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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 read across approach, oral acute toxicity studies show that oral LD50 is > 2000 mg/kg.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
read-across based on grouping of substances (category approach)
Adequacy of study:
key study
Justification for type of information:
The target substance is included in a category where a trend is identified. Data for the substances at the opposite sites indicate that they are not classified, therefore, the substance is not classified for acute oral toxicity for interpolation. See Category rationale for further details.
Key result
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Interpretation of results:
GHS criteria not met
Conclusions:
Based on read across approach, the derived oral toxicity of the substance is LD50 > 2000 mg/kg.

Additional information

Justification for classification or non-classification

Since the substance has kinematic viscosity lower than 20.5 mm²/s, it should be classified as "Asp. Tox. 1, H304" in accordance with Regulation EC n. 1272/2008.

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