Registration Dossier
Registration Dossier
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
