JP5718249B2 - 安定な殺虫剤組成物およびその製造方法 - Google Patents
安定な殺虫剤組成物およびその製造方法 Download PDFInfo
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- JP5718249B2 JP5718249B2 JP2011543496A JP2011543496A JP5718249B2 JP 5718249 B2 JP5718249 B2 JP 5718249B2 JP 2011543496 A JP2011543496 A JP 2011543496A JP 2011543496 A JP2011543496 A JP 2011543496A JP 5718249 B2 JP5718249 B2 JP 5718249B2
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- 239000002917 insecticide Substances 0.000 title description 62
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- 238000010438 heat treatment Methods 0.000 claims description 58
- 150000001875 compounds Chemical class 0.000 claims description 52
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- QZYSTPIBCDZBBH-UHFFFAOYSA-N 5-(1-methoxyethyl)-2-(trifluoromethyl)pyridine Chemical compound FC(C1=NC=C(C=C1)C(C)OC)(F)F QZYSTPIBCDZBBH-UHFFFAOYSA-N 0.000 claims description 17
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 14
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 14
- 229930185156 spinosyn Natural products 0.000 claims description 10
- 239000005929 Spinetoram Substances 0.000 claims description 8
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 claims description 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 6
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 claims description 6
- 239000005930 Spinosad Substances 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 125000001246 bromo group Chemical group Br* 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 229940014213 spinosad Drugs 0.000 claims description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 230000009466 transformation Effects 0.000 claims description 2
- 238000000844 transformation Methods 0.000 claims 1
- -1 for example Chemical group 0.000 description 136
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- 239000000243 solution Substances 0.000 description 50
- 238000006243 chemical reaction Methods 0.000 description 47
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 39
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- 239000012044 organic layer Substances 0.000 description 29
- 239000011734 sodium Substances 0.000 description 29
- 241000238631 Hexapoda Species 0.000 description 27
- 238000009472 formulation Methods 0.000 description 27
- 239000002904 solvent Substances 0.000 description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
- 239000007787 solid Substances 0.000 description 22
- 239000000575 pesticide Substances 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 17
- 241000607479 Yersinia pestis Species 0.000 description 17
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 17
- 239000003921 oil Substances 0.000 description 16
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- 239000000741 silica gel Substances 0.000 description 16
- 229910002027 silica gel Inorganic materials 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 15
- 235000019439 ethyl acetate Nutrition 0.000 description 14
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 241000196324 Embryophyta Species 0.000 description 13
- 239000012267 brine Substances 0.000 description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 229920006395 saturated elastomer Polymers 0.000 description 12
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- 125000005555 sulfoximide group Chemical group 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 239000003995 emulsifying agent Substances 0.000 description 9
- 238000000105 evaporative light scattering detection Methods 0.000 description 9
- 230000002829 reductive effect Effects 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000004587 chromatography analysis Methods 0.000 description 8
- 230000001276 controlling effect Effects 0.000 description 8
- 239000012043 crude product Substances 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- GLBQVJGBPFPMMV-UHFFFAOYSA-N sulfilimine Chemical compound S=N GLBQVJGBPFPMMV-UHFFFAOYSA-N 0.000 description 8
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- ZBIKORITPGTTGI-UHFFFAOYSA-N [acetyloxy(phenyl)-$l^{3}-iodanyl] acetate Chemical compound CC(=O)OI(OC(C)=O)C1=CC=CC=C1 ZBIKORITPGTTGI-UHFFFAOYSA-N 0.000 description 7
- 239000000417 fungicide Substances 0.000 description 7
- 239000008187 granular material Substances 0.000 description 7
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 6
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 6
- 239000012230 colorless oil Substances 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 230000000361 pesticidal effect Effects 0.000 description 6
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- RMBAVIFYHOYIFM-UHFFFAOYSA-M sodium methanethiolate Chemical compound [Na+].[S-]C RMBAVIFYHOYIFM-UHFFFAOYSA-M 0.000 description 6
- 239000004563 wettable powder Substances 0.000 description 6
- 241000193388 Bacillus thuringiensis Species 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- 235000019502 Orange oil Nutrition 0.000 description 5
- 238000003818 flash chromatography Methods 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 5
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- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 4
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- 239000002169 Metam Substances 0.000 description 4
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
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- 239000008346 aqueous phase Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 4
- CSJLBAMHHLJAAS-UHFFFAOYSA-N diethylaminosulfur trifluoride Chemical compound CCN(CC)S(F)(F)F CSJLBAMHHLJAAS-UHFFFAOYSA-N 0.000 description 4
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 4
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 4
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- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 4
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- 235000011181 potassium carbonates Nutrition 0.000 description 4
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- 150000001356 alkyl thiols Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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- 229910021538 borax Inorganic materials 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
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- 239000003054 catalyst Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229910000365 copper sulfate Inorganic materials 0.000 description 3
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 3
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- 201000010099 disease Diseases 0.000 description 3
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- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
- 230000014509 gene expression Effects 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 230000002363 herbicidal effect Effects 0.000 description 3
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
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- 244000144972 livestock Species 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
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- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000003880 polar aprotic solvent Substances 0.000 description 3
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- IUBQJLUDMLPAGT-UHFFFAOYSA-N potassium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([K])[Si](C)(C)C IUBQJLUDMLPAGT-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
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- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 3
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- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 2
- RLLPVAHGXHCWKJ-MJGOQNOKSA-N (3-phenoxyphenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-MJGOQNOKSA-N 0.000 description 2
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- JCIIKRHCWVHVFF-UHFFFAOYSA-N 1,2,4-thiadiazol-5-amine;hydrochloride Chemical compound Cl.NC1=NC=NS1 JCIIKRHCWVHVFF-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
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- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-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
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- CBEQULMOCCWAQT-WOJGMQOQSA-N triprolidine Chemical compound C1=CC(C)=CC=C1C(\C=1N=CC=CC=1)=C/CN1CCCC1 CBEQULMOCCWAQT-WOJGMQOQSA-N 0.000 description 1
- 229960001128 triprolidine Drugs 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 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
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/32—Sulfur atoms
- C07D213/34—Sulfur atoms to which a second hetero atom is attached
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/53—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/57—Nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
本出願は、2008年12月26日に出願された米国仮特許出願第61/203,600号の優先権を主張し、その内容は、その全体が参照により本明細書に組み込まれる。
(式中、
Xは、NO2、CNまたはCOOR4を表し;
Lは、単結合を表すか、または、R1、SおよびLは一緒になって、4、5もしくは6員環を表し;
R1は、(C1〜C4)アルキルを表し;
R2およびR3は、互いに異なり、個々に、水素、メチル、エチル、フルオロ、クロロまたはブロモを表し;
nは、Lが単結合を表す場合、1であるか、またはR1、SおよびLが一緒になって、4、5もしくは6員環を表す場合、0であり;
Yは、(C1〜C4)ハロアルキル、F、Cl、Br、またはIを表し;
R4は、(C1〜C3)アルキルを表す)
を有する化合物の立体異性体間の第1の比を含む組成物を提供する工程を含む。
(式中、
Xは、NO2、CNまたはCOOR4を表し;
R1は、(C1〜C4)アルキルを表し;
R2およびR3は、互いに異なり、個々に、水素、メチル、エチル、フルオロ、クロロまたはブロモを表し;
Yは、(C1〜C4)ハロアルキル、F、Cl、Br、またはIを表し;
R4は、(C1〜C3)アルキルを表す)
を有する式(I)の化合物を含む。
(式中、
Xは、NO2、CNまたはCOOR4を表し;
Yは、(C1〜C4)ハロアルキル、F、Cl、Br、またはIを表し;
R4は、(C1〜C3)アルキルを表す)
を有する式(I)の化合物を含む。
(1)Xが、NO2またはCN、最も好ましくはCNである式(I)の化合物、
(2)YがCF3である式(I)の化合物、
(3)R2およびR3が、互いに異なり、独立して、水素、メチルまたはエチルを表す式(I)の化合物、
(4)R1がCH3を表す式(I)の化合物
の1つまたは複数における式(I)の化合物を含む。
(式中、
Xは、NO2、CNまたはCOOR4を表し;
R1は、(C1〜C4)アルキルを表し;
R2およびR3は、互いに異なり、個々に、水素、メチル、エチル、フルオロ、クロロまたはブロモを表し;
Yは、(C1〜C4)ハロアルキル、F、Cl、Br、またはIを表し;
R4は、(C1〜C3)アルキルを表す)
を有する化合物の立体異性体混合物を含み、該混合物は、ジアステレオマーの第1の対およびジアステレオマーの第2の対で規定される組成物を提供する工程を含む。
置換基に対して与えられる例は、(ハロを除いて)非包括的であり、本文書に開示される本発明を限定すると解釈してはならない。
[1−(6−トリフルオロメチルピリジン−3−イル)エチル](メチル)−オキシド−λ4−スルファニリデンシアナミド(2)の調製
2−(6−トリフルオロメチルピリジン−3−イル)−1−オキシド−テトラヒドロ−1H−1λ4−チエン−1−イリデンシアナミド(3)の調製
(1−{6−[クロロ(ジフルオロ)メチル]ピリジン−3−イル}エチル)(メチル)−オキシド−λ4−スルファニリデンシアナミド(4)の調製
[1−(6−トリクロロメチルピリジン−3−イル)エチル(メチル)−オキシド−λ4−スルファニリデンシアナミド(5)の調製
[1−(6−ジフルオロメチルピリジン−3−イル)エチル](メチル)−オキシド−λ4−スルファニリデンシアナミド(6)の調製
[1−(6−ペンタフルオロエチルピリジン−3−イル)エチル](メチル)−オキシド−λ4−スルファニリデンシアナミド(7)の調製
2−トリフルオロメチル−5−(1−{メチル(オキシド)[オキシド(オキソ)ヒドラゾノ]−λ4−スルファニル}エチル)ピリジン(8)の調製
[6−(1,1−ジフルオロエチル)ピリジン−3−イル)エチル](メチル)−オキシド−λ4−スルファニリデンシアナミド(9)の調製
{1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}(メチル)オキシド−λ4−スルファニリデンシアナミドの立体異性体混合物を含む組成物の調製
ジアステレオマー群Aおよび群B間の約1:2の比を有する、240g/L濃度の{1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}(メチル)オキシド−λ4−スルファニリデンシアナミドを有する1リットルの総容量(〜1100gの総重量)のSC剤製品を、機械的撹拌機を備えた清浄なビーカーに脱イオン水を最初に添加することにより調製した。次いで、そのビーカーに以下の成分を連続撹拌下、特になく、添加した。:3.5gのAgnique(登録商標)DFM112S(Cognis Group(ドイツに本社を置くMonheim)から市販されているシリコン系消泡剤);20gのTersperse(登録商標)2500(Huntsman Performance Products(10003 Woodloch Forest Drive,The Woodlands,TX 77380)から市販されているポリマー界面活性剤);30gのMorwet(登録商標)D−360(Akzo Nobel Surfactants(525W,Van Buren St.,シカゴ,IL60607)から市販されている界面活性剤);20gのEthylan(登録商標)NS500LQ(Akzo Nobel Surfactants(525W,Van Buren St.,シカゴ,IL60607)から市販されている界面活性剤);40gのプロピレングリコール;1gのProxel(登録商標)GXL(Arch Chemicals,Inc.(1955 Lake Drive,Suite 100,スマーナ,GA30080)から市販されているマイクロバイオスタット溶液)。次いで、240gの{1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}(メチル)オキシド−λ4−スルファニリデンシアナミドをビーカーに添加し、続いて、10gのAvicel(登録商標)CL−611(FMC BioPolymer(1735 Market Street,フィラデルフィア,PA 19103)から市販されている安定剤)および2gのKelzan(CP Kelco(1000 Parkwood Circle,Suite 1000,アトランタ,GA 30339)から市販されているキサンタンガム)を添加した。均一な混合物が得られるまで、成分を撹拌した。次いで、この混合物をビーズミルで3〜5μmの平均粒径に粉砕した。このSC剤製品の最終処方を表1に示す。
本文書に開示される組成物は、昆虫を含む無脊椎動物の防除に有用である。したがって、本発明はまた、昆虫抑制量の本組成物を、昆虫の所在場所に、防護すべき領域に、または防除すべき昆虫に対して直接施用する工程を含む、昆虫を抑制する方法に関する。本発明の組成物は、ダニおよび線虫などの他の無脊椎有害生物を防除するためにも使用され得る。
鞘翅目(甲虫目)(Coleoptera)−ジアブロチカ属種(Diabrotica spp.)、レプチノタルサ・デセムリネアタ(Leptinotarsa decemlineata)、オウレマ・オリザエ(Oulema oryzae)、アントノムス・グランジス(Anthonomus grandis)、リッソルホプトルス・オリゾフィルス(Lissorhoptrus oryzophilus)、アグリオテス属種(Agriotes spp.)、メラノツス・コムニス(Melanotus communis)、ポピリア・ジャポニカ(Popillia japonica)、シクロセファラ属種(Cyclocephala spp.)、トリボリウム属種(Tribolium spp.)
