Abstract
The pulse polarographic behavior of N-nitrosopyrrolidine and two of its derivatives, N-nitrosoproline and N-nitroso-4-hydroxyproline, has been investigated in buffered solutions over a range of pH. The effects of temperature, mercury pressure, modulation amplitude, surfactant concentration, and solvent and supporting electrolyte have been studied. The reduction process is complicated and pH-dependent. In acid solutions, N-nitrosopyrrolidine and its derivatives give one irreversible reduction wave, while for pH greater than 6, only N-nitrosopyrrolidine itself is reduced. The reduction waves of N-nitrosoproline and N-nitroso-4-hydroxyproline at pH below 5 are diffusion-controlled in dc and normal pulse polarographic modes. In aqueous medium, N-nitrosopyrrolidine, N-nitrosoproline, and N-nitroso-4-hydroxyproline have been detected quantitatively at the 10-7 M level by differential pulse polarography with adequate precision and accuracy. The importance of examining electrochemical behavior to aid in selecting conditions for analysis is discussed. © 1975, American Chemical Society. All rights reserved.
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CITATION STYLE
Hasebe, K., & Osteryoung, J. (1975). Differential Pulse Polarographic Determination of Some Carcinogenic Nitrosamines. Analytical Chemistry, 47(14), 2412–2418. https://doi.org/10.1021/ac60364a002
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