Glycerol monostearate explained

Glycerol monostearate should not be confused with glycol monostearate.

Glycerol monostearate, commonly known as GMS, is a monoglyceride commonly used as an emulsifier in foods.[1] It takes the form of a white, odorless, and sweet-tasting flaky powder that is hygroscopic. Chemically it is the glycerol ester of stearic acid. It is also used as hydration powder in exercise formulas

Structure, synthesis, and occurrence

Glycerol monostearate exists as three stereoisomers, the enantiomeric pair of 1-glycerol monostearate and 2-glycerol monostearate. Typically these are encountered as a mixture as many of their properties are similar.

Commercial material used in foods is produced industrially by a glycerolysis reaction between triglycerides (from either vegetable or animal fats) and glycerol.[2]

Glycerol monostearate occurs naturally in the body as a product of the breakdown of fats by pancreatic lipase. It is present at very low levels in certain seed oils.

Uses

GMS is a food additive used as a thickening, emulsifying, anticaking, 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 somewhat responsible for giving ice cream and whipped cream their smooth texture. It is sometimes used as an antistaling agent in bread.

It can also be used as an additive in plastic, where GMS works as an antistatic and antifogging agent. This is common in food packaging.

See also

Compendial status

Notes and References

  1. Food emulsifiers: Surface activity, edibility, manufacture, composition, and application . Journal of the American Oil Chemists' Society . 53 . 6 . 1976 . 400–407 . Jens Birk Lauridsen . 10.1007/BF02605731. 86707965 .
  2. Sonntag. Norman O. V.. Glycerolysis of fats and methyl esters – Status, review and critique. Journal of the American Oil Chemists' Society. 59. 10. 1982. 795A–802A. 0003-021X. 10.1007/BF02634442. 84808531.
  3. http://www.intox.org/databank/documents/chemical/glycmono/cie536.htm Glycerol monostearate
  4. Web site: The British Pharmacopoeia Secretariat . Index, BP 2009 . 2009 . 18 March 2010 . dead . https://web.archive.org/web/20090411071437/http://www.pharmacopoeia.co.uk/pdf/2009_index.pdf . 11 April 2009.