Registration Dossier
Registration Dossier
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EC number: 232-391-0 | CAS number: 8013-07-8
Endpoint summary
Administrative data
Description of key information
The acute oral toxicity was observed in five male and five female rats over a period of 14 days. The LD50 was found to be greater than 5000 mg/kg.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 5 000 mg/kg bw
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Additional information
The acute oral LD50 was found to be greater than 5000 mg/kg. According to Directive 67/548/EEC, no classification is warranted. According to Regulation (EC) No. 1272/2008, no classification is warranted.
The only value given for dermal toxicity is that no effects occurred at greater than 20 mL/kg in rabbits - this is assumed to equate to greater than 2000 mg/kg bw
Justification for classification or non-classification
The acute oral LD50 was found to be greater than 5000 mg/kg. According to Directive 67/548/EEC, no classification is warranted. According to Regulation (EC) No. 1272/2008, no classification is warranted.
No classifiication is requiredfor dermal toxicity,based on limited information.
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