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1H,1H,2H,2H-Perfluorohexyl Iodide

    • Product Name 1H,1H,2H,2H-Perfluorohexyl Iodide
    • Alias PFHxI
    • Einecs 700-134-8
    • 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

    940455

    Productname 1H,1H,2H,2H-Perfluorohexyl Iodide
    Casnumber 2043-53-0
    Molecularformula C6H4F13I
    Molecularweight 427.98 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 110-112 °C at 760 mmHg
    Density 1.987 g/mL at 25 °C
    Refractiveindex n20/D 1.353
    Flashpoint >110 °C
    Purity ≥98%
    Meltingpoint -35 °C
    Solubility Insoluble in water; soluble in organic solvents

    As an accredited 1H,1H,2H,2H-Perfluorohexyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, securely sealed, labeled with hazard warnings and product details for 1H,1H,2H,2H-Perfluorohexyl Iodide.
    Shipping 1H,1H,2H,2H-Perfluorohexyl Iodide is shipped in tightly sealed containers, typically amber glass bottles, protected from light and moisture. It is handled as a hazardous chemical, following all regulatory guidelines. Packaging ensures containment to prevent leaks or exposure, with clear hazard labeling for safe transport by ground or air.
    Storage 1H,1H,2H,2H-Perfluorohexyl Iodide should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong bases and strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a specialized flammable or corrosive chemical storage cabinet. Proper labeling and secondary containment are recommended to prevent leaks or accidental exposure.
    Application of 1H,1H,2H,2H-Perfluorohexyl Iodide

    Applications of 1H,1H,2H,2H-Perfluorohexyl Iodide in Industrial Manufacturing

    1H,1H,2H,2H-Perfluorohexyl Iodide serves as a high-purity specialty intermediate for fluorochemical synthesis in complex industrial processes. As the direct manufacturer, we support downstream sectors that require advanced fluoroalkyl components for surface modification, specialty polymers, and emerging electronics.

    1. Fluorinated Surfactant Synthesis for Specialty Coatings

    This material provides the essential perfluoroalkyl segment for making advanced fluorinated surfactants. Manufacturers integrate it through telomerization or radical addition to create surface-active agents with high thermal and chemical stability. The surfactant products improve oil and water resistance in industrial coatings for textiles and engineered surfaces, offering long-term performance in harsh environments.

    Industry compliance standards

    • OECD PFAS Guidance (2023)
    • REACH Regulation (EC 1907/2006)
    • ISO 14001:2015 for Environmental Management
    • China RoHS 2.0

    Typical usage ratio

    • Intermediate input: 0.8–1.4 mol equivalent per mole of initiator, adjusted by chain length requirements and surfactant purity targets.

    Downstream process integration

    • Add material to the prepolymer reactor during telomerization or iodoperfluoroalkylation steps; introduce under inert atmosphere for controlled radical formation.
    • Monitor conversion by fluorine NMR and iodine content analysis at reaction checkpoint.

    Final product types

    • Nonionic and anionic fluorinated surfactants
    • Stain-resistant textile and carpet coatings
    • Repellent finishing for technical fabrics
    • Waterproofing agents for industrial laminates

    2. Fluorinated Acrylic and Methacrylic Monomer Manufacturing

    Downstream producers use this iodide as a fluoroalkylation reagent to synthesize perfluorohexyl acrylates and methacrylates. These high-value monomers feature prominently in specialty polymer formulations where low surface energy and hydrophobicity are critical. Manufacturers employ palladium-catalyzed coupling strategies for incorporation, controlling reactivity and substitution degree.

    Industry compliance standards

    • ISO 10993-18 for chemical characterization of medical-grade polymers
    • EU Regulation No 10/2011 on plastic materials in contact with food
    • REACH Annex XVII (Fluoropolymer applications)
    • FDA 21 CFR 177.1010 for resinous and polymeric coatings

    Typical usage ratio

    • Iodide: 1.0 molar equivalent per activated alkene group; adapt to palladium loading and desired molecular weight control.

