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1H,1H,2H,2H-Perfluorodecanethiol

    • Product Name 1H,1H,2H,2H-Perfluorodecanethiol
    • Alias FTD
    • Einecs 221-470-5
    • 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
    VTB
    Specifications

    HS Code

    785485

    Cas Number 78560-44-8
    Molecular Formula C10H5F17S
    Molecular Weight 526.28
    Appearance Colorless to pale yellow liquid
    Boiling Point ≥195°C (estimated, at 760 mmHg)
    Density 1.78 g/cm3 (at 25°C)
    Melting Point -15°C
    Refractive Index 1.323 (at 20°C)
    Flash Point >110°C
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Smiles C(C(C(C(C(C(C(C(C(F)(F)S)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F
    Synonyms 1H,1H,2H,2H-Perfluorodecanethiol; 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Octadecafluoro-1-decanethiol
    Ec Number 616-551-5
    Storage Temperature Store at 2-8°C

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

    Packing & Storage
    Packing The 25g 1H,1H,2H,2H-Perfluorodecanethiol is supplied in a sealed amber glass bottle with a secure screw cap.
    Shipping **1H,1H,2H,2H-Perfluorodecanethiol** is shipped in tightly sealed containers, typically made of glass or fluoropolymer to prevent leakage and contamination. It is transported as a hazardous chemical, requiring proper labeling and documentation. The packaging must comply with relevant regulations, including UN/DOT standards for chemicals, to ensure safe handling and delivery.
    Storage **1H,1H,2H,2H-Perfluorodecanethiol** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. It should be protected from moisture and direct sunlight. Proper chemical safety labeling is essential. Use in a fume hood and avoid prolonged exposure.
    Application of 1H,1H,2H,2H-Perfluorodecanethiol

    Applications of 1H,1H,2H,2H-Perfluorodecanethiol in Industrial Manufacturing

    1H,1H,2H,2H-Perfluorodecanethiol offers unique chemical and surface-modifying properties, supporting advanced manufacturing sectors that demand strong hydrophobic and oleophobic performance, chemical inertness, and precision coating technologies. Our application experience covers industries with proven large-scale adoption, where compliance, process control, and formulation integration clearly define the value added by this specialty raw material.

    1. Anti-Fingerprint and Anti-Smudging Coatings for Consumer Electronics

    In the consumer electronics sector, manufacturers apply this specialty thiol as a surface modifier in coatings to protect touchscreen panels, lenses, and display glass from fingerprints and smudging. Tailoring surface chemistry on such high-value substrates calls for reliable oleophobicity, chemical resistance, and optical transparency, making the inclusion of this material a fundamental step in achieving performance benchmarks required by global device brands.

    Industry compliance standards

    • IEC 60068-2-78 (Environmental Testing-Humidity, for coated surfaces)
    • REACH (EC) No 1907/2006 Registration and Safety Compliance
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • JEITA ED-4701/100 (Mechanical and Chemical Endurance of Device Surfaces)

    Typical usage ratio

    • 0.05–0.2% by weight in final coating mixture; precise dosage adapts to targeted surface energy and substrate type, with higher loading for increased oleophobic performance where higher friction resistance is specified.

    Downstream process integration

    • Added during final formulation stage of sol-gel or fluoropolymer-based coating recipes; applied by spray or dip onto cleaned touch panels, then cured by thermal or UV processes before device assembly.

    Final product types

    • Smartphone display panels
    • Tablet and laptop screen coverings
    • Wearable device touch interfaces
    • Camera lens glass modules

    2. Fluorinated Surface Treatment for Industrial Textiles

    Technical textile producers incorporate this fluorinated compound as part of durable water- and oil-repellent surface treatments for fabrics used in high-end protective garments, filtration materials, and outdoor performance wear. Its molecular structure provides long-chain perfluoroalkyl groups that bond with fabric fibers, imparting non-wetting characteristics while maintaining flexibility and breathability, meeting stringent standards for occupational and specialized textile applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Chemical Safety)
    • ISO 4920/14419 (Water and Oil Repellency, Spray Test Standard)
    • EU REACH Annex XVII (Perfluorochemical Regulation for Textiles)
    • bluesign® system criteria for chemical inputs

    Typical usage ratio

    • 0.1–0.5% by weight, calculated on dry fabric; dosage established after laboratory repellency and durability tests depending on fiber type and finishing process parameters.

    Downstream process integration

    • Dispersed in aqueous or solvent-based bath, the chemical is applied during padding or exhaustion step, followed by heat curing (typically 150–180°C) to anchor the treatment onto textile fibers.

    Final product types

    • High-visibility workwear
    • Oil- and chemical-resistant aprons and coveralls
    • Technical filter fabrics for industrial filtration
    • Premium outdoor sports jackets and pants

    3. Hydrophobic Treatment for Advanced Glass and Ceramic Surfaces

    The processed perfluorinated thiol is used by glass and ceramic manufacturers to form ultra-thin hydrophobic barriers on architectural, automotive, and laboratory glass components. The resulting nano-coatings ensure sustained water beading, resistance to staining agents, and preserved optical clarity, supporting rigorous requirements in environments exposed to moisture and contamination.

    Industry compliance standards

    • EN 1096-1: Glass in Building (Coated Glass Safety and Performance)
    • ISO 9211 (Optical Coating Durability, Abrasion & Chemical Resistance)
    • ISO 16293-3 (Durability of Hydrophobic Glass Surfaces)
    • Automotive OEM in-house glass surface testing protocols

    Typical usage ratio

    • Surface application yields 10–100 nanometers dry film thickness; solution concentration in silane or fluoroalkyl formulations typically ranges 0.02–0.15% wt/vol, subject to glass porosity and target repellency rating.

    Downstream process integration

    • Integrated in dip-coating, spray, or vapor-phase deposition units; the material is applied after primary surface cleaning and float glass annealing, then thermally or photochemically crosslinked for durability.

    Final product types

    • Self-cleaning architectural facade glass
    • Laboratory glassware with anti-fouling surfaces
    • Automotive windshields and sunroofs with rain-repellent treatment
    • Ceramic shower enclosures with long-life water barrier

    4. Reactive Modifier in Specialty Fluoropolymer Synthesis

    Industrial polymerization processes employ this thiol as a chain transfer agent or functional end-group supplier during the synthesis of high-performance fluoropolymers. It introduces reactive thiol or fluoroalkyl termini, enabling downstream cross-linking and surface energy adjustment in end-use engineering plastics. Controlled addition ensures compatibility with regulatory oversight of raw materials used in advanced composite and sealing applications.

    Industry compliance standards

    • ISO 9001:2015 (Polymer and Additive Manufacturing Quality Systems)
    • ASTM D5630 (Residue on Polymer Ignition – Fluoropolymer Purity)
    • 21 CFR 177.1550 (US FDA Polymer Additive Approvals, for indirect food contact plastics)
    • EU Regulation (EU) No 10/2011 for plastic materials and articles intended to come into contact with food (when polymer intended for such applications)

    Typical usage ratio

    • 0.02–0.1% by monomer weight; determined experimentally according to target molecular weight, fluorine content, and mechanical properties of the final polymer. Dosage may be lowered in high-reactivity, high-molecular-weight processes to avoid side reactions.

    Downstream process integration

    • Metered addition into the polymerization reactor (bulk, solution, or emulsion) as a functional modifier or chain transfer agent; incorporation occurs during the initial or mid-stage of synthesis, prior to final polymer purification, extrusion, or pelleting.

    Final product types

    • Fluoroelastomer seals for automotive and chemical processing
    • High-purity fluoropolymer tubing
    • Non-stick cookware coatings (PTFE-type dispersions)
    • Engineered membranes for fuel cells or microfiltration

    5. Anti-Corrosion Additive for High-Performance Metal Finishes

    Metal protection specialists use this raw material within advanced corrosion-resistant coatings engineered for high exposure components. By integrating with binder systems, especially in marine, chemical processing, and aerospace environments, it creates persistent hydrophobic films that limit water and aggressive ion ingress, extending substrate performance life and reducing maintenance intervals on ferrous and non-ferrous metals.

