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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 somatic cell study: cytogenicity / erythrocyte micronucleus
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1987
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to a guideline study and current standards but with limited documentation. Restricted to only one sampling time. Information taken from a secondary source (OECD, 2006).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987

Materials and methods

Principles of method if other than guideline:
Comparable to a guideline study but with only one sampling time.
GLP compliance:
not specified
Type of assay:
micronucleus assay

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
Methanol, reagent special grade from Junsei Chemicals Co., no further data.

Test animals

Species:
mouse
Strain:
ICR
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
No information
Duration of treatment / exposure:
single, 24 hours
Frequency of treatment:
once
Doses / concentrations
Remarks:
Doses / Concentrations:
1050, 2110, 4210 or 8410 mg/kg bw
Basis:
nominal conc.
No. of animals per sex per dose:
6 per dose level and positive control (TEM)
Control animals:
yes, concurrent no treatment
Positive control(s):
Yes, TEM

Examinations

Tissues and cell types examined:
Bone marrow

Results and discussion

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

Any other information on results incl. tables

There was no methanol-related increase in the induction of micronuclei: In treated groups, the mean MN rate varied from 0.5 to 2.2/1000 vs. 1.5/1000 in the neg. control and 45/1000 in the pos. control group.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative
There were no methanol-related increases in the induction of micronuclei in treated groups.