Abstract

The differential pulse polarographic behaviour of 2,4,6-trinitrophenyl (TNP) derivatives of several primary amines and amino acids was investigated in the presence of sulphite ion. All the derivatives produced a polarographic peak for their complexes with sulphite (1 × 10 −2 M) in pH 8.0 phosphate buffer (0.05 M)/0.1 M potassium chloride. The derivatives of proteins and peptides did not give such a peak. A 5-min reaction time at room temperature (or 50°C for lysine) and pH 10.5 using 1 × 10 −4 M 2,4,6-trinitrobenzene-1-sulphonic acid provides the optimal conditions for the determination of 5 × 10 −6−2.5 × 10 −5 M amines. The relative standard deviation for determining 1 × 10 −5 M glycine ( n = 5) was 1%.

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