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4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride

    • Product Name 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride
    • Alias 4-Bromo-3-(trifluoromethyl)benzenesulfonyl chloride
    • Einecs 409-040-1
    • 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
    VTB
    Specifications

    HS Code

    434669

    Product Name 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride
    Cas Number 705-35-9
    Molecular Formula C7H3BrClF3O2S
    Molecular Weight 327.52
    Appearance White to off-white solid
    Melting Point 65-69°C
    Purity Typically ≥98%
    Solubility Soluble in dichloromethane, chloroform
    Smiles C1=CC(=C(C=C1S(=O)(=O)Cl)C(F)(F)F)Br
    Storage Temperature Store below 30°C, keep container tightly closed

    As an accredited 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride, sealed in an amber glass bottle with hazard labels, screw cap, and desiccant.
    Shipping 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride is shipped in tightly sealed, corrosion-resistant containers to prevent moisture and air exposure. Classified as a hazardous material, it is handled according to international transport regulations, with appropriate labeling and documentation. Shipment is usually via ground or air freight, ensuring compliance with safety standards.
    Storage Store 4-Bromo-3-(trifluoromethyl)benzenesulfonyl chloride in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, in a cool, well-ventilated area. Keep away from moisture, heat, and incompatible materials such as strong bases and oxidizers. Handle with appropriate chemical-resistant gloves and safety equipment to avoid inhalation or contact with skin and eyes.
    Application of 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride

    Applications of 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride in Industrial Manufacturing

    4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride is a specialty intermediate widely adopted in several advanced chemical synthesis routes. As an established manufacturer, we supply this compound to industrial partners across critical downstream sectors that demand precise performance, stringent quality, and assured regulatory compliance. Below, we outline its principal applications in real-world manufacturing scenarios.

    1. Agrochemical Active Ingredient Synthesis

    This sulfonyl chloride serves as a selective sulfonation agent for the synthesis of novel herbicide and fungicide actives. Its unique halogen and trifluoromethyl substituents enable targeted modifications of aromatic systems, which are essential in developing crop protection products with improved stability and field performance. Typical processes involve aromatic substitution for core structural modification during the optimization of biological activity and patentable molecular designs.

    Industry compliance standards

    • REACH (EC 1907/2006) substance registration and safety assessment
    • US EPA FIFRA guidelines for pesticide intermediates
    • GB 2082-2005 (China Agrochemical Raw Material Requirements)
    • ISO 9001:2015 for raw material quality traceability

    Typical usage ratio

    • Range: 0.1 – 0.6 molar equivalents relative to target aromatic substrate, optimized per agrochemical synthesis step

    Downstream process integration

    • Added post-chlorination or nitration for aryl sulfonamide coupling
    • Integrated in nucleophilic substitution steps for structural diversification
    • Purification by controlled hydrolysis and crystallization before final product formulation

    Final product types

    • Active herbicidal compounds (e.g., triazole- or pyridyl-based ingredients)
    • Formulated fungicides with improved weather resistance
    • Patent-protected crop protection actives

    2. Pharmaceutical API Intermediate Manufacturing

    The compound is a key sulfonylation agent in several multi-step syntheses for drug intermediates, especially for generating aryl sulfonamide motifs in API scaffolds. Medicinal chemists exploit its electron-withdrawing features to fine-tune pharmacokinetic and bioactivity profiles of drug candidates. Large-scale production requires robust GMP control and precise stoichiometry in late-stage intermediate preparation to meet global regulatory standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. specifications for key intermediates
    • US FDA 21 CFR Part 211 for cGMP in drug substance manufacturing
    • Chinese Pharmacopoeia standards for pharma intermediates

    Typical usage ratio

    • 0.2 – 1.0 molar equivalents based on coupling partner and reaction stage
    • Lower ratios for late-stage modifications, higher for initial arylations

    Downstream process integration

    • Incorporated during sulfonamide ring closure or aryl sulfonyl coupling
    • Used in controlled batch or continuous flow reactors for GMP-compliant production
    • Batchwise in protected nitrogen or oxygen nucleophile reactions for clean impurity profiles

    Final product types

    • Sulfonamide-based API intermediates for antibiotics or antidiabetics
    • Advanced pharmaceutical building blocks for CNS and oncology drugs
    • Final-stage impurity markers used in pharmaceutical quality control

    3. Electronic Chemicals—Photoresist Additive Manufacturing

    In semiconductor fabrication, this specialty sulfonyl chloride is employed as a synthetic intermediate in the preparation of high-performance aryl sulfonate photoacid generators (PAGs). Its halogen and fluorinated functionalities impart superior stability and control over acid diffusion properties, enabling precise pattern transfer in advanced lithography processes for integrated circuits and panel displays.

