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Methanesulfonyl Fluoride

    • Product Name Methanesulfonyl Fluoride
    • Alias MSF
    • Einecs 214-208-6
    • 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

    188831

    CAS Number 558-25-8
    Chemical Formula CH3SO2F
    Molar Mass 114.09 g/mol
    Appearance Colorless liquid
    Boiling Point 93 °C
    Melting Point -34 °C
    Density 1.327 g/cm3
    Solubility in Water Hydrolyzes
    Refractive Index 1.397
    Vapor Pressure 38 mmHg (20 °C)
    Odor Pungent

    As an accredited Methanesulfonyl Fluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Methanesulfonyl Fluoride, 100g, is packaged in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling.
    Shipping Methanesulfonyl fluoride should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be transported as a hazardous chemical, following all relevant regulations for toxic and corrosive materials. Ensure the package is clearly labeled, with proper documentation, and handled by trained personnel during transit for safety.
    Storage Methanesulfonyl fluoride should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and clearly labeled. Store in glass or compatible plastic containers, protected from moisture. Avoid exposure to heat, direct sunlight, and sources of ignition, as this compound is volatile and may release toxic fumes.
    Application of Methanesulfonyl Fluoride

    Applications of Methanesulfonyl Fluoride in Industrial Manufacturing

    Methanesulfonyl fluoride serves as a specialty intermediate in several regulated and technically advanced chemical manufacturing sectors. Our facility produces methanesulfonyl fluoride with a focus on end-user needs in industrial synthesis, and we supply customers with supporting documentation for process integration and compliance audits.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Leading pharmaceutical producers utilize methanesulfonyl fluoride in synthesis routes for key APIs, especially as a reactive sulfonylating agent in the modification of heterocycles and formation of sulfonamide functional groups. The material enables selective fluorination steps under mild conditions, which is essential in the production of CNS-active compounds and enzyme inhibitors. Process safety, trace analysis of residuals, and impurity profiling demand precise control at each stage. We support tailored supply for batch, semi-batch, and continuous synthesis models used in cGMP facilities.

    Industry compliance standards

    • ICH Q7 — Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API production
    • USP Monograph Process Controls
    • FDA 21 CFR Part 211 — CGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 0.5–1.5 molar equivalents per sulfonamide or fluorination step, typically adjusted according to substrate reactivity and yield optimization. Excess is minimized for economic and waste compliance reasons.

    Downstream process integration

    • Stagewise addition during the key sulfonylation or fluorination reaction within multi-step API synthesis
    • In-line quenching and work-up using basic or aqueous solutions
    • Final API purification by crystallization or chromatography to eliminate unreacted material and byproducts

    Final product types

    • Central nervous system (CNS) therapeutics containing fluorinated motifs
    • Selective enzyme inhibitors for research and development
    • Sulfonamide class pharmaceuticals

    2. Agrochemical Intermediate Manufacturing

    Major crop protection manufacturers employ methanesulfonyl fluoride in the synthesis of selective herbicides, insecticides, and fungicidal actives, where it serves as a clean alternative for introducing sulfonyl fluoride groups. Its favorable reactivity profile helps maintain precise control of molecular architecture and process impurity levels. Downstream operations require robust solvent handling systems, and waste streams must be strictly managed under regional and international compliance protocols. Our technical support covers both process troubleshooting and traceability requirements for multi-ton campaigns.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO JMPS)
    • REACH Regulation (EC) No 1907/2006 concerning Registration and Evaluation of Chemicals
    • ISO 9001:2015 Quality Management Systems for chemical intermediates
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 1.0–2.0 equivalents per activated aromatic ring or heterocyclic precursor, with adjustment based on scale and analytic verification of end-point selectivity and conversion.

    Downstream process integration

    • Batch or continuous flow addition during key functionalization reactions
    • Immediate downstream purification (typically liquid-liquid extraction and distillation) to recover active intermediate
    • Incorporation into multi-step synthesis blocks for final agrochemical actives

    Final product types

    • Triazine-based herbicides
    • Sulfonylurea and sulfonamide fungicides
    • Fluorinated insecticidal agents

    3. Specialty Polymer and Resin Crosslinking

    Advanced polymer manufacturers incorporate methanesulfonyl fluoride as a crosslinking reagent for high-performance fluorinated or sulfonated resins. The raw material serves to introduce strong sulfonyl linkages, enhancing chemical resistance and thermal stability in specialty coatings, membranes, and engineered plastics. Strict QC is needed for purity and moisture content due to the high reactivity and potential for side-chain modification, and all operations require closed system handling for operator safety. Our production lot documentation includes detailed COAs and support for regulatory trace audits.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in chemical manufacturing
    • RoHS Directive (2011/65/EU) for restricted substances in end-use electronics
    • REACH Registration for polymers and reactive intermediates
    • ASTM D543 – Resistance of Plastics to Chemical Reagents

    Typical usage ratio

    • 0.2–1.0% by weight of total monomer or polymer resin, with precise dosing required for targeted crosslink density and uniform distribution throughout the matrix.

    Downstream process integration

    • Direct addition during bulk or solution polymerization
    • Post-polymerization grafting via reactive extrusion or batch treatment
    • Analytical monitoring for residuals and degree of crosslinking

    Final product types

    • Fluorinated ion-exchange membranes for water treatment and fuel cells
    • Chemically resistant specialty coatings for electronics and industrial components
    • High-strength engineering plastics

    4. Enzyme Inactivation Reagent Production for Diagnostics

    Specialty reagent suppliers use methanesulfonyl fluoride to produce irreversible enzyme inhibitors, primarily for application in proteomics, in vitro diagnostics, and biochemistry laboratories. The compound reacts selectively with active-site serine residues and serves as a critical component in buffers and extraction cocktails, with all output subject to batch traceability, endotoxin control, and validated shelf-life protocols. Manufacturing must ensure absence of trace solvents and high purity to avoid interference in sensitive downstream biological assays. Our batches ship with detailed QC data and statement of origin for regulated export markets.

    Industry compliance standards

    • ISO 13485 — Medical devices quality management for diagnostic reagents
    • CFR Title 21, Part 820 — Quality System Regulation for medical devices
    • IVD Directive 98/79/EC for European supply
    • USP General Chapter <85> Bacterial Endotoxins Test, as applicable

    Typical usage ratio

    • 0.5–2.0 mM concentration in lysis or extraction buffer formulations, with practical use depending on total protein load and buffer chemistry in downstream IVD assay kits.

    Downstream process integration

    • Dissolution and sterile filtration into ready-to-use buffer concentrates
    • Bulk packaging for kit manufacturers, with aliquot preparation for final device assembly
    • End-user integration into tissue and cell lysis protocols for biomarker discovery and clinical diagnostics

    Final product types

    • Protease inhibitor cocktail tablets and solutions
    • Biological sample preparation kits for clinical and research labs
    • IVD (in vitro diagnostic) extraction reagents
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    Certification & Compliance
    More Introduction

    Methanesulfonyl Fluoride: Reliable Production from Chemical Manufacturing Experts

    Introduction to Methanesulfonyl Fluoride from the Source

    In the field of organosulfur compounds, methanesulfonyl fluoride stands out for its precision and reactivity. Producing this compound in-house, we draw on years of hands-on experience with sulfonyl fluoride chemistry. Our team manages synthesis and purification at scale, delivering a model that consistently meets the needs of researchers and processing plants. Methanesulfonyl fluoride—known to chemists as MSF, or by its CAS number 557-24-2—presents itself as a clear, colorless, reactive liquid whose controlled volatility separates it from many other sulfonyl fluorides, both in laboratory and industrial contexts.

    Specifications and Handling Built on Industry Practice

    Day in and day out, we work with methanesulfonyl fluoride in our own facilities under strictly controlled conditions. Our batches comply with assay standards typically exceeding 98% purity, minimal water content, and tightly monitored levels of known impurities. Each lot undergoes gas chromatography (GC) and NMR analysis before release. We store and transport it in PTFE-lined containers, making sure the product remains as stable as possible during transit. Years of shipping experience have taught us the importance of rapid, temperature-controlled logistics, especially to international destinations where regulatory requirements demand full traceability and detailed export paperwork. Methanesulfonyl fluoride’s boiling point hovers around 162°C, meaning loss by evaporation occurs much more slowly than with lighter sulfonyl fluorides, and it avoids the abrupt fuming or loss that would complicate production-line dosing.

    Why We Make Methanesulfonyl Fluoride

    We choose to produce methanesulfonyl fluoride because end-users value consistent reactivity and reproducible purity in sulfonylation and fluorination chemistry. Over the past decade, demand from pharmaceutical developers has driven interest in MSF’s selectivity in enzyme inhibition and as a mild, controllable reactant for organic synthesis. Synthetic chemists use it to introduce methanesulfonyl groups under mild conditions. Its moderate reactivity balances ease of handling with high selectivity, giving a cleaner outcome than more aggressive sulfonyl chlorides or less stable analogues.

    We have walked researchers at all scales through its application, from gram-scale enzymology studies to multi-kilogram contract custom synthesis batches for clinical evaluation. The molecule’s small size and water solubility make it navigable by most standard lab equipment, with rotary evaporators and glassware sufficing for isolation and purification in most settings.

    Real-World Use Cases and Insights from Experience

    MSF finds a unique position in organic synthesis—particularly in the production of sulfonamides and sulfonyl fluorides. Lab chemists preparing specialty reagents cite its compatibility with basic and neutral media, unlike acyl fluorides or sulfonyl chlorides, which often degrade under similar conditions. We’ve seen formulation chemists value its ability to selectively activate peptides, carbohydrates, and other biologically active molecules, where other reagents can cause side reactions or unwanted hydrolysis.

    Early in our manufacturing history, academic collaborators approached us with requests for small, high-purity lots to support new enzyme labeling techniques. Rigorous toxicity and environmental persistence studies had already placed MSF in a different regulatory basket than more volatile or hydrolytically unstable reagents. Along the way, we provided technical support for protocols exploring MSF's performance in new labeling strategies, and our plant adapted to meet emerging purity demands quickly.

    As a fluorosulfonylating agent, MSF takes up a practical space: more stable in long-term storage than perfluoroalkyl analogues and less corrosive than sulfonyl chlorides. In our production, keeping water and reactive impurities low prevents unwanted side-product formation, especially important in pharmaceutical intermediates where residual toxicants spell failure at the release stage.

    Comparing Methanesulfonyl Fluoride to Other Sulfonylating Agents

    Competing reagents such as methanesulfonyl chloride, triflic anhydride, and tosyl chloride present unique handling hazards and reactivity profiles. Methanesulfonyl chloride releases acidic fumes and often demands acid scavengers or specialized glassware. In contrast, MSF remains less reactive to ambient moisture, offering a safer alternative for sensitive functional groups. Our packing line handles both MSF and its chloride cousin, yet we repeatedly observe lower frequency of glassware etching and less engineer call-out for corrosion after MSF campaigns.

    In proteomics research, triflic anhydride or tosyl chloride sometimes overshoot, giving too much background reactivity and generating unwanted sulfonated byproducts, whereas MSF hits the balance, modifying target residues without degrading valuable starting material. Our direct manufacturing experience makes these practical differences clear: we field questions about these issues daily from customers in academic and industrial R&D.

    Unlike difluoromethyl or trifluoromethyl analogues, MSF does not shed harmful degradation products, remaining stable and manageable if tightly contained. Over multiple years of direct observation and testing, we have watched MSF's breakdown profile—sulfamic acid and methanesulfonic acid, chiefly—pose far less persistence or threat in laboratory containment than the byproducts of perfluoroalkyl sulfonyl fluorides.

    MSF in Drug Development and Beyond

    MSF’s inhibition of acetylcholinesterase gained attention in the progression of research for cognitive disorders, especially Alzheimer’s disease. As industrial chemists, we know cost pressures matter. Many academic groups and startup biotech teams seek alternatives to more expensive, patented acetylcholinesterase inhibitors. With a reliable, proven manufacturing route and established analytical controls, we make it possible for innovators to secure uninterrupted access to high-quality MSF for their pilot studies, toxicology screens, and lead candidate developments.

    For mediation of allergic and inflammatory responses, as well as in proteomic labeling and neurological agent synthesis, our customers count on the low side-reaction rate of our MSF. In collaborative projects, we've routinely worked with formulation teams seeking predictable hydrolysis rates. By providing consistently pure lots, we've enabled these researchers to avoid troubleshooting that plagues other sulfonyl fluorides, cutting down on costly reruns.

    Quality assurance never stops at passing the assay. We regularly receive direct feedback: failed reactions caused by off-spec batches from less established suppliers. Our approach combines hands-on stewardship, routine inter-batch cross-checking, and, wherever needed, custom documentation of impurity profiles. Clients can track a lot back to individual reactor runs and analytical datasets.

    Manufacturing MSF: Challenges and Lessons Learned

    Producing methanesulfonyl fluoride at commercial scale demands strict temperature regulation and close monitoring of intermediate formation. In early process development, we adjusted feed rates and optimized solvent profiles to minimize byproducts, after persistent batch variability signaled a need for tighter process controls. Unlike simple batch distillations for sulfonyl chlorides, MSF’s volatility requires precision vacuum work, anti-corrosion lining, and active condenser management. Each design choice reflects years of accumulated lessons.

    On rare occasions, process upsets—such as a surge in water content or a spike in temperature during fluorination—expose the underlying fragility of the reaction. On these days, we pause production, investigate root causes, and retrain operators on predictive maintenance. Long-term reliability demands vigilance at every step, including tank farm monitoring, scheduled filter changes, and continuous investment in analytical calibration. These chores separate a reliable manufacturer from somebody just moving drums.

    We orient our safety procedures around real risks encountered during fluorination. Unlike sulfur tetrafluoride or fluorosulfonic acid, MSF can be managed without full-suit procedures for most operators. Still, splash hazards and inhalation risk lead us to maintain glove box handling under negative pressure, with scrubbers set up to neutralize accidental loss instantly. Training never becomes routine; we refresh drills so new and old hands alike know recovery actions down cold.

