1-(4-Vinylbenzyl)-1H-imidazole

95%

Reagent Code: #245377
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CAS Number 78430-91-8

science Other reagents with same CAS 78430-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.24 g/mol
Formula C₁₂H₁₂N₂
badge Registry Numbers
MDL Number MFCD28346936
thermostat Physical Properties
Boiling Point 351.3±11.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its vinyl group enables participation in free radical polymerization, while the imidazole ring provides coordination sites for metal ions, making it valuable in catalyst supports and metal-organic frameworks. Commonly employed in the development of ion-exchange membranes, antimicrobial coatings, and corrosion inhibitors. Also utilized in designing stimuli-responsive materials due to the pH-sensitive nature of the imidazole moiety. Finds application in dental composites and adhesives where improved durability and bioactivity are required.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,180.00
inventory 250mg
10-20 days ฿6,600.00

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1-(4-Vinylbenzyl)-1H-imidazole
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Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its vinyl group enables participation in free radical polymerization, while the imidazole ring provides coordination sites for metal ions, making it valuable in catalyst supports and metal-organic frameworks. Commonly employed in the development of ion-exchange membranes, antimicrobial coatings, and corrosion inhibitors. Also utilized in designing stimuli-responsive materials due to the p

Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its vinyl group enables participation in free radical polymerization, while the imidazole ring provides coordination sites for metal ions, making it valuable in catalyst supports and metal-organic frameworks. Commonly employed in the development of ion-exchange membranes, antimicrobial coatings, and corrosion inhibitors. Also utilized in designing stimuli-responsive materials due to the pH-sensitive nature of the imidazole moiety. Finds application in dental composites and adhesives where improved durability and bioactivity are required.

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