AR080350A1 - Mezclas de compuestos plaguicidas - Google Patents
Mezclas de compuestos plaguicidasInfo
- Publication number
- AR080350A1 AR080350A1 ARP100104843A ARP100104843A AR080350A1 AR 080350 A1 AR080350 A1 AR 080350A1 AR P100104843 A ARP100104843 A AR P100104843A AR P100104843 A ARP100104843 A AR P100104843A AR 080350 A1 AR080350 A1 AR 080350A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- carboxamide
- copper
- pyrazol
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 11
- 239000000203 mixture Substances 0.000 title abstract 7
- -1 etirimol Chemical compound 0.000 abstract 27
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 10
- 239000003112 inhibitor Substances 0.000 abstract 10
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 6
- 239000011717 all-trans-retinol Substances 0.000 abstract 5
- 235000019169 all-trans-retinol Nutrition 0.000 abstract 5
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- 239000011575 calcium Substances 0.000 abstract 4
- 229910052791 calcium Inorganic materials 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 239000011593 sulfur Substances 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 238000003786 synthesis reaction Methods 0.000 abstract 4
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 3
- 239000005766 Dodine Substances 0.000 abstract 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 3
- 230000015572 biosynthetic process Effects 0.000 abstract 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 238000002360 preparation method Methods 0.000 abstract 3
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 abstract 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 abstract 2
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 abstract 2
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 abstract 2
- JZRXHLPCGMDOOT-UHFFFAOYSA-N 3-(difluoromethyl)-n-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1OC(F)(F)C(F)C(F)(F)F JZRXHLPCGMDOOT-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 2
- 239000005745 Captan Substances 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 2
- 239000005750 Copper hydroxide Substances 0.000 abstract 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 2
- 239000005751 Copper oxide Substances 0.000 abstract 2
- 239000005752 Copper oxychloride Substances 0.000 abstract 2
- 239000005764 Dithianon Substances 0.000 abstract 2
- 239000005789 Folpet Substances 0.000 abstract 2
- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 abstract 2
- 239000005797 Iprovalicarb Substances 0.000 abstract 2
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 abstract 2
- 239000005802 Mancozeb Substances 0.000 abstract 2
- 239000005807 Metalaxyl Substances 0.000 abstract 2
- 239000005809 Metiram Substances 0.000 abstract 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 abstract 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 abstract 2
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 229930182764 Polyoxin Natural products 0.000 abstract 2
- 239000005821 Propamocarb Substances 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- JARYYMUOCXVXNK-UHFFFAOYSA-N Validamycin A Natural products OC1C(O)C(OC2C(C(O)C(O)C(CO)O2)O)C(CO)CC1NC1C=C(CO)C(O)C(O)C1O JARYYMUOCXVXNK-UHFFFAOYSA-N 0.000 abstract 2
- 239000005860 Valifenalate Substances 0.000 abstract 2
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 abstract 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 abstract 2
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 abstract 2
- 229940117949 captan Drugs 0.000 abstract 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 abstract 2
- 210000002421 cell wall Anatomy 0.000 abstract 2
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 229910001956 copper hydroxide Inorganic materials 0.000 abstract 2
- 229940120693 copper naphthenate Drugs 0.000 abstract 2
- 229910000431 copper oxide Inorganic materials 0.000 abstract 2
- 229910000365 copper sulfate Inorganic materials 0.000 abstract 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 abstract 2
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 abstract 2
- 230000007123 defense Effects 0.000 abstract 2
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 abstract 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract 2
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 abstract 2
- 229960002125 enilconazole Drugs 0.000 abstract 2
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 abstract 2
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 abstract 2
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 230000001939 inductive effect Effects 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 abstract 2
- 229920000940 maneb Polymers 0.000 abstract 2
- 230000008099 melanin synthesis Effects 0.000 abstract 2
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 abstract 2
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 abstract 2
- 229920000257 metiram Polymers 0.000 abstract 2
- HQUIFHINFGFWLJ-UHFFFAOYSA-N n-[(cyclopropylmethoxyamino)-[6-(difluoromethoxy)-2,3-difluorophenyl]methylidene]-2-phenylacetamide Chemical compound FC(F)OC1=CC=C(F)C(F)=C1C(NOCC1CC1)=NC(=O)CC1=CC=CC=C1 HQUIFHINFGFWLJ-UHFFFAOYSA-N 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 2
- JGCSKOVQDXEQHI-UHFFFAOYSA-N phenazine-1-carboxylic acid Chemical compound C1=CC=C2N=C3C(C(=O)O)=CC=CC3=NC2=C1 JGCSKOVQDXEQHI-UHFFFAOYSA-N 0.000 abstract 2
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 abstract 2
- 229920001021 polysulfide Polymers 0.000 abstract 2
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 abstract 2
- WTFXJFJYEJZMFO-UHFFFAOYSA-N propamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCOC1=CC=C(C(N)=N)C=C1 WTFXJFJYEJZMFO-UHFFFAOYSA-N 0.000 abstract 2
- 229960003761 propamidine Drugs 0.000 abstract 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 abstract 2
- 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 abstract 2
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 abstract 2
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 abstract 2
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 abstract 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 abstract 1
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 abstract 1
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 abstract 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 abstract 1
- URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 abstract 1
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 abstract 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 abstract 1
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 abstract 1
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 abstract 1
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 abstract 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 abstract 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 abstract 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 abstract 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 abstract 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 abstract 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 abstract 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 abstract 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 abstract 1
