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EC number: 248-580-6 | CAS number: 27619-97-2
- 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
- Endpoint:
- bioaccumulation in aquatic species: fish
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 305 (Bioaccumulation in Fish: Aqueous and Dietary Exposure) -II: Minimised Aqueous Exposure Fish Test
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.1730 (Fish Bioconcentration Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Potassium 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanesulphonate
- EC Number:
- 261-818-3
- EC Name:
- Potassium 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanesulphonate
- Cas Number:
- 59587-38-1
- Molecular formula:
- C8H5F13O3S.K
- IUPAC Name:
- potassium 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctane-1-sulfonate
- Test material form:
- solid: particulate/powder
- Details on test material:
- - Purity: 97.9%
Constituent 1
Test solutions
- Vehicle:
- yes
- Remarks:
- Dilution water
Test organisms
- Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
Study design
- Route of exposure:
- other: Aqueous and feed
- Test type:
- flow-through
- Water / sediment media type:
- natural water
- Total exposure / uptake duration:
- 56 d
- Total depuration duration:
- 28 d
Test conditions
- Hardness:
- 124 to 134 mg/L as CaCO3
- Test temperature:
- 11.9 to 12.1°C
- pH:
- 7.0 to 7.5
- Dissolved oxygen:
- 7.8 to 10.3 mg/L (air saturation at 12°C = 8.9 mg/L)
- Conductivity:
- 228 to 280 mhos/cm
- Nominal and measured concentrations:
- Aqueous
Nominal: 1 and 10 μg/L
Measured: 1.08 and 9.32 μg/L
Dietary
Nominal: 10 μg/kg
Measured: 13.1 μg/kg - Reference substance (positive control):
- not specified
Results and discussion
Lipid content
- Remarks on result:
- other: The lipid content of test fish was not measured because lipids are not a relevant partitioning phase for the class of chemistry represented by the test substance.
Bioaccumulation factoropen allclose all
- Key result
- Conc. / dose:
- 1 µg/L
- Type:
- BCF
- Value:
- 22 dimensionless
- Basis:
- other: whole fish
- Calculation basis:
- steady state
- Remarks on result:
- other: aqueous test
- Key result
- Conc. / dose:
- 10 µg/L
- Type:
- BCF
- Value:
- 3 dimensionless
- Basis:
- other: Whole fish
- Calculation basis:
- steady state
- Remarks on result:
- other: aqueous test
- Key result
- Conc. / dose:
- 1 µg/L
- Type:
- BCF
- Value:
- 36 dimensionless
- Basis:
- other: whole fish
- Calculation basis:
- kinetic
- Remarks on result:
- other: aqueous test
- Key result
- Conc. / dose:
- 10 µg/L
- Type:
- BCF
- Value:
- 3 dimensionless
- Basis:
- other: Whole fish
- Calculation basis:
- kinetic
- Remarks on result:
- other: aqueous test
- Key result
- Conc. / dose:
- 10 other: μg/kg
- Type:
- BMF
- Value:
- 0.295 dimensionless
- Basis:
- other: Whole fish
- Calculation basis:
- steady state
- Remarks on result:
- other: dietary test
Depurationopen allclose all
- Key result
- Parameter:
- other: Time to 95% Depuration
- Depuration time (DT):
- 23.5 d
- Remarks on result:
- other: Aqueous (1 μg/L)
- Key result
- Parameter:
- other: Time to 95% Depuration
- Depuration time (DT):
- 4.1 d
- Remarks on result:
- other: Aqueous (10 μg/L)
- Key result
- Parameter:
- other: Time to 95% Depuration
- Depuration time (DT):
- 17 d
- Remarks on result:
- other: Aqueous (10 μg/L)
- Remarks:
- Excluding day 63 depuration phase data
Rate constantsopen allclose all
- Key result
- Rate constant:
- growth rate constant (d-1)
- Remarks:
- Aqueous (1 μg/L)
- Value:
- 4.462
- Key result
- Rate constant:
- growth rate constant (d-1)
- Remarks:
- Aqueous (10 μg/L)
- Value:
- 0.452
- Key result
- Rate constant:
- overall depuration rate constant (d-1)
- Remarks:
- Aqueous (1 μg/L)
- Value:
- 0.125
- Key result
- Rate constant:
- overall depuration rate constant (d-1)
- Remarks:
- Aqueous (10 μg/L)
- Value:
- 0.727
- Key result
- Rate constant:
- growth-corrected depuration rate constant (d-1)
- Remarks:
- Dietary (10 μg/kg)
- Value:
- 0.029
- Key result
- Rate constant:
- growth-corrected half-life (d)
- Remarks:
- Dietary (10 µg/kg)
- Value:
- 23.5
- Key result
- Rate constant:
- growth rate constant (d-1)
- Remarks:
- Dietary (10 µg)
- Value:
- 0.057
- Key result
- Rate constant:
- other:
- Remarks:
- Overall elimination rate (d-1)
- Value:
- 0.057
- Reported statistics:
- Time to equilibrium was determined by ANOVA for each aqueous test substance concentration and the dietary test substance concentration
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Bioconcentration and dietary biomagnification potential are low for test substance. Hence, it would not be considered a bioaccumulative compound.
