Registration Dossier
Registration Dossier
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EC number: 215-951-9 | CAS number: 1459-93-4
Endpoint summary
Administrative data
Description of key information
The LD50 for acute oral toxicity in rats is > 2000 mg/kg bw. The acute dermal toxicity in rats is > 2000 mg/kg bw.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Additional information
In OECD guideline protocols, rats were administered the test material either orally or dermally at limit doses of 2000 mg/kg bw. There was no mortality and no adverse effects observed. The LD50 values are > 2000 mg/kg bw in rats.
Justification for selection of acute toxicity – oral endpoint
guideline method under GLP
Justification for selection of acute toxicity – dermal endpoint
guideline method under GLP
Justification for classification or non-classification
In OECD guideline protocols, rats were administered the test material either orally or dermally at limit doses of 2000 mg/kg bw. The LD50 values are > 2000 mg/kg bw in rats for both oral and dermal toxicity. According to Regulation EC No. 1272/2008, the values do not meet the criteria for classification. The substance is not classified for acute oral toxicity or acute dermal toxicity.
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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