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Diss Factsheets
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EC number: 433-480-9 | CAS number: 623-53-0
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
Short description of key information on bioaccumulation potential result:
Single oral administration to rats at 5000 mg/kg rapidly produced signs of lethargy, ataxia, hunched posture, disturbed respiration etc. (evident from 1 hour post-dose) but these proved transient, resolving by day 2 post-dose. Acute inhalation exposure of rats at 17.6 mg/l produced similarly rapid onset of transient reactions (disturbed respiration, hunched posture, piloerection) which had resolved by day 2 post-exposure.
An acute oral toxicity study of the close analogue diethyl carbonate also found rapid-onset but transient signs of sedation, which the investigators speculated might be related to metabolic conversion of the test substance to ethanol.
In an oral subacute toxicity test of methyl ethyl carbonate, rats dosed at 1000 mg/kg/day showed no signs of adverse reaction (males) or only hunched posture plus cases of transient, post-dose salivation (females). No clear evidence of toxicity and no effects in body tissues/organs were seen.
The close analogue diethyl carbonate also showed low repeat-dose toxicity: in a chronic mouse toxicity/carcinogenicity study, 1000 ppm in drinking water (approximately equal to 140 mg/kg/day) proved to be the NOAEL.
The close analogue dimethyl carbonate is said to be hydrolysed to methanol and carbon dioxide. Also, it is known that organic carbonates are a substrate for liver esterases, leading to hydrolysis and release of carbon dioxide (e.g. action of porcine liver esterase on diphenyl carbonate, described in various publications including US Patent 4892811, 1990).
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
Additional information
The evidence of rapid-onset signs of sedation and/or ataxia, disturbed respiration, etc. following acute exposure in rats suggests significant absorption may occur but the subsequent early recoveries, plus indications of low subacute or chronic toxicity, suggest significant metabolic detoxification. This is compatible with a hypothesis of hydrolysis to ethanol and methanol and carbon dioxide mediated by hepatic enzymes (e.g. esterases), with subsequent bioelimination via normal metabolic and excretory pathways.
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