    Downstream process integration

    • Charge with allylic or acrylic precursor under palladium(0) catalysis; maintain reaction temperature below 80°C for selectivity.
    • Purify product by silica gel column and monitor by GC-MS for residual iodine.

    Final product types

    • Perfluoroalkyl acrylate and methacrylate monomers
    • Specialty fluoropolymer dispersions
    • Low-surface-energy additives for release coatings
    • High-performance fluorinated resins for medical and electronics use

    3. Electronic Semiconductor Photoresist Additives

    IC fabrication plants utilize the compound in the synthesis of fluorinated aryl iodides and diaryl derivatives. These intermediates become specialty photoresist additives that combine low refractive index with high etch resistance, critical for high-density photolithography. Controlled introduction at the molecular level optimizes photochemical stability in next-generation microelectronic device manufacturing.

    Industry compliance standards

    • IATF 16949:2016 for automotive ICs
    • TUV SUD IECQ QC 080000 (Hazardous Substance Process Management)
    • JEDEC JESD46 for material change notification in semiconductor manufacturing
    • RoHS 3 (EU Directive 2015/863)

    Typical usage ratio

    • Intermediate: 0.2–0.9 wt% in functionalized aryl precursors, tuned for lithographic contrast and layer thickness.

    Downstream process integration

    • Add to organic synthesis stream under copper-catalyzed coupling reaction; react further with photoactive diazonium salts downstream.
    • Monitor incorporation by LC-MS and verify electrical neutrality by IC test wafers.

    Final product types

    • Advanced photoresist compounds for semiconductor wafers
    • Negative and positive tone resist systems
    • Photopatternable fluoropolymer dielectrics
    • Micro-patterned substrates for MEMS and sensor arrays

    4. Synthesis of Oil & Gas Well Intervention Fluorochemicals

    Energy sector chemical service firms introduce 1H,1H,2H,2H-Perfluorohexyl Iodide into flow modifier and tracer formulations. Its perfluorohexyl chain delivers pronounced chemical inertness and thermal stability in harsh downhole conditions, supporting performance in high-salinity reservoirs and thermally mature wells. The compound reliably enters nucleophilic substitution reactions to yield stable fluorinated tracers for well integrity diagnostics.

    Industry compliance standards

    • API Specification Q1 for Quality Management Systems
    • ISO 22241-3:2017 (chemical inspection for wellbore fluids)
    • REACH (EC 1907/2006) for oilfield specialty chemicals
    • OTC QHSE Guidance for environmental compatibility

    Typical usage ratio

    • 0.5–1.1 wt% as a precursor in well injection chemical blends; ratio varies by desired tracer detectability and reservoir depth.

    Downstream process integration

    • Introduce into the reactor vessel with alkylating agent; maintain inert conditions to prevent side-chain degradation.
    • QC using gas chromatography and fluorine analysis before product dispatch.

    Final product types

    • Perfluorinated tracer fluids for subsurface diagnostics
    • High-performance flow assurance additives
    • Wettability modifiers for enhanced oil recovery
    • Drilling fluid stabilizers for hostile environments

    5. Perfluorinated Lubricant Intermediate for Aerospace and Electronics

    Producers of specialty lubricants use this fluoroalkyl iodide to synthesize fully fluorinated ether and polyether oils. These intermediates enter etherification and coupling reactions, imparting low volatility and superior chemical resistance to the lubricant base. The resulting lubricants support aerospace and advanced electronic applications due to their non-flammability and high oxidative stability performance in thermal cycling environments.

    Industry compliance standards

    • ASTM D445 for kinematic viscosity
    • MIL-PRF-27617 (US Military specification for perfluorinated lubricants)
    • AS9100:2018 Quality Management for Aerospace
    • RoHS directives for electronics compatibility

    Typical usage ratio

    • 0.9–1.3 eq. per mol of polyether starting material; ratio adjusted for desired molecular weight and volatility of final lubricant.

    Downstream process integration

    • Add to fluoropolyether synthesis reaction during the final coupling stage, employing base-catalyzed etherification at 90–120°C.
    • Process stream undergoes vacuum stripping for purity, with QC by GPC and FTIR.

