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Benzyltriethylammonium Hydroxide

    • Product Name Benzyltriethylammonium Hydroxide
    • Alias BTEA
    • Einecs 211-691-5
    • 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

    211400

    Chemical Name Benzyltriethylammonium Hydroxide
    Cas Number 56-37-1
    Molecular Formula C13H21NO
    Molecular Weight 207.31 g/mol
    Appearance Colorless to yellow liquid
    Odor Amine-like
    Solubility In Water Miscible
    Density 0.98 g/mL at 20°C
    Ph Strongly basic
    Boiling Point Decomposes before boiling
    Synonyms BTEA hydroxide; Benzyltriethylammonium hydroxide solution
    Storage Temperature 2-8°C
    Hazard Statements Corrosive, causes burns
    Ec Number 200-269-2

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

    Packing & Storage
    Packing A 100 mL amber glass bottle with a secure screw cap, labeled "Benzyltriethylammonium Hydroxide Solution," includes hazard warnings.
    Shipping Benzyltriethylammonium Hydroxide is typically shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be transported under cool, dry conditions, away from incompatible materials. Due to its corrosive nature, proper labeling and adherence to safety regulations are essential during handling and shipping. Check local regulations for specific requirements.
    Storage Benzyltriethylammonium Hydroxide should be stored in a tightly closed, chemically resistant container, away from moisture and incompatible substances such as strong acids and oxidizers. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight and heat sources. Properly label the container and ensure access is restricted to trained personnel, using secondary containment to prevent leaks or spills.
    Application of Benzyltriethylammonium Hydroxide

    Applications of Benzyltriethylammonium Hydroxide in Industrial Manufacturing

    Benzyltriethylammonium hydroxide functions as a high-efficiency phase transfer catalyst and strong organic base in several advanced chemical manufacturing sectors. Our direct supply to industrial clients is based on verified field applications with stringent compliance, process optimization, and input formulation expertise across specialized production routes. The following sections present core deployment scenarios.

    1. Epoxide Synthesis for Epoxy Resin Production

    Epoxy resin manufacturers utilize benzyltriethylammonium hydroxide as a phase transfer catalyst in the key step of bisphenol-A epoxide formation, improving reaction speed and product selectivity in two-phase systems. The catalyst facilitates the transfer of nucleophilic reactants into the organic phase during the dehydrohalogenation of halohydrins, directly impacting the downstream resin’s molecular weight distribution and crosslinking profile. Adjustments to dosage reflect both batch and continuous process designs, resin end-use requirements, and targeted viscosity grade.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 (Quality Management Systems)
    • UL 746D (Polymeric Materials – Fabricated Parts)
    • GB/T 20028-2005 (Chinese Standard for Epoxy Resins)

    Typical usage ratio

    • 0.02% to 0.10% by weight, relative to the reactive halohydrin component, based on reactor configuration and process kinetics

    Downstream process integration

    • Added to the epoxidation reactor with stirring, after feeding aqueous caustic and halo-compound; catalyst quenched and separated during resin washing

    Final product types

    • Liquid and solid epoxy resins for coatings, electrical laminates, adhesives, and civil engineering composites

    2. Quaternary Ammonium Catalyst in Polycarbonate Interfacial Synthesis

    Large-scale polycarbonate manufacturers depend on this phase transfer agent to optimize the reaction of bisphenols with phosgene in an immiscible system. By promoting effective transfer of hydroxide ions into the organic phase, it enables higher molecular weight buildup and finer viscosity control of the resulting polycarbonate. Process engineers select the input ratio based on continuous or batch operation and the purity of raw bisphenol and other reaction medium parameters.

    Industry compliance standards

    • EN ISO 7391:2006 (Testing of Polycarbonates)
    • FDA 21 CFR 177.1580 (Polycarbonate resins for food contact)
    • ISO 14001:2015 (Environmental Management Systems)
    • CNAS L0564 (China National Accreditation Service – Polycarbonate Testing)

    Typical usage ratio

    • 0.01% to 0.05% based on total bisphenol mass, commonly optimized via pilot-scale trial runs

    Downstream process integration

    • Injected at the beginning of the interfacial polycondensation prior to the introduction of phosgene, co-dosed with aqueous caustic

    Final product types

    • Moldable polycarbonate pellets for automotive, optical disc, electrical housing, and food packaging sectors

    3. Zeolite Catalyst Precursor Modification in Petrochemical Processing

    Refineries and catalyst manufacturers utilize benzyltriethylammonium hydroxide as a structure-directing agent in the hydrothermal synthesis of high-silica zeolites (e.g., ZSM-5, Beta, Mordenite). This quaternary ammonium base selects for targeted crystal frameworks and particle morphologies during the gelation and aging steps, directly influencing surface area and acidity critical to catalytic cracking and isomerization activity. Dosage tuning occurs based on template-to-silica/alumina ratios and desired pore structure.

    Industry compliance standards

    • API RP 751 (Safe Operation of Hydrofluoric Acid Alkylation Units)
    • EN 12902:2004 (Water treatment products – Zeolites as filter media)
    • ISO/TS 16949:2009 (Automotive Quality Systems for Catalyst Producers)

    Typical usage ratio

    • 0.5 to 1.5 moles per mole of silica source, calculated based on crystallization study results and finished catalyst property targets

    Downstream process integration

    • Blended into the hydrothermal synthesis gel prior to crystallization; removed post-formation by calcination to yield catalytically active sites

    Final product types

    • FCC catalysts, petrochemical isomerization media, sorbents, hydrocracking and aromatics process catalysts

    4. Emulsion Polymerization Accelerator for Specialty Acrylics

    Producers of specialty acrylic emulsions employ benzyltriethylammonium hydroxide as a cationic process additive for improved rate of free-radical polymerization in waterborne systems. The compound increases monomer reactivity and assists in stabilizing the polymer latex, reducing coagulation in large-scale reactors. Use rates depend on targeted molecular weight, latex particle size, and residual monomer content to achieve designated end-product rheology for industrial coatings and pressure-sensitive adhesives.

    Industry compliance standards

    • EU Regulation (EC) No 1935/2004 (Materials Contacting Food)
    • GB/T 20102-2006 (Chinese Standard for Water-Based Acrylic Resins)
    • ASTM D6083 (Standard Specification for Acrylic Latex)
    • ISO 14021:2016 (Environmental labels and declarations)

    Typical usage ratio

    • 0.05%–0.12% by monomer weight, refined by pilot-batch flow properties and conversion completeness

    Downstream process integration

    • Metered into pre-emulsion feed with monomers and initiators, prior to emulsifier and buffer addition in continuous or batch reactor setups

    Final product types

    • High-performance acrylic dispersions for architectural coatings, textiles, waterborne adhesives, and PSA tapes

    5. Strong Organic Base for Halide Exchange and Quaternization Reactions

    Manufacturers of fine chemicals and specialty pharmaceuticals utilize this hydroxide as a strong organic base in nucleophilic halide exchange and quaternization steps, where strict pH control and minimal aqueous contamination are demanded. The use of this base supports high-yield formation of benzyl and alkyl quaternary ammonium compounds, with exact ratios adjusted to the required conversion efficiency and solvent system. The substance is favored where inorganic base residues are unacceptable in the final product.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP–NF (United States Pharmacopeia for pharmaceutical intermediates)
    • SFDA YBZ (Chinese Pharmacopoeia guidelines for fine chemicals)
    • ISO 9001:2015 (Quality management for chemical synthesis)

    Typical usage ratio

    • 1.05–1.20 equivalents versus halide or ammonium reactant, modified in-situ by reaction completeness and impurity profile analysis

    Downstream process integration

    • Charged to the reaction vessel post-alkylation or halide displacement feed, with quenching and aqueous-organic separation after completion

    Final product types

    • Pharmaceutical quaternary ammonium intermediates, phase transfer catalysts, specialty cationic surfactants, and dye intermediates
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