K08670606
Kromasil® AmyCoat® Chiral HPLC Column
5 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
product line
Kromasil®
manufacturer/tradename
Kromasil® KRWP-5-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
5 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, 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
Chiral liquid chromatography?tandem mass spectrometry assay to determine that dexpramipexole is not converted to pramipexole in vivo after administered in humans
Wei, Dong, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 971, 133-140 (2014)
Comparison of separation performances of amylose- and cellulose-based stationary phases in the high-performance liquid chromatographic enantioseparation of stereoisomers of ?-lactams
Pataj, Zoltan, et al.
Chirality, 2 (1), 116-119 (2010)
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