Chromatography visualization

Liquid chromatography Visual inspection of eluting fractions Ultraviolet analysis of eluted fractions... 

Hematoside was extracted from the cells, isolated by thin-layer chromatography, visualized with resorcinol spray, and quantitated by direct densitometry as described in Section II. 

Lipoproteins may denature on heating and if present during pasteurization can result in the formation of haze or turbidity in the final product. This material was removed traditionally by filtration through asbestos (qv) sheets (6) however, health hazards associated with asbestos have led to its replacement by alternative filter materials (23,37,193). These media have been less effective than asbestos and further measures have been required to ensure the visual clarity of albumin products, eg, further filtration developments for Hpid removal (194), preferential denaturation of contaminants using in-process heat treatment, and anion-exchange chromatography (49). 

Chemical stabiUty studies are monitored by siUca gel thin-layer chromatography (dc) or by high performance Hquid chromatography (hplc) using a reverse-phase C g coated column (24). Hplc peaks or dc spots are visualized by thek uv absorption at 245 nm the tic spots can also be detected by ceric sulfate or phosphomolybdic acid staining. 

An important publication by Kost et al. (63JGU525) on thin-layer chromatography (TLC) of pyrazoles contains a large collection of Rf values for 1 1 mixtures of petroleum ether-chloroform or benzene-chloroform as eluents and alumina as stationary phase. 1,3- and 1,5-disubstituted pyrazoles can be separated and identified by TLC (Rf l,3>i y 1,5). For another publication by the same authors on the chromatographic separation of the aminopyrazoles, see (63JGU2519). A-Unsubstituted pyrazoles move with difficulty and it is necessary to add acetone or methanol to the eluent mixture. Other convenient conditions for AH pyrazoles utilize silica gel and ethyl acetate saturated with water (a pentacyanoamine ferroate ammonium disodium salt solution can be used to visualize the pyrazoles). 

Fractions may be monitored by thin-layer chromatography on silica gel, developing with 10% v/v ethyl acetate in hexane and visualizing with iodine vapor. The following Rf values were observed famesol, 0.07 farnesyl acetate, 0.35 bromohydrin acetate, 0.20. 

TLC analysis of the crude product (elution with 50 1 pentane ether, visualization with iodine) showed three non-baseline spots Rf 0.65 (cis isomer), Rf 0.52 (unknown impurity), and Rf 0.32 (trans isomer). The unknown impurity is intensely sensitive to iodine and largely coelutes with the cw-isomer in the subsequent column chromatography. However, the ll NMR spectrum of this isomer shows excellent purity despite the presence of this spot on TLC. In 100 1 pentane ether, Rf values of the cis and trans isomers are about 0.50 and 0.15, respectively. 

Analysis by thin layer chromatography (TLC) indicates product formation and a small amount of starting material. TLC was performed on Merck Silica gel 60 F-254 coated on aluminum sheets. Product 3 has Rf = 0.44 (elution with 70 30 petroleum ether-ethyl acetate visualization with iodine vapor). 

Analytical thin-layer chromatography was performed on E. Merck silica gel 60 F254 plates (0.25 mm) and compounds were visualized by dipping the plates in a cerium sulfate-ammonium molybdate solution followed by heating. 

Besides the calculation of the different sulfonated species, it is also possible to determine them directly by chromatographic methods. Separation of the ester sulfonate and the disodium salt is achieved by thin-layer chromatography on silica gel plates. With a solvent mixture of acetone and tetrahydrofuran (90 10 v/v) the disodium salt stays at the start whereas the ester sulfonate has an R value of 0.2. With the more polar solvent 0.1 N H2S04 + methanol + chloroform the ester sulfonate and the disalt have Rf values of 0.36 and 0.14. For visualization, the plate is sprayed with pinacryptol yellow. In UV light (254 and... 

In these studies, choose different sets of affinities (SiB) and (S2B), and run these with the same parameters for the other ingredient encounters, as in Example 6.5. The cellular automata modeling of chromatographic separation produces a very realistic picture of the events taking place. It provides a visual and a tabular representation of the influence of variables on the process. The student is challenged to pursue these models and to compare them with some of the mathematical descriptions possible from chromatography. 

Visualization Techniques for Thin-Layer Chromatography.892 Qualitative Identification and Nicroreaction Techniques it ... 

The analysis of amino acids involves chromatographic issues similar to those encountered in analysis of simple amines. Underivatized amino acids have, with a few exceptions, weak UV absorbance and a strong tendency to interact with stationary phases in undesirable ways. Underivatized amino acids are normally separated with ion exchange chromatography, then visualized post-column by reaction with ninhydrin, o-phthaladehyde (OPA), or other agents. Underivatized tryptophan and the metabolites kynurenine, 3-hydroxykynurenine, kynurenic acid, and 3-hydroxyanthranilic acid, were separated on a Partisphere 5-p ODS column with fluorescent detection.121... 

Dichloromethane extraction of culture broth, thin layer chromatography of the extract, and visualization with 5% vanillin/sulfuric acid spray is effective for detecting cycloheximide in culture broth. Cycloheximide applied to TLC plates in amounts as low as 1 yg/spot will produce visible color with the vanillin spray. 

Caffeine was extracted from ficw varieties of roasted coffee beans and was determined in parallel by (1) measurement of spot area after thin layer chromatography on silica gel GF plates (development with chloroform/ cyclohexane/glacial acetic acid, 8 2 1, visualization in UV light), and (2) Kjeldahl N determination. Caffeine contents by (1) and (2), respectively, in the five varieties analyzed were (percent in DM) Santos lave 0, 1.10, and 1.12 Java Robusta 3, 1.19, and 1.22 Camerun Robusta 2, 1.16, and 1.19 Mocca 2, 1.21, and 1.26 Guatemala 0, 1.18, and 1.20. (1) is considered slightly less accurate than (2) but rather easier and more rapid.21... 

Analytical thin layer chromatography (TLC) was conducted on 10 x 2.5-cm precoated glass plates (silica gel GF, 0.25-mm thickness, Analtech), eluted with 10% ethyl acetate in hexane, and visualized with both UV (254 nm) and aqueous 50% sulfuric add spray/heating. The carbene complex moves as an orange spot on TLC the reaction is complete when this spot is no longer visible. 

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