SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri

ABSTRACT Candle nut oil could be transesterificated by methanol with concentrated H2S04 as a catalyst to form fatty acid methyl esther. Methyl linoleate could be separated by Column Chromatography mechanism technic partition from fatty acid methyl ester (FAME) mixture, then it was treated by ethanol...

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Main Author: Perpustakaan UGM, i-lib
Format: Article NonPeerReviewed
Published: [Yogyakarta] : Universitas Gadjah Mada 2009
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Online Access:https://repository.ugm.ac.id/28005/
http://i-lib.ugm.ac.id/jurnal/download.php?dataId=11068
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spelling id-ugm-repo.280052014-06-18T00:24:40Z https://repository.ugm.ac.id/28005/ SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri Perpustakaan UGM, i-lib Jurnal i-lib UGM ABSTRACT Candle nut oil could be transesterificated by methanol with concentrated H2S04 as a catalyst to form fatty acid methyl esther. Methyl linoleate could be separated by Column Chromatography mechanism technic partition from fatty acid methyl ester (FAME) mixture, then it was treated by ethanolamine at base condition in benzene as solvent and sodium methylate as a catalyst at reflux condition for 6 hours to form an alkanolamide. Alkanolamide could be epoxydized by tert-buthyl hydroperoxyde and peroxygenase as a catalyst and it was refluxed for 6 hours at 40°C and nitrogen gas condition to form the epoxy alkanolamide octadecanoate, and then it was hydrolyzed by HCI O.1 M to form alkanolamide tetrahidroxy octadecanoate (Polyol). Alkanolamide tetrahidroxy octadecanoate could be separated by Column Chromatography using silica gel H 40 and the eluent was the mixture of chloroform, ethyl acetate, formic acid in a ratio 90:10:1 (liNN/). Determination of HLB value from alknolamide tetrahydroxy octadecanoate is 13.096. Therefore, this compound was particularly suitable for application as an o/w emulsifiers. All af the reaction steps were confirmedby using FT-IR, 1H-NMR, GC-MS, Gas Chromatographyand TLC. Keywords: Esterification, Candle nut oil, Surfactant, Amidation, Polyol. [Yogyakarta] : Universitas Gadjah Mada 2009 Article NonPeerReviewed Perpustakaan UGM, i-lib (2009) SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri. Jurnal i-lib UGM. http://i-lib.ugm.ac.id/jurnal/download.php?dataId=11068
institution Universitas Gadjah Mada
building UGM Library
country Indonesia
collection Repository Civitas UGM
topic Jurnal i-lib UGM
spellingShingle Jurnal i-lib UGM
Perpustakaan UGM, i-lib
SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
description ABSTRACT Candle nut oil could be transesterificated by methanol with concentrated H2S04 as a catalyst to form fatty acid methyl esther. Methyl linoleate could be separated by Column Chromatography mechanism technic partition from fatty acid methyl ester (FAME) mixture, then it was treated by ethanolamine at base condition in benzene as solvent and sodium methylate as a catalyst at reflux condition for 6 hours to form an alkanolamide. Alkanolamide could be epoxydized by tert-buthyl hydroperoxyde and peroxygenase as a catalyst and it was refluxed for 6 hours at 40°C and nitrogen gas condition to form the epoxy alkanolamide octadecanoate, and then it was hydrolyzed by HCI O.1 M to form alkanolamide tetrahidroxy octadecanoate (Polyol). Alkanolamide tetrahidroxy octadecanoate could be separated by Column Chromatography using silica gel H 40 and the eluent was the mixture of chloroform, ethyl acetate, formic acid in a ratio 90:10:1 (liNN/). Determination of HLB value from alknolamide tetrahydroxy octadecanoate is 13.096. Therefore, this compound was particularly suitable for application as an o/w emulsifiers. All af the reaction steps were confirmedby using FT-IR, 1H-NMR, GC-MS, Gas Chromatographyand TLC. Keywords: Esterification, Candle nut oil, Surfactant, Amidation, Polyol.
format Article
NonPeerReviewed
author Perpustakaan UGM, i-lib
author_facet Perpustakaan UGM, i-lib
author_sort Perpustakaan UGM, i-lib
title SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
title_short SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
title_full SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
title_fullStr SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
title_full_unstemmed SYNTHESIS ALKANOLAMIDETETRAHIDROXYOCTADECANOATECOMPOUNDFROM CANDLE NUT OIL . . Pembuatan Senyawa Alkanolamida Tetrahidroksi Oktadekanoat yang Diturunkan dari M/nyak Kemiri
title_sort synthesis alkanolamidetetrahidroxyoctadecanoatecompoundfrom candle nut oil . . pembuatan senyawa alkanolamida tetrahidroksi oktadekanoat yang diturunkan dari m/nyak kemiri
publisher [Yogyakarta] : Universitas Gadjah Mada
publishDate 2009
url https://repository.ugm.ac.id/28005/
http://i-lib.ugm.ac.id/jurnal/download.php?dataId=11068
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