    Final product types

    • Perfluoropolyether lubricants for aerospace actuators
    • Non-migrating dielectric greases for microelectronics
    • High-temperature bearing oils
    • Vacuum pump fluids for cleanroom and analytical equipment

    6. Fluorinated Silane Coupling Agent Synthesis

    The compound serves as a key fluorine donor in the preparation of perfluorohexyl silane monomers. These functional silanes anchor to glass, metal, and ceramic substrates, forming ultra-thin low-energy surfaces. Manufacturers employ hydrosilylation or halogen exchange with trichlorosilane under anhydrous conditions to functionalize the silane moiety.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in silane manufacturing
    • REACH (Annex XIV – Fluorinated functional chemicals)
    • UL 94 for flammability of plastic components
    • ASTM C1087 for surface treatment

    Typical usage ratio

    • 0.7–1.1 molar equivalent based on silane core; optimize for target anchoring group loading and reactivity.

    Downstream process integration

    • React iodide under halogenation conditions with trichlorosilane, using dry solvent and sealed system to avoid hydrolysis.
    • Purge with nitrogen and purify by fractional distillation to achieve high monomer purity.

    Final product types

    • Perfluorohexyl silane coupling agents
    • Antifouling treatment for architectural glass
    • Corrosion-resistant coatings for metal parts
    • Hydrophobic agents for ceramic and stone surfaces
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    Certification & Compliance
    More Introduction

    Understanding 1H,1H,2H,2H-Perfluorohexyl Iodide: Function, Value, and Distinctions in Application

    What Sets 1H,1H,2H,2H-Perfluorohexyl Iodide Apart

    In the field of specialty fluorinated chemicals, 1H,1H,2H,2H-Perfluorohexyl Iodide stands out for its reliable behavior during advanced synthesis and for the opportunities it brings to fluorinated compound development. Our team manufactures this compound under conditions that emphasize not just purity, but also batch consistency — a priority driven by experience developing materials for industries committed to high performance. This compound, with the molecular formula C6F13CH2CH2I, has become a cornerstone intermediate across a range of applications, especially where robust thermal and chemical stability is required. Chemists and engineers working on next-level coatings, surfactants, and pharmaceuticals constantly press for cleaner reaction profiles, and this product fits into their process by offering efficient iodine transfer and manageable reactivity compared to other similar perfluoroalkyl iodides.

    Production at the Source: What Drives Quality

    The procedures and standards our team follows to create 1H,1H,2H,2H-Perfluorohexyl Iodide have evolved to serve the most demanding requirements. Decades of experience have underscored the need for stable supply chains and tight analytical controls. Over time, improvements in distillation and purification have made it possible to secure a product that fits seamless integration into multi-ton runs. Our manufacturing setup delivers narrow specification ranges, so downstream users see less variance in their own process windows. Reports from R&D partners have shown that minimizing iodine-containing side products is especially important; excess free iodine often endangers yield and by-product profiles in functionalization, so removing these traces has always belonged among our critical parameters.

    Why Purity and Traceability Matter

    Those working on advanced materials know that the difference between successful synthesis and failure sometimes depends on the purity and character of a single reagent. In recent years, the spotlight on trace impurities, particularly unreacted perfluoroalkyl chains or halide contaminants, has only grown brighter as regulatory pressures have intensified. Our own journey into improving product standards stems from years of troubleshooting, running pilot projects alongside customers, and seeing the actual impact small impurities can have — a factor that seldom appears in generic specifications but carries weight when it comes to isolating key intermediates or submitting data for regulatory clearance. Each batch of 1H,1H,2H,2H-Perfluorohexyl Iodide is documented and traced from raw material intake to packaging. Only by keeping these records and being transparent with audits have we built lasting trust with customers who manufacture fluorosurfactants for electronics, pharmaceutical intermediates, and custom fluoropolymers.

    Applications Informed by Practical Experience

    Decades on the production floor have demonstrated where 1H,1H,2H,2H-Perfluorohexyl Iodide exerts its value. Coatings developers seeking oil and water repellency in fabrics or engineered films count on the compound’s ability to deliver strong perfluoroalkyl end-groups onto their target molecules. In specialty surfactants, it provides the perfluoroalkyl tail group that creates extremely low surface energy, supporting foam control in fire-fighting agents and lubricants that deliver performance under the harshest industrial environments. Pharmaceutical process chemists seek out its unique iodine reactivity for introduction of hard-to-access perfluoroalkyl groups into active pharmaceutical ingredients. Teams manufacturing medical device coatings or diagnostic membranes turn to 1H,1H,2H,2H-Perfluorohexyl Iodide specifically because stability in harsh oxidative or acidic environments cannot be taken for granted — and perfluoroalkyl chains are chosen precisely to address this challenge.

    Working directly in synthesis and scale-up, we’ve seen how this iodide outperforms shorter and longer perfluoroalkyl analogues in many catalytic and nucleophilic substitution reactions. Lengthening the chain with additional CF2 units sometimes adds unnecessary cost without improvement in efficiency, while using shorter chains usually results in loss of hydrophobicity and electrochemical stability. From production runs, the feedback has consistently shown that six-carbon perfluoroalkyl iodide strikes the ideal balance for those chasing strong repellency effects, solubility in organic systems, and direct substitution chemistry.

    Comparison with Other Perfluoroalkyl Iodides and Halides

    Drawing on feedback from our customers and internal lab analysis, the most notable contrasts emerge in reaction kinetics, handling safety, and environmental persistence. Perfluorooctyl iodide (C8) and shorter chain analogues like perfluorobutyl iodide (C4) serve in some similar workflows, yet cost, toxicity, and physical properties force trade-offs. For example, C8 derivatives sit under more scrutiny by regulators due to their long-term persistence and bioaccumulation potential. The six-carbon (C6) length of our 1H,1H,2H,2H-Perfluorohexyl Iodide provides a practical escape: it delivers the performance sought in nonstick and anti-fouling technologies, avoids some of the most stringent regulatory concerns, and enables end-products that deliver reliable results in membrane fabrication, specialty lubricants, and more.

    From a chemistry standpoint, iodine’s reactivity offers users far better control versus bromine or chlorine-containing analogues. Nucleophilic substitution methods using 1H,1H,2H,2H-Perfluorohexyl Iodide typically proceed with milder conditions, which limits by-product formation. We’ve run head-to-head comparisons on laboratory and pilot scales, finding that the iodide consistently supports higher yields, shorter reaction times, and cleaner work-ups. This feeds directly into lower overall production costs and reduces the burden on downstream purification. Customers report this has tangible impact on throughput and waste minimization.

    Supporting Sustainable Progress

    Concerns about environmental persistence and toxicity of perfluorinated compounds mean open discussion about supply chain responsibility. As manufacturers, we do not simply watch these debates from the sidelines. The European Chemical Agency’s (ECHA) updated assessments and expanding lists of regulated PFAS substances force those in our field to revisit not just chemical selection but manufacturing practices. We have invested in containment, recovery, and destruction of process emissions following years of engagement with environmental authorities. External audits and our own internal reviews push continuous improvement. Several downstream clients now require us to certify that the product specifications rule out high-priority regulated PFAS, and our analytical team tracks these trace impurities down to parts-per-billion detection limits for full confidence.

    Years spent investigating emissions and workplace safety shaped our production plant design. We follow strict equipment protocols and build multi-layered monitoring into process runs, aiming not just for compliance, but for stewardship. The ability of 1H,1H,2H,2H-Perfluorohexyl Iodide to break down cleanly under controlled conditions eases the regulatory burden compared to some legacy fluorochemical compounds. We also developed recycling techniques, including reclaiming unused product from off-spec runs and using advanced chemical destruction units for end-of-life material, minimizing overall impact.

    Meeting the Demands of Advanced Markets

    The standards in electronics, healthcare, and high-value coatings force raw material suppliers to maintain more than just technical know-how. Over the years, working closely with partners in semiconductor, biotech, and aerospace markets, we have learned that documentation, reproducibility, and collaboration build the foundation for qualification and long-term contracts. Our experience shows that new application fields — for example, low-energy surface treatments or precision diagnostics — often start with a handful of trial runs where reagent availability, purity data, and reliable supply lines mean project go/no-go decisions ride on factors outside laboratory performance alone.

