ES2226778T3 - Combinaciones de productos activos fungicidas. - Google Patents
Combinaciones de productos activos fungicidas.Info
- Publication number
- ES2226778T3 ES2226778T3 ES00903619T ES00903619T ES2226778T3 ES 2226778 T3 ES2226778 T3 ES 2226778T3 ES 00903619 T ES00903619 T ES 00903619T ES 00903619 T ES00903619 T ES 00903619T ES 2226778 T3 ES2226778 T3 ES 2226778T3
- Authority
- ES
- Spain
- Prior art keywords
- combinations
- active
- formula
- active products
- methyl
- 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.)
- Expired - Lifetime
Links
- 239000000417 fungicide Substances 0.000 title claims description 9
- 230000000855 fungicidal effect Effects 0.000 title description 11
- 239000005774 Fenamidone Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 claims abstract description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical class CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 claims abstract description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000460 chlorine Substances 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 241000233866 Fungi Species 0.000 claims description 5
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- -1 Fencaramide Chemical compound 0.000 description 38
- 230000000694 effects Effects 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 10
- 238000009472 formulation Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000005660 Abamectin Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000005780 Fluazinam Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241001281803 Plasmopara viticola Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000000642 acaricide Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 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 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-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
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 229960003887 dichlorophen Drugs 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 2
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 2
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 229930195733 hydrocarbon Chemical class 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 description 2
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 description 2
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 2
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 2
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 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 description 2
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 2
- 229960004295 valine Drugs 0.000 description 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 description 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 description 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 description 1
- OTLLEIBWKHEHGU-TUNUFRSWSA-N (2R,3S,4S,5S)-2-[(2R,3R,4R,5S,6R)-5-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy]-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxyhexanedioic acid Chemical compound C([C@H]1O[C@H]([C@@H]([C@@H]1O)O)N1C=2N=CN=C(C=2N=C1)N)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]([C@H](O)[C@H](OP(O)(O)=O)[C@H](O)C(O)=O)C(O)=O)[C@H](O)[C@H]1O OTLLEIBWKHEHGU-TUNUFRSWSA-N 0.000 description 1
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- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 1
- FSJYRLHKLVGCNH-UHFFFAOYSA-N (3-tert-butylphenyl) n-methylcarbamate Chemical compound CNC(=O)OC1=CC=CC(C(C)(C)C)=C1 FSJYRLHKLVGCNH-UHFFFAOYSA-N 0.000 description 1
- YSEUOPNOQRVVDY-OGEJUEGTSA-N (5-benzylfuran-3-yl)methyl (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 YSEUOPNOQRVVDY-OGEJUEGTSA-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
- 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 description 1
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- 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 description 1
- PCKNFPQPGUWFHO-SXBRIOAWSA-N (Z)-flucycloxuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1)=CC=C1CO\N=C(C=1C=CC(Cl)=CC=1)\C1CC1 PCKNFPQPGUWFHO-SXBRIOAWSA-N 0.000 description 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 description 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 description 1
- RURQAJURNPMSSK-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3-{[2-(4-ethoxyphenyl)-3,3,3-trifluoropropoxy]methyl}benzene Chemical compound C1=CC(OCC)=CC=C1C(C(F)(F)F)COCC1=CC=CC(OC=2C=CC(Cl)=CC=2)=C1 RURQAJURNPMSSK-UHFFFAOYSA-N 0.000 description 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 description 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 description 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 description 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 description 1
- 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 description 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 description 1
- DELJNDWGTWHHFA-UHFFFAOYSA-N 1-azaniumylpropyl(hydroxy)phosphinate Chemical compound CCC(N)P(O)(O)=O DELJNDWGTWHHFA-UHFFFAOYSA-N 0.000 description 1
- KPNPDRFFWQBXGT-UHFFFAOYSA-N 1-dimethoxyphosphorylsulfanyl-2-ethylsulfanylethane;2-ethylsulfanylethoxy-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSCCOP(=S)(OC)OC.CCSCCSP(=O)(OC)OC KPNPDRFFWQBXGT-UHFFFAOYSA-N 0.000 description 1
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- 229960005322 streptomycin Drugs 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 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
- 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
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229940074152 thuringiensin Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-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
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 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 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 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 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 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 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 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 description 1
- 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 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 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
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
Abstract
Combinaciones de compuestos activos, que contienen al menos un derivado de valinamida de la fórmula (I) en la que R1 significa i-propilo o s-butilo y R2 significa cloro, metilo, etilo o metoxi, y Fenamidone de la fórmula (II)
Description
Combinaciones de productos activos
fungicidas.
La presente solicitud se refiere a nuevas
combinaciones de productos activos, que están constituidas por
derivados de valinamida por un lado y por Fenamidone por otro lado,
y que son adecuadas de una manera muy buena para la lucha contra los
hongos patógenos de las plantas.
Se sabe ya que los derivados de la valinamida
tienen propiedades fungicidas (véase la publicación
EP-A 472 996). La actividad de este producto es
buena; sin embargo deja que desear en algunos casos con ocasión de
cantidades de aplicación bajas.
Además se sabe ya que puede emplearse la
Fenamidone para la lucha contra los hongos (véase la publicación
EP-A 0 629 616). Sin embargo, el efecto de la
Fenamidone no es siempre satisfactorio con ocasión de cantidades de
aplicación bajas. La publicación WO 99/27788 describe composiciones
fungicidas, que contienen
2-imidazolin-5-ona y
otros fungicidas, tales como Fencaramide, que se emplea,
preferentemente, junto con Fesetyl-Al.
Se ha encontrado ahora que las nuevas
combinaciones de productos activos constituidas por derivados de
valinamida de la fórmula general (I)
en la
que
- R^{1}
- significa i-propilo o s-butilo y
- R^{2}
- significa cloro, metilo, etilo o metoxi,
y
Fenamidone de la fórmula (II)
tienen propiedades fungicidas muy
buenas.
Sorprendentemente el efecto fungicida de esta
combinación de productos activos según la invención es sensiblemente
mayor que la suma de los efectos de los productos activos
individuales. Se presenta un efecto realmente sinérgico no
previsible y no solamente un complemento de los efectos.
A partir de la fórmula estructural de los
productos activos de la fórmula (I) puede verse que los compuestos
presentan dos átomos de carbono asimétricamente substituidos. El
producto puede presentarse por lo tanto en forma de mezclas de
diversos isómeros o incluso en forma de isómeros individuales.
Los compuestos preferentes de la fórmula (I) son
los compuestos en los cuales la parte aminoácido está formada por
i-propiloxicarbonil-L-valina
o por sec.-butoxicarbonil-L-valina y
la parte fenetilamina bien es racémica o presenta la configuración
S(-), especialmente sin embargo la configuración R(+).
Compuestos de la fórmula (I) especialmente
preferentes son los compuestos en los cuales
- R^{1}
- significa i-propilo.
Especialmente pueden citarse los compuestos
[2-metil-1-[[[1-(4-clorofenil)etil]-amino]carbonil]-propil]-carbamidato
de 1-metiletilo de la fórmula (Ia)
[2-Metil-1-[[[-1-(4-metilfenil)etil]etil]amino]carbonil]-propil]-carbaminato
de 1-metiletilo de la fórmula (Ib)
[2-Metil-1-[[[-1-(4-etilfenil)etil]amino]carbonil]-propil]-carbaminato
de 1-metiletilo de la fórmula (Ic)
y
[2-metil-1-[[[-1-(4-metoxifenil)etil]amino]carbonil]-propil]-carbaminato
de 1-metiletilo de la fórmula
(Id)
y sus isómeros, tal como se ha
indicado
anteriormente.
Los productos activos de la fórmula (I) son
conocidos (véase la publicación
EP-A-472 996).
El producto fungicida, Fenamidone, presente
además en las combinaciones según la invención es igualmente
conocido (véase la publicación EP-A 0 629 616).
Las combinaciones de productos activos según la
invención contienen, además de al menos un producto activo de la
fórmula (I), Fenamidone de la fórmula (II). Además pueden contener
también otros componentes de mezcla de acción fungicida.
Cuando los productos activos están presentes en
las combinaciones de productos activos según la invención en
determinadas proporciones en peso, se muestra de manera
especialmente notable el efecto sinérgico. Sin embargo las
proporciones en peso de los productos activos pueden variar en las
combinaciones de productos activos en un intervalo relativamente
amplio. En general por una parte en peso del producto activo de la
fórmula (I) intervienen
desde 0,1 hasta 50 partes en peso,
preferentemente
desde 0,2 hasta 2 partes en peso
del producto activo de la fórmula
(II).
Las combinaciones de productos activos según la
invención tienen propiedades fungicidas muy buenas y pueden
emplearse para la lucha contra los hongos fitopatógenos, tales como
los plasmodioforomicetes, oomicetes, quitridiomicetes, cigomicetes,
ascomicetes, basidiomicetes, deuteromicetes, etc.
Las combinaciones de productos activos según la
invención son adecuadas de forma especialmente buena para la lucha
contra protectora contra Phytophthora infestans y Alternaria spec.
en tomates y patatas, así como contra Plasmopara viticola en
vides.
La buena compatibilidad con las plantas de las
combinaciones de los productos activos a las concentraciones
necesarias para la lucha contra las enfermedades de las plantas
permite un tratamiento de las partes aéreas de las plantas, de
plantones y semillas y del suelo.
Las combinaciones de productos activos pueden
transformarse en las formulaciones usuales tales como soluciones,
emulsiones, suspensiones, polvos, espumas, pastas, granulados,
aerosoles, microencapsulados en materiales polímeros y en masas de
recubrimiento para semillas así como formulaciones de volumen
ultrabajo (ULV).
Estas formulaciones se preparan de forma
conocida, por ejemplo por mezclado de los productos activos con
agentes extendedores, es decir disolventes líquidos, gases licuados
que se encuentran a presión y/o materiales de soporte sólidos, en
caso dado con empleo de agentes de superficie activa, es decir
emulsionantes y/o dispersantes y/o agentes generadores de espuma. En
el caso del empleo de agua como agente extendedor pueden emplearse
también disolventes orgánicos como disolventes auxiliares. Como
disolventes líquidos entran en consideración fundamentalmente:
hidrocarburos aromáticos, tales como xileno, tolueno o
alquilnaftalinas, hidrocarburos aromáticos clorados o hidrocarburos
alifáticos clorados. Tales como clorobencenos, cloroetileno o
cloruro de metileno, hidrocarburos alifáticos tales como ciclohexano
o parafinas, por ejemplo fracciones de petróleo, alcoholes tales
como butanol o glicol, así como éteres y ésteres, cetonas tales como
acetona, metiletilcetona, metilisobutilcetona o ciclohexanona,
disolventes fuertemente polares, tales como dimetilformamida y
dimetilsulfóxido, así como agua. Por agentes extendedores o
materiales de soporte gaseosos licuados se quieren indicar aquellos
que son gaseosos a temperatura normal y bajo presión normal, por
ejemplo gases propulsores para aerosol, tales como los hidrocarburos
halogenados así como butano, propano, nitrógeno y dióxido de
carbono. Como materiales de soporte sólidos entran en consideración,
por ejemplo, harinas minerales naturales, tales como caolines,
arcillas, talco, cretas, cuarzo, attapulgita, montmorillonita o
tierra de diatoméas y harinas minerales sintéticas, tales como ácido
silícico altamente dispersado, óxido de aluminio y silicatos. Como
materiales de soporte sólido para granulados entran en
consideración: por ejemplo minerales quebrados y fracciones tal como
calcita, mármol, pómez, sepiolita, dolomita así como granulados
sintéticos constituidos a partir de harinas inorgánicas y orgánicas
así como granulados constituidos a partir de material orgánico tales
como serrín, cáscaras de nueces de coco, panochas de maíz y tallos
de tabaco. Como agentes emulsionantes y/o generadores de espuma
entran en consideración: por ejemplo emulsionantes no iónicos y
aniónicos, tales como ésteres de ácidos grasos polioxietilenados,
por ejemplo alquilarilpoliglicoléter, alquilsulfonatos,
alquilsulfatos, arilsulfonatos, así como hidrolizados de albúmina.
Como dispersantes entran en consideración por ejemplo lejías
sulfíticas de lignina y metilcelulosa.
Pueden emplearse en las formulaciones adhesivos
tales como carboximetilcelulosa, polímeros naturales y sintéticos
pulverulentos, granulares o en forma de latex, tales como goma
arábiga, alcohol polivinílico, acetato de polivinilo así como
fosfolípidos naturales, tales como cefalina y lecitina y
fosfolípidos sintéticos. Otros aditivos pueden ser aceites minerales
y vegetales.
Pueden emplearse colorantes tales como pigmentos
inorgánicos, por ejemplo óxido de hierro, óxido de titanio, azul de
ferrocianuro y colorantes orgánicos tales como colorantes de
alizarina, azoicos y de ftalocianina metálicos y materiales
nutrientes en trazas, tales como sales de hierro, de manganeso, de
boro, de cobre, de cobalto, de molibdeno, de cinc.
Las formulaciones contienen en general entre 0,1
y 95% en peso de producto activo, preferentemente entre 0,5 y
90%.
Los productos activos de la fórmula (I) y las
combinaciones de productos activos según la invención pueden
presentarse en las formulaciones en mezclas con otros productos
activos tales como fungicidas, insecticidas, acaricidas y
herbicidas, así como en mezclas con abonos o reguladores del
crecimiento de las plantas.
Para tales mezclas entran en consideración, por
ejemplo:
2-Aminobutano;
2-anilino-4-metil-6-ciclopropilpirimidina;
2',6'-dibromo-2-metil-4'-trifluormetoxi-4'-trifluor-
metil-1,3-tiazol-5-carboxanilida; 2,6-dicloro-N-(4-trifluormetilbencil)benzaida; (E)-2-metoxiimino-N-metil-2-(2-fenoxifenil)acetamida; 8-hidroxiquinolinsulfato; metil-(E)-2-{2-[6-(2-cianofenoxi)pirimidin-4-iloxi]fenil}-3-metoxiacrilato; metil-(E)-metoxiimino [alfa-(o-toliloxi)-o-tolil]acetato; 2-fenilfenol (OPP), Aldimorph, Ampropylfos, Anilazin, Azaconazol, Benalaxyl, Benodanil, Benomyl, Binapacryl, Biphenyl, Bitertanol, Blasticidin-S, Bromuconazole, Bupirimate, Buthiobate, polisulfuro de calcio, Captafol, Captan, Carbendazim, Carboxin, Chinomethionat (Quinomethionat), Chloroneb, Chloropicrin, Chlorothalonil, Chlozolinat, Cufraneb, Cymoxanil, Cyproconazole, Cyprofuram, Dichlorophen, Diclobutrazol, Diclofuanid, Diclomezin, Dicloran, Diethofencarb, Di-fenoconazol, Dimethirimol, Dimethomorph, Diniconazol, Dinocap, Diphenylamin, Dipyrithion, Ditalimfos, Dithianon, Dodin, Drazoxolon,
metil-1,3-tiazol-5-carboxanilida; 2,6-dicloro-N-(4-trifluormetilbencil)benzaida; (E)-2-metoxiimino-N-metil-2-(2-fenoxifenil)acetamida; 8-hidroxiquinolinsulfato; metil-(E)-2-{2-[6-(2-cianofenoxi)pirimidin-4-iloxi]fenil}-3-metoxiacrilato; metil-(E)-metoxiimino [alfa-(o-toliloxi)-o-tolil]acetato; 2-fenilfenol (OPP), Aldimorph, Ampropylfos, Anilazin, Azaconazol, Benalaxyl, Benodanil, Benomyl, Binapacryl, Biphenyl, Bitertanol, Blasticidin-S, Bromuconazole, Bupirimate, Buthiobate, polisulfuro de calcio, Captafol, Captan, Carbendazim, Carboxin, Chinomethionat (Quinomethionat), Chloroneb, Chloropicrin, Chlorothalonil, Chlozolinat, Cufraneb, Cymoxanil, Cyproconazole, Cyprofuram, Dichlorophen, Diclobutrazol, Diclofuanid, Diclomezin, Dicloran, Diethofencarb, Di-fenoconazol, Dimethirimol, Dimethomorph, Diniconazol, Dinocap, Diphenylamin, Dipyrithion, Ditalimfos, Dithianon, Dodin, Drazoxolon,
Edifenphos, Epoxyconazole, Ethirimol, Etridiazol,
Fenarimol, Fenbuconazole, Fenfuram, Fenitropan, Fenpiclonil,
Fenpropidin, Fenpropimorf, Fentinacetate, Fentinhydroxyd, Ferbam,
Ferimzone, Fluazinam, Fludioxonil, Fluoromide, Fluquinconazole,
Flusilazole, Flusulfamide, Flutolanil, Flutriafol, Folpet,
Fosetyl-Aluminium, Fthalide, Fuberidazol, Furalaxil,
Furmecyclox,
Guazatine,
Hexaclorobenceno, Hexaconazol, Hymexazol,
Imazalil, Imibenconazol, Iminoctadin, Iprobenfos (IBP), Iprodion,
Isoprothiolan, Kasugamycin,
composiciones de cobre, tales como; hidróxido de
cobre, naftenato de cobre, oxicloruro de cobre, sulfato de cobre,
oxina de cobre y mezcla de Bordeux, Mancopper, Mancozeb, Maneb,
Mepanipyrim, Mepronil, Metalaxyl, Metconazol, Methasulfocarb,
Metiram, Metsulfovax, Myclobutanil,
dimetilditiocarbamato de níquel,
Nitrothal-isopropilo, Nuarimol, Ofurace, Oxadixyl,
Oxamocarb, Oxycarboxin,
Perfurazoat, Penconazol, Pencycuron, Phosdiphen,
Pimaricin, Piperalin, Polyoxin, Probenazol, Prochloraz, Procymidon,
Propamocarb, Propiconazole, Propineb, Pyrazophos, Pyrefenox,
Pyrimethanil, Pyroquilon,
Quintozen (PCNB), azufre y composiciones de
azufre, Tebuconazol, Tecloftalam, Techasen, Tetraconazol,
Thiabendazol, Thicyofen, Thiophanat-methyl, Thiram,
Tolclophos-metilo, Tolylfluanid, Triadimefon,
Triadimenol, Triazoxid, Trichlamid, Tricyclazol, Tridemorph,
Triflumizol, Triforin, Triticonazol, Validamycin A, Vinclozolin,
Zineb, Ziram.
