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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:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
weight of evidence
Study period:
28 Apr - 07 May 1992
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: GLP guideline study with acceptable restrictions (incomplete strain selection, E. coli strain is missing)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1996
Report date:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Version / remarks:
adopted in 1983
Deviations:
yes
Remarks:
(incomplete strain selection since E. coli strain is missing)
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Methyl hexanoate
EC Number:
203-425-1
EC Name:
Methyl hexanoate
Cas Number:
106-70-7
IUPAC Name:
methyl hexanoate
Details on test material:
- Name of test material (as cited in study report): Methylhexanoat
- Substance type: Fatty acid methyl ester
- Physical state: liquid, colourless
- Analytical purity: >98%
- Impurities: Not given
- Lot/batch No.: 1291191
- Expiration date of the lot/batch: 24.06.1992
- Stability: approx. 3 years
- Storage condition of test material: Room temperature

Method

Target gene:
his operon
Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Additional strain / cell type characteristics:
other: rfa-; uvrB- (R+ for TA 98)
Species / strain / cell type:
S. typhimurium TA 1538
Additional strain / cell type characteristics:
other: rfa-; uvrB-; R+
Metabolic activation:
with and without
Metabolic activation system:
cofactor supplemented post-mitochondrial fraction (S9 mix) prepared from the livers of rats treated with Aroclor 1254.
Test concentrations with justification for top dose:
8, 40, 200, 1000 and 5000 µg/plate
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: DMSO
- Justification for choice of solvent/vehicle: according to solubility properties tested before the start of the study
Controls
Untreated negative controls:
yes
Remarks:
untreated fresh cell suspension
Negative solvent / vehicle controls:
yes
Remarks:
DMSO
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: 2 µg/plate sodium azide (TA100 and 1535, -S9), 80 µg/plate 9-aminoacridine (TA1537, -S9), 40 µg/plate 4-nitro-o-phenylendiamine (TA98 and 1538, -S9), 2.5 µg/plate 2-aminoanthracene (TA1535, 1537, +S9), 5 µg/plate 2-aminoanthracene (TA98, 100, 1538, +S9)
Details on test system and experimental conditions:
METHOD OF APPLICATION: in medium; in agar (plate incorporation)

DURATION
- Exposure duration: 48 h
- Expression time (cells in growth medium): 48 h

NUMBER OF REPLICATIONS: triplicates in each of two independent experiments

DETERMINATION OF CYTOTOXICITY
- Method: Inspection of the bacterial background lawn wit a dissecting microscope


OTHER: The spontaneous mutation rates of each tester strain were within the characteristic spontaneous mutation rates
Evaluation criteria:
Revertant colonies were counted and the mean and standard deviation were calculated and compared to the controls. The tester strains were regulary tested for their genetic markers.
All cultures must demonstrate the characteristic mean number of spontaneous revertants in the vehicle controls.
Statistics:
Mean and standard deviation were calculated

Results and discussion

Test resultsopen allclose all
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:
cytotoxicity
Remarks:
at 5000 µg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 1538
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
at 5000 µg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
COMPARISON WITH HISTORICAL CONTROL DATA: Yes

Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

Table 1: Mutagenicity on bacteria - experiment I

With or without S9-Mix

Test substance concentration

(μg/plate)

Mean number of revertant colonies per plate

(average of 3 plates)

TA 1535

TA100

TA1537

TA1538

TA98

 

Buffer

7

95

7

5

13

-

Solvent (DMSO)

9

101

7

7

12

-

8

8

90

7

9

10

-

40

8

98

10

9

14

-

200

9

92

7

6

19

-

1000

7

84

5

7

13

 

5000

5

88

2

4

8

Positive

controls

- S9

Name

SA

SA

9AA

4ND

4ND

Concentrations

(μg/plate)

2

2

80

40

40

Number of colonies/plate

626

769

918

1972

1532

+

Buffer

14

92

6

11

33

+

Solvent (DMSO)

10

96

11

16

37

+

8

13

99

10

18

36

+

40

11

108

5

19

34

 

200

9

114

8

15

23

+

1000

6

99

6

17

25

+

5000

9

73

5

8

12

Positive

controls

+ S9

Name

2AA

2AA

2AA

2AA

2AA

Concentrations

(μg/plate)

2.5

5

2.5

5

5

Number of colonies/plate

221

1492

113

1465

1711

 

9AA = 9-Aminoacridine

2AA = 2-Aminoanthracene

SA = Sodium Acide

4ND = 4-Nitro-o-phenylendiamine

 

 

Table 2: Mutagenicity on bacteria - experiment II

With or without S9-Mix

Test substance concentration

(μg/plate)

Mean number of revertant colonies per plate

(average of 3 plates)

TA 1535

TA100

TA1537

TA1538

TA98

 

Buffer

10

112

14

11

19

-

Solvent (DMSO)

9

105

9

10

15

-

8

9

110

12

8

12

-

40

7

102

10

6

12

-

200

6

108

9

10

18

-

1000

9

101

7

8

16

 

5000

8

81

6

11

10

Positive

controls

- S9

Name

SA

SA

9AA

4ND

4ND

Concentrations

(μg/plate)

2

2

80

40

40

Number of colonies/plate

687

824

1016

1897

1418

+

Buffer

12

125

8

16

28

+

Solvent (DMSO)

7

109

7

18

27

+

8

8

113

7

14

27

+

40

11

117

9

14

25

 

200

11

98

11

18

28

+

1000

8

105

9

14

30

+

5000

8

68

6

6

13

Positive

controls

+ S9

Name

2AA

2AA

2AA

2AA

2AA

Concentrations

(μg/plate)

2.5

5

2.5

5

5

Number of colonies/plate

218

1584

125

1415

1967

9AA = 9-Aminoacridine

2AA = 2-Aminoanthracene

SA = Sodium Acide

4ND = 4-Nitro-o-phenylendiamine

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative