Reacts possibly explosively with halogens bromine chlorine or hydrogen halides hydrogen bromide hydrogen chloride baker 1980 p.
Methyl vinyl heat.
Flash point 20 f.
Vinyl methyl ether is used in copolymers for coatings and lacquers in polystyrene and ionomer resins in plasticizers and in adhesives.
This polymerization may cause violent ruptures in containers.
This structure is also available as a 2d mol file.
Methyl vinyl ketone appears as a clear colorless liquid with a pungent odor.
Vinyl methyl ketone 95 safety data sheet 06 09 2016 en english us sds id.
Workers that produce or use vinyl methyl ether may breathe in mists or have direct skin contact.
Fusuhkvfwtuube uhfffaoysa n cas registry number.
Conditions to avoid heat.
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.
Less dense than water.
It polymerizes spontaneously upon exposure to heat or sunlight.
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.
Vinyl methyl ether is a colorless gas.
Causes burns to skin eyes and mucous membranes.
30 f open cup in a wide range of concentrations flammable limits lower.
Vinyl methyl ether reacts vigorously with oxidizing materials.
May polymerize with the release of heat under exposure to heat or contamination.
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.
Methyl vinyl ketone is incompatible with strong oxidizers and strong bases.
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.
