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Ethyl Trans-3-Benzoylacrylate

    • Product Name Ethyl Trans-3-Benzoylacrylate
    • Alias Ethyl (E)-3-benzoylacrylate
    • Einecs 406-060-8
    • 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

    459264

    Productname Ethyl Trans-3-Benzoylacrylate
    Casnumber 3989-73-1
    Molecularformula C12H12O3
    Molecularweight 204.22 g/mol
    Appearance White to off-white solid
    Meltingpoint 76-78°C
    Boilingpoint 356.8°C at 760 mmHg
    Density 1.162 g/cm3
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles CCOC(=O)C=CC(=O)C1=CC=CC=C1
    Storagetemperature Store at room temperature, tightly closed

    As an accredited Ethyl Trans-3-Benzoylacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 grams of Ethyl Trans-3-Benzoylacrylate packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping Ethyl Trans-3-Benzoylacrylate is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is transported according to standard regulations for chemical safety, ensuring proper labeling and documentation. The product is typically shipped at ambient temperature, with precautions taken to prevent spillage or contamination during transit.
    Storage Ethyl Trans-3-Benzoylacrylate should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the compound away from strong oxidizers, acids, and bases. Ensure proper labeling and handle with appropriate personal protective equipment to prevent accidental exposure or contamination. Store at room temperature unless otherwise specified.
    Application of Ethyl Trans-3-Benzoylacrylate

    Applications of Ethyl Trans-3-Benzoylacrylate in Industrial Manufacturing

    Ethyl Trans-3-Benzoylacrylate serves as a specialized intermediate within several high-value industrial segments, where its distinct chemical profile fulfills targeted roles in advanced synthesis, polymer modification, and performance enhancement. Below, we detail its downstream adoption across verified application fields, referencing regulatory standards, formulation practices, integration stages, and typical finished products established by end-user industries.

    1. UV-Absorbing Polymer Additives for Specialty Plastics

    Major plastic manufacturers employ this compound in the design of UV-stable polymers, especially for automotive exteriors and electronics housings requiring sustained visual and structural performance under prolonged sunlight. Incorporators value its consistent compatibility with acrylic and styrenic matrices, utilizing its benzoyl functionality for tailored absorption spectra during masterbatch compounding. Sourcing from direct raw material producers helps ensure both regulatory compliance and reliable supply for mass-scale resin formulations.

    Industry compliance standards

    • EU REACH Regulation (EC) No. 1907/2006
    • RoHS 2011/65/EU for electronics-related polymers
    • ISO 4892-2:2013 Plastics — Methods of exposure to laboratory light sources

    Typical usage ratio

    • 0.2–1.0% w/w depending on UV stability requirements; engineers adjust with relation to polymer thickness and target lightfastness class.

    Downstream process integration

    • Blended into polymer matrix during melt mixing (extrusion or compounding), prior to pelletizing or sheet casting; often included in masterbatches for later dilution.

    Final product types

    • Automotive trim molds, outdoor electronics casings, architectural light diffusers, greenhouse glazing sheets

    2. Aromatic Building Block for Pharmaceutical Intermediates

    Within pharmaceutical synthesis, process chemists use this compound as a core aromatic precursor for targeted modifications in small molecule APIs, especially for molecules with benzoyl acrylate pharmacophores. Its geometric configuration and functional group chemistry enable precise coupling, supporting batch-to-batch consistency demanded in regulated markets. Dedicated GMP-compliant manufacturers ensure full traceability and minimize risk of synthetic side-products.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF and EP monograph guidance for starting materials
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, USA FDA)

    Typical usage ratio

    • Applied stoichiometrically as a primary reactant—generally 1.0 molar equivalent per API molecule; scale-up recipes may adjust loading based on targeted impurity profiles.

    Downstream process integration

    • Introduced during the intermediate coupling or condensation stage of multi-step organic synthesis, often within a controlled environment reactor under monitored temperature and solvent conditions.

