Preparation of heptadecenoic acid from Candida tropicallis yeast
In this paper a method is described for preparing 10 g or more of heptadecenoic acid (C17:1ω8) of 99 p.100 purity from Candida tripicallis yeast. Three cycles of treatment, based on crystallization techniques, were used successively: (1) Crystallization of fatty acids (in free form) from acetone at...
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Veröffentlicht in: | Journal of the American Oil Chemists' Society 1980-03, Vol.57 (3), p.121-124 |
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creator | Bauchart, D. Aurousseau, B. |
description | In this paper a method is described for preparing 10 g or more of heptadecenoic acid (C17:1ω8) of 99 p.100 purity from
Candida tripicallis
yeast. Three cycles of treatment, based on crystallization techniques, were used successively: (1) Crystallization of fatty acids (in free form) from acetone at −25 C induced the elimination of most of the saturated fatty acids, and at −60 C, of all of the poly‐unsaturated acids. (2) Inclusion formation of fatty acids (as methyl esters) with urea at hC induced the removal of all of the remaining saturated methyl esters and most of methyl oleate. (3) Crystallization of fatty acid methyl esters from acetone at −60 C removed almost all the remaining monounsaturated methyl esters (methyl palmitoleate and methyl oleate). Total efficiency of the preparation was about 17 p. 100. |
doi_str_mv | 10.1007/BF02678820 |
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Candida tripicallis
yeast. Three cycles of treatment, based on crystallization techniques, were used successively: (1) Crystallization of fatty acids (in free form) from acetone at −25 C induced the elimination of most of the saturated fatty acids, and at −60 C, of all of the poly‐unsaturated acids. (2) Inclusion formation of fatty acids (as methyl esters) with urea at hC induced the removal of all of the remaining saturated methyl esters and most of methyl oleate. (3) Crystallization of fatty acid methyl esters from acetone at −60 C removed almost all the remaining monounsaturated methyl esters (methyl palmitoleate and methyl oleate). Total efficiency of the preparation was about 17 p. 100.</description><identifier>ISSN: 0003-021X</identifier><identifier>EISSN: 1558-9331</identifier><identifier>DOI: 10.1007/BF02678820</identifier><language>eng</language><publisher>Springer Verlag</publisher><subject>Chemical Sciences ; Other</subject><ispartof>Journal of the American Oil Chemists' Society, 1980-03, Vol.57 (3), p.121-124</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c265t-115a35014a25f7515fe3c92c20797af9e673f7e428d0ddbd002555915d6c4fed3</citedby><cites>FETCH-LOGICAL-c265t-115a35014a25f7515fe3c92c20797af9e673f7e428d0ddbd002555915d6c4fed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.inrae.fr/hal-02732724$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Bauchart, D.</creatorcontrib><creatorcontrib>Aurousseau, B.</creatorcontrib><title>Preparation of heptadecenoic acid from Candida tropicallis yeast</title><title>Journal of the American Oil Chemists' Society</title><description>In this paper a method is described for preparing 10 g or more of heptadecenoic acid (C17:1ω8) of 99 p.100 purity from
Candida tripicallis
yeast. Three cycles of treatment, based on crystallization techniques, were used successively: (1) Crystallization of fatty acids (in free form) from acetone at −25 C induced the elimination of most of the saturated fatty acids, and at −60 C, of all of the poly‐unsaturated acids. (2) Inclusion formation of fatty acids (as methyl esters) with urea at hC induced the removal of all of the remaining saturated methyl esters and most of methyl oleate. (3) Crystallization of fatty acid methyl esters from acetone at −60 C removed almost all the remaining monounsaturated methyl esters (methyl palmitoleate and methyl oleate). Total efficiency of the preparation was about 17 p. 100.</description><subject>Chemical Sciences</subject><subject>Other</subject><issn>0003-021X</issn><issn>1558-9331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><recordid>eNpFkE9LAzEUxIMoWKsXP0GuCqsvL5vN7s1aWiss6EHB2_LMHxrZNkuyCP32tlT0NMzwmzkMY9cC7gSAvn9cAla6rhFO2EQoVReNlOKUTQBAFoDi45xd5Py1t7VENWEPr8kNlGgMccuj52s3jGSdcdsYDCcTLPcpbvictjZY4mOKQzDU9yHznaM8XrIzT312V786Ze_Lxdt8VbQvT8_zWVsYrNRYCKFIKhAlofJaCeWdNA0aBN1o8o2rtPTalVhbsPbTAqBSqhHKVqb0zsopuznurqnvhhQ2lHZdpNCtZm13yAC1RI3lt9izt0fWpJhzcv6vIKA7_NT9_yR_APOtWOw</recordid><startdate>198003</startdate><enddate>198003</enddate><creator>Bauchart, D.</creator><creator>Aurousseau, B.</creator><general>Springer Verlag</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope></search><sort><creationdate>198003</creationdate><title>Preparation of heptadecenoic acid from Candida tropicallis yeast</title><author>Bauchart, D. ; Aurousseau, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c265t-115a35014a25f7515fe3c92c20797af9e673f7e428d0ddbd002555915d6c4fed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Chemical Sciences</topic><topic>Other</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bauchart, D.</creatorcontrib><creatorcontrib>Aurousseau, B.</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of the American Oil Chemists' Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bauchart, D.</au><au>Aurousseau, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of heptadecenoic acid from Candida tropicallis yeast</atitle><jtitle>Journal of the American Oil Chemists' Society</jtitle><date>1980-03</date><risdate>1980</risdate><volume>57</volume><issue>3</issue><spage>121</spage><epage>124</epage><pages>121-124</pages><issn>0003-021X</issn><eissn>1558-9331</eissn><abstract>In this paper a method is described for preparing 10 g or more of heptadecenoic acid (C17:1ω8) of 99 p.100 purity from
Candida tripicallis
yeast. Three cycles of treatment, based on crystallization techniques, were used successively: (1) Crystallization of fatty acids (in free form) from acetone at −25 C induced the elimination of most of the saturated fatty acids, and at −60 C, of all of the poly‐unsaturated acids. (2) Inclusion formation of fatty acids (as methyl esters) with urea at hC induced the removal of all of the remaining saturated methyl esters and most of methyl oleate. (3) Crystallization of fatty acid methyl esters from acetone at −60 C removed almost all the remaining monounsaturated methyl esters (methyl palmitoleate and methyl oleate). Total efficiency of the preparation was about 17 p. 100.</abstract><pub>Springer Verlag</pub><doi>10.1007/BF02678820</doi><tpages>4</tpages></addata></record> |
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title | Preparation of heptadecenoic acid from Candida tropicallis yeast |
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