Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractChemical Tongues and Noses Based upon Conjugated Polymers    Next AbstractEffect of chlorination on the formation of odorous disinfection by-products »

Environ Sci Technol


Title:"Odorous products of the chlorination of phenylalanine in water: formation, evolution, and quantification"
Author(s):Freuze I; Brosillon S; Herman D; Laplanche A; Democrate C; Cavard J;
Address:"Laboratoire de Chimie des Nuisances et Genie de l'Environnement, Ecole Nationale Superieure de Chimie de Rennes, Av. du General Leclerq, 35700 Rennes, France. ingrid.freuze@ensc-rennes.fr"
Journal Title:Environ Sci Technol
Year:2004
Volume:38
Issue:15
Page Number:4134 - 4139
DOI: 10.1021/es035021i
ISSN/ISBN:0013-936X (Print) 0013-936X (Linking)
Abstract:"To explain some of the possible origins of an odor episode which took place in a drinking water supply in the region of Paris (France), the chlorination reaction in water of phenylalanine was studied. This amino acid was chosen for first experiments because of its physical and chemical particular properties. Changes in the different byproducts formed were followed by high-performance liquid chromatography (HPLC) over a period of time. N-chlorophenylalanine (mono-N-chlorinated amino acid) and then phenylacetaldehyde were the major products formed for the lower chlorine to nitrogen molar ratios. For Cl/N molar ratios of 1 and beyond, phenylacetonitrile and N-chlorophenylacetaldimine appeared and increased with the chlorination level. N-chlorophenylacetaldimine was quantified by using its difference of stability in various organic solvents. Our attention was first directed to the monochlorinated derivative but further examination indicated that it could not be responsible for odor troubles: it dissociated before reaching the consumer's tap and it was produced at consistently low yields under conditions relevant to drinking water treatment. On the contrary, chloroaldimine appeared to be a very odorous and water-stable product: it strongly smells of swimming pool with a floral background. The odor detection threshold is about 3 microg x L(-1) and it can persist for more than one week at 18 degrees C. It is now suspected of being a source of off-flavor concerns among consumers"
Keywords:Acetonitriles/analysis Chlorine/*chemistry Disinfectants/*chemistry Imines/analysis Odorants/*analysis Paris Phenylalanine/*chemistry Taste Ultraviolet Rays Water/*chemistry Water Purification Water Supply;
Notes:"MedlineFreuze, Ingrid Brosillon, Stephan Herman, Dorine Laplanche, Alain Democrate, Christian Cavard, Jacques eng Research Support, Non-U.S. Gov't 2004/09/09 Environ Sci Technol. 2004 Aug 1; 38(15):4134-9. doi: 10.1021/es035021i"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024