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Trimellitate Category; Revised Summaries - US Environmental ...

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5. Toxicity Id 53894-23-8<br />

5.1 .I ACUTE ORAL TOXICITY<br />

5.4<br />

5.5<br />

5.6<br />

5.8<br />

5.9<br />

Type<br />

Species<br />

Strain<br />

Sex<br />

Number of animals<br />

Vehicle<br />

Value<br />

Method<br />

Year<br />

GLP<br />

Test substance<br />

Remark<br />

Test condition<br />

Test substance<br />

Conclusion<br />

Reliability<br />

Flag<br />

28.12.2000<br />

REPEATED DOSE TOXICITY<br />

GENETIC TOXICITY ‘IN VITRO‘<br />

GENETIC TOXICITY ‘IN VITRO‘<br />

TOXICITY TO REPRODUCTION<br />

DEVELOPMENTAL TOXlClTY/TERATOGENlClTY<br />

Date 15.032002<br />

LD50<br />

rat<br />

Sprague-Dawley<br />

male<br />

20<br />

no data<br />

> 10000 mg/kg bw<br />

other<br />

1969<br />

no<br />

other TS<br />

No rats died during the study. At the two higher dose levels, decreased<br />

activity was observed one hour after dosing. Excessive urination and/or<br />

diarrhea were initially observed but decreased by 48 hours (5000 mglkg<br />

level) or by Day 5 (10,000 mg/kg level).<br />

Immediately following a 3-4 hour fasting period, animals were administered<br />

the test compound at doses of 417, 1450, 5000 and 10000 mg/kg of body<br />

weight. Observations were recorded immediately after dosing, then at I, 4<br />

and 24 hours; and once daily thereafter for 14 days. Gross necropsies<br />

were conducted on all animals that were sacrificed at the termination of the<br />

study.<br />

1,2,4-benzenetricarboxylic acid, triisononyl ester (triisononyl phthalate)<br />

Under the conditions of this study, the test material has a low order of<br />

acute oral toxicity.<br />

(2) valid with restrictions<br />

Critical study for SIDS endpoint<br />

(1)

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