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K08670372

Kromasil® CelluCoat® Chiral HPLC Column

3 μm particle size, L × I.D. 50 mm × 4.6 mm

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About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21

agency

suitable for USP L40

product line

Kromasil®

manufacturer/tradename

Kromasil® KRWP-3-CelluCoat-4.6X50

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 × 4.6 mm

matrix active group

carbamoyl phase

particle size

3 μm

pore size

>1000 Å

separation technique

chiral

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Legal Information

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

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Syame Khater et al.
Journal of chromatography. A, 1303, 83-93 (2013-07-11)
Since the expiration of the patent protection of Chiralcel OD, similar chiral stationary phases (CSPs), all based on the same chiral selector, have been introduced on the market with the promise to reproduce or improve the performance of the original
Chelating alkoxy NHC?Rh(I) complexes and their applications in the arylation of aldehydes
Denizalti, Serpil, et al.
Tetrahedron Letters, 55 (30), 4129-4132 (2014)
Hanna Nelander et al.
Journal of chromatography. A, 1218(52), 9397-9405 (2011-11-29)
The performance of four commercially available cellulose tris(3,5-dimethylphenylcarbamate) based chiral stationary phases (CSPs) was evaluated with parallel high performance liquid chromatography (HPLC) and super critical fluid chromatography (SFC). Retention, enantioselectivity, resolution and efficiency were compared for a set of neutral
Egor V Verbitskiy et al.
Bioorganic & medicinal chemistry letters, 25(3), 524-528 (2015-01-04)
The Petasis reaction of 6-hydroxy adducts of 1-alkyl-2,3-dicyano-5-arylpyrazinium salts with trans-styrylboronic acids proved to proceed smoothly at room temperature to give the corresponding 5-(hetero)aryl-6-styryl substituted 1,6-dihydropyrazine derivatives. Also it has been found that C(6) unsubstituted 1,6-dihydro- or 1,4,5,6-tetrahydropyrazine derivatives can
Diamidophosphites with remote P*-stereocentres and their performance in Pd-catalyzed enantioselective reactions
Gavrilov, Konstantin N., et al.
Tetrahedron Asymmetry, 25 (15), 1116-1121 (2014)

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