EP1830643A1 - Fungizide mischungen - Google Patents

Fungizide mischungen

Info

Publication number
EP1830643A1
EP1830643A1 EP05821560A EP05821560A EP1830643A1 EP 1830643 A1 EP1830643 A1 EP 1830643A1 EP 05821560 A EP05821560 A EP 05821560A EP 05821560 A EP05821560 A EP 05821560A EP 1830643 A1 EP1830643 A1 EP 1830643A1
Authority
EP
European Patent Office
Prior art keywords
compounds
compound
formula
case
combination
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05821560A
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German (de)
English (en)
French (fr)
Inventor
Markus Gewehr
Reinhard Stierl
Matthias NIEDENBRÜCK
Udo HÜNGER
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
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Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP1830643A1 publication Critical patent/EP1830643A1/de
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton

Definitions

  • the present invention relates to fungicidal mixtures containing as active components
  • Flumetover fluopicolide (picobenzamide), zoxamide, carpropamide, diclocymet, mandipropamide,
  • R 1 and R 2 are independently hydrogen, halogen, Ci-C 6 alkyl or C 1 -C 6 haloalkyl, cyano, nitro, methoxy, or trifluoromethoxy, with with the proviso that R 1 and R 2 are not simultaneously hydrogen, and R 3 is CF 3 or CHF 2 ;
  • the invention relates to a method for controlling harmful fungi
  • component 1 The strobilurin derivative of the formula I 1 2- ⁇ 2-, referred to above as component 1
  • Carboxin, 5,6-dihydro-2-methyl- ⁇ / -phenyl-1, 4-oxathiin-3-carboxamide (US 3,249,499), benalaxyl, methyl ⁇ / - (phenylacetyl) - ⁇ / - (2,6 -xylyl) -DL-alaninate (DE 29 03 612),
  • Mefenoxam methyl ⁇ / - (2,6-dimethylphenyl) - ⁇ - (methoxyacetyl) -D-alaninate; Ofurace, (RS) - ⁇ - (2-chloro- ⁇ / -2,6-xylylacetamido) - ⁇ -butyrolactone [CAS RN 58810-48-3];
  • R is methyl (M-A) or ethyl (H-B); and amides of the formula III, (WO 03/066609).
  • mixtures of the present invention were based on an improved effect against harmful fungi, in particular for certain indications, with a reduced total amount of applied active substances.
  • the mixtures of the compound I and of an active compound II, or the simultaneous joint or separate use of the compound I and an active compound II are distinguished by an outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes, Deuteromycetes , Oomycetes and Basidiomycetes. They are in part systemically effective and can be used in crop protection as foliar and soil fungicides.
  • the compound I and active compounds II can be applied simultaneously together or separately or in succession, the sequence in the case of separate application generally having no effect on the control result.
  • Halogen fluorine, chlorine, bromine and iodine
  • Alkyl saturated, straight-chain or branched hydrocarbon radicals having 1 to 6 carbon atoms, for example C r C 4 alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl;
  • Haloalkyl straight-chain or branched alkyl groups having 1 to 6 carbon atoms, where in these groups partially or completely the hydrogen atoms may be replaced by halogen atoms as mentioned above: in particular C 1 -C 2 -HaIo- genalkyl such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl , Difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroeth
  • Compound 2.1 - 2.22 Compounds of the formula IIIa in which R 1 is chlorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 3.1 - 3.22 Compounds of the formula IIIa in which R 1 is bromine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 4.1 - 4.22 Compounds of the formula IIIa in which R 1 is iodine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 7.1 - 7.22 Compounds of the formula IIIa in which R 1 is trifluoromethyl and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 10.1-10.22 Compounds of the formula IIIa in which R 1 is nitro and R 2 is in each case one row of Table A.
  • Compound 11.1-11.20 Compounds of the formula IIIa in which R 1 is hydrogen and the combination of R 2 and R 3 is in each case one of the rows 2 to 21 of Table A.
  • Compound 17.1-17.22 Compounds of the formula INb in which R 1 is methoxy and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 18.1-18.22 Compounds of the formula NIb, in which R 1 is trifluoromethyl and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 20.1 - 20.22 Compounds of the formula INb, in which R 1 is cyano and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 22.1-22.20 Compounds of the formula IIIb in which R 1 is hydrogen and the combination of R 2 and R 3 is in each case one of the rows 2 to 21 of Table A.
  • Compound 23.1-23.22 Compounds of the formula IHc in which R 1 is fluorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 25.1-25.22 Compounds of the formula NIc, in which R 1 is bromine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 25.1-25.22 Compounds of the formula IHc in which R 1 is methyl and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 28.1-28.22 Compounds of the formula IHc in which R 1 is methoxy and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 31.1-31.22 Compounds of the formula IIIc in which R 1 is cyano and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 32.1-32.22 Compounds of the formula IIIc in which R 1 is nitro and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 34.1-34.22 Compounds of the formula HId in which R 1 is fluorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 36.1-36.22 Compounds of the formula HId in which R 1 is bromine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 39.1-39.22 Compounds of the formula IHd in which R 1 is methoxy and the combination of R 2 and R 3 is in each case one row of Table A.
  • Table 40 Compound 40.1 - 40.22: Compounds of the formula IMd, in which R 1 is trifluoromethyl and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 41.1-41.22 Compounds of the formula IHd in which R 1 is trifluoromethoxy and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 42.1-42.22 Compounds of the formula HId in which R 1 is cyano and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 43.1-43.22 Compounds of the formula HId in which R 1 is nitro and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compounds 44.1-44.20 Compounds of the formula IHd in which R 1 is hydrogen and the combination of R 2 and R 3 is in each case one of lines 2 to 21 of Table A.