同翅目(ヨコバイ目)(Homoptera)−アフィス属種(Aphis spp.)、ミズス・ペルシカエ(Myzus persicae)、ロパロシフム属種(Rhopalosiphum spp.)、ジサフィス・プランタギネア(Dysaphis plantaginea)、トキソプテラ属種(Toxoptera spp.)、マクロシフム・ユーホルビアエ(Macrosiphum euphorbiae)、アウラコルタム・ソラニ(Aulacorthum solani)、シトビオン・アベナエ(Sitobion avenae)、メトポロフィウム・ジルホダム(Metopolophium dirhodum)、シザフィス・グラミヌム(Schizaphis graminum)、ブラキコルス・ノクシウス(Brachycolus noxius)、ネホテティクス属種(Nephotettix spp.)、ニラパルバタ・ルゲンス(Nilaparvata lugens)、ソガテラ・フルシフェラ(Sogatella furcifera)、ラオデルファクス・ストリアテルス(Laodelphax striatellus)、ベミシア・タバキ(Bemisia tabaci)、トリアロイロデス・バポラリオルム(Trialeurodes vaporariorum)、アロイロデス・プロレテラ(Aleurodes proletella)、アロイロスリキスス・フロッコスス(Aleurothrixus floccosus)、クアドラスピジオツス・ペルニシオスス(Quadraspidiotus perniciosus)、ウナスピス・ヤノネンシス(Unaspis yanonensis)、セロプラステス・ルベンス(Ceroplastes rubens)、アオニジエラ・アウランチイ(Aonidiella aurantii)
半翅目(カメムシ目)(Hemiptera)−リグス属種(Lygus spp.)、ユーリガステル・マウラ(Eurygaster maura)、ネザラ・ビリヅラ(Nezara viridula)、ピエゾドルス・ギルジンギ(Piezodorus guildingi)、レプトコリサ・バリコルニス(Leptocorisa varicornis)、シメクス・レクツラリウス(Cimex lectularius)、シメクス・ヘミプテルス(Cimex hemipterus)
総翅目(アザミウマ目)(Thysanoptera)−フランクリニエラ属種(Frankliniella spp.)、スリプス属種(Thrips spp.)、シルトスリプス・ドルサリス(Scirtothrips dorsalis)
等翅目(シロアリ目)(Isoptera)−レチクリテルメス・フラビペス(Reticulitermes flavipes)、コプトテルメス・フォルモサヌス(Coptotermes formosanus)、レチクリテルメス・ビルギニクス(Reticulitermes virginicus)、ヘテロテルメス・アウレウス(Heterotermes aureus)、レチクリテルメス・ヘスペルス(Reticulitermes hesperus)、コプトテルメス・フレンキイ(Coptotermes frenchii)、シェドリノテルメス属種(Shedorhinotermes spp.)、レチクリテルメス・サントネンシス(Reticulitermes santonensis)、レチクリテルメス・グラセイ(Reticulitermes grassei)、レチクリテルメス・バニュレンシス(Reticulitermes banyulensis)、レチクリテルメス・スペラツス(Reticulitermes speratus)、レチクリテルメス・ハゲニ(Reticulitermes hageni)、レチクリテルメス・チビアリス(Reticulitermes tibialis)、ゾオテルモプシス属種(Zootermopsis spp.)、インシシテルメス属種(Incisitermes spp.)、マルギニテルメス属種(Marginitermes spp.)、マクロテルメス属種(Macrotermes spp.)、ミクロセロテルメス属種(Microceroterm.es spp.)、ミクロテルメス属種(Microtermes spp.)
双翅目(ハエ目)(Diptera)−リリオミザ属種(Liriomyza spp.)、ムスカ・ドメスチカ(Musca domestica)、エデス属種(Aedes spp.)、クレクス属種(Culex spp.)、アノフェレス属種(Anopheles spp.)、ファニア属種(Fannia spp.)、ストモキシス属種(Stomoxys spp.)
