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Glycerol is the simplest alkane triol. It was historically called glycerine (or glycerin), but that name is misleading because the -ine suffix denotes an amine, not an alcohol.
Pioneering Swedish chemist Carl Wilhelm Scheele reported the discovery of glycerol in a 1783 article titled 鈥淔indings concerning a particular sweet substance in expressed oils and fatty substances鈥�. In doing so, he established that glycerol is sweet-tasting and that it is the alcohol portion of natural mono-, di-, and triglyceride esters.1
Glycerol/glycerine/glycerin appears in some 330,000 references listed in Chemical Abstracts Service鈥檚 . The earliest citations are from 1878, in an article titled 鈥淎 new test for glycerin鈥� and in patents titled 鈥淢anufacture of pigments鈥� and 鈥淔rees lime saccharate from salts and coloring matters鈥�.
Glycerol can be synthesized from propylene through intermediates such as epichlorohydrin, acrolein, or propylene oxide. But for economic reasons, almost all commercial glycerol comes from hydrolyzing glycerides in natural fats, especially since the advent of using fatty acids to make biodiesel fuels. Some now-inexpensive glycerol is used as a raw material for producing epichlorohydrin and acrolein.
Glycerol has myriad uses in foods, pharmaceuticals, personal-care products, antifreezes, inks, lubricants, industrial lubricants, and many more. It is a key starting material for preparing nitroglycerol2. As long ago as 1945, a book by Georgia Leffingwell and Milton A. Lesser titled listed 1583 specific uses3 of the compound.
Finally, glycerol is the base ingredient in commonly used face paints, as described in the . It is the medium in which the paint pigments are dispersed. If you paint your face for Halloween, Mardi Gras, or your favorite team鈥檚 game, give a shout-out for glycerol.
1. Similarly to the preference for glycerol over glycerine, one might conjecture that glycerides should be called 鈥済lycerates鈥� to conform with ester nomenclature.鈥擡d.
2. CAS Reg. No. 55-63-0.
3. The last four uses in the list are: 1580, poison gas indicators; 1581, skin protection against mustard gas; 1582, tattoo mark removal; and 1583, telephone mouthpiece.
Glycerol hazard information
Hazard class* | GHS code and hazard statement |
---|---|
Not a hazardous substance or mixture** | 听 |
*Globally Harmonized System (GHS) of Classification and Labeling of Chemicals.
**Most safety data sheets give this designation; but at least one reports 鈥渃auses eye irritation鈥�.
Gepotidacin1 is a topoisomerase type II inhibitor that is being studied for treating multiple diseases. It was first reported in world patent application by GlaxoSmithKline (GSK, London), which claimed gepotidacin and similar compounds as antibacterial agents.

This past February, Florian Wagenlehner at Justus Liebig University Giessen (Germany) and colleagues at several institutions, including GSK, found that gepotidacin , nitrofurantoin2, for treating uncomplicated urinary tract infection3. Then, in March, GSK announced that gepotidacin was likewise successful in a phase 3 clinical study against uncomplicated gonorrhea and could treatment.
1. CAS Reg. No. 1075236-89-3.
2. CAS Reg. No. 67-20-9.
3. GSK has since applied for US Food and Drug Administration approval for this use.
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Glycerol听fast facts
CAS Reg. No. | 56-81-5 |
SciFindern name | 1,2,3-Propanetriol |
Empirical formula | C3H8O3 |
Molar mass | 92.09 g/mol |
Appearance | Colorless viscous liquid |
Boiling point | 290 掳C |
Water solubility | Miscible |

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