MX2008001116A - Microemulsiones y concentrados que contienen fipronil. - Google Patents

Microemulsiones y concentrados que contienen fipronil.

Info

Publication number: MX2008001116A
Authority: MX; Mexico
Prior art keywords: spp; microemulsions; concentrates; fipronil; agrochemical composition
Prior art date: 2005-07-27

Application number

MX2008001116A

Other languages

English (en)

Spanish (es)

Inventor

Wang Bing

Ma Jufa

Guo Jingquan

Tong Xianming

Richard Dickmann

Original Assignee

Bayer Cropscience Sa

Priority date (The priority date 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 date listed.)

2005-07-27

Filing date

2006-07-14

Publication date

2008-03-13

2006-07-14 Application filed by Bayer Cropscience Sa filed Critical Bayer Cropscience Sa

2008-03-13 Publication of MX2008001116A publication Critical patent/MX2008001116A/es

Links

239000004530 micro-emulsion Substances 0.000 title claims abstract description 41
239000012141 concentrate Substances 0.000 title claims abstract description 28
ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 title claims abstract description 17
239000005899 Fipronil Substances 0.000 title claims abstract description 15
229940013764 fipronil Drugs 0.000 title claims abstract description 15
239000004480 active ingredient Substances 0.000 claims abstract description 8
239000003945 anionic surfactant Substances 0.000 claims abstract description 8
239000002736 nonionic surfactant Substances 0.000 claims abstract description 7
-1 alkyl ether sulphates Chemical class 0.000 claims description 91
239000000203 mixture Substances 0.000 claims description 48
125000000217 alkyl group Chemical group 0.000 claims description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
125000002947 alkylene group Chemical group 0.000 claims description 13
230000000749 insecticidal effect Effects 0.000 claims description 13
239000000654 additive Substances 0.000 claims description 12
229930195733 hydrocarbon Natural products 0.000 claims description 12
239000007921 spray Substances 0.000 claims description 11
239000004215 Carbon black (E152) Substances 0.000 claims description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
229910019142 PO4 Inorganic materials 0.000 claims description 9
235000021317 phosphate Nutrition 0.000 claims description 9
229920000151 polyglycol Polymers 0.000 claims description 9
239000010695 polyglycol Substances 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 8
125000002877 alkyl aryl group Chemical group 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
239000003921 oil Substances 0.000 claims description 6
229920001400 block copolymer Polymers 0.000 claims description 4
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 4
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 4
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 claims description 4
239000005946 Cypermethrin Substances 0.000 claims description 3
239000005892 Deltamethrin Substances 0.000 claims description 3
239000005906 Imidacloprid Substances 0.000 claims description 3
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 3
229960002587 amitraz Drugs 0.000 claims description 3
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims description 3
229960005424 cypermethrin Drugs 0.000 claims description 3
229960002483 decamethrin Drugs 0.000 claims description 3
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 3
229940056881 imidacloprid Drugs 0.000 claims description 3
YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims description 3
125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 claims description 3
150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 2
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims description 2
150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
238000007865 diluting Methods 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
229920000233 poly(alkylene oxides) Polymers 0.000 claims description 2
239000012872 agrochemical composition Substances 0.000 claims 8
238000004519 manufacturing process Methods 0.000 claims 2
150000008051 alkyl sulfates Chemical class 0.000 claims 1
239000010452 phosphate Substances 0.000 claims 1
239000003960 organic solvent Substances 0.000 abstract description 2
150000003254 radicals Chemical class 0.000 description 24
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 15
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 13
125000003342 alkenyl group Chemical group 0.000 description 13
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 12
125000004432 carbon atom Chemical group C* 0.000 description 11
238000009472 formulation Methods 0.000 description 11
241000196324 Embryophyta Species 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
239000012868 active agrochemical ingredient Substances 0.000 description 9
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
239000003905 agrochemical Substances 0.000 description 8
125000000304 alkynyl group Chemical group 0.000 description 7
239000004009 herbicide Substances 0.000 description 7
125000001624 naphthyl group Chemical group 0.000 description 7
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
239000002904 solvent Substances 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
125000003545 alkoxy group Chemical group 0.000 description 6
235000010290 biphenyl Nutrition 0.000 description 6
239000004305 biphenyl Substances 0.000 description 6
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
230000000694 effects Effects 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000003337 fertilizer Substances 0.000 description 5
125000004438 haloalkoxy group Chemical group 0.000 description 5
125000001188 haloalkyl group Chemical group 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
150000002367 halogens Chemical class 0.000 description 5
230000009261 transgenic effect Effects 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
150000005840 aryl radicals Chemical class 0.000 description 4
150000001768 cations Chemical class 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
238000005516 engineering process Methods 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
125000005842 heteroatom Chemical group 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
239000000126 substance Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical class OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000256248 Spodoptera Species 0.000 description 3
125000004448 alkyl carbonyl group Chemical group 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 3
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
125000001072 heteroaryl group Chemical group 0.000 description 3
125000000623 heterocyclic group Chemical group 0.000 description 3
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
239000012669 liquid formulation Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 2
125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
125000006736 (C6-C20) aryl group Chemical group 0.000 description 2
IQVNEKKDSLOHHK-FNCQTZNRSA-N (E,E)-hydramethylnon Chemical compound N1CC(C)(C)CNC1=NN=C(/C=C/C=1C=CC(=CC=1)C(F)(F)F)\C=C\C1=CC=C(C(F)(F)F)C=C1 IQVNEKKDSLOHHK-FNCQTZNRSA-N 0.000 description 2
241001143309 Acanthoscelides obtectus Species 0.000 description 2
241000239223 Arachnida Species 0.000 description 2
241000244186 Ascaris Species 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
241000555303 Mamestra brassicae Species 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
241001671714 Nezara Species 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
241001481703 Rhipicephalus <genus> Species 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
244000062793 Sorghum vulgare Species 0.000 description 2
241001414989 Thysanoptera Species 0.000 description 2
241000243774 Trichinella Species 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
CLSVJBIHYWPGQY-UHFFFAOYSA-N [3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-yl] ethyl carbonate Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)NC11CCC(OC)CC1 CLSVJBIHYWPGQY-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
229910001413 alkali metal ion Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
229910001420 alkaline earth metal ion Inorganic materials 0.000 description 2
125000003302 alkenyloxy group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
125000004644 alkyl sulfinyl group Chemical group 0.000 description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
125000005133 alkynyloxy group Chemical group 0.000 description 2
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
229910052921 ammonium sulfate Inorganic materials 0.000 description 2
235000011130 ammonium sulphate Nutrition 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000002585 base Substances 0.000 description 2
229960001901 bioallethrin Drugs 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
244000038559 crop plants Species 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 2
239000003906 humectant Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
125000004043 oxo group Chemical group O=* 0.000 description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000011591 potassium Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
125000006413 ring segment Chemical group 0.000 description 2
239000011734 sodium Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 1
SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 1
YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 description 1
AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 description 1
RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1r,3r)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-HKUYNNGSSA-N 0.000 description 1
RLLPVAHGXHCWKJ-MJGOQNOKSA-N (3-phenoxyphenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-MJGOQNOKSA-N 0.000 description 1
XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 1
VEMKTZHHVJILDY-WOJBJXKFSA-N (5-benzylfuran-3-yl)methyl (1s,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-WOJBJXKFSA-N 0.000 description 1
CSWBSLXBXRFNST-MQQKCMAXSA-N (8e,10e)-dodeca-8,10-dien-1-ol Chemical compound C\C=C\C=C\CCCCCCCO CSWBSLXBXRFNST-MQQKCMAXSA-N 0.000 description 1
125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
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CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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PYNKFIVDSJSNGL-UHFFFAOYSA-N thiosultap Chemical compound OS(=O)(=O)SCC(N(C)C)CSS(O)(=O)=O PYNKFIVDSJSNGL-UHFFFAOYSA-N 0.000 description 1
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229940116861 trichinella britovi Drugs 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

MX2008001116A 2005-07-27 2006-07-14 Microemulsiones y concentrados que contienen fipronil. MX2008001116A (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CNA2005100879344A CN1903029A (zh)	2005-07-27	2005-07-27	微乳剂
PCT/EP2006/006904 WO2007017040A2 (fr)	2005-07-27	2006-07-14	Micro-emulsions

Publications (1)

Publication Number	Publication Date
MX2008001116A true MX2008001116A (es)	2008-03-13

Family

ID=37606900

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
MX2008001116A MX2008001116A (es)	2005-07-27	2006-07-14	Microemulsiones y concentrados que contienen fipronil.

