EP1519651A1 - Associations de substances actives fongicides - Google Patents

Associations de substances actives fongicides

Info

Publication number
EP1519651A1
EP1519651A1 EP03735610A EP03735610A EP1519651A1 EP 1519651 A1 EP1519651 A1 EP 1519651A1 EP 03735610 A EP03735610 A EP 03735610A EP 03735610 A EP03735610 A EP 03735610A EP 1519651 A1 EP1519651 A1 EP 1519651A1
Authority
EP
European Patent Office
Prior art keywords
active ingredient
plants
formula
active
active substance
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
EP03735610A
Other languages
German (de)
English (en)
Inventor
Ulrike Wachendorff-Neumann
Astrid Mauler-Machnik
Manfred Jautelat
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.)
Bayer CropScience AG
Original Assignee
Bayer CropScience AG
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=29723409&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP1519651(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP1519651A1 publication Critical patent/EP1519651A1/fr
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • 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
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Definitions

  • the present invention relates to a new combination of active ingredients which is derived from the known 2- [ ⁇ - ⁇ [( ⁇ -memyl-3-trifluoromethyl-benzyl) imino] oxy ⁇ -o-tolyl] -glyoxylic acid methyl ester-O- methyloxime on the one hand and a known triazole derivative on the other hand and is very suitable for combating phytopathogenic fungi.
  • the fungicidal activity of the active compound combination according to the invention is considerably higher than the sum of the effects of the individual active compounds. So there is an unforeseeable, real synergistic effect and not just an addition.
  • the component present in the active ingredient combination according to the invention in addition to the active ingredient of the formula (I) is also known.
  • the active substances are described in detail in the following publications:
  • the active ingredients are present in the active ingredient combination according to the invention in certain weight ratios, the synergistic effect is particularly evident clear.
  • the weight ratios of the active ingredients in the active ingredient combination can be varied within a relatively wide range.
  • the active ingredient combination according to the invention has very good fungicidal properties and can be used to control phytopathogenic fungi, such as plasmidiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Deuteromycetes, etc.
  • the active ingredient combination according to the invention is particularly suitable for combating cereal diseases, such as Erysiphe, Cochliobolus, Pyrenophora,
  • Rhynchosporium Septoria, Fusarium, Pseudocercosporella and Leptosphaeria and for combating fungal attack on non-cereal crops such as wine, fruit, peanut, vegetables, for example Phythophthora, Plasmopara, Pythium as well as powdery mildew fungi such as Sphaerofheca or Uncinula and Ventineniaerre, as well as leaf stains, such as 'Leaf blemishes', as well as 'Leaf blemishes', as well as leaf stains, as well as leaf stains, as well as leaf stains and leaf stains, as well as leaf stains and leaf stains, as well as leaf stains and leaf stains, as well as leaf stains and leaf stains, as well as leaf stains, such as Sphaerofheca and Uncinula, as well as leaf stains and leaf stains, as well as leaf stains and leaf stains, such as Sphaerofheca and Un
  • the fact that the active ingredient combination is well tolerated by plants in the concentrations required to combat plant diseases permits treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil.
  • the active ingredient combination according to the invention can be used for leaf application or as a mordant.
  • the active ingredient combination according to the invention is also suitable for increasing the crop yield. It is also less toxic and has good plant tolerance. According to the invention, all plants and parts of plants can be treated. Plants are understood here to mean all plants and plant populations, such as desired and unwanted wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant cultivars which can or cannot be protected by plant breeders' rights.
  • Plant parts are to be understood to mean all above-ground and underground parts and organs of plants, such as shoots, leaves, flowers and roots, examples being leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes become.
