WO2008095890A2 - Fungicidal mixtures comprising substituted 1-methylpyrazol-4-ylcarboxanilides - Google Patents

Fungicidal mixtures comprising substituted 1-methylpyrazol-4-ylcarboxanilides Download PDF

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Publication number
WO2008095890A2
WO2008095890A2 PCT/EP2008/051331 EP2008051331W WO2008095890A2 WO 2008095890 A2 WO2008095890 A2 WO 2008095890A2 EP 2008051331 W EP2008051331 W EP 2008051331W WO 2008095890 A2 WO2008095890 A2 WO 2008095890A2
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WO
WIPO (PCT)
Prior art keywords
methyl
ustilago
pyrazole
carboxamide
chloro
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PCT/EP2008/051331
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French (fr)
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WO2008095890A3 (en
Inventor
Jochen Dietz
Siegfried Strathmann
Michael Vonend
Egon Haden
Original Assignee
Basf Se
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Publication date
Priority to CN200880004134A priority Critical patent/CN101631465A/en
Priority to EA200901035A priority patent/EA017319B1/en
Application filed by Basf Se filed Critical Basf Se
Priority to MX2009007605A priority patent/MX2009007605A/en
Priority to JP2009547706A priority patent/JP2010517974A/en
Priority to EP08708635A priority patent/EP2061320A2/en
Priority to KR1020097018607A priority patent/KR20090108735A/en
Priority to BRPI0807060-1A priority patent/BRPI0807060A2/en
Priority to NZ578585A priority patent/NZ578585A/en
Priority to AU2008212956A priority patent/AU2008212956A1/en
Priority to US12/525,591 priority patent/US20100035753A1/en
Priority to CA002675455A priority patent/CA2675455A1/en
Priority to UAA200908872A priority patent/UA100504C2/en
Publication of WO2008095890A2 publication Critical patent/WO2008095890A2/en
Publication of WO2008095890A3 publication Critical patent/WO2008095890A3/en
Priority to IL199802A priority patent/IL199802A0/en
Priority to MA32197A priority patent/MA31234B1/en

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • 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
    • A01N37/12—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 containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
    • 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
    • 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
    • A01N37/42—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 containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
    • 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
    • A01N37/44—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/46—N-acyl derivatives

Definitions

  • the present invention relates to fungicidal mixtures comprising, as active components,
  • X is hydrogen or fluorine
  • R 1 is Ci-C 4 -alkyl or Ci-C 4 -haloalkyl
  • R 2 is hydrogen or halogen
  • R 3 is hydrogen, cyano, nitro, halogen, Ci-C 4 -alkyl, Ci-C 4 -haloalkyl, Ci-C 4 -alkoxy,
  • B) strobilurins selected from the group consisting of 2-(2-(6-(3-chloro-2-methyl- phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl- acetamide and 3-methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane- carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester;
  • 2-amino-4-methyl-thiazole-5-carboxylic acid anilide 2-chloro-N-(1 ,1 ,3- trimethyl-indan-4-yl)-nicotinamide, N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3- dimethyl-5-fluoro-1 H-pyrazole-4-carboxylic acid amide, N-(4'-chloro-3',5- difluoro-biphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid amide, N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl- 1 H-pyrazole-4-carboxylic acid amide, N-(3',4'-dichloro-5-fluoro-biphenyl-2-yl)- 3-trifluoro
  • heterocyclic compounds selected from the group consisting of 2,3,5,6-tetra- chloro-4-methanesulfonyl-pyridine, 3,4,5-trichloropyridine-2,6-di-carbonitrile, N-(1 -( ⁇ -bromo-S-chloro-pyridin ⁇ -yO-ethyO ⁇ -dichloronicotinamide, N-[(5- bromo-S-chloro-pyridin ⁇ -y ⁇ -methy ⁇ -dichloro-nicotinamide, diflumetorim, nitrapyrin, dodemorph-acetate, fluoroimid, blasticidin-S, chinomethionat, de- bacarb, difenzoquat, difenzoquat-methylsulphat, oxolinic acid, piperalin, 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine
  • F) other fungicides selected from the group consisting of dodine free base, guaza- tine-acetate, iminoctadine-triacetate, iminoctadine-tris(albesilate), kasugamy- cin-hydrochlorid-hydrat, dichlorophen, N-(4-chloro-2-nitro-phenyl)-N-ethyl-4- methyl-benzenesulfonamide, dicloran, nitrothal-isopropyl, tecnazen, biphenyl, bronopol, diphenylamine, mildiomycin, oxin-copper, N-(cyclopropyl- methoxyimino-(6-difluoro-methoxy-2,3-difluoro-phenyl)-methyl)-2-phenyl acetamide, N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl
  • G plant growth regulators selected from the group consisting of clofibric acid, 4- CPA (4-chlorophenoxyacetic acid), 2,4-D, 2,4-DB, 2,4-DEP, dichlorprop, feno- prop, IAA (indole-3-acetic acid), IBA (4-indol-3-ylbutyric acid), naphtha- leneacetamide, ⁇ -naphthaleneacetic acid, 1-naphthol, naphthoxyacetic acid, potassium naphthenate, sodium naphthenate, 2,4,5-T, 2iP (N-(3-methylbut-2- enyl)-1 H-purin-6-amine), 6-benzylaminopurine (6-BA), 2,6-dimethylpuridine (N- oxide-2,6-lultidine), benzyladenine, kinetin, zeatin, calcium cyanamide, dime- thipin, endothal, ethephon, merphos, meto
  • the invention relates to a method for controlling harmful fungi using a mixture of at least one compound I and at least one of the active compounds II, to the use of the compound(s) I with active compound(s) Il for preparing such mixtures, and also to compositions and seed comprising such mixtures.
  • the 1-methylpyrazol-4-ylcarboxanilides of the formula I, referred to above as component 1 ), their preparation and their action against harmful fungi are known from the literature (cf., for example, EP-A 545 099, EP-A 589 301 , WO 99/09013 and WO 2003/70705), or they can be prepared in the manner described therein.
  • the active compounds Il mentioned above as component 2), their preparation and their action against harmful fungi are generally known (cf., for example, htlp://www.alanwood.net/pesticides/index .. cn .. frarrie.html); they are commercially available.
  • the compounds I can be used as synergists for a large number of different active compounds II.
  • simultaneous, that is joint or separate, application of compound(s) I with at least one active compound II the fungicidal activity is increased in a superadditive manner.
  • the compounds I can be present in different crystal modifications, which may differ in biological activity.
  • halogen is fluorine, chlorine, bromine or iodine, preferably fluorine or chlorine;
  • Ci-C 4 -alkyl is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2- methylpropyl or 1 ,1-dimethylethyl, preferably methyl or ethyl;
  • Ci-C 4 -haloalkyl is a partially or fully halogenated CrC 4 -alkyl radical, where the halogen atom(s) is/are in particular fluorine, chlorine and/or bromine, i.e., for example, chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2- dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethy
  • Ci-C 4 -alkoxy is OCH 3 , OC 2 H 5 , OCH 2 -C 2 H 5 , OCH(CH 3 ) 2 , n-butoxy, OCH(CH 3 )-C 2 H 5 , OCH 2 -CH(CH 3 ), or OC(CH 3 ) 3 , preferably OCH 3 or OC 2 H 5 ;
  • Ci-C 4 -haloalkoxy is a partially or fully halogenated Ci-C 4 -alkoxy radical, where the halogen atom(s) is/are in particular fluorine, chlorine and/or bromine, i.e., for example, chloromethoxy, bromomethoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chloro- difluoromethoxy, 1-chloroethoxy, 1-bromoethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2- difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroeth
  • Ci-C 4 -alkylthio is SCH 3 , SC 2 H 5 , SCH 2 -C 2 H 5 , SCH(CH 3 ) 2 , n-butylthio, SCH(CH 3 )-C 2 H 5 , SCH 2 -CH(CH 3 ), or SC(CH 3 ) 3 , preferably SCH 3 or SC 2 H 5 .
  • Preferred 1-methylpyrazol-4-ylcarboxanilides I are, on the one hand, those in which X is hydrogen. On the other hand, preferred compounds I are those in which X is fluorine.
  • R 1 is methyl or halomethyl, in particular CH 3 , CHF 2 , CH 2 F, CF 3 , CHFCl Or CF 2 CI.
  • R 2 is hydrogen, fluorine or chlorine, in particular hydrogen.
  • azoles selected from the group consisting of bitertanol, bromuconazole, cypro- conazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquin- conazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothiocon- azole, simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triti- conazole, prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid, benomyl, carbendazim, thiabendazole, fuberidazole, ethaboxam, etria
  • J) strobilurins selected from the group consisting of azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, enestroburin, methyl (2-chloro-5-[1-(3- methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1 -(6-methyl- pyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate and methyl 2-(ortho-(2,5-di- methylphenyloxymethylene)phenyl)-3-methoxyacrylate;
  • carboxamides selected from the group consisting of carboxin, benalaxyl, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, 3,4-dichloro-N-(2- cyanophenyl)isothiazole-5-carboxamide, penthiopyrad, dimethomorph, flumorph, flumetover, fluopicolide (picobenzamid), zoxamide, carpropamid, diclocymet, mandipropamid, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-ethoxyphenyl)ethyl)-
  • M) carbamates selected from the group consisting of mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram, diethofencarb, iprovalicarb, flub- enthiavalicarb, propamocarb, 4-fluorophenyl N-(1-(1-(4-cyanophenyl)ethane- sulfonyl)but-2-yl)carbamate, methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonyl- amino-3-methylbutyrylamino)propanoate and carbamate oxime ethers of the formula IV
  • Z is N or CH
  • N) other fungicides selected from the group consisting of guanidine, dodine, iminoctadine, guazatine, antibiotics: kasugamycin, streptomycin, polyoxin, validamycin A, nitrophenyl derivatives: binapacryl, dinocap, dinobuton, sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane, organometallic compounds: fentin salts such as fentin acetate, organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl, organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlor- benzene, phthalide, pencycuron, quintozene, thiophanate-methyl, tolylfluanid, inorganic
  • the active compounds III mentioned above, their preparation and their action against harmful fungi are generally known (cf., for example, htt ⁇ ://wvw.alanwoj ⁇ .nj ⁇
  • an active compound selected from the group of the azoles H) selected from the group consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazo
  • an active compound selected from the group of the azoles H) selected from the group consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, propiconazole, prothioconazole, triadi- mefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl and carbendazim.
  • an active compound selected from the group of the azoles H) selected from the group consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, propiconazole, prothioconazole, triadi- mefon
  • azoxystrobin dimoxystrobin
  • fluoxastrobin fluoxastrobin
  • kresoxim-methyl orysastrobin
  • picoxystrobin pyraclostrobin
  • trifloxystrobin azoxystrobin
  • an active compound selected from the group of the strobilurins J selected from the group consisting of kresoxim-methyl, orysastrobin and pyraclostrobin.
  • an active compound selected from the group of the carboxamides K) selected from the group consisting of fenhexamid, metalaxyl, mefenoxam, ofurace, dimethomorph, flumorph, fluopicolide (picobenzamid), zoxamide, carpropamid and mandipropamid.
  • an active compound selected from the group of the heterocyclic compounds L) selected from the group consisting of pyrimethanil, dodemorph, fenpropimorph, tridemorph, iprodione, vinclozolin and quinoxyfen.
  • an active compound selected from the group of the other fungicides N) selected from the group consisting of dithianon, fentin salts, such as fentin acetate, fosetyl, fosetyl- aluminum, phosphorous acid and its salts, chlorothalonil, dichlofluanid, thiophanate- methyl, copper acetate, copper hydroxide, copper oxy
  • the mixtures of the compound(s) I with at least one of the active compounds II, or the simultaneous, that is joint or separate, use of a compound I with at least one of the active compounds II, are/is distinguished by excellent activity against a broad spectrum of phytopathogenic fungi in particular from the classes of the Ascomycetes, Basidiomy- cetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). Some of them are systemically active and can be used in crop protection as foliar fungicides, as soil fungicides and as fungicides for seed dressing.
  • the plants or seed treated with the combinations of compounds I and Il may by wildlife types, plants or seed obtained by breeding and transgenic plants as well as their seed.
  • Rhizoctonia endophytica vor filicata Rhizoctonia solani forma specialis Rhizoctonia ferruginea Rhizoctonia solani var. cedri-deodorae Rhizoctonia floccosa Rhizoctonia solani var. fuchsiae Rhizoctonia fragariae Rhizoctonia solani var. hortensis Rhizoctonia fraxini Rhizoctonia stahlii Rhizoctonia fuliginea Rhizoctonia subtilis var.
  • Rhizoctonia nigra Rhizoctonia fumigata Rhizoctonia subtlilis Rhizoctonia globularis Rhizoctonia tomato Rhizoctonia goodyerae-repentis Rhizoctonia tuliparum Rhizoctonia gossypii Rhizoctonia veae Rhizoctonia gossypii vor.
  • Rhizoctonia anatolica Rhizoctonia versicolor Rhizoctonia gracilis Rhizoctonia cerealis Rhizoctonia griseo Rhynchosporium secalis Rhizoctonia hiemalis Sclerotina rolfsii Rhizoctonia juniperi Sclerotinia rolfsii Rhizoctonia lamallifera Sclerotinia sclerotiorum Rhizoctonia leguminicola Septoria glycines Rhizoctonia lilacina Septoria nodorum Rhizoctonia luoini Septoria tritici Rhizoctonia macrosclerotia Sphaerotheca fuliginea Rhizoctonia melongenae Stagonospora nodorum Rhizoctonia microsclerotia Stemphylium botryosum Rhizoctonia monilioides Thielaviopsis basicola Rhizoctonia monteithian
  • Ustilago eleocharidis Ustilago hieronymi var. insularis
  • Ustilago ischaemi-anthephoroides Ustilago maydis
  • Ustilago phlei-protensis Ustilago scutulata Ustilago secalis var. elymi Ustilago sumnevicziana
  • the i-methylpyrazol-4-ylcarboxanilides I and the combinations of compounds I and Il and optionally III are particularly suitable for controlling phytopathogenic fungi in barley (e.g. Pyrenophora teres, Rhynchosporium secalis,Puccinia hordei,Puccinia striiformis, Blumeria graminis, Ramularia collo-cygni / Physiological leaf spots, Microdochium nivale, Typhula incarnata, Pseudocercosporella herpotrichoides, Fusarium culmorum, Rhizoctonia cerealis, Gaeumannomyces graminis) and soybeans (e.g.
  • Phakopsora pachyrhizi Microsphaera diffusa, Septoria glycines, Cercospora sojina, Cercospora kikuchii, Corynespora cassiicola, Colletotrichum truncatum, Peronospora manshurica, Alternaria spp., Phomopsis phaseoli, Diaporthe phaseolorum, Phialophora gregata, Fusarium solani, Sclerotinia sclerotiorum, Sclerotinia rolfsii, Phytopthora megasperma, Rhizoctonia solani, Dematophora necatrix, Macrophomina phaseolina).
