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EC number: 201-993-5 | CAS number: 90-43-7
- 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
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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.13 (Bioconcentration: Flow-through fish test)
- Version / remarks:
- Cited as Directive 98/73/EC, C.13
- GLP compliance:
- yes
- Radiolabelling:
- no
- Vehicle:
- no
- Details on preparation of test solutions, spiked fish food or sediment:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: To produce the stock solution, the coarsly-particled test substance was pulverized, then weighed into water, treated in an ultrasonic bath for 1 hour and finally stirred with a magnetic stirrer for another hour. Stock solution was prepared daily. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: zebra fish
- Source: Bio International B.V., Netherlands
- Age at study initiation: 4 month
- Length at study initiation: 2.5-3.5 cm
- Feeding during test
- Food type: Tetra Min fish food, ground
- Amount: 1% of body weight, applicated in 2 portions
- Frequency: daily
KEEPING CONDITIONS
- Health during Keeping: < 5%
- Medical treatment: none - Route of exposure:
- aqueous
- Test type:
- flow-through
- Water / sediment media type:
- natural water: freshwater
- Total exposure / uptake duration:
- 53 h
- Total depuration duration:
- 19 h
- Test temperature:
- 20.0 - 20.4 °C
- pH:
- 7.8 - 7.9
- Dissolved oxygen:
- 8.7 - 9.4 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Material, size, fill volume: fish tank, 41 x 25 x 30 cm, 25 L
- Renewal rate of test solution (frequency/flow rate): about 20 times per day
- No. of organisms per vessel: 50
- No. of vessels per concentration (replicates): 1
- No. of vessels per control / vehicle control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: syntehtic fresh water in accordance with ISO 7346
- Intervals of water quality measurement: temperature, oxygen contnent and pH during acclimation, uptake and depuration phase
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light/ 8 hours dark
ANALYSIS
- Analysis: Analysis of test and control media as well as fish samples were conducted 2, 6, 23, 30 and 48 h after test start. After beginning of the depuration phase (53 h) analysis was carried out in water and in fish samples after 54 and 72 h.
- Detection limit test medium: 0.67 µg/L
- Detection limit test fish: 16.1 µg/L - Nominal and measured concentrations:
- Nominal test concentrations: control, 5, 50 µg/L
- Lipid content:
- 14.7 other: % ww
- Time point:
- start of exposure
- Remarks on result:
- other: control fish
- Lipid content:
- 21.1 other: % ww
- Time point:
- other: end of depuration phase
- Remarks on result:
- other: control fish
- Lipid content:
- 23.4 other: % ww
- Time point:
- other: end of depuration phase
- Remarks on result:
- other: 5 µg/L treatment group
- Lipid content:
- 22.9 other: % ww
- Time point:
- other: end of depuration phase
- Remarks on result:
- other: 50 µg/L treatment group
- Type:
- BCF
- Value:
- 21.7
- Basis:
- whole body w.w.
- Calculation basis:
- steady state
- Remarks on result:
- other: Conc.in environment / dose:both
- Type:
- BCF
- Value:
- 114
- Basis:
- other: lipid content of ww
- Calculation basis:
- steady state
- Remarks on result:
- other: Conc.in environment / dose:5 µg/L
- Type:
- BCF
- Value:
- 115
- Basis:
- other: lipid content of ww
- Calculation basis:
- steady state
- Remarks on result:
- other: Conc.in environment / dose:50 µg/L
- Details on results:
- - Mortality of test organisms: none
- Behavioural abnormalities: none
- Mortality and/or behavioural abnormalities of control: none
Reference
Stady state:
The time to reach steady-state conditions during the exposure period was very short. The first samples (water, fish) taken only two hours after the onset of the uptake phase yielded a CF/CW ratio (= steady-state BCF) of 20.8 in the lower concentration and 17.6 at the higher test concentration, respectively. The ratios for the low test concentration were 17.6 (after 6 h), 28.8 (after 23 h), 21.0 (after 30 h) and 20.5 (after 48 h). At the higher test concentration the respective CF/CW ratios were 25.0 (after 6 h), 22.0 (after 23 h), 22.3 (after 30 h) and 21.5 (after 48 h).
Depuration phase:
One hour after turning to clean water conditions the test substance concentration at the lower test level (5 µg a.i./L) had fallen below the analytical detection limit, both in water and in fish samples. At the higher test level (50 µg a.i./L), analytical values fell below the detection limits (water fish) 19 h after the start of the depuration phase, thus, not providing an appropriate data basis for the determination of the depuration rate constant (k2) nor of the uptake rate constant (k1).
Description of key information
The BCF value of 21.7 indicates a negligible potential of OPP to bioaccumulate.
Key value for chemical safety assessment
Additional information
To evaluate the bioaccumulation potential of OPP (CAS-No. 90-43-7) a flow-through study according to Directive 67/548/EC, C.13 was conducted. The Test was carried out with individuals of zebra fish (Danio rerio). A dosing system was used to maintain water concentrations (nominal) of 5.0 and 50 µg OPP/L for the 53-h exposure period. After exposure, the test fish were placed in clean water to determine the depuration of the test substance (Caspers, 1999).
At both test substance concentrations, the arithmetic means of five consecutive steady-state BCF were 21.7, indicating a negligible potential of the test substance to bioaccumulate. The achievement of steady-state conditions during the uptake (53 h exposure) phase as well as the subsequent depuration (19 h) were rapid processes.
The steady-state bioconcentration factor (BCF) of 21.7 indicates a negligible potential of OPP to bioaccumulate.
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