62502-71-0

62502-71-0 structure

Name: Glycerol-d5
Chemical Name: 1,1,2,3,3-pentadeuteriopropane-1,2,3-triol
CAS Number: 62502-71-0
Molecular Formula: C₃H₃D₅O₃
Molecular Weight: 97.12460
Create Date: 2018-07-02 21:40:41
Modify Date: 2024-01-03 14:14:21
Glycerol-d5 is the deuterium labeled Glycerol[1]. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis[2][3][4].

Name	1,1,2,3,3-pentadeuteriopropane-1,2,3-triol
Synonyms	1,1,2,3,3-D5-glycerol Bulbold-d5 Osmoglyn-d5 1,1,2,3,3-pentadeuterio-propane-1,2,3-triol Glycerin-d5 MFCD00084148 Glyceritol-d5 Propanetriol-d5 Glysanin-d5 Glycerol-1,1,2,3,3-d5 glycerol-d5 Glycerine-d5

Description	Glycerol-d5 is the deuterium labeled Glycerol[1]. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis[2][3][4].
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [2]. Pennings S, et al. Effect of glycerol on the separation of nucleosomes and bent DNA in low ionic strengthpolyacrylamide gel electrophoresis. Nucleic Acids Res. 1992 Dec 25;20(24):6667-72. [3]. Yazdani SS, et al. Anaerobic fermentation of glycerol: a path to economic viability for the biofuelsindustry. Curr Opin Biotechnol. 2007 Jun18(3):213-9. [4]. Huang ZH, et al. Expression and function of P-glycoprotein in rats with glycerol-induced acute renal failure. Eur J Pharmacol. 2000 Oct 20406(3):453-60.

Density	1.331 g/mL at 25ºC
Boiling Point	182ºC(lit.)
Melting Point	20ºC(lit.)
Molecular Formula	C₃H₃D₅O₃
Molecular Weight	97.12460
Flash Point	320 °F
Exact Mass	97.07870
PSA	60.69000
Index of Refraction	n20/D 1.472(lit.)
Storage condition	2-8°C

RIDADR	NONH for all modes of transport

56-81-5

~97%

62502-71-0

Literature: Maegawa, Tomohiro; Fujiwara, Yuta; Inagaki, Yuya; Monguchi, Yasunari; Sajiki, Hironao Advanced Synthesis and Catalysis, 2008 , vol. 350, # 14-15 p. 2215 - 2218

609-09-6

~61%

62502-71-0

Literature: Bersch, B.; Starck, J. P.; Milon, A.; Nakatani, Y.; Ourisson, G. Bulletin de la Societe Chimique de France, 1993 , vol. 130, p. 575 - 583

Precursor 2
56-81-5 609-09-6
DownStream 3
1838-59-1 102910-30-5 107-18-6

62502-71-0	946524-37-4
565183-24-6	1215168-37-8
1246523-69-2	1246523-63-6
928623-32-9	944795-74-8
2315262-46-3	5695-96-5