Registration Dossier
Registration Dossier
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EC number: 402-070-1 | CAS number: 88122-99-0 UVINUL T 150
Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Additional information
No further reproductive testing is required as there is an exisiting pre-natal development toxicity study.
Short description of key information:
No further reproductive testing is required as there is an exisiting pre-natal development toxicity study.
Effects on developmental toxicity
Description of key information
A pre-natal developmental toxicity was conducted. The NOAEL was determined to be 1000 mg/kg bw.day for both maternal and foetal toxicity.
Effect on developmental toxicity: via oral route
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
Additional information
A reliable GLP study (OECD 414) was conducted to determine the effect of the substance on pre-natal developmental toxicity. No maternal toxicity was seen up to 1000 mg/kg bw/day. Furthermore, the substance was no toxic to either the soft or sketal tissues in the foetuses up to 1000 mg/kg bw.day. As such the NOAEL was determined to be 1000 mg/kg bw.day for both maternal and foetal toxicity.
Justification for classification or non-classification
A pre-natal developmental toxicity was conducted and no developmental toxicity was observed. Thus classification according to Regulation (EC) No 1272/2008 is not required.
Additional information
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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