K08670601
Kromasil® AmyCoat® Chiral HPLC Column
10 μm particle size, L × I.D. 250 mm × 21.2 mm
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About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21
Pricing and availability is not currently available.
product line
Kromasil®
manufacturer/tradename
Kromasil® KRWP-10-AmyCoat-21.2X250
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.
250 mm × 21.2 mm
matrix active group
carbamoyl phase
particle size
10 μm
pore size
>1000 Å
separation technique
chiral
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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.
Imran Ali et al.
Chirality, 26(3), 136-143 (2014-01-28)
Solid phase extraction (SPE)-chiral separation of the important drugs pheniramine, oxybutynin, cetirizine, and brinzolamide was achieved on the C18 cartridge and AmyCoat (150 x 46 mm) and Chiralpak AD (25 cm x 0.46 cm id) chiral columns in human plasma. Pheniramine, oxybutynin, cetirizine
Imran Ali et al.
Combinatorial chemistry & high throughput screening, 15(6), 509-514 (2012-05-11)
Chiral analysis of profens in human plasma is an important area of research due to different pharmaceutical activities of their enantiomers. The solid phase extraction of ibuprofen and flurbiprofen from human plasma was carried out on C18 cartridges by using
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
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
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