WO2020007646A1 - Mélanges pesticides - Google Patents

Mélanges pesticides Download PDF

Info

Publication number
WO2020007646A1
WO2020007646A1 PCT/EP2019/066807 EP2019066807W WO2020007646A1 WO 2020007646 A1 WO2020007646 A1 WO 2020007646A1 EP 2019066807 W EP2019066807 W EP 2019066807W WO 2020007646 A1 WO2020007646 A1 WO 2020007646A1
Authority
WO
WIPO (PCT)
Prior art keywords
spp
cereals
mixture
corn
compound
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.)
Ceased
Application number
PCT/EP2019/066807
Other languages
English (en)
Inventor
Christian Winter
Markus Gewehr
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
Publication of WO2020007646A1 publication Critical patent/WO2020007646A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647Triazoles; Hydrogenated triazoles
    • A01N43/6531,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Definitions

  • the present invention relates to fungicidal mixtures comprising as active components, 4-[[6-[2- (2,4-difluorophenyl)-1 ,1-difluoro-2-hydroxy-3-(5-sulfanyl-1 ,2,4-triazol-1-yl)propyl]-3- pyridyl]oxy]benzonitrile as compound I and one fungicidal compound II, wherein compound II is selected from the group consisting of: pydiflumetofen, isoflucypram, inpyrfluxam, fluindapyr, pyraziflumid and pyrapropoyne.
  • the invention relates to an use of the mixture for controlling phytopathogenic harmful fungi and to a method for controlling phytopathogenic pests, wherein the pest, their habitat, breeding grounds, their locus or the plants to be protected against pest attack, the soil or plant propagation material are treated with an effective amount of the mixture.
  • plant propagation material is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e. g. pota- toes), which can be used for the multiplication of the plant.
  • vegetative plant material such as cuttings and tubers (e. g. pota- toes)
  • These young plants may also be protected before transplantation by a total or partial treatment by immersion or pouring.
  • the term propagation material denotes seeds.
  • pests embrace harmful fungi and animal pests.
  • Another problem encountered concerns the need to have available pest control agents which are effective against a broad spectrum of harmful fungi and harmful animal pests.
  • Another difficulty in relation to the use of pesticides is that the repeated and exclusive applica- tion of an individual pesticidal compound leads in many cases to a rapid selection of pests, that means animal pests, and harmful fungi, which have developed natural or adapted resistance against the active compound in question. Therefore, there is a need for pest control agents that help prevent or overcome resistance.
  • Another problem underlying the present invention is the desire for compositions that improve plants, a process which is commonly and hereinafter referred to as“plant health”.
  • plant health comprises various sorts of improvements of plants that are not connected to the control of pests.
  • advantageous properties are im- proved crop characteristics including: emergence, crop yields, protein content, oil content, starch content, more developed root system (improved root growth), improved stress tolerance (e.g.
  • tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less input needed (such as fertilizers or water), less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, enhanced plant vigor, increased plant stand and early and better germination; or any other advantages familiar to a person skilled in the art.
  • fungicidal mixtures corn- prising as active components comprising as active components, 4-[[6-[2-(2,4-difluorophenyl)- 1 ,1-difluoro-2-hydroxy-3-(5-sulfanyl-1 ,2,4-triazol-1-yl)propyl]-3-pyridyl]oxy]benzonitrile as corn- pound I and one fungicidal compound II, wherein compound II is selected from the group con- sisting of: pydiflumetofen, isoflucypram, inpyrfluxam, fluindapyr, pyraziflumid and pyrapropoyne.
  • the mixtures as defined in the outset show markedly en- hanced action against pests compared to the control rates that are possible with the individual compounds and/or is suitable for improving the health of plants when applied to plants, parts of plants, seeds, or at their locus of growth.
  • the ratio by weight of compound I and compound II in binary mixtures is from 10000:1 to 1 :10000, from 500:1 to 1 :500, preferably from 100:1 to 1 :100 more preferably from 50:1 to 1 :50, most preferably from 20:1 to 1 :20, including also ratios from 10:1 to 1 :10, 1 :5 to 5:1 , or 1 :1.
  • inventive mixtures can further contain one or more insecticides, fungicides, herbicides.
  • compositions e.g. solutions, emulsions, suspensions, dusts, powders, pastes, granules, pressings, capsules, and mixtures thereof.
  • composition types are suspensions (e.g. SC, OD, FS), emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME), capsules (e.g. CS, ZC), pastes, pastilles, wetable powders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g.
  • compositions types are defined in the“Catalogue of pesticide formulation types and international coding system”, Technical Monograph No. 2, 6 th Ed. May 2008, CropLife Interna- tional.
  • compositions are prepared in a known manner, such as described by Mollet and Grube- mann, Formulation technology, Wiley VCH, Weinheim, 2001 ; or Knowles, New developments in crop protection product formulation, Agrow Reports DS243, T&F Informa, London, 2005.
  • auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfactants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective colloids, adhe- sion agents, thickeners, humectants, repellents, attractants, feeding stimulants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers and binders.
  • Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil frac- tions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, al- kylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, benzylalcohol, cyclohexanol; glycols; DMSO; ketones, e.g. cyclohexanone; esters, e.g.
  • mineral oil frac- tions of medium to high boiling point e.g. kerosene, diesel oil
  • oils of vegetable or animal origin oils of vegetable or animal origin
  • aliphatic, cyclic and aromatic hydrocarbons e. g. toluene, paraffin, tetrahydrona
  • lactates carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.
  • Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, lime- stone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products ofvegetable origin, e.g. ce- real meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.
  • mineral earths e.g. silicates, silica gels, talc, kaolins, lime- stone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide
  • polysaccharides e.g. cellulose
  • Suitable surfactants are surface-active compounds, such as anionic, cationic, nonionic and am- photeric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emulsifier, dispersant, solubilizer, wetter, penetration enhancer, protective col- loid, or adjuvant. Examples of surfactants are listed in McCutcheon’s, Vol.1 : Emulsifiers & De- tergents, McCutcheon’s Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed.).
  • Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof.
  • sulfonates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of con- densed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates.
  • Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters.
  • Examples of phosphates are phosphate esters.
  • Examples of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates.
  • Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof.
  • alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents.
  • Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide.
  • Exam- pies of N-substituted fatty acid amides are fatty acid glucamides or fatty acid alkanolamides.
  • esters are fatty acid esters, glycerol esters or monoglycerides.
  • sugar- based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or al- kylpolyglucosides.
  • polymeric surfactants are home- or copolymers of vinylpyrroli- done, vinylalcohols, or vinylacetate.
  • Suitable cationic surfactants are quaternary surfactants, for example quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain primary amines.
  • Suitable amphoteric surfactants are alkylbetains and imidazolines.
  • Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide.
  • Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or pol- yethyleneamines.
  • Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity themselves, and which improve the biological performance of the inventive mixtures on the tar- get.
  • examples are surfactants, mineral or vegetable oils, and other auxilaries. Further examples are listed by Knowles, Adjuvants and additives, Agrow Reports DS256, T&F Informa UK, 2006, chapter 5.
  • Suitable thickeners are polysaccharides (e.g. xanthan gum, carboxymethylcellulose), inorganic clays (organically modified or unmodified), polycarboxylates, and silicates.
  • Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
  • Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
  • Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.
  • Suitable colorants are pigments of low water solubility and water- soluble dyes.
  • examples are inorganic colorants (e.g. iron oxide, titan oxide, iron hexacyanofer- rate) and organic colorants (e.g. alizarin-, azo- and phthalocyanine colorants).
  • Suitable tackifiers or binders are polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols, pol- yacrylates, biological or synthetic waxes, and cellulose ethers. Examples for composition types and their preparation are:
  • 10-60 wt% of an inventive mixture and 5-15 wt% wetting agent e.g. alcohol alkoxylates
  • a water-soluble solvent e.g. alcohols
  • an inventive mixture and 1-10 wt% dispersant e. g. polyvinylpyrrolidone
  • organic solvent e.g. cyclohexanone
  • emulsifiers e.g. calcium dodecylben- zenesulfonate and castor oil ethoxylate
  • water-insoluble organic solvent e.g. aromatic hydrocarbon
  • Emulsions (EW, EO, ES)
  • emulsifiers e.g. calcium dodecylbenzene- sulfonate and castor oil ethoxylate
  • water-insoluble organic solvent e.g. aromatic hydrocarbon
  • an inventive mixture 20-60 wt% are comminuted with addition of 2- 10 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate), 0.1- 2 wt% thickener (e.g. xanthan gum) and water ad 100 wt% to give a fine active substance sus- pension. Dilution with water gives a stable suspension of the active substance.
  • dispersants and wetting agents e.g. sodium lignosulfonate and alcohol ethoxylate
  • 0.1- 2 wt% thickener e.g. xanthan gum
  • water ad 100 wt% to give a fine active substance sus- pension.
  • Dilution with water gives a stable suspension of the active substance.
  • binder e.g. polyvinylalcohol
  • an inventive mixture 50-80 wt% of an inventive mixture are ground finely with addition of dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate) ad 100 wt% and prepared as water- dispersible or water-soluble granules by means of technical appliances (e. g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active sub- stance.
  • dispersants and wetting agents e.g. sodium lignosulfonate and alcohol ethoxylate
  • 50-80 wt% of an inventive mixture are ground in a rotor-stator mill with addition of 1-5 wt% dispersants (e.g. sodium lignosulfonate), 1-3 wt% wetting agents (e.g. alcohol ethoxylate) and solid carrier (e.g. silica gel) ad 100 wt%. Dilution with water gives a stable dispersion or solution of the active substance.
