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Bisphenol A Diacetate

    • Product Name Bisphenol A Diacetate
    • Alias 4,4'-Isopropylidenediphenol diacetate
    • Einecs 246-430-4
    • 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
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    Specifications

    HS Code

    948670

    Chemical Name Bisphenol A Diacetate
    Cas Number 5607-45-0
    Molecular Formula C19H20O4
    Molecular Weight 312.36 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 185-187 °C
    Solubility In Water Insoluble
    Density 1.18 g/cm³
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Synonyms 4,4'-Isopropylidenediphenol diacetate, BPA diacetate
    Ec Number 227-077-5

    As an accredited Bisphenol A Diacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for Bisphenol A Diacetate features a 500g amber glass bottle, tightly sealed, labeled with hazard warnings and product details.
    Shipping Bisphenol A Diacetate should be shipped in tightly sealed containers, away from direct sunlight, moisture, and incompatible substances. Ensure packaging complies with local and international transport regulations. During transit, keep upright and protect from physical damage. Label containers appropriately, and include relevant safety and hazard information according to Material Safety Data Sheet (MSDS) guidelines.
    Storage Bisphenol A Diacetate should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from direct sunlight, moisture, and heat sources. Ensure appropriate labeling and store at room temperature to maintain stability. Follow all relevant regulations and safety guidelines for chemical storage.
    Application of Bisphenol A Diacetate

    Applications of Bisphenol A Diacetate in Industrial Manufacturing

    Our Bisphenol A Diacetate, produced with strict in-house control and full batch traceability, serves critical roles across multiple chemical production sectors. Below, we detail main downstream application scenarios, covering integration points, compliance regimes, practical usage ratios, and the specific end products our material supports.

    1. Epoxy Resin Curing Agents for Advanced Composites

    Resin formulators utilise Bisphenol A Diacetate as a key co-curing agent in epoxy systems, specifically when manufacturing high-performance composites for industrial and automotive sectors. Its acetylated structure enhances compatibility with standard epoxy prepolymers, improving processability and final mechanical strength over unmodified bisphenol A. This additive enables accurate control of cure profiles, thermal stability, and processing windows in advanced prepreg and filament winding lines. Any shift in resin matrix chemistry or part design will require corresponding adjustment of additive level and process parameters, maintaining performance and compliance for each batch.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • REACH Regulation (EC) No 1907/2006 for European markets
    • RoHS Directive 2011/65/EU for electronics composite parts
    • UL 94: Flammability ratings for finished composite parts

    Typical usage ratio

    • 5–18 wt% of the total epoxy resin mix; formulation adjustments based on glass transition temperature and mechanical targets, as well as resin flow requirements for given composite geometries.

    Downstream process integration

    • Added directly to resin mixing vessels after pre-polymer and hardener addition; homogenised below 70°C to prevent premature crosslinking, followed by in-mold/post-mold thermal curing based on customer process windows.

    Final product types

    • CFRP automotive body panels
    • Industrial support beams and reinforcements
    • Glass fiber resin laminates
    • Thermal interface materials for electronics substrates

    2. Polyester and Polycarbonate Polymer Modification

    Major plastic compounding operations include Bisphenol A Diacetate in the synthesis of high-clarity copolyesters and modified polycarbonates. This role as a reactive chain-modifier and secondary monomer increases polymer flexibility or heat resistance, depending on molecular design. Granulators and extruders must closely manage dosing and thermal profiles to maintain reproducibility and regulatory compliance. The consistent purity and melt behavior of our product support stable runs in closed-loop production facilities focused on films, sheets, and injection-molded components.

    Industry compliance standards

    • FDA 21 CFR 177.1580 (Polycarbonate Resins, indirect food contact)
    • EN ISO 14001:2015 (environmental management for polymer manufacturing)
    • GB/T 12670-2008 (Chinese standard for polyester resins)
    • ASTM D1891 for polymer additive quality control

    Typical usage ratio

    • 0.3–2.0 mol% based on total diol input in the polymerisation feedstock; precise rates set after initial pilot trials and property profiling per resin grade.

    Downstream process integration

    • Metered into reactor kettles during esterification or transesterification step; undergoes full integration into backbone structure and is tracked via in-process FT-IR spectroscopy to confirm conversion and limit residual acetic species.

