1-(4-Vinylbenzyl)-1H-imidazole
95%
- Product Code: 245377
CAS:
78430-91-8
| Molecular Weight: | 184.24 g./mol | Molecular Formula: | C₁₂H₁₂N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28346936 | |
| Melting Point: | Boiling Point: | 351.3±11.0°C | |
| Density: | Storage Condition: | 2-8°C |
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.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿2,180.00 |
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| 0.250 | 10-20 days | ฿6,600.00 |
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1-(4-Vinylbenzyl)-1H-imidazole
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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