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1H,1H,5H-Octafluoropentyl Iodide

    • Product Name 1H,1H,5H-Octafluoropentyl Iodide
    • Alias Perfluoropentyl iodide
    • Einecs 206-579-9
    • 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
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    Specifications

    HS Code

    681339

    Product Name 1H,1H,5H-Octafluoropentyl Iodide
    Cas Number 423-61-2
    Molecular Formula C5H2F8I
    Molecular Weight 353.96 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 73-75°C at 30 mmHg
    Density 2.15 g/mL at 25°C
    Refractive Index n20/D 1.354
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms Perfluoropentyl iodide, Octafluoropentyl iodide
    Smiles C(C(C(C(CI)(F)F)(F)F)(F)F)(F)F
    Inchi InChI=1S/C5H2F8I/c6-1(7)2(8,9)3(10,11)4(12,13)5(14,15)16/h1H2
    Storage Temperature Store at 2-8°C

    As an accredited 1H,1H,5H-Octafluoropentyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25 g amber glass bottle, sealed with a Teflon-lined cap for light and moisture-sensitive protection.
    Shipping **Shipping Description for 1H,1H,5H-Octafluoropentyl Iodide:** 1H,1H,5H-Octafluoropentyl Iodide should be shipped in tightly sealed containers, protected from light and moisture. Transport under cool conditions, following all applicable regulations for hazardous chemicals. Properly label the package with hazard and handling information, and include safety documentation. Handle with care to avoid leaks or exposure.
    Storage 1H,1H,5H-Octafluoropentyl iodide should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent degradation. Keep it in a cool, dry, well-ventilated area, away from heat, light, and incompatible substances like strong bases or oxidizers. Refrigeration (2–8°C) is recommended for long-term storage. Handle in a fume hood.
    Application of 1H,1H,5H-Octafluoropentyl Iodide

    Applications of 1H,1H,5H-Octafluoropentyl Iodide in Industrial Manufacturing

    As an established manufacturer of 1H,1H,5H-Octafluoropentyl Iodide, we supply this critical fluorinated intermediate to specialized downstream sectors where its unique halogenation and perfluoroalkylating characteristics are indispensable for high-value chemical synthesis and performance formulations. Below, we detail the industrial application scenarios where our product is consistently specified and required by leading manufacturers to achieve advanced functionality in end products.

    1. Pharmaceutical Intermediate Synthesis

    This intermediate functions as a vital perfluoroalkylating agent in the synthesis of fluoroalkyl-containing pharmaceutical compounds, particularly where precise iodination and fluorination control is required. It is incorporated at key points in API production, especially for molecules targeting enhanced metabolic stability and cell permeability. Formulators utilize it for side-chain elongation and structural modification in late-stage synthesis, adhering to demanding impurity and residual solvent controls under strict operational cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph.Eur.) monographs for fluorinated pharmaceutical compounds
    • US FDA 21 CFR Part 210/211 (GMP for finished pharmaceuticals)
    • ChP (Chinese Pharmacopoeia) for process intermediates

    Typical usage ratio

    • Ranging from 0.1 to 3.0 molar equivalents, selected based on specific alkylation or iodination step requirements; adjusted for stoichiometry and desired yield optimization

    Downstream process integration

    • Introduced during late-stage intermediate coupling or during targeted functional group modification under controlled reaction temperatures, generally incorporated at the fluorination or iodination step after initial scaffold assembly

    Final product types

    • Small-molecule APIs with enhanced lipophilicity
    • Specialty fluorinated pharmaceutical intermediates
    • Active compounds in novel anti-inflammatory or antiviral drug candidates

    2. Electronic Liquid Crystal Material Manufacture

    In the production of high-performance liquid crystal materials, this iodoperfluoroalkyl compound is essential for constructing fluorinated side chains that impart low viscosity and precise refractive index control in advanced display technologies. Downstream users employ this material where robust chemical stability under varying voltage and temperature is needed in display molecule design. Strict compliance with purity and moisture content requirements is enforced to maintain uniform electro-optical characteristics in finished mixtures.

