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EC number: 213-059-4 | CAS number: 920-66-1
- 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:
- key study
- Study period:
- 7 May - 18 Jun 1985
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1985
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: Circular on Test Methods of New Chemical Substances (Japan)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 305 (Bioconcentration: Flow-through Fish Test)
- GLP compliance:
- not specified
Test material
- Reference substance name:
- 1,1,1,3,3,3-hexafluoropropan-2-ol
- EC Number:
- 213-059-4
- EC Name:
- 1,1,1,3,3,3-hexafluoropropan-2-ol
- Cas Number:
- 920-66-1
- Molecular formula:
- C3H2F6O
- IUPAC Name:
- 1,1,1,3,3,3-hexafluoropropan-2-ol
Constituent 1
- Radiolabelling:
- no
Sampling and analysis
- Details on sampling:
- - Sampling intervals/frequency for test organisms: Week 2, 3, 4 and 6
- Sampling intervals/frequency for test medium samples: twice per week
- Sample storage conditions before analysis: no storage
- Details on sampling and analysis of test organisms and test media samples: Test media and 2 fish were sampled for each concentration during the uptake phase. Sample preparation: 1) test media: NaCl and diethylether were added, cooled and shaken. The diethylether phase was used for GC-MS. 2) fish samples: After measurement of weight and length, and homogenization, urea and zeolite were added to distill. The first distilled fraction was collected in diethylether and NaCl was added. The diethylether phase was collected for GC-MS.
Test solutions
- Vehicle:
- no
- Details on preparation of test solutions, spiked fish food or sediment:
- Stock solution: 400 mg/L and 40 mg/L
Test organisms
- Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- TEST ORGANISM
- Common name: Koi
- Source: Fish farm, Yashiro-city, Japan
- Length at study initiation: 9.4 cm (mean)
- Weight at study initiation: 21.3 g (mean)
- Lipid content at test initiation: 4.0% (mean)
- Health status: 24 hrs Oxytetracyclin pre-treatment under static condition
- Feeding during test: yes
- Food type: mixture raising feed for young fish
- Amount: 2% body weight
- Frequency: twice a day
ACCLIMATION
- Acclimation period: 14 days
- Acclimation conditions: same as test
Study design
- Route of exposure:
- aqueous
- Test type:
- flow-through
- Water / sediment media type:
- natural water: freshwater
- Total exposure / uptake duration:
- 6 wk
Test conditions
- Test temperature:
- 25 ± 2 °C
- Dissolved oxygen:
- 5.2 - 6.7 mg/L (first concentration)
5.7 - 7.1 mg/L (second concentration) - Details on test conditions:
- TEST SYSTEM
- Test vessel: glass, 100 L
- Type: open
- Type of flow-through: propotional diluter
- Renewal rate of test solution: stock solution : test water = 2 mL/min : 800 mL/min
- No. of organisms per vessel: 20
- No. of vessels per concentration (replicates): 1
- No. of vessels per control / vehicle control (replicates): 0
RANGE-FINDING / PRELIMINARY STUDY
- Test concentrations: 48 h acute toxicity test in fish (Medaka)
- Results used to determine the conditions for the definitive study: LD 50 for 48 h was 270 mg/L - Nominal and measured concentrations:
- Nominal concentration: 1 and 0.1 mg/L
Measured concentration: 1.01 - 1.04 and 0.0961 - 0.0992 mg/L - Reference substance (positive control):
- no
Results and discussion
Bioaccumulation factoropen allclose all
- Conc. / dose:
- 1 mg/L
- Type:
- BCF
- Value:
- >= 1.1 - <= 1.4 L/kg
- Basis:
- whole body w.w.
- Calculation basis:
- steady state
- Conc. / dose:
- 0.1 mg/L
- Type:
- BCF
- Value:
- >= 1.3 - <= 2.7 L/kg
- Basis:
- whole body w.w.
- Calculation basis:
- steady state
- Details on results:
- - Mortality of test organisms: no mortality
- Behavioural abnormalities: no abnormalities
Any other information on results incl. tables
Table 1. Measured concentration of the test substance in test water (mg/L)
|
2 weeks |
3 weeks |
4 weeks |
6 weeks |
1stconcentration group |
1.04 |
1.04 |
1.03 |
1.01 |
2ndconcentration group |
0.0992 |
0.0974 |
0.0962 |
0.0961 |
Table 2. Bioconcentration factor (BCF) in fish
|
2 weeks |
3 weeks |
4 weeks |
6 weeks |
1stconcentration group |
1.3 |
1.4 |
1.1 |
1.2 |
|
1.2 |
1.2 |
1.1 |
1.1 |
2ndconcentration group |
1.3 |
2.7 |
1.7 |
1.5 |
|
1.7 |
2.1 |
1.3 |
1.7 |
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.