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Diss Factsheets
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EC number: 205-500-4 | CAS number: 141-78-6
- 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
Neurotoxicity
Administrative data
Description of key information
High concentrations of ethyl acetate vapor can produce acute transient sedation. Well-conducted rat studies have found no cumulative or enduring neurotoxic effects of ethyl acetate exposure.
Key value for chemical safety assessment
Additional information
No performance deficits in simple and choice reaction time, or in short-term memory, were detected during or after exposure in sixteen male volunteers exposed for four hours to 402 ppm ethyl acetate or to half this concentration in combination with acetone (Seeber, 1992a). The only significant finding reported was complaints that the volunteers found the exposures annoying and uncomfortable. Significant correlations were reported between subjective measures of ‘annoyance’ and ‘complaints’ and objective measures of urinary excretion of ethyl acetate (Seeber, 1992b).
The neurotoxicity of ethyl acetate has been evaluated in acute, repeated dose, and subchronic inhalation studies in rats. Diminished response to delivery of an alerting stimuli was noted during exposure at ethyl acetate concentrations of 750 ppm and above. The acute NOEC for neurobehavioural changes in this study was 600 ppm, and exceeded the NOEC for general toxicity (body weight loss). No cumulative or enduring effects to the nervous system were seen in 90-day rat studies that included exposures to 1500 ppm and evaluations of motor activity and functional observational battery, as well as schedule controlled operant behavior (Christoph, 2003).
The reported threshold limit for depressive effects of ethyl acetate on the vestibulo reflex in female Sprague-Dawley rats is 44 mg/l in blood (Tham, 1984). The reported neurotoxic dose in rabbits by the oral route is 4493 mg/kg (Munch, 1972) and the narcotic thresholds for mice and cats are reportedly 18 mg/l and 43 mg/l respectively by inhalation (Flury, 1933).
Justification for classification or non-classification
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.