    Industry compliance standards

    • SEMI C1/C30 purity and contamination control guidelines
    • ISO 14644 cleanroom production requirements
    • RoHS Directive 2011/65/EU for end-use in electronics
    • JPCA/IPC-4552A for chemical material traceability

    Typical usage ratio

    • 0.15 – 0.35 molar equivalents in PAG synthesis phase
    • Adjusted through in-process GC tracking and acid yield optimization

    Downstream process integration

    • Used post-arylation in the photoacid generator core preparation
    • Introduced before final sulfonation in mix-and-cure dry rooms
    • Combined with high-purity solvents for lithographic-grade output

    Final product types

    • Photoacid generator compounds for 193 nm/248 nm photoresists
    • Advanced i-line and DUV photoresist formulations
    • Specialty imaging resins for OLED, LCD, and microchip lithography

    4. Specialty Dyes and Pigment Intermediate Production

    The aromatic sulfonyl chloride plays a functionalization role in the manufacture of high-performance azo and anthracene-based dyes. Its electronic and steric features allow for selective sulfonation and halogenation, yielding pigment intermediates with enhanced lightfastness and solvent resistance. Industrial users apply it in tightly controlled batch processes tailored for textile, leather, and automotive finishes.

    Industry compliance standards

    • OEKO-TEX Standard 100 for dye raw materials
    • REACH Annex XVII for aryl halide intermediates
    • ZDHC MRSL for approved manufacturing chemical lists
    • ISO 9001:2015 pigment and dye production inspection

    Typical usage ratio

    • 0.3 – 0.7 molar equivalents calculated to adjust chromophore intensity and solubility

    Downstream process integration

    • Reacted in sulfonamide bridging step in pigment synthesis
    • Post-diazonium coupling for tailored azo dye profiles
    • Refined by multi-stage solvent extraction to meet color stability criteria

    Final product types

    • High-purity textile dyes for nylon and polyester
    • Solvent-resistant pigment dispersions for automotive coatings
    • UV-stable dyes for plastics and packaging inks

    5. Polymer Additive Manufacturing—Fluorinated Functional Polymers

    As a sulfonating and halogenating agent, 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride is chosen for the synthesis of specialty polymers with enhanced chemical and thermal resistance. Its use in surface modification and internal chain engineering permits manufacturers to produce advanced membranes and engineering plastics suited for demanding filtration, separations, and durable electronic component encapsulation.

    Industry compliance standards

    • UL 94 HB/V0 tests for flame-retardant polymer materials
    • ASTM D638 for mechanical and chemical resistance in final compounds
    • RoHS and REACH compliance for industrial polymer additives
    • ISO 14001 certified environmental performance in production

    Typical usage ratio

    • 1–5% weight/weight relative to polymer precursor, modified by application end-use (membranes vs. resins)

    Downstream process integration

    • Integrated during pre-polymer sulfonation and chain extension reactions
    • Fed into high-shear extruders for copolymer functionalization
    • Controlled dosing for consistent sulfonic acid group incorporation

    Final product types

    • Fluorinated ion-exchange membranes for fuel cells and water treatment
    • Engineering plastics with high solvent and flame resistance
    • Microfiltration and ultrafiltration membranes for chemical separations
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride

    Experience and Craftsmanship Shaped by Laboratory Realities

    Working at the bench and on the plant floor, we see how specialty intermediates shape outcomes both in R&D and production. 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride, with CAS number 222889-03-6, stands out in our catalog for its purity and consistency. Our process engineers tighten every part of the process, so each batch delivers on both analytically measured and practical aspects chemists care about. This isn’t just another exotic aryl sulfonyl chloride; from reactivity to storage stability, it fills a demanding role in advanced synthesis.

    Molecular Distinctiveness in Synthesis Routes

    Our chemists encounter design challenges daily—selectivity, yield, side product minimization. The bromo-trifluoromethyl arrangement on the aromatic ring doesn’t just impact the reactivity; it grants more control for directed sulfonylation and post-functionalization than simpler benzenesulfonyl chlorides. That extra handle speeds up protection or activation steps, which makes it a practical choice for teams building libraries or scaling new processes.

    This isn’t theory—it’s the pattern we see in customer feedback and our own continuous improvement work. Our in-process QC tracks not just the main peak on HPLC, but subtle impurity profiles that affect downstream coupling or cross-coupling efficiency. Medicinal chemistry labs and agrochemical developers leverage this compound for these reasons and get reliable results batch after batch.

    Analytical Profile: Detailed, Not Just Standard

    Instead of focusing simply on listed technical numbers, we learn from hands-on panel testing in both ambient and inert setups. With a melting point in the ballpark of 80–85°C and a white-to-off-white appearance, our product signals its quality visually—a key first check for any scale-up. NMR and GC-MS trace analyses show residuals trending below 0.5%, easing the burden on downstream purification. We monitor not just the sulfonyl chloride integrity but also decomposition markers—something overlooked in less stringently controlled material.

    From drum to vial, packaging integrity holds up under transit stress according to shipment logs. Our labs continually verify shelf-life against real-world temperatures, not just what’s written in the spec.

    Where Utility Exceeds Typical Benzenesulfonyl Chlorides

    Standard benzenesulfonyl chlorides fill their role in simple protecting group chemistry and arylation, but the molecule we produce opens more doors. Across years of customer projects, 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride excels in custom syntheses requiring both electron-withdrawing and steric fine-tuning. The bromo substituent adds a useful site for further functionalization—Suzuki, Sonogashira, or carbonylative couplings see particular benefit. Our QC records show a higher pass rate on coupling partners derived from this compound compared to less-substituted analogs.

    The trifluoromethyl group dramatically shifts the lipophilicity and electronic properties, which can help developers dial in ADMET performance or agrochemical selectivity. It’s a bench-proven building block when scaffold-hopping or tweaking lead candidates for improved potency and selectivity in pharmaceutical development. Because of its specialized structure, it unlocks routes unavailable to plain benzenesulfonyl chloride, and outperforms even para-substituted derivatives in complex multipurpose synthesis.

    Ease of Scale-Up and Consistency

    Lab scale might make use of a diverse set of building blocks, but industrial synthesis relies on reproducibility and minimal downtime. Reports from production chemists confirm that our 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride handles predictably during charging, minimizes dust due to granular control at drying, and dispenses without caking. This consistency reduces sieving steps and avoids bottlenecks in continuous or fed-batch systems.

    Our standard packaging, with nitrogen backfill, guards against hydrolysis and self-polymerization. Users confirm that the product retains its active sulfonyl chloride character, even after prolonged storage in ambient warehouses. We track trends in field complaints and proactively adjust drying cycles or packaging material when logistics data suggest improvement. This feedback loop sustains the quality across geographies and climates.

    Green Chemistry and Process Safety

    Process engineers want predictable behavior not only to protect yields but to maintain safe working environments. 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride stands out for its manageable volatility, smooth handling profile, and resistance to premature hydrolysis, when compared to more reactive or less stable sulfonyl chlorides. We’ve observed lower rates of off-gassing and aggressive fuming during dispensing in comparison to traditional benzenesulfonyl chloride.

    Our facility limits the formation of volatile byproducts by controlling reaction temperature and drying under filtered nitrogen. This aligns with both internal environmental targets and customer-driven sustainability audits. The waste streams from our process show lower levels of corrosive byproducts, reducing neutralization costs for our partners. We’ve shifted to batchwise containment protocols that protect operators and reduce spills—something seldom prioritized for small-volume specialty intermediates, but crucial in risk-averse sectors such as pharmaceuticals.

    Applications: Real-World Examples from Industrial Use

    Feedback from advanced pharmaceutical teams shows this molecule’s effectiveness for sulfonamide synthesis, even under harsh conditions that defeat regular benzenesulfonyl chloride. It enables the introduction of polar, electron-deficient aryl groups precisely where they’re needed in complex heterocyclic scaffolds or peptide mimics. The bromine functional handle can stay dormant until needed, giving medicinal chemistry groups valuable synthetic flexibility. Peptide and oligonucleotide chemists report success using this intermediate during side-chain capping and backbone modification strategies, where its dual high-activity and selectivity reduce the need for extra purification steps.

    Custom agrochemical workflows also benefit. Where typical aryl sulfonyl chlorides pause at the protecting step, this compound enables further modifications—fluorination, cross-coupling, or insertion—enabling designers to chase higher specificity or improved field activity profiles. Over hundreds of lots, our documentation shows uptimes above 98% for automated loading and dosing in process plants handling this compound, surpassing the metrics for less rigorously manufactured analogs.

