945943

N-(3,4-Dihydroxyphenethyl)methacrylamide

≥95%

• Synonym(s): N-(3,4-dihydroxyphenethyl)methacrylamide, N-[2-(3,4-Dihydroxyphenyl)ethyl]-2-methyl-2-propenamide, N-[2-(3,4-Dihydroxyphenyl)ethyl]-2-methylacrylamide, DMA, Dopamine Methacrylamide, Dopamine methacrylate

Properties

• InChI: 1S/C12H15NO3/c1-8(2)12(16)13-6-5-9-3-4-10(14)11(15)7-9/h3-4,7,14-15H,1,5-6H2,2H3,(H,13,16)
• SMILES string: O=C(NCCC1=CC=C(O)C(O)=C1)C(=C)C
• assay: ≥95%
• form: solid
• color: white to yellow
• storage temp.: 2-8°C
• Quality Level: 100

Description

General description

N-(3,4-Dihydroxyphenethyl)methacrylamide (DMA) is a specialized monomer characterized by its unique structure, which includes a 3,4-dihydroxyphenethyl group. This compound is designed for use in polymer synthesis, offering significant potential in the creation of functional polymers with diverse applications. Its chemical structure allows for easy incorporation into various polymer matrices, enhancing the properties of the resulting materials. The presence of hydroxyl groups contributes to increased hydrophilicity and the potential for further chemical modifications.

Application

N-(3,4-Dihydroxyphenethyl)methacrylamide is widely utilized in several key areas: Dopamine methacrylate-based materials can have a wide range of applications in biomedicine, such as drug delivery, tissue engineering, and biosensing. For example, dopamine methacrylate hydrogels have been used as a scaffold for the regeneration of injured tissues, while dopamine methacrylate coatings have been used to improve the biocompatibility and adhesion of medical implants. ; N-(3,4-Dihydroxyphenethyl)methacrylamide is valuable for creating polymer adhesives and surface coating polymers containing a catechol group. For instance, it is utilized in the development of wound dressing materials as well as in dry and wet adhesives ;

Safety Information

• Storage Class: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable