Feruloylated Products from Coconut Oil and Shea Butter

Abstract The synthesis of feruloylated coconut oil and feruloylated shea butter were demonstrated in 0.5‐L scale, shaken, batch reactions. Ethyl ferulate and the vegetable oil/fat were combined in a 1.0:1.3 mol ratio in the presence of Candida antartica lipase B immobilized on an acrylic resin (Novo...

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Published in:Journal of the American Oil Chemists' Society
Main Authors: Compton, David L., Goodell, John R., Berhow, Mark A., Kenar, James A., Cermak, Steven C., Evans, Kervin O.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2017
Subjects:
Online Access:http://dx.doi.org/10.1007/s11746-017-2953-7
http://link.springer.com/content/pdf/10.1007/s11746-017-2953-7.pdf
http://link.springer.com/article/10.1007/s11746-017-2953-7/fulltext.html
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spelling crwiley:10.1007/s11746-017-2953-7 2024-09-15T17:49:16+00:00 Feruloylated Products from Coconut Oil and Shea Butter Compton, David L. Goodell, John R. Berhow, Mark A. Kenar, James A. Cermak, Steven C. Evans, Kervin O. 2017 http://dx.doi.org/10.1007/s11746-017-2953-7 http://link.springer.com/content/pdf/10.1007/s11746-017-2953-7.pdf http://link.springer.com/article/10.1007/s11746-017-2953-7/fulltext.html https://onlinelibrary.wiley.com/doi/full/10.1007/s11746-017-2953-7 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor http://www.springer.com/tdm Journal of the American Oil Chemists' Society volume 94, issue 3, page 397-411 ISSN 0003-021X 1558-9331 journal-article 2017 crwiley https://doi.org/10.1007/s11746-017-2953-7 2024-07-18T04:25:09Z Abstract The synthesis of feruloylated coconut oil and feruloylated shea butter were demonstrated in 0.5‐L scale, shaken, batch reactions. Ethyl ferulate and the vegetable oil/fat were combined in a 1.0:1.3 mol ratio in the presence of Candida antartica lipase B immobilized on an acrylic resin (Novozym 435) at 60 °C. The transesterification of ethyl ferulate with coconut oil and shea butter reached equilibrium conversions, after 22 days, of 63 and 70%, respectively, with the shea butter transesterifications producing a white precipitate not observed in the coconut oil transesterifications. The faster transesterification rates, equilibrium conversions and white precipitate were shown to result from di‐ and monoacylglycerols (DAG and MAG) present in the shea butter. The transesterification of ethyl ferulate and coconut oil was also tested in a continuous, enzymatic, packed‐bed bioreactor using Novozym 435 at 60 °C to produce feruloylated coconut oil at rates of 0.5–0.9 kg/day over 4.5 months. The feruloylated coconut oil acylglycerol species were identified by LC–MS analysis of transesterification reactions of ethyl ferulate with medium chain triacylglycerol (TAG) standards, C8–C14. The feruloylated vegetable oils possessed an ultra violet (UV) absorbing λ max 328 nm, making them good UVAII absorbers, as defined by the U.S. Food and Drug Administration. The feruloylated coconut oil possessed a 17.5% higher absorption capacity than feruloylated shea butter on a per weight basis. All the feruloylated vegetable oils possessed rapid antioxidant capacity (50% reduction of initial radical concentration <5 min) at the concentrations tested, 0.5–2.5 mM. Feruloylated coconut oil possessed chemical and physical characteristics that suggested it would be fungible for feruloylated soybean oil in current retail formulations. Article in Journal/Newspaper antartic* Wiley Online Library Journal of the American Oil Chemists' Society 94 3 397 411
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract The synthesis of feruloylated coconut oil and feruloylated shea butter were demonstrated in 0.5‐L scale, shaken, batch reactions. Ethyl ferulate and the vegetable oil/fat were combined in a 1.0:1.3 mol ratio in the presence of Candida antartica lipase B immobilized on an acrylic resin (Novozym 435) at 60 °C. The transesterification of ethyl ferulate with coconut oil and shea butter reached equilibrium conversions, after 22 days, of 63 and 70%, respectively, with the shea butter transesterifications producing a white precipitate not observed in the coconut oil transesterifications. The faster transesterification rates, equilibrium conversions and white precipitate were shown to result from di‐ and monoacylglycerols (DAG and MAG) present in the shea butter. The transesterification of ethyl ferulate and coconut oil was also tested in a continuous, enzymatic, packed‐bed bioreactor using Novozym 435 at 60 °C to produce feruloylated coconut oil at rates of 0.5–0.9 kg/day over 4.5 months. The feruloylated coconut oil acylglycerol species were identified by LC–MS analysis of transesterification reactions of ethyl ferulate with medium chain triacylglycerol (TAG) standards, C8–C14. The feruloylated vegetable oils possessed an ultra violet (UV) absorbing λ max 328 nm, making them good UVAII absorbers, as defined by the U.S. Food and Drug Administration. The feruloylated coconut oil possessed a 17.5% higher absorption capacity than feruloylated shea butter on a per weight basis. All the feruloylated vegetable oils possessed rapid antioxidant capacity (50% reduction of initial radical concentration <5 min) at the concentrations tested, 0.5–2.5 mM. Feruloylated coconut oil possessed chemical and physical characteristics that suggested it would be fungible for feruloylated soybean oil in current retail formulations.
format Article in Journal/Newspaper
author Compton, David L.
Goodell, John R.
Berhow, Mark A.
Kenar, James A.
Cermak, Steven C.
Evans, Kervin O.
spellingShingle Compton, David L.
Goodell, John R.
Berhow, Mark A.
Kenar, James A.
Cermak, Steven C.
Evans, Kervin O.
Feruloylated Products from Coconut Oil and Shea Butter
author_facet Compton, David L.
Goodell, John R.
Berhow, Mark A.
Kenar, James A.
Cermak, Steven C.
Evans, Kervin O.
author_sort Compton, David L.
title Feruloylated Products from Coconut Oil and Shea Butter
title_short Feruloylated Products from Coconut Oil and Shea Butter
title_full Feruloylated Products from Coconut Oil and Shea Butter
title_fullStr Feruloylated Products from Coconut Oil and Shea Butter
title_full_unstemmed Feruloylated Products from Coconut Oil and Shea Butter
title_sort feruloylated products from coconut oil and shea butter
publisher Wiley
publishDate 2017
url http://dx.doi.org/10.1007/s11746-017-2953-7
http://link.springer.com/content/pdf/10.1007/s11746-017-2953-7.pdf
http://link.springer.com/article/10.1007/s11746-017-2953-7/fulltext.html
https://onlinelibrary.wiley.com/doi/full/10.1007/s11746-017-2953-7
genre antartic*
genre_facet antartic*
op_source Journal of the American Oil Chemists' Society
volume 94, issue 3, page 397-411
ISSN 0003-021X 1558-9331
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
http://www.springer.com/tdm
op_doi https://doi.org/10.1007/s11746-017-2953-7
container_title Journal of the American Oil Chemists' Society
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