K08971228
Kromasil® CelluCoat® Chiral HPLC Column
5 μm particle size, L × I.D. 50 mm × 2.1 mm
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52
agency
suitable for USP L40
product line
Kromasil®
manufacturer/tradename
Kromasil® KRWP-5-CelluCoat-2.1X50
availability
available only in USA, Canada and Puerto Rico
parameter
0-40 °C temperature
50 bar pressure (725 psi)
technique(s)
HPLC: suitable
L × I.D.
50 mm × 2.1 mm
particle size
5 μm
pore size
>1000 Å
separation technique
chiral
Looking for similar products? Visit Product Comparison Guide
Legal Information
CelluCoat is a registered trademark of EKA Chemicals AB
Kromasil is a registered trademark of EKA Chemicals AB
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.
If you need assistance, please contact Customer Support
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Syame Khater et al.
Journal of chromatography. A, 1303, 83-93 (2013-07-11)
Since the expiration of the patent protection of Chiralcel OD, similar chiral stationary phases (CSPs), all based on the same chiral selector, have been introduced on the market with the promise to reproduce or improve the performance of the original
Chelating alkoxy NHC?Rh(I) complexes and their applications in the arylation of aldehydes
Denizalti, Serpil, et al.
Tetrahedron Letters, 55 (30), 4129-4132 (2014)
Hanna Nelander et al.
Journal of chromatography. A, 1218(52), 9397-9405 (2011-11-29)
The performance of four commercially available cellulose tris(3,5-dimethylphenylcarbamate) based chiral stationary phases (CSPs) was evaluated with parallel high performance liquid chromatography (HPLC) and super critical fluid chromatography (SFC). Retention, enantioselectivity, resolution and efficiency were compared for a set of neutral
Egor V Verbitskiy et al.
Bioorganic & medicinal chemistry letters, 25(3), 524-528 (2015-01-04)
The Petasis reaction of 6-hydroxy adducts of 1-alkyl-2,3-dicyano-5-arylpyrazinium salts with trans-styrylboronic acids proved to proceed smoothly at room temperature to give the corresponding 5-(hetero)aryl-6-styryl substituted 1,6-dihydropyrazine derivatives. Also it has been found that C(6) unsubstituted 1,6-dihydro- or 1,4,5,6-tetrahydropyrazine derivatives can
Diamidophosphites with remote P*-stereocentres and their performance in Pd-catalyzed enantioselective reactions
Gavrilov, Konstantin N., et al.
Tetrahedron Asymmetry, 25 (15), 1116-1121 (2014)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service