1,3-Benzenedimethanamine, reaction products with glycidyl tolyl ether

Toxicity to microorganisms

Administrative data

Endpoint:

activated sludge respiration inhibition testing

Type of information:

experimental study

Adequacy of study:

key study

Study period:

This study was conducted between 21 February 2017 and 29 March 2017

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Reliability 1 is assigned because the study conducted according to OECD TG 209 in c ompliance with GLP, without deviations that influence the quality of the results

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2017

Report date:

2017

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test (Carbon and Ammonium Oxidation))

Version / remarks:

2010

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

2-​Propanol, 1-​[[[3-​(aminomethyl)​phenyl]​methyl]​amino]​-​3-​(2-​methylphenoxy)​-

Cas Number:

1617528-47-8

Molecular formula:

C18H24N2O2

IUPAC Name:

2-​Propanol, 1-​[[[3-​(aminomethyl)​phenyl]​methyl]​amino]​-​3-​(2-​methylphenoxy)​-

Constituent 2

Reference substance name:

3,3'-[benzene-1,3-diylbis(methanediylimino)]bis[1-(2-methylphenoxy)propan-2-ol]

Molecular formula:

C28H36N2O4

IUPAC Name:

3,3'-[benzene-1,3-diylbis(methanediylimino)]bis[1-(2-methylphenoxy)propan-2-ol]

Constituent 3

Reference substance name:

m-phenylenebis(methylamine)

EC Number:

216-032-5

EC Name:

m-phenylenebis(methylamine)

Cas Number:

1477-55-0

Molecular formula:

C8H12N2

IUPAC Name:

1,3-phenylenedimethanamine

impurity 1

Reference substance name:

2-Propanol, 1,3-bis(2-methylphenoxy)-

Cas Number:

17181-49-6

Molecular formula:

C17H20O3

IUPAC Name:

2-Propanol, 1,3-bis(2-methylphenoxy)-

impurity 2

Reference substance name:

1-{[2-hydroxy-3-(2-methylphenoxy)propyl][3-({[2-hydroxy-3-(2-methylphenoxy)propyl]amino}methyl)benzyl]amino}-3-(2-methylphenoxy)propan-1-ol

Molecular formula:

C38H48N2O6

IUPAC Name:

1-{[2-hydroxy-3-(2-methylphenoxy)propyl][3-({[2-hydroxy-3-(2-methylphenoxy)propyl]amino}methyl)benzyl]amino}-3-(2-methylphenoxy)propan-1-ol

impurity 3

Reference substance name:

3,3',3'',3'''-[benzene-1,3-diylbis(methanediylnitrilo)]tetrakis[1-(2-methylphenoxy)propan-2-ol]

Molecular formula:

C48H60N2O8

IUPAC Name:

3,3',3'',3'''-[benzene-1,3-diylbis(methanediylnitrilo)]tetrakis[1-(2-methylphenoxy)propan-2-ol]

Test material form:

liquid: viscous

Details on test material:

Identification:
1,3-Benzenedimethanamine, reaction products with glycidyl tolyl ether
Appearance/Physical state:
clear, colorless, viscous liquid
Batch:
WA 1508
Purity:
100% UVCB
Expiry date:
01 January 2021
Storage conditions:
room temperature, in the dark

Specific details on test material used for the study:

Identification: 1,3-Benzenedimethanamine, reaction products with glycidyl tolyl ether
Physical state/Appearance: clear colorless viscous liquid
Batch: WA 1508
Purity: not provided
Expiry Date: 01 January 2021
Storage Conditions: room temperature in the dark

Sampling and analysis

Analytical monitoring:

no

Remarks:

As it was not a requirement of the Test Guidelines, no analysis was conducted to determine the homogeneity, concentration or stability of the test item formulation. This is an exception with regard to GLP and is reflected in the GLP compliance statement.

