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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

A high quality, guideline- and GLP-compliant 28-day oral rat study is available.

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Study duration:
subacute
Species:
rat
Quality of whole database:
A high quality, guideline- and GLP-compliant 28-day rat study is available. A waiver is proposed for the 90-day study in the absence of any effects in the 28-day study and as systemic exposure is unlikely.

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available
Quality of whole database:
No study is available.

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion
Endpoint conclusion:
no study available
Quality of whole database:
No study is available.

Repeated dose toxicity: dermal - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available
Quality of whole database:
No study is available.

Repeated dose toxicity: dermal - local effects

Endpoint conclusion
Endpoint conclusion:
no study available
Quality of whole database:
No study is available.

Additional information

No effects of treatment were observed in a 28 -day oral (gavage) rat study at the limit dose of 1000 mg/kg bw/d. A waiver is proposed for the 90-day study in the absence of any effects in the 28-day study and as systemic exposure is unlikely.

Justification for classification or non-classification

The substance is of very low toxicity following repeated oral exposure; the available data do not warrant classification for STOT-RE under the CLP Regulation.