Registration Dossier
Registration Dossier
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EC number: 700-087-1 | CAS number: 201872-72-2
Endpoint summary
Administrative data
Description of key information
The acute oral toxicity to rats was evaluated by acute toxic class method. The test item was administerd to six female rats in a single dose by gavage at a dose fo 2000 mg/kg body weight. The animals were observed for mortality and any sub-lethal effects for 14 days after dosing.
Key value for chemical safety assessment
Additional information
No treatment related mortality or any other sublethal symptoms were observed within the 14 day post-dosing period at step 1 and 2. According to the acute toxic class method regime, no further testing was required. Under the conditions of this acute oral toxicity test the test item showed no acute oral toxic characteristics (LD50 rat, oral: >2000 mg/kg bw).
Justification for classification or non-classification
According to EU GHS (EC Regulation 1272/2008) criteria the test item has not to be classified.
According to EC Directive 67/548/EEC criteria the test item has not to be classified.
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