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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Genetic toxicity: in vivo

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Administrative data

Endpoint:
in vivo mammalian germ cell study: cytogenicity / chromosome aberration
Remarks:
Type of genotoxicity: chromosome aberration
Adequacy of study:
other information

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: OECD 474 / micronucleus test
GLP compliance:
yes
Type of assay:
other: Non-bacteriological test in vivo - 6th amendment data

Test animals

Species:
other: mus/ HSD/ Win: NMRI

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
maize germ oil
No. of animals per sex per dose:
Female: 2000 mg/kg; No. of animals: ; Sacrifice times: hours

Results and discussion

Test results
Toxicity:
yes
Remarks:
Doses producing toxicity: No clinical symptomes at 2000 mg/kg
Additional information on results:
Observations:
No toxicological or cytotoxical symptoms (PCE/ NCE in the
bone marrow) were induced. There were no signs of a
mutagenic potential.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative