2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine

99%

Reagent Code: #146932
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CAS Number 864377-31-1

science Other reagents with same CAS 864377-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.27 g/mol
Formula C₂₁H₁₄BrN₃
badge Registry Numbers
MDL Number MFCD22200060
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It effectively generates free radicals upon exposure to ultraviolet light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its ability to absorb UV light and undergo efficient cleavage allows for rapid curing even under low-intensity UV sources. It is especially valued in formulations requiring deep cure and good surface hardness. Additionally, due to its thermal stability in the dark, it offers long shelf life and processing safety. Commonly found in dental composites and electronic encapsulants where precise curing control is essential.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿500.00
inventory 25g
10-20 days ฿1,550.00
inventory 100g
10-20 days ฿5,880.00

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2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine
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Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It effectively generates free radicals upon exposure to ultraviolet light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its ability to absorb UV light and undergo efficient cleavage allows for rapid curing even under low-intensity UV sources. It is especially valued in formulations requiring deep cure and good surface hardness. Additionally, due to its therm

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It effectively generates free radicals upon exposure to ultraviolet light, making it suitable for initiating polymerization in coatings, inks, and adhesives. Its ability to absorb UV light and undergo efficient cleavage allows for rapid curing even under low-intensity UV sources. It is especially valued in formulations requiring deep cure and good surface hardness. Additionally, due to its thermal stability in the dark, it offers long shelf life and processing safety. Commonly found in dental composites and electronic encapsulants where precise curing control is essential.

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