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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

OECD406, GMPT, not skin sensitizer

Key value for chemical safety assessment

Skin sensitisation

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

The analogue substance 2 was tested for its sensitizing effect on the skin of the guinea pig in the Maximization Test based on the method of Magnusson and Kligman according to OECD guideline 406 (BASF 1988). After the challenge application, no cutaneous reactions were observed in the animals of the control and test groups at the 24-hour and 48-hour readings.

Justification for classification or non-classification

According to the CLP Regulation (EC n. 1272/2008) the following classifications apply:

skin sensitizer Cat 1A, with GPMT:

≥ 30 % is responsive to ≤ 0,1 % of the intradermal induction dose or

> 60 % is responsive to > 0,1 %- ≤ 1 % of the intradermal induction dose

 

skin sensitizer Cat 1B, with GPMT

≥ 30 % to < 60 % is responsive to > 0,1 % - ≤ 1 % of the intradermal induction dose or,

≥ 30 % is responsive to > 1 % of the intradermal induction dose

 

Based on the results of the skin sensitization test (GPMT) the substance is not classified as skin sensitizer