DE10015310A1 - Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften - Google Patents
Wirkstoffkombinationen mit insektiziden und akariziden EigenschaftenInfo
- Publication number
- DE10015310A1 DE10015310A1 DE10015310A DE10015310A DE10015310A1 DE 10015310 A1 DE10015310 A1 DE 10015310A1 DE 10015310 A DE10015310 A DE 10015310A DE 10015310 A DE10015310 A DE 10015310A DE 10015310 A1 DE10015310 A1 DE 10015310A1
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- halogen
- alkoxy
- spp
- 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- Withdrawn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
- 230000000895 acaricidal effect Effects 0.000 title claims abstract description 11
- 230000000749 insecticidal effect Effects 0.000 title claims abstract description 11
- 239000004480 active ingredient Substances 0.000 title description 41
- 229910052736 halogen Inorganic materials 0.000 claims description 44
- 150000002367 halogens Chemical class 0.000 claims description 44
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 22
- -1 C 1 -C 6 alkyl Chemical class 0.000 claims description 21
- 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 12
- 241000607479 Yersinia pestis Species 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 9
- 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
- 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
- 125000004435 hydrogen atom Chemical group [H]* 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
- 239000005951 Methiocarb Substances 0.000 claims description 3
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 claims description 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 2
- 239000005944 Chlorpyrifos Substances 0.000 claims description 2
- 239000005947 Dimethoate Substances 0.000 claims description 2
- 239000005898 Fenoxycarb Substances 0.000 claims description 2
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005948 Formetanate Substances 0.000 claims description 2
- 239000005949 Malathion Substances 0.000 claims description 2
- 239000005916 Methomyl Substances 0.000 claims description 2
- 239000005950 Oxamyl Substances 0.000 claims description 2
- 239000005921 Phosmet Substances 0.000 claims description 2
- 239000005923 Pirimicarb Substances 0.000 claims description 2
- 239000005924 Pirimiphos-methyl Substances 0.000 claims description 2
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 claims description 2
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 claims description 2
- MYPKGPZHHQEODQ-UHFFFAOYSA-N [3-(dimethylaminomethylideneamino)phenoxy]carbonyl-methylazanium;chloride Chemical compound Cl.CNC(=O)OC1=CC=CC(N=CN(C)C)=C1 MYPKGPZHHQEODQ-UHFFFAOYSA-N 0.000 claims description 2
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-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
- 229960005286 carbaryl Drugs 0.000 claims description 2
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 2
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 claims description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 claims description 2
- VEENJGZXVHKXNB-VOTSOKGWSA-N dicrotophos Chemical compound COP(=O)(OC)O\C(C)=C\C(=O)N(C)C VEENJGZXVHKXNB-VOTSOKGWSA-N 0.000 claims description 2
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 claims description 2
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 claims description 2
- DOFZAZXDOSGAJZ-UHFFFAOYSA-N disulfoton Chemical compound CCOP(=S)(OCC)SCCSCC DOFZAZXDOSGAJZ-UHFFFAOYSA-N 0.000 claims description 2
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 claims description 2
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 claims description 2
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 claims description 2
- RMFNNCGOSPBBAD-MDWZMJQESA-N formetanate Chemical compound CNC(=O)OC1=CC=CC(\N=C\N(C)C)=C1 RMFNNCGOSPBBAD-MDWZMJQESA-N 0.000 claims description 2
- 229960000453 malathion Drugs 0.000 claims description 2
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 claims description 2
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 claims description 2
- GEPDYQSQVLXLEU-AATRIKPKSA-N methyl (e)-3-dimethoxyphosphoryloxybut-2-enoate Chemical compound COC(=O)\C=C(/C)OP(=O)(OC)OC GEPDYQSQVLXLEU-AATRIKPKSA-N 0.000 claims description 2
- 229960001952 metrifonate Drugs 0.000 claims description 2
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 claims description 2
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 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
- PMCVMORKVPSKHZ-UHFFFAOYSA-N oxydemeton-methyl Chemical compound CCS(=O)CCSP(=O)(OC)OC PMCVMORKVPSKHZ-UHFFFAOYSA-N 0.000 claims description 2
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical group COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-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
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 claims description 2
- IOUNQDKNJZEDEP-UHFFFAOYSA-N phosalone Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=S)(OCC)OCC)C2=C1 IOUNQDKNJZEDEP-UHFFFAOYSA-N 0.000 claims description 2
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 claims description 2
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 claims description 2
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 claims description 2
- 229950001664 phoxim Drugs 0.000 claims description 2
- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 claims description 2
- QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 claims description 2
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 claims description 2
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 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
- 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
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 claims description 2
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 1
- 239000013543 active substance Substances 0.000 abstract description 12
- 125000004122 cyclic group Chemical group 0.000 abstract description 3
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- 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
- 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
- 230000011664 signaling Effects 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
- 239000004575 stone Substances 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
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 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
- 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
- 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
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 (23)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10015310A DE10015310A1 (de) | 2000-03-28 | 2000-03-28 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| PT01915355T PT1267619E (pt) | 2000-03-28 | 2001-03-15 | Combinacoes de substancias activas com propriedades insecticidas e acaricidas |
| AU2001242473A AU2001242473A1 (en) | 2000-03-28 | 2001-03-15 | Active substance combinations having insecticidal and acaricidal properties |
| BR0109541-2A BR0109541A (pt) | 2000-03-28 | 2001-03-15 | Combinações de subst ncias ativas com propriedades inseticidas e acaricidas |
| CNA2006100847210A CN1853469A (zh) | 2000-03-28 | 2001-03-15 | 具有杀昆虫和杀螨性能的活性化合物组合物 |
| EP01915355A EP1267619B1 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| HU0301516A HUP0301516A2 (hu) | 2000-03-28 | 2001-03-15 | Szinergetikus hatású inszekticid és akaricid készítmény előállítása és alkalmazása |
| CNB018072038A CN1267004C (zh) | 2000-03-28 | 2001-03-15 | 具有杀昆虫和杀螨性能的活性化合物组合物 |
