12100AST
Astec® CHIROBIOTIC® T Chiral (5 μm) HPLC Columns
L × I.D. 2 cm × 4 mm, HPLC Guard Cartridge
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UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52
L × i.d.:
2 cm × 4 mm
Particle size:
5 μm
Matrix active group:
teicoplanin glycopeptide phase
Pore size:
100 Å
Matrix:
fully porous particle
Servicio técnico
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Permítanos ayudarleNombre del producto
Astec® Chirobiotic® T Chiral HPLC Guard Column, Cartridge, 5 μm particle size, L × I.D. 2 cm × 4 mm
material
stainless steel column
Quality Level
agency
suitable for USP L63
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.
2 cm × 4 mm
matrix
fully porous particle
matrix active group
teicoplanin glycopeptide phase
particle size
5 μm
pore size
100 Å
operating pH
3.8-6.8
separation technique
chiral
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Clase de almacenamiento
13 - Non Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
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László Sipos et al.
Journal of chromatography. A, 1217(44), 6956-6963 (2010-09-25)
The enantiomers of five monoterpene-based 2-amino carboxylic acids were directly separated on chiral stationary phases containing macrocyclic glycopeptide antibiotics such as teicoplanin (Astec Chirobiotic T and T2) and teicoplanin aglycone (Chirobiotic TAG) as chiral selectors. The effects of pH, the
Xingxing Diao et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 939, 67-72 (2013-10-10)
A novel and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to determine the exposure of 3-n-butylphthalide (NBP) enantiomers in human plasma. The NBP enantiomers were extracted from human plasma using methyl tert-butyl ether. The baseline separation
Jolanta Flieger et al.
Journal of separation science, 40(11), 2374-2381 (2017-04-21)
We present the specific cooperative effect of a semisynthetic glycopeptide antibiotic teicoplanin and chiral ionic liquids containing the (1R,2S,5R)-(-)-menthol moiety on the chiral recognition of enantiomers of mandelic acid, vanilmandelic acid, and phenyllactic acid. Experiments were performed chromatographically on an