Chemistry:Hydroxylated lecithin
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| IUPAC name
[3-[(9R,10R)-9,10-dihydroxyoctadecanoyl]oxy-2-octadecanoyloxy-propyl] 2-(trimethylammonio)ethyl phosphate
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C44H88NO10P | |
| Molar mass | 822.159 g·mol−1 |
| Appearance | yellow-orange viscous liquid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Hydroxylated lecithin is chemically modified lecithin. It is made by treating lecithin with hydrogen peroxide and an organic acid such as acetic or lactic acid.[1] In the process, some of the organic acid becomes peroxy acid. The peroxy acid reacts with olefins in the fatty acid side chains creating intermediate epoxides. The epoxides react further with water, organic acid, or peroxy acid, to ultimately form vicinal diols. Because the natural fatty acid olefins have (Z)-configurations, the resulting vicinal diols have anti stereochemical configurations.
Fatty acids with hydroxyl groups on their hydrophobic tails are rare in nature. Compare hydroxylated lecithin to castor oil, which has 3 hydroxylated fatty acid chains in it. Hydroxyl groups give these oils unique polar properties that make them useful in a variety of applications, including cosmetics, pharmaceuticals, and foods.[2]
Synthesis
References
- ↑ F. D. Gunstone; John L. Harwood; Albert J. Dijkstra (2007). The Lipid Handbook. Boca Raton, FL: CRC Press. pp. 319–320. ISBN 978-0-8493-9688-5.
- ↑ "21 CFR 172.814". US Code of Federal Regulations. http://edocket.access.gpo.gov/cfr_2002/aprqtr/pdf/21cfr172.816.pdf. Retrieved 25 March 2011.
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