Yc. Fiamegos et al., Synthesis and analytical applications of 4-aminopyrazolone derivatives as chromogenic agents for the spectrophotometric determination of phenols, ANALYT CHIM, 403(1-2), 2000, pp. 315-323
The synthesis of simple, extensively conjugated chromophores as substitutes
for 4-aminoantipyrine (4-AAP) capable of causing hyperchromic shifts when
coupled with phenols is described. The 4-aminopyrazolone derivatives synthe
sised are subsequently applied for the spectrophotometric assay of phenolic
compounds and the advantages of each of the proposed systems are highlight
ed. No improvement is made on the detection of para-substituted phenols as
well as polychlorophenols (e.g. pentachlorophenol). An increase in the sens
itivity of coupling products is obtained for certain phenolic compounds as
indicated from the comparison of the individual responses. The proposed met
hods have analogous analytical features and in some cases show considerable
improvements compared to the 4-AAP method. Beer's law is obeyed over a wid
e dynamic range (up to ca. 500 mu g/l) and the relative standard deviations
are <3.4%. The methods are applied satisfactorily for phenol assay in real
samples, however, taking into account the intrinsic differences of the met
hods in the responses to the various phenolic compounds. (C) 2000 Elsevier
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