𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Isolation and identification of metabolites of 2-ethylhexyl diphenyl phosphate in rats

✍ Scribed by Tomoko Nishimaki-Mogami; Ken-ichiro Minegishi; Akira Tanaka; Michio Sato


Publisher
Springer-Verlag
Year
1988
Tongue
English
Weight
552 KB
Volume
61
Category
Article
ISSN
0340-5761

No coin nor oath required. For personal study only.

✦ Synopsis


The metabolic fate of 2-ethylhexyl diphenyl phosphate (EHDPP) was studied in male rats. Orally administered 14C-EHDPP was rapidly absorbed and about 80% of the radioactivity was excreted in the urine and feces in the first 24 h. By 7 days, 48% and 52% of the radioactivity was recovered in urine and feces, respectively. Since biliary excretion was low (6% for 2 days), urine seems to be the major excretion route of EHDPP. Radioactivity was widely distributed in all tissues examined. At 2 h, the concentration was relatively high in blood, liver kidney and adipose tissue. The elimination of radioactivity from adipose tissue and liver was somewhat delayed, but almost all the radioactivity was eliminated by 7 days. The major metabolites in the urine were diphenyl phosphate (DPP) and phenol. p-Hydroxyphenyl phenyl phosphate (OH-DPP) and monophenyl phosphate (MPP) were also identified as minor metabolites.


πŸ“œ SIMILAR VOLUMES


Isolation and Identification of Three Ur
✍ Ralph HΓ€nni; Felix Bigler; Walter Meister; Gerhard Englert πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 German βš– 432 KB πŸ‘ 1 views

## Abstract After the intraperitoneal administration of high doses of ^14^C‐ and ^3^H‐labelled retinoic acid (**1**) to rats three major urinary metabolites have been isolated in microgram amounts by use of column, thin‐layer and high‐pressure liquid chromatography. Their structures were elucidated

Cytogenetic evaluation of di-(2-ethylhex
✍ Putman, D. L. ;Moore, W. A. ;Schechtman, L. M. ;Hodgson, J. R. πŸ“‚ Article πŸ“… 1983 πŸ› Wiley (John Wiley & Sons) βš– 283 KB πŸ‘ 1 views

Di-(2-ethylhexyl)phthalate (DEHP) and its two major metabolites, mono-(2-ethyl-hexy1)phthalate (MEHP) and 2-ethylhexanol (EH), were evaluated for their ability to induce chromosomal damage in male Fischer 344 rats after oral administration. Dose levels, the highest of which represents one-tenth of t