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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

Produktlinie

Kromasil®

Hersteller/Markenname

Kromasil® KRWP-10-AmyCoat-21.2X250

Verfügbarkeit

available only in USA, Canada and Puerto Rico

Parameter

0-40 °C temperature
50 bar pressure (725 psi)

Methode(n)

HPLC: suitable

L × ID

250 mm × 21.2 mm

Aktive Matrixgruppe

carbamoyl phase

Partikelgröße

10 μm

Porengröße

>1000 Å

Trenntechnik

chiral

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Rechtliche Hinweise

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

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Analysenzertifikate (COA)

Lot/Batch Number

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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
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)
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
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