膜翅目(Hymenoptera)−イリドミルメクス・フミリス(Iridomyrmex humilis)、ソレノプシス属種(Solenopsis spp.)、モノモリウム・ファラオニス(Monomorium pharaonis)、アッタ属種(Atta spp.)、ポゴノミルメクス属種(Pogonomyrmex spp.)、カムポノツス種(Camponotus spp.)、モノモリウム属種(Monomorium spp.)、タピノマ・セシル(Tapinoma sessile)、テトラモリウム属種(Tetramorium spp.)、キシロカパ属種(Xylocapa spp.)、ベスプラ属種(Vespula spp.)、ポリステス属種(Polistes spp.)
食毛目(Mallophaga)(ハジラミ)
裸尾目(Anoplura)(シラミ)−プシルス・ピュービス(Pthirus pubis)、ペジクルス属種(Pediculus spp.)
直翅目(Orthoptera)(イナゴ類(grasshoppers)、コオロギ)−メラノプルス属種(Melanoplus spp.)、ロクスタ・ミグラトリア(Locusta migratoria)、シストセルカ・グレガリア(Schistocerca gregaria)、グリロタルピダエ(Gryllotalpidae)(ケラ)
ゴキブリ亜目(Blattoidea)(ゴキブリ)−ブラッタ・オリエンタリス(Blatta orientalis)、ブラテラ・ゲルマニカ(Blattella germanica)、ペリプラネタ・アメリカナ(Periplaneta americana)、スペラ・ロンギパルパ(Supella longipalpa)、ペリプラネタ・アウストララシアエ(Periplaneta australasiae)、ペリプラネタ・ブルンネア(Periplaneta brunnea)、パルコブラッタ・ペンシルバニカ(Parcoblatta pennsylvanica)、ペリプラネタ・フリギノサ(Periplaneta fuliginosa)、ピクノセルス・スリナメンシス(Pycnoscelus surinamensis)
隠翅目(ノミ目)(Siphonaptera)−クテノファリデス属種(Ctenophalides spp.)、プレクス・イリタンス(Pulex irritans)
ダニ目(Acari)−テトラニクス属種(Tetranychus spp.)、パノニクス属種(Panonychus spp.)、エオテトラニクス・カルピニ(Eotetranychus carpini)、フィロコプトルタ・オレイボラ(Phyllocoptruta oleivora)、アクルス・ペレカッシ(Aculus pelekassi)、ブレビパルプス・ホエニシス(Brevipalpus phoenicis)、ブーフィルス属種(Boophilus spp.)、デルマセントル・バリアビリス(Dermacentor variabilis)、リピセファルス・サングイネウス(Rhipicephalus sanguineus)、アンブリオマ・アメリカヌム(Amblyomma americanum)、イキソデス属種(Ixodes spp.)、ノトエドレス・キャティ(Notoedres cati)、サルコプテス・スカビエイ(Sarcoptes scabiei)、デルマトファゴイデス属種(Dermatophagoides spp.)
線形動物門(Nematoda)−ジロフィラリア・イミチス(Dirofilaria immitis)、メロイドジン属種(Meloidogyne spp.)、ヘテロデラ属種(Heterodera spp.)、ホプロライムス・コルムブス(Hoplolaimus columbus)、ベロノライムス属種(Belonolaimus spp.)、プラチレンクス属種(Pratylenchus spp.)、ロチレンクス・レニホルミス(Rotylenchus reniformis)、クリコネメラ・オルナタ(Criconemella ornata)、ジチレンクス属種(Ditylenchus spp.)、アフェレンコイデス・ベッセイ(Aphelenchoides besseyi)、ヒルシュマニエラ属種(Hirschmanniella spp.)。
ロフェン、スピロメシフェンおよびスピロテトラマート;チオ尿素系殺虫剤、例えばジアフェンチウロン;尿素系殺虫剤、例えばフルコフロンおよびスルコフロン;および未分類殺虫剤、例えばAKD−3088、クロサンテル、クロタミトン、シフルメトフェン、E2Y45、EXD、フェナザフロル、フェナザキン、フェノキサクリム、フェンピロキシメート、FKI−1033、フルベンジアミド、HGW86、ヒドラメチルノン、IKI−2002、イソプロチオラン、マロノベン、メタフルミゾン、メトキサジアゾン、ニフルリジド、NNI−9850、NNI−0101、ピメトロジン、ピリダベン、ピリダリル、Qcide、ラホキサニド、リナキシピル、SYJ−159、トリアラテンおよびトリアザメート、ならびにそれらの任意の組合せ。
Claims (13)
- 以下の式:
(式中、
Xは、NO2、CNまたはCOOR4を表し;
R1は、(C1〜C4)アルキルを表し;
R2は、メチル、エチル、フルオロ、クロロまたはブロモを表し、R3は、水素を表し;
Yは、(C1〜C4)ハロアルキル、F、Cl、Br、またはIを表し;
R4は、(C1〜C3)アルキルを表す)
を有する化合物のジアステレオマーの第1の対およびジアステレオマーの第2の対を含む組成物を提供する工程;および
前記化合物の安定性を改善するためのジアステレオマー変換を行うのに有効な手法で前記組成物を加熱する工程を含む、方法。 - XがNO2またはCNを表し、Yが−CF3を表し、R2が、メチルまたはエチルを表す、請求項1に記載の方法。
- 前記組成物が、スピネトラム、スピノサドおよびそれらの混合物からなる群から選択されるスピノシンをさらに含む、請求項1に記載の方法。
- 前記加熱が、最低50℃で4から72時間行われる、請求項1に記載の方法。
- ジアステレオマーの第1の対およびジアステレオマーの第2の対で規定される{1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}(メチル)オキシド−λ4−スルファニリデンシアナミドの立体異性体混合物を含み、前記ジアステレオマーの第1の対が{(R)−1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}−(R)−(メチル)オキシド−λ4−スルファニリデンシアナミドおよび{(S)−1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}−(S)−(メチル)オキシド−λ4−スルファニリデンシアナミドであり、前記ジアステレオマーの第2の対が{(R)−1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}−(S)−(メチル)オキシド−λ4−スルファニリデンシアナミドおよび{(S)−1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}−(R)−(メチル)オキシド−λ4−スルファニリデンシアナミドであり、前記ジアステレオマーの第1の対:ジアステレオマーの第2の対の比が、少なくとも3:1である、組成物。
- 前記ジアステレオマーの第1の対:ジアステレオマーの第2の対の比が、3:1から100:1である、請求項5に記載の組成物。
- 前記ジアステレオマーの第1の対:ジアステレオマーの第2の対の比が、3:1から40:1である、請求項5に記載の組成物。
- スピネトラム、スピノサドおよびそれらの混合物からなる群から選択されるスピノシンをさらに含む、請求項5に記載の組成物。
- {1−[6−(トリフルオロメチル)ピリジン−3−イル]エチル}(メチル)オキシド−λ4−スルファニリデンシアナミド:前記スピノシンの重量での比が、3:1から1:3である、請求項8に記載の組成物。
- 以下の式:
(式中、
Xは、NO 2 、CNまたはCOOR 4 を表し;
R 1 は、(C 1 〜C 4 )アルキルを表し;
R 2 は、メチル、エチル、フルオロ、クロロまたはブロモを表し、R 3 は、水素を表し;
Yは、(C 1 〜C 4 )ハロアルキル、F、Cl、Br、またはIを表し;
R 4 は、(C 1 〜C 3 )アルキルを表す)
を有する化合物の組成物中の安定性を改善するのに有効な手法で前記組成物を加熱する工程を含む、方法。 - XがNO 2 またはCNであり、Yが−CF 3 であり、R 2 がメチルまたはエチルである、請求項10に記載の方法。
- 前記組成物が、スピネトラム、スピノサドおよびそれらの混合物からなる群から選択されるスピノシンをさらに含む、請求項10に記載の方法。
- 前記加熱が、最低50℃で4から72時間行われる、請求項10に記載の方法。
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Families Citing this family (107)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201309635A (zh) * | 2006-02-10 | 2013-03-01 | Dow Agrosciences Llc | 殺蟲性之n-取代(6-鹵烷基吡啶-3-基)烷基磺醯亞胺(二) |
JP5718249B2 (ja) | 2008-12-26 | 2015-05-13 | ダウ アグロサイエンシィズ エルエルシー | 安定な殺虫剤組成物およびその製造方法 |
CN104222135B (zh) * | 2008-12-26 | 2017-04-26 | 美国陶氏益农公司 | 稳定的亚磺酰亚胺杀虫剂组合物 |
CN102971315B (zh) | 2010-05-05 | 2015-07-22 | 拜耳知识产权有限责任公司 | 作为害虫防治剂的噻唑衍生物 |
KR101808079B1 (ko) | 2010-06-18 | 2018-01-18 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 살충 및 살비성을 지니는 활성 물질 배합물 |
ES2626601T3 (es) | 2010-06-28 | 2017-07-25 | Bayer Intellectual Property Gmbh | Compuestos heterocíclicos como pesticidas |
CN103079407A (zh) | 2010-06-29 | 2013-05-01 | 拜耳知识产权有限责任公司 | 改进的包含环羰基脒的杀虫组合物 |
WO2012004293A2 (de) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
JP2012017289A (ja) | 2010-07-08 | 2012-01-26 | Bayer Cropscience Ag | 殺虫性ピロリン誘導体 |
CN104086528A (zh) | 2010-07-15 | 2014-10-08 | 拜耳知识产权有限责任公司 | 作为杀虫剂的新杂环化合物 |
JP2012062267A (ja) | 2010-09-15 | 2012-03-29 | Bayer Cropscience Ag | 殺虫性ピロリンn−オキサイド誘導体 |
JP2012082186A (ja) | 2010-09-15 | 2012-04-26 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
WO2012045680A2 (de) | 2010-10-04 | 2012-04-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
US9084424B2 (en) | 2010-10-21 | 2015-07-21 | Bayer Intellectual Property Gmbh | N-benzyl heterocyclic carboxamides |
JP5953308B2 (ja) | 2010-10-22 | 2016-07-20 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 殺害虫剤としての新規ヘテロ環式化合物 |
BR112013010683B1 (pt) | 2010-11-02 | 2018-06-26 | Bayer Intellectual Property Gmbh | Composto, composição fungicida e método para controlar fungos fitopatogênicos de safras |
MX2013005258A (es) | 2010-11-15 | 2013-07-05 | Bayer Ip Gmbh | N-aril pirazol(tio)carboxamidas. |
KR20130121904A (ko) | 2010-11-29 | 2013-11-06 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 알파,베타-불포화 이민 |
KR20180096815A (ko) | 2010-12-01 | 2018-08-29 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 작물에서 선충류를 구제하고 수확량을 증가시키기 위한 플루오피람의 용도 |
US20130317067A1 (en) | 2010-12-09 | 2013-11-28 | Bayer Intellectual Property Gmbh | Pesticidal mixtures with improved properties |
WO2012076471A1 (en) | 2010-12-09 | 2012-06-14 | Bayer Cropscience Ag | Insecticidal mixtures with improved properties |
TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種syht0h2及偵測其之組合物及方法 |
BR112013021019A2 (pt) | 2011-02-17 | 2019-02-26 | Bayer Ip Gmbh | uso de fungicidas sdhi em variedades de soja cultivadas de forma convencional com tolerância à ferrugem asiática da soja (asr), resistentes ao cancro da haste e/ou à mancha foliar olho-de-rã |
CN103492367B (zh) | 2011-02-17 | 2015-04-01 | 拜耳知识产权有限责任公司 | 用于治疗的取代的3-(联苯-3-基)-8,8-二氟-4-羟基-1-氮杂螺[4.5]癸-3-烯-2-酮 |
CA2827304C (en) | 2011-02-17 | 2018-11-13 | Bayer Intellectual Property Gmbh | Use of sdhi fungicides on conventionally bred asr-tolerant, stem canker resistant and/or frog-eye leaf spot resistant soybean varieties |
WO2012116960A1 (de) | 2011-03-01 | 2012-09-07 | Bayer Cropscience Ag | 2-acyloxy-pyrrolin-4-one |
AR085509A1 (es) | 2011-03-09 | 2013-10-09 | Bayer Cropscience Ag | Indol- y bencimidazolcarboxamidas como insecticidas y acaricidas |
WO2012120105A1 (en) | 2011-03-10 | 2012-09-13 | Bayer Cropscience Ag | Use of lipochito-oligosaccharide compounds for safeguarding seed safety of treated seeds |
MX350121B (es) | 2011-03-18 | 2017-08-28 | Bayer Ip Gmbh | Derivados de n-(3-carbamoilfenil)-1h-pirazol-5-carboxamida y el uso de los mismos para el control de plagas de animales. |
UA113851C2 (xx) * | 2011-06-07 | 2017-03-27 | Масляна дисперсія сульфоксімінів для боротьби з комахами | |
EP2535334A1 (de) | 2011-06-17 | 2012-12-19 | Bayer CropScience AG | Kristalline Modifikationen von Penflufen |
EP2540163A1 (en) | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematocide N-cyclopropyl-sulfonylamide derivatives |
AU2012288947B2 (en) | 2011-07-26 | 2016-03-31 | Clariant International Ltd | Etherified lactate esters, method for the production thereof and use thereof for enhancing the effect of plant protecting agents |
