34620-76-3 Usage
Description
Maltopentaose, a type of maltooligosaccharide, is a pentasaccharide composed of five glucose units linked by α-1,4-glycosidic bonds. It is characterized by its white powder form and has a unique structure where the glucose residue at the reducing end is in the aldehydo open-chain form.
Uses
Used in Research and Diagnostic Applications:
Maltopentaose is utilized as a research tool and for diagnostic purposes due to its specific chemical properties and structure. It aids in the study of various biological processes and the development of diagnostic tests.
Used in Nutrients and Healthcare Industry:
In the field of nutrition and healthcare, maltopentaose is used as a component in the formulation of nutritional supplements and healthcare products. Its properties make it a valuable addition to products aimed at promoting overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 34620-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,2 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34620-76:
(7*3)+(6*4)+(5*6)+(4*2)+(3*0)+(2*7)+(1*6)=103
103 % 10 = 3
So 34620-76-3 is a valid CAS Registry Number.
34620-76-3Relevant articles and documents
Regioselective glucosylation of inositols catalyzed by Thermoanaerobacter sp. CGTase
Miranda-Molina, Alfonso,Marquina-Bahena, Silvia,Alvarez, Laura,Lopez-Munguia, Agustin,Castillo, Edmundo
, p. 93 - 101,9 (2020/08/20)
Monoglucosylated products of l-chiro-, d-chiro-, muco-, and allo-inositol were synthesized by regioselective α-d-glucosylation with cyclodextrin glucosyl transferase from Thermoanaerobacter sp. after hydrolysis of by products with Aspergillus niger glucoamylase. While the reactions carried out with d-chiro-, muco-, and allo-inositol resulted in the regioselective formation of monoglucosylated products, two products were obtained in the reaction with l-chiro-inositol. Through the structural characterization of the glucosylated inositols here we demonstrated that the selectivity observed in the glucosylation of several inositols by Thermoanaerobacter sp. CGTase, is analogous to the specificity observed for the glucosylation of β-d-glucopyranose and equivalent glucosides.