Glycerol monostearate

Glycerol monostearate
Identifiers
CAS number 123-94-4 Y,  (pure grade)[1]
11099-07-3 (crude grade)[1]
31566-31-1 (generic)[1]
85666-92-8 (generic)[1]
85251-77-0 (glycerides, C16-18 mono- and di-)
ChemSpider 23095 Y
KEGG D01947 Y
ChEMBL CHEMBL255696 Y
Jmol-3D images Image 1
Properties
Molecular formula C21H42O4
Molar mass 358.57 g/mol
Appearance white, yellowish
Density 0.97
Melting point

58–59 °C (136–138 °F)

Boiling point

238–240 °C (460–464 °F)

Solubility in water Soluble in hot ethanol, diethyl ether, benzene, acetone, mineral or fixed oils, insoluble in water
Hazards
Flash point 230 °C (446 °F) (open cup)
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Glycerol monostearate, commonly known as GMS, is an organic molecule used as an emulsifier.[2] GMS is a colorless, odorless, and sweet-tasting flaky powder that is hygroscopic. It is a glycerol ester of stearic acid. It occurs naturally in the body as a by-product of the breakdown of fats, and is also found in fatty foods.

GMS is a food additive used as a thickening, emulsifying, anti-caking, and preservative agent; an emulsifying agent for oils, waxes, and solvents; a protective coating for hygroscopic powders; a solidifier and control release agent in pharmaceuticals; and a resin lubricant. It is also used in cosmetics and hair care products.[3] GMS is largely used in baking preparations to add "body" to the food. It is responsible for giving ice cream and whipped cream its smooth texture.

Compendial status

References

  1. ^ a b c d Ash, Michael; Ash, Irene (2004). Handbook of Preservatives. Synapse Information Resources. p. 404. ISBN 1890595667. http://books.google.com/books?id=XZ2QB7bu5LwC&pg=PA404. Retrieved 2008-11-06. 
  2. ^ Jens Birk Lauridsen (1976). "Food emulsifiers: Surface activity, edibility, manufacture, composition, and application". Journal of the American Oil Chemists' Society 53 (6): 400–407. doi:10.1007/BF02605731. 
  3. ^ Glycerol monostearate Cheminfo
  4. ^ The British Pharmacopoeia Secretariat (2009). "Index, BP 2009". http://www.pharmacopoeia.co.uk/pdf/2009_index.pdf. Retrieved 18 March 2010.