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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Additional information

There is no need for in-vivo testing because all in-vitro endpoints were clearly negative, with and without metabolic activation.

Short description of key information:
Di-2-EHTDG was negative in all in-vitro assays (gene mutation in bacteria, cytogenicity, and gene mutation in mammalian cells).

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Di-2 -EHTDG was negative in all in-vitro assays.