Improved TLC systems for rapid resolution of phenyl thiohydantoin amino acids
โ Scribed by R. Bhushan; V. K. Mahesh; P. V. Mallikharjun
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 243 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0269-3879
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โฆ Synopsis
Two new solvent systems, n-hexane + propionic acid (26: 5, v/v) and chloroform + acetone (29 : 3, v/v), for the rapid resolution and identification of an 18-component mixture of phenylthiohydantoin amino acids are reported. Using these systems certain difficult combinations of phenylthiohydantoin amino acids are resolved. Two more solvent systems, viz chloroform + acetic acid (27 : 3, v/v) and chloroform + methanol (30 : 4, v/v), are developed to resolve phenylthiodantoin derivatives of aspartic and glutamic acids. Detection of PTH-amino acids. After development, the chromatograms were removed from the chambers. These were dried and exposed to iodine vapours to locate the PTH-amino acid as light yellow-brown spots on the chromatograms.
๐ SIMILAR VOLUMES
An improved method is described for the resolution of enantiomeric isopropyl esters of N-trifluoroacetyl-u-amino acids of nonbasic amino acids using N-docosanoyl-L-valyl-rbutylamide and N-octadecanoyl-L-valyl-t.-valine cyclohexyl ester as mixed chiral phases on 150-ft stainless-steel capillary colum
## Rapid Communications intramolecular N{Hrrrp (aromatic) interactions are present (in a subsequent literature search we came through the x-ray diffraction work performed by Drew and Willey, 6 who also reported the occurrence of such a type of interaction in a phenylhydrazone derivative of benzophe