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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

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

A study was conducted to determine the acute oral toxicity of the test substance according to OECD Guideline 423. Male and female Wistar rats were exposed by oral gavage at a concentration of 2000 mg/kg bw. Treatment was followed by a 14 d observation period. No mortality, significant body weight changes, clinical signs or anomalies following gross pathology examination were observed. Under the study conditions, the LD50 of the test substance to rat was determined to be >2000 mg/kg bw (Müller, 2001).

Justification for classification or non-classification

Based on available acute oral toxicity data, the substance does not require classification for acute endpoints according to CLP (Regulation 1272/2008) criteria.