TW201234969A - Active compound combinations - Google Patents
Active compound combinations Download PDFInfo
- Publication number
- TW201234969A TW201234969A TW101113696A TW101113696A TW201234969A TW 201234969 A TW201234969 A TW 201234969A TW 101113696 A TW101113696 A TW 101113696A TW 101113696 A TW101113696 A TW 101113696A TW 201234969 A TW201234969 A TW 201234969A
- Authority
- TW
- Taiwan
- Prior art keywords
- active compound
- phenyl
- following formula
- plants
- plant
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 160
- 241000196324 Embryophyta Species 0.000 claims abstract description 137
- 239000000203 mixture Substances 0.000 claims abstract description 118
- 241000233866 Fungi Species 0.000 claims abstract description 20
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 18
- 239000004009 herbicide Substances 0.000 claims abstract description 17
- 244000068988 Glycine max Species 0.000 claims abstract description 16
- 230000009261 transgenic effect Effects 0.000 claims abstract description 14
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000003032 phytopathogenic effect Effects 0.000 claims abstract description 11
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims abstract description 7
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000005561 Glufosinate Substances 0.000 claims abstract description 6
- 239000005562 Glyphosate Substances 0.000 claims abstract description 6
- 229940097068 glyphosate Drugs 0.000 claims abstract description 6
- 239000007787 solid Substances 0.000 claims description 21
- 238000011282 treatment Methods 0.000 claims description 21
- 244000025254 Cannabis sativa Species 0.000 claims description 18
- 108090000623 proteins and genes Proteins 0.000 claims description 15
- 230000000855 fungicidal effect Effects 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 11
- 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 claims description 8
- 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 claims description 7
- 239000005785 Fluquinconazole Substances 0.000 claims description 7
- 239000005839 Tebuconazole Substances 0.000 claims description 7
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 7
- 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 claims description 6
- 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 claims description 6
- 239000005846 Triadimenol Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 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 claims description 6
- 239000005944 Chlorpyrifos Substances 0.000 claims description 5
- 239000005825 Prothioconazole Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims description 4
- 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 claims description 4
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 239000005757 Cyproconazole Substances 0.000 claims description 4
- 239000005767 Epoxiconazole Substances 0.000 claims description 4
- 239000005813 Penconazole Substances 0.000 claims description 4
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 claims description 4
- 229950000294 azaconazole Drugs 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 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 claims description 3
- 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 claims description 3
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 3
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 3
- OVFHHJZHXHZIHT-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)quinazolin-4-one Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C2=CC=CC=C2N=C1N1N=CN=C1 OVFHHJZHXHZIHT-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- 239000005741 Bromuconazole Substances 0.000 claims description 3
- 239000005775 Fenbuconazole Substances 0.000 claims description 3
- 239000005787 Flutriafol Substances 0.000 claims description 3
- 239000005796 Ipconazole Substances 0.000 claims description 3
- 239000005822 Propiconazole Substances 0.000 claims description 3
- 239000005840 Tetraconazole Substances 0.000 claims description 3
- 239000005859 Triticonazole Substances 0.000 claims description 3
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 3
- DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 claims description 3
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 3
