ES2712448T3 - Mezclas fungicidas sinérgicas para reprimir hongos en cereales - Google Patents
Mezclas fungicidas sinérgicas para reprimir hongos en cereales Download PDFInfo
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- ES2712448T3 ES2712448T3 ES16202262T ES16202262T ES2712448T3 ES 2712448 T3 ES2712448 T3 ES 2712448T3 ES 16202262 T ES16202262 T ES 16202262T ES 16202262 T ES16202262 T ES 16202262T ES 2712448 T3 ES2712448 T3 ES 2712448T3
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- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-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
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound 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
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 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
- 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
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-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
- 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-IMTORBKUSA-N validamycin 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-IMTORBKUSA-N 0.000 description 1
- 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 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
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- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- 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
- A01N47/06—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 containing —O—CO—O— groups; Thio analogues thereof
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- 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
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
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- 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
- A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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Abstract
Una mezcla fungicida sinérgica que comprende una cantidad fungicidamente eficaz de un compuesto de fórmula I-V y al menos un fungicida seleccionado entre el grupo que consiste en pentiopirad, y boscalida, o un compuesto de fórmula I y al menos un fungicida seleccionado de un grupo que consiste en isopirazam y bixafeno,**Fórmula**
Description
DESCRIPCION
Mezclas fungicidas sinergicas para reprimir hongos en cereales
Campo de la invencion
Esta invencion se refiere a una composition fungicida sinergica que contiene (a) un compuesto de formula I, II, III, IV o V y (b) al menos un fungicida seleccionado entre el grupo que consiste en pentiopirad y boscalida, o un compuesto de formula I y al menos un fungicida seleccionado del grupo que consiste en isopirazam y bixafeno.
Antecedentes de la invencion
Los fungicidas son compuestos, de origen natural o sintetico, que actuan para proteger las plantas contra el dano causado por los hongos. Los metodos actuales en la agricultura dependen en gran medida del uso de fungicidas. De hecho, algunas cosechas no pueden crecer de manera conveniente sin el uso de fungicidas. El uso de fungicidas permite a un agricultor aumentar el rendimiento y la calidad de la cosecha, y por consiguiente, aumentar el valor de la cosecha. En la mayoria de los casos, el aumento del valor de la cosecha vale al menos tres veces el coste del uso del fungicida.
Sin embargo, ningun fungicida es conveniente en todas las situaciones y el uso repetido de un unico fungicida conduce frecuentemente al desarrollo de resistencia frente a ese fungicida y otros relacionados. Por consiguiente, la investigation se encamina a producir fungicidas y combinaciones de fungicidas que sean seguros, que tengan una mayor eficacia, que requieran menos dosis, que sean mas faciles de usar, y que cuesten menos.
El sinergismo ocurre cuando la actividad de dos o mas compuestos excede las actividades de los compuestos cuando se usan solos. Las mezclas sinergicas de picolinamidas y un fungicida triazolico se describen en una contribution anonima titulada “Synergistic Fungicidal Compositions of Heterocyclic Aromatic Amides and Triazoles”, publicada en IP.COM el 20 de Julio de 2004.
Las mezclas fungicidas de picolinamidas y un segundo compuesto seleccionado de, entre otros, clorotalonil, se han descrito en una contribucion anonima titulada "Fungicidal Mixtures", publicada en IP.COM el 5 de julio de 2005.
Sumario de la invencion
Es un objetivo de esta invencion proporcionar composiciones sinergicas que comprendan compuestos fungicidas. Otro objetivo de esta invencion es proporcionar procedimientos que usen estas composiciones sinergicas. Las composiciones sinergicas son capaces de prevenir o curar, o ambos, enfermedades causadas por hongos de las clases Ascomycetes y Basidiomycetes. Ademas, las composiciones sinergicas tienen una eficacia mejorada contra patogenos Ascomycete y Basidiomycete, incluidos la septoriosis y la roya parda del trigo. De acuerdo con esta invencion, las composiciones sinergicas se proporcionan junto con metodos para su uso.
Description detallada de la invencion
La presente invencion se refiere a una mezcla fungicida sinergica que comprende una cantidad eficaz como antifungico de (a) un compuesto de formula I, II, III, IV o V, y (b) al menos un fungicida seleccionado entre el grupo que consiste en pentiopirad y boscalida, o un compuesto de formula I y al menos un fungicida seleccionado de un grupo que consiste en isopirazam y bixafeno.
Bixafeno es el nombre comun para N-(3',4'-dicloro-5-fluoro[1,1'-bifenil]-2-il)-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida. Bixafeno reprime una variedad de patogenos tales como Septoria tritici y roya.
Boscalida es el nombre comun para 2-cloro-N-(4'-clorobifenil-2-il)nicotinamida. Su actividad fungicida se describe en The Pesticide Manual, 15a edicion, 2009. Boscalida proporciona represion de oidio, Alternaria, Botrytis, Sclerotinia, Mycoshpaerella y Monilinia en fruta, cesped, cereales, colza, cacahuetes y patatas.
Isopirazam es el nombre comun para 3-(difluorometil)-1-metil-N-[1,2,3,4-tetrahidro-9-(1-metiletil)-1,4-metanonaftalen-5-il]-1H-pirazol-4-carboxamida. Su funcion fungicida se describe en The Pesticide Manual, 15a edicion, 2009. Isopirazam proporciona represion de Septoria y roya en trigo, asi como Ramularia en cebada.
Pentiopirad es el nombre comun para N-[2-(1,3-dimetilbutil)-3-tienil]-1-metil-3-(trifluorometil)-1H-pirazol-4-triazol carboxamida Su actividad fungicida se describe en The Pesticide Manual, 14a edicion, 2006. El pentiopirad proporciona represion de enfermedades de roya y Rhizoctonia, asi como moho gris, oidio y sarna del manzano.
En la composicion de esta invencion, la relacion en peso de los compuestos de formula I-V frente a epoxiconazol a la que el efecto fungicida es sinergico se encuentra dentro del intervalo entre 1:10 y 10:1. La relacion en peso de los compuestos de formula I-V frente a pentiopirad a la que el efecto fungicida es sinergico se encuentra dentro del intervalo entre 1:10 y 10:1. La relacion en peso del compuesto de formula I frente a isopirazam a la que el efecto fungicida es sinergico se encuentra dentro del intervalo entre 1:10 y 10:1. La relacion en peso del compuesto de formula I frente a bixafeno a la que el efecto fungicida es sinergico se encuentra dentro del intervalo entre 1:10 y 10:1. La relacion en peso de los compuestos de formula I-V frente a boscalida a la que el efecto fungicida es sinergico se encuentra dentro del intervalo entre 1:10 y 10:1.
La proporcion en la que se aplica la composicion sinergica dependera del tipo particular de hongo que se ha de reprimir, el grado de represion requerido y el momento y metodo de aplicacion. En general, la composicion de la invencion puede aplicarse en una proporcion de aplicacion entre 65 gramos por hectarea (g/ha) y 2300 g/ha basado en la cantidad total de ingredientes activos en la composicion. El pentiopirad se aplica en una proporcion entre 50 g/ha y 300 g/ha y el compuesto de formula I-V se aplica en una proporcion entre 35 g/ha y 300 g/ha. El isopirazam se aplica en una proporcion entre 30 g/ha y 125 g/ha y el compuesto de formula I se aplica en una proporcion entre 35 g/ha y 300 g/ha. El bixafeno se aplica en una proporcion entre 30 g/ha y 125 g/ha y el compuesto de fomula I se aplica en una proporcion entre 35 g/ha y 300 g/ha. La boscalida se aplica en una proporcion entre 50 g/ha y 350 g/ha y el compuesto de formula I-V se aplica en una proporcion entre 35 g/ha y 300 g/ha.
Los componentes de la mezcla sinergica de la presente invencion pueden aplicarse bien por separado o como parte de un sistema fungicida en varias partes.
La mezcla sinergica de la presente invencion puede aplicarse junto con uno o mas otros fungicidas para reprimir una amplia variedad de enfermedades no deseadas. Cuando se usa junto con otro(s) fungicida(s), los compuestos ahora reivindicados pueden formularse con el (los) otro(s) fungicida(s), mezclarse en el tanque con el (los) otro(s) fungicida(s) o aplicarse secuencialmente con el (los) otro(s) fungicida(s). Tales otros fungicidas pueden incluir 2-(tiocianometiltio)-benzotiazol, 2-fenilfenol, sulfato de 8-hidroxiquinolina, ametoctradina, amisulbrom, antimicina, Ampelomyces quisqualis, azaconazol, azoxistrobina, Bacillus subtilis, Bacillus subtilis cepa QST713, benalaxil, benomilo, bentiavalicarb-isopropil, sal de bencilaminobenceno-sulfonato (BABS), bicarbonatos, bifenilo, bismertiazol, bitertanol, bixafeno, blasticidin-S, borax, mezcla de Burdeos, boscalida, bromuconazol, bupirimato, polisulfuro de calcio, captafol, captan, carbendazim, carboxina, carpropamid, carvona, clazafenona, cloroneb, clorotalonil, clozolinato, Coniothyrium minitans, hidroxido de cobre, octanoato de cobre, oxicloruro de cobre, sulfato de cobre, sulfato de cobre (tribasico), oxido cuproso, ciazofamid, ciflufenamid, cimoxalil, ciproconazol, ciprodinil, dazomet,
debacarb, diamonio etilenbis-(ditiocarbamato), diclofluanid, diclorofeno, diclocimet, diclomezina, dicloran, dietofencarb, difenoconazol, difenzoquato ion, diflumetorim, dimetomorf, dimoxistrobina, diniconazol, diniconazol-M, dinotubon, dinocap, difenilamina, ditianon, dodemorf, dodemorf acetato, dodina, dodina base libre, edifenfos, enestrobina, enestroburina, epoxiconazol, etaboxam, etoxiquina, etridiazol, famoxadona, fenamidona, fenarimol, fenbuconazol, fenfuram, fenhexamida, fenoxanilo, fenpiclonilo, fenpropidin, fenpropimorf, fenpirazamina, fentin, fentin acetato, fentin hidroxido, ferbam, ferimzona, fluazinam, fludioxonil, flumorf, fluopicolida, fluopiram, fluoroimida, fluoxastrobina, fluquinconazol, flusilazol, flusulfamida, flutianilo, flutolanil, flutriafol, fluxapiroxad, folpet, formaldehido, fosetil, fosetil-aluminio, fuberidazol, furalaxilo, furametpir, guazatina, acetatos de guazatina, GY-81, hexaclorobenceno, hexaconazol, himexazol, imazalil, sulfato de imazalil, imibenconazol, iminoctadina, triacetato de iminoctadina, tris(albesilato) de iminoctadina, iodocarb, ipconazol, ipfenpirazolona, iprobenfos, iprodiona, iprovalicarb, isoprotiolano, isopirazam, isotianilo, kasugamicina, kasugamicina hidrocloruro hidrato, kresoxim-metil, laminarina, mancopper, mancozeb, mandipropamid, maneb, mefenoxam, mepanipirim, mepronilo, meptil-dinocap, cloruro de mercurio, oxido de mercurio, cloruro mercurioso, metalaxil, metalaxil-M, metam, metam-amonio, metampotasio, metam-sodio, metconazol, metasulfocarb, ioduro de metilo, metil-isotiocianato, metiram, metominostrobina, metrafenona, mildiomicina, miclobutanil, nabam, nitrotal-isopropil, nuarimol, octilinona, ofurace, acido oleico (acidos grasos), orisastrobina, oxadixilo, oxina-cobre, oxpoconazol fumarato, oxicarboxina, pefurazoato, penconazol, pencicuron, penflufeno, pentaclorofenol, laurato de pentaclorofenilo, pentiopirad, acetato de fenilmercurio, acido fosfonico, ftalida, picoxistrobina, polioxina B, polioxinas, polioxorim, bicarbonato de potasio, hidroxiquinolino-sulfato de potasio, probenazol, procloraz, procimidona, propamocarb, propamocarb hidrocloruro, propiconazol, propineb, proquinazid, protioconazol, piraclostrobina, pirametostrobina, piraoxistrobina, pirazofos, piribencarb, piributicarb, pirifenox, pirimetanil, piriofenona, piroquilona, quinoclamina, quinoxifen, quintozeno, extracto de Reynoutria sachalinensis, sedaxano, siltiofam, simeconazol, 2-fenilfenoxido de sodio, bicarbonato de sodio, pentaclorofenoxido de sodio, spiroxamina, azufre, SYP-Z048, aceites de alquitran, tebuconazol, tebufloquina, tecnazeno, tetraconazol, tiabendazol, tifluzamida, tiofanato-metil, tiram, tiadinil, tolclofos-metil, tolilfluanid, triadimefon, triadimenol, triazoxide, triciclazol, tridemorf, trifloxistrobina, triflumizol, triforina, triticonazol, validamicina, valifenalato, valifenal, vinclozolina, zineb, ziram, zoxamida, Candida oleophila, Fusarium oxysporum, Gliocladium spp, Phlebiopsis gigantea, Sreptomyces griseoviridis, Trichoderma spp., (RS)-W-(3,5-diclorofenil)-2-(metoximetil)-succinimida, 1,2-dicloropropano, hidrato de 1,3-dicloro-1,1,3,3-tetrafluroacetona, 1-cloro-2,4-dinitronaftaleno, 1-cloro-2-nitropropano, 2-(2-heptadecil-2-imidazolin-1-il)etanol, 2,3-dihidro-5-fenil-1,4-ditiino, 1,1,4,4-tetraoxido, acetato de 2-metoxietilmercurio, cloruro de 2-metoxietilmercurio, silicato de metoxietilmercurio, 3-(4-clorofenil)-5-metilrodanina, 4-(2-nitroprop-1-enil)fenil-tiocianatemo, ampropilfos, anilazina, azitiram, polisulfuro de bario, Bayer 32394, benodanilo, benquinox, bentaluron, benzamacrilo, benzamacrilo-isobutil, benzamorf, binapacrilo, sulfato de bis(metilmercurio), oxido de bis(tributilestano), butiobate, sulfato de cadmio calcio cobre cinc y cromato, carbamorf, CECA, clobentiazona, cloraniformetan, clorfenazol, clorquinox, climbazol, bis(3-fenilsalicilato) de cobre, cromato de cobre y cinc, cufraneb, sulfato cuprico de hidrazinio, cuprobam, ciclafuramid, cipendazol, ciprofuram, decafentina, diclona, diclozolina, diclobutrazol, dimetirimol, dinocton, dinosulfona, dinoterbon, dipiritiona, ditalimfos, dodicina, drazoxolona, EBP, ESBP, etaconazol, etem, etirim, fenaminosulf, fenapanilo, fenitropano, fluotrimazol, furcarbanilo, furconazol, furconazol-cis, furmeciclox, furofanato, gliodina, griseofulvina, halacrinato, Hercules 3944, hexiltiofos, ICIA0858, isopamfos, isovalediona, mebenilo, mecarbinzid, metazoxolona, metfuroxam, diciandiamida de metilmercurio, metsulfovax, milneb, anhfdrido mucoclorico, miclozolina, W-3,5-diclorofenil-succinimida, W-3-nitrofenilitaconimida, natamicina, W-etilmercurio-4-toluensulfonanilida, bis(dimetilditiocarbamato) de mquel, OCH, dimetilditiocarbamato de fenilmercurio, nitrato de fenilmercurio, fosdifeno, protiocarb; protiocarb hidrocloruro, piracarbolid, piridinitrilo, piroxiclor, piroxifur, quinacetol, sulfato de quinacetol, quinazamida, quinconazol, rabenzazol, salicilanilida, SSF-109, sultropeno, tecoram, tiadifluor, ticiofeno, tioclorfenfim, tiofanato, tioquinox, tioximid, triamifos, triarimol, triazbutilo, triclamida, urbacid, zarilamid, y una cualquiera de sus combinaciones.
Las composiciones de la presente invencion se aplican preferiblemente en forma de una formulacion que comprende una composicion de (a) un compuesto de formula I y (b) al menos un fungicida seleccionado entre el grupo que consiste en pentiopirad, isopirazam, bixafeno, y boscalida, junto con un vehfculo fitologicamente aceptable.
Las formulaciones concentradas pueden estar dispersas en agua, u otro lfquido, para su aplicacion, o las formulaciones pueden ser de en polvo o granulares, que pueden aplicarse luego sin ningun otro tratamiento. Las formulaciones se preparan segun los procedimientos que son convencionales en la tecnica de la qrnmica agncola, pero que son nuevos e importantes debido a la presencia de una composicion sinergica.
Las formulaciones que se aplican mas frecuentemente son suspensiones acuosas o emulsiones. Tales formulaciones solubles en agua, que se suspenden en agua, o emulsionables son solidas, habitualmente conocidas como polvos humectables, o lfquidos, habitualmente conocidas como concentrados emulsionables, suspensiones acuosas, o concentrados en suspension. La presente invencion contempla todos los vehfculos en los que las composiciones sinergicas pueden formularse para su administracion y uso como un fungicida.
Como se apreciara rapidamente, se puede emplear cualquier material que se puede anadir a estas composiciones sinergicas, siempre que proporcionen la utilidad deseada sin interferencia significativa con la actividad de estas composiciones sinergicas como agentes antifungicos.
Los polvos humectables, que pueden ser compactados para formar granulos que se dispersan en agua, comprenden una mezcla mtima de la composicion sinergica, un vehfculo y tensioactivos aceptables agncolamente. La
concentracion de la composicion sinergica en el polvo humectable es habitualmente de aproximadamente 10% a aproximadamente 90% en peso, mas preferiblemente aproximadamente 25% a aproximadamente 75% en peso, basado en el peso total de la formulacion. En la preparacion de las formulaciones de polvos humectables, la composicion sinergica puede ser combinada con uno cualquiera de los solidos finamente divididos, como pirofilita, talco, tiza, yeso, tierra de Fuller, bentonita, atapulgita, almidon, casema, gluten, arcillas montmorillonita, tierras diatomeas, silicatos purificados y similares. En tales operaciones, el vetuculo finamente dividido se pulveriza y se mezcla con la composicion sinergica en un disolvente organico volatil. Los tensioactivos eficaces, que comprenden de aproximadamente 0,5% a aproximadamente 10% en peso del polvo humectable, incluyen ligninas sulfonadas, naftalenosulfonatos, alquilbencenosulfonatos, alquilsulfatos, y tensioactivos no ionicos, como aductos de oxido de etileno de alquilfenoles.
Los concentrados emulsionables de la composicion sinergica comprenden una concentracion conveniente, de aproximadamente 10% a aproximadamente 50% en peso, un lfquido adecuado, basado en el peso total de la formulacion del concentrado emulsionable. Los componentes de las composiciones sinergicas, juntos o por separado, se disuelven en un vetuculo, que o bien es un disolvente miscible en agua o una mezcla de disolventes organicos inmiscibles en agua, y emulsionantes. Los concentrados pueden diluirse con agua y aceite para formar mezclas pulverizables en forma de emulsiones aceite-en-agua. Los disolventes organicos utiles incluyen aromaticos, especialmente las porciones naftalenicas y olefrnicas de alto punto de ebullicion del petroleo como el nafta aromatico pesado. Tambien se pueden usar otros disolventes organicos, como, por ejemplo, disolventes terpenicos, incluido derivados de colofonia, cetonas alifaticas, como ciclohexanona, y alcoholes complejos, como 2-etoxietanol.
Los emulsionantes que pueden emplearse ventajosamente en este texto pueden determinarse rapidamente por los expertos en la tecnica e incluyen varios emulsionantes no ionicos, anionicos, cationicos y anfoteros, o una mezcla de dos o mas emulsionantes. Los ejemplos de emulsionantes no ionicos utiles para preparar los concentrados emulsionables incluyen eteres de polialquilenglicol y productos de condensacion de alquil y arilfenoles, alcoholes alifaticos, aminas alifaticas o acidos grasos con oxido de etileno, oxidos de propileno como alquilfenoles etoxilados y esteres carboxflicos disueltos con el poliol o polioxialquileno. Los emulsionantes cationicos incluyen compuestos de amonio cuaternario y sales de aminas grasas. Los emulsionantes anionicos incluyen sales solubles en aceite (p.ej. calcio) de acidos alquilaril-sulfonicos, sales solubles en aceite o eteres de poliglicol sulfatados y sales apropiadas de eter de poliglicol fosfatado.
Los lfquidos organicos representativos que pueden emplearse para preparar los concentrados emulsionables de la presente invencion son los lfquidos aromaticos como xileno, fracciones de propilbenceno, o fracciones de mezclas de naftaleno, aceites minerales, lfquidos organicos aromaticos sustituidos como dioctil-ftalato, queroseno, dialquilamidas de varios acidos grasos, particularmente las dimetilamidas de glicoles grasos y derivados de glicol como n-butileter, etileter o metileter de dietilenglicol, y el metileter de trietilenglicol. Frecuentemente las mezclas de dos o mas lfquidos organicos se emplean tambien adecuadamente en la preparacion del concentrado emulsionable. Los lfquidos organicos preferidos son xileno, y fracciones de propilbenceno, siendo el xileno el mas preferido. Los agentes de dispersion activos de superficie que se emplean habitualmente en formulaciones lfquidas y en una cantidad de aproximadamente 0,1 a 20 por ciento en peso del peso combinado del agente de dispersion con las composiciones sinergicas. Las formulaciones pueden contener tambien otros aditivos compatibles, por ejemplo reguladores del crecimiento de plantas y otros compuestos activos biologicamente usados en agricultura.
Las suspensiones acuosas comprenden suspensiones de uno o mas compuestos solubles en agua, dispersos en un vetuculo acuoso a una concentracion dentro del intervalo de aproximadamente 5% a aproximadamente 70% en peso, basado en el peso total de la formulacion de la suspension acuosa. Las suspensiones se preparan triturando finamente los componentes de la combinacion sinergica o bien juntos o por separado, y mezclando vigorosamente el material triturado en un vehfculo que contiene agua y tensioactivos elegidos entre los mismos tipos abordados anteriormente. Tambien se pueden anadir otros ingredientes, como sales inorganicas y gomas sinteticas o naturales, para aumentar la densidad y viscosidad del vehfculo acuoso. Frecuentemente es mas eficaz triturar y mezclar al mismo tiempo al preparar la mezcla acuosa y homogeneizarla en un instrumento como un molino de arena, molino de bolas, o un homegeneizador de tipo piston.
