Browse > Article

GC-MS Analysis of Dyes Extracted from Turmeric  

Ahn Cheun-Soon (Department of Fashion & Industry, University of Incheon)
Obendorf S. Kay (Department of Textiles and Apparel, Cornell University)
Publication Information
Fibers and Polymers / v.7, no.2, 2006 , pp. 158-163 More about this Journal
Abstract
Standard extraction procedure for examining chromophoric substances of turmeric was investigated. Acetone and methanol were used as extracting solvents with different extraction procedures and pH levels. GC-MS analysis identified curcumene 2 (6.7 min), feruloylmethane 3 (8.3 min), coumaran 4 (6.09 min), vanillin 5 (6.2 min), and zingiberene 6 (10.5 min) as the major products. Curcumin 1 which has been known as the major chromophoric substance of turmeric was not detected in any samples. The maximum amount of curcumene 2, which was used as the fingerprint product for turmeric dye, was obtained by utilizing presoaking and decanting step with methanol prior to actual extraction step using a waterbath shaker (WMM). The highest relative abundance of curcumene 2 was detected in pH 6 sample followed by pH 5 indicating that the most appropriate pH level was in the range of pH 6-5.
Keywords
Turmeric; Curcumin; Curcumene; Dye extraction; GC-MS;
Citations & Related Records

Times Cited By Web Of Science : 1  (Related Records In Web of Science)
Times Cited By SCOPUS : 3
연도 인용수 순위
1 CambridgeSoft, 'The Merck Index', Merck & Co., N.J., 2001
2 P. C. Crews, Studies in Conservation, 32, 65 (1987)   DOI   ScienceOn
3 J. S. Jung and J. H. Sui, Journal ofthe Korean Society of Clothing and Textiles, 26(2), 325 (2002)
4 K. I. Priyadarsini, D. K. Maity, G. H. Naik, M. S. Kumar, M. K. Unnikrishnan, J. G. Satav, and H. Mohan, Free Radical Biology & Medicine, 35 (5), 475 (2003)   DOI   ScienceOn
5 K. I. Priyadarsini, Free Radical Biology & Medicine, 23(6),838 (1997)   DOI   ScienceOn
6 C. Ahn and S. K. Obendorf, Journal ofthe Korean Society of Clothing and Textiles, 27(11), 1350 (2003)
7 B. L. Ford, Studies in Conservation, 37, I (1992)   DOI   ScienceOn
8 Agilent Technologies, National Institute of Standards and Technology 98 Mass Spectral Libraries, NIST 98, Rev. D.02.00, 2000
9 Y. H. Lee and H. D. Kim, Fibers and Polymers, 5(4), 303 (2004)   DOI   ScienceOn
10 X. G. He, L. Z. Lin, L. Z. Lian, and M. Lindenmaier, Journal of Chromatography A, 818, 127 (1998)   DOI
11 S. Cho, H. Song, and B. Kim, Journal ofthe Korean Society of Clothing and Textiles, 21(6), 1051 (1997)
12 'Color Index', 3rd Ed., The Society of Dyers and Colourists, London, 1976
13 S. W.Nam, 'Natural Dyeing Class', Laboratory of Natural Dyeing, Sungkyunkwan University, Suwon, 1999
14 Y. C. Kim and K. S. Kim, 'Proceedings of the 2002 Joint Conference of the Korean Fiber Society and the Korean Society of Clothing and Textiles', pp.502-507, 2002
15 P. S. Negi, G. K. Jayaprakasha, L. Jagan Mohan Rao, and K. K. Sakariah, J. Agric. Food Chem., 47, 4297 (1999)   DOI   ScienceOn
16 C. Ahn and S. K. Obendorf, Text. Res. J.. 74(11), 949 (2004)   DOI   ScienceOn
17 E. K. Hwang, M. S. Kim, D. S. Lee, and K. B. Kim, J. Korean Fiber Soc., 35(8), 490 (1998)
18 R. Richmond and E. Pombo-Villar, Journal of Chromatography A, 760, 303 (1997)   DOI
19 D. Grosjean, P. M. Whitmore, P. D. Moor, G. R. Cass, and J. R. Druzik, Environ. Science and Technology, 22(11 ), 1357 (1988)   DOI   ScienceOn
20 Y. J. Chu and H. O. Soh, Journal ofthe Korean Society of Clothing and Textiles, 20(3),429 (1996)
21 Y. J. Wang, M. H. Pan, A. L. Cheng, L. I. Lin, Y. S. Ho, C. Y. Hsieh, and J. K. Lin, Journal of Pharmaceutical and Biomedical Analysis, 15, 1867 (1997)   DOI   ScienceOn