  • Compound 46.1-46.22 Compounds of the formula IH in which R 1 is chlorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 52.1-52.22 Compounds of the formula INe in which R 1 is trifluoromethoxy and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 53.1-53.22 Compounds of the formula IMe, in which R 1 is cyano and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 54.1-54.22 Compounds of the formula IH in which R 1 is nitro and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 56.1-56.22 Compounds of the formula HIf 1 in which R 1 is fluorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 57.1-57.22 Compounds of the formula Nif in which R 1 is chlorine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 59.1-59.22 Compounds of the formula IIIf in which R 1 is iodine and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 60.1-60.22 Compounds of the formula IIIf in which R 1 is methyl and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 64.1-64.22 Compounds of the formula IIIf in which R 1 is cyano and the combination of R 2 and R 3 is in each case one row of Table A.
  • Compound 65.1-65.22 Compounds of the formula IIIf in which R 1 is nitro and the combination of R 2 and R 3 is in each case one row of Table A.
  • Table 66 Compound 66.1-66.20: Compounds of the formula IIIf in which R 1 is hydrogen and the combination of R 2 and R 3 is in each case one of the rows 2 to 21 of Table A.
  • a preferred embodiment of the mixtures according to the invention relates to the combination of the compound of the formula I and one of the active compound from the group: carboxylic anilides, in particular fenhexamide, benalaxyl, boscalid, penthiopyrad, an anilide of the formula III.
  • the pure active ingredients which can be added as needed further active ingredients against harmful fungi or other pests such as insects, spider animals or nematodes, or herbicidal or growth-regulating agents or fertilizers as further active components.
  • mixtures of compound I with an active ingredient II are used. Under certain circumstances, however, mixtures of compound I with two or optionally several active components may be advantageous.
  • the compound I and the active compound II are usually employed in a weight ratio of 100: 1 to 1: 100, preferably 20: 1 to 1:20, in particular 10: 1 to 1:10. If desired, the further active components are added to the compound I in a ratio of from 20: 1 to 1:20.
  • the application rates of the mixtures according to the invention are from 5 g / ha to 2000 g / ha, preferably from 50 to 900 g / ha, in particular from 50 to 750 g / ha.
  • the application rates for the compound I are accordingly generally 1 to 1000 g / ha, preferably 10 to 900 g / ha, in particular 20 to 750 g / ha.
  • the application rates for the active compound II are correspondingly generally 1 to 2000 g / ha, preferably 10 to 900 g / ha, in particular 40 to 500 g / ha.
  • application rates of mixture of 1 to 1000 g / 100 kg of seed preferably 1 to 750 g / 100 kg, in particular 5 to 500 g / 100 kg, are generally used.
  • the method for controlling harmful fungi is carried out by the separate or combined application of the compound I and the active compound II or the mixtures of the compound I and the active ingredient II by spraying or dusting the seeds, the plants or the soil before or after sowing the plants or before or after emergence of the plants.
  • the mixtures according to the invention or the compound I and the active compound II can be converted into the customary formulations, e.g. Solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the application form depends on the respective purpose; It should in any case ensure a fine and uniform distribution of the compound according to the invention.
  • the formulations are prepared in a known manner, e.g. by stretching the active ingredient with solvents and / or carriers, if desired using emulsifiers and dispersants.
  • Suitable solvents / auxiliaries are essentially:
  • aromatic solvents eg Solvesso products, xylene
  • paraffins eg petroleum fractions
  • alcohols eg methanol, butanol, pentanol, benzyl alcohol
  • ketones eg cyclohexanone, gamma-butyrolactone
  • pyrrolidones NMP, NOP
  • Acetates glycols, dimethyl fatty acid amides, fatty acids and fatty acid esters.
  • solvent mixtures can also be used
  • - Carriers such as ground natural minerals (eg kaolins, clays, talc, crayons) and ground synthetic minerals (eg fumed silica, silicates); Emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkyl sulfonates and arylsulfonates) and dispersants such as lignin-sulphite liquors and methylcellulose.
  • ground natural minerals eg kaolins, clays, talc, crayons
  • ground synthetic minerals eg fumed silica, silicates
  • Emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkyl sulfonates and arylsulfonates) and dispersants such as lignin-sulphite liquors and methylcellulose.
  • the surface-active substances used are alkali metal, alkaline earth metal, ammonium salts of lignin sulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, and condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde , Condensation products of naphthalene or naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl
  • mineral oil fractions of medium to high boiling point such as kerosine or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strong polar solvents, e.g. Dimethylsulfoxide, N-methylpyrrolidone or water into consideration.
  • mineral oil fractions of medium to high boiling point such as kerosine or diesel oil, coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. Toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivative
  • Powders, dispersants and dusts may be prepared by mixing or co-grinding the active substances with a solid carrier.
  • Granules e.g. Coated, impregnated and homogeneous granules can be prepared by binding the active compounds to solid carriers.
  • Solid carriers are e.g. Mineral earths, such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics, fertilizers, e.g. Ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell meal, cellulose powder and other solid carriers.
  • Mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulphate, magnesium oxide, ground plastics
  • the formulations generally contain between 0.01 and 95 wt .-%, preferably between 0.1 and 90 wt .-% of the active ingredients.
  • the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • the formulations in question give, after dilution of from two to ten times, active compound concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations.
  • formulations according to the invention are: 1. Products for dilution in water
  • a Water-soluble concentrates (SL, LS)
  • DC Dispersible Concentrates
  • Emulsifiable Concentrates 15 parts by weight of the active compounds 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 in water results in an emulsion.
  • the formulation has 15% by weight active ingredient content.
  • the active compounds 25 parts by weight of the active compounds are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is added to water by means of an emulsifying machine (e.g., Ultraturax) in 30 parts by weight and made into a homogeneous emulsion. Dilution in water results in an emulsion.
  • the formulation has an active ingredient content of 25% by weight.
  • the active ingredients 20 parts by weight of the active ingredients are comminuted with the addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent in a stirred ball mill to a fine active substance suspension. Dilution in water results in a stable suspension of the active ingredient.
  • the active ingredient content in the formulation is 20% by weight.
  • Water-dispersible and water-soluble granules 50 parts by weight of the active ingredients are mixed with the addition of 50 parts by weight of dispersing and Wetting agents finely ground and produced by means of technical equipment (eg extrusion, spray tower, fluidized bed) as water-dispersible or water-soluble granules. Dilution in water results in a stable dispersion or solution of the active ingredient.
  • the formulation has an active ingredient content of 50% by weight.
  • WP 1 SP, SS, WS Water-dispersible and water-soluble powders 75 parts by weight of the active compounds are ground in a rotor-stator mill with the addition of 25 parts by weight of dispersing and wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient.
  • the active ingredient content of the formulation is 75% by weight.
  • 0.5 parts by weight of the active ingredients are finely ground and combined with 99.5 parts by weight of carriers. Common processes are extrusion, spray drying or fluidized bed. This gives a granulate for direct application with 0.5 wt .-% active ingredient content.
  • LS water-soluble concentrates
  • FS suspensions
  • DS dusts
  • WS water-dispersible and water-soluble powders
  • ES emulsifiable concentrates
  • GF gel formulations
  • such formulations contain 1 to 800 g / l active ingredient, 1 to 200 g / l surfactants, 0 to 200 g / l antifreeze, 0 to 400 g / l binder, 0 to 200 g / l dyes and solvents, preferably water.
  • the active compounds may be used as such, in the form of their formulations or the forms of use prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, scattering agents, granules by spraying, misting, dusting, scattering or pouring.
  • the forms of application depend entirely on the intended use; In any case, they should ensure the finest possible distribution of the active compounds according to the invention.
  • Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (spray powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agents, tackifiers, dispersants or emulsifiers.
  • wetting agents emulsions, pastes or oil dispersions
  • tackifiers tackifiers
  • dispersants or emulsifiers emulsifiers.
  • the active compound concentrations in the ready-to-use preparations can be varied within wide ranges. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1%.
  • the active ingredients can also be used with great success in the ultra-low-volume (ULV) process, it being possible to apply formulations containing more than 95% by weight of active ingredient or even the active ingredient without additives.
  • UUV ultra-low-volume
  • wetting agents To the active ingredients oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides, possibly also just immediately before use (tank mix), are added. These agents can be added to the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1:10 to 10: 1.
  • adjuvants in this sense are in particular: organically modified polysiloxanes, eg Break Thru S 240 ® ; Alcohol alkoxylates, eg. As Atplus 245 ®, Atplus MBA 1303 ®, Plurafac LF 300 ® and Lutensol ON 30 ®; EO-PO block polymers, eg. Eg Pluro- never RPE 2035 and Genapol ® B ®; Alcohol ethoxylates, eg. As Lutensol XP 80 ®; and sodium dioctylsulfosuccinate, e. B. Leophen RA ®.
  • organically modified polysiloxanes eg Break Thru S 240 ®
  • Alcohol alkoxylates eg. As Atplus 245 ®, Atplus MBA 1303 ®, Plurafac LF 300 ® and Lutensol ON 30 ®
  • EO-PO block polymers eg. Eg Pluro-
  • the compounds I and II, or the mixtures or the corresponding formulations are applied by mixing the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be kept free of them with a fungicidally effective amount of the mixture Compounds I and II with separate application, treated.
  • the application can be made before or after the attack by the harmful fungi.
  • the active compounds were prepared separately or together as a stock solution with 25 mg of active ingredient, which with a mixture of acetone and / or DMSO and the emulsifier Uniperol® EL (wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) in the volume ratio solvent- Emulsifier from 99 to 1 ad 10 ml was filled. It was then made up to 100 ml with water. This stock solution was diluted with the described solvent-emulsifier-water mixture to the drug concentration given below.
  • Uniperol® EL wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
  • the efficiency (W) is calculated according to the formula of Abbot as follows:
  • a corresponds to the fungal infestation of the treated plants in% and ß corresponds to the fungal infestation of the untreated (control) plants in%
  • the infestation of the treated plants corresponds to that of the untreated control plants; at an efficiency of 100, the treated plants have no infestation.
  • Leaves of potted tomato plants were sprayed to drip point with an aqueous suspension in the concentration of active compound specified below. Five days later, the leaves were infected with an aqueous sporangium suspension of Phytophthora infestans. Subsequently, the plants were saturated in a water vapor Chamber placed at temperatures between 18 and 20 0 C. After 6 days, the late blight on the untreated but infected control plants had developed so strongly that the infestation could be determined visually in%.

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)
EP05821560A 2004-12-23 2005-12-21 Fungizide mischungen Withdrawn EP1830643A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004063383 2004-12-23
PCT/EP2005/013813 WO2006069713A1 (de) 2004-12-23 2005-12-21 Fungizide mischungen

Publications (1)

Publication Number Publication Date
EP1830643A1 true EP1830643A1 (de) 2007-09-12

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EP05821560A Withdrawn EP1830643A1 (de) 2004-12-23 2005-12-21 Fungizide mischungen

Country Status (10)

Country Link
US (1) US20080188530A1 (ko)
EP (1) EP1830643A1 (ko)
JP (1) JP2008525351A (ko)
KR (1) KR20070093119A (ko)
CN (1) CN101080169A (ko)
AU (1) AU2005321579B2 (ko)
BR (1) BRPI0519234A2 (ko)
CA (1) CA2589787A1 (ko)
IL (1) IL183561A0 (ko)
WO (1) WO2006069713A1 (ko)

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JP5747542B2 (ja) * 2010-03-03 2015-07-15 住友化学株式会社 植物病害防除組成物及び植物病害防除方法
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CR20120543A (es) * 2010-04-15 2012-11-29 Basf Se Mezclas fungicidas ii que comprenden quinazolinas
WO2012077061A1 (en) * 2010-12-08 2012-06-14 Basf Se Pesticidal mixtures
CN102578090A (zh) * 2012-01-14 2012-07-18 陕西美邦农药有限公司 一种含有烯肟菌酯和甲霜灵的杀菌剂组合物
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CN102640761B (zh) * 2012-05-08 2013-11-20 陕西上格之路生物科学有限公司 一种含烯肟菌胺和防治卵菌纲类杀菌剂的杀菌组合物
CN106234367A (zh) * 2012-06-13 2016-12-21 陕西美邦农药有限公司 一种含氟吡菌胺与甲氧基丙烯酸酯类的杀菌组合物
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CA2589787A1 (en) 2006-07-06
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JP2008525351A (ja) 2008-07-17
WO2006069713A1 (de) 2006-07-06
IL183561A0 (en) 2007-09-20
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BRPI0519234A2 (pt) 2009-01-06

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