[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

WO2020120202A2 - Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole - Google Patents

Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole Download PDF

Info

Publication number
WO2020120202A2
WO2020120202A2 PCT/EP2019/083329 EP2019083329W WO2020120202A2 WO 2020120202 A2 WO2020120202 A2 WO 2020120202A2 EP 2019083329 W EP2019083329 W EP 2019083329W WO 2020120202 A2 WO2020120202 A2 WO 2020120202A2
Authority
WO
WIPO (PCT)
Prior art keywords
isoquinoline
dimethyl
difluoro
composition
mefentrifluconazole
Prior art date
Application number
PCT/EP2019/083329
Other languages
English (en)
Other versions
WO2020120202A3 (fr
Inventor
Mikael COQUILLER
Markus Gewehr
Original Assignee
BASF Agro B.V.
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 Agro B.V. filed Critical BASF Agro B.V.
Priority to EA202191562A priority Critical patent/EA202191562A1/ru
Priority to EP19816254.7A priority patent/EP3893642A2/fr
Priority to UAA202103803A priority patent/UA128261C2/uk
Publication of WO2020120202A2 publication Critical patent/WO2020120202A2/fr
Publication of WO2020120202A3 publication Critical patent/WO2020120202A3/fr

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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Definitions

  • the present invention relates to a method for controlling Sclerotinia spp. in oilseed rape or canola comprising treating the plants, their seed or the soil with a fungicidally effective amount of a composition comprising
  • mefentrifluconazole Owing to the basic character of its nitrogen atoms, mefentrifluconazole is capable of forming salts or ad ducts with inorganic or organic acids or with metal ions, in particular salts with inorganic acids. Mixtures of mefentrifluconazole are described in WO 2014/095994.
  • Mefentrifluconazole (I) comprises chiral centers and is generally obtained in the form of race- mates.
  • the R- and S-enantiomers of mefentrifluconazole (I) can be separated and isolated in pure form with methods known by the skilled person, e.g. by using chiral HPLC.
  • mefentrifluconazole (I) can be used in form of
  • Mefentrifluconazole (I) may be provided and used as (R)-enantiomer with an enantiomeric ex cess (e.e.) of at least 40%, for example, at least 50%, 60%, 70% or 80%, preferably at least 90%, more preferably at least 95%, yet more 25 preferably at least 98% and most preferably at least 99%. This applies to every composition detailed herein.
  • the (R)-enantiomer of mefentriflu conazole has the chemical name:
  • Mefentrifluconazole (I) may be further provided and used as (S)-enantiomer with an enantiomeric excess (e.e.) of at least 40%, for example, at least 50%, 60%, 70% or 80%, preferably at least 90%, more preferably at least 95%, yet more preferably at least 98% and most preferably at least 99%. This applies to every composition detailed herein.
  • the (S)-enantiomer of mefentrifluconazole has the chemical name:
  • Agriculturally acceptable salts encompass especially the salts of those cations or the acid addition salts of those acids whose cations and anions, respectively, have no adverse effect on the fungicidal action of said compounds.
  • Suitable cations are thus in particular the ions of the alkali metals, preferably sodium and potassium, of the alkaline earth metals, preferably calcium, magnesium and barium, of the transition metals, preferably manganese, copper, zinc and iron, and also the ammonium ion which, if desired, may carry one to four Ci-C4-alkyl substituents and/or one phenyl or benzyl substituent, preferably diisopropylammonium, tetramethylammonium, tet- rabutylammonium, trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(Ci-C4-alkyl)sulfonium, and sulfoxonium
  • Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogensulfate, sulfate, dihydrogenphosphate, hydrogenphosphate, phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate, and the anions of Ci-C4-alkanoic acids, preferably formate, acetate, propionate and butyrate. They can be formed by reacting such inventive compound with an acid of the corresponding anion, preferably of hydrochloric acid, hy- drobromic acid, sulfuric acid, phosphoric acid or nitric acid.
  • Sclerotinia spp. causes Sclerotinia stem rot (SSR) a major disease of oilseed rape or canola.
  • SSR Sclerotinia stem rot
  • SSR Sclerotinia stem rot
  • Sclerotinia spp. especially Sclerotinia sclerotiorum, can produce long-term storage structures and persist for long periods in the soil. Control of Sclerotinia spp. is becoming more and more difficult for farmers. In order to reduce crop losses and to obtain optimal crop yield proper pest management is required.
  • compositions comprising mefentrifluconazole ans at least one compound (II) as defined herein shows an unexpected fungicidal action towards Sclerotinia spp., especially towards Sclerotinia sclerotiorum.
  • the present invention relates to a method for controlling a phythopatogenic fungi selected from Sclerotinia spp. on oilseed rape or canola, comprising treating the plants, their seed or the soil with a fungicidally effective amount of a composition comprising
  • the invention relates to a use of the compositions comprising mefentrifluconazole (I) and at least one compound (II) as described herein for controlling a phythopatogenic fungi selected from Sclerotinia spp., especially Sclerotinia sclerotiorum, on oilseed rape or canola.
  • the present invention relates to a method for controlling Sclerotinia spp.. In a specific embodiment, the present invention relates to a method for controlling Sclerotinia sclerotiorum.
