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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity in vitro

Description of key information

No data is available on the substance.

However, information of Similar Substance is reported. Similar Substance, historically named as Acid Yellow 099 (EC 233-748-3), was tested in FAT 20'040/B. No determination of components of this FAT was carried out, thus no conclusion could be drawn whether Similar Substance is a multi-constituent or an UVCB. Accordingly, it was not possible to decide whether test substance and Similar Substance may be considered as the same.

In particular,

- FAT 20'040/B, certificate of analysis reported: 39.7 % main product and 41 % unknown coloured by-products giving a total of 77.7 %, reported as purity in studies.

Genetic toxicity in vitro

- gene mutation study in bacteria (AMES test): weak mutagenic on strain TA 102 of Salmonella typhimurium.

- gene mutation in mammalian cell (HPRT assay): non mutagenic.

AMES test was considered as inconclusive, while HPRT assay was found to be negative. Criteria for classification in the CLP Regulation (EC 1272/2008) were not met.

Based on available information from read across data, no concern was raised. Therefore, genetic toxicity was not further investigated and endpoints were not filled in, according to Article 12 of the REACH Regulation (EC 1907/2006).

Endpoint conclusion
Endpoint conclusion:
no study available

Genetic toxicity in vivo

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification