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2,3,5,6-Tetrafluorothiophenol

    • Product Name 2,3,5,6-Tetrafluorothiophenol
    • Alias 2,3,5,6-Tetrafluorobenzenethiol
    • Einecs 260-998-7
    • 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

    449944

    Chemical Name 2,3,5,6-Tetrafluorothiophenol
    Cas Number 1493-27-2
    Molecular Formula C6HF4SH
    Molecular Weight 182.13 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 148-150 °C
    Melting Point -8 °C
    Density 1.586 g/cm³
    Refractive Index 1.559
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., ether, chloroform)
    Smiles c1c(c(c(c(c1F)F)S)F)F
    Iupac Name 2,3,5,6-tetrafluorobenzenethiol
    Flash Point 50 °C
    Storage Temperature 2-8 °C

    As an accredited 2,3,5,6-Tetrafluorothiophenol 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 with a secure screw cap, labeled with hazard warnings and chemical identification for 2,3,5,6-Tetrafluorothiophenol.
    Shipping 2,3,5,6-Tetrafluorothiophenol is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material due to its toxic and corrosive properties, requiring proper labeling and documentation. Transport should comply with relevant regulations (such as DOT, IATA, or IMDG) to ensure safety and legal compliance.
    Storage 2,3,5,6-Tetrafluorothiophenol should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, and well-ventilated place away from sources of ignition and incompatible materials like strong oxidizers. Store at room temperature, protected from moisture and direct sunlight. Use proper personal protective equipment when handling.
    Application of 2,3,5,6-Tetrafluorothiophenol

    Applications of 2,3,5,6-Tetrafluorothiophenol in Industrial Manufacturing

    As a direct manufacturer of 2,3,5,6-tetrafluorothiophenol, we supply high-purity raw materials to specialized sectors where the unique chemical structure of this compound is required for critical synthesis steps. Below we outline major application scenarios in which our material is routinely integrated according to established industry standards and customers’ technical protocols.

    1. Advanced Agrochemical Production

    Our material is utilized as a key sulfur-containing building block in the synthesis of certain advanced agrochemical active ingredients, specifically fluorinated thiophene derivatives used in next-generation fungicide and herbicide molecules. The introduction of fluorine and thiol groups from this raw material enhances the metabolic stability and activity profile of downstream crop protection agents during industrial production.

    Industry compliance standards

    • REACH (EC) No 1907/2006
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • ISO 9001:2015 controlled manufacturing for starting materials
    • FAO/WHO specification requirements for pesticide active ingredients

    Typical usage ratio

    • 0.5%–2% by total batch weight in targeted fluorinated agrochemical intermediate synthesis; ratio determination based on stoichiometric calculations and yield optimization during scale-up.

    Downstream process integration

    • Dosed in early-stage sulfenylation or thiolation reactions in multi-step synthesis, typically fed into pressurized reactors under inert atmosphere to avoid oxidation before fluorination and post-treatment steps.

    Final product types

    • Active fungicidal and herbicidal ingredients bearing fluorinated thiophene moieties for formulation in wettable powders, SC, and granules
    • Precursor intermediates for further coupling and formulation in the agrochemical sector

    2. Pharmaceutical API Intermediates

    This specialty raw material is used in pharmaceutical manufacturing as a critical synthesis intermediate for introducing both thiol and fluorine functionalities into complex heterocyclic scaffold structures. These modifications improve the physiochemical properties of potential drug candidates and align with targeted small molecule development workflows in leading pharmaceutical research and production environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and Ph. Eur. monographs (where applicable to intermediate synthesis)
    • FDA 21 CFR Part 210/211 (where integrated into cGMP pharmaceutical production sites)
    • ISO 9001:2015 traceability controls

    Typical usage ratio

    • 0.3–1.2 molar equivalent relative to core substrate in specific API intermediate formations; precise ratios determined from structure-activity studies and process validation batches.

    Downstream process integration

    • Charged at the functionalization step—often thiolation or fluorine-exchange—in semi-batch reactors, prior to cyclization or coupling for lead compound development in clinical candidate synthesis.

    Final product types

    • API intermediates with tetrafluorinated thiophenol motifs incorporated in centrally acting pharmaceuticals and anti-infective agents
    • Reference compounds for medicinal chemistry and structure optimization

    3. Specialty Polymer Modification

    In the field of specialty polymer manufacturing, formulators incorporate our thiophenol derivative to modify polymer backbones, particularly in the synthesis of advanced fluorinated polymers and copolymers with enhanced thermal and chemical resistance. The compound introduces reactive sites for further cross-linking and provides significant benefits in engineering plastic and specialty membrane applications.

    Industry compliance standards

    • ISO 9001:2015 process certification
    • RoHS Directive 2011/65/EU on hazardous substances (applicable to electronics-grade polymers)
    • UL 94 standards for flammability in finished polymers
    • Industry-specific technical data sheet requirements for final polymer applications

    Typical usage ratio

    • 0.1–0.8% based on total monomer content for backbone modification; exact proportion defined by target cross-link density and molecular weight specifications.

    Downstream process integration

    • Directly co-polymerized through radical or condensation polymerization routes, added after initiator charging or during chain transfer stages, enabling controlled formation of fluorinated polymer blocks.

    Final product types

    • Specialty membranes with high chemical resistance for industrial filtration
    • Fluorinated engineering plastics for semiconductor and electronics fabrication

    4. Electronic Chemical Synthesis

    Our material serves as a precise precursor in the production of functionalized thiol ligands and fluorinated building blocks for the electronics and semiconductor sector. Manufacturers leverage its unique substitution pattern in surface modification, dielectric material preparation, and as a source for introducing sulfur functionality in etchant additives and microelectronic chemical blends.

    Industry compliance standards

    • SEMI Standards MS7 for chemical materials
    • IEC 62474:2018 for material declaration in electronic components
    • ISO 14001:2015 environmental management (for high-purity chemical plants)
    • Quality agreements for electronic chemical grade materials

    Typical usage ratio

    • Typically 0.02–0.25% of total solution or compound blend; ratio depends on desired sulfur incorporation and surface functional group density requirements.

    Downstream process integration

    • Introduced during formulation of photoresist additives, surface modifier solutions, or blending into etchant baths prior to wafer cleaning, patterning, or etching steps in fab lines.

    Final product types

    • Functionalized surface coatings for PCBs and semiconductor substrates
    • Microelectronic etching solutions containing custom ligand frameworks

    5. Fine Chemical Synthesis for Research and Specialty Applications

    Our tetrafluorothiophenol finds specific use as a building block in laboratory-scale and pilot-plant specialty chemical synthesis where highly fluorinated, sulfur-containing motifs are required. This includes the creation of analytical reference compounds, chiral auxiliaries, and unique organosulfur frameworks for chemical biology research and advanced material science studies.

    Industry compliance standards

    • ISO 9001:2015 for laboratory-scale chemical production
    • OECD GLP Principles (where substances are used for analytical standard production)
    • Customer-defined Certificate of Analysis (COA) and characterization standards
    • UN Model Regulations for handling and transport of chemical substances

    Typical usage ratio

    • 0.1–1.0 equivalent relative to principal substrate in customized multi-step organic synthesis; ratio selection based on desired fluorination and thiophenol integration intensity.

    Downstream process integration

    • Added in controlled stages of nucleophilic substitution or coupling reactions, enabling rapid generation of fluorinated organosulfur motifs under inert or anhydrous conditions, followed by downstream purification and isolation.

    Final product types

    • Analytical labeling standards for mass spectrometry and chromatography
    • Precursors for advanced ligands, sensors, and functional material components in R&D departments
    Free Quote

    Competitive 2,3,5,6-Tetrafluorothiophenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Tel: +8615371019725

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    Certification & Compliance
    More Introduction

    2,3,5,6-Tetrafluorothiophenol: A Reliable Building Block for Advanced Fluorinated Chemistry

    Our Firsthand Experience with 2,3,5,6-Tetrafluorothiophenol

    For over a decade, we have dedicated ourselves to the production and improvement of specialized fluorinated compounds. Through years in these labs and plants, our team has seen the unique challenges that chemists and formulators face when working with sulfur-bearing aromatic fluorides, particularly 2,3,5,6-tetrafluorothiophenol. Working with this product has taught us respect for both its sensitive handling requirements and its reliable reactivity in both laboratory and industrial settings.

    Consistent supply of high-purity 2,3,5,6-tetrafluorothiophenol remains a recurring challenge across the global chemical industry. Synthetically, this compound demands rigorous control at every step. Our chemists aren’t simply following recipes; they draw on years of bench-top experience to refine each run, using precise stoichiometry and repeated analytical checks. Every batch is measured to ensure minimal byproduct content, a clean odor profile, and clear liquid appearance, which reflect careful column purification and vacuum distillation.

    What Sets 2,3,5,6-Tetrafluorothiophenol Apart

    Direct contact with our customers and research partners has revealed that 2,3,5,6-tetrafluorothiophenol serves as a versatile precursor for a range of applications. In synthesis, its highly activated aromatic ring responds promptly to electrophilic and nucleophilic substitution, compared to classical thiophenols. The four electron-withdrawing fluorines draw attention from both pharmaceutical and materials science researchers; they often ask for this compound by name when they push towards new agrochemical ingredients or advanced polymer additives.

    Compared to non-fluorinated and partially fluorinated thiophenols, the 2,3,5,6-tetrafluoro variation imparts increased thermal and oxidative robustness to target molecules. The S–H group reacts predictably, whether forming custom thioethers, sulfoxides, or extending into more exotic cross-coupling chemistry. We have observed, in both our reactors and customer feedback, that final products made using this monomer resist degradation and chemical attack at greater rates than their trifluorinated cousins. In direct interaction with technical teams, we regularly calibrate our process to match not just quoted specs, but to real-world downstream requirements, such as solubility in various organic solvents and exceptionally narrow GC retention times for critical QC steps.

    Model and Specification: Guided by Experience, Not Guesswork

    “In the flask, on the kilo scale, and all the way to drums, quality means predictability.” This lesson recurs in our annual plant reviews. We supply batches labeled as TFTP-23-56, denoting purity above 98.5%, with residual fluoride and oxygenates kept near detection limit. By making GC-MS and NMR an integral part of our workflow, we reduce the likelihood of off-profile products and inconsistent odor, two issues that can become problematic due to the volatility and reactivity of the thiol functional group.

    Not every thiophenol in the market can claim such reproducibility. We have competitors that still work with benchmark procedures that ignore subtle thermal decomposition routes. Our in-house monitoring enables us to deliver TFTP-23-56 as a colorless to pale-yellow liquid, dense but low enough in viscosity for both bench and automated liquid-transfer systems. Internal standards are based on ppm-level detection of hydrolyzable sulfur and halogenated organics. Our team enforces a Quick-to-QC approach: tanks and barrels do not leave the plant until each passes verification, verified through high-throughput UPLC and Raman checks, a necessity for customers who run high-throughput or continuous reactors.

    Usage from the Perspective of Those Who Synthesize

    Years of batch testing and process scaling reveal the true value of 2,3,5,6-tetrafluorothiophenol. It acts as a nucleophile in key formation steps for fluorinated aryl thioethers, bridging the gap between sulfur chemistry and stabilized ring systems. Our R&D partners use this compound to introduce both the sulfur behavior and the fluorine effects found in advanced electronic materials, especially where moisture resistance and chemical inertness are required. Some of our earliest users ran into problems sourcing this niche precursor in the early 2010s, a time before direct-from-manufacturer supply chains stabilized. They brought those sourcing headaches to us, and we’ve maintained an uninterrupted flow since, even when upstream shortages shake the market.

    Real-world applications range from antistatic coatings to pharmaceutical intermediates. Polymer researchers value the unique behavior imparted by highly fluorinated sulfur rings, observing dramatic reductions in surface energy and permeability. For those working at the smaller scale, every drop counts; analytical chemists preparing reference standards rely on accurate mass balance and negligible side products. Industrial teams demand bulk supply, with minimal odor and easy clean-down, to avoid trace contamination in plastics processing equipment. We listen closely, providing both technical datasheets and practical suggestions on safe handling, blending, and downstream conversion for large- and lab-scale users alike.

    Comparison with Other Thiophenols: Insights from the Bench

    Chemists who have worked with non-fluorinated thiophenol or its difluoro and trifluoro analogs immediately notice the difference that four fluorines make. Our technical staff finds that the 2,3,5,6-tetrafluoro derivative behaves with more stability under aerobic conditions and shows sharper transitions in phase transfer during organic syntheses. Fewer side reactions complicate downstream purifications, leading to better predictability in creating target molecules. Testing reveals that even trace oxygen does not lead to rapid oxidation, making it friendlier to both synthesis and storage.

    Some clients seek alternatives for price reasons but come back after experiencing difficulties in final product durability or processing losses. For those calling for greener, higher-yield processes, 2,3,5,6-tetrafluorothiophenol stands apart. Less overreaction, more control; better stability in ambient air, fewer safety headaches. Fluorine’s addition changes solubility features, too: in our hands, this product dissolves smoothly in most halogenated and polar aprotic solvents, but also shows resistance to spontaneous oxidation that saves headaches in scale-up.

    Meeting Evolving Industry Expectations

    For many years, industry has moved toward safer, cleaner, and more sustainable chemicals, often at the cost of re-tooling entire processes. We’ve learned firsthand that robust process control, paired with open communication with customers, is irreplaceable. The tightly-held nature of tetrafluorothiophenols means only a handful of certified facilities manage scalable, reliable output according to international standards. Our response has been to make transparency a pillar, going beyond providing a certificate by itemizing trace impurities, offering batch-level stability data, and maintaining a log of customer feedback to improve future runs.

