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EC number: 291-001-7 | CAS number: 90295-11-7
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: inherent biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From June 13th to July 11th, 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with generally accepted scientific standards and described in sufficient detail
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
- Version / remarks:
- adopted on 17 July 1992
- Principles of method if other than guideline:
- The study was conducted in accordance with ISO/IEC 17025
- GLP compliance:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: municipal biological waste water treatment plant, ARA Werdhölzli, CH-8048 Zürich.
- Pre-conditioning: not pre-conditioned.
- Adaptation: the activated sludge was used immediately after sampling from the treatment plant without adaptation.
- Preparation of inoculum for exposure: prior to the test, the sludge was washed twice with tap water. - Duration of test (contact time):
- 28 d
- Initial conc.:
- ca. 50.6 mg/L
- Based on:
- DOC
- Initial conc.:
- ca. 146 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- DOC removal
- Details on study design:
- TEST CONDITIONS
- Composition of medium: aerobic mineral salts medium prepared with double distilled water (conductivity: < 1.5 µS/cm; DOC: < 0.3 mg/l).
Stock solution I, 10 ml/l (pH 7.4): Ammonium chloride 0.50 g, Di-sodium hydrogenphosphate 33.40 g, Potassium dihydrogenphosphate 8.50 g, Di-potassium monohydrogenphosphate 21.75 g
Stock solution Il, 1 ml/l: Calcium chloride, anhydrous 27.50 g
Stock solution III, 1 ml/l: Magnesium sulfate 22.50 g
Stock solution IV, 1 ml/l: Iron (III) chloride 0.25 g
- Test temperature: 22 ± 0.5 °C
- Additional substrate: none, test substance or procedure control as sole organic carbon source.
- Continuous darkness: yes.
- Oxyge: it was assured that during the test the oxygen concentration was greater than 6 mg/I.
- pH: the pH-value was checked periodically and adjusted to pH 6.5-8.0 with NaOH or HCI, if necessary.
TEST SYSTEM
- Inoculum: 0.2 g/l dry metter of activated sludge in final mixture.
- Test unit: 1200 ml closed glass bottle containing a total volume of test solution of 800 ml; aerated with CO2-free air and fitted to gas-absorption bottles containing 125 ml of 0.13 M KOH.
- Test suspension: two replicates containing activated sludge, test medium and the test substance.
- Stirring: the test vessels were stirred (100 r.p.m.)
- Aeration: the test vessels were areated with synthetic C02-free air for the test period.
SAMPLING
- Sampling: the elimination of the test material was followed by DOC determinations at regular intervals. First samples were analyzed at the beginning of and 3 h after starting the test.
- Air control: the air leaving the individual vessels was passed through gas-absorption bottles filled with NaOH. The trapped CO2 was determined as inorganic carbon (IC).
CONTROL AND BLANK SYSTEM
- Inoculum blank: two replicates containing activated sludge and test medium
- Reference compound: one replicate containing activated sludge, the test medium and the diethylene glycol as ready biodegradable reference compound. - Reference substance:
- diethylene glycol
- Remarks:
- 47.6 mg/l as DOC
- Parameter:
- % degradation (DOC removal)
- Value:
- 5
- Sampling time:
- 28 d
- Parameter:
- other: % degradation (ThCO2)
- Value:
- 3
- Sampling time:
- 28 d
- Details on results:
- No biodegradation of the test item based on the CO2 evolution and calculated as percentage ThCO was observed.
No significant elimination of the test substance due to adsorption to the activated sludge, on the glass surface or other physico-chemical processes was found as determined by means of DOC measurements 3 h after the start of the test. - Results with reference substance:
- The positive control, diethyleneglycol, showed 99 % biodegradation after 14 days of incubation thus confirming suitability of inoculum and test conditions.
- Validity criteria fulfilled:
- yes
- Remarks:
- reference compound reached more than 7 % of DOC removal within 14 days
- Interpretation of results:
- not inherently biodegradable
- Conclusions:
- DOC removal (28 days): 5 %
- Executive summary:
The biodegradability of the test compound exposed to activated sludge of a municipal sewage treatment plant was investigated under aerobic static conditions. The study was conducted according to the OECD guideline 302B. No significant elimination of the test substance due to adsorption to the activated sludge, on the glass surface or other physico-chemical processes was found as determined by means of DOC measurements 3 h after the start of the test. The positive control, diethyleneglycol, showed 99 % biodegradation after 14 days of incubation thus confirming suitability of inoculum and test conditions.