  • the compound (II) of the composition is selected from boscalid (II- 1 ), dimoxystrobin (II-2), fenpropimorph (II-3), fluxapyroxad (I I-4), inpyrfluxam (II-5), isoflucypram (II-6), kresoxym-methyl (II-7), metyltetraprole (II-8), quinofumelin (II-9), pyraclostrobin (11-10), 1 - (4, 5-dimethylbenzimidazol-1 -yl)-4, 4, 6-trifluoro-3, 3-dimethyl-isoquinoline (11-1 1 ), 6-chloro-1 -(4,5- dimethylbenzimidazol-1 -yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (11-12), 1 -(4,5- dimethylbenzimidazol-1 -yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline
  • the composition comprises mefentrifluconazole (I) and dimoxystrobin (II-2).
  • the composition comprises mefentrifluconazole (I) and fenpropimorph (II-3).
  • the composition comprises mefentrifluconazole (I) and fluxapyroxad (I I-4).
  • the composition comprises mefentrifluconazole (I) and inpyrfluxam (II-5).
  • the composition comprises mefentrifluconazole (I) and isoflucypram (II-6).
  • the composition comprises mefentrifluconazole (I) and kresoxym-methyl (II-7).
  • the composition comprises mefentrifluconazole (I) and metyltetraprole (II-8).
  • the composition comprises mefentrifluconazole (I) and quinofumelin (II-9).
  • the composition comprises mefentrifluconazole (I) and pyraclostrobin (11-10).
  • the composition comprises mefentrifluconazole (I) and 1-(4,5-dimethylbenzimidazol-1-yl)-4, 4, 6-trifluoro-3, 3-dimethyl-isoquinoline (11-1 1 ).
  • the composition comprises mefentrifluconazole (I) and 6-chloro-1 -(4, 5-dimethylbenzimidazol-1-yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (11-12).
  • the composition comprises mefentrifluconazole (I) and 1 -(4, 5-dimethylbenzimidazol-1-yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (11-13).
  • the composition comprises mefentrifluconazole (I) and 4,4-difluoro-3,3-dimethyl-1-(4-methylbenzimidazol-1-yl)isoquinoline (11-14).
  • the composition comprises mefentrifluconazole (I) and 1-(6-chloro-7-methyl-pyrazolo[1 ,5-a]pyridin-3-yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (II-
  • the composition comprises mefentrifluconazole (I) and 4, 4-difluoro-1-(6-fluoro-7-methyl-pyrazolo[1 ,5-a]pyridin-3-yl)-3, 3-dimethyl-isoquinoline (II-
  • the composition comprises mefentrifluconazole (I) and 4,4-difluoro-3,3-dimethyl-1-(6-methylpyrazolo[1 ,5-a]pyridin-3-yl)isoquinoline (11-17).
  • the composition comprises mefentrifluconazole (I) and 1 -(6, 7-dimethylpyrazolo[1 ,5-a]pyridin-3-yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (11-18).
  • the composition comprises mefentrifluconazole (I) and 1 -(7, 8-dimethylimidazo[1 ,2-a]pyridin-3-yl)-4,4-difluoro-3, 3-dimethyl-isoquinoline (11-19).
  • the composition comprises mefentrifluconazole (I) and one compound (II) as the only active ingredients of the composition.
  • the composition comprises mefentrifluconazole (I) and two compounds (II) differ ent from each other as the only active ingredients of the composition.
  • the weight ratio of compound I and compound II is usually from 500:1 to 1 :500, preferably from 100:1 to 1 :100, more preferably from 50:1 to 1 :50, even more preferably from 20:1 to 1 :20, most preferably from 10:1 to 1 :10.
  • the ratios can also be from 1 :5 to 5:1 , or 1 :1.
  • the compound (I) and compound (II) can be applied simultaneously, that is jointly or separately, or in succession. According to one embodiment, the compound (I) and compound (II) are ap plied simultaneously. According to another embodiment, compound (I) and compound (II) are applied in succession.
  • the method comprises treating oilseed rape or canola plants. (I)is In a further embodiment, the method comprises treating oilseed rape or canola seeds.
  • the method comprises treating the soil.
  • the present invention relates to a method for controlling Sclerotinia sclerotiorum on oilseed rape or canola, comprising treating the plants, their seed or the soil with a fungicidally effective amount of a composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein.
  • the method comprises treat ing the oilseed rape or canola plants.
  • the method comprises treating oilseed rape or canola seeds.
  • Treating the plants, their seed or the soil in the method according to present invention may be carried out in spray application, in seed treatment, in drip and drench applications, in-furrow applications, on-seed application and overall soil incorporation, chemigation, i.e. by addition of the active ingredients to the irrigation water, and in hydroponic/mineral systems.
  • plant propagation material is to be understood to denote all the generative parts of the plant in particular seeds
  • Plants and as well as the propagation material of said plants, which can be treated with fungi- cidally effective amount of a composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein include all genetically modified plants or transgenic plants, e.g. crops which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods, or plants which have modified characteristics in compar ison with existing plants, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures.
  • mixtures according to the present invention can be applied (as seed treatment, spray treatment, in furrow or by any other means) also to plants which have been modified by breeding, mutagenesis or genetic engineering including but not limiting to agricultural biotech products on the market or in development (cf.
  • Genetically modified plants are plants, which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or natural recombination. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant.