    Industry compliance standards

    • IEC 61249-2-21 (Materials for PCBs: requirements for Halogen Content)
    • ISO 9001:2015 (Quality Management for Materials Manufacturing)
    • JIS C6122 (Japanese LCD Material Specifications)
    • RoHS Directive (EU Restriction of Hazardous Substances for electronic components)

    Typical usage ratio

    • Used between 1% and 7% by weight in formulation mixes, dependent on final LC compound molar design and target blend properties

    Downstream process integration

    • Applied during fluorinated side-chain attachment by nucleophilic substitution in the core structure synthesis; typically purified and fractionated to electronic-grade before masterbatch blending with other mesogenic units

    Final product types

    • Liquid crystal display (LCD) panel mixtures for TVs and monitors
    • Thin-film transistor displays for mobile devices
    • Advanced optical shutter films

    3. Agrochemical Fine Chemical Synthesis

    Leading agrochemical manufacturers employ this raw material as a fluoroalkyl source when synthesizing highly hydrophobic and weather-resistant pesticide and herbicide active ingredients. The unique chain structure supports the design of molecules with low leaching potential and prolonged field persistence. Quality control closely monitors for residual iodine and perfluoroalkyl contaminants to meet regulatory residue limits in end-use agrochemical formulations.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) specifications
    • ISO 17025 (Testing/Calibration for Pesticide Ingredient Analysis)
    • China Ministry of Agriculture GB/T 1600 series (Safety requirements for pesticide raw materials)
    • EU Regulation (EC) No 1107/2009 (Authorization of plant protection products)

    Typical usage ratio

    • Employed from 0.2% to 2.5% by mass of total synthesis charge; varies according to the functional group demand in the targeted agrochemical backbone

    Downstream process integration

    • Introduced at the coupling stage for side-chain construction in active molecule assembly; typically reacted under controlled temperature with base catalysts and post-synthesis scrubbing to minimize free iodide residue

    Final product types

    • Fluorinated pesticide active ingredients for foliar and soil application
    • Herbicides with improved field stability
    • Protective fungicide agents for high-value crops

    4. Fluorinated Surface Treatment Agent Production

    This iodinated fluorocarbon is a key component in manufacturing specialized surface treatments, especially for imparting oleophobic and hydrophobic properties to substrates where solvent and contaminant resistance is important. It is processed under strict environmental and occupational hygiene controls to limit workplace exposure and byproduct release. Technicians adjust addition rates precisely based on substrate type and desired repellency metrics, with thorough product testing required for final release.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile chemical safety)
    • US EPA TSCA Inventory (Chemical import and processing rules)
    • ISO 14001 (Environmental Management Systems in Chemical Plants)
    • REACH Annex XVII restrictions for perfluorinated chemical use in surface treatments

    Typical usage ratio

    • Usually 1% to 5% by weight in the curing or finishing bath; final dosage based on desired contact angle and regulatory limits for perfluorochemicals

    Downstream process integration

    • Added during fluorinated chain grafting or blending step, before or during substrate application; industries use in both batch and continuous coating processes with final curing at elevated temperatures

    Final product types

    • Oleophobic textile finishers for uniforms and workwear
    • Hydrophobic coatings for glass and technical ceramics
    • Protective films for electronics housings and sensitive assembly components

    5. Specialty Polymer Fluorination

    Producers of specialty fluoropolymers utilize this halogenated precursor for controlled insertion of perfluoroalkyl side chains, enhancing chemical resistance and lowering surface energy in finished polymeric materials. This process requires precise monitoring of monomeric purity and low iodine residuals for consistency across polymer batches. Additive ratios respond to target molecular weight and end-use performance benchmarks, particularly in chemically aggressive environments.

