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Glycerol

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Glycerol
Chemical name
Chemical formula
Molecular mass
CAS number
HS number Crude: 1520.00.00
Pure: 2905.45.00
Density 3
Viscosity
Melting point
Boiling point
Food energy 4.32 kcal/g
SMILES
[Chemical infoboxDisclaimer and references]
Glycerol, also well known as glycerin and glycerine, and less commonly as propane-1,2,3-triol, 1,2,3-propanetriol, 1,2,3-trihydroxypropane, glyceritol, and glycyl alcohol is a colorless, odorless, hygroscopic, and sweet-tasting viscous liquid. Glycerol is a sugar alcohol and has three hydrophilic alcoholic hydroxyl groups (-OH) that are responsible for its solubility in water. Glycerol is prochiral. Glycerol is used in glycerol soap, in cosmetics and creams, in foods, in chemistry, and in glycerol fog machine mist. Glycerol is produced from dihydroxyacetone phosphate (DHAP) by the enzyme glycerol three-phosphate dehydrogenase (Gpd p) in the mitochondrion of the eukaryotic cell during glycolysis.[link]

Glycerol and triglycerides

Glycerol (3D model), showing the atoms and the lone electron pairs associated with the oxygen atoms (in pink)
Enlarge
Glycerol (3D model), showing the atoms and the lone electron pairs associated with the oxygen atoms (in pink)

When referring to its function in living organisms, the term glycerol is preferred. Glycerol is an important component of triglycerides (i.e. fats and oils) and of phospholipids. Glycerol is a three-carbon substance that forms the backbone of fatty acids in fats.(1) When the body uses stored fat as a source of energy, glycerol and fatty acids are released into the bloodstream. The glycerol component can be converted to glucose by the liver and provides energy for cellular metabolism.

A of saponification and transesterification to obtain biodiesel, this is produced by hydrolysis of three ester linkages and loss of three equivalents of fatty acid from fat or biological oil.

Fats and oils are insoluble in water, because the OH groups of glycerol are replaced by ester groups. They are hydrophobic.

Glycerol and biodiesel

As a byproduct of biodiesel production, each of the OH sites in HO-CH2-CH(-OH)-CH2-OH is one of the three places where a fatty acid chain is broken off the triglyceride molecule.

See: transesterification.

Purification

Like biodiesel by-product, the purification of the lower glycerol phase involves: neutralisation, separation of unreacted methanol, dilution with wash liquid stream coming from methylester washing, splitting of soaps and final concentration up to 80%. Partially refined glycerol can be delivered as such to specialized distillers.

Feedstock pre-treatment and upgrading of glycerol to pharmaceutical grade (>99.7%) can be optionally implemented within the biodiesel factory itself.

When used in food, care should be taken to use only pure vegetable glycerol that is specifically labeled for use in food. "External use only" warnings should be heeded.

Applications

Drugs

Personal care

: Glycerol is a component of glycerol soap, which is made from denatured alcohol, glycerol, sodium castorate (from castor), sodium cocoate, sodium tallowate, sucrose, water and parfum (fragrance). Sometimes one adds sodium laureth sulfate. This kind of soap is used by people with sensitive, easily irritated skin because it prevents skin dryness with its properties.
When used as an emollient, glycerol should never be applied undiluted to the skin. The same powerful hygroscopic property that draws moisture out of the air to moisten the skin will draw moisture out of the skin if the glycerol is too concentrated. A minimum of two or three parts water should be added to one part glycerol.

Foods and beverages

Glycerol has approximately 27 food 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. Glycerol should not be consumed undiluted, as unhydrated glycerol will draw water from tissues, causing blistering in the mouth and gastric distress. As food additive, glycerol is also known as E number E422.

Polyether polyols

Alkyd resins (plastics) and cellophane

Absolute alcohol

Other applications

: Use a mixture of one part glycerol to two parts water. Place the mixture in a flat pan, and totally submerge the leaves in a single layer in the liquid. You'll have to weigh them down to keep them submerged. In two to six days, they should have absorbed the liquid and be soft and pliable. Remove them from the pan and wipe off all the liquid with a soft cloth. Done correctly, the leaves will remain soft and pliable indefinitely.
  • Can be added to solutions of water and soap to increase that solution's ability to generate soap bubbles that will last a long time.
  • Used as an antifreeze or a cryoprotectant in cryogenic process.
  • Used in fog machine fluids
  • Used in hookah tobacco mixtures (called "ma'assel" or "shisha" tobacco), often along with molasses and/or honey.
  • Counteracts phenol burns
  • See also: oleochemicals.

    External links

    Sources

     


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