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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 />

<strong>UNEP</strong> Publications

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