My watch list  


The name polyols refers to alcohols containing multiple hydroxyl groups. In two technological disciplines polyols have special meaning: food science and polymer chemistry. For information as it pertains to food ingredients, please see the article on sugar alcohols.

Additional recommended knowledge

Polyols in food science

Sugar alcohols, a class of polyols, are commonly added to foods because of their lower caloric content than sugars; however, they are also, in general, less sweet, and are often combined with high-intensity sweeteners. They are also added to chewing gum because they are not metabolized (broken down) by bacteria in the mouth, so they do not contribute to tooth decay. Maltitol, sorbitol, and Isomalt are some of the more common types. Sugar alcohols may be formed under mild reducing conditions from their analogue sugars.

Polyols in polymer chemistry

In polymer chemistry, polyols are compounds with multiple hydroxyl functional groups available for organic reactions. A molecule with two hydroxyl groups is a diol, one with three is a triol, one with four is a tetrol and so on.

The main use of polymeric polyols is as reactants to make other polymers, They can be reacted with isocyanates to make polyurethanes, and this use consumes most polyether polyols[1] These material are ultimately used to make elastomeric shoe soles, fibers (Spandex for example), insulation for appliances (refrigerators and freezers), adhesives, mattresses, automotive seats and so on.

Monomeric polyols such as pentaerythritol, ethylene glycol and glycerin often serve as the starting point for polymeric polyols. Naturally occurring polyols like castor oil and sucrose can also be used to make synthetic polymeric polyols. These materials are often referred to as the "initiators" for the polymeric polyols, but they should not be confused with free radical "initiators" used to promote other polymerization reactions. The functional group used as the starting point for a polymeric polyol need not be a hydroxyl group; there are a number of important polyols which are built up from amines. A primary amino group (-NH2) often functions as the starting point for two polymeric chains, especially in the case of polyether polyols.

The polymeric chains built out from the initiator are usually polyesters or polyethers. Polyether polyols are made by reacting epoxides like ethylene oxide or propylene oxide with the multifunctional initiator in the presence of a catalyst, often a strong base such as potassium hydroxide or more exotic metal cyanides.[2] Common polyether diols are polyethylene glycol, polypropylene glycol, and poly(tetramethylene ether) glycol. The examples shown below are fairly low molecular weight triols based on glycerin (a triol) being reacted with propylene oxide, ethylene oxide or a combination of the two. In reality, the chains would not be of equal length in any one molecule and there would be a distribution of molecular weight polyols within the material. Polyether polyols account for about 90% of the polymeric polyols used industrially; the balance is polyester polyols.[3]

Another class of polymeric polyols is the polyesters. Polyesters are formed by condensation or step-growth polymerization of diols and dicarboxylic acids (or their derivatives), for example diethylene glycol reacting with phthalic acid.[4] Alternatively, the hydroxyl group and the carboxylic acid (or their derivatives) may be within the same molecule, as in the case of caprolactone. The example below is an idealized structure that could be obtained by reacting pentaerythritol (a tetrol) with gamma-butyrolactone.

A specialist class of polyol is the hydroxyl-terminated polybutadienes. These polyols are extensively used in formulations for polyurethanes.

The production of polyester polyols from vegetable oils is becoming increasingly important. These materials are known as natural oil polyols, or NOPs.


  1. ^ Chinn, Henry; Akihiro Kishi and Uwe Loechner (April, 2006). Polyether Polyols for Urethanes (abstract only without subscription). SRI Consulting.
  2. ^ Alper, H.; J. L. Garcia, E. J. Jang (4 Sep 2002). "New heterogeneous catalysis for the synthesis of poly(ether polyol)s". Journal of Applied Polymer Science 86 (7): 1553 - 1557. Retrieved on 2008-08-09.
  3. ^ Dow Polyurethanes and Thermoset Systems, uses and innovations. Retrieved on 2007-09-14.
  4. ^ Kaszynski, Poitr; Oleg Kadkin, Karol Osajda, Thomas A. Barber (2003). "Polyester Polyols: Synthesis and Characterization of Diethylene Glycol Terephthalate Oligomers". Journal of Polymer Science: Part A: Polymer Chemistry 41: 1114–1123. Retrieved on 2008-08-09.

  • Website
  • Food polyols overview
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Polyol". A list of authors is available in Wikipedia.
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE