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α-Malate radical, also known as L-malate radical, is a chemical species derived from L-malate, an organic compound that plays a crucial role in the citric acid cycle, also known as the Krebs cycle or the tricarboxylic acid (TCA) cycle. This cycle is a series of chemical reactions used by all aerobic organisms to release stored energy through the process of cellular respiration. The α-malate radical is formed when L-malate undergoes one-electron reduction, resulting in the formation of a radical species with an unpaired electron. This radical is involved in various biochemical processes, including electron transfer reactions and redox signaling, which are essential for maintaining cellular homeostasis and regulating metabolic pathways.

15906-66-8

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15906-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15906-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15906-66:
(7*1)+(6*5)+(5*9)+(4*0)+(3*6)+(2*6)+(1*6)=118
118 % 10 = 8
So 15906-66-8 is a valid CAS Registry Number.

15906-66-8Downstream Products

15906-66-8Relevant academic research and scientific papers

Rate constants for the OH reactions with oxygenated organic compounds in aqueous solution

Gligorovski,Rousse,George,Herrmann

, p. 309 - 326 (2009)

The kinetics of the oxidation of functionalized organic compounds of atmospheric relevance by the hydroxyl radical (OH) was measured in the aqueous phase. Competition kinetics, using the thiocyanate anion (SCN-) as competitor, was applied using both a las

A Pulse Radiolysis Study of Some Dicarboxylic Acids of the Citric Acid Cycle. The Kinetics and Spectral Properties of the Free Radicals Formed by Reaction with the OH Radical

Cabelli, Diane, E.,Bielski, Benon H. J.

, p. 1731 - 1737 (2007/10/02)

The reactions between the OH radical and fumaric acid, maleic acid, malic acid and succinic acid were studied using pulse radiolysis techniques.The rates of reaction, the absorption spectra of the resultant free radicals and the rates of disappearance of those radicals were determined as a function of pH over virtually the entire pH range (pH 2 - 14). - Key words: Pulse Radiolysis, Dicarboxylic Acid Radicals

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