Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 211-477-1 | CAS number: 647-42-7
- 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
Biodegradation in soil
Administrative data
- Endpoint:
- biodegradation in soil: simulation testing
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Although data provided have a report year after 2008, the data was obtained from a journal article which does not provide GLP information.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- 6-2 Fluorotelomer alcohol aerobic biodegradation in soil and mixed bacterial culture
- Author:
- Liu J, Wang N, Szostek B, Buck R, Paniciroli P, Folsom P, Sulecki L and Bellin C
- Year:
- 2 009
- Bibliographic source:
- Chemosphere 78: 437–444
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 307 (Aerobic and Anaerobic Transformation in Soil)
- Deviations:
- yes
- Remarks:
- (study run for 180 days)
- GLP compliance:
- not specified
- Test type:
- laboratory
Test material
- Reference substance name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctan-1-ol
- EC Number:
- 211-477-1
- EC Name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctan-1-ol
- Cas Number:
- 647-42-7
- Molecular formula:
- C8H5F13O
- IUPAC Name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctan-1-ol
- Details on test material:
- - Purity: 99%
Constituent 1
- Radiolabelling:
- no
Study design
- Oxygen conditions:
- aerobic
- Soil classification:
- USDA (US Department of Agriculture)
Soil properties
- Soil type:
- sandy loam
- % Clay:
- 14
- % Silt:
- 34
- % Sand:
- 52
- % Org. C:
- 3.8
- pH:
- 5.8
- Details on soil characteristics:
- SOIL COLLECTION AND STORAGE
- Collection details: Sassafras soil (Ultisol) was used. It was collected from a forested area undisturbed for at least 40 years in Newark, Delaware and sieved via a 2-mm sieve immediately upon collection and stored at 4 °C and used within 3 months.
PROPERTIES OF THE SOILS (in addition to defined fields)
- Moisture: The degradation study was conducted for 180 days at 40% of the field moisture capacity, corresponding to a gravimetric moisture content of 28%.
Duration of test (contact time)
- Duration:
- 180 d
Initial test substance concentration
- Initial conc.:
- 2.9 other: µg/g
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- test mat. analysis
- Details on experimental conditions:
EXPERIMENTAL DESIGN
- Test apparatus: The test substance was initially dosed at 2.9 µg/g soil. Parent and metabolites were measured in three compartments: volatile analytes in the headspace, volatile analytes absorbed onto the rubber septa, and study analytes in soil by exhaustive solvent extraction of the entire test vessel. 120-mL glass serum bottles were incubated statically in dark at 20 – 25 °C for 180 days. Approximately 10 g dry weight equivalent of sieved Sassafras soil was added to each vessel, and dosed with 10 µL of test substance stock solution prepared in ethanol. Sterile treatments were prepared by gamma irradiation (60Co) and additionally dosed with the triple antibiotics at respective 100 mg/kg final concentration. For each sampling time point, four treatments of triplicate vessels were prepared: (1) untreated (matrix) live soil with 10 µL ethanol; (2) test substance treated live soil; (3) test substance treated sterile soil; and (4) sterile soil treated with selected metabolites. In treatment group 4, the sterile soil was fortified with PFBA (0.13 nmol/g soil), PFPeA (0.10 nmol/g), and PFHxA (0.74 nmol/g) to evaluate the potential effects of abiotic processes on recovery of these three PFCAs over 120 days.
- Any indication of the test material adsorbing to the walls of the test apparatus: yes, septum and glass tube extracted
SAMPLING DETAILS
- Sampling intervals: 0, 2, 7, 14, 28 60, 90, 120, and 180 days
- Sampling method for soil samples: The O2 content was measured at each time point in untreated live soil to approximate O2 content in treated live sample bottles. Prior to opening the soil test vessels, the headspace gas of a sample bottle was pumped out through two needles inserted through the septum using an air pump at a rate of 1.5 L/min for 1 min. The outlet air went through two C18 cartridges in series to capture volatile fluorinated compound(s). Each cartridge was eluted with 5 mL acetonitrile and subject to chemical analysis. The rubber septum was then removed and extracted in 5 mL acetonitrile at 50 °C for 2 – 7 d. The soil was subjected to two sequential extractions in the test vessel sealed with a new rubber septum to enhance recovery.
