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N-Fluoro-4-Methylpyridinium-2-Sulfonate

    • Product Name N-Fluoro-4-Methylpyridinium-2-Sulfonate
    • Alias FMPy
    • Einecs 68489-09-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    324875

    Product Name N-Fluoro-4-Methylpyridinium-2-Sulfonate
    Molecular Formula C6H7FNO3S
    Molecular Weight 191.19 g/mol
    Appearance White to off-white solid
    Cas Number 77836-29-2
    Melting Point 160-164°C
    Solubility Soluble in water and polar organic solvents
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Storage Conditions Store in a cool, dry place, away from light
    Synonyms NFSI, F-TEDA-2-sulfonate
    Usage Electrophilic fluorinating agent
    Safety Precautions Irritant, use gloves and eye protection

    As an accredited N-Fluoro-4-Methylpyridinium-2-Sulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical "N-Fluoro-4-Methylpyridinium-2-Sulfonate, 5g" is packaged in a sealed amber glass bottle with a screw cap.
    Shipping N-Fluoro-4-Methylpyridinium-2-Sulfonate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be packaged in accordance with chemical safety regulations, with appropriate hazard labeling. Transport should comply with local and international guidelines for handling potentially reactive or irritant chemicals. Store upright, away from incompatible substances.
    Storage Store N-Fluoro-4-Methylpyridinium-2-Sulfonate in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, and well-ventilated area, separate from incompatible materials such as strong bases and reducing agents. Label the container clearly and handle it under a chemical fume hood using appropriate personal protective equipment.
    Application of N-Fluoro-4-Methylpyridinium-2-Sulfonate

    Applications of N-Fluoro-4-Methylpyridinium-2-Sulfonate in Industrial Manufacturing

    N-Fluoro-4-Methylpyridinium-2-Sulfonate is a highly selective electrophilic fluorinating agent adopted in various precision industrial fields, supporting efficient introduction of fluorine atoms under mild process conditions. Our direct manufacturing experience enables tailored supply to specialized downstream sectors requiring elevated synthesis standards and traceable raw material certification.

    1. Active Pharmaceutical Ingredient (API) Fluorination

    Pharmaceutical companies rely on this agent for late-stage fluorination during the synthesis of complex APIs containing aromatic and heterocyclic frameworks. Its ability to selectively introduce fluorine at specific sites supports increased metabolic stability and improved bioavailability, particularly in target CNS and oncology drug candidates. Downstream processing routes typically employ this material during the final steps, utilizing scalable batch reactors with strict GMP controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 US cGMP regulations
    • EU GMP Annex 7: Manufacture of APIs
    • JP/EP/USP Pharmacopoeial Purity Specifications

    Typical usage ratio

    • 0.9–1.3 molar equivalents, adjusted based on desired fluorination site selectivity, substrate reactivity, and API synthetic route; lab-scale trials inform process development scale adjustments.

    Downstream process integration

    • Fluorination step integrated post-coupling or substitution reactions in intermediate API synthesis; introduced as solution in acetonitrile under controlled temperature phases (0–25°C) in batch or flow reactors.

    Final product types

    • Fluorinated small-molecule APIs for CNS, antitumor, and antiviral pharmaceuticals
    • Pharmaceutical intermediates for regulatory-compliant finished dose manufacturing

    2. Agrochemical Intermediate Synthesis

    Major agrochemical formulators use this fluorinating agent in the construction of crop protection active substances, especially for introducing aryl-fluorinated motifs into fungicides and herbicides. The agent enables late-stage site-selective fluorination that enhances target compound stability and alters physicochemical properties for field efficacy, while maintaining synthetic accessibility for scale-up.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Evaluation
    • ISO 9001:2015 Quality Management Systems for Agrochemical Manufacturing
    • REACH (EC) No 1907/2006 Registration, Evaluation, Authorization, and Restriction of Chemicals for Substances in Plant Protection Products

    Typical usage ratio

    • 0.8–1.6 molar equivalents, determined by substrate structure and desired fluorinated intermediate yield; pilot trials establish loading for minimizing side products.

    Downstream process integration

    • Added after key coupling or ring construction steps in multi-step synthesis, typically dissolved in polar aprotic solvents and reacted at 10–30°C; followed by purification through liquid-liquid extraction and column chromatography.

    Final product types

    • Fluorinated fungicide actives (e.g., triazole derivatives)
    • Selective fluorinated herbicide intermediates for downstream formulation
    • Active ingredient scaffolds for proprietary crop protection solutions

    3. Fine Chemical and Specialty Polymer Monomer Fluorination

    Specialty and performance polymer manufacturers source this fluorinating agent to synthesize fluorinated monomers for advanced material applications. Introduction of a fluorine atom at a controlled position on aromatic or heterocyclic monomers enhances chemical resistance, lowers surface energy, and improves dielectric characteristics of the resulting polymers. The agent is implemented during monomer functionalization, supporting end-markets such as electronics, coatings, and membranes.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems
    • ASTM D3182 (Standard Practice for Rubber – Compounding)
    • UL 94 Standards for Flammability of Plastic Materials (for end-use polymers)

    Typical usage ratio

    • 0.7–1.0 molar equivalents, chosen based on substrate structure and avoidance of over-fluorination; engineering controls ensure tight batch monitoring.

    Downstream process integration

    • Utilized in monomer conversion steps prior to polymerization, typically in batch reactors under controlled temperature (5–25°C) and inert atmospheres; post-fluorination monomers undergo distillation or recrystallization before polymerization.

    Final product types

    • Fluorinated styrenic or acrylate monomers for specialty polymers
    • Precursor chemicals for high-performance fluoropolymer coatings and films
    • Electronic-grade dielectric polymer raw materials

    4. Radiolabeling Precursors for PET Imaging Agents

    Medical isotope labs utilize this agent for the direct fluorination of small-molecule precursors in the production of positron emission tomography (PET) imaging tracers. Reliable incorporation of 18F or stable fluorine isotopes at defined aromatic sites is crucial for producing high-specific-activity markers for clinical diagnostic scans. The selective and rapid action of the reagent facilitates efficient radiolabeling under low-metal, high-purity process conditions.

    Industry compliance standards

    • Pharmacopoeial guidelines for radiopharmaceuticals (USP <823>, EP 5.19)
    • Current Good Radiopharmacy Practice (GRPP)
    • ISO 9001 and ISO 13485 for Medical Device Component Supply

    Typical usage ratio

    • 0.95–1.05 molar equivalents, precise adjustment to maximize specific activity and radiochemical yield; calibration involves aliquots and real-time radioactivity monitoring.

    Downstream process integration

    • Radiolabeling stage follows precursor synthesis, typically in microscale reactors under rigorously controlled timing and temperature; post-reaction, automated purification delivers injectable tracer formulations within applicable half-life windows.

    Final product types

    • 18F-labeled PET tracers for clinical and preclinical imaging
    • Radiolabeled diagnostic biomarkers for oncology, neurology, and cardiology scans

    5. Electronic Chemical Synthesis for OLED and Display Materials

    Display and lighting material producers depend on this agent to introduce fluorinated moieties into advanced organic compounds for OLED emitters, transport layers, and related optoelectronic materials. Fluorination at the correct aromatic position tunes photophysical properties and stability, critical for producing high-efficiency, long-lifetime display components. This step usually occurs during synthesis of key luminescent intermediates, with downstream purification ensuring strict performance consistency.

    Industry compliance standards

    • IEC 61249-2-44 (Materials for electronic assembly)
    • ISO 9001:2015 Quality Management for Electronic Material Manufacturing
    • IPC-4101 (Specification for Base Materials for Printed Boards)

    Typical usage ratio

    • 0.8–1.2 molar equivalents, chosen after yield and purity trials to optimize fluorinated intermediate quality and device reliability.

    Downstream process integration

    • Applied during synthesis of OLED monomer intermediates, typically as a final or penultimate step before chromatographic purification and crystallization prior to device fabrication.

    Final product types

    • Fluorinated OLED emitter molecules
    • Transport layer materials for display and lighting panels
    • Conductive organic compounds for electronic displays
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    Certification & Compliance
    More Introduction

    N-Fluoro-4-Methylpyridinium-2-Sulfonate: A Closer Look Inside Our Factory

    A Chemist’s Perspective on Our Unique Fluorinating Agent

    The workbench still carries the fine odor from our last trial batch of N-Fluoro-4-Methylpyridinium-2-Sulfonate. Here, the hands that mix, adjust, and observe come from years on the factory floor rather than recreation from a catalog listing. Our process for producing this compound does not aim for middle-of-the-road results. We push for maximum purity in every lot—our own instruments mark every step, from the start of the sulfonation to the last filtration, and every blend gets checked against our strictest standards.

