Polyvinylidene Fluoride (PVDF) Syringe Filters - SPEC18217
Laboratory workflows requiring flexible sterilization options face limitations when pre-sterilized filters add unnecessary cost to routine sample preparation where you can autoclave before use. Nonsterile 0.22µm PVDF membrane construction delivers economical sterile-grade filtration capability with user sterilization flexibility. Hydrophobic polyvinylidene fluoride in compact 20mm ABS housing with threaded double luer lock connection provides chemical-resistant bacterial retention for HPLC mobile phases, organic solvents, and biological samples after autoclave sterilization.
Key PVDF Membrane Characteristics
- Hydrophobic membrane requires alcohol pre-wetting before aqueous processing, activating the surface for proper flow and preventing air-lock conditions during sample filtration
- Exceptional chemical compatibility resists degradation from acetonitrile, methanol, chlorinated solvents, and aggressive organic reagents that rapidly compromise cellulosic membrane alternatives
- 0.22µm absolute pore size provides sterile-grade bacterial retention after user sterilization, protecting analytical systems from microbial contamination in critical applications
- Ultra-low protein binding maintains biomolecule concentrations throughout filtration, preventing adsorptive losses that compromise quantitative accuracy in your protein analysis workflows
- Temperature stability to 80°C supports both elevated-temperature sample processing and autoclave sterilization cycles without membrane degradation or performance loss
Key Construction Characteristics
- ABS housing provides chemical resistance to common laboratory solvents while delivering mechanical strength for manual filtration operations in routine sample preparation
- Threaded double luer lock connection ensures secure, leak-proof attachment to syringes and transfer lines, preventing disconnection during processing workflows
- 72.5psi maximum operating pressure accommodates manual syringe filtration and integration with low-pressure pumping systems for automated sample preparation
- Nonsterile construction with autoclave capability allows user sterilization before first use, providing economical sterile filtration while eliminating gamma-irradiation costs
Designed for your routine analytical workflows where sterile-grade filtration matters but pre-sterilized filters add unnecessary costs to sample preparation budgets. PVDF's chemical versatility combined with autoclave sterilization capability delivers the flexibility your laboratory needs. Economical nonsterile units become sterile-ready after autoclaving, providing the solvent resistance and bacterial retention that protect analytical instrumentation, maintain sample integrity, and support reliable results across demanding HPLC, LC-MS, and pharmaceutical applications.
For more information about chemical and material compatibility, please review our Chemical Compatibility Chart.
- Bubble Point (psi)
- 7.25psi
- Burst Pressure (psi)
- 116psi
- Connection Type
- Double Luer Lock
- Construction
- Acrylonitrile Butadiene Styrene (ABS)
- Diameter
- 20mm
- Dimensions (W x D x H)
- 23mmx25.2mm
- Material
- Polyvinylidene Fluoride (PVDF)
- Maximum Operating Pressure
- 72.5psi
- Maximum Operating Temperature (°C)
- 80℃
- Pack Count
- 100
- Pore Size (µm)
- 0.22
- Sterility
- Nonsterile
- Weight
- 0.60
- Wetability
- Hydrophobic
- HPLC Mobile Phase Preparation — Sterilize and filter organic mobile phases after autoclaving, protecting columns from bacterial contamination
- LC-MS Sample Processing — Filter biological samples after sterilization, protecting mass spectrometry ionization sources from microbial contamination
- Organic Solvent Filtration — Process acetonitrile and methanol for analytical applications where chemical compatibility prevents membrane degradation
- Biological Sample Clarification — Remove particles from protein solutions after sterilization, maintaining sterile processing in biotechnology workflows
- Pharmaceutical Formulation — Filter heat-stable drug formulations after autoclave sterilization, providing economical sterile processing capability
- Quality Control Testing — Prepare samples for microbiology testing where user sterilization provides flexible contamination control at lower cost