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HS Code |
431807 |
| Cas Number | 821-08-9 |
| Molecular Formula | C6H6O2 |
| Molecular Weight | 110.11 g/mol |
| Iupac Name | Hexa-2,4-diyne-1,6-diol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 93-97 °C |
| Boiling Point | 229 °C at 760 mmHg |
| Solubility In Water | Slightly soluble |
| Density | 1.06 g/cm3 |
| Flash Point | 111.3 °C |
| Ec Number | 212-465-0 |
As an accredited 2,4-Hexadiyne-1,6-Diol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle, tightly sealed, labeled "2,4-Hexadiyne-1,6-Diol," with hazard pictograms and handling instructions. |
| Shipping | 2,4-Hexadiyne-1,6-Diol is shipped in tightly sealed containers under cool, dry conditions. It should be protected from heat, direct sunlight, and moisture. The chemical is classified as non-hazardous for transport, but appropriate labeling and documentation are required. Standard shipping regulations for laboratory chemicals must be followed to ensure safety. |
| Storage | **2,4-Hexadiyne-1,6-diol** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Store in a tightly closed container, protected from light and moisture. Ensure proper labeling and keep away from heat and direct sunlight. Follow all safety and regulatory guidelines when handling and storing this chemical. |
Applications of 2,4-Hexadiyne-1,6-Diol in Industrial Manufacturing2,4-Hexadiyne-1,6-Diol serves as a specialty intermediate in chemical manufacturing due to its unique diyne structure and reactivity. We supply this material directly for use in targeted industrial flows where its properties provide advantages in synthesis, polymer modification, crosslinking, and advanced electronics. Each downstream industry applies strict quality and process controls, and we tailor production consistency for reliable performance in customer applications. 1. Crosslinking Agent in UV-Curable CoatingsManufacturers of UV-curable coatings use this compound to develop high-performance materials for industrial flooring, electronic encapsulation, and specialized overprint varnishes. Its ability to participate in photo-induced crosslinking reactions allows for precise molecular tuning of film hardness, adhesion, and chemical resistance. Customers integrate our material in proprietary acrylate or methacrylate formulations, where controlled addition enables rapid cure times and lasting surface properties required in critical environments. Industry compliance standards
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2. Intermediate for Pharmaceutical Building BlocksFine chemical processors use this raw material as an intermediate in the synthesis of heterocyclic scaffolds and advanced pharmaceutical building blocks. The presence of terminal diol and diyne groups enables regioselective functionalization, supporting the preparation of kinase inhibitors and molecular probes. Manufacturers focusing on small-molecule drug R&D employ controlled batch processing to ensure high-purity conversion, in accordance with GMP and regulatory traceability protocols applicable to human therapeutic agents. Industry compliance standards
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3. Modifier in Advanced Polymer SynthesisSpecialty polymer manufacturers incorporate this diol as a chain-modifying monomer in the production of high-performance thermoplastic elastomers and engineering resins. Its linear diyne structure supports controlled branching and crystallinity modification, impacting tensile strength, flexibility, and thermo-oxidative stability. Production sites require batchwise or continuously metered dosing, often in conjunction with diacid chlorides or polyisocyanates, under precise reaction monitoring for reproducibility and consistent physical properties. Industry compliance standards
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4. Chemical Intermediate for Electronic MaterialsProducers in the electronic materials sector utilize this compound in the synthesis of specialty functional monomers and as a framework precursor in the production of organic semiconductors and photoresists. Its reactivity under controlled cyclization and coupling reactions forms π-conjugated structures with tailored electronic properties, critical for next-generation OLEDs and organic photovoltaic cells. Processing under anhydrous, controlled environments is standard to maintain defect-free semiconducting layers. Industry compliance standards
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5. Precursor for Specialty Surfactants and EmulsifiersManufacturers develop high-temperature and chemically resistant surfactants by functionalizing the diol with ethoxylation or sulfonation, leveraging the diyne core for stability in oilfield and metalworking applications. These specialty surfactants maintain emulsifying performance under aggressive process conditions where standard alkoxylates degrade. Strict process control is necessary to prevent side reactions and to achieve consistent hydrophile-lipophile balance (HLB), impacting downstream fluid performance and operational reliability. Industry compliance standards
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