Skip to Content
MilliporeSigma
All Photos(1)

Documents

K08670612

Kromasil® CelluCoat® Chiral HPLC Column

10 μm particle size, L × I.D. 150 mm × 4.6 mm

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21

agency

suitable for USP L40

product line

Kromasil®

manufacturer/tradename

Kromasil® KRWP-10-CelluCoat-4.6X150

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.

150 mm × 4.6 mm

matrix active group

carbamoyl phase

particle size

10 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

Sorry, we don't have COAs for this product available online at this time.

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.

Visit the Document Library

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)
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
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)

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