K08670346
Kromasil® AmyCoat® Chiral HPLC Column
3 μm particle size, L × I.D. 150 mm × 4.6 mm
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21
product line
Kromasil®
manufacturer/tradename
Kromasil® KRWP-3-AmyCoat-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
3 μm
pore size
>1000 Å
separation technique
chiral
Looking for similar products? Visit Product Comparison Guide
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.
Imran Ali et al.
Chirality, 22(1), 24-28 (2009-02-12)
Sixteen beta-adrenergic antagonists namely acebutalol, alprenolol, atenolol, bisoprolol, bopindolol, bufurolol, carazolol, celiprolol, indenolol, metaprolol, nebivolol, oxprenolol, practolol, propranolol, tertalol, and timolol, and two beta-adrenergic agonists namely cimeterol and clenbuterol were resolved on AmyCoat (150 x 46 mm, 3 microm size
Zeid A Al-Othman et al.
Biomedical chromatography : BMC, 26(6), 775-780 (2011-10-28)
A fast, economic, reproducible, accurate, effective, rugged and selective chiral-HPLC method was developed and validated for the enantiomeric resolution of nebivolol enantiomers [(+)-RRRS and (-)-SSSR)] in dosage formulation. The method was rapid as chiral separation occurred within only 12 min.
Martin Enmark et al.
Journal of chromatography. A, 1240, 123-131 (2012-05-01)
Enantiomeric separation of omeprazole has been extensively studied regarding both product analysis and preparation using several different chiral stationary phases. In this study, the preparative chiral separation of omeprazole is optimized for productivity using three different columns packed with amylose
A new organocatalyst derived from abietic acid and 4-hydroxy-l-proline for direct asymmetric aldol reactions in aqueous media
Bhowmick, Sudipto, et al.
Tetrahedron Asymmetry, 25 (18-19), 1292-1297 (2014)
Michal Douša et al.
Journal of separation science, 34(12), 1402-1406 (2011-05-07)
Separation of veterinary drug alaptide ((S)-8-methyl-6,9-diazaspiro(4,5)decane-7,10-dione) from a chiral impurity (R-enantiomer) was developed. Five chiral columns (three amylose and two cellulose type) were evaluated in a reversed-phase system. Three of them offered satisfactory enantiomeric resolution. Finally, three methods were validated
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