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EC number: 250-954-9 | CAS number: 32210-23-4
- 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
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1989/06/01
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods with acceptable restrictions
- Remarks:
- This study was performed according to a method developed in the laboratory, without GLP statement. This method is well documented in the report. The purity of the test substance is not mentionned in the report.
- Principles of method if other than guideline:
- This study is an oxygen consumption test, method developed at the HULS AG. Bacterial suspension of Pseudomonas putida was added to the test substance in sealed erlenmeyer flasks and incubated for 5-6 hours at 25 +/- 2°C in a brood cabinet. The difference between the oxygen content of the vessels containing solutions at time zero and after the incubation period results in the bacterial oxygen consumption. This comparison gives information about the concentration of the test substance influencing the oxygen consumption.
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- yes
- Test organisms (species):
- Pseudomonas putida
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 6 h
- Remarks on exposure duration:
- 5-6 hours
- Key result
- Duration:
- 6 h
- Dose descriptor:
- EC10
- Effect conc.:
- 1.15 other: mL/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- The EC10 value based on the inhibition of oxygen consumption was calculated at 1.15 mL/L.
- Executive summary:
This study, an oxygen consumption test, was performed according to a method developed in the laboratory HULS AG, without GLP statement. Bacterial suspension of Pseudomonas putida was added to the test substance (with a vehicle, Nonylphenolethoxypropoxylate) in sealed erlenmeyer flasks and incubated for 5-6 hours at 25 +/- 2°C in a brood cabinet. The difference between the oxygen content of the vessels containing solutions at time zero and after the incubation period results in the bacterial oxygen consumption. This comparison gives information about the concentration of the test substance influencing the oxygen consumption.
14 flasks were prepared: 4 flasks per test substance concentrations (173; 432; 860 and 1693 µL/L) - 2 of them were incubated with HgCl2; 4 flasks without test substance but with HgCl2 and 6 flasks without test substance and without HgCl2. HgCl2 solution was added to stop the biochemical reaction. After an incubation period of 5 -6 hours at 25 +/- 2°C, the oxygen concentration measurements were carried out.
The percentage of inhibition of oxygen consumption were 1.5% at 173 µL/L, 6.5% at 432 µL/L, 8.8% at 860 µL/L and 11.6% at 1693 µL/L. Based on these results, the EC10 was calculated (probit analysis) at 1151 µL/L, equivalent to 1.15 mL/L.
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 06-02-1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- This study was performed according to the EC Guideline 88/302/EC (similar to EU Method C.11) with GLP statement. All validity criteria were fulfilled.
- Qualifier:
- according to guideline
- Guideline:
- other: EC Guideline 88/302/EC (30.5.1988)
- Deviations:
- not specified
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Deviations:
- no
- Principles of method if other than guideline:
- The oxygen consumption of activated sludge, which was charged with a standardized amount of synthetic wastewater is measured after a contact time of 3 hours. Similarly, the oxygen consumption of the same activated sludge with synthetic wastewater and with different concentrations of the test substance is measured. The inhibitory effect of the test substance at a given concentration is expressed as a percentage of the average oxygen consumption of 2 controls. From tests with different test substance concentrations, the EC50 is calculated. Furthermore, the non-inhibitory concentrations of test substances can be used in biodegradability tests.
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- 1997-02-18
- Analytical monitoring:
- no
- Details on sampling:
- Not applicable
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: 250 µL, 50 µL and 25 μL of test substance was placed directly into the 100 mL of deionized water, and magnetic stirring was performed.
- Controls: 2 controls without test substance and without reference substance (initial and final determination) + 1 control with reference substance.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): not applicable
- Concentration of vehicle in test medium (stock solution and final test solution(s) including control(s)): not applicable
- Evidence of undissolved material (e.g. precipitate, surface film, etc): no data - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Preparation: Activated sludge (4-5 L) was, the day before the test, settle once and the supernatant was aspirated. The sludge was aerated for 10 minutes and stirring, allow to settle and washed with 2 L of drinking water and aerated and allowed to settle again briefly and filled with 200 mL of synthetic wastewater and drinking water to 4 L and aerated and stirred.
On the test day was the activated sludge can settle, the supernatant aspirated scum, washed with 2 L of drinking water, allow to settle again and refilled with potable water to 4L. After the quick-dry weight determination, the volume was concentrated to 3 L.
- Content of suspended solids: 3.22 g/L (activated sludge). This level gives a concentration of 1287 mg/L in the test medum. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Remarks on exposure duration:
- none
- Post exposure observation period:
- None
- Hardness:
- No data
- Test temperature:
- 18-22°C were hold by cooling the water in the incubation vessel with ice.
At the beginning of incubation: 18.5-19.5°C.
During the determination of oxygen content: 19.5-20.5°C. - pH:
- See table 6.1.7/2 in "Any other information on results incl. tables".
- Dissolved oxygen:
- No data
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal concentrations: 140.6, 234.3, 328.0, 468.5 and 702.8 mg/L.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: no data
- Material, size, headspace, fill volume: 500 mL
- Aeration: continuously (air flow = 0.5 to 1 L/min).
- 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): 1
- No. of vessels per control (replicates): 2
- No. of vessels per vehicle control (replicates): not applicable
TEST MEDIUM / WATER PARAMETERS
Drinking water.
OTHER TEST CONDITIONS
No data
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Respiration rate
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.40-1.67
- Range finding study: No - Reference substance (positive control):
- yes
- Remarks:
- 3,5 Dichlorophenol
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 302 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC10
- Effect conc.:
- 122 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Details on results:
- - See table 6.1.7/2 in "Any other information on results incl. tables".
- To calculate EC50 and EC10, 3 dose-effect pairs were evaluated in the range of concentration from 140.6, 234.4 and 328.0 mg/L. Increased concentration of 468.5 and 702.8 mg/L did not indicate a significant increased inhibition effect.
- The difference between oxygen consumption of control 1 and control 2 does not exceed 15%, here 3.5%. - Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- Relevant effect levels: EC50 = 5.5 mg/L. - Reported statistics and error estimates:
- Probit analysis was performed to determine EC50 values.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The EC50 and EC10 were determined to be 302 mg/L and 122 mg/L, respectivel.
- Executive summary:
This study was performed, according to the EC Guideline 88/302/EC (similar to EU Method C.11) with GLP statement, to determine the inhibition effect of the test substance on the respiration of activated sludge after 3 hours of exposure at 20 +/- 2°C.
The activated sludge was obtained from the sewage treatment plant Marl-West (Lippeverband), treating predominantly domestic sewage. The content of suspended solids was 3.22 g/L (activated sludge), equivalent to a concentration of 1287 mg/L in the test medium.
10 vessels were prepared: 2 controls vessels (without test substance and reference substance), 3 positive controls (with 3,5 -DCP at 5, 15 and 30 mg/L) and 5 test substance vessels (at 140.6, 234.3, 328.0, 468.5 and 702.8 mg/L). 16 mL of synthetic sewage and 200 mL of inoculum were added to each vessels and filled with water up to 500 mL.
The oxygen consumption in the controls vessels were 27.30 and 28.29 mg O2/L*h. The difference between these controls does not exceed 15%, here 3.5%.
The EC50 value of the reference substance (3,5 -DCP) was determined to be 5.5 mg/L.
For the test substance, the EC50 and EC10 values were determined at 302 mg/L and 122 mg/L, respectively. 3 dose-effect pairs were evaluated in the range of concentration from 140.6, 234.3 and 328.0 mg/L. Increased concentration of 468.5 and 702.8 mg/L did not indicate a significant increased inhibition effect.
Referenceopen allclose all
BSVn (%) = [(BSVo - BSVn)/BSVo]*100
Where,
BSVn (%): Indication of the percentage of inhibition (positive values) or promotion (negative values) of oxygen consumption.
BSVo: Biochemical oxygen demand of the controls within the incubation period
BSVn: Biochemical oxygen demand of the test substance concentrations within the incubation period.
Table 6.1.7/1: Oxygen concentration and calculation of the inhibitory concentration
|
Control |
173 µL/L |
432 µL/L |
860 µL/L |
1693 µL/L |
With HgCl2 O2- initial values |
8.28 8.27 8.24 8.20 |
8.26 8.21 |
8.13 8.25 |
8.25 8.23 |
8.19 8.20 |
Average |
8.25 |
8.24 |
8.19 |
8.24 |
8.20 |
Difference |
- |
0.01 |
0.06 |
0.01 |
0.05 |
Without HgCl2 O2- final values |
3.31 3.34 3.45 3.32 |
3.49 3.34 |
3.66 3.57 |
3.85 3.71 |
3.90 3.84 |
Average |
3.36 |
3.42 |
3.62 |
3.78 |
3.87 |
O2- consumption |
4.89 |
4.82 |
4.58 |
4.46 |
4.33 |
Difference |
- |
0.07 |
0.32 |
0.43 |
0.57 |
% effect |
- |
1.5 |
6.5 |
8.8 |
11.6 |
Table 6.1.7/2: Oxygen depletion and percentage of inhibition
|
Initial value (mg O2/L) |
Final value (mg O2/L) |
Respiration rate (mg O2/L*h) |
Inhibition (%) |
pH value |
|
Test substance |
702.8 mg/L |
8.02 |
6.11 |
13.48 |
51.5 |
7.9 |
468.5 mg/L |
8.22 |
6.31 |
12.73 |
54.2 |
7.9 |
|
328.0 mg/L |
7.90 |
6.10 |
12.71 |
54.3 |
7.8 |
|
234.3 mg/L |
7.83 |
5.48 |
17.63 |
36.6 |
7.9 |
|
140.6 mg/L |
7.41 |
4.20 |
24.08 |
13.4 |
8.1 |
|
Reference substance |
5 mg/L |
7.72 |
6.29 |
14.30 |
48.6 |
8.3 |
15 mg/L |
8.34 |
7.08 |
9.45 |
66 |
8.3 |
|
30 mg/L |
8.56 |
7.80 |
6.51 |
76.6 |
8.4 |
|
Control 1 |
7.53 |
4.80 |
27.30 |
- |
8.2 |
|
Control 2 |
7.05 |
3.75 |
28.29 |
- |
8.2 |
Description of key information
EC Guideline 88/302/EC, similar to EU Method C.11, GLP, key study, validity 1:
3h-EC50 = 302 mg/L;
3h-EC10 = 122 mg/L;
Key value for chemical safety assessment
- EC50 for microorganisms:
- 302 mg/L
- EC10 or NOEC for microorganisms:
- 122 mg/L
Additional information
Two studies are available to assess the toxicity of the registered substance to microorganisms.
The first study, assessed as a key study, was performed according to the EC Guideline 88/302/EC similar to the EU Method C.11 with GLP statement, to determine the inhibition effect of the test substance on the respiration of activated sludge after 3 hours of exposure at 20 +/- 2°C. The percentage of inhibition of oxygen consumption were 13.4% at 140.6 mg/L, 36.6% at 234.3 mg/L and 54.3% at 328.0 mg/L. Increased concentration of 468.5 and 702.8 mg/L did not indicate a significant increased inhibition effect. The EC50 and EC10 values were determined at 302 mg/L and 122 mg/L, respectively, for the test substance.
The second study, assessed as a supporting study, was performed according to a method developed in the laboratory HULS AG without GLP statement, to determine the inhibition of oxygen consumption of Pseudomonas putida after 5-6 hours of exposure at 25 +/- 2°C. The percentage of inhibition of oxygen consumption were 1.5% at 173 µL/L, 6.5% at 432 µL/L, 8.8% at 860 µL/L and 11.6% at 1693 µL/L. Based on these results, the EC10 value was calculated at 1.15 mL/L.
The result of the key study, performed similar to international guideline, is taken into account for chemical safety assessment.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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