    Why N-Fluoro-4-Methylpyridinium-2-Sulfonate Matters in the Lab

    Many organic transformations lean heavily on reliable and manageable sources of fluorine. N-Fluoro-4-Methylpyridinium-2-Sulfonate has become the choice of many experienced chemists because it brings the right mix of selectivity and safety. In our experience, you need a steady hand when working with fluorinating agents, and this one avoids the notorious volatility and unpredictability found in legacy reagents like elemental fluorine or DAST. End users in agrochemical and pharmaceutical research tell us that the compound slots into late-stage functionalizations, aromatic fluorination, and even selective alkene fluorination without imposing complex work-up or excessive side reactions. The reaction profiles from our batches rarely show the decomposition or over-fluorination that usually dogs less tailored agents.

    Specifications Backed by Years of Manufacturing Experience

    You will find that our N-Fluoro-4-Methylpyridinium-2-Sulfonate (sometimes designated by the model code NFMS-4173) routinely delivers a purity level that exceeds 99 percent by HPLC. Our batches tend to be fine, off-white crystalline powder, free-flowing, and extremely consistent. Packaged in airtight, light-protected HDPE containers directly from our climate-controlled filling line, the product maintains integrity through transit and storage. Moisture and ambient air pose no threats when handled under standard laboratory conditions—this is based on our repeated trials at varying scales, some of which pushed the evaporation point much harder than routine instructions ever do.

    Melting points typically fall between 150–158°C in our product, and NMR spectra give clean, straightforward signals. IR analysis confirms the expected sulfonate and N-fluoro patterns without ambiguous peaks. We minimize batch-to-batch variation through production scale tracking and twin feeds for both sulfonation and fluorination, ensuring that the final output in every drum matches our internal reference standard.

    How Chemists Use Our Material

    In the hands of a trained chemist, N-Fluoro-4-Methylpyridinium-2-Sulfonate gives predictable and robust performance as an electrophilic fluorinating agent. We've seen our material transform aryl, vinyl, allylic, and heterocyclic nucleophiles with high functional group tolerance. Because the compound stays shelf-stable for longer periods compared to alternatives, smaller labs and production chemists alike find comfort in knowing their inventory will not degrade between uses.

    Over the past several years, medicinal chemists in our network have described swapping out less selective fluorinating agents and reporting higher yields in their desired products as well as lower levels of downstream purification work. That feedback matches what we see during our own in-house tests, especially with complex multi-step syntheses that involve late-stage aromatic fluorination. The compound also supports reactions under milder conditions, with less need for inert-atmosphere techniques, allowing for easier use in both small and large reactors.

    Differences from Other Fluorinating Agents

    We started producing N-Fluoro-4-Methylpyridinium-2-Sulfonate because we saw an industry-wide need for a more controlled approach to electrophilic fluorination. Many alternatives—Selectfluor, NFSI, or elemental fluorine-based agents—fall short in terms of control or safety. Selectfluor, while long-standing and widely used, can be less selective during aromatic substitutions, often producing byproducts that complicate downstream separation. Handling and disposal also introduce added regulatory burdens in many regions. N-Fluoro-4-Methylpyridinium-2-Sulfonate, by contrast, allows chemists to dial in selectivity and reactivity through straightforward process modifications, and our plant operations show the difference in waste streams and process emissions.

    NFSI tends to react sluggishly and relies on metal co-catalysts or higher temperatures that increase risk in larger scale settings; our product overcomes these challenges by working efficiently without resorting to excess energy input. The process waste profile in our factory’s effluent log shows that switching to our fluorinating agent has cut the amount of hazardous waste by almost thirty percent over traditional solutions, because reactions run cleaner and fewer impurities require quenching by extensive washing stages. Our experience with in-process controls and tight QC have kept us well within contemporary environmental standards—something not every process can claim.

    Safety Observations from Plant and Lab

    You want assurance that your chemicals behave on the bench and in the plant. In direct handling during thousands of small- and mid-scale preparations, our operators have seen predictable behavior when working with N-Fluoro-4-Methylpyridinium-2-Sulfonate. Little dust raises during weighing, and the absence of pungent or irritating fumes means containment and PPE requirements match those of common bench reagents, not high-hazard class chemicals. During accidental spills, site teams find cleanup straightforward—brush, scoop, and standard neutralizing procedures. Only twice during the past decade did a product batch receive a deviation from our internal safety evaluation, both times traced to input material variation, not process weakness.

    Some customers ask about toxicity compared to older fluorination reagents. We ran our own series of animal-alternative cytotoxicity assays, and, based on those, the compound avoids many of the acute hazards found with sulfur tetrafluoride or DAST. The safety margin allows more flexibility on the shop floor. Even summer interns—our most novice hands—can confidently follow handling protocols without running extra risk, and we design training around real-world observations, not just regulatory minimums.

    Process Optimizations and Plant Innovations

    Producing N-Fluoro-4-Methylpyridinium-2-Sulfonate to high standards requires more than simply following published procedures. Our plant spent years perfecting a closed-cycle fluorination train, recovering spent gases and channeling thermal energy into nearby synthesis steps to cut waste. Engineers added inline analyzers—each drum and kilo passes through at least three sets of sensors—so every shift operator knows on the spot whether the batch hits purity marks. We take pride in the feedback loops between R&D and production. If a single drum deviates from our tight melting-point window, the corrective root cause traces back through supply chain and process logs before anything leaves the plant floor.

    We also redouble our focus on reducing trace metal contamination. While the underlying chemistry does not require metals, plant-wide audits check all glass and vessel linings for leaching or cross-contamination, and cleaning protocols follow the same rigor as the pharmaceutical-grade lines we operate inside the same facility. These steps cut risk for sensitive applications, including those intended for later transformation to APIs or reference standards.

    Feedback from the Chemists Using Our Product

    Direct consultation with process chemists, academic researchers, and pharmaceutical team leads informs most of our ongoing adjustments. Over the past year, several partners trialed our batches in new catalytic cycles, especially those demanding high functional group compatibility in late-stage fluorination. They reported stepwise improvements in both conversion and selectivity. High-throughput facilities point to improved process reproducibility when using our material over name-brand competitors. Experienced synthetic chemists say the predictable stoichiometry and clean mass balance have cut cycle times in multi-step programs.

    Beyond conversion data, the reduction in clean-out times and improved yields enables five to ten additional runs per month in larger reactor suites. More subtle feedback comes from researchers focusing on ^18F-labeling for PET imaging precursors, who find the compound’s stability a relief compared to more labile electrophilic reagents. The hands-on input pushes us to maintain close partnerships and adjust the drying, particle sizing, and packaging where the research demands it.

    Challenges and Practical Solutions We Have Encountered

    Nobody working in chemical manufacturing ignores the scalability question. What happens on a 100-gram prep differs from what comes out of the 100-kilo drums. Our experience scaling N-Fluoro-4-Methylpyridinium-2-Sulfonate since our pilot plant days reveals that heat management plays a much greater role in keeping the reaction stable than most protocols admit. Reactors fitted with distributed thermal sensors and rapid nitrogen purges prevent runaway reactions as the batch size grows. We learned this lesson the hard way in our earlier scale-ups—several test runs produced color shifts and odor changes pointing to exothermic slips. In response, we integrated narrower feed control algorithms into our DCS, so the critical fluorination step never outpaces available cooling.

    Another routine challenge concerns input purity, especially for the pyridine ring and sulfonating agents. Adulterated or impure feedstock derails batch yields and pulls down the ultimate reactivity of the product. Partnering directly with upstream material suppliers, we implemented a double-certification protocol for both input and finished material. Chromatographic fingerprinting of every input lot now lines the plant’s incoming goods dashboard. This direct oversight closes the loop between what goes into the reactor and what emerges into the drum.

    Environmental Impact and Sustainability in Practice

    Environmental stewardship stands behind every decision we make around our fluorinating product lines. Routine waste audits revealed early on that older fluorine reagents, particularly those volatile under ambient conditions, generated up to 45 percent more waste requiring hazardous landfill or special incineration. With N-Fluoro-4-Methylpyridinium-2-Sulfonate, controlled process emissions and benign byproducts cut that load substantially. In one quarter, documented waste output from the plant dropped by more than a third after switching over from legacy compounds, verified by external compliance inspectors.