Country Status (8)

Country	Link
EP (1)	EP1912505A2 (fr)
JP (1)	JP2009502826A (fr)
KR (1)	KR20080032225A (fr)
CN (1)	CN1903029A (fr)
BR (1)	BRPI0613908A2 (fr)
MX (1)	MX2008001116A (fr)
WO (1)	WO2007017040A2 (fr)
ZA (1)	ZA200800676B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN100433979C (zh) *	2007-01-18	2008-11-19	江苏太湖地区农业科学研究所	含氟虫腈和异丙威的杀虫组合物
AR067311A1 (es) *	2007-04-23	2009-10-07	Basf Ag	Metodo para el aumento de la productivdad de las plantas por combinacion de agentes quimicos con modificaciones transgenicas
KR101579846B1 (ko) *	2008-12-24	2015-12-24	주식회사 이엔에프테크놀로지	포토레지스트 패턴 제거용 조성물 및 이를 이용한 금속 패턴의 형성 방법
JP5590484B2 (ja) *	2009-05-25	2014-09-17	住友化学株式会社	殺虫組成物及び害虫防除方法
PE20140124A1 (es) *	2011-03-23	2014-02-06	Makhteshim Chem Works Ltd	Control sinergico de plagas agricolas
CN102428913B (zh) *	2011-11-11	2014-01-22	山东一览科技有限公司	一种微乳剂杀虫剂及其生产工艺
GB201707930D0 (en) *	2017-05-17	2017-06-28	Syngenta Participations Ag	Formulation component
CN109169644A (zh) *	2018-09-07	2019-01-11	东北农业大学	一种艾蒿微乳剂及其制备方法
MX2023004876A (es) *	2020-10-27	2023-05-11	Basf Se	Composiciones de microemulsion de plaguicidas.

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2119274A5 (en) *	1970-12-21	1972-08-04	Melle Bezons	Surfactants for microemulsions - contg a sulphocpd olein and an ethanolamine
IL116148A (en) *	1994-11-30	2001-03-19	Rhone Poulenc Agrochimie	Complexible composition for insect control
CN1308862A (zh) *	2000-02-16	2001-08-22	四川省农业科学院植物保护研究所	防治稻秆潜蝇等虫害的杀虫剂
DE10258867A1 (de) *	2002-12-17	2004-07-08	Bayer Cropscience Gmbh	Mikroemulsionskonzentrate
CN1225978C (zh) *	2003-11-03	2005-11-09	浙江新农化工有限公司	含三唑磷和氟虫腈复配杀虫微乳剂及其制备方法
US7531186B2 (en) *	2003-12-17	2009-05-12	Merial Limited	Topical formulations comprising 1-N-arylpyrazole derivatives and amitraz

2005
- 2005-07-27 CN CNA2005100879344A patent/CN1903029A/zh active Pending
2006
- 2006-07-14 EP EP06754725A patent/EP1912505A2/fr not_active Withdrawn
- 2006-07-14 JP JP2008523177A patent/JP2009502826A/ja not_active Withdrawn
- 2006-07-14 BR BRPI0613908-6A patent/BRPI0613908A2/pt not_active Application Discontinuation
- 2006-07-14 KR KR1020087004365A patent/KR20080032225A/ko not_active Withdrawn
- 2006-07-14 MX MX2008001116A patent/MX2008001116A/es unknown
- 2006-07-14 WO PCT/EP2006/006904 patent/WO2007017040A2/fr not_active Ceased
2008
- 2008-01-23 ZA ZA200800676A patent/ZA200800676B/xx unknown

Also Published As

Publication number	Publication date
EP1912505A2 (fr)	2008-04-23
WO2007017040A2 (fr)	2007-02-15
ZA200800676B (en)	2009-05-27
WO2007017040A3 (fr)	2007-12-06
KR20080032225A (ko)	2008-04-14
JP2009502826A (ja)	2009-01-29
CN1903029A (zh)	2007-01-31
BRPI0613908A2 (pt)	2011-02-15

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