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2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane

    • Product Name 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane
    • Alias Bisphenol B
    • Einecs EINECS 201-245-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    307381

    Chemical Name 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane
    Common Name Tetra-methyl Bisphenol A
    Molecular Formula C19H24O2
    Molecular Weight 284.39 g/mol
    Cas Number 79-97-0
    Appearance White to off-white crystalline powder
    Melting Point 171-174°C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in acetone, alcohol, and benzene
    Density 1.13 g/cm³
    Flash Point 227°C
    Synonyms Tetramethyl bisphenol A, TMBPA
    Usage Monomer for polymer synthesis (e.g., epoxy resins, polycarbonates)
    Structure Contains two 4-hydroxy-3,5-dimethylphenyl groups attached to a propane backbone

    As an accredited 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a screw cap, labeled "2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane," includes safety and handling instructions.
    Shipping 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane is shipped in tightly sealed containers to prevent contamination and moisture exposure. Containers are clearly labeled with product and hazard information. The chemical is typically transported as a solid at ambient temperature, following relevant regulatory guidelines for safe handling, storage, and transportation of chemicals.
    Storage 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Store at room temperature, in a cool, dry, and well-ventilated area. Handle with proper personal protective equipment to avoid skin and eye contact, as well as inhalation of dust. Always follow relevant safety guidelines and regulations.
    Application of 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane

    Applications of 2,2-Bis(4-Hydroxy-3,5-Dimethylphenyl)Propane in Industrial Manufacturing

    2,2-Bis(4-hydroxy-3,5-dimethylphenyl)propane is a specialty monomer used by advanced materials manufacturers to achieve targeted molecular performance attributes in sectors that require both chemical resistance and dimensional control. As an experienced producer of this compound, we detail below its established downstream applications, with a focus on real-world industrial practices, compliance frameworks, integration methods, and end product categories.

    1. Specialty Polycarbonate Resin Synthesis

    Polycarbonate suppliers use this bisphenol monomer to formulate resins with improved heat stability, UV endurance, and color retention for demanding optical and electronics applications. The material enables resin producers to balance flow properties and molecular rigidity during melt polymerization, supporting processability for intricate molding operations. Downstream users adopt this compound when customizing polycarbonate grades for LED diffusers, electrical domes, and high-wear housings exposed to persistent mechanical stress and heat cycles in professional environments.

    Industry compliance standards

    • ISO 7391-1 Polycarbonates—General Method for Determination of Properties
    • UL 94 Flammability Standard for Plastics Materials
    • RoHS Directive (2011/65/EU and amendments for electronic casings)
    • REACH Regulation (EC) No 1907/2006 (substance registration and safety dossier)

    Typical usage ratio

    • 5–15 mol% as a replacement or modifier for bisphenol A, depending on desired rigidity and colorfastness; formulators may decrease or increase the percentage in response to specified glass transition temperature values.

    Downstream process integration

    • Direct addition to the melt phase before transesterification or phosgenation steps in polycarbonate resin manufacturing lines; compound enters as a co-monomer in primary synthesis reactors.

    Final product types

    • Precision optical lenses for LED lighting units
    • Electrical housings for circuit protection in high-heat installations
    • Automotive instrument cluster covers
    • Structural sheets for railway and airport signage

    2. High-Performance Epoxy Systems for Electrical Encapsulation

    This monomer is selected by epoxy system manufacturers to reinforce the molecular network of potting compounds and encapsulation resins required for electrical component protection. The methyl-substituted structure enhances hydrophobicity and dielectric stability, ensuring encapsulation materials withstand repeated thermal cycling and extended field deployment. Such performance is critical in producing conformal coatings and encapsulation resins for medium- and high-voltage industrial modules.

    Industry compliance standards

    • IEC 60455-2 Resinous Compound—Systems for Electrical purposes
    • UL 746C Polymeric Materials—Use in Electrical Equipment Evaluations
    • EN 60216-1 Thermal Endurance Properties
    • RoHS 2011/65/EU Directive (electrical contact materials)

    Typical usage ratio

    • 2–6 parts per hundred resin (phr), calibrated against desired crosslink density and insulation grade as defined by dielectric constant specifications; adjustment permitted for product thickness and solidification window.

    Downstream process integration

    • Incorporation into prepolymer blending before addition of amine hardeners; it acts as a partial chain extender and crosslinking modifier during the resin curing step in vacuum casting or molding units.

