Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

approx. LD50 (oral, rat, screening level study): >300 mg/kg bw
approx. LD50 (dermal, rat, screening level study): > 2000 mg/kg bw

Key value for chemical safety assessment

Additional information

Available information from screening level studies:

approx. LD50 (oral, rat): >300 mg/kg bw

approx. LD50 (dermal, rat): > 2000 mg/kg bw

Only two screening level studies are available for acute oral and dermal toxicity. The results given above provide useful information about the corresponding properties of the substance. However the reliability, relevance and adequacy of the data are considered as limited and an overall reliability rating of 3 (= not reliable, according to the scoring system of Klimisch et al.) has been assigned. As a consequence, these data are not adequate for risk assessment and classification and labelling purposes.

Justification for classification or non-classification

Due to the low overall reliability rating of the available studies (see above under "Discussion"), the corresponding data are not adequate for a definitive decision about classification according to Regulation (EC) 1272/2008.

Based on the available information the substance does not meet the criteria for classification for "acute oral toxicity" under Regulation (EC) 1272/2008, Annex I, Part 3, 3.1.2; reason for non-classification: inconclusive.

Based on the available information the substance does not meet the criteria for classification for "acute dermal toxicity" under Regulation (EC) 1272/2008, Annex I, Part 3, 3.1.2; reason for non-classification: inconclusive.