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EC number: 267-051-0 | CAS number: 67774-74-7
- 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:
- 03 Apr 1995 to 26 May 1995
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Qualifier:
- according to guideline
- Guideline:
- other: ISO Guideline No. 9408
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): water treatment plant of Novara Italy
- Storage conditions: aerated at room temperature
- Storage length: collected 24 hrs before use - Duration of test (contact time):
- 28 d
- Initial conc.:
- 141.9 mg/L
- Based on:
- ThOD/L
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- - Test temperature: 22 +/- 0.2 degree C
- Biodegradability is measured by means of manometric respirometry. A measured volume of inoculated medium with a known amount of test substance is stirred in a closed flask. The consumption of oxygen is determined from the reduction in volume of the air contained in the apparatus. Evolved CO2 is adsorbed to soda lime and the amount of oxygen taken up by the substance (corrected for the blank) is expressed as a percentage of the theoretical oxygen demand calculated from the formula of the compound. A reference substance (sodium benzoate) was run in parallel to ensure viability of the inoculum. - Reference substance:
- benzoic acid, sodium salt
- Test performance:
- The reference substance, sodium benzoate, was within the expected range and the study is valid.
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 64
- Sampling time:
- 28 d
- Remarks on result:
- other: readily biodegradable, passes 10-day window
- Details on results:
- Mean degradation at plateau = 78.7%. The test substance was insoluble in water and therefore was added directly to the test flasks by microsyringe.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test substance was readily biodegradable.
- Executive summary:
The ready biodegradability of the test substance, was determined using the manometric respirometry test. A measured volume of inoculated medium with a known amount of test substance is stirred in a closed flask. The consumption of oxygen is determined from the reduction in volume of the air contained in the apparatus. Evolved CO2 is adsorbed to soda lime and the amount of oxygen taken up by the substance (corrected for the blank) is expressed as a percentage of the theoretical oxygen demand calculated from the formula of the compound. A reference substance (sodium benzoate) was run in parallel to ensure viability of the inoculum. The test substance was 64.1% degraded at the end of 28 days. The test substance met the 10 -day window and is therefore considered readily biodegradable. In accordance with the OECD Guidelines for Testing of Chemicals Revised Introduction to Section 3 Tests, Item 43, the 10 -day window criterion is not applicable because of the sequential degradation of different components fo the mixture. Therefore, LAB is readily biodegradable.
- Endpoint:
- biodegradation in water: screening tests
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- standard river die-away method
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- natural water / sediment
- Details on inoculum:
- - Source of inoculum: Illinois river water or Illinois river sediment
- Pretreatment: water was glass wool filtered - Duration of test (contact time):
- 42 d
- Initial conc.:
- 100 µg/L
- Based on:
- test mat.
- Initial conc.:
- 500 µg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- test mat. analysis
- Details on study design:
- TEST CONDITIONS
- Test temperature: ambient
TEST SYSTEM
- Culturing apparatus: 32 oz Boston round bottles
- Test performed in open system: bottles were loosely capped
SAMPLING
- Sampling frequency: weekly - Parameter:
- % degradation (test mat. analysis)
- Value:
- 99
- Sampling time:
- 42 d
- Remarks on result:
- other: 100 ppb initial concentration
- Parameter:
- % degradation (test mat. analysis)
- Value:
- 96.3
- Sampling time:
- 42 d
- Remarks on result:
- other: 500 ppb initial concentration
- Details on results:
- The half-life of Alkylate 225 was 4 days at 100 ppb and 9 days at 500 ppb. The removal rate varied from 0.076 to 0.170 per day.
- Validity criteria fulfilled:
- not specified
- Interpretation of results:
- other: rapidly biodegradable
- Conclusions:
- The substance rapidly biodegraded in natural river water.
- Executive summary:
Concentrations of 100 ppb or 500 ppb were added to samples of 500 ml of natural river water. Concentrations of various substance isomers were determined weekly. Total exposure was 42 days. At the end of this period, the substance was almost completely biodegraded (<96%). The half-life was 4 days for the 100 ppb initial concentration, and 9 days for the 500 ppb initial concentration. This shows that substance degrades more quickly at lower concentrations.
Referenceopen allclose all
The test substance was 64.1% degraded at the end of 28 days. The test substance met the 10 -day window and is therefore considered readily biodegradable.
Description of key information
The substance is readily biodegradable. The ready biodegradation of the substance was determined in an OECD 301F guideline study.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Additional information
The ready biodegradation of the substance was determined in an OECD 301F guideline study (manometric respirometry test). The substance reached 6.1% biodegradation in 28 days and passed the 10 day window. The substance is 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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