Its heavier than air vapor may travel to a source of ignition and flash back or result in the build up of explosive concentrations in enclosed spaces such as sewers.
Methyl vinyl heat.
The bdes reveal that the o h o ch3 c oh and c och3 bonds in vinyl alcohol and methyl vinyl ether are similar in energy to those in the aromatic molecules phenol and methyl phenyl ether being on average around 3 kcal mol 1 weaker in the vinyl systems.
Less dense than water.
Causes burns to skin eyes and mucous membranes.
Workers that produce or use vinyl methyl ether may breathe in mists or have direct skin contact.
This polymerization may cause violent ruptures in containers.
Vinyl methyl ether is used in copolymers for coatings and lacquers in polystyrene and ionomer resins in plasticizers and in adhesives.
Methyl vinyl ketone is incompatible with strong oxidizers and strong bases.
It polymerizes spontaneously upon exposure to heat or sunlight.
Methyl vinyl ketone appears as a clear colorless liquid with a pungent odor.
Highly toxic by inhalation.
There are three different types of eva copolymer which differ in the vinyl acetate va content and the way the materials are used.
It is soluble in water use.
Conditions to avoid heat.
Vinyl methyl ether reacts vigorously with oxidizing materials.
30 f open cup in a wide range of concentrations flammable limits lower.
Flash point 20 f.
Ethylene vinyl acetate eva also known as poly ethylene vinyl acetate peva is the copolymer of ethylene and vinyl acetate the weight percent of vinyl acetate usually varies from 10 to 40 with the remainder being ethylene.
Methyl vinyl ketone may be easily ignited by heat sparks or flame flash point.
Explosive in the form of vapor when exposed to heat flame or strong oxidizing agents.
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Reacts possibly explosively with halogens bromine chlorine or hydrogen halides hydrogen bromide hydrogen chloride baker 1980 p.
May polymerize with the release of heat under exposure to heat or contamination.
This structure is also available as a 2d mol file.