10-(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-10H-phenoxazine

>98%(HPLC), unsublimate

Reagent Code: #195746
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CAS Number 1411910-25-2

science Other reagents with same CAS 1411910-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.55398 g/mol
Formula C₃₃H₂₂N₄O
thermostat Physical Properties
Boiling Point 713.4±63.0 ℃(Predicted)
inventory_2 Storage & Handling
Density 1.264±0.06 g/cm3(Predicted)
Storage Room temperature, nitrogen

description Product Description

Used as a highly efficient photoinitiator in UV-curable systems, particularly in free radical and cationic polymerization processes. It exhibits strong absorption in the near-UV to visible light range, enabling curing under low-energy light sources, including LED lamps. Commonly applied in dental composites, coatings, inks, and adhesives where deep curing, low yellowing, and high stability are required. Its donor-acceptor molecular structure enhances electron transfer, improving initiation efficiency and reducing required concentrations. Also explored in 3D printing resins for improved surface quality and mechanical properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,280.00
inventory 100mg
10-20 days ฿9,880.00
inventory 500mg
10-20 days ฿34,590.00

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10-(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-10H-phenoxazine
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Used as a highly efficient photoinitiator in UV-curable systems, particularly in free radical and cationic polymerization processes. It exhibits strong absorption in the near-UV to visible light range, enabling curing under low-energy light sources, including LED lamps. Commonly applied in dental composites, coatings, inks, and adhesives where deep curing, low yellowing, and high stability are required. Its donor-acceptor molecular structure enhances electron transfer, improving initiation efficiency and

Used as a highly efficient photoinitiator in UV-curable systems, particularly in free radical and cationic polymerization processes. It exhibits strong absorption in the near-UV to visible light range, enabling curing under low-energy light sources, including LED lamps. Commonly applied in dental composites, coatings, inks, and adhesives where deep curing, low yellowing, and high stability are required. Its donor-acceptor molecular structure enhances electron transfer, improving initiation efficiency and reducing required concentrations. Also explored in 3D printing resins for improved surface quality and mechanical properties.

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