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:[[File:SaponificationGeneral.svg|400px]]
:[[File:SaponificationGeneral.svg|400px]]


It also is a byproduct of the production of [[biodiesel]] via [[transesterification]]. Triglycerides ('''1''') are reacted with an alcohol such as ethanol ('''2''') with catalytic base to give ethyl esters of fatty acids ('''3''') and glycerol ('''4'''):
It also is a byproduct of the production of [[biodiesel]] via [[transesterification]]. This form of crude glycerin in often dark in appearance with a thick, syrup-like consistency. Triglycerides ('''1''') are reacted with an alcohol such as ethanol ('''2''') with catalytic base to give ethyl esters of fatty acids ('''3''') and glycerol ('''4'''):


:[[File:Transesterification of triglycerides with ethanol.png|400px]]
:[[File:Transesterification of triglycerides with ethanol.png|400px]]

Revision as of 13:39, 23 June 2011

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Glycerol
Glycerol
Ball-and-stick model of glycerol
Space-filling model of glycerol
Names
IUPAC name
propan-1,2,3-triol
Other names
glycerin
glycerine
propane-1,2,3-triol
1,2,3-propanetriol
1,2,3-triglycerol
1,2,3-trihydroxypropane
glyceritol
glycyl alcohol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.263 Edit this at Wikidata
E number E422 (thickeners, ...)
KEGG
UNII
  • InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2 checkY
    Key: PEDCQBHIVMGVHV-UHFFFAOYSA-N checkY
  • InChI=1/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
    Key: PEDCQBHIVMGVHV-UHFFFAOYAF
  • C(C(CO)O)O
Properties
C3H8O3
Molar mass 92.094 g·mol−1
Appearance clear, colorless liquid
hygroscopic
Odor odorless
Density 1.261 g/cm3
Melting point 17.8 °C, 291.0 K, 64.0 °F
Boiling point 290 °C, 563 K, 554°F [1]
1.4746
Viscosity 1.412 Pa·s[2]
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
Flash point 160 °C (closed cup)
176 °C (open cup)
Supplementary data page
Glycerol (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Glycerol (or glycerin, glycerine) is a simple polyol compound. It is a colorless, odorless, viscous liquid that is widely used in pharmaceutical formulations. Glycerol has three hydrophilic hydroxyl groups that are responsible for its solubility in water and its hygroscopic nature. The glycerol backbone is central to all lipids known as triglycerides. Glycerol is sweet-tasting and of low toxicity. The term polyglycerol refers to many glycerol molecules together.

Production

Glycerol forms the backbone of triglycerides, and can be produced by saponification of fats, e.g. a byproduct of soap-making. Saponification is also referred to as the hydrolysis of esters in basic solutions or environments. The mechanism of this reaction involves a very rapid equilibrium where the alkoxide functions as a base deprotonating the carboxylic acid (an acidic work up would allow the carboxylic acid to be obtained from the reaction).

It also is a byproduct of the production of biodiesel via transesterification. This form of crude glycerin in often dark in appearance with a thick, syrup-like consistency. Triglycerides (1) are reacted with an alcohol such as ethanol (2) with catalytic base to give ethyl esters of fatty acids (3) and glycerol (4):

Glycerol is also produced by various routes from propylene. The epichlorohydrin process is the most important; it involves the chlorination of propylene to give allyl chloride, which is oxidized with hypochlorite to dichlorohydrins, which reacts with a strong base to give epichlorohydrin. Epichlorohydrin is then hydrolyzed to give glycerol.[3]

Because of the emphasis on biodiesel, where glycerol is a waste product, the market for glycerol is depressed, and the old epichlorohydrin process for glycerol synthesis is no longer economical on a large scale. Glycerol can be removed from the process by using a special enzyme that breaks down phytol and starches. This enzyme is biologically produced using a genetically engineered bacterium. Because there is no glycerin produced as a by-product, the biodiesel purity is greatly improved and costs can be reduced. [4]