    Final product types

    • Chemical intermediates for anti-inflammatory agents, photoreactive drug candidates, specialty benzoylated small molecules

    3. Photoinitiator Synthesis for UV-Curable Coatings

    Producers of advanced UV-curable surface coatings and inks base their photoinitiator development on specialty acrylate compounds, integrating this material as a key building block for fine-tuning curing profiles and stabilization. Its precise trans-configuration and functional diversity support customizable initiator packages, which align with evolving EU and North American regulatory frameworks for workplace and environmental safety during industrial-scale production.

    Industry compliance standards

    • EU Regulation No. 1272/2008 (CLP) for chemical classification and labeling
    • GHS (Globally Harmonized System of Classification and Labelling of Chemicals)
    • ISO 15397:2019 (Packaging and Environment — Requirements for UV-curable coatings)

    Typical usage ratio

    • Serves as up to 10–25% of the photoinitiator formulation by weight, dependent upon substrate type and desired reactivity under specific UV lamp wavelengths.

    Downstream process integration

    • Reacted in photoinitiator synthesis prior to blending into UV-curable coating or ink formulations; downstream users disperse these initiators into the resin matrix prior to application and curing.

    Final product types

    • Protective UV-cured coatings for consumer electronics, wood finishes, industrial metal coatings, digital inkjet inks

    4. Monomer Modifier in Specialty Acrylic Copolymerization

    Specialty acrylic producers utilize this material as a reactive comonomer in copolymerization processes to impart aromatic character and tailored thermal or barrier properties. This results in copolymers designed for advanced adhesive backings and specialty films. Process control during continuous polymerization lines, paired with precise dosing protocols, enables downstream partners to fine-tune copolymer microstructure with direct impact on the end-product’s application performance.

    Industry compliance standards

    • ISO 9001:2015 (Quality management system for process consistency)
    • CFR 21 177.1010 (US FDA - Polymers for food contact, when applicable)
    • European Plastics Regulation (EU) No. 10/2011 for plastics in contact with food (for food-packaging films)

    Typical usage ratio

    • Thermoplastic adhesive applications: 0.5–3.5% as feedstock monomer; packaging film modifications typically use 1.0–2.0% by monomer weight, with level set by desired balance of flexibility and UV resistance.

    Downstream process integration

    • Dosed into acrylic monomer feed stream prior to initiation of continuous or batch copolymerization; downstream batch parameters (temperature, initiator profile) optimized for aromatic comonomer inclusion.

    Final product types

    • Pressure-sensitive adhesive tapes, high-barrier packaging films, special-purpose lamination adhesives

    5. Intermediate for Synthesis of Liquid Crystal Materials

    Advanced display technology supply chains utilize this compound during liquid crystal material synthesis, exploiting its molecular geometry for subsequent esterification and functionalization steps. These processes demand stringent trace metal and impurity controls, as trace contaminants may impact electro-optical properties critical to liquid crystal display (LCD) panel performance. Direct sourcing from the synthetic origin ensures compliance with industry purity standards and enables scalable integration into downstream synthon preparation under statistical process control.

    Industry compliance standards

    • IEC 61290-1-1:2023 (Performance specifications for optoelectronic devices)
    • ISO 9001:2015 and ISO/TS 16949 (Automotive requirements, where display modules are integrated)
    • RoHS 2011/65/EU for restriction of hazardous substances in electronics

    Typical usage ratio

    • Relative feed: 1.05–1.10 molar equivalents with respect to intended core scaffold in LCD synthon preparation; the precise ratio fine-tuned to minimize by-product formation.

    Downstream process integration

    • Fed into multi-step organic synthesis, typically entering during the initial esterification or transesterification stage, followed by purification and functional group elaboration.

    Final product types

    • Liquid crystal mixtures for LCD panels, temperature-sensitive display fluids, optically active LCD formulation components
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