  • the 1-methylpyrazol-4-ylcarboxanilides I where X is fluorine and their combinations with compounds II, are particularly suitable for controlling phytopathogenic fungi in barley as mentioned above.
  • the combinations according to the invention are furthermore suitable for controlling harmful fungi in the protection of materials (for example wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products.
  • harmful fungi Ascomycetes, such as Ophio- stoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chae- tomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes, such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Po- ria spp., Serpula spp.
  • Tyromyces spp. Deuteromycetes, such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes, such as Mucor spp., additionally in the protection of materials the following yeasts: Candida spp. and Saccharomyces cerevisae.
  • Application of the inventive combinations to useful plants may also lead to an increase in the crop yield.
  • the compound(s) I and at least one of the active compounds Il can be applied simulta- neously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.
  • the pure active compounds I and II When preparing the mixtures, it is preferred to employ the pure active compounds I and II, to which further compounds active against harmful fungi or other pests, such as insects, arachnids or nematodes, or else herbicidal or growth-regulating active compounds or fertilizers can be added.
  • mixtures of a compound I and one active compound Il are employed. How- ever, in certain cases mixtures of at least one compound I with two or, if appropriate, more active components may be advantageous.
  • Suitable further active components in the above sense are in particular the active compounds II, mentioned at the outset, or fipronil, and in particular the preferred active compounds Il mentioned above.
  • the compound(s) I and the active compound(s) Il are usually employed in a weight ratio of from 100:1 to 1 :100, preferably from 20:1 to 1 :20, in particular from 10:1 to 1 :10.
  • the further active components are, if desired, added in a ratio of from 20:1 to 1 :20 to the compound I.
  • the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 20 to 1500 g/ha, in particular from 50 to 1000 g/ha.
  • the application rates for the compound I are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
  • the application rates for the active compound Il are generally from 1 to 2000 g/ha, preferably from 10 to 1500 g/ha, in particular from 40 to 1000 g/ha.
  • application rates of mixture are generally from 1 to 1000 g per 100 kg of seed, preferably from 1 to 750 g per 100 kg, in particular from 5 to 500 g per 100 kg of seed.
  • the method for controlling harmful fungi is carried out by the separate or joint application of a compound I or compounds I and active compound(s) Il or a mixture of a compound I or compounds I and at least one active compound Il by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
  • the mixtures according to the invention, or the compound(s) I and at least one active compound II, can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the use form depends on the particular intended purpose; in each case, it should ensure a fine and even dis- tribution of the mixture according to the invention.
  • the formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants.
  • Solvents/auxiliaries suitable for this purpose are essentially: - water, aromatic solvents (for example Solvesso® products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (N-methylpyrrolidone, N-octylpyrrolidone), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters.
  • solvent mixtures may also be used,
  • ground natural minerals for example kaolins, clays, talc, chalk
  • ground synthetic minerals for example highly disperse silica, silicates
  • emulsifiers such as nonionogenic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose.
  • Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphen
  • Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.
  • mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin
  • Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
  • Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
  • solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
  • mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth
  • the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compounds.
  • the active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • a mixture according to the invention 25 parts by weight of a mixture according to the invention are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion.
  • the formulation has an active compound content of 25% by weight.
  • a mixture according to the invention 20 parts by weight of a mixture according to the invention are comminuted with addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound.
  • the active compound content in the formulation is 20% by weight.
  • Water-dispersible granules and water-soluble granules (WG, SG) 50 parts by weight of a mixture according to the invention are ground finely with addition of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound.
  • the formulation has an active compound content of 50% by weight.
  • a mixture according to the invention is ground finely and associated with 99.5 parts by weight of carriers.
  • Current methods are extrusion, spray- drying or the fluidized bed. This gives granules to be applied undiluted having an active compound content of 0.5% by weight.
  • ULV solutions 10 parts by weight of a mixture according to the invention are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted having an active compound content of 10% by weight.
  • the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring.
  • the use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention.
  • Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier.
  • a wetting agent e.g., it is also possible to prepare concentrates composed of active substance, wetting agent, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
  • the active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 %.
  • the active compounds may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
  • Oils of various types, wetting agents or adjuvants may be added to the active compounds, even, if appropriate, not until immediately prior to use (tank mix). These agents are typically admixed with the compositions according to the invention in a weight ratio of from 1 :100 to 100:1 , preferably from 1 :10 to 10:1.
  • Suitable adjuvants in this sense are in particular: organically modified polysiloxanes, for example Break Thru S 240 ® ; alcohol alkoxylates, for example Atplus 245 ® , Atplus MBA 1303 ® , Plurafac LF 300 ® and Lutensol ON 30 ® ; EO/PO block polymers, for example Pluronic RPE 2035 ® and Genapol B ® ; alcohol ethoxylates, for example Lutensol XP 80 ® ; and sodium dioctylsulfosuccinate, for example Leophen RA ® .
  • the compounds I and Il or the mixtures or the corresponding formulations are applied by treating the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be kept free from them with a fungicidally effective amount of the mixture or, in the case of separate application, of the compounds I and II.
  • Application can be before or after the infection by harmful fungi.
  • the active compounds were prepared as a stock solution comprising 25 mg of active compound which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having an emulsifying and dispersing action based on ethoxylated alkylphenols) in a ratio by volume of solvent/emulsifier of 99:1.
  • the mixture was then made up to 100 ml with water.
  • This stock solution was diluted with the solvent/emulsifier/water mixture described to give the concentration of active compound stated below.
  • the efficacy (E) is calculated as follows using Abbot's formula:
  • ⁇ corresponds to the fungicidal infection of the treated plants in % and ⁇ corresponds to the fungicidal infection of the untreated (control) plants in %
  • An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants were not infected.
  • Use example 1 Preventative fungicidal control of early blight on tomatoes (Alternaria solani )
  • Young seedlings of tomato plants were grown in pots. These plants were sprayed to runoff with an aqueous suspension, containing the concentration of active ingredient or mixture mentioned in the table below. The next day, the treated plants were inoculated with an aqueous suspension of Alternaria solani. Then the trial plants were immediately transferred to a humid chamber. After 5 days at 20 to 22°C and a relative humidity close to 100 %, the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • Young seedlings of green pepper were grown in pots to the 2 to 3 leaf stage. These plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day the treated plants were inoculated with a spore suspension of Botrytis cinerea in a 2 % aqueous biomalt solution. Then the trial plants were immediately transferred to a dark, humid chamber. After 5 days at 22 to 24 0 C and a relative humidity close to 100 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • the first fully developed leaves of pot grown wheat were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below.
  • After cultivation in the greenhouse for 7 days at 22-26 0 C and a relative humidity between 60 to 90 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • Use example 5 Curative control of brown rust on wheat caused by Puccinia recondita
  • the first two developed leaves of pot-grown wheat seedling were dusted with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99 % and 20 to 22 0 C for 24 h. The next day the plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The plants were allowed to air-dry. Then the trial plants were cultivated for 8 days in a greenhouse chamber at 22-26 0 C and a relative humidity between 65 and 70 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • the first two developed leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their as described below.
  • the next day the plants were inoculated with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99 % and 20 to 22°C for 24 h. Then the trial plants were cultivated for 6 days in a greenhouse chamber at 22-26°C and a relative humidity between 65 and 70 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • Use example 7 Control of net blotch on barley caused by Pyrenophora teres
  • the first fully developed leaves of pot grown barley plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mentioned in the table below.
  • the next day the treated plants were inoculated with an aqueous spore suspension of Pyrenophora (syn. Drechslera) teres. Then the trial plants were immediately transferred to a humid chamber in the greenhouse. After 6 days of cultivation at 20-24 0 C and a relative humidity close to 70 %, the extent of fungal attack on the leaves was visually assessed as % leaf area.
  • Leaves of pot-grown soy bean seedlings were inoculated with spores of Phakopsora pachyrhizi .
  • the plants were transferred to a humid chamber with a relative humidity of about 95 % and 23 to 27 0 C for 24 h.
  • the next day the plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below.
  • the plants were allowed to air-dry.
  • the trial plants were cultivated for 14 days in a greenhouse chamber at 23-27 0 C and a relative humidity between 60 and 80 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • the active compounds were formulated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide.
  • Benalaxyl-M was used as commercial finished formulation and diluted with water to the stated concentration of the active compound.
  • the measured parameters were compared to the growth of the active compound-free control variant (100%) and the fungus-free and active compound-free blank value to determine the relative growth in % of the pathogens in the respective active compounds. These percentages were converted into efficacies.
  • the stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations.
  • MTP micro titer plate
  • a spore suspension of Phytophtora infestans containing a pea juice-based aqueous nutrient medium was then added.
  • the plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
  • MTP Botrytis cinerea
  • a spore suspension of Botrytis cinerea in 2 % aqueous biomalt solution was then added.
  • the plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.

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Abstract

Fungicidal mixtures, comprising as active components: 1) at least one 1-methylpyrazol-4-ylcarboxanilide of the formula (I) where X = hydrogen or fluorine, R1 = C1-C4-alkyl or C1-C4-haloalkyl, R2 = hydrogen or halogen, R3 = hydrogen, cyano, nitro, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy or C1-C4-alkylthio, R4 and R5 = independently of one another hydrogen, cyano, nitro, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, -CH=N-OR6 or -C(CH3)=N-OR6, where R6 is hydrogen, methyl or ethyl; and 2) at least one active compound II, selected from the active compound groups A) to G): A) azoles; B) strobilurins; C) carboxamides; D) heterocyclic compounds; E) carbamates; F) other fungicides; G) plant growth regulators; in a synergistically effective amount, methods for controlling harmful fungi using mixtures of at least one compound I and at least one active compound II, the use of a compound I or compounds I with active compounds Il for preparing such mixtures, and also compositions and seed comprising such mixtures.

Description

Fungicidal mixtures comprising substituted i-methylpyrazol-4-ylcarboxanilides
Description
The present invention relates to fungicidal mixtures comprising, as active components,
1 ) at least one 1 -methylpyrazol-4-ylcarboxanilides of the formula I
Figure imgf000002_0001
in which the substituents are as defined below: X is hydrogen or fluorine;
R1 is Ci-C4-alkyl or Ci-C4-haloalkyl;
R2 is hydrogen or halogen;
R3 is hydrogen, cyano, nitro, halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy,
Ci-C4-haloalkoxy or Ci-C4-alkylthio; R4 and R5 independently of one another are hydrogen, cyano, nitro, halogen,
Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, Ci-C4-haloalkoxy, Ci-C4-alkylthio, -CH=N-OR6 or -C(CH3)=N-OR6, where R6 is hydrogen, methyl or ethyl;
and
2) at least one active compound II, selected from the active compound groups A) to G):
A) azoles selected from the group consisting of azaconazole, diniconazole-M, oxpoconazol, paclobutrazol, uniconazol, 1-(4-chloro-phenyl)-2-([1 ,2,4]triazol-1- yl)-cycloheptanol and imazalil-sulfphate;
B) strobilurins selected from the group consisting of 2-(2-(6-(3-chloro-2-methyl- phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl- acetamide and 3-methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane- carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester;
C) carboxamides selected from the group consisting of benalaxyl-M,
2-amino-4-methyl-thiazole-5-carboxylic acid anilide, 2-chloro-N-(1 ,1 ,3- trimethyl-indan-4-yl)-nicotinamide, N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3- dimethyl-5-fluoro-1 H-pyrazole-4-carboxylic acid amide, N-(4'-chloro-3',5- difluoro-biphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid amide, N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1 -methyl- 1 H-pyrazole-4-carboxylic acid amide, N-(3',4'-dichloro-5-fluoro-biphenyl-2-yl)- 3-trifluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid amide, N-(3',5- difluoro-4'-methyl-biphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid amide, N-(3',5-difluoro-4'-methyl-biphenyl-2-yl)-3- trifluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid amide, N-(cis-2- bicyclopropyl-2-yl-phenyl)-3-di-fluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid amide, N-(trans-2-bi-cyclopropyl-2-yl-phenyl)-3-difluoromethyl- 1 -methyl-1 H-pyrazole-4-carboxylic acid amide, fluopyram, N-(3-ethyl-3,5-5- trimethyl-cyclohexyl)-3-formylamino-2-hydroxy-benzamide, oxytetracyclin, silthiofam, N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide, isotianil and 3-(difluoromethyl)-1 -methyl-N-[1 ,2,3,4-tetrahydro-9-(1 - methylethyl)-1 ,4-methano-naphthalen-5-yl]-1 H-pyrazole-4-carboxamide of the following formula:
Figure imgf000003_0001
heterocyclic compounds selected from the group consisting of 2,3,5,6-tetra- chloro-4-methanesulfonyl-pyridine, 3,4,5-trichloropyridine-2,6-di-carbonitrile, N-(1 -(δ-bromo-S-chloro-pyridin^-yO-ethyO^^-dichloronicotinamide, N-[(5- bromo-S-chloro-pyridin^-y^-methy^^^-dichloro-nicotinamide, diflumetorim, nitrapyrin, dodemorph-acetate, fluoroimid, blasticidin-S, chinomethionat, de- bacarb, difenzoquat, difenzoquat-methylsulphat, oxolinic acid, piperalin, 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine
Figure imgf000003_0002
and δ-amino^-iso-propyM-ortho-tolyl-pyrazol-S-on-i-thiocarboxylic acid allyl ester
Figure imgf000004_0001
E) carbamates selected from the group consisting of methasulphocarb, pyriben- carb and propamocarb hydrochlorid;
F) other fungicides selected from the group consisting of dodine free base, guaza- tine-acetate, iminoctadine-triacetate, iminoctadine-tris(albesilate), kasugamy- cin-hydrochlorid-hydrat, dichlorophen, N-(4-chloro-2-nitro-phenyl)-N-ethyl-4- methyl-benzenesulfonamide, dicloran, nitrothal-isopropyl, tecnazen, biphenyl, bronopol, diphenylamine, mildiomycin, oxin-copper, N-(cyclopropyl- methoxyimino-(6-difluoro-methoxy-2,3-difluoro-phenyl)-methyl)-2-phenyl acetamide, N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N- ethyl-N-methyl formamidine, N'-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5- dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'-(2-methyl-5-trifluormethyl- 4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine and N'-(5- difluormethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine;
G) plant growth regulators selected from the group consisting of clofibric acid, 4- CPA (4-chlorophenoxyacetic acid), 2,4-D, 2,4-DB, 2,4-DEP, dichlorprop, feno- prop, IAA (indole-3-acetic acid), IBA (4-indol-3-ylbutyric acid), naphtha- leneacetamide, α -naphthaleneacetic acid, 1-naphthol, naphthoxyacetic acid, potassium naphthenate, sodium naphthenate, 2,4,5-T, 2iP (N-(3-methylbut-2- enyl)-1 H-purin-6-amine), 6-benzylaminopurine (6-BA), 2,6-dimethylpuridine (N- oxide-2,6-lultidine), benzyladenine, kinetin, zeatin, calcium cyanamide, dime- thipin, endothal, ethephon, merphos, metoxuron, pentachlorophenol and its salts, thidiazuron, tribufos, aviglycine, 1-methylcyclopropene, ACC (1- aminocyclopropanecarboxylic acid), etacelasil, ethephon, glyoxime, gibberel- lins, gibberellic acid, abscisic acid, ancymidol, butralin, carbaryl, chlorphonium, chlorpropham, dikegulac, flumetralin, fluoridamid, fosamine, glyphosine, isopy- rimol, jasmonic acid, maleic hydrazide, mepiquat (mepiquat chloride, mepiquat pentaborate), piproctanyl, prohydrojasmon, propham, 2,3,5-tri-iodobenzoic acid, chlorfluren, chlorflurenol, dichlorflurenol, flurenol, chlormequat, dami- nozide, flurprimidol, mefluidide, paclobutrazol, tetcyclacis, uniconazole, brassi- nolide, forchlorfenuron, hymexazol, amidochlor, benzofluor, buminafos, car- vone, ciobutide, clofencet, cloxyfonac, cyanamide, cyclanilide, cycloheximide, cyprosulfamide, epocholeone, ethychlozate, ethylene, fenridazon, fluprimidol, heptopargil, holosulf, inabenfide, karetazan, lead arsenate, methasulfocarb, prohexadione (prohexadione calcium), pydanon, sintofen, triapenthenol and trinexapac (trinexapac-ethyl);
in a synergistically effective amount.
