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EC number: 201-188-9 | CAS number: 79-24-3
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation, other
- Remarks:
- We have only an in vivo study, no in vitro study. That is why we are using this in vivo study, in agreement with the requirements for this endpoint.
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 31 January 1989 - 3 February 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was not conducted according to guidelines but was conducted according to GLPs and the report contains sufficient data for interpretation of study results.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 989
- Report date:
- 1989
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: Federal Hazardous Substances Act Regulations (16 CFR Part 1500)
- Deviations:
- yes
- Remarks:
- Since a positive response was observed in 2 of 6 rabbits, the guideline indicates the test should be repeated. The test was not repeated.
- GLP compliance:
- yes
Test material
- Reference substance name:
- Nitroethane
- EC Number:
- 201-188-9
- EC Name:
- Nitroethane
- Cas Number:
- 79-24-3
- Molecular formula:
- C2H5NO2
- IUPAC Name:
- nitroethane
- Details on test material:
- Test material was described as Nitroethane - NC. No additional information available.
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- Young adult New Zealand White rabbits (Ace Animals, Inc., Boyertown, PA) were acclimated to the laboratory environment for at least five days prior to study initiation. They were observed daily during the acclimation period to assure their suitability as test animals. All housing and care conformed to the standards establisted in the "Guide for the Care and Use of Laboratory Animals" DHEW Publication No. (NIH) 85-23. Each animal was housed in a wire mesh cage and identified with an ear tag and color coded cage card. NIH 09 Rabbit Ration (Zeigler Brothers, Inc., Gardners, PA) and fresh tap water were selected randomly from the acclimated colony and assigned to the test group. The eyes of each rabbit were examined with sodium fluorescein and a slit light equipped with a cobalt blue filter prior to dosing to verify the absence of pre-existing ocular lesions.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not specified
- Amount / concentration applied:
- 0.1 ml was instilled into the right eye of each rabbit.
- Duration of treatment / exposure:
- According to the report the test material is allowed to remain on the eye till the study ends
- Observation period (in vivo):
- Primary eye irritation was evaluated 24, 48 and 72 hours after the test material was administered.
- Number of animals or in vitro replicates:
- 6 rabbits
- Details on study design:
- Eyes were examined with sodium fluorescein and a slit light equipped with a cobalt blue filter prior to dosing to verify the absence of pre-existing ocular lesions. The test material (0.1 ml) was instilled into the right conjunctival sac of each rabbit and the lids were held together for one second and released. The animals were observed twice daily for mortality at least 5 hours apart. Primary eye irritation was evaluated 24, 48 and 72 hours after the test material was administered. The cornea, iris and conjunctiva were scored separately according to the method of Draize. The total maximum score was 110.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 6.2
- Max. score:
- 18
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 4.2
- Max. score:
- 9
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not specified
- Irritant / corrosive response data:
- According to the report, 2 of 6 rabbits exhibited corneal irritation 24 hours after application. One of 6 rabbits exhibited iris and conjunctiva irritation 24 hrs after application. There was no evidence of corneal, iris or conjunctival irritation after 72 hours.
- Other effects:
- The untreated eyes of four animals exhibited diffuse areas of corneal opacity during the study.
Any other information on results incl. tables
Table 1 Summary of Primary Eye Irritation Scores
Number of | Mean Score +/- Standard Deviation after Test Article Instillation | ||
Animals Dosed | 24 hours | 48 hours | 72 hours |
6 | 6.2 + 6.4 | 4.2 + 3.1 | 1.0 + 1.1 |
Individual Draize Values | 4, 18, 2, 9, 2, 2 | 4, 6, 4, 9, 0, 2 | 2, 2, 0, 2, 0, 0 |
According to the classification used, the two most severe readings would equate to moderately and mildly irritating. In the case of the rabbit with a score of 18, the cornea opacity and area was rated a 1 and 1, respectively. Iris was rated a 1. Conjunctival rednes, chemosis, and discharge were 2, 1 and 1, respectively. By 48 hours, the only positive symptoms in this rabbit was conjunctival redness and chemosis which were 2 and 1, respectively. Thus the observed effects were considered to be minimal even though the rating scheme would classify the effect as moderate.
Applicant's summary and conclusion
- Interpretation of results:
- slightly irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- Based on the results of this test, nitroethane is equivocal as a primary eye irritant. The maximum average eye irritation score was 6.2 at 24 hours after dose administration. Based on this score, nitroethane is considered mildly irritating to rabbit eyes.
- Executive summary:
The eye irritation potential was evaluated using the U.S. Federal Hazardous Substances Act Regulation (16 CFR Part 1500). Based on the results of this test, nitroethane is equivocal as a primary eye irritant. The maximum average eye irritation score was 6.2 at 24 hours after dose administration. Based on this score, nitroethane is considered mildly irritating to rabbit eyes.
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