    Final product types

    • Encapsulated power relay coils
    • Insulating blocks for printed circuit boards (PCBs)
    • Hermetic modules for frequency control devices
    • Transformer and coil potting masses for industrial switchgear

    3. Modified Phenolic Resin Manufacture for Heat-Resistant Laminates

    Laminate manufacturers introduce this bisphenol derivative to adjust the flexibility–rigidity balance of high-performance phenolic resins. The methyl groups on the aromatic ring lend improved resistance against charring and micro-crack formation during thermal shock testing. Application in phenolic composite sheets demands exacting flow and curing profiles to achieve non-brittle, impact-resistant panels for specialty sectors such as rolling stock interiors and toxic-free fire barriers.

    Industry compliance standards

    • EN 438-7 High-Pressure Decorative Laminates for Railway Interiors
    • NFPA 130 (Standard for Fixed Guideway Transit and Passenger Rail Systems—Flammability and Smoke)
    • GB/T 2828.1-2012 Quality Control Standards for Batch Inspections
    • ASTM D2299 Standard Test Method for Haze and Luminous Transmittance

    Typical usage ratio

    • 7–12% by total phenolic monomer content, with fine-tuning based on the required flexural modulus and ignition resistance as determined by end-part testing protocols.

    Downstream process integration

    • Incorporated during alkali-catalyzed condensation in resin kettles before blending with cellulose or glass fiber mats for continuous sheet pressing lines.

    Final product types

    • Heat-resistant laminate boards for public transportation
    • High-density circuit board substrates
    • Fire-retardant wall panels for commercial buildings
    • Protective composite layers in aerospace interiors

    4. Advanced Polyarylate Synthesis for High-Clarity Film

    Producers of specialty engineering films leverage this diphenolic compound to raise inherent viscosity and maintain optical transparency in polyarylate formulations. Its presence ensures film webs resist yellowing, dimensional sag, and fracture during high-temperature thermoforming and vacuum shaping for flat panel display manufacturing. Use in this segment requires precise stoichiometric balance to achieve tensile uniformity and batch-to-batch color consistency.

    Industry compliance standards

    • ISO 15765 Polyarylate Molding and Extrusion Materials
    • JEDEC JESD22-B103C Thermal Testing Methods for Films in Electronics
    • JIS K6900 Test Methods for Engineering Plastics
    • IEC 61249-2-7 Halogen-Free Material Requirements

    Typical usage ratio

    • 3–10 mol% relative to total diol content, determined by clarity and mechanical strength targets; film producers adjust this range based on film gauge and substrate compatibility.

    Downstream process integration

    • Blend addition at the esterification or transesterification stage prior to chain extension in polyarylate batch reactors—followed by film casting and in-line polishing under inert atmosphere or controlled humidity curing ovens.

    Final product types

    • Transparent films for liquid crystal display (LCD) polarizers
    • Protective coating layers for capacitive touch screens
    • High-strength packaging films for semiconductor wafers
    • Flexible photographic substrate films

    5. UV-Curable Coating Additive for Printed Circuit Boards (PCB)

    Electronic material formulators utilize this bisphenol derivative as a reactive modifier in UV-curable coating matrices for PCBs requiring enhanced scratch resistance and anti-yellowing performance. The unique structural features support formation of dense polymer grids under rapid UV exposure, ensuring cured films offer both mechanical protection and long-term optical stability for surface-mounted and high-reliability PCBs.

    Industry compliance standards

    • IPC-4101B Specification for Base Materials for Rigid and Multilayer PCBs
    • IEEE-STD-802.3 Environmentally Safe Circuit Assembly
    • ASTM D3363 Pencil Hardness Test for Coatings
    • ISO 9242 Surface Insulation Resistance Measurement Procedures

    Typical usage ratio

    • 1–4% by total oligomer content; fine adjustments made according to degree of crosslinking, target hardness, and film thickness for each specific device line.

    Downstream process integration

    • Integration into monomer/oligomer blend tanks before photoinitiator and photoresist addition; enters the screen printing or curtain coating process preceding UV irradiation.

    Final product types

    • UV-cured solder mask films
    • Scratch-resistant top coats for surface-mount PCBs
    • Dielectric layers on power electronics substrates
    • Protective viscoelastic coatings for microelectronic assemblies
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