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2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol

    • Product Name 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol
    • Alias Perfluorooctane-1,8-diol
    • Einecs 700-216-4
    • 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

    715447

    Iupac Name 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorooctane-1,8-diol
    Cas Number 865-86-1
    Molecular Formula C8H6F12O2
    Molar Mass 394.12 g/mol
    Appearance White to off-white solid
    Melting Point 81-85 °C
    Density 1.81 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Synonyms Dodecafluorooctanediol; Perfluorinated octanediol
    Smiles OC(CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CO)O
    Inchi InChI=1S/C8H6F12O2/c9-3(10)1-2(20)4(11,12)5(13,14)6(15,16)7(17,18)8(19,21)22/h2-3,20-22H,1H2

    As an accredited 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g chemical is packaged in a sealed amber glass bottle with a secure cap and detailed label for safety and identification.
    Shipping 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-octanediol should be shipped in tightly sealed containers, protected from moisture and heat. It is typically transported as a non-hazardous chemical, but appropriate labeling and compliance with local, national, and international regulations are required. Avoid contact with incompatible substances during shipping.
    Storage 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-octanediol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat and sources of ignition. It should be kept away from incompatible materials such as strong oxidizing agents. Store in a designated chemical storage area with appropriate labeling and secondary containment to prevent spills.
    Application of 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol

    Applications of 2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol in Industrial Manufacturing

    2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoro-1,8-Octanediol serves as an advanced specialty intermediate in several critical industries requiring high performance and extreme chemical stability. Our direct manufacturing expertise supports technical partners in precisely controlled processes where conventional diols cannot deliver the necessary resistance, durability, or compatibility in harsh operational environments.

    1. Synthesis of Fluorinated Polyurethane Elastomers

    This material acts as a fluorinated chain extender in the synthesis of high-performance polyurethanes for elastomer applications. Its incorporation significantly improves oil resistance, chemical inertness, and low-temperature flexibility in elastomeric products. Customers dose it into pre-reacted polyisocyanate systems under moisture-free conditions to avoid unwanted side reactions. This enables the production of gaskets, seals, and rollers that maintain physicochemical integrity even after long-term exposure to aggressive solvents and fuels.

    Industry compliance standards

    • ISO 2178 Polyurethane Elastomers Requirements
    • ASTM D412 (Tensile Testing for Elastomers)
    • REACH Regulation (EC 1907/2006) for chemical substances
    • RoHS Directive 2011/65/EU for restricted substances

    Typical usage ratio

    • 5–20% by weight as a chain extender, with the exact ratio adjusted based on targeted fluorine content and final mechanical properties

    Downstream process integration

    • Added during polyol prepolymer preparation or directly into the isocyanate mixing stage, under inert conditions to maximize uniformity and prevent hydrolysis

    Final product types

    • Fuel hose liners
    • Chemical-resistant O-rings
    • Low-compression set seals for aerospace
    • Industrial elastomeric rollers

    2. Production of Fluorinated Acrylic Coatings

    In high-durability architectural and industrial coating formulations, this diol serves as a fluoropolymer-affording crosslinking monomer. By introducing this raw material during acrylic resin synthesis, downstream formulators achieve top-tier weatherability, superior hydrophobicity, and advanced anti-stain properties. Formulators benefit from the product's reactivity, which supports efficient copolymerization without excessive crosslinking side reactions.

    Industry compliance standards

    • ISO 12944 for protection of steel structures against corrosion by coatings
    • ASTM D6589 for accelerated weathering
    • VOC emission limits according to EU Directive 2004/42/EC
    • US EPA National Emission Standards for Hazardous Air Pollutants (NESHAP)

    Typical usage ratio

    • 2–8% by weight in the prepolymer backbone, modified depending on the required final surface energy and exposure grade

    Downstream process integration

    • Co-fed with acrylic or methacrylic monomers at the esterification or transesterification stage, with temperature control to prevent premature side reactions and degradation of fluorinated groups

    Final product types

    • Architectural topcoats for outdoor applications
    • Protective coil coatings for metal panels
    • Anti-graffiti clear coats
    • UHV equipment coatings

    3. Advanced Lithium Battery Electrolyte Additives

    Battery electrolyte manufacturers rely on this highly fluorinated diol for synthesis of specialty oligomers and dimers used in nonaqueous lithium battery systems. Its presence improves electrochemical stability, expands thermal performance, and suppresses flammability in electrolyte compositions. The physical and dielectric properties of the resulting additives allow safe operation at elevated voltages and in high-energy-density cells.

    Industry compliance standards

    • IEC 62660-x Electric Vehicle Battery Safety Standards
    • UN38.3 Transport of Dangerous Goods—Lithium Batteries
    • UL 2580 for electric vehicle battery systems
    • RoHS and REACH limits for residuals and leachables

    Typical usage ratio

    • Typically 0.5–5.0% by weight in lithium salt electrolytes, tuning for voltage window and temperature operating range

    Downstream process integration

    • Synthetic precursor added during polymer oligomerization or direct blending with liquid electrolytes under dry room conditions before cell filling

    Final product types

    • High-voltage lithium-ion pouch cells
    • Primary lithium batteries for metering devices
    • Automotive traction batteries
    • Nonflammable electrolyte blends for specialty markets

    4. Synthesis of Fluorinated Photoresist Binders

    This raw material finds controlled use in the fabrication of specialty fluorinated photoresist binders for semiconductor lithography. Its incorporation enables superior plasma etch resistance and pattern fidelity on silicon wafers during dry etching. Formulation chemists integrate this diol into the resin backbone with precise stoichiometry to balance high fluorine content and crosslink density, critical for advanced photolithography in sub-10 nm processes.

    Industry compliance standards

    • SEMI S2-0709 Safety Guidelines for Semiconductor Manufacturing
    • ISO 14644 Cleanroom Standards
    • JEITA ET-7307 for photoresist chemicals
    • Restriction of halogenated substances per customer foundry specifications

    Typical usage ratio

    • 0.5–6% by molar substitution of diol groups in the resin, with ratio adjustment for process line width and step coverage requirements

    Downstream process integration

    • Integrated via controlled polymerization during resin synthesis, often using two-step polycondensation under nitrogen atmosphere to ensure minimal moisture contamination

    Final product types

    • i-line and KrF photoresist binders
    • ArF excimer laser photoresist formulations
    • Immersion lithography resins
    • Nanoimprint template materials

    5. Manufacture of Anti-smudge, Oleophobic Surface Treatments

    Formulators use this diol for developing durable oleophobic and anti-smudge agents applied in electronics and touch-screen production. When reacted into siloxane or fluoropolymer frameworks, it imparts low surface energy, repelling oils and fingerprints. The integration step confines the raw material’s addition to the oligomerization stage, maximizing uniform functional group attachment for long-term stain protection on glass and plastic substrates.

    Industry compliance standards

    • IEC 62321-1 Test Methods for Hazardous Substance Restriction
    • EN 14362-1 Regulated Substance Content in Finished Goods
    • Customer-specific environmental and leaching protocols for device components

    Typical usage ratio

    • 1–10% by weight in the surface treatment concentrate, optimized per substrate roughness and desired repellency

    Downstream process integration

    • Introduced during siloxane or fluoropolymer condensation reactions, followed by dilution and spray or dip application on electronics assembly lines

    Final product types

    • Smartphone and tablet screens
    • Camera lens protectors
    • Display panels for automotive interiors
    • Protective glass sheets
    Free Quote

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