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EC number: 218-254-8 | CAS number: 2094-98-6
- 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:
- key study
- Study period:
- 4.8.2000-18.8.2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 000
- Report date:
- 2000
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- GLP compliance:
- no
- Test type:
- acute toxic class method
Test material
- Reference substance name:
- 1,1'-azobis(1-cyclohexanecarbonitrile)
- EC Number:
- 218-254-8
- EC Name:
- 1,1'-azobis(1-cyclohexanecarbonitrile)
- Cas Number:
- 2094-98-6
- Molecular formula:
- C14H20N4
- IUPAC Name:
- 1,1'-azobis(1-cyclohexanecarbonitrile)
- Test material form:
- solid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Crj: CD(SD)
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Quarantine and Animal Selection
Rats were quarantined after arrival for 6 days prior to testing. During the quarantine period, rats were weighed and observed for clinical signs of disease 3 times. Rats were obtained from the general population of stock rats released from quarantine and were selected for use on this study from those rats exhibiting a normal pattern of weight gain and no overt signs of disease.
Administration / exposure
- Route of administration:
- inhalation: aerosol
- Type of inhalation exposure:
- nose only
- Vehicle:
- air
- Mass median aerodynamic diameter (MMAD):
- 7 µm
- Geometric standard deviation (GSD):
- 2.4
- Remark on MMAD/GSD:
- Animals were exposed to H-24515 at a concentration of 8.0 mg/L. The mass median aerodynamic diameter (MMAD) of the aerosol particles collected during an inhalation exposure is generally targeted to be 1-4 μm. The dust atmospheres generated during this study were considered to be only moderately respirable in rats since the MMAD was 7.0 μm. However, 66% of the atmosphere was less than 10 μm.
Although attempts at grinding the test substance differently (e.g., sieving) and various generation systems were tried during the method development phase of the study, the physical properties of the test substance (e.g., granular texture) and safety concerns (e.g., explosivity), made it difficult to generate an atmosphere with a MMAD that was less than 7.0 μm. The atmospheres generated during this study were considered to be the best that could be generated, and acceptable for a hazard evaluation. - Details on inhalation exposure:
- Atmosphere Generation
Chamber atmospheres of H-24515 were generated by suspending the particulate test substance in air with a Fluid Energy Processing model 00 Jet-O-Mizer jetmill. The test substance was metered into the jetmill with a K-Tron model T-20 twin screw volumetric feeder. Nitrogen was introduced into the bin feeder to prevent moisture absorption by the test substance. Filtered, houseline air (37 L/min) introduced into the jetmill carried the resulting atmosphere into a 1.5 L glass cyclone elutriator and then into the exposure chamber. Chamber concentrations of H-24515 were controlled by varying the test substance feed rate to the jetmill.
Test atmospheres were exhausted through a high-capacity particle filter followed by an MSA charcoal/HEPA filter cartridge prior to discharge into the fume hood.
Chamber Construction and Design
The exposure chamber was constructed of glass (cylindrical) with a nominal internal volume of 29 L. A dispersion plate inside the chamber promoted uniform chamber distribution of the test atmosphere.
Exposure Mode
During exposure, rats were individually restrained in perforated plastic cylinders with conical nosepieces. The restrainers were inserted into the polymethylmethacrylate faceplate of the exposure chamber so that only the nose of each rat extended into the chamber. - Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- 4 h
- Concentrations:
- 8.0 mg/L
Range: 5.2-11 mg/L (s.d. 2.0, n=9) - No. of animals per sex per dose:
- 6
- Control animals:
- no
Results and discussion
Effect levels
- Key result
- Sex:
- male
- Dose descriptor:
- other: ALC / approximate lethal concentration
- Effect level:
- > 8 mg/L air
- Exp. duration:
- 4 h
- Mortality:
- All rats exposed to H-24515 survived the exposure and subsequent 14-day recovery period.
- Clinical signs:
- other: No abnormalities were observed in rats during the exposure. Immediately following the exposure and one day postexposure, most rats exposed to H-24515 exhibited stained/wet fur and nasal/ocular discharge. Stained fur and nasal/ocular discharge continued to
- Body weight:
- In addition, all rats had slight to severe weight loss (4 to 13% of initial body weight) on the day following the exposure, but had normal weight-gain patterns by the second day of recovery and experienced an overall weight gain by the end of recovery period.
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- Under the conditions of this study, the approximate lethal concentration (ALC) for H-24515 was greater than 8.0 mg/L. Because of the low respirability of the test atmosphere, this study should be considered a hazard evaluation of the test substance, rather than an accurate toxicity evaluation. However, H-24515, as tested, is considered to be no worse than very low in toxicity on an acute inhalation basis (ALC greater than 2.0 mg/L).
- Executive summary:
One group of 6 male Crl:CD®(SD)IGS BR rats was exposed nose-only for a single, 4-hour period to H-24515 in air. The test atmosphere was generated by suspension of H-24515 particulate in air. Gravimetric analysis was used to measure the concentration of the test substance in the exposure chamber. Rats were weighed and observed for clinical signs of toxicity during a 14-day recovery period.
Rats were exposed to a dust atmosphere of H-24515 at a concentration of 8.0 mg/L. The mass median aerodynamic diameter (MMAD) for the dust generated in the exposure chamber was 7.0 μm, with 66% of the particles less than 10 μm.
All rats exposed to H-24515 survived the exposure and subsequent 14-day recovery period. Stained/wet fur and nasal/ocular discharge were observed in rats up to 3 days following exposure. In addition, all rats had slight to severe weight loss (4 to 13% of initial body weight) on the day following the exposure, but had normal weight-gain patterns by the second day of recovery and experienced an overall weight gain by the end of recovery period.
Under the conditions of this study, the approximate lethal concentration (ALC) for H-24515 was greater than 8.0 mg/L. Because of the low respirability of the test atmosphere, this study should be considered a hazard evaluation of the test substance, rather than an accurate toxicity evaluation. However, H-24515, as tested, is considered to be no worse than very low in toxicity on an acute inhalation basis (ALC greater than 2.0 mg/L).
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