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14018AST

Supelco

Astec® CHIROBIOTIC® TAG Chiral (5 μm) HPLC Columns

L × I.D. 10 cm × 2.1 mm, HPLC Column

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1 EA
₹1,91,980.00

₹1,91,980.00


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1 EA
₹1,91,980.00

About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52

₹1,91,980.00


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Product Name

Astec® CHIROBIOTIC® TAG Chiral HPLC Column, 5 μm particle size, L × I.D. 10 cm × 2.1 mm

material

stainless steel column

Quality Level

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

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This Item
14019AST14020AST14022AST
L × I.D.

10 cm × 2.1 mm

L × I.D.

15 cm × 2.1 mm

L × I.D.

25 cm × 2.1 mm

L × I.D.

10 cm × 4.6 mm

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

matrix active group

teicoplanin aglycone phase

matrix active group

teicoplanin aglycone phase

matrix active group

teicoplanin aglycone phase

matrix active group

teicoplanin aglycone phase

matrix

High-purity silica gel particle platform, fully porous particle

matrix

High-purity silica gel particle platform, fully porous particle

matrix

High-purity silica gel particle platform, fully porous particle

matrix

High-purity silica gel particle platform, fully porous particle

agency

suitable for USP L63

agency

suitable for USP L63

agency

suitable for USP L63

agency

suitable for USP L63

General description

The removal of three carbohydrate moieties gives CHIROBIOTIC® TAG complementary selectivity to CHIROBIOTIC® T. Resolution is enhanced toward many of the amino acids, α, β, γ and cyclic, and especially sulfur-containing methionine, histidine and cysteine. A number of neutral molecules like the oxazolidinones, hydantoins and diazepines have shown enhanced resolution and, more remarkably, in the single solvents like methanol, ethanol and acetonitrile. Some acidic molecules have also shown increased selectivity.

  • Bonded phase: Teicoplanin aglycone
  • Operating pH range: 3.0 - 6.8
  • Particle diameter: 5, 10 or 16 μm
  • Pore size: 100 Å

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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

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    Ilaria D'Acquarica et al.
    Journal of chromatography. A, 1061(2), 167-173 (2005-01-12)
    We describe a new tandem-columns chiral-achiral HPLC arrangement by using a chiral column (CHIROBIOTIC TAG) connected in series with an achiral column (Spherisorb S5 SCX), based on a strong cationic exchange mechanism; this approach is very useful for the analysis
    Abdulrahman A Al-Majed
    Journal of pharmaceutical and biomedical analysis, 50(1), 96-99 (2009-05-19)
    A direct chiral high-performance liquid chromatography (HPLC) method was developed and validated for the resolution and quantification of antiepileptic drug enantiomers, R-(-)- and S-(+)-vigabatrin (gamma-vinyl-gamma-aminobutyric acid) in pharmaceutical products. The separation was optimized on a macrocyclic glycopeptide antibiotic chiral stationary
    Markus Fuereder et al.
    Journal of chromatography. A, 1236, 123-131 (2012-04-03)
    Teicoplanin aglycone-based chromatography columns (Chirobiotic TAG) enable amino acid enantioseparation with aqueous mobile phases, which perfectly accommodates the distinct hydrophilicity of most amino acids. Therefore, this stationary phase constitutes a promising option in particular for preparative-scale separations that require high
    Adsorption behavior of a teicoplanin aglycone bonded stationary phase under harsh overload conditions
    Bechtold, Matthias, et al.
    Journal of Chromatography A, 1154 (1-2), 2477-2286 (2007)
    Matthias Bechtold et al.
    Journal of chromatography. A, 1113(1-2), 167-176 (2006-02-28)
    The suitability of a teicoplanin-aglycone based chiral stationary phase for the simulated moving bed (SMB) enantioseparation of amino acids under enzyme-compatible conditions was shown following a procedure that is based solely on model-based simulations and HPLC experiments. A set of

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