Polar Columns in HPLC

Wavelength: 254nm
Temperature: 35°C
Flow Rte: 1.5ml/min
Injection Volume: 20μL

Availability: In Stock


Description of HPLC Columns in Polar

The traditional polar-embedded reverse-phase(RP) HPLC column is to bond the aminoamide group to the surface of the silica gel. This bonding method causes residual amino groups on the surface of the silica gel. The residual amino group exhibits a basic character, and when an acidic substance such as an organic acid is analyzed, a peak tail is caused.

With a unique bonding process, Hawach Polar-RP HPLC columns solve the problem of amino residue on the surface of traditionally processed silica gel, and adopt double tailing technology to obtain an excellent symmetrical peak shape.

Features of Polar-RP HPLC Column

  1. Unique selectivity different from ordinary RP C18 columns or C8 columns, especially when measuring polar substances such as phenols;
  2. 100% water can be used as a mobile phase, a better water column than the C18-Aqueous column;
  3. Excellent peak shape when measuring polar and alkaline substances;
  4. Better retention and selectivity for polar substances.

Polar-RP HPLC Columns Technical Parameters

  • Particle size: 1.8μm, 3μm, 5μm, 10μm;
  • Aperture: 120Å, 300Å;
  • Specific surface area: 120Å–320m²/g, 300Å–90m²/g;
  • Carbon loading: 18%;
  • pH range: 1.5-10.0;
  • Whether to seal: Yes.

New column activation

Rinse with 80% methanol 0.5ml/min for 4 hours, then change to analyze mobile phase equilibrium; if the mobile phase contains buffer salts, please use the transitional mobile phase transition and then analyze the mobile phase balance.

Routine maintenance

  1. It is recommended to filter the sample and mobile phase before testing;
  2. It is recommended to clean the samples in time after completing the samples;
  3. Routine testing, after the test, the column is directly connected by 90% organic phase washing for 45min, and finally

The use of buffer salt conditions:

  1. Isocratic conditions: before and after using the buffer salt, the transition mobile phase is used to rinse at an analytical flow rate for 45 min;
  2. Gradient conditions: use the same transition phase as the initial mobile phase before buffer salt to analyze the flow rate
    Rinse for 45 minutes;
    Note: The transition mobile phase means that the organic phase and the water phase are in the same ratio as the analytical mobile phase, but without buffer salts;
  3. After rinsing the buffer salt, rinse with 90% organic reverse for 60 min, and finally save;
    Note: The buffered saline solution cannot remain in the column overnight;

The preservation of the polar column

  1. Preservation of the column in a short time:
    If the time interval is less than four days, save it in the last organic solvent water.
  2. Preservation of long-term columns:
    If the column is not used for a long time, it is finally rinsed with 80% methanol-water for 45 minutes at the analytical flow rate, removed from the HPLC instrument, and sealed with a plastic plug to avoid solvent evaporation in the column.

Technical Data

Bonded PhaseUSP NoParticle size (μm)Pore sizeSurface Area (m²/g)Carbon
pH RangeEnd-capped
Polar-RPL11.8μm,3μm, 5μm, 10μm120Å, 300Å120Å –320m²/g,
300Å –90m2/g

Ordering Information

Item No.DescriptionDiameter(mm)Length(mm)Package (pcs/pk)
SLHPRP32130Polar-RP, 3μm, 120Å2.1301
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