Analysis and Enantioseparation of Amino Acids by Liquid Chromatography.
Amino Acids
/ chemistry
Chemical Fractionation
/ instrumentation
Chromatography, High Pressure Liquid
/ instrumentation
Chromatography, Thin Layer
/ instrumentation
Cross-Linking Reagents
/ chemistry
Dinitrofluorobenzene
/ analogs & derivatives
Erythromycin
/ chemistry
Stereoisomerism
Tartrates
/ chemistry
Triazines
/ chemistry
Amino acid analysis
Amino acids
Cyanuric chloride
DFDNB
Enantiomeric separation
Erythromycin
L-Tartaric acid
RP-HPLC
TLC
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
27
7
2019
pubmed:
28
7
2019
medline:
9
4
2020
Statut:
ppublish
Résumé
Enantioseparation studies of proteinogenic, non-proteinogenic, and dansyl amino acids are described herein by using liquid chromatographic techniques, i.e., HPLC and TLC. A researcher who wants to perform amino acid (AA) analysis or separate enantiomers of AAs by HPLC or TLC can follow the method. Figures included represent the actual experiments.Synthesis and application of chiral derivatizing reagents (CDRs) based on cyanuric chloride (CC) and difluorodinitrobenzene (DFDNB) have been described for AA analysis and enantioseparation by indirect approach. The methods represent pre-column derivatization of AAs and represent a good and less expensive substitute of AA analyzer. The application of commercial "Chiralplate" and use of erythromycin and L-tartaric acid have been described as chiral selector either as impregnating reagent in the stationary phase or as an additive in the mobile phase for direct enantioseparation by TLC. Application of the homemade TLC plates has also been described; the methods are successful in obtaining the native enantiomer as well.
Identifiants
pubmed: 31347121
doi: 10.1007/978-1-4939-9639-1_17
doi:
Substances chimiques
Amino Acids
0
Cross-Linking Reagents
0
Tartrates
0
Triazines
0
cyanuric chloride
5U4L4QHD6I
Erythromycin
63937KV33D
Dinitrofluorobenzene
D241E059U6
1,5-difluoro-2,4-dinitrobenzene
G5VV4MQ22V
tartaric acid
W4888I119H
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM