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Ursprungszeugnis (CoO)/Analysenzertifikate (CoA)

567573-U

Discovery^® HS F5 (3 µm) HPLC Columns

L × I.D. 2 cm × 4 mm, Supelguard Guard Cartridge Kit with 1 Cartridge holder + 1 Guard Cartridge

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About This Item

UNSPSC-Code:

41115700

eCl@ss:

32110501

NACRES:

SB.52

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Supelguard Vorsäulenhalter

product name

Discovery^® HS F5 Supelguard Kartusche, 3 μm particle size, L × I.D. 2 cm × 4 mm, pkg of 1 kit

Materialien

stainless steel column

Agentur

suitable for USP L43

Beschreibung

Supelguard Cartridge

Produktlinie

Discovery^®

Leistungsmerkmale

endcapped

Verpackung

pkg of 1 kit

Methode(n)

HPLC: suitable
LC/MS: suitable

L × ID

2 cm × 4 mm

Oberflächenbereich

300 m²/g

Matrix

fully porous particle

Aktive Matrixgruppe

PFP (pentafluorophenyl) phase

Partikelgröße

3 μm

Porengröße

120 Å

Betriebs-pH-Wert

2-8

Anwendung(en)

food and beverages

Kompatibilität

use to protect Discovery HS F5

Trenntechnik

reversed phase

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Fußnote

Das Kit enthält eine Kartusche, einen Stand-Alone-Halter, ein Stück Rohrleitung und zwei Verschraubungen mit Ferrules.

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Rechtliche Hinweise

Discovery is a registered trademark of Merck KGaA, Darmstadt, Germany

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Leider sind derzeit keine COAs für dieses Produkt online verfügbar.

Wenn Sie Hilfe benötigen, wenden Sie sich bitte an Kundensupport

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"Heart-cut" bidimensional achiral-chiral liquid chromatography applied to the evaluation of stereoselective metabolism, in vivo biological activity and brain response to chiral drug candidates targeting the central nervous system.

Umberto M Battisti et al.

Journal of chromatography. A, 1443, 152-161 (2016-03-30)

A "heart-cut" two-dimensional achiral-chiral liquid chromatography triple-quadrupole mass spectrometry method (LC-LC-MS/MS) was developed and coupled to in vivo cerebral microdialysis to evaluate the brain response to the chiral compound (±)-7-chloro-5-(3-furanyl)-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine-1,1-dioxide ((±)-1), a potent positive allosteric modulator (PAM) of AMPA receptor.

High-performance liquid chromatographic method with UV photodiode-array, fluorescence and mass spectrometric detection for simultaneous determination of galantamine and its phase I metabolites in biological samples.

Jana Maláková et al.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 853(1-2), 265-274 (2007-04-10)

Galantamine, an alkaloid isolated from the bulbs and flowers of Caucasian snowdrop (Galanthus woronowii, Amaryllidaceae) and related species, is employed in human medicine for the treatment of various neuromuscular and neurodegenerative diseases. After the administration, the products of oxidative biotransformation

HPLC method development, validation, and impurity characterization of a potent antitumor indenoisoquinoline, LMP776 (NSC 725776).

Jennie Wang et al.

Journal of pharmaceutical and biomedical analysis, 124, 267-273 (2016-03-13)

An HPLC method for the assay of a DNA topoisomerase inhibitor, LMP776 (NSC 725776), has been developed and validated. The stress testing of LMP776 was carried out in accordance with International Conference on Harmonization (ICH) guidelines Q1A (R2) under acidic

Chromatographic separation of arsenic species with pentafluorophenyl column and application to rice.

Koji Baba et al.

Journal of chromatography. A, 1354, 109-116 (2014-06-21)

Arsenic species, including arsenous acid, arsenic acid, methylarsonic acid, and dimethylarsinic acid, were determined using HPLC-ICPMS. The species were separated with a Discovery HS F5 column and a simple, volatile, and isocratic mobile phase of 0.1% (v/v) formic acid and

Fast high-performance liquid chromatography analysis of phenethylamine alkaloids in Citrus natural products on a pentafluorophenylpropyl stationary phase.

Federica Pellati et al.

Journal of chromatography. A, 1165(1-2), 58-66 (2007-08-07)

In this study, the chromatographic performance of a pentafluorophenylpropyl (PFPP) stationary phase was evaluated for the rapid separation of phenethylamine alkaloids (i.e. (+/-)-octopamine, (+/-)-synephrine, tyramine, N-methyltyramine and hordenine) in Citrus aurantium plant material (fruits and peel), various Citrus species, extracts

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