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Contents

   



(Top)
 


1 Use  





2 Production  





3 References  





4 External links  














Sodium stearate






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Sodium stearate
Names
Preferred IUPAC name

Sodium octadecanoate

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChemSpider
ECHA InfoCard 100.011.354 Edit this at Wikidata
EC Number
  • 212-490-5

PubChem CID

UNII

CompTox Dashboard (EPA)

  • 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

Chemical formula

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)

Solubility in water

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).

☒N verify (what is checkY☒N ?)

Infobox references

Sodium stearate (IUPAC: Sodium Octadecanoate) is the sodium saltofstearic acid. This white solid is the most common soap. It is found in many types of solid deodorants, rubbers, latex paints, and inks. It is also a component of some food additives and food flavorings.[1]

Use[edit]

Having the characteristics of soaps, sodium stearate has both hydrophilic and 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[edit]

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[edit]

  1. ^ Klaus Schumann, Kurt Siekmann, "Soaps" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a24_247

External links[edit]


Retrieved from "https://en.wikipedia.org/w/index.php?title=Sodium_stearate&oldid=1214641418"

Categories: 
Organic sodium salts
Stearates
Soaps
Anionic surfactants
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This page was last edited on 20 March 2024, at 06:26 (UTC).

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