Amines, N-(3- aminopropyl)-N’-[3-(C18 and C18-unsatd. alkyl amino)propyl]trimethylenedi and amines, N-(3-aminopropyl)-N’-(C18 and C18-unsatd. alkyl)trimethylenedi-

Genetic toxicity: in vitro

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

Study period:

16-jun-2009 to 29-jun-2009

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2009

Report date:

2009

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 471 (Bacterial Reverse Mutation Assay)

Deviations:

no

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Type of assay:

bacterial reverse mutation assay

Test material

Test material information

Constituent 1

Reference substance name:

Amines, N-(3- aminopropyl)-N’-[3-(C18 and C18-unsatd. alkyl amino)propyl]trimethylenedi and amines, N-(3-aminopropyl)-N’-(C18 and C18-unsatd. alkyl)trimethylenedi-

EC Number:

701-369-7

Molecular formula:

UVCB - No molecular formula;

IUPAC Name:

Amines, N-(3- aminopropyl)-N’-[3-(C18 and C18-unsatd. alkyl amino)propyl]trimethylenedi and amines, N-(3-aminopropyl)-N’-(C18 and C18-unsatd. alkyl)trimethylenedi-

Constituent 2

Reference substance name:

(Z)-N-(3-aminopropyl)-N'-[3-(9-octadecenylamino)propyl]propane-1,3-diamine

EC Number:

266-613-2

EC Name:

(Z)-N-(3-aminopropyl)-N'-[3-(9-octadecenylamino)propyl]propane-1,3-diamine

Cas Number:

67228-83-5

Molecular formula:

C27H58N4

IUPAC Name:

N-[3-[3-[[(E)-octadec-9-enyl]amino]propylamino]propyl]propane-1,3-diamine

Test material form:

solid

Details on test material:

- Name of test material (as cited in study report): Oleyl tripropylenetetramine
- Substance type: White paste (determined at NOTOX)
- Physical state: solid
- Analytical purity: 100% technical grade (UVCB)
- Impurities (identity and concentrations): See Certificate of Analysis
- Composition of test material, percentage of components: See Certificate of Analysis
- Purity test date: 5 Feb 2009
- Stability under test conditions: Stable
- Storage condition of test material: At room temperature in the dark under nitrogen

Specific details on test material used for the study:

Substance as described in Chapter 1.1

Method

Target gene:

- S. typhimurium: Histidine gene
- E. coli: Tryptophan gene

Species / strain

Species / strain 1

Species / strain / cell type:

S. typhimurium TA 1535, TA 1537, TA 98 and TA 100

Species / strain 2

Species / strain / cell type:

E. coli WP2 uvr A

Metabolic activation:

with and without

Metabolic activation system:

Rat liver S9-mix induced by a combination of phenobarbital and ß-naphthoflavone

Test concentrations with justification for top dose:

Experiment 1:
Preliminary test (without and with S9) TA100 and WP2uvrA: 3, 10, 33, 100, 333, 1000, 3330 and 5000 µg/plate
Main study: TA1535, TA1537, TA98 and TA100:
Without and with S9-mix: 0.3, 1, 3, 10, 33 and 66 µg/plate
Experiment 2:
TA1535
Without and with S9-mix: 0.3, 1, 3, 10, 20 and 33 µg/plate
TA1537, TA98 and TA100
Without and with S9-mix: 0.3, 1, 3, 10, 33 and 66 µg/plate
WP2uvrA
Without and with S9-mix: 1, 3, 10, 33, 100 and 200 µg/plate

Vehicle / solvent:

- Vehicle(s)/solvent(s) used: ethanol
- Justification for choice of solvent/vehicle: Accepted and approved by authorities and international guidelines

Controls

Controls 1

Untreated negative controls:

no

Negative solvent / vehicle controls:

yes

Remarks:

: ethanol

Positive controls:

yes

Positive control substance:

sodium azide

Remarks:

without S9 Migrated to IUCLID6: 5 µg/plate in saline for TA1535

Controls 2

Positive control substance:

9-aminoacridine

Remarks:

without S9 Migrated to IUCLID6: 60 µg/plate in water for TA1537

Controls 3

Positive control substance:

2-nitrofluorene

Remarks:

without S9 Migrated to IUCLID6: 10 µg/plate in DMSO for TA98

Controls 4

Positive control substance:

methylmethanesulfonate

Remarks:

without S9 Migrated to IUCLID6: 650 µg/plate in DMSO for TA100

Controls 5

Positive control substance:

4-nitroquinoline-N-oxide

Remarks:

without S9 Migrated to IUCLID6: 10 µg/plate in DMSO for WP2uvrA

Controls 6

Positive control substance:

other: 2-aminoanthracene in DMSO for all strains

Remarks:

with S9

Details on test system and experimental conditions:

METHOD OF APPLICATION: in agar (plate incorporation)

DURATION
- Exposure duration: 48 hours

NUMBER OF REPLICATIONS:
- Doses of the test substance were tested in triplicate in each strain. Two independent experiments were conducted.

