004283 biguanides Chemical class 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- DMVOXQPQNTYEKQ-UHFFFAOYSA-N biphenyl-4-amine Chemical compound C1=CC(N)=CC=C1C1=CC=CC=C1 DMVOXQPQNTYEKQ-UHFFFAOYSA-N 0.000 description 2
- 229940118790 boscalid Drugs 0.000 description 2
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 2
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000001793 charged compounds Chemical class 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- GCUVBACNBHGZRS-UHFFFAOYSA-N cyclopenta-1,3-diene cyclopenta-2,4-dien-1-yl(diphenyl)phosphane iron(2+) Chemical compound [Fe++].c1cc[cH-]c1.c1cc[c-](c1)P(c1ccccc1)c1ccccc1 GCUVBACNBHGZRS-UHFFFAOYSA-N 0.000 description 2
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 229960003887 dichlorophen Drugs 0.000 description 2
- 108010037444 diisopropylglutathione ester Proteins 0.000 description 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 2
- 235000021038 drupes Nutrition 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 229960002125 enilconazole Drugs 0.000 description 2
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 description 2
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 208000024386 fungal infectious disease Diseases 0.000 description 2
- 239000004478 grain bait Substances 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 244000000013 helminth Species 0.000 description 2
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 2
- 239000010903 husk Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 2
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- OVEHNNQXLPJPPL-UHFFFAOYSA-N lithium;n-propan-2-ylpropan-2-amine Chemical compound [Li].CC(C)NC(C)C OVEHNNQXLPJPPL-UHFFFAOYSA-N 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 2
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 2
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 description 2
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 2
- XYGTTXYQUMEHDB-UHFFFAOYSA-N n-(dimethoxymethyl)-n-methylethanamine Chemical compound CCN(C)C(OC)OC XYGTTXYQUMEHDB-UHFFFAOYSA-N 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- JIKUXBYRTXDNIY-UHFFFAOYSA-N n-methyl-n-phenylformamide Chemical compound O=CN(C)C1=CC=CC=C1 JIKUXBYRTXDNIY-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 150000002905 orthoesters Chemical class 0.000 description 2
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 description 2
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 2
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 2
- 150000002940 palladium Chemical class 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
- 230000001717 pathogenic effect Effects 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000002574 poison Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000015320 potassium carbonate Nutrition 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 2
- 235000021251 pulses Nutrition 0.000 description 2
- 208000029561 pustule Diseases 0.000 description 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 210000003491 skin Anatomy 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
- 208000004441 taeniasis Diseases 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 210000001550 testis Anatomy 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 description 2
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 description 1
- OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 description 1
- RQOCXCFLRBRBCS-UHFFFAOYSA-N (22E)-cholesta-5,7,22-trien-3beta-ol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CCC(C)C)CCC33)C)C3=CC=C21 RQOCXCFLRBRBCS-UHFFFAOYSA-N 0.000 description 1
- URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 description 1
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 1
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 description 1
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 description 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- NSCWRMLDSIVPGO-UHFFFAOYSA-N 1,2,5-oxadiazinane Chemical compound C1CNOCN1 NSCWRMLDSIVPGO-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-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
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 description 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 1
- LAOOXBLMIJHMFO-UHFFFAOYSA-N 1-[2-(diethylamino)ethylamino]-4-methylthioxanthen-9-one;hydron;chloride Chemical compound Cl.S1C2=CC=CC=C2C(=O)C2=C1C(C)=CC=C2NCCN(CC)CC LAOOXBLMIJHMFO-UHFFFAOYSA-N 0.000 description 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 1
- ULCWZQJLFZEXCS-UHFFFAOYSA-N 1-[[2-(2,4-dichlorophenyl)-5-(2,2,2-trifluoroethoxy)oxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1C(OCC(F)(F)F)CCC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-UHFFFAOYSA-N 0.000 description 1
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 description 1
- HJKLEAOXCZIMPI-UHFFFAOYSA-N 2,2-diethoxyethanamine Chemical compound CCOC(CN)OCC HJKLEAOXCZIMPI-UHFFFAOYSA-N 0.000 description 1
- BRXLVBSXVRDWQB-UHFFFAOYSA-N 2,3,5,6,6-pentamethylhepta-2,4-diene Chemical compound CC(C)=C(C)C=C(C)C(C)(C)C BRXLVBSXVRDWQB-UHFFFAOYSA-N 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- QKJJCZYFXJCKRX-HZHKWBLPSA-N 2-[(2s,3s,6r)-6-[4-amino-5-(hydroxymethyl)-2-oxopyrimidin-1-yl]-3-[[(2s)-2-amino-3-hydroxypropanoyl]amino]-3,6-dihydro-2h-pyran-2-yl]-5-(diaminomethylideneamino)-2,4-dihydroxypentanoic acid Chemical compound O1[C@H](C(O)(CC(O)CN=C(N)N)C(O)=O)[C@@H](NC(=O)[C@H](CO)N)C=C[C@@H]1N1C(=O)N=C(N)C(CO)=C1 QKJJCZYFXJCKRX-HZHKWBLPSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 description 1
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 description 1
- ZDRBJJNXJOSCLR-YZKQBBCCSA-N 2-amino-2-[(2r,3s,5s,6r)-5-amino-2-methyl-6-[(2r,3s,5s,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxyoxan-3-yl]iminoacetic acid;hydron;chloride Chemical compound Cl.N[C@H]1C[C@H](N=C(N)C(O)=O)[C@@H](C)O[C@@H]1OC1[C@H](O)[C@@H](O)C(O)[C@H](O)[C@@H]1O ZDRBJJNXJOSCLR-YZKQBBCCSA-N 0.000 description 1
- PVTHJAPFENJVNC-UHFFFAOYSA-N 2-amino-2-[5-amino-2-methyl-6-(2,3,4,5,6-pentahydroxycyclohexyl)oxyoxan-3-yl]iminoacetic acid Chemical compound NC1CC(N=C(N)C(O)=O)C(C)OC1OC1C(O)C(O)C(O)C(O)C1O PVTHJAPFENJVNC-UHFFFAOYSA-N 0.000 description 1
- CACOMUHPQMDEJQ-UHFFFAOYSA-N 2-amino-4-methyl-n-phenyl-1,3-thiazole-5-carboxamide Chemical class N1=C(N)SC(C(=O)NC=2C=CC=CC=2)=C1C CACOMUHPQMDEJQ-UHFFFAOYSA-N 0.000 description 1
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 1
- YOETUEMZNOLGDB-UHFFFAOYSA-N 2-methylpropyl carbonochloridate Chemical compound CC(C)COC(Cl)=O YOETUEMZNOLGDB-UHFFFAOYSA-N 0.000 description 1
- 229940061334 2-phenylphenol Drugs 0.000 description 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 description 1
- NRAYWXLNSHEHQO-UHFFFAOYSA-N 3-(1-benzothiophen-2-yl)-5,6-dihydro-1,4,2-oxathiazine 4-oxide Chemical compound O=S1CCON=C1C1=CC2=CC=CC=C2S1 NRAYWXLNSHEHQO-UHFFFAOYSA-N 0.000 description 1
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-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
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 description 1
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 description 1
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 description 1
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 description 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 description 1
- GABNAHQQEVWYNS-UHFFFAOYSA-N 5-phenyl-2,3-dihydro-1,4-dithiine 1,1,4,4-tetraoxide Chemical compound O=S1(=O)CCS(=O)(=O)C(C=2C=CC=CC=2)=C1 GABNAHQQEVWYNS-UHFFFAOYSA-N 0.000 description 1
- OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000881711 Acipenser sturio Species 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 241000819811 Acronicta major Species 0.000 description 1
- 241001014341 Acrosternum hilare Species 0.000 description 1
- 241000219066 Actinidiaceae Species 0.000 description 1
- 241001506009 Aculops Species 0.000 description 1
- 241000079319 Aculops lycopersici Species 0.000 description 1
- 241001506414 Aculus Species 0.000 description 1
- 241001227264 Adoretus Species 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- 241000484420 Aedia leucomelas Species 0.000 description 1
- 241001164222 Aeneolamia Species 0.000 description 1
- 241000902874 Agelastica alni Species 0.000 description 1
- 241000902467 Agonoscena Species 0.000 description 1
- 241001136265 Agriotes Species 0.000 description 1
- 241000218473 Agrotis Species 0.000 description 1
- 241000449794 Alabama argillacea Species 0.000 description 1
- 241001155864 Aleurolobus barodensis Species 0.000 description 1
- 241001136547 Aleurothrixus Species 0.000 description 1
- 241001398046 Amphimallon solstitiale Species 0.000 description 1
- 241000839189 Amrasca Species 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 241001511271 Ancylostoma braziliense Species 0.000 description 1
- 241000520197 Ancylostoma ceylanicum Species 0.000 description 1
- 241000380490 Anguina Species 0.000 description 1
- 241000693245 Antestiopsis Species 0.000 description 1
- 241001435074 Anthomyia Species 0.000 description 1
- 241000254177 Anthonomus Species 0.000 description 1
- 241000625764 Anticarsia gemmatalis Species 0.000 description 1
- 241001414827 Aonidiella Species 0.000 description 1
- 241001600407 Aphis <genus> Species 0.000 description 1
- 241001600408 Aphis gossypii Species 0.000 description 1
- 241001507652 Aphrophoridae Species 0.000 description 1
- 241000256844 Apis mellifera Species 0.000 description 1
- 241001161813 Aponogeton junceus Species 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000238901 Araneidae Species 0.000 description 1
- 241000838579 Arboridia Species 0.000 description 1
- 241001149932 Archaeognatha Species 0.000 description 1
- 241001162025 Archips podana Species 0.000 description 1
- 241001480748 Argas Species 0.000 description 1
- 241001480752 Argas persicus Species 0.000 description 1
- 241000237518 Arion Species 0.000 description 1
- 241000722809 Armadillidium vulgare Species 0.000 description 1
- 235000011330 Armoracia rusticana Nutrition 0.000 description 1
- 240000003291 Armoracia rusticana Species 0.000 description 1
- 241000244185 Ascaris lumbricoides Species 0.000 description 1
- 241000668391 Aspidiella Species 0.000 description 1
- 241000208838 Asteraceae Species 0.000 description 1
- 241001437124 Atanus Species 0.000 description 1
- 241001174347 Atomaria Species 0.000 description 1
- 241000131286 Attagenus Species 0.000 description 1
- 241001289510 Attagenus unicolor Species 0.000 description 1
- 241001166627 Aulacorthum Species 0.000 description 1
- 241001367049 Autographa Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 241000254123 Bemisia Species 0.000 description 1
- 239000005735 Benalaxyl-M Substances 0.000 description 1
- 239000005736 Benthiavalicarb Substances 0.000 description 1
- 241001142392 Bibio Species 0.000 description 1
- 241001142394 Bibio marci Species 0.000 description 1
- 241000237359 Biomphalaria Species 0.000 description 1
- 241000190150 Bipolaris sorokiniana Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000237519 Bivalvia Species 0.000 description 1
- 241000238659 Blatta Species 0.000 description 1
- 241001631693 Blattella asahinai Species 0.000 description 1
- 241000929635 Blissus Species 0.000 description 1
- 241001480060 Blumeria Species 0.000 description 1
- 241000895523 Blumeria graminis f. sp. hordei Species 0.000 description 1
- 239000005739 Bordeaux mixture Substances 0.000 description 1
- 241001669698 Bostrychus Species 0.000 description 1
- 241000273316 Brachycaudus Species 0.000 description 1
- 241000273318 Brachycaudus cardui Species 0.000 description 1
- 241001088081 Brachycolus Species 0.000 description 1
- 241001444260 Brassicogethes aeneus Species 0.000 description 1
- 241000233685 Bremia lactucae Species 0.000 description 1
- 239000005741 Bromuconazole Substances 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- 241001325378 Bruchus Species 0.000 description 1
- 241000244038 Brugia malayi Species 0.000 description 1
- 241000488564 Bryobia Species 0.000 description 1
- 241001517925 Bucculatrix Species 0.000 description 1
- 241000041029 Bulinus Species 0.000 description 1
- 241000931178 Bunostomum Species 0.000 description 1
- 241000931177 Bunostomum trigonocephalum Species 0.000 description 1
- 241001491790 Bupalus piniaria Species 0.000 description 1
- 239000005742 Bupirimate Substances 0.000 description 1
- 241000243770 Bursaphelenchus Species 0.000 description 1
- 125000004650 C1-C8 alkynyl group Chemical group 0.000 description 1
- 241000244203 Caenorhabditis elegans Species 0.000 description 1
- 241000906761 Calocoris Species 0.000 description 1
- 241001489688 Camponotus herculeanus Species 0.000 description 1
- 241000613201 Campylomma livida Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 241001350371 Capua Species 0.000 description 1