    1H,1H,2H,2H-Perfluorohexyl Iodide’s established track record in these advanced sectors comes from years prioritizing technical support. Scientists count on being able to phone in and get answers about previous batches, storage conditions, or compatibility with process additives developed since their last order. Changes in end-user regulation (such as evolving medical device rules in the US or new environmental thresholds in Europe) also drive our commitment to fast data turnaround. We involve regulatory teams early in the synthesis planning and batch release process for any new application, anchoring our operations in a culture of continual learning and adaptation.

    Performance in Synthetic Chemistry

    Synthetic chemists report that handling 1H,1H,2H,2H-Perfluorohexyl Iodide proves straightforward due to its stability under ambient conditions and manageable volatility. Compared to many highly fluorinated reagents, operators benefit from its reduced tendency to undergo decomposition or hazardous fume generation under normal laboratory conditions. Organic synthesis routes requiring introduction of a strong perfluoroalkyl group frequently turn to this compound when aromatic or aliphatic substrates must withstand harsh environments. Analytical feedback from our own in-process controls has shown that this reagent tolerates broad ranges of solvents, catalytic bases, and nucleophilic activators, providing process engineers flexibility during scale-up.

    Over years working alongside custom synthesis teams, we learned that minor differences in reagent purity, phase separation, or the presence of trace halides affect isolation and crystallization of sensitive intermediates. By focusing on these details during our own process design and by collaborating directly with end-users rather than leaving these discussions to trading agents, we’ve managed to support customers through several generations of process optimization. Reliable, direct feedback from those doing the work has driven us to tailor production controls to changing downstream needs — whether that’s in removing a troublesome UV-absorbing contaminant or verifying trace residue results to speed up regulatory filings.

    Scalability and Handling Efficiency

    Bringing a material from lab to plant scale brings out tough challenges that often go unnoticed at smaller quantities. Early in our production history, difficulties surfaced in scaling up 1H,1H,2H,2H-Perfluorohexyl Iodide. Managing phase equilibria, heat transfer across larger vessels, or even dealing with iodine residue in containment equipment introduced risk and variability. Refined techniques for iodine quenching, process ventilation, and on-site waste treatment have since been locked into standard operating protocols.

    Operators appreciate the compound’s relatively straightforward packaging and storage requirements. Its chemical robustness keeps storage problems at bay, even over long durations. By controlling ambient moisture and minimizing thermal cycling, our shipping team has delivered product worldwide to facilities operating across rigorous temperature and humidity regimes, with no significant complaints of degradation or loss of chemical potency. This reliability speaks to both the intrinsic stability of the molecule and the benefits of process experience gained after years supplying specialized industries.

    Lowering Waste and Reducing By-products

    Environmental responsibility guides our choice of feedstocks, recovery strategies, and effluent treatment steps. The manufacturing process prioritizes yield efficiency, with unreacted starting materials being continually recycled back into upstream production. This not only reduces chemical costs but also lowers the generation of perfluorinated waste. Process monitoring allows us to catch excursions early, so even if minor deviations occur, adjustments come swiftly and material stays within required specifications.

    We’ve refined distillation column design and real-time detection of by-products to maintain strict control over product composition. Any batch showing excess iodine, off-color, or unwanted fluorinated side-products is investigated. Over time, our internal audit data demonstrates steady improvement in product quality, supporting the transition to leaner, cleaner manufacturing. By collaborating with environmental partners, we regularly review and upgrade vapor capture, water treatment, and residue destruction procedures — easing both operational concerns and satisfying our commitment to environmental leadership in the fluorochemicals sector.

    Partnering Across the Supply Chain

    Supplying 1H,1H,2H,2H-Perfluorohexyl Iodide to global partners taught our team about the importance of communication across the value chain. Delays or errors in upstream precursors ripple directly into the timeframes and project costs for downstream users. By managing direct contracts for key starting materials and extending support through in-person technical workshops or remote troubleshooting, we have achieved more dependable project execution. Our logistics division invests time in regulatory compliance and customs clearance for each shipment, sparing customers from the stress of handling documentation or tracking import duties alone.

