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Title:
殺虫及び殺ダニ特性を有する活性物質の組合せ物
Document Type and Number:
Japanese Patent JP2007513103
Kind Code:
A
Abstract:
Composition (A) contains synergistic amounts of a phenylpyrazolone compound (I) or at least one insecticide (IA) comprising amitraz, buprofezin, triazamate, pymetrozin, pyriproxifen, flonicamide or pirimicarb and at least one anthranilic acid amide compound (II). Composition (A) contains synergistic amounts of a phenylpyrazolone compound of formula (I), its N oxides or salts or at least one insecticide (IA) comprising amitraz, buprofezin, triazamate, pymetrozin, pyriproxifen, flonicamide or pirimicarb and at least one anthranilic acid amide compound of formula (II). [Image] X : halo, alkyl, haloalkyl, alkoxy, haloalkoxy or cyano; W 1>, Y, Z : H or X; A 3> : H, alkyl, alkoxyalkyl or optionally substituted cycloalkyl in which at least one ring atom is optionally replaced by a heteroatom (all optionally substituted by halo); A 4> : H or alkyl, or A 3> + A 4> : a saturated or unsaturated ring optionally containing at least one heteroatom and optionally substituted; D : alkyl, alkenyl, alkoxyalkyl or cycloalkyl in at least 1 ring member is optionally replaced by heteroatoms (all optionally substituted) or H, or D + A 3> : a saturated or unsaturated ring optionally containing at least one heteroatom and optionally substituted; G 1> : e.g. H or COR 20>; R 20> : alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl or polyalkoxyalkyl (all optionally substituted by halo), cycloalkyl optionally including at least one heteroatom (optionally substituted by halo, alkyl or alkoxy), or phenyl, phenalkyl, hetaryl, phenoxyalkyl or hetaryloxyalkyl (all optionally substituted); A 1>, A 2> : O or S; X 1> : N or CR 10>; R 1> : 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl or 3-6C cycloalkyl (all optionally substituted) or H; R 2> : H, 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl, 3-6C cycloalkyl, 1-4C alkoxy, 1-4C alkylamino, 2-8C dialkylamino, 3-6C cycloalkylamino, 2-6C alkoxycarbonyl or 2-6C alkylcarbonyl; R 3> : H, R 11> or 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl or 3-6C cycloalkyl (all optionally substituted), or R 2> + R 3> : a ring; R 4> : e.g. 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl or 3-6C cycloalkyl (all optionally substituted), or H; R 5>, R 8> : 1-4C alkyl or 1-4C haloalkyl (both optionally substituted), H or halo; R 7> : H, halo or 1-4C alkyl, alkoxy or alkylS(O) x (all optionally substituted), with specified provisos. Full definitions are given in the Definitions Field (Full Definitions). ACTIVITY : Insecticide; Nematocide; Arachnicide; Acaricide; Antifouling. In a test against Aphis gossypii on cotton, results showed that N-(2-methyl-4-chloro-6-(dimethylaminocarbonyl)phenyl-1-(3-chloropyrid-2-yl)-3-trifluoromethyl-pyrrole-5-carboxamide, at 20 ppm, gave 55% kill after 6 days, while flonicamide at 20 ppm gave 40% kill. The specified amounts of both compounds, when applied together, gave a 99% kill, with 73% expected from an additive effect. MECHANISM OF ACTION : None given.

Inventors:
Funke, Cristian
Fisher, liner
Reishaiga, Fisher
Hungenberg, Heike
Andersilles, Bolframm
Tielate, Wolfgang
Claus, Anton
Application Number:
JP2006541833A
Publication Date:
May 24, 2007
Filing Date:
November 20, 2004
Export Citation:
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Assignee:
Bayer Crop Science Actien Gezershaft
International Classes:
A01N43/56; A01N43/00; A01N43/34; A01N43/36; A01N43/38; A01N43/40; A01N43/88; A01P7/02; A01P7/04
Domestic Patent References:
JPH0725222A1995-01-27
JP2000507564A2000-06-20
JP2002513002A2002-05-08
JP2000516927A2000-12-19
JPH07252222A1995-10-03
Foreign References:
WO2003015518A12003-02-27
WO2003024222A12003-03-27
Attorney, Agent or Firm:
Yoshio Kawaguchi
Makoto Ono
Chihiro Watanabe
Kenkyo Kanayama
Katsuma Osaki
Mitsuaki Tsubokura