Puretratech · P-PT69SPGAMS

Hydrophilic PES Membrane Filter Cartridges — Pharmaceutical intermediates

Hydrophilic PES Membrane Filter Cartridges for Pharmaceutical intermediates. Its construction, retention rating and operating limits are the same as the base model PT69SPGAMS.

Application field: PSterilizing grade: No
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SKU / ModelP-PT69SPGAMS
MOQ12 pcs
Lead time20 days
Country of originChina
HS code8421999090
Support / warranty3 years

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PRODUCT OVERVIEW

Hydrophilic PES Membrane Filter Cartridges for Pharmaceutical intermediates. Its construction, retention rating and operating limits are the same as the base model PT69SPGAMS.

If you are considering this product for Pharmaceutical intermediates, confirm process-fluid compatibility, retention rating, operating conditions and any sterilization or sanitization requirements before ordering.

Hydrophilic PES filter cartridges adopt full polypropylene construction with high retention performance, delivering excellent chemical compatibility and superior flow capacity.

Manufactured without adhesives, binders or surfactants, each cartridge is rinsed by high-purity water to cut extractables and system downtime.

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KEY FEATURES

  • High-retentive inherently hydrophilic PES membrane, no IPA pre-wetting required
  • All-polypropylene structure for broad chemical compatibility and high flow rate
  • Adhesive-free, binder-free & surfactant-free, low extractables after high-purity water rinse
  • Low-protein-binding, stable long-term filtration performance
  • Wide pore-size range: 0.04, 0.1, 0.2, 0.45, 0.65, 0.80, 1.2 μm
  • Minimize contamination risk and hazardous waste output

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APPLICATIONS

  • Pharmaceutical intermediates

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MATERIALS

ComponentMaterial / method
Filter MembranePES
Media SupportPolypropylene
End CapsPolypropylene
Inner CorePolypropylene
Outer CagePolypropylene
Sealing MethodThermal Bonding
O-ringsBuna, Viton (or FKM), EP, Silicone, Encapsulated Silicone, Encapsulated Viton (or FKM)

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BIOLOGICAL SAFETY

All components meet the biological-safety requirements of USP Class VI at 121 °C for plastics.

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FOOD SAFETY COMPLIANCE

Materials of construction comply with FDA regulations for food and beverage contact use as detailed in the US Code of Federal Regulations, Title 21 of the U.S. Code of Federal Regulations (21 CFR). Materials used to produce filter media and hardware are safe for use in contact with foodstuffs in accordance with EU 10/2011.

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MAXIMUM OPERATING PARAMETERS

  • Differential pressure: forward 50 psid (3.4 barg) at 20 °C (68 °F); reverse 40 psid (2.7 barg) at 20 °C (68 °F)
  • Operating temperature: 82 °C (180 °F) at 10 psid (0.69 barg) in water
  • Recommended change-out pressure: 35 psid (2.4 barg).

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SANITIZATION / STERILIZATION

  • Filtered hot water: 90 °C (194 °F), 30 minutes, multiple cycles, maximum 3 psid forward flow
  • Autoclave: 121 °C (250 °F), 30 minutes, multiple cycles
  • In-line steam: 135 °C (275 °F), 30 minutes, multiple cycles.

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Integrity Test

Pore sizeMinimum bubble point
0.05 µm31.9 psig / 2.2 bar (IPA)
0.1 µm24.7 psig / 1.5 bar (IPA)
0.2 µm45 psig / 3.1 bar
0.45 µm24 psig / 1.7 bar
0.65 µm19 psig / 1.3 bar
0.8 µm17 psig / 1.2 bar
1.2 µm11.6 psig / 0.8 bar

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Product Configuration / Ordering Information

Product number / modelPore sizeLengthEndcapsSealConnection support
P-PT69SPGAMS0X5=0.05µm05=5 inch7=226/finB=Buna-NS=SS reinforcement
001=0.1µm10=10 inch6=226/flatE=EPDM
002=0.2µm20=20 inch0=222/flatS=Silicone
004=0.45µm30=30 inch5=222/finV=Viton
006=0.65µm40=40 inchF=DOETV=FEP-encapsulated Viton
008=0.8µm2=224/finTS=FEP-encapsulated Silicone
012=1.2µm3=224/flat
4=222/fin (3 lugs)
8=222/flat (3 lugs)
x=213 internal O-ring