p-Tert-Butylphenol - UNEP Chemicals
p-Tert-Butylphenol - UNEP Chemicals
p-Tert-Butylphenol - UNEP Chemicals
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OECD SIDS P-TERT-BUTYLPHENOL<br />
B. Toxicodynamics, toxicokinetics<br />
122<br />
(a)<br />
Type: Metabolism<br />
14<br />
Results:<br />
C-labelled p-t-butylphenol was given intravenously to male Wistar rats at<br />
a single dose of 1.2 - 10.4 mg/kg b.w. Subsequently, bile and urine was<br />
collected for 4 hours. 65 - 71 % and 17 - 21 % of the applied dose were<br />
excreted as glucuronide conjugate and sulfate conjugate, respectively (total<br />
recovery of radioactivity: 91 - 93 %). The ratio of glucuronidation and<br />
sulfation was not dose-dependent.<br />
Remarks: D-Mannitol was infused to stimulate diuresis during the experiment. 14 Clabelled<br />
p-t-butylphenol dissolved in saline at pH 10.5 before dilution to<br />
the required concentration with saline.<br />
In vitro incubation of isolated hepatocytes with 3.6 - 120.2 mg/l at 37<br />
degree C for 1 hour supported these results concerning the ratio of<br />
conjugates and dose-dependency.<br />
Reference: Koster et al.: 1981<br />
(b)<br />
Type: Metabolism<br />
Results: [U- 14 C]p-t-butylphenol was given intravenously to rats at a dose of 18<br />
mg/kg b.w.. Urine and bile were collected during 24 hr and analyzed by<br />
thin layer chromatography. 1.5 ± 0.2 µmol was excreted as sulfate in the<br />
urine, while no significant amounts were found in the biliary excretes.<br />
Remarks:<br />
Reference: Nanbo: 1991<br />
(c)<br />
Type: Metabolism<br />
Results: In vitro incubation of 112.65 mg [U- 14 C]p-t-butylphenol with rat liver<br />
cytosol at 37 degree C for 1 h yielded 65.5 +/- 11.8 nmol/min/mg protein-1<br />
of sulfated TS.<br />
Remarks:<br />
Reference: Nanbo: 1991<br />
(d)<br />
Type: Distribution and Excretion<br />
14<br />
Results:<br />
C-labelled p-t-butylphenol (147 µg/kg/day) in Keltrol solution was<br />
administered to male Wistar rats by gavage daily for 3 days. Urine and<br />
feces were collected daily. 26.7 % and 72.9 % of the applied dose was<br />
eliminated via feces and urine, respectively. Distribution in tissues and<br />
organs was as follows: retention in abdominal adipose tissue: not<br />
detectable (< 0.01 %/g), liver: 0.02 %, lung: not detectable (< 0.01 %),<br />
carcass: 0.1 % (data in percent of the applied doses)<br />
Remarks: Post observation period was 4 days.<br />
Reference: Freitag et al.: 1982<br />
* 5.11 EXPERIENCE WITH HUMAN EXPOSURE<br />
A. Skin sensitization<br />
(a)<br />
Type: Patch Test<br />
Results: Sensitizing [X]; Not sensitizing [ ]; Ambiguous [ ] *See Remarks<br />
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