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A Manual of the Chemistry of the Carbon Compounds

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258 TEE CHEMISTRY OF<br />

Mon<strong>of</strong>ai'min C8H61 >ynffR ls f° rm ed by heating glycerin with<br />

oxalic acid. It is an oily liquid, soluble in water. Oti heating this<br />

solution, mon<strong>of</strong>onnin is resolved into glycerin and formic acid.<br />

Monaeetin C8H6 \ }cr J? |V an oily liquid, which is soluble in water<br />

and possesses an e<strong>the</strong>real smell, is formed by heating glycerin with<br />

acetic acid to 100°; while by heating <strong>the</strong> mixture to 200°, diacetin<br />

( OH<br />

CSH5 -j ,QQ JJ QV ia obtained, an oily liquid boiling at 280°. When<br />

this body is heated with a very large excess <strong>of</strong> acetic acid to 250°, it<br />

is couverfced into tviacetin CJH^OCJHJO^, a liquid which is insoluble<br />

in water and boils at 286°. This compound exists in <strong>the</strong> oil contained<br />

iu <strong>the</strong> seeds <strong>of</strong> <strong>the</strong> common spindle-tree (Jfotonymw mropceus),<br />

and has also been produced by heating propenyl tribromide witli<br />

silver acetate.<br />

The three bvtyrins are oily neutral liquids; tributyrin is found in<br />

butter, toge<strong>the</strong>r with trieapronin, tricapnjlin, and tricaprin; trimyristin<br />

occurs in nutmeg-butter.<br />

Monopabnitin melts at 49°, dipalmittn at 59°; both compounds are<br />

produced by heating glycerin with palmitic acid in sealed tubes. By<br />

using a large excess <strong>of</strong> palmitic acid and heating <strong>the</strong> mixture to 250°<br />

for twenty-four hours, tripalmitin is formed, a compound occurring<br />

in many fats. It is prepared by exposing olive oil to a stroug cold,<br />

and subjecting <strong>the</strong> solid mass to a strong pressure to remove liquid<br />

trioleia Tripalmitin crystallizes from alcohol iu pearly scales, melting<br />

at 61°,<br />

Tristearin occurs in almost all solid fats, and may be extracted<br />

from beet* or mutton suet by means <strong>of</strong> e<strong>the</strong>r. After being purified by<br />

repeated crystallizations, it is obtained in pearly crystals welting at<br />

66°*5 and solidifying to an auiorpjious mass.<br />

Lecithine C/JB^NPO,,.—Tlus complicated derivative <strong>of</strong> glycerin -<br />

phosphoric acid is found widely distributed in <strong>the</strong> animal organism,<br />

occurring iu <strong>the</strong> brain, in <strong>the</strong> nerves, in <strong>the</strong> yolk <strong>of</strong> eggs, in <strong>the</strong> bloodcorpuscles,<br />

&c. It is most conveniently prepared by exhausting <strong>the</strong><br />

yolk <strong>of</strong> eggs with a mixture <strong>of</strong> alcohol and e<strong>the</strong>r. The solution ia<br />

gently heated until all <strong>the</strong> e<strong>the</strong>r has volatilized, and alcohol added to<br />

<strong>the</strong> residue, by which fats are precipitated. The solution is filtered<br />

and platinum tetrachloride is added; a yellow precipitate having <strong>the</strong><br />

composition 2(C4aHg3NPO8Cl) + PW3L is formed, which is decomposed<br />

by hydrogen sulphide. The lecithine hydroohloride thus<br />

obtained is dissolved in a mixtuie <strong>of</strong> alcohol and e<strong>the</strong>r, and <strong>the</strong> solution<br />

shaken with silver oxide, aud, after filtration, again treated with<br />

hydrogen sulphide in order to precipitate silver which has gone in<br />

solution.<br />

Pure lecithine is a wnx-like, indistinctly crystalline mass, soluble<br />

in alcohol and e<strong>the</strong>r; iu watev it s<strong>of</strong>tens and becomes gelatinous, but<br />

does not dissulve. It combines uor nnlv with nc.\

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