Formation of ethyl nitrite in vivo after ethanol administration

Xin-Sheng Deng1, Pequita Bludeau, Richard A Deitrich

  • 1University of Colorado Health Sciences Center at Fitzsimons, School of Medicine, Alcohol Research Center and Department of Pharmacology, Mail Stop 8303, PO Box 6511, Aurora, CO 80045-0511, USA. xin-sheng.deng@uchsc.edu

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Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
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Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by water loss...
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Overview
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
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