Only one producer for synthetic glycerol is left, because high-quality glycerol is needed in highly sensitive pharmaceutical, technical and personal care applications. Raw materials used to make glycerol and glycerin include animal fats, such as beef tallow, and vegetable oils, such as coconut and soybean.[5] Approximately 950,000 tons per annum are produced in the USA and Europe; 350,000 tons of glycerol were produced per year in the United States alone from 2000-2004.[6] Production will increase as the EU directive 2003/30/EC is implemented, which requires the replacement of 5.75% of petroleum fuels with biofuel across all Member States by 2010. It is projected that by the year 2020, production will be six times more than demand.[3]

Applications

Food industry

In foods and beverages, glycerol serves as a humectant, solvent, and sweetener, and may help preserve foods. It is also used as filler in commercially prepared low-fat foods (e.g., cookies), and as a thickening agent in liqueurs. Glycerol and water are used to preserve certain types of leaves. As a sugar substitute, it has approximately 27 calories per teaspoon and is 60% as sweet as sucrose. Although it has about the same food energy as table sugar, it does not raise blood sugar levels, nor does it feed the bacteria that form plaques and cause dental cavities. As a food additive, glycerol is labeled as E number E422.

Glycerol is also used to manufacture mono- and di-glycerides for use as emulsifiers, as well as polyglycerol esters going into shortenings and margarine.

It is also used as a humectant (along with propylene glycol labelled as E1520 and/or E422) in the production of snus, a Swedish-style smokeless tobacco product.

As used in foods, glycerol is categorized by the American Dietetic Association as a carbohydrate. The U.S. Food and Drug Administration (FDA) carbohydrate designation includes all caloric macronutrients excluding protein and fat. Glycerin has a caloric density similar to table sugar, but a lower glycemic index and different metabolic pathway within the body, so some dietary advocates accept glycerin as a sweetener compatible with low carbohydrate diets.

Pharmaceutical and personal care applications

Glycerol is used in medical and pharmaceutical and personal care preparations, mainly as a means of improving smoothness, providing lubrication and as a humectant. It is found in allergen immunotherapies, cough syrups, elixirs and expectorants, toothpaste, mouthwashes, skin care products, shaving cream, hair care products, soaps and water-based personal lubricants. In solid dosage forms like tablets, glycerol is used as a tablet holding agent. For human consumption, glycerol is classified by the U.S. FDA among the sugar alcohols as a caloric macronutrient.

Glycerol is a component of glycerin soap, which is made from denatured alcohol, glycerol, sodium castorate (from castor), sodium cocoate, sodium tallowate, sucrose, and water. Sometimes one adds sodium laureth sulfate, or essential oils for fragrance. This kind of soap is used by people with sensitive, easily-irritated skin because it prevents skin dryness with its moisturizing properties. It draws moisture up through skin layers and slows or prevents excessive drying and evaporation. It is possible to make glycerol soap at home.

Used as a laxative when introduced into the rectum in suppository or small-volume (2–10 ml)(enema) form; irritates the anal mucosa and induces a hyperosmotic effect.

Topical pure or nearly pure glycerol is an effective treatment for psoriasis, burns, bites, cuts, rashes, bedsores, and calluses. It can be used orally to eliminate halitosis, as it is a contact bacterial desiccant. The same property makes it very helpful with periodontal disease; it penetrates biofilm quickly and eliminates bacterial colonies.

Botanical extracts

When utilized in 'tincture' method extractions specifically, as a 10% solution, glycerol prevents tannins from precipitating in ethanol extracts of plants (tinctures). It is also used as a substitute for ethanol as a solvent in preparing herbal extractions. It is less extractive when utilized in tincture methodology and is approximately 30% more slowly absorbed by the body resulting in a much lower glycemic load. Fluid extract manufacturers often extract herbs in hot water before adding glycerin to make glycerites.[7][8][9]

When used as a primary true alcohol-free botanical extraction solvent in innovative non-tincture based methodologies, glycerol has been shown, both in literature and through extraction applications, to possess a high degree of extractive versatility for botanicals including removal of numerous constituents and complex compounds, with an extractive power between water and ethanol. Glycerol is a stable preserving agent for botanical extracts that, when utilized in proper concentrations in an extraction solvent base, does not allow inverting or REDOX of a finished extract's constituents over several years. Both Glycerol and ethanol are viable preserving agents. Glycerol is bacteriostatic in its action, and ethanol is bactericidal in its action.[10][11][12]

