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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

No carcinogenicity data were available specifically on the test substance. According to Annex X of REACH, a carcinogenicity study may be required if the substance has a widespread dispersive use or if there is evidence of frequent or long-term human exposure and the substance is classified as mutagen category 3 or if 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, the test substance is not classified as a mutagen and there was no evidence of hyperplasia and/or pre-neoplastic lesions in a 90-day dermal toxicity study. Based on the weight of evidence, there are sufficient data to conclude that the test substance is not a carcinogen.

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

Additional information

No carcinogenicity data were available specifically on the test substance. According to Annex X of REACH, a carcinogenicity study may be required if the substance has a widespread dispersive use or if there is evidence of frequent or long-term human exposure and the substance is classified as mutagen category 3 or if 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, the test substance is not classified as a mutagen and there was no evidence of hyperplasia and/or pre-neoplastic lesions in a 90-day dermal toxicity study. Based on the weight of evidence, there are sufficient data to conclude that the test substance is not a carcinogen.