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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
in vivo mammalian germ cell study: cytogenicity / chromosome aberration
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: OECD method, GLP compliance

Data source

Reference
Reference Type:
other: inquiry result from ECHA
Title:
Unnamed
Year:
2013

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: OECD (MAY 26, 1983) 84/449/EEC, B.12
GLP compliance:
yes
Type of assay:
other: Non-bacteriological test in vivo-6th amendment data

Test material

Constituent 1
Chemical structure
Reference substance name:
Bis(η5-cyclopentadienyl)-bis(2,6-difluoro-3-[pyrrol-1-yl]-phenyl)titanium
EC Number:
412-000-1
EC Name:
Bis(η5-cyclopentadienyl)-bis(2,6-difluoro-3-[pyrrol-1-yl]-phenyl)titanium
Cas Number:
125051-32-3
Molecular formula:
C30H22F4N2Ti
IUPAC Name:
titanium(4+) bis(2,6-difluoro-3-(1H-pyrrol-1-yl)benzen-1-ide) bis(cyclopenta-2,4-dien-1-ide)

Test animals

Species:
other: MOUSE, Tif: MAGf (SPF)

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
CMC (0.5 %)
Duration of treatment / exposure:
SACRIFICE TIME 16, 24, 48
No. of animals per sex per dose:
8 MALES AND 8 FEMALES

Results and discussion

Test results
Genotoxicity:
negative
Toxicity:
yes
Remarks:
(Doses producing toxicity: NONE TESTED UP TO 5000 mg/kg)

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative