Abstract
In laboratory studies, the herbicide 3'-chloro-2-methyl-p-valerotoluidide (solan) when applied to soil was transformed in part to 3,3'-dichloro-4,4'-dimethylazobenzene. The biochemically mediated transformation followed the pattern established previously for 3,4-dichloroaniline-based acylanilides, but the 3-chloro-4-methylaniline intermediate did not accumulate. Compared to 3,4-dichloroaniline-based acylanilides, solan yielded less azo residue and did not inhibit soil respiration, even if applied at 200 times the recommended field rate.
Publisher
Cambridge University Press (CUP)
Subject
Plant Science,Agronomy and Crop Science
Cited by
12 articles.
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