1-Vinylimidazole

99%

Reagent Code: #245339
label
Alias 1-vinyl imidazole; 1-vinyl-1H-imidazole, N-vinyl imidazole
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CAS Number 1072-63-5

science Other reagents with same CAS 1072-63-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 94.11 g/mol
Formula C₅H₆N₂
badge Registry Numbers
EC Number 214-012-0
MDL Number MFCD00005297
thermostat Physical Properties
Melting Point <-50℃
Boiling Point 192-194 °C(lit.)
inventory_2 Storage & Handling
Density 1.039 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its ability to form coordination bonds with metal ions makes it valuable in catalyst supports and metal-chelating resins. Commonly employed in coatings, adhesives, and surface treatments where enhanced adhesion and chemical resistance are required. Plays a role in the production of biocidal polymers due to the antimicrobial properties associated with the imidazole ring. Utilized in pharmaceutical and biomedical applications, including drug delivery systems and hydrogels, thanks to its biocompatibility and pH-responsive behavior. Also serves as a building block in the development of ionic liquids and functional textiles.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿450.00
inventory 2.5kg
10-20 days ฿11,890.00
inventory 500g
10-20 days ฿3,280.00
inventory 100g
10-20 days ฿980.00
inventory 10g
10-20 days ฿290.00

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1-Vinylimidazole
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Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its ability to form coordination bonds with metal ions makes it valuable in catalyst supports and metal-chelating resins. Commonly employed in coatings, adhesives, and surface treatments where enhanced adhesion and chemical resistance are required. Plays a role in the production of biocidal polymers due to the antimicrobial properties associated with the imidazole ring. Utilized in pharma

Used as a reactive monomer in polymer chemistry, particularly in the synthesis of functional polymers and copolymers. Its ability to form coordination bonds with metal ions makes it valuable in catalyst supports and metal-chelating resins. Commonly employed in coatings, adhesives, and surface treatments where enhanced adhesion and chemical resistance are required. Plays a role in the production of biocidal polymers due to the antimicrobial properties associated with the imidazole ring. Utilized in pharmaceutical and biomedical applications, including drug delivery systems and hydrogels, thanks to its biocompatibility and pH-responsive behavior. Also serves as a building block in the development of ionic liquids and functional textiles.

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