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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

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2003
Report date:
2003

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
GLP compliance:
yes (incl. QA statement)
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
rel-((3aR,6R)-7,7-dimethyl-8-methyleneoctahydro-1H-3a,6-methanoazulen-3-yl)methyl acetate
Molecular formula:
C17H26O2
IUPAC Name:
rel-((3aR,6R)-7,7-dimethyl-8-methyleneoctahydro-1H-3a,6-methanoazulen-3-yl)methyl acetate
Constituent 2
Chemical structure
Reference substance name:
2-(8,8a-dimethyl-3,4,6,7,8,8a-hexahydronaphthalen-2(1H)-ylidene)propyl acetate
Molecular formula:
C17H26O2
IUPAC Name:
2-(8,8a-dimethyl-3,4,6,7,8,8a-hexahydronaphthalen-2(1H)-ylidene)propyl acetate
Constituent 3
Chemical structure
Reference substance name:
rel-(8R,8aS)-8,8a-dimethyl-2-(propan-2-ylidene)-1,2,3,7,8,8a-hexahydronaphthalene
Molecular formula:
C15H22
IUPAC Name:
rel-(8R,8aS)-8,8a-dimethyl-2-(propan-2-ylidene)-1,2,3,7,8,8a-hexahydronaphthalene
Constituent 4
Chemical structure
Reference substance name:
rel-(5R,10R)-6,10-dimethyl-2-(propan-2-ylidene)spiro[4.5]dec-6-en-8-one
Cas Number:
22196-46-9
Molecular formula:
C15H22O
IUPAC Name:
rel-(5R,10R)-6,10-dimethyl-2-(propan-2-ylidene)spiro[4.5]dec-6-en-8-one
Constituent 5
Chemical structure
Reference substance name:
rel-(4R,4aS)-4,4a-dimethyl-6-(propan-2-ylidene)-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one
Cas Number:
16981-90-1
Molecular formula:
C15H22O
IUPAC Name:
rel-(4R,4aS)-4,4a-dimethyl-6-(propan-2-ylidene)-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one
Constituent 6
Chemical structure
Reference substance name:
rel-(1R,8aS)-1,8a-dimethyl-7-(propan-2-ylidene)-1,2,3,7,8,8a-hexahydronaphthalene
Molecular formula:
C15H22
IUPAC Name:
rel-(1R,8aS)-1,8a-dimethyl-7-(propan-2-ylidene)-1,2,3,7,8,8a-hexahydronaphthalene
Constituent 7
Chemical structure
Reference substance name:
2-methoxy-4-prop-1-enylphenyl acetate
EC Number:
202-236-1
EC Name:
2-methoxy-4-prop-1-enylphenyl acetate
Cas Number:
93-29-8
Molecular formula:
C12H14O3
IUPAC Name:
2-methoxy-4-(prop-1-en-1-yl)phenyl acetate
Constituent 8
Chemical structure
Reference substance name:
rel-(1R,4aS,8aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
Molecular formula:
C15H24
IUPAC Name:
rel-(1R,4aS,8aR)-1,4a-dimethyl-7-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
Constituent 9
Chemical structure
Reference substance name:
rel-(3aR,6R,8aR)-7,7-dimethyl-8-methylenehexahydro-1H-3a,6-methanoazulen-3(2H)-one
Cas Number:
64550-95-4
Molecular formula:
C14H20O
IUPAC Name:
rel-(3aR,6R,8aR)-7,7-dimethyl-8-methylenehexahydro-1H-3a,6-methanoazulen-3(2H)-one
Constituent 10
Chemical structure
Reference substance name:
rel-(1R,4aS,8aR)-1-isopropyl-4,7-dimethyl-1,2,4a,5,6,8a-hexahydronaphthalene
Cas Number:
31983-21-8
Molecular formula:
C15H24
IUPAC Name:
rel-(1R,4aS,8aR)-1-isopropyl-4,7-dimethyl-1,2,4a,5,6,8a-hexahydronaphthalene
Constituent 11
Chemical structure
Reference substance name:
6-isopropyl-4,8a-dimethyl-1,2,3,7,8,8a-hexahydronaphthalene
Cas Number:
473-14-3
Molecular formula:
C15H24
IUPAC Name:
6-isopropyl-4,8a-dimethyl-1,2,3,7,8,8a-hexahydronaphthalene
Constituent 12
Chemical structure
Reference substance name:
rel-(4R,4aR)-4,4a-dimethyl-6-(prop-1-en-2-yl)-1,2,3,4,4a,7-hexahydronaphthalene
Molecular formula:
C15H22
IUPAC Name:
rel-(4R,4aR)-4,4a-dimethyl-6-(prop-1-en-2-yl)-1,2,3,4,4a,7-hexahydronaphthalene
Constituent 13
Chemical structure
Reference substance name:
rel-(1R,8aR)-1-isopropyl-4,7-dimethyl-1,2,3,5,6,8a-hexahydronaphthalene
Cas Number:
317819-82-2
Molecular formula:
C15H24
IUPAC Name:
rel-(1R,8aR)-1-isopropyl-4,7-dimethyl-1,2,3,5,6,8a-hexahydronaphthalene
Constituent 14
Reference substance name:
Likely sesquiterpine, MW 202
Molecular formula:
C15H22
IUPAC Name:
Likely sesquiterpine, MW 202
Constituent 15
Reference substance name:
Likely acetylated sesquiterpenes and acetylated sesquiterpene alcohols
IUPAC Name:
Likely acetylated sesquiterpenes and acetylated sesquiterpene alcohols
Constituent 16
Reference substance name:
Likely oxygenated sesquiterpenes
IUPAC Name:
Likely oxygenated sesquiterpenes
Constituent 17
Reference substance name:
Unknown constituent, MW 260
IUPAC Name:
Unknown constituent, MW 260
Test material form:
liquid
Specific details on test material used for the study:
Vetiveryl Acetate with 1% tocopherol alpha

