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| | N,N-Diethyl meta toluamide Basic information |
| | N,N-Diethyl meta toluamide Chemical Properties |
| | N,N-Diethyl meta toluamide Usage And Synthesis |
| Metabolic pathway | The phenobarbital-treated rat liver microsomal
incubation with N,N-diethyl-m-toluamide (DEET) yields
the three major metabolites, N-ethyl-m-toluamide, N,N-
diethyl-m-(hydroxymethyl)benzamide, and N-ethyl-m-
(hydroxymethyl)benzamide and the two minor
metabolites, toluamide and N,N-diethyl-m-formyl-
benzamide. The metabolic transformation involves N-dealkylation which is competitive with the oxidation
of the methyl group on the phenyl ring. The aldehydes
that are derived from the hydroxymethyl analogs are
reduced back to the corresponding alcohols. |
| | N,N-Diethyl meta toluamide Preparation Products And Raw materials |
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