N-(2-Aminoethyl)acrylamide hydrochloride
97%
- Product Code: 121361
CAS:
54641-27-9
| Molecular Weight: | 150.61 g./mol | Molecular Formula: | C₅H₁₁ClN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18380727 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
Used primarily in biochemical research, this compound is a key reagent in the synthesis of polymers and hydrogels with specific functional properties. It is particularly valuable in creating materials for drug delivery systems, where its ability to form cross-linked networks enhances controlled release mechanisms. Additionally, it is employed in surface modification processes to improve biocompatibility of medical devices. Its reactive acrylamide group allows for easy incorporation into various copolymers, making it a versatile building block in advanced material science and biomedical engineering applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Yellow Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £97.71 |
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| 0.250 | 10-20 days | £164.65 |
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| 1.000 | 10-20 days | £422.94 |
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| 5.000 | 10-20 days | £1,350.01 |
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N-(2-Aminoethyl)acrylamide hydrochloride
Used primarily in biochemical research, this compound is a key reagent in the synthesis of polymers and hydrogels with specific functional properties. It is particularly valuable in creating materials for drug delivery systems, where its ability to form cross-linked networks enhances controlled release mechanisms. Additionally, it is employed in surface modification processes to improve biocompatibility of medical devices. Its reactive acrylamide group allows for easy incorporation into various copolymers, making it a versatile building block in advanced material science and biomedical engineering applications.
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