Monolaurin

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Monolaurin
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Names
IUPAC name
Dodecanoic acid 2,3-dihydroxypropyl ester
Other names
Glyceryl laurate; Monolauroylglycerin; Glycerol monolaurate
Identifiers
27215-38-9 YesY
ChEMBL ChEMBL510533 YesY
ChemSpider 14181 YesY
Jmol 3D model Interactive image
PubChem 14871
UNII Y98611C087 YesY
  • InChI=1S/C15H30O4/c1-2-3-4-5-6-7-8-9-10-11-15(18)19-13-14(17)12-16/h14,16-17H,2-13H2,1H3 YesY
    Key: ARIWANIATODDMH-UHFFFAOYSA-N YesY
  • InChI=1/C15H30O4/c1-2-3-4-5-6-7-8-9-10-11-15(18)19-13-14(17)12-16/h14,16-17H,2-13H2,1H3
    Key: ARIWANIATODDMH-UHFFFAOYAD
  • O=C(OCC(O)CO)CCCCCCCCCCC
Properties
C15H30O4
Molar mass 274.40 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Monolaurin, also known as glycerol monolaurate, glyceryl laurate or 1-Lauroyl-glycerol, is a monoglyceride. It is the mono-ester formed from glycerol and lauric acid. Its chemical formula is C15H30O4.

Uses

Monolaurin is most commonly used as a surfactant in cosmetics, such as deodorants. As a food additive it is also used as an emulsifier.

Occurrence

Monolaurin is found in coconut oil and may be similar to other monoglycerides found in human breast milk.[1]

Pharmacology

Monolaurin has antibacterial, antiviral, and other antimicrobial effects in vitro.[2][3][4][5][6][7] It may therefore be useful in the treatment or prevention of various infections, but its clinical usefulness has not been established.

References

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