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A Manual of the Chemistry of the Carbon Compounds

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THE OABBON COMPOVNDS. 48!)<br />

(J/tolcslcnn C2OH4tO + H20 is found in <strong>the</strong> bile, <strong>the</strong> brain aud<br />

nefves, in blood and <strong>the</strong> yolk <strong>of</strong> eggs, aud forms <strong>the</strong> chief constituent<br />

<strong>of</strong> biliary calculi; it has also been found in plants. From alcohol it<br />

crystallizes in small, brilliant plates, and from e<strong>the</strong>r-alcohol in<br />

beautiful largo plates, which are tasteless, and colourless, and melt<br />

at 145°, and sublime when more strongly heated.<br />

Cholesterin is a monad alcohol, and apparently homologous with<br />

cinnyl alcohol.<br />

Clwlcstcryl Chlwide C^3.JJ\ is produced by heating eholesterin.<br />

with strong hydrochloric aciuand crystallises in colourless needles.<br />

Gholesterylaminc C^H^NH, ia obtained by heating <strong>the</strong> chloride with<br />

alcoholic ammonia. Ifc crystallizes in small iridescent plates, melting<br />

at 104°, and exhibiting ia <strong>the</strong> liquid state a fine bluish violet<br />

fluorescence.<br />

Clwlesteryl Acetate C2a HWO.C2H3O is formed by heatingcholcsterin<br />

with aoetyl chloride, anil crystallizes from hot alcohol in small<br />

needles, melting at 92°.<br />

Glwlesleryl BcnzoaCo C20H.3O.C7HBO is produced by heatiug<br />

choleaterine with benzoic acid in sealed tubes to 200°. It crystallizes<br />

from e<strong>the</strong>r in small, thick, rectangular plates, melting at 125°.<br />

OxycJwlic Add C24H10O,j is obtained by oxidizing cholesterin with<br />

a dilute solution <strong>of</strong> chromic acid. It ia an amorphous mass, lmving<br />

•a bitterish-sweet taste.<br />

Isochdestenn C^H^O is found toge<strong>the</strong>r with cholesterin and fatty<br />

acids in suint. It crystallizes from e<strong>the</strong>r in slender, transparent<br />

needles, melting at 137°.<br />

Iaoclwlesteryl Bensottte C^H^O.CJHJO crystallizes from acetone in<br />

tufts <strong>of</strong> brilliant needles, and troin e<strong>the</strong>r in microscopic needles.<br />

Bilhiibin G',pH,gN3O3 exists in small quantity in <strong>the</strong> bile <strong>of</strong> different<br />

animals, and in larger quantity combined with calcium in certain<br />

biliary calculi, and is best obtained from those <strong>of</strong> <strong>the</strong> ox. It is<br />

insoluble in water, sparingly solnble in alcohol and e<strong>the</strong>r, freely in<br />

chlor<strong>of</strong>orm, and foima dark-ied crystals. In alkalis it dissolves with<br />

a dark-orange colour; <strong>the</strong> salts <strong>of</strong> o<strong>the</strong>r metala produce dark-brown<br />

precipitates in this solution.<br />

BUvcerdin C10H2AN.1O5.~Wben an alkaline solution <strong>of</strong> bilirubin 19<br />

exposed to <strong>the</strong> air it turns green, and on addition <strong>of</strong> an acid a green<br />

precipitate ia formed, crystallizing from glacial acetic acid in green<br />

rhombic plates.<br />

Hydrobilirubin or Urobilin C32HMN4Oy is produced by <strong>the</strong> action<br />

<strong>of</strong> aodium-amalgain, and water on btttinbin, and biliverdin, and<br />

exists also in lirino, chiefly in <strong>the</strong> dark-colonred one <strong>of</strong> fever-patients.<br />

It dissolves in alcohol and chlor<strong>of</strong>orm with a yellowish-red colour,<br />

and in alkalis with a brown colour. By adding a little zinc sulphate<br />

to its aminoniacal solution <strong>the</strong> liquid assumes a red colour, and<br />

exhibits a green fluorescence.<br />

BUifuacin C,,,H2()N3O4 is an almost black, glistening, brittle mass,

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