    Environmental and Regulatory Considerations

    Sulfonyl fluorides, in general, bring a reputation for environmental persistence. Based on site audits and regulatory assessments, methanesulfonyl fluoride offers a reduced persistence profile, largely because of its controlled hydrolysis and lower bioaccumulation. In our region, local authorities require detailed reporting on organofluorine emissions: our scrubbed exhaust streams and water treatment facilities allow us to stay in compliance with evolving rules while passing audits on both sides of the supply chain.

    We’ve seen that customers often worry about possible listing changes and pre-authorization rules for shipping chemicals to certain destinations. By working at the interface of production and global regulatory compliance, we stay ready with all necessary documentation. Whether the shipment is bound for the United States under TSCA, reaches Europe’s REACH-compliant facilities, or targets a pharmaceutical intermediate registration, our team stays actively tuned to the latest tracking and labeling changes. We do not outsource these functions; regulatory vigilance remains a daily, in-house responsibility.

    Continual outreach to environmental and safety experts, as well as a willingness to adapt our practices to match or exceed government guidelines, lets us remain partners to our customers and neighbors. In post-marketing surveillance studies, no significant adverse impact from MSF has been confirmed under responsible operating conditions. Safety data updates feed directly into training, ensuring every drum that exits our gate comes with transparent risk communication.

    Supporting Scientific Progress and Innovation

    The development of new analytical methods and labeling strategies in proteomics, neuroscience, and pharmaceutical chemistry depends on reliable access to high-purity reagents. Our commitment to research partnerships goes beyond transactional supply; with every MSF shipment, we provide technical insights from our own scale-up experience, troubleshooting advice, and feedback on reaction conditions. Collaborative relationships with academic labs have led us to experiment with small-lot synthesis, on-demand purification techniques, and speeded shipment to match grant timelines or conference presentations.

    Methanesulfonyl fluoride’s growing role as a selective protease inhibitor drives new demand. Inside our labs, we’ve supported switchovers from older halogenated reagents to MSF, reducing hazardous waste generation and vapor exposure for benchtop workers. Transitioning to MSF also means less reliance on persistent, legacy chemicals with complex regulatory burdens. These process improvements reduce disposal costs and lessen environmental impact long after a synthesis project wraps up.

    In the pharmaceutical arena, shorter supply chains and the drive for local manufacturing favor direct-from-manufacturer supply. Researchers told us about delays when orders routed through layers of exporters led to product degradation or paperwork hold-ups. Handling end-to-end production allows us to respond swiftly, fine-tune batch sizes ahead of scale-outs, and lock in specification controls at each step. Security of supply runs alongside security of data: strict controls over who accesses plant documentation and product history shield proprietary information and build customer confidence.

    Future Developments and How We Adapt

    The market’s demand for MSF is changing. Drug research projects call for custom labeling, isotopically enriched versions, or special purity certifications. Our technical team works directly with customers to modify crystallization parameters, tailor packaging to unique regulatory geographies, and validate every change through in-house and third-party labs, based on real-world feedback not only from purchasing teams, but also from the chemists and engineers working at the bench.

    Process safety improvements never pause. Insights from other chemical plants—in corrosion resistance, sensor integration, or shipping compliance—flow directly into our own operations. After observing trace metal contamination in bulk storage tanks years ago, we invested in a complete lining overhaul across the plant, rolling out real-time conductivity and impurity detection in drum-filling stations. These investments cut down on customer rejections and saved time lost to post-shipment remediation.

    We’ve responded to calls for greener chemistry. Internally, we examine alternative fluorinating agents and process optimizations that cut down on reagent waste and energy use. With new reactor designs, we continue to drive the process toward higher yields and reduced emissions. Process intensification not only cuts costs but also means fewer trucks on the road, less storage at the customer site, and an easier path through regulatory review for all involved.

    Final Thoughts from the Production Floor

    Making methanesulfonyl fluoride isn’t just a matter of running a textbook reaction. Each batch brings its own challenges—from seasonal humidity shifts affecting reaction rates to changes in end-use demands from customers developing the next generation of pharmaceuticals and diagnostic tools. As a manufacturer, we learned early that attention to detail, willingness to invest in equipment and people, and genuine feedback from end users shape success far more than any brochure claim or sales pitch.

    Direct production experience produces insights that paperwork and secondhand reports never surface: the best condenser configuration to prevent loss, the timing of additions to dodge exotherms, the right analytics to catch trouble early. Our MSF leaves the plant informed by those hard-won lessons and backed by teams who know what rides on every shipment. We stand behind every drum, every bottle, and every ongoing partnership—and that, more than any commodity listing or catalog page, defines what it means to be a true manufacturer of methanesulfonyl fluoride.