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EC number: 274-393-4 | CAS number: 70209-96-0
- 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: inherent biodegradability
- Type of information:
- other: data on Acid Blue 225_constituent 1
- Adequacy of study:
- key study
- Study period:
- From May 25th to June 22nd, 1988
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Justification for type of information:
- The experiment was conducted on one of the substance components. It should be noted that the lot tested was characterized by the Acid Blue 225_constituent 1 as main component; however, the impurity profile (which includes also the Acid Blue 225_constituent 2) resulted to be similar to that characterizing the substance under assessment (details are given in the document attached to IUCLID section 13).
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
- GLP compliance:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- Activated sludge were taken from a municipal waste water treatment plant which has been rinsed with municipal water for 2 times. The sediment is taken to estimate the dry weight according to internal method.
The activated sludge was prepared one day before the start of the experiment, ventilated overnight and adjusted to a concentration of 600 mg/l. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 142 mg/L
- Based on:
- DOC
- Parameter followed for biodegradation estimation:
- DOC removal
- Details on study design:
- PRE-TEST
The day before the main test, a pre-test was conducted. A 3-liter beaker was prepared with 1900 ml of communal water an 100 ml of stock solution. After 1 minute of mixing a 15 ml sample is taken and filtered through a Whatman GF/A filter by centrifugation. Subsequently DOC was measured representing the 0-hour value. Three hours later a second sample is taken from the beaker andevaluated. The zero value was used to validate the DOCvalue, while the 3h-value was used to estimate the adsorption of the test substance to glass.
MAIN TEST
Test solutions and controls were prepared in duplicates.
Analysis of the activated sludge content
At least one day after the main test, 50 ml of the activated sludge was transferred to a measuring cylinder and the dry weight was measured.
Sampling and duration of the test:
Samples for DOC measurement were taken daily on working days until day 28.
Oxygen, pH and temperature measurements:
For oxygen measurements aeration and stirrer were stopped for the time of the measurement (about 30-60 sec.). Oxygen concentration was maintained over 2 mg/l. pH-valuewas taken between 7.0 and 8.0. If the pH-values were outside of this range, the pH was adjusted with NaOH or H2SO4 respectively.
The temperature was maintained in the range of 22 ± 3 °C. - Preliminary study:
- None
- Test performance:
- None
- Parameter:
- % degradation (DOC removal)
- Value:
- 22
- Sampling time:
- 28 d
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- Biodegradation (28d): 22 %, based on DOC removal.
- Executive summary:
The inherent biodegradability of the substance was determined in a 28 days, according to the OECD Guideline for Testing of Chemicals, No. 302B.
The test substance was tested in a concentration of 142 mg/l. Based on the findings of the study, biodegradation after 28 days of the test substance was 22 %.
Conclusion
Biodegradation (28d): 22 %, based on DOC removal.
Reference
DOC removal
Time | Substance DOC (mg/l) | Blank DOC (mg/l) | Substance DOC corrected by control (mg/l) | Elimination (%) |
Start | 142.0 | - | 142.0 | 0 |
3 hours | 121.9 | 9.0 | 112.9 | 20.49 |
Day 2 | 132.5 | 9.0 | 123.5 | 13.03 |
Day 5 | 131.8 | 9.4 | 122.4 | 13.8 |
Day 7 | 130.9 | 9.6 | 121.3 | 14.58 |
Day 9 | 131.7 | 7.8 | 123.9 | 12.75 |
Day 12 | 132.6 | 7.3 | 125.3 | 11.76 |
Day 14 | 132.6 | 8.7 | 123.9 | 12.75 |
Day 16 | 127.3 | 10.4 | 116.9 | 17.68 |
Day 19 | 128.8 | 10.3 | 118.5 | 16.55 |
Day 21 | 126.8 | 9.2 | 117.6 | 17.18 |
Day 23 | 123.1 | 9.4 | 113.7 | 19.93 |
Day 26 | 120.3 | 8.8 | 111.5 | 21.48 |
Day 28 | 119.1 | 8.9 | 110.2 | 22.39 |
Description of key information
Not readily biodegradable
Key value for chemical safety assessment
Additional information
Acid Blue 225 is an anthraquinone derivative dye; it is not expected to be ready biodegradable because of its chemical structure and its specific function. Commonly, dyes undergo a primary transformation, i.e. discolourization due to the interrupting the conjugation. Nevertheless, the degradation process involves more steps and take more time.
The assumption above mentioned is confirmed by the experimental data available on Acid Blue 225_constituent 1. It should be noted that the lot tested was characterized by the Acid Blue 225_constituent 1 as main component; however, the impurity profile (which includes also the Acid Blue 225_constituent 2) resulted to be similar to that characterizing the substance under assessment. Therefore, the data can be considered as adequate and the approach can be considered as suitable (details are given in the document attached to IUCLID section 13).
The inherent biodegradability of the Acid Blue 225_constituent 1 was determined in a 28 days test, conducted in accordance with the Zahn Wellens testing method, described into the OECD Guideline No. 302B. The test substance was tested in a concentration of 142 mg/l. Based on the findings of the study, biodegradation after 28 days of the test substance was 22 %.
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