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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

A skin sensitisation study with Glycolierral was performed according to an open epicutaneous test method. 21 consecutive days 3, 10, 30 and 100% test material was given to 8 animals for each concentration. The highest non irritant concentration after a single and after repeated applications was 3%. Higher concentrations caused very slight to slight irritation only.

No reactions were observed at the day 21 and 35 challenge in any of the test control group animals at any of the tested concentrations.

Based on these results Glycolierral is not regarded as a skin sensitizer.

Under the conditions of a repeated insult (occlusive) patch test procedure, the test substance 5% Sample D in DMP did not induce irritation nor show any evidence of induced allergic contact dermatitis in human subjects.


Migrated from Short description of key information:
A skin sensitisation study with Glycolierral was performed according to an open epicutaneous test method and a repeated insult (occlusive) patch test was performed.

Justification for selection of skin sensitisation endpoint:
Both studies showed no evidence of skin sensitisation.

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

Based on the results, Glycolierral does not have to be classified for skin sensitisation according to Regulation (EC) No 1272/2008.