ISOLATION AND IDENTIFICATION OF FLAVONOID COMPOUND EXTRACTIRE ETHYL ACETATE FRACTION EXTRACTED FROM THE RHIZOMES FINGERROOT OF (Boesenbergia pandurata (Roxb.) Schlecht) (Zingiberaceae)
Ochtavia Prima Sari(1*), Titik Taufiqurrohmah(2)
(1) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Surabaya State University, Jl. Ketintang Surabaya 60231
(2) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Surabaya State University, Jl. Ketintang Surabaya 60231
(*) Corresponding Author
Abstract
Boesenbergia pandurata (Roxb.) Schlecht is one of fingerroot plant in ginger family (Zingiberaceae). The rhizomes of the plant contained a lot of secondary metabolites compounds. Therefore, the purpose of the research is to isolate and identify the flavonoid compound from the plant. The rhizomes were extracted with metanol continued by partition using ethyl acetate-water (1:1). The ethyl acetate extract was chromatographed on a column of Si gel (Vacuum Liquid Chromatography and Gravitation Column Chromatography) using n-hexane-ethyl acetate (5:2) as eluents. Further purification by recristalization using benzene produced a compound as yellow powder (16 mg) having melting point of 294-295 oC. The spectra of isolated compound were determined by spectroscopic UV-Vis, FT-IR, and GC-MS. Spectrum UV-Vis of the isolated compound showed ultraviolet absorption at λmax (MeOH, nm) 290 and 322; λmax (MeOH+NaOH, nm) 322; λmax (MeOH+AlCl3, nm) 309; λmax (MeOH+AlCl3+HCl, nm) 310; λmax (MeOH+NaOAc, nm) 322 and λmax (MeOH+NaOAc+H3BO3, nm) 290. Its FT-IR spectrum represented a number of absorption lied on νmax (cm-1) : 3142.5; 3012.6; 2893; 2345.3; 1631.7; 1585.4; 1357.8; 1168.8; and 825.5. GC-MS spectrum of the isolated compound exhibited an [M]+ ion peak at m/z = 256 with retention time of 22,579. Based on the results of spectrum analysis it can be concluded that the compound is 5,7-dyhydroxyflavanone.
Keywords
Full Text:
Full Text PdfReferences
[1] Muhlisah, F., 1999, Temu – temuan dan Empon – emponan, Kanisus Yogyakarta.
[2] Trakoontivakorn, G., 2001, J. Agric Food Chem. 49, 3046-3050.
[3] Johansah, S., 2002, Perbandingan Reaksi Demitilasi Pinostrobin Hasil Isolasi Rimpang Temu Kunci (Boesenbergia pandurata) Dengan Pereaksi HBr dan Lil-KOlidina Serta Asetilasi dan Benzoilasi PInocembrin Hasil Reaks, Tesis, Universitas Airlangga Surabaya.
[4] Jaipetch, T., 1982, Phytochem., 22.
[5] Soegihardjo, C. J. 1984. Pemeriksaan Kandungan Flavonoid Dan Daya Antihepatotoksik Dari (Sonchus oleraceus L). 167.205.4.4/go.php?id= bptitbpp-gdl=S3-1984.cjsoegihar-1735-29k.
[6] Mulianingsih, L. 2004. Turunan Flavonoid Dari Nicolaia Speciosa Horan. 167.205.4.4/go.php?id= 2bptitbpp-gdl-52-2004-limulini-1734-26k.
[7] Achmad, S. A., 1986, Kimia Organik Bahan Alam. Modul 4-6, Karunia Universitas Terbuka Jakarta
[8] Markham, K.R., 1988, Cara Mengidentifikasi Flavonoid : Penerbit ITB Bandung.
[9] Mulja, M., Suharman. 1995, Analisa Instrumental, Airlangga University Press, Surabaya.
[10] Nekrasov, V.V., 1978, Practical Organic Chemistry. Second edition, MIR Publisher Moscow.
[11] Robinson, T. 1995, Kandungan Organik Tumbuhan Tinggi, ITB Bandung.
DOI: https://doi.org/10.22146/ijc.21764
Article Metrics
Abstract views : 6129 | views : 34798Copyright (c) 2010 Indonesian Journal of Chemistry
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.
View The Statistics of Indones. J. Chem.