- Executive summary:
The study was conducted to evaluate bioconcentration and bioaccumulation of test substance in Rainbow Trout, Oncorhynchus mykiss according to guidelines, OECD 305 and US EPA.OPPTS 850.1730. Rainbow trout, Oncorhynchus mykiss, were exposed to test substance under flow-through conditions for 56 days during the uptake (exposure) phase of the study followed by a 28-day depuration phase in clean dilution water. Two nominal aqueous test substance concentrations (1 and 10 µg/L), a single nominal spiked diet concentration (10 µg/kg), and a dilution water control were used for testing with 60 fish per exposure treatment and control. An error in preparation of the aqueous test concentrations and delay in analytical confirmation of the test substance concentrations resulted in the day 1-13 uptake phase aqueous test substance concentrations being below the analytical method limit of detection of 0.06 µg/L. This error was corrected upon discovery as reflected in the aqueous test substance concentrations for study days 14 through 56. The mean, measured concentrations of test substance in the aqueous test solutions from days 14-56 were 1.08 µg/L and 9.32 µg/L and the measured test substance concentration in the spiked trout chow diet used for the duration of the dietary uptake phase of the study was 13.1 µg/Kg. One-day after initiation of the depuration phase there were no detectable levels of test substance present in the aqueous test solution test chambers. The dilution water control and the control trout chow diet contained no detectable concentrations of test substance during the study.
Fish tissue residue concentrations of test substance reached steady-state equilibrium within 42 days or earlier in both aqueous and dietary exposures. The k1 values (uptake rate constant) for days 14-56 of the aqueous exposures in whole fish based on measured tissue residues were 4.462 and 0.452 day-1 for the nominal 1 and 10 µg/L nominal aqueous test concentrations while the day 14-56 depuration rate constants, k2, in whole fish based on measured tissue residues were 0.125 and 0.177 day-1, respectively. After a maximum of 24 days of depuration, the measured concentrations in the whole fish were approximately 95% or less of the whole fish tissue concentrations at the end of the uptake phase. However, measured concentrations in whole fish at the end of the uptake phase on day 56 were already less than 50% of the maximum uptake phase concentration in whole fish for both aqueous test concentrations and the dietary exposure concentration of test substance. The test substance steady-state bioconcentration factors (BCF) for the nominal 1 and 10 µg/L aqueous test substance concentrations were 22 and 3, respectively. The respective test substance kinetic bioconcentration factors were 36 and 3, respectively, for the nominal 1 and 10 µg/L aqueous test substance concentrations. The dietary assimilation efficiency for test substance, the growth corrected half-life, and the dietary biomagnification factor (BMF) for the dietary exposure were 0.435, 23.5 days, and 0.295, respectively.
Based on existing regulatory schemes in the United States and Europe, these results demonstrate that the bioconcentration and dietary biomagnification potential are low and test substance would not be considered a bioaccumulative compound
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