- ULCWZQJLFZEXCS-UHFFFAOYSA-N 1-[[2-(2,4-dichlorophenyl)-5-(2,2,2-trifluoroethoxy)oxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1C(OCC(F)(F)F)CCC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-UHFFFAOYSA-N 0.000 abstract 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 abstract 1
- WXDAGKGYVTVWAE-UHFFFAOYSA-N 1-methyl-n-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound FC(F)(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1OC(F)(F)C(F)F WXDAGKGYVTVWAE-UHFFFAOYSA-N 0.000 abstract 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 abstract 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 abstract 1
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- VZDKLOXSCIENND-UHFFFAOYSA-L n,n-dimethylcarbamothioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([O-])=S.CN(C)C([O-])=S VZDKLOXSCIENND-UHFFFAOYSA-L 0.000 abstract 1
- MEWYBGBLQURRNP-UHFFFAOYSA-N n-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide Chemical compound C1C(C)(C)CC(CC)(C)CC1NC(=O)C1=CC=CC(NC=O)=C1O MEWYBGBLQURRNP-UHFFFAOYSA-N 0.000 abstract 1
- GCIZLUZYQSYVSS-UHFFFAOYSA-N n-[(5-bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide Chemical compound ClC1=CC=NC(Cl)=C1C(=O)NCC1=NC=C(Br)C=C1Cl GCIZLUZYQSYVSS-UHFFFAOYSA-N 0.000 abstract 1
- AHJKPWGTBVOQFA-JOCHJYFZSA-N n-methyl-2-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]piperidin-4-yl]-n-[(1r)-1,2,3,4-tetrahydronaphthalen-1-yl]-1,3-thiazole-4-carboxamide Chemical compound CN([C@H]1C2=CC=CC=C2CCC1)C(=O)C(N=1)=CSC=1C(CC1)CCN1C(=O)CN1N=C(C(F)(F)F)C=C1C AHJKPWGTBVOQFA-JOCHJYFZSA-N 0.000 abstract 1
- OZGNYLLQHRPOBR-DHZHZOJOSA-N naftifine Chemical compound C=1C=CC2=CC=CC=C2C=1CN(C)C\C=C\C1=CC=CC=C1 OZGNYLLQHRPOBR-DHZHZOJOSA-N 0.000 abstract 1
- 229960004313 naftifine Drugs 0.000 abstract 1
- 235000010298 natamycin Nutrition 0.000 abstract 1
- 239000004311 natamycin Substances 0.000 abstract 1
- 229960003255 natamycin Drugs 0.000 abstract 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 abstract 1
- 230000001069 nematicidal effect Effects 0.000 abstract 1
- 235000005152 nicotinamide Nutrition 0.000 abstract 1
- 239000011570 nicotinamide Substances 0.000 abstract 1
- 102000039446 nucleic acids Human genes 0.000 abstract 1
- 108020004707 nucleic acids Proteins 0.000 abstract 1
- 150000007523 nucleic acids Chemical class 0.000 abstract 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 abstract 1
- 235000010292 orthophenyl phenol Nutrition 0.000 abstract 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 abstract 1
- 229960000321 oxolinic acid Drugs 0.000 abstract 1
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical compound NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 abstract 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 abstract 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 abstract 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 abstract 1
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 abstract 1
- 229960002132 pyrrolnitrin Drugs 0.000 abstract 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 abstract 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 abstract 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 abstract 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 abstract 1
- 229960002722 terbinafine Drugs 0.000 abstract 1
- 239000004308 thiabendazole Substances 0.000 abstract 1
- 235000010296 thiabendazole Nutrition 0.000 abstract 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 abstract 1
- 229960004546 thiabendazole Drugs 0.000 abstract 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 abstract 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 abstract 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 abstract 1
- 230000014616 translation Effects 0.000 abstract 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 abstract 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 abstract 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 abstract 1
- 229960004740 voriconazole Drugs 0.000 abstract 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 abstract 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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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)
Abstract
La presente se refiere a composiciones de plaguicidas que comprenden como componente A: transflutrina, como componente B: un componente fungicida, que muestran, sorprendentemente, actividades insecticidas, acaricidas, nematicidas y fungicidas. En particular, estas composiciones son adecuadas para el tratamiento de semillas. Reivindicacion 1: Composiciones que comprenden transflutrina de la formula (1), y un compuesto seleccionado del grupo (A), que está constituido por compuestos de los siguientes subgrupos (1) a (16); (1) Inhibidores de la síntesis de ácidos nucleicos, por ejemplo benalaxilo, benalaxilo-M, bupirimato, clozilacon, dimetirimol, etirimol, furalaxilo, himexazol, metalaxilo, metalaxilo-M, ofurace, oxadixilo y ácido oxolínico, (2) Inhibidores de la mitosis y de la division celular, por ejemplo benomilo, carbendazim, clorfenazol, dietofencarb, etaboxam, fuberidazol, pencicuron, tiabendazol, tiofanato, tiofanato-metilo y zoxamida, (3) Compuestos capaces de actuar como un desacoplador, como, por ejemplo, binapacrilo, dinocap, fluazinam y meptildinocap, (4) Inhibidores de la produccion de ATP, por ejemplo acetato de fentina, cloruro de fentina, hidroxido de fentina y siltiofam, (5) Inhibidores del aminoácido y/o biosíntesis de proteínas, por ejemplo andoprim, blasticidina-S, ciprodinilo, kasugamicina, hidrato de clorhidrato de kasugamicina, mepanipirim y pirimetanilo, (6) Inhibidores de la transduccion de la senal, por ejemplo fenpiclonilo, fludioxonilo y quinoxifeno, (7) Inhibidores de la síntesis de lípidos y de membranas, por ejemplo bifenilo, clozolinato, edifenfos, etridiazol, yodocarb, iprobenfos, iprodiona, isoprotiolano, procimidona, propamocarb, clorhidrato de propamocarb, pirazofos, tolclofos-metilo y vinclozolina, (8) Inhibidores de la síntesis de paredes celulares, por ejemplo bentiavalicarb, dimetomorf, flumorf, iprovalicarb, mandipropamida, polioxinas, polioxorim, protiocarb, validamicina A, y valifenalato, (9) Inhibidores de la biosíntesis de melanina, por ejemplo carpropamida, diciclomet, fenoxanilo, ftalida, piroquilon y triciclazol, (10) Compuestos capaces de inducir una defensa en el huésped, como, por ejemplo, acibenzolar-S-metilo, probenazol y tiadinilo, (11) Compuestos capaces de tener una accion multisitio, como por ejemplo caldo bordelés, captafol, captan, clorotalonilo, naftenato de cobre, oxido de cobre, oxicloruro de cobre, preparaciones de cobre tales como hidroxido de cobre, sulfato de cobre, diclofluanida, ditianon, dodina, base libre de dodina, ferbam, fluorofolpet, folpet, guazatina, acetato de guazatina, iminoctadina, albesilato de iminoctadina, triacetato de iminoctadina, mancobre, mancozeb, maneb, metiram, metiram cinc, oxina-cobre, propamidina, propineb, azufre y preparaciones de azufre incluyendo calcio, polisulfuro de calcio, tiram, tolilfluanida, zineb y ziram, inhibidores de la biosíntesis de ergosterol, por ejemplo aldimorf, azaconazol, bitertanol, bromuconazol, ciproconazol, diclobutrazol, difenoconazol, diniconazol, diniconazol-M, dodemorf, acetato de dodemorf, epoxiconazol, etaconazol, fenarimol, fenbuconazol, fenhexamida, fenpropidina, fenpropimorf, fluquinconazol, flurprimidol, flusilazol, flutriafol, furconazol, furconazol-cis, hexaconazol, imazalil, sulfato de imazalilo imibenconazol, ipconazol, metconazol, miclobutanilo, naftifina, nuarimol, oxpoconazol, paclobutrazol, pefurazoato, penconazol, piperalina, procloraz, propiconazol, protioconazol, piributicarb, pirifenox, quinconazol, simeconazol, espiroxamina, tebuconazol, terbinafina, tetraconazol, triadimefon, triadimenol, tridemorf, triflumizol, triforina, triticonazol, uniconazol, viniconazol y voriconazol, (12) Inhibidores de la síntesis de paredes celulares, por ejemplo, bentiavalicarb, dimetomorf, flumorf, iprovalicarb, mandipropamida, polioxinas, polioxorim, protiocarb, validamicina A, y valifenalato, (13) Inhibidores de la biosíntesis de melanina, por ejemplo carpropamid, diclocimet, fenoxanilo, ftalida, piroquilon y triciclazol, (14) Compuestos capaces de inducir una defensa en el huésped, como, por ejemplo, acibenzolar-S-metilo, probenazol y tiadinilo, (15) Compuestos capaces de tener una accion de multisitio, por ejemplo caldo bordelés, captafol, captan, clorotalonilo, naftenato de cobre, oxido de cobre, oxicloruro de cobre, preparaciones de cobre tales como hidroxido de cobre, sulfato de cobre, diclofluanida, ditianon, dodina, base libre de dodina, ferbam, fluorofolpet, folpet, guazatina, acetato de guazatina, iminoctadina, albesilato de iminoctadina, triacetato de iminoctadina, mancobre, mancozeb, maneb, metiram, metiram cinc, oxina-cobre, propamidina, propineb, azufre y preparaciones de azufre incluyendo polisulfuro de calcio, tiram, tolilfluanida, zineb y ziram, (16) Compuestos adicionales seleccionados de: 2,3-dibutil-6-clorotieno[2,3-d]pirimidin-4(3H)-ona, (2Z)-3-amino-2-ciano-3-fenilprop-2-enoato de etilo, N-[2-(1,3-dimetilbutil)fenil]-5-fluoro-1,3-dimetil-1H-pirazol-4-carboxamida, 3-(difluorometil)-1-metil-N-(3',4',5'-trifluorobifenil-2-il)-1 H-pirazol-4-carboxamida, 3-(difluorometil)-N-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxi)fenil]-1-metil-1H-pirazol-4-carboxamida, (2E)-2-(2-{[6-(3-cloro-2-metilfenoxi)-5-fluoropirimidin- 4-il]oxi}fenil)-2-(metoxiimino)-N-metiletanamida, (2E)-2-{2-[({[(2E,3E)-4-(2,6-diclorofenil)but-3-en-2-ilideno]amino}oxi)metil]fenil}-2-(metoxiimino)-N-metiletanamida, 2-cloro-N-(1,1,3-trimetil-2,3-dihidro-1H-inden-4-iI)piridina-3-carboxamida, N-(3-etil-3,5,5-trimetilciclohexil)-3-(formilamino)-2-hidroxibenzamida, 5-metoxi-2-metil-4-(2-{[({(1E)-1-[3-(trifluorometil)fenil]etilideno}amino)oxi]metil}fenil)-2,4-dihidro-3H-1,2,4-triazol-3-ona, (2E)-2-(metoxiimino)-N-metil-2-(2-{[({(1E)-1-[3-(trifluorometil)fenil]etilideno}amino)oxi]metil}fenil)etanamida, (2E)-2-(metoxiimino)-N-metil-2-{2-[(E)-({1-[3-(trifluorometil)fenil]etoxi}imino)metil]fenil}etanamida, (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-feniletenil]oxi}fenil)etilideno]amino}oxi)metil]fenil}-2-(metoxiimino)-N-metiletanamida, 