  • Such genetic modi fications also include but are not limited to targeted post-transitional modification of protein(s), oligo- or polypeptides e. g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.
  • a composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein can be converted into the customary formu lations, 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 distribution of the mixtures according to the present invention.
  • the formulations are prepared in a known manner (cf. US 3,060,084, EP-A 707 445 (for liquid concentrates), Brown ing: "Agglomeration”, Chemical Engineering, Dec.
  • the agrochemical formulations may also comprise auxiliaries which are customary in agro chemical formulations. The auxiliaries used depend on the particular application form and active substance, respectively.
  • auxiliaries are solvents, solid carriers, dispersants or emulsifiers (such as further solubilizers, protective colloids, surfactants and adhesion agents), organic and inorganic thickeners, bactericides, anti-freezing agents, anti-foaming agents, if appropriate colorants and tackifiers or binders (e. g. for seed treatment formulations).
  • Suitable solvents are water, organic solvents such as 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, e. g.
  • Solid carriers are mineral earths such as silicates, silica gels, talc, kaolins, limestone, lime, chalk, bole, loess, clays, dolomite, diatomaceous earth, calcium sulfate, magnesi-um sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e. g., ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as ce real meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid car riers.
  • mineral earths such as silicates, silica gels, talc, kaolins, limestone, lime, chalk, bole, loess, clays, dolomite, diatomaceous earth, calcium sulfate, magnesi-um sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e. g., ammoni
  • Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, such as ligninsoulfonic acid (Borresperse® types, Borregard, Norway) phenolsulfonic acid, naphthalenesulfonic acid (Mor- wet® types, Akzo Nobel, U.S.A.), dibutylnaphthalene-sulfonic acid (Nekal® types, BASF, Ger many), and fatty acids, alkylsulfonates, alkyl-arylsulfonates, alkyl sulfates, laurylether sulfates, fatty alcohol sulfates, and sulfated hexa-, hepta- and octadecanolates, sulfated fatty alcohol glycol ethers, furthermore conden
  • methylcellulose g. methylcellulose
  • hydrophobically modified starches polyvinyl alcohols (Mowiol® types, Clariant, Switzerland), polycarboxylates (Sokolan® types, BASF, Germany), polyalkoxylates, polyvinylamines (Lupasol® types, BASF, Germany), polyvinylpyrrolidone and the copolymers therof.
  • thickeners i. e. compounds that impart a modified flowability to formula-tions, i. e. high viscosity under static conditions and low viscosity during agitation
  • thickeners are polysaccharides and organic and inorganic clays such as Xanthan gum (Kelzan®, CP Kelco, U.S.A.), Rhodopol® 23 (Rhodia, France), Veegum® (R.T. Vanderbilt, U.S.A.) or Attaclay® (Engelhard Corp., NJ, USA).
  • Bactericides may be added for preservation and stabilization of the formulation.
  • suitable bactericides are those based on dichlorophene and benzylalcohol hemi formal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas) and isothia- zolinone derivatives such as alkylisothiazolinones and benzisothiazolinones (Acticide® MBS from Thor Chemie).
  • Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glyc erin.
  • anti-foaming agents examples include silicone emulsions (such as e. g. Silikon® SRE, Wacker, Germany or Rhodorsil®, Rhodia, France), long chain alcohols, fatty acids, salts of fatty acids, fluoroorganic compounds and mixtures thereof.
  • Suitable colorants are pigments of low water solubility and water-soluble dyes. Examples are rhodamin B, C. I. pigment red 112, C. I. solvent red 1 , pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pig ment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
  • tackifiers or binders examples include polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols and cellulose ethers (Tylose®, Shin-Etsu, Japan).
  • Powders, materials for spreading and dusts can be prepared by mixing or conco-mitantly grind ing composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein and, if appropriate, further active substances, with at least one solid carrier.
  • Granules e. g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein to solid carriers.
  • solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, dia- tomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic ma terials, fertilizers, such as, e.
  • ammonium sulfate ammonium phosphate, ammonium nitrate, ureas
  • products of vegetable origin such as cereal meal, tree bark meal, wood meal and nut-shell meal, cellulose powders and other solid carriers.
  • formulation types are suspensions (SC, OD, FS), emulsifiable concentrates (EC), emulsions (EW, EO, ES), pastes, pastilles, wettable powders or dusts (WP, SP, SS, WS, DP, DS) or granules (GR, FG, GG, MG), which can be water-soluble or wettable, as well as gel for mulations for the treatment of plant propagation materials such as seeds (GF), herein further below exemplified in detail: 1.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are dissolved in 90 parts by weight of water or in a water-soluble sol vent.
  • wetting agents or other auxiliaries are added.
  • the active substance dis solves upon dilution with water. In this way, a formulation having a content of 10% by weight of active substance is obtained.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, e. g. poly-vinylpyrrolidone. Dilution with water gives a disper sion.
  • a dispersant e. g. poly-vinylpyrrolidone. Dilution with water gives a disper sion.
  • the active substance content is 20% by weight.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein 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 composition has an active substance content of 15% by weight.
  • Emulsions (EW, EO, ES)
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein 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 mix ture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultra- turrax) and made into a ho-mogeneous emulsion. Dilution with water gives an emulsion.
  • the composition has an active substance content of 25% by weight.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein 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 substance sus-pension. Dilution with water gives a stable suspension of the active substance.
  • the active substance content in the composition is 20% by weight.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are ground finely with addi-tion of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of tech nical appliances (e. g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance.
  • the composition has an active substance content of 50% by weight.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein 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 solu tion of the active substance.
  • the active substance content of the composition is 75% by weight.
  • Dustable powders (DP, DS)
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable compo-sition having an active substance content of 5% by weight.
  • composition comprising mefentrifluconazole (I) and at least one com pound (II) as described herein is ground finely and associ-ated with 99.5 parts by weight of car riers.
  • Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted having an active sub-stance content of 0.5% by weight.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are dissolved in 90 parts by weight of an organic solvent, e. g. xylene.
  • an organic solvent e. g. xylene.
  • compositions generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, most preferably between 0.5 and 90%, by weight of active substances.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein can be used as such or in the form of their compositions, e. g. in the form of directly sprayable solutions, powders, suspensions, dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dust ing, spreading, brushing, immersing or pouring.
  • the application forms depend entirely on the intended purposes; it is intended to ensure in each case the finest possible distribution of the compounds present in composition comprising mefentrifluconazole (I) and at least one com pound (II) as described herein.
  • Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable 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 a wetter, tackifier, dispersant or emulsifier.
  • the active substance concentrations in the ready-to-use preparations can be varied within rela tively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.001 to 1% by weight of composition comprising mefentrifluconazole (I) and at least one compound (II) as de scribed herein.
  • compositions comprising mefentrifluconazole (I) and at least one compound (II) as described herein may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply compositions comprising over 95% by weight of active substance, or even to apply the active substance without addi-tives.
  • UUV ultra-low-volume process
  • oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds present in the composition comprising mefentriflucona zole (I) and at least one compound (II) as described herein, if appropriate not until immediately prior to use (tank mix).
  • These agents can be admixed with composition comprising mefentriflu conazole (I) and at least one compound (II) as described herein in a weight ratio of 1 : 100 to 100:1 , preferably 1 :10 to 10:1.
  • compositions of this invention may also contain fertilizers such as ammonium nitrate, urea, pot ash, and superphosphate, phytotoxicants and plant growth regulators and safeners. These may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a composition of this invention either before or after being treated with the fertilizers.
  • fertilizers such as ammonium nitrate, urea, pot ash, and superphosphate, phytotoxicants and plant growth regulators and safeners.
  • compositions are applied by treating the fungi or the plants, plant propagation materials (pref erably seeds), materials or soil to be protected from fungal attack with a pesticidally effective amount of composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein.
  • the application can be carried out both before and after the infection of the materials, plants or plant propagation materials (preferably seeds) by the pests.
  • pesticidally effective amount means the amount of composition comprising mefen trifluconazole (I) and at least one compound (II) as described herein or of compositions compris ing composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occur rence and activity of the target organism.
  • the pesticidally effective amount can vary.
  • a pesti cidally effective amount will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.
