EP2139335A2 - Mélanges fongicides - Google Patents

Mélanges fongicides

Info

Publication number
EP2139335A2
EP2139335A2 EP08735866A EP08735866A EP2139335A2 EP 2139335 A2 EP2139335 A2 EP 2139335A2 EP 08735866 A EP08735866 A EP 08735866A EP 08735866 A EP08735866 A EP 08735866A EP 2139335 A2 EP2139335 A2 EP 2139335A2
Authority
EP
European Patent Office
Prior art keywords
compound
compounds
weight
plants
species
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP08735866A
Other languages
German (de)
English (en)
Inventor
Dirk Voeste
Carola Reinecke
Frank Werner
Egon Haden
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to EP08735866A priority Critical patent/EP2139335A2/fr
Publication of EP2139335A2 publication Critical patent/EP2139335A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof

Definitions

  • the present invention relates to fungicidal mixtures containing as active components
  • the invention relates to a method for controlling harmful fungi with mixtures of the compound I with the compound II and the use of the compounds tileg I with the compound II for the preparation of such mixtures and compositions containing these mixtures.
  • the metconazole referred to above as component 1 is (1RS, 5RS, 1RS, 5SR) -5- (4-chlorobenzyl) -2,2-dimethyl-1 - (1H-1, 2,4-triazole-1 - ylmethyl) cyclopentanol, whose preparation and its action against harmful fungi are known from the literature (EP-A 267 778).
  • the active ingredient prochloraz mentioned above as component 2 is N-propyl-N- [2- (2,4,6-trichlorophenoxy) ethyl] imidazole-1-carboxamide, whose production and action against harmful fungi is likewise known (US Pat. No. 3,991,071).
  • a concentrated liquid fungicidal composition which consists of a carrier, an azole, which also comprises metconazole, another fungicidally active ingredient as a finely divided suspension, a solubilizing agent and a dispersant.
  • a solubilizing agent As other fungicidally active ingredients a long list of fungicides is listed, including prochloraz is called. Only metconazole with kresoxim-methyl and chlorotrhalonil are described as mixtures. The object of the invention underlying this application were concentrated, stable co-formulations.
  • the present invention mixtures were the object, which show an improved action against harmful fungi, especially for certain indications with reduced total amount of applied drugs.
  • the mixtures of the compound I and the compound II, or the simultaneous joint or separate use of the compound I and the compound II are distinguished by a strengthening and crop-increasing effect on plants, in particular legumes, and an outstanding activity against a broad spectrum of phytopathogenic Fungi, in particular from the class of the Ascomycetes, Deuteromycetes, Basidiomycetes and Peronosporomycetes (Syn. Oomycetes). They are partially systemically effective and can be used in crop protection as foliar, pickling and soil fungicides.
  • Bipolaris and Drechslera species on maize, cereals, rice and turf e.g. D. maydis on maize, • Blumeria graminis (powdery mildew) on cereals,
  • Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and vines
  • Cochliobolus species on corn, cereals, rice e.g. Cochliobolus sativus on cereals, Cochliobolus miyabeanus on rice,
  • Drechslera species Pyrenophora species on maize, cereals, rice and turf, e.g. D. teres to barley or D. tritici-repentis to wheat,
  • Fusarium and Verticillium species on various plants e.g. F. graminea rum or F. culmorum on cereal or F. oxysporum on a variety of plants such. Tomatoes,
  • Michrodochium nivale on cereals • Mycosphaerella species on cereals, bananas and peanuts, such as: M. graminicola on wheat or M. fijiensis on bananas,
  • Puccinia species on various plants such as P. triticina, P. striformins, P. hordei or P. graminis on cereals, or P. asparagi on asparagus,
  • the mixtures of compounds I and II are also 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 Ophiostoma spp., Ceratocystis spp., Aureosidium pullulans, Sclerophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp .; Basidiomycetes such as Coniophora spp., Coriolus spp., Gloeophlum spp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp.
  • Tyromyces spp. Deuteromycetes such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderm spp., Alternaria spp., Paecilomyces spp. and Zygomycetes such as Mucor spp., moreover, in the protection of the following yeasts: Candida spp. and Saccharomyces cerevisae.