- 241000131329 Carabidae Species 0.000 description 1
- NYSZJNUIVUBQMM-BQYQJAHWSA-N Cardamonin Chemical compound COC1=CC(O)=CC(O)=C1C(=O)\C=C\C1=CC=CC=C1 NYSZJNUIVUBQMM-BQYQJAHWSA-N 0.000 description 1
- 241001427143 Cavelerius excavatus Species 0.000 description 1
- 241001098608 Ceratophyllus Species 0.000 description 1
- 241001415293 Ceratovacuna Species 0.000 description 1
- 241001414824 Cercopidae Species 0.000 description 1
- 241001157813 Cercospora Species 0.000 description 1
- 241000530549 Cercospora beticola Species 0.000 description 1
- 241001450758 Ceroplastes Species 0.000 description 1
- 241000893172 Chabertia Species 0.000 description 1
- 241001094951 Chaetosiphon Species 0.000 description 1
- 241001436044 Chelifer Species 0.000 description 1
- 241000426499 Chilo Species 0.000 description 1
- 241000027435 Chlorophorus Species 0.000 description 1
- 241000359266 Chorioptes Species 0.000 description 1
- 241000255945 Choristoneura Species 0.000 description 1
- 241000255942 Choristoneura fumiferana Species 0.000 description 1
- 241000118402 Chromaphis juglandicola Species 0.000 description 1
- 241001367803 Chrysodeixis includens Species 0.000 description 1
- 241001124134 Chrysomelidae Species 0.000 description 1
- 241000668561 Chrysomphalus Species 0.000 description 1
- 241000123346 Chrysosporium Species 0.000 description 1
- 241001414836 Cimex 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
- 241001498622 Cixius wagneri Species 0.000 description 1
- 241000221751 Claviceps purpurea Species 0.000 description 1
- 241001152840 Cleonus Species 0.000 description 1
- 241001327942 Clonorchis Species 0.000 description 1
- 241001415288 Coccidae Species 0.000 description 1
- 241001478240 Coccus Species 0.000 description 1
- 241000933851 Cochliomyia Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- 241001509962 Coptotermes formosanus Species 0.000 description 1
- 241001212536 Cosmopolites Species 0.000 description 1
- 241000500845 Costelytra zealandica Species 0.000 description 1
- 241000720929 Creontiades dilutus Species 0.000 description 1
- WHPAGCJNPTUGGD-UHFFFAOYSA-N Croconazole Chemical compound ClC1=CC=CC(COC=2C(=CC=CC=2)C(=C)N2C=NC=C2)=C1 WHPAGCJNPTUGGD-UHFFFAOYSA-N 0.000 description 1
- 241001094916 Cryptomyzus ribis Species 0.000 description 1
- 241001152745 Cryptorhynchus lapathi Species 0.000 description 1
- 241001506147 Cryptotermes brevis Species 0.000 description 1
- 241001124552 Ctenolepisma Species 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000219104 Cucurbitaceae Species 0.000 description 1
- 241000256059 Culex pipiens Species 0.000 description 1
- 241000256057 Culex quinquefasciatus Species 0.000 description 1
- 241000338702 Cupido minimus Species 0.000 description 1
- 241000692095 Cuterebra Species 0.000 description 1
- 241001635274 Cydia pomonella Species 0.000 description 1
- 239000005758 Cyprodinil Substances 0.000 description 1
- 241000592374 Daktulosphaira vitifoliae Species 0.000 description 1
- 241001260003 Dalbulus Species 0.000 description 1
- 241000268912 Damalinia Species 0.000 description 1
- 239000005644 Dazomet Substances 0.000 description 1
- 241001523681 Dendrobium Species 0.000 description 1
- 241000238740 Dermatophagoides pteronyssinus Species 0.000 description 1
- 241001300085 Deroceras Species 0.000 description 1
- 241000878949 Deroceras agreste Species 0.000 description 1
- 241000489975 Diabrotica Species 0.000 description 1
- 241000108082 Dialeurodes Species 0.000 description 1
- 241000526124 Diaphorina Species 0.000 description 1
- 241001508802 Diaporthe Species 0.000 description 1
- 241001645342 Diaporthe citri Species 0.000 description 1
- 241000643949 Diaspis <angiosperm> Species 0.000 description 1
- 241001549096 Dichelops furcatus Species 0.000 description 1
- URDNHJIVMYZFRT-UHFFFAOYSA-N Diclobutrazol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)CC1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-UHFFFAOYSA-N 0.000 description 1
- 241000577452 Dicrocoelium Species 0.000 description 1
- 241001147667 Dictyocaulus Species 0.000 description 1
- 241000180412 Dictyocaulus filaria Species 0.000 description 1
- 241001273416 Didymella arachidicola Species 0.000 description 1
- 239000005760 Difenoconazole Substances 0.000 description 1
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 239000005762 Dimoxystrobin Substances 0.000 description 1
- 206010013029 Diphyllobothriasis Diseases 0.000 description 1
- 241001137876 Diphyllobothrium Species 0.000 description 1
- 241000866683 Diphyllobothrium latum Species 0.000 description 1
- 241001289269 Diplacanthus Species 0.000 description 1
- 241000511318 Diprion Species 0.000 description 1
- 239000005764 Dithianon Substances 0.000 description 1
- 239000005765 Dodemorph Substances 0.000 description 1
- 241000193907 Dreissena Species 0.000 description 1
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 1
- 241001425477 Dysdercus Species 0.000 description 1
- 241001516600 Dysmicoccus Species 0.000 description 1
- GKQLYSROISKDLL-UHFFFAOYSA-N EEDQ Chemical compound C1=CC=C2N(C(=O)OCC)C(OCC)C=CC2=C1 GKQLYSROISKDLL-UHFFFAOYSA-N 0.000 description 1
- 241000125118 Elsinoe fawcettii Species 0.000 description 1
- 241000995023 Empoasca Species 0.000 description 1
- 241001222563 Empoasca onukii Species 0.000 description 1
- 241000086608 Empoasca vitis Species 0.000 description 1
- 241000488562 Eotetranychus Species 0.000 description 1
- 241001301805 Epilachna Species 0.000 description 1
- DNVPQKQSNYMLRS-NXVQYWJNSA-N Ergosterol Natural products CC(C)[C@@H](C)C=C[C@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@H]3CC[C@]12C DNVPQKQSNYMLRS-NXVQYWJNSA-N 0.000 description 1
- 235000009008 Eriobotrya japonica Nutrition 0.000 description 1
- 244000061508 Eriobotrya japonica Species 0.000 description 1
- 241001558857 Eriophyes Species 0.000 description 1
- 241000415266 Ernobius mollis Species 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- 241001515686 Erythroneura Species 0.000 description 1
- 241001248531 Euchloe <genus> Species 0.000 description 1
- 241000060469 Eupoecilia ambiguella Species 0.000 description 1
- 241000483001 Euproctis chrysorrhoea Species 0.000 description 1
- 241000515838 Eurygaster Species 0.000 description 1
- 241000239245 Euscelis Species 0.000 description 1
- 241000098297 Euschistus Species 0.000 description 1
- 241001034433 Eutetranychus Species 0.000 description 1
- 241001488207 Eutrombicula Species 0.000 description 1
- 241000378864 Eutypa Species 0.000 description 1
- 241000378865 Eutypa lata Species 0.000 description 1
- 241000953886 Fannia canicularis Species 0.000 description 1
- 241000958182 Fannia scalaris Species 0.000 description 1
- 239000005774 Fenamidone Substances 0.000 description 1
- 239000005776 Fenhexamid Substances 0.000 description 1
- 239000005777 Fenpropidin Substances 0.000 description 1
- 241000218218 Ficus <angiosperm> Species 0.000 description 1
- 239000005781 Fludioxonil Substances 0.000 description 1
- 239000005782 Fluopicolide Substances 0.000 description 1
- 239000005785 Fluquinconazole Substances 0.000 description 1
- VEVZCONIUDBCDC-UHFFFAOYSA-N Flurprimidol Chemical compound C=1N=CN=CC=1C(O)(C(C)C)C1=CC=C(OC(F)(F)F)C=C1 VEVZCONIUDBCDC-UHFFFAOYSA-N 0.000 description 1
- 239000005787 Flutriafol Substances 0.000 description 1
- 239000005790 Fosetyl Substances 0.000 description 1
- 241000189565 Frankliniella Species 0.000 description 1
- 239000005791 Fuberidazole Substances 0.000 description 1
- 241001466042 Fulgoromorpha Species 0.000 description 1
- ULCWZQJLFZEXCS-KGLIPLIRSA-N Furconazole-cis Chemical compound O1[C@@H](OCC(F)(F)F)CC[C@@]1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-KGLIPLIRSA-N 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241001149475 Gaeumannomyces graminis Species 0.000 description 1
- 241000585112 Galba Species 0.000 description 1
- 241000982383 Gametis jucunda Species 0.000 description 1
- 241001660203 Gasterophilus Species 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- 241001057692 Geococcus coffeae Species 0.000 description 1
- 241001442498 Globodera Species 0.000 description 1
- 241001442497 Globodera rostochiensis Species 0.000 description 1
- 241000223247 Gloeocercospora Species 0.000 description 1
- 241000461774 Gloeosporium Species 0.000 description 1
- 241001620302 Glomerella <beetle> Species 0.000 description 1
- 241001243091 Gryllotalpa Species 0.000 description 1
- 241000241125 Gryllotalpa gryllotalpa Species 0.000 description 1
- 241000145313 Gymnocorymbus ternetzi Species 0.000 description 1
- 241000221557 Gymnosporangium Species 0.000 description 1
- 241001409809 Gymnosporangium sabinae Species 0.000 description 1
- 241000790933 Haematopinus Species 0.000 description 1
- 241000775881 Haematopota pluvialis Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 241001148481 Helicotylenchus Species 0.000 description 1
- 241000255990 Helicoverpa Species 0.000 description 1
- 241000256257 Heliothis Species 0.000 description 1
- 241000339323 Heliothrips Species 0.000 description 1
- 108010034145 Helminth Proteins Proteins 0.000 description 1
- 241001181537 Hemileia Species 0.000 description 1
- 241001181532 Hemileia vastatrix Species 0.000 description 1
- 241001659689 Hercinothrips Species 0.000 description 1
- 241001659688 Hercinothrips femoralis Species 0.000 description 1
- 241000920462 Heterakis Species 0.000 description 1
- 241000239389 Heterobostrychus brunneus Species 0.000 description 1
- 241001480224 Heterodera Species 0.000 description 1
- 241001176496 Heteronychus arator Species 0.000 description 1
- 241000697035 Heteropriacanthus cruentatus Species 0.000 description 1
- 241001124200 Heterotermes indicola Species 0.000 description 1
- 241001201623 Hofmannophila pseudospretella Species 0.000 description 1
- 241001288674 Holotrichia consanguinea Species 0.000 description 1
- 241000346653 Holotrichia parallela Species 0.000 description 1
- 241000995626 Homalodisca Species 0.000 description 1
- 241000957299 Homona magnanima Species 0.000 description 1
- 241001417351 Hoplocampa Species 0.000 description 1
- 241000218228 Humulus Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- 241001480803 Hyalomma Species 0.000 description 1
- 241001251958 Hyalopterus Species 0.000 description 1
- 241000115042 Hylamorpha elegans Species 0.000 description 1
- 241001464384 Hymenolepis nana Species 0.000 description 1
- 241000257176 Hypoderma <fly> Species 0.000 description 1
- 241001595209 Idiocerus Species 0.000 description 1
- 241000761334 Idioscopus Species 0.000 description 1
- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 description 1
- 241000692870 Inachis io Species 0.000 description 1
- 241001268508 Ioptera Species 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 239000005797 Iprovalicarb Substances 0.000 description 1
- VROYMKJUVCKXBU-UHFFFAOYSA-N Irumamycin Natural products CCC(=O)C1(C)OC1C(C)CC(C)C1C(C)C(O)C(C)C=CC(OC2OC(C)C(O)C(OC(N)=O)C2)CCCC=C(C)C(O2)C(C)=CCC2(O)CC(=O)O1 VROYMKJUVCKXBU-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 241000238681 Ixodes Species 0.000 description 1
- 235000013740 Juglans nigra Nutrition 0.000 description 1
- 244000184861 Juglans nigra Species 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 241000896288 Kakothrips Species 0.000 description 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 description 1
- 241001470016 Laodelphax Species 0.000 description 1
- 241001470017 Laodelphax striatella Species 0.000 description 1
- 241000256686 Lasius <genus> Species 0.000 description 1
- 241000599116 Lasius fuliginosus Species 0.000 description 1
- 241000948337 Lasius niger Species 0.000 description 1
- 241000051764 Lasius umbratus Species 0.000 description 1
- 241001163604 Latheticus oryzae Species 0.000 description 1
- 241000238866 Latrodectus mactans Species 0.000 description 1
- 241000669027 Lepidosaphes Species 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- 241000560153 Leptoglossus phyllopus Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 241000272320 Lipaphis Species 0.000 description 1
- 241000272317 Lipaphis erysimi Species 0.000 description 1
- 241000322707 Liposcelis Species 0.000 description 1
- 241000594036 Liriomyza Species 0.000 description 1
- 241000594033 Liriomyza bryoniae Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000004742 Lithophane antennata Species 0.000 description 1
- 241000532753 Lixus Species 0.000 description 1
- 241000255640 Loa loa Species 0.000 description 1
- 241000254023 Locusta Species 0.000 description 1
- 241000254022 Locusta migratoria Species 0.000 description 1
- 241001043195 Lyctus brunneus Species 0.000 description 1
- 241000656865 Lyctus linearis Species 0.000 description 1
- 241001414826 Lygus Species 0.000 description 1