  • dispersants e.g. sodium lignosulfonate
  • wetting agents e.g. alcohol ethoxylate
  • solid carrier e.g. silica gel
  • an inventive mixture 5-20 wt% are added to 5-30 wt% organic solvent blend (e.g. fatty ac- id dimethylamide and cyclohexanone), 10-25 wt% surfactant blend (e.g. alcohol ethoxylate and arylphenol ethoxylate), and water ad 100 %.
  • organic solvent blend e.g. fatty ac- id dimethylamide and cyclohexanone
  • surfactant blend e.g. alcohol ethoxylate and arylphenol ethoxylate
  • An oil phase comprising 5-50 wt% of an inventive mixture, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), 2-15 wt% acrylic monomers (e.g. methylmethacrylate, methacrylic acid and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radical initiator results in the formation of poly(meth)acrylate microcapsules.
  • an oil phase comprising 5-50 wt% of an inventive mixture according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), and an isocyanate monomer (e.g.
  • diphenylmethene-4,4’- diisocyanatae are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl al- cohol).
  • a protective colloid e.g. polyvinyl al- cohol
  • a polyamine e.g. hexamethylenediamine
  • the monomers amount to 1-10 wt%.
  • the wt% relate to the total CS corn- position.
  • Dustable powders (DP, DS)
  • an inventive mixture are ground finely and mixed intimately with solid carrier (e.g. finely divided kaolin) ad 100 wt%.
  • solid carrier e.g. finely divided kaolin
  • an inventive mixture is ground finely and associated with solid carrier (e.g. sil icate) ad 100 wt%.
  • Granulation is achieved by extrusion, spray-drying or fluidized bed.
  • organic solvent e.g. aromatic hydro- carbon
  • compositions types i) to xiii) may optionally comprise further auxiliaries, such as 0.1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0.1-1 wt% anti-foaming agents, and 0.1-1 wt% col- ora nts.
  • auxiliaries such as 0.1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0.1-1 wt% anti-foaming agents, and 0.1-1 wt% col- ora nts.
  • the resulting agrochemical compositions generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, and in particular between 0.5 and 75%, by weight of active substance.
  • the active substances are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).
  • Solutions for seed treatment (LS), Suspoemulsions (SE), flowable concentrates (FS), powders for dry treatment (DS), water-dispersible powders for slurry treatment (WS), water-soluble pow- ders (SS), emulsions (ES), emulsifiable concentrates (EC) and gels (GF) are usually employed for the purposes of treatment of plant propagation materials, particularly seeds.
  • the composi- tions in question give, after two-to-tenfold dilution, active substance concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40%, in the ready-to-use preparations. Application can be carried out before or during sowing.
  • Methods for applying the inventive mixtures and compo- sitions thereof, respectively, on to plant propagation material, especially seeds include dressing, coating, pelleting, dusting, soaking and in-furrow application methods of the propagation mate- rial.
  • the inventive mixtures or the compositions thereof, respectively 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 amounts of active substances applied are, depending on the kind of effect desired, from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg per ha, more preferably from 0.01 to 1.0 kg per ha, and in particular from 0.05 to 0.75 kg per ha.
  • amounts of active substance of from 0.01 -10kg, preferably from 0.1-1000 g, more prefer- ably from 1-100 g per 100 kilogram of plant propagation material (preferably seeds) are general- ly required.
  • the amount of active substance applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meter of treated material.
  • oils, wetters, adjuvants, fertilizer, or micronutrients, and further pesticides may be added to the active substances or the compositions comprising them as premix or, if appropriate not until immedi- ately prior to use (tank mix).
  • pesticides e.g. herbicides, insecticides, fungicides, growth regulators, safeners
  • These agents can be admixed with the compositions according to the invention in a weight ratio of 1 :100 to 100:1 , preferably 1 :10 to 10:1.
  • the user applies the composition according to the invention usually from a predosage device, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system.
  • the agrochemi- cal composition is made up with water, buffer, and/or further auxiliaries to the desired applica- tion concentration and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained.
  • 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of agricultural useful area.
  • individual components of the composition according to the in- vention such as parts of a kit or parts of a binary mixture may be mixed by the user himself in a spray tank or any other kind of vessel used for applications (e. g. seed treater drums, seed pel- leting machinery, knapsack sprayer) and further auxiliaries may be added, if appropriate.
  • a spray tank or any other kind of vessel used for applications (e. g. seed treater drums, seed pel- leting machinery, knapsack sprayer) and further auxiliaries may be added, if appropriate.
  • one embodiment of the invention is a kit for preparing a usable pesticidal corn- position, the kit comprising a) a composition comprising component 1 ) as defined herein and at least one auxiliary; and b) a composition comprising component 2) as defined herein and at least one auxiliary; and optionally c) a composition comprising at least one auxiliary and option- ally a further active component 3) as defined herein.
