2010
DOI: 10.2478/s11696-010-0026-6
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Visual spectroscopy detection of triclosan

Abstract: The azo coupling reaction with 2-aminonaphthalene-4,8-disulfonic acid (I) was used to develop a new cheap and rapid method of triclosan (II) determination in hygiene products. The calibration graph was linear in the range of 2.0−100 × 10−6 mol L−1. The detection limit was 2.0 μmol L−1.

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Cited by 3 publications
(1 citation statement)
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“…Literature survey reveals some analytical methods are developed for the determination of PPD by HPLC [10][11][12], GC/MS [13,14], voltametric method [15], emission spectroscopy [16] and some spectrophotometric method are reported. The spectrophotometric methods have their relative merits but the methods are carried out with time consuming in diazotization followed by coupling with N-(1-naphthyl) ethylenediamine [17], involves oxidation of the compound converted in to salt measured colorimetrically [18], coupling of triclosan with reagent 2-aminonaphthalene-4,8disulfonic acid with low level detection [19]. The another method was based on the reaction of sodium nitrite with p-sulfanilic acid in an acidic medium to form diazonium ion, with which triclosan further formed an azo compound in an alkaline medium [20].…”
Section: Introductionmentioning
confidence: 99%
“…Literature survey reveals some analytical methods are developed for the determination of PPD by HPLC [10][11][12], GC/MS [13,14], voltametric method [15], emission spectroscopy [16] and some spectrophotometric method are reported. The spectrophotometric methods have their relative merits but the methods are carried out with time consuming in diazotization followed by coupling with N-(1-naphthyl) ethylenediamine [17], involves oxidation of the compound converted in to salt measured colorimetrically [18], coupling of triclosan with reagent 2-aminonaphthalene-4,8disulfonic acid with low level detection [19]. The another method was based on the reaction of sodium nitrite with p-sulfanilic acid in an acidic medium to form diazonium ion, with which triclosan further formed an azo compound in an alkaline medium [20].…”
Section: Introductionmentioning
confidence: 99%