- 241001414823 Lygus hesperus Species 0.000 description 1
- 241000237354 Lymnaea Species 0.000 description 1
- 241000721715 Macrosiphum Species 0.000 description 1
- 241001344133 Magnaporthe Species 0.000 description 1
- 241001344131 Magnaporthe grisea Species 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000927670 Mahanarva fimbriolata Species 0.000 description 1
- 241000219071 Malvaceae Species 0.000 description 1
- 241000721708 Mastotermes darwiniensis Species 0.000 description 1
- 241000752141 Megaphorura arctica Species 0.000 description 1
- 241000726778 Melanaphis Species 0.000 description 1
- 241001415013 Melanoplus Species 0.000 description 1
- 240000000233 Melia azedarach Species 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 241000243785 Meloidogyne javanica Species 0.000 description 1
- 241000254043 Melolonthinae Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000131592 Metcalfiella Species 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- 239000005809 Metiram Substances 0.000 description 1
- 241000180212 Metopolophium Species 0.000 description 1
- 241001497122 Migdolus Species 0.000 description 1
- 241000656898 Minthea rugicollis Species 0.000 description 1
- 241001414825 Miridae Species 0.000 description 1
- 241001469521 Mocis latipes Species 0.000 description 1
- 241001668538 Mollisia Species 0.000 description 1
- 241001147402 Monachus Species 0.000 description 1
- 241001094463 Monellia Species 0.000 description 1
- 241001518729 Monilinia Species 0.000 description 1
- 241000862466 Monilinia laxa Species 0.000 description 1
- 241001442208 Monochamus Species 0.000 description 1
- 241000005782 Monographella Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- 240000002393 Murraya koenigii Species 0.000 description 1
- 241000234295 Musa Species 0.000 description 1
- 241000257229 Musca <genus> Species 0.000 description 1
- 241001477928 Mythimna Species 0.000 description 1
- 241000721623 Myzus Species 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- CYUIZYSKRBPGNU-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.[O].C1=CC=CC=C1 Chemical compound N1=CC=CC2=CC=CC=C12.[O].C1=CC=CC=C1 CYUIZYSKRBPGNU-UHFFFAOYSA-N 0.000 description 1
- JHXVRRJXCDAINK-UHFFFAOYSA-N NC(=O)N.N#CC#N Chemical compound NC(=O)N.N#CC#N JHXVRRJXCDAINK-UHFFFAOYSA-N 0.000 description 1
- 241000256807 Nasonia Species 0.000 description 1
- 241000133259 Nasonovia Species 0.000 description 1
- 241000133263 Nasonovia ribisnigri Species 0.000 description 1
- 241000196499 Naupactus xanthographus Species 0.000 description 1
- 241000041821 Necrobia Species 0.000 description 1
- 241000316646 Neomaskellia bergii Species 0.000 description 1
- 241000556984 Neonectria galligena Species 0.000 description 1
- 241000359016 Nephotettix Species 0.000 description 1
- 241001671709 Nezara viridula Species 0.000 description 1
- 241001556090 Nilaparvata Species 0.000 description 1
- 241001556089 Nilaparvata lugens Species 0.000 description 1
- VJAWBEFMCIINFU-UHFFFAOYSA-N Nitrothal-isopropyl Chemical group CC(C)OC(=O)C1=CC(C(=O)OC(C)C)=CC([N+]([O-])=O)=C1 VJAWBEFMCIINFU-UHFFFAOYSA-N 0.000 description 1
- 241001597008 Nomeidae Species 0.000 description 1
- WKELIVWALJPJGV-UHFFFAOYSA-N OBO.OB(O)O Chemical compound OBO.OB(O)O WKELIVWALJPJGV-UHFFFAOYSA-N 0.000 description 1
- 241000144610 Oculimacula acuformis Species 0.000 description 1
- 241001102020 Oebalus Species 0.000 description 1
- 241001446843 Oebalus pugnax Species 0.000 description 1
- 241000510960 Oesophagostomum Species 0.000 description 1
- 241000257191 Oestridae Species 0.000 description 1
- 241000488557 Oligonychus Species 0.000 description 1
- 241000243981 Onchocerca Species 0.000 description 1
- 241000243985 Onchocerca volvulus Species 0.000 description 1
- 241000777573 Oncometopia Species 0.000 description 1
- 241000963703 Onychiurus armatus Species 0.000 description 1
- 241001491877 Operophtera brumata Species 0.000 description 1
- 241000221671 Ophiostoma ulmi Species 0.000 description 1
- 241000238887 Ornithodoros Species 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 241001250072 Oryctes rhinoceros Species 0.000 description 1
- 241000975417 Oscinella frit Species 0.000 description 1
- 241000243795 Ostertagia Species 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 description 1
- 229910019213 POCl3 Inorganic materials 0.000 description 1
- 235000001591 Pachyrhizus erosus Nutrition 0.000 description 1
- 244000258470 Pachyrhizus tuberosus Species 0.000 description 1
- 235000018669 Pachyrhizus tuberosus Nutrition 0.000 description 1
- 241001510250 Panchlora Species 0.000 description 1
- 241000486438 Panolis flammea Species 0.000 description 1
- 241000488585 Panonychus Species 0.000 description 1
- 241000488581 Panonychus citri Species 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 241001516563 Paratrioza Species 0.000 description 1
- 241001523676 Parcoblatta Species 0.000 description 1
- 241001130603 Parlatoria <angiosperm> Species 0.000 description 1
- 241000541402 Pealius mori Species 0.000 description 1
- 241000517325 Pediculus Species 0.000 description 1
- 241000517306 Pediculus humanus corporis Species 0.000 description 1
- 239000005814 Pencycuron Substances 0.000 description 1
- 206010064458 Penicilliosis Diseases 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 241001123663 Penicillium expansum Species 0.000 description 1
- 208000022034 Penile disease Diseases 0.000 description 1
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 description 1
- 241000320508 Pentatomidae Species 0.000 description 1
- 239000005816 Penthiopyrad Substances 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- 241000256683 Peregrinus Species 0.000 description 1
- 241001510010 Periplaneta fuliginosa Species 0.000 description 1
- 241000201565 Peronospora viciae f. sp. pisi Species 0.000 description 1
- 241000218196 Persea Species 0.000 description 1
- 241001608567 Phaedon cochleariae Species 0.000 description 1
- 241000555275 Phaeosphaeria Species 0.000 description 1
- 241000440445 Phakopsora meibomiae Species 0.000 description 1
- 241000682645 Phakopsora pachyrhizi Species 0.000 description 1
- 241000250508 Phalangium Species 0.000 description 1
- 241000255129 Phlebotominae Species 0.000 description 1
- 241000722350 Phlebotomus <genus> Species 0.000 description 1
- 241000916811 Phloeomyzus Species 0.000 description 1
- 241001401863 Phorodon Species 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000005922 Phosphane Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 241001525654 Phyllocnistis citrella Species 0.000 description 1
- 241000497192 Phyllocoptruta oleivora Species 0.000 description 1
- 241001517955 Phyllonorycter blancardella Species 0.000 description 1
- 241001640279 Phyllophaga Species 0.000 description 1
- 241000210649 Phyllosticta ampelicida Species 0.000 description 1
- 241001396980 Phytonemus pallidus Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 241000351396 Picea asperata Species 0.000 description 1
- 239000005818 Picoxystrobin Substances 0.000 description 1
- 241000255972 Pieris <butterfly> Species 0.000 description 1
- 241000255969 Pieris brassicae Species 0.000 description 1
- 241000690748 Piesma Species 0.000 description 1
- 241000669426 Pinnaspis aspidistrae Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 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
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241001600434 Plectroglyphidodon lacrymatus Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000883286 Polydesmus Species 0.000 description 1
- 241000952063 Polyphagotarsonemus latus Species 0.000 description 1
- 241001660172 Polyrhachis Species 0.000 description 1
- 241000193943 Pratylenchus Species 0.000 description 1
- 241001384632 Priobium carpini Species 0.000 description 1
- 235000015926 Proboscidea louisianica ssp. fragrans Nutrition 0.000 description 1
- 235000015925 Proboscidea louisianica subsp. louisianica Nutrition 0.000 description 1
- 239000005820 Prochloraz Substances 0.000 description 1
- 239000005821 Propamocarb Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000005824 Proquinazid Substances 0.000 description 1
- 239000005825 Prothioconazole Substances 0.000 description 1
- 241001483625 Protopulvinaria pyriformis Species 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 235000005805 Prunus cerasus Nutrition 0.000 description 1
- 241001274600 Pseudacysta Species 0.000 description 1
- 241000721694 Pseudatomoscelis seriatus Species 0.000 description 1
- 241000668989 Pseudaulacaspis Species 0.000 description 1
- 241000722234 Pseudococcus Species 0.000 description 1
- 241001281802 Pseudoperonospora Species 0.000 description 1
- 241001281805 Pseudoperonospora cubensis Species 0.000 description 1
- 241000342307 Pseudoperonospora humuli 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
- 241001180370 Psylliodes chrysocephalus Species 0.000 description 1
- 241001454908 Pteromalus Species 0.000 description 1
- 241000396244 Ptilinus Species 0.000 description 1
- 241001105129 Ptinus Species 0.000 description 1
- 241000411574 Ptinus fur Species 0.000 description 1
- 239000005869 Pyraclostrobin Substances 0.000 description 1
- 241000228453 Pyrenophora Species 0.000 description 1
- 241000520648 Pyrenophora teres Species 0.000 description 1
- 241000932787 Pyrilla Species 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 241000944748 Quesada Species 0.000 description 1
- 241000201375 Radopholus similis Species 0.000 description 1
- 241000173769 Ramularia collo-cygni Species 0.000 description 1
- 241000549289 Rastrococcus Species 0.000 description 1
- 241001509970 Reticulitermes <genus> Species 0.000 description 1
- 241000590363 Reticulitermes lucifugus Species 0.000 description 1
- 241000590379 Reticulitermes santonensis Species 0.000 description 1
- 241001481703 Rhipicephalus <genus> Species 0.000 description 1
- 241000298314 Rhipiphorothrips cruentatus Species 0.000 description 1
- 241001617044 Rhizoglyphus Species 0.000 description 1
- 241000722251 Rhodnius Species 0.000 description 1
- 241000125162 Rhopalosiphum Species 0.000 description 1
- 241000125167 Rhopalosiphum padi Species 0.000 description 1
- 241001515790 Rhynchosporium secalis Species 0.000 description 1
- 241000752065 Rhyzobius Species 0.000 description 1
- 241000855013 Rotylenchus Species 0.000 description 1
- 241000231739 Rutilus rutilus Species 0.000 description 1
- 241001450655 Saissetia Species 0.000 description 1
- 241000509416 Sarcoptes Species 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- 241000254062 Scarabaeidae Species 0.000 description 1
- 241000365762 Scirtothrips Species 0.000 description 1
- 241000365764 Scirtothrips dorsalis Species 0.000 description 1
- 241001558929 Sclerotium <basidiomycota> Species 0.000 description 1
- 235000018519 Scolymus Nutrition 0.000 description 1
- 240000005687 Scolymus hispanicus Species 0.000 description 1
- 241000522594 Scorpio maurus Species 0.000 description 1
- 241000239226 Scorpiones Species 0.000 description 1
- 241001157780 Scutigera coleoptrata Species 0.000 description 1
- 241000883293 Scutigerella Species 0.000 description 1
- 241000669327 Selenaspidus Species 0.000 description 1
- 239000000877 Sex Attractant Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000005835 Silthiofam Substances 0.000 description 1
- 241001177138 Sinoxylon Species 0.000 description 1
- 241001365173 Sirex juvencus Species 0.000 description 1
- 241000254181 Sitophilus Species 0.000 description 1
- 241000336929 Sogata Species 0.000 description 1
- 241000176085 Sogatella Species 0.000 description 1
- 241000176086 Sogatella furcifera Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 241001250060 Sphacelotheca Species 0.000 description 1
- 241000532885 Sphenophorus Species 0.000 description 1
- 241000011575 Spilocaea Species 0.000 description 1
- 241001250070 Sporisorium reilianum Species 0.000 description 1
- 241001177161 Stegobium paniceum Species 0.000 description 1
- 241000283614 Stephanitis nashi Species 0.000 description 1
- 241000950030 Sternechus Species 0.000 description 1
- 241000532689 Stictocephala Species 0.000 description 1
- 241001494139 Stomoxys Species 0.000 description 1
- 241001494115 Stomoxys calcitrans Species 0.000 description 1
- 241000098292 Striacosta albicosta Species 0.000 description 1
- 229930182692 Strobilurin Natural products 0.000 description 1
- 241000244174 Strongyloides Species 0.000 description 1
- 241000244177 Strongyloides stercoralis Species 0.000 description 1
- 241001301282 Succinea Species 0.000 description 1
- 241001649248 Supella longipalpa Species 0.000 description 1
- 241000255626 Tabanus <genus> Species 0.000 description 1
- 241000244159 Taenia saginata Species 0.000 description 1
- 241000244157 Taenia solium Species 0.000 description 1
- 241000228446 Taphrina Species 0.000 description 1
- 241000228448 Taphrina deformans Species 0.000 description 1
- 239000005839 Tebuconazole Substances 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 241001454294 Tetranychus Species 0.000 description 1
- 241000239292 Theraphosidae Species 0.000 description 1
- 241000028626 Thermobia domestica Species 0.000 description 1
- 241000561282 Thielaviopsis basicola Species 0.000 description 1
- 102100034757 Thiol S-methyltransferase METTL7B Human genes 0.000 description 1
- 101710082490 Thiol S-methyltransferase METTL7B Proteins 0.000 description 1
- 239000005842 Thiophanate-methyl Substances 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 241000130764 Tinea Species 0.000 description 1
- 208000002474 Tinea Diseases 0.000 description 1
- 241001519477 Tinocallis Species 0.000 description 1
- 241001161507 Titanus Species 0.000 description 1
- 239000005845 Tolclofos-methyl Substances 0.000 description 1
- 241001238451 Tortrix viridana Species 0.000 description 1
- 241000271862 Toxoptera Species 0.000 description 1
- 239000005846 Triadimenol Substances 0.000 description 1
- 241000018135 Trialeurodes Species 0.000 description 1
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 1
- 241001414833 Triatoma Species 0.000 description 1
- 241001414831 Triatoma infestans Species 0.000 description 1
- 239000005847 Triazoxide Substances 0.000 description 1
- 241001439624 Trichina Species 0.000 description 1
- 241000243774 Trichinella Species 0.000 description 1
- 241000194297 Trichinella britovi Species 0.000 description 1
- 241000243776 Trichinella nativa Species 0.000 description 1
- 241000243779 Trichinella nelsoni Species 0.000 description 1
- NHTFLYKPEGXOAN-UHFFFAOYSA-N Trichlamide Chemical compound CCCCOC(C(Cl)(Cl)Cl)NC(=O)C1=CC=CC=C1O NHTFLYKPEGXOAN-UHFFFAOYSA-N 0.000 description 1
- 241001259047 Trichodectes Species 0.000 description 1
- 241001220308 Trichodorus Species 0.000 description 1
- 241000255985 Trichoplusia Species 0.000 description 1
- 241000610628 Trichoptilium incisum Species 0.000 description 1
- 241001414858 Trioza Species 0.000 description 1
- 235000019714 Triticale Nutrition 0.000 description 1
- 239000005859 Triticonazole Substances 0.000 description 1
- 241000267823 Trogoderma Species 0.000 description 1
- 241000215579 Trogoxylon Species 0.000 description 1
- 241001168740 Tychius Species 0.000 description 1
- 241000243782 Tylenchida Species 0.000 description 1
- 241000855019 Tylenchorhynchus Species 0.000 description 1
- 241001267618 Tylenchulus Species 0.000 description 1
- 241001267621 Tylenchulus semipenetrans Species 0.000 description 1
- 241000841223 Typhlocyba Species 0.000 description 1
- 241000959260 Typhula Species 0.000 description 1
- 241000333201 Typhula incarnata Species 0.000 description 1
- 241001106462 Ulmus Species 0.000 description 1
- 241000669245 Unaspis Species 0.000 description 1
- 241000122724 Urocerus augur Species 0.000 description 1
- 241000157667 Urocystis occulta Species 0.000 description 1
- 241000007070 Ustilago nuda Species 0.000 description 1
- 241000905623 Venturia oleaginea Species 0.000 description 1
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
- 241001274787 Viteus Species 0.000 description 1
- 241000609108 Wohlfahrtia Species 0.000 description 1
- 241000244002 Wuchereria Species 0.000 description 1
- 235000013447 Xanthosoma atrovirens Nutrition 0.000 description 1
- 240000001781 Xanthosoma sagittifolium Species 0.000 description 1
- 241000201423 Xiphinema Species 0.000 description 1
- 241001510583 Xyleborus Species 0.000 description 1
- 241001604425 Xylotrechus Species 0.000 description 1
- 241000792844 Xylotrupes Species 0.000 description 1
- 241001466337 Yponomeuta Species 0.000 description 1
- 241001466330 Yponomeuta malinellus Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000005870 Ziram Substances 0.000 description 1
- 241000964233 Zootermopsis nevadensis Species 0.000 description 1
- 239000005863 Zoxamide Substances 0.000 description 1
- 241001360088 Zymoseptoria tritici Species 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
- KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
- OYVABZRZDZPVQD-UHFFFAOYSA-N [F].C=1C=CSC=1 Chemical compound [F].C=1C=CSC=1 OYVABZRZDZPVQD-UHFFFAOYSA-N 0.000 description 1
- WHDHEVMINMZADQ-UHFFFAOYSA-N [F].N1C=CC=C1 Chemical compound [F].N1C=CC=C1 WHDHEVMINMZADQ-UHFFFAOYSA-N 0.000 description 1
- JSOJVSBOEOWZJX-UHFFFAOYSA-N [O].N1=CC=CC2=CC=CC=C21 Chemical compound [O].N1=CC=CC2=CC=CC=C21 JSOJVSBOEOWZJX-UHFFFAOYSA-N 0.000 description 1
- JSGLHKGTKZPJKI-UHFFFAOYSA-N [O]C(F)Cc1ccccc1 Chemical compound [O]C(F)Cc1ccccc1 JSGLHKGTKZPJKI-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical group 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000012872 agrochemical composition Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 125000006193 alkinyl group Chemical group 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 1
- BREATYVWRHIPIY-UHFFFAOYSA-N amisulbrom Chemical compound CN(C)S(=O)(=O)N1C=NC(S(=O)(=O)N2C3=CC(F)=CC=C3C(Br)=C2C)=N1 BREATYVWRHIPIY-UHFFFAOYSA-N 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 230000003698 anagen phase Effects 0.000 description 1
- 239000002152 aqueous-organic solution Substances 0.000 description 1
- 238000000065 atmospheric pressure chemical ionisation Methods 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910001423 beryllium ion Inorganic materials 0.000 description 1
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
- CXNPLSGKWMLZPZ-UHFFFAOYSA-N blasticidin-S Natural products O1C(C(O)=O)C(NC(=O)CC(N)CCN(C)C(N)=N)C=CC1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 1
- 229960003168 bronopol Drugs 0.000 description 1
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012677 causal agent Substances 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- JOXAXMBQVHFGQT-UHFFFAOYSA-J copper;manganese(2+);n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[Cu+2].[S-]C(=S)NCCNC([S-])=S.[S-]C(=S)NCCNC([S-])=S JOXAXMBQVHFGQT-UHFFFAOYSA-J 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 229960002042 croconazole Drugs 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 208000002925 dental caries Diseases 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 description 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 229940004812 dicloran Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 description 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 description 1
- JMXKCYUTURMERF-UHFFFAOYSA-N dodemorph Chemical compound C1C(C)OC(C)CN1C1CCCCCCCCCCC1 JMXKCYUTURMERF-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 1
- 229930184149 elsinochrome Natural products 0.000 description 1
- 206010014881 enterobiasis Diseases 0.000 description 1
- DNVPQKQSNYMLRS-SOWFXMKYSA-N ergosterol Chemical compound C1[C@@H](O)CC[C@]2(C)[C@H](CC[C@]3([C@H]([C@H](C)/C=C/[C@@H](C)C(C)C)CC[C@H]33)C)C3=CC=C21 DNVPQKQSNYMLRS-SOWFXMKYSA-N 0.000 description 1
- 230000012173 estrus Effects 0.000 description 1
- DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 description 1
- PQLFROTZSIMBKR-UHFFFAOYSA-N ethenyl carbonochloridate Chemical compound ClC(=O)OC=C PQLFROTZSIMBKR-UHFFFAOYSA-N 0.000 description 1
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical class CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 description 1
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 description 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 description 1
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 description 1
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
- NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 description 1
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 description 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 1
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 description 1
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 description 1
- 239000002316 fumigant Substances 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- LTVDTKRMOQDRCH-UHFFFAOYSA-N furan;1h-pyrrole Chemical compound C=1C=CNC=1.C=1C=COC=1 LTVDTKRMOQDRCH-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000004512 granular bait Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 150000005826 halohydrocarbons Chemical class 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011630 iodine 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
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- VROYMKJUVCKXBU-YACXGCCLSA-N irumamycin Chemical compound CCC(=O)[C@@]1(C)OC1[C@H](C)C[C@@H](C)[C@@H]1[C@H](C)C(O)[C@@H](C)/C=C/[C@H](OC2O[C@H](C)[C@@H](O)[C@H](OC(N)=O)C2)CCC/C=C(C)/[C@@H](O2)C(C)=CC[C@]2(O)CC(=O)O1 VROYMKJUVCKXBU-YACXGCCLSA-N 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 210000002752 melanocyte Anatomy 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- 150000002738 metalloids Chemical class 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- IXJOSTZEBSTPAG-UHFFFAOYSA-N methasulfocarb Chemical compound CNC(=O)SC1=CC=C(OS(C)(=O)=O)C=C1 IXJOSTZEBSTPAG-UHFFFAOYSA-N 0.000 description 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 1
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- 229920000257 metiram Polymers 0.000 description 1
- KCIRYJNISRMYFI-UHFFFAOYSA-N mildiomycin Natural products NC(CO)C(=O)NC1C=CC(OC1C(O)(CC(O)CNC(=N)N)C(=O)O)N2CN=C(N)C(=C2)CO KCIRYJNISRMYFI-UHFFFAOYSA-N 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 230000000394 mitotic effect Effects 0.000 description 1
- OZGNYLLQHRPOBR-DHZHZOJOSA-N naftifine Chemical compound C=1C=CC2=CC=CC=C2C=1CN(C)C\C=C\C1=CC=CC=C1 OZGNYLLQHRPOBR-DHZHZOJOSA-N 0.000 description 1
- 229960004313 naftifine Drugs 0.000 description 1
- 235000000010 nanu Nutrition 0.000 description 1
- 244000082862 nanu Species 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 239000004311 natamycin Substances 0.000 description 1
- 235000010298 natamycin Nutrition 0.000 description 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
- 229960003255 natamycin Drugs 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- DCUJJWWUNKIJPH-UHFFFAOYSA-N nitrapyrin Chemical compound ClC1=CC=CC(C(Cl)(Cl)Cl)=N1 DCUJJWWUNKIJPH-UHFFFAOYSA-N 0.000 description 1
- IBGCXOFOCKCBNQ-UHFFFAOYSA-N nitro cyanate Chemical compound [O-][N+](=O)OC#N IBGCXOFOCKCBNQ-UHFFFAOYSA-N 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- GVMDZMPQYYHMSV-UHFFFAOYSA-N octyl benzenesulfonate Chemical class CCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVMDZMPQYYHMSV-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 1
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N pentanoic acid group Chemical group C(CCCC)(=O)O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229940044652 phenolsulfonate Drugs 0.000 description 1
- 229910000064 phosphane Inorganic materials 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 229940093916 potassium phosphate Drugs 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 229960002132 pyrrolnitrin Drugs 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000001843 schistosomicidal effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000004509 smoke generator Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 210000004894 snout Anatomy 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- IHTAIAZIELSSOO-MKWAYWHRSA-N sodium (Z)-hydroxyimino-(1-hydroxypropan-2-yl)-oxidoazanium Chemical compound [Na+].CC(CO)[N+](\[O-])=N\O IHTAIAZIELSSOO-MKWAYWHRSA-N 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- QTENRWWVYAAPBI-YCRXJPFRSA-N streptomycin sulfate Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O QTENRWWVYAAPBI-YCRXJPFRSA-N 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- CMQCNTNASCDNGR-UHFFFAOYSA-N toluene;hydrate Chemical compound O.CC1=CC=CC=C1 CMQCNTNASCDNGR-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- 239000004559 tracking powder Substances 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- NTADARNNAPPIBY-UHFFFAOYSA-N triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=CC=NC2=CN=NN12 NTADARNNAPPIBY-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- 229940116861 trichinella britovi Drugs 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical class COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 239000004061 uncoupling agent Substances 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 239000004561 vapour releasing product Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000004549 water soluble granule Substances 0.000 description 1
- 239000004554 water soluble tablet Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- CHNQZRKUZPNOOH-UHFFFAOYSA-J zinc;manganese(2+);n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[Zn+2].[S-]C(=S)NCCNC([S-])=S.[S-]C(=S)NCCNC([S-])=S CHNQZRKUZPNOOH-UHFFFAOYSA-J 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/195—Radicals derived from nitrogen analogues of carboxylic acids
