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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