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Hydroxyethyl Acrylate (HEA)

Hydroxyethyl Acrylate (HEA) — химический продукт для промышленного производства и разработки рецептур. Ruifen Chemicals предлагает оптовые поставки, техническую документацию, документы качества и международную логистику. Свяжитесь с нами для получения спецификаций и информации о наличии.

Характеристики

Ключевые свойства и преимущества

  • Dual reactivity provided by the presence of both an acrylic double bond for polymerization and a primary hydroxyl group for condensation.
  • Exceptional adhesion promoters that enhance the bonding strength of coatings and adhesives to various polar substrates like metal and wood.
  • High transparency and low color value (typically less than 30 APHA), making it ideal for optical and clear coating applications.
  • Superior chemical resistance when cross-linked, providing durability against solvents and environmental stressors in the final polymer matrix.
  • Effective internal plasticization during copolymerization, which improves the impact resistance and overall flexibility of the resulting resin system.
Спецификации

Технические особенности

  • Molecular weight is 116.12 g/mol with a boiling point of approximately 197 degrees Celsius at atmospheric pressure conditions.
  • Specific gravity ranges between 1.106 and 1.110 at 20 degrees Celsius, ensuring predictable density for industrial volume formulations.
  • Standard moisture content is typically controlled below 0.2 percent to prevent premature polymerization or undesired side reactions during synthesis.
  • Flash point is recorded at 99 degrees Celsius (closed cup), requiring standard precautions for handling combustible liquids in plant environments.
  • Purity levels for industrial grades are generally maintained at a minimum of 97 percent via gas chromatography analysis.
Практическое применение в отраслях

Области применения

  • Formulation of thermosetting acrylic resins used extensively in high-performance automotive topcoats and industrial OEM finishes for metal surfaces.
  • Production of UV-curable monomers and oligomers where the hydroxyl functionality allows for subsequent acrylation or urethane acrylate synthesis.
  • Synthesis of pressure-sensitive adhesives (PSAs) where it improves shear strength and provides reactive sites for cross-linking agents.
  • Manufacturing of textile finishing agents and non-woven binders to enhance durability, wash-fastness, and softness of treated fiber materials.
  • Development of water-soluble polymers and hydrogels for medical or personal care applications, leveraging its inherent hydrophilic chemical character.
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