Antifreeze

Main article: antifreeze

Like ethylene glycol and propylene glycol, glycerol dissolved in water disrupts the hydrogen bonding between water molecules such that the mixture cannot form a stable crystal structure unless the temperature is significantly lowered. The minimum freezing point temperature is at about -36 °F / -37.8 °C corresponding to 60–70% glycerol in water.[13]

Glycerol was historically used as an anti-freeze for automotive applications before being replaced by ethylene glycol, which has a lower freezing point. While the minimum freezing point of a glycerol-water mixture is higher than an ethylene-glycol mixture, glycerol is not toxic and is being re-examined for use in automotive applications.[14][15]

In the laboratory, glycerol is a common component of solvents for enzymatic reagents stored at temperatures below 0 °C due to the depression of the freezing temperature of solutions with high concentrations of glycerol. It is also used as a cryoprotectant where the glycerol is dissolved in water to reduce damage by ice crystals to laboratory organisms that are stored in frozen solutions, such as bacteria, nematodes, and fruit flies.

Chemical intermediate

Glycerol is used to produce nitroglycerin, or glycerol-trinitrate (GTN), which is an essential ingredient of smokeless gunpowder and various explosives such as dynamite, gelignite and propellants like cordite. Reliance on soap-making to supply co-product glycerine made it difficult to increase production to meet wartime demand. Hence, synthetic glycerin processes were national defence priorities in the days leading up to World War II. GTN is commonly used to relieve angina pectoris, taken in the form of sub-lingual tablets, or as an aerosol spray.

A great deal of research is being conducted to try to make value-added products from crude glycerol (typically containing 20 % water and residual esterification catalyst) obtained from biodiesel production, as an alternative to disposal by incineration. The use of crude glycerin as an additive to biomass for a renewable energy source when combusted or gasified is also being explored.

Metabolism

Glycerol is a precursor for synthesis of triacylglycerols and of phospholipids in the liver and adipose tissue. When the body uses stored fat as a source of energy, glycerol and fatty acids are released into the bloodstream. In some organisms, the glycerol component can be converted into glucose by the liver and, thus, provide energy for cellular metabolism .

Before glycerol can enter the pathway of glycolysis or gluconeogenesis (depending on physiological conditions), it must be converted to their intermediate glyceraldehyde 3-phosphate in the following steps:

Glycerol Glycerol kinase Glycerol-3-phosphate Glycerol-3-phosphate dehydrogenase Dihydroxyacetone phosphate Triosephosphate isomerase Glyceraldehyde 3-phosphate
ATP ADP FAD FADH2
NAD+ NADH

The enzyme glycerol kinase is present only in the liver. In adipose tissue, glycerol 3-phosphate is obtained from dihydroxyacetone phosphate (DHAP) with the enzyme glycerol-3-phosphate dehydrogenase.

Glycerol has very low toxicity when ingested; its LD50 oral dose for rats is 12600 mg/kg and 8700 mg/kg for mice.[23]

Historical cases of contamination with diethylene glycol

Glycerine and diethylene glycol are similar in appearance, smell, and taste. The US Federal Food, Drug, and Cosmetic Act was passed following the 1937 "Elixir Sulfanilamide" incident of poisoning caused by diethylene glycol contamination of medicine.

On May 4, 2007, the US Food and Drug Administration advised all US makers of medicines to test all batches of glycerine for the toxic diethylene glycol.[24] This follows an occurrence of 100 fatal poisonings in Panama resulting from a Chinese factory deliberately falsifying records in order to export the cheaper diethylene glycol as the more expensive glycerol.[25]

Additional physical properties

Its surface tension is 64.00 mN/m at 20 °C , and it has a temperature coefficient of -0.0598 mN/(m K).[26]