- 150000003852 triazoles Chemical class 0.000 claims description 3
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 claims description 2
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 claims description 2
- 239000005727 Amisulbrom Substances 0.000 claims description 2
- 206010010144 Completed suicide Diseases 0.000 claims description 2
- 239000005868 Metconazole Substances 0.000 claims description 2
- 239000005811 Myclobutanil Substances 0.000 claims description 2
- 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 claims description 2
- 238000013329 compounding Methods 0.000 claims description 2
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims 2
- 241000254032 Acrididae Species 0.000 claims 1
- 101710136180 Galaxin Proteins 0.000 claims 1
- 240000001140 Mimosa pudica Species 0.000 claims 1
- 235000016462 Mimosa pudica Nutrition 0.000 claims 1
- 241000282320 Panthera leo Species 0.000 claims 1
- 238000004611 spectroscopical analysis Methods 0.000 claims 1
- 229960005322 streptomycin Drugs 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 abstract description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 99
- -1 1,3,3-trimethylbutyl Chemical group 0.000 description 71
- 238000009472 formulation Methods 0.000 description 48
- 239000003995 emulsifying agent Substances 0.000 description 39
- 239000002904 solvent Substances 0.000 description 39
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 34
- 238000012360 testing method Methods 0.000 description 34
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 32
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
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- 230000000694 effects Effects 0.000 description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
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- 229920000151 polyglycol Polymers 0.000 description 17
- 239000010695 polyglycol Substances 0.000 description 17
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 16
- 125000002877 alkyl aryl group Chemical group 0.000 description 16
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- 150000001412 amines Chemical class 0.000 description 13
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- IVHVNMLJNASKHW-UHFFFAOYSA-M Chlorphonium chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CC1=CC=C(Cl)C=C1Cl IVHVNMLJNASKHW-UHFFFAOYSA-M 0.000 description 9
- 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 9
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 8
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- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 8
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 7
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- 239000007900 aqueous suspension Substances 0.000 description 7
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 7
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 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 6
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- 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 6
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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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- 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)
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| DE200510026482 DE102005026482A1 (de) | 2005-06-09 | 2005-06-09 | Wirkstoffkombinationen |
| DE200510026483 DE102005026483A1 (de) | 2005-06-09 | 2005-06-09 | Wirkstoffkombinationen |
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| TW201234969A true TW201234969A (en) | 2012-09-01 |
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| TW095120327A TWI369950B (en) | 2005-06-09 | 2006-06-08 | Active compound combinations |
| TW101113697A TW201234970A (en) | 2005-06-09 | 2006-06-08 | Active compound combinations |
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| TW101113697A TW201234970A (en) | 2005-06-09 | 2006-06-08 | Active compound combinations |
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| AR (1) | AR054281A1 (enExample) |
| AT (1) | ATE484194T1 (enExample) |
| BR (1) | BRPI0612022B1 (enExample) |
| CA (2) | CA2916460C (enExample) |
| DE (1) | DE502006008090D1 (enExample) |
| EA (3) | EA017853B1 (enExample) |
| MX (2) | MX2007015376A (enExample) |
| PL (1) | PL1893024T3 (enExample) |
