Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Selective insecticides based on anthranilic acid diamides and safeners

An active, alkyl-based technology for use in biological control chemicals, biocides, biocides, etc.

Inactive Publication Date: 2008-12-31
BAYER CROPSCIENCE AG
View PDF70 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the activity of these mixtures is not always optimal

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Selective insecticides based on anthranilic acid diamides and safeners
  • Selective insecticides based on anthranilic acid diamides and safeners
  • Selective insecticides based on anthranilic acid diamides and safeners

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0182] In the definitions above and below, a saturated or unsaturated hydrocarbon group such as an alkyl, alkenyl or alkanediyl group - including in combination with a heteroatom as in an alkoxy group - may each be straight-chain or branched.

[0183] Unless stated otherwise, optionally substituted radicals can be monosubstituted or polysubstituted, where in the case of multiple substitution the substituents can be identical or different.

[0184] C 1 -C 20 The definition of alkyl includes the widest range of alkyl groups defined herein. Specifically, this definition includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, 1-methylbutyl, 2-methyl butylbutyl, 3-methylbutyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, and each All isomeric hexyl groups (such as n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,2-dimethylbutyl , 1,3-dimethylbutyl, 2,3-dimethylbutyl, 1,1-dimethylbut...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to the use of selective insecticides for controlling insects and / or arachnids. The selective insecticides are characterized by an active moiety of an active substance combination comprising: (a) at least one anthranilic acid amide of formula (III), wherein A1C, A2C, XC, R1C, R2C, R3C, R4C, R5C, R7C, R8C and R9C; have the meanings indicated in the description, and (b) at least one compound that improves crop plant tolerance and is part of the group of compounds indicated in the description, especially cloquintocet-mexyl, isoxadifen-ethyl, and mefenpyr-diethyl. The invention also discloses a method for controlling insects and / or arachnids using the inventive insecticides.

Description

[0001] This application is a divisional application of the No. 200580024810.X invention patent application submitted on July 18, 2005. technical field [0002] The present invention relates to a compound combination (combination) having selective insecticidal and / or acaricidal effects, said combination comprising, first, a halogenated alkyl nicotinic acid derivative, phthalamide or anthranilamide ( anthranilic acid diamide), and, secondly, at least one compound that improves the compatibility of crop plants, and also relates to the use of said combination for the selective control of insects and / or spider mites (spider mite) in various beneficial crop plants )the use of. Background technique [0003] Certain haloalkylnicotinic acid derivatives are known to have insecticidal properties (EP-A 0 580 374, JP-A 7-010841, JP-A 7-025853, JP-A 10-101648, JP-A 10-195072, JP-A 11-180957, JP-A 2002-205991, JP-A 2003-113179, JP-A 2004-035439, JP-A 2004-083415, WO 98 / 57969, WO 99 / 59993,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A01N47/34A01N43/40A01N47/12A01N41/10A01N43/56A01P7/00
CPCA01N37/20A01N41/10A01N43/56A01N47/34A01N47/30A01N47/28A01N47/16A01N43/80A01N43/76A01N43/653A01N43/54A01N43/42A01N41/06A01N25/32A01N47/12A01N43/40A01N2300/00A01N43/08A01N37/28
Inventor R·菲舍尔R·费希尔C·冯克A·亨赛W·安德施H·亨格伯格W·蒂勒特U·雷克曼L·威尔姆斯C·阿诺德
Owner BAYER CROPSCIENCE AG
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com