2-hydroxyethyl stearate
Structural formula | |||||||||||||
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General | |||||||||||||
Surname | 2-hydroxyethyl stearate | ||||||||||||
other names |
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Molecular formula | C 20 H 40 O 3 | ||||||||||||
Brief description |
white to yellowish solid |
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properties | |||||||||||||
Molar mass | 328.53 g mol −1 | ||||||||||||
Physical state |
firmly |
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density |
0.96 g cm −3 |
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Melting point |
55-57 ° C |
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boiling point |
149 ° C |
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solubility | |||||||||||||
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 . |
2-Hydroxyethyl stearate is a chemical compound from the group of stearates .
Extraction and presentation
2-Hydroxyethyl stearate can also be obtained by reacting stearic acid and ethylene glycol or by their enzymatic esterification.
properties
2-Hydroxyethyl stearate is a white to yellowish, waxy solid that is practically insoluble in water and n -hexane .
use
2-Hydroxyethyl stearate is used as a surfactant and emollient (for example in cosmetics).
Individual evidence
- ↑ a b c d e Michael Ash: Handbook of Fillers, Extenders, and Diluents . Synapse Info Resources, 2007, ISBN 978-1-890595-96-8 , pp. 479 ( limited preview in Google Book search).
- ↑ a b c d e f g data sheet 2-Hydroxyethyl stearate, technical grade from Sigma-Aldrich , accessed on December 4, 2018 ( PDF ).
- ↑ Tsinghua Tongfang Knowledge Network Technology: Synthesis of Ethylene Glycol Monostearate with p-Toluene Sulphonic Acid as Catalyst - 《Fine and Specialty Chemicals》 2005 年 11 期 , accessed December 4, 2018
- ↑ Gabriela N. Pereira, Jefferson P. Holz a. a .: Solvent-Free Production of Ethylene Glycol Monostearate through Enzymatic Esterification. In: Industrial & Engineering Chemistry Research. 57, 2018, p. 6627, doi : 10.1021 / acs.iecr.7b05365 .
- ^ William Arthur Poucher: Perfumes, Cosmetics and Soaps Modern Cosmetics . Springer, 2013, ISBN 978-1-4899-3055-2 , pp. 117 ( limited preview in Google Book search).