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Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate

Extraction of oil from the seed of Blighia unijugata gave a yield of 50.82 ± 1.20% using hexane in a soxhlet extractor. The iodine and saponification values were 67.60 ± 0.80 g iodine/100 g and 239.20 ± 1.00 mg KOH/g respectively with C18:1 being the dominant fatty acid. Unsaturated methyl esters of...

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Autores principales: Adewuyi, Adewale, Oderinde, Rotimi A, Rao, BVSK, Prasad, RBN, Nalla, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248850/
https://www.ncbi.nlm.nih.gov/pubmed/22145711
http://dx.doi.org/10.1186/1752-153X-5-79
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author Adewuyi, Adewale
Oderinde, Rotimi A
Rao, BVSK
Prasad, RBN
Nalla, M
author_facet Adewuyi, Adewale
Oderinde, Rotimi A
Rao, BVSK
Prasad, RBN
Nalla, M
author_sort Adewuyi, Adewale
collection PubMed
description Extraction of oil from the seed of Blighia unijugata gave a yield of 50.82 ± 1.20% using hexane in a soxhlet extractor. The iodine and saponification values were 67.60 ± 0.80 g iodine/100 g and 239.20 ± 1.00 mg KOH/g respectively with C18:1 being the dominant fatty acid. Unsaturated methyl esters of Blighia unijugata which had been previously subjected to urea adduct complexation was used to synthesize methyl 9, 10-dihydroxyoctadecanoate via hydroxylation in the presence of cetyltrimethylammonium permanganate (CTAP). The reaction was monitored and confirmed using FTIR and GC-MS. This study has revealed that oxidation reaction of mono unsaturated bonds using CTAP could be achieved under solvent free condition.
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spelling pubmed-32488502011-12-31 Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate Adewuyi, Adewale Oderinde, Rotimi A Rao, BVSK Prasad, RBN Nalla, M Chem Cent J Preliminary Communication Extraction of oil from the seed of Blighia unijugata gave a yield of 50.82 ± 1.20% using hexane in a soxhlet extractor. The iodine and saponification values were 67.60 ± 0.80 g iodine/100 g and 239.20 ± 1.00 mg KOH/g respectively with C18:1 being the dominant fatty acid. Unsaturated methyl esters of Blighia unijugata which had been previously subjected to urea adduct complexation was used to synthesize methyl 9, 10-dihydroxyoctadecanoate via hydroxylation in the presence of cetyltrimethylammonium permanganate (CTAP). The reaction was monitored and confirmed using FTIR and GC-MS. This study has revealed that oxidation reaction of mono unsaturated bonds using CTAP could be achieved under solvent free condition. BioMed Central 2011-12-06 /pmc/articles/PMC3248850/ /pubmed/22145711 http://dx.doi.org/10.1186/1752-153X-5-79 Text en Copyright ©2010 Adewuyi et al
spellingShingle Preliminary Communication
Adewuyi, Adewale
Oderinde, Rotimi A
Rao, BVSK
Prasad, RBN
Nalla, M
Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title_full Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title_fullStr Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title_full_unstemmed Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title_short Solvent free hydroxylation of the methyl esters of Blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
title_sort solvent free hydroxylation of the methyl esters of blighia unijugata seed oil in the presence of cetyltrimethylammonium permanganate
topic Preliminary Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248850/
https://www.ncbi.nlm.nih.gov/pubmed/22145711
http://dx.doi.org/10.1186/1752-153X-5-79
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