EP2101573A2 - Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation - Google Patents

Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation

Info

Publication number
EP2101573A2
EP2101573A2 EP07818202A EP07818202A EP2101573A2 EP 2101573 A2 EP2101573 A2 EP 2101573A2 EP 07818202 A EP07818202 A EP 07818202A EP 07818202 A EP07818202 A EP 07818202A EP 2101573 A2 EP2101573 A2 EP 2101573A2
Authority
EP
European Patent Office
Prior art keywords
spp
compositions
adjuvant
plants
agrochemical
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Withdrawn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
EP07818202A
Other languages
German (de)
English (en)
Inventor
Udo Reckmann
Peter Marczok
Peter Baur
Ronald Vermeer
Wolfgang Thielert
Heike Hungenberg
Dirk Ebbinghaus
Peter Lösel
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
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Priority to EP07818202A priority Critical patent/EP2101573A2/fr
Publication of EP2101573A2 publication Critical patent/EP2101573A2/fr
Withdrawn legal-status Critical Current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
    • A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/30—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues thereof
    • 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
    • A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
    • A01N31/14—Ethers
    • 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
    • A01N37/12—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 the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
    • 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
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10—Sulfones; Sulfoxides

Definitions

  • the present invention relates to the improvement of the action of agrochemical compositions in soil application, the agrochemical compositions suitable for this application, and their use for control of noxious insects.
  • compositions comprising corn syrup, methylated soybean oil and nonionic emulsifier, commercially available e.g. in the Süperb® product range.
  • Q B is hydrogen, halogen, cyano, nitro, C r C 8 haloalkyl, each optionally substituted C 3 -C 8 -Cyloalkyl, Ci-Cg--alkyl-carbonyl or Ci-Cg-alkoxy-carbonyl, 4B respectively T ⁇ _R optionally substituted phenyl, hetaryl or represents the group,
  • R 1B and R 28 together form an optionally substituted 4- to 7-membered ring which may optionally be interrupted by heteroatoms,
  • the phthalic diamides of the acaricidal and / or insecticidal agents are generally defined by the formula (II). Preferred substituents or ranges of the radicals listed in the formulas mentioned above and below are explained below:
  • X B is preferably fluorine, chlorine, bromine, iodine, cyano, C r C 6 alkyl, C r C 6 haloalkyl, C 1 - C ⁇ -alkoxy or Ci-C 6 haloalkoxy.
  • M 1B preferably represents achiral C r C 8 -alkylene, achiral C 3 -C 6 -alkenylene or achiral C 3 - C 6 -alkynylene.
  • R 4B particularly preferably represents hydrogen, in each case optionally mono- to trisubstituted by fluorine and / or chlorine, CpC 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl or
  • L 1B and L 3B independently of one another particularly preferably represent hydrogen, fluorine, chlorine,
  • L 2B particularly preferably represents hydrogen, fluorine, chlorine, bromine, iodine, cyano, in each case optionally monosubstituted to trisubstituted by fluorine and / or chlorine, C 1 -C 6 -MB R 6B
  • R 1B and R 2B are very particularly preferably hydrogen.
  • M ' B is very particularly preferably -C (CH 3 ) 2 CH 2 - or -C (C 2 Hj) 2 CH 2 -
  • R 4B very particularly preferably represents in each case optionally mono- to trisubstituted by fluorine and / or chlorine, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl or tert-butyl, allyl, Butenyl or isoprenyl.
  • L 1 B and L 3B very particularly preferably represent hydrogen, fluorine, chlorine, bromine, iodine, cyano, methyl, ethyl, n-propyl, isopropyl, tert-butyl, methoxy, ethoxy, trifluoromethyl, difluoromethoxy or trifluoromethoxy
  • L stands g anz particularly Favor g t represents hydrogen, fluorine, chlorine, bromine, iodine, cyano, represents in each case optionally substituted once to nine times by fluorine and / or chlorine-substituted methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, AHyI, M2B "6B
  • At least one nonionic surfactant and / or at least one anionic surfactant one or more additives from the groups of antifreezes, antifoaming agents, preservatives, antioxidants, spreading agents, dyes and / or thickeners.
  • compositions according to the invention are formulations which remain stable even after prolonged storage at elevated temperatures or in the cold, since no crystal growth is observed. They can be converted by dilution with water into homogeneous spray liquids.
  • the application rate of the compositions according to the invention can be varied within a relatively wide range. It depends on the particular agrochemical active ingredients and their content in the compositions.
  • compositions of the invention contain
  • compositions according to the invention are suitable with good plant tolerance, favorable toxicity to warm-blooded animals and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and mollusks in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
  • the above mentioned pests include:
  • Eriophyes spp. Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp. Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vasates lycopersici.
  • compositions according to the invention may optionally also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as anti-MLO agents ( Mycoplasma-like-organism) and RLO (Rickettsia-like-organism).
  • compositions according to the invention may contain other active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals as mixing partners.
  • active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • Particularly favorable mixing partners are, for example, the following:
  • Prothioconazole pyrifenox, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizole triforin, triticonazole, uniconazole, voriconazole, viniconazole,
  • Chloronicotinyls for example acetamipride, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
  • Chloride channel activators Mectins for example Abamectin, Emamectin, Emamectin benzoate, Ivermectin, Lepimectin,
  • Plant varieties are understood as meaning plants having new traits which have been bred by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, biotypes and genotypes.
  • Traits which are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT" gene).
  • the genes which confer the desired properties (“traits") can also occur in combinations with one another in the transgenic plants.
  • Examples of “Bt plants” are maize varieties, cotton varieties, soybean varieties and potato varieties which are sold under the trade names YIELD GARD® (eg corn, cotton, soya), KnockOut® (eg maize), StarLink® (eg maize), Bollgard® ( Cotton), Nucotn® (cotton) and NewLeaf® (potato).
  • compositions of the invention not only work against plant, hygiene and
  • Non-living materials such as preferably plastics, adhesives, glues, papers and cardboard, leather, wood, wood processing products and paints.
  • Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
  • Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.

