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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
in vitro cytogenicity / chromosome aberration study in mammalian cells
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
publication
Title:
Genotoxicity of hexamethylenetetraamine.
Author:
Girmanova, I., Chalupa, I., Sekerka, V.
Year:
1991
Bibliographic source:
Biologia (Bratislava), 46, 11, 1009-1015

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Not applicable
GLP compliance:
not specified
Type of assay:
in vitro mammalian chromosome aberration test

Test material

Constituent 1
Chemical structure
Reference substance name:
Methenamine
EC Number:
202-905-8
EC Name:
Methenamine
Cas Number:
100-97-0
Molecular formula:
C6H12N4
IUPAC Name:
1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane

Method

Target gene:
Not available
Species / strain
Species / strain / cell type:
Chinese hamster lung fibroblasts (V79)
Test concentrations with justification for top dose:
0.1, 1, 10, 50 mmol/L
Controls
Positive controls:
yes
Positive control substance:
mitomycin C

Results and discussion

Test results
Species / strain:
Chinese hamster lung fibroblasts (V79)
Metabolic activation:
not specified
Genotoxicity:
not specified
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
positive

In the highest analysable concentration of 10 mmol/l 17% aberrant cells (without gaps) were induced compared to 2% in control cultures.
(V79 positive results)