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Gas chromatographic analysis of amino acids as the N-Heptafluorobutyryl isobutyl esters

By: Material type: ArticleLanguage: English Publication details: United Kingdom : Oxford University Press, 1987.ISSN:
  • 1060-3271
  • 1944-7922 (Online)
Subject(s): In: Journal of Association of Official Analytical Chemists United Kingdom : Oxford University Press, 1987. v. 70, no. 1, p. 151–160Summary: The N-heptafluoroburyryl isobutyl derivatives of proteic amino acids are well resolved by gas chromatography and form the basis of a convenient, rapid assay. The derivatives are prepared by acid-catalyzed esterification at 120°C for 20 min in 3N HCl-isobutanol followed by acylation with heptafluorobutyric anhydride at 150°C for 10 min. The reaction sequence is performed without any transfers or extractions and thus is compatible with microscale analysis. A complete proteic amino acid profile can be completed in less than 20 min by using a packed column or less than 10 min by using a capillary column in combination with an elevated oven temperature program rate. Physiological sample matrixes, which frequently contain a complex mixture of components, and thus require maximum resolution, can be assayed in less than 1 h using a program rate of 4°C/min. A capillary column is recommended for this application. Capillary column chromatography, in combination with a nitrogen specific detector, is useful for identifying and assaying nonproteic amino acids in physiological sample matrixes. Frequently, a prior cleanup of the sample can be avoided.
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The N-heptafluoroburyryl isobutyl derivatives of proteic amino acids are well resolved by gas chromatography and form the basis of a convenient, rapid assay. The derivatives are prepared by acid-catalyzed esterification at 120°C for 20 min in 3N HCl-isobutanol followed by acylation with heptafluorobutyric anhydride at 150°C for 10 min. The reaction sequence is performed without any transfers or extractions and thus is compatible with microscale analysis. A complete proteic amino acid profile can be completed in less than 20 min by using a packed column or less than 10 min by using a capillary column in combination with an elevated oven temperature program rate. Physiological sample matrixes, which frequently contain a complex mixture of components, and thus require maximum resolution, can be assayed in less than 1 h using a program rate of 4°C/min. A capillary column is recommended for this application. Capillary column chromatography, in combination with a nitrogen specific detector, is useful for identifying and assaying nonproteic amino acids in physiological sample matrixes. Frequently, a prior cleanup of the sample can be avoided.

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