Test solutions

Vehicle:

no

Details on test solutions:

Range-Finding Test
Test Item Preparation
In the range-finding test, activated sewage sludge micro-organisms were exposed to a series of nominal test concentrations of 10, 100 and 1000 mg/L. The test item was dispersed directly in water.
Nominal amounts of test item (5, 50 and 500 mg (in triplicate)) were each separately dispersed in approximately 200 mL of deionized reverse osmosis water and subjected to ultrasonication for approximately 15 minutes followed by magnetic stirring for 24 hours, at temperatures of between 20 C and 21 C, in order to maximize the dissolved test item concentration. All test vessels were shielded from the light during mixing. Synthetic sewage (16 mL), activated sewage sludge (250 mL) and water were added to a final volume of
500 mL to give the required concentrations of 10, 100 and 1000 mg/L (3 replicates).
The pH of the test item dispersions was measured after stirring using a Hach HQ40d Flexi handheld meter and adjusted to between pH 7.0 and 8.0.
The exposure conditions for each flask were as described below.
The control group was maintained under identical conditions but not exposed to the test item.

Reference Item Preparation
A reference item, 3,5-dichlorophenol, was included in the range-finding test at concentrations of 3.2, 10 and 32 mg/L in order to confirm the suitability of the inoculum. A stock solution of 0.5 g/L was prepared by dissolving the reference item directly in water with the aid of ultrasonication for approximately 23 minutes. The pH of this stock solution was measured to be pH 6.4 and was adjusted to pH 7.0 using 1.0 M NaOH. The pH values were measured using a Hach HQ40d Flexi handheld meter. Aliquots (3.2, 10 and 32 mL) of the stock solution were removed and dispersed with activated sewage sludge (250 mL), synthetic sewage (16 mL) and water to a final volume of 500 mL to give the required concentrations of 3.2, 10 and 32 mg/L. The volumetric flask containing the reference item was inverted several times to ensure homogeneity of the solution.
The exposure conditions for each flask were as described below.

Definitive Test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 10, 32, 100, 320 and 1000 mg/L.

Test Item Preparation
The test item was dispersed directly in water.
Nominal amounts of test item (5.0, 16, 50, 160 and 500 mg (in triplicate)) were each separately dispersed in approximately 200 mL of deionized reverse osmosis water and subjected to ultrasonication for approximately 15 minutes followed by magnetic stirring for 24 hours, at temperatures between 20 C and 21 C, in order to maximize the dissolved test item concentration. All test vessels were shielded from the light during mixing. Synthetic sewage (16 mL), activated sewage sludge (250 mL) and water were added to a final volume of 500 mL to give the required concentrations of 10, 32, 100, 320 and 1000 mg/L
(3 replicates of each).
The pH of the test item dispersions were measured after stirring using Hach HQ40d Flexi handheld meter and adjusted to between pH 7.0 to pH 8.0.
As it was not a requirement of the Test Guidelines, no analysis was conducted to determine the homogeneity, concentration or stability of the test item formulation. This is an exception with regard to GLP and has been reflected in the GLP compliance statement.
The control group was maintained under identical conditions but not exposed to the test item.

Reference Item Preparation
For the purpose of the test a reference item, 3,5-dichlorophenol was used. A stock solution of 0.5 g/L was prepared by dissolving the reference item directly in water with the aid of ultrasonication for approximately 20 minutes. The pH of this stock solution was measured to be pH 6.6 and adjusted to pH 7.2 using 1.0 M NaOH. The pH values were measured using a Hach HQ40d Flexi handheld meter. Aliquots (3.2, 10 and 32 mL) of the stock solution were removed and dispersed with activated sewage sludge (250 mL), synthetic sewage (16 mL) and water to give the final concentrations of 3.2, 10 and 32 mg/L. The volumetric flask containing the reference item was inverted several times to ensure homogeneity of the solution.

Test organisms

Test organisms (species):

activated sludge of a predominantly domestic sewage

Details on inoculum:

A mixed population of activated sewage sludge micro-organisms was obtained on 22 February 2017 for the range-finding test and on 28 March 2017 for the definitive test from the aeration stage of the Severn Trent Water Plc sewage treatment plant at Loughborough, Leicestershire, UK which treats predominantly domestic sewage


Preparation of Inoculum
Preparation of Inoculum
The activated sewage sludge sample was maintained on continuous aeration in the laboratory at a temperature of approximately 21 ºC and was used on the day of collection. The pH of the sample was 7.6 measured using a Hach HQ40d Flexi handheld meter. Determination of the suspended solids level of the activated sewage sludge was carried out by filtering a sample (100 mL) of the activated sewage sludge by suction through a pre-weighed GF/A filter paper* using a Buchner funnel which was then rinsed 3 times with 10 mL of deionized reverse osmosis water and filtration continued for 3 minutes. The filter paper was then dried in an oven at approximately 105 ºC for at least one hour and allowed to cool before weighing. This process was repeated until a constant weight was attained. The suspended solids concentration was equal to 3.0 g/L.

