Sodium stearate

Source: Wikipedia, the free encyclopedia.
Sodium stearate
Names
Preferred IUPAC name
Sodium octadecanoate
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
ECHA InfoCard
100.011.354 Edit this at Wikidata
EC Number
  • 212-490-5
UNII
  • InChI=1S/C18H36O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h2-17H2,1H3,(H,19,20);/q;+1/p-1 checkY
    Key: RYYKJJJTJZKILX-UHFFFAOYSA-M checkY
  • InChI=1/C18H36O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h2-17H2,1H3,(H,19,20);/q;+1/p-1
    Key: RYYKJJJTJZKILX-REWHXWOFAA
  • [Na+].[O-]C(=O)CCCCCCCCCCCCCCCCC
Properties
C18H35NaO2
Molar mass 306.466 g·mol−1
Appearance white solid
Odor slight, tallow-like odor
Density 1.02 g/cm3
Melting point 245 to 255 °C (473 to 491 °F; 518 to 528 K)
soluble
Solubility slightly soluble in
ethanediol
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Flash point 176 °C (349 °F; 449 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Sodium stearate (

food additives and food flavorings.[1]

Use

Having the characteristics of

hydrophobic parts, a carboxylate and a long hydrocarbon chain. These two chemically different components induce the formation of micelles, which present the hydrophilic heads outwards and their hydrophobic (hydrocarbon) tails inwards, providing a lipophilic environment for hydrophobic compounds. The tail part dissolves the grease or dirt and forms the micelle. It is also used in the pharmaceutical industry as a surfactant
to aid the solubility of hydrophobic compounds in the production of various mouth foams.

Production

Sodium stearate is produced as a major component of soap upon saponification of oils and fats. The percentage of the sodium stearate depends on the ingredient fats. Tallow is especially high in stearic acid content (as the triglyceride), whereas most fats only contain a few percent. The idealized equation for the formation of sodium stearate from stearin (the triglyceride of stearic acid) follows:

(C18H35O2)3C3H5 + 3 NaOH → C3H5(OH)3 + 3 C18H35O2Na

Purified sodium stearate can be made by neutralizing stearic acid with sodium hydroxide.

C17H35COOH+NaOH→C17H35COONa+H2O

References

External links