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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:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Study period:
From September 2009 to October 2007
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Experimental studies reported in peer reviewed journal. For read-across justification see Section 13.

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1985

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
Chemical structure
Reference substance name:
Diundecyl phthalate
EC Number:
222-884-9
EC Name:
Diundecyl phthalate
Cas Number:
3648-20-2
Molecular formula:
C30H50O4
IUPAC Name:
diundecyl benzene-1,2-dicarboxylate
Details on test material:
- Name of test material (as cited in study report): Diundecyl phthalate
- Lot/batch No.:Not stated
- Purity: Not stated

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Metabolic activation system:
S9
Test concentrations with justification for top dose:
A maximum dose-level of 10000 ug/plate (unless limited by solubility of toxicity) and four lower concentrations separated by half-log intervals
Vehicle / solvent:
Solvent used: No data
Controlsopen allclose all
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
sodium azide
Remarks:
Strains TA100 and TA1535; -S9
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
9-aminoacridine
Remarks:
Strain TA1537; -S9
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: 4-nitro-o-phenylenediamine
Remarks:
Strain TA98; -S9
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: 2-Aminoanthracene
Remarks:
All strains; +S9
Details on test system and experimental conditions:
METHOD OF APPLICATION: in medium; Preincubation

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

SELECTION AGENT (mutation assays): Histidine

NUMBER OF REPLICATIONS: 3

DETERMINATION OF CYTOTOXICITY
- Method: Not reported but usually by reduced number of spontaneous revertants, microcolony formation, thinning of background lawn

Evaluation criteria:
For the test item to be considered mutagenic, a dose-related increase in revertant numbers must be observed.

Results and discussion

Test results
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not determined
Vehicle controls validity:
valid
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

It is concluded that the substance does not induce reverse mutation in Salmonella typhimurium under the reported experimental conditions.
Executive summary:

A bacterial reverse mutaion assay (Ames test) has been undertaken using methods similar to or equivalent to OECD test methods.

The substance does not induce reverse mutation in Salmonella typhimuriumi.