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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Skin sensitisation

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

The test substance registered was tested in an OECD 429 LLNA (Skin Sensitisation: Local Lymph Node Assay) test. The test substance was applied to the mouse ear at concentrations of 5%, 10% and 25 % in ethanol/ water, 7/3 v/v. No clinical signs were observed in any animal of groups 0% (control), 5% and 10%. On second application day a slight erythema was observed at both application sites of the 25% group persisting for a total of 2 days. The result obtained were the corresponding stimulation index (SI) with 0.9, 1.1 and 1.6, respectively. Based on this test results the test substance was found to be a non-sensitizer.


Migrated from Short description of key information:
With the test substance registered an OECD 429 LLNA (Skin Sensitisation: Local Lymph Node Assay) test was performed.

Respiratory sensitisation

Endpoint conclusion
Additional information:
Migrated from Short description of key information:
no data available

Justification for classification or non-classification

Based on an OECD 429 LLNA test (Skin Sensitisation: Local Lymph Node Assay) performed with the test substance registered the test substunce is not sensitizing and has not to be classified.