4,4'-Bis(diethylamino)benzophenone

99%

Reagent Code: #126898
label
Alias Tetraethyl Michler's Ketone ; 4,4'-Bis(diethylamino)benzophenone
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CAS Number 90-93-7

science Other reagents with same CAS 90-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.46 g/mol
Formula C₂₁H₂₈N₂O
badge Registry Numbers
EC Number 202-025-4
MDL Number MFCD00009044
thermostat Physical Properties
Melting Point 89-92 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily as a photosensitizer in photopolymerization processes, it plays a crucial role in the curing of inks, coatings, and adhesives when exposed to UV light. Its ability to absorb UV radiation and generate reactive species makes it valuable in the production of printed circuit boards and other electronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in reactions requiring light-induced transformations. Its stability and efficiency in initiating photochemical reactions have also led to its use in research and development of advanced materials.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 94-97
Purity (HPLC) 99-100%
Appearance White to yellow-green to light green powder
Infrared Spectrum Conforms to Structure
Transmittance (500 Nm) >=80%
Transmittance (590 nm) ≥80%

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿3,960.00
inventory 100g
10-20 days ฿980.00
inventory 2.5kg
10-20 days ฿18,560.00
inventory 25g
10-20 days ฿430.00

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4,4'-Bis(diethylamino)benzophenone
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Used primarily as a photosensitizer in photopolymerization processes, it plays a crucial role in the curing of inks, coatings, and adhesives when exposed to UV light. Its ability to absorb UV radiation and generate reactive species makes it valuable in the production of printed circuit boards and other electronic components. Additionally, it is employed in the synthesis of organic compounds, particularly in reactions requiring light-induced transformations. Its stability and efficiency in initiating photochemical reactions have also led to its use in research and development of advanced materials.
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