Registration Dossier
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EC number: 605-718-3 | CAS number: 174350-05-1
- 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

Bioaccumulation: aquatic / sediment
Administrative data
Link to relevant study record(s)
- Endpoint:
- bioaccumulation in aquatic species: fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Jun 30 - Aug 16, 2004
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study was performed according to GLP and the methods applied are fully compliant with OECD TG 305.
- Qualifier:
- according to guideline
- Guideline:
- other: METI Guideline: Concentration Test on Chemical Substances in Fish
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 305 (Bioconcentration: Flow-through Fish Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Radiolabelling:
- no
- Details on sampling:
- - Sampling intervals/frequency for test organisms: days 0, 7, 14, 21, 23, 25, 28- Sampling intervals/frequency for test medium samples: days 0, 7, 14, 21, 23, 25, 28- Details on sampling and analysis of test organisms and test media samples (e.g. sample preparation, analytical methods):LC analysis.Fish: two fish per sampling homogenised, and extracted with acetonitril/n-hexane. The analysis was performed using LC.
- Vehicle:
- yes
- Details on preparation of test solutions, spiked fish food or sediment:
- According to guideline PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)- Chemical name of vehicle (organic solvent, emulsifier or dispersant): SPAN 20- Concentration of vehicle in test medium (stock solution and final test solution(s) at different concentrations and in control(s)): Dose 1: Test item: 0.02 mg/L , Vehicle: 0.2 mg/LDose 2: Test item: 0.002 mg/L , Vehicle: 0.02 mg/LControl: Test item: --, Vehicle: 0.2 mg/L
- Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- Lot No. 40626 from 2004-05-26Weight: 0.8 +/- 0.09 gLength: 4.6 +/- 0.20 cm
- Route of exposure:
- aqueous
- Test type:
- flow-through
- Water / sediment media type:
- natural water: freshwater
- Total exposure / uptake duration:
- 28 d
- Total depuration duration:
- > 42 d
- Test temperature:
- 25.6 ° +/- 0.4 °C
- pH:
- 7.2 +/- 0.1
- Dissolved oxygen:
- 7.1 +/- 0.4 mg/L
- Salinity:
- According to guideline
- Details on test conditions:
- After acclimatisation period, the fish (Cyprinus carpio) were transferred into the test media under flow through conditions. Exposure concentrations were analytically verified at days 0, 7, 14, 21, 23, 25 and 28. The analytical values show that the nominal concentrations of 0.02 and 0.002 mg/L were maintained at about 100% using SPAN 20, respectively. At days 0, 7, 14, 21, 23, 25 and 28 two fish each were removed from each test group. Body weight was determined. The fish were homogenised and extracted The extract was analysed with LC.A depuration was followed from day 28 up to day 42.
- Nominal and measured concentrations:
- nominal concentration 0.02 mg/L: analytically measured concentrations: day 0: 0.0193 mg/Lday 7: 0.0172 mg/L day 14: 0.0180 mg/Lday 21: 0.0199 mg/Lday 23: 0.0203 mg/Lday 25: 0.0205 mg/Lday 28: 0.0164 mg/Lnominal concentration 0.002 mg/Lanalytically measured concentrations:day 0: 0.00197 mg/Lday 7: 0.00199 mg/L day 14: 0.00180 mg/Lday 21: 0.00199 mg/Lday 23: 0.00200 mg/Lday 25: 0.00198 mg/Lday 28: 0.00188 mg/L
- Details on estimation of bioconcentration:
- according to guideline
- Type:
- BCF
- Value:
- 1 162 dimensionless
- Basis:
- normalised lipid fraction
- Time of plateau:
- 14 d
- Calculation basis:
- steady state
- Remarks on result:
- other: analytical concentration
- Remarks:
- Conc.in environment / dose:0.02 mg/L
- Type:
- BCF
- Value:
- 1 221 dimensionless
- Basis:
- normalised lipid fraction
- Time of plateau:
- 7 d
- Calculation basis:
- steady state
- Remarks on result:
- other: analytical concentration
- Remarks:
- Conc.in environment / dose:0.002 mg/L
- Elimination:
- not specified
- Details on kinetic parameters:
- steady state was reached within 7 daysDepuration phase dropped below 100 at day 42
- Metabolites:
- none
- 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 steady state BCF values were at 1162 and 1221 (mean 1191). The test material showed no relevant bioaccumulation at concentrations at or above the water solubility (BCF < 2000).
Reference
Description of key information
BCFs from OECD TG 305 compliant GLP study: 1162 and 1221 (mean 1191).
The test material showed no relevant bioaccumulation (BCF < 2000).
Key value for chemical safety assessment
- BCF (aquatic species):
- 1 190 dimensionless
Additional information
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