Chromatography

Neutral molecules, amides, acids, esters and amines show considerable enantioselectivity on these vancomycin-based CSPs. A wide variety of secondary and tertiary amines have been separated on the CHIROBIOTIC &#174 V in the polar ionic mode.

Neutral molecules, amides, acids, esters and amines show considerable enantioselectivity on these vancomycin-based CSPs. A wide variety of secondary and tertiary amines have been separated on the CHIROBIOTIC &#174 V in the polar ionic mode.

CLC columns use the copper ligand concept described by Davankov to effect enantiomer separation (1). The method uses a small, chiral bidentate ligand attached to the silica surface and a copper sulphate-containing mobile phase.

CLC columns use the copper ligand concept described by Davankov to effect enantiomer separation (1). The method uses a small, chiral bidentate ligand attached to the silica surface and a copper sulphate-containing mobile phase.

CYCLOBOND I 2000 AC is used primarily for aromatic alcohols or amines that are chiral on the &#945 or &#946 carbon. Bonded phase: Acetylated beta-cyclodextrin Resources: CYCLOBOND FAQs CYCLOBOND Reference Bibliography Chiral Product Literature

CYCLOBOND I 2000 is bonded with &#946-cyclodextrin by a patented process to produce a stable matrix with the cyclodextrin arranged in such a way as to retain its most valuable property of forming inclusion complexes. This allows them to effect

CYCLOBOND I 2000 is bonded with &#946-cyclodextrin by a patented process to produce a stable matrix with the cyclodextrin arranged in such a way as to retain its most valuable property of forming inclusion complexes. This allows them to effect

CYCLOBOND I 2000 is bonded with &#946-cyclodextrin by a patented process to produce a stable matrix with the cyclodextrin arranged in such a way as to retain its most valuable property of forming inclusion complexes. This allows them to effect

CYCLOBOND I 2000 is bonded with &#946-cyclodextrin by a patented process to produce a stable matrix with the cyclodextrin arranged in such a way as to retain its most valuable property of forming inclusion complexes. This allows them to effect

The reaction of the 3,5-dimethylphenyl isocyanate with the hydroxyl groups of &#946-cyclodextrin results in a pi-basic phase similar in character to the naphthylethyl carbamate phases. The selectivity is greater for the CYCLOBOND I 2000 DMP when

The reaction of the 3,5-dimethylphenyl isocyanate with the hydroxyl groups of &#946-cyclodextrin results in a pi-basic phase similar in character to the naphthylethyl carbamate phases. The selectivity is greater for the CYCLOBOND I 2000 DMP when

The reaction of the 3,5-dimethylphenyl isocyanate with the hydroxyl groups of &#946-cyclodextrin results in a pi-basic phase similar in character to the naphthylethyl carbamate phases. The selectivity is greater for the CYCLOBOND I 2000 DMP when