EP1732388A1 - Ternäre fungizide mischungen - Google Patents
Ternäre fungizide mischungenInfo
- Publication number
- EP1732388A1 EP1732388A1 EP05729121A EP05729121A EP1732388A1 EP 1732388 A1 EP1732388 A1 EP 1732388A1 EP 05729121 A EP05729121 A EP 05729121A EP 05729121 A EP05729121 A EP 05729121A EP 1732388 A1 EP1732388 A1 EP 1732388A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- methyl
- compounds
- mixtures
- iii
- fungicidal
- 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- Withdrawn
Links
Classifications
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- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- 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
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
Definitions
- the present invention relates to ternary fungicidal mixtures containing as active components
- the invention relates to a method for controlling phytopathogenic harmful fungi with mixtures of the compounds I and II and III with a fungicidal active ingredient III and the use of the compounds I and II with III for the production of such mixtures and agents which contain these mixtures.
- the strobilurin derivatives II are also known from the literature (WO 96/01256; WO 97/15552. Mixtures of the strobilurin derivatives (I with various other fungicidal active ingredients are also described in the literature.
- the present invention was based on mixtures which, with a reduced total amount of active ingredients applied, have an improved action against the harmful fungi (synergistic mixtures).
- a preferred subject of the invention are mixtures of the compound I with pyracllostrobin 11-1 and a compound IM. They are particularly advantageous for combating harmful fungi from the Oomycetes class.
- Another preferred object of the invention are mixtures of compound I with orysastrobin II-2 and a compound IM. They are particularly advantageous for combating rice-pathogenic harmful fungi from the classes of the Ascomycetes, Deuteromycetes and Basidiomycetes.
- the aforementioned mixtures of the compounds I and II and the compounds III or the simultaneous joint or separate use of the compounds I, II and a compound IM are outstandingly effective against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes, Deuteromycetes , Oomycetes and Basidiomycetes. Some of them are systemically effective and can be used in plant protection as foliar, stain and soil fungicides. They are particularly important for combating a large number of fungi on various crops such as bananas, cotton, vegetables (e.g. cucumbers, beans and squashes), barley, grass, oats, coffee, potatoes, corn, fruit plants, rice, rye, soybeans, tomatoes , Wine, wheat, ornamental plants, sugar cane and a variety of seeds.
- bananas, cotton, vegetables e.g. cucumbers, beans and squashes
- barley grass, oats, coffee, potatoes, corn, fruit plants, rice, rye, soybeans, tomatoes
- the compounds I and II and the compounds III can be applied simultaneously together or separately or in succession, the sequence in the case of separate application generally not having any effect on the success of the control measures.
- Fungicides selected from the following groups are particularly suitable as fungicidal active ingredient III in the mixtures according to the invention:
- Acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,
- Amine derivatives such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph,
- Anionopyrimidines such as pyrimethanil, mepanipyrim or cyprodinil,
- Antibiotics such as cycloheximide, griseofulvin, kasugamycin, natamycin, polyoxin or streptomycin,
- Azoles such as bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquiconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazol, penocolazolol, myocazolol, myocazolol, myclazol, myclazol, myclazol, myocazolol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, myclazol, Tetraconazole, tri-dimefon, triadimenol, triflumizole, triticonazole, Dicarboximides such as iprodione, myclozolin, procymidone, vinclozol
- Dithiocarbamates such as Ferbam, Nabam, Maneb, Mancozeb, Metam, Metiram, Propineb, Polycarbamat, Thiram, Ziram, Zineb,
- Heterocyclic compounds such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, famoxadone, fenamidon, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolan, mepronazolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, proquinolifene, nuquin Pyroquilon, quinoxyfen, silthofam, thiabendazole, thifluzamide, thiophanate-methyl, tiadinil, tricyclazole, triforins,
- Copper fungicides such as Bordeaux broth, copper acetate, copper oxychloride, basic copper sulfate,
- Nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthal-isopropyl,
- Phenylpyrroie such as fenpiclonil or fludioxonil
- fungicides such as acibenzolar-S-methyl, benthiavalicarb, carpropamide, chlorothalonil, cyflufenamid, cymoxanil, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamide, fentin acetate, fenoxanil, feretorylyl, fosinone, foxam -Aluminium, iprovalicarb, hexachlorobenzene, metrafenone, pencycuron, penthiopyrad, propamocarb, phthalide, to-loclofos-methyl, quintozene, zoxamide, • strobilurins such as azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, methyl, creso-xostimim Picoxystrobin, pyraclostro
- Sulfenoic acid derivatives such as captafol, captan, dichlofluanid, folpet, tolylfluanid,
- Cinnamic acid amides and analogues such as dimethomorph, flumetover or flumorph.
- Guazatine mixture of the reaction products from the amidination of technical iminodi (octamethylene) diamine, containing various guanidines and polyamines
- Spiroxamine (8-tert-butyl-1,4-dioxa-spiro [4.5] dec-2-yl) diethylamine (EP-A 281 842); Tridemorph, 2,6-dimethyl-4-tridecylmorpholine (DE 11 64 152);
- Penconazole 1- [2- (2,4-dichlorophenyl) pentyl] -1H- [1, 2,4] triazole (Pesticide Manual, 12 th
- Prothioconazole 2- [2- (1-chloro-cyclopropyl) -3- (2-chlorophenyl) -2-hydroxypropyl] -2,4-dihydro- [1,2,4] triazol-3-thione (WO 96/16048);
- Triadimphone 1- (4-chlorophenoxy) -3,3-dimethyl-1- (1 tf-1, 2,4-triazol-1-yl) -2-butanone (BE 793 867);
- Triflumizole (4-chloro-2-trifluoromethyl-phenyl) - (2-propoxy-1- [1,2,4] triazol-1-yl-ethylidene) amine (JP-A 79/119462); Triticonazole, (£ 5) -5 - [(4-chlorophenyl) methylene] -2,2-dimethyl-1 - (1 H-1, 2,4-triazol-1-ylmethyl) cyclopentanol (FR 2641 277);
- Metiram zinc ammonium ethylene bis (dithiocarbamate) (US 3,248,400);
- Propineb, zinc propylene bis (dithiocarbamate) polymer (BE 611 960);
- Zineb zinc ethylene bis (dithiocarbamate) (US 2457674);
- Anilazine, 4,6-dichloro- / V- (2-chlorophenyl) -1, 3,5-triazin-2-amine (US 2,720,480); Benomyl, 2-acetylamino-benzoimidazole-1-carboxylic acid butylarnide (US 3631 176);
- Cyazofamide 4-chloro-2-cyano-V, ⁇ / -dimethyl-5- (4-methylphenyl) -1 H-imidazole-1 sulfonamide (CAS RN 120116-88-3];
- Furametpyr 5-chloro- ⁇ / - (1, 3-dihydro-1, 1, 3-trimethyl-4-isobenzofuranyl) -1, 3-dimethyl-1 H-pyrazole-4-carboxamide [CAS RN 123572-88- 3];
- Isoprothiolane, di-isopropyl 1, 3-dithiolan-2-ylidene malonate Proc. Insectic. Fungic. Conf.
- Tricyclazole 5-methyl-1, 2,4-triazolo [3,4-fc] [1,3] benzothiazole [CAS RN 41814-78-2];
- Copper oxychloride Cu 2 CI (OH) 3 [CAS RN 1332-40-7]; basic copper sulfate, CuSO 4 [CAS RN 1344-73-6];
- Nitrothal-isopropyl, 5-nitroisophthalic acid diisopropyl ester Proc. Br. Insectic. Fungic.
- Chlorothalonil, 2,4,5,6-tetrachloroisophthalonitrile (US 3290353);
- Cymoxanil 1- (2-cyano-2-methoxyiminoacetyl) -3-ethylurea (US 3,957847); Diclomezine, 6- (3,5-dichlorophenyl-p-tolyl) pyridazin-3 (2H) -one (US 4052395)
- Fentin acetate triphenyltin (US 3499086); Fenoxanil, ⁇ / - (1-cyano-1,2-dimethylpropyl) -2- (2,4-dichlorophenoxy) propanamide (EP
- Fosetyl, fosetyl aluminum, ethyl phosphonate (FR 22 54276);
- Penthiopyrad (RS) - ⁇ / - [2- (1,3-dimethylbutyl) -3-thienyl] -1-methyl-3- (trifluoromethyl) -1 H-pyrazole-4-carboxamide (JP 10130268); Propamocarb, 3- (dimethylamino) propyl carbamic acid propyl ester (DE 1567 169); Phthalide (DE 1643 347);
- Trifloxystrobin (£) -methoxyimino - ⁇ (£) - ⁇ - [1- ( ⁇ , ⁇ , ⁇ -trifluoro-m-tolyI) ethylidene aminooxy] -tolyl-acetic acid methyl ester (EP 460 575);
- Mixtures of the compounds I and II with an active ingredient III are preferred selected from the anilinopyrimidines, azoles, dithiocarbamates, heterocyclic compounds, sulfonic acid derivatives, cinnamic acid derivatives or the other fungicides mentioned, in particular the azoles mentioned.
- Mixtures of the compounds I and II with an active ingredient III are particularly preferred selected from the group cyprodinil, epoxiconazole, fluquiconazole, metconazole, prochloraz, prothioconazole, tebuconazole, triticonazole, Mancozeb, Metiram, boscalid, dithianon, chlorothalonil, metrafenone, and dimamethomol, propamocarb ,
- a further fungicide IV is added to compounds II and III.
- the aforementioned active ingredients III are suitable as component IV.
- the compounds I, II and IM are usually in a weight ratio of 100: 1: 5 to 1: 100: 20, preferably 20: 1: 1 to 1:20:20 to 1: 20: 1 to 20: 1: 20, in particular 10: 1: 1 to 1:10:10 to 1: 10: 1 to 10: 1: 10 applied.
- components IV are mixed in a ratio of 20: 1 to 1:20 to the mixtures of the compounds I, II and III.
- the application rates of the mixtures according to the invention are 5 g / ha to 2500 g / ha, preferably 5 g / ha to 1000 g / ha, in particular 50 to 750 g / ha.
- the application rates for the compound I are accordingly generally from 1 to 1000 g / ha, preferably from 10 to 900 g / ha, in particular from 20 to 750 g / ha.
- the application rates for the compounds II are generally from 1 to 1000 g / ha, preferably from 10 to 500 g / ha, in particular from 40 to 350 g / ha.
- the application rates for the compounds III are generally from 1 to 1000 g / ha, preferably from 10 to 500 g / ha, in particular from 40 to 350 g / ha.
- application rates of mixture of 1 to 1000 g / 100 kg of seed preferably 1 to 200 g / 100 kg, in particular 5 to 100 g / 100 kg, are generally used.
- the method for controlling harmful fungi is carried out by the separate or joint application of the compounds I and II and a compound III or the mixtures of the compounds I, II and a compound IM 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 compounds I, II and IM can be converted into the customary formulations, e.g. Solutions, emulsions, suspensions, dusts, powders, pastes and granules.
- the form of application depends on the respective purpose; in any case, it should 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.
- solvents / auxiliaries water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example petroleum fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butryolactone) , Pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, dimethyl fatty acid amides, fatty acids and fatty acid esters.
- aromatic solvents for example Solvesso products, xylene
- paraffins for example petroleum fractions
- alcohols for example methanol, butanol, pentanol, benzyl alcohol
- ketones for example cyclohexanone, gamm
- solvent mixtures can also be used, carriers such as natural stone powder (e.g. kaolins, clays, talc, chalk) and synthetic stone powder (e.g. highly disperse silica, silicates); Emulsifiers such as non-ionic and anionic emulsifiers (e.g. polyoxyethylene, fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste liquors and methyl cellulose.
- carriers such as natural stone powder (e.g. kaolins, clays, talc, chalk) and synthetic stone powder (e.g. highly disperse silica, silicates); Emulsifiers such as non-ionic and anionic emulsifiers (e.g. polyoxyethylene, fatty alcohol ethers, alkyl sulfonates and aryl sulfonates) and dispersants such as lignin sulfite waste
- Alkali metal, alkaline earth metal, ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkyl sulfonates, fatty alcohol sulfates, fatty acids and sulfated naphthalene glycol ethers and sulfonated etherifying products and sulfonated etherifying products are also used as surface-active substances, as well as sulfonated etherifying products and sulfonated etherifying products Formaldehyde, condensation products of naphthalene or naphthalene sulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol,
- Mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, also coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xy-, are used to produce directly sprayable solutions, emulsions, pastes or oil dispersions.
- lol paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
- Powders, materials for broadcasting and dusts can be prepared by mixing or grinding the active substances together with a solid carrier.
- Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers.
- Solid carriers are mineral earths such as silica gels, silicates, "talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, Caicium- and magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, Ammonium phosphate, ammonium nitrate, ureas and vegetable products, such as cereal flour, tree bark, wood and nutshell flour, cellulose powder and other solid carriers.
- the formulations generally contain between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight of the active ingredients, the active ingredients being used in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR spectrum).
- formulations are: 1. Products for dilution in water
- the active ingredients are dissolved in water or a water-soluble solvent. Alternatively, wetting agents or other aids are added. The active ingredient dissolves when diluted in water.
- the active ingredients are finely ground with the addition of dispersing and wetting agents and produced using technical equipment (e.g. 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.
- technical equipment e.g. extrusion, spray tower, fluidized bed
- WP, SP Water-dispersible and water-soluble powders 75 parts by weight of the active ingredients are ground in a RotorrStratpr mill with the addition of dispersing and wetting agents and silica gel. Dilution in water results in a stable dispersion or solution of the active ingredient.
- the active ingredients as such in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, Suspensions or dispersions, emulsions, oil dispersions, pastes, dusting agents, scattering agents, granules by spraying, atomizing, dusting, scattering or pouring can be used.
- the application forms depend entirely on the purposes; 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 (wettable 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, adhesives, dispersants or emulsifiers.
- concentrates composed of an active substance, wetting agents, adhesives, dispersants or emulsifiers and possibly solvents or oil, which are suitable for dilution with water.
- the active ingredient concentrations in the ready-to-use preparations can be varied over a wide range. 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 process (ULV), it being possible to apply formulations with more than 95% by weight of active ingredient or even the active ingredient without additives.
- UUV ultra-low-volume process
- Oils of various types, wetting agents, adjuvants, herbicides, fungicides, other pesticides, bactericides can be added to the active compounds, if appropriate also only immediately before use (tank mix). These agents are usually added to the agents according to the invention in a weight ratio of 1: 10 to 10: 1.
- the compounds I and II, or the mixtures or the corresponding formulations, are used in that the harmful fungi, the plants, seeds, soils, surfaces, materials or spaces to be kept free from them are mixed with a fungicidally effective amount of the mixture or the compounds I. and II when applied separately.
- the application can take place before or after the infestation by the harmful fungi.
- the fungicidal activity of the compound and the mixtures was demonstrated by the following tests:
- the active ingredients were prepared as a stock solution with 25 mg active ingredient, which was mixed 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 a volume ratio of solvent-emulsifier of 99 was filled to 1 ad 10 ml. Then ad 100 ml was made up with water. This stock solution was diluted with the solvent I-emulsifier / water mixture described to the concentration of active ingredient given below.
- Uniperol® EL wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
- ⁇ corresponds to the fungal attack of the treated plants in% and ß corresponds to the fungal attack of the untreated (control) plants in%
- the infection of the treated plants corresponds to that of the untreated control plants; with an efficiency of 100, the treated plants show no infection.
- Pots with wheat plants of the "Kanzler” variety were sprayed to runoff point with an aqueous suspension in the active compound concentration given below.
- the pots were inoculated with an aqueous spore suspension of Lepto-sphaeria nodorum (syn. Stagonospora nodorum, Septoria nodorum) the plants were placed in a chamber at 20 ° C. and maximum atmospheric humidity After 8 days the leaf spot disease on the untreated but infected control plants had developed in such a way that the infestation could be determined visually in% ,
- Leaves of potted plants were sprayed to runoff point with an aqueous suspension in the active compound concentration given below.
- the leaves were infected 5 days later with an aqueous spore suspension of Altemaria solani in 2% biomalt solution with a density of 0.17 x 10 B spores / ml.
- the plants were then placed in a water vapor-saturated chamber at temperatures between 20 and 22 ° C. After a further 5 days the disease had developed so strongly on the untreated but infected control plants that the infestation could be determined visually in%.
- the evaluation was carried out analogously to Example.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004016084 | 2004-03-30 | ||
PCT/EP2005/003213 WO2005094583A1 (de) | 2004-03-30 | 2005-03-26 | Ternäre fungizide mischungen |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1732388A1 true EP1732388A1 (de) | 2006-12-20 |
Family
ID=34963344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05729121A Withdrawn EP1732388A1 (de) | 2004-03-30 | 2005-03-26 | Ternäre fungizide mischungen |
Country Status (19)
Country | Link |
---|---|
US (1) | US20110136665A1 (de) |
EP (1) | EP1732388A1 (de) |
JP (1) | JP2007537156A (de) |
KR (1) | KR20070004068A (de) |
CN (1) | CN1937920A (de) |
AR (1) | AR049375A1 (de) |
AU (1) | AU2005227688A1 (de) |
BR (1) | BRPI0508965A (de) |
CA (1) | CA2558062A1 (de) |
EA (1) | EA200601674A1 (de) |
EC (3) | ECSP066617A (de) |
IL (1) | IL177654A0 (de) |
MA (1) | MA28540B1 (de) |
NO (1) | NO20064923L (de) |
TW (1) | TW200601972A (de) |
UA (2) | UA80509C2 (de) |
UY (1) | UY28832A1 (de) |
WO (1) | WO2005094583A1 (de) |
ZA (1) | ZA200608907B (de) |
Families Citing this family (22)
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EA012612B1 (ru) * | 2004-12-20 | 2009-10-30 | Басф Акциенгезельшафт | Способ борьбы с грибковыми заболеваниями бобовых культур |
NZ560376A (en) * | 2005-02-04 | 2010-03-26 | Mitsui Chemicals Inc | Plant pathogen control composition and method |
GB0508993D0 (en) | 2005-05-03 | 2005-06-08 | Syngenta Participations Ag | Pesticidal compositions |
NZ568508A (en) * | 2005-11-10 | 2011-11-25 | Basf Se | Use of pyraclostrobin as safener for triticonazole for controlling harmful fungi |
WO2007134777A2 (de) * | 2006-05-24 | 2007-11-29 | Bayer Cropscience Ag | Fungizide wirkstoffkombinationen |
DE102006024925A1 (de) * | 2006-05-24 | 2007-11-29 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
BRPI0807012A2 (pt) * | 2007-02-06 | 2014-04-22 | Basf Se | Uso de inseticidas, método de reduzir ou evitar o efeito fitotóxico de fungicidas, e, agente. |
KR101182617B1 (ko) * | 2007-08-06 | 2012-09-17 | 닛뽕소다 가부시키가이샤 | 농약 조성물, 농원예용 살균제 및 식물 병해의 방제 방법 |
PT2205082E (pt) * | 2007-09-26 | 2012-05-02 | Basf Se | Composições fungicidas ternárias compreendendo boscalide e clorotalonil |
BRPI0908358A8 (pt) * | 2008-02-05 | 2016-05-03 | Basf Se | mistura, composição pesticida, métodos para controlar pragas e/ou melhorar a saúde das plantas, e para proteção do material de propagação da planta contra pragas, e, material de propagação das plantas |
JP5359224B2 (ja) * | 2008-11-25 | 2013-12-04 | 住友化学株式会社 | 植物病害防除用組成物及び植物病害の防除方法 |
CN101779660B (zh) * | 2009-12-16 | 2013-03-20 | 福建新农大正生物工程有限公司 | 含有代森联的杀菌组合物 |
CN102150661A (zh) * | 2011-02-25 | 2011-08-17 | 陕西美邦农药有限公司 | 一种含有氰霜唑与***类化合物的杀菌组合物 |
JP5776294B2 (ja) * | 2011-04-15 | 2015-09-09 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
JP5997931B2 (ja) * | 2011-05-25 | 2016-09-28 | 石原産業株式会社 | 農園芸用殺菌剤組成物及び植物病害の防除方法 |
