Denigés' reagent explained

The Denigés' reagent is a reagent used for qualitative analysis. It was developed in 1898 by Georges Denigés (December 25, 1859 - February 20, 1951), a French biochemist.[1]

Uses

Denigés' reagent is used to detect isolefin or tertiary alcohols which can be easily dehydrated to form isoolefin in the presence of acid. Treatment of solutions containing either isolefin or tertiary alcohols with this reagent will result in the formation of a solid yellow or red precipitate.[2]

Synthesis

Despite the different stoichiometry in these mixtures which varies the concentration of the reagent, they all follow the same idea of adding HgO to distilled water and concentrated sulfuric acid. The Denigés' reagent is ultimately mercury(II) sulfate in an aqueous solution.

Health issues

Inhalation of the Denigés' reagent can result in acute poisoning: causing tightness in the chest, difficulties breathing, coughing and pain. Exposure of mercury sulfate to the eyes can cause ulceration of conjunctiva and cornea. If mercury sulfate is exposed to the skin it may cause sensitization dermatitis. Lastly, ingestion of mercury sulfate will cause necrosis, pain, vomiting, and severe purging. Ingestion can result in death within a few hours due to peripheral vascular collapse.[5]

Notes and References

  1. Web site: Georges Deniges . dead . https://web.archive.org/web/20130523195645/http://www.armb.be/index.php?id=2355 . 2013-05-23 . 2023-10-20 . Académie royale de Médecine de Belgique.
  2. Relations between Denigés Reaction and Oxymercuration. 2433/76026. Institute for Chemical Research, Kyoto University. Ichikawa, K.. Fujita, K. . Itoh, O. . Bulletin of the Institute for Chemical Research, Kyoto University. 1964. 42. 4. 221–226.
  3. Web site: Laboratory Reagents for Qualitative analysis. 2 May 2011.
  4. MARKS. E. M.. LIPKIN, D.. Reaction of Aliphatic Ethers with Deniges' Reagent. J. Org. Chem.. 1939. 3. 6. 598–602. 10.1021/jo01223a008.
  5. Web site: Chemicalbook . 2 May 2011.