    Industry compliance standards

    • ISO 10993 (Polymer Biocompatibility for medical/technical applications)
    • ASTM D543 (Chemical Resistance of Plastics)
    • UL 94 (Flammability Standard for Plastic Materials)
    • Japanese JIS K 6920 (Performance of fluorinated plastics)

    Typical usage ratio

    • Standard use ranges between 0.5% and 4.0% by monomer mass, adjusted upwards for high-resistance applications or copolymer structures

    Downstream process integration

    • Reacted as a perfluoroalkyl donor during reactor-phase polymerization, often under pressure with fluorinated co-monomers, or grafted during post-polymerization modifications

    Final product types

    • Low-surface-energy films for industrial processes
    • Highly chemical resistant gaskets and seals
    • Advanced wiring insulation and electronics coatings
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    Certification & Compliance
    More Introduction

    1H,1H,5H-Octafluoropentyl Iodide: Flawless Fluorination Starts Here

    Direct from the Source: How We Approach 1H,1H,5H-Octafluoropentyl Iodide

    Making specialty fluorinated intermediates has been at the core of our daily operations for years, and among the wide array of organofluorine compounds we produce, 1H,1H,5H-Octafluoropentyl Iodide stands out for its unique blend of reactivity, selectivity, and value. Years back, requests for this compound trickled in, mostly from groups pushing the boundaries of pharmaceutical development and fluorinated surfactant research. As more chemists found ways to use this molecule as a linchpin for further synthesis, we scaled up, optimized, and refined every step of our own process. The result: a consistently pure, precisely formulated organoiodide that meets demanding project goals in universities, research institutes, and manufacturing plants alike.

    Purity, Consistency, and Clarity — Where Quality Matters

    1H,1H,5H-Octafluoropentyl Iodide, with a molecular structure featuring eight fluorine atoms running along a five-carbon chain and a terminal iodine, seems straightforward until you try to make it without persistent byproducts or batch-to-batch fluctuation. In our plant, continuous monitoring and customized purification protocols prevent lingering impurities, especially critical since even low-level byproducts can disrupt downstream coupling, substitution, or cross-coupling processes. The boiling point and density measurements in our facility come from hands-on calibration work. At scale, small deviations mean lost yields and inconsistent performance. We make sure our product specification reflects what chemists observe during actual use—clean distillations, no precipitation, and stable handling over time.

    Using 1H,1H,5H-Octafluoropentyl Iodide in the Real World

    Researchers and process engineers gravitate to 1H,1H,5H-Octafluoropentyl Iodide for its utility as a reactive building block in synthesis. We see it shipped for organofluorine compound development, where it serves as a handle for introducing C–I functionality into fluorinated skeletons. That terminal iodine offers clean reaction pathways: nucleophilic substitutions, coupling reactions with transition metals, and transformations that keep difficult-to-handle perfluoroalkyl chains stable and efficient. Its performance shows up in everything from innovative agrochemical designs to new classes of surfactants. Recent projects have connected this compound to the fine-tuning of surface-active agents, allowing tunable hydrophobic and lipophobic properties, addressing challenges that simple hydrocarbon iodides or sulfonates cannot solve.

    Comparison with Other Alkyl Iodides and Perfluorinated Chains

    Working hands-on with a broad range of alkyl iodides, we notice that fully perfluorinated analogs, such as perfluoropentyl iodide, deliver excellent inertness but make downstream chemistry more cumbersome. Hydrogenated analogs bring higher reactivity but poor resistance to harsh environments. 1H,1H,5H-Octafluoropentyl Iodide falls into a sweet spot: its partial fluorination imparts both stability and tunability, something neither non-fluorinated nor completely fluorinated alkyl iodides manage. For instance, sulfonate end groups tend to build up too much hydrophilicity for some coatings and resists; we see users achieving fine control of surface and interfacial properties through the distinct fluoroalkyl and iodine combination in our product. The practical difference comes alive in polymerizations, where the chain end’s reactivity translates into well-defined block copolymers. This is not just theoretical—feedback from customers reveals improved incorporation rates and cleaner chain transfer when using our product versus less fluorinated or over-engineered alternatives.

    Scaling Up: Moving from Bench to Bulk

    Labs sometimes approach us after running into reproducibility walls with small-scale commercial samples of 1H,1H,5H-Octafluoropentyl Iodide. Achieving the same results from 100 grams up to tens of kilograms takes process foresight, not just technical capability. We faced our share of bottlenecks scaling the halogen exchange and purification steps. Over time, we invested in in-line analytics and cryogenic processing so we could watch byproduct evolution in real time and adapt conditions without pausing production. That is how shipping late orders or watching yields dip just never became part of our routine. This careful attention to real-world variables builds silent trust—people realize they do not have to adjust protocols or work up extra purifications midway through a project.

    Safety and Handling: Lessons Learned in Daily Operations

    No synthetic intermediate, especially those with reactive iodo groups and dense fluorination, should be treated like a shelf-stable commodity. We see regular interest in scaling up gram-to-kilogram operations among clients, often with limited in-house experience handling volatile or high-purity perfluoroalkyl iodides. Having run these procedures for years, we keep rigorous engineering controls in place: full local ventilation in bottle filling, closed-system transfers, and redundant monitoring for potential iodine evolution. The lessons are straightforward—fewer exposure incidents, lower waste, and no need for heavy quenching or post-reaction scavenging. Customers sometimes worry about specialized containers. Our investments in inert-gas-flushed glass ampoules and lined bottles have eliminated stability risks, supporting reliable cold-chain transport—discouraging sticky residues or sub-threshold decomposition, especially at the warehouse stage, where delays can trigger subtle quality loss.

    The Role in MedChem and Agrochemistry: Applied Value

    Innovators in pharmaceutical and agrochemical spaces look for building blocks that streamline complexity. In medicinal chemistry, installing a fluoroalkyl group at the right position on a scaffold can dramatically change pharmacokinetic properties, permeability, or metabolic stability. Perfluorinated options may look appealing at a glance, but medicinal chemists know the drawbacks: limited solubility and challenging downstream chemical modification. Our 1H,1H,5H-Octafluoropentyl Iodide addresses these everyday pain points. The partially fluorinated chain improves stability without choking functional group compatibility, while the terminal iodine enables selective substitution. Projects involving potent enzyme inhibitors, targeted delivery vehicles, or metabolically robust pesticides almost always come back to this compound—its properties make new motifs possible, giving researchers flexibility to push past the limitations of legacy alkyl chains.

    Supporting Next-Generation Surfactants and Polymers

    We have partnered with teams pioneering new surfactant designs for extreme environments. In these applications, full perfluorination delivers weather and chemical resistance, but expense soars and functionalization options shrink. Non-fluorinated analogs cannot approach the same performance in repellency or thermal stability. 1H,1H,5H-Octafluoropentyl Iodide enables the synthesis of fluorinated surfactant segments that resist breakdown and environmental leaching, while allowing tailored chain lengths and functional group placement through the reactive iodine. Our team works with polymer chemists who need initiators that survive tough conditions yet insert cleanly into macromolecular chains—our product consistently meets those needs, bringing reliable results across surface coatings, adhesives, and specialty membranes. Customer feedback points to improved durability and easier downstream processing even as regulatory scrutiny of fluorochemicals tightens.

    Environmental and Regulatory Realities

    Fluorinated organic chemicals receive increasing attention from regulatory bodies, especially as global awareness of persistent organic pollutants spreads. We pay close attention to what lands on lists of concern, both to stay in compliance and to support clients who need to explain supply chain choices. 1H,1H,5H-Octafluoropentyl Iodide has not faced the same restrictions as fully perfluorinated analogs, largely because partial fluorination supports improved degradability and reduces the risk associated with long-chain accumulation. Our regulatory staff keep up-to-date with REACH, TSCA, and other international frameworks, screening each production lot for legacy contaminants or precursor residues before shipment. Customers tell us this sort of proactive documentation makes customs clearance and downstream certification much smoother. Practical knowledge—born from real audits, not just paperwork—drives the quality control standards we maintain. We know, from both audits and conversations, that buyers and end users value traceability as much as chemical performance.

