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2-Methoxyethyl Acrylate

    • Product Name 2-Methoxyethyl Acrylate
    • Alias MEA
    • Einecs 221-499-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    171766

    Cas Number 3121-61-7
    Molecular Formula C6H10O3
    Molecular Weight 130.14 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 178-180 °C
    Melting Point -69 °C
    Density 1.029 g/cm3 at 20 °C
    Refractive Index 1.419 at 20 °C
    Flash Point 68 °C (closed cup)
    Solubility In Water Miscible
    Vapor Pressure 0.41 mmHg at 25 °C

    As an accredited 2-Methoxyethyl Acrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Methoxyethyl Acrylate is supplied in a 25 kg blue HDPE drum with a secure screw cap and clear hazard labeling.
    Shipping 2-Methoxyethyl Acrylate is shipped in tightly sealed, corrosion-resistant containers, typically drums or IBCs, to prevent leakage and moisture ingress. It is transported as a flammable liquid, requiring proper labeling and adherence to UN 2527 regulations. Store away from heat, sparks, and incompatible substances, with appropriate hazard documentation and safety precautions.
    Storage 2-Methoxyethyl Acrylate should be stored in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from oxidizing agents, acids, bases, and polymerization initiators. Use containers made of compatible material and ensure grounding to prevent static discharge. Handle under an inert atmosphere if possible.
    Application of 2-Methoxyethyl Acrylate

    Applications of 2-Methoxyethyl Acrylate in Industrial Manufacturing

    2-Methoxyethyl Acrylate finds established use among manufacturers of advanced polymers, specialty coatings, functional adhesives, and high-performance inks, where its chemical structure supports property optimization and defined performance outcomes. Application fields listed below reflect direct downstream transformations implemented in production-scale facilities, meeting sector-specific regulatory, engineering, and quality requirements.

    1. Radiation Curable Ink Formulations

    Ink formulators leverage 2-Methoxyethyl Acrylate for its high reactivity and ability to enhance flexibility and wetting on non-absorbent substrates, crucial in UV ink systems for packaging and digital print. Typical use involves precise ratio adjustments according to colorant load and press requirements, while safeguarding compliance with regional chemical safety assessments governing food contact and migration. Manufacturers integrate this monomer during the pre-polymerization phase, following pigment wetting and prior to photoinitiator addition, to tune viscosity and flow. Resulting products include UV-cured flexographic, screen, and inkjet inks for labels, folding cartons, and flexible food packs.

    Industry compliance standards

    • Swiss Ordinance on Materials and Articles in Contact with Food (SR 817.023.21, Annex 10-B)
    • European Printing Ink Association (EuPIA) Exclusion Policy
    • REACH Regulation (EC) No 1907/2006—classification and registration
    • EN 71-3:2013 For inks on toys and packaging

    Typical usage ratio

    • 5-20% by weight of total monomers, adjusted based on viscosity and final ink hardness targets

    Downstream process integration

    • Added to base resin synthesis or pre-polymer blend after pigment dispersion and before photoinitiator inclusion, under inert atmosphere to prevent premature cure

    Final product types

    • UV-curable inkjet inks
    • Flexographic UV inks
    • Screen-printed inks for plastics and metals
    • Food packaging exterior inks (non-direct contact)

    2. Pressure Sensitive Adhesive (PSA) Manufacture

    Producers of high-performance tapes and labels value this acrylate for imparting balanced tack, adhesive strength, and low-temperature flexibility, particularly in UV- and emulsion-polymerized PSAs where migration and odor limits matter. During co-polymerization, they regulate monomer ratios to achieve specific shear resistance and peel profiles. Addition occurs during the main feed to the polymerization reactor, alongside butyl acrylate or 2-ethylhexyl acrylate, after the emulsifiers and polymerization initiators have been charged. Finished PSAs target demanding uses such as automotive mounting tapes, electronics assembly films, and removable labels.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electrical/electronic tape adhesives
    • ASTM D3330 for Peel Adhesion Properties of Pressure-Sensitive Tape
    • FDA CFR 175.105 (indirect food-contact adhesives, US markets)
    • Toy Safety EN 71-3 for adhesives on children’s articles

    Typical usage ratio

    • 3-12% of monomer blend; reduced if more glass transition temperature (Tg) control is needed or if migration limits specify

    Downstream process integration

    • Co-fed as liquid monomer during emulsion or solution polymerization, or dosed via controlled feed for in-situ polymer builds after emulsifier and water have equilibrated