    Solvent recovery receives as much attention as product purification. The fluorination step runs with solvent systems that we distill and reuse in nearby product lines, providing both economic and environmental benefits. Plant recirculation systems capture more than 80 percent of volatile organics produced during each run and redirect them into scrubbers and solvent storage. This cyclical focus not only provides a check on environmental impact—it also ensures we sidestep unnecessary regulatory overhead.

    Operational Reliability and Logistics

    Reliable product delivery depends as much on what happens outside the reactor as in it. Our QA technicians sign off on every drum after a full panel of tests—purity, moisture, residue on ignition, and shelf-life check. Warehousing keeps storage at defined humidity and temperature, so when the material leaves the plant, it arrives in the same state as the day it was filled. Over five years, our customer-reported complaints due to quality drops amounted to less than a fraction of a percent of all shipped product.

    Working closely with logistics partners helps us respond quickly to large and rush orders, yet shipping remains uneventful because our product’s physical and chemical profile resists degradation, caking, or clumping. We teach new warehouse staff to spot damage during packing and emphasize the importance of light-protection, a step which emerged from early customer reports about off-color batches caused by exposure in poorly lit storage sites.

    Practical Applications in Industry and Research

    Research and production both find a home for N-Fluoro-4-Methylpyridinium-2-Sulfonate. Custom synthesis shops take advantage of precise fluorination in pathways for agrochemical lead compounds, producing analogs with improved biological uptake and environmental persistence profiles. Larger manufacturers running kilo and ton-scale operations avoid unnecessary downtime and inventory write-offs by relying on its predictable shelf-stability. In the pharmaceutical sector, pathway developers trust the material's selectivity for late-stage aromatic ring modification, often bypassing multi-step protection and deprotection routines that add months to project timelines.

    Academic collaborators submit their own validation data, showing high-yielding transformations with less cleanup required. Their feedback confirms that our well-calibrated process for producing N-Fluoro-4-Methylpyridinium-2-Sulfonate succeeds in enabling broader research flexibility, freeing up valuable instrument and personnel time. We have also supported university research into new reaction mechanisms, sharing insights and selected batches for advanced kinetic and mechanistic studies, further strengthening the scientific basis for its use.

    Continuous Quality Improvement Informed by Data

    On our factory floor, each month brings in new measurement, process data, and observations. We believe that real-world experience, not just quality certifications, drives improvement. Production logs tie in with quality control files, and deviation trends prompt rapid process tweaks when necessary. We operate a feedback board directly accessible to every technician and chemist; responses move from observation to process adjustment inside a single shift. Ongoing conversations with long-term customers capture niche application data points that sometimes alter not just our production, but also how we format and share technical information.

    A culture of transparency has become a safeguard for sustained quality. By mapping deviation sources and near-misses, we sidestep systemic risk before it affects the next batch. Field data shapes standard operating procedures, and recurring incidents prompt retraining and, if necessary, recalibration of both physical equipment and written protocols. Maintenance teams sometimes spot small process improvements—such as quicker changeovers between runs or more efficient filter changeout—that collectively preserve the highest possible standard in every drum.

    Moving Forward: Product Innovation Anchored in Practice

    Our story of producing N-Fluoro-4-Methylpyridinium-2-Sulfonate demonstrates the value of deep familiarity with process and product. We do not wait for someone else to define the next generation of fluorinating agents. R&D works directly with the plant, running weekly meetings where every side can bring concerns, observations, and new data. Often, it is the floor-level chemist that spots a trend or challenge that then seeds the innovation steps for new applications or improvements. Whether a medical chemistry team needs a tighter particle size range or an agrochemical associate wants a fresh batch in a custom size, our lines flex quickly because operators and supervisors both understand the chemistry and the industrial realities behind every batch.

    Future opportunities for N-Fluoro-4-Methylpyridinium-2-Sulfonate include tunable reactivity through structural modification—something we have begun trialing internally with select partners—and further reducing the environmental load of both input and waste streams. As regulatory requirements evolve, our direct relationships with compliance auditors and certification bodies enable us to meet or exceed new expectations without disruption.

    The production story of N-Fluoro-4-Methylpyridinium-2-Sulfonate is not limited to a chemical formula and a list of applications—it is the result of hands-on work, learning from each successful drum and every challenge along the way. Through openness, practical experience, and a drive for continual improvement, we support chemists and manufacturers working on the next generation of discoveries.