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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Key value for chemical safety assessment

Effects on fertility

Effect on fertility: via oral route
Endpoint conclusion:
no study available (further information necessary)
Effect on fertility: via inhalation route
Endpoint conclusion:
no study available
Effect on fertility: via dermal route
Endpoint conclusion:
no study available
Additional information

An OECD 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test) study has been conducted to address this endpoint. However, the study report was provided by the testing laboratory very close to the registration deadline and the content is still under discussion. As such, it is currently not possible to report these results and set final effect levels for this substance. In addition, there has not been sufficient time to develop a suitable strategy in order to determine any potential classification and labelling and/or further testing proposals.

These issues will be revisited once the results are confirmed and an appropriate registration update will be submitted as soon as possible.

Effects on developmental toxicity

Effect on developmental toxicity: via oral route
Endpoint conclusion:
no study available (further information necessary)
Effect on developmental toxicity: via inhalation route
Endpoint conclusion:
no study available
Effect on developmental toxicity: via dermal route
Endpoint conclusion:
no study available
Additional information

An OECD 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test) study has been conducted to address this endpoint. However, the study report was provided by the testing laboratory very close to the registration deadline and the content is still under discussion. As such, it is currently not possible to report these results and set final effect levels for this substance. In addition, there has not been sufficient time to develop a suitable strategy in order to determine any potential classification and labelling and/or further testing proposals.

These issues will be revisited once the results are confirmed and an appropriate registration update will be submitted as soon as possible.

Justification for classification or non-classification

In accordance with the criteria for classification as defined in Annex I, Regulation 1272/2008, the test material does not require classification for reproductive or developmental toxicity.

Additional information