Moreover, the invention relates to a method for controlling harmful fungi using a mixture of at least one compound I and at least one of the active compounds II, to the use of the compound(s) I with active compound(s) Il for preparing such mixtures, and also to compositions and seed comprising such mixtures.
The 1-methylpyrazol-4-ylcarboxanilides of the formula I, referred to above as component 1 ), their preparation and their action against harmful fungi are known from the literature (cf., for example, EP-A 545 099, EP-A 589 301 , WO 99/09013 and WO 2003/70705), or they can be prepared in the manner described therein.
However, the known 1-methylpyrazol-4-ylcarboxanilides of the formula I are, in particu- lar at low application rates, not entirely satisfactory.
The active compounds Il mentioned above as component 2), their preparation and their action against harmful fungi are generally known (cf., for example, htlp://www.alanwood.net/pesticides/index..cn..frarrie.html); they are commercially available.
It is an object of the present invention, with a view to reducing the application rates and broadening the activity spectrum of the active compounds I and II, to provide mixtures which, at a reduced total amount of active compounds applied, have improved activity against harmful fungi, in particular for certain indications.
We have accordingly found that this object is achieved by the mixtures, defined at the outset, of the active compounds I and II. Moreover, we have found that simultaneous, that is joint or separate, application of at least one compound I and at least one of the active compounds Il or successive application of the compound(s) I and at least one of the active compounds Il allows better control of harmful fungi than is possible with the individual compounds alone (synergistic mixtures).
The compounds I can be used as synergists for a large number of different active compounds II. By simultaneous, that is joint or separate, application of compound(s) I with at least one active compound II, the fungicidal activity is increased in a superadditive manner.
The compounds I can be present in different crystal modifications, which may differ in biological activity.
In the formula I, halogen is fluorine, chlorine, bromine or iodine, preferably fluorine or chlorine;
Ci-C4-alkyl is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2- methylpropyl or 1 ,1-dimethylethyl, preferably methyl or ethyl;
Ci-C4-haloalkyl is a partially or fully halogenated CrC4-alkyl radical, where the halogen atom(s) is/are in particular fluorine, chlorine and/or bromine, i.e., for example, chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2- dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl, heptafluoropropyl or nonafluorobutyl, in particular halomethyl, with particular preference CH2-CI, CH(CI)2, CH2-F, CHF2, CF3, CHFCI, CF2CI or CF(CI)2, in particular CHF2 or CF3;
Ci-C4-alkoxy is OCH3, OC2H5, OCH2-C2H5, OCH(CH3)2, n-butoxy, OCH(CH3)-C2H5, OCH2-CH(CH3), or OC(CH3)3, preferably OCH3 or OC2H5;
Ci-C4-haloalkoxy is a partially or fully halogenated Ci-C4-alkoxy radical, where the halogen atom(s) is/are in particular fluorine, chlorine and/or bromine, i.e., for example, chloromethoxy, bromomethoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chloro- difluoromethoxy, 1-chloroethoxy, 1-bromoethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2- difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy, heptafluoropropoxy or nonafluorobutoxy, in particular halomethoxy, particularly preferably OCH2-CI, OCH(CI)2, OCH2-F, OCH(F)2, OCF3, OCHFCI, OCF2CI Or OCF(CI)2;
Ci-C4-alkylthio is SCH3, SC2H5, SCH2-C2H5, SCH(CH3)2, n-butylthio, SCH(CH3)-C2H5, SCH2-CH(CH3), or SC(CH3)3, preferably SCH3 or SC2H5.
Preferred 1-methylpyrazol-4-ylcarboxanilides I are, on the one hand, those in which X is hydrogen. On the other hand, preferred compounds I are those in which X is fluorine.
For the mixtures according to the invention, preference is given to compounds of the formula I in which R1 is methyl or halomethyl, in particular CH3, CHF2, CH2F, CF3, CHFCl Or CF2CI.
Preference is furthermore given to compounds I in which R2 is hydrogen, fluorine or chlorine, in particular hydrogen.
Preference is furthermore given to those compounds I in which X is hydrogen and R3 is halogen, d-C4-alkyl, CrC4-haloalkyl, Ci-C4-alkoxy, Ci-C4-haloalkoxy or d-C4- alkylthio, preferably halogen, methyl, halomethyl, methoxy, halomethoxy or methylthio, in particular F, Cl, CH3, CF3, OCH3, OCHF2, OCF3 or SCH3, particularly preferably fluorine.
Preference is furthermore given to those compounds I in which X is fluorine and R3 is hydrogen.
Moreover, preference is given to those compounds I in which R4 is halogen, in particu- lar fluorine.
Preference is furthermore given to those compounds I in which R5 is halogen, in particular fluorine.
Particular preference is given to the compounds I, listed in Table 1 below, in which X is hydrogen.
Table 1
Figure imgf000007_0001
Figure imgf000008_0001
Figure imgf000009_0001
Figure imgf000010_0002
Particular preference is furthermore given to i-methylpyrazol-4-ylcarboxanilides of the formula Ia (I where X = H, R1 = CF3 and R2 = H)
Figure imgf000010_0001
in particular to the compounds Ia.1 to Ia.1010 listed in Table 2 below:
Table 2:
Figure imgf000010_0003
Figure imgf000011_0001
Figure imgf000012_0001
Figure imgf000013_0001
Figure imgf000014_0001
Figure imgf000015_0001
Figure imgf000016_0001
Figure imgf000017_0001
Figure imgf000018_0001
Figure imgf000019_0001
Figure imgf000020_0001
Figure imgf000021_0001
Figure imgf000022_0001
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
Figure imgf000033_0001
Figure imgf000034_0001
Figure imgf000035_0001
Figure imgf000036_0001
Figure imgf000037_0001
Figure imgf000038_0001
Figure imgf000039_0001
Figure imgf000040_0003
Particular preference is furthermore given to i-methylpyrazol-4-ylcarboxanilides of the formulae Ib to Im, in particular to the compounds Ib.1 to lb.1010 which differ from the corresponding compounds Ia.1 to la.1010 only in that R2 is fluorine:
Figure imgf000040_0001
the compounds Ic.1 to Ic.1010 which differ from the corresponding compounds Ia.1 to la.1010 only in that R2 is chlorine:
Figure imgf000040_0002
the compounds Id.1 to ld.1010 which differ from the corresponding compounds Ia.1 to la.1010 only in that R1 is difluoromethyl:
Figure imgf000041_0001
the compounds Ie.1 to Ie.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that R1 is difluoromethyl and R2 is fluorine:
Figure imgf000041_0002
the compounds lf.1 to If.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that R1 is difluoromethyl and R2 is chlorine:
Figure imgf000041_0003
the compounds Ig.1 to Ig.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that R1 is fluoromethyl:
Figure imgf000041_0004
the compounds Ih.1 to Ih.1010 which differ from the corresponding compounds Ia.1 to la.1010 only in that R1 is CF2CI:
Figure imgf000042_0001
the compounds Ij.1 to Ij.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that R1 is chlorofluoromethyl:
Figure imgf000042_0002
the compounds Ik.1 to Ik.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that X is 4-fluorine:
Figure imgf000042_0003
the compounds Im.1 to Im.1010 which differ from the corresponding compounds Ia.1 to Ia.1010 only in that X is 4-fluorine and R1 is difluoromethyl:
Figure imgf000042_0004
Among those 1-methylpyrazol-4-ylcarboxanilides I where X is hydrogen, particular preference is given to N-(2'-fluoro-4'-chloro-5'-methoxybiphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-(2'-fluoro-4'-chloro-5'-methylbiphenyl-2-yl)-
3-trifluoromethyl-1-methyl-1 H-pyrazole-4-carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)- 3-trifluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-(2',4',5'-trifluorobiphenyl-2-yl)- 3-trifluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N-(2'-fluoro-4'-chloro-5'- methoxybiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N- (2',3',4'-trifluorobiphenyl-2-yl)-3-trifluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, N- (2'-fluoro-4'-chloro-5'-methylbiphenyl-2-yl)-3-difluoromethyl-1-methyl-1 H-pyrazole- 4-carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(2',4',5'-trifluorobiphenyl-2-yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-fluoromethyl-1 -methyl-1 H-pyrazole-4- carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-chlorodifluoromethyl-1 -methyl-1 H- pyrazole-4-carboxamide, N-(3',4',5'-trifluorobiphenyl-2-yl)-3-chlorofluoromethyl-1- methyl-1 H-pyrazole-4-carboxamide, N-(2',3',4'-trifluorobiphenyl-2-yl)-3-fluoromethyl- 1 -methyl-1 H-pyrazole-4-carboxamide and N-(2',4',5'-trifluorobiphenyl-2-yl)-3-fluoro- methyl-1 -methyl-1 H-pyrazole-4-carboxamide.
Among those 1-methylpyrazol-4-ylcarboxanilides I where X is fluorine, particular preference is given to N-(3',4'-dichloro-3-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl- 1 H-pyrazole-4-carboxamide, N-(3',4'-dichloro-3-fluorobiphenyl-2-yl)-1 -methyl-3- difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'-difluoro-3-fluorobiphenyl-2-yl)-1- methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'-difluoro-3-fluorobiphenyl- 2-yl)-1 -methyl-3-difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3'-chloro-4'-fluoro-3- fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'- dichloro-4-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'-difluoro-4-fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H- pyrazole-4-carboxamide, N-(3',4'-difluoro-4-fluorobiphenyl-2-yl)-1-methyl-3- difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3'-chloro-4'-fluoro-4-fluorobiphenyl-2-yl)- 1 -methyl-3-difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'-dichloro-5- fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide,
N-(3',4'-difluoro-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H- pyrazole-4-carboxamide, N-(3',4'-difluoro-5-fluorobiphenyl-2-yl)-1-methyl-3- difluoromethyl-1 H-pyrazole-4-carboxamide, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1 ,3- dimethyl-1 H-pyrazole-4-carboxamide, N-(3'-chloro-4'-fluoro-5-fluorobiphenyl-2-yl)-1- methyl-3-difluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'-fluoro-4-fluorobiphenyl-2-yl)- 1 -methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'-fluoro-5-fluorobiphenyl-2- yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'-chloro-5- fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4-carboxamide, N-(4'-methyl-5-fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(4'-fluoro-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4- carboxamide, N-(4'-chloro-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4- carboxamide, N-(4'-methyl-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4- carboxamide, N-(4'-fluoro-6-fluorobiphenyl-2-yl)-1 -methyl-3-trifluoromethyl-1 H- pyrazole-4-carboxamide and N-(4'-chloro-6-fluorobiphenyl-2-yl)-1-methyl-3- trifluoromethyl-I H-pyrazole-4-carboxamide.
Preference is given to mixtures of a compound of the formula I with at least one active compound selected from the group of the A) azoles.
Preference is also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the B) strobilurins.
Preference is given to mixtures of a compound of the formula I with at least one active compound selected from the group of the C) carboxamides.
Preference is furthermore also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the D) heterocyclic compounds.
Preference is furthermore also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the E) carbamates.
Preference is furthermore also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the F) other fungicides.
Preference is furthermore also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the G) plant growth regulators.
Preference is also given to mixtures of a compound of the formula I with at least one active compound selected from the group of the F) other fungicides selected from the group consisting of N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N- ethyl-N-methyl formamidine and N'-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5- dimethyl-phenyl)-N-ethyl-N-methyl formamidine.
Preference is also given to mixtures of a compound of the formula I with at least one acitve compound selected from the group of the G) plant growth regulators selected from the group consisting of abscisic acid, amidochlor, ancymidol, 6- benzylaminopurine, brassinolide, butralin, chlormequat (chlormequat chloride), choline chloride, cyclanilide, daminozide, dikegulac, dimethipin, 2,6-dimethylpuridine, ethephon, flumetralin, flurprimidol, fluthiacet, forchlorfenuron, gibberellic acid, inaben- fide, indole-3-acetic acid, maleic hydrazide, mefluidide, mepiquat (mepiquat chloride), naphthaleneacetic acid, N-6 benzyladenine, prohexadione (prohexadione calcium), prohydrojasmon, thidiazuron, triapenthenol, tributyl phosphorotrithioate, 2,3,5-tri- iodobenzoic acid and trinexapac (trinexapac-ethyl). Preference is also given to three-component mixtures of one compound of the formula I with two of the active compounds Il mentioned above.
Preference is also given to three-component mixtures of one compound of the formula I with two of the active compounds Il mentioned above or with one active compound Il and a further fungicidally active compound III selected from active compound groups H) to N):
H) azoles selected from the group consisting of bitertanol, bromuconazole, cypro- conazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquin- conazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothiocon- azole, simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triti- conazole, prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid, benomyl, carbendazim, thiabendazole, fuberidazole, ethaboxam, etridiazole and hymexa- zole;
J) strobilurins selected from the group consisting of azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, enestroburin, methyl (2-chloro-5-[1-(3- methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1 -(6-methyl- pyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate and methyl 2-(ortho-(2,5-di- methylphenyloxymethylene)phenyl)-3-methoxyacrylate;
K) carboxamides selected from the group consisting of carboxin, benalaxyl, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, 3,4-dichloro-N-(2- cyanophenyl)isothiazole-5-carboxamide, penthiopyrad, dimethomorph, flumorph, flumetover, fluopicolide (picobenzamid), zoxamide, carpropamid, diclocymet, mandipropamid, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-ethoxyphenyl)ethyl)-
2-methanesulfonylamino-3-methylbutyramide, N-(2-(4-[3-(4-chlorophenyl)prop-2- ynyloxy]-3-methoxyphenyl)ethyl)-2-ethanesulfonylamino-3-methylbutyramide, methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)- propionate, N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carbox- amide, N-(4'-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methyl- thiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-difluoromethyl-1- methylpyrazole-4-carboxamide and N-(2-cyanophenyl)-3,4-dichloroisothiazole-5- carboxamide; L) heterocyclic compounds selected from the group consisting of fluazinam, pyrifenox, bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol, pyrimethanil, triforine, fenpiclonil, fludioxonil, aldimorph, dodemorph, fenpropi- morph, tridemorph, fenpropidin, iprodione, procymidone, vinclozolin, famoxadone, fenamidone, octhilinone, probenazole, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6- trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole, 2-butoxy-6-iodo-3-propylchromen-4-one, acibenzolar-S- methyl, captafol, captan, dazomet, folpet, fenoxanil, quinoxyfen and N,N-dimethyl- 3-(3-bromo-6-fluoro-2-methylindole-1 -sulfonyl)-[1 ,2,4]triazole-1 -sulfonamide;
M) carbamates selected from the group consisting of mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram, diethofencarb, iprovalicarb, flub- enthiavalicarb, propamocarb, 4-fluorophenyl N-(1-(1-(4-cyanophenyl)ethane- sulfonyl)but-2-yl)carbamate, methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonyl- amino-3-methylbutyrylamino)propanoate and carbamate oxime ethers of the formula IV
Figure imgf000046_0001
in which Z is N or CH;
N) other fungicides selected from the group consisting of guanidine, dodine, iminoctadine, guazatine, antibiotics: kasugamycin, streptomycin, polyoxin, validamycin A, nitrophenyl derivatives: binapacryl, dinocap, dinobuton, sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane, organometallic compounds: fentin salts such as fentin acetate, organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl, organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlor- benzene, phthalide, pencycuron, quintozene, thiophanate-methyl, tolylfluanid, inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur, others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine.
The active compounds III mentioned above, their preparation and their action against harmful fungi are generally known (cf., for example, httø://wvw.alanwoj^.nj^|Desticid^ they are commercially available. Preference is given to three-component mixtures of compounds I and Il with an active compound selected from the group of the azoles H).
Preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the strobilurins J).
Preference is given to three-component mixtures of compounds I and Il with an active compound selected from the group of the carboxamides K).
Preference is furthermore also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the heterocyclic compounds L).
Preference is furthermore also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the carbamates M).
Preference is furthermore also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the other fungicides N).
Preference is furthermore also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the azoles H) selected from the group consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl, carbendazim and ethaboxam.
Particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the azoles H) selected from the group consisting of cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, propiconazole, prothioconazole, triadi- mefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl and carbendazim.
Very particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the azoles H) selected from the group consisting of epoxiconazole, fluquinconazole, flutriafol, metconazole, tebuconazole, triticonazole, prochloraz and carbendazim.
Preference is also given to three-component mixtures of compounds I and Il with at least one active compound selected from the group of the strobilurins J) selected from the group consisting of azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin and trifloxystrobin. Particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the strobilurins J) selected from the group consisting of kresoxim-methyl, orysastrobin and pyraclostrobin.
Very particular preference is also given to three-component mixtures of compounds I and Il with pyraclostrobin.
Preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the carboxamides K) selected from the group consisting of fenhexamid, metalaxyl, mefenoxam, ofurace, dimethomorph, flumorph, fluopicolide (picobenzamid), zoxamide, carpropamid and mandipropamid.
Particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the carboxamides K) selected from the group consisting of fenhexamid, metalaxyl, mefenoxam, ofurace, dimethomorph, zoxamide and carpropamid.
Preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the heterocyclic compounds K) selected from the group consisting of fluazinam, cyprodinil, fenarimol, mepanipyrim, pyrimethanil, triforine, fludioxonil, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, vinclozolin, famoxadone, fenamidone, probenazole, 5-chloro-7-(4-methyl- piperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, proquinazid, acibenzolar-S-methyl, captafol, folpet, fenoxanil and quinoxyfen, in particular fluazinam, cyprodinil, fenarimol, mepanipyrim, pyrimethanil, triforine, fludioxonil, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, vinclozolin, famoxadone, fenamidone, probenazole, proquinazid, acibenzolar-S-methyl, captafol, folpet, fenoxanil and quinoxyfen.
Particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the heterocyclic compounds L) selected from the group consisting of pyrimethanil, dodemorph, fenpropimorph, tridemorph, iprodione, vinclozolin, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluoro- phenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine and quinoxyfen, in particular pyrimethanil, dodemorph, fenpropimorph, tridemorph, iprodione, vinclozolin and quinoxyfen.
Preference is also given to three-component mixtures of compounds I and Il with at least one active compound selected from the group of the carbamates M) selected from the group consisting of mancozeb, metiram, propineb, thiram, iprovalicarb, flubenthiavalicarb and propamocarb. Particular preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the carbamates M) selected from the group consisting of mancozeb and metiram.
Preference is also given to three-component mixtures of compounds I and Il with an active compound selected from the group of the other fungicides N) selected from the group consisting of dithianon, fentin salts, such as fentin acetate, fosetyl, fosetyl- aluminum, phosphorous acid and its salts, chlorothalonil, dichlofluanid, thiophanate- methyl, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur, cymoxanil, metrafenone and spiroxamine.
Particular preference is also given to three-component mixtures of compounds I and with an active compound selected from the group of the other fungicides N) selected from the group consisting of phosphorous acid and its salts, chlorothalonil and metrafenone.
Preference is also given to four-component mixtures of compounds I and Il with two futher active compounds selected from compounds Il and III mentioned above.
Preferred active compound combinations are listed in tables 3 to 8 below:
Table 3
Active compound combinations of compounds I with active compounds Il of group A):
Mixture Compound I Compound Il o. A.1 No. la.344 azaconazole o. A.2 No. la.719 azaconazole o. A.3 No. ld.344 azaconazole o. A.4 No. ld.667 azaconazole o. A.5 No. lj.344 azaconazole o. A.6 No. Im.1010 azaconazole o. A.7 No. la.344 diniconazole-M o. A.8 No. la.719 diniconazole-M o. A.9 No. ld.344 diniconazole-M o. A.10 No. ld.667 diniconazole-M o. A.11 No. lj.344 diniconazole-M o. A.12 No. Im.1010 diniconazole-M o. A.13 No. la.344 oxpoconazol o. A.14 No. la.719 oxpoconazol
Figure imgf000050_0001
Table 4
Active compound combinations of compounds I with active compounds Il of group B):
Figure imgf000050_0002
Figure imgf000051_0001
Table 5
Active compound combinations of compounds I with active compounds Il of group C):
Mixture Compounds I Compound Il
No. C.1 No. la.344 benalaxyl-M
No. C.2 No. la.719 benalaxyl-M
No. C.3 No. ld.344 benalaxyl-M
No. C.4 No. ld.667 benalaxyl-M
No. C.5 No. lj.344 benalaxyl-M
No. C.6 No. Im.1010 benalaxyl-M
No. C.7 No. la.344 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.8 No. la.719 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.9 No. ld.344 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.10 No. ld.667 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.11 No. lj.344 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.12 No. Im.1010 2-amino-4-methyl-thiazole-5-carboxylic acid anilide
No. C.13 No. la.344 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide
No. C.14 No. la.719 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide
No. C.15 No. ld.344 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide
No. C.16 No. ld.667 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide Mixture Compounds I Compound Il
No. C.17 No. lj.344 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide
No. C.18 No. Im.1010 2-chloro-N-(1 ,1 ,3-trimethyl-indan-4-yl)-nicotinamide
No. C.19 No. la.344 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyτazole-4-carboxylic acid amide
No. C.20 No. la.719 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyrazole-4-carboxylic acid amide
No. C.21 No. ld.344 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyrazole-4-carboxylic acid amide
No. C.22 No. ld.667 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyrazole-4-carboxylic acid amide
No. C.23 No. lj.344 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyrazole-4-carboxylic acid amide
No. C.24 No. Im.1010 N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3-dimethyl-5-fluoro-1 H- pyrazole-4-carboxylic acid amide
No. C.25 No. la.344 N-(4'-chloro-3\5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.26 No. la.719 N-(4'-chloro-3\5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.27 No. ld.344 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.28 No. ld.667 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.29 No. lj.344 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.30 No. Im.1010 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.31 No. la.344 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.32 No. la.719 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.33 No. ld.344 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.34 No. ld.667 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.35 No. lj.344 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.36 No. Im.1010 N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3-trifluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
Figure imgf000053_0001
Mixture Compounds I Compound Il
No. C.56 No. la.719 N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.57 No. ld.344 N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.58 No. ld.667 N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.59 No. lj.344 N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.60 No. Im.1010 N-(cis-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.61 No. la.344 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.62 No. la.719 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.63 No. ld.344 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.64 No. ld.667 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.65 No. lj.344 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.66 No. Im.1010 N-(trans-2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid amide
No. C.67 No. la.344 fluopyram
No. C.68 No. la.719 fluopyram
No. C.69 No. ld.344 fluopyram
No. C.70 No. ld.667 fluopyram
No. C.71 No. lj.344 fluopyram
No. C.72 No. Im.1010 fluopyram
No. C.73 No. la.344 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide
No. C.74 No. la.719 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide
No. C.75 No. ld.344 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide
No. C.76 No. ld.667 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide
No. C.77 No. lj.344 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide Mixture Compounds I Compound Il
No. C .78 No. Im.1010 N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-3-formylamino-2- hydroxy-benzamide
No. C .79 No. la.344 oxytetracyclin
No. C .80 No. la.719 oxytetracyclin
No. C .81 No. ld.344 oxytetracyclin
No. C .82 No. ld.667 oxytetracyclin
No. C .83 No. lj.344 oxytetracyclin
No. C .84 No. Im.1010 oxytetracyclin
No. C .85 No. la.344 silthiofam
No. C .86 No. la.719 silthiofam
No. C .87 No. ld.344 silthiofam
No. C .88 No. ld.667 silthiofam
No. C .89 No. lj.344 silthiofam
No. C .90 No. Im.1010 silthiofam
No. C .91 No. la.344 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. C .92 No. la.719 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. C .93 No. ld.344 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. C .94 No. ld.667 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. C .95 No. lj.344 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. C .96 No. Im.1010 N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide
No. Ic .97 la.344 isotianil
No. Ic .98 la.719 isotianil
No. Ic .99 ld.344 isotianil
No. Ic .100 ld.667 isotianil
No. Ic .101 lj.344 isotianil
No. Ic .102 Im. 1010 isotianil
Table 6
Active compound combinations of compounds I with active compounds Il of group D):
Figure imgf000055_0001
Figure imgf000056_0001
Mixture Compound I Compound Il
No. D.30 No. Im.1010 diflumetorim
No. D.31 No. la.344 nitrapyrin
No. D.32 No. la.719 nitrapyrin
No. D.33 No. ld.344 nitrapyrin
No. D.34 No. ld.667 nitrapyrin
No. D.35 No. lj.344 nitrapyrin
No. D.36 No. Im.1010 nitrapyrin
No. D.37 No. la.344 dodemorph-acetate
No. D.38 No. la.719 dodemorph-acetate
No. D.39 No. ld.344 dodemorph-acetate
No. D.40 No. ld.667 dodemorph-acetate
No. D.41 No. lj.344 dodemorph-acetate
No. D.42 No. Im.1010 dodemorph-acetate
No. D.43 No. la.344 fluoroimid
No. D.44 No. la.719 fluoroimid
No. D.45 No. ld.344 fluoroimid
No. D.46 No. ld.667 fluoroimid
No. D.47 No. lj.344 fluoroimid
No. D.48 No. Im.1010 fluoroimid
No. D.49 No. la.344 blasticidin-S
No. D.50 No. la.719 blasticidin-S
No. D.51 No. ld.344 blasticidin-S
No. D.52 No. ld.667 blasticidin-S
No. D.53 No. lj.344 blasticidin-S
No. D.54 No. Im.1010 blasticidin-S
No. D.55 No. la.344 chinomethionat
No. D.56 No. la.719 chinomethionat
No. D.57 No. ld.344 chinomethionat
No. D.58 No. ld.667 chinomethionat
No. D.59 No. lj.344 chinomethionat
No. D.60 No. Im.1010 chinomethionat
No. D.61 No. la.344 debacarb
No. D.62 No. la.719 debacarb
No. D.63 No. ld.344 debacarb
No. D.64 No. ld.667 debacarb
No. D.65 No. lj.344 debacarb
No. D.66 No. Im.1010 debacarb
No. D.67 No. la.344 difenzoquat Mixture Compound I Compound Il
No. D.68 No. la.719 difenzoquat
No. D.69 No. ld.344 difenzoquat
No. D.70 No. ld.667 difenzoquat
No. D.71 No. lj.344 difenzoquat
No. D.72 No. Im.1010 difenzoquat
No. D.73 No. la.344 difenzoquat-methylsulphat
No. D.74 No. la.719 difenzoquat-methylsulphat
No. D.75 No. ld.344 difenzoquat-methylsulphat
No. D.76 No. ld.667 difenzoquat-methylsulphat
No. D.77 No. lj.344 difenzoquat-methylsulphat
No. D.78 No. Im.1010 difenzoquat-methylsulphat
No. D.79 No. la.344 oxolinic acid
No. D.80 No. la.719 oxolinic acid
No. D.81 No. ld.344 oxolinic acid
No. D.82 No. ld.667 oxolinic acid
No. D.83 No. lj.344 oxolinic acid
No. D.84 No. Im.1010 oxolinic acid
No. D.85 No. la.344 piperalin
No. D.86 No. la.719 piperalin
No. D.87 No. ld.344 piperalin
No. D.88 No. ld.667 piperalin
No. D.89 No. lj.344 piperalin
No. D.90 No. Im.1010 piperalin
No. D.91 No. la.344 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.92 No. la.719 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.93 No. ld.344 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.94 No. ld.667 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.95 No. lj.344 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.96 No. Im.1010 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]- pyridine
No. D.97 No. la.344 δ-amino^-iso-propyl^-ortho-tolyl-pyrazol-S-on-i- thiocarboxylic acid allyl ester
No. D.98 No. la.719 δ-amino^-iso-propyl^-ortho-tolyl-pyrazol-S-on-i- thiocarboxylic acid allyl ester
Figure imgf000059_0001
Table 7
Active compound combinations of compounds I with active compounds Il of group E):
Mixture Compound I Compound Il
No. E.1 No. la.344 methasulphocarb
No. E.2 No. la.719 methasulphocarb
No. E.3 No. ld.344 methasulphocarb
No. E.4 No. ld.667 methasulphocarb
No. E.5 No. lj.344 methasulphocarb
No. E.6 No. Im.1010 methasulphocarb
No. E.7 No. la.344 pyribencarb
No. E.8 No. la.719 pyribencarb
No. E.9 No. ld.344 pyribencarb
No. E.10 No. ld.667 pyribencarb
No. E.11 No. lj.344 pyribencarb
No. E.12 No. Im.1010 pyribencarb
No. E.13 No. la.344 propamocarb hydrochloride
No. E.14 No. la.719 propamocarb hydrochloride
No. E.15 No. ld.344 propamocarb hydrochloride
No. E.16 No. ld.667 propamocarb hydrochloride
No. E.17 No. lj.344 propamocarb hydrochloride
No. E.18 No. Im.1010 propamocarb hydrochloride
Table 8
Active compound combinations of compounds I with active compounds Il of group F):
Figure imgf000059_0002
Mixture Compound I Compound Il
No. F.4 No. ld.667 dodine free base
No. F.5 No. lj.344 dodine free base
No. F.6 No. Im.1010 dodine free base
No. F.7 No. la.344 guazatine-acetate
No. F.8 No. la.719 guazatine-acetate
No. F.9 No. ld.344 guazatine-acetate
No. F.10 No. ld.667 guazatine-acetate
No. F.1 1 No. lj.344 guazatine-acetate
No. F.12 No. Im.1010 guazatine-acetate
No. F.13 No. la.344 iminoctadine-triacetate
No. F.14 No. la.719 iminoctadine-triacetate
No. F.15 No. ld.344 iminoctadine-triacetate
No. F.16 No. ld.667 iminoctadine-triacetate
No. F.17 No. lj.344 iminoctadine-triacetate
No. F.18 No. Im.1010 iminoctadine-triacetate
No. F.19 No. la.344 iminoctadine-tris(albesilate)
No. F.20 No. la.719 iminoctadine-tris(albesilate)
No. F.21 No. ld.344 iminoctadine-tris(albesilate)
No. F.22 No. ld.667 iminoctadine-tris(albesilate)
No. F.23 No. lj.344 iminoctadine-tris(albesilate)
No. F.24 No. Im.1010 iminoctadine-tris(albesilate)
No. F.25 No. la.344 kasugamycin-hydrochlorid-hydrat
No. F.26 No. la.719 kasugamycin-hydrochlorid-hydrat
No. F.27 No. ld.344 kasugamycin-hydrochlorid-hydrat
No. F.28 No. ld.667 kasugamycin-hydrochlorid-hydrat
No. F.29 No. lj.344 kasugamycin-hydrochlorid-hydrat
No. F.30 No. Im.1010 kasugamycin-hydrochlorid-hydrat
No. F.31 No. la.344 dichlorophen
No. F.32 No. la.719 dichlorophen
No. F.33 No. ld.344 dichlorophen
No. F.34 No. ld.667 dichlorophen
No. F.35 No. lj.344 dichlorophen
No. F.36 No. Im.1010 dichlorophen
No. F.37 No. la.344 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide
No. F.38 No. la.719 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide Mixture Compound I Compound Il
No. F.39 No. ld.344 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide
No. F.40 No. ld.667 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide
No. F.41 No. lj.344 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide
No. F.42 No. Im.1010 N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide
No. F.43 No. la.344 dicloran
No. F.44 No. la.719 dicloran
No. F.45 No. ld.334 dicloran
No. F.46 No. ld.667 dicloran
No. F.47 No. lj.344 dicloran
No. F.48 No. Im.1010 dicloran
No. F.49 No. la.344 nitrothal-isopropyl
No. F.50 No. la.719 nitrothal-isopropyl
No. F.51 No. ld.344 nitrothal-isopropyl
No. F.52 No. ld.667 nitrothal-isopropyl
No. F.53 No. lj.344 nitrothal-isopropyl
No. F.54 No. Im.1010 nitrothal-isopropyl
No. F.55 No. la.344 tecnazen
No. F.56 No. la.719 tecnazen
No. F.57 No. ld.344 tecnazen
No. F.58 No. ld.667 tecnazen
No. F.59 No. lj.344 tecnazen
No. F.60 No. Im.1010 tecnazen
No. F.61 No. la.344 biphenyl
No. F.62 No. la.719 biphenyl
No. F.63 No. ld.344 biphenyl
No. F.64 No. ld.667 biphenyl
No. F.65 No. lj.344 biphenyl
No. F.66 No. Im.1010 biphenyl
No. F.67 No. la.344 bronopol
No. F.68 No. la.719 bronopol
No. F.69 No. ld.344 bronopol
No. F.70 No. ld.667 bronopol
No. F.71 No. lj.344 bronopol
No. F.72 No. Im.1010 bronopol Mixture Compound I Compound Il
No. F.73 No. la.344 diphenylamine
No. F.74 No. la.719 diphenylamine
No. F.75 No. ld.344 diphenylamine
No. F.76 No. ld.667 diphenylamine
No. F.77 No. lj.344 diphenylamine
No. F.78 No. Im.1010 diphenylamine
No. F.79 No. la.344 mildiomycin
No. F.80 No. la.719 mildiomycin
No. F.81 No. ld.344 mildiomycin
No. F.82 No. ld.667 mildiomycin
No. F.83 No. lj.344 mildiomycin
No. F.84 No. Im.1010 mildiomycin
No. F.85 No. la.344 oxin-copper
No. F.86 No. la.719 oxin-copper
No. F.87 No. ld.344 oxin-copper
No. F.88 No. ld.667 oxin-copper
No. F.89 No. lj.344 oxin-copper
No. F.90 No. Im.1010 oxin-copper
No. F.91 No. la.344 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.92 No. la.719 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.93 No. ld.334 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.94 No. ld.667 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.95 No. lj.344 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.96 No. Im.1010 N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide
No. F.97 No. la.344 N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl- phenyl)-N-ethyl-N-methyl formamidine
No. F.98 No. la.719 N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl- phenyl)-N-ethyl-N-methyl formamidine
No. F.99 No. ld.344 N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl- phenyl)-N-ethyl-N-methyl formamidine
No. F.100 No. ld.667 N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl- phenyl)-N-ethyl-N-methyl formamidine
Figure imgf000063_0001
Figure imgf000064_0001
Table 9
Active compound combinations of compounds I with active compounds Il of group G):
Figure imgf000064_0002
Figure imgf000065_0001
Figure imgf000066_0001
Figure imgf000067_0001
Figure imgf000068_0001
Figure imgf000069_0001
The mixtures of the compound(s) I with at least one of the active compounds II, or the simultaneous, that is joint or separate, use of a compound I with at least one of the active compounds II, are/is distinguished by excellent activity against a broad spectrum of phytopathogenic fungi in particular from the classes of the Ascomycetes, Basidiomy- cetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). Some of them are systemically active and can be used in crop protection as foliar fungicides, as soil fungicides and as fungicides for seed dressing.
They are particularly important in the control of a large number of fungi on various crop plants and their seed, such as wheat, rye, barley, oats, rice, corn, grass, bananas, cotton, soybeans, coffee, sugar cane, grapevines, fruit and ornamental plants and vegetables, such as cucumbers, beans, tomatoes, potatoes and cucurbits, and also the seeds of these plants.
The plants or seed treated with the combinations of compounds I and Il may by wildlife types, plants or seed obtained by breeding and transgenic plants as well as their seed.
They are especially suitable for controlling the following phytopathogenic fungi: Alternaria atrans tenuissima Botrytis cinerea
Alternaria brassicae Bremia lactucae
Alternaria spp. Bremia lucinae
Ascochyta tritici Calonectria crotalariae
Blumeria graminis Cercospora canescens Cercospora kikuchii Physiological leaf spots Cercospora sojina Phythium ultimum Cercospora canescens Phytophthora megasperma Choanephora infundibulifera Phytophthora infestans Cladosporium herbarum Phytopthora megasperma Cochliobolus sativus Plasmopara viticola Cochliobolus sativus Podosphaera leucotricha Colletotrichum truncatum Podosphaera leucotricha Corynespora cassiicola Pseudocercospora herpotrichoides Dactuliophora glycines Pseudomonas lachrymans Dematophora necatrix Pseudomonas syringae Diaporthe phaseolorum Pseudoperonospora cubensis Diaporthe phaseolorum var. caulivora Pseudoperonospora humuli Drechslera glycini Puccinia hordei Epicoccum spp. Puccinia recondita Erwinia amylovora Puccinia striiformis Erysiphe graminis Puccinia triticina Frogeye sojina Pyrenochaeta glycines Fusarium solani Pyrenophora allosuri Fusarium culmorum Pyrenophora altermarina Fusarium graminearum Pyrenophora avenae Gaeumannomyces graminis Pyrenophora bartramiae Leptosphaeria nodorum Pyrenophora bondarzevii Leptosphaerulina trifolii Pyrenophora bromi Macrophomina phaseolina Pyrenophora bryophila Microdochium nivale Pyrenophora buddleiae Microsphaera diffusa Pyrenophora bupleuri Mycoleptodiscus terrestris Pyrenophora calvertii Neocosmospora vasinfecta Pyrenophora calvescens var. moravica Pellicularia sasakii Pyrenophora carthanie Peronospora brassicae Pyrenophora centranthi Peronospora manshurica Pyrenophora cerastii Peronospora brassicae Pyrenophora chengii Peronospora pisi Pyrenophora chrysamthemi Phakopsora pachyrhizi Pyrenophora convohuli Phakopsora meibomiae Pyrenophora coppeyana Phialophora gregata Pyrenophora cytisi Phomopsis phaseoli Pyrenophora dactylidis Phyllostica sojaecola Pyrenophora dictyoides Pyrenophora echinopis Pyrenophora semeniperda
Pyrenophora ephemera Pyrenophora semiusta
Pyrenophora eryngicola Pyrenophora seseli
Pyrenophora erythrospila Pyrenophora seseli f. poterii
Pyrenophora euphorbiae Pyrenophora subalpina
Pyrenophora freticola Pyrenophora sudetica
Pyrenophora graminea Pyrenophora suhantarctica
Pyrenophora graminea Pyrenophora syntrichiae
Pyrenophora heraclei Pyrenophora szaferiana
Pyrenophora hordei Pyrenophora teres
Pyrenophora horrida Pyrenophora teres f. makulata
Pyrenophora hyperici Pyrenophora teres subsp. graminea
Pyrenophora japonica Pyrenophora tetrahenae
Pyrenophora kugitangi Pyrenophora tranzschelii
Pyrenophora lithophila Pyrenophora trifulii
Pyrenophora lolii Pyrenophora triticil-repentis
Pyrenophora macrospora Pyrenophora ushuwaiensis
Pyrenophora metasequoiae Pyrenophora villose
Pyrenophora minuertiae hirsutae Pyrenophora graminea
Pyrenophora moravica Pyrenophora teres
Pyrenophora moroczkowskii Pyrenophora teres
Pyrenophora muscorum Pyrenophora teres
Pyrenophora osmanthi Pyrenophora tritici repentis
Pyrenophora phlei Pyricularia oryzae
Pyrenophora pimpinellae Pythium aphanidermatum
Pyrenophora pittospori Pythium debaryanum
Pyrenophora polytrichia Pythium irregulare
Pyrenophora pontresinerisis Pythium myriotylum
Pyrenophora pulsatillae Pythium ultimum
Pyrenophora raetica Ramularia collocygni
Pyrenophora rayssiae Rhizoctonia aerea
Pyrenophora rugosa Rhizoctonia alba
Pyrenophora ryohicola Rhizoctonia alpina
Pyrenophora saviczii Rhizoctonia anaticula
Pyrenophora schoeteri Rhizoctonia anomala
Pyrenophora scholevskii Rhizoctonia apocynacearum
Pyrenophora scirpi Rhizoctonia arachnion
Pyrenophora scirpicola Rhizoctonia asclerotica
Pyrenophora secalis Rhizoctonia batalicola Rhizoctonia borealis Rhizoctonia pini-insignis Rhizoctonia callae Rhizoctonia praticola Rhizoctonia carorae Rhizoctonia quercus Rhizoctonia cerealis Rhizoctonia ramicola Rhizoctonia choussii Rhizoctonia robusta Rhizoctonia coniothecioides Rhizoctonia rubi Rhizoctonia cundida Rhizoctonia ruhiginosa Rhizoctonia dichoroma Rhizoctonia sclerotica Rhizoctonia dimorpha Rhizoctonia solani Rhizoctonia endophytica Rhizoctonia solani f. paroketea Rhizoctonia endophytica vor. filicata Rhizoctonia solani forma specialis Rhizoctonia ferruginea Rhizoctonia solani var. cedri-deodorae Rhizoctonia floccosa Rhizoctonia solani var. fuchsiae Rhizoctonia fragariae Rhizoctonia solani var. hortensis Rhizoctonia fraxini Rhizoctonia stahlii Rhizoctonia fuliginea Rhizoctonia subtilis var. nigra Rhizoctonia fumigata Rhizoctonia subtlilis Rhizoctonia globularis Rhizoctonia tomato Rhizoctonia goodyerae-repentis Rhizoctonia tuliparum Rhizoctonia gossypii Rhizoctonia veae Rhizoctonia gossypii vor. anatolica Rhizoctonia versicolor Rhizoctonia gracilis Rhizoctonia cerealis Rhizoctonia griseo Rhynchosporium secalis Rhizoctonia hiemalis Sclerotina rolfsii Rhizoctonia juniperi Sclerotinia rolfsii Rhizoctonia lamallifera Sclerotinia sclerotiorum Rhizoctonia leguminicola Septoria glycines Rhizoctonia lilacina Septoria nodorum Rhizoctonia luoini Septoria tritici Rhizoctonia macrosclerotia Sphaerotheca fuliginea Rhizoctonia melongenae Stagonospora nodorum Rhizoctonia microsclerotia Stemphylium botryosum Rhizoctonia monilioides Thielaviopsis basicola Rhizoctonia monteithiana Tilletia aegilopis Rhizoctonia muneratii Tilletia aegopogonis Rhizoctonia nandorii Tilletia ahamadiana Rhizoctonia oryzae Tilletia airina Rhizoctonia oryzae-sativae Tilletia ajrekari Rhizoctonia pallida Tilletia alopecuri Tilletia anthaxanthi Tilletia echinosperma
Tilletia apludae Tilletia ehrhartae
Tilletia armdinellae Tilletia eleusines
Tilletia asperifolia Tilletia elymandrae
Tilletia asperitolioides Tilletia elymicola
Tilletia atacamensis Tilletia elyni
Tilletia baldrati Tilletia elythrophori
Tilletia bambusae Tilletia eragrostidis
Tilletia banarasae Tilletia euphorbiae
Tilletia bangalorensis Tilletia fahrendorfii
Tilletia barclayana Tilletia festinca-octoflorana
Tilletia biharica Tilletia foelida
Tilletia boliviensis Tilletia foliicola
Tilletia boutelouae Tilletia fusca
Tilletia brachypodii Tilletia fusca var. bromi-tectorum
Tilletia brachypodii-ramosi Tilletia fusca var. guyotiana
Tilletia braomi-tectorum Tilletia fusca var.paragonica
Tilletia brevifaciens Tilletia georfischeri
Tilletia bromi Tilletia gigaspora
Tilletia bromina Tilletia goloskokovii
Tilletia brunkii Tilletia haynaldiae
Tilletia buchloeana Tilletia heterospora
Tilletia bulayi Tilletia holci
Tilletia caries Tilletia hordei var.spontanei
Tilletia cathcariae Tilletia horrida
Tilletia cerebrina Tilletia hyalospora var.cuzcoensis
Tilletia chloridicola Tilletia hyparrheniae
Tilletia contaoversa Tilletia indica
Tilletia contraversa var. prostrata Tilletia iniermedia
Tilletia contraversa var. elyni Tilletia iovensis
Tilletia corona Tilletia ixophari
Tilletia cynasuri Tilletia koeleriae
Tilletia damacarae Tilletia kuznetzoviana
Tilletia deyeuxiae Tilletia laevis
Tilletia digitariicola Tilletia laguri
Tilletia durangensis Tilletia leptochlase
Tilletia earlei Tilletia lepturi
Tilletia echinochlave Tilletia macrotuberculata
Tilletia echinochloae Tilletia madeirensis Tilletia maglagonii Tilletia sphaerococca
Tilletia makutensis Tilletia sphenopie
Tilletia milti Tilletia sphenopodis
Tilletia milti-vernalis Tilletia sterilis
Tilletia montana Tilletia taiana
Tilletia montemartinii Tilletia texana
Tilletia nanifica Tilletia themedae-anatherae
Tilletia narasimhanii Tilletia themedicola
Tilletia narayanaoana Tilletia toguateei
Tilletia narduri Tilletia trachypogonis
Tilletia nigrifaciens Tilletia transiliensis
Tilletia obscura-reticulora Tilletia transvaalensis
Tilletia oklahomae Tilletia tritici f. monococci
Tilletia okudoirae Tilletia tritici var. controversa
Tilletia oplistneni-cristati Tilletia tritici var. nanifica
Tilletia paae Tilletia tritici var. laevis
Tilletia pachyderma Tilletia tritici-repentis
Tilletia pallida Tilletia triticoides
Tilletia panici Tilletia tuberculare
Tilletia panici. humilis Tilletia vertiveriae
Tilletia paonensis Tilletia viermotii
Tilletia paraloxa Tilletia vittara
Tilletia paspali Tilletia vittara var. burmahnii
Tilletia pennisetina Tilletia walkeri
Tilletia peritidis Tilletia youngii
Tilletia phalaridis Tilletia zundelii
Tilletia polypoganis Typhula incarnata
Tilletia prostrata Uromyces appendiculatus
Tilletia pulcherrima var. brachiariae Ustilago aaeluropodis
Tilletia redfieldiae Ustilago abstrusa
Tilletia rhei Ustilago aegilopsidis
Tilletia rugispora Ustilago affinis var. hilariae
Tilletia sabaudiae Ustilago agrestis
Tilletia salzmanii Ustilago agropyrina
Tilletia savilei Ustilago agrostis-palustris
Tilletia scrobiculata Ustilago airear-caespitosae
Tilletia setariae Ustilago alismatis
Tilletia setariae-palmiflorarae Ustilago almadina
Tilletia setariicola Ustilago alopecurivara Ustilago alsineae Ustilago bothriochloae
Ustilago altilis Ustilago bothriochloae-intermediae
Ustilago amadelpha var. glabriuscula Ustilago bouriqueti
Ustilago amphilophidis Ustilago braziliensis
Ustilago amplexa Ustilago brisae
Ustilago amthoxanthi Ustilago bromi-arvensis
Ustilago andropogonis-tectorum Ustilago bromi-erecti
Ustilago aneilemae Ustilago bromi-mallis
Ustilago anhweiona Ustilago bromina
Ustilago anomala var. avicularis Ustilago bromivora f. brachypodii
Ustilago anomala var. carnea Ustilago bromivora var. microspora
Ustilago anomala var. cordai Ustilago bullata f. brachypodii-distachyi
Ustilago anomala var. microspora Ustilago bullata var. bonariesis
Ustilago anomala var. muricata Ustilago bullata var. macrospora
Ustilago anomala var. tovarae Ustilago bungeana
Ustilago apscheronica Ustilago calanagrostidis
Ustilago arabidia.alpinae Ustilago calanagrostidis var. scrobiculata
Ustilago arandinellae-hirtae Ustilago calanagrostidis var. typica
Ustilago arctica Ustilago cardamines
Ustilago argentina Ustilago cariciphila
Ustilago aristidarius Ustilago caricis-wallichianae
Ustilago arotragostis Ustilago carnea
Ustilago asparagi-pygmaei Ustilago catherimae
Ustilago asprellae Ustilago caulicola
Ustilago avanae subsp. alba Ustilago cenrtodomis
Ustilago avenae Ustilago ceparum
Ustilago avenae Ustilago cephalariae
Ustilago avenae f. sp. perennars Ustilago chacoensis
Ustilago avenariae-bryophyllae Ustilago chloridii
Ustilago avicularis Ustilago chloridionis
Ustilago bahuichivoensis Ustilago chrysopoganis
Ustilago barbari Ustilago chubulensis
Ustilago beckeropsis Ustilago cichorii
Ustilago belgiana Ustilago cilmodis
Ustilago bethelii Ustilago clelandii
Ustilago bicolor Ustilago clintoniana
Ustilago bistortarum ustiloginea Ustilago coloradensis
Ustilago bistortarum var. pustulata Ustilago commelinae
Ustilago boreatis Ustilago compacta Ustilago concelata Ustilago eriocauli
Ustilago condigna Ustilago eriochloae
Ustilago consimilis Ustilago euphorbiae
Ustilago constantineanui Ustilago fagopyri
Ustilago controversa Ustilago festucae
Ustilago conventere-sexualis Ustilago festucorum
Ustilago cordai Ustilago filamenticola
Ustilago corlarderiae var. araucana Ustilago fingerhuthiae
Ustilago coronariaw Ustilago flectens
Ustilago coronata Ustilago flonersii
Ustilago courtoisii Ustilago foliorum
Ustilago crus-galli var. minor Ustilago formosana
Ustilago cryptica Ustilago fueguina
Ustilago curta Ustilago gageae
Ustilago custanaica Ustilago garcesi
Ustilago cynodontis Ustilago gardneri
Ustilago cynodontis Ustilago gausenii
Ustilago cyperi-lucidi Ustilago gayazana
Ustilago davisii Ustilago gigantispora
Ustilago deccanii Ustilago glyceriae
Ustilago decipiens Ustilago gregaria
Ustilago deformitis Ustilago grossheimii
Ustilago dehiscens Ustilago gunnerae
Ustilago delicata Ustilago haesendocki var. chloraphorae
Ustilago deyeuxiae Ustilago haesendocki var. vargasii
Ustilago dianthorum Ustilago halophiloides
Ustilago distichlidis Ustilago haynalodiae
Ustilago dubiosa Ustilago heleochloae
Ustilago dumosa Ustilago helictotrichi
Ustilago earlei Ustilago herteri var. Bicolor
Ustilago echinochloae Ustilago herteri var. vargasii
Ustilago ehrhartana Ustilago hierochloae-adoratae
Ustilago eleocharidis Ustilago hieronymi var. insularis
Ustilago eleusines Ustilago hieronymi var. minor
Ustilago elymicola Ustilago hilariicola
Ustilago elytrigiae Ustilago hilubii
Ustilago enneapogonis Ustilago himalensis
Ustilago epicampida Ustilago histortarum var. marginalis
Ustilago eragrostidis-japanicana Ustilago hitchcockiana Ustilago holci-avanacei Ustilago linderi
Ustilago hordei Ustilago linearis
Ustilago hordei f. sp. avenae Ustilago lirove
Ustilago hsuii Ustilago loliicola
Ustilago hyalino-bipolaris Ustilago longiflora
Ustilago hydropiperis Ustilago longiseti
Ustilago hyparrheniae Ustilago longissima var. dubiosa
Ustilago hypodyies f. congoensis Ustilago longissima var. paludificans
Ustilago hypodytes f. sporaboli Ustilago longissima var. typica
Ustilago hypodytes var. agrestis Ustilago lupini
Ustilago idonea Ustilago lychnidis-dioicae
Ustilago imperatue Ustilago lycoperdiformis
Ustilago induia Ustilago lyginiae
Ustilago inouyei Ustilago machili
Ustilago intercedens Ustilago machringiae
Ustilago iranica Ustilago magalaspora
Ustilago isachnes Ustilago magellanica
Ustilago ischaemi-akoensis Ustilago mariscana
Ustilago ischaemi-anthephoroides Ustilago maydis
Ustilago ixiolirii Ustilago melicae
Ustilago ixophori Ustilago merxmuellerana
Ustilago jacksonii Ustilago mesatlantica
Ustilago jacksonii var. vintonesis Ustilago michnoana
Ustilago jaczevskyana Ustilago microspora
Ustilago jaczevskyana van. typica Ustilago microspora var. paspalicola
Ustilago jaczevskyana var. sibirica Ustilago microstegii
Ustilago jagdishwari Ustilago microthelis
Ustilago jamalainentii Ustilago milli
Ustilago jehudana Ustilago mobtagnei var. minor
Ustilago johnstonii Ustilago modesta
Ustilago kairamoi Ustilago moenchiae-manticae
Ustilago kasuchstemica Ustilago monermae
Ustilago kenjiana Ustilago morinae
Ustilago kweichowensis Ustilago morobiana
Ustilago kylingae Ustilago mrucata
Ustilago lacjrymae-jobi Ustilago muda
Ustilago lepyrodiclidis Ustilago muehlenbergiae var. lucumanensis
Ustilago lidii Ustilago muscaribotryoidis
Ustilago liebenbergii Ustilago nagarnyi Ustilago nannfeldtii Ustilago phragmites
Ustilago nauda var. hordei Ustilago picacea
Ustilago nelsoniana Ustilago pimprina
Ustilago nepalensis Ustilago piperi (var.) rosulata
Ustilago neyraudiae Ustilago poae
Ustilago nigra Ustilago poae-bulbosae
Ustilago nivalis Ustilago poae-nemoralis
Ustilago nuda Ustilago polygoni-alati
Ustilago nuda Ustilago polygoni-alpini
Ustilago nuda var.tritici Ustilago polygoni-punctari
Ustilago nyassae Ustilago polygoni-serrulati
Ustilago okudairae Ustilago polytocae
Ustilago olida Ustilago polytocae-harbatas
Ustilago olivacea var. macrospora Ustilago pospelovii
Ustilago onopordi Ustilago prostrata
Ustilago onumae Ustilago pseudohieronymi
Ustilago opiziicola Ustilago puehlaensis
Ustilago oplismeni Ustilago puellaris
Ustilago orientalis Ustilago pulvertulensa
Ustilago otophora Ustilago raciborskiana
Ustilago ovariicola Ustilago radians
Ustilago overcemii Ustilago ravida
Ustilago pamirica Ustilago rechingeri
Ustilago panici-geminati Ustilago reticulara
Ustilago panjabensis Ustilago reticulispora
Ustilago pappophori Ustilago rhei
Ustilago pappophori var. magdalensis Ustilago rhynchelytri
Ustilago parasnothii Ustilago ruandenis
Ustilago parodii Ustilago ruberculata
Ustilago parvula Ustilago sabouriana
Ustilago paspalidiicola Ustilago salviae
Ustilago patagonica Ustilago sanctae-catharinae
Ustilago penniseti var. verruculosa Ustilago scaura
Ustilago perrara Ustilago scillae
Ustilago persicariae Ustilago scitaminea
Ustilago petrakii Ustilago scitaminea var. sacchar-officinorum
Ustilago phalaridis Ustilago scleranthi
Ustilago phlei Ustilago scrobiculata
Ustilago phlei-protensis Ustilago scutulata Ustilago secalis var. elymi Ustilago sumnevicziana
Ustilago seitaminea var. sacchari-barberi Ustilago superha
Ustilago semenoviana Ustilago sydowiana
Ustilago serena Ustilago symbiotica
Ustilago serpens Ustilago taenia
Ustilago sesleriae Ustilago taiana
Ustilago setariae-mambassanae Ustilago tanakue
Ustilago shastensis Ustilago tenuispora
Ustilago shimadae Ustilago thaxteri
Ustilago silenes-inflatae Ustilago tinontiae
Ustilago silenes-nutantis Ustilago togata
Ustilago sinkiangensis Ustilago tournenxii
Ustilago sitanil Ustilago tovarae
Ustilago sleuneri Ustilago trachophora var. pacifica
Ustilago sonoriana Ustilago trachyniae
Ustilago sorghi-stipoidei Ustilago trachypogonis
Ustilago spadicea Ustilago tragana
Ustilago sparoboli-indici Ustilago tragi
Ustilago sparti Ustilago tragica
Ustilago speculariae Ustilago tragi-racemosi
Ustilago spegazzinii Ustilago trichoneurana
Ustilago spegazzinii var. agrestis Ustilago trichophora var. crus-galli
Ustilago spermophora var. orientalis Ustilago trichophora var. panici-frumentacei
Ustilago spermophoroides Ustilago triseti
Ustilago spinulosa Ustilago tritici forma specialis
Ustilago sporoboli-trenuli Ustilago tucumariensis
Ustilago stellariae Ustilago tumeformis
Ustilago sterilis Ustilago turcomanica
Ustilago stewartli Ustilago turcomanica var. prostrata
Ustilago stipae Ustilago turcomanica var. typica
Ustilago striaeformis f. phlei Ustilago ugamica
Ustilago striaeformis f. poa... Ustilago ugandensis var. macrospora
Ustilago striaeformis f. poae-pratensis Ustilago underwoodii
Ustilago striiformis f. hierochloes-odoratae Ustilago urginede
Ustilago striiformis var. agrostidis Ustilago urochloana
Ustilago striiformis var. dactylidis Ustilago ustilaginea
Ustilago striiformis var. holci Ustilago ustriculosa var. cordai
Ustilago striiformis var. phlei Ustilago ustriculosa var. reticulata
Ustilago striiformis var. poae Ustilago valentula Ustilago vavilori Ustilago williamsii Ustilago verecunda Ustilago wynaadensis Ustilago verruculosa Ustilago zambettakisii Ustilago versatilis Ustilago zernae Ustilago vetiveriae Venturia inaequalis Ustilago violaceo-irregularis Xanthomonas campestris Ustilago violaceu var. stellariae Xanthomonas oryzae Ustilago violaceuverrucosa
The i-methylpyrazol-4-ylcarboxanilides I and the combinations of compounds I and Il and optionally III are particularly suitable for controlling phytopathogenic fungi in barley (e.g. Pyrenophora teres, Rhynchosporium secalis,Puccinia hordei,Puccinia striiformis, Blumeria graminis, Ramularia collo-cygni / Physiological leaf spots, Microdochium nivale, Typhula incarnata, Pseudocercosporella herpotrichoides, Fusarium culmorum, Rhizoctonia cerealis, Gaeumannomyces graminis) and soybeans (e.g. Phakopsora pachyrhizi, Microsphaera diffusa, Septoria glycines, Cercospora sojina, Cercospora kikuchii, Corynespora cassiicola, Colletotrichum truncatum, Peronospora manshurica, Alternaria spp., Phomopsis phaseoli, Diaporthe phaseolorum, Phialophora gregata, Fusarium solani, Sclerotinia sclerotiorum, Sclerotinia rolfsii, Phytopthora megasperma, Rhizoctonia solani, Dematophora necatrix, Macrophomina phaseolina).
