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HS Code |
665561 |
| Chemical Name | 1,2,4-Triacetoxybenzene |
| Molecular Formula | C12H12O6 |
| Molar Mass | 252.22 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 107-110 °C |
| Boiling Point | Decomposes before boiling |
| Density | 1.33 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Cas Number | 13218-42-3 |
| Pubchem Cid | 166953 |
| Smiles | CC(=O)OC1=CC=C(C(=O)OC)C(=C1)OC(=O)C |
| Inchi | InChI=1S/C12H12O6/c1-7(13)17-10-4-5-11(18-8(2)14)12(6-10)19-9(3)15/h4-6H,1-3H3 |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
| Hazard Status | Generally considered low hazard, avoid inhalation and prolonged contact |
As an accredited 1,2,4-Triacetoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,2,4-Triacetoxybenzene, 25g, is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | 1,2,4-Triacetoxybenzene should be shipped in tightly sealed containers, protected from moisture, heat, and incompatible substances. It is typically transported as a solid in chemical-resistant packaging. Ensure compliance with local, national, and international regulations, including hazardous material classifications if applicable. Always include safety data and proper labeling during shipping. |
| Storage | 1,2,4-Triacetoxybenzene should be stored in a cool, dry, well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protect from moisture. Store away from strong oxidizing agents and acids. Use appropriate chemical storage cabinets and clearly label the container. Follow all local regulations regarding chemical storage and safety guidelines. |
Applications of 1,2,4-Triacetoxybenzene in Industrial ManufacturingAs a direct manufacturer of 1,2,4-Triacetoxybenzene, we support key industrial customers across specialty polymers, advanced pharmaceutical synthesis, photographic chemistry, and custom crosslinking resins. Each application leverages distinct physical and chemical properties, with strict compliance, integration, and composition requirements. 1. Intermediate for Performance Polymer SynthesisMajor polymer producers use 1,2,4-Triacetoxybenzene as a functionalized core in high-performance epoxy and polyimide resin systems. The compound introduces acetoxy groups tailored for controlled crosslinking and improved mechanical and thermal properties. Integration typically involves solution blending at controlled temperatures, followed by in-situ polymerization to achieve target molecular weights suitable for electronics encapsulation and structural adhesives. The unique substitution pattern enhances compatibility with engineering-grade fillers, allowing precise adjustment of processing characteristics and composite performance. Industry compliance standards
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2. Reagent in Photographic Chemical ProductionProducers specializing in silver halide photographic materials use 1,2,4-Triacetoxybenzene as a key component for organic developer precursors and as a modifying agent in emulsion formulations. The acetoxy functional groups serve as protected intermediates during the multi-step organic synthesis for light-sensitive compounds. Reliable quality and uniform reactivity are essential due to the sensitivity of downstream emulsions to trace impurities. Industry compliance standards
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3. Pharmaceutical Process IntermediateSeveral pharmaceutical manufacturers utilize 1,2,4-Triacetoxybenzene as a protected benzene core within the synthesis route of active pharmaceutical ingredients (APIs), especially for specialty aromatic compounds where controlled deprotection is required. The material acts as a building block in multi-stage synthesis protocols, where each acetoxy substituent enables selective reactions and minimized side-product formation under cGMP conditions. Close quality monitoring ensures minimal carryover of residual solvents or contaminants that could impact downstream purification steps. Industry compliance standards
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4. Crosslinking Agent for Specialized Resin SystemsResin formulation plants rely on 1,2,4-Triacetoxybenzene as an efficient crosslinking additive in custom thermoset and UV-curable resin blends. Its multiple acetoxy groups promote fast crosslink development under catalyzed or photoinitiated curing, giving resins precise control over hardness and chemical resistance profiles. The position and reactivity of acetoxy substitutions allow formulators to fine-tune mechanical and thermal stability, and the material maintains low volatility during system mixing and casting for consistent batch quality. Industry compliance standards
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