2-(4-(Diethylamino)-2-methylbenzoyl)benzoic acid

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Reagent Code: #177496
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CAS Number 52830-65-6

science Other reagents with same CAS 52830-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.38 g/mol
Formula C₁₉H₂₁NO₃
badge Registry Numbers
MDL Number MFCD18970336
thermostat Physical Properties
Boiling Point 505.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Storage -20°C, dry

description Product Description

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It is especially effective in free-radical polymerization reactions triggered by ultraviolet or visible light. Common applications include inks, coatings, adhesives, and dental resins, where rapid curing under light exposure is required. Its ability to absorb light in the long-wavelength UV to visible range makes it suitable for formulations needing deep cure penetration and reduced oxygen inhibition. Often combined with co-initiators like tertiary amines to enhance efficiency.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,200.00

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2-(4-(Diethylamino)-2-methylbenzoyl)benzoic acid
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Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It is especially effective in free-radical polymerization reactions triggered by ultraviolet or visible light. Common applications include inks, coatings, adhesives, and dental resins, where rapid curing under light exposure is required. Its ability to absorb light in the long-wavelength UV to visible range makes it suitable for formulations needing deep cure penetration and reduced oxygen inhib

Used primarily as a photoinitiator in UV-curable systems, this compound plays a key role in polymer chemistry. It is especially effective in free-radical polymerization reactions triggered by ultraviolet or visible light. Common applications include inks, coatings, adhesives, and dental resins, where rapid curing under light exposure is required. Its ability to absorb light in the long-wavelength UV to visible range makes it suitable for formulations needing deep cure penetration and reduced oxygen inhibition. Often combined with co-initiators like tertiary amines to enhance efficiency.

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