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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study with GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
(only 2-aminoanthracene as positive control with metabolic activation)
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
N'-[3-(dimethylamino)propyl]-N,N-dimethylpropane-1,3-diamine
EC Number:
229-761-9
EC Name:
N'-[3-(dimethylamino)propyl]-N,N-dimethylpropane-1,3-diamine
Cas Number:
6711-48-4
Molecular formula:
C10H25N3
IUPAC Name:
N'-[3-(dimethylamino)propyl]-N,N-dimethylpropane-1,3-diamine
Details on test material:
- Name of test material (as cited in study report): Bis (3-dimethylaminopropyl) amin
- Physical state: Colourless liquid
- Analytical purity: 98.4%
- Lot/batch No.: 94-0675
- Storage condition of test material: Room temperature

Method

Target gene:
his operon and trp operon
Species / strain
Species / strain / cell type:
other: S. typhimurium TA 1535, TA 1537, TA 98 and TA 100 and E. coli WP2 uvr A
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:
Experiment 1: standard plate test 1: 0; 20; 100; 500; 2500 and 5000 µg/plate (with and without S9-mix); all strains
Experiment 2: standard plate test 2: 2000, 3000, 4000, 5000, 6000 µg/plate (with and without S9-mix); (TA100, E.coli WP2 uvrA)
Experiment 3: preincubation test : 0; 20; 100; 500; 2500 and 5000 µg/plate (with and without S9-mix); all strains
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: water
Controls
Untreated negative controls:
yes
Remarks:
sterility control
Negative solvent / vehicle controls:
yes
Remarks:
water control
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: (+ S9): 2-aminoanthracene, 2-AA (all strains); (- S9): N-methyl-N'-nitro-N-nitroso-guanidine, MNNG (TA 100, TA 1535); 4-nitro-o-phenylendiamine, NOPD (TA 98); 9-aminoacridine, AAC (TA 1537); N-ethyl-N'-nitro-N-nitrosoguanidin, ENNG (E.coli WP2 uvrA)
Remarks:
2-AA: 2 µg (TA100, TA 98, TA 1537, TA 1535), 60 µg (E. coli WP2 uvrA); MNNG: 5 µg; NOPD: 10 µg; AAC: 100 µg; ENNG: 10 µg; solvent for all positive control substances: DMSO
Details on test system and experimental conditions:
METHOD OF APPLICATION: standard plate test (first experiment), preincubation test (second experiment)

DURATION
- Preincubation period: 20 min (only preincubation test)
- Exposure duration: 48 - 72 h (in the dark, 37 °C)

NUMBER OF REPLICATIONS: 3 plates/concentration/experiment; 3 3experiments

DETERMINATION OF CYTOTOXICITY
- Method: reduction in the number of revertants or a clearing of the bacterial background lawn, reduction of the titer.
The titer is generally determined only in the experimental parts with S9 mix both for the negative controls (vehicle only) and for the two highest doses in all experiments.
Evaluation criteria:
The test chemical is considered positive in this assay if the following criteria are met: A dose-related and reproducible increase in the number of revertant colonies, i.e. about doubling of the spontaneous mutation rate in at least one tester strain either without S-9 mix or after adding a metabolizing system.

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:
A weak bacteriotoxic effect in the standard plate test at 6000 µg/plate (TA 100). In the preincubation assay bacteriotoxicity was found depending on the strain and test conditions at doses >= 500 µg/plate.
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
A weak bacteriotoxic effect in the standard plate test at 6000 µg/plate. In the preincubation assay bacteriotoxicity was found at doses >= 2500 µg/plate.
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: no test substance precipitation was found
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

Table 1: Test results of experiment 1 (plate incorporation)

 

With or without S9-Mix

Test substance concentration

(μg/plate)

Mean number of revertant colonies per plate

(average of 3 plates ± Standard deviation)

Base-pair substitution type

Frameshift type

TA 100

TA1535

WP2 uvrA

TA98

TA1537

0

116 ± 13

14 ± 2

30 ± 1

27 ± 5

9 ± 2

20

130 ± 32

13 ± 3

39 ± 3

25 ± 7

8 ± 2

100

153 ± 14

16 ± 5

41 ± 7

32 ± 5

8 ± 1

500

161 ± 23

20 ± 4

37 ± 8

22 ± 7

10 ± 2

2500

153 ± 13

18 ± 2

48 ± 4

25 ± 3

9 ± 3

5000

179 ± 3

21 ± 9

44 ± 7

27 ± 8

9 ± 2

Positive controls, –S9

Name

MNNG

MNNG

ENNG

NOPD

AAC

Concentrations

(μg/plate)

5

5

10

10

100

Mean No. of colonies/plate

(average of 3 ± SD)

1223 ± 268

1070 ± 278

698 ± 36

982 ± 16

575 ± 6

+

0

119 ± 13

15 ± 3

46 ± 5

42 ± 4

9 ± 2

+

20

171 ± 24

16 ± 5

56 ± 5

40 ± 8

11 ± 0

+

100

143 ± 23

15 ± 5

39 ± 4

40 ± 13

10 ± 3

+

500

138 ± 22

19 ± 5

44 ± 6

43 ± 6

12 ± 3

+

2500

154 ± 10

22 ± 3

54 ± 13

 40 ± 3

7 ± 1

+

5000

147 ± 17

21 ± 3

57 ± 7

33 ± 4

9 ± 3

Positive controls, +S9

Name

2AA

2AA

2AA

2AA

2AA

Concentrations

(μg/plate)

2.5

2.5

60

2.5

2.5

Mean No. of colonies/plate

(average of 3 ± SD)

1297 ± 57

112 ± 3

327 ± 37

577 ± 33

214 ± 21

ENNG = N-ethyl-N-nitro-N-nitrosoguanidine

MNNG = N-methyl-N-nitro-N-nitrosoguanidine

NOPD = 4-nitro-o-phenylendiamine

AAC = 9-aminoacridine

2AA = 2-Aminoanthracene

B = reduced background growth

Table 2: Test results of experiment 2 (plate incorporation)

 

With or without S9-Mix

Test substance concentration

(μg/plate)

 

 

 

 

TA 100

WP2 uvrA

0

117 ± 5

35 ± 2

2000

105 ± 5

38 ± 3

3000

120 ± 13

41 ± 2

4000

108 ± 11

38 ± 7

5000

90 ± 10

45 ± 4

6000

148 ± 20

31 ± 9

Positive controls, –S9

Name

MNNG

ENNG

Concentrations

(μg/plate)

5

10

Mean No. of colonies/plate

(average of 3 ± SD)

1307 ± 138

505 ± 6

+

0

126 ± 28

36 ± 6

+

2000

136 ± 11

32 ± 3

+

3000

142 ± 5

32 ± 4

+

4000

119 ± 19

36 ± 4

+

5000

97 ± 11

24 ± 3

+

6000

 0B

0B

Positive controls, +S9

Name

2AA

2AA

Concentrations

(μg/plate)

2.5

60

Mean No. of colonies/plate

(average of 3 ± SD)

1182 ± 66

220 ± 34

ENNG = N-ethyl-N-nitro-N-nitrosoguanidine

MNNG = N-methyl-N-nitro-N-nitrosoguanidine

NOPD = 4-nitro-o-phenylendiamine

AAC = 9-aminoacridine

2AA = 2-Aminoanthracene

B = reduced background growth

 

 

Table 3: Test results of experiment 3 (preincubation)

 

With or without S9-Mix

Test substance concentration

(μg/plate)

Mean number of revertant colonies per plate

(average of 3 plates ± Standard deviation)

Base-pair substitution type

Frameshift type

TA 100

TA1535

WP2 uvrA

TA98

TA1537

0

141 ± 10

22 ± 4

33 ± 4

31 ± 3

8 ± 2

20

117 ± 4

18 ± 1

36 ± 2

28 ± 7

9 ± 2

100

113 ± 13

19 ± 1

34 ± 4

30 ± 2

8 ± 1

500

94 ± 8

7 ± 2

34 ± 5

16 ± 2

8 ± 1

2500

0B

0B

14 ± 3

0B

0B

5000

0B

0B

0B

0B

0B

Positive controls, –S9

Name

MNNG

MNNG

ENNG

NOPD

AAC

Concentrations

(μg/plate)

5

5

10

10

100

Mean No. of colonies/plate

(average of 3 ± SD)

1104 ± 47

789 ± 44

521 ± 33

1087 ± 70

408 ± 42

+

0

138 ± 10

23 ± 0

41 ± 7

46 ± 4

9 ± 1

+

20

124 ± 10

20 ± 3

40 ± 3

41 ± 2

11 ± 3

+

100

103 ± 1

21 ± 3

40 ± 2

44 ± 9

13 ± 6

+

500

88 ± 8

21 ± 3

35 ± 3

36 ± 9

11 ± 5

+

2500

102 ± 5

13 ± 3

50 ± 4

30 ± 7

8 ± 2

+

5000

43 ± 9B

0B

18 ± 2

0B

7 ± 1

Positive controls, +S9

Name

2AA

2AA

2AA

2AA

2AA

Concentrations

(μg/plate)

2.5

2.5

60

2.5

2.5

Mean No. of colonies/plate

(average of 3 ± SD)

983 ± 31

121 ± 9

227 ± 14

574 ± 54

103 ± 11

ENNG = N-ethyl-N-nitro-N-nitrosoguanidine

MNNG = N-methyl-N-nitro-N-nitrosoguanidine

NOPD = 4-nitro-o-phenylendiamine

AAC = 9-aminoacridine

2AA = 2-Aminoanthracene

B = reduced background growth

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative