Highly reactive methacrylate monomer with pendant hydroxyl functionality for facile post-polymerization modification.
Excellent compatibility with common acrylic, styrenic, and vinyl monomers in free-radical copolymerization systems.
Enables synthesis of hydrophilic, crosslinkable, or adhesion-promoting polymers without requiring additional functionalization steps.
Low volatility and favorable handling characteristics compared to glycidyl methacrylate (GMA) or other epoxy-functional monomers.
Consistent batch-to-batch purity and low inhibitor residue, ensuring reliable polymerization kinetics and reproducible performance.
Functional comonomer in pressure-sensitive adhesives (PSAs) for enhanced cohesive strength and substrate adhesion.
Building block for waterborne acrylic dispersions used in architectural and industrial coatings.
Reactive diluent and hydroxyl source in UV-curable inks, overprint varnishes, and specialty resins.
Key ingredient in biomedical polymer design, including hydrogels and drug delivery carriers requiring biocompatible hydroxyl groups.
Modifier for thermoset acrylics and hybrid polymer systems targeting improved flexibility, toughness, and interfacial bonding.
| Chemical Type | Reactive hydroxyl-functional methacrylate monomer |
| Product Form | Liquid |
| Appearance | Colorless to pale yellow clear liquid |
| Primary Applications | Functional comonomer for acrylic copolymers, coatings, adhesives, and biomedical polymers |
| Key Features | Hydroxyl group reactivity, copolymerizability, low volatility, high purity |
| Stabilizer | Contains polymerization inhibitor (e.g., MEHQ) at industry-standard concentration |
| Storage Conditions | Store under nitrogen at 5–25 °C, protected from light and moisture |
| Handling Precautions | Use in well-ventilated areas; avoid contact with skin and eyes; refer to SDS for full safety guidance |
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