Study design

Test type:

static

Water media type:

freshwater

Limit test:

no

Total exposure duration:

3 h

Test conditions

Hardness:

Not reported

Test temperature:

21 - 22”C

pH:

7.2 - 8.0

Dissolved oxygen:

5.5 - 6.2 mg O2/L or 62 - 70% of Dissolved Oxygen Saturation Level of 8.9 mg O2/L

Salinity:

Not reported

Conductivity:

Not reported

Nominal and measured concentrations:

Range-Finding Test
Nominal test concentrations of 10, 100 and 1000 mg/L

Definitive Test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 10, 32, 100, 320 and 1000 mg/L

Details on test conditions:

Definitive Test
Based on the results of the range-finding test the following test concentrations were assigned to the definitive test: 10, 32, 100, 320 and 1000 mg/L.

Test Item Preparation
The test item was dispersed directly in water.
Nominal amounts of test item (5.0, 16, 50, 160 and 500 mg (in triplicate)) were each separately dispersed in approximately 200 mL of deionized reverse osmosis water and subjected to ultrasonication for approximately 15 minutes followed by magnetic stirring for 24 hours, at temperatures between 20 ”C and 21 ”C, in order to maximize the dissolved test item concentration. All test vessels were shielded from the light during mixing. Synthetic sewage (16 mL), activated sewage sludge (250 mL) and water were added to a final volume of 500 mL to give the required concentrations of 10, 32, 100, 320 and 1000 mg/L
(3 replicates of each).
The pH of the test item dispersions were measured after stirring using Hach HQ40d Flexi handheld meter and adjusted to between pH 7.0 to pH 8.0.
As it was not a requirement of the Test Guidelines, no analysis was conducted to determine the homogeneity, concentration or stability of the test item formulation. This is an exception with regard to GLP and has been reflected in the GLP compliance statement.
The control group was maintained under identical conditions but not exposed to the test item.

Reference Item Preparation
For the purpose of the test a reference item, 3,5-dichlorophenol was used. A stock solution of 0.5 g/L was prepared by dissolving the reference item directly in water with the aid of ultrasonication for approximately 20 minutes. The pH of this stock solution was measured to be pH 6.6 and adjusted to pH 7.2 using 1.0 M NaOH. The pH values were measured using a Hach HQ40d Flexi handheld meter. Aliquots (3.2, 10 and 32 mL) of the stock solution were removed and dispersed with activated sewage sludge (250 mL), synthetic sewage (16 mL) and water to give the final concentrations of 3.2, 10 and 32 mg/L. The volumetric flask containing the reference item was inverted several times to ensure homogeneity of the solution.

Preparation of Test System
At time "0" 16 mL of synthetic sewage was diluted to 250 mL with water and 250 mL of inoculum added in a 500 mL conical flask (first control). The mixture was aerated with clean, oil-free compressed air via narrow bore glass tubes at a rate of 0.5 to 1.0 liter per minute. Thereafter, at 15 minute intervals the procedure was repeated for the second control followed by the reference item vessels with appropriate amounts of the reference item being added. The test item vessels were prepared as described in above. Finally two further control vessels were prepared.
The test was conducted under normal laboratory lighting in a temperature controlled room at measured temperatures of between 21 and 22 ºC

Reference substance (positive control):

yes

Remarks:

Identification: 3,5-Dichlorophenol Physical state/Appearance: pale brown crystalline solid Batch: MKBV7274V Purity: 99.6% Expiry Date: 26 January 2022 Storage Conditions: room temperature

Results and discussion

Effect concentrations

Key result

Duration:

3 h

Dose descriptor:

EC50

Effect conc.:

160 mg/L

Nominal / measured:

nominal

Conc. based on:

test mat.