La composicion sinergica puede aplicarse tambien como una formulacion granular, que es particularmente util para su aplicacion en suelos. Habitualmente las formulaciones granulares contienen desde aproximadamente 0,5% a aproximadamente 10% en peso de los compuestos, basado en el peso total de la formulacion granular, dispersos en un vetuculo que consiste enteramente o en gran parte en atapulgita, bentonita, diatomita, arcilla divididas gruesamente o una sustancia economica similar. Habitualmente tales formulaciones se preparan disolviendo la composicion sinergica en un disolvente adecuado y aplicandolas sobre un vehfculo granular que se ha preparado con el tamano de partfcula apropiado, dentro del intervalo de aproximadamente 0,5 a aproximadamente 3 mm. Tales formulaciones pueden prepararse tambien preparando una masa o pasta del vehfculo y la composicion sinergica, y triturandola y secandola para obtener la partfcula granular deseada.
Los polvos que contienen la composicion sinergica se preparan sencillamente mezclando mtimamente la composicion sinergica en forma de polvo con un vehfculo polvoriento agncola adecuado, como, por ejemplo, arcilla de caolm, roca volcanica triturada, y similares. Los polvos pueden contener adecuadamente desde aproximadamente 1% a aproximadamente 10% en peso de la composicion sinergica/combinacion del vehfculo.
Las formulaciones pueden contener tensioactivos adyuvantes aceptables agncolamente para mejorar la deposicion, humectacion y penetracion de la composicion sinergica sobre la cosecha y organismo dianas. Estos tensioactivos adyuvantes pueden emplearse opcionalmente como un componente de la formulacion o como una mezcla extemporanea. La cantidad del tensioactivo adyuvante variara desde 0,01 por ciento a 1,0 por ciento volumen/volumen (v/v) basado en un volumen pulverizado de agua, preferiblemente 0,05 a 0,5 por ciento. Los tensioactivos adyuvantes adecuados incluyen nonilfenoles etoxilados, alcoholes etoxilados sinteticos o naturales, sales de los esteres o acidos sulfosuccrnicos, organosiliconas etoxiladas, aminas grasas etoxiladas y mezclas de tensioactivos con aceites minerales o vegetales.
Las formulaciones puedes incluir opcionalmente combinaciones que pueden comprender al menos 1% en peso de una o mas de las composiciones sinergicas con otro compuesto pesticida. Tales compuestos pesticidas adicionales pueden ser fungicidas, insecticidas, nematocidas, miticidas, artropodicidas, bactericidas o sus combinaciones que sean compatibles con las composiciones sinergicas de la presente invencion en el medio seleccionado para su aplicacion, y no antagonista con la actividad de los compuestos presentes. De acuerdo con esto, en tales realizaciones el otro compuesto pesticida se emplea como un toxico suplementario para el mismo o para un uso pesticida diferente. El compuesto pesticida y la composicion sinergica pueden mezclarse juntos generalmente en una relacion en peso de aproximadamente 1:100 a 100:1.
La presente invencion incluye dentro de su alcance metodos para la represion o prevencion de un ataque fungico. Estos metodos comprenden la aplicacion al locus del hongo, o a un locus donde se quiere prevenir la infeccion (por ejemplo la aplicacion a plantas de trigo o cebada), una cantidad eficaz como antifungico de la composicion sinergica. La composicion sinergica es adecuada para el tratamiento de varias plantas a niveles fungicidas, mientras exhibe una baja fitotoxicidad. La composicion sinergica es util de una manera protectora o erradicadora. La composicion sinergica se aplica mediante una cualquiera o varias tecnicas conocidas, bien como la composicion sinergica o como una formulacion que comprende la composicion sinergica. Por ejemplo, las composiciones sinergicas pueden aplicarse a las rafces, semillas o follaje de plantas para la represion de varios hongos, sin danar el valor comercial de las plantas. La composicion sinergica se aplica en forma de uno cualquiera de los tipos de formulacion usados generalmente por ejemplo, como disoluciones, polvos, polvos humectables, concentrados fluidos, o concentrados emulsionables. Estos materiales se aplican convenientemente de varias maneras conocidas.
Se ha visto que la composicion sinergica tiene un efecto fungicida significante, particularmente para su uso en la agricultura. La composicion sinergica es particularmente eficaz para su uso en cultivos agncolas y plantas de horticulture, o con madera, pintura, piel o el reverso de alfombras.
En particular, la composicion sinergica es eficaz para reprimir una variedad de hongos no deseables que infectan cultivos de plantas utiles. La composicion sinergica puede usarse contra una variedad de hongos Ascomycete y Basidiomycete, incluidas por ejemplo las especies representativas de hongos siguientes: roya parda del trigo (Puccinia recondita; codigo Bayer PUCCRT); roya amarilla del trigo (Puccinia striiformis; codigo Bayer PUCCST); mancha de la hoja del trigo (Mycosphaerella graminicola; anamorfo: Septoria tritici; codigo Bayer SEPTTR); septoriosis de la gluma del trigo (Leptosphaeria nodorum; codigo de Bayer LEPTNO; anamorfo: Stagonospora nodorum); mancha borrosa de la cebada (Cochliobolus sativum; codigo Bayer COCHSA; anamorfo: Helminthosporium sativum); cercosporiosis de la hoja de la remolacha (Cercospora beticola; codigo Bayer CERCBE); mancha de las hojas del cacahuete (Mycosphaerella arachidis; codigo Bayer MYCOAR; anamorfo: Cercospora arachidicola); antracnosis del pepino (Glomerella lagenarium; anamorfo: Colletotrichum lagenarium; codigo Bayer COLLLA) y enfermedad de la sigatoka negra del platano (Mycosphaerella fijiensis; codigo Bayer MYCOFI). Se entendera por los expertos en la tecnica que la eficacia de las composiciones sinergicas para uno o mas de los anteriores hongos establece la utilidad general de las composiciones sinergicas como fungicidas.
Las composiciones sinergicas tienen un amplio intervalo de eficacia como fungicida. La cantidad exacta de la composicion sinergica a aplicar depende no solamente de las cantidades relativas de los componentes, sino tambien de la accion particular deseada, las especies fungicas a reprimir, y del estadio de su crecimiento, al igual que la parte de la planta u otro producto en contacto con la composicion sinergica. Por ello, las formulaciones que contienen la composicion sinergica no pueden ser igualmente eficaces a concentraciones similares o contra las mismas especies de hongo.
Las composiciones sinergicas son eficaces en su uso con plantas en una cantidad aceptable fitologicamente y para inhibir una enfermedad. La expresion “cantidad aceptable fitologicamente y para inhibir una enfermedad” se refiere a una cantidad de la composicion sinergica que mata o inhibe la enfermedad de la planta que se desea reprimir, pero no es significativamente toxica para la planta. La concentracion exacta de la composicion sinergica requerida vana con la enfermedad fungica a reprimir, el tipo de formulacion empleada, el metodo de aplicacion, las especies de plantas particulares, las condiciones climaticas, y similar.
Las composiciones presentes pueden aplicarse a hongos o a su locus mediante el uso de pulverizadores terrestres convencionales, aplicadores de granulos, y por otros medios convencionales conocidos por el experto en la tecnica. Los ejemplos siguientes se proporcionan para mayor ilustracion de la invencion. No deben interpretarse como limitantes de la invencion.
Ejemplos
Evaluacion de la actividad curativa y protectora de las mezclas fungicidas vs. septoriosis de la hoja del trigo (Mycosphaerella graminicola; anamorfo: Septeria tritici; codigo Bayer: SEPTTR)
Las plantas de trigo (variedad Yuma) crecieron desde la semilla en un invernadero en macetas de plastico con un area superficial de 27,5 centfmetros cuadrados (cm2) que contema 50% de suelo mineral/50% de medio Metro mix sin sustrato, con 8-12 plantones por maceta. Las plantas se emplearon para el ensayo cuando la primera hoja habfa emergido totalmente, que tipicamente sucede en los 7 a 8 dfas despues de la siembra. Las plantas para ensayo fueron inoculadas con una suspension acuosa de esporas de Septoria tritici o bien 3 dfas antes (ensayo curativo a 3 dfas) o 1 dfa despues de los tratamientos fungicidas (ensayo protector a 1 dfa). Despues de la inoculacion, las plantas se mantuvieron en 100% de humedad relativa (un dfa en una camara oscura de rodo seguido de dos dfas en una camara de nebulizacion iluminada) para permitir que las esporas germinaran e infectaran la hoja. Luego las plantas fueron transferidas a un invernadero para que la enfermedad se desarrollara.
