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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Based on the result of the in-vitro skin corrosion study the test item is classified into Skin Corr. Category 1B. According to REACH Annex VII 8.5. column 2 acute toxicity studies do not need to be conducted if the substance is classified as corrosive to the skin.


Assessment of the test item concerning acute oral toxicity is not possible because no data are available for this toxicological endpoint. A data waiver is claimed.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for selection of acute toxicity – oral endpoint
According to REACH Annex VII 8.5. column 2 an acute oral toxicity study does not need to be conducted if the substance is classified as corrosive to skin.

Justification for classification or non-classification

According to REACH Annex VII 8.5. column 2 acute toxicity studies do not need to be conducted if the substance is classified as corrosive to skin. Therefore, no data are available for these toxicological endpoints. Due to the fact that there are no data available from structural analogues, the test item is not classified according to EC Regulation 1272/2008.