Showing 85–96 of 427 results

  • Catalog#
  • Description

  • C2, 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 5/pkg

    C2

    The ethyl functional group creates a polar sorbent, used for the extraction of hydrophobic compounds from aqueous matrices that are too strongly retained on the C8 and C18 sorbent phases. Typical sample types include plasma, serum, urine, and aqueous samples.

  • C4, 96 well plate, Orochem 2000, 100.0 mg/2.0 ml, 5/pkg

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    ─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.

  • C4, 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 5/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.

  • C4, 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 5/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, 5/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, 5/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, 5/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, 5/pkg

  • C8 (non-endcapped), 96-well plate, Orochem 2000, 25.0 mg/2.0 ml, 5/pkg

  • C8 (non-endcapped), 96-well plate, Orochem 2000, 50.0 mg/2.0 ml, 5/pkg

  • Cyclohexyl, 96-well plate, Orochem 2000, 100.0 mg/2.0 ml, 5/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, 5/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.