2,2',4-Tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4',5'-diphenyl-1,1'-biimidazole

95%

Reagent Code: #242114
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Alias 2,4-bis(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenylimidazol-1-yl]-5-(3,4-dimethoxyphenyl)imidazole
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CAS Number 100486-97-3

science Other reagents with same CAS 100486-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 754.102 g/mol
Formula C₄₄H₃₁Cl₃N₄O₂
badge Registry Numbers
EC Number 1312995-182-4
MDL Number MFCD08458465
thermostat Physical Properties
Melting Point 127-140 °C
Boiling Point 855.196 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3
Storage 2-8°C, dry, sealed

description Product Description

Used as a highly efficient photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry, especially in inks, coatings, and adhesives that cure upon exposure to ultraviolet light. Its strong absorption in the near-UV region and ability to generate free radicals make it effective in radical polymerization processes. It is particularly valued in applications requiring deep curing and high sensitivity, such as in printing technologies and electronic encapsulation. Additionally, due to its thermal stability and low migration tendency, it helps maintain the integrity and durability of the cured material, making it suitable for high-performance industrial formulations.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿10,870.00
inventory 25g
10-20 days ฿31,770.00

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2,2',4-Tris(2-chlorophenyl)-5-(3,4-dimethoxyphenyl)-4',5'-diphenyl-1,1'-biimidazole
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Used as a highly efficient photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry, especially in inks, coatings, and adhesives that cure upon exposure to ultraviolet light. Its strong absorption in the near-UV region and ability to generate free radicals make it effective in radical polymerization processes. It is particularly valued in applications requiring deep curing and high sensitivity, such as in printing technologies and electronic encapsulation. Additionally, d

Used as a highly efficient photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry, especially in inks, coatings, and adhesives that cure upon exposure to ultraviolet light. Its strong absorption in the near-UV region and ability to generate free radicals make it effective in radical polymerization processes. It is particularly valued in applications requiring deep curing and high sensitivity, such as in printing technologies and electronic encapsulation. Additionally, due to its thermal stability and low migration tendency, it helps maintain the integrity and durability of the cured material, making it suitable for high-performance industrial formulations.

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