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K08971229

Kromasil® AmyCoat® Chiral HPLC Column

3 μm particle size, L × I.D. 50 mm × 2.1 mm

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About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52

product line

Kromasil®

manufacturer/tradename

Kromasil® KRWP-3-Amycoat-2.1X150

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

3 μm

pore size

>1000 Å

separation technique

chiral

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Legal Information

AmyCoat is a registered trademark of EKA Chemicals AB
Kromasil is a registered trademark of EKA Chemicals AB

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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
A short enantioselective total synthesis of (R)- and (S)-pipecolic acid
Chavan, Subhash P., et al.
Tetrahedron Asymmetry, 25 (16-17), 1246-1251 (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

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