Bronopol, Dichlorophen, Nitrapyrin,
dimetilditiocarbamato de níquel, Kasugamycin, Octhilinon, ácido
furanocarboxílico, Oxytetracyclin, Probenazol, Streptomycin,
Tecloftalam, sulfato de cobre y otras preparaciones de cobre.
Abamectin, AC 303 630, Acephat, Acrinathrin,
Alanycarb, Aldicarb, Alphamethrin, Amitraz, Avermectin, AZ 60541,
Azadirachtin, Azinphos, A, Azinphos M, Azocyclotin, Bacillus
thuringiensis, Bendiocarb, Benfuracarb, Bensultap, Betacyluthrin,
Bifenthrin, BPMC, Brofenprox, Bromophos A, Bufencarb, Buprofezin,
Butocarboxin, Butylpiridaben, Cadusafos, Carbaryl, Carbofuran,
Carbophenothion, Carbosulfan, Cartap, CGA 157 419, CGA 184699,
Chloethocarb, Chlorethoxyfos, Chloretoxyfos, Chlorfenvinphos,
Chlor-fluazuron, Chlormephos, Chlorpyrifos,
Chlorpyrifos M, Cis-Resmethrin, Clocythrin,
Clofentezin, Cyanophos, Cycloprothrin, Cyfluthrin, Cyhalothrin,
Cyhexatin, Cypermethrin, Cyromazin,
Deltamethrin, Demeton M, Demeton S,
Demeton-S-metilo, Diafenthiuron,
Diazinon, Dichlofenthion, Dichlorvos, Dicliphos, Dicrotophos,
Diethion, Diflubenzuron, Dimethoat,
Dymethylvinphos, Dioxathioin, Disulfoton,
Edifenphos, Emamectin, Esfenvalerat,
Ethiofencarb, Ethion, Ethofenprox, Ethoprophos, Etofenprox,
Etrimphos,
Fenamiphos, Fenazaquin, Fenbutatinoxid,
Fenitrothion, Fenobucarb, Fenothiocarb, Fenoxycarb, Fenpropathrin,
Fenpyrad, Fenpyroximat, Fenthion, Fenvalerate, Fipronil, Fluazinam,
Flucycloxuron, Flucythrinat, Flufenoxuron, Flufenprox, Fluvalinate,
Fonophos, Formothion, Fosthiazat, Fubfenprox, Furathiocarb,
HCH, Heptenophos, Hexaflumuron, Hexythiazox,
Imidacloprid, Iprobenfos, Isazophos, Isofenphos,
Isoprocarb, Isoxathion, Ivemectin,
Lamda-cyhalothrin, Lufenuron,
Malathion, Mecarbam, Mervinphos, Mesulfenphos,
Metaldehyd, Methacrifos, Methamidophos, Methidathion,
Methomyl, Metolcarb, Milbemectin, Monocrotophos, Moxidectin,
Methomyl, Metolcarb, Milbemectin, Monocrotophos, Moxidectin,
Naled, NC 184, NI 25, Nitenpyram
Omethoat, Oxamyl, Oxydemethon M, Oxydeprofos,
Parathion A, Parathion M, Permethrin, Phenthoat,
Phorat, Phosalon, Phosmet, Phosphamdon, Phoxim, Pirimicarb,
Pirimiphos M, Primiphos A, Profenofos, Profenophos, Promecarb,
Propaphos, Propoxur, Prothiofos, Prothiophos, Prothoat, Pymetrozin,
Pyrachlophos, Pyraclofos, Pyraclophos, Pyradaphenthion,
Pyresmethrin, Pyrethrum, Pyridaben, Pyrimidifen, Pyriproxifen,
Quinalphos.
