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In organic chemistry, a polyol is an containing multiple (). The term "polyol" can have slightly different meanings depending on whether it is used in or polymer chemistry. Polyols containing two, three and four hydroxyl groups are , , and tetrols, respectively.


Classification
Polyols may be classified according to their chemistry. Some of these chemistries are polyether, polyester, polycarbonate and also acrylic polyols. Polyether polyols may be further subdivided and classified as polyethylene oxide or polyethylene glycol (PEG), polypropylene glycol (PPG) and Polytetrahydrofuran or PTMEG. These have 2, 3 and 4 carbons respectively per oxygen atom in the repeat unit. Polycaprolactone polyols are also commercially available. There is also an increasing trend to use biobased (and hence renewable) polyols.


Uses
Polyether polyols have numerous uses. As an example, polyurethane foam is a big user of polyether polyols.
(2025). 9780080878621, Elsevier.

Polyester polyols can be used to produce rigid foam. They are available in both aromatic and aliphatic versions. They are also available in mixed aliphatic-aromatic versions often made from recycled raw materials, typically polyethylene terephthalate (PET).

Acrylic polyols are generally used in higher performance applications where stability to light is required and also lower VOC coatings.

(2025). 9783110644104, De Gruyter.
Other uses include direct to metal coatings. As they are used where good UV resistance is required, such as automotive coatings, the component also tends to be UV resistant and hence isocyanate oligomers or based on Isophorone diisocyanate are generally used.

Caprolactone-based polyols produce polyurethanes with enhanced hydrolysis resistance.

Polycarbonate polyols are more expensive than other polyols and are thus used in more demanding applications. They have been used to make an isophorone diisocyanate based prepolymer which is then used in glass coatings. They may be used in reactive hotmelt .

All polyols may be used to produce polyurethane . These then find use in , , and .


Low molecular weight polyols
Low molecular weight polyols are widely used in polymer chemistry where they function as crosslinking agents and chain extenders. for example, use polyols in their synthesis and are used in and in molds for . They are the dominant or "binder" in most commercial "oil-based" coatings. Approximately 200,000 tons of alkyd resins are produced each year. They are based on linking reactive monomers through ester formation. Polyols used in the production of commercial alkyd resins are , trimethylolpropane, and . In polyurethane prepolymer production, a low molecular weight polyol- such as 1,4-butanediol may be used as a chain extender to further increase molecular weight though it does increase because more is introduced.

Low molecular weight polyols



Sugar alcohols
, a class of low molecular weight polyols, are commonly obtained by of sugars. They have the formula (CHOH)nH2, where n = 4–6.

Sugar alcohols are added to foods because of their lower caloric content than ; however, they are also, in general, less sweet, and are often combined with high-intensity . They are also added to because they are not broken down by bacteria in the mouth or to acids, and thus do not contribute to . , , , , and are common sugar alcohols.


Polymeric polyols
Polymeric polyols

(The oxygen atoms of the linkages

are shown in blue.)


(The oxygen and carbon atoms

of the are shown in blue.)

The term polyol is used for various chemistries of the molecular backbone. Polyols may be reacted with or polyisocyanates to produce . MDI finds considerable use in PU foam production. Polyurethanes are used to make flexible foam for and seating, rigid foam insulation for and , shoe soles, fibers (e.g. ), coatings, sealants and .

The term polyol is also attributed to other molecules containing hydroxyl groups. For instance, polyvinyl alcohol is (CH2CHOH) n with n hydroxyl groups where n can be in the thousands. is a polymer with many hydroxyl groups, but it is not referred to as a polyol.


Polyols from recycled or renewable sources
There are polyols based on renewable sources such as materials including and . Vegetable oils and biomass are also potential renewable polyol raw materials. Seed oil can even be used to produce polyester polyols.


Properties
Since the generic term polyol is only derived from chemical nomenclature and just indicates the presence of several hydroxyl groups, no common properties can be assigned to all polyols. However, polyols are usually viscous at room temperature due to hydrogen bonding.


See also


External links
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