Jump to content

Purpuric acid

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Spinningspark (talk | contribs) at 15:54, 2 March 2020 (copyedit + clarify and expand from source a sentence that currently does not make much sense. Improve ref details). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Purpuric acid is a nitrogenous acid.

  • Molecular formula: C8H5N5O6[1]
  • CAS Number: 121-08-4[1]
  • Molecular weight: 276.16[2]

Purpuric acid is a nitrogenous acid related to barbituric acid that yields alloxan and uramil on hydrolysis and is known especially in purple-red salts (as murexide) from which it is obtained as an orange-red powder.[3] Purpuric acid was first described in 1818 by the English chemist William Prout (1785-1850).[4] Though colourless itself, purpuric acid has a tendency to form red or purple-coloured salts with alkaline bases. This characteristic led the English doctor William Hyde Wollaston (1766-1828) to suggest the name purpuric acid.[5]

Purpuric acid can be synthesized by nitration of uric acid (previously known as lithic acid). In 1818 Prout obtained lithic acid from the excrement of a boa constrictor (which largely consists of this substance) or else used urinary calculi. He dissolved the lithic acid in dilute nitric acid and after an effervescence took place a purple liquid was formed. After neutralization of the solution with ammonia, granular crystals begin to separate out.[6]

Purpuric acid is insoluble in alcohol and ether. The mineral acids dissolve it only when they are concentrated. It does not affect litmus paper. Purpuric acid combines with the alkalis, alkaline earths and metallic oxides. It is capable of expelling carbonic acid from the alkaline carbonates, by the assistance of heat, and does not combine with any other acid. Wolllaston believed that these characterisitcs were sufficient to distinguish it from an oxide, and to establish its character as an acid.[6]

References

  1. ^ a b 121-08-4, CAS, ChemNet.com, retrieved 2 March 2020.
  2. ^ 5-[(2,4,6-Trioxo-1,3-diazinan-5-yl)imino&#93-1,3-diazinane-2,4,6-trione, PubChem, US National Library of Medicine, retrieved 2 March 2020.
  3. ^ "Purpuric acid", Philosophical Magazine, vol. 15, p. 491]
  4. ^ Edward Turner, Franklin Bache,"Animal acids", Elements of Chemistry, p. 594, Philadelphia: Desilver, Thomas & Co., 1835.
  5. ^ The Cyclopædia, Or, Universal Dictionary of Arts, Sciences, and Literature
  6. ^ a b Andrew Ure, "Acid (purpuric)", A Dictionary of Chemistry and Mineralolgy, London: Thomas Tegg & Son, 1835. Public Domain This article incorporates text from this source, which is in the public domain.