Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 263-606-6 | CAS number: 62570-50-7
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- >10% daphnids were immobilized/trapped at the surface of the control solution in the combined limit/range-finding test. In simultaneously performed tests no effects were observed in the control treatment, accept the results and use as a range-finder.
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- Readings taken every 24 hours for 48 hours
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna (Crustacea, Cladocera) (Straus 1820), at least third generation, obtained by a cyclical parthenogenesis under specified breeding conditions. Tests ran with new born daphnids, i.e. less than 3 days old, by placing about 250 of them into 5 litres of medium in an all-glass culture vessel.
- Test type:
- static
- Water media type:
- not specified
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- 180 mg/L expressed as CaCO3
- Test temperature:
- 18-22 °C
- pH:
- 7.7 ± 0.3
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 2.6 µg/L
- Nominal / measured:
- not specified
- Conc. based on:
- test mat. (dissolved fraction)
- Basis for effect:
- mobility
- Remarks on result:
- not determinable
- Remarks:
- The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6 µg/L)
- Details on results:
- The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6 µg/L)
- Validity criteria fulfilled:
- yes
- Conclusions:
A limit test was performed based on the results of a combined limit/range-finding test. Twenty daphnids per group (5 per replicate, quadruplicate) were exposed to an intreated control and to a saturated solution prepared at a loading rate of 100 mg/L. The total exposure period was 48 hours and samples or analytical confirmation of exposure concentrations were taken at the start and end of the test.
Samples taken from the limit concentration were analysed. The actual concentrations were below the LOD of the analytical method (LOD=5.1 µg/L) from the beginning of the exposure. Therefore, the effect parameters were expressed in terms of solubility in test medium, i.e. 2/6 µg/L (i.e. half of the LOD).
The study met the acceptability criteria prescribed by the study plan and was considered valid. The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6 µg/L).- Executive summary:
A limit test was performed based on the results of a combined limit/range-finding test. Twenty daphnids per group (5 per replicate, quadruplicate) were exposed to an intreated control and to a saturated solution prepared at a loading rate of 100 mg/L. The total exposure period was 48 hours and samples or analytical confirmation of exposure concentrations were taken at the start and end of the test.
Samples taken from the limit concentration were analysed. The actual concentrations were below the LOD of the analytical method (LOD=5.1µg/L) from the beginning of the exposure. Therefore, the effect parameters were expressed in terms of solubility in test medium, i.e. 2/6µg/L (i.e. half of the LOD).
The study met the acceptability criteria prescribed by the study plan and was considered valid. The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6µg/L).
Reference
Description of key information
A limit test was performed based on the results of a combined limit/range-finding test. Twenty daphnids per group (5 per replicate, quadruplicate) were exposed to an intreated control and to a saturated solution prepared at a loading rate of 100 mg/L. The total exposure period was 48 hours and samples or analytical confirmation of exposure concentrations were taken at the start and end of the test.
Samples taken from the limit concentration were analysed. The actual concentrations were below the LOD of the analytical method (LOD=5.1µg/L) from the beginning of the exposure. Therefore, the effect parameters were expressed in terms of solubility in test medium, i.e. 2/6µg/L (i.e. half of the LOD).
The study met the acceptability criteria prescribed by the study plan and was considered valid. The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6µg/L).
Key value for chemical safety assessment
Additional information
A limit test was performed based on the results of a combined limit/range-finding test. Twenty daphnids per group (5 per replicate, quadruplicate) were exposed to an intreated control and to a saturated solution prepared at a loading rate of 100 mg/L. The total exposure period was 48 hours and samples or analytical confirmation of exposure concentrations were taken at the start and end of the test.
Samples taken from the limit concentration were analysed. The actual concentrations were below the LOD of the analytical method (LOD=5.1µg/L) from the beginning of the exposure. Therefore, the effect parameters were expressed in terms of solubility in test medium, i.e. 2/6µg/L (i.e. half of the LOD).
The study met the acceptability criteria prescribed by the study plan and was considered valid. The 48h-EC50 was beyond range tested, i.e. exceeded the maximum solubility of Disperse Blue 359 in test medium (> 2.6µg/L).
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.