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PolyCap TC 150 Capsule Filter, 0.2/0.1um, Sterile, w/ 1/2in SB Inlet & Outlet

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    Purchase PolyCap TC 150 Capsule Filter, 0.2/0.1um, Sterile, w/ 1/2in SB Inlet & Outlet

    PolyCap TC 150 Capsule Filter, 0.2/0.1um, Sterile, w/ 1/2in SB Inlet & Outlet SKU: 6717-9501

    $213.99
    Ships in 10 business days
     

    Polyethersulfone (PES) Capsule Filters - 6717-9501

    When processing aqueous biologicals at volumes beyond syringe filter capacity, PES capsule filters provide the throughput and recovery performance that bench-scale devices cannot match. On the performance side, asymmetric PES membrane construction captures contaminants at the upstream surface while maintaining open pore channels beneath, extending capsule service life and reducing the frequency of mid-batch device changes. The outcome is a validated filtration barrier that arrives ready for process integration, supporting the single-use manufacturing strategies adopted by modern pharmaceutical and biotechnology facilities.

    Key Polyethersulfone (PES) Membrane Characteristics

    • Maximum operating pressure of 60 psi provides the differential pressure capacity needed for sustained filtration of viscous solutions and high-flow process streams.
    • The inherently hydrophilic PES membrane wets immediately on contact with aqueous solutions, eliminating alcohol pre-flush steps and reducing both startup time and solvent waste.
    • The 250 milliliter holdup volume reflects the capsule's internal fluid path geometry, relevant to recovery calculations for precious samples and small-batch pharmaceutical formulations.
    • The 121 degree Celsius temperature limit ensures reliable capsule performance for ambient and moderately heated filtration applications.
    • PES membrane construction supports integrity testing by forward flow, bubble point, or pressure decay methods, providing the post-use verification required by pharmaceutical quality systems.

    Key Capsule Construction Features

    • Polypropylene housing materials provide documented biocompatibility and low extractable profiles, supporting integration into pharmaceutical and food-processing filtration applications.
    • Thermally fused polypropylene construction eliminates adhesives, binders, and O-rings from the fluid path, reducing extractable contamination and simplifying material qualification.
    • Polypropylene capsule housing supports autoclave sterilization at 121 degrees Celsius and withstands gamma irradiation exposure, accommodating both user-sterilized and factory-sterilized device configurations.
    • Stepped hose barb design accommodates multiple tubing sizes on a single fitting, simplifying inventory management and enabling connection flexibility across different process configurations.

    When your filtration protocol calls for a validated, integrity-testable barrier that arrives ready to connect and begins filtering immediately, the capsule format delivers that capability without the overhead of traditional filter assemblies. When your filtration protocol demands both validated retention and maximum product recovery, PES membrane architecture balances performance with the low-adsorption surface chemistry your biologics require. Take control of your sample preparation variables and ensure that your data reflects the true nature of your work, rather than the quality of your consumables.

    Sterilization Guidance

    Factory sterilization ensures the device is ready for immediate use in aseptic applications, with validated sterility maintained through the sealed packaging until the labeled expiration date.

    For more information about chemical compatibility, please review our Chemical Compatibility Chart.

    Bubble Point (psi)
    46 psi
    Burst Pressure (psi)
    60 psi
    Capsule Format
    Polycap TC 150
    Compliance Standards
    ISO 9001; HIMA Challenge Test
    Construction
    Polypropylene
    Diameter
    15 cm
    Filling Bell (Yes/ No)
    No
    Filtration Area
    2200 cm²
    Holdup Volume
    250 mL
    Inlet Connection
    3/8 to 1/2 in. stepped barb
    Material
    PES
    Max Batch Volume
    Large-volume batch processing
    Maximum Operating Pressure
    60 psi
    Maximum Operating Temperature (°C)
    121 °C
    Outlet Connection
    3/8 to 1/2 in. stepped barb
    Pack Count
    1
    Pore Size (µm)
    0.1
    Pre-filter Pore Size
    0.2
    Prefilter (Yes/No)
    Yes
    Sterility
    Sterile
    Sterilization
    Do not re-sterilize (autoclavable if sterility expires)
    Vent (Yes/ No)
    No
    Wettability
    Hydrophilic
    • Process Intermediates - In-line capsule filtration of pharmaceutical intermediates with validated retention and low adsorptive losses.
    • Serum Processing - Capsule filtration of animal sera and biological supplements for cell culture and diagnostic reagent applications.
    • Water Purification - Membrane-grade filtration of purified water and water-for-injection systems in pharmaceutical manufacturing facilities.
    • Reagent Filtration - Removal of particulates and contaminants from laboratory reagents and process solutions before downstream use.
    • Biologics Protection - Ultra-low protein binding preserves antibody and growth factor concentrations through the membrane retention step.
    • Buffer Processing - Large-volume filtration of pharmaceutical buffers and process solutions with broad pH compatibility across pH 1-14.