  • mixtures of compounds I and II can be used in crops that tolerate the action of herbicides, fungicides or insecticides as a result of breeding, including genetic engineering methods.
  • the mixtures according to the invention can be applied to transgenic plants which are resistant to herbicides of the group of sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogues Active substances are resistant (EP-A 0 242 236, EP-A 0 242 246, WO 92/00377, EP-A 0 257 993, US 5,013,659).
  • they can be used in transgenic crops, for example wool, with the property of producing the Bacillus thuringiensis toxins (Bt toxins), which makes the plant resistant to certain pests (EP-A 0 142 924, EP-A 0 193 259) ,
  • the mixtures according to the invention can also be used for the treatment of plants which have modified properties. They can be prepared, for example, by conventional breeding methods by producing mutants. Known is also the recombinant modifications of crop plants for the purpose of modifying the starch synthesized in the plants (WO 92/1 1376, WO 92/14827, WO 91/19806). Furthermore, crops which produce a modified fatty acid (WO 91/13972) can be treated with the mixtures according to the invention.
  • the compounds I and II can be applied simultaneously together or separately or one after the other, the sequence in the case of separate application generally having no effect on the control result.
  • Triazoles bitertanol, bromuconazoles, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fenbuconazole, flusilazole, fluquinconazole, flutriol, hexaconazole, imibenconazole, ipconazole, myclobutanil, penconazole, propiconapazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadi - menol, triadimefon, triticonazole;
  • Benzimidazoles benomyl, carbendazim, fuberidazole, thiabendazole; - Other: Ethaboxam, Etridiazole, Hymexazole;
  • Azoxystrobin dimoxystrobin, enestroburine, fluoxastrobin, kresoxim-methyl, metominostrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, orysastrobin, (2-chloro-5- [1- (3-methyl-benzyloxyimino) -ethyl] -benzyl) -carbamic acid methyl ester, (2-Chloro-5- [1- (6-methyl-pyridin-2-ylmethoxyimino) -ethyl] -benzyl) -carbamic acid methyl ester, 2- (ortho- (2,5-dimethylphenyl-oxymethylene) -phenyl) -3- methoxy-methyl acrylate; carboxamides
  • Benzoic acid amides flumetover, fluopicolide (picobenzamide), zoxamide;
  • Pyridines Pyrifenox, 3- [5- (4-Chloro-phenyl) -2,3-dimethyl-isoxazolidin-3-yl] -pyridine;
  • pyrimidines bupirimate, ferimzone, fenarimol, mepanipyrim, nuarimol, pyrimethanil;
  • Morpholines aldimorph, dodemorph, fenpropimorph, tridemorph;
  • Dicarboximides iprodione, procymidone, vinclozolin;
  • acibenzolar-S-methyl anilazine, captan, captafol, dazomet, diclomethine, fenoxanil, folpet, fenpropidin, famoxadone, fenamidone, octhilinone, probenazole, proquinazide, pyroquilon, quinoxyfen, tricyclazole, 5-chloro-7- ( 4-methyl-piperidin-1-yl) -6- (2,4,6-trifluorophenyl) - [1,2,4] triazolo [1,5-a] pyrimidine, 2-butoxy-6- iodo-3-propyl-chromen-4-one, 3- (3-bromo-6-fluoro-2-methylindol-1-sulfonyl) - [1, 2,4] triazole-1-sulfonic acid dimethylamide;
  • guanidines dodine, iminoctadine, guazatine
  • - Antibiotics Kasugamycin, Polyoxins, Streptomycin, Validamycin A
  • Organometallic compounds fentin salts
  • Sulfur-containing heterocyclyl compounds isoprothiolanes, dithianone;
  • Organophosphorus compounds edifenphos, fosetyl, fosetyl-aluminum, Iprobenfos, pyrazophos, tolclofos-methyl, phosphorous acid and their salts;
  • Organochlorine compounds thiophanates methyl, chlorothalonil, dichlofluanid, toluylfluanid, flusulfamides, phthalides, hexachlorobenzene, pencycuron, quintozene;
  • Nitrophenyl derivatives binapacryl, dinocap, dinobuton;
  • the active compounds can also be used in the form of their agriculturally acceptable salts. Usually come for alkali or alkaline earth salts, such as sodium, potassium or calcium salts in question.
  • the compound I and the compound II are usually used in a weight ratio of 100: 1 to 1: 100, preferably 20: 1 to 1:20, in particular 10: 1 to 1:10 applied.
  • the further active components are added to compound I in a ratio of from 20: 1 to 1:20.
  • the application rates of the mixtures according to the invention are from 5 g / ha to 2000 g / ha, preferably from 50 to 900 g / ha, in particular from 50 to 750 g / ha.
  • the application rates for the compound I are accordingly generally 1 to 1000 g / ha, preferably 10 to 900 g / ha, in particular 20 to 750 g / ha.
  • the application rates for the active compound II are correspondingly generally 1 to 2000 g / ha, preferably 10 to 900 g / ha, in particular 40 to 500 g / ha.
  • seed treatment e.g. By dusting, coating or impregnating seeds, in general application rates of mixture of 1 to 1000 g / 100 kg of seed, preferably 1 to 750 g / 100 kg, in particular 5 to 500 g / 100 kg are used.
  • the application rate of active ingredient depends on the type of application and the desired effect. Usual application rates are, for example, 0.001 g to 2 kg, preferably 0.005 g to 1 kg of active ingredient per cubic meter of material treated in the protection of materials.
  • the method for controlling harmful fungi is carried out by the separate or combined application of the compound I and the compound II or the mixtures of the compound I and the compound II by spraying or dusting the seeds, the plants or the soil before or after sowing of the plants or before or after emergence of the plants.
  • the mixtures according to the invention, or compound I and compound II, can be converted into the customary formulations, e.g. Solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the application form depends on the respective purpose; It should in any case ensure a fine and uniform distribution of the compound according to the invention.
  • the formulations are prepared in a known manner, e.g. by stretching the active ingredient with solvents and / or carriers, if desired using emulsifiers and dispersants.
  • Suitable solvents / auxiliaries are essentially:
  • glycol diacetate glycols, dimethyl fatty acid amides, fatty acids and fatty acid esters.
  • solvent mixtures can also be used
  • Carriers such as ground natural minerals (e.g., kaolins, clays, talc, chalk) and ground synthetic minerals (e.g., fumed silica, silicates); Emulsifiers such as non-ionic and anionic emulsifiers (for example polyoxyethylene
  • the surface-active substances used are alkali metal, alkaline earth metal, ammonium salts of lignin sulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, and condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde , Condensation products of naphthalene or naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl
  • mineral oil fractions of medium to high boiling point such as or diesel oil, coal tar oils and oils of plant or animal origin
  • mineral oil fractions of medium to high boiling point such as or diesel oil, coal tar oils and oils of plant or animal origin
  • aliphatic, cyclic and aromatic hydrocarbons for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives
  • strongly polar solvents for example dimethyl sulfoxide, N-methylpyrrolidone or water into consideration.
  • Powders, dispersants and dusts may be prepared by mixing or co-grinding the active substances with a solid carrier.
  • Granules e.g. Coated, impregnated and homogeneous granules can be prepared by binding the active compounds to solid carriers.
  • Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics, fertilizers, e.g. Ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder and other solid carriers.
  • Mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics
  • the formulations generally contain between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight of the active ingredient.
  • the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • formulations are: 1. Products for dilution in water
  • a Water-soluble concentrates (SL, LS)
  • the active compounds 20 parts by weight are dissolved in 70 parts by weight of cyclohexanone with the addition of 10 parts by weight of a dispersant, e.g. Polyvinylpyrrolidone dissolved. Dilution in water results in a dispersion.
  • the active ingredient content is 20% by weight
  • the active compounds 25 parts by weight of the active compounds 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 added to water by means of an emulsifying machine (e.g., Ultraturax) in 30 parts by weight and made into a homogeneous emulsion. Dilution in water results in an emulsion.
  • the formulation has an active ingredient content of 25% by weight.
