DE10007411A1 - Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften - Google Patents
Wirkstoffkombinationen mit insektiziden und akariziden EigenschaftenInfo
- Publication number
- DE10007411A1 DE10007411A1 DE10007411A DE10007411A DE10007411A1 DE 10007411 A1 DE10007411 A1 DE 10007411A1 DE 10007411 A DE10007411 A DE 10007411A DE 10007411 A DE10007411 A DE 10007411A DE 10007411 A1 DE10007411 A1 DE 10007411A1
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- halogen
- spp
- alkoxy
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000000749 insecticidal effect Effects 0.000 title claims abstract description 12
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 11
- 239000004480 active ingredient Substances 0.000 title description 45
- 229910052736 halogen Inorganic materials 0.000 claims description 45
- 150000002367 halogens Chemical class 0.000 claims description 45
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 26
- -1 C 1 -C 6 alkyl Chemical class 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- 241001465754 Metazoa Species 0.000 claims description 14
- 241000607479 Yersinia pestis Species 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 125000001797 benzyl group Chemical class [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 125000006413 ring segment Chemical group 0.000 claims description 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 239000004606 Fillers/Extenders Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 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
- 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 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 2
- 239000005652 Acrinathrin Substances 0.000 claims description 2
- 239000005877 Alpha-Cypermethrin Substances 0.000 claims description 2
- 239000005884 Beta-Cyfluthrin Substances 0.000 claims description 2
- 239000005874 Bifenthrin Substances 0.000 claims description 2
- 239000005946 Cypermethrin Substances 0.000 claims description 2
- 239000005892 Deltamethrin Substances 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
- 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 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
- 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 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group 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
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
- 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 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
- 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 2
- 229960005424 cypermethrin Drugs 0.000 claims description 2
- 229960002483 decamethrin Drugs 0.000 claims description 2
- 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 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
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000005910 lambda-Cyhalothrin Substances 0.000 claims description 2
- 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 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
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 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
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 229940108410 resmethrin Drugs 0.000 claims description 2
- 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
- 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 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
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- 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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- 239000013543 active substance Substances 0.000 abstract description 10
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- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- 239000012716 precipitator Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 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
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical class CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- WVZPYZMQQDNINJ-UHFFFAOYSA-N tributyl(butylstannyloxy)stannane Chemical class CCCC[SnH](CCCC)O[SnH](CCCC)CCCC WVZPYZMQQDNINJ-UHFFFAOYSA-N 0.000 description 1
- 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
- 239000006200 vaporizer Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide 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
- A01N43/02—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
- A01N43/06—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 five-membered rings
