WO2001037668A2 - Combinaisons d'agents actifs fongicides - Google Patents

Combinaisons d'agents actifs fongicides Download PDF

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Publication number
WO2001037668A2
WO2001037668A2 PCT/EP2000/011088 EP0011088W WO0137668A2 WO 2001037668 A2 WO2001037668 A2 WO 2001037668A2 EP 0011088 W EP0011088 W EP 0011088W WO 0137668 A2 WO0137668 A2 WO 0137668A2
Authority
WO
WIPO (PCT)
Prior art keywords
formula
methyl
active
active ingredient
chloro
Prior art date
Application number
PCT/EP2000/011088
Other languages
German (de)
English (en)
Other versions
WO2001037668A3 (fr
Inventor
Karl-Heinz Kuck
Astrid Mauler-Machnik
Ulrike Wachendorff-Neumann
Wolfgang Krämer
Original Assignee
Bayer Aktiengesellschaft
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 Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Priority to AU11469/01A priority Critical patent/AU1146901A/en
Publication of WO2001037668A2 publication Critical patent/WO2001037668A2/fr
Publication of WO2001037668A3 publication Critical patent/WO2001037668A3/fr

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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
    • 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
    • A01N47/40—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 a double or triple bond to nitrogen, e.g. cyanates, cyanamides
    • 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
    • A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

Definitions

  • the present invention relates to new combinations of active ingredients consisting of the known 8-t-butyl-2- (N-ethyl-Nn-propylamino) methyl-1,4-dioxaspiro [5,4] decane on the one hand and two other known active ingredients on the other hand and are very suitable for combating phytopathogenic fungi.
  • the weight ratios of the active ingredients in the active ingredient combinations can be varied within a relatively wide range.
  • 0.1 to 1.5 parts by weight, preferably 0.1 to 1.2 parts by weight of active compound of the formula (II) and 0.1 to 1.5 parts by weight are in 1 part by weight of active compound of the formula (I), preferably 0.1 to 1.2 parts by weight of active ingredient of the formula (III-a),
  • the active compound combinations according to the invention have very good fungicidal properties and can be used to combat phytopathogenic fungi, such as plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes,
  • the active compound combinations according to the invention are particularly suitable for combating cereal diseases, such as Pyrenophora teres, Erysiphe graminis, Leptosphaeria nodorum, Rhynchosporium secalis, Septoria tritici, Pucci ⁇ ia spp.,
  • the active substance combinations can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, active substance-impregnated natural and synthetic substances, female capsules in polymeric substances and in coating compositions for seeds, furthermore in formulations with fuels sets, such as smoking cartridges, cans, spirals, etc., as well as ULV cold and warm mist formulations.
  • customary formulations such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, active substance-impregnated natural and synthetic substances, female capsules in polymeric substances and in coating compositions for seeds, furthermore in formulations with fuels sets, such as smoking cartridges, cans, spirals, etc., as well as ULV cold and warm mist formulations.
  • formulations are made in a known manner, e.g. by mixing the active ingredients with extenders, that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
  • extenders that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
  • surface-active agents that is to say emulsifiers and / or dispersants and / or foam-generating agents.
  • water e.g. organic solvents can also be used as auxiliary solvents.
  • aromatics such as
  • Xylene, toluene, or alkylnaphthalenes chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, e.g.
  • Petroleum fractions alcohols, such as butanol or glycol, and their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulfoxide, and water;
  • liquefied gaseous extenders or carriers mean liquids which are gaseous at normal temperature and pressure, e.g. Aerosol propellants, such as halogenated hydrocarbons, butane, propane, nitrogen and carbon dioxide; as solid carriers are possible: e.g. natural rock flour, like
  • Possible solid carriers for granules are: eg broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite as well as synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stalks;
  • Possible emulsifiers and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolyzates;
  • Possible dispersing agents
  • Adhesives such as carboxymethylcellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids can be used in the formulations.
  • Other additives can be mineral and vegetable oils.
  • dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes, such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron,
  • Copper, cobalt, molybdenum and zinc can be used.
  • the formulations generally contain between 0.1 and 95 percent by weight of active ingredients, preferably between 0.5 and 90%.
  • the active compound combinations according to the invention can be present in the formulations in a mixture with other known active compounds, such as fungicides, insecticides, acaricides and herbicides, and in mixtures with fertilizers or plant growth regulators.
  • the active compound combinations can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, emulsifiable concentrates, emulsions, suspensions, wettable powders, soluble powders and granules.
  • the application rates of active compound combination are generally between 0.1 and 10,000 g / ha, preferably between 10 and 1,000 g / ha.
  • the application rates of the active compound combination are generally between 0.001 and 50 g per kg of seed, preferably between 0.01 and 10 g per kg of seed.
  • the application rates of active ingredient combination are generally between 0.1 and 10,000 g / ha, preferably between 1 and 5,000 g / ha.
  • Fungicides always have a synergistic effect if the fungicidal activity of the active compound combinations is greater than the sum of the effects of the individually applied active compounds.