WO2013014227A1 (en) | 2011-07-27 | 2013-01-31 | Bayer Intellectual Property Gmbh | Seed dressing for controlling phytopathogenic fungi |
JP2013082632A (ja) | 2011-10-05 | 2013-05-09 | Bayer Cropscience Ag | 農薬製剤及びその製造方法 |
EP2604118A1 (en) | 2011-12-15 | 2013-06-19 | Bayer CropScience AG | Active ingredient combinations having insecticidal and acaricidal properties |
BR112014015002A2 (pt) | 2011-12-19 | 2017-06-13 | Bayer Cropscience Ag | uso de derivados de diamida de ácido antranílico para o controle de pragas em culturas transgênicas |
US9204645B2 (en) | 2011-12-20 | 2015-12-08 | Bayer Intellectual Property Gmbh | Insecticidal aromatic amides |
EP2606726A1 (de) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | N-Arylamidine-substituierte trifluoroethylsulfid-Derivate als Akarizide und Insektizide |
KR102243170B1 (ko) | 2012-01-21 | 2021-04-22 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 유용한 식물에서 박테리아성 유해 유기체를 방제하기 위한 숙주 방어 유도물질의 용도 |
TW201400452A (zh) | 2012-03-14 | 2014-01-01 | 拜耳智慧財產有限公司 | 除害之芳基吡咯啶類 |
IN2014DN09841A (ja) | 2012-05-16 | 2015-08-07 | Bayer Cropscience Ag | |
WO2013171201A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide öl-in-wasser (o/w) formulierung |
AR091104A1 (es) | 2012-05-22 | 2015-01-14 | Bayer Cropscience Ag | Combinaciones de compuestos activos que comprenden un derivado lipo-quitooligosacarido y un compuesto nematicida, insecticida o fungicida |
AR091202A1 (es) | 2012-05-30 | 2015-01-21 | Bayer Cropscience Ag | Composicion que comprende un agente de control biologico y un insecticida |
CN104540494B (zh) | 2012-05-30 | 2017-10-24 | 科莱恩金融(Bvi)有限公司 | N‑甲基‑n‑酰基葡糖胺作为增溶剂的用途 |
WO2013178662A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
WO2013178679A2 (de) | 2012-05-30 | 2013-12-05 | Clariant International Ltd. | N-methyl-n-acylglucamin enthaltende zusammensetzung |
BR112014030701A2 (pt) | 2012-06-08 | 2017-06-27 | Bayer Cropscience Ag | sistema de detecção para a identificação de resistência a inseticidas. |
NZ702435A (en) * | 2012-06-30 | 2016-07-29 | Dow Agrosciences Llc | Insecticidal n-substituted sulfilimine and sulfoximine pyridine n-oxides |
WO2014004094A1 (en) * | 2012-06-30 | 2014-01-03 | Dow Agrosciences Llc | Production of n-substituted sulfoximine pyridine n-oxides |
CN104602527B (zh) * | 2012-06-30 | 2018-09-25 | 美国陶氏益农公司 | 吡啶n-氧化物及其制备方法 |
KR20150040280A (ko) | 2012-07-31 | 2015-04-14 | 바이엘 크롭사이언스 아게 | 살충 테르펜 혼합물 및 살곤충제를 포함하는 조성물 |
US9345247B2 (en) | 2012-08-17 | 2016-05-24 | Bayer Cropscience Ag | Azaindole carboxylic acid amides and azaindole thiocarboxylic acid amides for use as insecticides and acaricides |
AU2013326600B2 (en) | 2012-10-02 | 2017-03-30 | Bayer Cropscience Ag | Heterocyclic compounds as pesticides |
WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
CN104884449A (zh) | 2012-10-31 | 2015-09-02 | 拜尔农作物科学股份公司 | 作为害虫防治剂的新的杂环化合物 |
DE102012021647A1 (de) | 2012-11-03 | 2014-05-08 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzungen |
UA117816C2 (uk) | 2012-11-06 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидна комбінація для толерантних соєвих культур |
EA201500580A1 (ru) | 2012-11-30 | 2016-01-29 | Байер Кропсайенс Акциенгезельшафт | Двойные фунгицидные смеси |
CN104837351A (zh) | 2012-11-30 | 2015-08-12 | 拜耳作物科学股份公司 | 二元杀真菌或杀虫混合物 |
US9730455B2 (en) | 2012-12-03 | 2017-08-15 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
CA2893027A1 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
WO2014086750A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086753A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
US9867377B2 (en) | 2012-12-03 | 2018-01-16 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014090765A1 (en) | 2012-12-12 | 2014-06-19 | Bayer Cropscience Ag | Use of 1-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]-5-amino-3-trifluoromethyl)-1 h-1,2,4 tfia zole for controlling nematodes in nematode-resistant crops |
AR093996A1 (es) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | Combinaciones bactericidas y fungicidas binarias |
AU2014214140B2 (en) | 2013-02-06 | 2017-08-31 | Vetoquinol Sa | Halogen-substituted pyrazol derivatives as pest-control agents |
