Hexadecanoic acidHexadecanoic acid
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Hexadecanoic acid

Palmitic acid; C16:0 Fatty acid

This high purity fatty acid is ideal as a standard and for biological studies. Hexadecanoic acid is considered the most abundant saturated fatty acid in nature comprising 20-30% of the lipids in many animal tissues. Palmitic acid has been found to cause reduced insulin activity due to its mediation of PKC-θ activation in the central nervous system.{50520} During the metabolism of hexadecanoic acid it is converted to the omegahydroxy hexadecanoic acid and then to the dicarboxylic hexadecanedioc acid. Long chain fatty acids have been found to inhibit the double-stranded DNA binding activity of p53 DNA binding domain suggesting that fatty acids in the cell membrane might regulate the activity of p53 for cell division, cell-cycle checkpoint, and tumor suppression.{31533} Saturated fatty acids, such as palmitic acid, induce apoptosis in beta-cells which can lead to the development of diabetes.{50521} Long chain fatty acids acylated to sphingolipids are critical in many biological functions and substantial amounts are found to be amide-linked to the long-chain sphingoid base sphinganine, forming a ceramide, which constitutes the lipid backbone of sphingomyelin and other sphingolipids. Long chain fatty acids can often be found in esterified linkages with cholesterol, gangliosides, galactocerebrosides, sphingomyelin, and phosphatidylcholine. Hexadecanoic acid, as a saturated fatty acid, has been found to cause moderate risk of coronary heart disease as compared with polyunsaturated fatty acids but does not change the total cholesterol/high density lipoprotein-cholesterol ratio as compared with carbohydrates.{50456} Saturated fatty acids can also lead to the development of atherosclerosis in obesity and type 2 diabetes.
Cat# Size Price Qty Buy
1014 1 gram £53.55

Additional Information

Property Value or Rating
Product Size 1 gram
Manufacturer Matreya, LLC
Empirical Formula C16H32O2
CAS# 57-10-3
Formula Weight 256.4
Solvent none
Source natural
Purity 99%
Analytical Methods GC, TLC
Natural Source Plant
Solubility chloroform, ethanol, ethyl ether
Physical Appearance A neat solid
Storage room temperature
References

1. S. Benoit et al. “Palmitic acid mediates hypothalamic insulin resistance by altering PKC- subcellular localization in rodents” Journal of Clinical Investigation, vol. 119 pp. 2577-2589, 2009 
2. H. Iijima et al. “The Inhibitory Action of Long-Chain Fatty Acids on the DNA Binding Activity of p53” Lipids, vol. 41 pp. 521-527, 2006 
3. H. Liang et al. “Palmitic acid-induced apoptosis in pancreatic -cells is increased by liver X receptor agonist and attenuated by eicosapentaenoate” In Vivo, vol. 25 pp. 711-718, 2011 
4. R. Micha and D. Mozaffarian “Saturated Fat and Cardiometabolic Risk Factors, Coronary Heart Disease, Stroke, and Diabetes: a Fresh Look at the Evidence” Lipids, vol. 45 pp. 893-905, 2010

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