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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Not skin sensitizer.

Key value for chemical safety assessment

Skin sensitisation

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

The Guinea Pig Maximisation Test was performed according to OECD 406 (1992). A total of 27 animals were used, 15 for the main study (10 test and 5 control) and 12 for the primary study.

The induction phase was accomplished by both intradermal and epicutaneous application. In the challenge phase, the test substance resulted in a sensitisation rate of 0 %, when tested at the maximum testable epidermal applications of 0.5 and 1 % v/v test article.


The substance did not show sensitising effects on tested animals.

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

According to the Regulation EC 1278/2008 (CLP) the substance does not meet the criteria for classification, since the sensitisation rate is lower than 30 %, minimum threshold value required for classification.