Lithium tetrakis(4-iodophenyl)borate

95%

Reagent Code: #202734
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CAS Number 852312-76-6

science Other reagents with same CAS 852312-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 829.75 g/mol
Formula C₂₄H₁₆BI₄Li
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a highly effective photoinitiator in radical polymerization reactions, particularly in UV-curable systems. It enables rapid curing of coatings, inks, and adhesives under mild light exposure due to its strong absorption in the near-UV to visible range. Its thermal stability makes it suitable for applications requiring long shelf life and controlled initiation. Also employed in advanced lithography and 3D printing technologies where precise spatial control of polymerization is needed. The presence of iodophenyl groups enhances both solubility in organic matrices and efficiency in electron transfer processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,240.00
inventory 250mg
10-20 days ฿9,030.00
inventory 1g
10-20 days ฿24,340.00

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Lithium tetrakis(4-iodophenyl)borate
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Used as a highly effective photoinitiator in radical polymerization reactions, particularly in UV-curable systems. It enables rapid curing of coatings, inks, and adhesives under mild light exposure due to its strong absorption in the near-UV to visible range. Its thermal stability makes it suitable for applications requiring long shelf life and controlled initiation. Also employed in advanced lithography and 3D printing technologies where precise spatial control of polymerization is needed. The presence

Used as a highly effective photoinitiator in radical polymerization reactions, particularly in UV-curable systems. It enables rapid curing of coatings, inks, and adhesives under mild light exposure due to its strong absorption in the near-UV to visible range. Its thermal stability makes it suitable for applications requiring long shelf life and controlled initiation. Also employed in advanced lithography and 3D printing technologies where precise spatial control of polymerization is needed. The presence of iodophenyl groups enhances both solubility in organic matrices and efficiency in electron transfer processes.

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