Registration Dossier
Registration Dossier
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EC number: 911-238-8 | CAS number: -
Endpoint summary
Administrative data
Description of key information
Acute oral toxicity (OECD 423, EU Method B.1 tris): LD50 >2000 mg/kg bw.
Acute dermal toxicity (OECD 402, EU Method B.3): >2000 mg/kg bw
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Additional information
Acute oral toxicity: The key study is a recent study (2005), performed according to actual guidelines. The test substance was administered in CMC/Tween 80 yielding a LD50 of >2000 mg/kg bw. There were no adverse effects noted in the animals.
Acute dermal toxicity: The key study is a recent study, performed according to actual guidelines. The LD50 was >2000 mg/kg bw and no adverse effects were noted in the animals.
Justification for classification or non-classification
According to REGULATION (EC) No 1272/2008 the test item does not require classification for acute oral or 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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