  • compositions comprising composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein, it is preferred to employ the pure active compound, to which optionally further active compounds against pests, such as insecticides, herbicides, fungicides or else herbicidal or growth-regulating active compounds or fertilizers can be added as further active components according to need.
  • pests such as insecticides, herbicides, fungicides or else herbicidal or growth-regulating active compounds or fertilizers can be added as further active components according to need.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein is employed by treating the fungi or the plants or soil to be protected from pes ticidal attack via foliar application with a pesticidally effective amount of composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein.
  • the ap plication can be carried out both before and after the infection of the plants by the pests.
  • the application rates of composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are from 0,1 g/ha to 10000 g/ha, preferably 2 g/ha to 2500 g/ha, more preferably from 5 to 1000 g/ha, most preferably from 10 to 750 g/ha, in particular from 20 to 700 g/ha.
  • composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein are used for the protection of the seed and the seedlings' roots and shoots, preferably the seeds as set forth above.
  • compositions which are especially useful for seed treatment are e.g.:
  • a Soluble concentrates (SL, LS)
  • compositions can be applied to plant propagation materials, particularly seeds, diluted or undiluted.
  • the compositions in question give, after two-to-tenfold dilution, active substance con centrations of from 0.01 to 60% by weight, prefer-ably from 0.1 to 40% by weight, in the ready- to-use preparations.
  • Application can be carried out before or during sowing.
  • Methods for apply ing or treating agrochemical compounds and compositions thereof, respectively, on to plant propagation material, especially seeds are known in the art, and include dressing, coating, pel leting, dusting and soaking application methods of the propagation material (and also in furrow treatment).
  • the compounds or the compositions thereof, respective ly are applied on to the plant propagation material by a method such that germination is not induced, e. g. by seed dressing, pelleting, coating and dusting.
  • the application rates of the in ventive mixture are generally for the formulated product (which usually comprises from10 to 750 g/l of the active(s)) .
  • the invention also relates to the propagation products of plants, and especially the seed com prising, that is, coated with and/or containing, a mixture as defined above or a composition con taining the mixture of two or more active ingredients or a mixture of two or more compositions each providing one of the active ingredients.
  • the plant propagation material (preferably seed) comprises composition comprising mefentrifluconazole (I) and at least one compound (II) as described herein in an amount of from 0.1 g to 10 kg per 100 kg of plant propagation material (preferably seed), preferably 0.1 g to 1 kg per 100 kg of plant propagation mate rial (preferably seed).
  • the compounds were dissolved in a mixture of acetone and/or dimethylsulfoxide and the wet ting agent/emulsifier Wettol, which is based on ethoxylated alkylphenoles, in a ratio (volume) solvent-emulsifier of 99 to 1 to give a total volume of 5 ml. Subsequently, water was added to total volume of 100 ml. This stock solution was then diluted with the described solvent- emulsifier-water mixture to the final concentration given in the table below.
  • Wettol which is based on ethoxylated alkylphenoles
  • Oilseed rapes were grown in pots to the 13 to 14 leaf stage.
  • the rape petals were fixed wit 25mI of 2.5% methylcellulose on leaf 1 and 2.
  • 25 mI of a spore suspension of Sclerotinia sclerotiorum was pipetted on each fixed rape petal.
  • the plants were transferred for 2 days in a greenhouse chamber at 20°C and a humidity of 60%. Then These plants were sprayed to run-off with previ ously described spray solution, containing the concentration of active ingredient or their mixture mentioned in the table below.
  • the trial plants were immediately transferred in the greenhouse chamber again. After 14 days the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
  • Oilseed rapes were grown in pots to the 13 to 14 leaf stage. These plants were sprayed to run off with previously described spray solution, containing the concentration of active ingredient or their mixture mentioned in the table below. The plants were allowed to air-dry. Three days later the applicated rape petals were fixed wit 25mI of 2.5% methylcellulose on leaf 1 and 2. 25 mI of a spore suspension of Sclerotinia sclerotiorum was pipetted on each fixed rape petal. After 14 days at 20°C and a relative humidity of 60 % the extent of fungal attack on the leaves was visu ally assessed as % diseased leaf area.
  • the disease ratings were converted into efficacies.
  • 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 trial was conducted under field conditions. Seeds of rape plants were planted and grown under standard conditions with adequate supply of water and nutrients. At the growth stage of 63-67, an application of the compounds was made once. No other compounds were applied for pathogen control. Infection with pathogens occurred naturally. The disease incidences were evaluated 56 days after the first application ( Sclesc ).
  • 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.

