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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

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:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: According to NICNAS source listed below, the study was conducted with methods similar to OECD guidelines.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
Prevention, Pesticides and Toxic Substances Reregistration Eligibility Decision (RED) Hydroxyethyl Octyl Sulfide
Author:
U.S. EPA
Year:
1995
Bibliographic source:
EPA 738-R-96-001
Reference Type:
secondary source
Title:
Full Public Report Ethyl Octyl Sulphide
Author:
National Industrial Chemicals Notification and Assessment Scheme
Year:
1998
Bibliographic source:
NA/487
Reference Type:
study report
Title:
Unnamed
Year:
1990

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Ethanol, 2-(octylthio)-
IUPAC Name:
Ethanol, 2-(octylthio)-
Constituent 2
Chemical structure
Reference substance name:
2-(octylthio)ethanol
EC Number:
222-598-4
EC Name:
2-(octylthio)ethanol
Cas Number:
3547-33-9
Molecular formula:
C10H22OS
IUPAC Name:
2-(octylsulfanyl)ethan-1-ol
Constituent 3
Reference substance name:
Hydroxyethyl octyl sulfide
IUPAC Name:
Hydroxyethyl octyl sulfide
Details on test material:
- Name of test material (as cited in study report): Hydroxyethyl octyl sulfide
- Substance type: Active
- Physical state: Liquid
- Analytical purity: 96.9 %

Method

Target gene:
Histidine locus
Species / strain
Species / strain / cell type:
S. typhimurium, other: TA98, TA100, TA1535 and TA1538
Metabolic activation:
with and without
Metabolic activation system:
Rat liver S9
Test concentrations with justification for top dose:
0, 3, 10, 33 and 333 ug/plate
Vehicle / solvent:
No data
Controls
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
not specified
Positive controls:
not specified
Positive control substance:
not specified
Details on test system and experimental conditions:
No data
Evaluation criteria:
No data
Statistics:
No data

Results and discussion

Test results
Species / strain:
S. typhimurium, other: TA98, TA100, TA1535 and TA1538
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Additional information on results:
ADDITIONAL INFORMATION ON CYTOTOXICITY: At doses above 100 ug/plate, in the absence of activation, toxicity was moderate to extreme.
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

NICNAS also lists TA1537 as having been tested.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

Based on the results of the study, the test substance failed to induce a mutagenic response in the Ames assay either in the presence or absence of metabolic activation up to a concentration level of 333 ug/plate.
Executive summary:

In a bacterial reverse mutation assay,Salmonella typhimurium, conducted with methods similar to OECD 471 guidelines, S. typhimurium strains TA98, TA100, TA1535 and TA1538 were treated with ethanol, 2-(octylthio) (96.9%) at concentrations of 0, 3, 10, 33 and 333 µg/plate in the presence and absence of rat liver S9 activation. No induced mutations were observed in the indicator strains in either the presence or absence of metabolic activation. At doses above 100 µg/plate, in the absence of activation, toxicity was moderate to extreme.