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Metal complexes of fenoterol drug

Preparation, spectroscopic, thermal, and biological activity characterization

Journal of Thermal Analysis and Calorimetry
Authors: M. Soliman, Gehad Mohamed, and Eman Mohamed

(II) complex are recorded in d 6 -dimethylsulfoxide (DMSO) solution using tetramethylsilane (TMS) as internal standard. The chemical shifts of the different types of protons of the FEN drug and its diamagnetic Zn(II) complex are listed in Table 3

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study. All the other reagents: methanol, xylenol orange, arsenazo I, chloric(VII) acid, NaOH, dimethyloformamide (DMF), and dimethylsulfoxide (DMSO) were analytically pure. Synthesis of the compounds The complexes of

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bilateral CVS on behavioral parameters, changes in dopamine levels and histopathological changes in the striatum of rats with rotenone-induced PD. Material and methods Drugs and chemicals Rotenone, dimethylsulfoxide (DMSO), reference standard dopamine and

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divergence slit was used. Analysis in solution phase Nuclear Magnetic Resonance (NMR) Spectroscopy NMR spectra were obtained in deuterated dimethylsulfoxide on Bruker Advance II 400 NMR

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eluents such as acetone, chloroform, DMF, dimethylsulfoxide, ethyl acetate, methylene chloride and THF (and any basic solvent modifiers) may destroy the CSP if they are present, even in residual quantities, in the system, and (ii) the entire HPLC system

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