2922-61-4 Usage
Uses
Used in Cell Culture Media:
Pyruvic acid lithium salt is used as a growth and metabolism supporter for cells, enhancing their viability and function in various cell culture applications.
Used in Energy Provision:
In certain cell types, pyruvic acid lithium salt is used as an energy source, contributing to their metabolic processes and overall health.
Used in Buffering Agents:
Pyruvic acid lithium salt is utilized as a buffering agent in biological and chemical research, maintaining pH stability and ensuring accurate experimental conditions.
Used in Pharmaceutical Research:
Pyruvic acid lithium salt is investigated for its potential therapeutic use in treating conditions such as cancer, diabetes, and neurological disorders, showcasing its diverse applications in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 2922-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2922-61:
(6*2)+(5*9)+(4*2)+(3*2)+(2*6)+(1*1)=84
84 % 10 = 4
So 2922-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H4O3.Li/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1
2922-61-4Relevant academic research and scientific papers
Complete conversion of l-lactate into d-lactate. A generic approach involving enzymatic catalysis, electrochemical oxidation of NADH, and electrochemical reduction of pyruvate
Biade, Azz-Eddine,Bourdillon, Christian,Laval, Jean-Marc,Mairesse, Gilles,Moiroux, Jacques
, p. 893 - 897 (2007/10/02)
L-Lactate was converted into D-lactate with a yield better than 97%, the system involving stereospecific catalysis of L-lactate oxidation by the rather cheap L-lactate dehydrogenase plus electrochemical regeneration of NAD+ at the anode and electrochemical reduction of pyruvate at the cathode. Such an approach can be extended to mere deracemization or complete inversion of all types of chiral α-alcohol-acids provided that the dehydrogenase related to the isomer to be inverted is available. Efficiency was not limited by enzyme or coenzyme deactivations.
