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4-Bromo-2-Fluorobenzenesulfonamide

    • Product Name 4-Bromo-2-Fluorobenzenesulfonamide
    • Alias 4-Bromo-2-fluorobenzenesulfonamide
    • Einecs 629-731-5
    • 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

    179445

    Product Name 4-Bromo-2-Fluorobenzenesulfonamide
    Cas Number 851386-75-1
    Molecular Formula C6H5BrFNO2S
    Molecular Weight 254.08
    Appearance White to off-white solid
    Melting Point 128-132°C
    Purity Typically ≥97%
    Solubility Slightly soluble in organic solvents
    Storage Temperature Store at 2-8°C
    Synonyms 4-Bromo-2-fluorobenzenesulphonamide
    Smiles NS(=O)(=O)C1=C(Br)C=CC(F)=C1
    Inchi InChI=1S/C6H5BrFNO2S/c7-4-1-2-5(8)6(3-4)12(9,10)11/h1-3H,9H2
    Hs Code 29350090

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

    Packing & Storage
    Packing White, sealed 25g HDPE bottle with tamper-evident cap, labeled with chemical name, CAS number, hazard warnings, and manufacturer details.
    Shipping 4-Bromo-2-Fluorobenzenesulfonamide is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous chemical, following all applicable regulations for transport. Proper labeling and documentation are included to ensure safe handling during transit, and emergency procedures are specified in the shipping paperwork.
    Storage 4-Bromo-2-Fluorobenzenesulfonamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from sources of heat or ignition and protect it from moisture and direct sunlight. Store at room temperature, following all applicable chemical safety protocols and local regulations.
    Application of 4-Bromo-2-Fluorobenzenesulfonamide

    Applications of 4-Bromo-2-Fluorobenzenesulfonamide in Industrial Manufacturing

    As a manufacturer specializing in fine chemical intermediates, we supply 4-Bromo-2-Fluorobenzenesulfonamide to sectors requiring specific halogenated sulfonamide functionalities for advanced synthesis. Below we present verified industrial uses across pharmaceutical, agrochemical, and specialty chemical value chains, based on current practice and formulation standards.

    1. Pharmaceutical Intermediate for API Synthesis

    Our material functions as a key sulfonamide building block in the synthesis pathway of specific pharmaceutical APIs, including certain kinase inhibitors and anti-inflammatory agents. Medicinal chemistry teams utilize its unique halogenation pattern to introduce selectivity in lead optimization and final bulk synthesis. Formulation requirements specify the sulfonamide moiety for subsequent arylation, amination, or amide coupling reactions. QC teams verify controlled introduction at the second-step intermediate stage, ensuring batch traceability and meeting stringent impurity thresholds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monograph guidelines for sulfonamide intermediates
    • European Pharmacopoeia General Chapter 5.10 (Contaminants)
    • cGMP Certification under Chinese NMPA for export compliance

    Typical usage ratio

    • 10–25 mol% in target API intermediate coupling reactions, optimized by desired substitution degree and by-product minimization

    Downstream process integration

    • Enters as the arylsulfonamide partner during Suzuki, Buchwald-Hartwig, or reductive amination step in the multi-stage bulk synthesis process

    Final product types

    • Branded and generic kinase inhibitor APIs (oncology sector)
    • Non-steroidal anti-inflammatory drug intermediates
    • Advanced sulfonamide-based pharmaceutical APIs under preclinical/clinical development

    2. Agrochemical Synthesis: Herbicide and Fungicide Precursors

    Major agrochemical formulators require our compound in the design chain of next-generation sulfonylurea herbicides and selective fungicide precursors. Its dual halogenation allows for backbone modification, enabling construction of active molecules with improved crop safety and reduced resistance. R&D formulators integrate this intermediate at early-stage tosylation, followed by transformation into heterocycles or alkylated derivatives.

    Industry compliance standards

    • ISO 9001:2015 for Agricultural Chemical Production
    • China National Standards for Pesticide Raw Materials (GB 2763)
    • European Union Regulation (EC) 1107/2009 (Plant Protection Products)
    • OECD Test Guidelines for industrial chemical intermediates

    Typical usage ratio

    • 5–18 mol% based on final molecule design and active ingredient potency in crop applications

    Downstream process integration

    • Used as a core intermediate in the tosylation or diazotization step, enabling late-stage elaboration of the target molecule framework

    Final product types

    • Halogenated sulfonylurea herbicides
    • Broad-spectrum fungicide actives
    • Crop protection pre-mixes and commercial seed-coating concentrates

    3. Electronic Chemical Precursors for OLED Materials

    Component manufacturers in the electronics sector incorporate this aromatic sulfonamide in the synthesis of custom substituted aryl scaffolds for organic light-emitting diode (OLED) emitter molecules and hole-transport materials. Its high electron-withdrawing capacity assists in band-gap engineering and material property tuning. The material is dosed into functionalization reactions during specialty small-molecule design.

    Industry compliance standards

    • IPC-6012 (Qualification of Printed Boards for Device Producers)
    • RoHS Directive (2011/65/EU) for restricted substance content
    • ISO 14001 for Environmental Management in Electronic Material Production
    • SEMI S2 Chemical Safety Guidelines

    Typical usage ratio

    • 2–12 mol% relative to final aromatic unit count, adjusted for emission wavelength and transport property specification

    Downstream process integration

    • Acts as a nucleophile or aryl donor in Suzuki coupling or Ullmann amination for formation of π-conjugated OLED building blocks

    Final product types

    • OLED emitter molecules for display panels
    • Hole-transport layer materials
    • Active organic semiconductors for flexible electronics

    4. Specialty Dye and Pigment Manufacturing

    Producers of specialty dyes select this sulfonamide intermediate to introduce robust electron-withdrawing groups into advanced pigment backbones, particularly for the synthesis of high-performance azo, phthalocyanine, and anthraquinone-based pigments. It serves key roles in controlling hue stability, solvent fastness, and light absorption properties. Formulators introduce the substance during the diazotization or coupling reaction phases.

    Industry compliance standards

    • EU REACH Regulation (EC 1907/2006) for dye and pigment registration
    • OEKO-TEX® Standard 100 (Class II/IV) for textile dye applications
    • ISO 18451 for Composition of Colourants
    • EN 71-3 (Safety requirements for toys: migration of certain elements) for pigment use in consumer goods

    Typical usage ratio

    • 8–15 mol% depending on desired dye structure and target extinction coefficient in end use

    Downstream process integration

    • Used in primary diazotization or coupling steps for modification of parent aromatic rings in dye intermediate manufacture

    Final product types

    • Azo and phthalocyanine-based textile dyes
    • High-fastness pigments for automotive and printing inks
    • Electron-acceptor dyes for technical coatings and industrial plastics
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    Certification & Compliance
    More Introduction

    4-Bromo-2-Fluorobenzenesulfonamide: Practical Insights From The Manufacturing Floor

    Understanding 4-Bromo-2-Fluorobenzenesulfonamide From the Source

    4-Bromo-2-Fluorobenzenesulfonamide walks a fine line in the landscape of specialty chemicals. For everyday operators on the shop floor in our facility, clarity around a product’s value and fit for use means more than ticking boxes from a technical sheet. Our work with this compound provides a direct look at its real-world impact. Known under the model designation C6H5BrFNO2S, this sulfonamide blends two strategically positioned halogens – bromine at the 4-position and fluorine at the 2-position – on a benzenesulfonamide backbone. The design itself brings clear differences compared to older or more common sulfonamides. That interplay produces reasons for its rising demand in pharmaceutical research, chemical intermediates, and specialized agrochemical synthesis.

    Holding Quality To A Real Standard

    From synthesis to drying and final packaging, daily attention to raw material choice sets the foundation. Consistency doesn’t come by chance in this room. Decisions often depend on how well 4-Bromo-2-Fluorobenzenesulfonamide separates during purification and whether the final material clears HPLC purity benchmarks that exceed 98% by weight. Some in the market speak often of “high purity”; here, batch-to-batch reproducibility and absence of residual solvents draw the real line between research-grade and process-grade products. Our daily testing follows a strict protocol, using direct GC-MS and NMR analysis. Staff confirm the melting point range between 142° and 145°C, spot moisture content using Karl Fischer titration, and check every drum for visual uniformity before labeling. This ground-level approach means repeat customers rarely encounter unexpected variances.

    Why Real Halogen Placement Matters

    Design choices impact performance, especially in building blocks for pharmaceutical intermediates. Bromine at the 4-position on a benzenesulfonamide ring delivers distinct steric and electronic effects over 2-bromo analogs. Switching that position changes the way downstream coupling partners react during Suzuki, Buchwald, or Ullmann cross-couplings. In our own reactors, this position gives cleaner conversions and less by-product drag in late-stage API intermediates. The fluorine atom at the 2-position influences not just reactivity but also stability, since it pulls electron density and helps manage unwanted decomposition in higher temperature steps.

    Applications That Go Beyond A Label

    Pharma clients bring us questions month after month, ranging from quick-batch needs in medicinal chemistry, to multi-ton lots for pilot plant scaling. The molecular design behind 4-Bromo-2-Fluorobenzenesulfonamide offers more than just another node in a benzenesulfonamide family tree. It often takes a central place in the construction of kinase inhibitors and related heterocycle scaffolds. We’ve seen this compound picked for building blocks in sulfonamide-linked ureas and carbamates, especially where halogen substitution directly influences receptor binding, metabolic profile, or synthetic tractability. On the agrochemical side, several project managers have shifted from plain benzenesulfonamides to our 4-bromo, 2-fluoro variant after noticing stronger downstream yields in sulfonylurea precursors. Sometimes a subtle tweak in substitution pattern reshapes costs in multi-step syntheses and shortens process validation, leading to a clear cost advantage on the factory floor.

    Workmanship and Handling You Notice

    No sulfonamide survives the scale-up process without presenting some wrinkles in handling. We find our 4-Bromo-2-Fluorobenzenesulfonamide forms a crystalline white to off-white solid, with practical flowability that beats out some stickier sulfonamides we have handled in the past. Dosing machines run with fewer clogs. Filtration and drying stages progress without excessive downtime. Operators mention that the dust profile stays low, so less material escapes during collection and less cleaning shuts down lines. The compound maintains its solid-state integrity in both fiberboard drums and foil pouches meant for long-term storage. Test lots left at room temperature for six months have consistently passed all retests, suggesting stable shelf life under proper dry-box conditions.

    Purity Control and Troubleshooting: Ground Realities

    Managing reaction by-products is a quiet challenge with any substituted benzenesulfonamide. We run regular impurity profiling, targeting 2-bromo or 3-bromo side products that creep in if the bromination sequence varies. Real world experience shows that blank sheet methods posted online rarely match up with shop floor realities, which often demand stepwise control of reaction time, temperature, and solvent ratios. Our technical staff adapts workup protocols after every abnormal batch. If a process generates more than 0.2% total impurities in GC-MS, we recycle or re-work barrels rather than push inferior product. Recognizing trouble spots early comes only from handling thousands of kilos across multiple campaigns.

    Comparing Alternatives: Not All Sulfonamides React The Same

    Plenty of customers believe that any halogen-substituted benzenesulfonamide serves the same role. Daily lab and pilot scale experience says otherwise. Single-fluorine or single-bromine analogs show different rates of nucleophilic substitution and sometimes require harsh bases, driving up failure rates or scaling costs. The combined 4-bromo, 2-fluoro pattern delivers a set of properties that brings cleaner crystallization, tighter melting point spread, and higher loading efficiency in solid-phase reactions. We have also compared the compound to more common multi-halogenated sulfonamides, such as 2,4-difluoro or 3,4-dibromo analogs. The 2-fluoro/4-bromo configuration maintains a practical balance between stability and reactivity, avoiding over-activation that sometimes leads to poor product selectivity. Many teams have shifted to this compound for late-stage functionalization, remarking on its lower incidence of side chain scission or 'over-reaction' in coupling and condensation steps.

    Sustainable Production and Responsible Stewardship

    Over decades, regulatory trends have placed the environmental profile of fine chemicals under greater scrutiny. We track the solvent and energy inputs for the manufacture of each kilo of 4-Bromo-2-Fluorobenzenesulfonamide. Our routes employ controlled addition of reagents, often using greener alternatives to traditional halogenation and sulfonation steps. Rather than relying on legacy washout methods, we recycle reaction mother liquors where possible. Waste minimization training runs deep on our crew, so fewer hazardous residues leave our gates. In parallel, audit trails track every drum from production to shipment, supporting traceability and compliance checks from both authorities and clients. This focus creates real trust: major pharmaceutical and agrochemical projects continue to source directly from us year after year.

    Feedback From End-Users and Continuous Improvement

    We’ve learned that no process or material stands still. Our research partners often come back with process data highlighting minor differences batch to batch, sometimes sparked by a shift in supplier among precursor chemicals. These signals prompt targeted root-cause analysis in our labs, using side-by-side testing with competitor batches. Performance feedback has led us to update particle size specifications, adjust drying cycles to improve bulk density, or modify our sieving process. We treat end-user process performance—such as yield data, reaction time, or product color changes—as ammunition to keep tuning our internal SOPs. Some specialty projects have even prompted us to build custom filtration units or accelerate a shift from glass-lined to stainless steel reactors, depending on customer purity or cross-contamination concerns.

    Handling Safety and User Experience

    While technical data sheets carry standard warnings, daily reality on the shop floor shapes safe practice. Granular sulfonamides can pose inhalation risks, so direct loading under local extraction remains essential. Operators wear fitted masks and gloves, and open bags only inside controlled hoods. This hands-on approach catches leaks or moisture issues earlier. Real hazard comes from transitory steps—especially initial bromination, not in the final product itself—which leads us to maintain a rigorous, in-house training program for every production shift. Regular maintenance of weighing, blending, and packaging lines prevents exposure and upholds an accident-free record, even on weeks pushing out multiple metric tons.

    Looking Forward: Customer Needs Drive Material Choices

    Market trends show steady interest in fine-tuned intermediates, especially materials engineered for specific coupling and derivatization steps in pharma and agro. Shorter innovation cycles put a premium on building blocks that bring flexible reactivity and storable purity. Our experience guiding client projects, fielding trouble-shooting calls, and delivering emergency rush orders forms the backbone of ongoing improvements across supply, packaging, and support. We believe a sharp focus on feedback—combined with honest reporting of both strengths and limits—sets real chemical manufacturers apart from middlemen.

    Meeting Changing Regulatory and Technical Demands

    Ephemeral shifts in international regulations around halogenated compounds push factories to sharpen processes. As environmental, safety, and quality standards keep rising, we welcome audits and routine sampling by institutional partners. Regular investment in external lab certification and digital traceability matches increased scrutiny in the market. This compound, in particular, stands close to the edge of new pharmaceutical and crop protection pathways, so our customers rely on us to quickly supply purity certifications, characterization data, and custom packaging for both kilo- and multi-ton shipments.

    Limiting Counterfeits and Securing Authentic Material

    Proliferation of intermediates through resellers or brokers increases the risk of counterfeit or sub-specification batches entering the supply chain. Direct manufacturers use batch-coded tamper-proof containers and maintain identity documentation. We recommend buyers always verify chain of custody and request real-time analytics, especially for high-value process intermediates. It’s not just about liability; it’s about production success. Each shipment’s documentation ties back to work in our reactor rooms, letting any discrepancies be traced and rectified. Experienced staff flag authenticity issues swiftly. Long-term partners insist on direct purchase—this tradition serves both sides in transparency and trust.

    Logistical Realities: Getting The Material Where It Counts

    Shipping specialized sulfonamides calls for more than pushing inventory out the door. We monitor ambient temperature and humidity during dispatch, switching to thermal-insulated packaging on long-haul or ocean routes. Each drum bears internal desiccant packs. Expedited handling for sensitive projects comes with batch-level documentation, and all our drivers know how to flag delays. For urgent deliveries, our crew prepares split shipments. No theoretical guarantee matches the relief felt once a client confirms receipt and successful QC in their hands.

    In Summary: Craftsmanship Borne Of Use

    4-Bromo-2-Fluorobenzenesulfonamide moves beyond generic catalog presence, earning its place through actual application and performance. Over years in manufacture, our team recognizes it as a backbone building block with proven output across fine chemical synthesis, research, and upscaling. The value emerges through careful production, vigilant in-process checks, and an eye for the small details that shift performance from routine to reliable. Our experience stands as a reminder that genuine material, made and tested at the source, underpins the progress of both science and industry.