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EC number: 812-244-2 | CAS number: 957209-18-6
- 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

Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 2012
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
- Principles of method if other than guideline:
- - Principle of test: Repeated-dose inhalation toxicity.
- Short description of test conditions: The test method was based on a custom protocol. Rats (3 males) were exposed, whole body, to 100 ppm (vapor) of the test article for 6 hours per day for 5 consecutive days. Control rats (3 males) were treated in a similar manner with the exclusion of exposure to the test material.
- Parameters analysed / observed: Clinical observation were recorded continuously during each exposure period. Body weights were recorded for all animals each day prior to exposure. Animals were euthanized immediately following Day 5 exposure and gross necropsy, liver tissue collection, serum collection and body weight measurements were performed. - GLP compliance:
- no
- Test type:
- other: Screening study.
- Limit test:
- no
Test material
- Reference substance name:
- 2,3,3,4,4-pentafluoro-2,5-bis(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-5-methoxyoxolane
- EC Number:
- 812-244-2
- Cas Number:
- 957209-18-6
- Molecular formula:
- C11H3F19O2
- IUPAC Name:
- 2,3,3,4,4-pentafluoro-2,5-bis(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-5-methoxyoxolane
Constituent 1
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: 3M Company, NB#159571-76, Purity: 99.9%
- Expiration date of the lot/batch: Not specified
- Purity test date: 17 February, 2012
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: The test article was unchanged.
FORM AS APPLIED IN THE TEST: A vapor of the test article was generated.
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan
- Age at study initiation: 6-8 weeks
- Weight at study initiation: 170-178 g
- Fasting period before study: None
- Housing: All rats were group housed in solid bottom cages after each daily exposure.
- Diet (e.g. ad libitum): Harlan Tedland Rat/Mouse 2018 Diet (Harlan Teklad, Madison, WI), ad libitum.
- Water (e.g. ad libitum): Tap water, ad libitum.
- Acclimation period: At least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20.6-23.9
- Humidity (%): 30-70
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 12 March, 2012 To: 16 March, 2012
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
Vapor was generated by adding a calculated amount of the test article to a test chamber of known volume containing the animals. The atmosphere was supplemented with oxygen if necessary to maintain a level of at least 18%. No other parameters specified in the study report.
TEST ATMOSPHERE
- Brief description of analytical method used: Not specified.
- Samples taken from breathing zone: Not specified
VEHICLE: Air - Analytical verification of test atmosphere concentrations:
- not specified
- Duration of exposure:
- ca. 6 h
- Concentrations:
- 0 (control), 100 ppm
- No. of animals per sex per dose:
- 3 males per dose
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: Animals were dosed for 6 hours a day for 5 days and necropsied following the final exposure.
- Frequency of observations and weighing: Observations were made continually during exposures and body weights were recorded daily prior to exposure.
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, liver weights were recorded, serum samples collected for clinical chemistry analysis.
Results and discussion
Effect levels
- Key result
- Sex:
- male
- Dose descriptor:
- LC0
- Effect level:
- 100 ppm
- Based on:
- test mat.
- Exp. duration:
- 6 h
- Mortality:
- No mortality occurred during the study.
- Clinical signs:
- other: No treatment-related clinical signs were observed during the study.
- Body weight:
- There was no statistically significant difference in average group body weight gain.
- Gross pathology:
- No macroscopic abnormalities were observed in any of the treated animals at necropsy.
- Other findings:
- Clinical chemistry: A statistically significant increase in calcium was noted in treated rats compared to controls.
Liver weights: Liver weights were similar between treated and control animals.
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- Based on the results of the study, the 6 hour, 5-day inhalation LD50 value of the test article is greater than 100 ppm (2.16 mg/L, vapor).
- Executive summary:
The acute inhalation toxicity of the test article was evaluated in a 5-day repeat inhalation toxicity test in Sprague-Dawley rats. Rats (3 males) were exposed, whole body, to 100 ppm (vapor) of test article for 6 hours per day for 5 consecutive days. Control rats (3 males) were treated in a similar manner with the exclusion of exposure to the test material. Rats were weighed daily and were euthanized immediately following the Day 5 exposure. Animals were subject to a gross necropsy, livers collected and weighed, and serum samples collected for clinical chemistry evaluation. All animals survived the 5-day exposure period and showed no clinical signs of toxicity or macroscopic abnormalities at necropsy. The test article treated rats showed statistically significant increases in calcium blood serum levels as compared to the controls (p<0.05); however, it should be noted that both the control and exposed groups serum calcium values were above those recognized as the normal range for Wistar rats. Liver weights and body weights were in normal ranges and similar for all animals. Based on the results of the study, the 6 hour, 5-day inhalation LC50 value of the test article is greater than 100 ppm (2.16 mg/L, vapor).
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