581394-U
Discovery® HS C18 (10 µm) HPLC Columns
L × I.D. 1 cm × 21.2 mm HPLC Prep Guard Cartridge
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About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52
Productos recomendados
product name
Discovery® HS C18 Prep Guard Cartridge, 10 μm particle size, L × I.D. 1 cm × 21.2 mm
material
stainless steel column
agency
suitable for USP L1
description
Prep Cartridge
product line
Discovery®
feature
endcapped
packaging
pkg of 1 ea
technique(s)
HPLC: suitable
LC/MS: suitable
L × I.D.
1 cm × 21.2 mm
surface area
300 m2/g
matrix
fully porous particle
matrix active group
C18 (octadecyl) phase
particle size
10 μm
pore size
120 Å
operating pH
2-8
application(s)
food and beverages
compatibility
use to protect Discovery HS C18 Prep
separation technique
reversed phase
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Jolanta Flieger et al.
Journal of separation science, 34(7), 733-739 (2011-03-02)
Highly hydrophilic compounds belonging to biogenic amines were analysed in the reversed-phase system, modified with the addition of ionic liquids: 1-ethyl-3-methyl-imidazolium hexafluorophosphate (EMIM PF(6)) and chaotropic salt NaPF(6) on Discovery HS C18 column at acidic conditions. The effect of the
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A new, simple, economical and validated high-performance liquid chromatography linked with electrochemical detector (HPLC-ECD) method has been developed and optimized for different experimental parameters to analyze the most common monothiols and disulfide (cystine, cysteine, homocysteine, methionine, reduced (GSH) and oxidized
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A simple, precise and accurate assay for the determination of 6-methoxy-2-naphthylacetic acid (6-MNA), an active metabolite of nabumetone in human plasma, was developed and validated using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The analyte (6-MNA) and propranolol (internal standard, IS) were
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 944, 114-122 (2013-12-10)
A simple, specific, precise and rapid RP-HPLC-UV method was developed for simultaneous determination of lumefantrine and its metabolite desbutyl lumefantrine in human plasma. Experimental parameters were optimized and the method was validated according to standard guidelines. The method showed adequate
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