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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

NOEL (28 days): 1000 mg/kg/day

Key value for chemical safety assessment

Toxic effect type:
dose-dependent

Repeated dose toxicity: via oral route - systemic effects

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
1 000 mg/kg bw/day
Study duration:
subacute
Species:
rat

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

In this subacute 28-day toxicity study, the test item was administered daily by gavage to SPF-bred Wistar rats. The study comprised of four groups.


FINDINGS:


At 50 mg/kg/day: No treatment-related changes detected.


At 200 mg/kg/day: No treatment-related changes detected.


At 1000 mg/kg/ day: No treatment-related changes detected.

Justification for classification or non-classification

Based on the information available for repeated dose toxicity and according to the CLP Regulation n.1272/2008, table 3.9.1 ,  the substance is not classified for specific target organ toxicity-repeated exposure.