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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data is from peer reviewed publication

Data source

Reference
Reference Type:
publication
Title:
Mutagenicity Produced by Aqueous Chlorination of Organic Compounds
Author:
W. Howard Rapson, Mark A. Nazar, and Victor V. Butsky
Year:
1980
Bibliographic source:
Bull. Environm. Contam. Toxicol, 24,590-596 (1980)

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: as mentioned below
Principles of method if other than guideline:
Ames assay was performed to evaluated the mutagenic nature of the test compound m-Methoxyacetophenone
GLP compliance:
not specified
Type of assay:
bacterial gene mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
3-methoxyacetophenone
EC Number:
209-573-3
EC Name:
3-methoxyacetophenone
Cas Number:
586-37-8
Molecular formula:
C9H10O2
IUPAC Name:
1-(3-methoxyphenyl)ethan-1-one
Constituent 2
Reference substance name:
m-Methoxyacetophenone
IUPAC Name:
m-Methoxyacetophenone
Test material form:
other: Liquid
Details on test material:
- Name of test material (as cited in study report): m-Methoxyacetophenone
- Molecular formula (if other than submission substance): C10H12O2
- Molecular weight (if other than submission substance): 164.2028 g/mol
- Substance type: Organic
- Physical state: No data available
Purity No data available
- Impurities (identity and concentrations): No data available

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 100
Details on mammalian cell type (if applicable):
No data available
Additional strain / cell type characteristics:
not specified
Metabolic activation:
not specified
Metabolic activation system:
No data
Test concentrations with justification for top dose:
103, 102, 101, 100 and 10-1 µg per plate.
Vehicle / solvent:
No data available
Controls
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
not specified
True negative controls:
not specified
Positive controls:
not specified
Positive control substance:
not specified
Details on test system and experimental conditions:
METHOD OF APPLICATION: in agar (plate incorporation)

DURATION
- Preincubation period: No data available
- Exposure duration: No data available
- Expression time (cells in growth medium): No data available
- Selection time (if incubation with a selection agent): No data available
- Fixation time (start of exposure up to fixation or harvest of cells): No data available

SELECTION AGENT (mutation assays): No data available
SPINDLE INHIBITOR (cytogenetic assays): No data available
STAIN (for cytogenetic assays): No data available

NUMBER OF REPLICATIONS: No replications were performed

NUMBER OF CELLS EVALUATED: No data available

DETERMINATION OF CYTOTOXICITY
- Method: mitotic index; cloning efficiency; relative total growth; other: No data available

OTHER EXAMINATIONS:
- Determination of polyploidy: No data available
- Determination of endoreplication: No data available
- Other: No data available

OTHER: No data available
Evaluation criteria:
Increase in the number of revertants, Toxicity toward the Ames Salmonella TA100 strain used was roughly estimated by visual comparison of the background lawn on the plate under a microscope, with 100% representing the same number of bacteria per unit area as the blank with no test solution (no toxicity) and 0 representing death of all bacteria.
Statistics:
No data available

Results and discussion

Test results
Species / strain:
S. typhimurium TA 100
Metabolic activation:
not specified
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified
Remarks on result:
other: strain/cell type:
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

The test compound failed to induce mutation in the Salmonella typhimurium TA100 and hence is not a mutagen.
Executive summary:

Ames assay was performed to evaluate the mutagenic nature of the test compound m-Methoxyacetophenone usingSalmonella typhimuriumTA100. The test compound was tested at dose levels of 103, 102, 101, 100and 10-1ug per plate.

 

The test compoundm-Methoxyacetophenonefailed to induce mutation in theSalmonella typhimuriumTA100 and hence is not a mutagen.