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Cyclodextrins in chromatography / Tibor Cserháti and Esther Forgács.

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Royal Society of Chemistry eBooks 1968-2026 Available online

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Format:
Book
Author/Creator:
Cserháti, Tibor.
Contributor:
Forgács, Esther, 1957-
Royal Society of Chemistry (Great Britain)
Series:
RSC Chromatography Monographs
RSC chromatography monographs
ISSN
Language:
English
Subjects (All):
Chromatographic analysis.
Cyclodextrins.
Physical Description:
1 online resource (168 p.)
Edition:
1st ed.
Place of Publication:
Cambridge : Royal Society of Chemistry, c2003.
Language Note:
English
Summary:
Cyclodextrins can form complexes with a wide variety of organic and inorganic compounds, a property which can prove useful when trying to separate complex mixtures. This book provides an up-to-date and critical evaluation of the application of cyclodextrins in many fields of chromatography (including thin layer, gas-liquid, high performance liquid and supercritical fluid chromatography; capillary electrophoresis; and isotacophoresis). Whilst mainly practical in nature, the book also looks briefly at the theoretical background for the various techniques.Any professional working with chromatogra
Contents:
BK9780854045402-FX001; CIC; Figure 1; Figure 1; Figure 1; Figure 1; Figure 1; Table 1; Figure 2; Table 2; Table 1; Figure 2; Table 2; Figure 2; Figure 2; Table 1; Table 2; Figure 2; Table 1; Table 2; 1&X; Selector Properties; heading01; References; 1&X; Thin-layer Chromatography; 1&X; Capillary Zone Electrophoresis; 2&X; Solubility of Cyclodextrins; Figure 3; 2&X; Separation of Optical and Positional Isomers with Cyclodextrins; Figure 3; Figure 3; Modification of Retention Be-hav-iour; Figure 3; Separation of Positional and Optical Isomers of Pesticides; Figure 3; 3&X; Dielectric Properties
4&XThermal Properties; Separation of Positional and Optical Isomers of Pesticides; Separation of Toxaphenes; Determination of the Strength of Cyclodextrin; Separation of positional and Optical Isomers; Separation of Positional and Optical Isomers of Other Environmental Pollutants; Separation of Positional and Optical Isomers of Amino Acids and Related Com-pounds; Figure 4; Figure 4; Figure 4; Figure 4; Figure 4; 5&X; Chemically Modified Cyclodextrins (Cyclodextrin Derivatives); Table 3; Separation of HCH; Table 3; 2&X; High Per-form-ance Liquid Chromatography
Separation of Positional and Optical Isomers of PharmaceuticalsTable 3; 6&X; Cyclodextrin Polymers; Table 4; Separation of Positional and Optical Isomers of Other Environmental Pollutants; Table 4; Cyclodextrin Stationary Phases; Table 4; Separation of Positional and Optical Isomers of Miscellaneous Organic Com-pounds; References; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; Other Organohalogen Analytes or PCB and Arylhalogen Analy-sis; mkr1; mkr2; mkr3
mkr4mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; Determination of the Strength of inter-action Be-tween CD-Bonded Stationary Phase and solutes; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; Acids; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16
mkr17mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; Figure 5; Figure 5; Figure 5; Other Analytes; Separation of Positional and Optical Isomers of Pesticides and Other Environmental Pollutants; Anions; Figure 6; Figure 6; Figure 6; Figure 7; Figure 7; Figure 7; Figure 8; Figure 8; Figure 8; Separation of Positional and Optical Isomers of Pharmaceuticals; Figure 9; Separation of Positional and Optical Isomers of Pharmaceuticals; Figure 9; Figure 9; 2&X; Micellar Electrokinetic Chromatography
Separation of Positional and Optical Isomers of Aroma Com-pounds and Food Com-po-nents
Notes:
Description based upon print version of record.
Includes bibliographical references and index.
ISBN:
9781847550675
1847550673
OCLC:
843641050

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