Glyceryl Monostearate
While the names glyceryl monostearate and mono- and diglycerides are used for a variety of esters of long-chain fatty acids, the esters fall into two distinct grades: 40-55 percent monoglycerides The PhEur describes glyceryl monostearate 40-55 as a mixture of monoacylglycerols, mostly monostearoylglycerol, together with quantities of di- and triacylglycerols. It contains 40-55% of monoacylglycerols, 30-45% of diacylglycerols, and 5-15% of triacylglycerols.
Supplier | CD Formulation |
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Product # | PE-0518 |
Pricing | , Inquire for price |
product1 | Emulsifier Excipients |
Molecular Formula | C21H42O4 |
Molecular Weight | 358.6 |
Applications | The many varieties of glyceryl monostearate are used as nonionic emulsifiers, stabilizers, emollients, and plasticizers in a variety of food, pharmaceutical, and cosmetic applications. It acts as an effective stabilizer, that is, as a mutual solvent for polar and nonpolar compounds that may form water-in-oil or oil-in-water emulsions.These properties also make it useful as a dispersing agent for pigments in oils or solids in fats, or as a solvent for phospholipids, such as lecithin. Glyceryl monostearate has also been used in a novel fluidized hot-melt granulation technique for the production of granules and tablets. Glyceryl monostearate is a lubricant for tablet manufacturing and may be used to form sustained-release matrices for solid dosage forms. Sustained-release applications include the formulation of pellets for tablets or suppositories, and the preparation of a veterinary bolus. Glyceryl monostearate has also been used as a matrix ingredient for a biodegradable, implantable, controlledrelease dosage form. When using glyceryl monostearate in a formulation, the possibility of polymorph formation should be considered. The a form is dispersible and foamy, useful as an emulsifying agent or preservative. The denser, more stable, b-form is suitable for wax matrices. This application has been used to mask the flavor of clarithromycin in a pediatric formulation. |
Safety | Glyceryl monostearate is widely used in cosmetics, foods, and oral and topical pharmaceutical formulations, and is generally regarded as a nontoxic and nonirritant material. LD50 (mouse, IP): 0.2 g/kg |
Incompatibilities | The self-emulsifying grades of glyceryl monostearate are incompatible with acidic substances. |
Synonyms | Capmul GMS-50; Cutina GMS; 2, 3-dihydroxypropyl octadecanoate; Geleol; glycerine monostearate; glycerin monostearate; glycerol monostearate; glyceroli monostearas; glycerol stearate; glyceryl stearate; GMS; HallStar GMS; Imwitor 191; Imwitor 900; Kessco GMS; Lipo GMS; monoester with 1, 2, 3-propanetriol; monostearin; Myvaplex 600P; Myvatex; 1, 2, 3-propanetriol octadecanoate; Protachem GMS-450; Rita GMS; stearic acid, monoester with glycerol; stearic monoglyceride; Stepan GMS; Tegin; Tegin 503; Tegin 515; Tegin 4100; Tegin M; Unimate GMS |
CAS Number | 31566-31-1 |
Category | Emollient; Emulsifying Agents; Solubilizing Agents; Stabilizing Agents; Sustained-release Agents; Tablet and Capsule Lubricant |
Chemical Name | Octadecanoic acid, monoester with 1, 2, 3-propanetriol |
Grade | Pharmceutical Excipients |
Administration route | Oral; ophthalmic, otic, rectal, topical, transdermal, and vaginal |
Dosage Form | Oral capsules and tablets; ophthalmic, otic, rectal, topical, transdermal, and vaginal preparations |
Stability and Storage Conditions | If stored at warm temperatures, glyceryl monostearate increases in acid value upon aging owing to the saponification of the ester with trace amounts of water. Effective antioxidants may be added, such as butylated hydroxytoluene and propyl gallate. Glyceryl monostearate should be stored in a tightly closed container in a cool, dry place, and protected from light. |
Source and Preparation | Glyceryl monostearate is prepared by the reaction of glycerin with triglycerides from animal or vegetable sources, producing a mixture of monoglycerides and diglycerides. The diglycerides may be further reacted to produce the 90% monoglyceride grade. Another process involves reaction of glycerol with stearoyl chloride. The starting materials are not pure substances and therefore the products obtained from the processes contain a mixture of esters, including palmitate and oleate. Consequently, the composition, and therefore the physical properties, of glyceryl monostearate may vary considerably depending on the manufacturer. |