  • the plant parts also include crops and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment of the plants and parts of plants with the active compounds according to the invention is carried out directly or by acting on their surroundings, living space or storage space according to the customary treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, scattering, spreading and, in the case of propagation material, in particular seeds, furthermore by single- or multi-layer coating.
  • the active ingredient combination according to the invention can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in
  • formulations are prepared in a known manner, for example by mixing the active ingredients or combinations of active ingredients with extenders, that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, ie Emulsifiers and / or dispersants and / or foaming agents. If water is used as an extender, organic solvents can, for example, also be used as auxiliary solvents.
  • extenders that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, ie Emulsifiers and / or dispersants and / or foaming agents.
  • surface-active agents ie Emulsifiers and / or dispersants and / or foaming agents.
  • organic solvents can, for example, also be used as auxiliary solvents.
  • aromatics such as xylene, toluene or allylnaphthalamine
  • chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride
  • aliphatic hydrocarbons such as cyclohexane or paraffins, for example 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 under normal pressure, for example aerosol propellants such as butane, propane, nitrogen and carbon dioxide.
  • Solid carrier materials come into question: for example natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock powders such as highly disperse silica, aluminum oxide and silicates.
  • Solid carriers for granules are possible: e.g.
  • 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 alkyl aryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolysates.
  • Possible dispersants are, for example, lignin sulfite liquor and methyl cellulose.
  • Adhesives such as carboxymethyl cellulose, natural and synthetic polymers in the form of powders, granules or latices, such as Giimmiarabicum, polyvinyl alcohol, polyvinyl acetate and natural ones, can be used in the formulations.
  • Phospholipids such as cephalins and lecithins, and synthetic phospholipids.
  • Other additives can be mineral and vegetable oils.
  • Dyes such as inorganic pigments, for example 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% by weight of active ingredients, preferably between 0.5 and 90%.
  • the active ingredient combination according to the invention can be used as such or in its formulations also in hybrid with known fungicides, bactericides, acaricides, nematicides or insecticides, in order, for example, to broaden the spectrum of activity or to prevent the development of resistance. In many cases, synergistic effects are obtained, i.e. the effectiveness of the mixture is greater than the effectiveness of the individual components.
  • the active substance 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. They are used in the usual way, e.g. by pouring, spraying, spraying, scattering, spreading, dry pickling, wet pickling, wet pickling, slurry pickling or incrusting.
  • the application rates can be varied within a substantial range, depending on the type of application.
  • the application rates of active compound combination are generally between 0.1 and 10000 g / ha, preferably between
  • the amount of active ingredients Combination of substances generally between 0.001 and 50 g per kg of seed, preferably between 0.01 and 10 g per kg of seed.
  • the active compound combination application rates 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 ingredient combinations is greater than the sum of the effects of the individually applied active ingredients.
  • X means the efficiency when using the active ingredient A in an application rate of m g / ha
  • Y means the efficiency when using the active ingredient B in an application rate of n g / ha and
  • the efficiency is determined in%. It means 0% an efficiency that corresponds to that of the control, while an efficiency of 100% means that no infection is observed. If the actual fungicidal activity is greater than calculated, the combination of the combination is superadditive, ie there is a synergistic effect. In this case, the actually observed efficiency must be greater than the value for the expected efficiency E ⁇ calculated from the above formula.
  • Emulsifier 0.6 part by weight of alkylaryl polyglycol ether
  • the plants are placed in a greenhouse at a temperature of approx. 15 ° C and a relative humidity of 80%.
  • Emulsifier 0.6 part by weight of alkylaryl polyglycol ether
  • the plants are placed in a greenhouse at a temperature of approx. 20 ° C and a relative humidity of approx. 80% in order to promote the development of rust pustules.

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

L'invention concerne une nouvelle association de substances actives qui comprend le composé méthylester-O-méthyloxime d'acide 2-[ alpha {[( alpha -méthyl-3-trifluorométhyl-benzyl)imino]oxy}-o-tolyl]-glyoxalique de formule (I) (trifloxystrobine) ainsi que la substance active de formule (II) (prothioconazole) qui est spécifiée dans la description, et présente d'excellentes propriétés fongicides.
EP03735610A 2002-06-24 2003-06-12 Associations de substances actives fongicides Ceased EP1519651A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10228102 2002-06-24
DE10228102A DE10228102A1 (de) 2002-06-24 2002-06-24 Fungizide Wirkstoffkombinationen
PCT/EP2003/006174 WO2004000021A1 (fr) 2002-06-24 2003-06-12 Associations de substances actives fongicides

Publications (1)

Publication Number Publication Date
EP1519651A1 true EP1519651A1 (fr) 2005-04-06

Family

ID=29723409

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03735610A Ceased EP1519651A1 (fr) 2002-06-24 2003-06-12 Associations de substances actives fongicides

Country Status (14)

Country Link
US (1) US20060004070A1 (fr)
EP (1) EP1519651A1 (fr)
JP (1) JP2005530831A (fr)
AR (1) AR039701A1 (fr)
AU (1) AU2003237930A1 (fr)
BR (1) BR0312103A (fr)
CA (1) CA2490303A1 (fr)
DE (1) DE10228102A1 (fr)
GT (1) GT200300123A (fr)
PL (1) PL374390A1 (fr)
RU (1) RU2331192C2 (fr)
TW (1) TWI274549B (fr)
WO (1) WO2004000021A1 (fr)
ZA (1) ZA200410269B (fr)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
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DE4426753A1 (de) * 1994-07-28 1996-02-01 Bayer Ag Mittel zur Bekämpfung von Pflanzenschädlingen
DE19716257A1 (de) 1997-04-18 1998-10-22 Bayer Ag Fungizide Wirkstoffkombination
HU230539B1 (hu) 1998-06-10 2016-11-28 Bayer Intellectual Property Gmbh Növényvédőszer-készítmény
DE10140108A1 (de) 2001-08-16 2003-03-06 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
ATE397860T1 (de) 2002-03-01 2008-07-15 Basf Se Fungizide mischungen auf der basis von prothioconazole und picoxystrobin
DE10228104A1 (de) * 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungizide Wirkstoffkombination
DE10228103A1 (de) * 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
DE10335183A1 (de) * 2003-07-30 2005-02-24 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
DE10341945A1 (de) * 2003-09-11 2005-04-21 Bayer Cropscience Ag Verwendung von fungiziden Mitteln zur Beizung von Saatgut
DE10347090A1 (de) * 2003-10-10 2005-05-04 Bayer Cropscience Ag Synergistische fungizide Wirkstoffkombinationen
DE10347440A1 (de) * 2003-10-13 2005-05-04 Bayer Cropscience Ag Synergistische insektizide Mischungen
KR100870174B1 (ko) * 2003-12-04 2008-11-24 바이엘 크롭사이언스 아게 살충 및 살비성을 가지는 활성 물질 배합물
EP1691611A1 (fr) * 2003-12-04 2006-08-23 Bayer CropScience Aktiengesellschaft Combinaisons d'agents presentant des proprietes insecticides
AP2006003662A0 (en) * 2003-12-12 2006-06-30 Bayer Corpscience Ag Synergistic insecticidal mixtures
EP1563731A1 (fr) 2004-02-12 2005-08-17 Bayer CropScience S.A. Composition fongicide comprenant un composé pyridylethylbenzamide et un inhibiteur de la synthèse d'ergosterol
DE102004020840A1 (de) * 2004-04-27 2005-11-24 Bayer Cropscience Ag Verwendung von Alkylcarbonsäureamiden als Penetrationsförderer
DE102004049041A1 (de) 2004-10-08 2006-04-13 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
