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Lauric acid
Laurostearic acid, Vulvic acid, 1-Undecanecarboxylic acid, Duodecylic acid, C12:0 (Lipid numbers) 0.8744 g/cm3 (41.5 °C) 0.8679 g/cm3 (50 °C) 282.5 C at 512 mmHg 225.1 C at 100 mmHg 5.37 cP (60 °C) 1.4183 (82 °C) 55 mg/L (20 °C) 63 mg/L (30 °C) 72 mg/L (45 °C) 83 mg/L (100 °C) 0.42 kPa (150 °C) 6.67 kPa (210 °C) 120 g/100 g (20 °C) 2250 g/100 g (40 °C) 60.5 g/100 g (20 °C) 1590 g/100 g (40 °C) 52 g/100 g (20°C) 1250 g/100 g (40°C) 97 g/100 g (20°C) 1410 g/100 g (40°C) 0.1921 W/m·K (72.5 °C) 0.1748 W/m·K (106 °C) P, No. 2 (γ-form) (γ-form) 7425.8 kJ/mol (292 K) | NFPA-H = 1 | NFPA-F = 1 | NFPA-R = 1 | NFPA-S = Tridecanoic acid Dodecanol Dodecanal Sodium lauryl sulfate Lauric acid, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids. It is a bright white, powdery solid with a faint odor of bay oil or soap. The salts and esters of lauric acid are known as laurates. Lauric acid accounts for nearly half of the fat in coconut oil and palm kernel oil.
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 Attalea speciosa, a species 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 47-49%
- 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%
- Viburnum opulus 0.24-0.33%
- Citrullus lanatus (egusi melon)
- Pumpkin flower 205 ppm, pumpkin seed 472 ppm
Insect
- Black soldier fly Hermetia illucens 30–50 mg/100 mg fat.
Uses
Like many other fatty acids, lauric acid is inexpensive, has a long shelf-life, is nontoxic, 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.
Lauric acid is a precursor to dilauroyl peroxide, a commercial initiator of polymerizations.
Production and reactions
Lauric acid is mainly isolated from natural sources. It transesterifies with vinyl acetate. Treatment with sulfur trioxide gives the α-sulfonic acid.
As a dietary fat and cardiovascular risk factor
Lauric acid increases total serum lipoproteins more than many other fatty acids, including LDL and high-density lipoprotein (HDL), making it a risk factor for cardiovascular diseases. Lauric acid has been characterized as having "a more favorable effect on total HDL than any other fatty acid [examined], either saturated or unsaturated", which may favor a lower cardiovascular disease risk. However, given the prominence of lauric acid in palm kernel and coconut oil (about 47% of total fat), replacing dietary coconut oil and its high lauric acid content with oils containing mostly unsaturated fats would alter total blood lipids in a way that reduces cardiovascular disease risk.
Although 95% of medium-chain triglycerides are absorbed through the portal vein, only 25–30% of lauric acid is absorbed through this vein.
References
References
- {{CRC90
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- (1952). "Solubilities of inorganic and organic compounds". D. Van Nostrand Company.
- {{PubChemLink. 3893
- (2000). "Engineering data on mixing". Elsevier Science B.V..
- Sydow, Erik von. (1956). "On the structure of the crystal form A of lauric acid". Acta Chemica Scandinavica.
- (1951). "The crystal structure of lauric acid". Acta Crystallographica.
- {{nist
- {{Sigma-Aldrich
- (2001). "Lexicon of lipid nutrition (IUPAC Technical Report)". Pure and Applied Chemistry.
- David J. Anneken, Sabine Both, Ralf Christoph, Georg Fieg, Udo Steinberner, Alfred Westfechtel "Fatty Acids" in Ullmann's Encyclopedia of Industrial Chemistry 2006, Wiley-VCH, Weinheim. {{doi. 10.1002/14356007.a10_245.pub2
- Dijkstra, D.J.. (2015). "Lauric Oils".
- Amri, Ibrahim Nuzul. (2011). "Vegetable Oils in Food Technology: Composition, Properties and Uses".
- (2019). "Variation in volatile and fatty acid contents among Viburnum opulus L. Fruits growing different locations". Scientia Horticulturae.
- (2019). "Black soldier fly (Hermetia illucens L.): effect on the fat integrity using different approaches to the killing of the prepupae.". Journal of Insects as Food and Feed.
- J. C. Sauer. (1951). "Laurone". Organic Syntheses.
- (1950). "Vinyl Laurate and Other Vinyl Esters". Organic Syntheses.
- (1956). "α-Sulfopalmitic Acid". Organic Syntheses.
- (2016). "Coconut oil consumption and cardiovascular risk factors in humans". [[Nutrition Reviews]].
- (May 2003). "Effects of dietary fatty acids and carbohydrates on the ratio of serum total to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials". American Journal of Clinical Nutrition.
- 978-3-540-22569-0.
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