Showing 49–60 of 427 results

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  • Description

  • C4, 96 well plate, Orochem 2000, 50.0 mg/2.0 ml, 1/pkg

    |

    ─Si ─(CH2)3-CH3

    It is silica based bonded with butyl function group. It has lower hydrophobicity than C8 and C18 columns, and provides better retention for some polar compounds which do not retain on C8 or C18 column. It applies in proteomics and metabolites analysis.

  • C8, 96-well plate, Orochem 2000, 100.0 mg/2.0 ml, 1/pkg

    c-8
    Reversed phase retention mechanism of the C8 elute allows for the extraction of hydrophobic compounds from aqueous matrices that are too strongly retained on C18 sorbent. Provides for the quick release of hydrophobic molecules using weaker organic solvents. Typical applications includes peptide extraction from biological matrices (serum, plasma, urine), nutraceutical extractions from food and beverages.

  • C8, 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 1/pkg

    c-8
    Reversed phase retention mechanism of the C8 elute allows for the extraction of hydrophobic compounds from aqueous matrices that are too strongly retained on C18 sorbent. Provides for the quick release of hydrophobic molecules using weaker organic solvents. Typical applications includes peptide extraction from biological matrices (serum, plasma, urine), nutraceutical extractions from food and beverages.

  • C8, 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 1/pkg

    c-8
    Reversed phase retention mechanism of the C8 elute allows for the extraction of hydrophobic compounds from aqueous matrices that are too strongly retained on C18 sorbent. Provides for the quick release of hydrophobic molecules using weaker organic solvents. Typical applications includes peptide extraction from biological matrices (serum, plasma, urine), nutraceutical extractions from food and beverages.

  • C8 (non-endcapped), 96-well plate, Orochem 2000, 100.0 mg/2.0 ml, 1/pkg

  • C8 (non-endcapped), 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 1/pkg

  • C8 (non-endcapped), 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 1/pkg

  • Cyclohexyl, 96-well plate, Orochem 2000, 100.0 mg/2.0 ml, 1/pkg

    phenyal
    The moderately non-polar retention mechanism of the bonded cyclohexyl functional group provides unique selectivity to retain polar analytes. Typical sample types include water, and other aqueous samples.

  • Cyclohexyl, 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 1/pkg

    phenyal
    The moderately non-polar retention mechanism of the bonded cyclohexyl functional group provides unique selectivity to retain polar analytes. Typical sample types include water, and other aqueous samples.

  • Cyclohexyl, 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 1/pkg

    phenyal
    The moderately non-polar retention mechanism of the bonded cyclohexyl functional group provides unique selectivity to retain polar analytes. Typical sample types include water, and other aqueous samples.

  • Cyanopropyl(CN), 96-well plate, Orochem 2000, 100.0 mg/2.0 ml, 1/pkg

    Cyanopropyl(CN)
    Reversed-phase or normal phase retention mechanism. Ideal for extraction of polar compounds retained too strongly on more non-polar sorbents such as C18. Typical samples include aqueous solutions in reversed-phase and organic solvents in normal phase.

  • Cyanopropyl(CN), 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 1/pkg

    Cyanopropyl(CN)
    Reversed-phase or normal phase retention mechanism. Ideal for extraction of polar compounds retained too strongly on more non-polar sorbents such as C18. Typical samples include aqueous solutions in reversed-phase and organic solvents in normal phase.