AcroPrep Advance PTFE Filter Plate, 0.45 µm, 5/Pk - 8688
Filter plates clarify withdrawn samples across a multi-well format, delivering analysis-ready aliquots in parallel throughout an automated sampling run. Chemically inert PTFE resists attack from the harshest process chemistries while suiting solvent filtration where other membranes fail and delivers absolute particle cutoff at the rated pore size. Analysis-ready fractions move directly to chromatographic or spectroscopic measurement, shortening the path from sample collection to reportable result.
Key Characteristics
- Absolute pore size rating gives consistent results across protocols
- Stable across a wide operating temperature range for demanding methods
- Low extractables keep the chromatographic background clean
- Surface-treated for direct aqueous wetting without alcohol pre-wetting
- Filters aggressive organic solvents without swelling or breakdown
Clarifying organic mobile phases before injection protects your chromatography while standing up to the solvent. Solvent-stream filtration handles the solvents and reagents your methods rely on so your filter holds its integrity through the run. Reach out to the Tisch Scientific team for application support, volume pricing, and technical assistance with your filtration product selection.
- Capacity
- 1mL
- Pore Size (µm)
- 0.45
- Sterility
- Nonsterile
- Wettability
- Hydrophilic
- Unattended Sampling Runs - Single-use plates paired with automated instruments enable clean, hands-off sample collection through a full test.
- Analytical Sample Prep - Turbid samples reduce to clean, injection-ready fractions for reproducible chromatographic and spectroscopic assays.
- High-Throughput Cleanup - Plate-based clarification prepares large analytical batches in parallel and cuts hands-on preparation time per sample.
- Automated Dissolution Sampling - Filtered aliquots pulled from dissolution vessels arrive analysis-ready with no manual clarification step.
- Parallel Sample Processing - Multiple vessel samples clarify at once, tightening run-to-run consistency across a full analytical sequence.
- Pharmaceutical Release Testing - Clarified samples meet USP, EP, and JP method requirements for routine QC and batch release workflows.