Herbicidal Compositions With Safeners for Crop Tolerance
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Solution Overview
Problem
Existing herbicidal compositions exhibit unfavorable biological properties, such as herbicidal action, tolerance by crop plants, and toxicological and ecotoxicological issues.
Innovation Solution
Development of herbicidal compositions comprising a specific N-(1,3,4-oxadiazol-2-yl)arylcarboxamide compound with absolute configuration (component A) and one or more herbicides (component B) selected from groups B1, B2, B5, B6, B8, and B9, optionally combined with safeners (component C) like benoxacor or cyprosulfamide, applied in various formulations for pre- and post-emergence weed control.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If existing N-(1,3,4-oxadiazol-2-yl)arylcarboxamide herbicidal compositions are used, then herbicidal activity is achieved, but unfavorable biological properties including poor crop plant tolerance and toxicological issues occur
Solution Approach 1:
The patent applies parameter changes by specifying a particular absolute configuration (enantiomer or diastereomer) of the N-(1,3,4-oxadiazol-2-yl)arylcarboxamide compound. This stereochemical parameter change results in improved crop plant tolerance while maintaining herbicidal activity, directly resolving the contradiction between herbicidal efficacy and phytotoxicity
Solution Approach 2:
The patent combines the specific enantiomer or diastereomer of N-(1,3,4-oxadiazol-2-yl)arylcarboxamide with safeners (such as benoxacor, cyprosulfamide, or dichlormid) to create a composite herbicidal composition. This composite approach enhances crop plant tolerance through synergistic protection while maintaining effective weed control
2Reliability
If existing herbicidal compositions are used, then weed control is achieved, but unfavorable toxicological and ecotoxicological properties occur
Solution Approach 1:
The patent changes the stereochemical parameter of the herbicidal composition by using a specific enantiomer or diastereomer of the N-(1,3,4-oxadiazol-2-yl)arylcarboxamide compound. This parameter change improves the toxicological and ecotoxicological profile while preserving herbicidal efficacy against weeds
Solution Approach 2:
The patent converts the potential harm of racemic or mixed stereoisomer compositions into benefit by isolating and using only the beneficial enantiomer or diastereomer. This selective approach eliminates or reduces toxicological and ecotoxicological issues while maintaining or improving weed control effectiveness
Data Source
AI summary
Herbicidal compositions are described, comprising an N-(1,3,4-oxadiazol-2-yl)arylcarboxamide and further herbicides.


