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EC number: 203-389-7 | CAS number: 106-36-5
- 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:
- key study
- Study period:
- 2003
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to OECD guideline 203, EU 92/69/EEC, C.1, U.S Toxic Substances Control Act Test Guidelines. 40 CFR 797.1400 and in accordance with Good Laboratory Pracice (GLP).
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 003
- Report date:
- 2003
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OTS 797.1400 (Fish Acute Toxicity Test)
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes
Test material
- Reference substance name:
- Propyl propionate
- EC Number:
- 203-389-7
- EC Name:
- Propyl propionate
- Cas Number:
- 106-36-5
- Molecular formula:
- C6H12O2
- IUPAC Name:
- propyl propanoate
- Details on test material:
- - Name of test material (as cited in study report): n-propyl propionate
- Molecular formula: C6H12O2
- Physical state: liquid
- Analytical purity: 99.96%
- Lot/batch No.: QC1355V1C1
Constituent 1
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
Not applicable
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 (water control), 2.33, 3.89, 6.48, 10.8, 18.0, and 30.0 mg n-propyl propionate/L
Test solutions
- Vehicle:
- no
- Details on test solutions:
- For the definitive test, two replicate aquaria were prepared in laboratory dilution water (LDW) at each of six nominal (target) exposure concentrations of 2.33, 3.89, 6.48, 10.8, 18.0, and 30.0 mg npropyl propionate/L, in addition to two aquaria each of control laboratory dilution water.
Aquaria were replenished on a regular intermittent cycle with test solutions delivered from a flow-through proportional diluter.
Test organisms
- Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
- Details on test organisms:
- TEST ORGANISM
- Common name: Rainbow trout (Oncorhynchus mykiss)
- Strain: Walbaum
- Source: Osage Catfisheries Inc., Osage Beach, Missouri.
- Length at study initiation (length definition, mean, range and SD): 4.3 ± 0.2 cm
- Weight at study initiation (mean and range, SD): 0.683 ± 0.134 g
- Feeding during test: Yes
- Food type: standard diet (Aquatic Diet Number 1 Lot #218452, Harlan-Teklad, Madison, Wisconsin)
- Frequency: at least once daily
ACCLIMATION
- Acclimation period: atleast 7 days
- Acclimation conditions (same as test or not): yes
- Type and amount of food: standard diet (Aquatic Diet Number 1 Lot #218452, Harlan-Teklad, Madison, Wisconsin)
- Feeding frequency: at least once daily
Study design
- Test type:
- flow-through
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- Not applicable
Test conditions
- Hardness:
- 88–92 mg/L CaCO3
- Test temperature:
- 12.8–13.9°C
- pH:
- 7.2–7.4
- Dissolved oxygen:
- 7.0–8.8 (7.8 ± 0.5), averaged 76% of saturation and remained greater than or equal to 68% over the 96-hour exposure period
- Salinity:
- No data
- Nominal and measured concentrations:
- Nominal concentrations: 0 (water control), 2.33, 3.89, 6.48, 10.8, 18.0, and 30.0 mg npropyl propionate/L.
Measured concentrations: less than the lowest level quantified of 0.244 mg/L for the water control and 1.73, 2.86, 5.73, 9.20, 15.5, and 26.7 mg/L for the treatment solutions. - Details on test conditions:
- TEST SYSTEM
- Test vessel: Test aquaria were constructed of double-strength glass held together with clear silicone adhesive and measured approximately 30 x 15.5 x 12.5 cm.
- Type: Each vessel had a cover and a Nitex (Tetko, Elmsford, New York) screen-covered drain guard
- Material, size, headspace, fill volume: approximately 3.7-L
- Aeration: No
- Type of flow-through : proportional diluter
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 2
- Biomass loading rate: The resulting average instantaneous biological loading rate was 0.9-g fish/L of test solution and the average standard loading rate (based on total solution flow in a 24-hour period) was 0.06-g fish/L/day
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: The laboratory dilution water (LDW) is Lake Huron water supplied to The Dow Chemical Company by the City of Midland Water Treatment Plant. The water is obtained from the upper Saginaw Bay of Lake Huron near Whitestone Point and is limed and flocculated with ferric chloride. The water is pumped to the laboratory prior to treatment for municipal use.