  • the active ingredients 20 parts by weight of the active ingredients are comminuted with the addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent in a stirred ball mill to a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient.
  • the active ingredient content in the formulation is 20% by weight.
  • the active ingredients are finely ground with the addition of 50 parts by weight of dispersants and wetting agents and prepared by means of industrial equipment (for example extrusion, spray tower, fluidized bed) as water-dispersible or water-soluble granules. Dilution in water results in a stable dispersion or solution of the active substance.
  • the formulation has an active ingredient content of 50% by weight.
  • Water-dispersible and water-soluble powders 75 parts by weight of the active compounds are ground in a rotor-stator mill with the addition of 25 parts by weight of dispersing and wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient.
  • the active ingredient content of the formulation is 75% by weight.
  • 0.5 parts by weight of the active ingredients are finely ground and treated with 99.5 parts by weight of connected. Common processes are extrusion, spray drying or fluidized bed. This gives a granulate for direct application with 0.5 wt .-% active ingredient content.
  • LS water-soluble concentrates
  • FS suspensions
  • DS dusts
  • WS water-dispersible and water-soluble powders
  • ES emulsions
  • EC emulsifiable concentrates
  • gel formulations GF
  • the active compounds may be used as such, in the form of their formulations or the forms of use prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, litter, granules by spraying, misting, dusting, scattering or pouring.
  • the forms of application depend entirely on the intended use; In any case, they should ensure the finest possible distribution of the active compounds according to the invention.
  • Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (spray powders, oil dispersions) by adding water.
  • the substances as such or dissolved in an oil or solvent, can be homogenized in water by means of wetter, tackifier, dispersant or emulsifier.
  • the active compound concentrations in the ready-to-use preparations can be varied within wide ranges. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1%.
  • the active ingredients can also be used with great success in the ultra-low-volume (ULV) process, it being possible to apply formulations containing more than 95% by weight of active ingredient or even the active ingredient without additives.
  • UUV ultra-low-volume
  • the active substances may include oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides, if appropriate only be added immediately before application (tank mix). These agents can be added to the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1:10 to 10: 1.
  • the active compounds were prepared separately or together as a stock solution with 25 mg of active ingredient, which with a mixture of acetone and / or DMSO and the emulsifier Wettol EM 31 (wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) in the volume ratio solvent- Emulsifier from 99 to 1 ad 10 ml was filled. It was then made up to 100 ml with water. This stock solution was diluted with the described solvent-emulsifier-water mixture to the drug concentration given below.
  • Wettol EM 31 wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
  • Paprika seedlings were, after 2-3 leaves had developed well, sprayed to drip point with an aqueous suspension in the drug concentration below. The next day, the treated plants were inoculated with a spore suspension of Botrytis cinerea in 2% biomalt solution. Subsequently, the test plants were placed in a climatic chamber at 22 to 24 ° C, darkness and high humidity. After 5 days, the extent of fungal attack on the leaves could be determined visually in%.
  • the efficiency (W) is calculated according to the formula of Abbot as follows:
  • ⁇ corresponds to the fungal infestation of the treated plants in% and ⁇ corresponds to the fungal infestation of the untreated (control) plants in%
  • ⁇ corresponds to the fungal infestation of the untreated (control) plants in%
  • the infestation of the treated plants corresponds to that of the untreated control plants; at an efficiency of 100, the treated plants have no infestation.

