<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Ruth A. Davis</dc:contributor>
  <dc:creator>Verdel K. Dawson</dc:creator>
  <dc:date>1997</dc:date>
  <dc:description>&lt;p class="chapter-para"&gt;&lt;i&gt;N&lt;/i&gt;-sodium-&lt;i&gt;N&lt;/i&gt;-chloro-ρ-toiuenesulfonamide (chloramine-T) effectively controls bacterial gill disease (BGD) in cultured fishes. BGD, a common disease of hatchery-reared salmonids, causes more fish losses than any other disease among these species. This study describes a liquid chromatographic (LC) method that is capable of direct, simultaneous analysis of chloramine-T and its primary degradation product, ρ-toluenesulfonamide (ρ-TSA), in water. The procedure involves reversed-phase (C&lt;sub&gt;18&lt;/sub&gt;) LC analysis with ion suppression, using 0.01 M phosphate buffer at pH 3. The mobile phase is phosphate buffer-acetonitrile (60 + 40) at 1 mL/min. Both chemicals can be detected with a UV spectrophotometer at 229 nm; the method is linear up to 40 mg chloramine-T or ρ-TSA/L. Mean recoveries were 96.4 ± 6.1% for water samples fortified with 0.03 mg chloramine-T/L and 95.3 ± 4.6% for water samples fortified with 0.005 mg ρ-TSA/L. Limits of detection without sample enrichment for chloramine-T and ρ-TSA are 0.01 mg/L and 0.001 mg/L, respectively.&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1093/jaoac/80.2.316</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Oxford Academic</dc:publisher>
  <dc:title>Liquid chromatographic determination of chloramine-T and its primary degradation product, p-toluenesulfonamide, in water</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>