    Advanced electronics and materials synthesis teams leverage the electron-withdrawing attributes for charged ion transport layers in OLED and specialty polymer work. In these cases, purity and stability go beyond technical specs—impurities threaten device performance. Our statistical process control correlates sub-ppm impurity levels with thin film efficacy, giving materials scientists more confidence in their downstream work.

    Batch Records, Traceability, and Expert Collaboration

    From the start, every production batch receives a traceability record integrating starting material lots, operator shifts, and environmental controls. Our logs don’t just sit on a shelf; we draw on them to troubleshoot, accommodate new solvent restrictions, and tailor advice for customers encountering deviations. Over time, this strengthens relationships and hastens resolution of rare quality questions in regulatory filings or investigational projects.

    Collaboration doesn’t stop at delivery. We regularly host joint technical reviews with buyers—walking through HPLC trace data, storage trends, and even transport conditions. For users scaling from grams to multiple kilograms, our process chemists offer tailored procedure suggestions, grounded in real-time observations rather than template advice. Lessons from one sector often transfer into breakthrough applications in another—our staff’s hands-on experience feeds directly into the guidance we offer.

    Differentiation: Real Benchmarks, Not Just Claims

    Against the generic alternatives, our 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride scores consistently on four practical points: impurity control, packaging integrity, reliable reactivity, and responsive support. Feedback surveys and internal audits document a customer satisfaction rate north of 95% for the last five years. Not every manufacturer invests this time or effort into process optimization; too many focus only on COA specs. In contrast, our approach centers on bridging the gap between analytical purity and in-use performance. That’s how we’ve carved out loyalty among high-end synthesis groups.

    Technical differentiators—such as low hydrolysis residue and stable bromo/trifluoromethyl pattern—directly impact on-stream time for industrial campaigns. Our emphasis on deep process understanding offers a clear return: less downtime, fewer batch recalls due to off-target side products, and simpler compliance with cGMP and ISO standards.

    Continuous Improvement: Learning from Each Batch

    Real-world manufacturing teaches humility. Each customer application feeds back into process adjustments, whether through minor tweaks in crystallization temperature or enhanced drying protocols. We respond to raw material market shifts by qualifying alternative sources, running parallel pilot reactions, and comparing downstream impact. Our teams keep both eyes on changing environmental standards, so each improvement boosts both quality and compliance over time.

    This commitment is reflected in our incident reporting and open communication culture. Customers don’t just get a vial or drum—they gain a partner in troubleshooting and problem prevention. This reduces overall project risk, especially for high-stakes synthesis where lead times are tight and budgets inflexible.

    Supporting Innovation: Customization and New Directions

    Researchers exploring novel reaction cascades or unusual substrate couplings require tools beyond off-the-shelf intermediates. We support these efforts, adapting particle size, drying level, or even reactivity via custom synthesis for select users. These orders require direct collaboration between our technical staff and client labs, blending process expertise with end-use creativity.

    Newer collaborations include process intensification projects, aiming to streamline multi-step syntheses by integrating activation and protection steps using this compound. Joint development agreements enrich our own process knowledge and set new industry benchmarks for reliability.

    Challenges Ahead: Meeting Future Demands

    Demand for highly specialized sulfonyl chlorides is growing, driven by needs in drug discovery and advanced materials. Meeting these demands means staying agile in process development, expanding capacity smartly, and reducing environmental impacts wherever possible. Frequent audits and customer visits reveal the tight timeframes and stringent requirements end-users now expect; this drives us to constantly reevaluate raw material choices, introduce real-time monitoring, and shorten feedback cycles.

    We recognize the pressure to further reduce trace metals, residual solvents, and cross-contamination—a persistent challenge, especially as equipment is pushed for ever-higher throughput. Our capital expenditure plan addresses these problems head-on, adding dedicated equipment trains, tighter cleaning validation, and automated micro-batch testing for high-sensitivity applications.

    Shaping Tomorrow’s Chemistry from the Production Line Up

    Our team’s expertise grows with each lot shipped—not just in producing material that meets spec, but in solving problems alongside researchers across sectors. Each drum of 4-Bromo-3-(Trifluoromethyl)Benzenesulfonyl Chloride carries a legacy of trial, adaptation, and service that supports scientific progress. Our commitment is to maintain this momentum, anchoring every advancement in hard-earned experience and open dialogue with users.

    By focusing on deep process knowledge, stringent controls, and continuous learning, we deliver more than a chemical—we contribute a dependable link in the innovation chain. Through consistency, transparency, and technical partnership, we keep pushing forward what’s possible in fine chemicals manufacturing.