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HS Code |
207169 |
| Productname | 3,4-Difluorobenzenesulfonamide |
| Casnumber | 57326-00-8 |
| Molecularformula | C6H5F2NO2S |
| Molecularweight | 193.17 |
| Appearance | White to off-white solid |
| Meltingpoint | 99-103°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | NS(=O)(=O)c1ccc(F)c(F)c1 |
| Inchi | InChI=1S/C6H5F2NO2S/c7-4-1-2-5(6(8)3-4)12(9,10)11/h1-3H,9H2 |
| Synonyms | 3,4-Difluoro-benzenesulfonamide |
| Storagetemperature | Room temperature |
As an accredited 3,4-Difluorobenzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package contains 3,4-Difluorobenzenesulfonamide in a sealed amber glass bottle with a secure screw cap and hazard label. |
| Shipping | 3,4-Difluorobenzenesulfonamide is shipped in tightly sealed containers to prevent moisture and contamination. It is transported according to standard chemical safety regulations, typically at ambient temperature. Proper labeling and documentation are included. Handle with care, ensuring the package avoids excessive heat, direct sunlight, and incompatible substances during shipment. |
| Storage | 3,4-Difluorobenzenesulfonamide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep within a cool, dry, well-ventilated area. Avoid incompatible materials such as strong oxidizers and bases. Ensure proper labelling and store at room temperature unless otherwise specified by safety data. Use secondary containment to prevent spills or leaks. |
Applications of 3,4-Difluorobenzenesulfonamide in Industrial Manufacturing3,4-Difluorobenzenesulfonamide serves as a specialized chemical intermediate in several advanced manufacturing sectors. With well-characterized structural features, it contributes to complex synthesis routes where strict process and quality controls define production outcomes. Below we outline established downstream application scenarios, each grounded in precise industry practice and compliance standards. 1. Pharmaceutical Intermediate for Sulfonamide-Based APIsWithin pharmaceutical synthesis, 3,4-difluorobenzenesulfonamide enters as a building block for active pharmaceutical ingredients (APIs) based on sulfonamide scaffolds. It supports synthesis where positioning of fluorine atoms affects pharmacological activity and bioavailability. Process chemists add it during multi-step reactions leading to final drug intermediates, adjusting its ratio to optimize yield and reaction selectivity according to the specific molecular target. Validation under regulated environments, including batch documentation and impurity profiling, is mandatory for API supply chains. Industry compliance standards
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2. Agrochemical Intermediate for Synthesis of HerbicidesAgrochemical manufacturers introduce 3,4-difluorobenzenesulfonamide as a key intermediate in the multi-step construction of sulfonylurea and related herbicide active substances. Its fluorinated sulfonamide group confers high selectivity and environmental persistence, making it essential in proprietary process schemes. Process engineers incorporate it during cyclization or coupling with other aromatic or heterocyclic units, streamlining production workflows for regulatory-conforming agrochemical actives. Industry compliance standards
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3. Specialty Intermediate for Electronic ChemicalsAdvanced microelectronics fabrication relies on ultra-high purity precursors during production of photoresist and etching agents. 3,4-difluorobenzenesulfonamide functions as a precursor in developing fluorinated sulfonamide additives, which modulate resist sensitivity and process window in lithography. It enters downstream formulation via solution mixing or melt compounding, followed by stringent purification and QC for trace metal, anion, and organic contaminant elimination. Product lots must pass exacting particle size and residue release specifications. Industry compliance standards
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4. Intermediate for Synthesis of Performance PolymersManufacturers of fluorinated engineering polymers and specialty elastomers utilize 3,4-difluorobenzenesulfonamide for introduction of sulfonamide groups which significantly alter polymer dielectric and surface energy properties. Formulators add this compound during copolymerization, usually via solution or bulk polymerization routes, ensuring precise stoichiometric balance for structural integrity and final polymer property targets. Extensive pre-polymerization quality checks and batch records govern its controlled input and traceability. Industry compliance standards
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5. Intermediate for Fluorinated Chemical Synthesis in Fine ChemicalsProducers of advanced fluorinated fine chemicals deploy 3,4-difluorobenzenesulfonamide at key points in the synthesis of custom molecules for dyes, UV stabilizers, or specialty reagents. Chemists rely on its unique substitution pattern to fine-tune electronic effects in end-molecules, integrating the raw material at precise stages such as sulfonamide introduction or as a leaving group. Application batches observe careful solvent selection and reaction parameter optimization to suppress byproduct formation and enhance downstream material performance. Industry compliance standards
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As a manufacturer with decades of experience in the aromatic sulfonamide sector, our team brings hands-on perspective to the production and application of 3,4-Difluorobenzenesulfonamide. Through the years, we’ve witnessed changes in the chemical market, shifts in research priorities, and the rising demand for specialized intermediates. Our own facility produced the first kilogram of this compound more than ten years ago, back when requests from pharmaceutical labs and agrochemical companies still trickled in as small, custom orders. Over time, 3,4-Difluorobenzenesulfonamide has worked its way into broader markets, drawing steady attention from R&D teams, early-stage process engineers, and scientists developing new molecules.
The push for halogenated benzene derivatives stems from their utility in pharmaceutical synthesis. The fluorine atoms at the 3 and 4 positions of this sulfonamide ring enable chemists to build more stable, selective, and sometimes more potent drug candidates. Our chemists often remark how a seemingly simple structural change, such as adding two fluorines, impacts the compound’s metabolic profile and reactivity. In our experience, this difference leads to fewer off-target effects when used in drug discovery applications. In the field of materials science, the same features offer predictable electronic properties.
We manufacture 3,4-Difluorobenzenesulfonamide under strict process control, drawing on both traditional and modern chemical engineering. By controlling temperature and pressure profiles at each stage, we maximize yield and minimize by-products. These controls also avoid problems like sulfone formation via over-oxidation, which we learned to address only after considerable troubleshooting in our earlier years.
Our production lines focus on delivering material to tightly defined specifications. Every batch undergoes HPLC and GC-MS checks, not just for documentary purposes but because even trace impurities can affect synthesis in a pharma-grade setting. Over many runs, we finetuned our drying process to consistently hit moisture levels below 0.3%. From experience, we know that excessive water can impact subsequent coupling reactions or cause issues during crystallization. The product presents as a white to off-white crystalline solid, with a melting range that sits comfortably within the specification window required by most end-users.
Solubility challenges always surface with aromatic sulfonamides. In the early days, customers repeatedly contacted us about solubility profiles in various organic solvents. Our R&D team tracked stability and dissolution in acetonitrile, DMSO, ethyl acetate, and even less common solvents, so we could provide reliable guidance instead of generic statements. This practical insight helped customers avoid frustrating delays during pilot experiments.
Over time, we shifted from small glassware reactions to multi-hundred kilogram reactor runs. At each scale, a unique roster of hurdles appeared—from mixing issues in larger vessels to challenges with heat transfer. Our engineers implemented modifications to stir settings to keep the sulfonamide fully suspended and to prevent clumping, especially during temperature ramps. Waste management techniques adapted too: rather than relying on wasteful solvent extraction, we invested in vacuum distillation lines, capturing volatile by-products efficiently and reducing our environmental impact. Direct feedback from established partners in the pharma sector helped us sharpen our specifications, tightening acceptable impurity levels and adjusting particle size to meet evolving standards.
Pharmaceutical chemists often leverage 3,4-Difluorobenzenesulfonamide as a versatile building block. It fits into synthetic pathways that create enzyme inhibitors, antifungal agents, and even kinase modulators. The presence of difluoro groups confers distinct metabolic stability, something medicinal chemists prize when screening compound libraries. We’ve seen research teams streamline their workflows by starting with our material, shaving weeks off their timelines by sidestepping extra purification steps.
Apart from pharmaceuticals, agricultural companies reach out for this sulfonamide when developing crop protection agents. We’ve heard repeated stories from partners whose leads reached testing stage faster because of the consistent quality of our batches. Some found that comparable compounds, lacking substitution in the 3 and 4 positions, showed reduced biological activity or less favorable environmental profiles.
We also supply universities, where students and faculty explore new cross-coupling techniques and reaction mechanisms. It’s rewarding to see papers published on new methods that started with material shipped from our production floor.
Working with both fluorinated and non-fluorinated sulfonamide derivatives taught us to appreciate subtle differences that make substantial downstream impact. The 3,4-difluoro configuration makes this material less reactive under standard nucleophilic aromatic substitution compared to less substituted rings, which pushes chemists to adjust their conditions. We’ve tested dozens of reaction scenarios in our own labs, sharing findings with partners who seek to optimize transformations involving metal catalysts or specific coupling agents.
Compared to mono-fluorinated or unfluorinated derivatives, the 3,4-difluoro variant displays earlier onset of melting, which translates to easier purification by recrystallization under suitable conditions. Its increased resistance to oxidative degradation also allows for longer shelf life—feedback we often hear from storage facility managers and warehouse teams. Handling is safer because the sulfonamide core resists hydrolysis better, especially important when bulk drums might travel across different climates during shipping.
Our philosophy centers on bringing the customer’s voice into every production and R&D meeting. Feedback on real-world usage—good or bad—drives continuous process updates. More than once, a customer call about an unexpected impurity or handling issue spurred investigation, leading to a new purification step or process tweak. One agricultural scientist reported trouble forming a crucial intermediate; by tracing the issue, we discovered a minor side-reaction unique to that scale, which we now routinely check before release.
