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Diss Factsheets
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EC number: 701-164-2 | CAS number: -
- 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: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- November 2016 - June 2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Version / remarks:
- 1992
- Deviations:
- yes
- Remarks:
- The incorrect concentration of Ammonium Chloride (NH4Cl) was used in the preparation of stock solution (a) which was used to prepare the mineral medium.
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-C (Determination of the "Ready" Biodegradability - Carbon Dioxide Evolution Test)
- Version / remarks:
- 2008
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, adapted
- Details on inoculum:
- -Inoculum
A mixed population of activated sewage sludge micro-organisms was obtained on 6 March 2017 from the aeration stage of the Severn Trent Water Plc sewage treatment plant at Loughborough, Leicestershire, UK, which treats predominantly domestic sewage.
Sewage sludge/treatment micro-organisms were selected following the recommendations of guidelines. Pre-adaption of the inoculum was not performed.
-Preparation of Inoculum
The activated sewage sludge sample was washed twice by settlement and re-suspension in mineral medium to remove any excessive amounts of dissolved organic carbon (DOC) that may have been present. The washed sample was then maintained on continuous aeration in the laboratory at a temperature of approximately 21 ºC and used on the day of collection. The suspended solids concentration was equal to 3.0 g/L prior to use. - Duration of test (contact time):
- 35 d
- Initial conc.:
- 13.9 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- Preparation of Test System
Based upon the results of the preliminary solubility work and following the recommendations of the International Standards Organisation (ISO, 1995), the test item was dispersed directly on filter paper prior to dispersion in mineral medium.
An amount of test item (41.7 mg) was adsorbed onto a filter paper*, added to inoculated mineral medium and the volume was adjusted to 3 liters to give a final concentration of 13.9 mg/L, equivalent to 10 mg carbon/L.
A filter paper was added to each control vessel in order to maintain consistency between the test and procedure control vessels.
The following test preparations were prepared and inoculated in 5 liter glass test culture vessels each containing 3 liters of solution:
a) Duplicate inoculated control vessels consisting of inoculated mineral medium plus a filter paper.
b) Duplicate procedure control vessels containing the reference item (sodium benzoate) in inoculated mineral medium plus a filter paper* to give a final concentration of 10 mg carbon/L.
c) Duplicate test item vessels containing test item on a filter paper* in inoculated mineral medium to give a final concentration of 10 mg carbon/L.
d) A single toxicity control consisting of the test item on a filter paper* plus the reference item in inoculated mineral medium to give a final concentration of 20 mg carbon/L to act as a toxicity control (one vessel only).
A filter paper was added to the inoculum control and procedure control vessels in order to maintain consistency between these vessels and the test item vessels.
Each test vessel was inoculated with the prepared inoculum at a final concentration of 30 mg suspended solids (ss)/L. The test was carried out in a temperature controlled room, in darkness, and the temperature of the additional vessel containing water which was incubated under the same conditions as the test vessels ranged from 20 to 24 °C.
Approximately 24 hours prior to addition of the test and reference items the vessels were filled with 2400 mL of mineral medium and 30 mL of inoculum and aerated overnight.
The pH was adjusted to pH 7.4 ± 0.2 using diluted hydrochloric acid or sodium hydroxide solution prior to the volume in all the vessels being adjusted to 3 liters by the addition of mineral medium which had been purged overnight with CO2 free air.
The test vessels were sealed and CO2-free air bubbled through the solution at a rate of 30 to 100 mL/min per vessel and stirred continuously by magnetic stirrer.
The CO2 produced by degradation was collected in two 500 mL Dreschel bottles containing 350 mL of 0.05 M NaOH. The CO2 absorbing solutions were prepared using purified water. - Reference substance:
- benzoic acid, sodium salt
- Key result
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 31
- Sampling time:
- 28 d
- Key result
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 32
- Sampling time:
- 36 d
- Details on results:
- The results of the inorganic carbon analysis of samples from the first absorber vessels on Day 36 showed an increase in all replicate vessels.
Inorganic carbon analysis of the samples from the second absorber vessels on Day 36 confirmed that no significant carry-over of CO2 into the second absorber vessels occurred.
The test item attained 31% biodegradation after 28 days and 32% biodegradation after 35 days and therefore cannot be considered to be readily biodegradable under the strict terms and conditions of OECD Guideline No. 301B.
The toxicity control attained 62% biodegradation after 14 days, 57% biodegradation after 28 days and 71% biodegradation after 35 days thereby confirming that the test material did not exhibit an inhibitory effect on the sewage treatment micro-organisms used in the test.
The reference item, sodium benzoate, attained 82% biodegradation after 14 days, 78% biodegradation after 28 days, and 77% biodegradation after 35 days, thereby confirming the suitability of the inoculum and test conditions. The slight decrease in biodegradation between Days 28 and 35 was attributed to sampling/analytical variation. - Validity criteria fulfilled:
- yes
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The test material attained 31% biodegradation after 28 days and 32% biodegradation after 35 days and therefore cannot be considered to be readily biodegradable under the strict terms and conditions of OECD Guideline No. 301B.
- Executive summary:
A study was performed to assess the ready biodegradability of the test item in an aerobic aqueous medium. The method followed was designed to be compatible with the OECD Guidelines for Testing of Chemicals (1992) No. 301B, "Ready Biodegradability; CO2 Evolution Test".
The test item, at a concentration of 10 mg carbon/L, was exposed to activated sewage sludge micro-organisms with mineral medium in sealed culture vessels in the dark at temperatures of between 20 and 24°C for 35 days. At the request of the Sponsor the study was extended from 28 to 35 days for biodegradation of the test item to reach a plateau.
Based on the results of a preliminary solubility/dispersibility trial and following the recommendations of the International Standards Organisation (ISO 10634, 1995) and Handley et al (2002), the test item was adsorbed onto filter paper prior to addition to the test medium to aid dispersion of the test item in the test medium and to increase the surface area of the test item exposed to the test organisms.
The biodegradation of the test item was assessed by the determination of carbon dioxide produced. Control solutions with inoculum and the reference item, sodium benzoate, together with a toxicity control were used for validation purposes.
The test item attained 31% biodegradation after 28 days and 32% biodegradation after 35 days and therefore cannot be considered to be readily biodegradable under the strict terms and conditions of OECD Guideline No. 301B.
Reference
% Biodegradation | |||
Day | Procedure Control | Test Item | Toxicity Control |
0 | 0* | 0 | 0 |
2 | 49 | 0* | 28 |
6 | 71 | 0* | 37 |
8 | 80 | 4 | 47 |
10 | 73 | 4 | 46 |
14 | 82 | 6 | 62 |
21 | 82 | 26 | 65 |
28 | 78 | 31 | 57 |
35 | 76 | 28 | 67 |
36** | 77 | 32 | 71 |
*Negative biodegradation values reported as 0% biodegradation
** Day 36 values were corrected to include carry-over of CO2 detected in absorber 2, if any
Description of key information
An experimental study was carried out to determine the ready biodegradation property of the registered substance according the CO2 Evolution Test (OECD 301B) and GLP.
The test material, attained 31% biodegradation after 28 days and 32% biodegradation after 35 days and therefore cannot be considered to be readily biodegradable under the strict terms and conditions of OECD Guideline No. 301B.
Key value for chemical safety assessment
- Biodegradation in water:
- not biodegradable
- Type of water:
- freshwater
Additional information
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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