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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
in vivo mammalian cell study: DNA damage and/or repair
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
2000
Report date:
2000

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 478 (Genetic Toxicology: Rodent Dominant Lethal Test)
GLP compliance:
yes
Type of assay:
rodent dominant lethal assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Atrazine
EC Number:
217-617-8
EC Name:
Atrazine
Cas Number:
1912-24-9
Molecular formula:
C8H14ClN5
IUPAC Name:
6-chloro-N-ethyl-N'-isopropyl-1,3,5-triazine-2,4-diamine
Details on test material:
- Purity: 97.4%
- Batch No.: SG 8029 BA10
Specific details on test material used for the study:
- Purity: 97.4%
- Batch No.: SG 8029

Test animals

Species:
mouse
Strain:
Tif:MAGf
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Duration of treatment / exposure:
8 weeks
Doses / concentrationsopen allclose all
Dose / conc.:
500 mg/kg bw/day
Dose / conc.:
1 000 mg/kg bw/day
Dose / conc.:
2 000 mg/kg bw/day
Dose / conc.:
2 400 mg/kg bw/day

Results and discussion

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

Applicant's summary and conclusion