Basis for effect:

inhibition of total respiration

Details on results:

Range-Finding Test
The dissolved oxygen concentrations in all vessels after 30 minutes contact time are given in Table 1. Oxygen consumption rates and percentage inhibition values for the control, test and reference item after 3 hours contact time are given in Table 2.
The dissolved oxygen concentrations after 30 minutes contact time in all vessels were above 60% of the dissolved oxygen saturation level of 8.9 mg O2/L.
No statistically significant toxic effects were shown at the test concentration of 10 mg/L, however statistically significant toxic effects were shown at the test concentrations of 100 and 1000 mg/L.
Based on these results and after discussion with the Sponsor, it was considered necessary to perform a definitive test in order to obtain an EC50 value for the test item. Based on this information test concentrations of 10, 32, 100, 320 and 1000 mg/L were selected for the definitive test.

Definitive Test
The dissolved oxygen concentrations in all vessels after 30 minutes contact time are given in Table 3. Oxygen consumption rates and percentage inhibition values for the control, test and reference items after 3 hours contact time are given in Table 4.

Validation Criteria
The coefficient of variation of oxygen uptake in the control vessels was 6.2% and the specific respiration rate of the controls was 30.28 mg oxygen per gram dry weight of sludge per hour. The validation criteria have therefore been satisfied.
The validation criterion for the reference item EC50 value was also satisfied

Inhibition of Respiration Rate
The following results were derived:

1,3-Benzenedimethanamine, reaction products 3,5-dichlorophenol
ECx (3 hours)(mg/mL) 95% Confidence LImits (mg/mL) ECx (3 hours)(mg/mL) 95% Confidence Limits (mg/mL)
EC10 75 - 1.6 -
EC20 100 - 2.4 -
EC50 160 - 7.6 5.9 - 9.8
EC80 260 - 24 -

In some instances, the initial and final dissolved oxygen concentrations were outside those recommended in the test guidelines (7 mg O2/L and 2 mg O2/L respectively). This was considered to have had no adverse effect on the results of the study given that in all cases the oxygen consumption rate was determined over the linear portion of the oxygen consumption trace.

Results with reference substance (positive control):

See "Details on Results" (above)

Any other information on results incl. tables

Table 1: Dissolved Oxygen Concentrations of the Test Preparations after 30 Minutes Contact Time in the Range-Finding Test

Dissolved Oxygen Concentrations of the Test Preparations after 30 Minutes Contact Time in the Definitive Test		Dissolved Oxygen Concentration (mg O2/L)	Expressed as a Percentage of a Dissolved Oxygen Saturation Level of 8.9 mg O2/L
Control	R1	6.0	67
	R2	6.1	69
	R3	5.9	66
	R4	5.5	62
Test Item	10	6.4	72
	100	6.2	70
	1000 R1	7.7	87
	1000 R2	7.9	89
	1000 R3	7.9	89
3,5 -dichlorophenol	3.2	6.3	71
	10	7.6	85
	32	8.2	92

Table 2: Oxygen Consumption Rates and Percentage Inhibition Values after 3 Hours Contact Time in the Range-Finding Test

Nominal Concentration (mg/L)	Initial O^2 Reading (mg O2/L)	Measurement Period (minutes)	Final O2 Reading (mg O2/L)	O2 Consumption Rates (mg O2/L/hour)	% Inhibition
Control R1	6.3	7	2.0	36.86	-
R2	6.0	7	1.9	35.14	-
R3	6.0	6	2.3	37.00	-
R4	5.0	5	1.8	38.40	-
Test Item 10	5.5	5	2.2	39.60	[7]
100	6.1	10	2.5	21.60	41
1000 R1	8.3	10	8.3	0.00	100
1000 R2	8.6	10	8.5	0.60	98
1000 R3	8.6	10	8.5	0.60	98
3,5 -dichlorophenol 3.2	6.2	8	2.1	30.75	17
10	6.6	10	4.0	15.60	58
32	7.6	10	6.8	4.80	87

R1 – R4 = Replicates 1 to 4

[Increase in respiration rate as compared to controls]