RH 5992.
Salithion, Sebufos, Silafluofen, Sulfotep,
Sulprofos,
Tebufenozid, Tebufenpyrad, Tebupirimphos,
Teflubenzuron, Tefluthrin, Temephos, Terbam, Terbufos,
Tetrachlorvinphos, Thiafenox, Thiodicarb, Thiofanox, Thiomethon,
Thionazin, Thuringiensin, Tralomethrin, Triarathen, Triazophos,
Triazuron, Trichlorfon, Triflumuron, Trimethacarb,
Vamidothion, XMC, Xylylcarb, YI 5301/5302,
Zetamethrin.
Las combinaciones de productos activos pueden
emplearse como tales en forma de sus formulaciones o de las formas
de aplicación preparadas a partir de las anteriores, tales como
soluciones listas para su empleo, concentrados emulsionables,
emulsiones, suspensiones, polvos inyectables, polvos solubles y
granulados. El empleo se efectúa de forma usual, por ejemplo por
regado, pulverizado, empolvado, esparcido, aplicación a brocha,
macerado en seco, macerado en húmedo, macerado por remojo, macerado
en suspensión o incrustación.
Cuando se tratan partes de las plantas las
concentraciones de productos activos puede variar en las formas de
aplicación dentro de un amplio margen. Se encuentran en general
entre 1 y 0,0001% en peso, preferentemente entre 0,5 y 0,001%.
En el caso del tratamiento de las semillas se
requieren en general cantidades de producto activo de 0,001 hasta 50
g por cada kilogramo de semillas, preferentemente de 0,01 hasta 10
g.
Cuando se trata el suelo se requieren
concentraciones del producto activo de 0,00001 hasta 0,1% en peso,
preferentemente de 0,0001 hasta 0,02% en el lugar de actuación.
El buen efecto fungicida de las combinaciones de
productos activos según la invención se desprende de los ejemplos
siguientes. Mientras que los productos activos individuales
presentan puntos débiles en su efecto fungicida, las combinaciones
presentan un efecto que va mas allá de una simple suma de los
efectos.
Se presenta un efecto sinérgico en los fungicidas
siempre que el efecto fungicida de las combinaciones de productos
activos sea mayor que la suma de los efectos de los productos
activos aplicados individualmente.
El efecto esperable para una combinación dada de
dos productos activos puede calcularse (véase Colby, S.R.,
"Calculating Synergistic and Antagonistic Responses of Herbicide
Combinations", Weeds 15, páginas 20-22,
1967) de la manera siguiente:
si
- X
- representa el grado de actividad expresado en % de los controles no tratados, cuando se emplea el producto activo A en una concentración de \underline{m} ppm,
- Y
- representa el grado de actividad, expresado en % de los controles no tratados, cuando se emplea el producto activo B en una concentración de \underline{n} ppm,
- E
- representa el grado de actividad expresado en % de los controles no tratados, cuando se emplean los productos activos A y B en una concentración de \underline{m} y \underline{n} ppm,
entonces se da la relación
E = X + Y
-\frac{X.
Y}{100}
Si el efecto fungicida real es mayor que el
calculado, entonces la combinación es sobreaditiva en cuanto a su
efecto, es decir que existe un efecto sinérgico. En este caso el
grado de actividad real observado debe ser mayor que el valor
calculado a partir de la fórmula anteriormente indicada para el
grado de actividad esperado (E).
Para la obtención de una preparación conveniente
de producto activo se diluyen con agua hasta la concentración
deseada bien formulaciones de producto activo usuales en el comercio
(productos activos individuales o combinaciones de productos
activos), o 1 parte en peso de producto activo con 4,7 partes en
peso de disolvente (acetona) y 0,3 partes en peso de emulsionante
(alquilarilpoliglicoléter).
Para ensayar la actividad protectora se
pulverizan plantas jóvenes con la preparación de producto activo en
la cantidad de aplicación indicada. Tras secado del recubrimiento
aplicado por pulverización se inoculan las plantas con una
suspensión acuosa de esporas de Plasmopara viticola y
permanecen 1 día en una cabina de incubación aproximadamente a 201C
y una humedad relativa del aire del 100%. Seguidamente se disponen
las plantas durante 5 días en el invernadero a 211C aproximadamente
y una humedad del aire del 90%. Las plantas se humedecen
seguidamente y se disponen durante 1 día en una cabina de
incubación.
Al cabo de 6 días desde la inoculación se lleva a
cabo la evaluación. En este caso 0% significa un grado de actividad
que corresponde al de los controles, mientras que un grado de
actividad del 100% significa que no se observa ningún ataque.
El efecto encontrado de la combinación de
productos activos según la invención es mayor que el calculado, es
decir que se presenta un efecto sinérgico. La combinación de
Iprovalicarb y Fenamidone tiene, con una proporción de mezcla de 1:1
y con una cantidad de aplicación de 5 g/ha un grado de actividad
real del 98%. El valor esperado según la fórmula de Colby es del
45%, significativamente menor.
Claims (6)
1. Combinaciones de compuestos activos, que
contienen al menos un derivado de valinamida de la fórmula (I)
en la
que
- R^{1}
- significa i-propilo o s-butilo y
- R^{2}
- significa cloro, metilo, etilo o metoxi,
y
Fenamidone de la fórmula (II)
2. Combinación de compuestos activos según la
reivindicación 1, caracterizada porque en las combinaciones
de productos activos la proporción en peso entre el producto activo
de la fórmula (I) y el producto activo de la fórmula (II) es de
1:0,1 hasta 1:10.
3. Procedimiento para la lucha contra los hongos,
caracterizado porque se dejan actuar combinaciones de
productos activos, como se han definido en la reivindicación 1 sobre
los hongos y/o sobre su medio ambiente.
4. Agentes fungicidas que tienen un contenido de
una combinación de productos activos como se ha definido en la
reivindicación 1.
5. Empleo de combinaciones de productos activos o
bien de los agentes, como se han definido en las reivindicaciones 1
hasta 4 para la lucha contra los hongos.
6. Procedimiento para la obtención de agentes
fungicidas caracterizado porque se mezclan combinaciones de
productos activos según la reivindicación 1 con extendedores y/o
productos tensioactivos.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19904081 | 1999-02-02 | ||
DE19904081A DE19904081A1 (de) | 1999-02-02 | 1999-02-02 | Fungizide Wirkstoffkombinationen |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2226778T3 true ES2226778T3 (es) | 2005-04-01 |
Family
ID=7896135
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES00903619T Expired - Lifetime ES2226778T3 (es) | 1999-02-02 | 2000-01-24 | Combinaciones de productos activos fungicidas. |
Country Status (21)
Country | Link |
---|---|
US (1) | US6444693B1 (es) |
EP (1) | EP1150568B1 (es) |
JP (1) | JP3841264B2 (es) |
KR (1) | KR100446912B1 (es) |
CN (1) | CN1204811C (es) |
AR (1) | AR022294A1 (es) |
AT (1) | ATE276659T1 (es) |
AU (1) | AU2543600A (es) |
BR (1) | BR0007910A (es) |
CO (1) | CO5210898A1 (es) |
DE (2) | DE19904081A1 (es) |
ES (1) | ES2226778T3 (es) |
HK (1) | HK1042827A1 (es) |
HU (1) | HU228792B1 (es) |
ID (1) | ID30023A (es) |
PL (1) | PL195817B1 (es) |
PT (1) | PT1150568E (es) |
RU (1) | RU2237996C2 (es) |
TR (1) | TR200102212T2 (es) |
WO (1) | WO2000045638A1 (es) |
ZA (1) | ZA200105255B (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2789551B1 (fr) | 1999-02-12 | 2002-06-21 | Aventis Cropscience Sa | Compositions fongicides pour la protection des fruits |
MXPA03006033A (es) | 2001-01-22 | 2003-09-10 | Basf Ag | Mezclas fungicidas. |
DE10141618A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
FR2832031A1 (fr) * | 2001-11-14 | 2003-05-16 | Aventis Cropscience Sa | Composition fongicide a base d'au moins un derive de pyridylmethylbenzamide et d'au moins un derive de type valinamide |
ITMI20012430A1 (it) * | 2001-11-19 | 2003-05-19 | Isagro Spa | Composizioni a base di sali rameici sali rameici e loro utilizzo per il controllo di fitopatogeni |