Evaluacion de la actividad curativa de las mezclas fungicidas vs. roya parda del trigo (Puccinia recondita; codigo Bayer: PUCCRT)
Las semillas de trigo Yuma crecieron como se ha descrito anteriormente, y se las inoculo con una suspension acuosa de esporas de Puccinia recondita 3 dfas antes o 1 dfa despues del tratamiento fungicida. Despues de la inoculacion, las plantas se mantuvieron en una humedad relativa del 100% durante 24 horas en una camara oscura de rodo para permitir que las esporas germinaran e infectaran las plantas. Luego las plantas se transfirieron a un invernadero para que se desarrollara la enfermedad.
Los tratamientos consistieron en los compuestos fungicidas I, II, III, IV, V, pentiopirad, y boscalida, o bien usados individualmente o como una mezcla de dos con los compuestos I-V. Para el compuesto I, isopirazam y bixafeno tambien se incluyeron en los estudios. Las calidades tecnicas de los materiales se disolvieron en acetona para preparar disoluciones madre, que luego se usaron para llevar a cabo disoluciones en acetona bien para cada componente fungicida individual o para la mezcla de dos. Las relaciones de fungicidas deseadas se obtuvieron despues de mezclar las disoluciones con 9 volumenes de agua que conteman 110 partes por millon (ppm) de Triton X-100. Se aplicaron veinte mililitros (mL) de disoluciones de fungicida sobre 12 macetas de plantas usando una camara de pulverizacion automatica, que utilizaba dos toberas pulverizadoras modelo 6218-1/4 JAUPM operando ajustado a 20 libras por pulgada cuadrada (psi) en angulos opuestos para recubrir ambas superficies de las hojas. Se dejaron secar al aire todas las plantas pulverizadas antes de su posterior manejo. Las plantas testigo se pulverizaron de la misma manera con el blanco de disolvente.
Cuando la enfermedad se desarrollo totalmente en las plantas testigo, se evaluaron visualmente los niveles de infeccion de las plantas tratadas y se puntuaron en una escala de 0 a 100 por ciento. Luego se calculo el porcentaje de represion de la enfermedad usando la relacion de la enfermedad de las plantas tratadas frente a las plantas testigo.
Se uso la ecuacion de Colby para determinar los efectos fungicidas esperados de las mezclas. (Vease Colby, S. R. Calculation of the synergistic y antagonistic response of herbicide combinations. Weeds 1967, 15, 20-22).
La siguiente ecuacion se uso para calcular la actividad esperada de las mezclas que conteman dos ingredientes activos, A y B:
Esperado = A B - (Ax B/100)
A= eficacia observada de componente activo A a la misma concentracion empleada en la mezcla;
B= eficacia observada de componente activo B a la misma concentracion empleada en la mezcla.
Las interacciones sinergicas representativas se presentan en las siguientes tablas 1-3 y 5-12.
%DC Obs= porcentaje de represion observada de la enfermedad
%DC Esp= porcentaje de represion esperada de la enfermedad
Factor de sinergismo= %DC Obs / %DC Esp
Tabla 1: Interacciones sinergicas del compuesto I y otros fungicidas en ensayos curativos de 3 dfas (3DC) con Septoria tritici (SEPTTR)
Tabla 2: Interacciones sinergicas del compuesto I y otros fungicidas en ensayos protectores de 1 dfa (1DP) con
SEPTTR
Tabla 3: Interacciones sinergicas del compuesto I y otros fungicidas en ensayos de 3DC con Puccinia recondita
(PUCCRT)
Tabla 5: Interacciones sinergicas del compuesto II y boscalida en ensayos de 1DP con SEPTTR
Tabla 6: Interacciones sinergicas del compuesto II y boscalida en ensayos de 3DC con SEPTTR
Tabla 7: Interacciones sinergicas del compuesto III y otros fungicidas en ensayos de 1DP con SEPTTR
Tabla 8: Interacciones sinergicas del compuesto III y otros fungicidas en ensayos de 3DC con SEPTTR
Tabla 9: Interacciones sinergicas del compuesto IV y boscalida en ensayos de 1DP con SEPTTR
Tabla 10: Interacciones sinergicas del compuesto IV y otros fungicidas en ensayos de 3DC con SEPTTR
Tabla 11: Interacciones sinergicas del compuesto V y otros fungicidas en ensayos de 1DP con SEPTTR
Tabla 12: Interacciones sinergicas del compuesto V y otros fungicidas en ensayos de 3DC con SEPTTR
Para todas las tablas, %DC = % represion de enfermedad
Aspectos de la invencion
1. Una mezcla fungicida sinergica que comprende una cantidad eficaz fungicidamente de un compuesto de fomula I V y al menos un fungicida seleccionado del grupo que consiste en pentiopirad y boscalida, procloraz y clorotalonil o un compuesto de formula I y al menos un fungicida seleccionado del grupo que consiste en isopirazam y bixafeno,
2. La mezcla del aspecto 1, en la que la relacion en peso del compuesto I-V frente al pentiopirad esta entre 1:10 y 10:1.
3. La mezcla del aspecto 1, en la que la relacion en peso del compuesto I frente al isopirazam esta entre 1:10 y 10:1.
4. La mezcla del aspecto 1, en la que la relacion en peso del compuesto I frente al bixafeno esta entre 1:10 y 10:1. 5. La mezcla del aspecto 1, en la que la relacion en peso del compuesto I-V frente a la boscalida esta entre 1:10 y 10:1.
6. Una composition fungicida que comprende una cantidad fungicidamente eficaz de una mezcla fungicida del aspecto 1 y un vehiculo o adyuvante agricolamente aceptable.
Claims (11)
1. Una mezcla fungicida sinergica que comprende una cantidad fungicidamente eficaz de un compuesto de formula I-V y al menos un fungicida seleccionado entre el grupo que consiste en pentiopirad, y boscalida, o un compuesto de formula I y al menos un fungicida seleccionado de un grupo que consiste en isopirazam y bixafeno,
2. La mezcla de la reivindicacion 1, en la que la relacion en peso del compuesto I-V frente a pentiopirad esta entre 1:10 y 10:1.
3. La mezcla de la reivindicacion 1, en la que la relacion en peso del compuesto I frente a isopirazam esta entre 1:10 y 10:1.
4. La mezcla de la reivindicacion 1, en la que la relacion en peso del Compuesto I-V frente a bixafeno esta entre 1:10 y 10:1.
5. La mezcla de la reivindicacion 1, en la que la relacion en peso del Compuesto I-V frente a boscalida esta entre 1:10 y 10:1.
6. Una composition fungicida que comprende una cantidad fungicidamente eficaz de la mezcla fungicida de la reivindicacion 1, y un adyuvante o vehiculo agricolamente aceptable.
7. El uso de la mezcla o la composicion de una cualquiera de las reivindicaciones precedentes para reprimir los hongos que infectan los cultivos de plantas.