| TW (3) | TW201234969A (enExample) |
| WO (1) | WO2006131230A2 (enExample) |
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| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| WO2005102057A2 (en) | 2004-03-30 | 2005-11-03 | Monsanto Technology Llc | Methods for controlling plant pathogens using n-phosphonomethylglycine |
| PT1885176T (pt) | 2005-05-27 | 2016-11-28 | Monsanto Technology Llc | Evento mon89788 de soja e métodos para a sua deteção |
| EP2255650A3 (de) | 2005-06-09 | 2011-04-27 | Bayer CropScience AG | Wirkstoffkombinationen |
| AU2006278210B2 (en) * | 2005-08-09 | 2012-04-26 | Syngenta Participations Ag | Method for controlling phytopathogenic organisms |
| WO2007071656A1 (de) * | 2005-12-20 | 2007-06-28 | Basf Aktiengesellschaft | Verfahren zur bekämpfung des rostbefalls bei leguminosen |
| EP1922927A1 (en) * | 2006-10-26 | 2008-05-21 | Syngeta Participations AG | A method for controlling soybean rust |
| BRPI0808447A2 (pt) * | 2007-03-20 | 2014-08-12 | Basf Se | Método para proteger plantas de soja de serem infectadas por fungos prejudiciais, composição fungicida, agente fungicida, semente, e, uso de uma composição. |
| BRPI0809045A2 (pt) * | 2007-03-23 | 2014-09-02 | Basf Se | Combinações de substância ativa, uso de combinações de substância ativa, métodos para combater fungos fitopatogênicos indesejáveis, para preparar agentes pesticidas, e para tratar sementes, e, produto de revestimento de semente |
| AU2008263925A1 (en) * | 2007-06-12 | 2008-12-18 | Basf Se | Use of fungicides for making the phenological development of oil plants more coherent |
| CN103250712A (zh) | 2008-07-04 | 2013-08-21 | 巴斯夫欧洲公司 | 包含取代的1-甲基吡唑-4-基甲酰苯胺的杀真菌混合物 |
| TWI526535B (zh) * | 2008-09-12 | 2016-03-21 | 住友化學股份有限公司 | 噻唑菌胺對於基因轉殖植物在植物病害之防治方法的用途 |
| EP2239331A1 (en) * | 2009-04-07 | 2010-10-13 | Bayer CropScience AG | Method for improved utilization of the production potential of transgenic plants |
| WO2010135324A1 (en) | 2009-05-18 | 2010-11-25 | Monsanto Technology Llc | Use of glyphosate for disease suppression and yield enhancement in soybean |
| JP5642786B2 (ja) * | 2009-07-16 | 2014-12-17 | バイエル・クロップサイエンス・アーゲーＢａｙｅｒ Ｃｒｏｐｓｃｉｅｎｃｅ Ａｇ | フェニルトリアゾール類を含む相乗的活性化合物組み合わせ |
| CN101697727B (zh) * | 2009-10-28 | 2013-02-06 | 陕西上格之路生物科学有限公司 | 一种含环丙唑醇的农用杀菌组合物 |
| CN105394046B (zh) | 2010-10-25 | 2019-03-01 | 范德比尔特大学 | 用于抑制昆虫宿主感觉的组合物 |
| BR112013012082A2 (pt) * | 2010-11-15 | 2016-07-19 | Bayer Ip Gmbh | 5-halogenopirazolcarboxamidas |
| BR112013012080A2 (pt) * | 2010-11-15 | 2016-07-19 | Bayer Ip Gmbh | n-aril pirazol (tio) carboxamidas |
| JP5511093B2 (ja) * | 2010-12-22 | 2014-06-04 | ダウ グローバル テクノロジーズ エルエルシー | グリホサート化合物とｔｂｚとの相乗的組み合わせ |
| WO2012154403A2 (en) | 2011-05-06 | 2012-11-15 | Vanderbilt University | Composition for inhibition of insect sensing |
| EP2524600A1 (en) * | 2011-05-17 | 2012-11-21 | Bayer CropScience AG | Active compound combinations comprising phosphorous acid or a derivative thereof and Tebuconazole or Myclobutanil |
| US9801374B2 (en) | 2012-10-19 | 2017-10-31 | Bayer Cropscience Ag | Active compound combinations comprising carboxamide derivatives |
| CN103081924A (zh) * | 2013-02-27 | 2013-05-08 | 海利尔药业集团股份有限公司 | 一种含有烯肟菌胺与噻酰菌胺的杀菌组合物 |
| CN103271049A (zh) * | 2013-04-27 | 2013-09-04 | 广东中迅农科股份有限公司 | 吡唑醚菌酯和氟啶胺农药组合物 |
| UA126917C2 (uk) * | 2013-11-26 | 2023-02-22 | Юпл Лімітед | Фунгіцидна композиція |
| CA2843032A1 (en) * | 2014-02-19 | 2015-08-19 | Yangdou Wei | Use of glyphosate to control clubroot disease |
| AU2016238305B2 (en) | 2015-03-25 | 2020-10-08 | Vanderbilt University | Binary compositions as disruptors of ORco-mediated odorant sensing |
| EP3162208A1 (en) | 2015-10-29 | 2017-05-03 | Helm AG | Fungicidal composition for controlling fungal infections in the soybean plant |
| RU2623264C1 (ru) * | 2016-07-07 | 2017-06-23 | Михаил Михайлович Акулин | Инсектофунгицидная пиротехническая композиция |
| EA201991994A1 (ru) | 2017-03-07 | 2020-01-30 | Юпл Лтд | Фунгицидные комбинации |
| JP2021176818A (ja) * | 2018-07-31 | 2021-11-11 | 住友化学株式会社 | Ｑｏ阻害剤に対して耐性を有するダイズさび病菌の防除方法 |
| CN109769831A (zh) * | 2019-01-28 | 2019-05-21 | 刘丽丽 | 一种环保低残留的农药及其制备方法 |
| US11937601B2 (en) * | 2020-08-13 | 2024-03-26 | Globachem Nv | Method for treatment of soybean rust |
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| CA500788A (en) | 1948-05-18 | 1954-03-16 | R. Kittleson Allen | Preparation of n-trichloromethylthioimides |
