High-performance liquid chromatography /nuclear magnetic resonance

High-Performance Liquid Chromatography-Nuclear Magnetic Resonance... 24... [Pg.1]

D. Bao, V.Thanabal, and W. F. Pool, Determination of tacrine metabolites in microsomal incubate by high-performance liquid chromatography-nuclear magnetic resonance/mass spectrometry with a column trapping system, /. Pharma. Biomed. Anal. 28 (2002), 23-30. [Pg.935]

There are a variety of analytical methods commonly used for the characterization of neat soap and bar soaps. Many of these methods have been published as official methods by the American Oil Chemists Society (29). Additionally, many analysts choose United States Pharmacopoeia (USP), British Pharmacopoeia (BP), or Pood Chemical Codex (FCC) methods. These methods tend to be colorimetric, potentiometric, or titrametric procedures. However, a variety of instmmental techniques are also frequendy utilized, eg, gas chromatography, high performance liquid chromatography, nuclear magnetic resonance spectroscopy, infrared spectroscopy, and mass spectrometry. [Pg.159]

Albert, K. Schlotterbeck, G. Tseng, L.-H. Braumann, U. Application of on-line capillary high-performance liquid chromatography-nuclear magnetic resonance spectrometry coupling for the analysis of vitamin A derivatives. [Pg.1350]

Laude DA Jr and Wilkins CL (1984) Direct-linked analytical scale high-performance liquid chromatography/ nuclear magnetic resonance spectroscopy. Analytical Chemistry 56 2471-2475. [Pg.311]

Although saponification was found to be unnecessary for the separation and quantification of carotenoids from leafy vegetables by high performance liquid chromatography (HPLC) or open column chromatography (OCC), saponification is usually employed to clean the extract when subsequent purification steps are required such as for nuclear magnetic resonance (NMR) spectroscopy and production of standards from natural sources. [Pg.452]

D2O = deutered water. HPLC = high performance liquid chromatography. IS = internal standard. MeOH = methanol. MS = mass spectrometry. NMR = nuclear magnetic resonance. PDA = photodiode array detector. TEA = triethylamine. MTBE = methyl tert-butyl ether. [Pg.461]

Strohschein, S., Pursch, M., and Albert, K., Hyphenation of high performance liquid chromatography with nuclear magnetic resonance spectroscopy for the characterization of (3-carotene isomers employing a Cjq stationary phase, J. Pharm. Biom. Anal., 21, 669, 1999. [Pg.476]

Hentschel, P. et ah. Structure elucidation of deoxylutein 11 isomers by on-line capillary high performance liquid chromatography- H nuclear magnetic resonance spectroscopy, J. Chromatogr. A, 1112, 285, 2006. [Pg.477]

M.E. Lacey, Z. J. Tan, A. G. Webb, J. V. Sweedler 2001, (Union of capillary high-performance liquid chromatography and microcoil nuclear magnetic resonance spectroscopy applied to the separation and identification of terpenoids), J. Chromatogr. A 922(1-2), 139. [Pg.139]

FID = flame ionization detection GC = gas chromatography HPLC = high performance liquid chromatography ITMS = ion trap mass spectrometry MS = mass spectrometry PNMR = proton nuclear magnetic resonance TLC = thin-layer chromatography... [Pg.134]

Because carotenoids are light- and oxygen-sensitive, a closed-loop hyphenated technique such as the on-line coupling of high performance liquid chromatography (HPLC) together with nuclear magnetic resonance (NMR) spectroscopy can be used for the artifact-free structural determination of the different isomers. [Pg.61]

In addition to the above prescriptions, many other quantities such as solution phase ionization potentials (IPs) [15], nuclear magnetic resonance (NMR) chemical shifts and IR absorption frequencies [16-18], charge decompositions [19], lowest unoccupied molecular orbital (LUMO) energies [20-23], IPs [24], redox potentials [25], high-performance liquid chromatography (HPLC) [26], solid-state syntheses [27], Ke values [28], isoelectrophilic windows [29], and the harmonic oscillator models of the aromaticity (HOMA) index [30], have been proposed in the literature to understand the electrophilic and nucleophilic characteristics of chemical systems. [Pg.180]