    Final product types

    • Acrylic-based pressure-sensitive adhesives for label stock
    • Mounting tapes for automotive and industrial use
    • Protective films for electronics assembly
    • Peelable and repositionable office labels

    3. Automotive Clearcoat and Refinish Coatings

    Makers of original equipment and refinish automotive coatings incorporate this acrylate as a functional comonomer to impart enhanced leveling, chemical resistance, and durability required for long-lasting topcoats. Quality control targets film uniformity, resistance to weathering, and controlled VOC levels, ensuring compliance with evolving regional automotive coatings standards and green chemistry mandates. The raw material is typically charged into the batch reactor during the oligomer synthesis or blended post-polymerization prior to crosslinker addition for two-component clearcoats. The final surface finish meets gloss, hardness, and environmental exposure specification of global automotive OEMs and refinish bodyshops.

    Industry compliance standards

    • ISO 12944-6 (Corrosion protection—paint systems for steel structures)
    • GB/T 22374-2018 (Chinese automotive coating specification)
    • Directive 2004/42/EC (EU VOC regulations for vehicle refinishing products)
    • SAE J2334 (Automotive corrosion laboratory test)

    Typical usage ratio

    • 2-8% of total acrylate composition, based on crosslink density and gloss specification of target clearcoat

    Downstream process integration

    • Blended into acrylic polyol or acrylate copolymer base during bulk synthesis or mixed into formulated topcoat prior to catalyzation and application

    Final product types

    • Automotive OEM clearcoats (2K systems)
    • Aftermarket refinish topcoats
    • Scratch-resistant coatings
    • Protective clear films for vehicle exteriors

    4. Specialty Fiber and Performance Textile Coatings

    Technical textile finishers and fiber producers employ 2-Methoxyethyl Acrylate in the synthesis of specialty acrylic latexes and copolymers formulated for low-temperature processing and soft hand feel. The material enables hydrophilic modification and elastic recovery in coated fabrics or nonwovens, crucial for medical, filtration, and high-comfort apparel applications. The acrylate enters at the emulsion polymerization stage, following surfactant charging and prior to initiator dosing, where it dictates final latex film flexibility, absorption, and grip. End use comprises nonwoven medical staples, hygiene coverstock, and breathable functional apparel coatings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile product safety)
    • ISO 9001:2015 (textile manufacturing quality management)
    • REACH Annex XVII (restricted substances for textiles)
    • FDA 21 CFR Part 177.1630 (polymer coatings for food contact fibers, if applicable)

    Typical usage ratio

    • 1-7% of latex or copolymer solids, adjusted for hand feel, breathability, and drape

    Downstream process integration

    • Fed during latex polymerization or as a post-polymer modification agent, post-surfactant and prior to final initiator charge

    Final product types

    • Medical and surgical nonwovens
    • Hygiene product coverstock (e.g., diapers, sanitary pads)
    • Breathable technical textiles for athletic apparel
    • Filter media base coatings

    5. Functional Acrylic Resin Synthesis for Electronics Encapsulation

    Producers of encapsulants and potting compounds in the electronics industry utilize this raw material to engineer acrylic resins with improved flow and thermal stability, supporting fine-pitch device filling and moisture resistance. The monomer is metered directly into the solution or bulk acrylic resin polymerization, following initiator addition and prior to chain transfer agent feed, allowing for molecular weight control and dielectric property adjustment. Strict adherence to electronics-grade purity and outgassing limits are observed in compliance with international standards. Output includes thin-film encapsulants, structural adhesives, and conformal coatings for printed circuit boards and optoelectronic modules.

    Industry compliance standards

    • IPC-CC-830 (Conformal Coating for Printed Boards)
    • UL 94 (Flammability standards for electronics potting compounds)
    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • IEC 60695 (Electrical insulation—flammability test)

    Typical usage ratio

    • 2-10% of acrylic resin backbone; higher content for encapsulants requiring increased penetration, lower for rigid structural resins

    Downstream process integration

    • Co-polymerized into acrylic resins during bulk or solution-phase synthesis, preceding chain transfer agent dosing to control molecular weight distribution

    Final product types

    • Electronic potting compounds for PCBs
    • Encapsulants for LED and sensor modules
    • Conformal coatings for moisture-sensitive electronics
    • Structural adhesives for device assembly
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