    On the safety front, both our on-site and remote partners commonly ask about storage and transport risks. Strong odor, potential for oxidation, and handling volatility require guidance drawn from hard-won plant knowledge, not just the text of an SDS. We’ve invested in improved drum linings, nitrogen-blanketed transfers, and specialized PPE recommendations. Periodic staff drills enforce practical standards, so accidents are kept rare and our product ships with minimal risk. Real-life tests, not just simulations, have flagged storage temperature sensitivity, leading us to recommend controlled environments even for short duration shipments. Small lessons, learned from spilled barrels and near-miss documentation, keep our risk low and the end-user’s experience positive.

    Quality Control: Not Only an Objective, But a Discipline

    Each kilogram of 2,3,5,6-tetrafluorothiophenol that leaves our facility represents dozens of decisions made by chemists on the line and QC staff with real accountability. We dig deeper than the industry average for lot-to-lot tracking. Our experienced synthesis teams track upstream fluoride and thiol sources, rejecting material that even hints at off-odor or impurity profile drift. Incoming calls from customers reporting any abnormality—color shift, odor note, solubility change—are logged and flagged for both management review and analytical reruns.

    Delivering reliability takes troubleshooting engrained in daily operation. Equipment upgrades—new distillation columns, high-purity argon blanketing, digital flowmeters—are selected after real-world yield tracking, not just vendor presentations. Root-cause analysis, for example, revealed a once-invisible source of trace water ingress, now tightly countered by dual-point vacuum drying and increased desiccant checks. Each iteration of our process reflects a partnership between those who run the plant and those who synthesize with the product in the field. This dialogue shapes our continuous improvement strategy.

    Sustainability and Strategic Sourcing

    As global demand grows for materials with aggressive performance targets and environmental goals, we face constant scrutiny over our feedstock choices and waste minimization efforts. We keep mapping new sourcing partnerships for key raw materials, selecting only stable, low-impurity suppliers. This creates resilience against region-specific shortages or quality surprises. Investment in recovery and reuse of fluorinated intermediates cuts the waste profile and enables us to offer a more sustainable option compared to less refined market entrants.

    On the energy front, process intensification helps us reach higher yields at lower solvent volumes. Integration of heat exchangers and closed-loop chilling for the critical S–H introduction step substantially cuts direct emissions and keeps the total environmental footprint low. Several partner companies have engaged with us on joint pilot projects to reclaim spent catalyst and recycle it for further runs, contributing to a more circular model in specialty chemical manufacturing.

    Supporting Advanced R&D and Commercial Growth

    Researchers and industrial engineers working at the top of their fields regularly push the limits of what’s known about sulfur-fluorine interactions. Our goal is to offer not just material, but direct support: technical calls, troubleshooting on-site, and step-by-step synthesis advice for both novel molecules and scaled-up processes. We make laboratory samples available for early-phase work, backed by expedited analytical turnaround and candid communication about lot variability or potential scale-up bottlenecks.

    Several years ago, an R&D group at a major electronics manufacturer reached out with a problem: competitor lots were producing inconsistent results in their thin-film processes. Our team worked through their entire workflow, identifying a spectral impurity missed by standard QA—trace dibenzothiophene that seemed invisible to routine analysis. A new purification protocol, keyed by our own analytical team, solved the issue. Since then, they’ve imported all their fluorinated thiophenol from us, reporting greater reproducibility in device yield.

    The Future for 2,3,5,6-Tetrafluorothiophenol

    Regional and global regulations continue to shift, raising the stakes for chemical traceability and safety performance. We see a growing need for self-certifications, third-party audits, and joint customer-lab verification. We aim to stay ahead by documenting not just what’s required, but anticipated changes in both performance requirements and regulatory frameworks. Our familiarity with REACH, TSCA, and other environmental standards enables us to serve multinational partners that require more than basic compliance.

    Looking forward, continual exchange with end-users, research teams, and fellow production chemists will shape advances in how 2,3,5,6-tetrafluorothiophenol is offered and improved. We stand by every liter shipped and welcome partner input as we explore new frontiers in material science, green chemistry, and high-reliability production. Those looking to move beyond commodity raw materials find in our process and this molecule a partner for the long run. Direct engagement and attention to real pain points keep us learning every month, shaping our path to deliver real value from synthesis bench to final application—always with both a scientific and practical approach.