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EC number: 459-550-9 | CAS number: -
- 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
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Jan 16th to Feb 16th 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, performed in conformity with GLP-principles
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-C (Determination of the "Ready" Biodegradability - Carbon Dioxide Evolution Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Details on test material:
- Identity: LZ 1780
Chemical name: L-Carnitine L-tartrate
Lot number: 21205
Expiry date: 09 December 2007
Appearance: White crystalline powder
Storage conditions: Room temperature
Date received: 4 January 2006
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- A sample of activated sludge was collected from a sewage treatment works, which treats predominantly domestic waste. Aliquots (25 ml) of a homogenised sample were filtered through dried (approximately 105OC) and pre-weighed Whatman GFIC filter papers. The filters were dried for at least one hour, allowed to cool and re-weighed. The solids level in the sludge was determined and then an appropriate volume used to inoculate control and
test vessels to give a fmal suspended solids concentration of 30 mg/l. - Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 10 mg/L
- Based on:
- other: carbon
Parameter followed for biodegradation estimation
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- The test item was added to two, five-litre vessels containing three litres of mineral salts medium inoculated with activated sludge (30 mg solids/l) to give a nominal test concentration of 10 mg Carbon [C]/l. Two control vessels contained inoculated mineral salts medium alone and one contained inoculated mineral salts medium plus the reference substance, sodium benzoate (10 mg C/l). An additional mixture containing sodium benzoate (10 mg C/l) and LZ 1780 (10 mg C/l) was established in order to assess the potential inhibitory effects of the test substance on the activity of the microbial inoculum.
Test, control and reference mixtures were aerated for 29 days with air that had been treated to remove carbon dioxide (C02). The COz produced by each culture was trapped in a series of Dreschel bottles containing barium hydroxide, which were connected to the outlet fiom each test vessel. The residual barium hydroxide was determined at intervals by titration.
The pH of control, reference and test mixtures was measured at the start of the test and after 28 days. The pH of the test plus reference mixture was measured at the start of the test and on the day of its termination (Day 5).
Reference substance
- Reference substance:
- benzoic acid, sodium salt
Results and discussion
- Preliminary study:
- None.
- Test performance:
- See details on study design.
% Degradationopen allclose all
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 12
- Sampling time:
- 2 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 69
- Sampling time:
- 6 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 82
- Sampling time:
- 14 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 86
- Sampling time:
- 21 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 90
- Sampling time:
- 28 d
BOD5 / COD results
- Results with reference substance:
- 22 % degradation after 2 d
43 % degradation after 3 d
57 % degradation after 4 d
65 % degradation after 5 d
70 % degradation after 6 d
73 % degradation after 7 d
75 % degradation after 9 d
78 % degradation after 14 d
81 % degradation after 21 d
84 % degradation after 28 d
85 % degradation after 29 d
Any other information on results incl. tables
Sodium benzoate had been biodegraded by 65% after 5 days and 85% after 29 days in the absence of the test item, and by 60% after 5 days in its presence, which confirmed that the test item was not inhibitory to the activity of the microbial inoculum. Cumulative levels of CO2 production in the controls after 29 days (65.5 and 70.4 mg C02) were within the acceptable range for this assay system (recommended maximum = 120 mg C02 for a three-litre culture). These results confirm that the inoculum was viable and that the test was valid. Mean cumulative C02 production by mixtures containing the test item was rapid and equivalent to 10% of the theoretical value (TC02, 110.1 mg CO2) after approximately 2 days of incubation, 61% after 5 days and 79% by Day 9. The rate of CO2 evolution then slowed and had achieved 91% of the TCOz by the end of the test on Day 29.
Substances are considered to be readily biodegradable in this test if CO2 production is equal to or greater than 60% of the theoretical value within ten days of the level achieving 10%. The test item can, therefore, be considered to be readily biodegradable.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test item showed a biodegradation rate of 90% after 28 days. Based upon the results of this test, the test substance can be considered to be readily biodegradable.
- Executive summary:
The test item was tested for ist ready biodegradability according to OECD-Guideline No. 301B, EU-Testing Method C.4 -C and in conformity with GLP-principles. The study was performed from January - February 2006.
Based on the mean biodegradation rate of 90% after 28 days, the test item was found to be readily biodegradable in this test system.
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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