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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

In the LLNA assay, no signs of systemic toxicity were noticed. The test substance neither induced a concentration dependent and biologically relevant response in the auricular lymph node cell counts, nor an increase in ear weights. The lymph node weights changes followed the lymph node cell count. The increase of 3H-thymidine incorporation into the cells was neither concentration dependent, nor biologically relevant at the concentrations tested.


Migrated from Short description of key information:
A Local Lymph Node Assay (LLNA) according to OECD guideline 429 was conducted in compliance with GLP. The test substance was demonstrated to be no sensitizer.

Respiratory sensitisation

Endpoint conclusion
Additional information:

No data available.


Migrated from Short description of key information:
No data available.

Justification for classification or non-classification

It is concluded that ULS-611 does not show a skin sensitizing effect in the LLNA under the test conditions chosen and thus classification is not warranted.