Table 3       Dissolved Oxygen Concentrations of the Test Preparations after 30 Minutes Contact Time in the Definitive Test

Dissolved Oxygen Concentrations of the Test Preparations after 30 Minutes Contact Time in the Definitive Test		Dissolved Oxygen Concentration (mg O2/L)	Expressed as a Percentage of a Dissolved Oxygen Saturation Level of 8.9 mg O2/L
Control	R1	5.6	63
	R2	6.0	67
	R3	5.7	64
	R4	6.2	70
	R5	5.5	62
	R6	5.5	62
Test Item	10 R1	6.1	69
	10 R2	6.2	70
	10 R3	6.2	70
	32 R1	5.5	62
	32 R2	5.8	65
	32 R3	5.5	62
	100 R1	5.9	66
	100 R2	5.7	64
	100 R3	6.2	70
	320 R1	5.8	65
	320 R2	6.4	72
	320 R3	6.2	70
	1000 R1	7.1	80
	1000 R2	5.9	80
	1000 R3	5.8	65
3,5 -dichlorophenol	3.2	5.5	62
	10	7.0	79
	32	8.5	96

R1 – R3 = Replicates 1 to 3

Table 4       Oxygen Consumption Rates and Percentage Inhibition Values after 3 Hours Contact Time in the Definitive Test

Concentration (mg/L)	Initial O^2 Reading (mg O2/L)	Measurement Period (minutes)	Final O2Reading (mg O2/L)	O2Consumption Rates (mg O2/L/hour)	% Inhibition
Control R1	3.6	2	1.9	51.00	-
R2	4.2	3	2.0	44.00	-
R3	4.2	3	2.0	44.00	-
R4	4.9	4	2.0	43.50	-
R5	5.1	4	2.1	45.00	-
R6	5.0	4	2.0	45.00	-
Test Item 10 R1	4.0	3	1.7	46.00	[1]
10 R2	4.9	4.	1.9	45.00	1
10 R3	5.4	4	2.5	43.50	4
32 R1	4.8	4	1.9	43.50	4
32 R2	4.9	4	2.0	43.50	4
32 R3	4.9	4	2.1	42.00	8
100 R1	4.9	5	1.8	37.20	18
100 R2	5.4	5	2.4	36.00	21
100 R3	5.0	5	1.9	37.20	18
320 R1	7.4	10	6.0	8.40	82
320 R2	8.0	10	7.2	4.80	89
320 R3	8.0	10	7.2	4.80	89
1000 R1	8.3	10	8.0	1.80	96
1000 R2	8.3	10	7.9	2.40	95
1000 R3	8.4	10	8.2	1.20	97
3,5 -dichlorophenol 3.2	5.6	6	2.3	33.00	27
10	6.5	10	3.3	19.20	58
32	7.9	10	6.9	6.00	87

R1 – R3 = Replicates 1 to 3

Applicant's summary and conclusion

Validity criteria fulfilled:

yes

Conclusions:

The effect of the test item on the respiration of activated sewage sludge micro-organisms gave a 3-Hour EC50 value of 160 mg/L, 95% confidence limits 140 to 190 mg/L.

Executive summary:

A study was performed to assess the effect of the test item on the respiration of activated sewage sludge.  The method followed was designed to be compatible with the OECD Guidelines for Testing of Chemicals (2010) No. 209 "Activated Sludge, Respiration Inhibition Test (Carbon and Ammonium Oxidation)".

Methods

Following a preliminary range-finding test, activated sewage sludge was exposed to an aqueous dispersion of the test item at concentrations of 10, 32, 100, 320 and 1000 mg/L for a period of 3 hours at measured temperatures of between 21 and 22 deg C with the addition of a synthetic sewage as a respiratory substrate.

The rate of respiration was determined after 3 hours contact time and compared to data for the control and a reference item, 3,5-dichlorophenol.

Results

The effect of the test item on the respiration of activated sewage sludge gave a 3 Hour EC50 value of 160 mg/L, 95% confidence limits 140 to 190 mg/L.  

The reference item gave a 3-Hour EC50 value of 7.6 mg/L, 95% confidence limits 5.9 to 9.8 mg/L.