sodium palmitate

Product Information

Molecular Formula
C16H31NaO2
Molecular Weight
278.412
Description
sodium palmitate is commonly used to produce cosmetics, soaps and release agents.
Synonyms
Palmitic Acid Sodium Salt
IUPAC Name
sodiumhexadecanoate
Canonical SMILES
CCCCCCCCCCCCCCCC(=O)[O-].[Na+]
InChI
InChI=1S/C16H32O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18;/h2-15H2,1H3,(H,17,18);/q;+1/p-1
InChI Key
GGXKEBACDBNFAF-UHFFFAOYSA-M
Melting Point
283-290°C(lit.)
Flash Point
154.1°C
Purity
>97.0%(GC)(T)
Solubility
water, 33.32 mg/L @ 25 °C (est)
Appearance
White to Almost white powder to crystal
Application
Used as polymerization catalyst (synthetic rubbers) and emulsifier; Used in laundry and toilet soaps, detergents, cosmetics, pharmaceuticals, and printing inks.
Storage
2-8°C
Decomposition
When heated to decomposition it emits acrid smoke and irritating fumes.

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
14
Exact Mass
278.22217451 g/mol
Monoisotopic Mass
278.22217451 g/mol
Topological Polar Surface Area
40.1Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
184
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114177152-A Digoxin micro tablet and preparation method thereof 2021-12-16
CN-114045119-A Flexible acrylic acid foam adhesive tape 2021-12-07
CN-114146812-A Beneficiation method for recovering weighting agent of petroleum drilling 2021-11-30
CN-114058191-A Environment-friendly antioxidant master batch, preparation method thereof and rubber product 2021-11-06
CN-114010519-A A method for improving stability of p-hydroxyacetophenone in cosmetic composition 2021-11-05
CN-114129527-A Miniature tablet and preparation method and preparation thereof 2021-11-02
CN-114146059-A Levothyroxine sodium micro-tablet and preparation method and preparation thereof 2021-11-02
CN-114159397-A Oseltamivir phosphate micro-tablet and preparation method and preparation thereof 2021-11-02
CN-113930223-A PH-sensitive tackifier, preparation method and application thereof, plugging agent and drilling plugging method 2021-10-29
CN-113999543-A Preparation method of calcium-silicon core-shell structure nano calcium carbonate 2021-10-29

Literatures

PMID Publication Date Title Journal
36347319 2022-12-01 Isosilybin regulates lipogenesis and fatty acid oxidation via the AMPK/SREBP-1c/PPARα pathway Chemico-biological interactions
34968464 2022-02-15 Leptin and adiponectin synthesis and secretion in mature 3T3-L1 adipocytes are differentially down-regulated by arsenic and palmitic acid exposure throughout different stages of adipogenesis Life sciences
34774660 2022-01-15 Palmitate impairs the autophagic flux to induce p62-dependent apoptosis through the upregulation of CYLD in NRCMs Toxicology
34678374 2021-12-01 Carnosol alleviates nonalcoholic fatty liver disease by inhibiting mitochondrial dysfunction and apoptosis through targeting of PRDX3 Toxicology and applied pharmacology
33736254 2021-05-15 Combined effects of arsenic and palmitic acid on oxidative stress and lipid metabolism disorder in human hepatoma HepG2 cells The Science of the total environment
33604948 2021-05-01 Increased oxidative stress and mitochondrial impairments associated with increased expression of TNF-α and caspase-3 in palmitic acid-induced lipotoxicity in myoblasts Journal of biochemical and molecular toxicology
32347412 2021-02-01 Roles of acyl-CoA synthetase long-chain family member 5 and colony stimulating factor 2 in inhibition of palmitic or stearic acids in lung cancer cell proliferation and metabolism Cell biology and toxicology
32976987 2021-01-01 Palmitate exacerbates bisphenol A toxicity via induction of ER stress and mitochondrial dysfunction Biochimica et biophysica acta. Molecular and cell biology of lipids
34485530 2021-01-01 Morroniside Promotes PGC-1α-Mediated Cholesterol Efflux in Sodium Palmitate or High Glucose-Induced Mouse Renal Tubular Epithelial Cells BioMed research international
33236894 2020-12-21 A Proteomics- and Metabolomics-Based Study Revealed That Disorder of Palmitic Acid Metabolism by Aconitine Induces Cardiac Injury Chemical research in toxicology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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