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EC number: 413-110-2 | CAS number: 135861-56-2
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Toxicity to microorganisms
Administrative data
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 8th January 2002 (range finding test); 24th January 2002 (definitive test)
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.6800 (Modified Activated Sludge, Respiration Inhibition Test for Sparingly Soluble Chemicals)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Details on test material:
- Sponsor's identification: Experimental 11334-18
Data relating to the identity, purity and stability of the test material are the responsibility of the Sponsor.
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
- Details on sampling:
- Not applicable
Test solutions
- Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: For the purpose of the definitive test, the test material was dispersed directly in water or prepared using a preliminary solution in dimethylformamide.
An amount of test material (500 mg) was dispersed in approximately 250 mL of water and subjected to ultrasonication (approximately 30 minutes). Synthetic sewage (16 mL), activated sewage sludge (200 mL) and water were added to a final volume of 500 mL to give the required concentration of 1000 mg/L. This method of preparation was performed for each of 3 replicate vessels.
Additionally, the definitive test also consisted of a single test concentration prepared using a preliminary solution in dimethylformamide. An amount of test material (47.6 mg) was dissolved in dimethylformamide and the volume adjusted to 10 mL to give an 47.6 mg/10 mL stock solution from which a dilution was made to give a 4.76 mg/10 mL solvent stock solution. An aliquot (50 µL) of the 4.76 mg/10 mL stock solution was dispersed with activated sewage sludge (200 mL), synthetic sewage (16 mL) and water, to a final volume of 500 mL to give the test concentration of 0.0476 mg/L.
The volumetric flasks containing the solvent stock solutions were inverted several times to ensure homogeneity of the stock solutions.
Analysis of the concentration, homogeneity and stability of the test material in the test preparations was not appropriate to the Test Guideline.
A standard synthetic sewage was added to each test vessel to act as a respiratory substrate.
- Controls: At time "0" 16 mL of synthetic sewage was diluted to 300 mL with water and 200 mL of inoculum added in a 500 mL conical flask (first control). The mixture was aerated with compressed air via narrow bore glass tubes at a rate of approximately 0.5 - 1 litre per minute. Thereafter, at 15 minute intervals the procedure was repeated with appropriate amounts of the reference material being added. A solvent control vessel was prepared containing 16 mL synthetic sewage, 300 mL water, 50 µL of dimethylformamide and 200 mL of inoculum in a 500 mL conical flask. Finally a second control was prepared.
- Chemical name of vehicle (organic solvent): Dimethylformamide
- Concentration of vehicle in test medium (stock solution and final test solution(s) including control(s)): Not specified
- Evidence of undissolved material (e.g. precipitate, surface film, etc): The 0.0476 mg/L test samples were dark brown dispersions with no undissolved test material visible. The 1000 mg/L test samples were dark brown dispersions with many white particles of undissolved test material on the surface and dispersed throughout the test medium.
Test organisms
- Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Laboratory culture: Not applicable
- Source: A mixed population of activated sewage sludge micro-organisms was obtained on 24 January 2002 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 for exposure: The activated sewage sludge sample was maintained on continuous aeration in the laboratory at a temperature of 21°C and was used on the day of collection. The pH of the sample was 7.6 measured using a WTW pH 320 pH 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 piece of pre-weighed GFIA filter paper using a Buchner funnel. The paper was then dried in an oven at approximately 110°C for approximately 1 hour and allowed to cool before re-weighing. The suspended solids was equal to 3.9 g/L prior to use.
- Pretreatment: None specified
- Initial biomass concentration: Not specified
Study design
- Test type:
- other: aerobic
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 3 h
- Post exposure observation period:
- Not performed
Test conditions
- Hardness:
- Mean: 176 mg/L CaCO3
- Test temperature:
- 21 °C
- pH:
- pH of the inoculum: 7.6
pH values of the test preparations at the end of the exposure period:7.6-7.9 - Dissolved oxygen:
- Not specified
- Salinity:
- Not specified
- Nominal and measured concentrations:
- 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.
Based on the results of the range-finding test a "limit test" was conducted at a concentration of 1000 mg/L (three replicate vessels) to confirm that at this concentration no effect on respiration of the activated sewage sludge was observed.
In addition to this a test concentration of 0.0476 mg/L was prepared using a preliminary solution in auxiliary solvent to confirm that at the limit of water solubility (data supplied by the Sponsor) no effect on respiration of the activated sewage sludge was observed. - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (open / closed): Not specified
- Material, size, headspace, fill volume: Standard glass conical flasks of 500 mL capacity.
- Aeration: The mixtures were aerated with compressed air via narrow bore glass tubes at a rate of approximately 0.5 - 1 litre per minute.