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/12—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to hydrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Description
说明
本发明涉及联苯脒衍生物及其制备方法,以及它们作为杀真菌剂或杀虫剂活性试剂的用途,特别是以杀真菌或杀虫组合物或的形式,以及用这些化合物或它们的组合物来控制植物病原真菌或害虫(尤其是植物的植物病原真菌或害虫)的方法。
在国际专利申请WO-00/46184中,揭示了某些苯脒衍生物。但是,该文献中没有具体揭示,也没有提出选择这类其中苯环依据本发明被取代因而具有出乎意料且明显提高的杀真菌活性的化合物。
在农业领域中,为了避免或控制对活性成分有耐药性的菌株产生,人们对于使用新型农药化合物一直很感兴趣。而且,为了减少活性化合物的用量,同时保持与已知化合物至少等同的效力,人们对于使用比那些已知的农药活性更高的化合物也很感兴趣。
同样,人们对于使用新颖的杀虫剂、杀线虫剂或杀螨剂以控制害虫或其它有害生物也非常感兴趣。
本发明人已经发现一类具有上述效果或益处的新化合物。
因此,本发明提供通式(I)的联苯脒衍生物及其盐、N-氧化物(N-oxydes)、金属络合物、准金属络合物和光学活性或几何异构体:
式中:
R1表示H、取代或未取代的C1-C12-烷基、取代或未取代的C2-C12-烯基、取代或未取代的C2-C12-炔基、SH或取代或未取代的S-C1-C12-烷基;
R2表示取代或未取代的C1-C12-烷基;
R3表示取代或未取代的C2-C12-烷基、取代或未取代的C3-C6-环烷基、取代或未取代的C2-C12-烯基、取代或未取代的C2-C12-炔基、卤代-C1-C12-烷基;或者
R1和R2、R1和R3或R2和R3可以一起形成取代或未取代的5-至7-元杂环;
R4表示取代或未取代的C1-C12-烷基、卤原子、卤代-C1-C12-烷基、取代或未取代的O-C1-C12-烷基或氰基;
m表示0、1、2、3、4或5;
R5表示H、取代或未取代的C1-C12-烷基、卤原子、卤代-C1-C12-烷基、取代或未取代的O-C1-C12-烷基或氰基;
R6可相同或不同,表示H、卤原子、硝基、氰基;三烷基甲硅烷基、C1-C8-烷基、取代或未取代的C1-C4-烷基-苯基、取代或未取代的苯基、C1-C4-烷氧基、C1-C4-烷氧基-C1-C4-烷基、C1-C8-烷硫基、C1-C6-卤代烷基、C1-C6-卤代烷氧基或C1-C6-卤代烷硫基、取代或未取代的C1-C4-烷氧基-苯基如苄氧基、取代或未取代的苯氧基、取代或未取代的烷氨基-C1-C8-NR7R8、取代或未取代的NR7R8、C1-C8-烷基-S(O)nR9、-S(O)nR9、C1-C8-烷基-SO2NR7R8、-SO2NR7R8、C1-C8-烷基-C(O)R10、-CR9=N-O-R11;
两个取代基R6可形成碳环或杂环,所述杂环可包含一个或多个选自O、N、S的杂原子;
n表示0、1或2;
R7和R8可相同或不同,表示H、取代或未取代的C1-C6-烷基;
R7和R8可形成杂环,该杂环可包含一个或多个选自O、N、S的杂原子;
R9表示H、取代或未取代的直链型或支链型C1-C8-烷基、C1-C8-烯基、C1-C8-炔基(alkinyl);
R10表示H、取代或未取代的直链型或支链型C1-C8-烷基、C1-C8-烷氧基、NR7R8;
R11表示H、取代或未取代的直链型或支链型C1-C8-烷基、C1-C4-烷基-苯基、C1-C4-烷氧基-C1-C4-烷基、取代或未取代的C1-C4-烷基-苯基、取代或未取代的苯基;
R9和R11可形成杂环,该杂环可包含一个或多个选自O、N、S的杂原子。
本发明的任何化合物可根据化合物中不对称中心的数目以一种或多种光学、几何或手性异构体的形式存在。因此,本发明同样涉及所有光学异构体和它们的外消旋或非外消旋(scalemic)混合物(术语“非外消旋”指对映异构体以不同比例混合的混合物),还涉及所有可能的立体异构体以任何比例混合的混合物。可根据本领域技术人员已知的方法分离非对映异构体和/或光学异构体。
本发明的任何化合物可根据化合物中双键的数目以一种或多种几何异构体的形式存在。因此,本发明同样涉及所有几何异构体和它们以所有可能的比例混合的所有可能的混合物。可通过本领域技术人员已知的常规方法分离几何异构体。
对于本发明的化合物,卤素表示氟、溴、氯或碘中的一种,杂原子可以是氮、氧或硫。
优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R1表示H;C1-C12-烷基,优选C1-C12-烷基如甲基;或SH。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R3表示C2-C12-烷基,优选未取代的C2-C4-烷基如乙基、正丙基、异丙基;C2-C12-烯基,优选C3-C4-烯基如丙烯基或烯丙基;C3-C6-环烷基如环丙基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R2和R3可一起形成取代或未取代的5-至7-元杂环,优选6-元杂环,更优选哌啶基或吡咯烷基(pyrolidinyl),更优选2-烷基化的-吡咯烷基如2-甲基-吡咯烷基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R4表示C1-C12-烷基,优选未取代的C1-C12-烷基如甲基和乙基;卤原子如氟原子和氯原子;三氟甲基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R5表示H,C1-C12-烷基,优选未取代的C1-C12-烷基如甲基和乙基;卤原子如氟原子和氯原子;三氟甲基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:m表示1、2、3或4;更优选m表示1、2或3。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R6可相同或不同,表示H;F、Cl、Br、I;硝基;氰基;C1-C6-烷基;C1-C4-烷基-苯基,其可以未被取代或被卤素、C1-C4-烷基或C1-C4-卤代烷基取代;苯基,其可以未被取代或被卤素、C1-C4-烷基或C1-C4-卤代烷基取代;C1-C6-烷氧基;C1-C4-烷氧基-C1-C4-烷基;C1-C6-烷硫基;C1-C6-卤代烷基;C1-C6-卤代烷氧基;C1-C6-卤代烷硫基;C1-C6-烷氧基;C1-C4-烷氧基-C1-C4-烷基;C1-C6-烷硫基;苄氧基,其可以未被取代或被卤素取代;苯氧基,其可以未被取代或被卤原子或CF3取代;NR7R8;C1-C4-烷基-NR7R8;S(O)nR9;C1-C4-烷基-S(O)nR9;OR10;C1-C4-烷基-COR10;-CR9=N-O-R11。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R7和R8可相同或不同,表示H、C1-C6烷基,或者R7和R8可形成还包含选自O、S、N的杂原子的杂环。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R9表示H、甲基或乙基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R10表示H;C1-C4-烷基;C1-C4-烷氧基;NR7R8。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R11表示H;C1-C4-烷基;C1-C4-卤代烷基;C1-C4-烷基-苯基,其中苯基可被F、Cl、Br、I、C1-C4-烷基、C1-C4-卤代烷基或C1-C4-卤代烷氧基取代基;C1-C4-烷氧基-C1-C4-烷基;苯氧基;苄氧基。
更优选的依据本发明的通式(I)的化合物是具有以下特征的化合物:R9和R11可形成还包含选自O、S、N的杂原子的5-或6-元杂环。
上述关于化合物的取代基的优选方案可以任何方式组合。因此这些优选特征的组合提供了多种类别的依据本发明的化合物。这些类别的本发明优选化合物的例子可具有以下组合特征:
R1的优选特征与R2至R6或至R11(如果合适)的优选特征;
R2的优选特征与R1至R6或至R11(如果合适)的优选特征;
R3的优选特征与R1至R6或至R11(如果合适)的优选特征;
R4的优选特征与R1至R6或至R11(如果合适)的优选特征;
R5的优选特征与R1至R6或至R11(如果合适)的优选特征。
在这些依据本发明的化合物的取代基的优选特征的组合中,所有优选特征还可选自各m、n和R1-R11的更优选特征,以形成最优选的依据本发明的化合物类别。
本发明还涉及一种制备通式(I)的化合物的方法。通常,依据本发明的通式(I)的化合物的制备可按照流程1进行。
流程1
因此,依据本发明的其它方面,提供一种通过通式(IIa)或(Va)的苯胺衍生物与通式(IV)的硼酸衍生物的反应来制备通式(I)或(VII)的苯胺衍生物的方法:
式中
R1、R2、R3、R4和R5如文中所定义,
X表示卤素、甲苯磺酸基(tosylate)、SOMe、甲磺酸基(mesylate)或三氟甲磺酸基(triflate);
式中
m和R6如文中所定义;
A1和A2各自表示氢,或者一起表示四甲基亚乙基(tetramethylethylene)。
依据本发明的方法(a)还包括一个或多个以下特征:
存在酸结合剂;
存在惰性有机稀释剂;
存在催化剂。
依据本发明的方法(a)使用2,3-二甲基-4-溴代-苯胺和4-叔丁基-苯基-硼酸作为原料和催化剂进行。方法(a)可依据流程2进行:
流程2
为了依据本发明进行方法(a),通式(IIa)或(Va)的苯胺或脒衍生物分别用作原料。
优选用于进行本发明的方法(a)的原料是通式(IIa)或(Va)的化合物,其中R1、R2、R3、R4和R5表示文中在描述本发明的通式(I)的优选化合物中所定义的取代基。
X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基。
通式(IIa)的苯胺衍生物和通式(IV)的硼酸衍生物以及它们各自的制备方法是已知的。
通式(IV)提供更需要用作进行本发明的方法(a)的硼酸衍生物的一般定义。在通式(IV)中,R6和m优选地表示在说明本发明的通式(I)的化合物中已经描述的取代基,对于A1和A2优选各自表示氢,或者一起表示通式(IV)的化合物的四甲基亚乙基
通式(IV)的硼酸衍生物是已知的,可通过例如WO-01/90084或US-5,633,218描述的已知方法制备。这些衍生物可通过例如使通式(VI)的苯基衍生物与通式(XI)的硼酸酯或4,4,4′,4′,5,5,5′,5′-八甲基-2,2′-二-1,3,2-二杂氧戊硼烷(dioxaborolane)在镁或烷基锂存在下反应来制得:
式中R6和m如文中所定义,X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基;
B(O-Alk)3
(XI)
式中Alk表示C1-C4-烷基。可以使用四氢呋喃之类的稀释剂。
通式(XI)提供可用于制备本发明的通式(IV)的硼酸(boronic acid)衍生物的硼酸酯的一般定义。在通式(XI)中,Alk优选表示甲基、乙基、正丙基、异丙基,更优选是甲基或乙基,通式(XI)的硼酸酯是已知的化合物。
本发明的另一方面涉及通过使通式(IIb)或(Vb)的硼酸衍生物与通式(VI)的苯基衍生物反应来制备通式(I)或(VII)的苯胺衍生物的方法(b):
式中
R1、R2、R3、R4和R5如文中所定义,
A1和A2各自表示氢,或者一起表示四甲基亚乙基;
通式(VI)
式中
R6和m如文中所定义;
X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基。
依据本发明的方法(b)还包括一个或多个以下特征:
存在酸结合剂;
存在惰性有机稀释剂;
存在催化剂。
依据本发明的另一方面涉及通过使通式(IIa)或(Va)的苯胺衍生物与通式(VI)的苯基衍生物在钯、镍或铂催化剂存在下且在4,4,4′,4′,5,5,5′,5′-八甲基-2,2′-二-1,3,2-二杂氧戊硼烷存在下反应来制备通式(I)或(VII)的苯胺衍生物的方法:
式中
R1、R2、R3、R4和R5如文中所定义,
X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基;
式中
R6和m如文中所定义;
X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基。
依据本发明的方法(c)还包括一个或多个以下特征:
存在酸结合剂;
存在惰性有机稀释剂。
通式(IIa)和(Va)提供可用作进行本发明的方法(a)或(c)的反应组分的取代胺衍生物的一般定义。在这些通式中,R1、R2、R3、R4和R5优选表示在描述本发明的通式(I)的化合物中所定义的取代基。
卤素优选表示氯、溴或碘,更优选是溴或碘。
通式(II)的苯胺衍生物是已知化合物,可通过已知方法由相应的硝基化合物通过还原来制备,或者通过相应的苯胺衍生物的卤化来制备。
可用作进行本发明的方法(a)的原料的通式(IV)的硼酸衍生物是已知的,或者是可商购的试剂。
通式(IIb)和(Vb)提供可用作进行本发明的方法(b)的反应组分的硼酸衍生物的一般定义。在这些通式中,R1、R2、R3、R4和R5优选表示在描述本发明的通式(I)的化合物中所定义的取代基。A1和A2优选各自表示氢,或者一起表示四甲基亚乙基。
通式(IIb)、(Vb)的硼酸衍生物或通式(VI)的苯基衍生物是已知的,可通过已知方法制备。
通式(I)和(Va)的脒衍生物可通过本发明的其它方法制得。可以考虑依据本发明的方法(d)的不同选择形式,它们称为依据本发明的方法(d1)、方法(d2)和方法(d3)。
依据本发明的方法(d)包括使通式(VII)或(IIa)的苯胺衍生物与不同试剂反应,从而分别定义为方法(d1)、(d2)和(d3):
式中
R4、R5、R5、R6和m如文中所定义;
X表示卤素、三氟甲磺酸基、SOMe、甲磺酸基或甲苯磺酸基。
还使用通式(VIII)的酰胺衍生物进行方法(d1):
式中
R1、R2、R3如文中所定义。
依据本发明的方法(d1)还包括一个或多个以下特征:
存在卤化剂,例如PCl5、PCl3、POCl3、SOCl2;
存在稀释剂。
使用4′-叔丁基-2,5-二甲基联苯-4-胺、哌啶-2-酮和三氯化磷作为原料以及酸进行本发明的方法(d1)。方法(d1)可依据流程3进行。
流程3
通式(VII)提供可用作进行本发明的方法(d1)的原料的联苯胺的一般定义。在此通式中,R1、R2、R3、R4、R5、R6和m优选表示在描述本发明的通式(I)的化合物中所定义的取代基或数值。
使用通式(IX)的氨基-缩醛衍生物进行方法(d2):
式中
R1、R2、R3如文中所定义;
B1和B2分别表示烷基,或者一起形成环烷基。
依据本发明的方法(d2)还包括一个或多个以下特征:
存在酸或碱;
存在稀释剂。
使用4′-叔丁基-2,5-二甲基联苯-4-胺和N-(二甲氧基甲基)-N-甲基乙胺作为原料进行本发明的方法(d2)。方法(d2)可依据流程4进行。
流程4
还可使用通式(X)的胺衍生物,在通式(XI)的原酸酯存在下进行方法(d3):
式中
R2和R3如文中所定义;
式中
R1如文中所定义;
B1、B2和B3各自表示烷基。
通式(VII)提供用作进行本发明的方法(d3)的原料的联苯胺的一般定义。在此通式中,R1、R2、R3、R4、R5、R6和m优选表示文中在描述本发明的通式(I)的化合物中所定义的取代基或数值。
使用4′-叔丁基-2,5-二甲基联苯-4-胺、原酸三甲酯和N-甲基-乙胺作为原料以及酸进行本发明的方法(d3)。方法(d3)可依据流程5进行。
流程5
通式(VII)提供用作进行本发明的方法(d3)的原料的联苯胺的一般定义。在此通式中,R1、R2、R3、R4、R5、R6和m优选表示文中在描述本发明的通式(I)的化合物中所定义的取代基或数值。
依据本发明的方法(d)、(d1)、(d2)或(d3)还包括一个或多个以下特征:
存在酸或碱;
存在稀释剂。
适用于进行本发明的方法(a)、(b)和(c)的稀释剂是所有普通惰性有机溶剂。优选使用脂族、脂环族或芳族烃,例如石油醚、己烷、庚烷、环己烷、甲基环己烷、苯、甲苯、二甲苯或萘烷;卤代烃,例如氯苯、二氯苯、二氯甲烷、氯仿、四氯化碳、二氯乙烷或三氯乙烷;醚,例如二乙醚、二异丙醚、甲基叔丁基醚、甲基叔戊基醚、二噁烷、四氢呋喃、1,2-二甲氧基乙烷、1,2-二乙氧基乙烷或茴香醚;腈,例如乙腈、丙腈、正丁腈或异丁腈、或苯甲腈;酰胺,例如N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、N-甲基甲酰苯胺、N-甲基吡咯烷酮或六甲基磷酸三酰胺;它们与水的混合物,或者纯水。
在各种情况下,适用于进行本发明的方法(d1)、(d2)和(d3)的稀释剂都是所有普通惰性有机溶剂。优选使用脂族、脂环族或芳族烃,例如石油醚、己烷、庚烷、环己烷、甲基环己烷、苯、甲苯、二甲苯或萘烷;醚,例如二乙醚、二异丙醚、甲基叔丁基醚、甲基叔戊基醚、二噁烷、四氢呋喃、1,2-二甲氧基乙烷、1,2-二乙氧基乙烷或茴香醚;腈,例如乙腈、丙腈、正丁腈或异丁腈、或苯甲腈;酰胺,例如N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、N-甲基甲酰苯胺、N-甲基吡咯烷酮或六甲基磷酸三酰胺;酯,例如乙酸甲酯或乙酸乙酯;亚砜,例如二甲亚砜;或者砜,例如环丁砜(sulpholane);醇,例如甲醇、乙醇、正丙醇或异丙醇、正丁醇、异丁醇、仲丁醇或叔丁醇、乙二醇、丙烷-1,2-二醇、乙氧基乙醇、甲氧基乙醇、二甘醇单甲醚、二甘醇单乙醚;它们与水的混合物,或者纯水。
适用于进行本发明的方法(a)、(b)和(c)的酸结合剂(acid binder)是所有常用于这类反应的无机碱和有机碱。优选使用碱土金属或碱金属氢化物、氢氧化物、氨基化合物、醇盐、乙酸盐、碳酸盐或碳酸氢盐,例如氢化钠、氨基钠、二异丙基氨基锂、甲醇钠、乙醇钠、叔丁醇钾、乙酸钠、乙酸钾、乙酸钙、氢氧化钠、氢氧化钾、碳酸钠、碳酸钾、碳酸氢钾、碳酸氢钠或碳酸铵;以及叔胺,例如三甲胺、三乙胺、三丁胺、N,N-二甲基苯胺、N,N-二甲基-苄胺、吡啶、N-甲基哌啶、N-甲基吗啉、N,N-二甲基氨基吡啶、二氮杂二环辛烷(DABCO)、二氮杂二环壬烯(DBN)或二氮杂二环十一碳烯(DBU)。
在各情况中,适用于进行本发明的方法(d1)、(d2)和(d3)的酸结合剂都是所有常用于这类反应的无机碱和有机碱。优选使用碱土金属或碱金属氢化物、氢氧化物、氨基化合物、醇盐、乙酸盐、氟化物、磷酸盐、碳酸盐或碳酸氢盐,例如氢化钠、氨基钠、二异丙基氨基锂、甲醇钠、乙醇钠、叔丁醇钾、氢氧化钠、氢氧化钾、乙酸钠、磷酸钠、磷酸钾、氟化钾、氟化铯、碳酸钠、碳酸钾、碳酸氢钾、碳酸氢钠、碳酸氢钠或碳酸铯;以及叔胺,例如三甲胺、三乙胺、三丁胺、N,N-二甲基苯胺、N,N-二甲基-苄胺、吡啶、N-甲基哌啶、N-甲基吗啉、N,N-二甲基氨基吡啶、二氮杂二环辛烷(DABCO)、二氮杂二环壬烯(DBN)或二氮杂二环十一碳烯(DBU)。
适用于进行本发明的方法(d3)的酸是常用于这类反应的所有无机酸和有机酸。优选使用对甲苯磺酸、甲磺酸、盐酸(气体、水溶液或有机溶液)或硫酸。
适用于进行本发明的方法(d1)的缩合剂(condensing agent)是常用于这类氨基化反应的所有缩合剂。优选使用酰卤形成剂,例如光气、三溴化磷、三氯化磷、五氯化磷、三氯氧磷或亚硫酰氯;酸酐形成剂,例如氯甲酸乙酯、氯甲酸甲酯、氯甲酸异丙酯、氯甲酸异丁酯或甲磺酰氯;碳二亚胺,例如N,N′-二环己基碳二亚胺(DCC)或其它常用缩合剂,例如五氧化二磷、多磷酸、N,N′-羰基二咪唑、2-乙氧基-N-乙氧基羰基-1,2-二氢喹啉(EEDQ)、三苯膦/四氯甲烷或溴代三吡咯烷基六氟磷酸_(phosphonium-hexafluorophosphate)。
本发明的方法(a)、(b)和(c)可以在催化剂存在下进行。优选的是钯盐或络合物,例如氯化钯、乙酸钯、四-(三苯基膦)钯、二氯化二-(三苯基膦)钯或氯化1,1′-二(二苯基膦基)二茂铁钯(II)。
还可以通过分别向反应混合物中加入钯盐和络合配体而直接在反应混合物中生成钯络合物,所述络合配体如三乙基膦(phosphane)、三叔丁基膦、三环己基膦、2-(二环己基膦)联苯、2-(二叔丁基膦)联苯、2-(二环己基膦)-2′-(N,N-二甲基氨基)-联苯、三苯基膦、三-(邻甲苯基)膦、3-(二苯基膦基)苯磺酸钠、三-2-(甲氧基苯基)膦、2,2′-二-(二苯基膦)-1,1′-联萘、1,4-二-(二苯基膦)丁烷、1,2-二-(二苯基膦)乙烷、1,4-二-(二环己基膦)丁烷、1,2-二-(二环己基膦)乙烷、2-(二环己基膦)-2′-(N,N-二甲基氨基)-联苯、二(二苯基膦基)二茂铁或三-(2,4-叔丁基苯基)-亚磷酸酯。
当进行本发明的方法(d)时,反应温度可以在较宽的范围内变化。通常,所述方法在0-150℃的温度下进行,优选在0-120℃的温度下进行,更优选在10-90℃的温度下进行。
当进行本发明的方法(a)、(b)时,反应温度在各情况中可以在较宽的范围内变化。通常,所述方法在0-180℃的温度下进行,优选在10-150℃的温度下进行,更优选在20-120℃的温度下进行。
当进行本发明的方法(a)时,通常每摩尔通式(IIa)或(Va)的胺或脒,使用0.5-15摩尔、优选0.8-8摩尔的通式(IV)的硼酸衍生物,1-5摩尔的酸结合剂和0.2-5摩尔%的催化剂。但是,还可以其它比例使用反应组分。按照常规方法进行操作(work-up)。通常,向反应物中加入水,分离沉淀物,干燥。如果合适,可使用常规方法(例如色谱或重结晶)除去残留的残余物中任何可能仍存在的杂质。
当进行本发明的方法(b)时,通常每摩尔通式(IIb)或(Vb)的硼酸衍生物,使用0.8-15摩尔、优选0.8-8摩尔的通式(VI)的苯基衍生物,1-10摩尔的酸结合剂和0.5-5摩尔%的催化剂。但是,还可以其它比例使用反应组分。按照常规方法进行操作。通常,向反应物中加入水,分离沉淀物,干燥。如果合适,可使用常规方法(例如色谱或重结晶)除去残留的残余物中任何可能仍存在的杂质。
当进行本发明的方法(c)时,通常每摩尔通式(VI)的苯基衍生物,使用0.8-15摩尔、优选0.8-8摩尔的通式(IIa)或(Va)的胺或脒衍生物,0.8-15摩尔、优选0.8-8摩尔的4,4,4′,4′,5,5,5′,5′-八甲基-2,2′-二-1,3,2-二杂氧戊硼烷,1-5摩尔的酸结合剂和1-5摩尔%的催化剂。但是,还可以其它比例使用反应组分。按照常规方法进行操作。通常,向反应物中加入水,分离沉淀物,干燥。如果合适,可使用常规方法(例如色谱或重结晶)除去残留的残余物中任何可能仍存在的杂质。
当进行本发明的方法(d1)时,通常每摩尔通式(VII)或(Va)的胺,使用0.8-50摩尔、优选1-10摩尔的通式(VIII)的酰胺和1-10摩尔的卤化剂。但是,还可以其它比例使用反应组分。按照常规方法进行操作。
当进行本发明的方法(d2)时,通常每摩尔通式(VII)或(Va)的胺,使用0.8-50摩尔、优选1-10摩尔的通式(IX)的氨基缩醛。但是,还可以其它比例使用反应组分。按照常规方法进行操作。
当进行本发明的方法(d3)时,通常每摩尔通式(VII)或(Va)的胺,使用1-10摩尔的通式(XI)的原酸酯,0.8-50摩尔、优选1-10摩尔的通式(X)的胺和催化量的酸。但是,还可以其它比例使用反应组分。按照常规方法进行操作。
所有依据本发明的方法一般都在大气压下进行。但是,在各情况中,还可以在加压或减压的情况下进行,通常在0.1巴至10巴之间。
本发明的通式(I)的化合物可依据文中所描述的方法制备。然而要理解,本领域技术人员基于其所掌握的常识和可获得的出版物,可以根据所需合成的各化合物的特殊性对本发明方法进行调整。
另一方面,本发明还涉及含有有效且非植物毒性量的通式(I)的活性化合物的杀真菌或杀虫组合物。
“有效且非植物毒性量”的表达方式指本发明的组合物量足以控制或破坏存在于或易于出现在农作物上的真菌,而该剂量并不会使所述农作物产生任何可以观察到的植物毒性症状。该量根据以下因素会在很宽的范围内变化:要控制的真菌、农作物的类型、气候条件和包含在本发明的杀真菌组合物中的化合物。
这种用量可通过系统田间试验来确定,这在本领域技术人员的能力范围内。
因此,依据本发明,提供一种杀真菌或杀虫组合物,该组合物包含有效量的上述通式(I)的化合物作为活性组分和农业上可接受的担体(support)、载体或填充物(filler)。
依据本发明,术语“担体”表示天然或合成的有机或无机化合物,它与通式(I)的活性化合物组合或联合使用,使活性材料更容易施用,特别是施用到植物部分上。因此,此担体通常是惰性的,并且应该是农业上可接受的。担体可为固体或液体。合适的担体的例子包括粘土、天然或合成的硅酸盐、二氧化硅、树脂、蜡、固体肥料、水、醇(特别是丁醇)、有机溶剂、矿物油和植物油以及它们的衍生物。也可以使用此类担体的混合物。
依据本发明的组合物也可以包含其它的组分。具体地,组合物还可包含表面活性剂。表面活性剂可为离子或非离子型乳化剂、分散剂或润湿剂或此类表面活性剂的混合物。例如,聚丙烯酸盐、木质素磺酸盐、苯酚磺酸盐或萘磺酸盐、环氧乙烷与脂肪醇或脂肪酸或脂肪胺的缩聚物、取代的苯酚(特别是烷基苯酚或芳基苯酚)、磺基琥珀酸酯的盐、牛磺酸衍生物(特别是牛磺酸烷基酯(alkyl taurate))、聚氧乙基化醇或苯酚的磷酸酯、多元醇的脂肪酸酯,和含有硫酸、磺酸和磷酸官能团的上述化合物的衍生物。当活性物质和/或惰性担体是不溶于水,并且当施用的媒介剂是水时,存在至少一种表面活性剂通常是至关重要的。较佳地,表面活性剂的含量以组合物的重量为基准计在5重量%至40重量%之间。
任选地,也可包括附加的组分,例如,保护性胶体、胶粘剂、增稠剂、触变剂、渗透剂、稳定剂(stabilisers)、螯合剂(sequestering agent)。更一般地,活性化合物可根据常用的配方技术与任何固体或液体添加剂相混合。
一般来说,本发明的组合物可含有0.05重量%至99重量%的活性化合物,较佳为10重量%至70重量%。
本发明的组合物可以各种形式使用,诸如气雾分散剂、饵剂(即刻可使用)、浓饵剂、块饵,微囊悬浮剂、冷雾浓缩剂、可撒粉剂、可乳化的浓缩剂、水包油乳剂、油包水乳剂、微囊粒剂、细粒剂、种子处理用可流动的浓缩剂、压缩气体(在压力下)制剂、气体发生剂、谷粒毒饵(grain bait)、粒饵(granular bait)、颗粒剂、热雾浓缩剂、大粒剂、微粒剂、油可分散性粉剂、油可混溶性可流动的浓缩剂、油可混溶剂、糊剂、植物棒剂、片饵、干种子处理用粉剂、农药包衣的种子、熏烟烛、熏烟匣、熏烟剂(smoke generator)、熏烟丸、熏烟棒、熏烟片、熏烟罐、可溶性液剂、可溶性粉剂、种子处理用溶液、悬浮剂(=可流动的浓缩剂)、追踪粉、超低量(ulv)液体、超低量(ulv)悬浮剂、熏蒸剂(vapourreleasing product)、水可分散粒剂或片剂、浆液处理用水可分散粉剂、水溶性粒剂或片剂、种子处理用水溶性粉剂、和可润湿性粉剂。
这些组合物不仅包括通过合适的设备如喷雾或撒粉设备施用到待处理的植物或种子上的现成组合物,还包括在施用到农作物之前必须稀释的浓缩商品组合物。
依据本发明的化合物还可与一种或多种杀虫剂、杀真菌剂、杀细菌剂、引诱剂、杀螨剂或信息素活性物质或其它有生物活性的化合物混合。这样得到的混合物具广谱的活性。
与其它杀真菌化合物的混合物尤其有利。合适的可进行混合的杀真菌剂的例子选自以下:
B1)能抑制核酸合成的化合物,例如苯霜灵、苯霜灵-M(benalaxyl-M)、乙嘧酚磺酸酯、赤拉灵(chiralaxyl)、柯罗泽尔昆(clozylacon)、甲菌定、乙嘧酚、呋霜灵、恶霉灵、甲霜灵、高效甲霜灵、呋酰胺、恶霜灵、喹菌酮;
B2)能够抑制有丝分裂和细胞分裂的化合物,例如苯菌灵、多菌灵、乙霉威、麦穗宁、戊菌隆、噻菌灵、甲基硫菌灵、苯酰菌胺;
B3)能抑制呼吸的化合物,例如
作为CI-呼吸抑制剂,如氟嘧菌胺(diflumetorim);
作为CII-呼吸抑制剂,如啶酰菌胺(boscalid)、萎锈灵、甲呋酰胺、氟酰胺、呋吡菌胺(furametpyr)、灭锈胺、氧化萎锈灵(oxycarboxine)、吡噻菌胺(penthiopyrad)、噻氟菌胺;
作为CIII-呼吸抑制剂,如嘧菌酯、氰霜唑、醚菌胺(dimoxystrobin)、厄内斯卓宾(enestrobin)、恶唑菌酮、咪唑菌酮、氟嘧菌酯(fluoxastrobin)、醚菌酯、苯氧菌胺、肟醚菌胺(orysastrobin)、唑菌胺酯(pyraclostrobin)、啶氧菌酯(picoxystrobin)、肟菌酯;
B4)能起着解偶联剂作用的化合物,例如消螨普、氟啶胺;
B5)能抑制ATP产生的化合物,例如三苯基乙酸锡、三苯基氯化锡、三苯基氢氧化锡、硅噻菌胺(silthiofam);
B6)能抑制AA和蛋白质生物合成的化合物,例如胺扑灭(andoprim)、杀稻瘟菌素-S、嘧菌环胺、春雷霉素、水合盐酸春雷霉素(kasugamycinhydrochloride hydrate)、嘧菌胺、嘧霉胺;
B7)能抑制信号转导的化合物,例如拌种咯、咯菌腈、苯氧喹啉;
B8)能抑制脂和膜合成的化合物,例如乙菌利、异菌脲、腐霉利、乙烯菌核利、吡菌磷、敌瘟磷、异稻瘟净(IBP)、稻瘟灵、甲基立枯磷、联苯、依杜卡(iodocarb)、霜霉威、霜霉威盐酸盐;
B9)能抑制麦角固醇生物合成的化合物,例如环酰菌胺、氧环唑、联苯三唑醇、糠菌唑、环丙唑醇、苄氯三唑醇(diclobutrazole)、苯醚甲环唑、烯唑醇、烯唑醇-M(diniconazole-M)、氟环唑、乙环唑、腈苯唑、氟喹唑、氟硅唑、粉唑醇、呋菌唑、呋醚唑、己唑醇、亚胺唑、种菌唑、叶菌唑、腈菌唑、多效唑、戊菌唑、丙环唑、丙硫菌唑(prothioconazole)、硅氟唑、戊唑醇、四氟醚唑、三唑酮、三唑醇、灭菌唑、烯效唑、伏立康唑、抑霉唑、抑霉唑硫酸盐(imazalil sulfate)、恶咪唑、氯苯嘧啶醇、呋嘧醇、氟苯嘧啶醇、啶斑肟、嗪胺灵、稻瘟酯、咪鲜胺、氟菌唑、烯霜苄(viniconazole)、阿尔迪莫(aldimorph)、十二环吗啉、十二环吗啉乙酸盐(dodemorph acetate)、丁苯吗啉(fenpropimorph)、十三吗啉、苯锈啶、螺环菌胺、萘替芳、稗草丹、特比萘芬;
B10)能抑制细胞壁合成的化合物,例如苯噻菌胺(benthiavalicarb)、双丙氨膦、烯酰吗啉、氟吗啉、异丙菌胺、多抗霉素(polyoxins)、多氧霉素(polyoxorim)、有效霉素A;
B11)能抑制黑素生物合成的化合物,例如环丙酰菌胺、双氯氰菌胺、氰菌胺、四氯苯酞(phtalide)、咯喹酮、三环唑;
B12)能诱导宿主防御的化合物,例如活化酯-S-甲基(acibenzolar-S-methyl)、噻菌灵、噻酰菌胺(tiadinil);
B13)具有多位点(multisite)作用的化合物,例如敌菌丹、克菌丹、百菌清、铜制剂如氢氧化铜、环烷酸铜、氯氧化铜、硫酸铜、氧化铜、喹啉铜和波尔多液、苯氟磺胺、二氰蒽醌、多果定、多果定游离碱、福美铁、氟佛匹特(fluorofolpet)、灭菌丹、双胍辛(guazatine)、双胍辛乙酸盐、双胍辛胺、双胍三辛烷基苯磺酸盐(iminoctadine albesilate)、双胍辛胺乙酸盐、代森锰铜、代森锰锌、代森锰、代森联(metiram)、代森联锌(metiram zinc)、丙森锌、硫和硫制品,包括多硫化钙、福美双、甲苯氟磺胺、代森锌、福美锌;
B14)选自以下的化合物:阿密布洛姆朵尔(amibromdole)、苯噻硫氰、贝斯氧杂嗪(bethoxazin)、卡巴西霉素、香芹酮、灭螨猛、氯化苦、硫杂灵(cufraneb)、环氟菌胺(cyflufenamid)、霜脲氰、棉隆、咪菌威、哒菌酮、双氯酚、氯硝胺、野燕枯、野燕枯甲基硫酸盐(difenzoquat methylsulphate)、二苯胺、噻唑菌胺、嘧菌腙、氟酰菌胺、磺菌胺、藻菌磷铝、藻菌磷钙、藻菌磷钠、氟吡菌胺(fluopicolide)、氟氯菌核利(fluoroimide)、六氯苯、8-羟基喹啉硫酸盐、人间霉素(irumamycin)、磺菌威(methasulphocarb)、苯菌酮(metrafenone)、异硫氰酸甲酯、灭粉霉素、那他霉素、二甲基二硫代氨基甲酸镍、酞菌酯、辛噻酮、奥克斯莫卡宾(oxamocarb)、氧代奋欣(oxyfenthiin)、五氯苯酚和盐、2-苯基苯酚和盐、亚磷酸及其盐、病花灵、普罗帕诺欣(propanosine)-钠、丙氧喹啉(proquinazid)、吡咯叠氮(pyrrolnitrine)、五氯硝基苯、叶枯酞、四氯硝基苯、咪唑嗪、水杨菌胺、氰菌胺和2,3,5,6-四氯-4-(甲基磺酰基)-吡啶、N-(4-氯-2-硝基苯基)-N-乙基-4-甲基-苯磺酰胺、2-氨基-4-甲基-N-苯基-5-噻唑羧酰胺、2-氯-N-(2,3-二氢-1,1,3-三甲基-1H-茚-4-基)-3-吡啶羧酰胺、3-[5-(4-氯苯基)-2,3-二甲基异_唑烷-3-基]吡啶、顺式-1-(4-氯苯基)-2-(1H-1,2,4-三唑-1-基)-环庚醇、1-(2,3-二氢-2,2-二甲基-1H-茚-1-基)-1H-咪唑-5-羧酸甲酯、3,4,5-三氯-2,6-吡啶二腈、2-[[[环丙基[(4-甲氧基苯基)亚氨基]甲基]硫基(thio)]甲基]-α-(甲氧基亚甲基)-苯乙酸甲酯、4-氯-α-丙炔氧基-N-[2-[3-甲氧基-4-(2-丙炔氧基)苯基]乙基]-苯乙酰胺、(2S)-N-[2-[4-[[3-(4-氯苯基)-2-丙炔基]氧基(oxy)]-3-甲氧基苯基]乙基]-3-甲基-2-[(甲基磺酰基)氨基]-丁酰胺、5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)[1,2,4]三唑并[1,5-a]嘧啶、5-氯-6-(2,4,6-三氟苯基)-N-[(1R)-1,2,2-三甲基丙基][1,2,4]三唑并[1,5-a]嘧啶-7-胺、5-氯-N-[(1R)-1,2-二甲基丙基]-6-(2,4,6-三氟苯基)[1,2,4]三唑并[1,5-a]嘧啶-7-胺、N-[1-(5-溴-3-氯吡啶-2-基)乙基]-2,4-二氯烟酰胺、N-(5-溴-3-氯吡啶-2-基)甲基-2,4-二氯烟酰胺、2-丁氧基-6-碘代-3-丙基-苯并吡喃-4-酮、N-{(Z)-[(环丙基甲氧基)亚氨基][6-(二氟甲氧基)-2,3-二氟苯基]甲基}-2-苯基乙酰胺、N-(3-乙基-3,5,5-三甲基-环己基)-3-甲酰氨基-2-羟基-苯甲酰胺、2-[[[[1-[3(1氟-2-苯基乙基)氧基]苯基]亚乙基]氨基]氧基]甲基]-α-(甲氧基亚氨基)-N-甲基-αE-苯乙酰胺、N-{2-[3-氯-5-(三氟甲基)吡啶-2-基]乙基}-2-(三氟甲基)苯甲酰胺、N-(3′,4′-二氯-5-氟联苯-2-基)-3-(二氟甲基)-1-甲基-1H-吡唑-4-羧酰胺、2-(2-{[6-(3-氯-2-甲基苯氧基)-5-氟嘧啶-4-基]氧基}苯基)-2-(甲氧基亚氨基)-N-甲基乙酰胺、1-[(4-甲氧基苯氧基)甲基]-2,2-二甲基丙基-1H-咪唑-1-羧酸、O-[1-[(4-甲氧基苯氧基)甲基]-2,2-二甲基丙基]-1H-咪唑-1-硫代羟酸。
包含通式(I)的化合物和杀细菌剂化合物的混合物的本发明组合物是特别有利的。合适的可进行混合的杀细菌剂的例子可选自以下:溴硝醇、双氯酚、氯定、二甲基二硫代氨基甲酸镍、春雷霉素、辛噻酮、呋喃羧酸、土霉素、噻菌灵、链霉素、叶枯酞、硫酸铜和其它铜制备物。
本发明的通式(I)的化合物和杀真菌组合物可用来治疗性或预防性地控制植物或农作物的植物病原真菌。因此,依据本发明的其它方面,提供一种治疗性或预防性地控制植物或农作物植物病原真菌的方法,该方法的特征在于将本发明的通式(I)的化合物或杀真菌组合物施用到种子、植物和/或植物的果实或植物正在生长或需要生长的土壤中。
同样,依据本发明的通式(I)的化合物和杀虫组合物可用于治疗性或预防性地控制害虫,特别是植物或农作物的害虫。因此,依据本发明的其它方面,提供一种治疗性或预防性地控制害虫,尤其是植物或农作物的害虫的方法,该方法的特征在于将本发明的通式(I)的化合物或杀虫组合物施用到种子、植物和/或植物的果实或植物正在生长或需要生长的土壤中。
本发明的处理方法还可用于处理繁殖材料如块茎或根茎,以及种子、幼苗或移植(pricking out)苗和植物或移植植物。该处理方法也可用于处理根。本发明的处理方法也可用于处理植物的地上部分如有关植物的干、茎或梗、叶子、花和果实。
在可用本发明的方法保护的植物中,包括棉花;亚麻;葡萄藤;果实或蔬菜作物,诸如蔷薇科(Rosaceae sp.)(例如,仁果类水果,诸如苹果和梨,还有核果,诸如杏、杏仁和桃子)、茶蔗子科(Ribesioidae sp.)、胡桃科(Juglandaceae sp.)、桦木科(Betulaceae sp.)、漆树科(Anacardiaceae sp.)、山毛榉科(Fagaceae sp.)、桑科(Moraceae sp.)、木犀科(Oleaceae sp.)、猕猴桃科(Actinidaceae sp.)、樟科(Lauraceae sp.)、芭蕉科(Musaceae sp.)(例如香蕉树和粉芭蕉(plantins))、茜草科(Rubiaceae sp.)、山茶科(Theaceae sp.)、梧桐科(Sterculiceae sp.)、芸香科(Rutaceae sp.)(例如柠檬、橙子和葡萄柚);茄科(Solanaceae sp.)(例如,西红柿)、百合科(Liliaceae sp.)、紫菀科(Asteraceaesp.)(例如莴苣)、伞形科(Umbelliferae sp.)、十字花科(Cruciferae sp.)、藜科(Chenopodiaceae sp.)、葫芦科(Cucurbitaceae sp.)、蝶形花科(Papilionaceaesp.)(例如豌豆)、蔷薇科(Rosaceae sp.)(例如草莓);大作物,诸如禾本科(Graminae sp.)(例如玉米、菌苔或谷物如小麦、稻、大麦和黑小麦)、紫菀科(Asteraceae sp.)(例如向日葵)、十字花科(Cruciferae sp.)(例如油菜)、豆科(Fabacae sp.)(例如花生)、蝶形花科(Papilionaceae sp.)(例如大豆)、茄科(Solanaceae sp.)(例如马铃薯)、藜科(Chenopodiaceae sp.)(例如甜菜根);园艺作物和森林作物;以及这些作物的遗传修饰的同系物。
在可通过本发明方法控制的植物或农作物疾病中,可提及的有:
白粉病(powdery mildew),例如:
小麦白粉病(Blumeria diseases),例如由小麦白粉菌(Blumeria graminis)引起;
叉丝单囊壳属病(Podosphaera diseases),例如由白叉丝单囊壳(Podosphaera leucotricha)引起;
单丝壳属病(Sphaerotheca diseases),例如由苍耳单丝壳(Sphaerothecafuliginea)引起;
钩丝壳属病(Uncinula diseases),例如由葡萄钓丝壳(Uncinula necator)引起;
锈病,例如:
胶锈属病(Gymnosporangium diseases),例如由Gymnosporangiumsabinae引起;
驼孢锈病(Hemileia diseases),例如由咖啡驼孢锈菌(Hemileia vastatrix)引起;
层锈菌属病(Phakopsora diseases),例如由豆薯层锈菌(Phakopsorapachyrhizi)或山马蝗层锈菌(Phakopsora meibomiae)引起;
柄锈菌属病(Puccinia diseases),例如由隐匿柄锈菌(Puccinia recondita)引起;
单孢锈菌属病(Uromyces diseases),例如由疣顶单胞锈菌(Uromycesappendiculatus)引起;
卵菌病(Oomycete diseases),例如:
盘梗霉属病(Bremia diseases),例如由莴苣盘梗霉(Bremia lactucae)引起;
霜霉属病(Peronospora diseases),例如由豌豆霜霉(Peronospora pisi)或芸苔霜霉(P.brassicae)引起;
疫霉属病(Phytophthora diseases),例如由致病疫霉(Phytophthorainfestans)引起;
单轴霉属病(Plasmopara diseases),例如由葡萄生单轴霉(Plasmoparaviticola)引起;
假霜霉属(Pseudoperonospora diseases),例如由葎草假霜霉(Pseudoperonospora humuli)或古巴假霜霉(Pseudoperonospora cubensis)引起;
腐霉属病(Pythium diseases),例如由终极腐霉(Pythium ultimum)引起;
叶斑病(Leafspot disease)、污叶病(leaf blotch disease)和叶枯病(leafblight disease),例如:
支链孢属病(Alternaria diseases),例如由茄链格孢(Alternaria solani)引起;
尾孢霉属病(Cercospora diseases),例如由甜菜生尾孢(Cercosporabeticola)引起;
金孢子菌属病(Cladiosporum diseases),例如由瓜枝孢(Cladiosporiumcucumerinum)引起;
旋孢腔菌病(Cochliobolus diseases),例如由禾旋孢腔菌(Cochliobolussativus)引起;
刺盘孢属病(Colletotrichum diseases),例如由豆刺盘孢(Colletotrichumlindemuthanium)引起;
油橄榄孔雀斑病(Cycloconium diseases),例如由Cycloconium oleaginum引起;
腐皮壳菌层病(Diaporthe diseases),例如由桔柑间座壳(Diaporthe citri)引起;
痂囊腔菌属病(Elsinoe diseases),例如由桔柑痂囊腔菌(Elsinoe fawcettii)引起;
长孢属病(Gloeosporium diseases),例如由悦色盘长孢(Gloeosporiumlaeticolor)引起;
小丛壳属病(Glomerella diseases),例如由围小丛壳(Glomerellacingulata)引起;
球座菌属病(Guignardia diseases),例如由葡萄球座菌(Guignardiabidwelli)引起;
小球腔菌属病(Leptosphaeria diseases),例如由十字花科小球腔菌(Leptosphaeria maculans);颖枯小球腔菌(Leptosphaeria nodorum)引起;
稻瘟病(Magnaporthe),例如由稻瘟菌(Magnaporthe grisea)引起;
球腔菌属病(Mycosphaerella diseases),例如由禾生球腔菌(Mycosphaerella graminicola);落花生球腔菌(Mycosphaerella arachidicola);香蕉黑条叶斑病菌(Mycosphaerella fijiensisi)引起;
壳针孢属病(Phaeosphaeria diseases),例如由颖枯壳针孢(Phaeosphaerianodorum)引起;
核腔菌属病(Pyrenophora diseases),例如由圆核腔菌(Pyrenophora teres)引起;
柱隔孢属病(Ramularia diseases),例如由Ramularia collo-cygni引起;
喙孢属病(Rhynchosporium diseases),例如由黑麦喙孢(Rhynchosporiumsecalis)引起;
壳针孢属病(Septoria diseases),例如由芹菜小壳针孢(Septoria apii)或番茄壳针孢(Septoria lycopercisi)引起;
核瑚菌属病(Typhula diseases),例如由肉孢核瑚菌(Typhula incarnata)引起;
黑星菌属病(Venturia diseases),例如由苹果黑星菌(Venturia inaequalis)引起;
根和茎疾病,例如:
伏革菌病(Corticium diseases),例如由禾伏革菌(Corticium graminearum)引起;
镰孢菌(霉)属病(Fusarium diseases),例如由尖镰孢(Fusarium oxysporum)引起;
鲟形属病(Gaeumannomyces diseases),例如由禾顶囊壳(Gaeumannomycesgraminis)引起;
丝核菌属病(Rhizoctonia diseases),例如由立枯丝核菌(Rhizoctonia solani)引起;
Tapesia病,例如由Tapesia acuformis引起;
根串珠霉属病(Thielaviopsis diseases),例如由根串珠霉(Thielaviopsisbasicola)引起;
耳穗和圆锥花序疾病,例如:
链格孢属病(Alternaria diseases),例如由链格孢(Alternaria spp.)引起;
曲霉病(Aspergillus diseases),例如由黄曲霉(Aspergillus flavus)引起;
枝孢属病(Cladosporium diseases),例如由枝孢(Cladosporium spp.)引起;
麦角菌属病(Claviceps diseases),例如由麦角菌(Claviceps purpurea)引起;
镰孢菌(霉)属病(Fusarium diseases),例如由大刀镰孢菌(Fusariumculmorum)引起;
赤霉属病(Gibberella diseases),例如由玉米赤霉(Gibberella zeae)引起;
水稻云形病(Monographella),例如由Monographella nivalis引起;
黑穗病和腥黑穗病,例如:
轴黑粉菌属病(Sphacelotheca diseases),例如由丝轴黑粉菌(Sphacelotheca reiliana)引起;
腥黑粉菌属病(Tilletia diseases),例如由小麦网腥黑粉菌(TiHetia caries)引起;
条黑粉菌属病(Urocystis diseases),例如由隐条黑粉菌(Urocystis occulta)引起;
黑粉菌属病(Ustilago diseases),例如由裸黑粉菌(Ustilago nuda)引起;
果实腐烂和霉菌病,例如:
曲霉病(Aspergillus diseases),例如由黄曲霉(Aspergillus flavus)引起;
葡萄孢属病(Botrytis diseases),例如由灰葡萄孢(Botrytis cinerea)引起;
青霉菌病(Penicillium diseases),例如由扩展青霉(Penicillium expansum)引起;
核盘菌属病(Sclerotinia diseases),例如由核盘菌(Sclerotinia sclerotiorum)引起;
轮枝孢属病(Verticilium diseases),例如由黑白轮枝孢(Verticiliumalboatrum)引起;
种子和土壤传播的腐烂,霉菌,枯萎,腐烂和猝倒病:
镰孢菌(霉)属病(Fusarium diseases),例如由大刀镰孢菌(Fusariumculmorum)引起;
疫霉属病(Phytophthora diseases),例如由恶疫霉(Phytophthora cactorum)引起;
腐霉属病(Pythium diseases),例如由终极腐霉(Pythium ultimum)引起;
丝核菌属病(Rhizoctonia diseases),例如由立枯丝核菌(Rhizoctonia solani)引起;
小核菌病(Sclerotium diseases),例如由齐整小核菌(Sclerotium rolfsii)引起;
微结节菌属病(Microdochium diseases),例如由雪腐微座孢(Microdochiumnivale)引起;
溃疡病(Canker)、松碎(broom)和梢枯病,例如:
丛赤壳属病(Nectria diseases),例如由干癌丛赤壳菌(Nectria galligena)引起;
枯萎病,例如:
链核盘菌属病(Monilinia diseases),例如由核果链核盘菌(Monilinia laxa)引起;
叶疱病或缩叶病,例如:
外囊菌属病(Taphrina diseases),例如由畸形外囊菌(Taphrina deformans)引起;
木质植物的衰退病,例如:
Esca病,例如由Phaemoniella clamydospora引起;
葡萄顶枯病(Eutypa dyeback),例如由Eutypa lata引起;
榆树荷兰病(Dutch elm disease),例如由榆枯萎病菌(Ceratocystis ulmi)引起;
花和种子的疾病,例如:
葡萄孢属病(Botrytis diseases),例如由灰葡萄孢(Botrytis cinerea)引起;
根茎类疾病,例如:
丝核菌属病(Rhizoctonia diseases),例如由立枯丝核菌(Rhizoctonia solani)引起。
在依据本发明的杀虫方法,可以在任何生长阶段控制的有害病虫或有害昆虫中,可提及的有:
虱目(Anoplura(Phthiraptera)),例如畜虱(Damalinia spp.)、血虱(Haematopinus spp.)、长颚虱(Linognathus spp.)、体虱(Pediculus spp.)、啮毛虱(Trichodectes spp.);
蛛形纲(Arachnida),例如粗脚粉螨(Acarus siro)、桔芽瘤螨(Aceriasheldoni)、刺皮瘿螨(Aculops spp.)、刺瘿螨(Aculus spp.)、钝眼蜱(Amblyommaspp.)、锐缘蜱(Argas spp.)、牛蜱(Boophilus spp.)、短须螨(Brevipalpusspp.)、苜蓿苔螨(Bryobia praetiosa)、皮螨(Chorioptes spp.)、鸡皮刺螨(Dermanyssus gallinae)、东方叶螨(Eotetranychus spp.)、梨叶锈螨(Epitrimeruspyri)、真叶螨(Eutetranychus spp.)、瘿螨(Eriophyes spp.)、跗线螨(Hemitarsonemusspp.)、璃眼蜱(Hyalomma spp.)、硬蜱(Ixodes spp.)、黑寡妇(Latrodectusmactans)、Metatetranychus spp.、小爪螨(Oligonychus spp.)、钝缘蜱(Ornithodorosspp.)、全爪螨(Panonychus spp.)、柑锈螨(Phyllocoptruta oleivora)、侧多食趺线螨(Polyphagotarsonemus latus)、痒螨(Psoroptes spp.)、扇头蜱(Rhipicephalusspp.)、根嗜螨(Rhizoglyphus spp.)、疥螨(Sarcoptes spp.)、中东金蝎(Scorpiomaurus)、狭跌线螨(Stenotarsonemus spp.)、趺线螨(Tarsonemus spp.)、叶螨(Tetranychus spp.)、Vasates lycopersici;
双壳纲(Bivalva),例如斑马贝(Dreissena spp.);
唇足亚纲(Chilopoda),例如地蜈蚣(Geophilus spp.)、蚰蜒(Scutigeraspp.);
鞘翅目(Coleoptera),例如菜豆象(Acanthoscelides obtectus)、丽金龟(Adoretus spp.)、赤杨紫跳甲(Agelastica alni)、叩甲(Agriotes spp.)、六月金龟(Amphimallon solstitialis)、家具窃蠹(Anobium punctatum)、星天牛(Anoplophoraspp.)、象甲(Anthonomus spp.)、皮蠹(Anthrenus spp.)、鳃角金龟(Apogoniaspp.)、隐食甲(Atomaria spp.)、黑皮蠹(Attagenus spp.)、Bruchidius obtectus、豆象(Bruchus spp.)、Ceuthorhynchus spp.、Cleonus mendicus、叩甲(Conoderusspp.)、象甲(Cosmopolites spp.)、Costelytra zealandica、象鼻虫(Curculiospp.)、杨干象甲(Cryptorhynchus lapathi)、皮蠹(Dermestes spp.)、叶甲(Diabro-tica spp.)、瓢虫(Epilachna spp.)、蛀茎象甲(Faustinus cubae)、裸蛛甲(Gibbiumpsylloides)、非洲独角仙(Heteronychus arator)、Hylamorpha elegans、北美家天牛(Hylotrupes bajulus)、苜蓿叶象甲(Hypera postica)、果小蠹(Hypothenemusspp.)、暗黑鳃金龟(Lachnosterna consanguinea)、科罗拉多金花虫(Leptinotarsadecemlineata)、稻水象甲(Lissorhoptrus oryzophilus)、象甲(Lixus spp.)、粉蠹(Lyctus spp.)、油菜露尾甲(Meligethes aeneus)、大栗鳃角金龟(Melolontha melo-lontha)、Migdolus spp.、墨天牛(Monochamus spp.)、白缘象(Naupactusxanthographus)、黄蛛甲(Niptus hololeucus)、椰蛀犀金龟(Oryctes rhinoceros)、锯谷盗(Oryzaephilus surinamensis)、黑耳喙鼻(Otiorrhynchus sulcatus)、小青花金龟(Oxycetonia jucunda)、辣根猿叶甲(Phaedon cochleariae)、金龟子(Phyllophaga spp.)、日本金龟子(Popillia japonica)、安第斯马铃薯象甲(Premnotrypes spp.)、油菜兰跳甲(Psylliodes chrysocephala)、蛛甲(Ptinusspp.)、黑根瓢虫(Rhizobius ventralis)、谷蠹(Rhizopertha dominica)、米象(Sitophilus spp.)、黑楔象(Sphenophorus spp.)、Sternechus spp.、Symphyletesspp.、黄粉虫甲(Tenebrio molitor)、谷蛀虫(Tribolium spp.)、斑皮蠹(Trogo-derma spp.)、籽象(Tychius spp.)、脊虎天牛(Xylotrechus spp.)、步甲(Zabrusspp.)。
弹尾目(Collembola),例如武装棘跳虫(Onychiurus armatus);
革翅目(Dermaptera),例如地蜈蚣(Forficula auricularia);
倍足亚纲(Diplopoda),例如具斑马陆(Blaniulus guttulatus);
双翅目(Diptera),例如伊蚊(Aedes spp.)、疟蚊(Anopheles spp.)、全北毛蚊(Bibio hortulanus)、红头丽蝇(Calliphora erythrocephala)、地中海实蝇(Ceratitis capitata)、金蝇(Chrysomyia spp.)、锥蝇(Cochliomyia spp.)、嗜人瘤蝇(Cordylobia anthropophaga)、库蚊(Culex spp.)、黄蝇(Cuterebra spp.)、油橄榄实蝇(Dacus oleae)、人皮蝇(Dermatobia hominis)、果蝇(Drosophilaspp.)、厕蝇Fannia spp.)、胃蝇(Gastrophilus spp.)、黑蝇(Hylemyia spp.)、虱蝇(Hyppobosca spp.)、皮蝇(Hypoderma spp.)、斑潜蝇(Liriomyza spp.)、绿蝇(Lucilia spp.)、蝇(Musca spp.)、蝽(Nezara spp.)、狂蝇(Oestrus spp.)、瑞典蝇(Oscinella frit)、甜菜潜叶蝇(Pegomyia hyoscyami)、草种蝇(Phorbia spp.)、刺蝇(Stomoxys spp.)、牛虻(Tabanus spp.)、Tannia spp.、沼泽大蚊(Tipulapaludosa)、污蝇(Wohlfahrtia spp);
腹足纲(Gastropoda),例如蛞蝓(Arion spp.)、扁卷螺(Biomphalaria spp.)、水泡螺(Bulinus spp.)、野蛞蝓(Deroceras spp.)、土蜗(Galba spp.)、椎实螺(Lymnaea spp.)、钉螺(Oncomelania spp.)、椎实蜗牛(Succinea spp.);
肠虫(helminths),例如十二指肠钩虫(Ancylostoma duodenale)、锡兰钩口线虫(Ancylostoma ceylanicum)、猫钩虫(Acylostoma braziliensis)、钩口线虫(Ancylostoma spp.)、人蛔虫(Ascaris lubricoides)、蛔虫(Ascaris spp.)、马来丝虫(Brugia malayi)、帝汶布鲁丝虫(Brugia timori)、仰口线虫(Bunostomum spp.)、夏氏线虫(Chabertia spp.)、支睾吸虫(Clonorchis spp.)、古柏线虫(Cooperiaspp.)、双腔吸虫(Dicrocoelium spp.)、丝圆线虫(Dictyocaulus filarial)、阔节裂头绦虫(Diphyllobothrium latum)、麦地那龙线虫(Dracunculus medinensis)、细粒棘球绦虫(Echinococcus granulosus)、多房棘球绦虫(Echinococcusmultilocularis)、蛲虫(Enterobius vermicularis)、形吸虫(Faciola spp.)、血矛线虫(Haemonchus spp.)、异刺线虫(Heterakis spp.)、短膜壳绦虫(Hymenolepisnana)、猪圆形线虫(Hyostrongulus spp.)、非洲眼线虫(Loa Loa)、细颈属(Nematodirus spp.)、结节线虫(Oesophagostomum spp.)、后睾吸虫(Opisthorchisspp.)、旋盘尾丝虫(Onchocerca volvulus)、胃线虫(Ostertagia spp.)、并殖吸虫(Paragonimus spp.)、血吸虫(Schistosomen spp.)、费氏类圆线虫(Strongyloidesfuelleborni)、粪类圆线虫(Strongyloides stercoralis)、类圆线虫(Stronyloidesspp.)、牛肉绦虫(Taenia saginata)、猪肉绦虫(Taenia solium)、旋毛线虫(Trichinella spiralis)、本地毛形线虫(Trichinella nativa)、布氏旋毛虫(Trichinella britovi)、纳氏旋毛虫(Trichinella nelsoni)、伪旋毛形线虫(Trichinella pseudopsiralis)、毛圆线虫(Trichostrongulus spp.)、鞭虫(Trichuristrichuria)、斑氏线虫(Wuchereria bancrofti);
原生动物,例如艾美球虫属(Eimeria);
异翅目(Heteroptera),例如南瓜缘蝽(Anasa tristis)、Antestiopsis spp.、长椿(Blissus spp.)、盲蝽(Calocoris spp.)、Campylomma livida、长蝽(Caveleriusspp.)、臭虫(Cimex spp.)、绿盲蝽(Creontiades dilutus)、胡椒缘蝽(Dasynuspiperis)、Dichelops furcatus、Diconocoris hewetti、红蝽(Dysdercus spp.)、Euschistus spp.、Eurygaster spp.、Heliopeltis spp.、Horcias nobilellus、稻缘蝽(Leptocorisa spp.)、叶足缘蝽(Leptoglossus phyllopus)、草盲蝽(Lygus spp.)、蔗黑长蝽(Macropes excavatus)、盲椿科(Miridae)、绿蝽(Nezara spp.)、稻蝽(Oebalus spp.)、蝽科(Pentomidae)、蝽象(Piesma quadrata)、纹蝽(Piezodorusspp.)、Psallus seriatus、Pseudacysta persea、红猎蝽(Rhodnius spp.)、可可褐盲蝽(Sahlbergella singularis)、黑椿(Scotinophora spp.)、梨冠网蝽(Stephanitisnashi)、Tibraca spp.、锥蝽(Triatoma spp);
同翅目(Homoptera),例如蚜科(Acyrthosipon spp.)、Aeneolamia spp.、隆脉木虱(Agonoscena spp.)、粉虱(Aleurodes spp.)、蔗粉虱(Aleurolobusbarodensis)、毛粉虱(Aleurothrixus spp.)、叶蝉(Amrasca spp.)、Anuraphiscardui、园蚧(Aonidiella spp.)、梨瘤蚜(Aphanostigma piri)、蚜虫(Aphis spp.)、葡萄浮尘子(Arboridia apicalis)、小园盾蚧(Aspidiella spp.)、圆盾蚧(Aspidiotusspp.)、Atanus spp.、茄沟无网蚜(Aulacorthum solani)、粉虱(Bemisia spp.)、李短尾蚜(Brachycaudus helichrysii)、短蝽(Brachycolus spp.)、甘蓝蚜(Brevicorynebrassicae)、小稻褐飞虱(Calligypona marginata)、丽黄头大叶蝉(Carneocephalafulgida)、甘蔗绵蚜(Ceratovacuna lanigera)、沬蝉科(Cercopidae)、蜡蚧(Cero-plastes spp.)、草莓毛管蚜(Chaetosiphon fragaefolii)、蔗黄雪盾蚧(Chionaspistegalensis)、茶绿叶蝉(Chlorita onukii)、核桃黑斑蚜(Chromaphisjuglandicola)、褐圆介壳虫(Chrysomphalus ficus)、玉米叶蝉(Cicadulinambila)、Coccomytilus halli、软蚧(Coccus spp.)、茶蔍隐瘤额蚜(Cryptomyzusribis)、叶蝉(Dalbulus spp.)、粉虱(Dialeurodes spp.)、木虱(Diaphorina spp.)、白蚧(Diaspis spp.)、Doralis spp.、草履蚧(Drosicha spp.)、圆尾蚜(Dysaphisspp.)、粉蚧(Dysmicoccus spp.)、小绿叶蝉(Empoasca spp.)、绵蚜(Eriosomaspp.)、斑叶蝉(Erythroneura spp.)、Euscelis bilobatus、咖啡地粉蚧(Geococcuscoffeae)、琉璃叶蝉(Homalodisca coagulate)、桃粉蚜(Hyalopterus arundinis)、吹绵蚧(Icerya spp.)、片角叶蝉(Idiocerus spp.)、扁喙叶蝉(Idioscopus spp.)、灰飞虱(Laodelphax striatellus)、蜡蚧(Lecanium spp.)、蛎蚧(Lepidosaphes spp.)、萝卜蚜(Lipaphis erysimi)、长管蚜(Macrosiphum spp.)、Mahanarvafimbriolata、高粱蚜(Melanaphis sacchari)、Metcalfiella spp.、麦无网长管蚜(Metopolophium dirhodum)、黑缘平翅斑蚜(Monellia costalis)、Monelliopsispecanis、蚜虫(Myzus spp.)、莴苣蚜(Nasonovia ribisnigri)、黑尾叶蝉(Nepho-tettix spp.)、褐飞虱(Nilaparvata lugens)、Oncometopia spp.、旗蚧(Ortheziapraelonga)、桑粉虱(Parabemisia myricae)、准个木虱(Paratrioza spp.)、片蚧(Parlatoria spp.)、天疱疮(Pemphigus spp.)、玉米飞虱(Peregrinus maidis)、绵粉蚧(Phenacoccus spp.)、杨平翅棉蚜(Phloeomyzus passerinii)、忽布疣额蚜(Phorodon humuli)、木虱(Phylloxera spp.)、柑桔并盾蚧(Pinnaspisaspidistrae)、动性球菌属(Planococcus spp.)、梨形原绵腊蚧(Protopulvinariapyriformis)、桑白蚧(Pseudaulacaspis pentagona)、粉蚧(Pseudococcus spp.)、木虱(Psylla spp.)、金小蜂(Pteromalus spp.)、璐蜡蝉(Pyrilla spp.)、圆盾蚧(Quadraspidiotus spp.)、Quesada gigas、平刺粉蚧(Rastrococcus spp.)、缢管蚜(Rhopalosiphum spp.)、硬蚧(Saissetia spp.)、Scaphoides titanus、麦二叉蚜(Schizaphis graminum)、刺盾蚧(Selenaspidus articulatus)、Sogata spp.、白背飞虱(Sogatella furcifera)、飞虱(Sogatodes spp.)、牛角蝉(Stictocephala festina)、Tenalaphara malayensis、美核桃黑蚜(Tinocallis caryaefoliae)、沫蝉(Tomaspisspp.)、二岔蚜(Toxoptera spp.)、温室粉虱(Trialeurodes vaporariorum)、木虱(Trioza spp.)、红闪小叶蝉(Typhlocyba spp.)、矢尖蚧(Unaspis spp.)、葡萄根瘤蚜(Viteus vitifolii);
膜翅目,例如锯角叶缝(Diprion spp.)、实叶峰(Hoplocampa spp.)、黑蚁(Lasius spp.)、厨蚁(Monomorium pharaonis)、胡蜂(Vespa spp.);
等足目(Isopoda),例如鼠妇(Armadillidium vulgare)、潮虫(Oniscusasellus)、球鼠妇(Porcellio scaber);
等翅目(Ioptera),例如白蚁(Reticulitermes spp.)、白蚁(Odontotermesspp.);
鳞翅目(Lepidoptera),例如桑剑纹夜蛾(Acronicta major)、甘薯烦夜蛾(Aedia leucomelas)、地虎(Agrotis spp.)、Alabama argillacea、夜蛾(Anticarsiaspp.)、甘兰夜蛾(Barathra brassicae)、棉叶穿孔潜蛾(Bucculatrix thurberiella)、松尺蠖(Bupalus piniarius)、黄尾卷叶蛾(Cacoecia podana)、烟卷蛾(Capuareticulana)、苹果矗蛾(Carpocapsa pomonella)、Cheimatobia brumata、螟(Chilo spp.)、云杉卷叶蛾(Choristoneura fumiferana)、葡萄果蠢蛾(Clysia ambi-guella)、纵卷叶野螟(Cnaphalocerus spp.)、埃及金刚钻(Earias insulana)、地中海粉螟(Ephestia kuehniella)、黄毒蛾(Euproctis chrysorrhoea)、切夜蛾(Euxoaspp.)、脏切夜蛾(Fltia spp.)、大蜡螟(Galleria mellonella)、Helicoverpa spp.、夜蛾(Heliothis spp.)、褐织叶蛾(Hofmannophila pseudospretella)、茶长卷蛾(Homona magnanima)、苹巢蛾(Hyponomeuta padella)、Laphygma spp.、潜叶细蛾(Lithocolletis blancardella)、绿果冬夜蛾(Lithophane antennata)、Loxagrotisalbicosta、毒蛾(Lmantria spp.)、天幕毛虫(Malacosoma neustria)、甘兰夜蛾(Mamestra brassicae)、稻毛胫夜蛾(Mocis repanda)、腹夜蛾(Mythimnaseparata)、麦杆夜蛾(Oria spp.)、稻负泥虫(Oulema oryzae)、松夜蛾(Panolisflammea)、红铃虫(Pectinophora gossypiella)、桔细潜蛾(Phyllocnistis citrella)、粉蝶(Pieris spp.)、菜蛾(Plutella xylostella)、尺蠖夜蛾(Prodenia spp.)、粘虫(Pseudaletia spp.)、大豆夜蛾(Pseudoplusia includens)、玉米螟(Pyraustanubilalis)、夜蛾(Spodoptera spp.)、Thermesia gemmatalis、织网夜蛾(Tineapellionella)、负袋夜蛾(Tineola bisselliella)、栎绿卷叶蛾(Tortrix viridana)、粉夜蛾(Trichoplusia spp.);
直翅目(Orthoptera),例如家蟋蟀(Acheta domesticus)、东方蜚蠊(Blattaorientalis)、德国小蠊(Blattella germanica)、蝼蛄虫(Gryllotalpa spp.)、马德拉蜚蠊(Leucophaea maderae)、飞蝗(Locusta spp.)、蚱蜢(Melanoplus spp.)、美洲大蠊(Periplaneta americana)、沙漠蝗(Schistocerca gregaria);
蚤目(Siphonaptera),例如角叶蚤(Ceratophyllus spp.)、开皇客蚤(Xenopsyllacheopis)。
综合纲(Symphyla),例如庭园幺蚰(Scutigerella immaculate);
缨翅目(Thysanoptera),例如稻蓟马(Baliothrips biformis)、Enneothripsflavens、花蓟马(Frankliniella spp.)、阳蓟马(Heliothrips spp.)、温室条蓟马(Hercinothrips femoralis)、豌豆蓟马(Kakothrips spp.)、腹钩蓟马(Rhipiphorothrips cruentatus)、黄蓟马(Scirtothrips spp.)、枇杷带蓟马(Taeniothrips cardamoni)、蓟马(Thrips spp.);
缨尾目(Thysanura),例如西洋衣鱼(Lepisma saccharina);
植物寄生线虫,包括例如鳗属(Anguina spp.)、滑刃线虫(Aphelenchoidesspp.)、刺线虫(Belonoaimus spp.)、伞滑刃线虫(Bursaphelenchus spp.)、续断双垫刃线虫(Ditylenchus dipsaci)、球形胞囊线虫(Globodera spp.)、螺旋线虫(Heliocotylenchus spp.)、异皮线虫(Heterodera spp.)、长针线虫(Longidorusspp.)、根结线虫(Meloidogyne spp.)、根线虫(Pratylenchus spp.)、据穴线虫(Radopholus similis)、盘旋线虫(Rotylenchus spp.)、轮胎虫(Trichodorus spp.)、矮化线虫(Tylenchorhynchus spp.)、麦线虫(Tylenchulus spp.)、桔垫刃线虫(Tylenchulus semipenetrans)、剑线虫(Xiphinema spp);
甲虫,例如家天牛(Hylotrupes bajulus)、Chlorophorus pilosis、家具窃蠹(Anobium punctatum)、红毛窃蠹(Xestobium rufovillosum)、Ptilinus pecticornis、Dendrobium pertinex、粉窃蠹(Ernobius mollis)、Priobium carpini、欧洲足粉蠹(Lyctus brunneus)、非洲粉蠹(Lctus africanus)、平颈粉蠹(Lyctus planicollis)、桴粉蠹(Lyctus linearis)、Lyctus pubescens、Trogoxylon aequale、鳞毛粉蠹(Minthes rugicollis)、小蠹(Xyleborus spec.)、Tryptodendron spec.、咖啡黑长蠹(Apate monachus)、Bostrychus capucins、棕异翅长蠹(Heterobostrychusbrunneus)、长蠹(Sinoxylon spec.)、竹长蠹(Dinoderus minutus);
膜翅目(Hymenopterons),例如小树峰(Sirex juvencus)、枞大树峰(Urocerusgigas)、大树蜂(Urocerus gigas taignus)、Urocerus augur;
白蚁,例如欧洲木白蚁(Kalotermes flayicollis)、麻头砂白蚁(Cryptotermesbrevis)、印巴结构木异白蚁(Heterotermes indicola)、黄胸散白蚁(Reticulitermesflavipes)、Reticulitermes santonensis、南欧网纹白蚁(Reticulitermes lucifugus)、达尔文澳白蚁(Mastotermes darwiniensis)、内华达古白蚁(Zootermopsisnevadensis)、家白蚁(Coptotermes formosanus);
蠹虫(Bristletails),例如西洋衣鱼(Lepisma saccharina);
螨目(Acarina),例如波斯锐缘蜱(Argaspersicus)、鸽锐缘蜱(Argasreflexus)、苔螨(Bryobia ssp.)、鸡皮刺螨(Dermanyssus gallinae)、家甜食螨(Glyciphagus domesticus)、非洲钝缘蜂(Ornithodorus moubat)、血红扇头蜱(Rhipicephalus sanguineus)、阿氏真恙螨(Trombicula alfreddugesi)、Neutrombicula autumnalis、屋尘螨(Dermatophagoides pteronissimus)、粉皮螨(Dermatophagoides forinae);
蜘蛛目(Araneae),例如Aviculariidae、金蛛(Araneidae);
盲蛛目(Opiliones),例如Pseudoscorpiones chelifer、Pseudoscorpionescheiridium、Opiliones phalangium;
等足目(Isopoda),例如潮虫(Oniscus asellus)、球鼠妇(Porcellio scaber);
倍足纲(Diplopoda),例如具斑马陆(Blaniulus guttulatus)、山蛩虫(Polydesmus spp).;
唇足纲(Chilopoda),例如地蜈蚣(Geophilus spp.);
衣鱼目(Zygentoma),例如毛衣鱼(Ctenolepisma spp.)、西洋衣鱼(Lepismasaccharina)、盗火虫(Lepismodes inquilinus);
蜚蠊目(Blattaria),例如东方蜚(Blatta orientalies)、德国小蠊(Blattellagermanica)、亚洲蟑螂(Blattella asahinai)、马德拉蜚蠊(Leucophaea maderae)、Panchlora spp.、木蠊(Parcoblatta spp.)、澳洲大蠊(Periplaneta australasiae)、美洲大蠊(Periplaneta Americana)、褐色大蠊(Periplaneta brunnea)、烟色大蠊(Periplaneta fuliginosa)、长须蜚蠊(Supella longipalpa);
Saltatoria,例如家蟋蟀(Acheta domesticus);
革翅目(Dermaptera),例如欧洲球螋(Forficula auricularia);
等翅目(Isoptera),例如木白蚁(Kalotermes spp.)、网白蚁(Reticulitermesspp);
啮虫目(Psocoptera),例如网翅书虱(Lepinatus spp.)、书虱(Liposcelis spp);
鞘翅目(Coleoptera),例如圆皮蠹(Anthrenus spp.)、黑皮囊(Attagenusspp.)、皮蠹(Dermestes spp.);云杉籽小蠹蛾(Latheticus oryzae)、郭公虫(Necrobia spp.)、蛛甲(Ptinus spp.)、谷蠹(Rhizopertha dominica)、谷象(Sitophilus granarius)、米象(Sitophilus oryzae)、玉米象(Sitophilus zeamais)、药材谷盗(Stegobium paniceum)。
双翅目(Diptera),例如埃及伊蚊(Aedes aegypti)、白纹伊蚊(Aedesalbopictus)、带喙伊蚊(Aedes taeniorhynchus)、疟蚊(Anopheles spp.)、红头丽蝇(Calliphora erythrocephala)、Chrysozona pluvialis、五带淡色库纹(Culexquinquefasciatus)、尖音库蚊(Culex pipiens)、环跗库蚊(Culex tarsalis)、果蝇(Drosophila spp.)、黄腹厕蝇(Fannia canicularis)、家蝇(Musca domestica)、白蛉(Phlebotomus spp.)、肉蝇(Sarcophaga carnaria)、蚋属(Simulium spp.)、厩螫蝇(Stomoxys calcitrans)、沼泽大蚊(Tipula paludosa);
鳞翅目(Lepidoptera),例如小蜡螟(Achroia grisella)、大蜡螟(Galleriamellonella)、印度谷螟(Plodia interpunctella)、Tinea cloacella、织网衣蛾(Tineapellionella)、负袋衣蛾(Tineola bisselliella);
蚤目(Siphonaptera),例如犬栉头蚤(Ctenocephalides canis)、猫栉头蚤(Ctenocephalides felis)、人蚤(Pulex irritans)、穿皮蚤骚(Tunga penetrans)、开皇客蚤(Xenopsylla cheopis)。
膜翅目(Hymenoptera),例如大黑蚁(Camponotus herculeanus)、黑草蚁(Lasius fuliginosus)、黑蚁(Lasius niger)、Lasius umbratus、厨蚁(Monomoriumpharaonis)、Paravespula spp.、铺道蚁(Tetramorium caespitum);
虱目(Anoplura),例如头虱(Pediculus humanus capitis)、衣虱(Pediculushumanus corporis)、天疱疮(Pemphigus spp.)、Phylloera vastatrix、阴虱(Phthirus pubis);
异翅目(Heteroptera),例如热带臭虫(Cimex hemipterus)、温带臭虫(Cimexlectularius)、长红猎蝽(Rhodinus prolixus)、骚扰锥蝽(Triatoma infestans)。
本发明的杀真菌或杀虫组合物还可以用来抵抗易于生长在木材上或木材内部或者容易攻击木材的真菌疾病。术语“木材”指所有种类的木材,和所有用于建筑的此类木材的加工材料,例如实木、高密度木材、层压木材和胶合板。本发明的处理木材的方法主要包括:使木材与本发明的一种或多种化合物或本发明的组合物接触;这包括例如直接施涂、喷涂、浸涂、注入或任何其它合适的方式。
在根据本发明的处理方法中,对于叶处理应用,活性化合物通常施用剂量优选为10-800克/公顷,优选为50-300克/公顷。对于种子处理,活性物质的施用剂量通常优选为2-200克/100千克种子,优选为3-150克/100千克种子。
应该清楚地理解,上述剂量是作为本发明方法的说明性例子给出。本领域技术人员知道如何根据待处理植物或农作物的性质调节施用剂量。
本发明的杀真菌或杀虫组合物也可以用于处理用本发明的化合物或本发明的农用化学组合物遗传修饰的生物体。遗传修饰的植物是其基因组被稳定地整合入编码感兴趣蛋白的异源基因的植物。“编码感兴趣蛋白的异源基因”主要是指给予转化植物新的农学性质的基因,或指改善改良植物的农学性质的基因。
本发明的化合物或混合物也可以用于制备对于治疗或预防人或动物真菌疾病有用的组合物,这些疾病例如霉菌病(mycose)、皮肤病、藓菌病和念珠菌病或由曲霉属(Aspergillus spp.)如烟曲霉(Aspergillus fumigatus)引起的疾病。
本发明的各方面将参考下表中的化合物和实施例进行说明。下表中列举了本发明的化合物的非限制性实施例。
在以下实施例中,质谱中所观察到的M+1(或M-1)分别指正或负1a.m.u.(原子质量单位)的分子离子峰,M(ApcI+)指通过质谱中的正大气压化学电离发现的分子离子峰。
在以下实施例中,依据HPLC(高效液相色谱)EEC Directive 79/831Annex V.A8,使用以下方法在反相柱(C18)上测量logP值:
温度:40℃;流动相:0.1%的甲酸和乙腈的水溶液;线性梯度为10%乙腈至90%乙腈。
使用logP值已知的直链型烷-2-酮(包括3-16个碳原子)进行校准(logP值是通过使用两个连续烷酮之间的线性内插的保留时间确定的)。
使用紫外光谱时,从190纳米至400纳米的色谱信号中的最大值确定λmax值。
表1:
以下实施例非限制性地说明了依据本发明的通式(I)的化合物的制备和药效。
制备实施例1-方法(a)-化合物(IIa)-化合物(VII):4′-叔丁基-2,5-二甲基联苯
-4-胺-中间体(VII-1)
使用惰性条件(氩气或氮气气氛,干溶剂)进行反应。将6.4克(36.0毫摩尔)(4-叔丁基苯基)硼酸、6.0克(30.0毫摩尔)4-溴代-2,5-二甲基苯胺、29.3克(90毫摩尔)碳酸铯和0.7克(0.6毫摩尔)四(三苯基膦)钯在75毫升1,2-二甲氧基乙烷中形成的悬浮液在80℃搅拌16小时。在室温下,加入25毫升水和75毫升甲苯。分离有机层,使用75毫升甲苯再次萃取水层。用硫酸镁干燥合并的有机层,并在真空下浓缩。进行柱色谱处理(环己烷/乙酸乙酯:2/1),得到5.5克(21.7毫摩尔)72%的4′-叔丁基-2,5-二甲基联苯-4-胺(log P(pH 2.3)=3.65)。
制备实施例2-方法(a)-化合物(Va)-化合物(I):N′-(4′-叔丁基-2,5-二甲基联苯
-4-基)-N-乙基-N-甲基亚氨基甲酰胺-化合物8
使用惰性条件(氩气或氮气气氛,干溶剂)进行反应。将0.3克(1.8毫摩尔)(4-叔丁基苯基)硼酸、0.4克(1.5毫摩尔)N′-(4-溴代-2,5-二甲基苯基)-N-乙基-N-甲基亚氨基甲酰胺、1.5克(4.5毫摩尔)碳酸铯和0.03克(0.3毫摩尔)四(三苯基膦)钯在3.5毫升1,2-二甲氧基乙烷中形成的悬浮液在80℃搅拌16小时。在室温下,加入5毫升水和15毫升甲苯。分离有机层,使用15毫升甲苯再次萃取水层。用硫酸镁干燥合并的有机层,并在真空下浓缩。进行柱色谱处理(环己烷/丙酮:4/1),得到0.23g(0.7毫摩尔)47%的N′-(4′-叔丁基-2,5-二甲基联苯-4-基)-N-乙基-N-甲基亚氨基甲酰胺;log P(pH 2.3)=2.67。
制备实施例3-方法(d3)-化合物(IIa)-化合物(Va):N′-(4-溴代-2,5-二甲基苯
基)-N-乙基-N-甲基亚氨基甲酰胺-中间体(Va-1)
向10.0克(50毫摩尔)4-溴代-2,5-二甲基苯胺和126毫升(1.15摩尔)三甲氧基甲烷的混合物中加入0.86克(5毫摩尔)对甲苯磺酸。将该反应混合物回流16小时,并在真空下浓缩。将该粗产物溶解在50毫升二氯甲烷中,加入5.9克(100毫摩尔)N-甲基乙胺。将该反应混合物在室温下搅拌16小时。将该反应混合物在真空下浓缩。进行柱色谱处理(梯度:石油醚->甲基-叔丁基醚),得到5.2克(19.5毫摩尔)39%的N′-(4-溴代-2,5-二甲基苯基)-N-乙基-N-甲基亚氨基甲酰胺;log P(pH 2.3)=1.36。
制备实施例4-方法(d1)-化合物(VII)-化合物(I):4′-叔丁基-2,5-二甲基-N-[哌
啶-2-亚基(piperidin-2-lidene)]联苯-4-胺-化合物121
将0.2克(1.5毫摩尔)三氯化磷在5毫升甲苯中形成的溶液加入到0.3克(3.0毫摩尔)哌啶-2-酮的混合物中,该放热反应在环境温度下搅拌2小时。然后加入0.38克(1.5毫摩尔)4′-叔丁基-2,5-二甲基联苯-4-胺在5毫升甲苯中的溶液,将该反应混合物回流5小时。在环境温度下,加入5毫升10%的氢氧化钠水溶液。分离各层,用10毫升甲苯萃取水层,用硫酸镁干燥,在真空下浓缩,进行柱色谱处理(梯度:环己烷->乙酸乙酯),得到0.3克(1.0毫摩尔)63%的4′-叔丁基-2,5-二甲基-N-[哌啶-2-亚基]联苯-4-胺;log P(pH 2.3)=2.6。
制备实施例5-方法(d2)-化合物(VII)-化合物(I):N′-(4′-叔丁基-2,5-二甲基联
苯-4-基)-N-乙基-N-甲基亚氨基甲酰胺-化合物8
向2.1克(6.3毫摩尔)4′-叔丁基-2,5-二甲基联苯-4-胺在2.5毫升甲醇中形成的混合物中加入8.8毫摩尔N-(二甲氧基甲基)-N-甲基乙胺的溶液(60%,在甲醇中)。将该反应混合物在45℃搅拌24小时。将该反应混合物在真空下浓缩。进行柱色谱处理(梯度:环己烷->乙酸乙酯),得到0.96克(3.0毫摩尔)47%的N′-(4′-叔丁基-2,5-二甲基联苯-4-基)-N-乙基-N-甲基亚氨基甲酰胺;log P(pH 2.3)=2.67。
药效实施例A:小麦隐匿柄锈菌(Puccinia recondita f.Sp.Tritici)(小麦褐锈病)
的体内预防性测试
溶剂:50重量份N,N-二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试预防性活性,用小麦隐匿柄锈菌的孢子悬浮液(浓度为0.1%的水性琼脂溶液)对树苗进行接种。在喷洒的涂层干燥后,用活性化合物制剂以一定的施用率喷洒植物。将所述植物在20℃、相对大气湿度为100%的培养箱中放置24小时。
将所述植物放置在约20℃、相对大气湿度约80%的温室中,以促进锈脓包(rust pustule)的生长。
在培养后10天,对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为1000ppm的情况下表现出等于或高于70%的药效:1、2、3、7、8、10、16、17、21、28、31、33、34、35、39、4、47、64、73、96、97、98、106、107、108、109、110、112、114、115、116、122、123、125、127、129、131、132、133、136、145、146、149、151、155、156、160、162、163、164、165、167、169。
