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EC number: 205-055-6 | CAS number: 132-27-4
- 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:
- other: GLP guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Deviations:
- yes
- Remarks:
- Concentration of test material was reduced to 0.2 and 1.0 mg/L.
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: A sample of activated sludge mixed Iiquor was obtained from the Midland Municipal Wastewater Treatment Plant (Midland, Michigan. USA) on April 28, 1997.
- Concentration of sludge: mixed liquor suspended solids (MLSS) concentration of the activated sludge sample was determined to be 2190 ± 160 mg/L: Based on this determination, the mineral medium (3 liters) was inoculated with 41 ml of activated sludge to yield a final MLSS concentration of 30 ± 1 mg/L. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 0.2 mg/L
- Based on:
- test mat.
- Initial conc.:
- 1 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Composition of medium: according to guideline
- Test temperature: 23 ± 1°C
- pH adjusted: yes, the pH of the inoculated mineral medium was adjusted from 7.01 to 7.37 with 5N NaOH.
TEST SYSTEM
- Culturing apparatus: 1 L flasks were sealed with rubber stoppers fitted with CO2 traps containing 4 ml of 1N NaOH.
CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Abiotic sterile control: yes
- Toxicity control: yes
- Other: non labelled control
- Reference substance:
- benzoic acid, sodium salt
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 33.5
- St. dev.:
- 1.5
- Sampling time:
- 3 d
- Remarks on result:
- other: 0.2 mg [14C]-OPP
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 62.5
- St. dev.:
- 0.5
- Sampling time:
- 11 d
- Remarks on result:
- other: 0.2 mg [14C]-OPP
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 70.8
- St. dev.:
- 0.3
- Sampling time:
- 28 d
- Remarks on result:
- other: 0.2 mg [14C]-OPP
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 35.2
- St. dev.:
- 0.2
- Sampling time:
- 3 d
- Remarks on result:
- other: 1.0 mg [14C]-OPP
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 67.7
- St. dev.:
- 0.8
- Sampling time:
- 11 d
- Remarks on result:
- other: 1.0 mg [14C]-OPP
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 75.7
- St. dev.:
- 0.5
- Sampling time:
- 28 d
- Remarks on result:
- other: 1.0 mg [14C]-OPP
- Details on results:
- 70.8 and 75.7% biodegradation (CO2 formation as percentage of theoretical value) after 28 days at low (0.2 mg/L) and high (1.0 mg/L) concentration
- Results with reference substance:
- Kinetic of control substance: 81% after 2 days
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- Please refer to analogue justification provided in IUCLID section 13
- Reason / purpose for cross-reference:
- read-across source
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 75.7
- St. dev.:
- 0.5
- Sampling time:
- 28 d
- Remarks on result:
- other: 1.0 mg [14C]-OPP
- Interpretation of results:
- readily biodegradable
Referenceopen allclose all
Biodegradation rates of o-phenylphenol (percentage of added radioactivity mineralized to 14CO2):
Day |
Abiotic control |
Biodegradation at different OPP concentrations |
|
1.0 mg [14C]-OPP |
0.2 mg [14C]-OPP |
1.0 mg [14C]-OPP |
|
0 |
0.0% |
0.0% |
0.0% |
3 |
0.2% |
33.5% (± 1.5) |
35.2% (± 0.2) |
11 |
0.3% |
62.5% (± 0.5) |
67.7% (± 0.8) |
28 |
0.6% |
70.8% (± 0.3) |
75.7% (± 0.5) |
Description of key information
Readily biodegradable: 70.8 – 75.7% in 28 days (OECD 301B); read across
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
Reliable experimental data on the biodegradability of sodium 2-biphenylate are not available. The assessment was therefore based on a study conducted with the analogue substance 2-phenylphenol (CAS 90-43-7). The read across approach is in accordance with Regulation (EC) No. 1907/2006, Annex XI, 1.5. Please refer to the analogue justification attached to IUCLID section 13 for a detailed justification.
The biodegradability of the source substance 2-phenylphenol (CAS 90-43-7) was tested according to OECD 301B under GLP conditions using non-adapted activated sludge as inoculum (Gonsior and Tryska, 1997). To avoid potential inhibitory effects the tested substance, concentrations were lower than specified in the guideline (i.e. 0.2 mg and 1 mg test material/L). The test substance was radiolabelled (14C-OPP) and the degradation was followed by measuring the amount of evoluted14CO2. Furthermore the concentration of the test substance was determined at day 28 by HPLC. Based on the CO2evolution a biodegradation rate of 70.8% was determined at a test substance concentration of 0.2 mg/L. The determined degradation rate at a substance concentration of 1 mg/L was 75.7%.The 10-day window was met (degradation rate at day 11: > 60%). Thus the substance is considered as readily biodegradable.
The results are supported by data available for sodium 2-biphenylate. The ready biodegradability of the substance was tested based on the oxygen consumption in a study design similar to OECD 301D (Hamburger, 1976). At a test substance concentration of 2.4 mL/L a degradation rate of 84% was determined after 20 days. The results were not considered for assessment because of insufficient study documentation. However, the results are a further indication of a ready biodegradability of the substance.
Based on the results for the source substance (in accordance to Regulation (EC) No 1907/2006 Annex XI, 1.5) sodium 2-biphenylate is considered as readily biodegradable.
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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