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2,4-Hexadiyne-1,6-Diol

    • Product Name 2,4-Hexadiyne-1,6-Diol
    • Alias DIYNE DIOL
    • Einecs 204-621-1
    • 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

    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 & Storage
    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.
    Application of 2,4-Hexadiyne-1,6-Diol

    Applications of 2,4-Hexadiyne-1,6-Diol in Industrial Manufacturing

    2,4-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 Coatings

    Manufacturers 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

    • REACH Regulation (EC) No 1907/2006—Registration and use in Europe
    • US EPA TSCA—Chemical substance inventory and reporting
    • ISO 9001:2015—Production quality management systems
    • Directive 2004/42/EC—Limitation of VOC emissions for paints and varnishes

    Typical usage ratio

    • 0.5–3.0 wt% of total resin composition, adjusted based on required crosslink density, film thickness, and UV lamp energy

    Downstream process integration

    • Introduced during the resin blending step before photoinitiator charging
    • Dosed under nitrogen atmosphere to avoid oxidative degradation
    • Homogenized at 25–40°C for even dispersion within pre-polymer matrix
    • Exposed to controlled UV irradiation after application to substrate

    Final product types

    • Industrial floor coatings
    • Microelectronic overprint varnishes
    • Automotive headlamp sealants
    • PCB conformal coatings

    2. Intermediate for Pharmaceutical Building Blocks

    Fine 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

    • ICH Q7—Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 211—Current Good Manufacturing Practice in Manufacturing, Processing, Packaging, or Holding of Drugs
    • USP General Chapter <797>—Pharmaceutical Compounding
    • GLP—OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • Varies from 0.1–1.5 molar equivalents relative to the target synthetic pathway; precise ratio determined by stepwise reaction stoichiometry of the customer's process

    Downstream process integration

    • Charged into intermediate coupling or cycloaddition steps following the initial activation of starting aromatics or alkenes
    • Reacts under inert atmosphere (argon or nitrogen) in polar aprotic solvents
    • Careful temperature control within 0–40°C to maintain selectivity and yield
    • Subsequent purification by crystallization, chromatography, or distillation

    Final product types

    • Small-molecule kinase inhibitors
    • Advanced pharmaceutical active intermediates (APIs)
    • Research reagents for drug discovery
    • Medicinal chemistry library compounds

    3. Modifier in Advanced Polymer Synthesis

    Specialty 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

    • ISO 9001—Quality management for polymer plants
    • ASTM D638—Standard Test Method for Tensile Properties of Plastics
    • RoHS Directive (2011/65/EU)—Restriction of hazardous substances, for electronics-related polymers
    • FDA 21 CFR 177.1680—Polymers for food contact, where applicable

    Typical usage ratio

    • 0.25–2.0 mole % based on total monomer feed; ratio depends on desired flexibility, crosslinking density, and end-use specification

    Downstream process integration

    • Fed to polyester or polyurethane synthesis reactors after initial oligomerization stage
    • Reacted at 80–150°C under controlled vacuum to drive polycondensation
    • Integrated with continuous process analytics to monitor molecular weight distribution
    • Filtered and pelletized before downstream compounding

    Final product types

    • High-performance thermoplastic elastomers
    • Polyamide modification resins
    • Flexible cable insulation
    • Impact-resistant engineering plastics

    4. Chemical Intermediate for Electronic Materials

    Producers 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

    • IEC 61249-2-21:2017—Electronic materials for printed circuit boards
    • IPC-4101C—Specification for Base Materials for Rigid and Multilayer Boards
    • ISO 14001—Environmental management in electronic chemical production
    • Cleanroom ISO Class 7 or better, as required for device integration

    Typical usage ratio

    • Typically 1–10% by weight in monomer or pre-polymer feed formulation; adjusted by target electronic mobility and desired thin film morphology

    Downstream process integration

    • Introduced during monomer synthesis or as crosslinker in spin coating solutions
    • Further processed via thermal or photoinitiated cyclization under inert conditions
    • Purified to 99.9%+ to limit trace metal and particle contamination
    • Formulated into coating solutions immediately before substrate application

    Final product types

    • Organic semiconducting layers for OLED pixels
    • Photoresists for advanced lithography
    • Thin-film transistors (TFTs)
    • Organic photovoltaic cells (OPVs)

    5. Precursor for Specialty Surfactants and Emulsifiers

    Manufacturers 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

    • OECD Guideline 301B—Readily biodegradable surfactants
    • EPA 40 CFR Part 435—Effluent Guidelines for Oil and Gas Extraction Point Source Category
    • ISO 9001—Quality management in specialty chemical production
    • API RP 13M—Recommended Practice for Testing of Surface-Active Agents

    Typical usage ratio

    • 1–7 weight % in final surfactant formulation; precise level determined by test of emulsification and temperature tolerance

    Downstream process integration

    • Activated via base- or acid-catalyzed ethoxylation or sulfonation reactors following initial purification
    • Undergoes final neutralization and phase separation before product blending
    • Quality-checked for residual diyne and free diol content
    • Packaged in corrosion-inhibited containers for direct shipment

    Final product types

    • Oilfield drilling fluid surfactants
    • Metalworking fluid emulsifiers
    • Engineered wetting agents for industrial cleaning
    • Specialty dispersants for high-temperature applications
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