Enantiomeric purity test of bevantolol by reversed-phase high performance liquid chromatography after derivatization with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
✍ Scribed by Kyeong Ho Kim; Sung Young Heo; Seon-Pyo Hong; Beom-Chan Lee
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 450 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0253-6269
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📜 SIMILAR VOLUMES
A novel method for reversed-phase high-performance liquid chromatographic resolution of amino acid enantiomers by the formation of diastereomers using 8 new chiral reagent, 2,3,4,6-tetra-O-acetyl+D-glucopyranosyl isothiocyanate (GITC), is described. GITC reacts readily with enantiomeric amino acids
## Abstract Resolution of isomers of 2,3,4,6‐tetra‐__O__‐acetyl‐β‐D‐glucopyranosyl isothiocyanate (GITC)–derivatized DL‐amino acids was accomplished using micellar electrokinetic chromatography with sodium dodecyl sulfate (SDS) solutions. These solutes were not separated by the usual capillary zone