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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

No acutely toxic effects were observed in rats via oral, inhalation and dermal exposure.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

Justification for classification or non-classification

The substance did not cause any signs of toxicity in rats via oral, inhalation or dermal exposure. The lowest LD50 (oral, gavage) is >5000 mg/kg bw. The LC0 (inhalation, saturated vapour, 8 h) is > saturation limit. The lowest LD50 (dermal) is >2500 mg/kg bw. The substance does not meet the classification criteria of the CLP Regulation.