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and TA 102
Details on mammalian cell type (if applicable):
not applicable
Additional strain / cell type characteristics:
not applicable
Cytokinesis block (if used):
not applicable
Metabolic activation:
with and without
Metabolic activation system:
Sodium phenobarbitone and beta napthoflavone
Test concentrations with justification for top dose:
Experiment 1: 33, 100, 333, 1000, 2500 and 5000 ug/plate.

Toxic effects were evident as a reduction in revertants colonies.
No reduction in bacterial lawn was noted.
Vehicle / solvent:
DMSO
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
not specified
Positive controls:
yes
Positive control substance:
4-nitroquinoline-N-oxide
sodium azide
methylmethanesulfonate
other: "-Aminoanthracene
Details on test system and experimental conditions:
METHOD OF APPLICATION: in medium; in agar (plate incorporation).
DURATION
- Exposure duration: 3 days

SELECTION AGENT (mutation assays): Frame shift mutations and base-pair substitutions.

NUMBER OF REPLICATIONS: 3 per concentration.

DETERMINATION OF CYTOTOXICITY
- Bactericial effects.
Rationale for test conditions:
Standard OECD 471 test conditions.
Evaluation criteria:
Fold increase over the standard concurrent solvent control.
Dose dependent increase.
Historical range.
Statistics:
Fold increase over the standard concurrent solvent control.

Results and discussion

Test resultsopen allclose all
Key result
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Key result
Species / strain:
S. typhimurium TA 102
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Remarks on result:
other: Negative

Applicant's summary and conclusion

Conclusions:
In conclusion, it can be stated that during the described mutagenicity test and under the experimental conditions reported, the test item did not induce mutations by base-pair substitutions or frames shift mutation in the genome of the tester strains.
Executive summary:

Negative for in vitro mutagencity.