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Butanone, also known as methyl ethyl ketone (MEK) or ethyl methyl ketone, [a] is an organic compound with the formula CH 3 C(O)CH 2 CH 3. This colorless liquid ketone has a sharp, sweet odor reminiscent of acetone. It is produced industrially on a large scale, but occurs in nature only in trace amounts. [7]
Butanone (methyl ethyl ketone) organic compound; similar solvent properties to acetone but has a significantly slower evaporation rate Butylated hydroxytoluene: a fat-soluble organic compound that is primarily used as an antioxidant food additive: n-Butyllithium
Methylethyl ketone oxime is the organic compound with the formula C 2 H 5 C(NOH)CH 3.This colourless liquid is the oxime derivative of methyl ethyl ketone. MEKO, as it is called in the paint industry, is used to suppress "skinning" of paints: the formation of a skin on paint before it is used.
2-Hexanone (methyl butyl ketone, MBK) is a ketone used as a general solvent and in paints. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins. It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins.
2,3-Butanediol is the organic compound with the formula (CH 3 CHOH) 2. ... 2,3-Butanediol undergo dehydration to form butanone (methyl ethyl ketone): [10]
Methyl ethyl ketone, also known as MEK or 2-butanone (CH3COCH2CH3), boasts a flash point of 16 degrees F (-9 degrees C) and an ignition temperature of 759 degrees F (404 degrees C). Its explosive limits range from 1.9% to 10.0%, with a vapor density of 2.5 and a specific gravity of 0.8.
Methyl ethyl ketone peroxide (MEKP) is an organic peroxide with the formula [(CH 3)(C 2 H 5)C(O 2 H)] 2 O 2. MEKP is a colorless oily liquid. It is widely used in vulcanization (crosslinking) of polymers. [3] It is derived from the reaction of methyl ethyl ketone and hydrogen peroxide under acidic conditions.
The size and nature of these fragments depends upon the stability of the generated radicals; for instance, the cleavage of 2-butanone largely yields ethyl radicals in favor of less stable methyl radicals. [4] Norrish type I reaction. Several secondary reaction modes are open to these fragments depending on the exact molecular structure.