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HS Code |
635702 |
| Product Name | (Perfluoro-N-Propyl)Phenyliodonium Trifluoromethanesulfonate |
| Cas Number | 1602691-00-0 |
| Molecular Formula | C9H5F9IOS |
| Molecular Weight | 510.09 g/mol |
| Appearance | White to off-white powder |
| Purity | Typically ≥98% |
| Solubility | Soluble in acetonitrile, DMSO |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Uses | Reagent for trifluoromethylation and fluoroalkylation |
| Synonyms | Perfluoro-n-propylphenyliodonium triflate |
| Sensitivity | Moisture sensitive |
| Hazard Class | Irritant |
| Supplier Example | Sigma-Aldrich |
| Smiles | C1=CC=C(C=C1)[I+](C(C(C(F)(F)F)(F)F)(F)F)[O-]S(CF3)(=O)=O |
As an accredited (Perfluoro-N-Propyl)Phenyliodonium Trifluoromethanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 1-gram (Perfluoro-N-Propyl)Phenyliodonium Trifluoromethanesulfonate is supplied in an amber glass vial with a tightly sealed cap. |
| Shipping | Shipping of (Perfluoro-N-Propyl)phenyliodonium trifluoromethanesulfonate requires compliance with hazardous material regulations. It should be packaged in sealed, compatible containers, labeled appropriately, and shipped with necessary safety documentation. Handle with care to avoid exposure, following both local and international guidelines for the transport of potentially hazardous organoiodine compounds. |
| Storage | (Perfluoro-N-Propyl)phenyliodonium trifluoromethanesulfonate should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture uptake and degradation. Store in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong bases or nucleophiles. Protect from physical damage and dispose of following proper chemical waste procedures. |
Applications of (Perfluoro-N-Propyl)Phenyliodonium Trifluoromethanesulfonate in Industrial Manufacturing(Perfluoro-N-Propyl)Phenyliodonium Trifluoromethanesulfonate has achieved stable implementation in demanding photochemical and electronics industry settings that require high-performance photoacid generators (PAGs) for next-generation lithographic and imaging processes. Each application scenario below details the integration of this compound in real-world industrial workflows, highlighting compliance, formulation, process stages, and the range of finished goods manufactured by downstream partners. 1. Photolithography Resists for Semiconductor FabricationSemiconductor manufacturing relies heavily on advanced chemically amplified resists for patterning sub-10nm features. As a PAG, this compound delivers controlled acid generation upon deep UV or EUV exposure, supporting the industry’s migration to ever-smaller nodes. Precision dosing and reproducibility define its function in automotive, memory chip, and logic processor lines, where layer integrity and defect minimization are critical for downstream wafer yields. Industry compliance standards
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2. Microelectromechanical Systems (MEMS) Device ManufacturingMEMS device producers deploy photoacid generators in thick-film photoresists to enable accurate definition of microstructures, such as pressure sensors and actuators. Performance reflects in clean development, undercut control, and minimal residual contamination, supporting volume manufacturing for automotive, industrial, and biomedical sensor markets. Industry compliance standards
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3. Printed Circuit Board (PCB) Photoimageable Solder Mask ProductionIn PCB fabrication, consistent formation of solder mask patterns ensures circuit protection and minimizes solder bridging. This photoacid generator allows high sensitivity and sharp resolution for photoimageable solder masks that undergo UV imaging, essential for high-density interconnect and package substrates in telecommunications and computing hardware. Industry compliance standards
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4. Optical Waveguide and Micro-Optics FabricationTelecom and data center markets use this compound in photo-patternable organosilane and epoxy resins to precisely define waveguide structures and micro-lenses. The compound’s acid generation controls phase changes at micrometer resolution, critical in minimizing optical loss and enhancing device efficiency. Industry compliance standards
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5. Advanced Printed Organic Electronics (Photopatterning Conductive Polymers)Manufacturers of organic LEDs (OLEDs), organic field effect transistors (OFETs), and flexible displays utilize this material to photopattern high-purity conductive polymers. Its photoacid function supports selective doping and maskless etching steps demanded by inkjet and roll-to-roll printing platforms. Industry compliance standards
Typical usage ratio
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