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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Study period:
1996
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1996
Report date:
1996

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no
Type of assay:
chromosome aberration assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Sulfapyridine
EC Number:
205-642-7
EC Name:
Sulfapyridine
Cas Number:
144-83-2
Molecular formula:
C11H11N3O2S
IUPAC Name:
4-amino-N-pyridin-2-ylbenzenesulfonamide
Test material form:
not specified
Details on test material:
No data

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
No data

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
corn oil
Details on exposure:
500 mg/kg
Duration of treatment / exposure:
6, 24 and 48h
Frequency of treatment:
No data
Post exposure period:
6, 24 and 48 hours
Doses / concentrations
Remarks:
Doses / Concentrations:
500 mg/kg
Basis:
nominal conc.
No. of animals per sex per dose:
No data
Control animals:
not specified
Positive control(s):
No data

Examinations

Details of tissue and slide preparation:
bone marrow
Evaluation criteria:
No data
Statistics:
No data

Results and discussion

Test results
Sex:
male/female
Genotoxicity:
negative
Toxicity:
not specified

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative
The test substance did not cause chromosome Aberrations in in vivo in rat bone marrow cells under the experimental condition.
Executive summary:

The study were performed to assess the chromosome aberration of the test substance to rat bone marrow cells.500 mg/kg was applied orally to male and female rats. The rats were killed after 6, 24 and 48 hours later. No chromosome damaging was found. Thus, we can conclude the test substance dose not cause chromosome Aberrations in in vivo in rat bone marrow cells.