Waters PAH Columns optimized for HPLC analysis of Polyaromatic hydrocarbons (PAHs).

SKU: 186002015
Atlantis Silica HILIC Column, 100Å, 3 µm, 2.1 mm X 150 mm, 1/pk

Atlantis Silica HILIC Column | 186002015


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Product Description

Atlantis HILIC Silica columns are used in combination with high organic mobile phases (>80% acetonitrile) to provide retention of analytes that are simply too polar to be retained by reverse-phase chromatography. HILIC separation mechanisms provide orthogonal analyte selectivity compared to traditional chromatographic reversed-phase approaches.

Specifications

  • Chemistry

    HILIC

  • Separation Mode

    Hydrophilic Interaction (HILIC)

  • Particle Substrate

    Silica

  • pH Range Min

    1 pH

  • pH Range Max

    5 pH

  • Maximum Pressure

    6000 psi (415 Bar)

  • Endcapped

    No

  • Silanol Activity

    High

  • Particle Shape

    Spherical

  • Particle Size

    3 µm

  • Endfitting Type

    Waters

  • Pore Size

    100 Å

  • Format

    Column

  • Surface Area

    330

  • System

    HPLC

  • Particle Technology

    Silica

  • USP Classification

    L3

  • Inner Diameter

    2.1 mm

  • Length

    150 mm

  • UNSPSC

    41115709

  • Brand

    Atlantis

  • Product Type

    Columns

  • Units per Package

    1 pk

Product Support

Documents

Documents



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Atlantis Silica HILIC Column, 100Å, 3 µm, 2.1 mm X 150 mm, 1/pk

Use the Atlantis Silica HILIC Column in combination with high organic mobile phases (>80% acetonitrile) to provide retention of analytes that are simply too polar to be retained by reverse-phase chromatography. HILIC (Hydrophilic Interaction Chromatography) separation mechanisms provide orthogonal analyte selectivity compared to traditional chromatographic reversed-phase approaches. The compounds that can be separated by the Atlantis Silica HILIC Column include peptides, metabolites, and actives. In addition to providing retention of very polar compounds, HILIC offers improved LC/ESI-MS response and direct compatibility with SPE solvents. When it is compared to reversed-phase HPLC, the lab equipment also offers complimentary selectivity.

Using reversed-phase chromatography, it is extremely difficult to retain and separate very basic polar analytes, owing to their hydrophilic nature combined with their net positive charge at acidic pH. The use of HILIC resolves these challenging separation problems, which is why the Atlantis Silica HILIC Column is of crucial importance as the ideal lab equipment that can be used in metabolism, drug discovery, and combinatorial chemistries.

The Atlantis Silica HILIC Column enables you to retain highly polar basic analytes with volatile mobile phases that are suitable for compound ionization by ESI-MS. This means you get results that exhibit higher sensitivity and lower limits of detection, which is especially useful in drug metabolism studies as metabolites are often more polar than their parent compounds and are present in a much lower concentration.

Other than offering improved LC/ESI-MS response, the Atlantis Silica HILIC Column also offers direct compatibility with SPE solvents and complementary selectivity when compared to the traditional reversed-phase HPLC columns. In addition to this, in contrast to the traditional reversed-phase HPLC columns where severe peak tailing for polar bases is observed, the use of Atlantis Silica HILIC Column gives superior peak shapes for polar bases while leveraging faster and easier method development.

Shop for lab equipment directly from our website to ensure that you get the authentic Waters lab equipment at the best possible price in the market. You can also read up on our latest and upcoming technological developments using the Waters catalog and website.

You may also want to learn more about the HILIC QC Reference Material.

What Is The Principle of Mass Spectrometry?

The principle of mass spectrometry (MS) is to generate ions from either inorganic or organic compounds by any suitable method, as well as to separate these ions by their mass-to-charge ratio (m/z) and to detect them qualitatively and quantitatively by their respective m/z and abundance.