59629
SUPELCOSIL™ LC-18-S (5 µm) HPLC Columns
L × I.D. 2 cm × 4 mm Supelguard Guard Cartridge pkg of 2 ea, Guard Cartridge holder required for use
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About This Item
UNSPSC Code:
41115700
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product name
SUPELCOSIL™ LC-18-S Supelguard Cartridge, 5 μm particle size, L × I.D. 2 cm × 4 mm
agency
suitable for USP L1
Quality Level
description
Supelguard Cartridge
packaging
pkg of 1 kit
technique(s)
HPLC: suitable
L × I.D.
2 cm × 4 mm
matrix active group
C18 (octadecyl) phase
particle size
5 μm
pore size
120 Å
application(s)
food and beverages
separation technique
reversed phase
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General description
SUPELCOSIL™ LC-18-S Supelguard Cartridges [5 μm particle size, L × I.D. 2 cm × 4 mm] contain a SUPELCOSIL packing, in a 2 cm stainless steel body, enclosed by polyether ether ketone (PEEK) encapsulated stainless steel frits (2 μm porosity). A Supelguard kit (one cartridge, a stand-alone holder, tubing, and 2 nuts and ferrules) enables one to use the cartridge with any analytical column. A direct-connect guard cartridge holder can directly connect a Supelguard cartridge to a Supelco analytical column. 3.0 mm cartridges are available in packs of two only-purchase a stand-alone or modular holder separately. Low volume 3.0 mm ID cartridges are a good choice for protecting an analytical column containing 3 μm particles.
Footnote
Kit includes one cartridge, a stand-alone holder, a piece of tubing, and 2 nuts and ferrules.
Legal Information
SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC
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M Crozatier et al.
Molecular and biochemical parasitology, 31(2), 127-131 (1988-11-01)
We have digested trypanosome DNA with a combination of pancreatic DNase I, nuclease P1 and bovine alkaline phosphatase and fractionated the resulting nucleosides on a Supelcosil LC-18-S column by high pressure liquid chromatography. We find less than 0.1% unusual nucleosides
Catrina L Dupard-Julien et al.
Analytical and bioanalytical chemistry, 387(3), 1027-1032 (2007-01-06)
A reversed-phase, high-performance liquid chromatography (RP-HPLC) method that allows quantitation of low levels of epoxides has been described. The method involved derivatization of epoxides using 100- to 1,000-fold excess N,N-diethyldithiocarbamate (DTC) at 60 degrees C for 20 min at neutral
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