- A01N43/08—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 five-membered rings with oxygen as the ring hetero atom
-
- 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
- A01N43/06—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 five-membered rings
- A01N43/12—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 five-membered rings condensed with a carbocyclic ring
-
- 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)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (28)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10007411A DE10007411A1 (de) | 2000-02-18 | 2000-02-18 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EG20010129A EG22825A (en) | 2000-02-18 | 2001-01-14 | Active compound combinations having insecticidal and acaricidal properties |
| ARP010100417A AR031553A1 (es) | 2000-02-18 | 2001-01-30 | Composiciones insecticidas y acaricidas, su empleo para la lucha contra las pestes animales, procedimiento para la lucha contra las pestes animales, y procedimiento para la obtencion de estas composiciones |
| AT01902414T ATE301931T1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| DE50107115T DE50107115D1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| CA2400425A CA2400425C (en) | 2000-02-18 | 2001-02-06 | Active substance combinations comprising insecticidal and acaricidal properties |
| US10/204,011 US6653343B2 (en) | 2000-02-18 | 2001-02-06 | Active substance combinations comprising insecticidal and acaricidal properties |
| JP2001559265A JP4928700B2 (ja) | 2000-02-18 | 2001-02-06 | 殺虫性及び殺ダニ性を含む活性物質の組合わせ |
| CNB018049605A CN1262187C (zh) | 2000-02-18 | 2001-02-06 | 具有杀虫和杀螨活性的活性化合物组合物 |
| PL01356369A PL356369A1 (en) | 2000-02-18 | 2001-02-06 | Active substance combinations comprising insecticidal and acaricidal properties |
| EP01902414A EP1263287B1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| PCT/EP2001/001237 WO2001060158A1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| HU0204343A HUP0204343A3 (en) | 2000-02-18 | 2001-02-06 | Insecticidal and acaricidal synergetic mixture preparation and use thereof |
| IL15106801A IL151068A0 (en) | 2000-02-18 | 2001-02-06 | Active substance combinations comprising insecticidal and acaricidal properties |
| ES01902414T ES2244581T3 (es) | 2000-02-18 | 2001-02-06 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
| AU30249/01A AU775704B2 (en) | 2000-02-18 | 2001-02-06 | Active substance combinations comprising insecticidal and acaricidal properties |
| MXPA02008011A MXPA02008011A (es) | 2000-02-18 | 2001-02-06 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
| BRPI0108427-5A BR0108427B1 (pt) | 2000-02-18 | 2001-02-06 | composiÇço contendo misturas de substÂncias ativas com propriedades inseticidas e acaricidas, sua aplicaÇço e seu processo de preparaÇço, bem como processo para combater pragas animais. |
| KR1020027009781A KR100740977B1 (ko) | 2000-02-18 | 2001-02-06 | 살충 및 살비성을 갖는 활성 물질의 배합물 |
| GT200100024A GT200100024A (es) | 2000-02-18 | 2001-02-07 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
| TW090102993A TWI310300B (en) | 2000-02-18 | 2001-02-12 | Active compound combinations having insecticidal and acaricidal properties |
| HN2001000025A HN2001000025A (es) | 2000-02-18 | 2001-02-15 | Combinaciones de productos activos con propiedades insecticidas y acaricidas |
| CO01012557A CO5231190A1 (es) | 2000-02-18 | 2001-02-16 | Combinaciones de compuestos activos del tipo de los cetoenoles ciclicos con piretroides |
| SV2001000315A SV2002000315A (es) | 2000-02-18 | 2001-02-16 | Combinaciones de productos activos con propiedades insecticidas y acaricidas ref. lea 34226-sv |
| ZA200205784A ZA200205784B (en) | 2000-02-18 | 2002-07-19 | Active substance combinations comprising insecticidal and acaricidal properties. |
| IL151068A IL151068A (en) | 2000-02-18 | 2002-08-05 | Active substance combinations containing toxic substances against insects and mites |
| US10/652,153 US7091233B2 (en) | 2000-02-18 | 2003-08-29 | Active substance combinations comprising insecticidal and acaricidal properties |
| US11/349,681 US7232845B2 (en) | 2000-02-18 | 2006-02-08 | Active substance combinations comprising insecticidal and acaricidal properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10007411A DE10007411A1 (de) | 2000-02-18 | 2000-02-18 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10007411A1 true DE10007411A1 (de) | 2001-08-23 |
Family
ID=7631416
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10007411A Withdrawn DE10007411A1 (de) | 2000-02-18 | 2000-02-18 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE50107115T Expired - Fee Related DE50107115D1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE50107115T Expired - Fee Related DE50107115D1 (de) | 2000-02-18 | 2001-02-06 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US6653343B2 (https=) |
| EP (1) | EP1263287B1 (https=) |
| JP (1) | JP4928700B2 (https=) |
| KR (1) | KR100740977B1 (https=) |
| CN (1) | CN1262187C (https=) |
| AR (1) | AR031553A1 (https=) |
| AT (1) | ATE301931T1 (https=) |
| AU (1) | AU775704B2 (https=) |
| BR (1) | BR0108427B1 (https=) |
| CA (1) | CA2400425C (https=) |
| CO (1) | CO5231190A1 (https=) |
| DE (2) | DE10007411A1 (https=) |
| EG (1) | EG22825A (https=) |
| ES (1) | ES2244581T3 (https=) |
| GT (1) | GT200100024A (https=) |
| HN (1) | HN2001000025A (https=) |
| HU (1) | HUP0204343A3 (https=) |
| IL (2) | IL151068A0 (https=) |
| MX (1) | MXPA02008011A (https=) |
| PL (1) | PL356369A1 (https=) |
| SV (1) | SV2002000315A (https=) |
| TW (1) | TWI310300B (https=) |
| WO (1) | WO2001060158A1 (https=) |
| ZA (1) | ZA200205784B (https=) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10007411A1 (de) * | 2000-02-18 | 2001-08-23 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10013914A1 (de) * | 2000-03-21 | 2001-09-27 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10015310A1 (de) * | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10017881A1 (de) * | 2000-04-11 | 2001-10-25 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10018370A1 (de) * | 2000-04-14 | 2001-10-18 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| AU2007101011B9 (en) * | 2002-12-05 | 2008-04-17 | Osmose (Australia) Pty Limited | Superficial Treatment for Wood and Wood Products |
| AU2002953128A0 (en) * | 2002-12-05 | 2002-12-19 | Osmose (Australia) Pty Ltd | Surface treatment for wood and wood products |
| US8637089B2 (en) | 2003-04-09 | 2014-01-28 | Osmose, Inc. | Micronized wood preservative formulations |
| US7674481B2 (en) | 2003-04-09 | 2010-03-09 | Osmose, Inc. | Micronized wood preservative formulations |
| US8701743B2 (en) | 2004-01-02 | 2014-04-22 | Water Gremlin Company | Battery parts and associated systems and methods |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| DE102006008691A1 (de) * | 2006-02-24 | 2007-08-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| WO2008062413A2 (en) * | 2006-11-21 | 2008-05-29 | Mitam Ltd. | Formulations of entomopathogenic fungi for insect control |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| WO2010036882A1 (en) * | 2008-09-29 | 2010-04-01 | The Hartz Mountain Corporation | Photo-stable pest control |
| PL3059785T3 (pl) | 2009-04-30 | 2020-03-31 | Water Gremlin Company | Części akumulatora mające cechy utrzymujące i uszczelniające |
| WO2011066505A2 (en) * | 2009-11-30 | 2011-06-03 | Pathak Holdings Llc | Methods and compositions for filling fleshy fruits and vegetables |
| EP2525658B1 (de) * | 2010-01-22 | 2017-03-01 | Bayer Intellectual Property GmbH | Akarizide und/oder insektizide wirkstoffkombinationen |
| US8927547B2 (en) | 2010-05-21 | 2015-01-06 | Noviga Research Ab | Pyrimidine derivatives |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| DK2688883T3 (en) | 2011-03-24 | 2016-09-05 | Noviga Res Ab | pyrimidine |
| US9748551B2 (en) | 2011-06-29 | 2017-08-29 | Water Gremlin Company | Battery parts having retaining and sealing features and associated methods of manufacture and use |
| CN103621548B (zh) * | 2012-08-28 | 2015-10-28 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与拟除虫菊酯类的杀虫组合物 |
| CN103621509B (zh) * | 2012-08-28 | 2015-10-21 | 陕西美邦农药有限公司 | 一种含螺甲螨酯的农药组合物 |
| CN105248421B (zh) * | 2012-08-29 | 2017-08-25 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与双酰肼类的农药组合物 |
| US9954214B2 (en) | 2013-03-15 | 2018-04-24 | Water Gremlin Company | Systems and methods for manufacturing battery parts |
| CN105746570A (zh) * | 2016-03-31 | 2016-07-13 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和四氟苯菊酯的杀虫组合物 |
| CN105766910A (zh) * | 2016-03-31 | 2016-07-20 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和杀虫双的杀虫组合物 |
| CN105831118A (zh) * | 2016-03-31 | 2016-08-10 | 太仓市璜泾华南农机作业专业合作社 | 一种含螺环季酮酸类化合物和杀虫环的杀虫组合物 |
| CN108976215B (zh) * | 2017-05-31 | 2022-02-11 | 河北兰升生物科技有限公司 | 苯基酮烯醇衍生物的晶体及其制备方法、以及包含该晶体的农药组合物 |
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|---|---|---|---|---|
| US462237A (en) * | 1891-11-03 | Electric-lighting system | ||
