p-hydroxyphenyl methacrylate

I.Product information

Producr manager email: eva@coreychem.com

II. Application

1. Polymer Materials Synthesis

(1) Ultraviolet (UV) Curable Systems

• High-Performance Coatings: Automotive clear coats, metal coatings, plastic coatings
  • Performance Enhancement: Excellent adhesion, scratch resistance, and chemical resistance
  • Benzene Ring Structure: Increases coating hardness and heat deflection temperature
• Electronic Inks: Solder mask inks for printed circuit boards, marking inks
  • Phenolic Hydroxyl Function: Improves adhesion to metal substrates like copper foil
  • Curing Characteristics: Participates in free radical polymerization, forming dense network structures
• Adhesives: Structural adhesives, instant adhesives, pressure-sensitive adhesives
  • Dual Functional Advantage: Participates in polymerization while providing polar groups for enhanced adhesion

(2). Dental Restorative Materials

• Functional Characteristics:
  • Good biocompatibility and low cytotoxicity
  • Appropriate hydrophilic/hydrophobic balance for handling and curing
  • Provides sufficient mechanical strength (compressive, flexural)
• Application Forms:
  • Mixed with dimethacrylates (e.g., Bis-GMA)
  • Modifies resin viscosity and curing shrinkage
  • Acts as diluent and comonomer

(3). Optical Materials

• Optical Resin Lenses: Increases refractive index, reduces lens thickness
• Fiber Optic Coatings: Functional layer enhancing mechanical strength and durability
• Optical Adhesives: For optical component bonding with good light transmission and low stress

(4). Polymer Modifier

• Antioxidant Functionalization: Introduces phenolic hydroxyl groups into polymer backbone via copolymerization
  • Antioxidant modification of polyolefins, polyesters, polyamides
  • Prevents thermal oxidative degradation, extends service life
• Polarity Adjustment: Increases surface polarity of non-polar polymers
  • Improves printability, coatability, and adhesion
  • Enhances interfacial bonding with fillers and reinforcing fibers

2. Fine Chemicals & Intermediates

(1). Polymeric Antioxidant Precursor

• Synthesis of Hindered Phenol Antioxidants: e.g., Irganox series
• Functionalized Antioxidants: Preparation of reactive antioxidant monomers
  • Can be grafted onto polymers for permanent antioxidant function
  • Avoids migration and leaching issues of small-molecule antioxidants

(2). Specialty Surfactant Synthesis

• Acts as hydrophobic segment for preparing reactive surfactants
• Serves as emulsifier in emulsion polymerization that can participate in polymerization

(3). Chromatographic Stationary Phase Functionalization

• Precursor for bonding phases on silica gel and other chromatographic supports
• Preparation of reversed-phase HPLC columns

3. Electronics & Semiconductor Industry

(1). Photoresist Component

• Chemically Amplified Photoresists: As monomer or additive
  • Improves film-forming properties and adhesion of photoresists
  • Participates in crosslinking reactions during post-exposure baking
• Negative Photoresists: Used as crosslinking agent

(2). Electronic Encapsulation Materials

• Chip Encapsulation Resins: Modifier for epoxy or silicone resins
  • Improves heat resistance and oxidation resistance of encapsulation materials
  • Reduces curing stress and moisture absorption
• Potting Compounds: Protection for sensitive electronic components

(3). Printed Electronics Materials

• Binder phase for conductive inks
• Protective coatings for flexible circuit boards

4. Medical & Biomaterials

(1). Drug Delivery Carriers

• Functional monomer for preparing pH-responsive or enzyme-responsive polymeric carriers
• Design of targeted drug delivery systems

(2). Tissue Engineering Scaffolds

• Component of photocurable hydrogels
• Tunable mechanical properties and degradation characteristics

(3). Medical Adhesives

• Surgical incision bonding, tissue adhesion
• Functional component of hemostatic materials