Bis-(4-tert-butylphenyl)-iodonium hexafluoroantimonate

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Reagent Code: #151814
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CAS Number 61358-23-4

science Other reagents with same CAS 61358-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 629.08 g/mol
Formula C₂₀H₂₆F₆ISb
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a highly efficient photoacid generator in advanced photolithography processes, particularly in semiconductor manufacturing. Upon exposure to deep UV or EUV light, it releases strong protic acids that catalyze chemical transformations in photoresists, enabling precise patterning of microelectronic circuits. Also employed in cationic polymerization reactions, where it initiates the curing of epoxies and vinyl ethers under light exposure, making it valuable in coatings, inks, and adhesives. Its thermal stability and high acid strength upon activation make it suitable for high-performance imaging systems and specialty polymer synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,440.00
inventory 5g
10-20 days ฿4,320.00
inventory 25g
10-20 days ฿18,720.00

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Bis-(4-tert-butylphenyl)-iodonium hexafluoroantimonate
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Used as a highly efficient photoacid generator in advanced photolithography processes, particularly in semiconductor manufacturing. Upon exposure to deep UV or EUV light, it releases strong protic acids that catalyze chemical transformations in photoresists, enabling precise patterning of microelectronic circuits. Also employed in cationic polymerization reactions, where it initiates the curing of epoxies and vinyl ethers under light exposure, making it valuable in coatings, inks, and adhesives. Its thermal
Used as a highly efficient photoacid generator in advanced photolithography processes, particularly in semiconductor manufacturing. Upon exposure to deep UV or EUV light, it releases strong protic acids that catalyze chemical transformations in photoresists, enabling precise patterning of microelectronic circuits. Also employed in cationic polymerization reactions, where it initiates the curing of epoxies and vinyl ethers under light exposure, making it valuable in coatings, inks, and adhesives. Its thermal stability and high acid strength upon activation make it suitable for high-performance imaging systems and specialty polymer synthesis.
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