Uses
Copolymer with 3–5% polyvinyl chloride
for plastic products such as clear plastic bottles;
medicine (anesthetic, for brief operations only).
General Description
A clear colorless liquid with a characteristic odor. Flash point below -22°F. Less dense than water. Autoignition temperature 680°F. Slightly soluble in water; miscible with alcohol, acetone, chloroform, and ether. Must be protected from light.Vapors heavier than air. Toxic by inhalation.
Air & Water Reactions
Highly flammable. Slightly soluble in water. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164].
Reactivity Profile
Ethers, such as DIVINYL ETHER, can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert. Vinyl ether is miscible with alcohol, acetone, chloroform and ether and must be protected from light [Hawley].
Health Hazard
Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
Description
Divinyl ether is a mobile,
colorless, inflammable liquid with a characteristic
sweet odor, bp 28.4 ?C. Approximately 4 %
ethanol is added as a stabilizer. Divinyl ether
may contain 0.0077 % of a stabilizer, phenyl-α-
naphthylamine, that produces a slightly reddish
fluorescence.
Chemical Properties
Clear, colorless liquid with a characteristicodor; boils at 28.5°C (83°F); density 0.774[at 20°C (68°F)]; soluble in most organicsolvents, slightly soluble in water [0.53 g/dLat 37°C (98°F)].
Definition
ChEBI: Vinyl ether is an ether.
Indications
Divinyl ether is used for minor
surgery, obstetrics, dentistry, and inducing anesthesia.
A certain degree of hepatotoxicity rules
out long-term use. Hypersecretion has also been
observed. Divinyl ether increases and decreases
in tissue levels faster than diethyl ether.
Fire Hazard
Highly flammable; flash point (closed cup) <
-30°C (<-22°F); vapor density 2.4 (air =
1); the vapor is heavier than air and can travel
a considerable distance to a source of igni tion and flash back; autoignition temperature
360°C (680°F); can be ignited by lightning
or static electricity; fire-extinguishing agent:
dry chemical, foam, or CO2; use a water
spray to keep fire-exposed containers cool
and to disperse the vapors
Vinyl ether forms explosive mixtures with
air, with LEL and UEL values of 1.7%
and 27% by volume of air, respectively. It
forms unstable peroxides on long standing or
in the presence of oxygen. These peroxides
can explode spontaneously or when heated.
It decomposes to acetaldehyde (toxic and
highly flammable) when exposed to light.
Synthesis
Divinyl ether is prepared by the reaction of
liquefied alkali hydroxide or sodium alkoxide
on β,β_x0002_-dihalodiethyl ether or by pyrolysis
of α,α_x0002_-dichlorodiethyl ether in the gas phase at
600 – 800 ?C in the presence of barium chloride
catalyst .
storage
Vinyl ether is stored in a flammable-liquidsstorage room or cabinet separated from oxidizing and combustible materials. It shouldbe protected from physical damage andfrom static electricity or lightning. It isshipped in amber glass bottles or metaldrums.
Waste Disposal
Vinyl ether is mixed with an excess ofhigher-boiling solvent and burned in a chem ical incinerator equipped with an afterburnerand scrubber. Small amounts, free of peroxides, can be evaporated in a fume hood awayfrom a source of ignition.
