Butyraldehyde Butyric anhydride

Butyric alcohol. See Butyl alcohol Butyric aldehyde. See n-Butyraldehyde Butyric anhydride... [Pg.654]

Butyl peroxylri methyl acetate, see Butyl peroxypivalate Butyl vinyl ether n-Butyraldehyde iso-Butyraldehyde n-Butyric acid iso-Butyric acid n-Butyric anhydride 2-Butyrolactone n-Butyronitrile Butyryl chloride Camphor Caproic acid... [Pg.112]

The selective hydrogenation of an olefinic bond in crotonaldehyde gives n-butyraldehyde in presence of a suitable catalyst n-butyraldehyde reacts with poly (vinyl alcohol) to form poly (vinyl butyral) which is used as an interlayer for safety glass as well as for coating fabrics and for injection-moulding compositions. Butyraldehyde also finds use in making oil-soluble and alcohol-soluble resins. Butyraldehyde is a raw material for the manufacture of butyric acid and butyric anhydride... [Pg.851]

Bromo-2-fluoro biphenyl intermediate, foam builders Alkenyl succinic anhydride intermediate, food additives Soy acid Stearyl alcohol intermediate, food emulsifiers Caprylic/capric acid Tallow acid intermediate, food supplements (tablet form) Cetyl alcohol intermediate, food wrap Vinylidene chloride monomer intermediate, fragrances p-t-Butyl toluene t-Butyl-m-xylene Citral Cyclopentanone Diethyl toluene diamine Dimethyl hexynediol 1,2-Methylenedioxybenzene 2-Methylpentanal Myrcene n-Propyl bromide intermediate, fragrances cosmetics Acetic anhydride n-Butyraldehyde n-Butyric acid Butyric anhydride 2-Ethylhexoic acid Isobutyric anhydride 2-Methylpropanal Propionic anhydride intermediate, fragrances personal care Butyric anhydride Isobutyric anhydride intermediate, free-radical polymerization initiators... [Pg.5398]

Ethyl alcohol has been made by the hydration of ethylene (9) since 1930. Like isopropyl alcohol, part of the output is used as a solvent, but most is converted to other oxygenated chemicals. Its most important raw material use is conversion to acetaldehyde by catalytic air oxidation. Acetaldehyde, in turn, is the raw material source of acetic acid, acetic anhydride, pentaerythritol, synthetic n-butyl alcohol (via aldol condensation), butyraldehyde, and other products. Butyraldehyde is the source of butyric acid, polyvinyl butyral resin, and 2-ethylhexanol (octyl alcohol). The last-named eight-carbon alcohol is based on the aldol condensation of butyraldehyde and is used to make the important plasticizer di-2-ethylhexyl phthalate. A few examples of the important reactions of acetaldehyde are as follows ... [Pg.294]

A powerful oxidizer. Explosive reaction with acetaldehyde, acetic acid + heat, acetic anhydride + heat, benzaldehyde, benzene, benzylthylaniUne, butyraldehyde, 1,3-dimethylhexahydropyrimidone, diethyl ether, ethylacetate, isopropylacetate, methyl dioxane, pelargonic acid, pentyl acetate, phosphoms + heat, propionaldehyde, and other organic materials or solvents. Forms a friction- and heat-sensitive explosive mixture with potassium hexacyanoferrate. Ignites on contact with alcohols, acetic anhydride + tetrahydronaphthalene, acetone, butanol, chromium(II) sulfide, cyclohexanol, dimethyl formamide, ethanol, ethylene glycol, methanol, 2-propanol, pyridine. Violent reaction with acetic anhydride + 3-methylphenol (above 75°C), acetylene, bromine pentafluoride, glycerol, hexamethylphosphoramide, peroxyformic acid, selenium, sodium amide. Incandescent reaction with alkali metals (e.g., sodium, potassium), ammonia, arsenic, butyric acid (above 100°C), chlorine trifluoride, hydrogen sulfide + heat, sodium + heat, and sulfur. Incompatible with N,N-dimethylformamide. [Pg.365]

Acetylated hydrogenated tallow glyceride Acetylated hydrogenated tallow glycerides Adipic acid Alkenyl succinic anhydride Ammonium citrate dibasic Behenic acid Behenyl alcohol Benzoic acid Benzothiazyl disulfide Benzyl butyrate Benzyltriethyl ammonium chloride 1-Butoxyethoxy-2-propanol Butoxytriglycol Butyl benzoate Butylcarbitol formal Butyl diglycol carbonate Butylene glycol n-Butyraldehyde C6-10 alcohols C8-10 alcohols... [Pg.5534]