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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
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1994-07-06 - 1994-10-08
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1994
Report date:
1994

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
range of strains does not comply with current guideline
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
3-(trimethoxysilyl)propyl isocyanate
EC Number:
239-415-9
EC Name:
3-(trimethoxysilyl)propyl isocyanate
Cas Number:
15396-00-6
Molecular formula:
C7H15NO4Si
IUPAC Name:
(3-isocyanatopropyl)trimethoxysilane
Test material form:
liquid
Details on test material:
.

Method

Target gene:
Histidine
Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Species / strain / cell type:
S. typhimurium TA 1538
Metabolic activation:
with and without
Metabolic activation system:
Aroclor induced rat liver S9
Test concentrations with justification for top dose:
Test 1: 0.003 - 0.30 µg/plate. Test 2: 0.03 - 3.0 µg/plate
Vehicle / solvent:
DMSO
Controlsopen allclose all
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: 4-Nitro-o-Phenylenediamine 0.01 µg/plate
Remarks:
TA98, TA1538 without metabolic activation
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
sodium azide
Remarks:
TA100, TA1535 without metabolic activation; 0.01 µg/plate
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
9-aminoacridine
Remarks:
TA1537 without metabolic activation 0.06 µg/plate
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: 2-Aminoanthracene 2.5 µg/plate
Remarks:
TA 98, TA100, TA1535, TA1537 and TA1538 with metabolic activation
Details on test system and experimental conditions:
METHOD OF APPLICATION: in medium; in agar (plate incorporation); preincubation

DURATION
- Preincubation period: ?
- Exposure duration: 48 - 72 hours


SELECTION AGENT (mutation assays):

NUMBER OF REPLICATIONS:
3 plates per dose, experiment repeated


DETERMINATION OF CYTOTOXICITY
- Method: Revertant colonies were counted


OTHER:
Evaluation criteria:
A chemical is considered positive if it shows a statistically significant dose dependent and reproducible increase in the number of revertants relative to the solvent control.
Statistics:
None used

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 98
Metabolic activation:
without
Genotoxicity:
positive
Remarks:
Produced a weak but consistent mutagenic effect
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 1538
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid

Any other information on results incl. tables

Table 1a Experiment 1 Number of revertants per plate (mean of 3 plates)

Concentration

µg/plate

TA98

TA100

TA1535

-MA

+MA

-MA

+MA

-MA

+MA

Solvent control

7

18

90

88

25

8

Positive control

294

1500

645

1310

596

90

3

10

-

1

-

3*

-

10

10

14

64

80

134

5

30

12

15

69

72

3*

6

100

17

14

60

71

9*

6

300

12

9

69

50

4*

2*

3000

-

3*

-

8*

-

0*

* Toxic, absence of background lawn, or mean number of colonies < ½ solvent control values.

 

Table 1b Experiment 1 Number of revertants per plate (mean of 3 plates)

Concentration

TA1537

TA1538

µg/plate

-MA

+MA

-MA

+MA

Solvent control

4

3

9

14

Positive control

76

150

451

1285

3

4

-

5

3

10

4

4

11

11

30

4

5

7

9

100

3

5

12

12

300

2

3

2

6*

3000

-

*

2*

0*

* Toxic: absence of background lawn, or mean number of colonies < ½ solvent control values.

 

Table 2a Experiment 2 Number of revertants per plate (mean of 3 plates)

Concentration

TA98

TA100

TA1535

µg/plate

-MA

+MA

-MA

+MA

-MA

+MA

Solvent control

11

17

59

83

3

5

Positive control

341

1508

688

1572

664

101

3

12

-

59

-

4

-

10

13

20

53

65

4

7

30

15

17

66

74

5

4

100

22

18

65

76

2

1*

300

6

15

57

40*

1*

4

3000

-

0*

-

14*

-

3*

* Toxic, absence of background lawn, or mean number of colonies < ½ solvent control values.

 

Table 2b Experiment 2 Number of revertants per plate (mean of 3 plates)

Concentration

TA1537

TA1538

µg/plate

-MA

+MA

-MA

+MA

Solvent control

3

6

10

9

Positive control

100

175

338

1340

3

2

-

9

-

10

4

5

9

9

30

5

3

11

11

100

5

5

10

12

300

2

3

4*

6

3000

-

2*

-

2*

* Toxic, absence of background lawn, or mean number of colonies < ½ solvent control values.

Applicant's summary and conclusion

Conclusions:
3-(trimethoxysilyl)propyl isocyanate has been tested according to a protocol that is similar to OECD 471, and under GLP in Salmonella typhimurium strains TA 98, TA 100, TA 1535, TA 1537 and TA 1538. A slight increase in the number of revertants was observed in strain TA 98 in the absence of metabolic activation, in the initial experiment at a single dose. This result was reproducible in the second experiment, in which the response appeared to be weakly dose-dependent. This was considered to be evidence of a weak mutagenic potential. It is concluded that the test substance is positive for mutagenicity to Salmonella typhimurium TA 98 in the absence of metabolic activation under the conditions of the test.