Published October 13, 2021 | Version v1
Journal article

Fluorescein isothiocyanate stability in different solvents

  • 1. Charles University. Department of Physiology and Biochemistry, Faculty of Physical Education and Sport (Czech Republic)
  • 2. Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences (Czech Republic)
  • 3. University of Helsinki. Department of Chemistry, Faculty of Science (Finland)
  • 4. Czech University of Life Sciences Prague. Department of Agro-Environmental Chemistry and Plant Nutrition, Faculty of Agrobiology, Food and Natural Resources (Czech Republic)

Description

Well-established label in biomolecules analysis, fluorescein isothiocyanate is commercially available in its two different isomers with equal fluorescence sensitivity, differing in meta- vs. para-isothiocyanate position. It was found in this study that the stability of the isomers depends on the polarity of different solvents and the pyridine (stabiliser) presence. The lowest stability has fluorescein isothiocyanate in water solvent. In acidic solution, their quinoid (acid) form switches to the lactone form. The p-quinoid form has higher tendency to create dimers and trimers and is less soluble in acetone than the lactone form. Graphic abstract:

Additional details

Identifiers

Publishing Information

Journal Title
Monatshefte fuer Chemie
Journal Volume
152
Journal Issue
11
Journal Page Range
p. 1299-1306
ISSN
0026-9247
CODEN
MOCHAP

Optional Information

Copyright
Copyright (c) 2021 © Springer-Verlag GmbH Austria, part of Springer Nature 2021