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Ascentis^® Express 90 Å C18 (2.7 μm) HPLC Columns

Name: Ascentis<SUP>&#174;</SUP> Express 90 Å C18 (2.7 μm) HPLC Columns
Brand: SUPELCO

L × I.D. 15 cm × 100 μm HPLC Capillary Column

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About This Item

Código UNSPSC:

41115700

eCl@ss:

32110501

NACRES:

SB.52

product name

Ascentis^® Express C18, 2.7 Micron Capillary HPLC Column, 2.7 μm particle size, L × I.D. 15 cm × 100 μm

Materiales

stainless steel column

Agency

suitable for USP L1

Línea del producto

Ascentis^®

Características

endcapped

fabricante / nombre comercial

Ascentis^®

envase

1 ea of

Parámetros

400 bar pressure (5801 psi)
60 °C temp. range

técnicas

HPLC: suitable
LC/MS: suitable
UHPLC-MS: suitable
UHPLC: suitable

L × D.I.

15 cm × 100 μm

superficie

135 m²/g

impurezas

<5 ppm metals

matriz

Fused-Core particle platform
superficially porous particle

grupo activo de la matriz

C18 (octadecyl) phase

tamaño de partícula

2.7 μm

tamaño de poro

90 Å pore size

pH operativo

2-9

aplicaciones

food and beverages

técnica de separación

reversed phase

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Otras notas

The capillary housing for Ascentis^® Express capillary columns is PEEK with stainless steel end fittings.

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Información legal

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

Producto relacionado

Referencia del producto

Descripción

Precios

14274

Acetonitrile with 0.1% ammonium acetate, tested for UHPLC-MS

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Development and Validation of an LC-MS-MS Method for Determination of Simvastatin and Simvastatin Acid in Human Plasma: Application to a Pharmacokinetic Study.

Pankaj Partani et al.

Journal of chromatographic science, 54(8), 1385-1396 (2016-05-27)

A liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous determination of simvastatin (SV) and simvastatin acid (SVA) in human plasma. To improve assay sensitivity and achieve simultaneous analysis, SVA monitored in (-)ESI (electrospray ionization) mode within

Determination of tropane alkaloids atropine and scopolamine by liquid chromatography-mass spectrometry in plant organs of Datura species.

Silvia Jakabová et al.

Journal of chromatography. A, 1232, 295-301 (2012-03-07)

Hyoscyamine (atropine) and scopolamine are the predominant tropane alkaloids in the Datura genus, occurring in all plant organs. The assessment of the alkaloid content of various plant parts is essential from the viewpoint of medical use, but also as a

Development of a new high-performance liquid chromatography method with diode array and electrospray ionization-mass spectrometry detection for the metabolite fingerprinting of bioactive compounds in Humulus lupulus L.

Francesco Pio Prencipe et al.

Journal of chromatography. A, 1349, 50-59 (2014-05-27)

The study was aimed at developing a new analytical method for the metabolite fingerprinting of bioactive compounds in Humulus lupulus L. (hop), together with a simple extraction procedure. Different extraction techniques, including maceration, heat reflux extraction (HRE), ultrasound-assisted extraction (UAE)

Development of a rapid and sensitive method for the determination of aluminum by reverse-phase high-performance liquid chromatography using a fluorescence detector.

Heena et al.

Journal of chromatographic science, 53(5), 800-806 (2014-10-18)

This study represents a new analytical high-performance liquid chromatography-fluorescence detector method for the determination of Al(III) as Al(III) complex with 8-hydroxyquinoline-5-sulfonic acid in a tap water sample and a coke sample. A micellar liquid chromatographic method is proposed for the

Practical comparison of 2.7 microm fused-core silica particles and porous sub-2 microm particles for fast separations in pharmaceutical process development.

Ahmed Abrahim et al.

Journal of pharmaceutical and biomedical analysis, 51(1), 131-137 (2009-09-18)

Fused-core silica stationary phases represent a key technological advancement in the arena of fast HPLC separations. These phases are made by fusing a 0.5 microm porous silica layer onto 1.7 microm nonporous silica cores. The reduced intra-particle flow path of

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