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CN103210937A (zh) * | 2013-02-06 | 2013-07-24 | 吉林省八达农药有限公司 | 一种含有丁香菌酯与其它杀菌剂的组合物 |
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CN103783055B (zh) * | 2014-02-28 | 2015-09-23 | 浙江农林大学 | 含啶酰菌胺的三元复配杀菌剂及其用途 |
CN104126595B (zh) * | 2014-08-21 | 2016-04-13 | 陕西上格之路生物科学有限公司 | 一种含有吡唑醚菌酯的杀菌剂组合物 |
CN105941395A (zh) * | 2016-04-30 | 2016-09-21 | 广东中迅农科股份有限公司 | 含有吡唑醚菌酯和咪鲜胺的农药组合物 |
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CN1145418C (zh) * | 1996-08-30 | 2004-04-14 | 巴斯福股份公司 | 杀真菌混合物 |
TWI252231B (en) * | 1997-04-14 | 2006-04-01 | American Cyanamid Co | Fungicidal trifluorophenyl-triazolopyrimidines |
US6316480B1 (en) * | 1997-05-28 | 2001-11-13 | Basf Aktiengesellschaft | Fungicidal mixtures |
BR9909002A (pt) * | 1998-03-24 | 2000-11-28 | Basf Ag | Mistura fungicida e processo para controlar fungos nocivos |
SI0988790T1 (en) * | 1998-09-25 | 2003-10-31 | Basf Aktiengesellschaft | Fungicidal mixtures |
DE10063046A1 (de) * | 2000-12-18 | 2002-06-20 | Basf Ag | Fungizide Mischungen |
US7687434B2 (en) * | 2000-12-22 | 2010-03-30 | Monsanto Technology, Llc | Method of improving yield and vigor of plants |
WO2002054870A2 (de) * | 2001-01-16 | 2002-07-18 | Basf Aktiengesellschaft | Fungizide mischungen auf der basis von imidazolderivaten |
CZ301050B6 (cs) * | 2001-01-18 | 2009-10-21 | Basf Aktiengesellschaft | Fungicidní smesi |
CA2505498A1 (en) * | 2002-11-15 | 2004-06-03 | Basf Aktiengesellschaft | Fungicidal mixtures for controlling rice pathogens |
OA12957A (en) * | 2002-11-15 | 2006-10-13 | Basf Ag | Fungicidal mixtures. |
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2005
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- 2005-03-26 CN CNA2005800106414A patent/CN1937920A/zh active Pending
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- 2005-03-26 WO PCT/EP2005/003213 patent/WO2005094583A1/de active Application Filing
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- 2005-03-26 JP JP2007505466A patent/JP2007537156A/ja not_active Withdrawn
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- 2005-03-26 US US10/591,290 patent/US20110136665A1/en not_active Abandoned
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- 2006-10-18 MA MA29395A patent/MA28540B1/fr unknown
- 2006-10-27 NO NO20064923A patent/NO20064923L/no not_active Application Discontinuation
- 2006-10-27 ZA ZA200608907A patent/ZA200608907B/xx unknown
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Also Published As
Publication number | Publication date |
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ECSP066890A (es) | 2006-12-29 |
AR049375A1 (es) | 2006-07-26 |
MA28540B1 (fr) | 2007-04-03 |
US20110136665A1 (en) | 2011-06-09 |
UA80509C2 (en) | 2007-09-25 |
JP2007537156A (ja) | 2007-12-20 |
IL177654A0 (en) | 2006-12-31 |
EA200601674A1 (ru) | 2007-04-27 |
UA80931C2 (en) | 2007-11-12 |
WO2005094583A1 (de) | 2005-10-13 |
CA2558062A1 (en) | 2005-10-13 |
BRPI0508965A (pt) | 2007-08-21 |
UY28832A1 (es) | 2005-10-31 |
KR20070004068A (ko) | 2007-01-05 |
AU2005227688A1 (en) | 2005-10-13 |
TW200601972A (en) | 2006-01-16 |
ECSP066617A (es) | 2006-10-25 |
NO20064923L (no) | 2006-10-27 |
CN1937920A (zh) | 2007-03-28 |
ECSP066891A (es) | 2006-12-29 |
ZA200608907B (en) | 2008-07-30 |
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