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EC number: 446-620-9 | CAS number: 120983-72-4
- 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

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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- Deviations:
- not applicable
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-E (Determination of the "Ready" Biodegradability - Closed Bottle Test)
- Deviations:
- no
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- - Type: mixed population of aquatic microorganisms
- Source of sewage effluent: secondary effluent of a domestic sewage treatment plant (Odenthal)
- Date of collection: 2001-08-24
- Preconditioning: seperation of coarse particles by filtratio, aeration of mineral medium plus inoculum (filtrate) for 4 days
- Effluent concentration in reaction mixture: 5 mL/L - Duration of test (contact time):
- 28 d
- Initial conc.:
- 2 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- Pretreatment of the test substance:
- The test substance was weighed out on aluminium foil. This substance inclusive the aluminium foil was added to the test vessels.
- Initial concentration of the test substance 2.0 mg test substance/L
Reference compound:
- Initial concentration of the reference compound : 2.9 test substance/L
Exposure conditions:
- Incubation time: 28 days
- Incubation temperature: 20 ± 1 °C - Reference substance:
- benzoic acid, sodium salt
- Remarks:
- purity 99 %
- Preliminary study:
- The initial concentration of the test substance has been reduced in the main test, because the test substance showed a toxic effect against bacteria in the preliminary test.
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 28 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 7 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 14 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 21 d
- Results with reference substance:
- 68 % degradation after 7 d
76 % degradation after 14 d
81 % degradation after 21 d
81 % degradation after 28 d - Validity criteria fulfilled:
- yes
- Remarks:
- for details see 'overall remarks'
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The substance showed 0 % degradation after 28 days. Therefore the substance has to be classified as "Not Readily Biodegradable".
- Executive summary:
The study was conducted in accordance with the Council Directive 92/69/EEC Method C.4-E: Closed Bottle Test. This test method is in all essential parts identical with OECD Guideline 301 D. The test substance in a mineral medium was inoculated with secondary effluent and incubated for 28 d under aerobic conditions in completely full, closed bottles. During this period the biodegradation is followed by analysis of dissolved oxygen. The amount of oxygen taken up by the test chemical, corrected for uptake by the blank inoculum run in parallel, is expressed as a percentage of theoretical oxygen demand (ThOD) or chemical oxygen demand (COD). The substance showed 0 % degradation after 28 days. Therefore the substance has to be classified as "Not Readily Biodegradable". The reference compound showed 76 % degradation after 14 days.
Reference
Toxicity Control:
No toxicity of the test substance was observed.
Description of key information
The study was conducted in accordance with the Council Directive 92/69/EEC Method C.4-E: Closed Bottle Test. This test method is in all essential parts identical with OECD Guideline 301 D. The test substance in a mineral medium was inoculated with secondary effluent and incubated for 28 d under aerobic conditions in completely full, closed bottles. During this period the biodegradation is followed by analysis of dissolved oxygen. The amount of oxygen taken up by the test chemical, corrected for uptake by the blankinoculum run in parallel, is expressed as a percentage of theoretical oxygen demand (ThOD) or chemical oxygen demand (COD). The substance showed 0 % degradation after 28 days. Therefore the substance has to be classified as "Not Readily Biodegradable".
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
- Type of water:
- freshwater
Additional information
The reference compound showed 76 % degradation after 14 days.
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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