Ion-pairing reagents, when used as mobile phase additives, promote the analysis of ionic and highly polar substances on reversed phase HPLC columns. The purity of mobile phase additives is of highest significance for their effective application. Sigma-Aldrich makes available a variety of tailor-made reagents for anionic (quaternary ammonium and phosphonium salts) and cationic (alkanesulfonates) separations. All mobile phase additives are tested thoroughly with special consideration on the demands of modern reversed phase HPLC:
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pH Standardization in Analytical Chemistry: Buffers serve as critical components in the batch-to-batch reproducibility studies for primary pH methods, ensuring high precision in pH measurement across various scientific disciplines, from pharmaceuticals to environmental science (Asakai et al., 2024).
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LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
Elucidating dissolution kinetics and mechanisms at carbonate mineral-water interfaces is essential to many environmental and geochemical processes, including geologic CO(2) sequestration in deep aquifers. In the present work, effects of background electrolytes on dolomite (CaMg(CO(3))(2)) reactivity were investigated by measuring
Lignocellulosic biomass was submitted to a biological pretreatment prior to a catalytic hydroliquefaction in order to produce biofuel. The biodegradation process was conducted over 3 months in a reactor under controlled conditions. During the biodegradation process the organic matter was
Journal of neuroscience methods, 205(1), 110-118 (2012-01-11)
Numerous brain structures are composed of distinct layers and such stratification has a profound effect on extracellular diffusion transport in these structures. We have derived a more general form of diffusion equation incorporating inhomogeneities in both the extracellular volume fraction
A strategy for changing plasma pralidoxime kinetics and, perhaps, effect in organophosphorus insecticide poisoning.
Michael Eddleston et al.
Critical care medicine, 39(4), 908-909 (2011-05-27)
Chemistry (Weinheim an der Bergstrasse, Germany), 18(18), 5552-5557 (2012-04-11)
The non-covalent interactions of different upper-rim-substituted C(2)-resorcinarenes with tetramethylammonium salts were analyzed in the gas phase in an Electrospray Ionization Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometer and by (1)H NMR titrations. The order of binding strengths of the hosts towards the