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AU2005321567A1 (en) * 2004-12-23 2006-07-06 Basf Aktiengesellschaft Fungicidal mixtures containing enestroburin and at least one active substance from the group of azoles
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DE102005023835A1 (de) * 2005-05-24 2006-12-07 Bayer Cropscience Ag Fungizide Wirkstoffkombination
MX2008003071A (es) * 2005-09-09 2008-03-19 Bayer Cropscience Ag Formulacion solida de mezclas fungicidas.
DE102006031978A1 (de) * 2006-07-11 2008-01-17 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
US20090281157A1 (en) * 2006-07-11 2009-11-12 Bayer Cropscience Ag Active Ingredient Combinations With Insecticidal and Acaricidal Properties
DE102006031976A1 (de) * 2006-07-11 2008-01-17 Bayer Cropscience Ag Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
RU2326878C1 (ru) * 2006-11-17 2008-06-20 Российский химико-технологический университет (РХТУ им. Д.И. Менделеева) Замещенные 2-(1,2,4-триазол-1-илметил)-6-бензилиден-1,4-диоксаспиро[4.5]деканы, способ их получения, фунгицидная композиция на их основе
PT2124557E (pt) * 2007-02-02 2015-02-27 Plant Health Care Inc Composições fungicidas sinérgicas compreendendo formononetina
EP2036438A1 (fr) * 2007-09-12 2009-03-18 Bayer CropScience AG Traitement post-récolte
EP2224810A2 (fr) * 2007-11-05 2010-09-08 Basf Se Procédé, utilisation et agent pour protéger une plante contre phakospora
US8683346B2 (en) * 2008-11-17 2014-03-25 Sap Portals Israel Ltd. Client integration of information from a supplemental server into a portal
EP2269454A1 (fr) * 2009-06-24 2011-01-05 Bayer CropScience AG Combinaisons de levures fongicides et de fongicides
CA2808333C (fr) * 2010-08-11 2016-02-16 Randy Allen Myers Procede d'amelioration de la croissance de plantes par reduction des infections fongiques
WO2014082950A1 (fr) * 2012-11-30 2014-06-05 Bayer Cropscience Ag Mélanges fongicides ternaires
CN102960347A (zh) * 2012-12-14 2013-03-13 江苏七洲绿色化工股份有限公司 一种含有丙硫菌唑和肟菌酯的杀菌组合物
EP3932206A1 (fr) * 2013-11-26 2022-01-05 UPL Ltd Procede de lutte contre de la rouille
AR102987A1 (es) * 2014-12-16 2017-04-05 Bayer Cropscience Ag Combinaciones de compuestos activos que comprenden un derivado de (tio)carboxamida y compuesto(s) fungicida(s)
BR112018076864A2 (pt) * 2016-06-22 2019-04-02 Bayer Cropscience Ag combinações de composto ativo
EA202191023A3 (ru) 2017-03-07 2021-10-29 Юпл Лтд Фунгицидные комбинации
CN109042682A (zh) * 2018-06-11 2018-12-21 上海农乐生物制品股份有限公司 一种含豆科素和肟菌酯的杀菌组合物
CN109042701A (zh) * 2018-09-21 2018-12-21 贵州道元生物技术有限公司 一种防治黄瓜褐斑病的丙硫唑和肟菌酯的杀菌组合物及其用途
CA3139524A1 (fr) 2019-05-10 2020-11-19 Bayer Cropscience Lp Combinaisons de composes actifs

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Patent Citations (3)

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Publication number Priority date Publication date Assignee Title
EP0460575A1 (fr) * 1990-06-05 1991-12-11 Ciba-Geigy Ag Composés aromatiques
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CA2490303A1 (fr) 2003-12-31
RU2331192C2 (ru) 2008-08-20
AU2003237930A1 (en) 2004-01-06
TW200406153A (en) 2004-05-01
ZA200410269B (en) 2006-02-22
GT200300123A (es) 2004-03-08
DE10228102A1 (de) 2004-01-15
AR039701A1 (es) 2005-03-09
TWI274549B (en) 2007-03-01
RU2005101615A (ru) 2005-07-20
WO2004000021A1 (fr) 2003-12-31
JP2005530831A (ja) 2005-10-13
BR0312103A (pt) 2005-03-29
PL374390A1 (en) 2005-10-17
US20060004070A1 (en) 2006-01-05

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