Select a Size
$3,200.00
$3,200.00
Available to ship TODAYDetails
About This Item
Skip To
Product Name
Astec® CHIROBIOTIC® TAG Chiral HPLC Column, 5 μm particle size, L × I.D. 15 cm × 4.6 mm
material
stainless steel column
agency
suitable for USP L63
description
HPLC column
product line
Astec®
packaging
pkg of 1 ea
manufacturer/tradename
Astec®
parameter
0-45 °C temperature, 241 bar pressure (3500 psi)
technique(s)
HPLC: suitable, LC/MS: suitable
L × I.D.
15 cm × 4.6 mm
matrix
High-purity silica gel particle platform, fully porous particle
matrix active group
teicoplanin aglycone phase
particle size
5 μm
pore size
100 Å
operating pH range
3.0-6.8
separation technique
chiral
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
1 of 4
This Item | 14018AST | 14019AST | 14020AST |
|---|---|---|---|
| particle size 5 μm | particle size 5 μm | particle size 5 μm | particle size 5 μm |
| matrix active group teicoplanin aglycone phase | matrix active group teicoplanin aglycone phase | matrix active group teicoplanin aglycone phase | matrix active group teicoplanin aglycone phase |
| separation technique chiral | separation technique chiral | separation technique chiral | separation technique chiral |
| L × I.D. 15 cm × 4.6 mm | L × I.D. 10 cm × 2.1 mm | L × I.D. 15 cm × 2.1 mm | L × I.D. 25 cm × 2.1 mm |
| pore size 100 Å | pore size 100 Å | pore size 100 Å | pore size 100 Å |
| agency suitable for USP L63 | agency suitable for USP L63 | agency suitable for USP L63 | agency suitable for USP L63 |
General description
- Bonded phase: Teicoplanin aglycone
- Operating pH range: 3.0 - 6.8
- Particle diameter: 5, 10 or 16 μm
- Pore size: 100 Å
Application
- High-performance liquid chromatographic enantioseparation of 2-aminomono- and dihydroxycyclopentanecarboxylic and 2-aminodihydroxycyclohexanecarboxylic acids on macrocyclic glycopeptide-based phases.: This study emphasizes the effectiveness of the Astec® CHIROBIOTIC® TAG Chiral HPLC Column in the enantioseparation of complex cyclic amino acids. The methodology detailed provides profound insights into the chirality aspects of biochemical molecules, which is crucial for the synthesis of novel pharmaceutical agents and the study of biochemical pathways. This research supports analytical chemists in academia focused on developing chiral analytical methods and advancing chemical synthesis (Berkecz et al., 2009).
Legal Information
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service


