DE102004021564A1 - Wirkstoffkombinationen mit insektiziden Eigenschaften - Google Patents
Wirkstoffkombinationen mit insektiziden Eigenschaften Download PDFInfo
- Publication number
- DE102004021564A1 DE102004021564A1 DE102004021564A DE102004021564A DE102004021564A1 DE 102004021564 A1 DE102004021564 A1 DE 102004021564A1 DE 102004021564 A DE102004021564 A DE 102004021564A DE 102004021564 A DE102004021564 A DE 102004021564A DE 102004021564 A1 DE102004021564 A1 DE 102004021564A1
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- Germany
- Prior art keywords
- alkyl
- independently
- haloalkyl
- halogen
- haloalkoxy
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 241001465754 Metazoa Species 0.000 title claims abstract description 15
- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 15
- 239000002728 pyrethroid Substances 0.000 title claims abstract description 13
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 title abstract 3
- 239000011885 synergistic combination Substances 0.000 title abstract 3
- -1 Nitro, Hydroxy Chemical group 0.000 claims abstract description 60
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 47
- 150000002367 halogens Chemical class 0.000 claims abstract description 47
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 32
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims abstract description 31
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 26
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 24
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims abstract description 23
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract description 19
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 19
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 18
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims abstract description 17
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 16
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 14
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 11
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims abstract description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 6
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims abstract description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 4
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims abstract description 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims abstract description 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims abstract description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 3
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 3
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 61
- 125000001424 substituent group Chemical group 0.000 claims description 48
- 239000004480 active ingredient Substances 0.000 claims description 47
- 229910052739 hydrogen Inorganic materials 0.000 claims description 47
- 239000001257 hydrogen Substances 0.000 claims description 43
- 239000013543 active substance Substances 0.000 claims description 30
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 24
- 150000002431 hydrogen Chemical class 0.000 claims description 23
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 13
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 12
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 claims description 9
- 239000005884 Beta-Cyfluthrin Substances 0.000 claims description 9
- 239000005946 Cypermethrin Substances 0.000 claims description 9
- 239000005892 Deltamethrin Substances 0.000 claims description 9
- 239000005903 Gamma-cyhalothrin Substances 0.000 claims description 9
- QQODLKZGRKWIFG-RUTXASTPSA-N [(R)-cyano-(4-fluoro-3-phenoxyphenyl)methyl] (1S)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-RUTXASTPSA-N 0.000 claims description 9
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 9
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 9
- 229960005424 cypermethrin Drugs 0.000 claims description 9
- 229960002483 decamethrin Drugs 0.000 claims description 9
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 9
- ZXQYGBMAQZUVMI-GCMPRSNUSA-N gamma-cyhalothrin Chemical compound CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-GCMPRSNUSA-N 0.000 claims description 9
- 239000005910 lambda-Cyhalothrin Substances 0.000 claims description 9
- 239000005652 Acrinathrin Substances 0.000 claims description 8
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 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 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 4
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- PXBFMLJZNCDSMP-UHFFFAOYSA-N 2-Aminobenzamide Chemical class NC(=O)C1=CC=CC=C1N PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 claims description 3
- INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 claims description 3
- 229940079593 drug Drugs 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims description 2
- 239000005877 Alpha-Cypermethrin Substances 0.000 claims description 2
- 239000005874 Bifenthrin Substances 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 claims description 2
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 claims description 2
- 229960001591 cyfluthrin Drugs 0.000 claims description 2
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims description 2
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 claims description 2
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 claims description 2
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 claims description 2
- GBIHOLCMZGAKNG-CGAIIQECSA-N flucythrinate Chemical compound O=C([C@@H](C(C)C)C=1C=CC(OC(F)F)=CC=1)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-CGAIIQECSA-N 0.000 claims description 2
- WIFXJBMOTMKRMM-UHFFFAOYSA-N halfenprox Chemical compound C=1C=C(OC(F)(F)Br)C=CC=1C(C)(C)COCC(C=1)=CC=CC=1OC1=CC=CC=C1 WIFXJBMOTMKRMM-UHFFFAOYSA-N 0.000 claims description 2
- 229960000490 permethrin Drugs 0.000 claims description 2
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 2
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
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- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 claims description 2
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 claims description 2
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- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 claims 1
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 10
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- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
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- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical class C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
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- YDUBPEZBWPRJJL-UHFFFAOYSA-M tributyl-(4-chloro-2-phenylphenoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OC1=CC=C(Cl)C=C1C1=CC=CC=C1 YDUBPEZBWPRJJL-UHFFFAOYSA-M 0.000 description 1
- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- SMBZJSVIKJMSFP-UHFFFAOYSA-N trifluoromethyl hypofluorite Chemical compound FOC(F)(F)F SMBZJSVIKJMSFP-UHFFFAOYSA-N 0.000 description 1
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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
- 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
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)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004021564A DE102004021564A1 (de) | 2003-11-14 | 2004-05-03 | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| EP04791083A EP1686859B1 (de) | 2003-11-14 | 2004-10-30 | Wirkstoffkombinationen mit insektiziden eigenschaften |
| BRPI0416560-8A BRPI0416560B1 (pt) | 2003-11-14 | 2004-10-30 | Agente compreendendo combinação de substâncias ativas com propriedades inseticidas, seu uso, e processo para preparação de defensivos |
| RU2006120438/04A RU2381651C2 (ru) | 2003-11-14 | 2004-10-30 | Комбинация действующих веществ с инсектицидными свойствами |
| AU2004290502A AU2004290502C1 (en) | 2003-11-14 | 2004-10-30 | Combination of active substances with insecticidal properties |
| KR1020067011507A KR101140334B1 (ko) | 2003-11-14 | 2004-10-30 | 살충성을 가지는 활성 물질의 배합물 |
| CN2004800336924A CN1882245B (zh) | 2003-11-14 | 2004-10-30 | 具有杀昆虫特性的活性物质结合物 |
