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12100AST

Supelco

Astec® CHIROBIOTIC® T Chiral HPLC Guard Column

Cartridge, 5 μm particle size, L × I.D. 2 cm × 4 mm

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eCl@ss:
32110501
NACRES:
SB.52

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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This Item
11100AST14100AST12024AST
matrix active group

teicoplanin glycopeptide phase

matrix active group

vancomycin phase

matrix active group

teicoplanin aglycone phase

matrix active group

teicoplanin glycopeptide phase

particle size

5 μm

particle size

5 μm

particle size

5 μm

particle size

5 μm

separation technique

chiral

separation technique

chiral

separation technique

chiral

separation technique

chiral

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 L88

agency

suitable for USP L63

agency

suitable for USP L63

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Legal Information

Astec is a registered trademark of Merck KGaA, Darmstadt, Germany
CHIROBIOTIC is a registered trademark of Sigma-Aldrich Co. LLC

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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
Róbert Berkecz et al.
Journal of chromatography. A, 1216(6), 927-932 (2008-12-27)
The direct separation of the enantiomers of four 2-aminomono- or dihydroxycyclopentanecarboxylic acids and four 2-aminodihydroxycyclohexanecarboxylic acids was performed on chiral stationary phases containing macrocyclic glycopeptide antibiotics such as teicoplanin (Astec Chirobiotic T and T2), teicoplanin aglycone (Chirobiotic TAG) or ristocetin
László Sipos et al.
Journal of chromatography. A, 1232, 142-151 (2011-12-20)
The enantiomers of four unusual isoxazoline-fused 2-aminocyclopentanecarboxylic acids were directly separated on chiral stationary phases containing macrocyclic glycopeptide antibiotics teicoplanin (Astec Chirobiotic T and T2), teicoplanin aglycone (Chirobiotic TAG), vancomycin (Chirobiotic V) and vancomycin aglycone (Chirobiotic VAG) as chiral selectors.

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