7325-16-8
7325-16-8
Chemical Structure
Glycerol-d3
Synonym(s): Trihydroxypropane-d3
- CAS No.: 7325-16-8
- Formula:C3H5D3O3
- Molecular Weight:95.11
IUPAC Name: prop-1-yne-d4
InChIKey: PEDCQBHIVMGVHV-WVALGTIDSA-N
SMILES: [2H]OCC(O[2H])CO[2H]
Biological Activity: Glycerol-d3 is the deuterium labeled Glycerol[1]. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis[2][3][4].
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Glycerol-d3 | Glycerol-d3 is the deuterium labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | |||||||||||||||||||||
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Glycerol (Standard) | 98.91% | Glycerol (Standard) is the analytical standard of Glycerol. This product is intended for research and analytical applications. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | ||||||||||||||||||||
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D-Glycerol-13C-3 | D-Glycerol-3-13C is the 13C labeled D-Glycerol. | |||||||||||||||||||||
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Glycerol-d5 | 99.06% | Glycerol-d5 is the deuterium labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | ||||||||||||||||||||
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Glycerol-13C | 99.29% | Glycerol-13C is the 13C labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. The product specifications provided below refer solely to the active content of Glycerol-13C. |
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Glycerol-13C-1 | Glycerol-13C-1 (Trihydroxypropane-13C-1) is the 13C-labeled Glycerol (HY-B1659). Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | |||||||||||||||||||||
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Glycerol-13C2 | 99% | Glycerol-13C2 is the 13C labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | ||||||||||||||||||||
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Glycerol-13C3 | 99.69% | Glycerol-13C3 is the 13C labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | ||||||||||||||||||||
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Glycerol-13C3,d8 | Glycerol-13C3,d8 is the deuterium and 13C labeled Glycerol. | |||||||||||||||||||||
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Glycerol-d8 | 99.98% | Glycerol-d8 is the deuterium labeled Glycerol. | ||||||||||||||||||||
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Glycerol-13C-1 (90% in water) | 99.3% | Glycerol-13C-1 (90% in water) is the 13C labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. The product specifications provided below indicate the total amount only; they do not represent the actual content of Glycerol-13C-1. |
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Glycerol-d1 | Glycerol-d is the deuterium labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | |||||||||||||||||||||
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Glycerol | 99.97% | Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.89
HY-Y0921S(±)-1,2-Propanediol-d8 -
Similarity Score 0.88
HY-W017758S11,3-Propanediol-d8 -
Similarity Score 0.88
HY-W017310S3-Bromopropane-1,2-diol-d5 -
Similarity Score 0.88
HY-W585827S2-Chloro-1,3-propanediol-d5 -
Similarity Score 0.88
HY-146567Smeso-Erythritol-d6 -
Similarity Score 0.88
HY-W007357S1Serinol-d5 -
Similarity Score 0.88
HY-Y0921S2(±)-1,2-Propanediol-d6 -
Similarity Score 0.87
HY-W017758S1,3-Propanediol-d6 -
Similarity Score 0.84
HY-Y0338S2Ethylene glycol-d4 -
Explore the MedChemAI to find more analogs
References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [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. [Content Brief]
- [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. [Content Brief]
- [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. [Content Brief]
