Characterization of sacha inchi (Plukenetia volubilis L.) oil by FTIR spectroscopy and 1H NMR. Comparison with linseed oil

Three oil samples obtained from sacha inchi (Plukenetia volubilis L.) seeds were studied by means of FTIR and 1H NMR. Frequency data of the most significant bands of the IR spectrum of this oil are given. These data show that sacha inchi oil has a high degree of unsaturation. The same fact is deduce...

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Veröffentlicht in:Journal of the American Oil Chemists' Society 2003-08, Vol.80 (8), p.755-762
Hauptverfasser: Guillén, María D., Ruiz, Ainhoa, Cabo, Nerea, Chirinos, Rosana, Pascual, Gloria
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Ruiz, Ainhoa
Cabo, Nerea
Chirinos, Rosana
Pascual, Gloria
description Three oil samples obtained from sacha inchi (Plukenetia volubilis L.) seeds were studied by means of FTIR and 1H NMR. Frequency data of the most significant bands of the IR spectrum of this oil are given. These data show that sacha inchi oil has a high degree of unsaturation. The same fact is deduced from the ratio between the absorbance of the bands due to the stretching vibrations of the cis olefinic CH double bonds at 3010.5 cm−1 and to the methylene symmetrical stretching vibrations at 2855.1 cm−1. The proportions of monounsaturated, polyunsaturated, and saturated acyl groups were predicted from the frequency of some IR bands, and these were in satisfactory agreement with the values obtained through FAME generation and their quantification by GC. Likewise, simple observation of the 1H NMR spectra provided a great deal of information about sacha inchi oil, with regard not only to the relative proportions of the different acyl groups but also to their nature. Thus, the presence of γ‐linolenic acyl groups was discounted. Furthermore, the area of some 1H NMR signals was used to determine the proportion of saturated and mono‐, di‐, and triunsaturated acyl groups, which also were in satisfactory agreement with the values obtained by classical methods. IR and 1H NMR determinations take very little time in comparison with classical methods and do not require chemical manipulation or transformation of the sample. A comparison was also made between the compositions of sacha inchi and linseed oil. Both oils are important sources of the healthful n−3 linolenic acyl groups, and sacha inchi also contains high proportions of the n−6 linoleic acyl groups.
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The proportions of monounsaturated, polyunsaturated, and saturated acyl groups were predicted from the frequency of some IR bands, and these were in satisfactory agreement with the values obtained through FAME generation and their quantification by GC. Likewise, simple observation of the 1H NMR spectra provided a great deal of information about sacha inchi oil, with regard not only to the relative proportions of the different acyl groups but also to their nature. Thus, the presence of γ‐linolenic acyl groups was discounted. Furthermore, the area of some 1H NMR signals was used to determine the proportion of saturated and mono‐, di‐, and triunsaturated acyl groups, which also were in satisfactory agreement with the values obtained by classical methods. IR and 1H NMR determinations take very little time in comparison with classical methods and do not require chemical manipulation or transformation of the sample. A comparison was also made between the compositions of sacha inchi and linseed oil. Both oils are important sources of the healthful n−3 linolenic acyl groups, and sacha inchi also contains high proportions of the n−6 linoleic acyl groups.</description><identifier>ISSN: 0003-021X</identifier><identifier>EISSN: 1558-9331</identifier><identifier>DOI: 10.1007/s11746-003-0768-z</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>1H nuclear magnetic resonance ; Biological and medical sciences ; Characterization ; composition ; Fat industries ; Food industries ; Fourier transform infrared spectroscopy ; Fundamental and applied biological sciences. 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Comparison with linseed oil</title><title>Journal of the American Oil Chemists' Society</title><description>Three oil samples obtained from sacha inchi (Plukenetia volubilis L.) seeds were studied by means of FTIR and 1H NMR. Frequency data of the most significant bands of the IR spectrum of this oil are given. These data show that sacha inchi oil has a high degree of unsaturation. The same fact is deduced from the ratio between the absorbance of the bands due to the stretching vibrations of the cis olefinic CH double bonds at 3010.5 cm−1 and to the methylene symmetrical stretching vibrations at 2855.1 cm−1. The proportions of monounsaturated, polyunsaturated, and saturated acyl groups were predicted from the frequency of some IR bands, and these were in satisfactory agreement with the values obtained through FAME generation and their quantification by GC. Likewise, simple observation of the 1H NMR spectra provided a great deal of information about sacha inchi oil, with regard not only to the relative proportions of the different acyl groups but also to their nature. Thus, the presence of γ‐linolenic acyl groups was discounted. Furthermore, the area of some 1H NMR signals was used to determine the proportion of saturated and mono‐, di‐, and triunsaturated acyl groups, which also were in satisfactory agreement with the values obtained by classical methods. IR and 1H NMR determinations take very little time in comparison with classical methods and do not require chemical manipulation or transformation of the sample. A comparison was also made between the compositions of sacha inchi and linseed oil. 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Psychology</topic><topic>sacha inchi oil</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guillén, María D.</creatorcontrib><creatorcontrib>Ruiz, Ainhoa</creatorcontrib><creatorcontrib>Cabo, Nerea</creatorcontrib><creatorcontrib>Chirinos, Rosana</creatorcontrib><creatorcontrib>Pascual, Gloria</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Journal of the American Oil Chemists' Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guillén, María D.</au><au>Ruiz, Ainhoa</au><au>Cabo, Nerea</au><au>Chirinos, Rosana</au><au>Pascual, Gloria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of sacha inchi (Plukenetia volubilis L.) oil by FTIR spectroscopy and 1H NMR. 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The proportions of monounsaturated, polyunsaturated, and saturated acyl groups were predicted from the frequency of some IR bands, and these were in satisfactory agreement with the values obtained through FAME generation and their quantification by GC. Likewise, simple observation of the 1H NMR spectra provided a great deal of information about sacha inchi oil, with regard not only to the relative proportions of the different acyl groups but also to their nature. Thus, the presence of γ‐linolenic acyl groups was discounted. Furthermore, the area of some 1H NMR signals was used to determine the proportion of saturated and mono‐, di‐, and triunsaturated acyl groups, which also were in satisfactory agreement with the values obtained by classical methods. IR and 1H NMR determinations take very little time in comparison with classical methods and do not require chemical manipulation or transformation of the sample. A comparison was also made between the compositions of sacha inchi and linseed oil. Both oils are important sources of the healthful n−3 linolenic acyl groups, and sacha inchi also contains high proportions of the n−6 linoleic acyl groups.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><doi>10.1007/s11746-003-0768-z</doi><tpages>8</tpages></addata></record>
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subjects 1H nuclear magnetic resonance
Biological and medical sciences
Characterization
composition
Fat industries
Food industries
Fourier transform infrared spectroscopy
Fundamental and applied biological sciences. Psychology
sacha inchi oil
title Characterization of sacha inchi (Plukenetia volubilis L.) oil by FTIR spectroscopy and 1H NMR. Comparison with linseed oil
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