    Process Development and Continuous Improvement

    Proudly manufacturing this class of intermediates means more than just hitting purity and volume targets. Over the years, we identified mi-solvent azeotrope issues, byproduct entrapment, and even subtle batch-to-batch color shifts, which, while not always affecting chemical performance, can cloud downstream analytics. Feedback from manufacturing clients revealed how minor batch differences can upset chromatographic separations or high-throughput screening workflows. These insights prompted upgrades—not just to mainline reactors, but to washing, solvent exchange, and fill-finish setups, resulting in visually consistent batches that inspire confidence all the way from receiving dock to synthetic bench. No batch leaves the facility without passing both instrumental assay and direct inspection in real light for color and clarity. Everyone here understands that daily improvement never ends. This attitude trickles down to support staff and maintenance teams, who spot operational issues long before they show up as product variability, ensuring delivery deadlines remain intact through seasonal, demand, or supplier fluctuation.

    Operational Insights: Supply, Lead Times, and Forecasting

    Looking out across our facility, materials move, people coordinate, and the world beyond our gates demands ever-shorter lead times. For project managers or buyers lining up multi-step syntheses, supply stability trumps every theoretical metric. We organize production of 1H,1H,5H-Octafluoropentyl Iodide in a flexible scheduling model, allowing small- and large-volume runs to overlap without cross-contamination or bottlenecking. Based on demand data, most clients prefer regular, pre-booked shipments. We respond with a schedule that rewards predictable planning for everyone up and down the supply chain. Emergency requests—rushed shipments, unexpected upswings in consumption, or late-stage scale-ups—get immediate coordination, drawing on both buffer stock and rapid extra runs. These organizational strengths stem from close engagement with the real world of chemistry: missed batches or delays ripple through R&D, creating problems no spreadsheet or planning software can prevent. From order entry to outbound logistics, hands-on staff track each order, so questions and updates get answers from people who know both the product and the manufacturing context.

    Continuous Feedback Drives Better Chemistry

    Building a reputation for quality does not come from marketing—it starts with chemists who share feedback about their reactions and product performance. We make ourselves available to discuss specifics. Problems like phase separation in preparative chromatography, low HRMS purity readings, or subtle end-use inconsistencies spark troubleshooting sessions with our technical specialists. Tracking complaint rates and quality returns over the years has not just kept our batch success at the top of the sector—it has put us directly next to the end users who turn 1H,1H,5H-Octafluoropentyl Iodide into tomorrow’s advanced materials. Every improvement in isolation, container choice, or shipping method came directly from these partnerships.

    The Path Ahead: Evolving with the Market

    The field for high-quality, partially fluorinated intermediates shows no sign of shrinking. We see new projects cropping up in sustainable electronics, advanced coatings, and biomedical engineering, fueled by the drive to combine chemical stability with next-level reactivity. This trend puts 1H,1H,5H-Octafluoropentyl Iodide in the crosshairs for innovation—a molecule that bridges old boundaries between inertness and functionality. Our work never stays static. Ongoing investment in cleaner, safer, and more efficient production keeps our plant competitive in a market where demands grow more complex every year. As new regulations emerge and the scientific landscape shifts, our commitment rests on three constants: quality, reliability, and close connection with the real-world users of our products.

    Direct Dialogue: Supporting Users, Supporting Progress

    Those who handle and transform 1H,1H,5H-Octafluoropentyl Iodide—whether at a bench in a university lab, a pilot plant, or a full-scale specialty chemical facility—face real challenges: tight schedules, shifting requirements, regulatory hurdles, and tough targets for yield or selectivity. We see ourselves as more than a source of containers with white labels. We stay in touch about best practices, improvements, and tweaks to purification or reaction conditions. If a researcher needs insight into reducing hydrodeiodination, or a project manager needs documentation for a customs clearance, they do not get a form letter or a generic answer—they get real input from the people who ship, synthesize, and test the product daily. This two-way street is grounded in our experience as direct manufacturers—a perspective that keeps the industry advancing at speed and assures the chemists who depend on our products never have to face problems alone.