Title of article :
Determination of the Reactivity of the Anti-cancer Nitrogen Mustard-Mechlorethamine: A Cyclic Voltammetric Investigation
Author/Authors :
Setiyanto Henry نويسنده Analytical Chemistry Research Group, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesha No.10 Bandung 40132, Indonesia , Saraswaty Vienna نويسنده Research Centre for Chemistry, Indonesian Institute of Sciences Jl. Cisitu Sangkuriang Bandung 40135, Indonesia , Hertadi Rukman نويسنده Biochemistry Research Group, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesha No.10 Bandung 40132, Indonesia , Buchari Buchari نويسنده Analytical Chemistry Research Group, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesha No.10 Bandung 40132, Indonesia
Pages :
9
From page :
657
To page :
665
Abstract :
We have investigated the electrochemical interaction between mechlorethamine and organic solvents i.e. acetone and acetonitrile, in the presence and absence of 4-chloro butyronitrile (CBN) using cyclic voltammetric technique. We found the reactivity (chemical reactivity) of mechlorethamine through the value of the forward reaction rate constants (Kf) in acetone and acetonitrile, in the presence and absence of CBN were 0.1601 s-1, 0.4828 s-1, 0.1365 s-1, 0.2724 s-1, respectively. These values of Kf were determined from the curves of Kft versus t with correlation coefficient values are higher than 0.9500. The values of Kf affected by the donor number (DN) of solvents and also the structure of the nucleophilic compound were added. This is due to acetone has a larger DN than acetonitrile therefore Kf in acetone is higher than that in acetonitrile. CBN reduces the value of the chemical reactivities of mechlorethamine in both solvents. This can occur because CBN is a simple structure that is why it can interact directly with mechlorethamine
Journal title :
Astroparticle Physics
Serial Year :
2015
Record number :
2412510
Link To Document :
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