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(prō`pāntrī'ŏl), CH2OHCHOHCH2OH, colorless, odorless, sweet-tasting, syrupy liquid. Glycerol is a trihydric alcoholalcohol,
any of a class of organic compounds with the general formula R-OH, where R represents an alkyl group made up of carbon and hydrogen in various proportions and -OH represents one or more hydroxyl groups.
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. It melts at 17.8°C;, boils with decomposition at 290°C;, and is miscible with water and ethanol. It is hygroscopic; i.e., it absorbs water from the air; this property makes it valuable as a moistener in cosmetics. Glycerol is present in the form of its estersester,
any one of a group of organic compounds with general formula RCO2R′ (where R and R′ are alkyl groups or aryl groups) that are formed by the reaction between an alcohol and an acid.
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 (glycerides) in all animal and vegetable fats and oils. It is obtained commercially as a byproduct when fats and oils are hydrolyzed to yield fatty acids or their metal salts (soaps). Glycerol is also synthesized on a commercial scale from propylene (obtained by cracking petroleum), since supplies of natural glycerol are inadequate. Glycerol can also be obtained during the fermentation of sugars if sodium bisulfite is added with the yeast. Glycerol is widely used as a solvent; as a sweetener; in the manufacture of dynamite, cosmetics, liquid soaps, candy, liqueurs, inks, and lubricants; to keep fabrics pliable; as a component of antifreeze mixtures; as a source of nutrients for fermentation cultures in the production of antibioticsantibiotic,
any of a variety of substances, usually obtained from microorganisms, that inhibit the growth of or destroy certain other microorganisms. Types of Antibiotics
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; and in medicine. It has many other uses as well.
The Columbia Electronic Encyclopedia™ Copyright © 2013, Columbia University Press. Licensed from Columbia University Press. All rights reserved.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.



(1,2,3-trihydroxypropane; 1,2,3-propanetriol), the simplest trihydric alcohol HOCH2—CHOH—CH2OH; a syrupy, colorless, nontoxic, sweet, odorless liquid. Melting point, 17.9° C; boiling point, 290° C; density, 1.26 g/cm3(25° C). Upon supercooling, it forms a glassy mass at about -100° C. Glycerol may be distilled without decomposition only under vacuum or with superheated steam. It is miscible with water in all proportions (the boiling point of aqueous glycerol solutions decreases with decreasing glycerol concentration; these solutions are characterized by low freezing points), as well as with methanol, ethanol, and acetone. It is soluble in mixtures of alcohol with ether or chloroform but is insoluble in fats, petroleum ether, benzene, and carbon disulfide. It dissolves many inorganic and organic materials, such as salts, alkalies, and sugars; it is hygroscopic and absorbs water from the air up to 40 percent (by weight). Glycerol forms mono-, di-, and tri-derivatives. Like other alcohols, it forms metallic derivatives—glycerates. On reacting with hydrogen halides or phosphorus halides, halohydrins are formed—for example, α-chlorohydrin, C1CH2CHOHCH2OH, and α, γ-dichloro-hydrin, ClCH2CHOHCH2Cl. Glycerol oxidizes to glyceraldehyde (CH2OH—CHOH—CH=O), dihydroxyacetone (CH2OH—CO—CH2OH), and glyceric acid (CH2OH— CHOH—COOH), as well as CO2 and water.

The dehydration of glycerol leads to the formation of polyglycerols or acrolein. Glycerol reacts with aldehydes and ketones to give the corresponding acetals and ketals (for example, acetaldehyde-glycerol acetal and acetone-glycerol ketal). Reaction with mineral acids gives esters—for example, the treatment of glycerol with a mixture of nitric and sulfuric acids yields glycerol trinitrate, so-called nitroglycerin. Acylation with organic acids, or with their derivatives gives mono-, di-, and triglycerides. The triglycerides of higher fatty acids comprise the main part of fats and oils of vegetable and animal origin.

Glycerol was first prepared by the saponification of natural fats (K. Scheele, 1779). It is produced mainly by synthetic methods based on propylene:

Other methods for the synthesis of glycerol are also known. Glycerol is used in the production of explosives and synthetic resins. Epichlorohydrin, Glycerol which is produced from glycerol or from the intermediates in its synthesis, is the raw material for the production of epoxy resins. Glycerol is an important component of many food, cosmetic, and pharmaceutical products. It is used in the printing, leather, textile, and paper industries. Aqueous solutions of glycerol are used as antifreezes.

In medicine, glycerol is used locally as a skin softener, as well as in suppositories and enemas as a laxative. It serves as a base for the preparation of ointments and liniments. Glycerol derivatives, such as fats and lipids, play an important biological role.

The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.


(organic chemistry)
CH2OHCHOHCH2OH The simplest trihedric alcohol; when pure, it is a colorless, odorless, viscous liquid with a sweet taste; it is completely soluble in water and alcohol but only partially soluble in common solvents such as ether and ethyl acetate; used in manufacture of alkyd resins, explosives, antifreezes, medicines, inks, perfumes, cosmetics, soaps, and finishes. Also known as glycerin; Also known as glycerin; glycerine; glycyl alcohol. glycyl alcohol.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.

glycerol, glycerin, glycerine

Colorless, odorless fluid used in mixing synthetic and natural resins for paints and varnishes; used for making distempers more pliable; used in the manufacture of some adhesives.
McGraw-Hill Dictionary of Architecture and Construction. Copyright © 2003 by McGraw-Hill Companies, Inc.


a colourless or pale yellow odourless sweet-tasting syrupy liquid; 1,2,3-propanetriol: a by-product of soap manufacture, used as a solvent, antifreeze, plasticizer, and sweetener (E422). Formula: C3H8O3
Collins Discovery Encyclopedia, 1st edition © HarperCollins Publishers 2005
References in periodicals archive ?
helicoides hyphae using 3% staining solution, however, when we added 1% glycerol to the 5% solution there was better sharpness when compared to cotton blue (Figures 1O, P and Q).
[2] To assess urea and glycerol transport, NR's solutions containing urea (5 mM) and glycerol (90 mM) each were placed on the mucosal side, ADH added on the serosal side.
In order to reduce computational work load, a series of three steady flow rates were applied to determine the nozzle angle-fluid resistance relationship for both blood and water glycerol. The three steady flow rates simulated onset ventricular systole (5L/min), mid-systole (15L/min), and peak systole (25 L/min) [10].
Monitoring metabolites, including glycerol and ethanol, during fermentation can reveal whether yeasts are efficiently converting the substrate into the desired product.
On the other side, dried biomass and glycerol elemental composition were used to calculate the term [eta], which represents biomass formation energy yield and corresponds to the ratio of biomass heat of combustion to the heat of combustion of the corresponding amount of substrate metabolized [19].
Using the sum of squares model, cell viability results (Table 3) showed that glycerol, adenosine, and antimycin-A alone, as well as the combination of glycerol and l-ascorbic acid, had a significant effect on the number of viable cells.
In this work novel Pd supported on cerium oxide composites' catalytic activity in the liquid phase glycerol oxidation with molecular oxygen was studied.
Twenty-four hours after glycerol injection, the results of Western blotting and reverse transcriptase-qPCR (RT-qPCR) analysis indicated that the expression of TLR4 and NF-?B was significantly increased in glycerol-treated group [ P < 0.01; [Figure 2].
Glycerol was estimated according to the method described and adapted by Mansour 14.
The aim of this work is to study the etherification of glycerol with propylene or 1-butene over commercial heterogeneous acid catalysts, that is, Amberlyst-15 and S100 and S200 ion exchange resins.