Improved reagent for trimethylsilylation of sphingolipid bases

This paper describes the trimethylsilylation of sphingolipid bases under conditions that give derivatives of improved stability. The retention times of the common C18 and C20 long-chain bases, including the anhydro bases, obtained on a commercially available gas-liquid chromatographic column with a...

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Main Authors: H.E. Carter, R.C. Gaver
Format: Article
Language:English
Published: Elsevier 1967-07-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520395717
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spelling doaj-a91bca1b074a4016ab8530edfa2bb6662021-04-23T06:11:37ZengElsevierJournal of Lipid Research0022-22751967-07-0184391395Improved reagent for trimethylsilylation of sphingolipid basesH.E. Carter0R.C. Gaver1Division of Biochemistry, Noyes Laboratory of Chemistry, University of Illinois, Urbana, Illinois 61801Division of Biochemistry, Noyes Laboratory of Chemistry, University of Illinois, Urbana, Illinois 61801This paper describes the trimethylsilylation of sphingolipid bases under conditions that give derivatives of improved stability. The retention times of the common C18 and C20 long-chain bases, including the anhydro bases, obtained on a commercially available gas-liquid chromatographic column with a nonpolar stationary phase are given. Data are also presented on the separation of the erythro and threo isomers of sphingosine and dihydrosphingosine, as the trimethylsilyl ethers of the N-acetyl derivatives.http://www.sciencedirect.com/science/article/pii/S0022227520395717sphingolipid basesgas-liquid chromatographytrimethylsilyl ether derivativesseparationlong-chain baseserythro and threo isomers
collection DOAJ
language English
format Article
sources DOAJ
author H.E. Carter
R.C. Gaver
spellingShingle H.E. Carter
R.C. Gaver
Improved reagent for trimethylsilylation of sphingolipid bases
Journal of Lipid Research
sphingolipid bases
gas-liquid chromatography
trimethylsilyl ether derivatives
separation
long-chain bases
erythro and threo isomers
author_facet H.E. Carter
R.C. Gaver
author_sort H.E. Carter
title Improved reagent for trimethylsilylation of sphingolipid bases
title_short Improved reagent for trimethylsilylation of sphingolipid bases
title_full Improved reagent for trimethylsilylation of sphingolipid bases
title_fullStr Improved reagent for trimethylsilylation of sphingolipid bases
title_full_unstemmed Improved reagent for trimethylsilylation of sphingolipid bases
title_sort improved reagent for trimethylsilylation of sphingolipid bases
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1967-07-01
description This paper describes the trimethylsilylation of sphingolipid bases under conditions that give derivatives of improved stability. The retention times of the common C18 and C20 long-chain bases, including the anhydro bases, obtained on a commercially available gas-liquid chromatographic column with a nonpolar stationary phase are given. Data are also presented on the separation of the erythro and threo isomers of sphingosine and dihydrosphingosine, as the trimethylsilyl ethers of the N-acetyl derivatives.
topic sphingolipid bases
gas-liquid chromatography
trimethylsilyl ether derivatives
separation
long-chain bases
erythro and threo isomers
url http://www.sciencedirect.com/science/article/pii/S0022227520395717
work_keys_str_mv AT hecarter improvedreagentfortrimethylsilylationofsphingolipidbases
AT rcgaver improvedreagentfortrimethylsilylationofsphingolipidbases
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