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A Manual of the Chemistry of the Carbon Compounds

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TEE CARBON COMPOUNDS. 475<br />

soluble in water. It baa <strong>the</strong> properties <strong>of</strong> an aldehyde, and yields on<br />

oxidation hemijainic acid C^H^Og, which is also obtained toge<strong>the</strong>r<br />

with meconin when opianic acid is heated with potash-solution.<br />

Heawpimric Add C10H10O9 crystallizes in large four-sided prisms,<br />

which melt at 180°, and sublime without decomposition. By heating<br />

it with, concentrated hydriodic acid it yields oxalic acid, methyl<br />

iodide, and two isomeric acids CMHM06.<br />

Opvwk Add crystallizes from hot water in brilliant prisms, and<br />

gives with ferric chloride a lilac colour.<br />

Isopinie Add forms small warty needles, dissolving more freely<br />

than opinic acid, and yielding a deep-blue colour with ferric chloride.<br />

Thebaine C10HaNOs crystallizes from dilute alcohol in plates resembling<br />

beuzoic acid, and from strong alcohol in thick prisms, melting<br />

at 193°. It is a strong base and a violent poison, producing tetanus.<br />

In concentrated sulphuric acid it dissolves with a blood-red colour.<br />

By heating it with hydrochloric acid it is converted into <strong>the</strong>bmine<br />

hydrochloridc, crystallizing in large laminee having a bitter taste, and<br />

consisting <strong>of</strong> CwHaNO8.GlH + 3H..O. On adding normal sodium<br />

sulphide to its solution, <strong>the</strong>benine is obtained as a white flocculent<br />

precipitate, which rapidly oxidizes in <strong>the</strong> air. It is isomeric with<br />

<strong>the</strong>baiine, but differs from it, by dissolving in sulphuric acid with a<br />

splendid blue colour.<br />

Codamine G^B^NO^ crystallizes from benzene in email prisms<br />

melting at 126°, and giving with ferric chloride or concentrated<br />

nitric acid a deep-green solution.<br />

Lcmdanine C^H^N®* forms small prisms melting at 166°; it gives<br />

with concentrated nitric acid an orange-red solution, and with ferrio<br />

ohloride an emerald-green colour.<br />

Frotopine C^H^NO, forms small prisms melting at 202°; it gives<br />

no colour with feme chloride, and dissolves in sulphuric acid containing<br />

ferric sulphate with a dark-violet colour.<br />

Papaverine CgiH81NO4 crystallizes from alcohol in colourless prisms,<br />

dissolving in hot sulphuric acid with a dark-violet colour; on adding<br />

water to this solution brown amorphous flakes separate out, dissolving<br />

in alkalis with a splendid purple colour.<br />

Nitropa/paveriw COTH^NO^NO^ + H2O is obtained by <strong>the</strong> action<br />

<strong>of</strong> strong nitric acid oo papavenne, and crystallizes in yellowish<br />

needles. It is a base forming crystalline salts.<br />

Mcconidine C^H^NO^ is an amorphous mass which is soluble in<br />

caustic potash. It forms amorphous unstable salts, and dissolves in<br />

sulphuric acid with an olive-green colour.<br />

haudanosine C^H^NO^ is very soluble in e<strong>the</strong>r, and crystallizes<br />

from benzene in beautiful white needles melting at 89°. It dissolves<br />

in sulphuric acid containing ferric sulphate with a brownish-red<br />

colour, which on heating first becomes green and <strong>the</strong>n dark-violet.<br />

Rfueadine C^H^NO,, exists in Papaver Ilhasas, and also sometimes<br />

in opium. It is a tasteless crystalline powder, and has no poisonous<br />

properties.

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