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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 | 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. |
Applications of 1,2,3-Triacetoxybenzene in Industrial Manufacturing1,2,3-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) SynthesisProcess 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
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2. High-Performance Polymer Additive ManufacturingPolymer 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
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3. Specialty Coating and Varnish FormulationProducers 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
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4. Fine Chemical Intermediates for Custom SynthesisCustom 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
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