Zingerone

Zingerone, also called vanillylacetone, is thought by some to be a key component of the pungency of ginger, but imparts the "sweet" flavor of cooked ginger.[1] Zingerone is a crystalline solid that is sparingly soluble in water and soluble in ether. When synthesized and tasted does not have any pungency, suggesting it is more likely that zingerone is a decomposition product of, rather than the direct source of, the pungency of ginger.[2]

Zingerone
Names
IUPAC name
4-(4-hydroxy-3-methoxyphenyl)-butan-2-one
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.136
UNII
Properties
C11H14O3
Molar mass 194.22 g/mol
Melting point 40 to 41 °C (104 to 106 °F; 313 to 314 K)
Boiling point 187 to 188 °C (369 to 370 °F; 460 to 461 K) at 14 mmHg
Insoluble
Solubility Miscible in ether
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Zingerone is similar in chemical structure to other flavor chemicals such as vanillin and eugenol. It is used as a flavor additive in spice oils and in perfumery to introduce spicy aromas.

Fresh ginger does not contain zingerone, but it is produced by cooking or drying of the ginger root, which causes a reverse aldol reaction on gingerol.

Production

History

Zingerone was first isolated from the ginger root in 1917 by Hiroshi Nomura, a chemistry professor at Tokyo Imperial University.[3] Nomura named the compound and identified the empirical formula of zingerone in his studies at the laboratory of the Agricultural College.

Current methods

Nomura identified and later patented a method for the synthesis of zingerone, in which vanillin and acetone are reacted under basic conditions to form dehydrozingerone. This compound is obtained in about 95% quantity.[4] This reaction is followed by catalytic hydrogenation of the intermediate compound in order to form zingerone, obtained in approximately 100% quantity.[5]

Biological effects

Ginger compounds have been shown to be active against enterotoxigenic Escherichia coli heat-labile enterotoxin-induced diarrhea. This type of diarrhea is the leading cause of infant death in developing countries. Zingerone is likely the active constituent responsible for the antidiarrheal efficacy of ginger.[6]

Zingerone is recognized as being a particularly efficient free radical scavenger. It is able to scavenge and degrade free radicals and reactive oxygen species in the body, and inhibits enzymes involved in the generation of these reactive oxygen species.[7]

It is used by some flowers to attract pollinating fruit flies by mimicking the sex pheremone of the fly [8]

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References
  1. Monge, P; Scheline, R; Solheim, E (1976). "The metabolism of zingerone, a pungent principle of ginger". Xenobiotica. 6 (7): 411–23. doi:10.3109/00498257609151654. PMID 997589.
  2. Steffen Arctander, Perfume and Flavor Materials of Natural Origin, pg. 280
  3. Nomura, Hiroshi (1917). "The pungent principles of ginger. Part I. A new ketone, zingerone (4-hydroxy-3-methoxyphenylethyl methyl ketone) occurring in ginger". Journal of the Chemical Society, Transactions. 111: 769–776. doi:10.1039/ct9171100769.
  4. Wu, Anxin; Wang, Zihua; Yin, Guodong; Qin, Jing; Gao, Meng; Cao, Liping (2008). "An Efficient Method for the Selective Iodination of α,β-Unsaturated Ketones". Synthesis. 2008 (22): 3675–3681. doi:10.1055/s-0028-1083200.
  5. Nomura, Hiroshi. "Method of preparing 'zingerone' (methyl-3-methoxy-4-hydroxyphenyl-ethyl ketone." U.S. Patent 1,263,796. Issued April 23, 1918.
  6. Chen, Jaw-Chyun; Li-Jiau Huang; Shih-Lu Wu; Sheng-Chu Kuo; Tin-Yun Ho; Chien-Yun Hsiang (2007). "Ginger and Its Bioactive Component Inhibit Enterotoxigenic Escherichia coli Heat-Labile Enterotoxin-Induced Diarrhea in Mice". Journal of Agricultural and Food Chemistry. 55 (21): 8390–7. doi:10.1021/jf071460f. PMID 17880155.
  7. Rajan, Iyappan; Narayanan, Nithya; Rabindran, Remitha; Jayasree, P. R.; Kumar, P. R. Manish (2013-12-01). "Zingerone Protects Against Stannous Chloride-Induced and Hydrogen Peroxide-Induced Oxidative DNA Damage In Vitro". Biological Trace Element Research. 155 (3): 455–459. doi:10.1007/s12011-013-9801-x. ISSN 0163-4984. PMID 24006104.
  8. Tan, Keng-hong; Nishida, Ritsuo (2000). "[No title found]". Journal of Chemical Ecology. 26 (2): 533–546. doi:10.1023/A:1005477926244.
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