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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Effects on fertility

Effect on fertility: via oral route
Endpoint conclusion:
no study available
Effect on fertility: via inhalation route
Endpoint conclusion:
no study available
Effect on fertility: via dermal route
Endpoint conclusion:
no study available

Effects on developmental toxicity

Effect on developmental toxicity: via oral route
Endpoint conclusion:
adverse effect observed
Dose descriptor:
NOAEL
30 mg/kg bw/day
Species:
rat
Effect on developmental toxicity: via inhalation route
Endpoint conclusion:
no study available
Effect on developmental toxicity: via dermal route
Endpoint conclusion:
no study available

Justification for classification or non-classification

One key study is available for this endpoint. In a developmental toxicity study according to OECD testing guideline 414, the test item was administered to female rats by gavage from days 6 through 19 of gestation. On the basis of the effects observed in this study, the LOEL for maternal toxicity was determined at 10 mg/kg/day (effects on maternal body weight) and the NOAEL for fetal and developmental toxicity at 30 mg/kg/day (growth retardation at 100 mg/kg bw/day).

Based on this data, no classification is required for the test item concerning the developmental toxicity endpoint according to the CLP criteria.

Additional information