40762-22-9 Usage
Description
D-Glucose-1-13C is a stable isotope-labeled monosaccharide that is present in plants and plays a crucial role in various metabolic processes. It may exist in open chain or cyclic conformation if in solution and is involved in photosynthesis and cellular respiration.
Uses
Used in Metabolic Studies:
D-Glucose-1-13C is used as a tracer compound for studying metabolic pathways and enzymatic reactions in various organisms. It helps in understanding the primary reaction mechanism in pyrolysis of glucose and the conversion of labeled glucose into alkanediols using Ni-MgO-ZnO catalyst.
Used in Diagnostic Applications:
D-Glucose-1-13C is used as a diagnostic tool for detecting type 2 diabetes mellitus and potentially Huntington's disease through the analysis of blood-glucose levels in type 1 diabetes mellitus.
Used in Tracer Enrichment Determination:
D-Glucose-1-13C is used in tracer enrichment determination in blood plasma using high-resolution mass spectrometry, providing valuable insights into metabolic processes and disease mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 40762-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40762-22:
(7*4)+(6*0)+(5*7)+(4*6)+(3*2)+(2*2)+(1*2)=99
99 % 10 = 9
So 40762-22-9 is a valid CAS Registry Number.
40762-22-9Relevant articles and documents
HYDROXIDE-CATALYZED ISOMERIZATION OF D-(1-13C)MANNOSE: EVIDENCE FOR THE INVOLVEMENT OF 3,4-ENEDIOLS
King-Morris, Melinda J.,Serianni, Anthony S.
, p. 29 - 36 (2007/10/02)
The KOH-catalyzed isomerization of D-(1-13C)mannose under anaerobic conditions was studied by 13C-n.m.r. spectroscopy.D-(1-13C)Glucose and D-(1-13C)fructose are generated during the reaction, as expected.In addition, however, (6-13C)glucose, (6-13C)mannose, and (6-13C)fructose are produced in small proportions, possibly via symmetrical 3,4-enediol intermediates.The involvement of the latter structures in 13C-label shifting is inferred from the observation of (1-13C)sorbose and (6-13C)sorbose in the reaction mixture.