N-(3-Aminophenyl)acrylamide
97%
- Product Code: 121327
CAS:
16230-24-3
| Molecular Weight: | 162.19 g./mol | Molecular Formula: | C₉H₁₀N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20696452 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
N-(3-Aminophenyl)acrylamide is widely used in the synthesis of polymers and copolymers, particularly in the development of advanced materials with specific functional properties. Its acrylamide group allows it to participate in polymerization reactions, making it valuable in creating coatings, adhesives, and hydrogels. The compound is also utilized in the preparation of molecularly imprinted polymers (MIPs), which are employed in selective recognition and separation processes, such as in sensors or purification systems. Additionally, its amino group provides a reactive site for further chemical modifications, enabling its use in the production of dyes, pharmaceuticals, and bioactive compounds. In research, it serves as a building block for designing novel materials with tailored properties for industrial and biomedical applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Light Yellow To Yellow Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $50.73 |
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| 1.000 | 10-20 days | $125.06 |
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| 5.000 | 10-20 days | $460.51 |
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N-(3-Aminophenyl)acrylamide
N-(3-Aminophenyl)acrylamide is widely used in the synthesis of polymers and copolymers, particularly in the development of advanced materials with specific functional properties. Its acrylamide group allows it to participate in polymerization reactions, making it valuable in creating coatings, adhesives, and hydrogels. The compound is also utilized in the preparation of molecularly imprinted polymers (MIPs), which are employed in selective recognition and separation processes, such as in sensors or purification systems. Additionally, its amino group provides a reactive site for further chemical modifications, enabling its use in the production of dyes, pharmaceuticals, and bioactive compounds. In research, it serves as a building block for designing novel materials with tailored properties for industrial and biomedical applications.
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