| EP12178036A EP2540164A1 (de) | 2003-11-14 | 2004-10-30 | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| ES04791083T ES2391019T3 (es) | 2003-11-14 | 2004-10-30 | Combinaciones de principios activos con propiedades insecticidas |
| US10/579,076 US8268751B2 (en) | 2003-11-14 | 2004-10-30 | Combination of active substances with insecticidal properties |
| PCT/EP2004/012330 WO2005048713A1 (de) | 2003-11-14 | 2004-10-30 | Wirkstoffkombinationen mit insektiziden eigenschaften |
| JP2006538722A JP4949031B2 (ja) | 2003-11-14 | 2004-10-30 | 殺虫特性を有する活性物質の組合せ物 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10353280 | 2003-11-14 | ||
| DE10353280.3 | 2003-11-14 | ||
| DE102004021564A DE102004021564A1 (de) | 2003-11-14 | 2004-05-03 | Wirkstoffkombinationen mit insektiziden Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102004021564A1 true DE102004021564A1 (de) | 2005-07-07 |
Family
ID=34621290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102004021564A Withdrawn DE102004021564A1 (de) | 2003-11-14 | 2004-05-03 | Wirkstoffkombinationen mit insektiziden Eigenschaften |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8268751B2 (https=) |
| EP (2) | EP1686859B1 (https=) |
| JP (1) | JP4949031B2 (https=) |
| KR (1) | KR101140334B1 (https=) |
| CN (1) | CN1882245B (https=) |
| AU (1) | AU2004290502C1 (https=) |
| BR (1) | BRPI0416560B1 (https=) |
| DE (1) | DE102004021564A1 (https=) |
| ES (1) | ES2391019T3 (https=) |
| RU (1) | RU2381651C2 (https=) |
| WO (1) | WO2005048713A1 (https=) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4426753A1 (de) * | 1994-07-28 | 1996-02-01 | Bayer Ag | Mittel zur Bekämpfung von Pflanzenschädlingen |
| CA2334618C (en) | 1998-06-10 | 2010-01-12 | Bayer Aktiengesellschaft | Agents for combating plant pests |
| MY142967A (en) | 2001-08-13 | 2011-01-31 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| TWI283164B (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| DE10228103A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| DE10228102A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| SI1599463T1 (sl) | 2003-01-28 | 2013-10-30 | E.I. Du Pont De Nemours And Company | Ciano antranilamidni insekticidi |
| DE10335183A1 (de) * | 2003-07-30 | 2005-02-24 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| DE10341945A1 (de) * | 2003-09-11 | 2005-04-21 | Bayer Cropscience Ag | Verwendung von fungiziden Mitteln zur Beizung von Saatgut |
| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10347440A1 (de) * | 2003-10-13 | 2005-05-04 | Bayer Cropscience Ag | Synergistische insektizide Mischungen |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE102004006075A1 (de) | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| DE10356550A1 (de) * | 2003-12-04 | 2005-07-07 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| WO2005053405A1 (de) * | 2003-12-04 | 2005-06-16 | Bayer Cropscience Aktiengesellschaft | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| BRPI0417322B1 (pt) * | 2003-12-04 | 2015-11-24 | Bayer Cropscience Ag | agente inseticida, seu processo de preparação, e processo para combate de parasitas animais |
| US20070155797A1 (en) * | 2003-12-12 | 2007-07-05 | Bayer Cropscience Aktiengesellschaft | Synergistic insecticidal mixtures |
| DE102004005786A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | Haloalkylcarboxamide |
| MXPA06012897A (es) * | 2004-05-10 | 2007-01-26 | Syngenta Participations Ag | Mezclas plaguicidas. |
| EP1606999A1 (de) * | 2004-06-18 | 2005-12-21 | Bayer CropScience AG | Saatgutbehandlungsmittel für Soja |
| GT200500179A (es) * | 2004-07-01 | 2006-02-23 | Mezclas sinergistas de agentes de antranilamida para el control de plagas de invertebrados | |
| DE102004035134A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern |
| GB0514652D0 (en) * | 2005-07-15 | 2005-08-24 | Syngenta Ltd | Pesticidal mixtures |
| DE102006031976A1 (de) * | 2006-07-11 | 2008-01-17 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006031978A1 (de) * | 2006-07-11 | 2008-01-17 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US20090281157A1 (en) * | 2006-07-11 | 2009-11-12 | Bayer Cropscience Ag | Active Ingredient Combinations With Insecticidal and Acaricidal Properties |
| WO2008034787A2 (en) | 2006-09-18 | 2008-03-27 | Basf Se | Pesticidal mixtures comprising an anthranilamide insecticide and a fungicide |
| JP5449669B2 (ja) | 2006-12-14 | 2014-03-19 | 石原産業株式会社 | 有害生物防除組成物 |
| DE102006061538A1 (de) * | 2006-12-27 | 2008-07-03 | Bayer Healthcare Ag | Kombinationsprodukt zur Bekämpfung von Parasiten an Tieren |
| PT2124557E (pt) * | 2007-02-02 | 2015-02-27 | Plant Health Care Inc | Composições fungicidas sinérgicas compreendendo formononetina |
| RU2384065C2 (ru) * | 2007-12-10 | 2010-03-20 | Общество с ограниченной ответственностью "ЯДЖУР-ВЕДА" | Инсектоакарицидное средство |
| US8496256B2 (en) * | 2007-12-17 | 2013-07-30 | Deere & Company | Steering assist for a rear caster wheel on a work machine |
| US8683346B2 (en) * | 2008-11-17 | 2014-03-25 | Sap Portals Israel Ltd. | Client integration of information from a supplemental server into a portal |
| MX341267B (es) * | 2010-06-18 | 2016-08-09 | Bayer Ip Gmbh | Combinaciones de principios activos con propiedades insecticidas y acaricidas. |
| RU2485776C1 (ru) * | 2012-02-03 | 2013-06-27 | Открытое акционерное общество "Чебоксарское производственное объединение им. В.И. Чапаева" | Пиротехнический дымообразующий инсектицидный состав |
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| CN103478162A (zh) * | 2012-06-11 | 2014-01-01 | 陕西美邦农药有限公司 | 一种含溴虫苯甲酰胺与拟除虫菊酯类的杀虫组合物 |
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| CN106818844A (zh) * | 2016-12-14 | 2017-06-13 | 安徽东健化工科技有限公司 | 一种除草剂 |
| RU2748469C1 (ru) * | 2020-10-29 | 2021-05-26 | федеральное государственное бюджетное образовательное учреждение высшего образования "Ставропольский государственный аграрный университет" | Инсектоакарицидная паста |
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| FR2805971B1 (fr) * | 2000-03-08 | 2004-01-30 | Aventis Cropscience Sa | Procedes de traitement et/ou de protection des cultures contre les arthropodes et compositions utiles pour de tels procedes |
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| DE60236600D1 (de) | 2001-08-13 | 2010-07-15 | Du Pont | Substituierte 1h-dihydropyrazole, ihre herstellung und verwendung |
| TWI327566B (en) | 2001-08-13 | 2010-07-21 | Du Pont | Novel substituted ihydro 3-halo-1h-pyrazole-5-carboxylates,their preparation and use |
| AR036872A1 (es) * | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
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-
2004
- 2004-05-03 DE DE102004021564A patent/DE102004021564A1/de not_active Withdrawn
- 2004-10-30 CN CN2004800336924A patent/CN1882245B/zh not_active Expired - Lifetime
- 2004-10-30 KR KR1020067011507A patent/KR101140334B1/ko not_active Expired - Lifetime
- 2004-10-30 RU RU2006120438/04A patent/RU2381651C2/ru not_active IP Right Cessation
- 2004-10-30 US US10/579,076 patent/US8268751B2/en not_active Expired - Lifetime
- 2004-10-30 AU AU2004290502A patent/AU2004290502C1/en not_active Expired
- 2004-10-30 WO PCT/EP2004/012330 patent/WO2005048713A1/de not_active Ceased
- 2004-10-30 JP JP2006538722A patent/JP4949031B2/ja not_active Expired - Lifetime
- 2004-10-30 ES ES04791083T patent/ES2391019T3/es not_active Expired - Lifetime
- 2004-10-30 BR BRPI0416560-8A patent/BRPI0416560B1/pt not_active IP Right Cessation
- 2004-10-30 EP EP04791083A patent/EP1686859B1/de not_active Revoked
- 2004-10-30 EP EP12178036A patent/EP2540164A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004290502B2 (en) | 2011-07-21 |
| JP4949031B2 (ja) | 2012-06-06 |
| BRPI0416560A (pt) | 2007-01-23 |
| US20080070863A1 (en) | 2008-03-20 |
| AU2004290502C1 (en) | 2014-07-03 |
| EP1686859B1 (de) | 2012-08-01 |
| US8268751B2 (en) | 2012-09-18 |
| BRPI0416560B1 (pt) | 2014-09-23 |
| ES2391019T3 (es) | 2012-11-20 |
| KR20060126498A (ko) | 2006-12-07 |
| CN1882245B (zh) | 2011-12-07 |
| RU2006120438A (ru) | 2008-01-10 |
| AU2004290502A1 (en) | 2005-06-02 |
| EP2540164A1 (de) | 2013-01-02 |
| WO2005048713A1 (de) | 2005-06-02 |
| EP1686859A1 (de) | 2006-08-09 |
| JP2007510683A (ja) | 2007-04-26 |
| KR101140334B1 (ko) | 2012-05-03 |
| RU2381651C2 (ru) | 2010-02-20 |
| CN1882245A (zh) | 2006-12-20 |
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