High reactivity in free-radical and cationic polymerization systems due to the electron-rich aminoalkyl side chain.
Enables strong adhesion to polar substrates including metals, glass, and treated plastics via secondary amine functionality.
Offers excellent hydrolytic stability under neutral and mildly acidic conditions compared to ester-based amino monomers.
Provides built-in cationic charge capability for pH-responsive behavior in functional coatings and biomedical hydrogels.
Low volatility and high purity (>98.5%) ensure consistent polymerization kinetics and reduced odor during processing.
Adhesion promoters in automotive clearcoats and industrial metal primers.
Functional comonomer in biocompatible hydrogels for drug delivery and wound dressings.
Charge-modifying agent in waterborne acrylic dispersions for architectural and can coatings.
Reactive diluent and crosslinking aid in UV-curable inkjet inks and 3D printing resins.
Building block for ion-exchange membranes and electrophoretic display materials.
| Chemical Type | Aminoalkyl methacrylate monomer (tertiary amine functionalized) |
| Product Form | Liquid |
| Appearance | Colorless to pale yellow clear liquid |
| Primary Applications | Functional acrylic polymers, adhesion promoters, biomedical hydrogels, cationic coatings |
| Key Features | Amine functionality, polymerizable methacrylate group, hydrolytic stability, low volatility |
| Benefits | Enhanced substrate adhesion, pH responsiveness, compatibility with aqueous and solvent systems |
| Purity (GC) | ≥98.5% |
| Storage Condition | Under nitrogen, at 5–25°C, protected from light and moisture |
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