DE602008003921D1 (de) | 2007-04-25 | 2011-01-20 | Syngenta Participations Ag | Fungizidzusammensetzungen |
EP2292094A1 (en) * | 2009-09-02 | 2011-03-09 | Bayer CropScience AG | Active compound combinations |
BR112013002081A2 (pt) | 2010-07-27 | 2018-01-30 | S Ginn Richard | sistema para estabilização sacro-ilíaca |
EP2622961A1 (en) * | 2012-02-02 | 2013-08-07 | Bayer CropScience AG | Acive compound combinations |
CN106259347A (zh) * | 2012-06-14 | 2017-01-04 | 陕西美邦农药有限公司 | 一种含咪唑菌酮的杀菌组合物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4304172A1 (de) * | 1993-02-12 | 1994-08-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
FR2722652B1 (fr) * | 1994-07-22 | 1997-12-19 | Rhone Poulenc Agrochimie | Composition fongicide comprenant une 2-imidazoline-5-one |
UA61064C2 (uk) * | 1997-12-02 | 2003-11-17 | Рон-Пуленк Агро | Синергічна фунгіцидна композиція, що містить 2-інідазолін-5-он та спосіб боротьби з фітопатогенними грибками культур |
-
1999
- 1999-02-02 DE DE19904081A patent/DE19904081A1/de not_active Withdrawn
-
2000
- 2000-01-14 AR ARP000100177A patent/AR022294A1/es active IP Right Grant
- 2000-01-24 ES ES00903619T patent/ES2226778T3/es not_active Expired - Lifetime
- 2000-01-24 EP EP00903619A patent/EP1150568B1/de not_active Expired - Lifetime
- 2000-01-24 JP JP2000596771A patent/JP3841264B2/ja not_active Expired - Fee Related
- 2000-01-24 PT PT00903619T patent/PT1150568E/pt unknown
- 2000-01-24 WO PCT/EP2000/000505 patent/WO2000045638A1/de active IP Right Grant
- 2000-01-24 AT AT00903619T patent/ATE276659T1/de not_active IP Right Cessation
- 2000-01-24 CN CNB008033811A patent/CN1204811C/zh not_active Expired - Fee Related
- 2000-01-24 DE DE50007895T patent/DE50007895D1/de not_active Expired - Lifetime
- 2000-01-24 RU RU2001124421A patent/RU2237996C2/ru not_active IP Right Cessation
- 2000-01-24 TR TR2001/02212T patent/TR200102212T2/xx unknown
- 2000-01-24 ID IDW00200101682A patent/ID30023A/id unknown
- 2000-01-24 US US09/890,404 patent/US6444693B1/en not_active Expired - Fee Related
- 2000-01-24 AU AU25436/00A patent/AU2543600A/en not_active Abandoned
- 2000-01-24 KR KR10-2001-7009674A patent/KR100446912B1/ko not_active IP Right Cessation
- 2000-01-24 PL PL00349862A patent/PL195817B1/pl not_active IP Right Cessation
- 2000-01-24 BR BR0007910-3A patent/BR0007910A/pt not_active Application Discontinuation
- 2000-01-24 HU HU0105229A patent/HU228792B1/hu unknown
- 2000-02-01 CO CO00005914A patent/CO5210898A1/es not_active Application Discontinuation
-
2001
- 2001-06-26 ZA ZA200105255A patent/ZA200105255B/en unknown
-
2002
- 2002-06-20 HK HK02104613.7A patent/HK1042827A1/zh unknown
Also Published As
Publication number | Publication date |
---|---|
ATE276659T1 (de) | 2004-10-15 |
EP1150568A1 (de) | 2001-11-07 |
TR200102212T2 (tr) | 2001-12-21 |
KR20010104336A (ko) | 2001-11-24 |
CN1204811C (zh) | 2005-06-08 |
HU228792B1 (en) | 2013-05-28 |
BR0007910A (pt) | 2001-11-06 |
ZA200105255B (en) | 2002-06-26 |
CN1338897A (zh) | 2002-03-06 |
HUP0105229A2 (hu) | 2002-04-29 |
RU2237996C2 (ru) | 2004-10-20 |
AU2543600A (en) | 2000-08-25 |
EP1150568B1 (de) | 2004-09-22 |
PL349862A1 (en) | 2002-09-23 |
JP3841264B2 (ja) | 2006-11-01 |
KR100446912B1 (ko) | 2004-09-04 |
CO5210898A1 (es) | 2002-10-30 |
HUP0105229A3 (en) | 2004-06-28 |
PL195817B1 (pl) | 2007-10-31 |
ID30023A (id) | 2001-11-01 |
DE50007895D1 (de) | 2004-10-28 |
WO2000045638A1 (de) | 2000-08-10 |
HK1042827A1 (zh) | 2002-08-30 |
JP2002536303A (ja) | 2002-10-29 |
US6444693B1 (en) | 2002-09-03 |
PT1150568E (pt) | 2005-02-28 |
DE19904081A1 (de) | 2000-08-03 |
AR022294A1 (es) | 2002-09-04 |
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