ENG

    ARION

    -High quality silica particle shape and circularity

    -Tight particle and pore size distribution

    -The closest proximity to the shape of circle

    -420 m2/g surface area with C (Plus C18)

     

    Stationary phases at ARION columns:

    Plus C18 & C8-L1

    PolarC18-L1

    Biphenyl, Phenyl-Butyl-L11

    PFP –Pentafluorphenyl-L43

    NH2 -L8

    CN-L10

    SCX –Strong cation exchange-L50

    SAX-Strong anion exchange-L14

    Si-Silica-L3

    HILIC Plus (Hydrophilic Interactionin Liquid Chromatography)-L3

    • Ideal for: Pharmaceutical, Environmental, and Nutraceutical applications
    • Outstanding performance and peak shapes
    • pH rangestability 1 to 10 / 2 to 7,0 (C8)
    • Unique selectivity: for Amino Acids and small molecules
    • Outstanding performance and peak shapes
    • pH range stability 1 to 7,0
    • Designedt o run analysis in 100% aqueous mobile phase
    • Ideal for: for variety of analytes including aromatic, polycyclic and unsaturated compounds
    • The π-π interactions between the electron rich double bounds within the analyte and stationary phase phenyl moieties
    • Relative retention compared to more hydrophobic phases is reported to increase in the order: aliphatics < substituted benzenes < polyaromatic hydrocarbons ≅ nitroaromatics
    • pH stability: 1,5 to 7
    • Separation at PFP stationary phase is controlled by hydrogen bonding along with π-π interactions. This stationary phase may be used to analyze both aromatic and aliphatic analytes.
    • Significant separationat supramolecular level (ibuprophen, omeprazole with LC-MS)
    • Delivers High-Resolution separation and low back pressures
    • pH range stability 1,5 to 7,5
    • Use for selective analysis of non-halogenated compounds, such as polar compounds containing hydroxyl, carboxyl, nitro, or other polar groups.
    • Ideal for: Sugars, Sugar Alcohols, Vitamins, Steroids, Anionic Compounds, Oligomers (< 30mer), Hydrogen-bonding compounds
    • Great stability in Normal and Reversed Phase Mode
    • pH rangestability 2 to 6,5
    • Outstanding buffer stability
    • Ideal for: Compounds with COOH, CO, NH2, NHR2 or NR2 groups, Explosives, Esters and Steroids, Plasticizers
    • Great stability in Normal and Reversed Phase Mode
    • pH rangestability 2 to 7,0
    • Ideal for: Amine and polyamine containing compounds, cough and cold compounds, morphine, drugs of abuse, nucleosides, peptides and peptide maps
    • Provides sharper peaks
    • Great pH range stability 2 to 7,5
    • Phenyl-sulfonic acid bonded phase – phenyl gives some reversed phase character that can be enhanced with METHANOL
    • Ideal for: separating and analyzing anionic species, such as Sb(III) and Sb(V), in aqueous environmental samples
    • Common method for protein and peptide separation
    • Suited to the analysis of smaller organic molecules including nucleotides and organic acids
    • pH rangestability 1 to 7,5
    • Ideal for: Polar compounds, adsorption chromatography under normal phase conditions
    • High loading capacity vs. Other silicas
    • pH rangestability 1 to 7
    • Outstanding mechanical stability
    • Low with metal content
    • HILIC is intended to apply for polar compounds (Neutral and Ionic)
    • Ideal for polar drugs and their metabolites (as metabolites are more polar than their drug parents)
    • Ideal for Mass spectrophotometric detection
    • Different selectivity than in Reversed Phase Chromatography – as polar compounds are retained with high organic concentration
    • pH rangestability 1,5 to 7
    • Increased retention with increasing organic concentration
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