- Total organic carbon: <2000 microgram/L
- Culture medium different from test medium: No
OTHER TEST CONDITIONS
- Photoperiod: 16-hour light/8-hour dark
TEST CONCENTRATIONS
- Range finding study: Yes
- Results used to determine the conditions for the definitive study: yes - Reference substance (positive control):
- no
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 10.8 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 9.53–12.3 mg/L
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 2.86 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- Fish were observed and any mortality and sublethal effects recorded at 24, 48, 72, and 96 hours of exposure. All biological results are expressed in terms of mean measured concentrations of n-propyl propionate. Sublethal effects were observed down through the 5.73 mg/L dose level during the conduct of this 96-hour exposure study and included lethargy, partial and complete loss of equilibrium, exophthalmia, and immobility.
Mortality following 24 hours of exposure was observed in 100% (10/10) of the fish at the 26.7 mg/L dose level. Mortality was observed in 90% (9/10)and 100% (10/10) of the fish at the 15.5 mg/L dose level following 48 and 72 hours of exposure, respectively.
Following 96 hours of exposure, mortality was observed in 20% (2/10) of the fish at the 9.20 mg/L dose level. Therefore, fish mortality, as a result from 96-hours of exposure (test termination), totaled 100% (10/10), 100% (1/10), and 20% (2/10) for fish exposed at the 26.7 mg/L, 15.5 mg/L, and
9.20 mg/L dose levels, respectively.
No fish mortality was observed in any of the remaining treatment or control solutions during the conduct of this study.
The 24-hour LC50 value was 20.3 mg/L with a Spearman-Karber trim of 0.0%; no reliable 95% confidence interval could be determined.
The 48-hour LC50 value was 12.6 mg/L, with a 95% confidence interval of 11.4-13.9 mg/L; the Spearman-Karber trim was 0.0%.
The 72-hour LC50 value was 11.9 mg/L with a Spearman-Karber trim of 0.0%; no reliable 95% confidence interval could be determined. - Results with reference substance (positive control):
- Not applicable
- Reported statistics and error estimates:
- Standard statistical methods were employed
Any other information on results incl. tables
- Sublethal observations / clinical signs:
Preliminary study-
A 72-hour probe study was conducted under flowthrough conditions. The study was conducted with one replicate of five fish per dose level exposed to nominal test concentrations of 0 (water control), 17.5, 29.2, 48.6, 81.0, 135, and 225 mg n-propyl propionate/L. The study was terminated on day 3 since the npropyl propionate vessel feeding the diluter emptied sometime between the evening of day 2 and day 3 of the study. However, sufficient information was obtained from this probe study and a repeat probe study not deemed necessary.
Following ~72-hours of exposure, mortality was observed in 100% of the fish at the 29.2, 48.6, 81.0, 135, and 225 mg/L dose levels. No mortalities or sublethal effects were observed in the 17.5 mg/L dose level or the water control during the conduct of the study.
The information derived from this study was used to set the range of concentrations for the definitive test.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Under the conditions of the study, the 96-hour LC50 of n-propyl propionate for fish was 10.8 mg/L, with a 95% confidence interval of 9.53-12.3 mg/L; and the NOEC being 2.86 mg/L.
- Executive summary:
The purpose of this study was to evaluate the acute toxicity of n-propyl propionate to the rainbow trout (Oncorhynchus mykiss) over a 96-hour flow-through exposure period. These data were used to calculate 24-, 48-, 72-, and 96-hour LC50 values and a 96-hour no-observed-effect concentration or NOEC.
The study was conducted with two groups of five fish exposed to nominal test concentrations of 0 (water control), 2.33, 3.89, 6.48, 10.8, 18.0, and 30.0 mg n-propyl propionate/L, over a 96-hour exposure period. Observations were made every 24 hours for mortality. These data were statistically evaluated, where applicable, using mean measured n-propyl propionate concentrations.
Based on mean measured concentrations, the 96-hour LC50 of n-propyl propionate for fish was 10.8 mg/L, with a 95% confidence interval of 9.53-12.3 mg/L; and the NOEC being 2.86 mg/L.
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