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2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide

    • Product Name 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide
    • Alias 2-Bromo-4-(trifluoromethyl)benzenesulfonamide
    • Einecs 697-183-4
    • 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

    662066

    Productname 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide
    Casnumber 877399-88-3
    Molecularformula C7H5BrF3NO2S
    Molecularweight 320.08
    Appearance White to off-white solid
    Meltingpoint 109-113°C
    Purity ≥98%
    Solubility Slightly soluble in DMSO or DMF
    Storagetemperature 2-8°C
    Smiles NS(=O)(=O)c1ccc(C(F)(F)F)cc1Br
    Inchi InChI=1S/C7H5BrF3NO2S/c8-5-1-2-6(7(9,10)11)4(3-5)16(12,13)14/h1-3H, (H2,12,13,14)
    Synonyms N-(2-Bromo-4-trifluoromethylphenyl)sulfonamide

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed, hazard-labeled, with chemical name, CAS number, and safety instructions clearly displayed.
    Shipping 2-Bromo-4-(Trifluoromethyl)benzenesulfonamide is shipped in sealed, chemical-resistant containers, compliant with regulatory standards. Packaging ensures protection from moisture and light. The chemical is labeled for hazardous material transport, accompanied by a safety data sheet (SDS). Shipping adheres to DOT, IATA, and IMDG guidelines for safe handling and delivery.
    Storage 2-Bromo-4-(trifluoromethyl)benzenesulfonamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Store away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and access only to trained personnel. Follow standard safety protocols for handling hazardous chemicals.
    Application of 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide

    Applications of 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide in Industrial Manufacturing

    As an established manufacturer, we supply 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide to leading companies engaged in advanced chemical synthesis. This specialty intermediate finds application in highly regulated technical sectors where sulfonamide functionalities and fluorinated moieties are critical for molecule design. Below, we detail verified downstream segments incorporating this raw material.

    1. Pharmaceutical Intermediates for Small-Molecule Drug Development

    Leading API and CDMO facilities utilize this compound as a sulfonamide source in the synthesis of kinase inhibitors, CNS modulators, and other bioactive scaffolds. Medicinal chemists value its electron-withdrawing trifluoromethyl group and bromine substitution, which serve as directing groups for regioselective functionalization in complex heterocycles. Batch QC requires traceability to ICH Q7 guidelines, with final usage defined in multi-step syntheses for investigational medications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <791> pH, <621> Chromatography specifications
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • 0.2–0.7 molar equivalents based on targeted sulfonamidation reactions; ratios adjusted per specific synthetic route and target molecule complexity

    Downstream process integration

    • Introduced post-halogenation or amidation steps in API synthesis; directly coupled in palladium- or copper-mediated cross-coupling reactions; applied in late-stage derivatization for SAR studies

    Final product types

    • Clinical trial APIs (oncology, neurology, metabolic diseases)
    • Reference standard compounds
    • Pharmacological screening libraries
    • Regulatory filing substances for IND and NDA

    2. Agrochemical Building Blocks for Herbicide and Fungicide Synthesis

    Global agrochemical producers employ this specialty sulfonamide as a core scaffold or side-chain modifier in the manufacture of new-generation crop protection chemicals. The reactivity of the bromine and trifluoromethyl moieties facilitates step-efficient generation of active ingredients with increased metabolic stability, meeting updated environmental standards for reduced persistence and improved selectivity in the field.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials and formulations
    • REACH (EC) No 1907/2006
    • EPA Title 40 CFR, Part 180 (Tolerances and exemptions for pesticide residues)
    • ISO 9001:2015 (Process traceability and quality assurance)

    Typical usage ratio

    • 5–15% w/w in precursor stage; final loading varies by active ingredient structure and regulatory residue limits

    Downstream process integration

    • Fed into active ingredient synthesis prior to sulfonylation or fluorination; supports introduction of pendant groups in structure–activity relationship optimization campaigns; processed under controlled conditions—post-reaction purification ensures removal of unreacted intermediate

    Final product types

    • Selective herbicides (e.g., sulfonylurea, triazole classes)
    • Systemic fungicides with enhanced bioavailability
    • Crop treatment agents with reduced toxicity profiles
    • Formulated agrochemical concentrates for seed conditioning

    3. Advanced Electronic Materials for Photoresist and Dielectric Polymer Manufacturing

    Specialty electronics and materials companies source this compound to engineer sulfonamide-functionalized aryl monomers, enabling precise tuning of photoresist sensitivity and dielectric constant in microelectronics processes. Its robust fluorinated structure imparts performance attributes required for EUV and ArF lithography, especially in high-aspect ratio pattern transfer and barrier layer enhancement for advanced chip designs.

    Industry compliance standards

    • SEMI S2 (EHS guidelines for semiconductor manufacturing equipment)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • JIS Standards for photoresist materials
    • ISO 14001 (Environmental management for electronic materials)

    Typical usage ratio

    • 1–3% by weight in aryl monomer production; adjusted to achieve specific polymer architecture and patterning fidelity in lithography resists

    Downstream process integration

    • Used in precursor polymerization stages before chain extension and cross-linking; integrated into resist formulations by solution blending and subsequent, solvent-cast processing; monitored using GPC and FTIR for inclusion verification

    Final product types

    • Photoresist polymers for DUV/EUV lithography
    • High-k dielectric thin films
    • Barrier layer components in IC manufacturing
    • Plug fill materials for advanced packaging

    4. Specialty Chemical Synthesis for Fluorinated Fine Chemical Production

    Producers of advanced fine chemicals rely on this intermediate to construct bespoke fluorinated and sulfonamide frameworks demanded in high-value sectors such as liquid crystal displays, specialty catalysts, and analytical standards. The unique electron-withdrawing nature of its substituents accelerates targeted substitution, sulfonamidation, and cross-coupling reactions, supporting synthesis projects that demand high purity and consistent reactivity.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for specialty chemical plants)
    • ECHA REACH registration and downstream user communication
    • Custom specifications on trace metals and halide impurities as required by application sector
    • Internal QC per ASTM E288 (Purity determination by mass loss)

    Typical usage ratio

    • 0.5–2.5% by mass in stepwise libraries; tailored by reaction scale, substitution pattern, and targeted functional group content

    Downstream process integration

    • Introduced in building block assembly lines as a halogenated activator or sulfonylation partner; used in both batch and continuous synthesis environments, with in-process analytics to guarantee complete transformation

    Final product types

    • Fluorinated liquid crystal intermediates
    • Chiral catalyst precursors and ligand libraries
    • Analytical reference chemicals
    • Specialty dyes and pigments for technical applications
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    Certification & Compliance
    More Introduction

    2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide: A Manufacturer’s Insight

    Introduction to a Reliable Intermediate

    Producing specialty chemicals starts with a precise approach to raw materials. In the shop floors and synthesis units where the rubber meets the road, 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide has secured its place as a trusted building block for more than a decade. Every kilogram carries the weight of tight batch-to-batch consistency, because the stakes are higher than simple cost per unit: process reproducibility saves time, resources, and often a lot of headaches. This compound features a trifluoromethyl group and a bromo substituent on a benzenesulfonamide backbone, creating a unique reactivity profile that process chemists lean on to solve downstream problems.

    Practical Handling & Formulation Behavior

    The real test of any aromatic sulfonamide lies in how it handles under actual plant conditions. We spend as much time refining granule size, moisture control, and filtration ease as we do on polishing purity metrics. In our experience, 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide takes the challenge of scale-up smoothly. Once, on trial scale, we saw clumping and caking with certain sulfonamides, but this compound continues to show stable, free-flowing characteristics, even with only modest desiccant precautions.

    Operators report that it dispenses through metering hoppers without bridging, whether melting or charging directly to reactors under nitrogen. From an engineering standpoint, less downtime spent clearing blocked lines translates directly into lower cost of goods. During solvent washes or aqueous work-ups, it doesn’t produce stubborn emulsions, and filtration moves quickly. These points matter to operators tasked with keeping a campaign moving on deadline.

    Purity, Consistency, and Real-World Specifications

    Some suppliers advertise purity above 99%, but we take this deeper by working closely with our in-house QC team to monitor impurity profiles, including residual halides and byproduct amines. Most manufacturers, including us, keep HPLC purity above 99% and loss on drying below 0.5%. This tight control means less background interference for customers, who often use this intermediate upstream in pharmaceutical or agrochemical synthesis.

    Early on, we realized our clients saw fewer side reactions with our product: bromine exchange and undesired coupling generally dropped out of the analytical noise. That’s no accident. The underlying purity speaks as much for the raw materials as it does for the actual process. We maintain synthesis routes free from unwanted isomers or colored impurities, knowing full well that a yellow tint might create batch rejections or extra work.

    Responsibility in Manufacturing: Batch Integrity and Documentation

    Our clients frequently visit to audit our traceability and documentation system. They want more than a certificate of analysis. What matters most for regulatory filings and customer peace of mind is robust traceability and a clear chain of custody through each production run. Every reactor log, operator entry, and sample analysis bridges the gap between a paper specification and boots-on-the-ground compliance. Documenting every batch, storing retained samples, and keeping training logs updated have become part of our daily discipline.

    Inside the plant, we operate closed handling systems for halide-bearing chemicals, mindful of both workplace safety and cross-contamination. We treat every campaign of 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide as a potential for validation, not just a commodity run. Our process engineers actively run side-by-side tests of new process improvements, sometimes capturing subtle gains—a few degrees cooler on crystallization, a gentler workup, a shift in anti-solvent selection—that end up protecting yield or purity.

    Comparisons to Similar Intermediates

    It’s easy to lump all sulfonamides together, but subtle differences in reactivity and processability quickly separate one intermediate from another. Over years of feedback from our partners, we’ve seen where 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide outpaces related compounds. Compared with 2-Bromo-benzenesulfonamide (which lacks the trifluoromethyl group), this compound consistently delivers higher selectivity in certain coupling or amide-forming reactions, likely due to the electron-withdrawing effect of the CF3 substituent.

    One project—a multinational in pesticide R&D—shared that their yield for a key heterocycle went up by over 15% after switching to our 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide. Their case also highlighted improved impurity rejection at downstream stages, reducing the need for additional purifications and washing solvents. For pharma clients, this intermediate proves more forgiving in scale-up, especially where minimization of byproducts containing free amine or residual halide is critical to meeting ICH Q3A/B guidelines.

    We’ve tested performance head-to-head against alternatives such as 4-Trifluoromethylbenzenesulfonamide and 2-Bromobenzenesulfonamide in standard palladium-catalyzed couplings. Our compound’s unique combination grants better solubility profiles—neither too hydrophobic nor prone to premature precipitation. It stands up to reaction temperatures above 100°C without marked decomposition, which gives chemists a wider process window for trickier transformations.

    Role in Synthetic Pathways and End Uses

    Process chemists and R&D teams use 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide primarily in constructing aryl-substituted sulfonamides, biaryl frameworks, and complex heterocycles. Cleaner reactivity shortens route scouting. We’ve seen it employed in Suzuki and Buchwald–Hartwig coupling reactions, where the bromo function serves as a convenient leaving group, and the trifluoromethyl group tunes the reactivity for more selective conversion. A few of our agrochemical clients choose it to build core scaffolds for herbicides and fungicides, taking advantage of its dual halide and sulfonamide function for multi-point derivatization.

    Batch records from catalog and custom synthesis show that, in many peptide-coupling runs, it resists hydrolysis, maintaining integrity against a range of acid and base strengths. Unlike some other benzenesulfonamide variants, it tolerates high concentrations of nucleophiles and stays manageable in both protic and aprotic solvents.

    Environmental and Safety Observations from Plant Floor

    Handling any aromatic sulfonamide, particularly one with both bromo and trifluoromethyl groups, calls for solid wastewater treatment and fume management procedures. Our operators don’t just follow written SOPs—they shape them. Over the years, we’ve switched to closed filling lines fitted with HEPA filtration after a spike in operator complaints about localized irritation. We invested early in cold-trapping volatile byproducts, capturing residual halides before they could enter the vent system.

    Effluent treatment remains a day-to-day priority. Removing halogenated organics from plant wastewater is never trivial. Our on-site system draws on activated carbon followed by advanced oxidation units tailored for bromo and trifluoromethyl contaminants, cutting our emissions sharply below local limits. Putting care into this area supports both compliance and public trust, and makes permit renewals smoother.

    Inside the facility, we use personal badge monitors to track air quality throughout each campaign. We noticed lower overall exposure rates after switching to direct-to-reactor powder handling for the benzenesulfonamide series. Updating safety protocols and keeping a tight dialogue with frontline workers has led to more practical improvements than anything dictated top-down from management.

    Raw Material Sourcing and Supply Chain Stability

    The market for starting materials—like bromobenzene derivatives and trifluoromethylating agents—can turn volatile. Early disruptions taught us to dual-source critical raw materials, expanding our inventory buffers during periods of market stress. Our supply team maintains strong relationships with producers in both Asia and Europe, which insulates us from the capacity swings that sometimes hit the market for fluorinated and halogenated aromatic intermediates.

    In years when freight costs spiked or shipping lanes slowed down, we adjusted production schedules to prevent line stoppages, keeping our downstream partners in the loop with regular updates. Our plant planners routinely audit our vendor panels and ensure we only accept lots with the right levels of trace impurities. If a critical supply looks at risk, we notify long-term customers early and propose mutually agreed adjustments, ensuring no one faces a sudden shortfall.

    Supporting Innovation: From Lab Bench to Commercial Scale

    Researchers tackling new pharma or crop protection targets often need small batches quickly, then larger lots for pilot scale-up and registration batches. We’ve worked side-by-side with customers from all over the globe to match lab-scale quality with ton-scale runs. This close involvement includes shipping additional samples from retained inventory, sharing in-process results, and accommodating specs not captured in standard certificates of analysis.

    We keep an open-door approach: customers routinely request differences in salt form, particle fraction, or packaging, and we update our protocols to deliver. One case involved a pharma company launching a new sulfonamide-linked kinase inhibitor; we ramped up their requirements from a few hundred grams to several hundred kilograms, helping the project stay on its critical path through regulatory hurdles.

    As a manufacturer, our lab team digs deep into method development, optimizing for new reaction endpoints or discovering faster workups. Every process improvement—fewer steps, less solvent, improved stirrability—ends up benefiting the end user, turning what used to be “hard-to-make” molecules into straightforward, reliable feedstocks.

    Quality Commitment and Performance Feedback

    In manufacturing, open feedback from end users keeps us honest. Whether it’s a call in the middle of a campaign or samples brought in by customers who want tweaks, our team values every data point. Living up to end-use demands, not just book specs, keep our batch records and operator logs meaningful.

    Sometimes, customers re-test our intermediates on their own platforms—running new impurity checks, blending into complex mixtures, stress-testing stability. We don’t leave these requests unresolved; responding to in-the-field feedback often catches edge cases—trace discoloration, unforeseen byproduct formation, or filtration sluggishness. Acting on these reports shapes how we refine both process and QC controls. The end result is more confidence on both sides of the supply chain.

    Global Reach and Cross-Border Logistics

    Supplying 2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide to dozens of countries presents its own hurdles. Each region has its own paperwork, labeling, and compliance steps. We’ve learned the hard way how to avoid pitfalls—missing customs forms, incorrect labeling, or underestimating temperature stability in transit. Our logistics team tracks every shipment, staying ready to reroute or re-chill freight in real time. After losing a load once to unseasonable heat damage, we switched to cooled packaging for warm climate destinations, giving customers peace of mind on delivery.

    Clear, honest communication with customs and regulators in advance of each shipment prevents clearance bottlenecks. Providing accurate, compliance-focused documentation avoids stops and delays that can undermine even the best production scheduling. Over years of export and import, our in-house regulatory team honed rapid response abilities, supported by a depth of knowledge accumulated from hundreds of campaigns.

    Looking Ahead: Adapting to Market Changes

    The wider chemical market faces challenges. Regulatory pressure on certain halides and perfluoro compounds tightens each year, with new registration or notification requirements. We stay proactive, tracking emerging rules and cooperating with customers on updated compliance packages. Developing greener process options, collecting new process safety data, and minimizing waste streams, shapes the sustainability profile of our entire product line.

    Genuine partnership with customers—built on feedback, trust, and shared technical knowledge—remains our foundation. We invest in both technology and people, aiming for improvements that show up in the customer’s own yields, timelines, and audit results. Our production philosophies come from hard-earned in-plant lessons: listen, document, refine, and always support the downstream process.

    2-Bromo-4-(Trifluoromethyl)Benzenesulfonamide is more than a stock item. Each batch represents dozens of hands and minds across R&D, manufacturing, shipping, and QA. Every specification and tweak grows from years of actual scale-up, hard-won process improvements, and feedback from the researchers and operators who rely on its consistent performance. This intermediate continues to evolve as high-value applications emerge, keeping us focused on delivering reliable, transparent, and practical solutions to our partners across the world.