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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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- 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:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.5400 (Algal Toxicity, Tiers I and II) (January 2012)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0.5, 1.0, 2.0, 4.0, 8.0 mg a.i./L
- Sampling time: at 0, 72 and 96 hours - Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): Acetone
- Concentration of vehicle in test medium: 0.01% v/v - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: green alga
- Strain: UTEX 1648
- Source: Department of Botany, University of Texas, USA
- Age of inoculum (at test initiation): 3-7 days
- Method of cultivation: cultured in freshwater algal nutrient medium under continuous illumination of approx. 4300 Lux at a temperature of 24 ± 2°C. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Test temperature:
- 24 ± 2 °C
- pH:
- After 0 hours: 7.4 - 7.5
After 72 hours: 7.7 -8.1 - Nominal and measured concentrations:
- Nominal test concentrations: 0.5, 1.0, 2.0, 4.0 and 8.0 mg a.i./L
Mean measured concentrations (72 h, % of nominal): 86- 94
Mean measured concentrations (96 h, % of nominal): 83 - 89 - Details on test conditions:
- TEST SYSTEM
- Test vessel: 250 ml Erlenmeyer flasks containing 100 ml test solution
- Initial cells density: 10 000 cells/ml
- Control end cells density: 57E+04 cells/ml after 72 h; 147E+04 after 96 hours
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 3
- No. of vessels per vehicle control (replicates): 3
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Test medium was freshwater algal nutrient medium (FWAM), prepared by the addition of appropriate reagent nutrients to ABC reagent water
OTHER TEST CONDITIONS
- Photoperiod: permanent
- Light intensity and quality: cool-white fluorescent lightning, 4300 ± 430 lx
EFFECT PARAMETERS MEASURED: cell densities after 24, 48, 72 and 96 hours - Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.468 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 3.57 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.35 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- biomass
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.432 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- 3.78 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.32 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- biomass
- Validity criteria fulfilled:
- yes
- Executive summary:
The study from Hicks (2002) was conducted according to OECD 201 and revealed a EC50 (72 h) of 3.57 mg/L for the growth rate of Selenastrum capricornutum. The NOEC (72 h) is 0.468 mg/L.
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP study according to a national standard method with some missing details
- Qualifier:
- according to guideline
- Guideline:
- other: Scenedesmus-Zellvermehrungs-Hemmtest, DIN 38412 Teil 9, Bestimmung der Hemmwirkung von Wasserinhaltsstoffen auf Gruenalgen (method of the German Standards Institution, Berlin, Germany)
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Reference substance (positive control):
- no
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 0.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.98 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 0.38 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.85 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Validity criteria fulfilled:
- not specified
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP guideline study, some test details are missing
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Vehicle:
- not specified
- Test organisms (species):
- Chlorella pyrenoidosa
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Reference substance (positive control):
- not specified
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.35 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 1 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 3.8 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 5 mg/L
- Basis for effect:
- growth rate
- Validity criteria fulfilled:
- not specified
Referenceopen allclose all
Description of key information
ErC50 (72 h) = 3.57 mg a.i./L and NOEC (72 h) = 0.468 mg i.a./L for Pseudokirchneriella subcapitata (nominal, OECD 201)
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 3.57 mg/L
- EC10 or NOEC for freshwater algae:
- 0.468 mg/L
Additional information
To investigate the influence of OPP (CAS-No. 90-43-7) on the growth of aquatic algae the results of a GLP study according to OECD 201 are available (Hicks, 2002). Based on growth rate a 72- hour ErC50 of 3.57 mg a.i./L (measured) for Pseudokirchneriella subcapitata was determined. The corresponding NOEC (72 h) was 0.468 mg a.i./L
Additionally, effects of OPP on another green algae Desmodesmus subspicatus (formerly Scenedesmus subspicatus) were investigated by Caspers (1989). Due to significant deficiencies found in the methodology, (e.g. no analytical measurements) the test results should only be regarded as additional information and will not be used for the risk assessment.
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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