Registration Dossier
Registration Dossier
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EC number: 407-250-3 | CAS number: -
Endpoint summary
Administrative data
Description of key information
oral (rat): >5000 mg/kg bw (m+f)
dermal (rat): >2000 mg/kg bw (m+f)
Key value for chemical safety assessment
Additional information
The test substance was tested for acute toxicity via oral and dermal application to rats.
Acute oral toxicity:
The test substance was applied to male and female rats at 5000 mg/kg bw. No mortality or signs of toxicity occured.
An LD50 of > 5000 mg/kg bw was therefore identified via oral application for rats.
Acute dermal toxicity:
The test substance was applied to male and female rats at 2000 mg/kg bw. No mortality or signs of toxicity occured.
An LD50 of > 2000 mg/kg bw was therefore identified via dermal application for rats.
The substance is considered not acute toxic.
The studies were found to be adequate to fufill the purposes of this endpoint.
Justification for classification or non-classification
There are conclusive but not sufficient data for classification of the test substance with regard to acute toxicity.
The substance is not classified for acute toxicity via oral or dermal route in accordance to Directive 67/548/EEC or the CLP Regulation (EC) No 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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