Results and discussion
% Degradation
- % Degr.:
- >= 93.8 - <= 96.5
- Parameter:
- test mat. analysis
- Remarks:
- (Primary biodegradation)
- Sampling time:
- 28 d
Half-life / dissipation time of parent compound
- DT50:
- 1.6 d
- Type:
- (pseudo-)first order (= half-life)
- Transformation products:
- yes
Identity of transformation productsopen allclose all
- No.:
- #1
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- perfluoropentanoic acid (PFPeA)
- Identifier:
- common name
- Identity:
- perfluoropentanoic acid (PFPeA)
- No.:
- #2
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- 5:3 acid [F(CF2)5CH2CH2COOH]
- Identifier:
- other: Formula
- Identity:
- 5:3 acid [F(CF2)5CH2CH2COOH]
- No.:
- #3
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- perfluorohexanoic acid (PFHxA)
- Identifier:
- common name
- Identity:
- perfluorohexanoic acid (PFHxA)
- No.:
- #4
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- 5-2 Secondary alcohol (5-2 sFTOH)
- Identifier:
- common name
- Identity:
- 5-2 Secondary alcohol (5-2 sFTOH)
- No.:
- #5
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- perfluorobutanoic acid (PFBA)
- Identifier:
- common name
- Identity:
- perfluorobutanoic acid (PFBA)
- No.:
- #6
Reference
- Reference substance name:
- Unnamed
- IUPAC name:
- 4:3 acid [F(CF2)4CH2CH2COOH]
- Identifier:
- other: Formula
- Identity:
- 4:3 acid [F(CF2)4CH2CH2COOH]
- Evaporation of parent compound:
- yes
- Volatile metabolites:
- yes
- Residues:
- yes
- Details on results:
- TEST CONDITIONS
- Aerobicity, moisture, temperature and other experimental conditions maintained throughout the study: Yes
Any other information on results incl. tables
In soil, the treated sterile control samples showed satisfactory ≈87 – 113% test substance mass balance over 180 days. At the end of the study, ≈52% of the test substance was recovered from the rubber septa, ≈29% recovered from soil plus inner glass walls, and the remaining ≈3.5% was recovered from the headspace in sterile controls. The gradual decrease of the test substance in soil and increase in the rubber septum of the sterile control indicated that the septum was a preferred phase for partitioning when there was no microbial activity. The treated live soil samples had a mass balance of ≈67 – 88% from day 1 to 180, showing a slow decline of recovery over time. The declining overall mass balance in live soil is indicative of some metabolites irreversibly bound to soil and non-extractable with organic solvent plus alkaline treatment that may not be available for further biodegradation.
At day 180, the major terminal metabolites were PFPeA, [F(CF2)4COOH, 30%], PFHxA (8%), PFBA [F(CF2)3COOH, 2%], and 5-3 acid (15%). A new metabolite 4-3 acid [F(CF2)4CH2CH2COOH] accounted for 1%, the test substance for 3%, and 5-2 sFTOH for 7%.
Test substance biodegradation in the aerobic soil was rapid with an estimated half-life of 1.6 days assuming first-order kinetics. After an initial sharp decline, the test substance concentration gradually levelled off after 28 days at ≈3.5 – 6.2% of the total mass applied at day 0. This would be equal to 93.8- 96.5% primary degradation by day 28. Metabolite levels reached steady-state at 120 days.
Applicant's summary and conclusion
- Conclusions:
- This study and the conclusions which are drawn from it fulfill the quality criteria (validity, reliability, repeatability).
93.8- 96.5% primary degradation by day 28 - Executive summary:
Test substance biodegradation was evaluated at 2.9 µg/mL for 180 days in aerobic soil . Test vessels were 120-mL glass serum bottles sealed with natural rubber septa and the vessels were incubated statically in dark at 20 – 25 °C. The replicate test and control vessels were extracted and analysed at 0, 2, 7, 14, 28, 60, 90, 120 and 180 days for the test substance and metabolites.
Biodegradation in the aerobic soil was rapid with an estimated half-life of 1.6 days assuming first-order kinetics. After an initial sharp decline, the test substance concentration gradually levelled off after 28 days at ≈3.5 – 6.2% of the total mass applied at day 0. This would be equal to 93.8- 96.5% primary degradation by day 28. Metabolite levels reached steady-state at 120 days.
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.