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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Description of key information

Acute oral: LD50(rat): > 2000 mg/kg bw

Key value for chemical safety assessment

Additional information

In an acute oral toxicity study performed according to the Acute Toxic Class method, 2000 mg/kg bw of the undiluted test item EEIM Acetate were administered to two test groups of three fasted Wistar rats by gavage.
The following test substance-related clinical observations were recorded:
2000 mg/kg (first test group): No mortality occurred. Impaired general state in two out of three animals. Dyspnoea in two out of three animals. Piloerection in two out of three animals.
2000 mg/kg (second test group): Mortality in one out of three animals. No clinical signs. Macroscopic pathological findings in the animal that died: -Liquid clear content in the stomach; -Enhanced bleeding in the glandular stomach.
The mean body weight of the surviving animals increased within the normal range throughout the study period. There were no macroscopic pathological findings in the surviving animals sacrificed at the end of the observation period. The acute oral LD50 was calculated to be LD50, oral, rat > 2000 mg/kg bw.

Justification for classification or non-classification

Based on the results, the test item is no subject to classification and labelling according to Regulation (EC) No 1272/2008 (CLP).