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Supelco

SUPELCOGEL™ C610 (9 µm) HPLC Columns

L × I.D. 30 cm × 7.8 mm

Synonym(s):

SUPELCOGEL™ 6% Cross Linked HPLC Columns

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About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52

product name

SUPELCOGEL™ C610H, 6% Crosslinked HPLC Column, 9 μm particle size, L × I.D. 30 cm × 7.8 mm

material

stainless steel column

agency

suitable for USP L17

product line

SUPELCOGEL™

feature

endcapped: no

packaging

1 ea of

parameter

85 °C max. temp.

technique(s)

HPLC: suitable

L × I.D.

30 cm × 7.8 mm

matrix

sulfonated polystyrene/divinylbenzene, spherical particle platform
polymeric

particle size

9 μm

separation technique

ion exclusion

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General description

SUPELCOGEL™ C-610H, 6% crosslinked HPLC columns are prepared specifically for the analysis of organic acids. They are also used in the separation of acetic, propionic, butyric, formic, malic, citric, succinic, lactic, and other acids using a simple isocratic mobile phase and minimal sample preparation.

Legal Information

SUPELCOGEL is a trademark of Sigma-Aldrich Co. LLC

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Product No.
Description
Pricing

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Erika C Pavarina et al.
Applied biochemistry and biotechnology, 98-100, 663-677 (2002-05-23)
Four soil fungi able to grow under low oxygenation conditions were selected and used in studies to determine the production of enzymes that promote the degradation of lignocellulosic materials. The capacity of these fungi to ferment such materials was also
M Zecevic et al.
Journal of chromatography. A, 949(1-2), 61-64 (2002-05-10)
A new high-performance liquid chromatography (HPLC) method was developed for the quality control of pancuronium bromide and its degradation products. The HPLC method used a 5-microm Supelcogel ODP-50 (150x4 cm) column with acetonitrile-CH3OH-water-F3CCOOH (20.5:74.9:0.1, v/v) as the mobile phase (pH
François Becher et al.
Rapid communications in mass spectrometry : RCM, 16(6), 555-565 (2002-03-01)
There is still a need for direct determination (i.e. without dephosphorylation) of nucleoside reverse transcriptase inhibitor (NRTI) triphosphorylated nucleotides in the peripheral-blood mononuclear cells (PBMCs) of HIV-positive patients. The objective of this paper was first to improve our previously described

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