    Industry compliance standards

    • ISO 12944-6 (Paints and varnishes—Protective paint systems for steel structures)
    • ASTM B117 (Salt Spray Testing for Coating Durability)
    • IMO PSPC (Performance Standard for Protective Coatings, marine use)
    • REACH Annex XVII (Substance usage on metal surfaces)

    Typical usage ratio

    • 0.03–0.12% by solids in the protective coating binder; actual ratio defined by salt fog resistance targets and compatibility with resins such as epoxies or fluoropolymers.

    Downstream process integration

    • Added at pigment and additive premix step; disperses in resin system followed by high-shear mixing, then applied to metal substrates by spray, roller, or dip, with subsequent curing in accordance with customer OEM schedules.

    Final product types

    • Offshore oil platform structural beams
    • Bridge steel coatings
    • Aerospace aluminum parts
    • Chemical plant reactor vessels
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    Certification & Compliance
    More Introduction

    1H,1H,2H,2H-Perfluorodecanethiol: Meeting Modern Demands in Surface Chemistry

    Understanding Perfluorodecanethiol and Its Place in Surface Modification

    In our years producing specialized fluorinated materials, the journey behind 1H,1H,2H,2H-Perfluorodecanethiol has always revolved around real-world challenges that surface engineers, chemists, and product developers face in the laboratory and on the production floor. For many, fluorinated thiols may sound esoteric, but they represent an essential solution for those chasing the twin goals of control and reliability in surface modification. This compound, designated as C10H5F17S and known by CAS number 78560-44-8, fills a niche that traditional alkyl thiols and non-fluorinated analogs fail to occupy.

    Why Experts Choose 1H,1H,2H,2H-Perfluorodecanethiol

    It only takes a day working in a lab or manufacturing setting to see how critical surface energy is in advanced materials science. Surface energy governs adhesion, wetting, and chemical resistance. Our customers demand surfaces that repel water, oils, organic solvents, and resist contamination and corrosion over long cycles—especially in electronics, MEMS, microfluidics, and advanced coatings. Many experiment with alkyl thiols, but the leap to fluorinated chains brings a whole new level of performance that non-fluorinated thiols cannot match.

    1H,1H,2H,2H-Perfluorodecanethiol stands out because its perfluorinated segment grants both low surface energy and significant chemical inertness. Typical hexane- or octanethiols lack the power to drive true hydrophobic or oleophobic effects. In developing this product line, we saw that researchers using shorter chain thiols returned with feedback about insufficient repellency and unstable self-assembled monolayers (SAMs) under operation conditions. Extending to perfluorodecanethiol directly addressed that gap, offering a longer perfluorinated tail with a terminal thiol that binds strongly—often irreversibly—to gold, silver, platinum, and other noble metal surfaces.

    Key Specifications and Practical Application

    Our production lines set quality benchmarks by delivering 1H,1H,2H,2H-Perfluorodecanethiol with a purity greater than 97%, usually confirmed by GC and NMR analysis. Molecular weight remains consistent at about 538.27 g/mol, while the compound itself appears as a clear to yellowish liquid at room temperature, boasting a faint, characteristic odor. The product’s performance window lies within normal laboratory conditions, without special storage requirements beyond avoiding prolonged light or extreme heat.

    Users typically encounter this compound in solutions of ethanol, dichloromethane, or tetrahydrofuran, though our customers regularly explore new solvent systems aiming for compatibility with more delicate substrates. The thiol head group forms reliable self-assembled monolayers on coinage metals, forming a densely packed film. It is recognized for its long-lasting hydrophobic and oleophobic properties, making it a staple in fabricating anti-fingerprint, anti-smudge, and chemical-resistant surfaces—key in touch panels, wearable electronics, photonics, and laboratory chips for bioscience. The molecule’s tail structure, packed with fluorine, ensures very low surface tension: droplets bead easily, particles fail to stick, and stains wipe clean with minimal effort.