| DE1081446B (de) | 1955-09-20 | 1960-05-12 | Montedison Spa | Verfahren zur Herstellung von kristallinem Zinkaethylen-bisdithiocarbamat |
| NL230587A (enExample) | 1957-08-17 | |||
| US3010968A (en) | 1959-11-25 | 1961-11-28 | Du Pont | Process for manufacture of certain alkyl esters of benzimidazole carbamic acids |
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| NL157191C (nl) | 1966-12-17 | Schering Ag | Werkwijze voor het bereiden van een preparaat met fungicide en fungistatische werking. | |
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| UA85690C2 (ru) * | 2003-11-07 | 2009-02-25 | Басф Акциенгезелльшафт | Смесь для применения в сельском хозяйстве, содержащая стробилурин и модулятор этилена, способ обработки и борьбы с инфекциями в бобовых культурах |
| EP1570736A1 (en) * | 2004-03-05 | 2005-09-07 | Bayer CropScience S.A. | Fungicide composition comprising an arylamidine derivative and known fungicide compounds |
| WO2005102057A2 (en) * | 2004-03-30 | 2005-11-03 | Monsanto Technology Llc | Methods for controlling plant pathogens using n-phosphonomethylglycine |
| BRPI0512118A (pt) | 2004-06-18 | 2008-02-06 | Basf Ag | composto, processo para combater fungos nocivos, e, agente fungicida |
| DE502005009089D1 (de) | 2004-06-18 | 2010-04-08 | Basf Se | 1-methyl-3-trifluormethyl-pyrazol-4-carbonsäure-(ortho-phenyl)-anilide und ihre verwendung als fungizid |
| DE102004037506A1 (de) * | 2004-08-03 | 2006-02-23 | Bayer Cropscience Ag | Methode zur Verbesserung der Pflanzenverträglichkeit gegenüber Glyphosate |
| GB0418047D0 (en) | 2004-08-12 | 2004-09-15 | Syngenta Participations Ag | Fungicidal compositions |
| PT1885176T (pt) * | 2005-05-27 | 2016-11-28 | Monsanto Technology Llc | Evento mon89788 de soja e métodos para a sua deteção |
| EP2255650A3 (de) | 2005-06-09 | 2011-04-27 | Bayer CropScience AG | Wirkstoffkombinationen |
| EP2064952A1 (en) * | 2007-11-29 | 2009-06-03 | Bayer CropScience AG | Method for reducing mycotoxin contamination in maize |
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2006
- 2006-05-27 EP EP10169127A patent/EP2255650A3/de not_active Withdrawn
- 2006-05-27 EA EA201001074A patent/EA017853B1/ru not_active IP Right Cessation
- 2006-05-27 KR KR1020087000482A patent/KR20080018943A/ko not_active Ceased
- 2006-05-27 JP JP2008515094A patent/JP5101496B2/ja not_active Expired - Fee Related
- 2006-05-27 WO PCT/EP2006/005094 patent/WO2006131230A2/de not_active Ceased
- 2006-05-27 CA CA2916460A patent/CA2916460C/en active Active
- 2006-05-27 PL PL06791516T patent/PL1893024T3/pl unknown
- 2006-05-27 US US11/921,667 patent/US8754009B2/en active Active
- 2006-05-27 CA CA2611178A patent/CA2611178C/en active Active
- 2006-05-27 AT AT06791516T patent/ATE484194T1/de active
- 2006-05-27 EP EP10169123A patent/EP2255648A3/de not_active Withdrawn
- 2006-05-27 MX MX2007015376A patent/MX2007015376A/es active IP Right Grant
- 2006-05-27 CN CN201410335143.8A patent/CN104170838B/zh not_active Expired - Fee Related
- 2006-05-27 BR BRPI0612022A patent/BRPI0612022B1/pt not_active IP Right Cessation
- 2006-05-27 EP EP06791516A patent/EP1893024B1/de not_active Not-in-force
- 2006-05-27 EA EA201270781A patent/EA201270781A1/ru unknown
- 2006-05-27 EP EP10169126A patent/EP2255649B1/de not_active Not-in-force
- 2006-05-27 EP EP10169114A patent/EP2255645A3/de not_active Withdrawn
- 2006-05-27 DE DE502006008090T patent/DE502006008090D1/de active Active
- 2006-05-27 EA EA200702661A patent/EA014410B1/ru not_active IP Right Cessation
- 2006-06-05 AR AR20060102338A patent/AR054281A1/es active IP Right Grant
- 2006-06-08 TW TW101113696A patent/TW201234969A/zh unknown
- 2006-06-08 TW TW095120327A patent/TWI369950B/zh not_active IP Right Cessation
- 2006-06-08 TW TW101113697A patent/TW201234970A/zh unknown
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2007
- 2007-12-05 MX MX2013012756A patent/MX336614B/es unknown
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2012
- 2012-02-21 JP JP2012035302A patent/JP2012140441A/ja not_active Withdrawn
- 2012-08-08 JP JP2012175670A patent/JP2013006844A/ja not_active Withdrawn
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2014
- 2014-03-28 US US14/229,174 patent/US9414600B2/en active Active
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