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About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21
L × i.d.:
3.3 cm × 4.6 mm
Particle size:
3 μm
Matrix active group:
cyano phase
Pore size:
120 Å
Matrix:
silica gel, spherical particle platform
Product Name
SUPELCOSIL™ LC-CN HPLC Column, 3 μm particle size, L × I.D. 3.3 cm × 4.6 mm
agency
suitable for USP L10
Quality Level
feature
endcapped
manufacturer/tradename
SUPELCOSIL™
extent of labeling
4% Carbon loading
parameter
≤70 °C temp. range, 400 bar pressure (5801 psi)
technique(s)
HPLC: suitable
L × I.D.
3.3 cm × 4.6 mm
surface area
170 m2/g
surface coverage
surface coverage 3.5 μmol/m2
matrix
silica gel, spherical particle platform
matrix active group
cyano phase
particle size
3 μm
pore size
120 Å
pH range
2-7.5
application(s)
food and beverages
separation technique
hydrophilic interaction (HILIC), normal phase, reversed phase
General description
The LC-CN phase is often used as a substitute for silica because it offers the advantages of a bonded phase (such as quick equilibration, and less sensitivity to small changes of the water content in the mobile phase). More often, however, the LC-CN column is operated under reversed-phase mobile phase conditions.
Legal Information
SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC
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Storage Class
13 - Non Combustible Solids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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D Paczkowski et al.
Polish journal of pharmacology, 47(5), 429-434 (1995-09-01)
This paper describes a simple high-performance liquid chromatographic (HPLC) method for the determination of diltiazem and desacetyldiltiazem in human serum. After basic methyl-tert-butyl ether extraction and back-extraction with hydrochloric acid, the drug and its metabolite was injected into a Supelcosil
S Fogli et al.
Therapeutic drug monitoring, 21(3), 367-375 (1999-06-12)
A single high-performance liquid chromatography (HPLC) method, suitable for the analysis of daunorubicin, idarubicin, doxorubicin, epirubicin, and their 13-dihydro metabolites is validated in the present study. Preparation of plasma samples was performed by a first extraction of analytes with a
H Kataoka et al.
Journal of analytical toxicology, 24(4), 257-265 (2000-06-29)
A simple and rapid method for the determination of amphetamine, methamphetamine, and their 3,4-methylenedioxy derivatives in urine samples was developed using automated in-tube solid-phase microextraction (SPME) coupled with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS). In-tube SPME is an extraction technique
Global Trade Item Number
| SKU | GTIN |
|---|---|
| U1752-1G | 04061837409363 |
| 58979 | 04061833669587 |