8. El uso segun la reivindicacion 7, donde los hongos son de las clases Ascomycetes y Basidiomycetes.
9. El uso segun la reivindicacion 7, donde los hongos se seleccionan entre el grupo que consiste en la roya parda del trigo (Puccinia recondita; PUCCRT); roya lineal del trigo (Puccinia striiformis; PUCCST); septoriosis de la hoja del trigo (Mycosphaerella graminicola: anamorfo: Septoria tritici; SEPTTR); septoriosis de la gluma del trigo (Leptospheria nodorum; LEPTNO; anamorfo: Stagonospora nodorum); mancha borrosa de la cebada (Cochliobolus sativum; COCHSA; anamorfo: Helminthosporium sativum); cercosporiosis de la hoja de la remolacha (Cercospora beticola; CERCBE); mancha de las hojas del cacahuete (Mycosphaerella arachidis; MYCOAR; anamorfo: Cercospora arachidicola); antracnosis del pepino (Glomerella lagenarium; anamorfo: Colletotrichum lagenarium; COLLLA) y enfermedad de la sigatoka negra del platano (Mycosphaerella fijiensis; MYCOFI).
10. El uso segun la reivindicacion 7, donde la composicion se aplica en una proportion de aplicacion de entre 65 gramos por hectarea (g/ha) y 2300 g/ha, basado en la cantidad total de los ingredientes activos en la composicion.
11. El uso segun la reivindicacion 7, donde el pentiopirad se aplica en una proporcion entre 50 g/ha y 300 g/ha, el isopirazam se aplica en una proporcion entre 30 g/ha y 125 g/ha, el bixafeno se aplica en una proporcion entre 30 g/ha y 125 g/ha, o la boscalida se aplica en una proporcion entre 50 g/ha y 350 g/ha y el compuesto de formula I-V se aplica en una proporcion entre 35 g/ha y 300 g/ha.
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Families Citing this family (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY159237A (en) * | 2009-09-01 | 2016-12-30 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
PT3178321T (pt) * | 2009-10-07 | 2019-08-01 | Dow Agrosciences Llc | Misturas fungicidas sinérgicas de epoxiconazol para o controlo de fungos em cereais |
AU2010303832B2 (en) * | 2009-10-07 | 2015-02-12 | Dow Agrosciences Llc | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
PL2847185T3 (pl) | 2012-05-07 | 2017-06-30 | Dow Agrosciences Llc | Makrocykliczne pikolinamidy jako fungicydy |
JP6129300B2 (ja) | 2012-05-07 | 2017-05-17 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
BR112014027515A2 (pt) * | 2012-05-07 | 2017-06-27 | Dow Agrosciences Llc | uso de pró-fungicidas de uk-2a para controle de sigatoka negra |
KR20150013692A (ko) * | 2012-05-07 | 2015-02-05 | 다우 아그로사이언시즈 엘엘씨 | 살진균제로서 매크로시클릭 피콜린아미드 |
WO2013169658A1 (en) * | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llc | Use of pro-fungicides of uk-2a for control of soybean rust |
KR20150027107A (ko) | 2012-06-22 | 2015-03-11 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 살진균제 4-메틸아닐리노 피라졸 |
CN104883884B (zh) | 2012-12-28 | 2018-03-23 | 美国陶氏益农公司 | 用于谷物里的真菌防治的协同增效杀真菌混合物 |
US10455835B2 (en) | 2012-12-31 | 2019-10-29 | Dow Agrosciences Llc | Fungicidal compositions for controlling leaf spots in sugar beets |
US9247742B2 (en) * | 2012-12-31 | 2016-02-02 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
US9750248B2 (en) * | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
US9482661B2 (en) | 2012-12-31 | 2016-11-01 | Dow Agrosciences Llc | Synthesis and use of isotopically labeled macrocyclic compounds |
JP2016507511A (ja) * | 2012-12-31 | 2016-03-10 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
WO2014130409A2 (en) | 2013-02-21 | 2014-08-28 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazole mixtures |
CN103988840A (zh) * | 2013-03-20 | 2014-08-20 | 海南正业中农高科股份有限公司 | 含有吡噻菌胺与咪鲜胺的杀菌组合物 |
KR20150143650A (ko) | 2013-04-15 | 2015-12-23 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 살진균성 카르복스아미드 |
US9730447B2 (en) | 2013-04-15 | 2017-08-15 | E I Du Pont De Nemours And Company | Fungicidal amides |
TW201542089A (zh) * | 2013-07-10 | 2015-11-16 | Meiji Seika Pharma Co Ltd | 含有吡啶羧酸衍生物而成之協同作用植物病害防治用組成物 |
EP3052490A4 (en) | 2013-10-01 | 2017-06-07 | Dow AgroSciences LLC | Macrocyclic picolinamide compounds with fungicidal activity |
US9265253B2 (en) | 2013-10-01 | 2016-02-23 | Dow Agrosciences Llc | Use of macrocyclic picolinamides as fungicides |
WO2015100184A1 (en) * | 2013-12-26 | 2015-07-02 | Dow Agrosciences Llc | Use of macrocyclic picolinamides as fungicides |
CN106061256A (zh) | 2013-12-26 | 2016-10-26 | 美国陶氏益农公司 | 具有杀真菌活性的大环吡啶酰胺化合物 |
CN106061262A (zh) * | 2013-12-31 | 2016-10-26 | 阿达玛马克西姆股份有限公司 | 用防治谷类中真菌的协同杀真菌混合物 |
CN106061260A (zh) * | 2013-12-31 | 2016-10-26 | 美国陶氏益农公司 | 用于谷类中真菌防治的协同杀真菌混合物 |
GB201401117D0 (en) * | 2014-01-23 | 2014-03-12 | Univ Sussex The | Antifungal composition |
WO2015123193A1 (en) | 2014-02-12 | 2015-08-20 | E. I. Du Pont De Nemours And Company | Fungicidal benzodipyrazoles |
WO2015157005A1 (en) | 2014-04-10 | 2015-10-15 | E I Du Pont De Nemours And Company | Substituted tolyl fungicide mixtures |
US20150322051A1 (en) | 2014-05-06 | 2015-11-12 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
US20170037014A1 (en) | 2014-05-06 | 2017-02-09 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
US9955691B2 (en) | 2014-07-08 | 2018-05-01 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
TWI689498B (zh) | 2014-07-08 | 2020-04-01 | 美商陶氏農業科學公司 | 用於製備4-烷氧基-3-羥基吡啶甲酸之方法(三) |
EP3166935A4 (en) | 2014-07-08 | 2017-11-22 | Dow AgroSciences LLC | Macrocyclic picolinamides as fungicides |
MX2016017124A (es) | 2014-07-08 | 2017-05-10 | Dow Agrosciences Llc | Proceso para la preparacion de acidos 3-hidroxipicolinicos. |
US20160037774A1 (en) * | 2014-08-08 | 2016-02-11 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
ES2815673T3 (es) | 2014-12-30 | 2021-03-30 | Dow Agrosciences Llc | Compuestos de picolinamida con actividad fungicida |
AU2015374459A1 (en) | 2014-12-30 | 2017-06-29 | Dow Agrosciences Llc | Picolinamide compounds with fungicidal activity |
RU2703402C2 (ru) | 2014-12-30 | 2019-10-16 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Пиколинамиды с фунгицидной активностью |
WO2016109304A1 (en) | 2014-12-30 | 2016-07-07 | Dow Agrosciences Llc | Picolinamides as fungicides |
