Date published: 2026-4-20

1-800-457-3801

SCBT Portrait Logo
Seach Input

α-D-Glucose 1-phosphate dipotassium salt (CAS 5996-14-5)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Cori Ester Dipotassium Salt
Application:
α-D-Glucose 1-phosphate dipotassium salt is a α-anomeric form of glucose which contains a phosphate group on the primary carbon
CAS Number:
5996-14-5
Molecular Weight:
336.32
Molecular Formula:
C6H11O9P•2K
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

α-D-Glucose 1-phosphate dipotassium salt is a widely used chemical compound in scientific research. It is derived from glucose, a vital source of energy for living organisms. One of its primary uses is as a substrate for enzyme assays, particularly for studying enzymes involved in glycogen metabolism. Additionally, it plays a role in the synthesis of various important molecules. In scientific research, α-D-Glucose 1-phosphate dipotassium salt serves as a substrate for measuring enzyme activity, particularly those related to glycogen metabolism. Moreover, it is utilized in the synthesis of essential molecules like nucleotides and glycosaminoglycans. The mechanism of action of α-D-Glucose 1-phosphate dipotassium salt stems from its ability to act as a substrate for enzymes involved in glycogen metabolism. Through the action of the enzyme phosphoglucomutase, Alpha-Glucose-1-phosphate is converted into glucose-6-phosphate, which can further be metabolized to provide energy for cellular processes.


α-D-Glucose 1-phosphate dipotassium salt (CAS 5996-14-5) References

  1. Structural analysis of amylose tris(3,5-dimethylphenylcarbamate) by NMR relevant to its chiral recognition mechanism in HPLC.  |  Yamamoto, C., et al. 2002. J Am Chem Soc. 124: 12583-9. PMID: 12381203
  2. NMR and computational studies of chiral discrimination by amylose tris(3,5-dimethylphenylcarbamate).  |  Ye, YK., et al. 2007. J Phys Chem B. 111: 1189-98. PMID: 17266274
  3. Immobilized polysaccharide derivatives: chiral packing materials for efficient HPLC resolution.  |  Ikai, T., et al. 2007. Chem Rec. 7: 91-103. PMID: 17394175
  4. [Optimization of enzymatic preparation of glucose 1-phosphate by response surface methodology].  |  Wang, X., et al. 2013. Sheng Wu Gong Cheng Xue Bao. 29: 107-10. PMID: 23631123
  5. Synthesis and application of immobilized polysaccharide-based chiral stationary phases for enantioseparation by high-performance liquid chromatography.  |  Shen, J., et al. 2014. J Chromatogr A. 1363: 51-61. PMID: 24997110
  6. Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC.  |  Enomoto, N., et al. 1996. Anal Chem. 68: 2798-804. PMID: 8794916
  7. Enantioseparation using selected polysaccharides as chiral buffer additives in capillary electrophoresis.  |  Chankvetadze, B., et al. 1997. J Chromatogr A. 773: 331-8. PMID: 9228803

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

α-D-Glucose 1-phosphate dipotassium salt, 2 g

sc-222432
2 g
$198.00

α-D-Glucose 1-phosphate dipotassium salt, 5 g

sc-222432A
5 g
$303.00