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Diss Factsheets
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EC number: 248-363-6 | CAS number: 27247-96-7
- 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: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2005
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 310 (Ready Biodegradability - CO2 in Sealed Vessels (Headspace Test)
- Version / remarks:
- ISO 14593
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, adapted
- Details on inoculum:
- Sewage sludge microorganisms from a domestic wastewater treatment plant. Sample filtered through coarse filter paper, filtrate purged with CO2 free air for approximately 1 hour while maintaining pH at 6.5 using concentrated orthophosphoric acid. The pH was then adjusted to 7.6 with sodium hydroxide and the inoculum allowed to settle for approximately 1 hour prior to the removal of the supernatant for use in the study.
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 36.5 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- 107 mL of inoculated culture medium added to each of 25 replicate test vessels which were then sealed using Teflon lined silicon septa and aluminum crimp caps. After sealing 4.0 μl of test material was injected through the septum of each vessel to give test material concentration of 36.5 mg/L (20 mg carbon/L). 29 control vessels prepared as above without the addition of the test material.
Replicates: Duplicates for the control, standard material, test material and toxicity control at each sampling point (5 replicates were available for day 28 analysis). Headspace to liquid ratio was 1:2.
Temperature of incubation: 20+1 °C
Study initiation: Test cultures provided with CO2 free air and placed on a rotary shaker and mixed at 150 rpm for the study duration.
Sampling: Days 2, 6, 8, 10, 14, 16, 20, 22, 24, 28 (after acidification on day 28)
Concentration of test substance: 36.5 mg/L (20 mg carbon/L)
Controls: Toxicity, blank and positive controls used per guideline. Positive control was sodium benzoate added to the control vessel at a loading of 20 mg C/L. Both test substance and reference material were added to the toxicity controls to obtain a maximum concentration of 40 mg C/L
Study termination: An aliquot of concentrated orthophosphoric acid was injected through the septum of each vessel taken for analysis in order to reduce pH to <3. The vessels were then shaken at ~150 rpm for 1 hour at 20+1 °C prior to samples being withdrawn from the headspace for analysis.
Method of calculating biodegradation values: Percent biodegradation calculated as percent ratio of cumulative net carbon dioxide to theoretical carbon dioxide as determined from elemental analysis of test material. - Reference substance:
- benzoic acid, sodium salt
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 0
- Sampling time:
- 28 d
- Details on results:
- The test substance was not considered readily biodegradable under the criteria that requires 60% biodegradation within 28 days, achieved within 10 days of reaching 10% biodegradation. The CO2 production from the reference chemical exceeded the 60% of theoretical necessary to consider the test valid. The degradation for the toxicity control was 34% as of day 28 therefore the test substance was not considered to be inhibitory at the concentration tested. The water solubility of this test material is relatively low and coupled with the volatile nature of the test material, this may have resulted in the majority of the test material being present in the headspace and not proportionally dissolving in the test media. The test material may not hav been bioavailable and this may have contributed to the lack of biodegradation.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- not inherently biodegradable
- Conclusions:
- The test material attained 0% degradation after 28 days and therefore cannot be considered to be readily biodegradable.
Reference
Description of key information
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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