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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

oral: The median lethal dose (LD50) of EMIM Methansulfonat after oral administration was found to be greater than 2000 mg/kg bw in rats.

Key value for chemical safety assessment

Additional information

acute toxicity (oral):

In an acute oral toxicity study performed according to the Acute Toxic Class method, 2000 mg/kg bw of the undiluted test item EMIM Methansulfonat was administered to two test groups of three fasted Wistar rats by gavage. The mean body weight increased within the normal range throughout the study period. There were no macroscopic pathological findings in the animals sacrificed at the end of the observation period. The acute oral LD50 was calculated to be greater than 2000 mg/kg bw. [BASF, 2011]

Justification for classification or non-classification

Classification for acute oral toxicity is not warranted according to the criteria of EU Directive 67/548/EEC and EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No 1272/2008.