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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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

No studies for acute toxicity with sodium 2-methylbutan-2-olate are available. According to the REACh Regulation (EC) No 1907/2006, Article 18.2 no further studies need to be conducted. The available data regarding skin irritation demonstrate that Sodium 2-methylbutan-2-olate has a corrosive potential to skin. According to the REACh Regulation (EC) No 1907/2006, Annex VII and Annex VII, column 2 point 8.5 a study of acute toxicity does not need to be performed if the substance is classified as corrosive to skin. The test substance hydrolyses rapidly in contact with water into 2-methylbutan-2-ol and sodium hydroxide. Therefore, the hydrolysis products are considered to be relevant for acute toxicity.

Justification for classification or non-classification

The test substance hydrolyses rapidly in contact with water. Therefore, the hydrolysis products are considered to be relevant for classification according to CLP Regulation (EC) No 1272/2008. For both hydrolysis products disseminated dossiers are available on the homepage of ECHA.

The hydrolysis product sodium hydroxide (CAS No. 1310-73-2) showed no acute toxicity and is not classified for acute toxicity. The second product 2-methylbutan-2-ol (CAS No. 75-85-4) is not classified as orally toxic. However, it is classified as acute toxic category 4 by inhalation route according to Annex VI of the CLP Regulation (EC) No 1272/2008 and is classified as acute toxic by the dermal exposure route according to the disseminated dossier. Based on this data, the test substance should also be classified as acute toxic, category 4 by dermal and inhalative route.