Based on the data of the individuaL DOC determinations no biodegradability of the test compound was observed after 28 days. Furthermore, no biodegradation of the test substance based on CO2 evolution and calculated as % ThCO2 was observed, confirming that no biodegradation occurred.
Conclusion
Based on these results, the test substance is not inherently biodegradable under the conditions, since less than 20 % degradation was attained after 28 days of contact time.
Reference
DOC concentrations of test suspension, inoculum blank and procedure control and calculation of degradation data.
Inoculum blank (B)* | Procedure control with diethylene glycol (R) | Test suspension with test material (T)* | |||||
Time | DOC | DOC | DOC net. | Degradation | DOC | DOC net. | Degradation |
(days) | (mg/I) | (mg/I) | (mg/I) | (%) | (mg/I) | (mg/I) | (%) |
0 | 0.8 | 48.7 | 47.9 | - | 49.9 | 49.0 | - |
0.125 | 0.6 | 47.7 | 47.1 | 1 | 50.2 | 49.6 | 0 |
1 | 0.9 | 46.6 | 45.7 | 4 | 49.9 | 49.1 | 1 |
3 | 1.1 | 37.3 | 36.2 | 24 | 49.0 | 47.9 | 3 |
7 | 1.4 | 1.9 | 0.5 | 99 | 49.7 | 48.4 | 3 |
10 | 2.3 | 3.3 | 1.0 | 98 | 50.0 | 47.7 | 4 |
14 | 1.4 | 1.9 | 0.5 | 99 | 49.5 | 48.1 | 3 |
17 | 1.4 | 1.8 | 0.4 | 99 | 49.4 | 48.0 | 3 |
21 | 1.5 | 2.0 | 0.5 | 99 | 49.2 | 47.7 | 4 |
24 | 1.5 | 1.7 | 0.2 | 100 | 48.5 | 46.9 | 5 |
27 | 1.5 | 1.8 | 0.3 | 99 | 48.5 | 46.9 | 5 |
28 | 1.8 | 1.9 | 0.1 | 100 | 49.1 | 47.3 | 5 |
*Mean of two replicates
IC concentration, calculated from the concentrations in the gas absorption bottles, of test suspension, inoculum blank and procedure control and corresponding degradation data
Time | Test suspension (IC) | Procedure control with diethylene glycol IC | Inoculum blank IC | Biodegradation test suspension | Biodegradation procedure control |
(days) | (mg/I) | (mg/I) | (mg/I) | (% ThCO2) | (% ThCO2) |
0 | nd | nd | nd | - | - |
7 | 23.1 | 58.9 | 22.7 | 1 | 76 |
14 | 32.4 | 76.6 | 31.9 | 1 | 94 |
21 | 39.5 | 82.0 | 38.3 | 2 | 92 |
28 | 42.7 | 86.4 | 41.4 | 3 | 95 |
Description of key information
neither readily nor inherently biodegradable
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
Additional information
Direct Blue 199 Na was exposed to activated sludge of a municipal sewage treatment plant was investigated under aerobic static conditions. The study was conducted according to the OECD guideline 302B. No significant elimination of the test substance due to adsorption to the activated sludge, on the glass surface or other physico-chemical processes was found as determined by means of DOC measurements 3 h after the start of the test. The positive control, diethyleneglycol, showed 99 % biodegradation after 14 days of incubation thus confirming suitability of inoculum and test conditions. Based on the data of the individual DOC determinations no biodegradability of the test compound was observed after 28 days. Furthermore, no biodegradation of the test substance based on CO2evolution and calculated as % ThCO2was observed, confirming that no biodegradation occurred.
Since less than 20 % of degradation was attained after 28 days of contact time, Direct Blue 199 Na is considered as not inherently biodegradable.
The ration BOD5:COD of Direct Blue 199 Na resulted lower than 0.5 in all of the test available, confirming that Direct Blue 199 Na is not readily biodegradable.
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