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Diss Factsheets
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EC number: 203-466-5 | CAS number: 107-13-1
- 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
Health surveillance data
Administrative data
- Endpoint:
- health surveillance data
- Type of information:
- other: review
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Unpublished review of the available data
Data source
Reference
- Reference Type:
- grey literature
- Title:
- Unnamed
- Year:
- 2 010
Materials and methods
- Study type:
- other: review
- Endpoint addressed:
- neurotoxicity
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- Literature review
- GLP compliance:
- no
- Remarks:
- : not relevant
Test material
- Reference substance name:
- Acrylonitrile
- EC Number:
- 203-466-5
- EC Name:
- Acrylonitrile
- Cas Number:
- 107-13-1
- Molecular formula:
- C3H3N
- IUPAC Name:
- prop-2-enenitrile
Constituent 1
Method
- Type of population:
- occupational
- Ethical approval:
- not applicable
- Details on study design:
- Review and critical appraisal of relevant luterature data relating to the neurotoxicity of acrylonitrile.
Results and discussion
Any other information on results incl. tables
Wilson (1944) reports health problems encountered in workers exposed to acrylonitrile in the synthetic rubber industry. Reported symptoms included nausea, vomiting, diarrhoea, weakness, fatigue, headache, nasal irritation and oppressive feeling. Workers were also likely exposed to a number of other compounds used in the manufacture of synthetic rubbers, such as butadiene, styrene, hydrogen peroxide and carbon tetrachloride. The same author (Wilson et al., 1948) reports that workers exposed to acrylonitrile at concentrations of 6-100 ppm for 20-45 minutes had headaches, irritation of mucous membranes and nervous irritability. However potential exposure to multiple chemicals may also have contributed to this symptomatology.
Sakurai et al (1978) studied the effects of acrylonitrile in workers exposed for over 5 years, and in matched controls. Although the authors were very careful in selecting the subjects for this study, the sample sizes in this study are small (three groups of 20 exposed workers; exposure levels of 2.1, 7.4 and 14.1 ppm). No evidence for an effect of acrylonitrile was found, but the possibility of a palpable liver and conjunctival reddening effects cannot be entirely excluded.
Muto et al. (1992) report that medical examination failed to detect any health effects attributable to long-term exposure to acrylonitrile at 0.27 and 0.84 ppm, but symptoms of irritation could not be ruled out. Some symptoms such as heaviness in the stomach were reported in the absence of other gastrointestinal symptoms. Eye pain or lacrimation were also seen in one factory; decreased libido, poor memory and reddening of the conjunctiva were reported in another factory. These signs and symptoms were not reported in the other factories and were not considered related to acrylonitrile as the level of exposure was considerably lower than past levels, according to the authors.
Kaneko et al. (1992) investigated the relationship between long-term exposure to acrylonitrile and symptoms as measured with a questionnaire (modified Cornell Medical Index) in seven acrylic fibre factories (504 males divided into three exposure groups of 1.8, 7.4 or 14.1 ppm for 5-9 years) and in a reference group of 255 males. The authors conclude that there were no differences between the exposed and referenced groups.
Cheng et al. (2004) examined olfactory function in 52 injection-moulding workers exposed to acrylonitrile-butadiene-styrene (ABS) thermal decomposition products (7.3 years at unknown exposure levels) and in 72 control workers. The Connecticut Chemosensory Clinical Research Center method was used to test olfactory functions. Threshold scores were significantly reduced in the exposed workers compared to controls, but they recovered after one night of rest. Due to the concurrent exposure to other respiratory irritants, the authors concluded that it was impossible to speculate on the cause of the lower threshold scores in this study.
Rongzhu et al. (2005) examined the neurobehavioral effects in 3 groups of workers exposed to acrylonitrile by inhalation (175 workers from two departments exposed to 0.11 or 0.91 ppm (no personal sampling and with expousre to other substances). The matched control group consisted of 174 unexposed workers. Several psychological tests were used in this study and gave ambiguous data (contradictory results, no relation to exposure duration). Simple reaction time (attention/response speed) and motor steadiness tests showed reduced performance in both exposed groups compared to controls, as well as a duration-related decrease. Among the many tests, several statistically significant differences were flagged, and the multiplicity problem was neither controlled nor addressed. The authors conclude that due to limitations, further studies are needed to determine the presence of a neurotoxic effect.
Applicant's summary and conclusion
- Conclusions:
- It is concluded that irritation is often reported in human studies, however other reported signs or symptoms were nonspecific (headache, fatigue, weakness). It is noted that olfactory function can be reversibly affected in workers exposed to ABS products for several years, but that no convincing evidence has been provided to support neurobehavioural effects in workers exposed to AN by inhalation at ambient concentrations of 0.91 ppm.
- Executive summary:
The author reviews the available health surveillance data relating to the neurotoxicity of acrylonitrile. It is concluded that irritation is often reported in human studies, however other reported signs or symptoms were nonspecific (headache, fatigue, weakness).
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