Utilization of Folin-Ciocalteu phenol reagent for the detection of certain nitrogen compounds
Abstract
To determine in more detail the reaction of Folin-Ciocalteu phenol reagent with nitrogen compounds, a number of hydroxylamine-related compounds and a large number of guanidine-containing compounds were tested. In general, guanidine compounds did not react strongly unless they were hydroxyamino or hydrazino derivatives. The non-hydroxyamino paralytic shellfish poison saxitoxin, however, reacted to a significant extent. This may be due to the presence of a five-membered ring structure and its analogy to 2-aminopurines, which react strongly. A number of simpler amines were also tested. Tertiary aliphatic amines, but not primary, secondary, or quaternary amines, reacted strongly with the reagent. Primary, secondary, and tertiary aromatic amines all reacted strongly with the reagent. Reactivity was extended to pyrroles and indole derivatives but not to imidazole and benzimidazole derivatives. Defining the reactivity of Folin-Ciocalteau phenol reagent with nitrogen compounds extends the usefulness of the reagent for the detection and determination of certain nitrogen compounds in basic extracts by colorimetric means and by thin-layer chromatography.
Publication Date
2-28-2003
Journal Title
Journal of Agricultural and Food Chemistry
Publisher
American Chemical Society
Digital Object Identifier (DOI)
10.1021/jf021099r
Scientific Contribution Number
2051
Document Type
Article
Rights
Copyright © 2003 American Chemical Society
Recommended Citation
Ikawa, Miyoshi; Schaper, Timothy D.; Dollard, Catherine A.; and Sasner, John J., "Utilization of Folin-Ciocalteu phenol reagent for the detection of certain nitrogen compounds" (2003). Journal of Agricultural and Food Chemistry. 78.
https://scholars.unh.edu/nhaes/78