Landscapes

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

Abstract

La présente invention concerne un procédé de lutte contre des champignons phythopatogènes choisis parmi Sclerotinia spp., en particulier le Sclerotinia sclerotibio, sur le colza oléagineux, comprenant le traitement des plantes, de leur graine ou du sol avec une quantité efficace du point de vue fongicide de la composition comprenant du méféntrifluconazole et un autre composé actif (II) choisi parmi boscalide, dimoxystrobine, fenpropimorphe, fluxapyroxade, inpyrfluxame, isoflucyprame, kresoxym-méthyle, metyltétraprole, quinofumeline, pyraclostrobine, 1-(4,5-diméthylbenzimidazol-1-yl)-4,4,6-trifluoro-3,3-diméthyl- isoquinoline, 6-chloro-1-(4,5-diméthylbenzimidazol-1-yl)-4,4-difluoro-3,3-diméthyl-isoquinoline, -(4,5-diméthylbenzimidazol-1-yl)-4,4-difluoro-3,3-diméthyl-isoquinoline, 4,4-difluoro-3,3- diméthyl-1-(4-méthylbenzimidazol-1-yl)isoquinoline, 1-(6-chloro-7-méthyl-pyrazolo[1,5-a]pyridin- 3-yl)-4,4-difluoro-3,3-diméthyl-isoquinoline, 4,4-difluoro-1-(6-fluoro-7-méthyl-pyrazolo[1,5-1 a]pyridin-3-yl)-3,3-diméthyl-isoquinoline, 4,4-difluoro-3,3-diméthyl-1-(6-méthylpyrazolo[1,5- a]pyridin-3-yl)isoquinoline, 1-(6,7-diméthylpyrazolo[1,5-a]pyridin-3-yl)-4,4-difluoro-3,3-diméthyl- isoquinoline et 1-(7,8-diméthylimidazo[1,2-a]pyridin-3-yl)-4,4-difluoro-3,3-diméthyl-isoquinoline.
PCT/EP2019/083329 2018-12-11 2019-12-02 Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole WO2020120202A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EA202191562A EA202191562A1 (ru) 2018-12-11 2019-12-02 Способ борьбы с sclerotinia spp. в масличном рапсе или каноле композициями, содержащими мефентрифлуконазол
EP19816254.7A EP3893642A2 (fr) 2018-12-11 2019-12-02 Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole
UAA202103803A UA128261C2 (uk) 2018-12-11 2019-12-02 Спосіб боротьби з sclerotinia spp. в олійному ріпаку або канолі композиціями, що містять мефентрифлуконазол

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18211681 2018-12-11
EP18211681.4 2018-12-11

Publications (2)

Publication Number Publication Date
WO2020120202A2 true WO2020120202A2 (fr) 2020-06-18
WO2020120202A3 WO2020120202A3 (fr) 2020-07-23

Family

ID=64664894

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2019/083329 WO2020120202A2 (fr) 2018-12-11 2019-12-02 Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole

Country Status (4)

Country Link
EP (1) EP3893642A2 (fr)
EA (1) EA202191562A1 (fr)
UA (1) UA128261C2 (fr)
WO (1) WO2020120202A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111955464A (zh) * 2020-08-14 2020-11-20 陕西上格之路生物科学有限公司 一种含有氯氟醚菌唑的杀菌组合物