  • the present invention comprises an use of the mixture for controlling phytopath- ogenic harmful fungi and to a method for controlling phytopathogenic pests, wherein the pest, their habitat, breeding grounds, their locus or the plants to be protected against pest attack, the soil or plant propagation material are treated with an effective amount of the mixture.
  • inventive mixtures are suitable for controlling the following fungal plant diseases:
  • Albugo spp. white rust on ornamentals, vegetables (e. g. A. Candida) and sunflowers (e. g. A. tragopogonis), A Hern aria spp. (Alternaria leaf spot) on vegetables (e.g. A. dauciox A. porri), oilseed rape (A. brass icicoia or brassicae ), sugar beets (A. tenuis ), fruits (e.g. A. grandis ), rice, soybeans, potatoes and tomatoes (e. g. A. soiani, A. grandis or A. alternate), tomatoes (e. g. A. soiani ox A. aiternata) and wheat (e.g. A.
  • sorokiniana and rice (e. g. C. miyabeanus, anamorph: H. ory- zae) Coiietotrichum (teleomorph: Giomereiia) spp. (anthracnose) on cotton (e. g. C. gossypii), corn (e. g. C. graminicoia: Anthracnose stalk rot), soft fruits, potatoes (e. g. C. coccodes. black dot), beans (e. g. C. Hndemuthianum), soybeans (e. g. C. truncatumox C. gioeosporioides), vegetables (e.g. C. iagenariumox C.
  • fruits e.g. C. acutatum
  • coffee e.g. C. coffeanum or C. kahawae
  • C. gioeosporioides on various crops
  • Corticiums . e. g. C. sasakii (sheath blight) on rice
  • Corynespora cassiicoia leaf spots
  • Cy- cioconium spp. e. g. C. oieaginumox ⁇ olive trees
  • Cyiindrocarpon spp. e. g.
  • teleomorph Nectria ox Neonectria spp.) on fruit trees, vines (e. g. C. iirio- dendri, teleomorph: Neonectria Hriodendri. Black Foot Disease) and ornamentals; Dematophora (teleomorph: Roseiiinia) necatrix (root and stem rot) on soybeans; Diaporthe spp., e. g. D. phaseoiorum (damping off) on soybeans; Drechsiera (syn. Helminthosporium, teleomorph: Pyr- enophora) spp.
  • Fusarium) nivaie pink snow mold on cereals (e. g. wheat or barley); Micro- sphaera diffusa (powdery mildew) on soybeans; MoniUnia spp., e. g. M. laxa, M. fructicda and M. fructigena (syn. Monilia spp. ⁇ bloom and twig blight, brown rot) on stone fruits and other ro- saceous plants; Mycosphaerella spp. on cereals, bananas, soft fruits and ground nuts, such as e. g. M. graminicda (anamorph: Zymoseptoria M/c/formerly Septoria tritici.
  • Septoria blotch on wheat or M. fijiensis (syn. Pseudocercospora fijiensis. black Sigatoka disease) and M. musicda on bananas, M. arachidicda (syn. M. a ra chid is or Cercospora arachidis), M. berkeieyi on pea- nuts, M. pis ion peas and M. brassicioia on brassicas; Peronospora spp. (downy mildew) on cabbage (e. g. P. brassicae), oilseed rape (e. g. P. parasitica), onions (e. g. P.
  • betae root rot, leaf spot and damping-off
  • P. zeae-maydis (syn. Phyiiostica zeae) on corn
  • Phomopsis spp. on sunflowers, vines (e. g. P. viticoia. can and leaf spot)
  • soybeans e. g. stem rot: P. phase i, teleomorph: Diaporthe phasedorum) ⁇ , Physoderma maydis (brown spots) on corn
  • Phytophthora spp. tilt, root, leaf, fruit and stem root
  • various plants such as papri- ka and cucurbits (e. g. P. capsid), soybeans (e.
  • P. xanthii Pdymyxa spp., e. g. on cereals, such as barley and wheat ( P graminis) and sugar beets ( P betae) and thereby transmitted viral dis- eases; Pseudocercosporella herpotrichoides (syn. Oculimacula yallundae, O. acuformis. eye- spot, teleomorph: Tapesia yallundae) on cereals, e. g. wheat or barley; Pseudoperonospora (downy mildew) on various plants, e. g. P.
  • kuehnii orange rust
  • Pyrenopeziza spp. e.g. P. brassicae on oilseed rape
  • Pyrenophora anamorph: Drechslera
  • tritici-repentis tan spot
  • P. teres ⁇ net blotch barley
  • Pyricu /aria spp. e. g. P. oryzae (teleomorph: Magnaporthe grisea. rice blast) on rice and P. grisea on turf and cereals
  • soiani ⁇ roo ⁇ and stem rot on soybeans, R. solani (sheath blight) on rice or R. cerealis (Rhizoctonia spring blight) on wheat or barley; Rhizopus stolonifer (black mold, soft rot) on strawberries, carrots, cabbage, vines and tomatoes; Rhynchosporium seca/is and R. ses (scald) on barley, rye and triticale; Sarodadium oryzae and S. attenua- tum (sheath rot) on rice; Sderotinia spp. (stem rot or white mold) on vegetables (S. minor and S.
  • sderotiorum and field crops, such as oilseed rape, sunflowers (e. g. S. sderotiorum) and soy- beans, S. roifsii ⁇ syn. Atheiia roifsii) on soybeans, peanut, vegetables, corn, cereals and orna- mentals; Septoria spp. on various plants, e. g. S. glycines (brown spot) on soybeans, S. tritici (syn. Zymoseptoria tritici, Septoria blotch) on wheat and S. (syn.
  • Stagonospora nodorum (Stagonospora blotch) on cereals; Uncinuia (syn. Erysiphe) necator (powdery mildew, ana- morph: Oidium tucker i) on vines; Setosphaeria spp. (leaf blight) on corn (e. g. S. turcicum, syn. Heiminthosporium turcicum) and turf; Sphaceiotheca spp. (smut) on corn, (e. g. S. reiiiana, syn. Ustiiago reiiiana.
  • Sphaerotheca fuiiginea (syn. Podo- sphaera xanthii powdery mildew) on cucurbits; Spongospora subterranea (powdery scab) on potatoes and thereby transmitted viral diseases; Stagonospora s . on cereals, e. g. S. r io- dorum (Stagonospora blotch, teleomorph: Leptosphaeria [syn. Phaeosphaeria] nodorum, syn.
  • Septoria nodorum on wheat; Synchytrium endobioticum on potatoes (potato wart disease); Ta- phrina spp., e. g. T. deformans (leaf curl disease) on peaches and T. pruni (plum pocket) on plums; Thieiaviopsis spp. (black root rot) on tobacco, pome fruits, vegetables, soybeans and cotton, e. g. T. basicoia (syn. Chaiara eiegans), Tiiietia spp. (common bunt or stinking smut) on cereals, such as e. g. T. tritici ⁇ syn. T.