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

Abstract

L'invention concerne des mélanges fongicides contenant comme composants actifs : 1) du metconazole de formule (I) et 2) du prochloraze de formule (II) dans des quantités garantissant un effet synergique, ainsi que des agents contenant ces mélanges.
EP08735866A 2007-04-25 2008-04-07 Mélanges fongicides Withdrawn EP2139335A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP08735866A EP2139335A2 (fr) 2007-04-25 2008-04-07 Mélanges fongicides

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP07106953 2007-04-25
EP08735866A EP2139335A2 (fr) 2007-04-25 2008-04-07 Mélanges fongicides
PCT/EP2008/054132 WO2008132021A2 (fr) 2007-04-25 2008-04-07 Mélanges fongicides

Publications (1)

Publication Number Publication Date
EP2139335A2 true EP2139335A2 (fr) 2010-01-06

Family

ID=39789794

Family Applications (1)

Application Number Title Priority Date Filing Date
EP08735866A Withdrawn EP2139335A2 (fr) 2007-04-25 2008-04-07 Mélanges fongicides

Country Status (12)

Country Link
US (1) US8288315B2 (fr)
EP (1) EP2139335A2 (fr)
JP (1) JP5166514B2 (fr)
CN (1) CN101668427A (fr)
AR (1) AR066320A1 (fr)
AU (1) AU2008244436B2 (fr)
BR (1) BRPI0810236A2 (fr)
CA (1) CA2682922A1 (fr)
EA (1) EA016291B1 (fr)
UA (1) UA99615C2 (fr)
UY (1) UY31051A1 (fr)
WO (1) WO2008132021A2 (fr)

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JP5530428B2 (ja) 2008-07-04 2014-06-25 ビーエーエスエフ ソシエタス・ヨーロピア 置換１−メチルピラゾール−４−イルカルボキシアニリドを含んでいる殺菌剤混合物
CN102067859A (zh) * 2011-02-19 2011-05-25 陕西美邦农药有限公司 一种含有种菌唑与硫代氨基甲酸酯类化合物的杀菌组合物
JP5940369B2 (ja) * 2011-05-27 2016-06-29 石原産業株式会社 植物病害の防除方法
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EP2719281A4 (fr) * 2011-06-07 2014-11-19 Kureha Corp Agent chimique pour l'agriculture ou l'horticulture, composition pour lutter contre les maladies des plantes, procédé pour lutter contre les maladies des plantes et produit pour lutter contre les maladies des plantes
NZ729081A (en) * 2014-07-14 2022-07-01 Adjuvants Plus Usa Inc Clonostachys rosea inoculated plant materials with fungicides and adjuvants
CN105724393B (zh) * 2016-04-07 2018-06-05 陕西上格之路生物科学有限公司 含叶菌唑的杀菌组合物在防治小麦赤霉病上的应用
CN106719767A (zh) * 2017-01-17 2017-05-31 上海悦联生物科技有限公司 一种含叶菌唑和咪鲜胺的农药组合物

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JP5166514B2 (ja) 2013-03-21
AR066320A1 (es) 2009-08-12
WO2008132021A2 (fr) 2008-11-06
US20100062938A1 (en) 2010-03-11
AU2008244436B2 (en) 2013-03-14
EA200901443A1 (ru) 2010-04-30
BRPI0810236A2 (pt) 2014-09-30
UA99615C2 (ru) 2012-09-10
WO2008132021A3 (fr) 2009-04-16
CN101668427A (zh) 2010-03-10
US8288315B2 (en) 2012-10-16
AU2008244436A1 (en) 2008-11-06
UY31051A1 (es) 2008-10-31
JP2010525004A (ja) 2010-07-22
EA016291B1 (ru) 2012-03-30
CA2682922A1 (fr) 2008-11-06

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