Abstract

Selon l'invention, les nouvelles combinaisons d'agents actifs composées A) de spiroxamine, B) de quinoxyfène, et C) d'imidaclopride, de thiaclopride ou de thiaméthoxame, sont particulièrement adaptées à la lutte contre les champignons phytopathogènes.
PCT/EP2000/011088 1999-11-22 2000-11-09 Combinaisons d'agents actifs fongicides WO2001037668A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU11469/01A AU1146901A (en) 1999-11-22 2000-11-09 Fungicidally active substance combinations

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19956098.6 1999-11-22
DE1999156098 DE19956098A1 (de) 1999-11-22 1999-11-22 Fungizide Wirkstoffkombinationen

Publications (2)

Publication Number Publication Date
WO2001037668A2 true WO2001037668A2 (fr) 2001-05-31
WO2001037668A3 WO2001037668A3 (fr) 2002-02-14

Family

ID=7929893

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2000/011088 WO2001037668A2 (fr) 1999-11-22 2000-11-09 Combinaisons d'agents actifs fongicides

Country Status (4)

Country Link
AR (1) AR026546A1 (fr)
AU (1) AU1146901A (fr)
DE (1) DE19956098A1 (fr)
WO (1) WO2001037668A2 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2314225T3 (es) * 2002-03-08 2009-03-16 Basf Se Mexclas fungicidas a base de prothioconazol con un insecticida.

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4426753A1 (de) * 1994-07-28 1996-02-01 Bayer Ag Mittel zur Bekämpfung von Pflanzenschädlingen
DE19649459A1 (de) * 1996-11-26 1998-05-28 Bayer Ag Fungizide Wirkstoffkombinationen
DE19716256A1 (de) * 1997-04-18 1998-10-22 Bayer Ag Fungizide Wirkstoffkombinationen
WO1998051146A2 (fr) * 1997-05-15 1998-11-19 Novartis Ag Combinaisons fongicides comprenant un 4-phenoxyquinoline
WO1999048366A1 (fr) * 1998-03-24 1999-09-30 Basf Aktiengesellschaft Melanges fongicides a base de derives d'oximether de diatomite et d'insecticides

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2832482B2 (ja) * 1990-03-19 1998-12-09 日本バイエルアグロケム株式会社 殺虫殺菌剤組成物

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4426753A1 (de) * 1994-07-28 1996-02-01 Bayer Ag Mittel zur Bekämpfung von Pflanzenschädlingen
DE19649459A1 (de) * 1996-11-26 1998-05-28 Bayer Ag Fungizide Wirkstoffkombinationen
DE19716256A1 (de) * 1997-04-18 1998-10-22 Bayer Ag Fungizide Wirkstoffkombinationen
WO1998051146A2 (fr) * 1997-05-15 1998-11-19 Novartis Ag Combinaisons fongicides comprenant un 4-phenoxyquinoline
WO1999048366A1 (fr) * 1998-03-24 1999-09-30 Basf Aktiengesellschaft Melanges fongicides a base de derives d'oximether de diatomite et d'insecticides

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 016, no. 081 (C-0915), 27. Februar 1992 (1992-02-27) & JP 03 271207 A (NIPPON TOKUSHU NOYAKU SEIZO KK), 3. Dezember 1991 (1991-12-03) *

Also Published As

Publication number Publication date
DE19956098A1 (de) 2001-05-23
AR026546A1 (es) 2003-02-19
AU1146901A (en) 2001-06-04
WO2001037668A3 (fr) 2002-02-14

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