药效实施例B:禾白粉菌(Erysiphe gramini)(大麦白粉病)的体内预防性测试
溶剂:50重量份N,N-二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物或活性化合物组合与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试预防性活性,以一定的施用率将活性化合物或活性化合物组合的制剂喷洒到树苗上。
在喷洒的涂层干燥后,将禾白粉菌(Erysiphe graminis f.sp.hordei)的孢子撒在所述植物上。
将所述植物放置在约20℃,相对大气湿度约为80%的温室中,以促进霉脓疱(mildew pustule)的生长。
在接种后7天,对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为1000ppm的情况下表现出等于或高于70%的药效:1、2、7、8、10、17、18、21、28、31、33、34、35、40、47、73、96、97、100、106、107、108、109、112、114、115、116、123、127、129、132、133、138。
药效实施例C:茄链格孢(Alternaria solani)(番茄叶斑病)的体内保护性测试
溶剂:49重量份N,N-二甲基甲酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试保护性活性,以一定的施用率将活性化合物的制剂喷洒到树苗上。在喷洒的涂层干燥后,用茄链格孢的水性孢子悬浮液接种所述植物。将所述植物在约20℃、相对大气湿度100%的培养箱中保持一天。然后将所述植物放置在约20℃、相对大气湿度96%的培养箱中。
在接种后7天对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为500ppm的情况下表现出等于或高于70%的药效:8、31、35、36、39、40、41、43、47、76、77、78、106、119、123、129、132、133。
药效实施例D:白叉丝单囊壳(Podosphaera leucotricha)(苹果)的体内保护性
测试
溶剂:24.5重量份丙酮
24.5重量份二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试保护性活性,以一定的施用率将活性化合物的制剂喷洒到树苗上。在喷洒的涂层干燥后,用苹果霉病(白叉丝单囊壳)的致病剂(causal agent)的水性孢子悬浮液接种所述植物。然后将所述植物放置在约23℃、相对大气湿度70%的温室中。
在接种后10天对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为100ppm的情况下表现出等于或高于70%的药效:1、8、27、28、40、106、112、129、132、133、155、160。
药效实施例E:苍耳单丝壳(Sphaerotheca fuliginea)(黄瓜)的体内保护性测试
溶剂:24.5重量份丙酮
24.5重量份二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试保护性活性,以一定的施用率将活性化合物的制剂喷洒到树苗上。在喷洒的涂层干燥后,用苍耳单丝壳的水性孢子悬浮液接种所述植物。然后将所述植物放置在约23℃、相对大气湿度70%的温室中。
在接种后7天对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为100ppm的情况下表现出等于或高于70%的药效:1、8、17、27、28、40、106、112、114、122、123、124、129、132、133、145、155。
药效实施例F:灰葡萄孢(Botrytis cinerea)(豆类)的体内保护性测试
溶剂:24.5重量份丙酮
24.5重量份二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试保护性活性,用活性化合物的制剂喷洒树苗。在喷洒的涂层干燥后,将2小片覆盖了灰葡萄孢生长物的琼脂放在各叶子上。将接种植物放在20℃、相对大气湿度为100%的暗箱中。
在接种后2天,评价叶子损害的大小。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为500ppm的情况下表现出等于或高于70%的药效:8、40、7、106、129、132、133。
药效实施例G:疣顶单胞锈菌(Uromyces appendiculatus)(豆类)的体内保护性
测试
溶剂:24.5重量份丙酮
24.5重量份二甲基乙酰胺
乳化剂:1重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用水稀释该浓缩物至所需浓度。
为了测试保护性活性,以一定的施用率将活性化合物的制剂喷洒到树苗上。在喷洒的涂层干燥后,用豆类锈病(疣顶单胞锈菌)的致病剂的水性孢子悬浮液接种所述植物,然后将所述植物在约20℃、相对大气湿度为100%的培养箱中放置1天。
然后将所述植物放置在约21℃、相对大气湿度90%的温室中。
在接种后10天对测试结果进行评价。0%表示相当于对照样的药效,100%的药效表示无病症出现。
在该测试中,依据本发明的以下化合物在活性成分浓度为100ppm的情况下表现出等于或高于70%的药效:129、132、133、155、160。
药效实施例H:埃及伊蚊(Aedes Aegypti)(AEDSAE U)的体内保护性测试
溶剂:1%N-甲基吡咯烷酮(NMP)
1%双丙酮醇
染料:用于着色水的布莱斯伏温(brillantsulfoflavin)
为了生产活性化合物的合适制剂,将活性化合物与一定量的溶剂混合,用着色水稀释该浓缩物至所需浓度。
用所需浓度的活性成分的制剂处理埃及伊蚊幼虫。
在特定时间后,确定死亡率%。100%表示所有幼虫被杀死,0%表示无幼虫被杀死。
在该测试中,以下来自制备实施例的化合物表现出良好的活性:9、18、19、26、47、54、77、99、100、104、105、127、128、129。
药效实施例I:烟芽夜蛾(Heliotis virescens)-烟芽夜蛾的测试(HELIVI喷洒施
用)
溶剂:78重量份丙酮
1.5重量份二甲基甲酰胺
润湿剂:0.5重量份烷基芳基聚乙二醇醚
为了生产活性化合物的合适制剂,将1重量份活性化合物与一定量的溶剂和乳化剂混合,用含乳化剂的水稀释该浓缩物至所需浓度。
将活性成分的制剂以所需浓度喷洒在大豆(Glycine max.)叶部分上。干燥后,立即用棉花暝蛉(烟芽夜蛾)的卵感染该叶部分。
在特定时间后,确定死亡率%。100%表示所有卵被杀死;0%表示无卵被杀死。
在此测试中,以下来自制备实施例的化合物表现出良好的活性:26。
Claims (5)
1.一种通式(I)的苯脒衍生物:
式中:
R1表示H、C1-C12-烷基或SH;或
R2表示甲基;或
R3表示C2-C12-烷基、C2-C12-烯基、C3-C6-环烷基;或
R2和R3可一起形成哌啶基或吡咯烷基;或
R4表示C1-C12-烷基、卤原子或三氟甲基;或
R5表示H、C1-C12-烷基、卤原子或三氟甲基;或
R6可相同或不同,表示H;F、Cl、Br、I;硝基;氰基;C1-C6-烷基;C1-C4-烷基-苯基,其可以未取代或被卤素、C1-C4-烷基或C1-C4-卤代烷基取代;苯基,其可以未取代或被卤素、C1-C4-烷基或C1-C4-卤代烷基取代;C1-C6-烷氧基;C1-C4-烷氧基-C1-C4-烷基;C1-C6-卤代烷基;C1-C6-卤代烷氧基;苄氧基,其可以未取代或被卤素取代;苯氧基,其可以未取代或被卤原子或CF3取代;OR10;-CR9=N-O-R11;或
R9表示H、甲基或乙基;或
R10表示H、C1-C4-烷基或C1-C4-烷氧基;或
R11表示H;C1-C4-烷基;C1-C4-卤代烷基;C1-C4-烷基-苯基,其中苯基可被F、Cl、Br、I、C1-C4-烷基、C1-C4-卤代烷基或C1-C4-卤代烷氧基取代;C1-C4-烷氧基-C1-C4-烷基;苯氧基;苄氧基;或
m表示1、2、3或4。
2.如权利要求1所述的通式(I)的化合物,其特征在于,
R1表示C1-C12-烷基;或
R3表示未取代的C2-C4-烷基、C3-C4-烯基或环丙基;或
R4表示未取代的C1-C12-烷基、氟原子或氯原子;或
R5表示未取代的C1-C12-烷基、氟原子或氯原子;或
m表示1、2或3。
3.如权利要求1所述的通式(I)的化合物,其特征在于,
R1表示甲基;或
R3表示乙基、正丙基、异丙基、丙烯基或烯丙基;或
R4表示甲基或乙基;或
R5表示甲基或乙基。
5.一种控制农作物中植物病原真菌的方法,其特征在于,将农药有效且非植物毒性量的如权利要求1至3中任一项所述的化合物施用到植物生长或能够生长的土壤中,施用到植物叶子和/或植物果实上,或者施用到植物种子上。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05356153.6 | 2005-09-13 | ||
EP05356153 | 2005-09-13 | ||
PCT/EP2006/066271 WO2007031512A2 (en) | 2005-09-13 | 2006-09-12 | Pesticide bi-phenyl-amidine derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101287703A CN101287703A (zh) | 2008-10-15 |
CN101287703B true CN101287703B (zh) | 2012-11-07 |
Family
ID=35840629
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2006800330715A Expired - Fee Related CN101287703B (zh) | 2005-09-13 | 2006-09-12 | 农药联苯脒衍生物 |
Country Status (16)
Country | Link |
---|---|
US (1) | US7999137B2 (zh) |
EP (1) | EP1926706B1 (zh) |
JP (1) | JP2009507813A (zh) |
KR (1) | KR20080045749A (zh) |
CN (1) | CN101287703B (zh) |
AR (1) | AR058041A1 (zh) |
AT (1) | ATE550315T1 (zh) |
BR (1) | BRPI0616002B1 (zh) |
CA (1) | CA2619607A1 (zh) |
CR (1) | CR9780A (zh) |
EA (1) | EA200800817A1 (zh) |
EC (1) | ECSP088312A (zh) |
IL (1) | IL189259A0 (zh) |
MX (1) | MX2008003432A (zh) |
WO (1) | WO2007031512A2 (zh) |
ZA (1) | ZA200800694B (zh) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2399721T5 (es) | 2004-03-05 | 2016-05-25 | Univ Pennsylvania | Métodos para tratar trastornos o enfermedades asociados a la hiperlipidemia e hipercolesterolemia minimizando los efectos adversos |
JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
EP1969931A1 (de) | 2007-03-12 | 2008-09-17 | Bayer CropScience Aktiengesellschaft | Fluoalkylphenylamidine und deren Verwendung als Fungizide |
WO2009053250A1 (de) | 2007-10-26 | 2009-04-30 | Basf Se | Fungizide verbindungen, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
EP2282742A1 (en) * | 2008-04-09 | 2011-02-16 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
WO2010115758A2 (en) | 2009-04-03 | 2010-10-14 | Basf Se | Fungicidal compounds |
CA2757622A1 (en) | 2009-04-07 | 2010-10-14 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
WO2010118155A1 (en) | 2009-04-07 | 2010-10-14 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
MX336742B (es) | 2010-02-03 | 2016-01-29 | Infinity Pharmaceuticals Inc | Inhibidores de amida hidrolasa de acido graso. |
EP2552889A1 (en) | 2010-03-29 | 2013-02-06 | Basf Se | Fungicidal iminoderivatives |
ITMI20101564A1 (it) | 2010-08-23 | 2012-02-24 | Isagro Ricerca Srl | Fenilammidine ad elevata attivita' fungicida e relativo uso |
CA3006745C (en) | 2010-11-05 | 2021-03-30 | Oat Agrio Co., Ltd. | Ethynylphenylamidine compound or salt thereof, method for producing same, and fungicide for agricultural and horticultural use |
ITMI20120405A1 (it) | 2012-03-15 | 2013-09-16 | Chemtura Corp | "composizioni sinergiche ad attivita' fungicida e relativo uso" |
LT3307707T (lt) | 2015-06-15 | 2021-01-11 | Syngenta Crop Protection Ag | Halogeninti fenoksifenilamidinai ir jų naudojimas kaip fungicidų |
US10252977B2 (en) | 2015-06-15 | 2019-04-09 | Bayer Cropscience Aktiengesellschaft | Halogen-substituted phenoxyphenylamidines and the use thereof as fungicides |
BR112018000390A2 (pt) | 2015-07-08 | 2018-09-11 | Bayer Cropscience Ag | fenoxihalogenofenilamidinas e o uso dessas como fungicidas |
CN108368543B (zh) | 2015-10-12 | 2023-06-13 | 领先细胞医疗诊断有限公司 | 高噪声样品中原位检测核苷酸变体及相关的组合物和方法 |
WO2018109002A1 (en) | 2016-12-14 | 2018-06-21 | Bayer Cropscience Aktiengesellschaft | Active compound combinations |
AU2017375006A1 (en) | 2016-12-14 | 2019-07-04 | Bayer Aktiengesellschaft | Phenoxyphenylamidines and the use thereof as fungicides |
US20190308933A1 (en) | 2016-12-14 | 2019-10-10 | Bayer Cropscience Aktiengesellschaft | Phenylamidines and the use thereof as fungicides |
EP3335559A1 (en) | 2016-12-14 | 2018-06-20 | Bayer CropScience Aktiengesellschaft | Active compound combinations |
TW201838965A (zh) | 2017-04-20 | 2018-11-01 | 印度商Pi工業公司 | 新穎的苯胺化合物 |
WO2018211442A1 (en) | 2017-05-18 | 2018-11-22 | Pi Industries Ltd. | Formimidamidine compounds useful against phytopathogenic microorganisms |
CN108640857B (zh) * | 2018-06-07 | 2021-03-30 | 烟台新秀化学科技股份有限公司 | 一种n-(乙氧基羰基苯基)-n’-甲基-n’-苯基脒的合成工艺 |
EP3708565A1 (en) | 2020-03-04 | 2020-09-16 | Bayer AG | Pyrimidinyloxyphenylamidines and the use thereof as fungicides |
EP3915971A1 (en) | 2020-12-16 | 2021-12-01 | Bayer Aktiengesellschaft | Phenyl-s(o)n-phenylamidines and the use thereof as fungicides |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5064846A (en) * | 1988-10-31 | 1991-11-12 | Ici Americas Inc. | Heterocyclic insecticides |
WO2000046184A1 (en) * | 1999-02-06 | 2000-08-10 | Aventis Cropscience Gmbh | N2-phenylamidine derivatives |
WO2002055510A1 (fr) * | 2001-01-12 | 2002-07-18 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derives de 2-arylimino-2,3-dihydrothiazoles, leurs procedes de preparation et leur utilisation therapeutique |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2202034A1 (de) * | 1971-01-22 | 1972-07-27 | Ciba Geigy Ag | Neue Kondensationsprodukte |
US5633218A (en) | 1995-05-24 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Herbicidal benzodioxoles and benzodioxanes |
EP1178038A1 (en) * | 2000-08-04 | 2002-02-06 | Aventis Cropscience S.A. | Fungicidal phenylamidine derivatives |
FR2812633A1 (fr) * | 2000-08-04 | 2002-02-08 | Aventis Cropscience Sa | Derives de phenyl(thio)urees et phenyl(thio)carbamates fongicides |
EP1570736A1 (en) * | 2004-03-05 | 2005-09-07 | Bayer CropScience S.A. | Fungicide composition comprising an arylamidine derivative and known fungicide compounds |
AU2008226094A1 (en) * | 2007-03-12 | 2008-09-18 | Bayer Cropscience Ag | Use of N2-phenylamidines as herbicides and herbicidal agents comprising the same |
EP1969931A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience Aktiengesellschaft | Fluoalkylphenylamidine und deren Verwendung als Fungizide |
-
2006
- 2006-09-12 EP EP06793447A patent/EP1926706B1/en not_active Not-in-force
- 2006-09-12 US US12/063,659 patent/US7999137B2/en not_active Expired - Fee Related
- 2006-09-12 AT AT06793447T patent/ATE550315T1/de active
- 2006-09-12 MX MX2008003432A patent/MX2008003432A/es not_active Application Discontinuation
- 2006-09-12 CN CN2006800330715A patent/CN101287703B/zh not_active Expired - Fee Related
- 2006-09-12 AR ARP060103970A patent/AR058041A1/es unknown
- 2006-09-12 JP JP2008529647A patent/JP2009507813A/ja not_active Withdrawn
- 2006-09-12 EA EA200800817A patent/EA200800817A1/ru unknown
- 2006-09-12 CA CA002619607A patent/CA2619607A1/en not_active Abandoned
- 2006-09-12 BR BRPI0616002A patent/BRPI0616002B1/pt not_active IP Right Cessation
- 2006-09-12 WO PCT/EP2006/066271 patent/WO2007031512A2/en active Application Filing
- 2006-09-12 KR KR1020087008716A patent/KR20080045749A/ko not_active Application Discontinuation
-
2008
- 2008-01-23 ZA ZA200800694A patent/ZA200800694B/xx unknown
- 2008-02-04 IL IL189259A patent/IL189259A0/en unknown
- 2008-02-29 CR CR9780A patent/CR9780A/es unknown
- 2008-03-26 EC EC2008008312A patent/ECSP088312A/es unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5064846A (en) * | 1988-10-31 | 1991-11-12 | Ici Americas Inc. | Heterocyclic insecticides |
WO2000046184A1 (en) * | 1999-02-06 | 2000-08-10 | Aventis Cropscience Gmbh | N2-phenylamidine derivatives |
WO2002055510A1 (fr) * | 2001-01-12 | 2002-07-18 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derives de 2-arylimino-2,3-dihydrothiazoles, leurs procedes de preparation et leur utilisation therapeutique |
Also Published As
Publication number | Publication date |
---|---|
KR20080045749A (ko) | 2008-05-23 |
JP2009507813A (ja) | 2009-02-26 |
WO2007031512A2 (en) | 2007-03-22 |
ZA200800694B (en) | 2009-01-28 |
EP1926706A2 (en) | 2008-06-04 |
IL189259A0 (en) | 2008-08-07 |
AR058041A1 (es) | 2008-01-23 |
CA2619607A1 (en) | 2007-03-22 |
EA200800817A1 (ru) | 2008-08-29 |
EP1926706B1 (en) | 2012-03-21 |
MX2008003432A (es) | 2008-03-27 |
BRPI0616002B1 (pt) | 2016-04-19 |
US7999137B2 (en) | 2011-08-16 |
CN101287703A (zh) | 2008-10-15 |
ECSP088312A (es) | 2008-05-30 |
BRPI0616002A2 (pt) | 2011-05-31 |
US20080280992A1 (en) | 2008-11-13 |
WO2007031512A3 (en) | 2008-06-26 |
CR9780A (es) | 2010-03-08 |
ATE550315T1 (de) | 2012-04-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101287703B (zh) | 农药联苯脒衍生物 | |
CN101263129A (zh) | 农药噻唑氧基取代的苯脒衍生物 | |
JP5261181B2 (ja) | 殺虫剤フェニルオキシ置換フェニルアミジン誘導体 | |
JP5849074B2 (ja) | 三元活性化合物組合せ | |
KR101361189B1 (ko) | 살충성을 갖는 활성 물질의 배합물 | |
US20090197918A1 (en) | Pesticide benzyloxy- and phenetyl-substituted phenyl-amidine derivatives | |
EP1931623B1 (en) | Pesticide naphthyloxy substituted phenylamidine derivatives | |
JP2009541378A (ja) | 殺虫剤及び殺真菌剤の相乗的な混合物 | |
TW200812489A (en) | Active compound combinations having insecticidal and acaricidal properties | |
KR20080023738A (ko) | 살충 활성이 있는 벤즈아닐리드 | |
TW200803729A (en) | Active compound combinations having insecticidal and acaricidal properties | |
CN101460056A (zh) | 具有杀虫特性的活性物质结合物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20121107 Termination date: 20160912 |