N’-(4-Chloro-o-tolyl)-N,N-Dimethylformamidine-14C (Galecron) and 4-Chloro-o-touidine-14C Metabolism in the White Rat1

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Abstract
The systemic acaricide Galecron® and a Galecron metabolite, 4-chloro-o-toluidine-14C, were given orally to white rats at a radioactivity level of 3µCi per rat. 4-Chlorootoluidine was absorbed and degraded more slowly than was Galecron. Galecron and 4-chloro-o-toluidine were Callverted to more polar metabolites, and by 72 hr after treatment, 96% of the administered dose was eliminated in the urine and feces in both cases.