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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Acceptable publication which meets basic scientific principles

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Unnamed
Year:
1988
Reference Type:
publication
Title:
No information
Author:
National Toxicology Program
Year:
1984
Bibliographic source:
http://www.niehs.nih.gov/

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Method: other: nach Haworth, S. et al.: Environ. Mutagen. 5, Suppl. 1, 3-142
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
3-(2-ethylhexyloxy)propylamine
EC Number:
226-420-6
EC Name:
3-(2-ethylhexyloxy)propylamine
Cas Number:
5397-31-9
Molecular formula:
C11H25NO
IUPAC Name:
3-[(2-ethylhexyl)oxy]propan-1-amine

Method

Target gene:
his-operon
Species / strain
Species / strain / cell type:
S. typhimurium, other: TA97, TA98, TA100, TA1535
Metabolic activation:
with and without
Metabolic activation system:
S9 mix of Aroclor 1254-induced rat and hamster livers
Test concentrations with justification for top dose:
3, 10, 33, 100, 166, 333, 1000 µg/plate
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: DMSO
Controls
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
9-aminoacridine
sodium azide
other: 4-nitro-o-phenylenediamine; 2-aminoanthracene
Details on test system and experimental conditions:
METHOD OF APPLICATION: preincubation

DURATION
- Preincubation period: 20 minutes
- Exposure duration: 48 hours

NUMBER OF REPLICATIONS: 3

DETERMINATION OF CYTOTOXICITY
- Method: number of his+ colonies, clearing in the density of the background lawn

Evaluation criteria:
A chemical was judged mutagenic (+) or weakly mutagenic (+W) if it produced a reproducible dose-related reponse over the solvent control in replicate trials. A chemical was judged questionable (?) if the results of individual trials were not reproducible, if increases in his + revertants did not meet the criteria for a "+W" response, or if only single dose produced increases in his+ revertants in repeat trials. Chemicals were judged nonmutagenic (-) if they did not meet the criteria for a mutagenic or questionable response.

Results and discussion

Test results
Species / strain:
S. typhimurium, other: TA97, TA98, TA100, TA1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
Positive controls validity:
valid
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative