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Diss Factsheets
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EC number: 203-872-2 | CAS number: 111-46-6
- 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
Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Inhalation of Aerosolized Ethylene Glycol by Man
- Author:
- Wills J.H.
- Year:
- 1 974
- Bibliographic source:
- CLINICAL TOXICOLOGY 7( 5), pp. 463-476 ( 1974)
Materials and methods
- Endpoint addressed:
- respiratory irritation
- repeated dose toxicity: inhalation
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- Twenty volunteers were exposed during 20 to 22 hr per day to aerosolized ethylene glycol in mean daily concentrations between 3 and 67 mg/m3.
- GLP compliance:
- no
Test material
- Reference substance name:
- Ethane-1,2-diol
- EC Number:
- 203-473-3
- EC Name:
- Ethane-1,2-diol
- Cas Number:
- 107-21-1
- Molecular formula:
- C2H6O2
- IUPAC Name:
- ethylene glycol
Constituent 1
Method
- Ethical approval:
- not applicable
- Details on study design:
- Twenty volunteers were exposed during 20 to 22 hr per day to aerosolized ethylene glycol in mean daily concentrations between 3 and 67 mg/m3 in an unused ward of a prison hospital. Fourteen other volunteers, as a control group, were kept in another ward of the prison hospital facility and were fed and otherwise treated as similarly as possible to the exposed group.
The volunteers left this chamber only for meals and toilet purposes; they spent at least 20 hr each day within the chamber, and more commonly about 22. Moderate smoking within the chamber was permitted.
Both the control and the exposed groups were held under their particular experimental conditions for 30 days. Follow-up observations were made on both groups two weeks after the end of the exposure period. Before admission to the study, all subjects underwent complete physical examinations, including slit-lamp, electrocardiographic, and electroencephalographic studies. A battery of psychological tests designed to reveal effects on simple reaction time, reaction time with discrimination, visual-motor coordination, perception, and mental ability was applied also. These examinations were repeated at the end of the first two weeks of exposure in the main study and at the termination of the exposure. Blood and urine samples were collected and examined. - Exposure assessment:
- measured
- Details on exposure:
- An unused ward of the prison hospital was converted into an exposure chamber.
Aerosol jet nozzles were mounted to force mists ol ethylene glycol into the cooled air streams of the three air conditioners. Air compressed to 50 psi was supplied to the jet nozzles through pipelines from a compressor in an adjacent room. The ethylene glycol was aspirated from reservoirs below each nozzle; these reservoirs were refilled by hand as necessary.
The sizes of the droplets of the aerosol were estimated at intervals by exposing three clean glass slides simultaneously in various parts of the chamber. These slides were stored in a moist chamber until they could be examined. The diameters of the droplets were measured with a calibrated microscope, and were found always to be within the range 1-5 μm.
Polyethylene bottles of 250 ml capacity were evacuated by a motor driven pump and were then allowed to fill with air from the room, the cycle of evacuation and filling being repeated 15 times. Samples were collected during each of the three periods during the day at which the volunteers left the chamber to eat. Samples were collected from five stations within the chamber at each sampling time.
For estimation of the ethylene glycol within the bottle, 2 mL of distilled water were injected into the bottle with a syringe and needle. The bottle was then shaken vigorously for several minutes; an aliquot of the aqueous solution was analyzed calorimetrically. The concentrations of ethylene glycol measured within the five air samples collected at each sampling time were averaged, the means for the three sampling times being averaged to obtain a mean daily value. The daily means were averaged to obtain mean weekly or fortnightly values.
Results and discussion
- Results:
- The results of intensive exposure for four weeks to aerosolized ethylene glycol were satisfactorily negative. No evidence was found that a tolerable concentration during virtually uninterrupted exposure for that length of time had any deleterious effect on psychologic or other functions of the human body. The subject who consistently excreted the highest mean concentration of the glycol in his urine (18 mg/100 mL) may be calculated to have absorbed about 0.8 g/day. On the assumption that man excretes unchanged about one-quarter of that which is absorbed. This would represent between 1 and 2 % of the estimated Single lethal dose.
The most common complaint during the exposure was irritation of the upper respiratory tract. This symptom of exposure to ethylene glycol seemed to correlate well with the concentration of the glycol in the ambient air. Concentrations of about 200 mg/m3 or more were intolerable due to strong irritation of the upper respiratory tract, with a burning sensation along the trachea and a burning cough. On the basis of this study, we judge that it would be impossible for an individual with reasonably normal sensory apparatus to absorb through his respiratory tract enough aerosolized ethylene glycol to cause damage to any important functional systems or organs.
Applicant's summary and conclusion
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.
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