BR112015018419A2 (pt) | 2013-02-11 | 2017-07-18 | Bayer Cropscience Lp | composições compreendendo um agente de controle biológico à base de streptomyces e um outro agente de controle biológico |
CA2898725A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising a streptomyces-based biological control agent and an insecticide |
BR112015021342A2 (pt) | 2013-03-12 | 2017-07-18 | Bayer Cropscience Ag | uso de ditiina-tetracarboximidas para controle de microrganismos bacterianos nocivos em plantas úteis |
EP2986117A1 (en) | 2013-04-19 | 2016-02-24 | Bayer CropScience Aktiengesellschaft | Binary insecticidal or pesticidal mixture |
EP2986121A1 (en) | 2013-04-19 | 2016-02-24 | Bayer CropScience Aktiengesellschaft | Active compound combinations having insecticidal properties |
CN103333101B (zh) * | 2013-06-08 | 2015-06-17 | 北京格林凯默科技有限公司 | 吡啶基亚磺酰亚胺化合物及其制备方法 |
CN103333102B (zh) * | 2013-06-08 | 2015-06-17 | 北京格林凯默科技有限公司 | 吡啶基-n-氰基磺基肟化合物及其制备方法 |
WO2014202510A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
EP3010889B1 (de) | 2013-06-20 | 2018-10-03 | Bayer CropScience Aktiengesellschaft | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
JP6423873B2 (ja) | 2013-07-08 | 2018-11-14 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての6員c−n−結合アリールスルフィド誘導体及びアリールスルホキシド誘導体 |
DE202014008415U1 (de) | 2014-02-19 | 2014-11-25 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzung zur Wirkungssteigerung von Elektrolyt-Wirkstoffen |
DE202014008418U1 (de) | 2014-02-19 | 2014-11-14 | Clariant International Ltd. | Schaumarme agrochemische Zusammensetzungen |
WO2015160618A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and a biological control agent |
WO2015160620A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and an insecticide |
DE102014005771A1 (de) | 2014-04-23 | 2015-10-29 | Clariant International Ltd. | Verwendung von wässrigen driftreduzierenden Zusammensetzungen |
WO2016001129A1 (de) | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Verbesserte insektizide zusammensetzungen |
DE102014012022A1 (de) | 2014-08-13 | 2016-02-18 | Clariant International Ltd. | Organische Ammoniumsalze von anionischen Pestiziden |
DE102014018274A1 (de) | 2014-12-12 | 2015-07-30 | Clariant International Ltd. | Zuckertenside und deren Verwendung in agrochemischen Zusammensetzungen |
AU2015367344A1 (en) | 2014-12-19 | 2017-07-13 | Clariant International Ltd | Aqueous electrolyte-containing adjuvant compositions, active ingredient-containing compositions and the use thereof |
EP3240423B1 (en) | 2014-12-22 | 2020-10-21 | Bayer CropScience LP | Method for using a bacillus subtilis or bacillus pumilus strain to treat or prevent pineapple disease |
GB2536650A (en) | 2015-03-24 | 2016-09-28 | Augmedics Ltd | Method and system for combining video-based and optic-based augmented reality in a near eye display |
TW201639453A (zh) * | 2015-03-31 | 2016-11-16 | 陶氏農業科學公司 | 殺蟲組成物及相關方法(一) |
DE102015219608B4 (de) | 2015-10-09 | 2018-05-03 | Clariant International Ltd | Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen |
DE102015219651A1 (de) | 2015-10-09 | 2017-04-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Zuckeramin und Fettsäure |
CN105503672A (zh) * | 2015-12-06 | 2016-04-20 | 杨秀娟 | 一种药物中间体芳基砜类化合物的合成方法 |
MX2018012994A (es) | 2016-04-24 | 2019-01-28 | Bayer Cropscience Ag | Uso de fluopiram y/o de bacillus subtilis para controlar el marchitamiento por fusarium en plantas de la familia musaceae. |
DE102016207877A1 (de) | 2016-05-09 | 2017-11-09 | Clariant International Ltd | Stabilisatoren für Silikatfarben |
WO2018005756A1 (en) | 2016-07-01 | 2018-01-04 | Mclaughlin Gormley King Company | Mixtures of sabadilla alkaloids and bacillus thuringiensis and uses thereof |
EP3490379A1 (en) | 2016-07-29 | 2019-06-05 | Bayer CropScience Aktiengesellschaft | Active compound combinations and methods to protect the propagation material of plants |
CN107254920B (zh) * | 2016-11-11 | 2019-11-01 | 新沂市金达木业有限公司 | 一种能够预防蛀虫的室内装饰用防火板的制备方法 |
