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EC number: 260-375-3 | CAS number: 56773-42-3
- 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

Epidemiological data
Administrative data
- Endpoint:
- epidemiological data
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: secondary literature
Data source
Reference
- Reference Type:
- secondary source
- Title:
- Unnamed
- Year:
- 2 001
- Report date:
- 2001
Materials and methods
- Study type:
- cross sectional study
- Endpoint addressed:
- not applicable
- Principles of method if other than guideline:
- cross-sectional data used to determine PFOS levels in the general population
- GLP compliance:
- no
Test material
- Reference substance name:
- PFOS
- IUPAC Name:
- PFOS
- Details on test material:
- Identity: PFOS and 6 other fluorochemicals
Constituent 1
Method
- Details on study design:
- Study design: Cross-sectional
Manufacturing/Processing/Use: N/A
Hypothesis tested: To determine the levels of PFOS in the serum of American Red Cross blood banks in
6 regions of the U.S.
Study period: 2000
Setting: N/A
Total population: Serum pooled from 6 ARC blood banks in various geographic regions in the US: Los
Angeles, CA; Minneapolis/St. Paul, MN; Charlotte, NC; Boston, MA; Portland, OR, and Hagerstown, MD.
Subject selection criteria: Unknown
Total # of subjects in study: 652 donors, age 20-69 years
Comparison population: N/A
Participation rate: N/A
Subject description: No information was provided on the individuals from whom the sera samples were
taken.
Health effects studied: PFOS levels in blood
Data collection methods: Blood sera samples were analyzed using high-pressure liquid
chromatography/electrospray tandem mass spectrometry (HPLC/ESMSMS).
Details on data collection: No information was provided as to how the blood was drawn, stored, etc.
Exposure period: Unknown--PFOS serum levels used as surrogate for exposure.
Description/delineation of exposure groups/categories: N/A
Measured or estimated exposure: N/A
Exposure levels: N/A
Statistical methods: Arithmetic means, ranges, geometric means and 95% confidence intervals were
calculated. Central tendency and distribution of the data by age, gender, location
and their respective interaction terms will be done in the final report. A reliability assessment is also being analyzed.
Other methodological information: N/A - Exposure assessment:
- not specified
Results and discussion
- Results:
- The mean serum PFOS level was 43.7 ppb. The range was 4.27 to 1656 ppb. Analyses stratified by age, gender, and geographic location will be forthcoming in the final report.
- Confounding factors:
- no data
- Strengths and weaknesses:
- These data are cross-sectional data used to determine PFOS levels in the general population. No other descriptive information about the subjects is available in this preliminary report. The sample size is relatively small.
Blood donors cannot be considered representative of the general population of the US.
Any other information on results incl. tables
no data
Applicant's summary and conclusion
- Executive summary:
In a cross sectional study PFOS levels in the serum of American Red Cross blood banks in 6 regions of the U.S. were determined.
The mean serum PFOS level was 43.7 ppb. The range was 4.27 to 1656 ppb.
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