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1,2,3-Triacetoxybenzene

    • Product Name 1,2,3-Triacetoxybenzene
    • Alias Benzene-1,2,3-triyl triacetate
    • Einecs 221-844-8
    • 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
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    Specifications

    HS Code

    190618

    Chemicalname 1,2,3-Triacetoxybenzene
    Molecularformula C12H12O6
    Molarmass 252.22 g/mol
    Casnumber 1672-12-4
    Appearance White to off-white solid
    Meltingpoint 93-96 °C
    Boilingpoint Decomposes before boiling
    Density 1.31 g/cm³ (estimated)
    Solubility Soluble in organic solvents such as ethanol, chloroform, and acetone
    Synonyms 1,2,3-Benzenetriol triacetate
    Structure Benzene ring with acetoxy groups at positions 1, 2, and 3
    Smiles CC(=O)Oc1cc(OC(=O)C)c(OC(=O)C)cc1

    As an accredited 1,2,3-Triacetoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 1,2,3-Triacetoxybenzene is packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 1,2,3-Triacetoxybenzene is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. The packaging follows regulations for non-hazardous organic chemicals. During transport, containers should be kept upright and protected from physical damage, heat, and direct sunlight. Appropriate documentation and labeling ensure safe handling and regulatory compliance.
    Storage **1,2,3-Triacetoxybenzene** should be stored in a cool, dry, well-ventilated area away from incompatibles such as strong oxidizers and moisture. Keep the container tightly closed and protected from light. Store in a chemical-resistant, labeled container and avoid exposure to heat or open flames. Always follow appropriate safety protocols and wear suitable personal protective equipment when handling the compound.
    Application of 1,2,3-Triacetoxybenzene

    Applications of 1,2,3-Triacetoxybenzene in Industrial Manufacturing

    1,2,3-Triacetoxybenzene serves as a critical intermediate in selected chemical processes within the pharmaceutical, advanced polymer, performance coatings, and specialty chemical sectors. Our production facilities maintain tight controls over purity and batch reproducibility, ensuring stable integration into demanding downstream manufacturing environments.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Process engineers use 1,2,3-Triacetoxybenzene as a functionalized aromatic building block for the synthesis of specialty APIs, especially in multi-step benzene core modification routes. In regulated facilities, this compound supports esterification, acylation, and downstream deprotection strategies to achieve the required molecular complexity for patented pharmaceutical actives. Integration occurs before the final coupling, allowing for selective installation of protected functional groups, facilitating high-yield synthesis with strict traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) General Chapters on Residual Solvents and Organic Impurities
    • EU GMP EudraLex Volume 4 - Part II: Basic Requirements for Active Substances
    • FDA 21 CFR Part 211 and Part 210 (if used in drug substance production for US market)

    Typical usage ratio

    • 5% to 15% molar equivalent in pre-final functional group installation; adjusted based on target molecule complexity and protecting group strategy

    Downstream process integration

    • Stepwise introduced as a protected phenyl ester intermediate prior to deprotection and final coupling reaction in multi-step API synthesis

    Final product types

    • Antifungal pharmaceutical actives
    • Ortho-substituted benzene-based APIs
    • Advanced intermediate catalog compounds for contract manufacturing organizations (CMOs)

    2. High-Performance Polymer Additive Manufacturing

    Polymer compounders utilize 1,2,3-Triacetoxybenzene as a reactive modifier in the manufacture of specialty engineering plastics and thermosetting resins. The compound allows for precise introduction of acetoxy-functional groups, improving the crosslink density and imparting specific chemical resistance to the final matrix. During melt-processing, formulation chemists tune additive ratios based on the final mechanical property targets, balancing processability against end-use requirements for high-temperature and chemical-resistant applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Plastics Processing
    • REACH (EC Regulation No 1907/2006) Registration for Additive Use
    • Specific Food-Contact Approval (EU 10/2011 or FDA 21 CFR 177.2600) when producing food-grade polymers

    Typical usage ratio

    • 0.5% to 3% by weight in polymer blends; tailored to achieve the required crosslinking or functional group density, verified by QC rheometry

    Downstream process integration

    • Direct addition during melt-compounding or resin formulation prior to extrusion, molding, or curing

    Final product types

    • High chemical-resistance thermoset resins
    • Engineering plastics for automotive under-hood applications
    • Specialty coatings powders
    • Thermally stable laminates for electronics

    3. Specialty Coating and Varnish Formulation

    Producers employ 1,2,3-Triacetoxybenzene as a functional aromatic additive for high-performance coatings and varnish systems where controlled hydrolytic stability and specific film characteristics are required. This raw material participates in the esterification reactions within the vehicle portion of coatings, refining the viscosity and enhancing surface hardness in the cured finish. Formulators precisely dose based on desired drying time, gloss, and durability outcomes, especially in products intended for wood, plastics, or industrial fabricated metals.

    Industry compliance standards

    • ISO 12944-6 Corrosion Protection of Steel Structures by Protective Paint Systems
    • ASTM D3022 for Automotive Paints and Coatings
    • RoHS 2011/65/EU for Hazardous Substance Restrictions
    • EU REACH for permitted substances in coatings

    Typical usage ratio

    • 1% to 7% by weight in the total binder content depending on film thickness, targeted drying profile, and balance of mechanical properties

    Downstream process integration

    • Added to the resin or varnish solvent blend phase prior to pigment and additive incorporation

    Final product types

    • Industrial corrosion-resistant topcoats
    • Clear wood varnishes for furniture finishing
    • Specialty plastic primers and sealers
    • Protective metal coatings for equipment

    4. Fine Chemical Intermediates for Custom Synthesis

    Custom synthesis laboratories and bulk chemical producers include 1,2,3-Triacetoxybenzene in aromatic substitution reactions as a strategic precursor for accessing ester-protected derivatives. The triacetoxy pattern provides temporary protection for subsequent nitration, halogenation, or organometallic functionalization, after which selective deacetylation yields multi-functionalized intermediates. Process chemists optimize input ratios to minimize byproduct formation, ensuring target selectivity in complex molecule construction projects.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems (for process emissions management)
    • OECD Guidelines for Chemical Process Safety
    • Responsible Care Global Charter Adherence in bulk intermediates manufacture

    Typical usage ratio

    • 10% to 30% by mass relative to total aromatic substrate input, scaled according to the number and type of target functionalization reactions

    Downstream process integration

    • Inserted prior to the major aromatic substitution (nitration, halogenation, lithiation), enabling selective functional-group manipulation before further downstream derivatization or deprotection steps

    Final product types

    • Trimethoxybenzene derivatives for dyes and pigments
    • Halogenated aromatics for agrochemical synthesis
    • Multi-step intermediates for fragrance or specialty chemicals
    • Precursor blocks for contract research projects
    Free Quote

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