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EC number: 205-599-4 | CAS number: 143-33-9
- 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 based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Similar to a guideline study, but precedes development of OECD protocols. Well documented study performed in a laboratory wthe significant expertise in inhalation toxicology.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 981
- Report date:
- 1981
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Version / remarks:
- precedes establishment of guideline
- Deviations:
- yes
- Remarks:
- no data on characterization of material; no necropsies performed, however, some clinical chemistry data was obtained.
- GLP compliance:
- no
- Remarks:
- precedes establishment of GLP standards, but is of high quality
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Hydrogen cyanide
- EC Number:
- 200-821-6
- EC Name:
- Hydrogen cyanide
- Cas Number:
- 74-90-8
- IUPAC Name:
- cyanide
- Details on test material:
- Hydrocyanic acid gas, Matheson Gas Products Co., Haskell No. 13,697.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Crj: CD(SD)
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Test Animals: Rats were housed in pairs in stainless steel cages with food and water available ad libitum The animal room temperature (26 oC), humidity (60-70%) and light cycle (7 AM 0 5 PM) were controlled automatically. After a quarantine and acclimatization period, rats weighing 250 ± 25 g were selected for the test exposures. During the exposure, rats were either restrained in whole body holders and exposed head only to the test gas, or were allowed free movement inside the chamber. During some exposures, restrained and unrestrained rats were exposed simultaneously.
For selected non-lethal exposures, polyethylene cannulas were placed in the femoral arteries of rats anesthetized with 50 mg/kg sodium pentobarbital. The cannulated rats were caged individually and used after a 24-hour post-surgery recovery peiod.
Administration / exposure
- Route of administration:
- inhalation: gas
- Type of inhalation exposure:
- other: head only and whole body
- Vehicle:
- not specified
- Details on inhalation exposure:
- Exposure system: The rectangular exposure chamber was constructed of ½ inch sheets of polymethylmethacrylate, 48 inches long and 18 inches tall by 14 inches deep, and had an approximate internal volume of 175 liters.
The animal exposure ports were located medially on the front panel. The animal head space was separated from the rest of the chamber by a hinged box which was swung down to start an exposure. This permitted the exposure to begin instantenously once a satisfactory steady state chamber concentration of the test material was obtained.
The test-gas chamber atmospheres were obtained with continuous flow-through generation. Gas concentrations were generated by dilution of commercial bottled gas (Matheson Gas Products, East Rutherford, NJ).
Chamber Analytical: Concentrations of HCN were continuously monitored by infrared spectrophotometry. This method was validated by gas chromatography.
Respiratory Rate: Respiratory rate was monitored by recording pressure fluctuations due to breathing in a body plethysmograph. A pressure transducer (Gould Statham PM6) coupled the plethysmograph to a signal amplifier and recorder (Gould 2800). Respiratory rate (breaths/minute) was measured for 1 minute every 5 minutes for the 10-minute control period prior to exposure. Respiratory rate was monitored continuously during the first 5 minutes of exposure and thereafter recorded at 5-minute intervals. A mean percent decrease in respiratory rate was calculated for each rat. The groupmean, a mean of the individual means, was used to graphically determine the RD25. - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- Continuously by infrared spectrophotometry. The method was validated by gas chromatography
- Duration of exposure:
- > 5 - < 60 min
- Remarks on duration:
- 4 groups: 5, 15, 30 and 60 min
- Concentrations:
- up to approximately 11,000 ppm HCN. The principle of "concentration x time" was employed.
- No. of animals per sex per dose:
- 4-7
- Control animals:
- no
- Statistics:
- Statistical Methods: The LC50 (median lethal concentration) was calculated by the method described in Probit analysis (D.J. Finney, Cambridge University Press, Cambridge, 1977). The RD25 (concentration causing a 25% reduction in respiratory rate) was obtained by graphical methods.
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 63 ppm
- Based on:
- test mat.
- 95% CL:
- > 52 - < 79
- Exp. duration:
- 1 h
- Remarks on result:
- other: In restrained rats. See data table for LC50 for other time periods.
- Mortality:
- Significantly lower LC50s for restrained rats were observed for the 30- and 60-minute exposure periods, compared with free-moving rats.
HCN exposure caused death during exposure periods, compared with other noxious gases which result in death in the 14-day period after exposure ceases. - Clinical signs:
- other: The concentration at which the respiratory rate decreased 50% is 125 ppm
- Body weight:
- In rats which survived for 7 days after exposure, body weight was significantly decreased. In restrained rats exposed for 60 min, average weight loss was about 34%, while in free-moving rats, average weight loss was about 15%.
- Gross pathology:
- No necropsy performed.
Any other information on results incl. tables
Lapin CA 1981 LC50s in Study of Inhalation Toxicity of Common Combustion Gases | ||||||
Group | Time (min) | Concentration (ppm) resulting in LD50 (Average and 95% CI) | ||||
Restrained | Unrestrained | |||||
1 | 5 | 398 | 369 | |||
370-431 | 350-395 | |||||
2 | 15 | 163 | 196 | |||
131-189 | 181-209 | |||||
3 | 30 | 85 | 173 | |||
59-110 | 163-188 | |||||
4 | 60 | 63 | 139 | |||
52-79 | 120-155 |
Applicant's summary and conclusion
- Interpretation of results:
- Toxicity Category II
- Remarks:
- Migrated information as listed in Table 3.1 of Regulation (EC) No. 1272/2008 Criteria used for interpretation of results: EU
- Conclusions:
- Hydrogen cyanide is a highly toxic compound by the inhalation route. Toxicity is higher in restrained animals compared with free-moving animals. There is a clear (concentration x time) relationship: the longer the exposure time, the lower the concentration which results in lethality of exposed animals. The LC50 for 60 min in restrained rats is 63 ppm. For a 30 min time period, the LC50 is 85 ppm, and for a 5 min time period, the LC50 is 369 ppm.
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