4-Methylbenzophenone

98%

Reagent Code: #204740
label
Alias 4-methylbenzophenone; p-methylbenzophenone
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CAS Number 134-84-9

science Other reagents with same CAS 134-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.24 g/mol
Formula C₁₄H₁₂O
badge Registry Numbers
EC Number 205-159-1
MDL Number MFCD00008553
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a photoinitiator in UV-curable systems such as inks, coatings, and adhesives. It absorbs UV light and generates free radicals that initiate polymerization, enabling fast curing under UV exposure. Commonly found in printing inks and protective films where rapid drying and strong adhesion are required. Also serves as an intermediate in organic synthesis for pharmaceuticals and fine chemicals. Its methyl group enhances solubility and reactivity in certain formulations compared to unsubstituted analogs.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿280.00
inventory 50g
10-20 days ฿710.00
inventory 250g
10-20 days ฿1,590.00
inventory 1kg
10-20 days ฿3,580.00
inventory 10g
10-20 days ฿310.00

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4-Methylbenzophenone
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Used primarily as a photoinitiator in UV-curable systems such as inks, coatings, and adhesives. It absorbs UV light and generates free radicals that initiate polymerization, enabling fast curing under UV exposure. Commonly found in printing inks and protective films where rapid drying and strong adhesion are required. Also serves as an intermediate in organic synthesis for pharmaceuticals and fine chemicals. Its methyl group enhances solubility and reactivity in certain formulations compared to unsubstitute
Used primarily as a photoinitiator in UV-curable systems such as inks, coatings, and adhesives. It absorbs UV light and generates free radicals that initiate polymerization, enabling fast curing under UV exposure. Commonly found in printing inks and protective films where rapid drying and strong adhesion are required. Also serves as an intermediate in organic synthesis for pharmaceuticals and fine chemicals. Its methyl group enhances solubility and reactivity in certain formulations compared to unsubstituted analogs.
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