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EC number: 603-522-2 | CAS number: 131819-23-3
- 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
Long-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- adult fish: sub(lethal) effects
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2000-09-14 to 2000-12-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Guideline 305 (Bioconcentration: Flow-through Fish Test)
- Qualifier:
- according to guideline
- Guideline:
- other: METI Guideline: Concentration Test on Chemical Substances in Fish
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch: E998833
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling intervals/frequency for test organisms: days 0, 7, 14, 21, 28, 35, 42, 49, and 60
- Vehicle:
- yes
- Details on test solutions:
- According to guideline
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): HCO-40
- Concentration of vehicle in test medium (stock solution and final test solution(s) at different concentrations and in control(s)):
Test solution 1: 0.02 mg/L mg/L test material, 0.4 mg/L HCO-40
Test solution 2: 0.002 mg/L test material, 0.04 mg/L HCO-40
Control: 0.4 mg/L HCO-40 - Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- Weight: 5 g
Length: 8 +/- 4 cm
Lot: 00-K-0630 - Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 60 d
- Test temperature:
- 23.4-24.2°C
- pH:
- 7.2-7.7
- Dissolved oxygen:
- 7.1-7.5 mg/L
- Nominal and measured concentrations:
- nominal concentration
0.02 mg/L:
analytically measured concentrations:
day 7: 0.0203 mg/L;
day 14: 0.0201 mg/L
day 21: 0.0204 mg/L
day 28: 0.0202 mg/L
day 35: 0.0203 mg/L
day 42: 0.0202 mg/L
day 49: 0.0199 mg/L
day 60: 0.0198 mg/L
nominal concentration
0.002 mg/L:
analytically measured concentrations:
day 7: 0.00179 mg/L;
day 14: 0.00182 mg/L
day 21: 0.00182 mg/L
day 28: 0.00186 mg/L
day 35: 0.00189 mg/L
day 42: 0.00191 mg/L
day 49: 0.00189 mg/L
day 60: 0.00189 mg/L - Reference substance (positive control):
- no
- Key result
- Duration:
- 60 d
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 0.02 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: solubilzer HCO-40 was applied
- Key result
- Duration:
- 14 d
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 0.02 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: solubilzer HCO-40 was applied
- Details on results:
- - Mortality of test organisms: no effects
- Behavioural abnormalities:no effects
- Observations on body length and weight:no effects
- Other biological observations: no effects
- Bound residues forming a plateau: no
- Mortality and/or behavioural abnormalities of control: no
- Loss of test substance during test period: no
- Results with vehicle control: no effects - Validity criteria fulfilled:
- yes
- Conclusions:
- The test material showed no relevant toxic potential at a concentration of 0.02 mg/L. The NOEC was >= 0.02 mg/L and the EC (48 h) clearly exceeds 0.02 mg/L.
- Executive summary:
The informtion for this endpoint study record was obtained from an experimental study. The OECD GLP criteria were met and the methods applied are fully compliant with OECD TG 305.
The test material showed no relevant toxic potential at a concentration of 0.02 mg/L. The NOEC was >= 0.02 mg/L and the EC (48 h) clearly exceeds 0.02 mg/L.
Reference
Purpose
The purpose of this study was to determine the bioconcentration potential of the test material in fish under flow-through conditions. During the GLP compliant test the lethal and other effects in fish were determined during the exposure period of 60 days.
Study Design
The study was performed according to the OECD Guideline for Testing of Chemicals 305 (Bioconcentration: Flow-through Fish Test) adopted on June 14, 1996 using two test material concentrations for exposure to Cyprinus carpio. Two environmental concentrations of the test material of 0.02 and 0.002 mg/Lwere used in this study. The exposure was concentration was maintained using HCO-40 as solubiliser. The concentrations were verified analytically using a GC method with MS detection.
Results
There were no mortality and no signs of toxicity detected throughout the study in any dose group up to 60 days of exposure.
Conclusion
The test material showed no relevant toxic potential at a concentration of 0.02 mg/L. The NOEC was >= 0.02 mg/L and the EC (48 h) clearly exceeds 0.02 mg/L.
Description of key information
For this endpoint data from a long term (60 d) bioconcentration study provide adequate information.
This study has used HCO-40 as vehicle to increase water solubility. In the long term 60 days study no mortality was observed up to 0.02 mg/L. Therefore, the test material does not exhibit a significant potential for toxicity up to 0.02 mg/L. To ensure maximum exposure above the water solubility of the pure substance, solubiliser HCO-40 was applied.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 0.02 mg/L
Additional information
NOEC (BCF, 28d) >= 0.02 mg/L (with HCO-40 as solubiliser).
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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