Naphthalene-2,3-dicarbaldehyde derivatization of amino acids - an improved technique for minimization of benzoin condensation

Investor logo
Investor logo

Warning

This publication doesn't include Faculty of Medicine. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

DĚDOVÁ Tereza CELÁ Andrea MÁDR Aleš GLATZ Zdeněk

Year of publication 2013
Type Article in Periodical
Magazine / Source Chemické listy
MU Faculty or unit

Faculty of Science

Citation
Field Biochemistry
Keywords capillary electrophoresis; LIF; Amino acids;
Description Amino acids (AA) have no native fluorescence thus chemical modification (so called derivatization) of AA has to be performed prior the detection by a fluorescent detector. There is a lot of derivatization reagents commercially available differing in reactivity, excitation and emission wavelengths, quantum yield, product stability etc. Naphtalene-2,3-dicarbaldehyde (NDA) is a non-fluorescent reagent giving fluorescent product of primary amines. Derivatization procedure is quite simple, however has to be optimized to minimize undesired by-products of benzoin condensation. The by-products can exhibit fluorescence or form crystals which can clog capillary. The novel derivatization protocol using NDA for AA derivatization is subject of this contribution.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info