See also

References

  1. ^ Lide, D. R., Ed. CRC Handbook of Data on Organic Compounds, 3rd ed.; CRC Press: Boca Raton, FL, 1994; p 4386.
  2. ^ "Viscosity of Glycerol and its Aqueous Solutions". Retrieved 2011-04-19.
  3. ^ a b Christoph, Ralf; Schmidt, Bernd; Steinberner, Udo; Dilla, Wolfgang; Karinen, Reetta (2006). "Glycerol". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a12_477.pub2.
  4. ^ "Biosynthesis of Biodiesel without Glycerin By-Product". University of Minnesota. Retrieved 27 May 2011.
  5. ^ Information of the DOW Chemical Company http://www.dow.com/glycerine/advantage/index.htm
  6. ^ Dave Nilles (2005). "A Glycerin Factor". Biodiesel Magazine.
  7. ^ Walter S. Long. The Composition of Commercial Fruit Extracts Transactions of the Kansas Academy of Science (1903-), Vol. 28, Jan. 14, 1916 – Jan. 13, 1917 (Jan. 14, 1916 - Jan. 13, 1917), pp. 157–161 doi:10.2307/3624347
  8. ^ David Winston www.herbaltherapeutics.com
  9. ^ Does Alcohol Belong In Herbal Tinctures?
  10. ^ GLYCEROL AND THE GLYCOLS – Production, Properties and Analysis by, James W. Lawrie, Ph.D. (1928 The Chemical Catalog Company, Inc., New York, NY)
  11. ^ GLYCERIN – Its Industrial and Commercial Applications, by Georgia Leffingwell, Ph.D. and Miton Lesser, B.S. (1945 Chemical Publishing Co., Inc., Brooklyn, NY)
  12. ^ The Manufacture of GLYCEROL – Vol. III (1956 The Technical Press, LTD., London, UK)
  13. ^ Glycerol Freezing Point
  14. ^ Hudgens, R. Douglas; Hercamp, Richard D.; Francis, Jaime; Nyman, Dan A.; Bartoli, Yolanda (2007). doi:10.4271/2007-01-4000. {{cite journal}}: Cite journal requires |journal= (help); Missing or empty |title= (help)
  15. ^ [1]
  16. ^ A. T. Marshall and R. G. Haverkamp (2008). "Production of hydrogen by the electrochemical reforming of glycerol-water solutions in a PEM electrolysis cell". International Journal of Hydrogen Energy. 33 (17): 4649–4654. doi:10.1016/j.ijhydene.2008.05.029.
  17. ^ J. A. Melero, R. vanGrieken, G. Morales and M. Paniagua (2007). "Acidic mesoporous silica for the acetylation of glycerol: Synthesis of bioadditives to petrol fuel". Energy Fuels. 21 (3): 1782–1791. doi:10.1021/ef060647q.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  18. ^ "Dow achieves another major milestone in its quest for sustainable chemistries" (Press release). Dow Chemical Company. 15 March 2007.
  19. ^ L. Ott, M. Bicker and H. Vogel (2006). "The catalytic dehydration of glycerol in sub- and supercritical water: a new chemical process for acrolein production". Green Chemistry. 8 (2): 214–220. doi:10.1039/b506285c.
  20. ^ Watanabe, M.; et al. (2007). "Acrolein synthesis from glycerol in hot-compressed water". Bioresource Technology. 98 (6): 1285–1290. doi:10.1016/j.biortech.2006.05.007. PMID 16797980. {{cite journal}}: Explicit use of et al. in: |author= (help)
  21. ^ S. S. Yazdani and R. Gonzalez (2007). "Anaerobic fermentation of glycerol: a path to economic viability for the biofuels industry". Current Opinion in Biotechnology. 18 (3): 213–219. doi:10.1016/j.copbio.2007.05.002. PMID 17532205. {{cite journal}}: Unknown parameter |laydate= ignored (help); Unknown parameter |laysource= ignored (help); Unknown parameter |laysummary= ignored (help)
  22. ^ "Dow Epoxy advances glycerine-to-epichlorohydrin and liquid epoxy resins projects by choosing Shanghai site" (Press release). Dow Chemical Company. 26 March 2007.
  23. ^ Safety data for glycerol http://msds.chem.ox.ac.uk/GL/glycerol.html
  24. ^ U.S. Food and Drug Administration. "FDA Advises Manufacturers to Test Glycerin for Possible Contamination." Released May 4, 2007. Last retrieved May 8, 2007.
  25. ^ Walt Bogdanich. "From China to Panama, a Trail of Poisoned Medicine." New York Times. Published: May 6, 2007. Last retrieved May 8, 2007.
  26. ^ "Surface tension values of some common test liquids for surface energy analysis". Retrieved 2010-09-05.
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