Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 hazard was identified after one administration by oral or dermal route in rodents according to OECD tests n° 423 and 402 (tests were performed with the registered substance at 25%)

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
Quality of whole database:
Klimich 1: the study was conducted according to OECD guideline 423, GLP study

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw
Quality of whole database:
Klimich 1: the study was conducted according to OECD guideline 402, GLP study

Additional information

Justification for selection of acute toxicity – inhalation endpoint
Acute toxicity data are already available for the oral route and for the dermal route.
Vapor pressure is expected to be low

Justification for classification or non-classification

The registered substance is not classified for health