Harman Patil (Editor)

Lauric acid

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Related compounds
  
Glyceryl laurate

Melting point
  
43.2 °C

Boiling point
  
298.9 °C

Appearance
  
White powder

Formula
  
C12H24O2

Molar mass
  
200.3178 g/mol

Density
  
880 kg/m³

Lauric acid wwwchemfacescomstructuralLauricacidCFN90493jpg

Coconut oil the benefits of lauric acid health hacks thomas delauer


Lauric acid or systematically, dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus falling into the medium chain fatty acids, is a white, powdery solid with a faint odor of baby oil or soap. The salts and esters of lauric acid are known as laurates.

Contents

Lauric acid coconut oil 1


Occurrence

Lauric acid, as a component of triglycerides, comprises about half of the fatty acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil), Otherwise, it is relatively uncommon. It is also found in human breast milk (6.2% of total fat), cow's milk (2.9%), and goat's milk (3.1%).

In various plants

  • The palm tree Orbignya phalerata Mart, a species popularly known in Brazil as babassu - 50% in babassu oil.
  • Attalea cohune, the cohune palm (also rain tree, American oil palm, corozo palm or manaca palm) - 46.5% in cohune oil.
  • Astrocaryum murumuru (Arecaceae) a palm native to the Amazon - 47.5% in "murumuru butter".
  • Coconut oil 49%
  • Pycnanthus kombo (African nutmeg)
  • Virola surinamensis (wild nutmeg) 7.8–11.5%
  • Peach palm seed 10.4%
  • Betel nut 9%
  • Date palm seed 0.56–5.4%
  • Macadamia nut 0.072–1.1%
  • Plum 0.35–0.38%
  • Watermelon seed 0.33%
  • Citrullus lanatus (egusi melon)
  • Pumpkin flower 205 ppm, pumpkin seed 472 ppm
  • Properties

    Like many other fatty acids, lauric acid is inexpensive, has a long shelf-life, is non-toxic and is safe to handle. It is used mainly for the production of soaps and cosmetics. For these purposes, lauric acid is reacted with sodium hydroxide to give sodium laurate, which is a soap. Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil. These precursors give mixtures of sodium laurate and other soaps.

    Niche uses

    In the laboratory, lauric acid may be used to investigate the molar mass of an unknown substance via the freezing-point depression. The choice of lauric acid is convenient because the melting point of the pure compound is relatively high (43.8 °C). Its cryoscopic constant is 3.9 °C·kg/mol. By melting lauric acid with the unknown substance, allowing it to cool, and recording the temperature at which the mixture freezes, the molar mass of the unknown compound may be determined.

    Potential medicinal properties

    In vitro experiments have suggested that some fatty acids including lauric acid could be a useful component in a treatment for acne, but no clinical trials have yet been conducted to evaluate this potential benefit in humans.

    Lauric acid increases total serum cholesterol more than many other fatty acids. But most of the increase is attributable to an increase in high-density lipoprotein (HDL) (the "good" blood cholesterol). As a result, lauric acid has been characterized as having "a more favorable effect on total HDL cholesterol than any other fatty acid [examined], either saturated or unsaturated". In general, a lower total/HDL serum cholesterol ratio correlates with a decrease in atherosclerotic risk. Nonetheless, an extensive meta-analysis on foods affecting the total/LDL serum cholesterol ratio found in 2003 that the net effects of lauric acid on coronary artery disease outcomes remained uncertain.

    References

    Lauric acid Wikipedia