1997Journal of Liquid Chromatography & Related TechnologiesRequires access

Separation of D and L Enantiomers of [(Phenylsulfonyl)amino]-3-oxo-1-octadecanol by Chiral High Performance Liquid Chromatography

Fred G. Rojas, Russell C. Klix, A. V. BHATIA

Open publisher page 1 citations

Abstract

A convenient and rapid method has been developed for the separation of the D and L enantiomers of [(phenyl-sulfonyl)amino]-3-oxo-octadecanol using chiral High Performance Liquid Chromatography (HPLC). An amylose tris(3,5-dimethylphenylcarbamate) chiral HPLC column was used for the separation. The two enantiomers were fully resolved from each other with approximate retention times of 11 and 13 minutes for the L and the D forms respectively. The total run time per sample was 30 minutes.

About this research paper

What this paper is about

A convenient and rapid method has been developed for the separation of the D and L enantiomers of [(phenyl-sulfonyl)amino]-3-oxo-octadecanol using chiral High Performance Liquid Chromatography (HPLC). An amylose tris(3,5-dimethylphenylcarbamate) chiral HPLC column was used for the separation. The two enantiomers were fully resolved from each other with approximate retention times of 11 and 13 minutes for the L and the D forms respectively. The total run time per sample was 30 minutes.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A convenient and rapid method has been developed for the separation of the D and L enantiomers of [(phenyl-sulfonyl)amino]-3-oxo-octadecanol using chiral High Performance Liquid Chromatography (HPLC). An amylose tris(3,5-dimethylphenylcarbamate) chiral HPLC column was used for the separation. The two enantiomers were fully resolved from each other with approximate retention times of 11 and 13 minutes for the L and the D forms respectively. The total run time per sample was 30 minutes.

Key concepts: Chemistry, Enantiomer, Chromatography, High-performance liquid chromatography, Chiral column chromatography, Chiral derivatizing agent, Sulfonyl, Chiral stationary phase

Related papers

Back to paper searchBrowse research topicsOriginal source
Separation of D and L Enantiomers of [(Phenylsulfonyl)amino]-3-oxo-1-octadecanol by Chiral High Performance Liquid Chromatography — Research Paper | ScholarLens