Bio LC Prepacked Chiral Columns

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

In the design of this new chemistry, it was an objective to create a very stable and reproducible phase with shorter retention times, while maintaining or improving selectivity over CYCLOBOND I 2000 RSP. With that goal and more achieved, CYCLOBOND

In the design of this new chemistry, it was an objective to create a very stable and reproducible phase with shorter retention times, while maintaining or improving selectivity over CYCLOBOND I 2000 RSP. With that goal and more achieved, CYCLOBOND

The hydroxyl groups on the surface of the &#946-cyclodextrin are reacted with (R,S)-propylene oxide to yield a general purpose chiral stationary phase. It has the added property of separating non-aromatic structures such as t-boc amino acids, for

Consisting of eight glucopyranose units arranged in a truncated cone shape, CYCLOBOND II is an excellent chiral selector for multi-ring structures. It is useful for isomeric compounds based on anthracene, chrysene and pyrene type ring structures.