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3060084A (en) 1961-06-09 1962-10-23 Du Pont Improved homogeneous, readily dispersed, pesticidal concentrate
US3299566A (en) 1964-06-01 1967-01-24 Olin Mathieson Water soluble film containing agricultural chemicals
US3920442A (en) 1972-09-18 1975-11-18 Du Pont Water-dispersible pesticide aggregates
US4144050A (en) 1969-02-05 1979-03-13 Hoechst Aktiengesellschaft Micro granules for pesticides and process for their manufacture
US4172714A (en) 1976-12-20 1979-10-30 E. I. Du Pont De Nemours And Company Dry compactible, swellable herbicidal compositions and pellets produced therefrom
GB2095558A (en) 1981-03-30 1982-10-06 Avon Packers Ltd Formulation of agricultural chemicals
WO1991013546A1 (fr) 1990-03-12 1991-09-19 E.I. Du Pont De Nemours And Company Granules pesticides dispersibles ou solubles dans l'eau, obtenus a partir de liants thermo-actives
US5180587A (en) 1988-06-28 1993-01-19 E. I. Du Pont De Nemours And Company Tablet formulations of pesticides
US5208030A (en) 1989-08-30 1993-05-04 Imperial Chemical Industries Plc Active ingredient dosage device
US5232701A (en) 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
EP0707445A1 (fr) 1993-07-03 1996-04-24 Basf Ag Formulation aqueuse polyphasee et stable prete a l'emploi pour produits phytosanitaires et procede de preparation
WO2013007767A1 (fr) 2011-07-13 2013-01-17 Basf Se Composés fongicides 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol substitués
WO2014095994A1 (fr) 2012-12-20 2014-06-26 Basf Se Compositions comprenant un composé triazole
WO2018060039A1 (fr) 2016-09-28 2018-04-05 Syngenta Participations Ag Compositions fongicides
WO2018149851A1 (fr) 2017-02-16 2018-08-23 Syngenta Participations Ag Compositions fongicides

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2019004930A (es) * 2016-10-26 2019-06-06 Bayer Cropscience Ag Uso de piraziflumid para el control de sclerotinia spp en aplicaciones de tratamiento de semillas.
WO2018105663A1 (fr) * 2016-12-06 2018-06-14 株式会社クレハ Agent chimique agricole et horticole, procédé de lutte contre des maladies de plantes et produit de lutte contre des maladies de plantes
CN108541711A (zh) * 2018-06-27 2018-09-18 佛山市瑞生通科技有限公司 一种含氯氟醚菌唑与氟唑菌酰胺的杀菌组合物

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3060084A (en) 1961-06-09 1962-10-23 Du Pont Improved homogeneous, readily dispersed, pesticidal concentrate
US3299566A (en) 1964-06-01 1967-01-24 Olin Mathieson Water soluble film containing agricultural chemicals
US4144050A (en) 1969-02-05 1979-03-13 Hoechst Aktiengesellschaft Micro granules for pesticides and process for their manufacture
US3920442A (en) 1972-09-18 1975-11-18 Du Pont Water-dispersible pesticide aggregates
US4172714A (en) 1976-12-20 1979-10-30 E. I. Du Pont De Nemours And Company Dry compactible, swellable herbicidal compositions and pellets produced therefrom
GB2095558A (en) 1981-03-30 1982-10-06 Avon Packers Ltd Formulation of agricultural chemicals
US5180587A (en) 1988-06-28 1993-01-19 E. I. Du Pont De Nemours And Company Tablet formulations of pesticides
US5208030A (en) 1989-08-30 1993-05-04 Imperial Chemical Industries Plc Active ingredient dosage device
WO1991013546A1 (fr) 1990-03-12 1991-09-19 E.I. Du Pont De Nemours And Company Granules pesticides dispersibles ou solubles dans l'eau, obtenus a partir de liants thermo-actives
US5232701A (en) 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
EP0707445A1 (fr) 1993-07-03 1996-04-24 Basf Ag Formulation aqueuse polyphasee et stable prete a l'emploi pour produits phytosanitaires et procede de preparation
WO2013007767A1 (fr) 2011-07-13 2013-01-17 Basf Se Composés fongicides 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol substitués
WO2014095994A1 (fr) 2012-12-20 2014-06-26 Basf Se Compositions comprenant un composé triazole
WO2018060039A1 (fr) 2016-09-28 2018-04-05 Syngenta Participations Ag Compositions fongicides
WO2018149851A1 (fr) 2017-02-16 2018-08-23 Syngenta Participations Ag Compositions fongicides

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
"Perry's Chemical Engineer's Handbook", 1963, MCGRAW-HILL, pages: 8 - 57
BROWNING: "Agglomeration", CHEMICAL ENGINEERING, 4 December 1967 (1967-12-04), pages 147 - 48
HANCE ET AL.: "Weed Control Handbook", 1989, BLACKWELL SCIENTIFIC
KLINGMAN: "Weed Control as a Science", 1961, J. WILEY & SONS
MOLLET, H.GRUBEMANN, A.: "Formulation technology", 2001, WILEY VCH VERLAG
R.S. COLBY: "Calculating synergistic and antagonistic responses of herbicide combinations", WEEDS, vol. 15, 1967, pages 20 - 22, XP001112961

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111955464A (zh) * 2020-08-14 2020-11-20 陕西上格之路生物科学有限公司 一种含有氯氟醚菌唑的杀菌组合物
CN111955464B (zh) * 2020-08-14 2022-03-04 陕西上格之路生物科学有限公司 一种含有氯氟醚菌唑的杀菌组合物

Also Published As

Publication number Publication date
WO2020120202A3 (fr) 2020-07-23
EP3893642A2 (fr) 2021-10-20
EA202191562A1 (ru) 2021-10-18
UA128261C2 (uk) 2024-05-22

Similar Documents

Publication Publication Date Title
WO2020120206A2 (fr) Procédé de lutte contre un champignon phytopathogène choisi parmi des espèces de phakopsora. du soja par des compositions comprenant du méfentrifluconazole
JP5502854B2 (ja) 菌類感染から大豆を保護する方法
EP3893643A2 (fr) Procédé de lutte contre des champignons phythopatogènes choisis parmi septoria tritici et puccinia spp. dans les céréales au moyen de compositions comprenant du méfentrifluconazole
WO2020120205A2 (fr) Procédé de lutte contre un champignon phythopatogène choisi parmi uncinula necator, plasmopara viticola et gloeosporium ampelophagum pour le raisin au moyen de compositions comprenant du méfentrifluconazole
US20100099559A1 (en) Method for protecting soybeans from being infected by fungi
EP3099166B1 (fr) Procede pour le contrôle de septoria tritici resistante a la strobilurine
EP2280604A2 (fr) Procédé de protection de céréales d'une infection par des champignons
US20230200389A1 (en) Synergistic fungicidal interactions of a picolinamide fungicide with other fungicides against asian soybean rust
EP3525585B1 (fr) Procédé de régulation de septoria tritici résistante aux fongicides inhibiteurs de succinate déshydrogénase
CN103210922A (zh) 一种含氨基寡糖素和稻瘟酰胺的杀菌组合物
WO2008135480A2 (fr) Lutte contre un pathogène fongique spécifique au soja avec du bénodanile
PL204905B1 (pl) Kompozycja chwastobójcza, sposób zwalczania niepożądanych roślin i zastosowanie kompozycji chwastobójczej
EP3701794A1 (fr) Procédé de lutte contre un champignon phytopathogène choisi parmi rhizoctonia solani, magnaporthe grisea, helminthosporium oryzae, xanthomonas oryzae pv.oryza, sclerotium oryzae ou saro-cladium oryzae dans le riz par des compositions comprenant du méfentrifluconazole
WO2010015578A1 (fr) Procédé de lutte contre des maladies fongiques dans les légumineuses
EP3666073A1 (fr) Procédé de lutte contre un champignon phytopathogène choisi parmi rhizoctonia solani et peronosclerospora sorghi dans le maïs par des compositions comprenant du méfentrifluconazole
AU2011269037B2 (en) Nematicidal mixtures for use in sugar cane
WO2020120202A2 (fr) Procédé de lutte contre sclerotinia spp dans le colza oléagineux ou la canola au moyen de compositions comprenant du méfentrifluconazole
EP3718406B1 (fr) Procédé de lutte contre la rayure réticulée et/ou la ramulariose résistante aux fongicides inhibiteurs de succinate déshydrogénase
WO2009056620A2 (fr) Procédé pour protéger des céréales contre des infections par des champignons
ZA200504841B (en) Fungicidal mixtures for controlling rice pahtogens
US20130090360A1 (en) Method for protecting rice from being infected by fungi
EA044292B1 (ru) Способ борьбы с sclerotinia spp. в масличном рапсе или каноле композициями, содержащими мефентрифлуконазол
CN110859189B (zh) 一种组合物、制剂及其应用、制备方法
EA044290B1 (ru) Способ борьбы с фитопатогенными грибами, выбранными из septoria tritici и puccinia spp., в зерновых культурах с помощью композиций, которые содержат мефентрифлуконазол
KR20230156356A (ko) 새로운 오일 현탁 농축액 조성물

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19816254

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2019816254

Country of ref document: EP

Effective date: 20210712