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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1988
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1988
Report date:
1988

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
464-510-9
EC Name:
-
Cas Number:
147768-39-6
Molecular formula:
C10H23O3P
IUPAC Name:
3-[(3-hydroxypropyl)(2-methylpropyl)phosphoryl]propan-1-ol
Test material form:
liquid: viscous

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
Metabolic activation system:
Aroclor 1254 induced rat liver S9
Test concentrations with justification for top dose:
Concentration range in the main test (with metabolic activation): 50 ... 5000 µg/plate
Concentration range in the main test (without metabolic activation): 50 ... 5000 µg/plate
Vehicle / solvent:
Solvent: Sterile distilled water

Results and discussion

Test results
Species / strain:
other: all strains
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
(> 5000 µg/plate)
Additional information on results:
Observations:
The vehicle control plates produced counts of revertant colonies within the normal range.


All of the positive control chemicals used in the test
induced marked increases in the frequency of revertant
colonies, both with and without metabolic activation.


The test substance caused no visible reduction in the growth
of the bacterial lawn at any dose level either with or
without metabolic activation, it was, therefore, tested up
to the maximum recommended dose level of 5000 µg/plate.

Applicant's summary and conclusion

Conclusions:
Interpretation of results
negative with metabolic activation
negative without metabolic activation
Executive summary:

No clasification is required for the test item according to the Ames test performed.