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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity in vitro

Description of key information

The test material was not genotoxic to Salmonella and E. Coli strains with and without metabolic activation.

No cytotoxic response was seen in the dose range finding study.

The positive control exhibited at least a 3 fold increase in revertant colonies.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

Additional information from genetic toxicity in vitro:

All of the data available for the registered substance to assess the mutagenic, clastogenic and genotoxic effects

of the substance in vitro and in vivo. All the studies achieved negative results.

Data have been included that were conducted on sodium and magnesium salts. The sodium and magnesium ions

are considered likely to be more active than calcium and the data is therefore considered suitable as supporting

data for the endpoint.

The following information is taken into account for any hazard / risk assessment:

A number of genotoxicity studies have been conducted in vitro and in vivo to determine the genotoxic effects of

the registered substance

Justification for selection of genetic toxicity endpoint

The test material was not genotoxic to Salmonella and E. Coli strains with and without metabolic activation.

Justification for classification or non-classification

Based on the in vitro and in vivo data available for the substance, the substance is considered to be not

genotoxic.