1960
DOI: 10.1007/bf01221839
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D�nnschichtchromatographie in der Toxikologie

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Cited by 58 publications
(5 citation statements)
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“…A spray method may be used after chromatography, including such fluorescent reagent sprays as a solution of 2',7'-dichlorofluorescein in ethanol (Mangold, 1961), a solution of fluorescein in water (Kirchner et al, 1951;Stahl, 1958), a solution of Rhodamine B in water (Manchata, 1960;Huneck, 1962) or a solution of morin in methanol (Schellenberg, 1962). Compounds containing conjugated double bonds appear as colored spots when viewed under ultraviolet light.…”
Section: Sawickimentioning
confidence: 99%
See 1 more Smart Citation
“…A spray method may be used after chromatography, including such fluorescent reagent sprays as a solution of 2',7'-dichlorofluorescein in ethanol (Mangold, 1961), a solution of fluorescein in water (Kirchner et al, 1951;Stahl, 1958), a solution of Rhodamine B in water (Manchata, 1960;Huneck, 1962) or a solution of morin in methanol (Schellenberg, 1962). Compounds containing conjugated double bonds appear as colored spots when viewed under ultraviolet light.…”
Section: Sawickimentioning
confidence: 99%
“…Alternative processes incorporate organic fluorescent agents in the slurry during the preparation. These include the use of aqueous sodium fluorescein solution instead of water (Stahl, 1958), Rhodamine 6G in adsorbent (Reitsema, 1954; Avigan et al, 1963), and a solution of 2',7'-dichlorofluorescein (Brown and Johnson, 1962).A spray method may be used after chromatography, including such fluorescent reagent sprays as a solution of 2',7'-dichlorofluorescein in ethanol (Mangold, 1961), a solution of fluorescein in water (Kirchner et al, 1951;Stahl, 1958), a solution of Rhodamine B in water (Manchata, 1960;Huneck, 1962) or a solution of morin in methanol (Schellenberg, 1962). Compounds containing conjugated double bonds appear as colored spots when viewed under ultraviolet light.…”
mentioning
confidence: 99%
“…Salts of various alkaloids have been separated on adsorption columns of basic and neutral alumina (166-169) or silicic acid (29), but most investigators prefer partition columns, usually with a buffer as the stationary phase (279, 358, 861-863, 927, 1350, 1594, 1662). Similarly, while adsorption chromatography on paper (320) or thin lay ers of adsorbents (296,306,387,449,722,867,965,1068,1130,1283) is used to some extent, paper partition chromatography is apparently superior (943) and the bulk of the research work on alkaloid separations continues to be done in this area (1135).…”
Section: Carbohydratesmentioning
confidence: 99%
“…Thin-layer chromatography has been used by Cochin & Daly (1963) to identify 16 commercially available barbiturates after their extraction from urine into methylene chloride, and Machata (1960) separated various barbiturates from common pharmaceutical mixtures. A simple method for the identification of barbiturate mixtures when present in blood was devised by Petzold, Camp & Kirch (1963), a procedure which was especially useful in differentiating between amylobarbitone and pentobarbitone.…”
mentioning
confidence: 99%