| DE50104210T DE50104210D1 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| US10/239,332 US6900190B2 (en) | 2000-03-28 | 2001-03-15 | Active substance combinations having insecticidal and acaricidal properties |
| MXPA02009530A MXPA02009530A (es) | 2000-03-28 | 2001-03-15 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
| JP2001570094A JP5002106B2 (ja) | 2000-03-28 | 2001-03-15 | 殺昆虫および殺ダニ性を有する活性物質の組み合わせ |
| PCT/EP2001/002977 WO2001072125A2 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| AT01915355T ATE279861T1 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| IL15175001A IL151750A0 (en) | 2000-03-28 | 2001-03-15 | Active substance combinations having insecticidal and acaricidal properties |
| KR1020027012220A KR100730001B1 (ko) | 2000-03-28 | 2001-03-15 | 살충 및 살비성을 갖는 활성 물질의 배합물 |
| TW090106531A TWI241887B (en) | 2000-03-28 | 2001-03-21 | Active compound combinations having insecticidal and acaricidal properties |
| GT200100046A GT200100046A (es) | 2000-03-28 | 2001-03-23 | Combinaciones de productos activos con propiedades insecticidas y acaricidas. |
| EG20010302A EG23185A (en) | 2000-03-28 | 2001-03-27 | Active compound combinations having insecticidal and acaricidal properties. |
| ZA200206765A ZA200206765B (en) | 2000-03-28 | 2002-08-23 | Active substance combinations having insecticidal and acaricidal properties. |
| IL151750A IL151750A (en) | 2000-03-28 | 2002-09-12 | Combinations of active ingredients with insecticidal and acaricidal properties |
| US11/074,156 US20050147639A1 (en) | 2000-03-28 | 2005-03-07 | Active substance combinations having insecticidal and acaricidal properties |
| US12/548,731 US20090318386A1 (en) | 2000-03-28 | 2009-08-27 | Active compound combinations having insecticidal and acaricidal properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10015310A DE10015310A1 (de) | 2000-03-28 | 2000-03-28 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10015310A1 true DE10015310A1 (de) | 2001-10-04 |
Family
ID=7636645
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10015310A Withdrawn DE10015310A1 (de) | 2000-03-28 | 2000-03-28 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE50104210T Expired - Fee Related DE50104210D1 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE50104210T Expired - Fee Related DE50104210D1 (de) | 2000-03-28 | 2001-03-15 | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US6900190B2 (enExample) |
| EP (1) | EP1267619B1 (enExample) |
| JP (1) | JP5002106B2 (enExample) |
| KR (1) | KR100730001B1 (enExample) |
| CN (2) | CN1267004C (enExample) |
| AT (1) | ATE279861T1 (enExample) |
| AU (1) | AU2001242473A1 (enExample) |
| BR (1) | BR0109541A (enExample) |
| DE (2) | DE10015310A1 (enExample) |
| EG (1) | EG23185A (enExample) |
| GT (1) | GT200100046A (enExample) |
| HU (1) | HUP0301516A2 (enExample) |
| IL (2) | IL151750A0 (enExample) |
| MX (1) | MXPA02009530A (enExample) |
| PT (1) | PT1267619E (enExample) |
| TW (1) | TWI241887B (enExample) |
| WO (1) | WO2001072125A2 (enExample) |
| ZA (1) | ZA200206765B (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19948129A1 (de) * | 1999-10-07 | 2001-04-12 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE19953775A1 (de) * | 1999-11-09 | 2001-05-10 | 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 |
| US20040185212A1 (en) * | 2003-03-20 | 2004-09-23 | Bogrett Blake Boyd | Fungi resistant sheet, facing and faced insulation assembly |
| US20040192132A1 (en) * | 2003-03-20 | 2004-09-30 | Fay Ralph Michael | Fungi resistant asphalt and asphalt sheet materials |
| DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10353281A1 (de) * | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| KR100870174B1 (ko) † | 2003-12-04 | 2008-11-24 | 바이엘 크롭사이언스 아게 | 살충 및 살비성을 가지는 활성 물질 배합물 |
| DE102004001112A1 (de) * | 2004-01-07 | 2005-08-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektizide und akariziden Eigenschaften |
| DE102006014480A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006014489A1 (de) * | 2006-03-29 | 2007-10-04 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) * | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027730A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| EA022553B1 (ru) | 2010-01-22 | 2016-01-29 | Байер Интеллектуэль Проперти Гмбх | Применение комбинации биологически активных веществ, набор и средство, содержащие комбинацию биологически активных веществ, для борьбы с вредителями животного происхождения и способ улучшения использования продукционного потенциала трансгенного растения |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| 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 |
| CN103651484B (zh) * | 2012-08-31 | 2015-04-15 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与氨基甲酸酯类的农药组合物 |
| CN105613559A (zh) * | 2012-08-31 | 2016-06-01 | 陕西美邦农药有限公司 | 一种含螺甲螨酯与新烟碱类的杀虫组合物 |
| CN111295094A (zh) | 2017-10-09 | 2020-06-16 | 泰尔茂比司特生物技术有限公司 | 冻干容器及使用冻干容器的方法 |
| WO2020185916A1 (en) | 2019-03-14 | 2020-09-17 | Terumo Bct Biotechnologies, Llc | Lyophilization container fill fixture, system and method of use |
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|---|---|---|---|---|
| DE814152C (de) | 1951-07-26 | I arbenfabriken Bayer | everkusen I Verfahren zur Herstellung von Estern der Phosphorsaure und Thiophosphor saure | |
| BE552284A (enExample) | ||||
| US2498283A (en) * | 1945-01-30 | 1950-02-21 | United Aircraft Corp | Drive for helicopters |
| BE487705A (enExample) | 1947-05-21 | |||
| CA494562A (en) | 1948-02-04 | 1953-07-21 | American Cyanamid Company | Carbamylalkyl phosphates and method of preparation |
| US2586655A (en) | 1948-03-26 | 1952-02-19 | American Cyanamid Co | S-alkoxymethyl-o, o'-dialkyldithiophosphates |
| NL80825C (enExample) | 1950-03-02 | |||
| BE637016A (enExample) | 1951-04-20 | 1900-01-01 | ||
| GB775085A (en) | 1951-09-25 | 1957-05-22 | Ciba Ltd | Preparations for combating pests |
| US2754246A (en) * | 1952-02-25 | 1956-07-10 | Phillips Petroleum Co | Stripping still control according to specific gravity of liquid and vapors introduced into column |
| US2685552A (en) | 1952-02-29 | 1954-08-03 | Shell Dev | Dimethyl 1-carbomethoxy-1-propen-2-yl phosphate |
| DE917668C (de) | 1952-08-01 | 1954-09-09 | Bayer Ag | Verfahren zur Herstellung von neutralen Estern der Dithiophosphorsaeure |
| CA529379A (en) | 1952-09-20 | 1956-08-21 | Farbenfabriken Bayer Aktiengesellschaft | Phosphonic ester |
| DE947368C (de) | 1954-11-06 | 1956-08-16 | Bayer Ag | Verfahren zur Herstellung von Sulfoxydgruppen enthaltenden Estern der Phosphor- und Thiophosphorsaeuren |
| US2758115A (en) | 1955-02-10 | 1956-08-07 | Bayer Ag | Derivatives of thiophosphoric acid |
| US2767194A (en) | 1955-03-18 | 1956-10-16 | Stauffer Chemical Co | Compositions of matter |
| GB834814A (en) | 1955-06-14 | 1960-05-11 | Montedison Spa | ª‡-substituted o, o-dialkyl-dithiophosphorylacetic esters and process for their preparation |
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| BE587481A (enExample) | 1958-08-07 | |||
| BE593564A (enExample) | 1959-07-31 | |||
| NL105160C (enExample) | 1959-09-03 | |||
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| NL292088A (enExample) | 1962-04-30 | 1900-01-01 | ||
| BE635767A (enExample) | 1962-08-02 | |||
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| DE1567137C3 (de) | 1965-08-20 | 1979-01-25 | Sankyo Co. Ltd., Tokio | Insektizides Mittel auf der Basis von Phosphorsäureisoxazolyiestern |
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| CH478152A (de) | 1966-07-05 | 1969-09-15 | Agripat Sa | Verfahren zur Herstellung heterozyklischer Thiophosphor- und Thiophosphonsäureester |
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| JPS4924656B1 (enExample) | 1970-03-13 | 1974-06-25 | ||
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| BR0017618B1 (pt) * | 1999-03-12 | 2013-04-09 | composiÇço inseticida sinÉrgica, e, processos para controle de insetos, e para proteger plantas contra infestaÇço e ataque de insetos. | |
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| CL2007003746A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende propamocarb-hcl y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| DE102007018452A1 (de) * | 2007-04-17 | 2008-10-23 | Bayer Cropscience Ag | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
| TW200904331A (en) * | 2007-06-15 | 2009-02-01 | Bayer Cropscience Sa | Pesticidal composition comprising a strigolactone derivative and an insecticide compound |
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| KR20120027265A (ko) * | 2009-04-27 | 2012-03-21 | 다우 아그로사이언시즈 엘엘씨 | 살충성 피리딘 화합물 |
| AR079609A1 (es) * | 2009-11-17 | 2012-02-08 | Bayer Cropscience Ag | Combinaciones de compuestos activos |
-
2000
- 2000-03-28 DE DE10015310A patent/DE10015310A1/de not_active Withdrawn
-
2001
- 2001-03-15 AT AT01915355T patent/ATE279861T1/de not_active IP Right Cessation
- 2001-03-15 PT PT01915355T patent/PT1267619E/pt unknown
- 2001-03-15 EP EP01915355A patent/EP1267619B1/de not_active Expired - Lifetime
- 2001-03-15 MX MXPA02009530A patent/MXPA02009530A/es active IP Right Grant
- 2001-03-15 AU AU2001242473A patent/AU2001242473A1/en not_active Abandoned
- 2001-03-15 WO PCT/EP2001/002977 patent/WO2001072125A2/de not_active Ceased
- 2001-03-15 JP JP2001570094A patent/JP5002106B2/ja not_active Expired - Fee Related
- 2001-03-15 CN CNB018072038A patent/CN1267004C/zh not_active Expired - Lifetime
- 2001-03-15 KR KR1020027012220A patent/KR100730001B1/ko not_active Expired - Fee Related
- 2001-03-15 DE DE50104210T patent/DE50104210D1/de not_active Expired - Fee Related
- 2001-03-15 BR BR0109541-2A patent/BR0109541A/pt not_active Application Discontinuation
- 2001-03-15 IL IL15175001A patent/IL151750A0/xx active IP Right Grant
- 2001-03-15 HU HU0301516A patent/HUP0301516A2/hu unknown
- 2001-03-15 CN CNA2006100847210A patent/CN1853469A/zh active Pending
- 2001-03-15 US US10/239,332 patent/US6900190B2/en not_active Expired - Fee Related
- 2001-03-21 TW TW090106531A patent/TWI241887B/zh not_active IP Right Cessation
- 2001-03-23 GT GT200100046A patent/GT200100046A/es unknown
- 2001-03-27 EG EG20010302A patent/EG23185A/xx active
-
2002
- 2002-08-23 ZA ZA200206765A patent/ZA200206765B/en unknown
- 2002-09-12 IL IL151750A patent/IL151750A/en not_active IP Right Cessation
-
2005
- 2005-03-07 US US11/074,156 patent/US20050147639A1/en not_active Abandoned
-
2009
- 2009-08-27 US US12/548,731 patent/US20090318386A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN1267004C (zh) | 2006-08-02 |
| MXPA02009530A (es) | 2003-05-14 |
| GT200100046A (es) | 2002-01-11 |
| HUP0301516A2 (hu) | 2003-08-28 |
| PT1267619E (pt) | 2005-03-31 |
| EP1267619B1 (de) | 2004-10-20 |
| IL151750A (en) | 2006-08-20 |
| ATE279861T1 (de) | 2004-11-15 |
| TWI241887B (en) | 2005-10-21 |
| US20090318386A1 (en) | 2009-12-24 |
| JP2003528116A (ja) | 2003-09-24 |
| CN1419412A (zh) | 2003-05-21 |
| WO2001072125A3 (de) | 2002-02-28 |
| WO2001072125A8 (de) | 2004-03-04 |
| US20050147639A1 (en) | 2005-07-07 |
| EP1267619A2 (de) | 2003-01-02 |
| US20030100604A1 (en) | 2003-05-29 |
| EG23185A (en) | 2004-07-31 |
| DE50104210D1 (de) | 2004-11-25 |
| BR0109541A (pt) | 2003-06-10 |
| IL151750A0 (en) | 2003-04-10 |
| CN1853469A (zh) | 2006-11-01 |
| JP5002106B2 (ja) | 2012-08-15 |
| KR20020084209A (ko) | 2002-11-04 |
| US6900190B2 (en) | 2005-05-31 |
| AU2001242473A1 (en) | 2001-10-08 |
| WO2001072125A2 (de) | 2001-10-04 |
| ZA200206765B (en) | 2003-08-25 |
| KR100730001B1 (ko) | 2007-06-20 |
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