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EC number: 224-957-0 | CAS number: 4573-50-6
- 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:
- 24 Aug - 21 Sep 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-E (Determination of the "Ready" Biodegradability - Closed Bottle Test)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: Kläranlage Odenthal, Germany
- Preparation of inoculum for exposure: aeration of mineral medium plus inoculum (filtrate) for 6 days (effluent concentration in reaction mixture 5 ml/L)
- Pretreatment: seperation of coarse particles by filtration - Duration of test (contact time):
- 28 d
- Initial conc.:
- 2.5 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium: mineral medium (no further specification)
- Test temperature: 20 ± 1 °C
- Continuous darkness: yes
TEST SYSTEM
- Culturing apparatus: closed bottles
- Number of culture flasks/concentration: 10
CONTROL AND BLANK SYSTEM
- Inoculum blank: 10 bottles
- Procedure control: 10 bottles
- Toxicity control: 10 replicates - Reference substance:
- benzoic acid, sodium salt
- Remarks:
- 2.9 mg/L
- Key result
- Parameter:
- other: % degradation (dissolved oxygen)
- Value:
- 77
- Sampling time:
- 28 d
- Details on results:
- Theoretical oxygen demand: 2838 mg O2/g
Test item samples: 47, 59, 74 and 77% biodegradation was determined after 7, 14, 21 and 28 d, respectively
Toxicity control: 62, 64, 77 and 77% degradation was determined after 7, 14, 21 and 28 d - Results with reference substance:
- Theoretical oxygen demand: 1665 mg O2/g
69, 79, 82 and 84% degradation was determined after 7, 14, 21 and 28 d. - Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The substance is readily biodegradable (77% degradation after 28 days).
Reference
Description of key information
Readily biodegradable: 77% within 28 d (EU Method C.4-E, activated sludge, domestic)
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
There is one GLP study available investigating the ready biodegradability of the test substance in an aerobic, aqueous medium, according to the Council Directive 92/69/EEC Method C.4-E.
In a closed bottle test a nominal concentration of 2.5 mg/L test substance was inoculated with 5 mL/L secondary effluent from a local, domestic sewage treatment plant for 28 d under aerobic conditions in completely full, closed bottles. A procedure and toxicity control as well as an inoculum blank were run in parallel. Biodegradation was followed by analysis of dissolved oxygen and was expressed as % of the theoretical oxygen demand (ThOD).
The biodegradation of the test substance was 47%, 59%, 74% and 77% after 7, 14, 21, and 28 d. Therefore, the test substance is classified as readily biodegradable (77% within 28 d, 14-d window passed). The toxicity control indicated that the test substance did not inhibit the biodegradation of the reference substance.
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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