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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Carcinogenicity

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Administrative data

Description of key information

Based on the available data of sodium tungstate for read-across, ammonium metatungstate is not classified as a mutagen and there is no evidence from repeat dose oral studies on sodium tungstate to indicate that it would induce hyperplasia and/or pre-neoplastic lesions.

Key value for chemical safety assessment

Carcinogenicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no study available

Carcinogenicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Carcinogenicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

No data of sufficient quality data on the carcinogenicity of ammonium metatungstate are available. Classification is not possible due to data lacking.

Additional information

No data of sufficient quality on the carcinogencity of ammonium metatungstate (target substance) are available. However, toxicity data are available for sodium tungstate (source substance).

 

Due to similar or lower transformation/dissolution results for ammonium metatungstate (target substance) than sodium tungstate (source substance), the resulting toxicity potential is expected to be similar or lower, so read-across is appropriate. In addition, read-across is justified because the classification and labelling is the same or less severe for the target substance and the PBT/vPvB profile is the same. Finally, the dose descriptors are, or are expected to be, sufficiently similar or higher for the target substance, and read-across to the source substance is adequately protective. For more details, refer to the read-across category approach description in the Category section of this IUCLID submission or Annex 3 of the CSR.

 

According to Column 2 of REACH Annex X, a carcinogenicity study may be required if the substance has a widespread dispersive use or there is evidence of frequent or long-term human exposure and the substance is classified as mutagen category 3 or there is evidence from the repeated dose study(ies) that the substance is able to induce hyperplasia and/or pre-neoplastic lesions. Based on the available data from read across to sodium tungstate, hexaaamonium metatungstate is not classified as a mutagen and there is no evidence from repeat dose oral studies on sodium tungstate to indicate that it would induce hyperplasia and/or pre-neoplastic lesions.