Regulatory challenges evolve year to year. Clients in Europe and North America, facing stricter limits on residual solvents and metal contamination, prompted upgrades to our in-line monitoring equipment. As we adapted, batch records became more comprehensive, with lot-specific traceability linking QC results to each production run. Researchers using our 3,4-Difluorobenzenesulfonamide can trace every drum to origin, supporting compliance and audit readiness. This practical transparency, more than stackable certificates or statements, ensures trust and long-term partnerships.
Many requests now focus on the interface between research and industrial scale. Early-stage scientists often face disconnect between small-scale lab results and the logistics of kilogram-level synthesis. We help bridge this gap, sharing our production experience, including quirks like agitation profiles, drying times, and scale-specific safety checks. Chemists coming from academia benefit from insights on solvent selection based on observations across our own plant shifts.
We equipped our facility with flexible reactor setups that can shift between pilot and semi-commercial scales quickly. This setup supports projects that start at a few grams and grow into multi-ton campaigns. We encourage open dialogue—if a customer faces yield drops or purification bottlenecks, our technical support often walks through possible process improvements based on our site experience. Our QA technicians, who run all final checks, periodically visit production lines for cross-training, keeping quality and field needs in sync.
Every batch of 3,4-Difluorobenzenesulfonamide represents a partnership between chemistry, engineering, and logistics. Consistency depends on trained operators, robust process recipes, and rigorous final checks. Process safety remains front and center—not just for regulatory compliance, but to protect our staff handling halogenated compounds daily. Maintenance crews routinely inspect transfer lines, gaskets, and filtration systems for signs of corrosion or blockages, catching issues early before they reach critical stages.
Environmental stewardship motivates upgrades to both process and site infrastructure. Our plant teams installed energy-efficient distillation columns, redesigned scrubbers to minimize emissions, and launched campaigns for solvent recycling. Waste streams from 3,4-Difluorobenzenesulfonamide are mapped at each process node, so nothing escapes unnoticed. Ongoing work with local environmental agencies shaped better containment and monitoring protocols.
Early on, the limited availability of key starting materials strained lead times, often frustrating both us and our clients. To ease these supply chain bottlenecks, our purchasing teams developed direct partnerships with upstream chemical producers, sidestepping layers of intermediaries. Inventory systems now operate in real time, alerting production planners to tight raw material balances so no order stalls without notice.
Global shipping brings its own hurdles, with customs hold-ups threatening timely delivery. By sharing reliable Certificates of Analysis and shipment history, as well as clear packaging data, we reduce delays. Some regions demand specialized documentation or more robust drums; we adjust packaging and labeling to fit with local transportation protocols, drawing from years of export experience.
Customers, especially those from newer markets, sometimes require extra technical information or validation data before introducing a new building block into their process. We maintain an internal database of reaction data, stability studies, and reference samples to support customer inquiries fast—direct from the manufacturing site, not a faceless data aggregator. Lab notebooks from our own runs become valuable resources in tackling unusual challenges submitted by R&D partners worldwide.
Our continued investment in production technology ensures 3,4-Difluorobenzenesulfonamide remains both accessible and reliable, even as demand spikes. Competing compounds, whether from alternative sources or adjacent chemistries, often lack the structure-specific documentation or real-world test data we offer from firsthand experience. Having spent years troubleshooting everything from crystallization failures to bottlenecked filtration, our plant teams understand what it takes to keep supply secure.
The compound’s unique difluoro arrangement cannot be simply swapped for other substitutions without consequence. Chemists who tried alternatives often returned, citing lower yields, more difficult work-ups, or inconsistent analytical results. Our synthesis route minimizes these inconsistencies, giving users a reproducible experience batch after batch.
Technologists in pharma, agrochemicals, and academia recognize these differences, not just through datasheets but via hands-on lab work. Routine customer visits, shipments of joint test samples, and open seminars in collaboration with local researchers reinforce direct knowledge transfer. It is this ongoing interaction between manufacturer and user that supports progress in both basic science and commercial research.
The chemistry behind 3,4-Difluorobenzenesulfonamide is well established within our facility, yet our teams continually reevaluate synthetic steps, looking for cleaner, safer, and more efficient options. The ever-changing regulatory landscape demands flexibility, both in formulation and reporting. Our operators participate in continuous education programs to stay current with evolving practice standards, learning about changes in exposure limits, transport rules, and documentation needs as soon as they arise.
Each drum that leaves our plant tells a story of adaptation—of process scale-up, feedback-driven modifications, and lessons learned across hundreds of batches. We support customers large and small, from global pharmaceuticals to early-phase startups, financing everything from new mixing equipment to process chemist training programs. Experience from the manufacturer’s bench makes all the difference in transforming 3,4-Difluorobenzenesulfonamide from just another entry on a catalog into a reliable foundation for innovative research.
In the end, partnering directly with those who make the compound, rather than through a remote reseller, brings transparency, traceability, and rapid response to changing needs. Our doors remain open to technical exchanges, new project requests, and collaboration, because behind every batch—beyond the molecule itself—stands a manufacturer invested in chemistry’s future.