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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Oral acute toxicity study show that oral LD50 is > 2000 mg/kg. 
Dermal acute toxicity study show that dermal LD50 is > 2000 mg/kg.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 001 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 001 mg/kg bw

Additional information

Acute oral and dermal toxicity were evaluated in accordance with EU and OECD guidelines. The substance, under the test conditions, did not appear toxic by oral and dermal route.

Justification for classification or non-classification

According to Directive 67/548/EEC and to Regulation (EC) n. 1272/2008, the substance should not be classified for acute oral toxicity.

According to Directive 67/548/EEC and to Regulation (EC) n. 1272/2008, the substance should not be classified for acute dermal toxicity.