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Catalog No. MN723382.10
Part No. 723382.10
Supplier MACHEREY‑NAGEL
GC column, LIPODEX E, 10 m L, 0.10 mm ID, proprietary df
Net Price
Special offer
Availability

6 weeks

PROPERTIES
  • Method
    Gas chromatography (GC)
  • Composition
    Octakis-(2,6-di-O-pentyl-3-O-butyryl)-γ-cyclodextrin
  • Recommended application(s)
    Alcohols, Alkyl halides, Amines, Diols, Enantiomers, Gas chromatography, GC, Hydroxycarboxylic acid esters, Ketones, Lactones, Pheromones (Cyclic acetals), α-amino acids
  • Storage temperature
    RT
  • Hazardous material
    No
  • Scope of delivery
    1x GC column coiled/wound on metal cage, user manual, certificate of analysis
  • Type
    GC column
  • Brand
    LIPODEX
  • Phase
    LIPODEX E
  • USP listing
    Not available or proprietary
  • Polarity
    Not available or proprietary
  • Column inner diameter
    0.10 mm
  • Film thickness
    Not available or proprietary
  • Column length
    10 m
  • Tmax isotherm
    200 °C
  • Tmax temp. program
    220 °C
  • Housing type
    Wall coated open tubular (WCOT) capillary column, internal wall of capillary is coated with a very fine film of liquid stationary phase
  • Hardware
    Fused Silica coated with polyimide coiled/wound on metal cage
  • Cage size
    7" (inch)
  • Integrated precolumn
    No
DESCRIPTION
Capillary columns for GC enantiomer separation. LIPODEX cyclodextrin phases are made of cyclic oligosaccharides consisting of six (α-cyclodextrin), seven (β-cyclodextrin) or eight (γ-cyclodextrin) glucose units bonded through α-1,4-linkages. Regioselective alkylation and/or acylation of the hydroxyl groups leads to lipophilic phases with varying enantioselectivity, which are well suited for chiral analyses. Important advantage - many compounds can be analyzed without derivatization (however, for certain substances enantioselectivity can be favorably influenced by formation of derivatives). A large number of separations have been achieved, however, it is not possible to make a general prediction, which phase could solve a given separation task. Even for compounds with small structural differences or within homologous series the enantiodifferentiation can be quite different.
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