DETERMINATION OF CYTOTOXICITY
- The reduction of the bacterial background lawn, the increase in the size of the microcolonies and the reduction of the revertant colonies

OTHER:
- Precipitation of the test substance on the plate

Evaluation criteria:

A test substance is considered negative (not mutagenic) in the test if:
a) The total number of revertants in tester strain TA100 is not greater than two (2) times the concurrent control, and the total number of revertants in tester strains TA1535, TA1537, TA98 or WP2uvrA is not greater than three (3) times the concurrent control.
b) The negative response should be reproducible in at least one independently repeated experiment.

A test substance is considered positive if:
b) A two-fold (TA100) or more or a three-fold (TA1535, TA1537, TA98, WP2uvrA) or more increase above solvent control in the mean number of revertant colonies is observed in the test substance group.
b) The increase in the mean number of revertant colonies follows the concentration of test substance (dose-response relationship).

Results and discussion

Test results

Test results 1

Key result

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

Vehicle controls validity:

valid

Positive controls validity:

valid

Test results 2

Key result

Species / strain:

E. coli WP2 uvr A

Metabolic activation:

with and without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

cytotoxicity

Vehicle controls validity:

valid

Positive controls validity:

valid

Additional information on results:

TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: Slight precipitation was observed at the top dose of 5000 µg/plate

RANGE-FINDING/SCREENING STUDIES:
- In tester strain TA100, toxicity was observed at dose levels of 33 μg/plate and above in the absence and presence of S9-mix. In tester strain WP2uvrA, toxicity was observed at dose levels of 100 μg/plate and above in the absence of S9-mix and at 333 µg/plate and above in the presence of S9-mix.

COMPARISON WITH HISTORICAL CONTROL DATA:
- The negative and strain-specific positive control values were within our laboratory historical control data ranges indicating that the test conditions were adequate and that the metabolic activation system functioned properly.

ADDITIONAL INFORMATION ON CYTOTOXICITY:
TA1535: without S9: 33 µg/plate and above and with S9: 33 µg/plate and above
TA1537: without S9: 33 µg/plate and above and with S9: 66 µg/plate and above
TA98: without S9: 33 µg/plate and above and with S9: 33 µg/plate and above
TA100: without S9: 33 µg/plate and above and with S9: 33 µg/plate and above
WP2uvrA: without S9: 100 µg/plate and above and with S9: 200 µg/plate and above

Applicant's summary and conclusion

Conclusions:

Based on the results of this study it is concluded that Oleyl tripropylenetetramine is not mutagenic in the Salmonella typhimurium reverse mutation assay and in the Escherichia coli reverse mutation assay.

Executive summary:

Evaluation of the mutagenic activity of Oleyl tripropylenetetramine in the Salmonella typhimurium reverse mutation assay and the Escherichia coli reverse mutation assay (with independent repeat).

 

Oleyl tripropylenetetramine was tested in the Salmonella typhimurium reverse mutation assay with four histidine-requiring strains of Salmonella typhimurium (TA1535, TA1537, TA98 and TA100) and in the Escherichia coli reverse mutation assay with a tryptophan-requiring strain of Escherichia coli (WP2uvrA). The test was performed in two independent experiments in the presence and absence of S9-mix (rat liver S9-mix induced by a combination of phenobarbital and ß-naphthoflavone).

 

The study procedures described in this report were based on the most recent OECD and EC guidelines.

 

Batch S001029 of Oleyl tripropylenetetramine was a white paste. The test substance was dissolved in ethanol. Table 1 gives an overview of the experiments conducted.

 

Table 1 Overview of experiments

Experiment	Tester strains	Metabolic activation	Concentration range (µg/plate)
Dose range finding	TA100 and WP2uvrA	- 5% (v/v) S9	Up to 5000 µg/plate Up to 5000 µg/plate
Experiment 1	TA1535, TA1537, TA98 and TA100	- 5% (v/v) S9	Up to 66 µg/plate Up to 66 µg/plate
Experiment 2	TA1535	- 10% (v/v) S9	Up to 33 µg/plate Up to 33 µg/plate
	TA1537, TA98 and TA100	- 10% (v/v) S9	Up to 66 µg/plate Up to 66 µg/plate
	WP2uvrA	- 10% (v/v) S9	Up to 200 µg/plate Up to 200 µg/plate

-  no S9-mix added.

 

Oleyl tripropylenetetramine precipitated on the plates at the top dose of 5000 µg/plate.

Cytotoxicity, as evidenced by a decrease in the number of revertants and/or a reduction of the

bacterial background lawn, was observed in all tester strains in the absence and presence of S9-

mix.

 

Oleyl tripropylenetetramine did not induce a significant dose-related increase in the number of revertant (His+) colonies in each of the four tester strains (TA1535, TA1537, TA98 and TA100) and in the number of revertant (Trp+) colonies in tester strain WP2uvrA both in the absence and presence of S9-metabolic activation. These results were confirmed in an independently repeated experiment.

 

In this study, the negative and strain-specific positive control values were within the laboratory historical control data ranges indicating that the test conditions were adequate and that the metabolic activation system functioned properly.

 

Based on the results of this study it is concluded that Oleyl tripropylenetetramine is not mutagenic in the Salmonella typhimurium reverse mutation assay and in the Escherichia coli reverse mutation assay.