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See also:ACETONE, or DIMETHYL KETONE , CH3•CO•CH3, in See also:chemistry, the simplest representative of the aliphatic See also:ketones. It is See also:present in very small quantity in normal urine, in the See also:blood, and in larger quantities in diabetic patients. It is found among the products formed in the destructive See also:distillation of See also:wood, See also:sugar, See also:cellulose, &c., and for this See also:reason it is always present in crude wood spirit, from which the greater portion of it may be re-covered by fractional distillation. On the large See also:scale it is pre-pared by the dry distillation of See also:calcium acetate (CH3CO2)2Ca= CaCO3+CH3000H3. E. R. Squibb (Journ. Amer. Chem. See also:Soc., 1895, 17, p. 187) manufactures it by passing the vapour of acetic See also:acid through a rotating See also:iron See also:cylinder containing a mixture of See also:pumice and precipitated See also:barium carbonate, and kept at a temperature of from 500° C. to 600° C. The mixed vapours of acetone, acetic acid and See also:water are then led through a. condensing apparatus so that the acetic acid and water are first condensed, and then the acetone is condensed in a second See also:vessel. The barium carbonate used in the See also:process acts as a contact substance, since the temperature at which the operation is carried out is always above the decomposition point of barium acetate. Crude acetone may be purified by converting it into the crystal-See also:line See also:sodium bisulphite See also:compound, which is separated by filtration and then distilled with sodium carbonate. 2 CHa\C< +Na2CO3=2CH3>C0+2Na2S03+See also:CO2+H20. See also:CH3/ S03Na CH3 It is then dehydrated and redistilled. Acetone is largely used in the manufacture of See also:cordite (q.v.). For this purpose the crude distillate is redistilled over sulphuric acid and then fractionated. Acetone is a colourless See also:mobile liquid of pleasant See also:smell, boiling at 56.53°C., and has a specific gravity o• 819 (o%4° C.) . It is readily soluble in water, See also:alcohol, See also:ether, &c. In addition to its application in the cordite See also:industry, it is used in the manufacture of See also:chloroform (q.v.) and See also:sulphonal, and as a solvent. It forms a See also:hydrazone with phenyl See also:hydrazine, and an oxime with hydroxyl-amine. Reduction by sodium See also:amalgam converts it into isopropyl alcohol; oxidation by chromic acid gives See also:carbon dioxide and acetic acid. With See also:ammonia it reacts to See also:form di- and triacetoneamines. It also unites directly with hydrocyanic acid to form the nitrile of a-oxyisobutyric acid. By the See also:action of various reagents such as See also:lime, See also:caustic potash, hydrochloric acid, &c., acetone is converted into condensation products, mesityl See also:oxide C6H160, phorone C9H140, &c., being formed. On distillation with sulphuric acid, it is converted into mesitylene C9H12(symmetrical trimethyl See also:benzene). Acetone has also been used in the artificial See also:production of See also:indigo. In the presence of See also:iodine and an See also:alkali it gives See also:iodoform. Acetone has been employed medicinally in cases of dyspnoea. With See also:potassium iodide, See also:glycerin and water, it forms the preparation spirone, which has been used as a spray inhalation in paroxysmal See also:sneezing and See also:asthma. Additional information and CommentsThere are no comments yet for this article.
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