Registration Dossier
Registration Dossier
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EC number: 700-857-7 | CAS number: -
Endpoint summary
Administrative data
Description of key information
Two studies are available for acute oral toxicity: one in rats showing a combined oral LD50 equal to 3170 mg/kg bw with 95% confidence limits between 2260 and 4000 mg/kg bw, and one supporting study in mice showing an oral LD50 of 3600 mg/kg bw.
In an acute dermal toxicity study similar to OECD guideline 402, mortality was 0/5 male and 0/5 female at 2000 mg/kg bw and 4/5 males and 1/5 female at 5000 mg/kg bw.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 3 170 mg/kg bw
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Additional information
Two studies are available for acute oral toxicity: one in rats showing a combined oral LD50 equal to 3170 mg/kg bw with 95% confidence limits between 2260 and 4000 mg/kg bw, and one supporting study in mice showing an oral LD50 of 3600 mg/kg bw.
In an acute dermal toxicity study similar to OECD guideline 402, mortality was 0/5 male and 0/5 female at 2000 mg/kg bw and 4/5 males and 1/5 female at 5000 mg/kg bw.
Justification for classification or non-classification
LD50 in acute oral and dermal toxicity studies conducted similar to OECD guidelines were higher than 2000 mg/kg bw therefore the substance is not classified according to the Annex VI to the Directive 67/548/EEC and the CLP Regulation (EC) N° (1272-2008).
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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