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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Endpoint summary

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Administrative data

Description of key information

The test article is not considered to be a sensitizer.

Key value for chemical safety assessment

Skin sensitisation

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

No information are available for the substance, but there is a study that was conducted with a substance made by the same components , but different mixture; therefore the similarity is very high. The test was conducted with international guidelines and it is GLP compliant; the purity of the substance is 94 %. In this study 15% of the animals were positive after treatment with a non irritant test substance concentration of 15 % in bi-distilled water.

Justification for selection of skin sensitisation endpoint:

The study was conducted with a substance made by the same components , but different mixture; therefore the similarity is very high. The test was conducted with international guidelines and it is GLP compliant.

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

According to the CLP Regulation (EC n. 1272/2008) section 3.4.1.2: Skin sensitiser means a substance that will lead to an allergic response following skin contact.

The substance is capable to induce allergic reactions to 15 % of the animals. The table 3.4.4 of the CLP Regulation (EC n. 1272/2008) shows that the trigger value for classification is 30 % responding at > 1 % intradermal induction dose. The substance is below the trigger value, therefore no classification is warranted for skin sensitisation according to the CLP Regulation (EC n. 1272/2008)