2009
DOI: 10.3329/jsr.v1i2.1635
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Isolation of (+)-Catechin from Acacia Catechu (Cutch Tree) by a Convenient Method

Abstract: Biologically important polyphenol (+)-catechin was isolated from catechu, the extract of the red heartwood of Acacia Catechu tree (Khoiyer tree). The isolation procedure was developed to get better yield (25%) and to reduce the isolation cost and time. The structure of the isolated (+)-catechin was confirmed with several spectral analyses and chemical studies. Keywords:  Acacia Catechu; (+)-catechin; Polyphenol. © 2009 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved. DOI: 1… Show more

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Cited by 59 publications
(38 citation statements)
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“…Based on the resonance for C-2 at d C 82.9, strong H-2/H-3 correlations in the COSY experiment, 1 H-NMR, 13 C-NMR, and data in literature, [15] compound 3 was identified as (C)-catechin. This was confirmed by GC-MS, IR, and UV-Vis spectroscopy.…”
Section: Structure Elucidationmentioning
confidence: 99%
“…Based on the resonance for C-2 at d C 82.9, strong H-2/H-3 correlations in the COSY experiment, 1 H-NMR, 13 C-NMR, and data in literature, [15] compound 3 was identified as (C)-catechin. This was confirmed by GC-MS, IR, and UV-Vis spectroscopy.…”
Section: Structure Elucidationmentioning
confidence: 99%
“…Based on the above mentioned data, and based on the comparison with the data of literature [6], compound 1 was confirmed to be (+)-catechin. Catechin has been isolated from Camellia sinensis [7] and known to possess a variety of biological activities, such as anti-inflammatory [8], antimicrobial [9] and antioxidant [10].…”
Section: Resultsmentioning
confidence: 64%
“…It was proposed to be 7‐O‐rhamno‐acetylglucosyl diosmetin structure, science standards of these compounds were not available, we depend on the literature data of a compound with a near structure and defined as 7‐O‐(acetyl)‐pento‐hexosyl‐diosmetin (Ferreres and others 2006). Flavan 3‐ols in n ‐butanol fraction, according to their UV and mass spectral data, were identified as: catechin 7 , epicatechin 8 , epicatechin gallate 11, and epigallocatechin gallate 13 (Hye and others 2009; Hasslauer and others 2010; Long‐Ze and Harnly, 2010). The loss of 162 u (hexosyl radical) and 180 u (hexose + water) facilitated the identification of compound 9 and was confirmed by its UV spectra as ferulyl hexose (Ferreres and others 2006).…”
Section: Resultsmentioning
confidence: 99%