HPLC, uses

Schematic diagrams of flow cell detectors for HPLC using (a) UVA/is absorption spectrophotometry and (b) amperometry.

The amount of caffeine in an analgesic tablet was determined by HPLC using a normal calibration curve. Standard solutions of caffeine were prepared and analyzed using a lO-pL fixed-volume injection loop. Results for the standards are summarized in the following table. 

Instmmental methods of analysis provide information about the specific composition and purity of the amines. QuaUtative information about the identity of the product (functional groups present) and quantitative analysis (amount of various components such as nitrile, amide, acid, and deterruination of unsaturation) can be obtained by infrared analysis. Gas chromatography (gc), with a Hquid phase of either Apiezon grease or Carbowax, and high performance Hquid chromatography (hplc), using siHca columns and solvent systems such as isooctane, methyl tert-huty ether, tetrahydrofuran, and methanol, are used for quantitative analysis of fatty amine mixtures. Nuclear magnetic resonance spectroscopy (nmr), both proton ( H) and carbon-13 ( C), which can be used for quaHtative and quantitative analysis, is an important method used to analyze fatty amines (8,81). 

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. 

Proteoglycans (from cultured human muscle cells). Separated by ion-exchange HPLC using a Biogel TSK-DEAE 5-PW analytical column. [Harper et al. Anal Biochem 159 150 1986.]... 

Xylanase (from Streptomyces lividans) [37278-89-0] Mr 43,000 [EC 3.2.1.8]. Purified by anion-exchange chromatography on an Accell QMA column and finally by HPLC using a ProteinPak DEAE 5PW anion-exchange column. Solutions were stored frozen at -70°. [Morosoli et al. Biochem J 239 587 79S6 Wong et al. Microbiol Rev 52 305 1988.]... 

Determined by HPLC using diode array detection of a sample taken directly from the reaction mixture. b (< = 1, CHClj). 

A method offering the possibility for the separation, identification, and determination of alkyl- and alkylphenol ether carboxylates, even in mixtures with other nonionic and amphoteric substances, is carried out by HPLC using a reverse phase RP18 column and a mixture of methanol, water, and acetonitrile with the addition of an ion-pairing reagent as mobile phase working under isocratic conditions [242]. 

MacMillan and Wright [133] identified and measured saturated and unsaturated 1,3- and saturated 1,4-sultones in anionic surfactants by a series of separation maneuvers. Ion exchange treatment separates sultones from the bulk of the ionic surfactant. TLC concentrates the sultones systems for HPLC analysis. They found that pentane-ether is preferable to the usual hexane-ether system and that the addition of a little methanol sharpens the separations. Finally, HPLC using a micro-Porasil column with 90 1 isooctane/ethanol provides quali-... 

The sulfanes are soluble in carbon disulfide, benzene, tetrachloromethane, and dry diethylether (decreasingly so in that order) while alcohols and aqueous systems initiate rapid decomposition. For this reason a report on the chromatographic separation of the sulfanes H2S by reversed-phase HPLC using methanol as an eluent [35] was shown to be in error The peaks observed in the chromatogram have to be assigned to bismethoxy oligosulfanes... 

The activated carbonyl of anhydrides can acylate alcohols or amines at the temperatures necessary for polymer processing. These reactions have been verified by HPLC using the polymer system described in Table 2. An examination of the HPLC chromatograms in Fig. 25 indicates that the phthalic anhydride peak (3.2 min) diminishes with increasing injection-molding temperatures and that two new peaks (4.6 and 6.9 min) increase in intensity. These new peaks corresponded to the half phthalate esters of 1,6-hexanediol and trans-... 

The most direct method is the separation of the enantiomers by HPLC using chiral columns. It has the advantage that there is no risk of contamination from chiral resolving agents. The formation of diastereoisomers... 

A dansyl-containing lysine analogue, monodansylcadaverine (MDC), was used in initial TGase linking, because the dansyl UV absorption peak allowed quantification by reverse-phase HPLC using the absorbance at 280 nm. The reacted Qll was dissolved in TFA along with a known dansyl standard. Peak areas of the standard were then compared with product to establish the amormt of MDC present into Qll. Six Qll peaks were measured and ascribed to Qll with zero to five MDCs attached (Fig. 33). 

Below the dotted line in Table I we list less fundamental differences between the two methods. Column lengths tend to be somewhat shorter in HPLC using small particle PB as a consequence of the high efficiencies that can be generated with the smaller particle sizes. For analytical scale HPLC, tube diameters of 3-4 mm are selected however, for preparative scale, tube diameters of 1 cm or above are not uncommon. 

Grootveld, M. and Halliwell, B. (1986a). An aromatic hydroxy-lation assay for hydroxyl radicals utilising high performance liquid chromatography (HPLC). Use to investigate the effect... 

Jorg, E. and Sontag, G. (1992). Determination of phenolic acids in honey by HPLC using coulometric dual electrode detection. Dtsch. Lebensm. Rundsh. 88,179-183. 

Bispyribac in water samples can be directly quantifled by high-performance liquid chromatography (HPLC) using an ultravilot (UV) detector without methylation. 

The increased use of IV-methyl carbamate insecticides in agriculture demands the development of selective and sensitive analytical procedures to determine trace level residues of these compounds in crops and other food products. HPLC is the technique most widely used to circumvent heat sensitivity of these pesticides. However, HPLC with UV detection lacks the selectivity and sensitivity needed for their analysis. In the late 1970s and early 1980s, HPLC using post-column hydrolysis and derivatization was developed and refined with fluorescence detection to overcome these problems. The technique relies on the post-column hydrolysis of the carbamate moiety to methylamine with subsequent derivatization to a fluorescent isoindole product. This technique is currently the most widely used HPLC method for the determination of carbamates in water" and in fruits and vegetables." " ... 

Several applications of on-line HPLC used as temporary installations for process monitoring are presented in this section. These case histories include... 

Inman, E. L. and Tenbarge, H. J., High-low chromatography estimating impurities in HPLC using a pair of sample injections, /. Chromatogr. Sci., 26, 89,... 

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