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2,6-Difluorobenzenesulfonamide

    • Product Name 2,6-Difluorobenzenesulfonamide
    • Alias DFBSA
    • Einecs 238-601-1
    • 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

    607224

    Substance Name 2,6-Difluorobenzenesulfonamide
    Cas Number 825-34-3
    Molecular Formula C6H5F2NO2S
    Molecular Weight 193.17
    Appearance White to off-white solid
    Melting Point 96-99 °C
    Smiles NS(=O)(=O)C1=C(F)C=CC=C1F
    Iupac Name 2,6-difluorobenzenesulfonamide
    Solubility Slightly soluble in water; soluble in organic solvents such as methanol and ethanol
    Synonyms 2,6-Difluorobenzenesulfonamide; Benzenesulfonamide, 2,6-difluoro-

    As an accredited 2,6-Difluorobenzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,6-Difluorobenzenesulfonamide, with a tamper-evident screw cap and hazard labeling.
    Shipping 2,6-Difluorobenzenesulfonamide is typically shipped in sealed, chemical-resistant containers to prevent contamination and moisture absorption. The package should comply with national and international regulations for non-hazardous laboratory chemicals, including proper labeling and documentation. Storage during shipping should be at ambient temperature, away from strong acids, bases, and oxidizing agents.
    Storage 2,6-Difluorobenzenesulfonamide should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store at room temperature whenever possible, avoiding extremes of heat or cold. Clearly label the container and ensure easy access for authorized personnel only.
    Application of 2,6-Difluorobenzenesulfonamide

    Applications of 2,6-Difluorobenzenesulfonamide in Industrial Manufacturing

    2,6-Difluorobenzenesulfonamide serves as a specialized intermediate in multiple advanced chemical sectors. As a manufacturer directly supplying this material, we support customers in pharmaceutical, agrochemical, polymer modification, and specialty chemical synthesis channels. The following sections present the detailed industrial applications, focusing on genuine downstream integration, process controls, and real-world compliance demands.

    1. Pharmaceutical Intermediate for Antibacterial Drug Synthesis

    Pharmaceutical manufacturers incorporate 2,6-difluorobenzenesulfonamide in the multi-step synthesis of select fluoroquinolone derivatives and sulfonamide-based antibacterial agents. The specific substitution pattern on the aniline nucleus aids in achieving high activity and pharmacokinetic profiles. This intermediate enters initial or penultimate steps, depending on the molecule design, and must meet strict impurity limits and traceability documentation under cGMP operations.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: US FDA Current Good Manufacturing Practice (cGMP) for Finished Pharmaceuticals
    • EP Monograph 203: General Requirements for Pharmaceutical Intermediates
    • USP General Chapter <467>: Residual Solvents

    Typical usage ratio

    • 10%–25% by mass relative to final API structure, adjusted according to target compound molecular weight and synthetic route.

    Downstream process integration

    • Utilized in nucleophilic substitution or amidation step prior to cyclization or final functionalization.
    • Controlled addition via batch or semi-batch reactors under dry, inert atmosphere.
    • In-process QC monitored by HPLC for byproduct analysis and residual starting material.
    • Integration into solid-liquid separation and crystallization steps for purification.

    Final product types

    • Oral and parenteral fluoroquinolone antibiotics (e.g., levofloxacin, ciprofloxacin derivatives)
    • Second-generation sulfonamide drugs
    • Combination antibacterial therapies (fixed-dose combinations)
    • Pharmaceutical grade intermediates for contract manufacturing

    2. Agrochemical Active Ingredient Intermediate

    Agrochemical formulators rely on 2,6-difluorobenzenesulfonamide in the synthesis of select fluorinated sulfonylurea herbicide actives and fungicidal agents. Its difluoro-substituted benzene ring enhances biological activity and environmental stability of downstream crop protection chemicals. We supply material with defined particle size and purity for direct integration into laboratory-scale synthesis or industrial pilot stages.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006 Registration
    • ISO 9001:2015 Quality Management Systems
    • EPA 40 CFR Part 158: Data Requirements for Pesticide Registration (USA)

    Typical usage ratio

    • 5%–15% by mol in the synthesis step, exact proportion selected per stoichiometric demand of sulfonylurea coupling.

    Downstream process integration

    • Charged directly into the condensation step with urea or amino-pyrimidine derivatives.
    • Utilized under inert conditions with acid or base catalysis as defined by the agrochemical synthetic protocol.
    • Feeds into continuous or batch production lines, adapted for pilot to commercial scale.
    • Monitored by GC-MS for process residue and in-line HPLC for intermediate verification.