    Frequent interaction with research laboratories, production facilities, and waste handlers has surfaced new concerns most distributors overlook. For example, batch traceability frequently plays into research project success: if a trial fails, the project team wants to know exactly which lot contributed and whether any anomalies surfaced during production. Detailed data supply, fast-acting customer service, and transparency make these investigations possible. By working directly with our end-users, rather than through resellers, we have preserved critical feedback loops that help shape each product upgrade.

    Developing New Uses Through Collaboration

    Collaboration with application researchers often begins with requests for custom cuts, experimental grades, or reevaluation of storage protocols for 1H,1H,2H,2H-Perfluorohexyl Iodide. Lately, we’ve fielded more requests for tailored reactivity, especially as downstream customers seek cutting-edge fluorinated building blocks for ultra-thin film coatings, medical diagnostics, and niche surfactant systems with ever-tighter residue requirements. Our willingness to experiment with alternative purification strategies, custom batch sizes, or even fast-turnaround analytical results has been shaped directly by these practitioner needs.

    By funding joint process development efforts with collaborators, we have contributed to advances in controlled radical polymerization, diagnostic chemistry, and designer surfactant creation. The product serves not just as a final component, but also as the starting point for a host of new chemistries under study by research teams across sectors. The gains realized by these shared efforts inform our own manufacturing techniques and improve future product development in ways no isolated market summary or specification sheet ever could.

    Commitment to Transparency and Data Sharing

    Customers need to know the full profile of every shipment. In recent years, requests for expanded analytical data and regulatory support have outpaced traditional needs for just physical property information. Our analytical division provides batches of 1H,1H,2H,2H-Perfluorohexyl Iodide with comprehensive characterization: NMR spectra, halide and water content, GC-MS breakdown, and trace metals analysis. We’re prepared to furnish COAs containing batch-specific analytical methods so users can cross-check data using their preferred instrumentation.

    Service doesn’t end when a batch is shipped. Technical staff remain available for feedback and troubleshooting at all stages, from feasibility trials to end-use qualification testing. This integrated approach has helped customers achieve smoother regulatory audits, win quality certificates more readily, and meet the evolving expectations of end-users in strict regulatory environments — including advanced electronics and regulated medical markets.

    Real-World Lessons from Production and Application

    Looking back on years of manufacturing, real advances come not from incremental changes in batch size or changes in supplier lists, but from sustained engagement with the most challenging projects and difficult customers. Every time our 1H,1H,2H,2H-Perfluorohexyl Iodide finds its way into a new process — be it a breakthrough in water-repellency for technical textiles or a synthons for medicinal chemistry — we learn from application engineers and production supervisors who don’t hesitate to share what works and where pain points persist.

    Failures and setbacks drive process improvement. A single incident of product instability or downstream reaction stalling prompts reviews, not just of immediate chemical purity, but also of shipping practices, storage conditions, and supplier reliability. This operational discipline creates closer relationships up and down the value chain, ensuring that the lessons gleaned from demanding industrial clients and methodical laboratory technicians shape each new batch and inspire upgrades in technology, safety, and documentation standards.

    Future Focus and Ongoing Innovation

    Manufacturing 1H,1H,2H,2H-Perfluorohexyl Iodide means never standing still. Ongoing regulatory developments and rising expectations from customers in every industry nudge us to keep pushing: shorter lead times, greener processes, even higher purity requirements, and smarter packaging solutions. Investments in process intensification, new waste minimization techniques, and automation of analytical controls have changed what our team is able to promise, and deliver, with each passing year.

    Collaborations with leading research centers, daily feedback from end-users, and steady investment in process controls position us to keep evolving alongside the fast-changing needs of industries relying on specialty fluorinated intermediates. The story of this compound does not end with its molecular structure: it continues to unfold through the hands of those using it to pioneer new chemistry, create novel materials, and protect both human health and the environment one batch, and one innovation, at a time.