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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
Study period:
September 1987
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study performed equivalent or similar to OECD 471 guideline, but predating GLP. A fifth strain to detect certain oxidising mutagens, cross-linking agents and hydrazines was not included.

Data source

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

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
No fifth strain was tested (E. coli or TA102).
GLP compliance:
no
Remarks:
Study performed around/just before the time GLP was introduced in Europe, but internal QA statement.
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Reaction mass of 5-[(2R)-butan-2-yl]-2-[(1R,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1R,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1S,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1S,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2S)-butan-2-yl]-2-[(1S,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2S)-butan-2-yl]-2-[(1S,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane
EC Number:
700-927-7
Molecular formula:
C17H30O2
IUPAC Name:
Reaction mass of 5-[(2R)-butan-2-yl]-2-[(1R,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1R,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1S,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2R)-butan-2-yl]-2-[(1S,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2S)-butan-2-yl]-2-[(1S,2R)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane and 5-[(2S)-butan-2-yl]-2-[(1S,2S)-2,4-dimethylcyclohex-3-en-1-yl]-5-methyl-1,3-dioxane
Test material form:
other: liquid
Details on test material:
- Name of test material (as cited in study report): PM 968
- Physical state: liquid
- Storage condition of test material: no data available

Method

Target gene:
Histidine gene
Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Metabolic activation system:
Rat liver S9-mix induced with Aroclor 1254
Test concentrations with justification for top dose:
Preliminary toxicity assay (all strains):
Without and with S9-mix: 0, 0.5, 5, 50, 500 and 5000 µg/plate

Main study 1 and 2:
TA1535 (without and with S9-mix) and TA1537 (without S9-mix): 0, 5, 15, 50, 150 and 500 µg/plate
TA1537 (with S9-mix) and TA100 (without and with S9-mix): 0, 15, 50, 150, 500 and 1500 µg/plate
TA98 (without and with S9-mix): 0, 50, 150, 500, 1500 and 5000 µg/plate
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: DMSO
- Justification for choice of solvent/vehicle: DMSO is accepted and approved by authorities and international guidelines.
Controlsopen allclose all
Negative solvent / vehicle controls:
yes
Remarks:
water
Positive controls:
yes
Positive control substance:
sodium azide
Remarks:
Without S9-mix: 10 µg/plate in water for TA1535 and TA100
Negative solvent / vehicle controls:
yes
Remarks:
DMSO
Positive controls:
yes
Positive control substance:
9-aminoacridine
Remarks:
Without S9-mix: 40 µg/plate in DMSO for TA1537
Negative solvent / vehicle controls:
yes
Remarks:
DMSO
Positive controls:
yes
Positive control substance:
2-nitrofluorene
Remarks:
Without S9-mix: 10 µg/plate in DMSO for TA98
Negative solvent / vehicle controls:
yes
Remarks:
DMSO
Positive controls:
yes
Positive control substance:
other: 2-aminoanthracene 2 µg/plate in DMSO for all tester strains
Remarks:
With S9-mix
Details on test system and experimental conditions:
METHOD OF APPLICATION: preincubation

DURATION
- Preincubation period: 60 minutes
- Exposure duration: 48 or 72 hour

NUMBER OF REPLICATIONS:
- Doses of the test substance were tested in triplicate in each strain. Two independent experiments were conducted.

NUMBER OF CELLS EVALUATED: 10E8 per plate

DETERMINATION OF CYTOTOXICITY
- Method: The reduction of the revertant colonies.
Evaluation criteria:
The average number of mutant colonies per plate is compared with the average number of spontaneous revertants in the control. A dose-related
increase in the number of colonies which reaches at least a doubling of the control values is usually considered to be a positive response.

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Remarks:
of 5000 µg/plate
Vehicle controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium, other: TA1535, TA1537 and TA100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Positive controls validity:
valid
Additional information on results:
TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: No information on precipitation in doses tested.

RANGE-FINDING/SCREENING STUDIES:
- Toxicity was observed at the top dose of 5000 µg/plate in strain TA1535 (with and without S9-mix), TA1537 (without S9-mix) and TA100 (without S9-mix)

COMPARISON WITH HISTORICAL CONTROL DATA:
- The positive control substances produced the expected mutagenic results.

ADDITIONAL INFORMATION ON CYTOTOXICITY MAIN STUDY:
- No toxicity or mutagenicity was observed up to and including the top dose of 5000 µg/plate in strain TA98.
- No toxicity or mutagenicity was observed up to and including the top dose of 500 µg/plate in strain TA1535 (with and without S9-mix), TA1537 (without S9-mix).
- No toxicity or mutagenicity was observed up to and including the top dose of 1500 µg/plate in strain TA1537 (with S9-mix) and TA100 (with and without S9-mix).

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

The substance was tested in the Salmonella typhimurium assay with strains TA1535, TA1537, TA98 and TA100 equivalent or similar to OECD 471 guideline. The substance is not mutagenic in strain TA1535, TA1537, TA98 and TA100 with and without S9-mix.
Executive summary:

The substance was tested in the Salmonella typhimurium assay with strains TA1535, TA1537, TA98 and TA100 equivalent or similar to OECD 471 guideline. In a preliminary toxicity test all four strains were tested up to 5000 ug/plate with and without metabolic activation. In the mutagenicity assay concentrations used were chosen on data obtained in the preliminary toxicity assay. In the mutagenicity assay no toxicity and no increase in the number of revertant colonies was observed in strain TA98 up to and including the top dose of 5000 µg/plate, with and without S9 -mix. No toxicity and no increase in the number of revertant colonies was observed up to and including the top dose of 500 µg/plate in strain TA1535 (with and without S9-mix), TA1537 (without S9-mix), and no toxicity and no increase in the number of revertant colonies was observed up to and including the top dose of 1500 µg/plate in strain TA1537 (with S9 -mix) and TA100. From this it can be concluded that the substance is not mutagenic in strains TA1535, TA1537, TA98 and TA100 with and without S9-mix in two main experiments.