Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well documented publication which meets basic scientific principles
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
publication
Title:
Mutagenicity tests with styrene oxide in mammals.
Author:
Fabry L et al
Year:
1978
Bibliographic source:
Mutat Res. 1978 Sep;51(3):377-81.

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 478 (Genetic Toxicology: Rodent Dominant Lethal Test)
GLP compliance:
no
Remarks:
study performed before implementation of GLP
Type of assay:
rodent dominant lethal assay

Test material

Constituent 1
Chemical structure
Reference substance name:
(epoxyethyl)benzene
EC Number:
202-476-7
EC Name:
(epoxyethyl)benzene
Cas Number:
96-09-3
Molecular formula:
C8H8O
IUPAC Name:
2-phenyloxirane

Test animals

Species:
mouse
Strain:
Balb/c
Sex:
male

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
Paraffin oil
Details on exposure:
To test the ability of styrene oxide to induce chromosomal aberrations in male post-meiotic germ cells, each male was caged, after injection, with three virgin females from the same strain which were replaced after 7 and 14 days.
Duration of treatment / exposure:
250 mg/kg bw
Frequency of treatment:
once prior to mating
Doses / concentrations
Remarks:
Doses / Concentrations:250 mg/kg bwBasis:no data
No. of animals per sex per dose:
7 treated animals; 10 control animals
Control animals:
yes, concurrent vehicle

Examinations

Tissues and cell types examined:
The males were then kept for another two months, killed and their dividing spermatocytes examined for the presence of reciprocal translocations induced in the pre-meiotic cells. The females were dissected 17 days after mating had started, and pre- and post-implantation losses were determined by conventional methods.

Results and discussion

Test results
Sex:
male
Genotoxicity:
negative
Toxicity:
not specified
Vehicle controls validity:
valid
Negative controls validity:
not applicable
Positive controls validity:
not specified

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negativeStyrene oxide did not induce dominant lethal mutations or translocations in meiotic germ cells of male BALB/c mice
Executive summary:

Styrene oxide did not induce dominant lethal mutations or translocations in meiotic germ cells of male BALB/c mice administered styrne oxide by intraperitoneal injection at a dose of 250 mg/kg bw.