Glycerol (Glycerine)

Référence G8145-1L

Conditionnement : 1L

Marque : US Biological

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G8145 Glycerol (Glycerine)

Clone Type
Polyclonal
Grade
Molecular Biology Grade
Shipping Temp
RT
Storage Temp
RT

Glycerol is a chemical compound also commonly called glycerin or glycerine. It is a colorless, odorless, viscous liquid that is widely used in pharmaceutical formulations. Glycerol is a sugar alcohol, and is sweet-tasting and of low toxicity. Glycerol has three hydrophilic alcoholic hydroxyl groups that are responsible for its solubility in water and its hygroscopic nature. Its surface tension is 64.00mN/m at 20°C, and it has a temperature coefficient of -0.0598mN/(mK). The glycerol substructure is a central component of many lipids.

Glycerol is used both in sample preparation and gel formation for polyacrylamide gel electrophoresis. Glycerol (5-10%) increases the density of a sample so that the sample will layer at the bottom of a gel’s sample well. Glycerol is also used to aid in casting gradient gels and as a protein stabilizer and storage buffer component.

Synonyms:
1,2,3-Propanetriol; 1,3-dihydroxy-2-propanol; Propanetriol; 1,2,3-Trihydroxypropane; Bulbold; Cognis G; Cristal; DG; DG Glycerin; E 422; Emery 916; GL 300; Glycerin; Glycerin DG; Glycerine; Glyceritol; Glycyl Alcohol; Glyrol; Glysanin; IFP; M 314429; Mackstat H 66; NSC 9230; Osmoglyn; rine 9088; rine 9091; RG; RG-S; Trihydroxypropane

CAS No:
56-81-5

Molecular Formula:
C3H8O3

Molecular Weight:
92.09

Purity:
≥99.7%

Appearance:
Clear, viscous liquid

Identification (IR):
Conforms to reference

Water:
≤0.3%

Heavy Metals:
≤0.0005%

Specific Gravity @25°C:
1.2607-1.2650

Sulfate:
≤0.002%

Chloride:
≤0.003%

RNase:
None Detected

DNase:
None Detected

Protease:
None Detected

Storage and Stability:
Store at RT. Stable for 12 months.

Meets or exceeds USP Specifications

Applications
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. ||Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures.
References
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|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.|Dow Chemical Company (15 Mar 2007). "Dow Achieves Another Major Milestone in its Quest for Sustainable Chemistries". Press release.|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.|Watanabe, M. et al (2007). "Acrolein synthesis from glycerol in hot-compressed water". Bioresource Technology 98: 1285-1290.|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. Lay summary – ScienceDaily (27 Jun 2007).|Dow Chemical Company (26 March 2007). "Dow Epoxy Advances Glycerine-To-Epichlorohydrin and Liquid Epoxy Resins Projects by Choosing Shanghai Site". Press release.|U.S. Food and Drug Administration. "FDA Advises Manufacturers to Test Glycerin for Possible Contamination." Released May 4, 2007. Last retrieved May 8, 2007.|WALT BOGDANICH and JAKE HOOKER. "From China to Panama, a Trail of Poisoned Medicine." New York Times. Published: May 6, 2007. Last retrieved May 8, 2007.

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abx082383-25g
 25g