| US403680A (en) * | 1889-05-21 | Hinge-screw coupling for fishing-net frames | ||
| US3264177A (en) | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
| GB1168797A (en) | 1965-12-09 | 1969-10-29 | Nat Res Dev | Cyclopropane Carboxylic Acid Derivatives and their use as Insecticides |
| JPS515450B1 (https=) | 1971-06-29 | 1976-02-20 | ||
| DE2326077C2 (de) | 1972-05-25 | 1985-12-12 | National Research Development Corp., London | Ungesättigte Cyclopropancarbonsäuren und deren Derivate, deren Herstellung und diese enthaltende Insektizide |
| US4024163A (en) | 1972-05-25 | 1977-05-17 | National Research Development Corporation | Insecticides |
| US4622337A (en) | 1972-05-25 | 1986-11-11 | National Research Development Corporation | 2,2-dimethyl-3-(2-halovinyl)cyclopropane carboxlic acid ester pesticides |
| US4039680A (en) | 1972-07-11 | 1977-08-02 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| US4062968A (en) | 1972-07-11 | 1977-12-13 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| US4058622A (en) | 1972-07-11 | 1977-11-15 | Sumitomo Chemical Company, Limited | Substituted phenyl acetate, insecticidal composition and method of use |
| US4031235A (en) | 1972-07-11 | 1977-06-21 | Sumitomo Chemical Company, Limited | Insecticidal substituted acetate compounds |
| EG11383A (en) | 1972-07-11 | 1979-03-31 | Sumitomo Chemical Co | Novel composition for controlling nixious insects and process for preparing thereof |
| US4016179A (en) | 1972-07-11 | 1977-04-05 | Sumitomo Chemical Co | Certain esters of 2-substituted-4-hydroxy-cyclopent-2-enones |
| US4055661A (en) | 1974-12-11 | 1977-10-25 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4148918A (en) | 1974-05-10 | 1979-04-10 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4070481A (en) | 1975-09-15 | 1978-01-24 | E. I. Du Pont De Nemours And Company | Substituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides |
| US4053634A (en) | 1975-09-15 | 1977-10-11 | E. I. Du Pont De Nemours And Company | Miticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters |
| US4220591A (en) | 1975-11-26 | 1980-09-02 | Commonwealth Scientific And Industrial Research Organization | Insecticidal esters |
| SE7610038L (sv) | 1976-03-29 | 1977-09-20 | Du Pont | Miticida och aficida karboxylsyraestrar |
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-
2000
- 2000-02-18 DE DE10007411A patent/DE10007411A1/de not_active Withdrawn
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2001
- 2001-01-14 EG EG20010129A patent/EG22825A/xx active
- 2001-01-30 AR ARP010100417A patent/AR031553A1/es active IP Right Grant
- 2001-02-06 BR BRPI0108427-5A patent/BR0108427B1/pt not_active IP Right Cessation
- 2001-02-06 CN CNB018049605A patent/CN1262187C/zh not_active Expired - Lifetime
- 2001-02-06 IL IL15106801A patent/IL151068A0/xx active IP Right Grant
- 2001-02-06 DE DE50107115T patent/DE50107115D1/de not_active Expired - Fee Related
- 2001-02-06 US US10/204,011 patent/US6653343B2/en not_active Expired - Lifetime
- 2001-02-06 MX MXPA02008011A patent/MXPA02008011A/es active IP Right Grant
- 2001-02-06 PL PL01356369A patent/PL356369A1/xx not_active Application Discontinuation
- 2001-02-06 AU AU30249/01A patent/AU775704B2/en not_active Expired
- 2001-02-06 WO PCT/EP2001/001237 patent/WO2001060158A1/de not_active Ceased
- 2001-02-06 AT AT01902414T patent/ATE301931T1/de not_active IP Right Cessation
- 2001-02-06 KR KR1020027009781A patent/KR100740977B1/ko not_active Expired - Lifetime
- 2001-02-06 JP JP2001559265A patent/JP4928700B2/ja not_active Expired - Lifetime
- 2001-02-06 HU HU0204343A patent/HUP0204343A3/hu unknown
- 2001-02-06 CA CA2400425A patent/CA2400425C/en not_active Expired - Fee Related
- 2001-02-06 ES ES01902414T patent/ES2244581T3/es not_active Expired - Lifetime
- 2001-02-06 EP EP01902414A patent/EP1263287B1/de not_active Expired - Lifetime
- 2001-02-07 GT GT200100024A patent/GT200100024A/es unknown
- 2001-02-12 TW TW090102993A patent/TWI310300B/zh not_active IP Right Cessation
- 2001-02-15 HN HN2001000025A patent/HN2001000025A/es unknown
- 2001-02-16 SV SV2001000315A patent/SV2002000315A/es not_active Application Discontinuation
- 2001-02-16 CO CO01012557A patent/CO5231190A1/es not_active Application Discontinuation
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- 2002-08-05 IL IL151068A patent/IL151068A/en unknown
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2003
- 2003-08-29 US US10/652,153 patent/US7091233B2/en not_active Expired - Lifetime
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