US10925286B2 (en) * | 2017-03-17 | 2021-02-23 | Telluris Biotech India Private Limited | Synergistic chalcone containing composition of a nematicide |
WO2019211741A1 (en) | 2018-05-02 | 2019-11-07 | Augmedics Ltd. | Registration of a fiducial marker for an augmented reality system |
US11766296B2 (en) | 2018-11-26 | 2023-09-26 | Augmedics Ltd. | Tracking system for image-guided surgery |
US11980506B2 (en) | 2019-07-29 | 2024-05-14 | Augmedics Ltd. | Fiducial marker |
US11382712B2 (en) | 2019-12-22 | 2022-07-12 | Augmedics Ltd. | Mirroring in image guided surgery |
US11896445B2 (en) | 2021-07-07 | 2024-02-13 | Augmedics Ltd. | Iliac pin and adapter |
WO2024057210A1 (en) | 2022-09-13 | 2024-03-21 | Augmedics Ltd. | Augmented reality eyewear for image-guided medical intervention |
CN115466208B (zh) * | 2022-11-01 | 2024-05-14 | 安徽宁亿泰科技有限公司 | 提纯螺虫乙酯顺式中间体的方法 |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050038501A1 (en) * | 2003-08-12 | 2005-02-17 | Moore James E. | Dynamic stent |
UY28506A1 (es) | 2003-09-12 | 2005-04-29 | Basf Ag | 6-halógeno-(1,2,4)triazolo(1,5-a)pirimidinas para combatir plagas animales. |
AU2005310314B2 (en) * | 2004-04-08 | 2011-07-21 | Corteva Agriscience Llc | Insecticidal N-substituted sulfoximines |
TW200626532A (en) | 2004-09-21 | 2006-08-01 | Syngenta Participations Ag | Novel insecticides |
TW201309635A (zh) * | 2006-02-10 | 2013-03-01 | Dow Agrosciences Llc | 殺蟲性之n-取代(6-鹵烷基吡啶-3-基)烷基磺醯亞胺(二) |
TWI381811B (zh) * | 2006-06-23 | 2013-01-11 | Dow Agrosciences Llc | 用以防治可抵抗一般殺蟲劑之昆蟲的方法 |
TWI383973B (zh) * | 2006-08-07 | 2013-02-01 | Dow Agrosciences Llc | 用於製備2-取代-5-(1-烷硫基)烷基吡啶之方法 |
TWI387585B (zh) * | 2006-09-01 | 2013-03-01 | Dow Agrosciences Llc | 殺蟲性之n-取代(雜芳基)烷基烴基硫亞胺 |
TWI409256B (zh) * | 2006-09-01 | 2013-09-21 | Dow Agrosciences Llc | 殺蟲性之n-取代(雜芳基)環烷基磺醯亞胺 |
TWI395737B (zh) * | 2006-11-08 | 2013-05-11 | Dow Agrosciences Llc | 作為殺蟲劑之雜芳基(取代的)烷基n-取代的磺醯亞胺 |
TWI383970B (zh) * | 2006-11-08 | 2013-02-01 | Dow Agrosciences Llc | 多取代的吡啶基磺醯亞胺及其作為殺蟲劑之用途 |
TW200820902A (en) * | 2006-11-08 | 2008-05-16 | Dow Agrosciences Llc | Use of N-substituted sulfoximines for control of invertebrate pests |
EP2364971B1 (en) * | 2006-11-30 | 2014-04-30 | Dow AgroSciences LLC | 2,5-Disubstituted pyridines for the preparation of 2-substituted 5-(1-alkylthio)-alkylpyridines |
US7709648B2 (en) * | 2007-02-09 | 2010-05-04 | Dow Agrosciences Llc | Process for the preparation of 2-substituted-5-(1-alkylthio)alkylpyridines |
US7511149B2 (en) * | 2007-02-09 | 2009-03-31 | Dow Agrosciences Llc | Process for the oxidation of certain substituted sulfilimines to insecticidal sulfoximines |
CA2678028C (en) | 2007-02-26 | 2015-02-03 | Dow Agrosciences Llc | Process for the preparation of certain substituted sulfilimines |
JP5511393B2 (ja) | 2007-03-01 | 2014-06-04 | ビーエーエスエフ ソシエタス・ヨーロピア | アミノチアゾリン化合物を含む殺有害生物活性混合物 |
AR066366A1 (es) * | 2007-05-01 | 2009-08-12 | Dow Agrosciences Llc | Mezclas sinergicas plaguicidas |
US7844777B2 (en) * | 2007-06-26 | 2010-11-30 | Intel Corporation | Cache for a host controller to store command header information |
US20090006676A1 (en) * | 2007-06-29 | 2009-01-01 | Intel Corporation | Method for Scheduling a Device Notification Time Slot for a Wireless USB System |
BRPI0816422A2 (pt) | 2007-09-04 | 2017-05-16 | Segetis Inc | compostos de cetal a partir de polióis e oxocarboxilatos. |
ES2554768T3 (es) | 2007-11-16 | 2015-12-23 | Basf Se | Mezclas de pesticidas que comprenden compuestos cianosulfoximina |
TWM332793U (en) * | 2007-11-28 | 2008-05-21 | Cooler Master Co Ltd | Heat radiating structure and the lighting apparatus |
MX2009011860A (es) * | 2008-05-01 | 2009-12-18 | Dow Agrosciences Llc | Mezclas pesticidas sinergicas. |
CN104604922B (zh) * | 2008-05-07 | 2016-05-11 | 拜耳作物科学股份公司 | 活性化合物组合及其组合物、防治动物害虫的方法 |
US20110160054A1 (en) * | 2008-08-28 | 2011-06-30 | Basf Se | Pesticidal Mixtures Comprising Cyanosulfoximine Compounds and Spinetoram |
JP5718249B2 (ja) | 2008-12-26 | 2015-05-13 | ダウ アグロサイエンシィズ エルエルシー | 安定な殺虫剤組成物およびその製造方法 |
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