Palmitic acid ethyl ester
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Palmitic acid ethyl ester | ||||||||||||||||||
other names |
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Molecular formula | C 18 H 36 O 2 | ||||||||||||||||||
Brief description |
white odorless mass or liquid |
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properties | |||||||||||||||||||
Molar mass | 284.48 g mol −1 | ||||||||||||||||||
Physical state |
liquid or solid, depending on the room temperature |
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density |
0.86 g cm −3 |
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Melting point |
24-26 ° C |
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boiling point |
192–194 ° C (13 hPa) |
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solubility |
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Refractive index |
1.440 (20 ° C) |
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safety instructions | |||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
Palmitic acid ethyl ester is a chemical compound from the group of fatty acid esters .
Occurrence
Ethyl palmitate is one of the major volatile compounds found in cooked rice , wine, and Luzhou raw liquor (and other brandies ). It occurs naturally in licorice root and chamomile .
Extraction and presentation
Palmitic acid ethyl ester can be obtained by passing hydrogen chloride through an alcoholic solution of palmitic acid .
properties
Palmitic acid ethyl ester is a flammable, hardly flammable, deliquescent, white and odorless solid mass, which melts at a slightly elevated temperature and which is practically insoluble in water. The compound decomposes above 300 ° C. It occurs in two forms that have a melting point of 19 ° C and 24 ° C.
use
Palmitic acid ethyl ester is used in the production of pharmaceutical creams, ointments, skin and hair oils. It acts as a lubricant on the surface of the skin to keep it soft and smooth. The detection of ethyl myristate , ethyl palmitate, ethyl oleate and ethyl stearate in human hair is determined in medicine as a marker for excessive alcohol consumption .
Individual evidence
- ↑ a b c d e f g h i Entry on ethyl palmitate in the GESTIS substance database of the IFA , accessed on December 17, 2018(JavaScript required) .
- ↑ a b Data sheet Ethyl palmitate, 97% from AlfaAesar, accessed on December 19, 2018 ( PDF )(JavaScript required) .
- ↑ a b Data sheet Ethyl palmitate, ≥95%, FG from Sigma-Aldrich , accessed on December 17, 2018 ( PDF ).
- ↑ Hans-Dieter Belitz, Werner Grosch: Textbook of food chemistry . Springer-Verlag, 2013, ISBN 978-3-662-08308-6 , pp. 743 ( limited preview in Google Book search).
- ↑ H.-D. Belitz, W. Grosch: Textbook of food chemistry . Springer-Verlag, 2013, ISBN 978-3-662-08306-2 , pp. 697 ( limited preview in Google Book search).
- ↑ George Fownes: A Manual of Elementary Chemistry, Theoretical and Practical From the 10th Revised and Corrected English Ed . HC Lea, 1870, p. 622 ( limited preview in Google Book search).
- ↑ a b Entry on ethyl palmitate. In: Römpp Online . Georg Thieme Verlag, accessed on December 19, 2018.
- ↑ Axel M. Gressner, Torsten Arndt: Lexicon of Medical Laboratory Diagnostics . Springer-Verlag, 2013, ISBN 978-3-642-12921-6 , pp. 480 ( limited preview in Google Book Search).