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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The sensitizing potential of the test item was assessed in vivo in a non-adjuvant Buehler test (OECD 406). No skin reactions were observed after the challenge exposure during the entire observation period of 48 hours (the sensitisation rate was 0%).

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not sensitising)
Additional information:

Skin Sensitisation study with the substance

The potential skin sensitising properties of the test item were assessed in the guinea pig sensitisation test carried out as the non-adjuvant Buehler test using 20 test and 10 control animals. Following three epidermal induction exposures to the test article at 100 %, the animals were subjected two weeks later to a epidermal challenge exposure with the test article at the concentration of 25 %. Responses to the challenge procedure were evaluated 24 and 48 h after the end of the exposure period. No allergic or other skin reactions were observed during the entire observation period. The sensitisation rate was 0 % at 24 and 48 h after the end of the exposure period. No other signs of clinical toxicity were observed (Toxlabs Bioscience GmbH 1998).

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

The test item was not sensitising to skin. Therefore no classification and labelling is warranted according to EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008