Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy

Introduction: Nuclear magnetic resonance (NMR) spectroscopy is an analytical chemistry technique used for the chemical structural determination. This valuable tool is used to study nuclei, commonly hydrogen (1H) and carbon (13C). NMR provides information about the number of atoms of the studied nucl...

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Main Authors: Ab. Hadi, Hazrina, Azmar, Hawa Mas
Format: Proceeding Paper
Language:English
English
English
Published: 2016
Subjects:
Online Access:http://irep.iium.edu.my/52614/
http://irep.iium.edu.my/52614/1/NMR%20Poster_Hawa.pdf
http://irep.iium.edu.my/52614/2/Abstract_PP_Hawa.pdf
http://irep.iium.edu.my/52614/3/Cover%20page.pdf
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author Ab. Hadi, Hazrina
Azmar, Hawa Mas
author_facet Ab. Hadi, Hazrina
Azmar, Hawa Mas
author_sort Ab. Hadi, Hazrina
building IIUM Repository
collection Online Access
description Introduction: Nuclear magnetic resonance (NMR) spectroscopy is an analytical chemistry technique used for the chemical structural determination. This valuable tool is used to study nuclei, commonly hydrogen (1H) and carbon (13C). NMR provides information about the number of atoms of the studied nuclei that are magnetically separated as well as the nature of the environment of the nuclei. Aims: In this study, NMR is used to identify the isolated hydroxychavicol. The isolated hydroxychavicol was dissolved in deuterated methanol. Methods: The sample is analyzed for 1D NMR (1H and 13C) spectra using 500 MHz NMR (Bruker; Avance III Ultrashield Plus; Switzerland) located in Universiti Malaysia Pahang. The target directed isolation of hydroxychavicol was performed by comparing bioautographic profile of hydroxychavicol-rich fraction to that of hydroxychavicol standard. Hydroxychavicol is a known compound with molecular formula of C9H10O2 and molecular weight of 150.174 g/mol. Results and discussion: 1H and 13C NMR elucidated the structure of the isolated hydroxychavicol. The 1H NMR spectrum furnished 10 protons at chemical shifts of δH 3.21, 4.90, 4.98, 5.9, 6.49, 6.61, and 6.67 ppm. Based on the spectrum, a broad spectrum was displayed meaning there is a hydroxyl group in the structure. The 13C NMR spectrum displayed the nine carbons at chemical shifts δC 40.64, 115.33, 116.31, 116.76, 120.87, 132.99, 139.57, 144.46, and 146.17 ppm. Conclusion: The isolated hydroxychavicol was successfully being authenticated by NMR.
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institution International Islamic University Malaysia
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language English
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English
last_indexed 2025-11-14T16:31:41Z
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spelling iium-526142017-03-10T17:37:24Z http://irep.iium.edu.my/52614/ Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy Ab. Hadi, Hazrina Azmar, Hawa Mas RS Pharmacy and materia medica Introduction: Nuclear magnetic resonance (NMR) spectroscopy is an analytical chemistry technique used for the chemical structural determination. This valuable tool is used to study nuclei, commonly hydrogen (1H) and carbon (13C). NMR provides information about the number of atoms of the studied nuclei that are magnetically separated as well as the nature of the environment of the nuclei. Aims: In this study, NMR is used to identify the isolated hydroxychavicol. The isolated hydroxychavicol was dissolved in deuterated methanol. Methods: The sample is analyzed for 1D NMR (1H and 13C) spectra using 500 MHz NMR (Bruker; Avance III Ultrashield Plus; Switzerland) located in Universiti Malaysia Pahang. The target directed isolation of hydroxychavicol was performed by comparing bioautographic profile of hydroxychavicol-rich fraction to that of hydroxychavicol standard. Hydroxychavicol is a known compound with molecular formula of C9H10O2 and molecular weight of 150.174 g/mol. Results and discussion: 1H and 13C NMR elucidated the structure of the isolated hydroxychavicol. The 1H NMR spectrum furnished 10 protons at chemical shifts of δH 3.21, 4.90, 4.98, 5.9, 6.49, 6.61, and 6.67 ppm. Based on the spectrum, a broad spectrum was displayed meaning there is a hydroxyl group in the structure. The 13C NMR spectrum displayed the nine carbons at chemical shifts δC 40.64, 115.33, 116.31, 116.76, 120.87, 132.99, 139.57, 144.46, and 146.17 ppm. Conclusion: The isolated hydroxychavicol was successfully being authenticated by NMR. 2016 Proceeding Paper NonPeerReviewed application/pdf en http://irep.iium.edu.my/52614/1/NMR%20Poster_Hawa.pdf application/pdf en http://irep.iium.edu.my/52614/2/Abstract_PP_Hawa.pdf application/pdf en http://irep.iium.edu.my/52614/3/Cover%20page.pdf Ab. Hadi, Hazrina and Azmar, Hawa Mas (2016) Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy. In: Pharma BioAsia Conference 2016, 28-29 Sep 2016, Kuala Lumpur. (Unpublished)
spellingShingle RS Pharmacy and materia medica
Ab. Hadi, Hazrina
Azmar, Hawa Mas
Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title_full Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title_fullStr Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title_full_unstemmed Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title_short Authentication of isolated hydroxychavicol from p. Betle linn. Leaves using nuclear magnetic resonance spectroscopy
title_sort authentication of isolated hydroxychavicol from p. betle linn. leaves using nuclear magnetic resonance spectroscopy
topic RS Pharmacy and materia medica
url http://irep.iium.edu.my/52614/
http://irep.iium.edu.my/52614/1/NMR%20Poster_Hawa.pdf
http://irep.iium.edu.my/52614/2/Abstract_PP_Hawa.pdf
http://irep.iium.edu.my/52614/3/Cover%20page.pdf