    Final product types

    • Selective post-emergence herbicides (sulfonylurea class)
    • Systemic fungicidal actives with high environmental persistence tolerance
    • Pre-formulation intermediates for seed treatment products
    • Bulk agrochemical reagents for tolling and contract crop science applications

    3. Monomer Modifier in High-Performance Polymers

    Polymer compounders introduce 2,6-difluorobenzenesulfonamide as a monomeric modifier or chain-terminating group for engineering plastics with tailored chemical resistance and thermal properties. Its unique difluoro functionality imparts enhanced hydrophobicity and improved flame retardance in select copolymer matrices. Careful control of inclusion level ensures property consistency and regulatory compliance in high-value, performance-driven markets.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for Chemical Products
    • ROHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94: Standard for Tests for Flammability of Plastic Materials
    • ISO 9001:2015 for process and batch documentation

    Typical usage ratio

    • 0.5%–2% by weight in the polymer batch, optimized by molecular weight and target mechanical or flame-resistance properties.

    Downstream process integration

    • Added at the initial polymerization feed stage or during reactive extrusion processes.
    • Mixing performed under nitrogen atmosphere to avoid hydrolysis of sulfonamide group.
    • Continuous monitoring by FT-IR for incorporation efficacy and batch-to-batch consistency.
    • Post-polymerization purification for removal of unreacted modifier as per QC protocols.

    Final product types

    • High-temperature resistant engineering plastics (e.g., polyaryl ether ketones, fluorinated polyamides)
    • Flame-retardant wire coatings
    • Specialty polymer foams for electronics encapsulation
    • Modified copolymers for aerospace and automotive parts

    4. Fine Chemical Synthesis for Specialty Dyes and Pigments

    Producers of specialty dyes and high-performance pigments use 2,6-difluorobenzenesulfonamide as a building block in synthesizing fluorinated azo and sulfonamide-functional colorants. Its reactive sulfonamide group enables targeted coupling and post-functionalization steps, yielding pigments with high lightfastness and chemical inertness. Manufacturers require strict lot-to-lot purity and metal trace control to prevent color deviations in downstream coatings or inks.

    Industry compliance standards

    • ETAD Code of Practice for Responsible Care in the Dye and Pigment Industry
    • REACH Annex XVII: Substances of Very High Concern (SVHC) Requirements
    • EN 71-3:2019 for Toy Safety (Migration of Certain Elements in Pigments)
    • ISO 14001:2015 for dyehouse and pigment production environmental management

    Typical usage ratio

    • 2%–10% by mol relative to primary diazo component in the pigment molecule; variable based on molecular design and end-use lightfastness targets.

    Downstream process integration

    • Entry as a coupling partner during diazotization or transsulfonamidation stages.
    • Reaction staged in glass-lined reactors under temperature control for pigment homogeneity.
    • Success tracked via UV-vis analysis and batch colorimetry.
    • Final purification by solvent extraction and membrane filtration for inclusion in masterbatches.

    Final product types

    • Solvent-resistant fluorinated azo dyes for plastics and fibers
    • Sulfonamide-bridged pigments for industrial paints and coatings
    • High-stability printing inks for commercial printers
    • Specialty colorants for automotive and high-visibility textile markets
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    Certification & Compliance
    More Introduction

    2,6-Difluorobenzenesulfonamide: Reliable Chemistry for Advanced Applications

    Direct Insight from the Manufacturer’s Lab Bench

    Chemical manufacturing walks a fine line between creativity and precision. Every compound we make leaves a trace of our practical knowledge and commitment. 2,6-Difluorobenzenesulfonamide stands out for us not only because of its reliable behavior in the lab, but also its consistent performance under demanding industrial conditions. We have been routinely producing this compound in our dialyzed reactors for nearly a decade. From the earliest syntheses, we saw how minute tweaks in temperature or solvent selection could tip the yield or purity, teaching us everything worth knowing about its chemical quirks.

    This compound carries the chemical formula C6H5F2NO2S, with fluorine atoms settled at the 2 and 6 positions on the benzene ring. The difference is more than symbolic — that precise placement makes all the difference in a molecule’s reactivity, melting point, and compatibility with other reagents. Over many production runs, our technical staff noticed that even minor impurities can affect downstream activity, especially in pharmaceutical or agrochemical synthesis. Control isn’t just a catchphrase here; we verify each lot using a combination of HPLC, NMR, and GC, ensuring our clients gain predictable performance batch after batch.

    Over time, chemists have found sulfonamides indispensable when they need both stability and specific reactivity. 2,6-Difluorobenzenesulfonamide, in particular, is favored for its unique profile. Compare it to its mono-fluorinated cousins or the non-fluorinated sulfonamides; they don’t match its electronic influence on the benzene ring. This has a practical consequence: reactions tend to proceed differently, especially nucleophilic substitutions, because those two fluorines at ortho positions sharply reduce the electron density. Through hundreds of kilogram-scale syntheses, we have verified that its crystalline form packs tightly, flows easily from storage bins, and withstands temperature variance across shipping routes.

    Production Realities and Specification Insights

    Every chemist asks about purity, but only a few push for the truth behind those numbers. Our production batches regularly reach >99% chemical purity as established by calibrated HPLC methods against certified standards. Water content tends to hover under 0.2% due to rigorous rotary vacuum drying. If left unchecked, small amounts of water threaten condensation reactions that clients need to avoid, so we maintain moisture control systems at every filtration stage.

    Compared to other sulfonamide derivatives, 2,6-Difluorobenzenesulfonamide doesn’t behave as a simple analog. The presence of two fluorines means it resists hydrolysis and displays an elevated melting point in the neighborhood of 140-145°C, depending on residual solvent traces. Customers in Japan and North America have told us that this robustness leads to fewer line stoppages during processing, as the compound resists breakdown under standard conditions.

    Years ago, in the early years of our scale-up, we learned this molecule demands patience and care in its reaction workup. Filtration speed slows slightly compared to non-halogenated sulfonamides because the product tends to form a dense cake. Our operators have adapted filtration methods, adjusting vacuum pressures and optimizing filter media to match this specific tendency. It may sound trivial, but these adaptations eliminate reprocessing steps for our customers downstream, saving hours of lost time.

    Where 2,6-Difluorobenzenesulfonamide Finds Its Value

    This compound plays a background but essential role in a range of industries. Medicinal chemistry teams rely on its unique balance of hydrophobicity and reactivity; it finds its place as a starting material for enzyme inhibitors, herbicides, and anti-microbial candidates.

    Many research teams tell us their projects live or die by the consistency of sulfonamide intermediates. Any batch-to-batch variability — even at ppm levels — can derail scale-up projects or force revalidation in regulated environments. Over the years, our production floor received detailed feedback from scientists troubleshooting unexpected assay drop-offs or LC-MS anomalies traced back to trace contaminants. These conversations pushed us to refine our recrystallization protocols and invest in higher-resolution analytical tools, not just to fill a spec sheet but to meet the real expectations of working chemists.

    Agricultural chemistry also finds value in 2,6-Difluorobenzenesulfonamide. Its two fluorines confer environmental persistence, helping downstream products function under challenging field conditions. We understand these requirements because we have worked alongside formulating teams struggling to stabilize active ingredients under high UV or humidity exposure. Our compound performs reliably, letting formulation chemists focus energy on other complex tasks.

    Distinctives That Set This Sulfonamide Apart

    It’s tempting to look at a chemical family and assume close cousins behave the same way. With sulfonamides, subtlety matters. By positioning fluorines at the 2 and 6 spots, we alter the entire reactivity landscape. From our hands-on work, we see how this compound offers greater resistance to nucleophilic attack and boosts shelf-stability. 4-Fluorobenzenesulfonamide or 3,5-difluoro analogs, which we’ve also synthesized, don’t match the stubborn longevity of the 2,6 version.

    Formulators manufacturing API intermediates or agrochemicals gain more than just another fluorinated building block. The difference shows up in every stage: mixing, dissolving, reacting, and isolating. Just last year, one customer reported that switching to our 2,6-difluoro variant shaved several steps off their isolation protocol, improving throughput without additional stabilizers or additives.

    Why Consistency Really Matters

    Process engineers judge a supplier’s worth on more than price. Repeatability, no surprises, and genuine technical backup make the difference on a busy plant floor. We have lived through the consequences of minor deviations. One winter, an abnormally cold storage room led to crystal agglomeration, complicating redispersion for a customer’s pilot batch. We built contingency plans, retrained warehouse staff, and installed backup heaters. From experience, we know sharp eyes at every stage can head off downstream complications.

    Each shipment undergoes a gauntlet of tests, beyond standard specs. White crystalline powder means nothing if elemental impurities or batch memory creep in. Using ICP-MS and qNMR, our QC staff hunt down trace metals or legacy solvents. This level of scrutiny is no longer just for pharmaceutical lots; crop science innovators demand the same rigor, and we believe every client deserves nothing less.

    Clients draw heavily on our technical support to troubleshoot new reactions. Internally, we keep detailed production logs, dating back years, to support troubleshooting and root-cause analysis. This transparency and retention of institutional memory directly supports research teams working against tight deadlines.

    Practical Tips from Hands-on Production

    Years of batch records and operator logbooks taught us more than any textbook. Every run tells a different story. By working directly with the organic phase, our staff learned that solvent quality and degassing matter more than theoretical purity, particularly at scale. High-purity solvents prevent side reactions, but fresh solvent stocks also reduce the risk of introducing moisture, which is always the enemy in sulfonamide chemistry.

    Temperature control isn’t just about hitting the right number on the PID readout. Certain steps during sulfonation demand slow addition and tight control to prevent overreaction or decomposition, especially with electron-deficient aromatics like this one. Over-cooling could trigger premature crystallization, complicating downstream isolation, so our reactors use both active cooling and heating jackets for rapid response. These improvements cut down batch times and help maintain close to theoretical yields.

    Safety stays front and center. Fluorinated organics deserve respect, not only for their stability but also for their sometimes stubborn persistence in the environment. Our production lines feature specialized scrubbers and waste handling to capture trace fluorinated emissions. These precautions go beyond regulatory minimums and come from firsthand experience, not a checklist.

    Looking Beyond Purity: Customer-Driven Adjustments

    Sometimes, customers require tighter specs or tailor-made physical forms. We have retooled our crystallization procedures to deliver customized particle sizes or flow characteristics, depending on process needs. By working with clients on collaborative pilot runs, we share learnings and co-develop methods to address nonstandard requests, whether that involves semi-bulk packaging, direct charging, or integrating into closed systems. These adaptations emerge from customer partnership, not marketing formulas.

    Over the past few years, data-driven QC initiatives sharpened our sense of what really matters to end-users. Trend tracking flagged subtle links between storage rh and batch stability, prompting us to update our warehouse humidity controls. It’s not just about ticking off a requirements list — every practical improvement stems from real feedback.

    Tracing the Full Production and Supply Chain

    Supply chain reliability enters every product conversation, whether explicitly or not. From our location close to core chemical precursors, we control sourcing for both benzene sulfonation and fluorination sources. Over time, we’ve built direct partnerships with upstream raw material producers, which improves risk management and lets us enforce traceability all the way back to base chemicals. Process audits and periodic supplier visits keep standards high, heading off issues before they reach the shop floor.

    Real events tested these connections. During a raw material crunch two years ago, our advance purchases and strong supplier links meant we haven’t missed a delivery window, even as market prices surged. Such resilience doesn’t happen by accident; it grows from consistent, direct supply relationships and an understanding of both upstream chemistry and logistics.

    Regulatory and Compliance Mindset

    Chemicals cross more than international borders. They move through a maze of regulatory, customs, and safety checks. Clients in pharmaceutical, agrochemical, and specialty materials sectors expect nothing less than full documentation. Over the years, our compliance team built a playbook for international shipments of 2,6-Difluorobenzenesulfonamide, backed by certified COAs, SDS, and specialized transportation packaging. Audits — both planned and impromptu — have shaped our document control and record-keeping practices.

    Compliance stays current, adapting as safety regulations evolve. As global chemical controls grow stricter, our teams stay ahead by monitoring policy developments and anticipating reporting requirements. It’s not about what’s enough for now; it’s about what’s necessary for the future of responsible chemistry.

    Why Chemists Keep Turning to 2,6-Difluorobenzenesulfonamide

    After years of manufacturing, we have heard stories of breakthrough syntheses, last-minute project rescues, and successful product launches — all enabled by the qualities of this compound. Though 2,6-Difluorobenzenesulfonamide may seem like a niche product in a crowded market, its value is proven by the repeat orders, detailed technical queries, and customer loyalty we see year after year.

    In any line of chemical manufacturing, the best-laid plans can falter if the raw materials do not deliver as expected. Scientists need not only purity but also process reliability, stable physical handling, and swift support when troubleshooting is required. That perspective shapes every stage of our operation. From raw material selection to the last shipment off the loading dock, we take every measure to keep variables in check, letting researchers and engineers focus on discovery, production, and progress.

    Conclusion: A Compound Forged in Real-World Chemistry

    2,6-Difluorobenzenesulfonamide represents more than a name on a bottle or a line on a balance sheet. It is the outcome of years of practical learning and adaptation, forged in the challenges of daily production and relentless problem-solving. Its unique arrangement of atoms offers the chemical world a distinct tool, one shaped as much by hands-on experience as by molecular diagrams. We remain committed to supplying this key product, standing by both its reliability and the collaborative spirit that built it into what it is today.