10300AST
Astec® CHIROBIOTIC® (5 μm) HPLC Column Screening Kit
L × I.D. 10 cm × 4.6 mm
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About This Item
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52
L × i.d.:
10 cm × 4.6 mm
Particle size:
5 μm
Pore size:
100 Å pore size
Matrix:
fully porous particle
Product Name
Astec® CHIROBIOTIC® HPLC Column Screening Kit, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
material
stainless steel column
product line
Astec®
packaging
pkg of 1 kit
manufacturer/tradename
Astec®
parameter
0-45 °C temperature, 241 bar pressure (3500 psi)
technique(s)
HPLC: suitable, LC/MS: suitable
L × I.D.
10 cm × 4.6 mm
matrix
fully porous particle
particle size
5 μm
pore size
100 Å pore size
operating pH
3.5-6.8
separation technique
chiral
Quality Level
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Kit Components Also Available Separately
Product No.
Description
SDS
- 15022ASTAstec® CHIROBIOTIC® V2 Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
- 12022ASTAstec® CHIROBIOTIC® T Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
- 13022ASTAstec® CHIROBIOTIC® R Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
- 14022ASTAstec® CHIROBIOTIC® TAG Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 4.6 mm
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Chromatographic Separations and Analysis: Macrocyclic Glycopeptide Chiral Stationary Phases
Berthod, A.
Comprehensive Chirality, 8, 227-262 (2012)
Chromatography Liquid Chiral Separations
Xiao, T.L., et al.
Encyclopedia of Separation Science, 1-15 (2000)
Ying Liu et al.
Journal of chromatography. A, 978(1-2), 185-204 (2002-12-03)
The chiral recognition capabilities of three macrocyclic glycopeptide chiral selectors, namely teicoplanin (Chirobiotic T), its aglycone (Chirobiotic TAG) and ristocetin (Chirobiotic R), were evaluated with supercritical and subcritical fluid mobile phases. A set of 111 chiral compounds including heterocycles, analgesics
Carla Fernandes et al.
Journal of chromatography. A, 1241, 60-68 (2012-05-04)
A chiral HPLC method using four macrocyclic antibiotic chiral stationary phases (CSPs) has been investigated for determination of the enantiomeric purity of fourteen new chiral derivatives of xanthones (CDXs). The separations were performed with the CSPs Chirobiotic T, Chirobiotic TAG
High-performance liquid chromatographic enantioseparation of bicalutamide and its related compounds.
Roland Török et al.
Journal of chromatography. A, 1098(1-2), 75-81 (2005-11-30)
Direct high-performance liquid chromatographic methods were developed for the enantioseparation of (R,S)-bicalutamide (1) and its analogs (+/-)-3-chloro-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide (2), (+/-)-N-(4-cyano-3-(trifluoro-methyl)phenyl)-2-methyloxirane-2-carboxamide (3), (+/-)-4-fluorophenylsulfonyl-2-hydroxy-2-methylpropionic acid (4) and (+/-)-3-hydroxy-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide (5). The methods involved the use of a cellulose-based Chiralcel OD-H, macrocyclic glycopeptide-based Chirobiotic T
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