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

95%

Reagent Code: #163563
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CAS Number 77989-14-1

science Other reagents with same CAS 77989-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.81 g/mol
Formula C₂₁H₁₄ClN₃
badge Registry Numbers
MDL Number MFCD00521478
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It efficiently 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 cleavage or hydrogen abstraction reactions allows rapid curing under low-intensity UV sources. It is especially effective in formulations where deep cure and good film formation are required. Due to its molecular structure, it exhibits good compatibility with various monomers and oligomers, enhancing the curing speed and final material properties in acrylate-based systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,890.00
inventory 250mg
10-20 days ฿7,480.00
inventory 1g
10-20 days ฿17,820.00

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2-(2-Chlorophenyl)-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 efficiently 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 cleavage or hydrogen abstraction reactions allows rapid curing under low-intensity UV sources. It is especially effective in formulations where deep cure and good film formation are required. Due t

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It efficiently 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 cleavage or hydrogen abstraction reactions allows rapid curing under low-intensity UV sources. It is especially effective in formulations where deep cure and good film formation are required. Due to its molecular structure, it exhibits good compatibility with various monomers and oligomers, enhancing the curing speed and final material properties in acrylate-based systems.

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