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EC number: 239-590-1 | CAS number: 15541-60-3
- 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
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- 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 fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 4-8 April 2005
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study conducted in accordance with an internationally recognised method
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: it was decided that the definitive study be conducted as a limit test with test concentrations of 0 (Control) and 100mg/l only. A stock solution of 1000 mg/1 was prepared and stirred to mix. Appropriate volumes of the stock solution were then made up to 10 litres by addition of dechlorinated tap water to achieve the desired concentration. The test solutions were stirred to mix.
- Sampling method: samples of the test solutions in which the fish were exposed were taken for analytical verification at the start of the definitive study, before and after renewal of solutions at 24, 48, 72 hours, and at the end of the 96 hour exposure period.
- Sample storage conditions before analysis: test substance specific analysis of each test concentration was carried out as soon as possible after sampling. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: when the study was conducted using dechlorinated tap water as the dilution water analysis of the test solution indicated that only 7% of the nominal concentration could be recovered. The study was at the same test concentration of 0 (Control) and 100mg/1 using bottled natural spring water as the dilution water. A stock solution of 1000 mg/1 was prepared and stirred to mix. Appropriate volumes of the stock solution were then made up to 10 litres by addition of bottled natural spring water to achieve the desired concentration. The test solutions were stirred to mix
- Controls: as for test solution but without addition of test substance
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): not applicable, none used
- Concentration of vehicle in test medium (stock solution and final test solution(s) including control(s)): 1000mg/L stock. 100mg/L test solution.
- Evidence of undissolved material (e.g. precipitate, surface film, etc): all test solutions were slightly cloudy white solutions when prepared using dechlorinated tap water but were clear colourless solutions when prepared using natural bottled spring water. - Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
- Details on test organisms:
- TEST ORGANISM
- Common name: rainbow trout
- Source: reputable supplier
- Age at study initiation (mean and range, SD):
- Length at study completion: 55.5 mm (mean of 10 fish measured)
- Weight at study completion: 1.53g (mean of 10 fish weighed)
ACCLIMATION
- Acclimation period: 5 days
- Acclimation conditions): same as test
- Health during acclimation (any mortality observed): 6.67% mortality - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- Declorinated tap water: 240 mg CaCO3/L
Bottle Spring water: 34 mg CaCO3/L - Test temperature:
- 15 ± 2°C
- pH:
- Control: 7.2 - 8.0
Test: 5.2 - 6.7 - Dissolved oxygen:
- Control: 98-100 air saturated value
Test: 98-100 air saturated value - Salinity:
- Not applicable - freshwater study
- Nominal and measured concentrations:
- Analytical measurement of the exposure solutions showed the mean measured concentrations were not within 20% of the nominal concentrations. Therefore in accordance with OECD Guidelines, the measured concentrations should be used in the determination of the LC50, LOEC and NOEC values.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 12 litre volume aquaria
- Renewal rate of test solution): every 24 hours
- No. of organisms per vessel: 7
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: dechlorinated tap water and bottled natural spring water
OTHER TEST CONDITIONS
- Adjustment of pH: none
- Photoperiod: 16 hours light and 8 hours dark
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Observations and records of mortalities were made every 24 hours, as close to test initiation time as possible
TEST CONCENTRATIONS
- Spacing factor for test concentrations: not applicable (limit test)
- Justification for using less concentrations than requested by guideline: see range finding results below
- Range finding study: yes
- Test concentrations:0.1, 1.0, 10, 100mg/L
- Results used to determine the conditions for the definitive study: no abnormalities or mortalities observed up to and including 100mg/L (three fish per concentration) - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 74.96 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- - Behavioural abnormalities:
- Observations on body length and weight:
- Other biological observations:
- Mortality of control:
- Other adverse effects control:
- Abnormal responses:
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values:
- Effect concentrations exceeding solubility of substance in test medium: - Results with reference substance (positive control):
- LC50: 154 mg/L (confidence limits 128-185)
NOEC (96 hrs): 60 mg/L
100% mortality (96 hrs): 240 mg/L - Sublethal observations / clinical signs:
No abnormalities or mortalities were observed in the range finding study nor in a definitive study conducted using bottle spring water.
An initial study using dechlorinated tap water as the dilution water was conducted, the result of this study was no mortalities or abnormal behaviour recorded from any of the exposed Rainbow trout. Due to the poor solubility of MPP in dechlorinated tap water the test was repeated using bottled natural spring water as the dilution water.
- Validity criteria fulfilled:
- no
- Remarks:
- Analytical measurement of the exposure solutions showed the mean measured concentrations were not within 20% of the nominal concentrations.
- Conclusions:
- No abnormality or mortality was observed in any fish exposed to 100mg/L nominal concentration of test substance (>74.96% measured concentration).
Reference
Description of key information
The 96 hour EC50 for fish was estimated to be >74.96 mg/L based on measured concentration and >100mg/l based upon nominal concentrations.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Dose descriptor:
- LC50
- Effect concentration:
- 74.96 mg/L
Additional information
In an acute toxicity study with rainbow trout, MPP was initially tested using dechlorinated tap water, but due to poor water solubility in this medium, the test was repeated using bottled natural spring water as the dilution water. No abnormalities or mortalities were observed in the range finding study nor in the definitive study conducted using bottle spring water at 100mg/L nominal concentration of test substance (>74.96% measured concentration).
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