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EC number: 287-494-3 | CAS number: 85536-14-7
- 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:
- 1992
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP laboratory study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD DOC-Die away test (EG-Richtlinie 92/69 EWG, Tiel II, C.4-A)
- Principles of method if other than guideline:
- Equivalent to OECD 301A
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 11.3 mg/L
- Based on:
- DOC
- Parameter followed for biodegradation estimation:
- DOC removal
- Details on study design:
- A measured volume of inoculated mineral medium, containing a known concentration of the test substance (10-40 mg DOC/l) as the nominal sole source of organic carbon, is aerated in the dark or diffuse light at 22 ± 2°C. Degradation is followed by DOC analysis at frequent intervals over a 28-day period. The degree of biodegradation is calculated by expressing the concentration of DOC removed (corrected for that in the blank inoculum control) as a percentage of the concentration initially present.
- Reference substance:
- benzoic acid, sodium salt
- Remarks:
- 99.5% purity
- Key result
- Parameter:
- % degradation (DOC removal)
- Value:
- 94
- Sampling time:
- 28 d
- Details on results:
- readily biodegradable
- Results with reference substance:
- Biodegradation with the reference substance, sodium benzoate, at 11.8 mg DOC/L resulted in 96% degradation in 28 days.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Executive summary:
The substance was tested in a 28 -day DOC-die away test and found to be degraded by 94% in 28 days. The substance is readily biodegradable.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- Nov. 18, 2002-Dec. 19, 2002
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Marl-Ost municipal sewage treatment plant
- Initial cell/biomass concentration: 3.94 g/l dry matter - Duration of test (contact time):
- 29 d
- Initial conc.:
- 34.3 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Test temperature: 19.7-21.9 degree C
- pH: 7.4-7.5
- Aeration of dilution water: yes, overnight
- Suspended solids concentration: 26.3 mg/L
TEST SYSTEM
- Culturing apparatus: 5000 ml Woullf flasks
- Number of culture flasks/concentration: 2 flasks
SAMPLING
- Sampling frequency: 0, 2, 5, 9, 12, 14, 21, 28, and 29 days
CONTROL AND BLANK SYSTEM
- Inoculum blank: 2 flasks
STATISTICAL METHODS: Results were calculated using the EXCEL computer program. - Reference substance:
- benzoic acid, sodium salt
- Key result
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 85
- Sampling time:
- 29 d
- Details on results:
- The test substance was 85% degraded on day 29.
- Results with reference substance:
- The reference substance was 89% degraded in 29 days.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test substance was 85% degraded in 29 days, and is considered readily biodegradable.
- Executive summary:
This study examined the biodegradability of the test substance. 34.3 mg/L of test substance was added to flasks containing activated sludge. The amount of CO2 evolved was then measured over the next 29 days. Sodium benzoate was used as a reference substance. The reference substance was 89% degraded in 29 days. Therefore the test is valid. The test substance was 85% degraded in 29 days. The test substance is readily biodegradable.
Referenceopen allclose all
% Degradation
Test Duration (days) |
Sodium Benzoate | Test Vessel 1 | Test Vessel 2 | Test Vessel Mean |
0 | 0 | 0 | -1 | -1 |
2 | 32 | 1 | -5 | -2 |
5 | 59 | 24 | 19 | 22 |
9 | 76 | 57 | 46 | 52 |
12 | 84 | 73 | 66 | 70 |
14 | 84 | 72 | 67 | 70 |
21 | 93 | 76 | 79 | 78 |
28 | 95 | 86 | 80 | 83 |
29 | 89 | 84 | 85 | 85 |
Description of key information
The key study examined the biodegradability of LAS-acid. The substance (initial concentration at 11.3 mg/L DOC) was tested in a 28 -day DOC-die away test and found to be degraded by 94% in 28 days. The substance is readily biodegradable. The supporting study examined the biodegradability of LAS. The amount of CO2 evolved was measured over 29 days. The test substance was 85% degraded in 29 days. The reference substance (sodium benzoate) was 89% degraded in 29 days. Thus, the LAS is readily biodegradable as well.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
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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