DiphenyliodoniumTetrafluoroborate

≥98%

Reagent Code: #180126
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CAS Number 313-39-3

science Other reagents with same CAS 313-39-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.92 g/mol
Formula C₁₂H₁₀BF₄I
badge Registry Numbers
MDL Number MFCD00154992
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a photoacid generator in photopolymerization processes, particularly in UV-curable coatings, inks, and resins. Upon exposure to light, it releases strong acid that initiates polymerization, making it valuable in advanced lithography for microelectronics and in dental composites. Also serves as an arylating agent in organic synthesis, transferring phenyl groups to various substrates under mild conditions. Its stability and reactivity make it suitable for use in radical reactions and as a precursor in the preparation of hypervalent iodine-based catalysts.

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Test Parameter Specification
Appearance White to Light Yellow Solid, Powder or Crystals
Purity (%) 98-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,630.00
inventory 25g
10-20 days ฿66,740.00
inventory 5g
10-20 days ฿13,450.00

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DiphenyliodoniumTetrafluoroborate
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Used as a photoacid generator in photopolymerization processes, particularly in UV-curable coatings, inks, and resins. Upon exposure to light, it releases strong acid that initiates polymerization, making it valuable in advanced lithography for microelectronics and in dental composites. Also serves as an arylating agent in organic synthesis, transferring phenyl groups to various substrates under mild conditions. Its stability and reactivity make it suitable for use in radical reactions and as a precursor

Used as a photoacid generator in photopolymerization processes, particularly in UV-curable coatings, inks, and resins. Upon exposure to light, it releases strong acid that initiates polymerization, making it valuable in advanced lithography for microelectronics and in dental composites. Also serves as an arylating agent in organic synthesis, transferring phenyl groups to various substrates under mild conditions. Its stability and reactivity make it suitable for use in radical reactions and as a precursor in the preparation of hypervalent iodine-based catalysts.

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