    Final product types

    • Optical-grade polyester films for electronics
    • High-impact polycarbonate enclosures
    • Bottle preforms for beverage packaging
    • Flame-retardant engineering plastics for electrical housings

    3. UV-Curable Coating Formulations

    Bisphenol A Diacetate is integrated by coating producers as a reactive monomer in UV-initiated acrylate and epoxy-acrylate systems, serving industries such as optical fiber protection, PCB varnishes, and specialty wood coatings. The acetylated bisphenol structure minimises volatility and improves UV transparency, allowing formulators to achieve precise film properties including surface hardness and resistance to yellowing. Expansion or tightening of coating parameters depends on the intended substrate, line speed, and customer-specific durability requirements.

    Industry compliance standards

    • EN 71-3:2019 (safety of toy coatings)
    • GB 18581-2020 (Chinese VOC limits for architectural coatings)
    • FDA 21 CFR 175.300 (indirect food contact coatings, if applicable)
    • RoHS Directive for coatings on electronic circuit boards

    Typical usage ratio

    • 3–12 wt% of total acrylate/aliphatic epoxy content; rate adjusted for targeted crosslink density and final application thickness.

    Downstream process integration

    • Mixed into resin base at the let-down stage before photoinitiator addition; disperses at ambient or slightly elevated temperature, followed by curing under UV lamps at line speeds up to 60 m/min.

    Final product types

    • Digital print-compatible overprint varnishes
    • Scratch-resistant optical fiber coatings
    • PCB solder mask resins
    • High-gloss UV-curable wood lacquers

    4. Specialty Adhesives for Electronics Assembly

    Electronics adhesive formulators use Bisphenol A Diacetate in thermosetting and light-cure adhesive development, where it provides controlled flexibility and improved dielectric performance. Its presence optimises bond-line thickness and reduces the risk of voiding during automated dispensing or screen-printing applications. Consistent supply and narrow purity specifications are essential, as downstream QC includes rigorous microelectronic reliability and compatibility testing with sensitive substrates like polyimide and glass-reinforced laminates.

    Industry compliance standards

    • IPC-4101D (laminate material specification for printed boards)
    • IEC 61249-2-7 (halogen-free requirements)
    • UL 746E (adhesive components in electrical equipment)
    • ISO/TS 16949 (automotive electronic adhesive suppliers)

    Typical usage ratio

    • 2–10 wt% in total binder matrix; lower percentages for fine-pitch component glue, higher for mechanical PCB assembly adhesives.

    Downstream process integration

    • Pre-blended into base resin before final adjustment with fillers and thixotropic agents; processed through vacuum degassing and then packaged for one- or two-component dispensing systems according to OEM customer workflow.

    Final product types

    • Surface-mount adhesives for PCB assembly lines
    • Die attach pastes for semiconductor packaging
    • Structural microelectronic component glues
    • Smart device module assembly tapes

    5. Intermediate for Fine Chemical Synthesis

    Chemical synthesis plants employ Bisphenol A Diacetate as a protected bisphenol building block or masking agent in processes where direct hydroxy functional groups would otherwise interfere. The diacetate group enables selective deprotection in subsequent synthetic steps, supporting manufacture of advanced intermediates for pharmaceutical, agricultural, and functional monomer segments. Detailed trace impurity data and controlled moisture content are vital for maintaining process yields and regulatory documentation in these applications.

    Industry compliance standards

    • GMP (Good Manufacturing Practice) for intermediates (ICH Q7)
    • Ph. Eur. General Chapters (where active intermediates are destined for pharma)
    • ISO 9001 for batch-controlled synthesis
    • EPA SARA Title III compliance (for chemical handling and reporting)

    Typical usage ratio

    • Stoichiometric equivalence; calculated per mole of desired masked bisphenol in the synthetic route, typically ranging from 1.0–1.2 molar equivalents per reaction stage.

    Downstream process integration

    • Introduced at the condensation or protection step; controls downstream side reactions in presence of strong acids or bases, then removed by selective hydrolysis or transesterification as the target molecule progresses to next API or specialty chemical stage.

    Final product types

    • Fine chemical intermediates for pharmaceuticals
    • Agrochemical precursor compounds
    • Functional monomers for specialty polymer synthesis
    • Protected ligand sets for advanced coordination chemistry
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