Sodium laurate

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Sodium laurate
Sodium laurate.svg
Names
Preferred IUPAC name
Sodium dodecanoate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.010.076 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 211-082-4
PubChem CID
RTECS number
  • OF0700000
UNII
  • InChI=1S/C12H24O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12(13)14;/h2-11H2,1H3,(H,13,14);/q;+1/p-1
    Key: BTURAGWYSMTVOW-UHFFFAOYSA-M
  • [Na+].[O-]C(=O)CCCCCCCCCCC
Properties
C12H23NaO2
Molar mass 222.304 g·mol−1
Density 1.102 g/ml [1]
Melting point 244 to 246 °C (471 to 475 °F; 517 to 519 K) [2]
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg
Danger
H315, H318, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Sodium laurate is a chemical compound with formula CH3(CH2)10CO2Na. As the sodium salt of a fatty acid (lauric acid), it is classified as a soap. It is a white solid.

Use

Sodium laurate is frequently used in bars of soap as an ingredient. Sodium laurate is also a permitted bleaching, washing and peeling agent.

Sodium Laurate has also been used to induce peripheral arterial disease in rats. [3]

Related Research Articles

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An acetate is a salt formed by the combination of acetic acid with a base. "Acetate" also describes the conjugate base or ion typically found in aqueous solution and written with the chemical formula C
2
H
3
O
2
. The neutral molecules formed by the combination of the acetate ion and a positive ion are also commonly called "acetates". The simplest of these is hydrogen acetate with corresponding salts, esters, and the polyatomic anion CH
3
CO
2
, or CH
3
COO
.

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Lauric acid, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids. It is a bright white, powdery solid with a faint odor of bay oil or soap. The salts and esters of lauric acid are known as laurates.

<span class="mw-page-title-main">Sodium chlorite</span> Chemical compound

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<span class="mw-page-title-main">Magnesium stearate</span> Chemical compound

Magnesium stearate is the chemical compound with the formula Mg(C
18
H
35
O
2
)
2
. It is a soap, consisting of salt containing two equivalents of stearate (the anion of stearic acid) and one magnesium cation (Mg2+). Magnesium stearate is a white, water-insoluble powder. Its applications exploit its softness, insolubility in many solvents, and low toxicity. It is used as a release agent and as a component or lubricant in the production of pharmaceuticals and cosmetics.

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Sodium bisulfite (or sodium bisulphite, sodium hydrogen sulfite) is a chemical mixture with the approximate chemical formula NaHSO3. Sodium bisulfite in fact is not a real compound, but a mixture of salts that dissolve in water to give solutions composed of sodium and bisulfite ions. It appears in form of white or yellowish-white crystals with an odor of sulfur dioxide. Regardless of its ill-defined nature, sodium bisulfite is used in many different industries such as a food additive with E number E222 in the food industry, a reducing agent in the cosmetic industry, and a decomposer of residual hypochlorite used in the bleaching industry.

Copper(II) laurate is an metal-organic compound with the chemical formula Cu(C
11
H
23
COO)
2
. It is classified as a metallic soap, i.e. a metal derivative of a fatty acid.

Cobalt laurate is an metal-organic compound with the chemical formula C
24
H
48
CoO
4
. It is classified as a metallic soap, i.e. a metal derivative of a fatty acid.

Manganese laurate is an metal-organic compound with the chemical formula C
24
H
48
MnO
4
. The compound is classified as a metallic soap, i.e. a metal derivative of a fatty acid.

Potassium laurate is a metal-organic compound with the chemical formula C
12
H
23
KO
2
. The compound is classified as a metallic soap, i.e. a metal derivative of a fatty acid.

References

  1. Pathak, K. D.; Journal of the Indian Chemical Society 1953, V30, P47-51
  2. Zacharie, Boulos; Organic Process Research & Development 2009, V13(3), P581-583
  3. Wang Z (2018-01-10). "Low molecular weight fucoidan ameliorates hindlimb ischemic injury in type 2 diabetic rats". Journal of Ethnopharmacology. 210: 434–442. doi:10.1016/j.jep.2017.09.014. PMID   28917976. S2CID   2299321.