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EC number: 412-550-2 | CAS number: 85776-14-3 GRAPHTOL ORANGE 3RT; PERMANENT ORANGE 2 RLD; PERMANENT ORANGE 3 RTN
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1993
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study compliant to GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OCDE n° 202 (1984) Directive CEE 84/449 (1984) - annexe V - méthode C2
- GLP compliance:
- yes
Test material
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
Test solutions
- Vehicle:
- yes
- Details on test solutions:
- Identity and concentration of auxiliary solvent for dispersal: Dimethyl sulfoxyde 50 mg/l
Test organisms
- Test organisms (species):
- other aquatic crustacea: DM
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- 180 mg CaCO3/L
- Test temperature:
- measurement of temperature was performed at the start of the study for each test media and for the control, then at the end of the study:
1) start: 19.4 - 20 °C
2) 48 h: 20.3 - 20.1 °C - pH:
- measurement of pH was performed at the start of the study for each test media and for the control, then at the end of the study:
1) start: 7.88 - 7.93
2) 48 h: 7.7 - 7.79 - Dissolved oxygen:
- measurement of dissolved oxygen was performed at the start of the study for each test media and for the control, then at the end of the study:
1) start: 7.9 - 8.2 mg/L
2) 48 h: 7.8 - 8.1 mg/L - Nominal and measured concentrations:
- To obtain 25 - 50 - 75 - 90 and 100% of test substance extract in test medium, and the single auxiliary substance concentration of 50 mg/L, appropriate volumes of extract were mixed into dilution water added with auxiliary substances, to give final volumes of 100 mL per concentration
- Reference substance (positive control):
- no
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.1 mg/L
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.1 mg/L
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 0.1 mg/L
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 0.1 mg/L
- Details on results:
- No immobilization of Daphnia was recorded during the 48 hour study period, until 100% of test substance extract, maximum possible concentration of exposure
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- EC(I)50 -48 hours for Daphnia: Higher than limit of solubility.
- Executive summary:
The Daphnia (Daphnia magna) were exposed to a test substance extract for 48 hours.
The extract was prepared for the study by coarse filtration (paper filter) of a test substance saturated solution. This suspension, added with 50 mgll of Dimethyl sulfoxide, had been previously submitted to magnetic stirring for 4 hours. The study (range-finding study) was performed using 25 - 50 - 75 - 90 and 100% of test substance extract in test medium (20 Daphnia per group. A control group (not exposed to any substance) and an "auxiliary control" group (exposed only to the auxiliary substance at the same concentration as that
used for the test media) were also employed under the same experimental conditions.
As no immobilization was recorded during the 48-hour period, until 100% of test substance extract, the study was considered as completed and no EC (I) 50 - 48 hour evaluation could be performed.
The percentage of immobilization was noted approximately 24 and 48 hours after the start of the study. Measurements of pH, dissolved oxygen and temperature were performed at the start of the study for each test medium and for the control, then at the end of the study.
The study concentrations were expressed as percent of the test substance extract in test medium (volume by volume). Each test medium was twice sampled (at the beginning and at the end of the study).
The quality criteria for the study as notified in the O.E.C.D. and E.E.C. protocols relative to the dissolved oxygen concentration, the degree of immobiliz.ation of Daphnia in the control media and their absence from the surface, were respected.
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.
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