CHGL71TP3 Durapore® Cartridge Filter 10 in. 0.45/0.22 µm Code 7

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CHGL71TP3
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      Overview

      Replacement Information

      Key Specifications Table

      Description
      Catalogue NumberCHGL71TP3
      Trade Name
      • Durapore®
      DescriptionDurapore® Cartridge Filter 10 in. 0.45/0.22 µm Code 7
      References
      Product Information
      Device ConfigurationCartridge
      Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
      Maximum Inlet Pressure, bar (psi)Forward - 5.5 bar (80 psi) @ 25 °C; 1.7 bar (25 psi) @ 80 °C; 0.35 bar (5 psi) @ 135 °C; Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent
      Cartridge CodeCode 7 (2-226) O-rings w/locking-tabs
      Good Manufacturing PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
      Quality LevelMQ400
      Applications
      Biological Information
      Bacterial EndotoxinsAqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaMultilayer Durapore®
      SterilityOther
      Sterilization30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C
      Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
      WettabilityHydrophilic
      Physicochemical Information
      Pore Size0.45 / 0.22 µm
      Air Diffusion at 23 °C≤10.8 mL/min @ 2.75 bar (40 psig) in water
      Bubble Point at 23 °C≥3450 mbar (50 psig) air with water
      Indirect Food AdditiveAll component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
      Non-Fiber ReleasingThis product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
      TOC/ConductivityAfter sterilization and a controlled water flush of 16 L per 10-inch cartridge, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 °C.
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Dimensions
      Cartridge Nominal Length10 in. (25 cm)
      Diameter6.9 cm (2.7 in.)
      Filtration Area0.55 m²
      Device Size10 in.
      Materials Information
      Chemistry
      • Polyvinylidene Fluoride (PVDF)
      Device Material
      • Polypropylene
      Seal MaterialSilicone (SI)
      Support MaterialPolypropylene
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Packaging Information
      Material Size3
      Transport Information
      Supplemental Information
      Specifications
      Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥1.5 L

      Documentation

      Durapore® Cartridge Filter 10 in. 0.45/0.22 µm Code 7 SDS

      Title

      Safety Data Sheet (SDS) 

      Certificates of Quality

      Title
      Mulitlayer Durapore Cartridge - C6BA25009
      Multilayer Dupore Cartridge C8AA16728
      Multilayer Durapore Cartridge
      Multilayer Durapore Cartridge C7BA83213
      Multilayer Durapore Cartridge C7EA94798
      Multilayer Durapore Cartridge C7KA49669
      Multilayer Durapore Cartridge C7PA98316
      Multilayer Durapore Cartridge C5CA82844
      Multilayer Durapore Cartridge C5DA03429
      Multilayer Durapore Cartridge C7KA45566

      Technical Info

      Title
      Application Note: Integrity Test Troubleshooting - Beyond Rewet and Retest
      Filter Integrity Test Methods

      Data Sheet

      Title
      Hydrophilic Multilayer Durapore® 0.45/0.22μm Filters

      User Guides

      Title
      Hydrophilic Durapore® Cartridges and Capsules User Guide