Page:Treatise on poisons in relation to medical jurisprudence, physiology, and the practice of physic (IA treatiseonpoison00chriuoft).pdf/538

From Wikisource
Jump to navigation Jump to search
This page needs to be proofread.

Meconic acid, as procured by evaporation, is usually in little scales of a pale brown or yellowish tint, being rendered so by adhering resin or extractive matter; but when nearly colourless, it forms long, extremely delicate tabular crystals, which in mass have a fine silky appearance like spermaceti. 1. When heated in a tube, it is partly decomposed, and partly sublimed; and the sublimate condenses in filamentous, radiated crystals. 2. When dissolved even in a very large quantity of water, the solution acquires an intense cherry-red colour with the perchloride of iron. The sublimed crystals have the same property. Only one other acid is so affected, namely, the sulpho-cyanic, a very rare substance. It has been repeatedly stated,[1] that the redness produced by meconic acid may be distinguished by the effect of an alkali, which is said to bleach the colour produced by sulpho-cyanic acid, but to deepen the cherry-red tint occasioned by the meconic. This is not correct; an alkali added to the red solution of meconate of iron precipitates oxide of iron and renders the liquid colourless. The best distinction yet proposed is the following which has been suggested by Dr. Percy. Acidulate the red fluid with sulphuric acid, drop in a bit of pure zinc, and suspend at the mouth of the tube a bit of paper moistened with solution of acetate of lead: If the redness be caused by sulphocyanic acid, hydrosulphuric acid gas is evolved, and blackens the paper; but no such effect ensues, it the redness be owing to meconic acid.[2]—According to Dr. Pereira, solutions of the acetates, an infusion of white mustard, decoctions of Iceland moss, and of the Gigantina helminthocorton, besides other more rare substances, are reddened, like solution of meconic acid, by the salts of peroxide of iron.[3] 3. The solution of meconic acid gives a pale-green precipitate with the sulphate of copper, and, if the precipitate is not too abundant, it is dissolved by boiling, but reappears on cooling.

Of the Tests for Morphia and its Salts.—Morphia, when pure, is in small, beautiful, white crystals. Various forms have been ascribed to it; but in the numerous crystallizations I have made, it has always assumed when pure the form of a slightly flattened hexangular prism. It has a bitter taste, but no smell.

A gentle heat melts it, and if the fluid mass is then allowed to cool, a crystalline radiated substance is formed. A stronger heat reddens and then chars the fused mass, white fumes of a peculiar odour are disengaged, and at last the mass kindles and burns brightly.—Morphia is very little soluble in water. It is more soluble, yet still sparingly so, in ether. But its proper solvents are alcohol, or the diluted acids, mineral as well as vegetable. All its solutions are intensely bitter, and that in alcohol has an alkaline reaction.—From its solutions in the acids crystallizable salts may be procured; and morphia may be separated by the superior affinity of any of the inorganic alkalis; but it is easily redissolved by an excess of potash.—Morphia when treated with nitric acid is dissolved with effervescence, and becomes instantly orange-red, which, if too much acid be used,

  1. London Medical Gazette, viii. 47.
  2. Lancet, July 31, 1841.
  3. Elements of Materia Medica, 1842, p. 1738.