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See also:CHLOROFORM (trichlor-methane), CHC13 , a valuable an-aesthetic, a colourless liquid, possessing an agreeable See also:smell and a pleasant See also:taste. It may be prepared by the See also:action of See also:bleaching See also:powder on many See also:carbon compounds, such, for example, as See also:ethyl See also:alcohol and See also:acetone (E. Soubeiran, See also:Ann. chim. phys., 1831 [2], 48, p. 131; J. V. See also:Liebig, Ann., 1832, 1, p. 199), by See also:heating See also:chloral with alkalis (Liebig), CCI3CHO + NaHO= CHCI3 + NaHCO2, or by heating trichloracetic See also:acid with See also:ammonia (J. See also:Dumas, Ann., 1839, 32, p. 113). In the preparation of chloroform by the action of bleaching powder on ethyl alcohol it is probable that the alcohol is first -oxidized to acetaldehyde, which is subsequently chlorinated and then decomposed. Chloroform solidifies in the See also:cold and then melts at -62 C.; it boils at 61.2° C., and has a specific gravity 1.52637 (0 /4°) (T. E. See also:Thorpe). It is an exceedingly See also:good solvent, especially for fats, alkaloids and See also:iodine. It is not inflammable. The vapour of chloroform when passed through a red-hot See also:tube yields hexachlorbenzene C6C16, .perchlorethane C2CI6i and some perchlorethylene C2C14 (W. See also:Ramsay and S. See also:Young, Jahresberichte, 1886, p. 628). Chromic acid converts it into phosgene (carbonyl chloride, COC12). It reacts with See also:sodium ethylate to See also:form ortho-formic ester, CH(OC2H5)3, and when heated with aqueous ammonia for some See also:hours at 200-220° C. gives carbon monoxide and ammonium formate, 2CHCI3 + 7NH3 + 3H2O = NH4•HCO2 + CO+6NH4C1 (G. See also:Andre, Jahresb., 1886, p. 627). When digested with phenols and See also:caustic soda it forms oxyaldehydes (K. Reimer, Ber., 1876, 9, p. 423); and when heated with alcoholic potash it is converted into See also:potassium formate, CHC13 + 4KHO=KHCO2 + 3KC1+ 2H20. It combines with acetoacetic ester to form the aromatic See also:compound See also:meta-oxyuvitic acid, C6H2•CH3.OH•(COOH)2. A See also:hydrate, of See also:composition CHC13.18H2O, has been described (G. See also:Chancel, See also:Fresenius Zeitschrift f. anal. Chemie, 1886, 25, p. 118) ; it forms hexagonal crystals which melt at 1.6° C. Chloroform may be readily detected by the See also:production of an isonitrile when it is heated with alcoholic potash and a See also:primary amine; thus with See also:aniline, phenyl isocyanide (recognized by its nauseating smell) is produced, CHCI3+See also:C6H 5N H2+3KHO = C6H 5NC+3KCI+3H20. For the action and use of chloroform as an anaesthetic, see See also:ANAESTHESIA. Chloroform may be given internally in doses of from one to five drops. The See also:British See also:Pharmacopoeia contains a watery solution—the Aqua Chloroformi—which is useful in disguising the taste of nauseous drugs; a liniment which consists of equal parts of camphor liniment and chloroform, and is a useful See also:counter-irritant; the Spiritus Chloroformi (erroneously known as " chloric See also:ether "), which is a useful See also:anodyne in doses of from five to See also:forty drops; and the Tinctura Chloroformi et Morphinae Composita, which is the See also:equivalent of a proprietary See also:drug called chlorodyne. This See also:tincture contains chloroform, See also:morphine and prussic acid, and must be used with the greatest care. Externally chloroform is an antiseptic, a See also:local anaesthetic if allowed to evaporate, and a rubefacient, causing the vessels of the skin to dilate, if rubbed in. Its action on the See also:stomach is practically identical with that of alcohol (q.v.), though in very much smaller doses. The uses of chloroform which fall to be mentioned here are:—as a counter-irritant; as a local anaesthetic for toothache due to See also:caries, it being applied on a See also:cotton- VI. 9CHM IELNICKI 257 See also:wool plug which is inserted into the carious cavity; as an antispasmodic in See also:tetanus and See also:hydrophobia; and as the best and most immediate and effective antidote in cases of See also:strychnine poisoning. Additional information and CommentsThere are no comments yet for this article.
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