Microanalysis of Si,S and Zn in GaSb by use of direct observation of (p,p′γ) reactions

The use of direct observation of nuclear reactions (p,p′γ) is discussed. The main characteristics of this method are presented and applied to the case of the miroanalysis of Si, S and Zn in GaSb.     

Investigations in the imidazole series

Imidazo[1,2-a]imidazole derivatives were synthesized by the reaction of 1-acylmethyl-2-bromo-4,5-diphenylimidazoles with ammonia and primary amines.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1243–1247, September, 1971.     

Structure and PMR spectra of isoquercitrin and hirsutrin

Chemistry of Natural Compounds - 1. Two isomers of quercetin 3-glucoside are present in the flowers and leaves of the cotton plant of variety 108-F: hirsutrin, quercetin 3-β-D-glucopyranoside;...     

Use of p-dimethylaminobenzalhyde as a colored reagent for determination of procaine hydrochloride by spectrophotometry

Spectrophotometric determination of procaine hydrochloride is described. The procaine hydrochloride reacts with p-dimethylaminobenzalhyde in glacial acetic acid to form an Schiff base which is a yellow compound, and its maximum absorption wavelength is at 455nm, ₄₅₅=3.46×10⁴. The absorbance for procaine hydrochloride from 0.2 to 15 μg ml⁻¹ obeys Beer's law. The linear regression equation of the calibration graph is C=5.866A−0.02, with a linear regression correlative coefficient is 0.9994 and relative standard deviation (RSD) of 1.7%; the detection limit is 0.1 μg ml⁻¹; recovery is from 92.0 to 110.0%. Effects of reaction medium, temperature, gentamycin, beneylpenicillin, kanamycin, streptomycin, foreign ions, and stand for time on the determination of procaine hydrochloride have been examined. The results obtained by this method agreed with those by the official method (dead-stop titration). This method is rapid and simple, and can be used for the determination of procaine hydrochloride in injection solution of procaine hydrochloride.     

Morestan (6-Methyl-2,3-chinoxalindithiolcarbonat) als Rückstand auf Orangenschalen

Analytical and Bioanalytical Chemistry -     

Reaction of quinoxaline with benzopyridines in acetic anhydrides in the presence of Zn dust

The reaction between quinoxaline and benzopyridine in acetic anhydride in the presence of zinc dust gives a quinoxaline anion and a benzopyridine N-acetyl radical, which recombine to give the previously unknown N-acetyl dihydrobenzo-pyridine derivative of 1,2-dihydroquinoxaline. Under these conditions, quinoxaline alone gives 1,4-diacetyl-1,4-dihydroquinoxaline and 1-acetyl-2-(1,2-dihydroquinoxalyl-2)-1,2-dihydroquinoxaline.Previous communication, [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 967–973, July, 1985.