The 1-methylpyrazol-4-ylcarboxanilides I where X is fluorine and their combinations with compounds II, are particularly suitable for controlling phytopathogenic fungi in barley as mentioned above. For example, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1-methyl- 3-difluoromethyl-1 H-pyrazole-4-carboxamide, solo or in combination with an active compound II, exhibits an excellent activity against Ramularia collo-cygni / Physiological leaf spots .
The combinations according to the invention are furthermore suitable for controlling harmful fungi in the protection of materials (for example wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products. In the protection of wood, particular attention is paid to the following harmful fungi: Ascomycetes, such as Ophio- stoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chae- tomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes, such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Po- ria spp., Serpula spp. and Tyromyces spp., Deuteromycetes, such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes, such as Mucor spp., additionally in the protection of materials the following yeasts: Candida spp. and Saccharomyces cerevisae. Application of the inventive combinations to useful plants may also lead to an increase in the crop yield.
The compound(s) I and at least one of the active compounds Il can be applied simulta- neously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.
When preparing the mixtures, it is preferred to employ the pure active compounds I and II, to which further compounds active against harmful fungi or other pests, such as insects, arachnids or nematodes, or else herbicidal or growth-regulating active compounds or fertilizers can be added.
Usually, mixtures of a compound I and one active compound Il are employed. How- ever, in certain cases mixtures of at least one compound I with two or, if appropriate, more active components may be advantageous.
Suitable further active components in the above sense are in particular the active compounds II, mentioned at the outset, or fipronil, and in particular the preferred active compounds Il mentioned above.
The compound(s) I and the active compound(s) Il are usually employed in a weight ratio of from 100:1 to 1 :100, preferably from 20:1 to 1 :20, in particular from 10:1 to 1 :10.
The further active components are, if desired, added in a ratio of from 20:1 to 1 :20 to the compound I.
Depending on the type of compound and the desired effect, the application rates of the mixtures according to the invention, in particular in the case of agricultural crop areas, are from 5 g/ha to 2000 g/ha, preferably from 20 to 1500 g/ha, in particular from 50 to 1000 g/ha.
Correspondingly, the application rates for the compound I are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
Correspondingly, the application rates for the active compound Il are generally from 1 to 2000 g/ha, preferably from 10 to 1500 g/ha, in particular from 40 to 1000 g/ha. In the treatment of seed, application rates of mixture are generally from 1 to 1000 g per 100 kg of seed, preferably from 1 to 750 g per 100 kg, in particular from 5 to 500 g per 100 kg of seed.
The method for controlling harmful fungi is carried out by the separate or joint application of a compound I or compounds I and active compound(s) Il or a mixture of a compound I or compounds I and at least one active compound Il by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
The mixtures according to the invention, or the compound(s) I and at least one active compound II, can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The use form depends on the particular intended purpose; in each case, it should ensure a fine and even dis- tribution of the mixture according to the invention.
The formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants. Solvents/auxiliaries suitable for this purpose are essentially: - water, aromatic solvents (for example Solvesso® products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (N-methylpyrrolidone, N-octylpyrrolidone), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used,
- carriers such as ground natural minerals (for example kaolins, clays, talc, chalk) and ground synthetic minerals (for example highly disperse silica, silicates); emulsifiers such as nonionogenic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose.
Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, tristearyl phenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.
Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.
Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compounds. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
The following are examples of formulations: 1. Products for dilution with water
A) Water-soluble concentrates (SL)
10 parts by weight of a mixture according to the invention are dissolved in 90 parts by weight of water or in a water-soluble solvent. As an alternative, wetting agents or other auxiliaries are added. The active compound dissolves upon dilution with water. In this way, a formulation having a content of 10% by weight of active compound is obtained.
B) Dispersible concentrates (DC)
20 parts by weight of a mixture according to the invention are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion. The active compound content is 20% by weight. C) Emulsifiable concentrates (EC)
15 parts by weight of a mixture according to the invention are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The formulation has an active compound content of 15% by weight.
D) Emulsions (EW, EO)
25 parts by weight of a mixture according to the invention are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion. The formulation has an active compound content of 25% by weight.
E) Suspensions (SC, OD)
In an agitated ball mill, 20 parts by weight of a mixture according to the invention are comminuted with addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound. The active compound content in the formulation is 20% by weight.
F) Water-dispersible granules and water-soluble granules (WG, SG) 50 parts by weight of a mixture according to the invention are ground finely with addition of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound. The formulation has an active compound content of 50% by weight.
G) Water-dispersible powders and water-soluble powders (WP, SP)
75 parts by weight of a mixture according to the invention are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetting agents and silica gel. Dilution with water gives a stable dispersion or solution of the active compound. The active compound content of the formulation is 75% by weight. 2. Products to be applied undiluted
H) Dustable powders (DP)
5 parts by weight of a mixture according to the invention are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having an active compound content of 5% by weight.
J) Granules (GR, FG, GG, MG)
0.5 part by weight of a mixture according to the invention is ground finely and associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray- drying or the fluidized bed. This gives granules to be applied undiluted having an active compound content of 0.5% by weight.
K) ULV solutions (UL) 10 parts by weight of a mixture according to the invention are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted having an active compound content of 10% by weight.
The active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention.
Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetting agent, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 %.
The active compounds may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives. Oils of various types, wetting agents or adjuvants may be added to the active compounds, even, if appropriate, not until immediately prior to use (tank mix). These agents are typically admixed with the compositions according to the invention in a weight ratio of from 1 :100 to 100:1 , preferably from 1 :10 to 10:1.
Suitable adjuvants in this sense are in particular: organically modified polysiloxanes, for example Break Thru S 240®; alcohol alkoxylates, for example Atplus 245®, Atplus MBA 1303®, Plurafac LF 300® and Lutensol ON 30®; EO/PO block polymers, for example Pluronic RPE 2035® and Genapol B®; alcohol ethoxylates, for example Lutensol XP 80®; and sodium dioctylsulfosuccinate, for example Leophen RA®.
The compounds I and Il or the mixtures or the corresponding formulations are applied by treating the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be kept free from them with a fungicidally effective amount of the mixture or, in the case of separate application, of the compounds I and II. Application can be before or after the infection by harmful fungi.
The fungicidal action of the individual compounds and of the mixtures according to the invention was demonstrated by the tests below.
The active compounds, separately or jointly, were prepared as a stock solution comprising 25 mg of active compound which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having an emulsifying and dispersing action based on ethoxylated alkylphenols) in a ratio by volume of solvent/emulsifier of 99:1. The mixture was then made up to 100 ml with water. This stock solution was diluted with the solvent/emulsifier/water mixture described to give the concentration of active compound stated below.
The visually determined percentages of infected leaf areas were converted into efficacies in % of the untreated control:
The efficacy (E) is calculated as follows using Abbot's formula:
E = (1 - α/β ) ■ 100
α corresponds to the fungicidal infection of the treated plants in % and β corresponds to the fungicidal infection of the untreated (control) plants in % An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants were not infected.
The expected efficacies of active compound combinations were determined using Colby's formula (Colby, S. R. " Calculating synergistic and antagonistic responses of herbicide combinations", Weeds, ^5, pp. 20-22, 1967) and compared with the observed efficacies.
Colby's formula: E = x + y - X- y/100
E expected efficacy, expressed in % of the untreated control, when using the mixture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active compound A at the concentration a y efficacy, expressed in % of the untreated control, when using the active compound B at the concentration b
Use example 1 - Preventative fungicidal control of early blight on tomatoes (Alternaria solani )
Young seedlings of tomato plants were grown in pots. These plants were sprayed to runoff with an aqueous suspension, containing the concentration of active ingredient or mixture mentioned in the table below. The next day, the treated plants were inoculated with an aqueous suspension of Alternaria solani. Then the trial plants were immediately transferred to a humid chamber. After 5 days at 20 to 22°C and a relative humidity close to 100 %, the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000087_0001
Figure imgf000088_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 2 - Preventative control of grey mold (Botrytis cinerea) on leaves of green pepper
Young seedlings of green pepper were grown in pots to the 2 to 3 leaf stage. These plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day the treated plants were inoculated with a spore suspension of Botrytis cinerea in a 2 % aqueous biomalt solution. Then the trial plants were immediately transferred to a dark, humid chamber. After 5 days at 22 to 240C and a relative humidity close to 100 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000089_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 3 - Control of late blight on tomatoes caused by Phytophthora infestans Young seedlings of tomato plants were grown in pots. These plants were sprayed to runoff with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day, the treated plants were inoculated with an aqueous suspension of sporangia of Phytophthora infestans. After inoculation, the trial plants were immediately transferred to a humid chamber. After 6 days at 18 to 200C and a relative humidity close to 100 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000090_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 4 - Control of powdery mildew on wheat caused by Blumeria graminis f. sp. tritici
The first fully developed leaves of pot grown wheat were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day the treated plants were inoculated with spores of Blumeria graminis f. sp. tritici (= syn. Erysiphe garminis f. sp. tritici) by shaking heavily infestated stock plants over the treated pots. After cultivation in the greenhouse for 7 days at 22-260C and a relative humidity between 60 to 90 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000091_0001
Figure imgf000092_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby' s formula.
Use example 5 - Curative control of brown rust on wheat caused by Puccinia recondita The first two developed leaves of pot-grown wheat seedling were dusted with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99 % and 20 to 220C for 24 h. The next day the plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The plants were allowed to air-dry. Then the trial plants were cultivated for 8 days in a greenhouse chamber at 22-260C and a relative humidity between 65 and 70 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000092_0002
Figure imgf000093_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby' s formula.
Use example 6 - Preventative control of brown rust on wheat caused by Puccinia recondita
The first two developed leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their as described below. The next day the plants were inoculated with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99 % and 20 to 22°C for 24 h. Then the trial plants were cultivated for 6 days in a greenhouse chamber at 22-26°C and a relative humidity between 65 and 70 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000094_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby' s formula.
Use example 7 - Control of net blotch on barley caused by Pyrenophora teres The first fully developed leaves of pot grown barley plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mentioned in the table below. The next day the treated plants were inoculated with an aqueous spore suspension of Pyrenophora (syn. Drechslera) teres. Then the trial plants were immediately transferred to a humid chamber in the greenhouse. After 6 days of cultivation at 20-240C and a relative humidity close to 70 %, the extent of fungal attack on the leaves was visually assessed as % leaf area.
Figure imgf000094_0002
Figure imgf000095_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 8 - Curative control of soy bean rust on soy beans caused by Phakopsora pachyrhizi
Leaves of pot-grown soy bean seedlings were inoculated with spores of Phakopsora pachyrhizi . To ensure the success the artificial inoculation, the plants were transferred to a humid chamber with a relative humidity of about 95 % and 23 to 270C for 24 h. The next day the plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The plants were allowed to air-dry. Then the trial plants were cultivated for 14 days in a greenhouse chamber at 23-270C and a relative humidity between 60 and 80 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Figure imgf000095_0002
Figure imgf000096_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 9 - Microtest
The active compounds were formulated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide.
Benalaxyl-M was used as commercial finished formulation and diluted with water to the stated concentration of the active compound.
The measured parameters were compared to the growth of the active compound-free control variant (100%) and the fungus-free and active compound-free blank value to determine the relative growth in % of the pathogens in the respective active compounds. These percentages were converted into efficacies.
The expected efficacies of active compound mixtures were determined using Colby's formula [R. S. Colby, " Calculating synergistic and antagonistic responses of herbicide combinations", Weeds 15, 20-22 (1967)] and compared with the observed efficacies.
9.1 : Activity against the late blight pathogen Phytophthora infestans in the microtiter test
The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Phytophtora infestans containing a pea juice-based aqueous nutrient medium was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
Figure imgf000097_0001
9.2: Activity against the grey mold Botrytis cinerea in the microtiterplate test
The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate
(MTP) and diluted with water to the stated concentrations. A spore suspension of Botrytis cinerea in 2 % aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
Figure imgf000098_0001
9.3: Activity against rice blast Pyricularia oryzae in the microtiterplate test The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Pyricularia oryzae in 2 % aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
Figure imgf000098_0002
9.4: Activity against leaf blotch on wheat caused by Septoria tritici The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Septoria tritici in 2 % aqueous biomalt solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
Figure imgf000099_0001
All microtiter tests make it clear that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 10 - Control of Phytophthora infestans
The stock solutions were mixed according to the ratio listed in the following table.
Figure imgf000099_0002
Figure imgf000100_0001
Figure imgf000101_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 11 - Control of Botrytis cinerea
The stock solutions were mixed according to the ratio listed in the following table.
Figure imgf000101_0002
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula. Use example 12 - Control of Pyricularia oryzae
The stock solutions were mixed according to the ratio listed in the following table.
Figure imgf000102_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.
Use example 13 - Control of Septoria tritici
The stock solutions were mixed according to the ratio listed in the following table.
Figure imgf000102_0002
Figure imgf000103_0001
The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more active than had been predicted using Colby's formula.