- Type of flow-through (e.g. peristaltic or proportional diluter): Not applicable
- Renewal rate of test solution (frequency/flow rate): Not applicable
- No. of organisms per vessel: Not applicable
- No. of vessels per concentration (replicates): 3 replicates at the 1000 mg/L dose level; 1 vessel at the 0.0476 mg/L dose level in the definitive test.
- No. of vessels per control (replicates): 2 replicates
- No. of vessels per vehicle control (replicates): 1 vessel (the solvent control was exposed to 100 µL/L of dimethylformamide)
- Biomass loading rate: Not specified
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: The test water used for both the range-finding and definitive tests was laboratory tap water dechlorinated by passage through an activated carbon filter and partly softened.
- Total organic carbon: Mean value: 1 mg/L
- Particulate matter: Not specified
- Metals: Various metals are present in the water at differing concentrations
- Pesticides: <0.01 µg/L
- Chlorine: Total chlorine (mean value): 0.156 mg/L
- Alkalinity: Mean pH: 7.804
- Ca/mg ratio: Ca: 54 mg/L; Mg: 10 mg/L
- Conductivity: Mean value: 413267 µS/cm
- Culture medium different from test medium: No
- Intervals of water quality measurement: Observations were made on the test preparations throughout the test period, and the pH of the control, reference material and test material preparations were measured at the end of the exposure period prior to measurement of the oxygen consumption rate.
OTHER TEST CONDITIONS
- Adjustment of pH: No
- Photoperiod: None specified
- Light intensity: Normal laboratory lighting
EFFECT PARAMETERS MEASURED:
As each vessel reached 30 minutes contact time an aliquot was removed from the conical flask and poured into the measuring vessel (250 mL darkened glass Biological Oxygen Demand (BOD) bottle) and the rate of respiration measured using a Yellow Springs dissolved oxygen meter fitted with a BOD probe. The contents of the measuring vessel were stirred constantly by magnetic stirrer. The rate of respiration for each flask was measured over the linear portion of the oxygen consumption trace for an approximate 10 minute period (between approximately 8.9 mg O2/L and 1.3 mg O2/L). After measurement the contents of the BOD bottle were returned to the test vessel.
This procedure was repeated after 3 hours contact time.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: The test concentrations to be used in the definitive test were determined by a preliminary range-finding test.
- Justification for using less concentrations than requested by guideline: The definitive study was performed as a limit test.
- Range finding study
- Test concentrations: 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 material was dispersed directly in water. Amounts of test material (5.0, 50 and 500 mg) were separately dispersed in approximately 250 mL of water and subjected to ultrasonication (approximately 30 minutes). Synthetic sewage (16 mL), activated sewage sludge (200 mL) and water were added to a final volume of 500 mL to give the required concentrations of 10, 100 and 1000 mg/L.
The control group was maintained under identical conditions but not exposed to the test material.
A reference material, 3.5-dichlorophenol, was included in the range-finding test at concentrations of 3.2 and 32 mg/L in order to confirm the suitability of the inoculum.
Oxygen consumption rates were measured after 3 hours contact time only.
- Results used to determine the conditions for the definitive study: Oxygen consumption rates and percentage inhibition values for the control, test and reference materials in the range-finding test are given in Table 1.
No significant effect on respiration was observed at any of the test concentrations employed. Based on this information, a single test concentration, in triplicate, of 1000 mg/L was selected for the definitive test.
Data supplied by the Sponsor indicated the water solubility of the test material to be 0.0476 mg/L therefore in order to satisfy the requirements of all Competent Authorities worldwide a single test concentration of 0.0476 mg/L prepared using a preliminary solution in auxiliary solvent was also included in the study.
Using this approach the effect of an excess amount of undissolved test material can be assessed in order to determine whether the test material has any effect on the activated sewage sludge micro-organisms exoenzymes, or whether the uptake of undissolved test material by processes such as phagocytosis has any adverse effect on the activated sewage sludge. In addition the use of a test vessel at the maximum attainable test concentration that is a solution can show whether soluble test material has an adverse effect on the activated sewage sludge. - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 3 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.048 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: Test performed at the limit of water solubility
- Details on results:
- - Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: Observations made throughout the study period, showed that at the test concentration of 1000 mg/L, white particles of undissolved test material were visible on the surface and dispersed throughout the test media at 0 hours, 30 minutes and 3 hours contact time. This was considered to be due to the insoluble nature of the test material in the test media. However at the test concentration of 0.0476 mg/L no undissolved test material was visible in a dark brown dispersion at 0 hours, 30 minutes and 3 hours contact time.
- Effect concentrations exceeding solubility of substance in test medium: The 1000 mg/L test samples exceeded the solubility of the test material in the test medium. - Results with reference substance (positive control):
- - Results with reference substance valid?: Yes
- Relevant effect levels:
EC50 (30 minutes): 20 mg/L
EC50 (3 hours): 13 mg/L - Reported statistics and error estimates:
- No data available
Any other information on results incl. tables
Variation in respiration rates of controls 1 and 2 after 30 minutes: 2%.
Variation in respiration rates of controls 1 and 2 after 3 hours: ± 4%.
The validation criteria for the control respiration rates and reference material EC50 values have been satisfied.
Table 1: Oxygen Consumption Rates and Percentage Inhibition Values in the Range-finding Test
Nominal concentration (mg/L) |
Initial O2reading (mg O2/L) |
Measurement period (minutes) |
Final O2reading (mg O2/L) |
O2consumption rates (mg O2/L/min) |
% inhibition |
|
Control |
R1 |
6.9 |
9 |
2.7 |
0.47 |
- |
|
R2 |
7.1 |
9 |
2.6 |
0.50 |
- |
Test material |
10 |
7.1 |
8 |
2.6 |
0.56 |
[15] |
|
100 |
6.6 |
8 |
2.3 |
0.54 |
[11] |
|
1000 |
6.1 |
7 |
2.5 |
0.51 |
[5] |
3,5-dichlorophenol |
3.2 |
6.5 |
9 |
2.5 |
0.44 |
9 |
|
32 |
8.1 |
10 |
7.2 |
0.09 |
81 |
Table 2:Oxygen Consumption Rates and Percentage Inhibition Values in theDefinitive Test after 3 Hours Contact Time
Nominal concentration (mg/L) |
Initial O2reading (mg O2/L) |
Measurement period (minutes) |
Final O2reading (mg O2/L) |
O2consumption rates (mg O2/L/min) |
% inhibition |
|
Control |
R1 |
7.1 |
8 |
2.3 |
0.60 |
- |
R2 |
6.7 |
8 |
2.3 |
0.55 |
- |
|
Solvent control |
7.3 |
9 |
2.2 |
0.57 |
- |
|
Test material |
0.0476 |
7.2 |
10 |
1.9 |
0.53 |
7 |
1000 R1 |
6.5 |
9 |
1.5 |
0.56 |
3 |
|
1000 R2 |
6.3 |
8 |
1.8 |
0.56 |
3 |
|
1000 R3 |
6.3 |
9 |
1.3 |
0.56 |
3 |
|
3,5-dichlorophenol |
3.2 |
6.8 |
8 |
2.4 |
0.55 |
4 |
10 |
7.9 |
10 |
4.2 |
0.37 |
36 |
|
32 |
8.9 |
10 |
8.0 |
0.09 |
84 |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The effect of the test material on the respiration of activated sewage sludge micro-organisms gave a 3 hour EC50 of greater than 1000 mg/L. The NOEC after 3 hours exposure was 1000 mg/L.
In the single test vessel prepared using a preliminary solution in auxiliary solvent to give a test concentration of 0.0476 mg/L (limit of water solubility), no significant inhibition of the respiration rate of activated sewage sludge was observed and hence the 3-Hour EC50 value was determined to be greater than 0.0476 mg/L. Correspondingly the NOEC determined from this vessel was 0.0476 mg/L. These results show that at the limit of water solubility no effect on the respiration rate of activated sewage sludge micro-organisms was observed. - Executive summary:
The inhibitory effect of Millad 3988 on the respiration of activated sewage sludge was assessed in a study performed in accordance with OECD Guideline No. 209.
In the single test vessel prepared using a preliminary solution in auxiliary solvent to give a test concentration of 0.0476 mg/L (the limit of water solubility supplied by the Sponsor) no significant inhibition of the respiration rate of activated sewage sludge was observed and hence the 3-Hour EC50 value was determined to be greater than 0.0476 mg/L. Correspondingly the NOEC determined from this vessel was 0.0476 mg/L. These results show that at the limit of water solubility of the test material, the test material has no effect on the respiration rate of activated sewage sludge.
The effect of the test material on the respiration rate of activated sewage sludge at concentrations in excess of the water solubility level of the test material was also assessed using a single test concentration of 1000 mg/L prepared by direct dispersion of the test material in water with the aid of ultrasonication. At a test concentration in excess of the water solubility level of the test material inhibition of respiration of the activated sewage sludge did not occur and the 3-Hour EC50 value was determined to be greater than 1000 mg/L. Correspondingly the NOEC was determined to be 1000 mg/L. These results show that at a concentration in excess of the water solubility level of the test material, the test material does not have an effect on the respiration rate of activated sewage sludge.
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