Name: Enantiomeric separation of Valganciclovir by HPLC and LC/MS methods (en Inglés)
Price: 57.26 USD
Availability: InStock
Author: Gowramma, Byran ; Meyyanathan, Subramania Nainar ; Kalirajan, Rajagopal
ISBN: 9786202554305

portada Enantiomeric separation of Valganciclovir by HPLC and LC/MS methods (en Inglés)

Enantiomeric separation of Valganciclovir by HPLC and LC/MS methods (en Inglés)

Formato

Libro Físico

Autor

Byran Gowramma

Subramania Nainar Meyyanathan

Rajagopal Kalirajan

Editorial

LAP Lambert Academic Publishing

Idioma

Inglés

N° páginas

Encuadernación

Tapa Blanda

Dimensiones

22.9 x 15.2 x 0.5 cm

Peso

0.14 kg.

ISBN13

9786202554305

Categorías

Empresa y gestión

Enantiomeric separation of Valganciclovir by HPLC and LC/MS methods (en Inglés)

Byran Gowramma (Autor) · Subramania Nainar Meyyanathan (Autor) · Rajagopal Kalirajan (Autor) · LAP Lambert Academic Publishing · Tapa Blanda

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Reseña del libro "Enantiomeric separation of Valganciclovir by HPLC and LC/MS methods (en Inglés)"

Chiral separations occupy an important sector of HPLC-type analyses since many bioorganic molecules, as well as many pharmaceutical drugs, are chiral.However, the selection of a column in chiral separation and the development of a successful HPLC procedure remain a rather difficult subject. The differences in the interaction forces between enantiomers are typically small, and specific phases are more suitable than others for a specific separation.he selection of a chiral column for developing a separation is typically based on manufacturer recommendations. The selection of a chiral column for developing a separation is typically based on manufacturer recommendations. Among the different chiral stationary phases (CSPs) used in chiral HPLC, the polysaccharide CSPs have proved to be very useful and might be recommended as first-choice columns when one wants to develop chiral separations. These CSPs know many applications, both in normal-phase and reversed-phase mode. The chiral selectors of these CSPs have a broad enantiorecognition range (80% of marketed drugs), which makes them excellent candidates for developing both screening strategies and individually optimized separations.