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PALMITIC ACID SODIUM SALT

  • CasNo:408-35-5

Product Description

Factory supply PALMITIC ACID SODIUM SALT 408-35-5 with low price

  • Molecular Formula: C16H32NaO2
  • Molecular Weight: 278.411
  • Appearance/Colour: white powder 
  • Melting Point: 283-290 °C(lit.) 
  • Boiling Point: 340.6 °C at 760 mmHg 
  • Flash Point: 154.1 °C 
  • PSA: 40.13000 
  • LogP: 4.21760 

PALMITIC ACID SODIUM SALT(Cas 408-35-5) Usage

Hazard

A poison. Combustible.

Biochem/physiol Actions

Sodium palmitate is the sodium salt of palmitic acid, a component in hard soaps. Palmitic acid is a common saturated fatty acid and produced during fatty acid synthesis. Sodium palmitate enhances lipogenesis, cellular steatosis in various cell lines. Palmitate induces cell death in human epidermal growth factor receptor 2 (HER2)/neu-positive cells and breast cancer cell lines like MCF-7 due to enhanced fatty acid accumulation. Sodium palmitate induces lipoapoptosis in L02 and HepG2 liver cells by inducing glycogen synthase kinase-3β (GSK3β) expression.

Safety Profile

A poison by intravenous route. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

It crystallises from EtOH and is dried in an oven. [Beilstein 2 IV 1157.]

InChI:InChI=1/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);

408-35-5 Relevant articles

Micellar Dynamics and Organization. A Multifield 13C NMR Spin-Lattice Relaxation and /1H/13C Nuclear Overhauser Effect Study

Walderhaug, Harald,Soederman, Olle,Stilbs, Peter

, p. 1655 - 1662 (1984)

An extensive 13C spin-relaxation study i...

The salts of fatty acids as precursors for preparation of silver nanoparticles in organic solvents

Glushko,Anisimova,Blokhina

, p. 1759 - 1764 (2016/10/24)

The silver salts of fatty acids were stu...

Photolysis of phenacyl esters in a two-phase system

Ruzicka, Radovan,Zabadal, Miroslav,Klan, Petr

, p. 2581 - 2590 (2007/10/03)

Phenacyl esters are useful photoremovabl...

Salt effects on solvolysis reactions of p-nitrophenyl alkanoates catalyzed by 4-(dialkylamino)pyridine-functionalized polymer in buffered water and aqueous methanol solutions

Wang, Guang-Jia,Ye, Donghao,Fife, Wilmer K.

, p. 12536 - 12540 (2007/10/03)

Specific salting-in effects that lead to...

408-35-5 Process route

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

sodium palmitate
408-35-5

sodium palmitate

Conditions
Conditions Yield
With sodium hydroxide; In water; at 60 - 80 ℃;
91%
With potassium ethoxide; In ethanol;
p-toluenesulfonic acid

p-toluenesulfonic acid

8-chloro-11-[4-(2-ethoxyethanol)-1-piperazinyl]-5H-dibenzo[b,e][1,4]diazepine

8-chloro-11-[4-(2-ethoxyethanol)-1-piperazinyl]-5H-dibenzo[b,e][1,4]diazepine

sodium carbonate
497-19-8

sodium carbonate

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

sodium palmitate
408-35-5

sodium palmitate

hexadecanoic acid 2-{2-[4-(8-chloro-5<i>H</i>-dibenzo[<i>b</i>,<i>e</i>][1,4]diazepin-11-yl)-piperazin-1-yl]-ethoxy}-ethyl ester
68465-70-3

hexadecanoic acid 2-{2-[4-(8-chloro-5H -dibenzo[b ,e ][1,4]diazepin-11-yl)-piperazin-1-yl]-ethoxy}-ethyl ester

Conditions
Conditions Yield
In 5,5-dimethyl-1,3-cyclohexadiene;

408-35-5 Upstream products

  • 141-53-7
    141-53-7

    sodium formate

  • 57-10-3
    57-10-3

    1-hexadecylcarboxylic acid

  • 1492-30-4
    1492-30-4

    4-nitrophenyl palmitate

  • 477218-70-5
    477218-70-5

    2,5-dimethylphenacyl palmitate

408-35-5 Downstream products

  • 502-52-3
    502-52-3

    hexadecanoic acid, 2-hydroxy-1,3-propanediyl ester

  • 555-44-2
    555-44-2

    glyceroltripalmitate

  • 502-73-8
    502-73-8

    palmitone

  • 623-65-4
    623-65-4

    palmitic anhydride

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