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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The substance fusanus spicatus, ect. has been tested in an OECD 471 study (Ames study) for in vitro mutagenicity to bacterial strains Salmonelly typhimuirion TA98, TA100, TA102, TA 1535 abd TA 1537 and was found negative for mutagenic effects in all strains, irrespective when tested with or without metabolic activation using S9 mix. Thus, based on available data, the substance is not to be classified for mutagenicity.

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

Genetic toxicity in vivo

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

Based on the results of an in vitro mutagenicity study according to OECD 471, the substance is not subject to classification and labelling for mutagenicity according to CLP (Regulation EC No 1272/2088).