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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Near guideline study, GLP status unknown, published in peer reviewed literature, minor restrictions in design and / or reporting but otherwise adequate for assessment.

Data source

Reference
Reference Type:
publication
Title:
Assay of 855 test chemicals in ten tester strains using a new modification of the Ames test for bacterial mutagens
Author:
McMahon RE, Cline JC and Thompson CZ
Year:
1979
Bibliographic source:
Cancer Research 39, 682-693

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
assessment of mutagenic potential in 8 histidine auxotrophs of S. typhimurium and 2 trytophan auxotrophs of E. coli over a 10000-fold concentration range using a gradient plate method.
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Acetic anhydride
EC Number:
203-564-8
EC Name:
Acetic anhydride
Cas Number:
108-24-7
Molecular formula:
C4H6O3
IUPAC Name:
acetyl acetate

Method

Species / strain
Species / strain / cell type:
other: S. typhimurium LT-2, TA1535, TA100, C3076, TA1537, D3052, TA1538, TA98. E. coli WP2 and WP2 uvrA-
Metabolic activation:
with and without
Metabolic activation system:
S9 from Arochlor induced rat liver
Test concentrations with justification for top dose:
Approximately 0.1 - 1.0, 1-10, 10-100 and 100-1000 µg/mL using concentration gradient plates.
Vehicle / solvent:
dimethyl sulfoxide.
Controls
Untreated negative controls:
yes
Positive controls:
yes
Positive control substance:
other: streptozotocin (mutagenic - activation) and 2-acetylaminofluorene (mutagenic + activation)
Details on test system and experimental conditions:
METHOD OF APPLICATION: in agar (plate incorporation using gradient plates)

DURATION
- Exposure duration: 48 hours at 37°C

NUMBER OF REPLICATIONS: Not reported

Evaluation criteria:
The concentration range over which chemically induced mutant colonies are present was recorded. when the plates are read the operator has a series of 4 plates covering a 10,000-fold concentration range on which to base his judgment. If the test chemical is toxic to the auxotroph, minimal inhibitory concentrations can be observed as clear zones and were also recorded.

Results and discussion

Test results
Species / strain:
other: S. typhimurium LT-2, TA1535, TA100, C3076, TA1537, D3052, TA1538, TA98. E. coli WP2 and WP2 uvrA-
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
valid
Positive controls validity:
valid
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

In a modified Ames test, acetic anhydride, at concentrations of up to 1000 µg/mL, was negative, ie non-mutagenic

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative with metabolic activation
negative without metabolic activation

In a modified Ames test using a gradient plate method, acetic anhydride, at concentrations of up to 1000 µg/mL, was negative, ie non-mutagenic
Executive summary:

In a modified Ames test using a gradient plate method, acetic anhydride, at concentrations of up to 1000 µg/mL, was negative, ie non-mutagenic