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 l'amélioration de l'action des pesticides agricoles contenant des ingrédients actifs appartenant à la classe des diamides d'acide phtalique insecticides grâce à l'utilisation d'additifs. L'invention concerne les procédés de fabrication correspondants ainsi que les compositions adaptées.
EP07818202A 2006-09-30 2007-09-18 Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation Withdrawn EP2101573A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP07818202A EP2101573A2 (fr) 2006-09-30 2007-09-18 Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06020678 2006-09-30
EP07818202A EP2101573A2 (fr) 2006-09-30 2007-09-18 Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation
PCT/EP2007/008096 WO2008037374A2 (fr) 2006-09-30 2007-09-18 Amélioration de l'action biologique de compositions agrochimiques, lorsqu'elles sont appliquées dans un substrat de culture, formulations adaptées et leur utilisation

Publications (1)

Publication Number Publication Date
EP2101573A2 true EP2101573A2 (fr) 2009-09-23

Family

ID=38960806

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07818202A Withdrawn EP2101573A2 (fr) 2006-09-30 2007-09-18 Amelioration de l'action biologique de compositions chimiques, lorsqu'elles sont appliquees sur un substrat de culture, formulations ainsi obtenues et leur utilisation

Country Status (13)

Country Link
US (1) US20100087542A1 (fr)
EP (1) EP2101573A2 (fr)
JP (1) JP2010505752A (fr)
KR (1) KR20090060446A (fr)
CN (1) CN101522024A (fr)
AR (1) AR063055A1 (fr)
BR (1) BRPI0717153A2 (fr)
CL (1) CL2007002822A1 (fr)
CO (1) CO6160262A2 (fr)
MX (1) MX2009003071A (fr)
TW (1) TW200822864A (fr)
WO (1) WO2008037374A2 (fr)
ZA (1) ZA200902118B (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008043185A1 (de) * 2008-10-27 2010-04-29 Evonik Goldschmidt Gmbh Nicht schäumende organische Tenside als Additive für Tankmischungszubereitungen im Pflanzenschutz
CN102480946A (zh) * 2009-06-03 2012-05-30 拜尔农作物科学股份公司 氟虫双酰胺和有益生物的结合物
AR084149A1 (es) * 2010-12-13 2013-04-24 Akzo Nobel Chemicals Int Bv Composicion de adyuvantes para insecticidas y proceso para controlar poblaciones de insectos de cultivos
JPWO2012115070A1 (ja) * 2011-02-25 2014-07-07 株式会社クレハ 農業用薬剤およびその製造方法
WO2012169473A1 (fr) * 2011-06-06 2012-12-13 日本農薬株式会社 Régulateur de la croissance végétale et procédé pour son utilisation
ES2733112T3 (es) * 2013-05-23 2019-11-27 Syngenta Participations Ag Formulaciones de mezcla de tanque
CN107056447B (zh) * 2017-04-17 2020-12-08 南陵县生产力促进中心 一种根系促生园林绿化育苗基质

