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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
developmental toxicity
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because the substance is of low toxicological activity (no evidence of toxicity seen in any of the tests available), it can be proven from toxicokinetic data that no systemic absorption occurs via relevant routes of exposure (e.g. plasma/blood concentrations below detection limit using a sensitive method and absence of the substance and of metabolites of the substance in urine, bile or exhaled air) and there is no or no significant human exposure
Justification for type of information:
Data of developmental toxicity on humans are available (see section 7.10)

Data source

Materials and methods

Test animals

Species:
other: no data
Strain:
not specified

Results and discussion

Results (fetuses)

Effect levels (fetuses)

Remarks on result:
not measured/tested
Remarks:
Data of developmental toxicity on humans are available (see section 7.10)

Fetal abnormalities

Abnormalities:
not examined
Description (incidence and severity):
Data of developmental toxicity on humans are available (see section 7.10)

Overall developmental toxicity

Developmental effects observed:
not specified

Applicant's summary and conclusion