  • Ustiiago spp. loose smut on cereals (e. g. U. nuda and U. avaenae), corn (e. g. U. maydis. corn smut) and sugar cane; Venturia spp. (scab) on apples (e. g. V. inaequaiis) and pears; and Vertidiiium spp. (wilt) on various plants, such as fruits and ornamentals, vines, soft fruits, vegetables and field crops, e. g. V. tongisporum on oilseed rape, V. dahliae on strawberries, oilseed rape, potatoes and tomatoes, and 14 fungicola on mushrooms; Zymoseptoria tritici on cereals; Phaeosphaeria maydis und Puccinia polysora.
  • the mixtures according to the present invention are also suitable for controlling harmful fungi in the protection of stored products or harvest and in the protection of materials.
  • protection of materials is to be understood to denote the protection of technical and non-living materials, such as adhesives, glues, wood, paper and paperboard, textiles, leather, paint dispersions, plastics, cooling lubricants, fiber or fabrics, against the infestation and de- struction by harmful microorganisms, such as fungi and bacteria.
  • harmful microorganisms such as fungi and bacteria.
  • Ascomycetes such as Ophiostoma spp., Ceratocystis s p p .
  • Tyromyces spp. Deuteromycetes such as Aspergillus s ., Cladosporium spp., Pen ici Ilium spp., Trichoderma spp., A /tern aria spp., Paecilomyces spp. and Zygomycetes such as /corspp., and in addition in the protection of stored products and harvest the following yeast fungi are worthy of note: Candida spp. and Saccharomyces cerevisae.
  • the inventive mix- tures are used in soya (soybean), cereals and corn.
  • pesticidally effective amount means the amount of the inventive mixtures or of compositions comprising the mixtures needed to achieve an observable effect on growth, in- cluding the effects of necrosis, death, retardation, prevention, and removal, destruction, or oth- erwise diminishing the occurrence and activity of the target organism.
  • the pesticidally effective amount can vary for the various mixtures / compositions used in the invention.
  • a pesticidally effective amount of the mixtures / compositions will also vary according to the prevailing condi- tions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.
  • the present invention comprises a method for improving the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propaga- tion material, from which the plant grows, is treated with an plant health effective amount of an inventive mixture.
  • plant effective amount denotes an amount of the inventive mixtures, which is suffi- cient for achieving plant health effects as defined herein below. More exemplary information about amounts, ways of application and suitable ratios to be used is given below. Again, the skilled artisan is well aware of the fact that such an amount can vary in a broad range and is dependent on various factors, e.g. the treated cultivated plant or material and the climatic condi- tions.
  • active compounds to which 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.
  • inventive mixtures are employed by treating the fungi or the plants, plant propagation materials (preferably seeds), materials or soil to be protected from fungal attack with a pesticidally effective amount of the active compounds.
  • 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.
  • the term plant refers to an entire plant, a part of the plant or the propagation material of the plant.
  • inventive mixtures and compositions thereof are particularly important in the control of a multitude of phytopathogenic fungi on various cultivated plants, such as cereals, e. g. wheat, rye, barley, triticale, oats or rice; beet, e. g. sugar beet or fodder beet; fruits, such as pomes, stone fruits or soft fruits, e. g.
  • cereals e. g. wheat, rye, barley, triticale, oats or rice
  • beet e. g. sugar beet or fodder beet
  • fruits such as pomes, stone fruits or soft fruits, e. g.
  • the inventive mixtures and compositions thereof are used for control- ling a multitude of fungi on field crops, such as potatoes, sugar beets, tobacco, wheat, rye, bar- ley, oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee or sugar cane; fruits; vines; ornamentals; or vegetables, such as cucumbers, tomatoes, beans or squashes.
  • field crops such as potatoes, sugar beets, tobacco, wheat, rye, bar- ley, oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee or sugar cane; fruits; vines; ornamentals; or vegetables, such as cucumbers, tomatoes, beans or squashes.
  • treatment of plant propagation materials with the inventive mixtures and compo- sitions thereof, respectively is used for controlling a multitude of fungi on cereals, such as wheat, rye, barley and oats; potatoes, tomatoes, vines, rice, corn, cotton and soybeans.
  • inventive mixtures for the combinations 1-1 to 1-138 as disclosed in Table 1 :
  • cultiva plants is to be understood as including 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. http://cera-gmc.org/, see GM crop database therein).
  • 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.
  • 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 modifications also include but are not limited to tar- geted post-translational modification of protein(s), oligo- or polypeptides e. g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.
  • herbicides e. bromoxynil or ioxynil herbicides as a result of conventional methods of breeding or genetic engineering. Furthermore, plants have been made resistant to multiple classes of herbicides through multiple genetic modifications, such as resistance to both glyphosate and glufosinate or to both glyphosate and a herbicide from anoth- er class such as ALS inhibitors, HPPD inhibitors, auxin herbicides, or ACCase inhibitors. These herbicide resistance technologies are e. g. described in Pest Management Sci. 61 , 2005, 246; 61 , 2005, 258; 61 , 2005, 277; 61 , 2005, 269; 61 , 2005, 286; 64, 2008, 326; 64, 2008, 332;
  • plants are also covered that are by the use of recombinant DNA techniques capa- ble to synthesize one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus thuringiensis, such as d-endotoxins, e. g. CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, Cryl 11 B(b1 ) or Cry9c; vegetative insecticidal pro- teins (VIP), e. g. VIP1 , VIP2, VIP3 or VIP3A; insecticidal proteins of bacteria colonizing nema- todes, e. g. Photorhabdus spp.
  • VIP vegetative insecticidal pro- teins
  • toxins produced by animals such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins pro- prised by fungi, such Streptomycetes toxins, plant lectins, such as pea or barley lectins; aggluti nins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdyster- oid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ion channel blockers, such as 3-hydroxysteroid oxidase,
  • these insecticidal proteins or toxins are to be understood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins.
  • Hybrid proteins are characterized by a new combination of protein domains, (see, e. g. WO 02/015701 ).
  • Further examples of such toxins or genetically modified plants ca- pable of synthesizing such toxins are disclosed, e. g., in EP-A 374 753, WO 93/007278,
  • WO 95/34656 EP-A 427 529, EP-A 451 878, WO 03/18810 und WO 03/52073.
  • the methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g. in the publications mentioned above.
  • These insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins toler- ance to harmful pests from all taxonomic groups of athropods, especially to beetles (Coelop- tera), two-winged insects (Diptera), and moths (Lepidoptera) and to nematodes (Nematoda).
  • Genetically modified plants capable to synthesize one or more insecticidal proteins are, e.
  • Agrisure ® CB and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the CrylAb toxin and PAT enzyme), MIR604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the CrylAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).
  • plants are also covered that are by the use of recombinant DNA techniques capa- ble to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens.
  • proteins are the so-called“pathogenesis- related proteins” (PR proteins, see, e. g. EP-A 392 225), plant disease resistance genes (e. g. potato cultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potato Solarium bulbocastanum) or T4-lysozym (e. g. potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Er- winia amylvora).
  • PR proteins so-called“pathogenesis- related proteins”
  • plant disease resistance genes e. g. potato cultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potato Solarium bulbocastanum
  • T4-lysozym
  • plants are also covered that are by the use of recombinant DNA techniques capa- ble to synthesize one or more proteins to increase the productivity (e. g. bio mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral patho- gens of those plants.
  • productivity e. g. bio mass production, grain yield, starch content, oil content or protein content
  • plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, e. g. oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e. g. Nexera ® rape, DOW Agro Sciences, Cana- da).
  • plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve raw material production, e. g. potatoes that produce increased amounts of amylopectin (e. g. Amflora ® potato, BASF SE, Germany).
  • the separate or joint application of the compounds of the inventive mixtures is carried out by spraying or dusting the seeds, the seedlings, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
  • inventive mixtures and the compositions comprising them can be used for protecting wood- en materials such as trees, board fences, sleepers, etc. and buildings such as houses, out- houses, factories, but also construction materials, furniture, leathers, fibers, vinyl articles, elec- tric wires and cables etc. from ants and/or termites, and for controlling ants and termites from doing harm to crops or human being (e.g. when the pests invade into houses and public facili ties).
  • Customary application rates in the protection of materials are, for example, from 0.01 g to 1000 g of active compound per m 2 treated material, desirably from 0.1 g to 50 g per m 2 .
  • the content of the mixture of the active ingredients is from 0.001 to 80 weight %, preferably from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight %.
  • the active compounds were formulated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide.
  • Example 1 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.
  • MTP micro titer plate
  • a spore suspension of Botrci cinerea in an aqueous biomalt or yeast-bactopeptone-sodiumacetate 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.
  • 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 a Qol resistant iso- late of Pyrenophora teres in an aqueous biomalt or yeast-bactopeptone-glycehne or DOB solu- tion was then added.
  • the plates were placed in a water vapor-saturated chamber at a tempera- ture of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
  • 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 rela- tive growth in % of the pathogens in the respective active compounds.
  • An efficacy of 0 means that the growth level of the pathogens corresponds to that of the un- treated control; an efficacy of 100 means that the pathogens were not growing.
  • 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.

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)

Abstract

La présente invention concerne des mélanges fongicides comprenant, en tant que composants actifs, 1) du 4-[[6- [2-(2,4-difluorophényl)-1,1-difluoro-2-hydroxy-3-(5-sulfanyl-1,2,4-triazol-1-yl)propyl]-3-pyridyl] oxy]benzonitrile en tant que composé I et 2) un composé fongicide II, le composé II étant choisi dans le groupe constitué par : le pydiflumétofène, l'isoflucypram, l'inpyrfluxam, le fluindapyr, le pyraziflumide et le pyrapropoyne, et des procédés pour lutter contre des champignons phytopathogènes sur la base de ces mélanges.
PCT/EP2019/066807 2018-07-02 2019-06-25 Mélanges pesticides Ceased WO2020007646A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18181059 2018-07-02
EP18181059.9 2018-07-02

Publications (1)

Publication Number Publication Date
WO2020007646A1 true WO2020007646A1 (fr) 2020-01-09

Family

ID=62841900

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2019/066807 Ceased WO2020007646A1 (fr) 2018-07-02 2019-06-25 Mélanges pesticides

Country Status (1)

Country Link
WO (1) WO2020007646A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4066643A1 (fr) * 2021-03-30 2022-10-05 Basf Se Mélanges de pesticides
CN117088948A (zh) * 2023-08-23 2023-11-21 中国农业大学 辣椒疫霉调控游动孢子发育相关蛋白及其编码基因与应用

Citations (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
WO2007072999A1 (fr) 2005-12-22 2007-06-28 Nihon Nohyaku Co., Ltd Derives pyrazinecarboxamide et agents de lutte contre les parasites les contenant
WO2011162397A1 (fr) 2010-06-24 2011-12-29 Sumitomo Chemical Company, Limited Composition de lutte contre une maladie des plantes et procédé de lutte contre une maladie des plantes
WO2012084812A1 (fr) 2010-12-20 2012-06-28 Isagro Ricerca S.R.L. Amides d'aminoindanes présentant une forte activité fongicide et leurs compositions phytosanitaires
WO2012143127A1 (fr) 2011-04-22 2012-10-26 Bayer Cropsciences Ag Combinaisons de composés actifs comprenant un dérivé de (thio)carboximide et un composé fongicide
WO2014060502A1 (fr) 2012-10-19 2014-04-24 Bayer Cropscience Ag Combinaisons de composés actifs comprenant des dérivés carboxamide
WO2015119246A1 (fr) 2014-02-07 2015-08-13 日産化学工業株式会社 Composition bactéricide ou de stérilisation et méthode de lutte contre les maladies
WO2016187201A2 (fr) 2015-05-18 2016-11-24 Viamet Pharmaceuticals, Inc. Composés antifongiques
WO2018098216A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Utilisation d'un composé difluoro-(2-hydroxypropyl)pyridine en tant que fongicide pour lutter contre les champignons phytopathogènes de l'orge
WO2018098235A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides pour la lutte contre les maladies fongiques dans des céréales
WO2018098243A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Utilisation d'un composé difluoro-(2-hydroxypropyl)pyridine en tant que fongicide pour lutter contre les champignons phytopathogènes du blé
WO2018098245A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Composé difluoro-(2-hydroxypropyl)pyridine utilisé comme fongicide pour lutter contre les champignons phytopathogènes du maïs
WO2018098236A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés fongicides et mélanges de régulation des champignons dans les céréales
WO2018098218A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés fongicides et mélanges de régulation des champignons dans les céréales
WO2018098224A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides pour la lutte contre les maladies fongiques dans des céréales
WO2018098222A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides destinés à lutter contre les champignons dans les céréales

Patent Citations (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
WO2007072999A1 (fr) 2005-12-22 2007-06-28 Nihon Nohyaku Co., Ltd Derives pyrazinecarboxamide et agents de lutte contre les parasites les contenant
WO2011162397A1 (fr) 2010-06-24 2011-12-29 Sumitomo Chemical Company, Limited Composition de lutte contre une maladie des plantes et procédé de lutte contre une maladie des plantes
WO2012084812A1 (fr) 2010-12-20 2012-06-28 Isagro Ricerca S.R.L. Amides d'aminoindanes présentant une forte activité fongicide et leurs compositions phytosanitaires
WO2012143127A1 (fr) 2011-04-22 2012-10-26 Bayer Cropsciences Ag Combinaisons de composés actifs comprenant un dérivé de (thio)carboximide et un composé fongicide
WO2014060502A1 (fr) 2012-10-19 2014-04-24 Bayer Cropscience Ag Combinaisons de composés actifs comprenant des dérivés carboxamide
WO2015119246A1 (fr) 2014-02-07 2015-08-13 日産化学工業株式会社 Composition bactéricide ou de stérilisation et méthode de lutte contre les maladies
WO2016187201A2 (fr) 2015-05-18 2016-11-24 Viamet Pharmaceuticals, Inc. Composés antifongiques
WO2018098216A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Utilisation d'un composé difluoro-(2-hydroxypropyl)pyridine en tant que fongicide pour lutter contre les champignons phytopathogènes de l'orge
WO2018098235A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides pour la lutte contre les maladies fongiques dans des céréales
WO2018098243A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Utilisation d'un composé difluoro-(2-hydroxypropyl)pyridine en tant que fongicide pour lutter contre les champignons phytopathogènes du blé
WO2018098245A1 (fr) 2016-11-22 2018-05-31 Vps-3, Inc. Composé difluoro-(2-hydroxypropyl)pyridine utilisé comme fongicide pour lutter contre les champignons phytopathogènes du maïs
WO2018098236A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés fongicides et mélanges de régulation des champignons dans les céréales
WO2018098218A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés fongicides et mélanges de régulation des champignons dans les céréales
WO2018098224A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides pour la lutte contre les maladies fongiques dans des céréales
WO2018098222A1 (fr) * 2016-11-22 2018-05-31 Vps-3, Inc. Composés et mélanges fongicides destinés à lutter contre les champignons dans les céréales

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
"Technical Monograph No. 2", May 2008, CROPLIFE INTERNATIONAL, article "Catalogue of pesticide formulation types and international coding system"
AUSTRAL. J. AGRICULT. RES., vol. 58, 2007, pages 708
KNOWLES: "Agrow Reports DS243", 2005, T&F INFORMA, article "New developments in crop protection product formulation"
KNOWLES: "Agrow Reports DS256", 2006, T&F INFORMA, article "Adjuvants and additives"
MOLLETGRUBE-MANN: "Formulation technology", 2001, WILEY VCH
PEST MANAGEMENT SCI., vol. 61, 2005, pages 246
PEST MANAGEMENT SCI., vol. 61, 2005, pages 286
PEST MANAGEMENT SCI., vol. 64, 2008, pages 332
R.S. COLBY: "Calculating synergistic and antagonistic responses of herbicide combinations", WEEDS, vol. 15, 1967, pages 20 - 22, XP001112961
SCIENCE, vol. 316, 2007, pages 1185
WEED SCI., vol. 57, 2009, pages 108

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4066643A1 (fr) * 2021-03-30 2022-10-05 Basf Se Mélanges de pesticides
WO2022207373A1 (fr) * 2021-03-30 2022-10-06 Basf Se Mélanges pesticides
CN117088948A (zh) * 2023-08-23 2023-11-21 中国农业大学 辣椒疫霉调控游动孢子发育相关蛋白及其编码基因与应用
CN117088948B (zh) * 2023-08-23 2024-05-14 中国农业大学 辣椒疫霉调控游动孢子发育相关蛋白及其编码基因与应用

Similar Documents

Publication Publication Date Title
EP3648604B1 (fr) Mélanges fongicides de méfentrifluconazole
EP4255189B1 (fr) Mélanges contenant du métarylpicoxamide
EP3214937B1 (fr) Mélanges de pesticides
EP3675638A1 (fr) Mélanges pesticides
WO2020078797A1 (fr) Mélanges ternaires contenant des inhibiteurs de fenpropimorphe, de succinate déshydrogénase et un autre composé
WO2018050508A1 (fr) Mélanges pesticides
WO2018011112A1 (fr) Mélanges fongicides contenant un carboxamide
WO2019007717A1 (fr) Mélanges pesticides
WO2018189001A1 (fr) Mélanges fongicides destinés à être utilisés dans le riz
EP3412150A1 (fr) Mélanges de meptyldinocap avec fongicides sdhi
WO2020030454A1 (fr) Utilisation d'un dérivé de composé i actif fongicide et de mélanges de celui-ci dans une application de semence et procédés de traitement
WO2019166252A1 (fr) Mélanges fongicides comprenant de la fenpropidine
EP3643175A1 (fr) Mélanges pesticides ternaires contenant du metyltetraprole et du fenpropimorphe
EP3533331A1 (fr) Melanges fongicides comprenant du pydiflumetofen
US20190208783A1 (en) Fungicidal Mixtures Comprising a Formamidine
DK3048888T3 (en) PESTICIDE MIXTURES
WO2020007646A1 (fr) Mélanges pesticides
EP3698634A1 (fr) Mélanges de pesticides
EP3817553B1 (fr) Mélanges pesticides
WO2022128554A1 (fr) Mélanges contenant du n-méthoxy-n-[[4-[5-(trifluorométhyl)-1,2,4-oxadiazol-3-yl]phényl]méthyl]cyclopropanecarboxamide
EP3533333A1 (fr) Mélanges fongicides comprenant du pydiflumetofène
WO2020078794A1 (fr) Mélanges ternaires contenant du fenpropimorphe, des azoles et un fongicide multilatéral
WO2020078795A1 (fr) Mélanges ternaires contenant du fenpropimorphe, des inhibiteurs de succinate déshydrogénase et des azoles
EP3536150A1 (fr) Mélanges fongicides contenant du fluxapyroxade
EP3530116A1 (fr) Mélanges fongicides contenant du xemium

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: 19735508

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19735508

Country of ref document: EP

Kind code of ref document: A1