Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Toxicity to reproduction

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Administrative data

Endpoint:
screening for reproductive / developmental toxicity
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because a pre-natal developmental toxicity study is available
Cross-reference
Reason / purpose for cross-reference:
data waiving: supporting information
Reference
Endpoint:
developmental toxicity
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Justification for type of information:
Based on the explanation given in the read-across assessment framework document (attached in IUCLID section 13.2) an analogue approach for read-across of the endpoint “developmental toxicity" from the structural analogues to the target substance is considered justified.
Reason / purpose for cross-reference:
read-across source
Reason / purpose for cross-reference:
read-across source
Species:
rat
Key result
Remarks on result:
not determinable due to absence of adverse toxic effects
Remarks:
no effects where observed with neither of the two source substances (managnese alumina pink corundum and chromium iron oxide)
Abnormalities:
no effects observed
Key result
Remarks on result:
not determinable due to absence of adverse toxic effects
Remarks:
no effects where observed with neither of the two source substances (managnese alumina pink corundum and chromium iron oxide)
Abnormalities:
no effects observed
Developmental effects observed:
no

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion