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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 481<br />

hydrdberhmiic C^H^NO^ which separates from an alcoholic solution<br />

in very brilliant, colourless crystals.<br />

Oxyacanthine occurs in <strong>the</strong> root <strong>of</strong> berlieris, and crystallizes from<br />

alcohol in colourless prisms, which, wlien exposed to <strong>the</strong> sunshine,<br />

assume a yellow tint; its composition is not known.<br />

BEBEEMNE C'10HMN03.<br />

This base is found in <strong>the</strong> bark <strong>of</strong> <strong>the</strong> bebeero, or greenhart-tree<br />

<strong>of</strong> British Guiana (Ncctandra Roddei) and <strong>of</strong> Gc<strong>of</strong>frmja jamaieensis,<br />

and in <strong>the</strong> trunk and roots <strong>of</strong> dssampclos Pareira, and in Bnxits<br />

sempmmvcns. It is a colourless amorphous powder, and insoluble in<br />

water, but dissolves in alcohol; its solution lias a very bitter taste,<br />

and an alkaline reaction. Bcbeerine sulphate 2(C10H2,NO3)SO4H2 is<br />

sometimes used as a substitute for quinine.<br />

PIPERISK N | p 6l ?, w n .<br />

(. "-IJ 11 !) 1 -';!<br />

This weak base exists in different kinds <strong>of</strong> pepper, and is prepared<br />

by exhausting white pepper with alcohol and evaporating <strong>the</strong> solution;<br />

<strong>the</strong> residue is dissolved in alcoholic potash, and <strong>the</strong> impure<br />

piperiue, which, on concentrating this solution, crystallizes out, is<br />

purified by recrystallization from alcohol.<br />

Piperine forms colourless, tasteless, nnd inodorous prisms; its<br />

alcoholic solution possesses a sharp peppery taste, and a nqutral<br />

reactioa<br />

On boiling with alcoholic potash it is resolved into pvpcru&nc<br />

eriHuN, and kittle acid. C,2H,0O4.<br />

{ C* TT<br />

,, 5 l0 is a colourless liquid, which is soluble in<br />

water, and boils at 10f>°; it has a pungent and caustic tnste, and an<br />

anunoniacal and peppery smell. It is a powerful base, forming<br />

erystallizaMe salts. When treated with benzoyl chloride it is con-<br />

verted into Inizoyl-pipcridinc N \ r>\^% "wliitili is ft compound corre-<br />

sponding to pipeline.<br />

Pipette Add C'^HJOO., is a monobasic acid, crystallizing from hot<br />

alcohol in long needles, melting nt 210°. Nascent hydrogen converts<br />

it into hydropipene acid C,;H,o04, which consists <strong>of</strong> needles, melting<br />

at 64°.<br />

By adding potassium permanganate to a solution <strong>of</strong> potassium<br />

pipcrate, piperonaldchyde is formed :—<br />

Ci2H10O4 + 40, = CH.0, + C.H2O4 + 2C0, + H,0<br />

0 I I

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