THE PREPARATION AND PROPERTIES OF THE POTASSIUM SKATOLYL SULFATES (THE "SULFATOXYSKATOLES")

1965 ◽  
Vol 43 (4) ◽  
pp. 469-478 ◽  
Author(s):  
R. A. Heacock ◽  
O. Hutzinger

The four isomeric potassium skatolyl sulfates, with the sulfate residue attached to the 4-, 5-, 6-, and 7-positions in the benzene moiety of the skatole molecule, have been synthesized. The four isomers were prepared by the sulfation of the corresponding hydroxyskatoles with either (a) the pyridine – sulfur trioxide complex in pyridine or (b) chlorosulfonic acid in pyridine. The ultraviolet spectroscopy of this group of compounds is discussed together with their paper chromatographic behavior in several different solvent systems.

1979 ◽  
Vol 6 (4) ◽  
pp. 485 ◽  
Author(s):  
MG Smart ◽  
TP O'brien

Fractions enriched in the cell walls of wheat and barley scutella were prepared from isolated, ungerminated scutella. The cell-wall fractions were subjected to hot, alkaline extraction under an inert atmosphere. An ether extract was investigated for phenolic compounds by thin-layer chromatography using three solvent systems and by ultraviolet spectroscopy. The major autofluorescent component of the scutella of both wheat and barley is ferulic acid. There is apparently no p-coumaric acid.


2020 ◽  
pp. 5-15
Author(s):  
Yuriy Nikolayevich Malyar ◽  
Natal'ya Yur'yevna Vasil'yeva ◽  
Aleksandr Sergeyevich Kazachenko ◽  
Galina Pavlovna Skvortsova ◽  
Irina Vladimirovna Korol'kova ◽  
...  

In this work, we optimized the process of sulfating abies ethanol lignin with complexes of sulfuric anhydride with pyridine and 1,4-dioxane. Experimentally found are the conditions for the implementation of the process of sulfation of abies ethanol lignin by complexes of sulfur trioxide with 1,4-dioxane and pyridine, providing a high sulfur content (12.0–12.6%). It was shown that a high sulfur content of 12.0–13.5% (mass.) in the obtained ethanol lignin sulfate is achieved when the ratio of the amount of chlorosulfonic acid to the amount of abies ethanol lignin is 20.22 : 1 mmol : g and the duration of the sulfation process is 60–120 min and independent of the nature of the sulfating complex. The structure and composition of water-soluble sulfated abies ethanol lignin are confirmed by FTIR spectroscopy, gel permeation chromatography and elemental analysis. In the FTIR spectra of sulfated abies ethanol lignin, in comparison with the FTIR spectra of the initial abies ethanol lignin, there are absorption bands in the region of 1270–1260, 1220–1212, 861–803 cm-1, corresponding to vibrations of sulfate groups. Compared to the initial lignin, sulfated abies ethanol lignin has a low degree of polydispersity. In particular, there was an increase in Mw c ~1.5 kDa to ~3.4 kDa in lignin sulfated for 30 min and a decrease in polydispersity from 2.59 to 1.22 compared to the initial abies ethanol lignin. With an increase in the sulfation time, the profile of the molecular mass distribution curve shifts to a high molecular weight region, with a simultaneous increase in polydispersity to 1.5 and Mw increases to ~4.3 kDa.


1974 ◽  
Vol 20 (2) ◽  
pp. 155-161 ◽  
Author(s):  
B. Vaks ◽  
A. Zuckerberg ◽  
E. Rosenberg

A strain of Myxococcus xanthus, referred to as M. xanthus TA, has been isolated which produces an antibiotic capable of inhibiting growth of certain Gram-positive and Gram-negative bacteria. Antibiotic production was significantly inhibited when the concentration of protein hydrolysate in the production medium exceeded 1%. The antibiotic was purified over 1000 times to apparent homogeneity by silicic acid chromatography and by a variety of preparative alumina thin-layer chromatographic procedures. The purified antibiotic was partially characterized by its chromatographic behavior in six solvent systems, stability to acid, alkali and heat, infrared, ultraviolet, and mass spectra. The antibiotic has a λmax of 242 nm in methanol.


1976 ◽  
Vol 59 (6) ◽  
pp. 1416-1418
Author(s):  
Jitendra J Shah ◽  
Ramila J Shah

Abstract Thin layer chromatographic behavior of some sympathomimetic amines in the presence of acids in neutral and organic solvent systems is reported. The sympathomimetic amines were dissolved in 0.1N HCl or ethanol and treated with bromocresol green or p-nitrobenzoyl chloride reagents on fiber sheets or precoated glass plates. Two-, 3-, and 4-component solvent systems were tested. Benzene-ethyl acetate gave 2 spots for each amine standard; the more polar spots were satisfactorily separated. Amines in pharmaceuticals were not separated by any solvent system tested.


1950 ◽  
Vol 22 (4) ◽  
pp. 549-552 ◽  
Author(s):  
William. Seaman ◽  
J. T. Woods ◽  
H. N. Bank

1958 ◽  
Vol 36 (5) ◽  
pp. 853-857 ◽  
Author(s):  
R. A. Heacock ◽  
C. Nerenberg ◽  
A. N. Payza

The preparation of adrenochrome in a pure stable crystalline form has been carried out by the silver oxide oxidation of adrenaline in methanol with the use of an anion-exchange resin (Dowex-1(Cl−)) to remove heavy metal ions from the reaction mixture prior to the isolation of the product. Its paper chromatographic behavior together with that of three derivatives (adrenolutin, adrenochrome monosemicarbazone, and adrenochrome monoisonicotinic acid hydrazide) in six different solvent systems has been examined. Water was found to be the best paper chromatographic solvent so far examined for this series of compounds.


1964 ◽  
Vol 42 (8) ◽  
pp. 1177-1182 ◽  
Author(s):  
F. Hertelendy ◽  
R. H. Common

16-Epiestriol has been isolated in crystalline form from hen urine and characterized on the basis of the melting points of the isolated product and of two of its derivatives (acetonide, triacetate) and on the chromatographic behavior of the isolated product and five of its derivatives in each of three different solvent systems.


1969 ◽  
Vol 67 (1_3) ◽  
pp. 168-168
Author(s):  
H. G. Hertz

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