CA2972430C (en) * | 2014-12-30 | 2023-08-29 | Dow Agrosciences Llc | Fungicidal compositions |
RU2702697C2 (ru) | 2014-12-30 | 2019-10-09 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Использование пиколинамидных соединений с фунгицидной активностью |
CN107428694A (zh) | 2015-03-19 | 2017-12-01 | 杜邦公司 | 杀真菌吡唑 |
EP3141118A1 (en) | 2015-09-14 | 2017-03-15 | Bayer CropScience AG | Compound combination for controlling control phytopathogenic harmful fungi |
AU2016381095B2 (en) * | 2015-12-30 | 2020-11-12 | Corteva Agriscience Llc | Fungal control of white mold |
WO2017194363A1 (en) * | 2016-05-10 | 2017-11-16 | Bayer Cropscience Aktiengesellschaft | Compound combination for controlling phytopathogenic harmful fungi |
EP3245872A1 (en) * | 2016-05-20 | 2017-11-22 | BASF Agro B.V. | Pesticidal compositions |
AR109429A1 (es) * | 2016-08-26 | 2018-11-28 | Dow Agrosciences Llc | Uso de profungicidas de uk-2a para el control de añublo de arroz |
US20180055049A1 (en) * | 2016-08-26 | 2018-03-01 | Dow Agrosciences Llc | Use of pro-fungicides of uk-2a for control of brown rot diesease on stone and pome fruits |
WO2018044991A1 (en) | 2016-08-30 | 2018-03-08 | Dow Agrosciences Llc | Thiopicolinamide compounds with fungicidal activity |
WO2018045010A1 (en) | 2016-08-30 | 2018-03-08 | Dow Agrosciences Llc | Pyrido-1,3-oxazine-2,4-dione compounds with fungicidal activity |
US10244754B2 (en) | 2016-08-30 | 2019-04-02 | Dow Agrosciences Llc | Picolinamide N-oxide compounds with fungicidal activity |
US10214490B2 (en) | 2016-08-30 | 2019-02-26 | Dow Agrosciences Llc | Picolinamides as fungicides |
EP3558984B1 (en) | 2016-12-20 | 2023-08-02 | FMC Corporation | Fungicidal oxadiazoles |
BR102018000183B1 (pt) | 2017-01-05 | 2023-04-25 | Dow Agrosciences Llc | Picolinamidas, composição para controle de um patógeno fúngico, e método para controle e prevenção de um ataque por fungos em uma planta |
PE20211981A1 (es) * | 2017-03-07 | 2021-10-05 | Upl Ltd | Combinaciones fungicidas |
TWI829634B (zh) | 2017-04-06 | 2024-01-21 | 美商富曼西公司 | 殺真菌之噁二唑 |
TWI774760B (zh) * | 2017-05-02 | 2022-08-21 | 美商科迪華農業科技有限責任公司 | 用於蔬菜中的真菌防治之協同性混合物 |
CA3062074A1 (en) | 2017-05-02 | 2018-11-08 | Dow Agrosciences Llc | Use of an acyclic picolinamide compound as a fungicide for fungal diseases on turfgrasses |
TW201842851A (zh) * | 2017-05-02 | 2018-12-16 | 美商陶氏農業科學公司 | 用於穀類中的真菌防治之協同性混合物 |
TWI774761B (zh) * | 2017-05-02 | 2022-08-21 | 美商科迪華農業科技有限責任公司 | 用於穀物中的真菌防治之協同性混合物 |
AR112221A1 (es) | 2017-07-05 | 2019-10-02 | Fmc Corp | Oxadiazoles fungicidas, composición que los comprende y un método para controlar fitoenfermedades que los emplea |
MA50787A (fr) | 2017-11-21 | 2020-09-30 | Syngenta Participations Ag | Compositions fongicides |
US11319553B2 (en) | 2017-11-29 | 2022-05-03 | Rahan Meristem (1998) Ltd. | Compositions and methods conferring resistance to fungal diseases |
RU2672493C1 (ru) * | 2018-02-14 | 2018-11-15 | ООО "Агро Эксперт Груп" | Фунгицидная композиция (варианты) |
RU2661392C1 (ru) * | 2018-02-14 | 2018-07-16 | Общество с ограниченной ответственностью "Агро Эксперт Груп" | Фунгицидная композиция (Варианты) |
BR102019004480B1 (pt) | 2018-03-08 | 2023-03-28 | Dow Agrosciences Llc | Picolinamidas como fungicidas |
TWI819078B (zh) | 2018-09-06 | 2023-10-21 | 美商富曼西公司 | 殺真菌之經硝苯胺基取代之吡唑 |
TWI843750B (zh) | 2018-09-14 | 2024-06-01 | 美商富曼西公司 | 殺真菌劑鹵甲基酮及水合物 |
CN113286513A (zh) | 2018-09-27 | 2021-08-20 | 0903608Bc有限公司 | 协同农药组合物和用于递送杀昆虫活性成分的方法 |
WO2020081382A1 (en) | 2018-10-15 | 2020-04-23 | Dow Agrosciences Llc | Methods for sythesis of oxypicolinamides |
TWI832917B (zh) | 2018-11-06 | 2024-02-21 | 美商富曼西公司 | 經取代之甲苯基殺真菌劑 |
MX2022008688A (es) | 2020-01-15 | 2022-08-04 | Fmc Corp | Amidas fungicidas. |
EP4103554A1 (en) | 2020-02-14 | 2022-12-21 | Fmc Corporation | Substituted 5,6-diphenyl-3(2h)-pyridazinones for use as fungicides |
RU2763596C1 (ru) * | 2021-07-19 | 2021-12-30 | Акционерное общество "Щелково Агрохим" | Фунгицидная синергетическая комбинация биологически активных веществ |
CN115299449B (zh) * | 2022-09-20 | 2023-10-27 | 允发化工(上海)有限公司 | 一种农药组合物及其应用 |
Family Cites Families (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4051173A (en) | 1974-04-02 | 1977-09-27 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Phenoxyalkanol derivatives |
EP0612754B1 (de) | 1993-02-25 | 1998-08-19 | Th. Goldschmidt AG | Organopolysiloxanpolyether und deren Verwendung als hydrolysestabile Netzmittel in wässrigen Systemen |
EP0862856B1 (en) | 1997-03-03 | 2003-06-18 | Rohm And Haas Company | Pesticide compositions |
WO1999011127A1 (fr) * | 1997-08-29 | 1999-03-11 | Meiji Seika Kaisha, Ltd. | Agent de lutte contre la piriculariose du riz et agent de lutte contre la tavelure du ble |
TW491686B (en) | 1997-12-18 | 2002-06-21 | Basf Ag | Fungicidal mixtures based on amide compounds and tetrachloroisophthalonitrile |
CA2319807C (en) | 1998-02-06 | 2010-04-06 | Meiji Seika Kaisha Ltd. | Novel antifungal compound and process for producing the same |
US7183278B1 (en) | 1998-11-04 | 2007-02-27 | Meiji Seika Kaisha, Ltd. | Picolinamide derivative and harmful organism control agent comprising said picolinamide derivative as active component |
US6521622B1 (en) | 1999-07-20 | 2003-02-18 | Dow Agrosciences Llc | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
US20030018052A1 (en) | 1999-07-20 | 2003-01-23 | Ricks Michael J. | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
US6355660B1 (en) | 1999-07-20 | 2002-03-12 | Dow Agrosciences Llc | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
EP1516875A1 (en) | 1999-07-20 | 2005-03-23 | Dow AgroSciences LLC | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
PL205059B1 (pl) | 1999-08-20 | 2010-03-31 | Dow Agrosciences Llc | Heterocykliczny amid aromatyczny, jego kompozycja grzybobójcza oraz sposób zwalczania lub zapobiegania zakażeniom grzybami |
US20050239873A1 (en) | 1999-08-20 | 2005-10-27 | Fred Hutchinson Cancer Research Center | 2 Methoxy antimycin a derivatives and methods of use |