1-(4-clorofenil)-2-(1H-1,2,4-triazol-1-il)cicloheptanol, 1-(2,2-dimetil-2,3-dihidro-1H-inden-1-il)-1H-imidazol-5-carboxilato de metilo, N-etil-N-metil-N'-{2-metil-5-(trifluorometil)-4-[3-(trimetilsilil)propoxi]fenil}imidoformamida, N'-{5-(difluorometil)-2-metil-4-[3-(trimetilsilil)propoxi]fenil}-N-etil-N-metilimidoformamida, O-{1-[(4- metoxifenoxi)metil]-2,2-dimetilpropil} 1H-imidazol-1-carbotioato, N-[2-(4-{[3-(4-clorofenil)prop-2-in-1-il]oxi}-3-metoxifenil)etil]-N2-(metilsulfonil)valinamida, 5-cloro-7-(4-metilpiperidin-1-il)-6-(2,4,6-trifluorofenil)[1,2,4]triazolo[1,5-a]pirimidina, 5-amino-1,3,4-tiadiazol-2-tiol, propamocarb-fosetil, 1-[(4-metoxifenoxi)metil]-2,2-dimetilpropil-1H-imidazol-1-carboxilato, 1-metil-N-[2-(1,1,2,2-tetrafluoroetoxi)fenil]-3-(trifluorometil)-1H-pirazol-4-carboxamida, 2,3,5,6-tetracloro-4-(metilsulfonil)piridina, 2-butoxi-6-yodo-3-propil-4H-cromen-4-ona, 2-fenilfenol y sales, 3-(difluorometil)-1-metil-N-[2-(1,1,2,2-tetrafluoroetoxi)fenil]-1H-pirazol-4-carboxamida, 3,4,5-tricloropiridina-2,6-dicarbonitrilo, 3-[5-(4-clorofenil)2,3-dimetilisoxazolidin-3-iI]piridina, 3-cloro-5-(4-clorofenil)-4-(2,6-difluorofenil)-6-metilpiridazina, 4-(4-clorofenil-5-(2,6-difluorofenil)-3,6-dimetilpiridazina, quinolin-8-ol, sulfato de quinolin-8-ol (2:1) (sal), tebufloquina, 5-metil-6-octil-3,7-dihidro[1,2,4]triazolo[1,5-a]pirimidin-7-amina, 5-etil-6-octil-3,7-dihidro[1,2,4]triazoIo[1,5-a]pirimidin-7-amina, ametoctradina, bentiazol, betoxazina, capsimicina, carvona, cinometionat, cloroneb, cufraneb, ciflufenamid, cimoxanilo, ciprosulfamida, dazomet, debacarb, diclorofeno, diclomezina, dicloran, difenzoquat, difenzoquat metilsulfato, difenilamina, ecomato, ferimzone, flumetover, fluopicolida, fluoroimida, flusulfamida, flutianilo, fosetil-aluminio, fosetil-calcio, fosetil-sodio, hexaclorobenceno, irumamicina, isotianilo, metasulfocarb, metoxiacrilato de (2E)-2-{2-[({ciclopropil[(4-metoxifenil)imino]metil}tio)metil]fenil}-3-fenilo, isotioacetato de metilo, metrafenona, (5-cloro-2-metoxi-4-metilpiridin-3-il)(2,3,4-trimetoxi-6-metilfenil)metanona, mildiomicina, tolnifanida, N-(4-clorobencil)-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, N-[(4-clorofenil)(ciano)metil]-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, N-[(5-bromo-3-cloropiridin-2-il)metil]-2,4-dicloropiridina-3-carboxamida, N[1-(5-bromo-3-cloropiridin-2-iI)etil]-2,4-dicloropiridina-3-carboxamida, N-[1-(5-bromo-3-cloropiridin-2-il)etil]-2-fluoro-4-yodopiridina-3-carboxamida, N-{(Z)-[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, N-{(E)-[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, natamicina, dimetiltiocarbamato de níquel, nitrotal-isopropilo, octilinona, oxamocarb, oxifentiina, pentaclorofenol y sales, ácido fenazina-1-carboxílico, fenotrina, ácido fosforico y sus sales, fosetilato de propamocarb, propanosina-sodio, proquinazid, pirrolnitrina, quintozeno, 5-amino-2-(1-metiletil)-4-(2-metilfenil)-3-oxo-2,3-dihidro-1 H-pirazol-1-carbotioato de S-prop-2-en-1-ilo, tecloftalam, tecnazeno, triazoxida, triclamida, 5-cloro-N'-fenil-N'-prop-2-in-1-iltiofeno-2-sulfonohidrazida, zarilamida, N-metil-2-(1-{[5-metil-3-(trifluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-N-[(1R)-1,2,3,4-tetrahidronaftalen-1-il]-1,3-tiazol-4-carboxamida, N-metil-2-(1-{[5-metil-3-(trifluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-N-(1,2,3,4-tetrahidronaftalen-1-il)-1,3-tiazol-4-carboxamida, 3-(difluorometil)-N-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxi)fenil]-1-metil-1H-pirazol-4-carboxamida y {6-[({[(1-metil-1H-tetrazol- 5-il)(fenil)metilideno]amino}oxi)metil]piridin-2-iI}carbamato de pentilo. Reivindicacion 2: Composicion de acuerdo con la reivindicacion 1, en la que el compuesto del grupo (A) es fludioxonilo. Reivindicacion 3: Composicion de acuerdo con la reivindicacion 1, en la que el compuesto del grupo (A) es metalaxilo. Reivindicacion 4: Composicion de
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| Application Number | Priority Date | Filing Date | Title |
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| EP09180534 | 2009-12-23 | ||
| US29038209P | 2009-12-28 | 2009-12-28 |
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| Publication Number | Publication Date |
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| AR080350A1 true AR080350A1 (es) | 2012-04-04 |
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| Application Number | Title | Priority Date | Filing Date |
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| ARP100104843A AR080350A1 (es) | 2009-12-23 | 2010-12-21 | Mezclas de compuestos plaguicidas |
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| Country | Link |
|---|---|
| US (1) | US20110152079A1 (es) |
| AR (1) | AR080350A1 (es) |
| WO (1) | WO2011076726A2 (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103027058A (zh) * | 2011-10-08 | 2013-04-10 | 安徽众邦生物工程有限公司 | 一种防治水稻病害的杀菌剂组合物 |
| JP5873298B2 (ja) * | 2011-11-04 | 2016-03-01 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 移植稲の病害防除方法 |
| CN103125504B (zh) * | 2011-11-28 | 2014-02-26 | 深圳诺普信农化股份有限公司 | 一种含有噻酰菌胺的杀菌组合物 |
| CN102771485A (zh) * | 2012-07-02 | 2012-11-14 | 南通帝星化工有限公司 | 精甲霜灵和霜霉威盐酸盐和噁草酮复合乳油 |
| CN103053530B (zh) * | 2013-01-06 | 2014-09-17 | 广东中迅农科股份有限公司 | 丙烷脒和氟啶胺的杀菌组合物 |
| CN103109814A (zh) * | 2013-03-04 | 2013-05-22 | 中化蓝天集团有限公司 | 一种含咯菌腈和氟啶胺的防病悬浮种衣剂 |
| CN103190432B (zh) * | 2013-03-19 | 2014-06-04 | 本溪经济开发区壮苗科技开发有限公司 | 一种杀菌剂的组合物 |
| CN103168781B (zh) * | 2013-03-26 | 2015-01-07 | 河北省农林科学院植物保护研究所 | 一种含氟吡菌胺和咯菌腈的复配杀菌剂及其应用 |
| CN103416402B (zh) * | 2013-07-22 | 2015-08-19 | 杨凌农科大无公害农药研究服务中心 | 一种丙烷脒水分散粒剂及其制备方法 |
| CN104705319A (zh) * | 2013-12-12 | 2015-06-17 | 南京华洲药业有限公司 | 一种含戊菌唑和苯噻菌胺的杀菌组合物及其应用 |
| CN104705320A (zh) * | 2013-12-12 | 2015-06-17 | 南京华洲药业有限公司 | 一种含戊菌唑和霜霉威的杀菌组合物及其应用 |
| CN105724398B (zh) * | 2014-12-11 | 2018-12-14 | 沈阳中化农药化工研发有限公司 | 一种杀真菌组合物及其应用 |
| CN104839180B (zh) * | 2015-01-12 | 2017-01-18 | 四川利尔作物科学有限公司 | 杀菌组合物及其应用 |
| CN111393227B (zh) * | 2020-04-08 | 2022-07-08 | 黑龙江八一农垦大学 | 一种种衣剂 |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
| US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
| US4339456A (en) | 1980-01-14 | 1982-07-13 | Gustafson, Inc. | Peanut seed treating |
| US4383391A (en) | 1981-09-21 | 1983-05-17 | Celanese Corporation | Seed coating composition based on carbamate pesticide and non-alkaline amorphous carbon |
| US4634587A (en) | 1982-07-09 | 1987-01-06 | Key Pharmaceuticals, Inc. | Sustained release quinidine dosage form |
| US4465017A (en) | 1983-03-09 | 1984-08-14 | Simmons John J | Seed coating machine |
| US4735015A (en) | 1983-11-25 | 1988-04-05 | Basf Corporation | Seed protective coating |
| DE3616010A1 (de) | 1986-05-13 | 1987-11-19 | Bayer Ag | Verfahren zum beizen und/oder inkrustieren von saatgutkoernern |
| DE3705224A1 (de) * | 1987-02-19 | 1988-09-01 | Bayer Ag | (+)1r-trans-2,2-dimethyl-3-(2,2-dichlorvinyl) -cyclopropancarbonsaeure-2,3,5,6- tetrafluorbenzylester |
| US4808430A (en) | 1987-02-27 | 1989-02-28 | Yazaki Corporation | Method of applying gel coating to plant seeds |
| FR2618041B1 (fr) | 1987-07-16 | 1991-06-21 | Ceres Ets | Dispositif pour le traitement des semences |
| JPH0646887B2 (ja) | 1988-11-08 | 1994-06-22 | 矢崎総業株式会社 | 種子のゲル被覆装置 |
| US5300127A (en) | 1989-01-06 | 1994-04-05 | Agricultural Genetics Company Limited | Seed coatings |
| EP0539588A1 (en) | 1990-07-05 | 1993-05-05 | Nippon Soda Co., Ltd. | Amine derivative |
| DE69206993T2 (de) | 1991-07-19 | 1996-05-30 | Uniroyal Chem Co Inc | Zusammensetzungen zur verwendung von filmen auf saatgut |
| SK44894A3 (en) | 1991-10-18 | 1995-04-12 | Monsanto Co | Trisubstituted aromatic compounds, method of their preparation and fungicidal agents |
| FI93687C (fi) | 1992-07-29 | 1995-05-26 | Novasso Oy | Menetelmä siementen päällystämiseksi |
| US5661103A (en) | 1992-11-05 | 1997-08-26 | Donlar Corporation | Seed treatment composition and method |
| US5882713A (en) | 1994-04-26 | 1999-03-16 | The United States Of America As Represented By The Secretary Of Agriculture | Non-separable compositions of starch and water-immiscible organic materials |
| US5580544A (en) | 1995-03-29 | 1996-12-03 | Uniroyal Chemical Company, Inc. | Paste formulation useful for seed treatment and foliar treatment of plants |
| JP3125847B2 (ja) | 1995-06-15 | 2001-01-22 | 矢崎総業株式会社 | ゲル被覆種子のゲル層易崩壊処理方法 |
| US5622003A (en) | 1995-07-11 | 1997-04-22 | Isp Investments Inc. | Seed coating containing Mn (NO3)2 ·6H2 O |
| US5849320A (en) | 1996-06-13 | 1998-12-15 | Novartis Corporation | Insecticidal seed coating |
| US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
| US5939356A (en) | 1996-06-21 | 1999-08-17 | Southwest Research Institute | Controlled release coated agricultural products |
| JP3185133B2 (ja) | 1997-02-13 | 2001-07-09 | タキイ種苗株式会社 | 造粒コーティング種子およびその製造方法 |
| US5891246A (en) | 1997-08-15 | 1999-04-06 | Gustafson, Inc. | Seed coating apparatus |
| WO1999055668A1 (en) | 1998-04-27 | 1999-11-04 | Kumiai Chemical Industry Co., Ltd. | 3-arylphenyl sulfide derivatives and insecticides and miticides |
| US6503904B2 (en) | 1998-11-16 | 2003-01-07 | Syngenta Crop Protection, Inc. | Pesticidal composition for seed treatment |
| RU15525U1 (ru) | 2000-07-04 | 2000-10-20 | Федеральный научно-производственный центр закрытое акционерное общество "Научно-производственный концерн (объединение) "ЭНЕРГИЯ" | Электродвигатель постоянного тока |
| US6660690B2 (en) | 2000-10-06 | 2003-12-09 | Monsanto Technology, L.L.C. | Seed treatment with combinations of insecticides |
| US20020134012A1 (en) | 2001-03-21 | 2002-09-26 | Monsanto Technology, L.L.C. | Method of controlling the release of agricultural active ingredients from treated plant seeds |
| DE102005008021A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
| TWI398433B (zh) | 2006-02-10 | 2013-06-11 | Dow Agrosciences Llc | 殺蟲性之n-取代(6-鹵烷基吡啶-3-基)烷基磺醯亞胺 |
| DE102006015470A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015468A1 (de) * | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015467A1 (de) * | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| TWI381811B (zh) | 2006-06-23 | 2013-01-11 | Dow Agrosciences Llc | 用以防治可抵抗一般殺蟲劑之昆蟲的方法 |
-
2010
- 2010-12-20 WO PCT/EP2010/070221 patent/WO2011076726A2/en not_active Ceased
- 2010-12-21 AR ARP100104843A patent/AR080350A1/es unknown
- 2010-12-21 US US12/974,888 patent/US20110152079A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20110152079A1 (en) | 2011-06-23 |
| WO2011076726A2 (en) | 2011-06-30 |
| WO2011076726A3 (en) | 2011-11-17 |
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