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HS Code |
168850 |
| Chemical Name | 2,2,4,6,7-Pentamethyldihydrobenzofuran |
| Molecular Formula | C13H20O |
| Molecular Weight | 192.30 g/mol |
| Cas Number | 1759-58-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 229-230 °C |
| Melting Point | -47 °C |
| Density | 0.929 g/cm3 (20 °C) |
| Refractive Index | 1.495 (20 °C) |
| Solubility In Water | Insoluble |
| Flash Point | 93 °C |
| Odor | Characteristic aromatic odor |
As an accredited 2,2,4,6,7-Pentamethyldihydrobenzofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams, sealed with a screw cap, labeled with chemical name, CAS number, and hazard warnings. |
| Shipping | 2,2,4,6,7-Pentamethyldihydrobenzofuran should be shipped in tightly sealed containers, protected from light and moisture. Packaging must comply with applicable chemical transport regulations. It should be clearly labeled, and handled using standard precautions for organic liquids. Avoid shipping with incompatible substances, preferably using ground transportation to minimize risk of spillage or exposure. |
| Storage | 2,2,4,6,7-Pentamethyldihydrobenzofuran should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separated from strong oxidizing agents and acids. Proper chemical labeling and secondary containment are recommended. Use in accordance with established chemical hygiene and safety guidelines to prevent accidental exposure or release. |
Applications of 2,2,4,6,7-Pentamethyldihydrobenzofuran in Industrial Manufacturing2,2,4,6,7-Pentamethyldihydrobenzofuran serves as an advanced functional intermediate in various mature industrial supply chains due to its aromatic stability, hydrophobic methyl substitution pattern, and compatibility with catalytic systems. As a chemical manufacturer, we supply this material in bulk for well-established downstream transformations where its performance parameters match industry requirements for purity, reactivity, and batch consistency. Below, we detail several industrial segments with established applications involving this compound, outlining the regulatory framework, composition practices, production integration points, and the principal downstream articles manufactured. 1. Specialty Lubricant Additives for High-Temperature FluidsBlenders in the specialty lubricant sector employ this compound for its chemical inertness and volatility performance in polyalphaolefin- and ester-based lubricants engineered for industrial and automotive applications. The methyl-protected core enhances oxidative stability and viscosity control for lubricants operating in sealed, high-temperature environments, helping end users meet extended maintenance intervals in critical machinery. Industry compliance standards
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2. Aromatic Polymer Modifier for High-Performance PlasticsProducers of engineering polymers utilize this molecule as a structural modifier in aromatic ring-containing thermoplastics—most notably in the synthesis of high-gloss, thermally stable resins for automotive interiors or appliance housings. Its configuration confers resistance to discoloration under heat, while the methyl groups disrupt crystallinity, letting compounders fine-tune impact properties and optical clarity. Industry compliance standards
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3. High-Purity Solvent in Electronic Photoresist SynthesisManufacturers of advanced electronic-grade photoresists adopt this compound for its controlled volatility and solvent window in the preparation of positive and negative resists used in semiconductor wafer fabrication. The methyl-substituted structure ensures low metal impurity migration and favorable evaporation dynamics during spin-coating, essential for lithography resolution and process reproducibility. Industry compliance standards
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4. Chemical Intermediate in Advanced Agrochemical SynthesisLarge-scale agrochemical manufacturers use this molecule as a protected aromatic intermediate for downstream synthesis of specialty fungicides and plant growth regulators, leveraging its resistance to oxidation and ready reactivity in Friedel-Crafts-type alkylation and acylation reactions. The controlled substitution pattern enables precise functional group introduction in multi-step processes under cGMP or ISO-qualified facilities. Industry compliance standards
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5. Synthetic Fragrance Precursor for Fine Chemical BlendingFragrance compound houses incorporate this molecule as a central motif in the construction of musk-like and woody accords for high-end perfumery and aroma chemicals. Its poly-methylated structure allows perfumers to produce stable, high-boiling base notes, resistant to oxidative degradation, by constructing complex ethers and lactone derivatives through established synthetic protocols. Industry compliance standards
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Competitive 2,2,4,6,7-Pentamethyldihydrobenzofuran prices that fit your budget—flexible terms and customized quotes for every order.
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