WO2001014365A1 (en) | 1999-08-20 | 2001-03-01 | Fred Hutchinson Cancer Research Center | COMPOSITIONS AND METHODS FOR MODULATING APOPTOSIS IN CELLS OVER-EXPRESSING bcl-2 FAMILY MEMBER PROTEINS |
FR2803592A1 (fr) | 2000-01-06 | 2001-07-13 | Aventis Cropscience Sa | Nouveaux derives de l'acide 3-hydroxypicolinique, leur procede de preparation et compositions fongicides les contenant. |
US20020119979A1 (en) | 2000-10-17 | 2002-08-29 | Degenhardt Charles Raymond | Acyclic compounds and methods for treating multidrug resistance |
EP1275653A1 (en) * | 2001-07-10 | 2003-01-15 | Bayer CropScience S.A. | Oxazolopyridines and their use as fungicides |
KR20040018538A (ko) * | 2001-07-31 | 2004-03-03 | 다우 아그로사이언시즈 엘엘씨 | Uk-2a의 엑소사이클릭 에스테르 또는 이의 유도체의환원성 분해 및 이로부터 형성된 생성물 |
US6903219B2 (en) | 2001-10-05 | 2005-06-07 | Dow Agrosciences Llc | Process to produce derivatives from UK-2A derivatives |
AR037328A1 (es) * | 2001-10-23 | 2004-11-03 | Dow Agrosciences Llc | Compuesto de [7-bencil-2,6-dioxo-1,5-dioxonan-3-il]-4-metoxipiridin-2-carboxamida, composicion que lo comprende y metodo que lo utiliza |
OA13171A (en) * | 2003-05-28 | 2006-12-13 | Basf Ag | Fungicidal mixtures for controlling rice pathogens. |
CN1794914A (zh) * | 2003-05-28 | 2006-06-28 | 巴斯福股份公司 | 用于防治稻病原体的杀真菌混合物 |
DE10347090A1 (de) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
RU2361400C2 (ru) * | 2004-02-04 | 2009-07-20 | Янссен Фармацевтика Н.В. | Синергические противогрибковые композиции ддах |
GB0419694D0 (en) | 2004-09-06 | 2004-10-06 | Givaudan Sa | Anti-bacterial compounds |
AU2006211239B2 (en) * | 2005-02-04 | 2011-04-07 | Mitsui Chemicals, Inc. | Composition for preventing plant diseases and method for preventing the diseases |
EP2363421B1 (de) * | 2005-04-18 | 2013-09-18 | Basf Se | Copolymere CP für die Herstellung von Zubereitungen, enthaltend wenigstens ein Conazolfungizid |
AR054143A1 (es) * | 2005-06-21 | 2007-06-06 | Cheminova Agro As | Combinacion sinergica de un herbicida de glifosato y un fungicida de triazol |
MX2008000801A (es) | 2005-08-05 | 2008-03-18 | Basf Ag | Mezclas fungicidas que contienen anilidas sustituidas de acido 1-metilpirazol-4-ilcarboxilico. |
US8008231B2 (en) | 2005-10-13 | 2011-08-30 | Momentive Performance Materials Inc. | Extreme environment surfactant compositions comprising hydrolysis resistant organomodified disiloxane surfactants |
WO2008105964A1 (en) | 2007-02-26 | 2008-09-04 | Stepan Company | Adjuvants for agricultural applications |
UA103008C2 (ru) * | 2007-09-26 | 2013-09-10 | Басф Се | Трехкомпонентные фунгицидные композиции, содержащие боскалид и хлороталонил |
HUE028586T2 (en) * | 2008-05-30 | 2016-12-28 | Dow Agrosciences Llc | Methods for controlling Qoi-resistant fungal pathogens |
TWI504598B (zh) | 2009-03-20 | 2015-10-21 | Onyx Therapeutics Inc | 結晶性三肽環氧酮蛋白酶抑制劑 |
JP5784603B2 (ja) | 2009-08-07 | 2015-09-24 | ダウ アグロサイエンシィズ エルエルシー | N1−スルホニル−5−フルオロピリミジノン誘導体 |
UA112284C2 (uk) | 2009-08-07 | 2016-08-25 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Похідні 5-фторпіримідинону |
MY159237A (en) | 2009-09-01 | 2016-12-30 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
US20110070278A1 (en) | 2009-09-22 | 2011-03-24 | Humberto Benito Lopez | Metconazole compositions and methods of use |
UA109416C2 (xx) | 2009-10-06 | 2015-08-25 | Стабільні емульсії типу "масло в воді" | |
PT3178321T (pt) * | 2009-10-07 | 2019-08-01 | Dow Agrosciences Llc | Misturas fungicidas sinérgicas de epoxiconazol para o controlo de fungos em cereais |
AU2010303832B2 (en) | 2009-10-07 | 2015-02-12 | Dow Agrosciences Llc | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
WO2011069893A1 (en) | 2009-12-08 | 2011-06-16 | Basf Se | Pesticidal mixtures |
PL2563771T3 (pl) | 2010-04-24 | 2016-06-30 | Viamet Pharmaceuticals Nc Inc | Związki inhibitora metaloenzymu |
WO2011159067A2 (en) | 2010-06-18 | 2011-12-22 | Green Cross Corporation | Thiazole derivatives as sglt2 inhibitors and pharmaceutical composition comprising same |
US20130130898A1 (en) | 2010-08-03 | 2013-05-23 | Markus Gewehr | Fungicidal Compositions |
UA111167C2 (uk) | 2010-08-05 | 2016-04-11 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Пестицидні композиції мезорозмірних частинок з підсиленою дією |
US9155305B2 (en) | 2010-08-05 | 2015-10-13 | Bayer Intellectual Property | Active compounds combinations comprising prothioconazole and fluxapyroxad |
JP2012036143A (ja) | 2010-08-10 | 2012-02-23 | Sumitomo Chemical Co Ltd | 植物病害防除組成物およびその用途 |
AU2011333311A1 (en) | 2010-11-24 | 2013-07-04 | Stemergie Biotechnology Sa | Inhibitors of the activity of Complex III of the mitochondrial electron transport chain and use thereof for treating diseases |
JP6013032B2 (ja) | 2011-07-08 | 2016-10-25 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
AU2013209520A1 (en) | 2012-01-20 | 2014-08-28 | Viamet Pharmaceuticals (NC), Inc. | Metalloenzyme inhibitor compounds |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
PL2847185T3 (pl) | 2012-05-07 | 2017-06-30 | Dow Agrosciences Llc | Makrocykliczne pikolinamidy jako fungicydy |
BR112014027515A2 (pt) | 2012-05-07 | 2017-06-27 | Dow Agrosciences Llc | uso de pró-fungicidas de uk-2a para controle de sigatoka negra |
KR20150013692A (ko) | 2012-05-07 | 2015-02-05 | 다우 아그로사이언시즈 엘엘씨 | 살진균제로서 매크로시클릭 피콜린아미드 |
WO2013169658A1 (en) | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llc | Use of pro-fungicides of uk-2a for control of soybean rust |
JP6129300B2 (ja) | 2012-05-07 | 2017-05-17 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
CN104883884B (zh) | 2012-12-28 | 2018-03-23 | 美国陶氏益农公司 | 用于谷物里的真菌防治的协同增效杀真菌混合物 |
JP2016507511A (ja) | 2012-12-31 | 2016-03-10 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
US9750248B2 (en) | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
US9265253B2 (en) | 2013-10-01 | 2016-02-23 | Dow Agrosciences Llc | Use of macrocyclic picolinamides as fungicides |
CN106061256A (zh) | 2013-12-26 | 2016-10-26 | 美国陶氏益农公司 | 具有杀真菌活性的大环吡啶酰胺化合物 |
CN106061260A (zh) | 2013-12-31 | 2016-10-26 | 美国陶氏益农公司 | 用于谷类中真菌防治的协同杀真菌混合物 |
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