Metabolism of derivatives of toluene. 3. o-, m- and p-xylenes
- 1 January 1949
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 45 (2) , 241-244
- https://doi.org/10.1042/bj0450241
Abstract
All 3 xylenes are mainly oxidized to the corresponding toluic acids (60, 81 and 88%, respectively). The resulting o-toluic acid is excreted mainly unconjugated and as an ester glucuronide (30% of the dose), but a small amt. (0.3% by isolation) is conjugated. The toluic acids from m- and p-xylenes are excreted chiefly as glycine conjugates, only small amts. being excreted free or conjugated with glucuronic acid. Evidence of hydroxylation was obtained in the case of all 3 isomers: 6 and 4% of doses of o- and m-xylenes, respectively, are excreted as ethereal sulfate and 10-15% of o-xylene is probably excreted as an ether glucuronide. p-Xylene may give rise to a xylenol.Keywords
This publication has 4 references indexed in Scilit:
- Metabolism of derivatives of toluene. 1. The metabolism of acetotoluidides in the rabbitBiochemical Journal, 1948
- Quantitative aspects of benzoyl glucuronate formation in normal individuals and in patients with liver disordersThe American Journal of Medicine, 1947
- The fate of certain organic acids and amides in the rabbitBiochemical Journal, 1947
- The fate of certain organic acids and amides in the rabbitBiochemical Journal, 1946