    Firsthand Experience in Surface Chemistry Labs

    Across dozens of surface science projects, our team learned how variable conventional thiols behave when film thickness, stability, and uniformity matter. Conventional alkanethiols sometimes fail to deliver the expected water contact angle, even with stringent preparation routines. Perfluorodecanethiol repeatedly succeeds in pushing contact angles above 110 degrees, often reaching beyond 115–120 degrees using optimized conditions. This figure comes directly from in-house testing done in collaboration with process engineers building devices for consumer and industrial markets.

    The thiol group’s strong affinity for gold and silver makes this compound a mainstay in single-molecule electronics research and biosensor development. Labs performing DNA immobilization or protein assays on modified metal substrates rely on predictable surface behavior. 1H,1H,2H,2H-Perfluorodecanethiol delivers a platform that resists non-specific binding, cutting false positives and reagent waste.

    Comparing to Other Surface Modifiers

    We often see questions about how perfluorodecanethiol differs in practice from widely used alkanethiols or shorter-chain fluorinated thiols. To make sense of this, consider durability and repellency. Non-fluorinated thiols, such as octadecanethiol (ODT), create hydrophobic surfaces, but their hydrocarbon tails remain susceptible to degradation by strong solvents, ozone, and UV. In contrast, perfluorodecanethiol’s saturated fluorocarbon backbone shrugs off aqueous acids, alkalis, most organic solvents, and atmospheric oxidative agents, maintaining its performance for months under regular duty.

    Another issue arises in wetting behavior and contamination resistance. Devices coated with non-fluorinated thiols readily stain with oils from fingerprints or airborne hydrophobic particulates. In contrast, the perfluorinated version offers a much stronger resistance to common contaminants, showing cleanability and anti-fouling effects that endure after repeated handling and even ultrasonic or chemical cleaning. This advantage turns especially valuable in biosensing, microfluidics, and photonics, where protein fouling or organic contamination can halt an expensive experiment or short out entire batches of sensor arrays.

    Some users start with less expensive, shorter-chain fluorinated thiols like perfluorohexanethiol or perfluorooctanethiol, only to discover their films deliver slightly lower water and oil repellency, and in some cases, less robust binding or ordering than the longer C10 chain delivers. By investing in the longer perfluorinated tail, researchers get a more cohesive SAM, with reduced lacunae or defects, ultimately leading to more consistent and reliable results.

    Industrial Use Cases: From Touch Screens to Lab-on-a-Chip

    Products incorporating our perfluorodecanethiol coating can be found in sectors ranging from touchscreen panel manufacturing to precision optical components. Commercial touch screens treated with this material retain their anti-fingerprint properties longer, endure harsher cleaning chemicals without degrading, and maintain responsiveness by reducing the “drag” effect that contaminant films can cause. In laboratory settings, users report significant reductions in sample carryover and improved droplet control in digital microfluidics, boosting workflow efficiency and reproducibility.

    Flat panel display manufacturers have pointed out the benefit of using perfluorodecanethiol-based coatings to cut long-term maintenance costs by reducing cleaning frequency and extending product life. In biosensors, device surfaces resist protein fouling and interference from biological matrices. This impact ripples outward: less downtime in maintenance, more reliable data, longer product lifespans, and, by seeing fewer lot-to-lot discrepancies, smoother technology transfer from prototype to full-scale production.

    Challenges in Scaling and Handling

    Scaling up production and finding robust supply chains for highly fluorinated thiols presents hurdles. Creating these molecules involves multiple-step synthesis under tightly controlled atmospheres, often involving hazardous intermediates and energetic fluorinating reagents. Over the years, our site invested in closed-system reactors, real-time monitoring, and enhanced worker training to prevent leaks and guarantee batch purity. Routine checks on residual solvents, byproducts, and impurities ensure our customers receive consistent material, safeguarding their process yields and regulatory compliance.

    Handling and dosing perfluorodecanethiol requires care in the lab as even a minor spill on the wrong material can impart lasting surface effects. Our instructions always encourage the use of Teflon-coated tools and glassware, and we supply advice on cleaning and disposal to avoid contamination in sensitive labs. Those lessons come from cleaning up after a single overlooked drop can impart months-long hydrophobicity to benchtop surfaces. Working with this compound, you quickly develop a healthy respect for its power—and its longevity.

    Long-Term Perspective and Regulatory Considerations

    Interest in perfluorinated compounds has surged, driving both innovation and closer regulatory scrutiny. Our technical and regulatory teams regularly review evolving local and international standards on handling, environmental fate, and residuals. We observe strict internal controls on emissions, waste, and byproduct disposal—not just to meet compliance thresholds, but because environmental impact and sustainable chemistry shape future demand and market access.

    Though the molecule itself is not volatile and resists breakdown, responsible handling and disposal remain paramount throughout its lifecycle. Discussions with customers have strengthened partnerships in green chemistry initiatives. Where possible, we support research into recoverable and recyclable coatings, or surface treatments with lower environmental footprints. Forward-looking projects look at how much perfluorinated thiol is truly necessary: can monolayer formation be pushed to lower loading, or can dual-layer approaches with less resource-intensive underlayers be used? Some customers now reclaim and repurpose coated substrates, minimizing discard—especially important in prototyping or lab-scale work.

    Emerging Trends in High-Performance Surfaces

    Innovation continues apace thanks to demands from device miniaturization, wearables, and point-of-care diagnostics. Smaller devices with exposed circuitry or microchannels encounter more aggressive cleaning, handling, and exposure conditions. Technicians and engineers working in these fields recognize the advantages perfluorodecanethiol brings: superior robustness in confined spaces, and resistance to even the tiniest particulate intrusion. Conversations with design engineers over the past few years point to growing requirements for omniphobicity—where both water and a wide array of low-surface-tension solvents must bead up and roll away. This compound answers that call, performing far better than what can be achieved with silanes or basic alkyl thiols.

    Our internal R&D has also pushed boundaries experimenting with patterning technologies: inkjet, microcontact printing, and advanced photolithographic methods. 1H,1H,2H,2H-Perfluorodecanethiol offers excellent pattern resolution thanks to its affinity for noble metals and tendency to self-limit monolayer growth. Work with academic researchers confirms photopatterned SAMs can yield pixel-level repellency changes, enabling new applications in flexible displays and diagnostic multiplexing.

    Supporting Real-World Problem Solving

    Through customer feedback, failed first attempts, and iterative improvements, one theme emerges: the best chemical innovations come when manufacturers listen to practical details from the lab and field. Every batch of 1H,1H,2H,2H-Perfluorodecanethiol shipped has been shaped by hundreds of conversations about what worked, what didn’t, and what might improve process efficiency or finished-product reliability.

    Reports from production floors noted issues with early SAM formation methods—pinholes, patchy coverage, or rapid degradation on poorly cleaned surfaces. We took these to heart, investing in deeper purification and offering technical support to optimize application parameters: concentration, solvent choice, rinsing procedures, and curing conditions. By emphasizing dialogue over mere delivery, our chemists share nuanced application notes that often save customers hours or days in troubleshooting. That level of technical partnership pays forward, generating insight and better outcomes for entire supply chains.

    For example, a thin-film sensor manufacturer once highlighted the challenge of achieving reproducible low-background signals. After reviewing their protocols, we supported their switch to shorter immersion times, higher-purity solvents, and post-coating annealing—cutting signal drift in half and slashing reject rates. Such hands-on collaboration reinforces our belief that chemistry manufacturing never ends at the loading dock; it continues in every wiped-down benchtop, every well-sorted data set, and every next-generation product iteration.

    Conclusion: Delivering Long-Term Value in Advanced Materials

    Manufacturing 1H,1H,2H,2H-Perfluorodecanethiol places us at the crossroads of chemical innovation, advanced manufacturing, and practical user support. There’s no secret sauce—just years of careful process development, a commitment to purity and reproducibility, and close attention to users’ evolving needs. The future for fluorinated thiols looks dynamic as industries chase new surface properties with lower environmental costs.

    By producing this compound, we contribute to scientific breakthroughs, industrial efficiency, and sustained product excellence. With every inquiry and every delivery, new applications come into view. This product, shaped by practical experience and real-world problem solving, stands as a direct bridge between molecular design and daily advances in research and manufacturing.