82425-96-5

Basic information

• Product Name: GLYCEROL-2-13C
• Synonyms: 13C Labeled glycerol;Glycerin-2-13C;GLYCEROL-2-13C;[2-13C]GLYCEROL;GLYCEROL-2-13C, 99 ATOM % 13C;1,2,3-Propanetriol-2-13C
• CAS NO: 82425-96-5
• Molecular Formula: C3H8O3
• Molecular Weight: 93.1
• Product Categories: 13C & 2H Sugars;Fatty Acids;Metabolic Research;Stable Isotopes;Alphabetical Listings;G-H
• Mol File: 82425-96-5.mol
• Article Data: 1

Chemical Properties

• Melting Point: 20 °C(lit.)
• Boiling Point: 182 °C(lit.)
• Flash Point: 320 °F(lit.)
• Appearance: /
• Density: 1.275 g/mL at 25 °C
• Refractive Index: n20/D 1.474(lit.)
• Storage Temp.: Refrigerator
• Solubility: DMSO, Methanol, Water
• CAS DataBase Reference: GLYCEROL-2-13C(CAS DataBase Reference)
• NIST Chemistry Reference: GLYCEROL-2-13C(82425-96-5)
• EPA Substance Registry System: GLYCEROL-2-13C(82425-96-5)

Safety Data

• WGK Germany: 1
• Hazardous Substances Data: 82425-96-5(Hazardous Substances Data)

Upstream product

• 71122-43-5 [2-13C]-DL-glyceraldehyde 

Downstream Products

• 1213780-65-4 rac-1,2-di-O-stearoyl-3-O-tritylglycerol-2,1',1-13C3 
• 1213780-55-2 rac-1,2-di-O-stearoyl-3-O-tritylglycerol-1,3,1',1-13C4 
• 1213780-64-3 rac-3-O-tritylglycerol-2-13C 
• 1213780-53-0 rac-3-O-tritylglycerol-1,3-13C₂ 
• 64-18-6 formic acid 
• 1633-56-3 (¹³C)-formic acid 
• 81277-96-5 1-¹³C-glycolic acid 

Relevant articles and documents

Synthesis of Sugars by Aldolase-Catalyzed Condensation Reactions

Dihydroxyacetone phosphate was prepared in 200-mmol scale from dihydroxyacetone by two procedures: reaction with phosphorus oxytrichloride and glycerol kinase catalyzed phosphorylation using ATP with in situ regeneration of ATP by phosphoenolpyruvate or acetyl phosphate.Dihydroxyacetone phosphate was converted to fructose 6-phosphate in 80percent yield by exposure to a mixture of co-immobilized triosephosphate isomerase and aldolase followed by acid hydrolysis of the condensation product fructose 1,6-bisphosphate.Fructose 6-phosphate was subsequently converted by chemical and enzymatic schemes into fructose, glucose 6-phosphate, and glucose.Practical procedures are described for the preparation of D- and L-glyceraldehyde 3-phosphate and for several hexoses labeled with 13C in the C-2 and C-2,5 positions.