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Diss Factsheets
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EC number: 908-081-2 | 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
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 14 September 2016 - 12 October 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 835.3110 (Ready Biodegradability)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-E (Determination of the "Ready" Biodegradability - Closed Bottle Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch/Lot Number: 150205
Description: Blue powder
Purity: As a UVCB, purity is considered as 100%
Expiry date: 05 February 2019
Storage condition: Controlled room temperature (15-25°C, below 70 RH%) - Oxygen conditions:
- aerobic
- Inoculum or test system:
- sewage, domestic, adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: Secondary effluent, microorganisms from a domestic waste water treatment plant
- Preparation of inoculum for exposure: The secondary effluent used for this study was allowed to settle for half an hour, then the decanted effluent was aerated until use (not later than an hour).
- Pretreatment: mechanical stirring and using ultrasonic bath
- Initial cell/biomass concentration: 0.5 mL per litre
- Water filtered: yes - Duration of test (contact time):
- 28 d
- Initial conc.:
- 6.055 mg/L
- Based on:
- COD
- Initial conc.:
- 3.5 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks:
- chemical oxygen demand
- Details on study design:
- TEST CONDITIONS
- Composition of medium: Reconstituted Water
- Test temperature: 22 ± 2°C
- pH: 7.22
- Aeration of dilution water: yes
- Other: The secondary effluent was allowed to settle for half an hour, then the decanted effluent was aerated until use
TEST SYSTEM
- Culturing apparatus: BOD bottles (300 ml) with special neck and glass stoppers
- Number of culture flasks/concentration: 10
- Method used to create aerobic conditions: aeration
- Measuring equipment: suitable instruments
- Test performed in closed vessels due to significant volatility of test substance: yes
SAMPLING
The respective amount of the test item was weighed directly to reach the required test item concentration of 3.5 mg/L. During the preparation of the test solutions they were mixed by mechanical stirring and using ultrasonic bath to ensure a good dispersion
CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Abiotic sterile control: no
- Toxicity control: yes
- Other: toxicity control - Reference substance:
- benzoic acid, sodium salt
- Test performance:
- Concentration of Test item: 3.5 mg/L
BOD:
- 7 days: 0.07; 0.04
- 14 days: 0.03; 0.00
- 21 days: 0.06; 0.06
- 28 days: 0.09; 0.03 - Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 3.3
- Sampling time:
- 28 d
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 3.3
- Sampling time:
- 21 d
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0.8
- Sampling time:
- 14 d
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 3.3
- Sampling time:
- 7 d
- Details on results:
- Biodegradation % = ((BOD (mg O /mg Test item or Reference item))/(COD (mg O /mg Test item) or ThOD (mg O /mg Reference item)) x100
- Key result
- Parameter:
- COD
- Value:
- ca. 1.73 other: mg O2/mg test item
- Results with reference substance:
- Concentration: 3.6 mg/L
Mean percent of biodegradation:
- 7 days: 74.2
- 14 days: 80.0
- 21 days: 84.2
- 28 days: 83.3 - Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- Under the test conditions the percentage biodegradation of the test item reached a mean of 3.3 % after 28 days based on the measured COD of the test item. Therefore the test item is considered not readily biodegradable.
According to the test guidelines the test item can be assumed to be not inhibitory at the applied concentration level of 3.5 mg/L on the secondary effluent microorganisms because degradation was >25 % within 14 days.
The study met the validity criteria.
The test item was not considered to have significant inhibitory effects on the secondary effluent microorganisms.
Based on the results of this study, the test item is considered not readily biodegradable.
Reference
Description of key information
Mean percentage of biodegradation based on the the measured COD of the test item after 28 days: 3.3 %
The test item is considered not readily biodegradable.
Degradation within 14 days for 3.5 mg/L applied concentration level on the secondary effluent microorganisms: >25 %
The test item can be assumed to be not inhibitory.
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
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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