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EC number: 232-029-1 | CAS number: 7783-82-6
- 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:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1963
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study done before GLP was established. Read across justification is given in section 13 assessment reports: WF6 justification for read across
Data source
Reference
- Reference Type:
- publication
- Title:
- A toxicopathologic study in animals after brief single exposures to hydrogen fluoride
- Author:
- Rosenholtz MJ, Carson TR, Weeks MH, Wilinski F, Ford DF & Oberst FW; Rosenholtz MJ, Carson TR, Weeks MH, Wilinski F, Ford DF & Oberst FW;
- Year:
- 1 963
- Bibliographic source:
- publication Am. Ind. Hyg. Assoc. J. 24:253-261, 1963
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Acute inhalation toxicity in the rat.
Maximum exposure: 60 min. - GLP compliance:
- no
- Remarks:
- done before GLP was established
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Hydrogen fluoride
- EC Number:
- 231-634-8
- EC Name:
- Hydrogen fluoride
- Cas Number:
- 7664-39-3
- IUPAC Name:
- fluoride
- Test material form:
- other: HF vapour
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Weight: 100 - 120 g
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: no vehicle
- Details on inhalation exposure:
- Volume of the exposure chamber/housing was 400 l with an air flow of 200 l/min. An expansion tank and a manometer were used.
Constant temperature at 20 degree Celsius. - Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- 60 min
- Remarks on duration:
- 5, 15, 30 and 60 min
- Concentrations:
- various
- No. of animals per sex per dose:
- 20 male rats per group/concentration
- Control animals:
- yes
- Details on study design:
- Groups of rats were exposed to various concentrations of hydrogen fluoride vapour for either 5, 15, 30 or 60 minutes. Surviving rats were weighed daily and observed for 14 days after exposure. Clinical observations were made following exposure, body weights were recorded daily and mortalities recorded.
- Statistics:
- The LC50 values for each exposure time were calculated using the method of Bliss (1952).
Results and discussion
Effect levelsopen allclose all
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 4 970 ppm
- Based on:
- test mat.
- 95% CL:
- 4 584 - 5 388
- Exp. duration:
- 5 min
- Remarks on result:
- other: slope: 11.8 std. dev. +/- 4.2
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 2 689 ppm
- Based on:
- test mat.
- 95% CL:
- 2 397 - 3 016
- Exp. duration:
- 15 min
- Remarks on result:
- other: slope: 9.4 std. dev. +/- 2.1
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 2 042 ppm
- Based on:
- test mat.
- 95% CL:
- 1 901 - 2 192
- Exp. duration:
- 30 min
- Remarks on result:
- other: slope: 14.0 std. dev. +/- 3.3
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 1 307 ppm
- Based on:
- test mat.
- 95% CL:
- 1 212 - 1 410
- Exp. duration:
- 60 min
- Remarks on result:
- other: slope: 10.7 std. dev. +/- 3.8
- Mortality:
- Mortality occurred, but count of rats that passed away was not reported. Some deaths were reported to occur during the post-exposure observation period.
- Clinical signs:
- other: Conjunctival and nasal irritation as shown by reddened conjunctivae, pawing at the nose, marked lacrimation, nasal secretion and sneezing. These signs were not seen 1 week following exposure (in surviving animals). Respiratory distress and general weaknes
- Body weight:
- Body weight loss was observed in surviving animals. Compared to controls, surviving rats exhibited a 10-15% reduction in body weight during the first 3-7 days after exposure, after which weights returned to normal.
- Gross pathology:
- Lesions were found (differing quantitatively from that of controls) in the kidneys, liver, nasal passage, bone marrow and skin of exposed rats.
Any other information on results incl. tables
The LC50 values were 4970, 2690, 2040 and 1310 ppm for rats exposed to hydrogen fluoride vapour for 5, 15, 30 and 60 minutes, respectively.
Applicant's summary and conclusion
- Interpretation of results:
- very toxic
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The LC50 values were 4970, 2690, 2040 and 1310 ppm for rats exposed to hydrogen fluoride vapour for 5, 15, 30 and 60 minutes, respectively.
1310 ppm HF equals 218 ppm WF6 and 2700 mg/m³ of WF6 at 20 °C and 1,013 bar - Executive summary:
Male Wistar rats were exposed to lethal concentrations of hydrogen fluoride vapour, at various concentrations for either 5, 15, 30 or 60 minutes. The LC50 values were 4970, 2690, 2040 and 1310 ppm for rats exposed to hydrogen fluoride vapour for 5, 15, 30 and 60 minutes, respectively. Exposure resulted in mortalities, although numbers and times of death are not reported. Lesions were observed in the kidneys, liver, nasal passages, bone marrow and skin. Exposure resulted in conjunctival and nasal irritation, respiratory distress and general weakness and body weight loss.
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