Claims

Claims
1. A fungicidal mixture for controlling phytopathogenic harmful fungi, comprising
1 ) at least one 1 -methylpyrazol-4-ylcarboxanilide of the formula I
Figure imgf000104_0001
in which the substituents are as defined below: X is hydrogen or fluorine; R1 is Ci-C4-alkyl or Ci-C4-haloalkyl; R2 is hydrogen or halogen;
R3 is hydrogen, cyano, nitro, halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C1-C4- alkoxy, Ci-C4-haloalkoxy or Ci-C4-alkylthio; R4 and R5 independently of one another are hydrogen, cyano, nitro, halogen,
Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, Ci-C4-haloalkoxy, Ci-C4- alkylthio, -CH=N-OR6 or -C(CHs)=N-OR6, where R6 is hydrogen, methyl or ethyl;
and
2) at least one active compound II, selected from the active compound groups
A) to G):
A) azoles selected from the group consisting of azaconazole, diniconazole- M, oxpoconazol, paclobutrazol, uniconazol, 1-(4-chloro-phenyl)-2- ([1 ,2,4]triazol-1-yl)-cycloheptanol and imazalil-sulfphate;
B) strobilurins selected from the group consisting of 2-(2-(6-(3-chloro-2- methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N- methyl-acetamide and 3-methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclo- propanecarboximidoylsulfanylmethy^-pheny^-acrylic acid methyl ester;
C) carboxamides selected from the group consisting of benalaxyl-M, 2-amino-4-methyl-thiazole-5-carboxylic acid anilide, 2-chloro-N-(1 ,1 ,3- trimethyl-indan-4-yl)-nicotinamide, N-(2-(1 ,3-dimethylbutyl)-phenyl)-1 ,3- dimethyl-5-fluoro-1 H-pyrazole-4-carboxylic acid amide, N-(4'-chloro-3',5- difluoro-biphenyl-2-yl)-3-difluoromethyl-1-methyl-1 H-pyrazole-4- carboxylic acid amide, N-(4'-chloro-3',5-difluoro-biphenyl-2-yl)-3- trifluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid amide, N-(3\4'-dichloro-5-fluoro-biphenyl-2-yl)-3-trifluoromethyl-1-methyl-1 H- pyτazole-4-carboxylic acid amide, N-(3',5-difluoro-4'-methyl-biphenyl-2- yl)-3-difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid amide,
N-(3',5-difluoro-4'-methyl-biphenyl-2-yl)-3-trifluoromethyl-1-methyl-1 H- pyrazole-4-carboxylic acid amide, N-(cis-2-bicyclopropyl-2-yl-phenyl)-3- difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid amide, N-(trans- 2-bicyclopropyl-2-yl-phenyl)-3-difluoromethyl-1-methyl-1 H-pyrazole-4- carboxylic acid amide, fluopyram, N-(3-ethyl-3,5-5-trimethyl-cyclohexyl)-
3-formylamino-2-hydroxy-benzamide, oxytetracyclin, silthiofam, N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide, isotianil and 3-(difluoromethyl)-1 -methyl-N-[1 ,2,3,4-tetrahydro-9-(1 -methylethyl)- 1 ,4-methano-naphthalen-5-yl]-1 H-pyrazole-4-carboxamide of the follow- ing formula:
Figure imgf000105_0001
heterocyclic compounds selected from the group consisting of 2,3,5,6- tetrachloro-4-methanesulfonyl-pyridine, 3,4,5-trichloro-pyridine-2,6-di- carbonitrile, N-(1 -(5-bromo-3-chloro-pyridin-2-yl)-ethyl)-2,4-dichloro- nicotinamide, N-((5-bromo-3-chloro-pyridin-2-yl)-methyl)-2,4-dichloro- nicotinamide, diflumetorim, nitrapyrin, dodemorph-acetate, fluoroimid, blasticidin-S, chinomethionat, debacarb, difenzoquat, difenzoquat- methylsulphat, oxolinic acid, piperalin, 3-[5-(4-chloro-phenyl)-2,3- dimethyl-isoxazolidin-3-yl]-pyridine
Figure imgf000105_0002
and 5-amino-2-iso-propyl-4-ortho-tolyl-pyrazol-3-on-1 -thiocarboxylic acid allyl ester
Figure imgf000106_0001
E) carbamates selected from the group consisting of methasulphocarb, pyribencarb and propamocarb hydrochlorid;
F) other fungicides selected from the group consisting of dodine free base, guazatine-acetate, iminoctadine-triacetate, iminoctadine-tris(albesilate), kasugamycin-hydrochlorid-hydrat, dichlorophen, N-(4-chloro-2-nitro- phenyl)-N-ethyl-4-methyl-benzenesulfon-amide, dicloran, nitrothal- isopropyl, tecnazen, biphenyl, bronopol, diphenylamine, mildiomycin, oxin-copper, N-(cyclopropylmethoxyimino-(6-difluoromethoxy-2,3- difluoro-phenyl)-methyl)-2-phenyl acetamide, N'-(4-(4-chloro-3- trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl forma- midine, N'-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N- ethyl-N-methyl formamidine, N'-(2-methyl-5-trifluormethyl-4-(3- trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl formamidine and N'- (5-difluormethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl- N-methyl formamidine;
G) plant growth regulators selected from the group consisting of clofibric acid, 4-CPA (4-chlorophenoxyacetic acid), 2,4-D, 2,4-DB, 2,4-DEP, di- chlorprop, fenoprop, IAA (indole-3-acetic acid), IBA (4-indol-3-ylbutyric acid), naphthaleneacetamide, α-naphthaleneacetic acid, 1-naphthol, naphthoxyacetic acid, potassium naphthenate, sodium naphthenate,
2,4, 5-T, 2iP (N-(3-methylbut-2-enyl)-1 H-purin-6-amine), 6- benzylaminopurine (6-BA), 2,6-dimethylpuridine (N-oxide-2,6-lultidine), benzyladenine, kinetin, zeatin, calcium cyanamide, dimethipin, endothal, ethephon, merphos, metoxuron, pentachlorophenol and its salts, thidia- zuron, tribufos, aviglycine, 1-methylcyclopropene, ACC (1- aminocyclopropanecarboxylic acid), etacelasil, ethephon, glyoxime, gib- berellins, gibberellic acid, abscisic acid, ancymidol, butralin, carbaryl, chlorphonium, chlorpropham, dikegulac, flumetralin, fluoridamid, fosa- mine, glyphosine, isopyrimol, jasmonic acid, maleic hydrazide, mepiquat (mepiquat chloride, mepiquat pentaborate), piproctanyl, prohydrojasmon, propham, 2,3,5-tri-iodobenzoic acid, chlorfluren, chlorflurenol, dichlor- flurenol, flurenol, chlormequat, daminozide, flurprimidol, mefluidide, pa- clobutrazol, tetcyclacis, uniconazole, brassinolide, forchlorfenuron, hy- mexazol, amidochlor, benzofluor, buminafos, carvone, ciobutide, clofencet, cloxyfonac, cyanamide, cyclanilide, cycloheximide, cyprosul- famide, epocholeone, ethychlozate, ethylene, fenridazon, fluprimidol, heptopargil, holosulf, inabenfide, karetazan, lead arsenate, methasulfo- carb, prohexadione (prohexadione calcium), pydanon, sintofen, triapen- thenol and trinexapac (trinexapac-ethyl)
in a synergistically effective amount.
2. The fungicidal mixture according to claim 1 , comprising as component 1 ) a i-methylpyrazol-4-ylcarboxanilide of the formula I where X is hydrogen and R3, R4 and R5 independently of one another are cyano, nitro, halogen, Ci-C4-alkyl,
Ci-C4-haloalkyl, CrC4-alkoxy, CrC4-haloalkoxy, CrC4-alkylthio, -CH=N-OR6 or -C(CH3)=N-OR6, where R6 is hydrogen, methyl or ethyl.
3. The fungicidal mixture according to claim 2, comprising as component 1) a 1-methylpyrazol-4-ylcarboxanilide of the formula I where R1 is methyl or ha- lomethyl, R2 is hydrogen, fluorine or chlorine and R3, R4 and R5 are each halogen.
4. The fungicidal mixture according to claim 2, comprising as component 1 ) N-(3',4',5'-trifluorobiphenyl)-1 ,3-dimethylpyrazol-4-ylcarboxamide,
N-(3',4',5'-trifluorobiphenyl)-1 ,3-dimethyl-5-fluoropyrazol-4-ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-5-chloro-1 ,3-dimethylpyrazol-4-ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-3-fluoromethyl-1-methylpyrazol-4-ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-3-(chlorofluoromethyl)-1-methylpyrazol-4- ylcarboxamide,
N-(3',4',5'-trifluorobiphenyl)-3-difluoromethyl-1-methylpyrazol-4-ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-3-difluoromethyl-5-fluoro-1-methylpyrazol-4- ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-5-chloro-3-difluoromethyl-1-methylpyrazol-4- ylcarboxamide,
N-(3',4',5'-trifluorobiphenyl)-3-(chlorodifluoromethyl)-1-methylpyrazol-4- ylcarboxamide,
N-(3',4',5'-trifluorobiphenyl)-1-methyl-3-trifluoromethylpyrazol-4-ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-5-fluoro-1-methyl-3-trifluoromethylpyrazol-4- ylcarboxamide, N-(3',4',5'-trifluorobiphenyl)-5-chloro-1-methyl-3-trifluoromethylpyrazol-4- ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-1 ,3-dimethylpyrazol-4-ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-1 ,3-dimethyl-5-fluoropyrazol-4-ylcarboxamide, N-(2',4',5'-trifluorobiphenyl)-5-chloro-1 ,3-dimethylpyrazol-4-ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-3-fluoromethyl-1-methylpyrazol-4-ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-3-(chlorofluoromethyl)-1-methylpyrazol-4- ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-3-difluoromethyl-1-methylpyrazol-4-ylcarboxamide, N-(2',4',5'-trifluorobiphenyl)-3-difluoromethyl-5-fluoro-1 -methylpyrazol-4- ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-5-chloro-3-difluoromethyl-1-methylpyrazol-4- ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-3-(chlorodifluoromethyl)-1-methylpyrazol-4- ylcarboxamide,
N-(2',4',5'-trifluorobiphenyl)-1-methyl-3-trifluoromethylpyrazol-4-ylcarboxamide,
N-(2\4\5'-trifluorobiphenyl)-5-fluoro-1-methyl-3-trifluoromethylpyrazol-4- ylcarboxamide or
N-(2',4',5'-trifluorobiphenyl)-5-chloro-1-methyl-3-trifluoromethylpyrazol-4- ylcarboxamide.
5. The fungicidal mixture according to claim 1 , comprising as component 1 ) a i-methylpyrazol-4-ylcarboxanilide of the formula I where X is fluorine and R3 is hydrogen.
6. The fungicidal mixture according to claim 5, comprising as component 1 ) a 1-methylpyrazol-4-ylcarboxanilide of the formula I where X is fluorine in 5- position, and R1 is methyl or halomethyl, R2 is hydrogen, fluorine or chlorine, R3 is hydrogen and R4 and R5 are each halogen.
7. The fungicidal mixture according to claim 5, comprising as component 1) N-(3',4'-dichloro-3-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4'-dichloro-3-fluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-3-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-3-fluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide, N-(3'-chloro-4'-fluoro-3-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H- pyrazole-4-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-4-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-4-fluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3'-chloro-4'-fluoro-4-fluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H- pyrazole-4-carboxamide,
N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-difluoro-5-fluorobiphenyl-2-yl)-1-methyl-3-difluoromethyl-1 H-pyrazole-4- carboxamide,
N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4-carboxamide, N-(3'-chloro-4'-fluoro-5-fluorobiphenyl-2-yl)-1 -methyl-3-difluoromethyl-1 H- pyrazole-4-carboxamide,
N-(4'-fluoro-4-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(4'-fluoro-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(4'-chloro-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide,
N-(4'-methyl-5-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide, N-(4'-fluoro-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4-carboxamide,
N-(4'-chloro-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4-carboxamide,
N-(4'-methyl-5-fluorobiphenyl-2-yl)-1 ,3-dimethyl-1 H-pyrazole-4-carboxamide,
N-(4'-fluoro-6-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H-pyrazole-4- carboxamide or N-(4'-chloro-6-fluorobiphenyl-2-yl)-1-methyl-3-trifluoromethyl-1 H- pyrazole-4-carboxamide.
8. The fungicidal mixture according to claims 1 to 7, comprising an additional active compound III, selected from the groups H) to N):
H) azoles selected from the group consisting of bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imiben- conazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, triadimefon, triadimenol, tebuconazole, tet- raconazole, triticonazole, prochloraz, pefurazoate, imazalil, triflumizole, cya- zofamid, benomyl, carbendazim, thiabendazole, fuberidazole, ethaboxam, et- ridiazole and hymexazole;
J) strobilurins selected from the group consisting of azoxystrobin, dimoxy- strobin, enestroburin, fluoxastrobin, kresoxim-methyl, methominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, enestroburin, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)- carbamate and methyl 2-(ortho-(2,5-dimethylphenyloxymethylene)phenyl)-3- methoxyacrylate;
K) carboxamides selected from the group consisting of carboxin, benalaxyl, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, me- fenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, 3,4-dichloro-N-(2-cyanophenyl)isothiazole-5-carboxamide, dimethomorph, flumorph, flumetover, fluopicolide (picobenzamid), zoxamide, carpropamid, diclocymet, mandipropamid, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3- methoxyphenyl)ethyl)-2-methanesulfonylamino-3-methylbutyramide, N-(2-(4- [3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2- ethanesulfonylamino-3-methylbutyramide, methyl 3-(4-chlorophenyl)-
3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)propionate, N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methyl- thiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-difluoro- methyl-1-methylpyrazole-4-carboxamide, N-(3',4'-dichloro-5-fluorobiphenyl- 2-yl)-3-difluoromethyl-1 -methylpyrazole-4-carboxamide and N-(2-cyano- phenyl)-3,4-dichloroisothiazole-5-carboxamide;
L) heterocyclic compounds selected from the group consisting of fluazinam, pyrifenox, bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuari- mol, pyrimethanil, triforine, fenpiclonil, fludioxonil, aldimorph, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, procymidone, vinclozolin, famoxadone, fenamidone, octhilinone, probenazole, 5-chloro-7-(4-methyl- piperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole, 2-butoxy-6-iodo- 3-propylchromen-4-one, acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil, quinoxyfen and N,N-dimethyl-3-(3-bromo-6-fluoro-2- methylindole-1 -sulfonyl)-[1 ,2,4]triazole-1 -sulfonamide;
M) carbamates selected from the group consisting of mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram, diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb, 4-fluorophenyl N-(1-(1-(4- cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, methyl 3-(4-chlorophenyl)- 3-(2-isopropoxycarbonylamino-3-methyl-butyrylamino)propanoate and carbamate oxime ethers of the formula IV
Figure imgf000111_0001
in which Z is N or CH;
N) other fungicides selected from the group consisting of guanidine, dodine, iminoctadine, guazatine, antibiotics: kasugamycin, streptomycin, polyoxin, validamycin A, nitrophenyl derivatives: binapacryl, dinocap, dinobuton, sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane, organometallic compounds: fentin salts, organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos, tolclofos- methyl, organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate-methyl, tolylfluanid, inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur, others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine.
9. The fungicidal mixture according to any of claims 1 to 8, comprising the components 1 ) and 2) in a weight ratio of from 100:1 to 1 :100.
10. A composition, comprising at least one liquid or solid carrier and a mixture according to any of claims 1 to 8.
1 1. A method for controlling phytopathogenic harmful fungi, wherein the fungi, their habitat or the plants to be protected against fungal attack, the soil, seed, areas, materials or spaces are/is treated with an effective amount of at least one compound I and at least one compound Il according to any of claims 1 to 8.
12. The method according to claim 11 , wherein the components 1 ) and 2) according to any of claims 1 to 8 are applied simultaneously, that is jointly or separately, or in succession.
13. The method according to claim 11 or 12, wherein the components 1) and 2) according to any of claims 1 to 8 are applied in an amount of from 5 g/ha to 2000 g/ha.
14. The method according to claim 1 1 or 12, wherein the components 1) and 2) according to any of claims 1 to 8 are applied in an amount of from 1 g to 1000 g per 100 kg of seed.
15. Seed, comprising the mixture according to any of claims 1 to 8 in an amount of from 1 g to 1000 g per 100 kg of seed.
16. The use of the compounds I and Il according to any of claims 1 to 8 for preparing a composition suitable for controlling harmful fungi.
17. The use of the compounds I and Il according to any of claims 1 to 8 for treating transgenic plants or the seed thereof.
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AR065200A1 (en) 2009-05-20
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EP2061320A2 (en) 2009-05-27
UA100504C2 (en) 2013-01-10
MA31234B1 (en) 2010-03-01
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KR20090108735A (en) 2009-10-16
TW200843640A (en) 2008-11-16
BRPI0807060A2 (en) 2015-06-16
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CL2008000363A1 (en) 2008-06-13
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CA2675455A1 (en) 2008-08-14
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