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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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)

Data source

Reference
Reference Type:
publication
Title:
STUDY OF ARTIFICIAL FLAVOURING SUBSTANCES FOR MUTAGENICITY IN THE SALMONELLA/MICROSOME, BASC AND MICRONUCLEUS TESTS.
Author:
D. WILD, M.-T. KING, E. GOCKE and K. ECKHARDT
Year:
1983
Bibliographic source:
Fd Chem. Toxic'. Vol. 21, No. 6, pp. 707-719, 1983

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: as mentioned below principle
Principles of method if other than guideline:
Toxicity of 2 Phenylpropionaldehyde was study using Salmonella/mammalian microsome test (Ames test).
GLP compliance:
not specified
Type of assay:
bacterial gene mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Hydratropaldehyde
EC Number:
202-255-5
EC Name:
Hydratropaldehyde
Cas Number:
93-53-8
Molecular formula:
C9H10O
IUPAC Name:
hydratropaldehyde
Constituent 2
Reference substance name:
2 Phenylpropionaldehyde
IUPAC Name:
2 Phenylpropionaldehyde
Test material form:
other: Liquid
Details on test material:
Details on test material
- Name of test material (as cited in study report): 2 Phenylpropionaldehyde (synonym-Hydratropic aldehyde)
- Molecular formula (if other than submission substance): C9-H10-O
- Molecular weight (if other than submission substance): 134.177 g/mol
- Substance type: Organic
- Physical state: Liquid
- Purity: No data available
- Impurities (identity and concentrations): No data available

Method

Target gene:
No data available
Species / strain
Species / strain / cell type:
other: Salmonella typhimurium TA 1535, TA 100, TA 1537,TA1538 and TA98
Details on mammalian cell type (if applicable):
No data available
Additional strain / cell type characteristics:
not specified
Metabolic activation:
with and without
Metabolic activation system:
Aroclor-pretreated rats
Test concentrations with justification for top dose:
up to 3.6 mg/plate(Five doses were taken)
Vehicle / solvent:
DMSO
Controls
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
not specified
True negative controls:
not specified
Positive controls:
yes
Positive control substance:
sodium azide
benzo(a)pyrene
Remarks:
No other data available
Details on test system and experimental conditions:
Details on test system and conditions
METHOD OF APPLICATION: plate incorporation method using Vogel Bonnet Medium
DURATION
- Preincubation period: No data available
- Exposure duration: 48 hrs
- Expression time (cells in growth medium): No data available
- Selection time (if incubation with a selection agent): No data available
- Fixation time (start of exposure up to fixation or harvest of cells): No data available

SELECTION AGENT (mutation assays): No data available
SPINDLE INHIBITOR (cytogenetic assays): No data available
STAIN (for cytogenetic assays): No data available

NUMBER OF REPLICATIONS:
No data available
NUMBER OF CELLS EVALUATED: No data available
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index; cloning efficiency; relative total growth; other: No data available

OTHER EXAMINATIONS:
- Determination of polyploidy: No data available
- Determination of endoreplication: No data available
- Other:

OTHER:
Evaluation criteria:
numbers of revertants/plate were calculated

Results and discussion

Test results
Species / strain:
other: Salmonella typhimurium TA 1535, TA 100, TA 1537,TA1538 and TA98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified
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):
other: Negative (with and without)

After experiment, end point for genetic toxicity for 2 Phenylpropionaldehyde(93-53-8) was determined to be negative with and without activation.
Executive summary:

2 Phenylpropionaldehyde artificial flavouring substance in food products was studied for mutagenic properties by the use of the Salmonella/mammalian microsome test (Ames test).

 

The test was performed by plate incorporation method at 5 different dosesupto 3600 µg/plate and the plates were incubated for 48hrs.

 

2 Phenylpropionaldehyde is non mutagenic when Salmonella/microsome AMES test is performed.