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6362369B2 (en) * 1997-11-25 2002-03-26 Nihon Nohyaku Co., Ltd. Phthalic acid diamide derivatives fluorine-containing aniline compounds as starting material, agricultural and horticultural insecticides, and a method for application of the insecticides
WO2001046124A1 (fr) * 1999-12-22 2001-06-28 Nihon Nohyaku Co., Ltd. Derives de diamide aromatique, produits chimiques utilises en agriculture ou en horticulture et utilisations de ces derniers
CZ299375B6 (cs) * 1998-11-30 2008-07-09 Nihon Nohyaku Co., Ltd. Ftalamidové deriváty nebo jejich soli, zemedelsko-zahradnický insekticid je obsahující a jeho použití
IL146967A0 (en) * 1999-06-24 2002-08-14 Nihon Nohyaku Co Ltd Heterocyclic dicarboxylic acid diamide derivatives, agricultural and horticultural insecticides and method of using the same
CN1142152C (zh) * 1999-06-25 2004-03-17 日本农药株式会社 苯甲酰胺衍生物、农业与园艺用杀虫剂及其用途
AR030154A1 (es) * 1999-07-05 2003-08-13 Nihon Nohyaku Co Ltd Derivado de ftalamida, derivado de amina heterociclico util como intermediario para la produccion del mismo, insecticida agrohorticola y metodo para utilizar dicho insecticida
ES2239035T3 (es) * 1999-09-24 2005-09-16 Nihon Nohyaku Co., Ltd. Derivados de diamida aromatica o sales de estos derivados, productos quimicos para la agricultura/horticultura y procedimiento de utilizacion de estos productos.
DE50204181D1 (de) * 2001-02-06 2005-10-13 Bayer Cropscience Ag Phthalsäurediamide, ein verfahren zu ihrer herstellung und ihre verwendung als schädlingsbekämpfungsmittel
DK1380209T3 (da) * 2001-04-17 2012-09-24 Nihon Nohyaku Co Ltd Sammensætning til et middel til bekæmpelse af skadelige organismer og fremgangsmåde til anvendelse af samme
US20040097595A1 (en) * 2001-04-26 2004-05-20 Hayami Nakao Phthalamide derivatives, insecticides for agricultural and horticultural use and method for application thereof
US20040116299A1 (en) * 2001-04-26 2004-06-17 Hiroto Harayama Phthalamide derivates, insecticides for agricultural and horticultural use and method for application thereof
AR035884A1 (es) * 2001-05-18 2004-07-21 Nihon Nohyaku Co Ltd Derivado de amida aromatico sustituido, derivado de amina aromatico sustituido con un grupo fluoroalquilo util como intermediario para obtener el mismo, insecticida para agrohorticultura que lo contiene y metodo para usar este ultimo
DE10129855A1 (de) * 2001-06-21 2003-01-02 Bayer Ag Suspensionskonzentrate auf Ölbasis
DE10310906A1 (de) * 2003-03-13 2004-09-23 Bayer Cropscience Ag Synergistische Wirkstoffkombinationen
EP1782689A1 (fr) * 2004-08-23 2007-05-09 Nihon Nohyaku Co., Ltd. Dérivé optiquement actif de phtalimide, insecticide pour l'agriculture ou l'horticulture et procédé d'utilisation de celui-ci
JP4977607B2 (ja) * 2004-08-31 2012-07-18 バイエル・クロップサイエンス・アーゲー 光学活性フタルアミド
EP1688039A3 (fr) * 2005-02-08 2006-10-11 Nihon Nohyaku Co., Ltd. Préparation d' un appât toxique pour l'agriculture et l'horticulture
DE102005059466A1 (de) * 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
DE102005059467A1 (de) * 2005-12-13 2007-06-14 Bayer Cropscience Ag Insektizide Zusammensetzungen mit verbesserter Wirkung
TWI324908B (en) * 2006-01-05 2010-05-21 Du Pont Liquid formulations of carboxamide arthropodicides

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2008037374A2 *

Also Published As

Publication number Publication date
WO2008037374A2 (fr) 2008-04-03
WO2008037374A3 (fr) 2009-02-12
BRPI0717153A2 (pt) 2013-10-15
AR063055A1 (es) 2008-12-23
US20100087542A1 (en) 2010-04-08
JP2010505752A (ja) 2010-02-25
WO2008037374A8 (fr) 2009-05-22
MX2009003071A (es) 2009-04-02
CN101522024A (zh) 2009-09-02
KR20090060446A (ko) 2009-06-12
CO6160262A2 (es) 2010-05-20
CL2007002822A1 (es) 2008-04-18
ZA200902118B (en) 2010-06-30
TW200822864A (en) 2008-06-01

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