Nucleosil Chiral Columns
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- Published on 18 May 2013
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Nucleosil Chiral Columns
Nucleosil Chiral 1
Nucleosil Chiral-1 has been developed to control optical purity and separate optically- active
compounds. This is achieved by ligand exchange in aqueous solvent systems. The stationary phase
matrix is Nucleosil 120Å bonded chemically with L-hydroxyproline -Cu2+ complexes. The principal
interaction mode between the solute enantiomers to be separated and the chiral selector is the
formation of ternary, mixed-ligand complexes with a transition metal cation, Cu(ll).
This chiral column has been developed for control of optical purity of compounds soluble only in
organic solvents.
Nucleosil Chiral 2 and Chiral 3
The stationary phase matrix is Nucleosil silica, chemically bonded with Ddinitrobenzoylphenylglycine
via a propyl spacer resulting in three chiral centres. This is a 'brush type' phase. Applications include
control of optical purity of plant protectives (pesticides), pharmaceuticals and production control in chiral
organic synthesis, using nonpolar organic mobile phase.1
The chiral-3 column carries the opposite optical isomeric chiral phase to Nucleosil Chiral-2, i.e.,
L-dinitrobenzoylphenylglycine. This allows the elution order of a pair of enantiomers to be
reversed to that obtained using Nucleosil Chiral-2 under the same elution conditions.
Nucleosil - Chiral Columns
Phase 2cm 5cm 10cm 15cm 20cm 25cm |
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(guard) |
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ChiralI n/a n/a n/a 5K5115 n/a 5K5125 |
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ChiralII n/a n/a n/a 5L5115 n/a 5L5125 |
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PRICE/£ seepricelistpa |
ge17-18 |