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EC number: 210-539-5 | CAS number: 617-94-7
- 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
Short-term toxicity to fish
Administrative data
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- disregarded due to major methodological deficiencies
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: Screening test, with multiple effects reported as one result
Data source
Reference
- Reference Type:
- publication
- Title:
- Toxicity of 4,346 Chemicals to Larval Lampreys and Fishes
- Author:
- Applegate, V.C., J.H. Howell, A.E.,Jr. Hall, and M.A. Smith
- Year:
- 1 957
- Bibliographic source:
- Spec.Sci.Rep.Fish.No.207, Fish Wildl.Serv., U.S.D.I., Washington, DC(): -
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- not detailed
- GLP compliance:
- not specified
Test material
- Reference substance name:
- 2-phenylpropan-2-ol
- EC Number:
- 210-539-5
- EC Name:
- 2-phenylpropan-2-ol
- Cas Number:
- 617-94-7
- Molecular formula:
- C9H12O
- IUPAC Name:
- 2-phenylpropan-2-ol
- Test material form:
- liquid
Constituent 1
Test organisms
- Test organisms (species):
- other: Lepomis macrochirus, Oncorhynchus mykiss and Petromyzon marinus
- Details on test organisms:
- Observations on the toxic effect of compounds were made on larvae of the sea lamprey (Petromyzon marinus), rainbow trout (Salmo gairdnerii) and bluegill sunfish (Lepomis macrochirus). Larval lamphreys varied from 3 to 5 inches in total length. Test fishes were of fingerling size, 4 inches or slightly less in length. Every effort was made to keep size variation at a minimum. Larval lamphreys were collected by means of an electrci shocker in the Ocqueoc River, Michigan and were held in running water in aquaria and small races under conditions which simulated their natural stream habitat. Test fishes were obtained from the stocks of local state and federal fish hatcheries and were held in large raceways. These specimens were maintained in the best possible physical condition until used in the laboratory.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Remarks:
- Water (consistently clear and of relatively uniform quality) used in all tests was drawn from a supply pumped directly from Hammond Bay of Lake Huron. The suction line intake of this pumping sytems was located 250 feet offshore at a depth of about 9 feet.
- Total exposure duration:
- 24 h
Test conditions
- Test temperature:
- 55 Fahrenheit
- pH:
- 7.5 - 8.2
- Dissolved oxygen:
- 8.6;13.7 parts per million
- Details on test conditions:
- Durng a typical year while tests were being conducted (November 1953 to December 1954) , pH varied from 7.5 to 8.2, dissolved oxygen from 8.6 to 13.7 ppm and free carbon dioxide from 5.0 to 9 ppm.
- Reference substance (positive control):
- not specified
Results and discussion
Effect concentrations
- Remarks on result:
- other: see Any Other Information
Any other information on results incl. tables
- Sublethal observations / clinical signs:
Repeated experiments were performed in which larvae, trout, and blue gills were exposed to the maximum concentration of each solvent that could occur in any screening test. No adverse effect on any species was observed at any time. Observations of each test were made approximately six times, at various intervals, during the 24-hour test period. At each observation, the condition of every test specimen was determined and recorded. Chronological histories were thus obtained of any symptoms of illness and the occurrence of death. Any chemical killing the larval lampreys in eight hours or less at a concentration of 5 ppm. (regardless of the effects on other fishes) was tested further at levels of 1 and 0.1 ppm. Water temperature, test period, and procedures were identical with those described for the initial test at 5 ppm.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not specified
- Conclusions:
- Repeated experiments were performed in which larvae, trout, and blue gills were exposed to the maximum concentration of each solvent that could occur in any screening test. No adverse effect on any species was observed at any time. Observations of each test were made approximately six times, at various intervals, during the 24-hour test period. At each observation, the condition of every test specimen was determined and recorded. Chronological histories were thus obtained of any symptoms of illness and the occurrence of death. Any chemical killing the larval lampreys in eight hours or less at a concentration of 5 ppm. (regardless of the effects on other fishes) was tested further at levels of 1 and 0.1 ppm. Water temperature, test period, and procedures were identical with those described for the initial test at 5 ppm.
- Executive summary:
Repeated experiments were performed in which larvae, trout, and blue gills were exposed to the maximum concentration of each solvent that could occur in any screening test. No adverse effect on any species was observed at any time. Observations of each test were made approximately six times, at various intervals, during the 24-hour test period. At each observation, the condition of every test specimen was determined and recorded. Chronological histories were thus obtained of any symptoms of illness and the occurrence of death. Any chemical killing the larval lampreys in eight hours or less at a concentration of 5 ppm. (regardless of the effects on other fishes) was tested further at levels of 1 and 0.1 ppm. Water temperature, test period, and procedures were identical with those described for the initial test at 5 ppm.
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