867-55-0 Usage
Uses
Used in Pharmaceutical Industry:
Lithium Lactate is used as a mood stabilizer for the treatment of bipolar disorder. It is believed to work by altering the levels of certain chemicals in the brain, such as serotonin and norepinephrine, which help regulate mood.
Used in Research:
Lithium Lactate is used as an electron spin resonance (ESR) dosimeter material. It is employed in the measurement of radiation doses in various research applications.
Used in Analytical Chemistry:
Lithium Lactate is used as a lactic acid standard in the determination of lactic acid. It serves as a reference material for the accurate quantification of lactic acid in various samples.
Used in Enzymatic Assays:
Lithium Lactate is used as a lactic acid standard in the determination of lactic acid with muscle lactic dehydrogenase by an enzymatic method. It provides a reliable reference for the accurate measurement of lactic acid levels in biological samples.
Safety Profile
Moderately toxic by
ingestion and subcutaneous routes. When
heated to decomposition it emits acrid
smoke and irritating fumes. See also
LITHIUM COMPOUNDS.
Check Digit Verification of cas no
The CAS Registry Mumber 867-55-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 867-55:
(5*8)+(4*6)+(3*7)+(2*5)+(1*5)=100
100 % 10 = 0
So 867-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O3.Li/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1
867-55-0Relevant 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.
