Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary Phase
The use of novel polysiloxanes as stationary phase carrying chiral groups enables the separation of most amino acid enantiomers in a much shorter time than ever reported previously. Phases of this type exhibit very low volatility and high thermal stability and may be used in routine analysis with op...
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Veröffentlicht in: | Journal of chromatographic science 1977-05, Vol.15 (5), p.174-176 |
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container_title | Journal of chromatographic science |
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creator | Frank, Hartmut Nicholson, Graeme J. Bayer, Ernst |
description | The use of novel polysiloxanes as stationary phase carrying chiral groups enables the separation of most amino acid enantiomers in a much shorter time than ever reported previously. Phases of this type exhibit very low volatility and high thermal stability and may be used in routine analysis with open tubular columns at temperatures of at least 175°C. Most protein amino acids are separated in a temperature program between 90 and 175°C, thus obviating the need for multiple injections. Resolution factors are somewhat lower than those of other diamide phases containing the L-valine t-butylamide group, but are sufficient for resolution of almost all protein amino acid enantiomers. |
doi_str_mv | 10.1093/chromsci/15.5.174 |
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Phases of this type exhibit very low volatility and high thermal stability and may be used in routine analysis with open tubular columns at temperatures of at least 175°C. Most protein amino acids are separated in a temperature program between 90 and 175°C, thus obviating the need for multiple injections. Resolution factors are somewhat lower than those of other diamide phases containing the L-valine t-butylamide group, but are sufficient for resolution of almost all protein amino acid enantiomers.</description><identifier>ISSN: 0021-9665</identifier><identifier>EISSN: 1945-239X</identifier><identifier>DOI: 10.1093/chromsci/15.5.174</identifier><identifier>PMID: 863993</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Amino Acids - analysis ; Chromatography, Gas - methods ; Drug Stability ; Isomerism ; Siloxanes</subject><ispartof>Journal of chromatographic science, 1977-05, Vol.15 (5), p.174-176</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-aaca9b8713e8a16bb721a1dc760c6bb38cac2367b3e42e9bb95fdd8a70cd05a03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/863993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frank, Hartmut</creatorcontrib><creatorcontrib>Nicholson, Graeme J.</creatorcontrib><creatorcontrib>Bayer, Ernst</creatorcontrib><title>Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary Phase</title><title>Journal of chromatographic science</title><addtitle>Journal of Chromatographic Science</addtitle><description>The use of novel polysiloxanes as stationary phase carrying chiral groups enables the separation of most amino acid enantiomers in a much shorter time than ever reported previously. Phases of this type exhibit very low volatility and high thermal stability and may be used in routine analysis with open tubular columns at temperatures of at least 175°C. Most protein amino acids are separated in a temperature program between 90 and 175°C, thus obviating the need for multiple injections. Resolution factors are somewhat lower than those of other diamide phases containing the L-valine t-butylamide group, but are sufficient for resolution of almost all protein amino acid enantiomers.</description><subject>Amino Acids - analysis</subject><subject>Chromatography, Gas - methods</subject><subject>Drug Stability</subject><subject>Isomerism</subject><subject>Siloxanes</subject><issn>0021-9665</issn><issn>1945-239X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMlOwzAQhi3EVpYHQOLgE7cUO64T-1hVpUWq2AoS4mJNHJcakjjYKcvb41LgNJr5F40-hE4o6VMi2bleelcHbc8p7_M-zQdbqEflgCcpk4_bqEdIShOZZXwfHYTwsl6p4HtoV2RMStZD-g5aW-IJBDxad0Hnnj20S6vx3LTgobOuwW6Bh7VtHB7qaB430MRzbXzAH7ZbYsBX7t1UscF6qPC8-0mB_8I3SwjmCO0soArm-HceooeL8f1omsyuJ5ej4SzRjLEuAdAgC5FTZgTQrCjylAItdZ4RHTcmNOiUZXnBzCA1sigkX5SlgJzoknAg7BCdbXpb795WJnSqtkGbqoLGuFVQgkmaMiGjkW6M2rsQvFmo1ts6_qsoUWuu6o-rolxxFbnGzOlv-aqoTfmf2ICMcrKRbejM578K_lVlOcu5mj4-qVsxvx2J6UxN2Dc6FYbE</recordid><startdate>19770510</startdate><enddate>19770510</enddate><creator>Frank, Hartmut</creator><creator>Nicholson, Graeme J.</creator><creator>Bayer, Ernst</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19770510</creationdate><title>Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary Phase</title><author>Frank, Hartmut ; Nicholson, Graeme J. ; Bayer, Ernst</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-aaca9b8713e8a16bb721a1dc760c6bb38cac2367b3e42e9bb95fdd8a70cd05a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Amino Acids - analysis</topic><topic>Chromatography, Gas - methods</topic><topic>Drug Stability</topic><topic>Isomerism</topic><topic>Siloxanes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frank, Hartmut</creatorcontrib><creatorcontrib>Nicholson, Graeme J.</creatorcontrib><creatorcontrib>Bayer, Ernst</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of chromatographic science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frank, Hartmut</au><au>Nicholson, Graeme J.</au><au>Bayer, Ernst</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary Phase</atitle><jtitle>Journal of chromatographic science</jtitle><addtitle>Journal of Chromatographic Science</addtitle><date>1977-05-10</date><risdate>1977</risdate><volume>15</volume><issue>5</issue><spage>174</spage><epage>176</epage><pages>174-176</pages><issn>0021-9665</issn><eissn>1945-239X</eissn><abstract>The use of novel polysiloxanes as stationary phase carrying chiral groups enables the separation of most amino acid enantiomers in a much shorter time than ever reported previously. Phases of this type exhibit very low volatility and high thermal stability and may be used in routine analysis with open tubular columns at temperatures of at least 175°C. Most protein amino acids are separated in a temperature program between 90 and 175°C, thus obviating the need for multiple injections. Resolution factors are somewhat lower than those of other diamide phases containing the L-valine t-butylamide group, but are sufficient for resolution of almost all protein amino acid enantiomers.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>863993</pmid><doi>10.1093/chromsci/15.5.174</doi><tpages>3</tpages></addata></record> |
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issn | 0021-9665 1945-239X |
language | eng |
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source | Oxford University Press Journals Digital Archive legacy; MEDLINE |
subjects | Amino Acids - analysis Chromatography, Gas - methods Drug Stability Isomerism Siloxanes |
title | Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary Phase |
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