2',5'-Dimethoxyacetophenone

97%

Reagent Code: #170392
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CAS Number 1201-38-3

science Other reagents with same CAS 1201-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₁₀H₁₂O₃
badge Registry Numbers
MDL Number MFCD00008728
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a photoinitiator in UV-curable systems, enabling rapid polymerization of inks, coatings, and adhesives upon exposure to ultraviolet light. Its ability to generate free radicals under UV irradiation makes it valuable in printing inks, electronic coatings, and dental materials where quick curing and low yellowing are desired. Also employed in the synthesis of fine chemicals and pharmaceuticals as an intermediate due to its reactive carbonyl group and stable methoxy substituents.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿450.00
inventory 100g
10-20 days ฿1,740.00
inventory 500g
10-20 days ฿5,196.00
inventory 5g
10-20 days ฿168.00

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2',5'-Dimethoxyacetophenone
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Used primarily as a photoinitiator in UV-curable systems, enabling rapid polymerization of inks, coatings, and adhesives upon exposure to ultraviolet light. Its ability to generate free radicals under UV irradiation makes it valuable in printing inks, electronic coatings, and dental materials where quick curing and low yellowing are desired. Also employed in the synthesis of fine chemicals and pharmaceuticals as an intermediate due to its reactive carbonyl group and stable methoxy substituents.

Used primarily as a photoinitiator in UV-curable systems, enabling rapid polymerization of inks, coatings, and adhesives upon exposure to ultraviolet light. Its ability to generate free radicals under UV irradiation makes it valuable in printing inks, electronic coatings, and dental materials where quick curing and low yellowing are desired. Also employed in the synthesis of fine chemicals and pharmaceuticals as an intermediate due to its reactive carbonyl group and stable methoxy substituents.

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