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Sartolon® Cartridge

Sartolon filters are designed for broad chemical compatibility for specific applications in the pharmaceutical and chemical industry. The double-layer design leads to superior filtration performance compared to other nylon membrane filters and thereby allows more economical design of your filtration process. Sartolon filter elements are ideal for filtration of a broad range of solvents and solvent-containing liquids.

Item no.:  5102607H2---E

Availability:  On Request

Sterilizing-Grade, 0.2 µm Rated Filters

Sartolon
Pore size: 0.45 | 0.2 µm (heterogeneous Polyamide double layer)

Your Benefits:

  • High chemical compatibility for the filtration of solvents
  • High filter capacity by in-built pre-filter (double-layer construction)
  • Excellent performance for oily formulations
  • Highly economic solution e.g. for antibiotics processes

For highest process flexibility all Sartolon filters are available for conventional or single use applications. All filter elements are available in various sizes and adapter combinations. Please review the selection guide in the supporting resources literature.

Datasheet

Sartolon ® 0,2 µm Cartridges & Midicaps & MaxiCaps
en 619.8 kB

Product properties

  • Connector Inlet
    Double Bayonet Adapter with 2 O-rings (26)
  • Connector Outlet
    Double Bayonet Adapter with 2 O-rings (26)
  • Material o-ring | seal
    EPDM
  • Vent Valve
    N/A
  • Capsule/Cartridge Format
    Cartridges
  • Filter Size
    20" (1.2 m² / 12.9 ft²)
  • Material Prefilters
    Nylon (NY)
  • Pore Size Final-filter
    0.2 µm
  • Pore Size Pre-filter
    0.45 µm
  • Outer Diameter
    70 mm

Technical attributes

  • Sterilization Method
    Autoclavable & In-Line Steam Sterilizable
  • Bacterial Endotoxins
    < 0.25 EU/mL as determined by the LAL test
  • Bacterial Retention
    Quantitative Retention of 1 × E7 CFU/cm² Brevundimonas Diminuta ATCC® 19146 per ASTM methodology
  • GMP Compliance
    This product was manufactured in conformance with established Current Good Manufacturing Practice (cGMP) standards.
  • Maximum Differential Pressure
    20 °C: 5 bar; 80 °C: 2 bar
  • Biosafety
    All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
  • Extractables
    The total amount of extractables is well below the limits established by the current USP unter "Sterile Water for Injection".
  • Housing Material
    Polypropylene (PP)
  • Maximum Diffusion
    26 mL/min at 2.5 bar | 36 psi
  • Non-Fiber Releasing
    This filter product complies with the title 21 of the Code of Federal Regulations (CFR), section 210.3(b)(6) and 211.72.
  • Support Fleece
    Polypropylene (PP)
  • Maximum Allowable Back Pressure (at 20°C)
    2 bar / 29 psi at 20°C; 1 bar / 14.5 psi at 80°C
  • Application
    Filtration of antibiotics and organic solvents
  • Industry
    Pharma/Biotech
  • Sterilization Procedures
    • In-Line Steam Sterilization: at 134 °C, 20 min., 0.5 bar, min. 25 Cycles
    • Autoclaving: at 134°C, 30 min, 2 bar, min. 25 Cycles
  • Minimum Required Bubble Point
    3.0 bar