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4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride

    • Product Name 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride
    • Alias BTMOSC
    • Einecs 629-383-7
    • 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

    203266

    Chemical Name 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride
    Molecular Formula C7H3BrClF3O3S
    Molecular Weight 357.52 g/mol
    Cas Number 1422369-42-7
    Appearance White to off-white solid
    Solubility Slightly soluble in polar organic solvents
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Purity Typically >97%
    Smiles COC(F)(F)C1=CC(Br)=CC(S(=O)(=O)Cl)=C1
    Inchi InChI=1S/C7H3BrClF3O3S/c8-4-1-2-5(16(9,13)14)6(3-4)15-7(10,11)12/h1-3H

    As an accredited 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure blue cap, labeled with chemical name, hazard symbols, and quantity: 25 grams, sealed for safety.
    Shipping **Shipping Description:** 4-Bromo-2-(trifluoromethoxy)benzene-1-sulfonyl chloride should be shipped in tightly sealed containers under dry, cool conditions. It is moisture-sensitive and corrosive; handle as a hazardous chemical (UN3261, Corrosive Solid, n.o.s.). Appropriate labeling and documentation are required. Comply with all local and international transport regulations for hazardous materials.
    Storage 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, heat, and sources of ignition. Protect from light and incompatible substances such as strong bases, strong oxidizers, and water. Handle under inert atmosphere if possible, and avoid contact with air and humidity to prevent decomposition.
    Application of 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride

    Applications of 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride, we focus on real, established industrial segments where this intermediate is vital for downstream product performance, compliance, and processing efficiency. Below are key application areas, each mapped to their actual industrial context, regulatory framework, formulation practices, production schemes, and finished goods.

    1. Pharmaceutical API Synthesis (Sulfonamide Segment)

    This specialty sulfonyl chloride serves as a key sulfonating agent in the synthesis of advanced sulfonamide building blocks for selective pharmaceutical actives, particularly within anti-infective and CNS agent research pipelines. Its high reactivity enables the formation of critical S–N bonds under controlled process schemes, ensuring precise sulfonamide functionality and site-selectivity for medicinal chemistry and scale-up labs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU EMA Guidelines for Intermediates
    • WHO Technical Report Series No. 986

    Typical usage ratio

    • 1.10–1.25 molar equivalents relative to amine substrates
    • Adjusted based on amine reactivity and process yield requirements

    Downstream process integration

    • Undergoes controlled sulfonylation post-amination stage in multi-step API processes
    • Integrated after deprotection or amidation where selective S–N bond introduction is required

    Final product types

    • Sulfonamide-substituted active pharmaceutical ingredients
    • Intermediate scaffolds for heterocyclic drugs
    • Small molecule CNS agents
    • Antibacterial agents under IND development

    2. Agrochemical Intermediate Production

    This compound functions as a sulfonylating and halogenating intermediate in the targeted synthesis of agrochemical actives, especially for sulfur-containing herbicide and fungicide molecular classes. Its trifluoromethoxy and bromo groups impart unique electron-withdrawing effects, benefiting downstream substitution, coupling, and crystallization steps in modern agroscience R&D.

    Industry compliance standards

    • EPA Title 40 CFR Part 158 (Pesticide Registration Requirements)
    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO JMPR agrochemical standards
    • ISO 9001:2015 for process monitoring

    Typical usage ratio

    • 1.05–1.18 molar equivalents in condensation steps
    • Fine-tuned for target yield vs. side reaction minimization

    Downstream process integration

    • Reacted with amines or phenols post-halogenation in core molecule construction
    • Used during key-stage sulfonylation in multi-functional crop protection synthesis

    Final product types

    • Sulfonylurea herbicide actives
    • Trifluoromethoxy-substituted fungicides
    • Herbicide meta-intermediates for post-patent product lines
    • Pre-formulation intermediates for custom agro R&D contracts

    3. Specialty Polymer Additive Manufacture

    In the specialty polymers market, this sulfonyl chloride is indispensable for introducing sulfonated aromatic units into engineering plastics or ionomers, creating unique chemical resistance or ionic conduction characteristics. The material’s strong electron-withdrawing nature helps tailor the final polymer’s physical performance and processing parameters.

    Industry compliance standards

    • REACH Annex XVII (EU Chemical Safety Requirements)
    • ASTM F2026 (Standard for High-performance Polymers)
    • RoHS 2 Directive 2011/65/EU
    • ISO 14001:2015 for environmental impact control

    Typical usage ratio

    • 0.7–3.0 wt% relative to monomer feed in copolymerization or post-functionalization
    • Ratio optimized following targeted sulfonation degree and mechanical property needs

    Downstream process integration

    • Post-polymerization sulfonation in resin modification units
    • Direct copolymerization with aromatic/heterocyclic monomers for new polymer grades

    Final product types

    • Sulfonated aromatic engineering plastics
    • Ionomer electrolyte membranes for fuel cells
    • Functional polymer beads for chromatography media
    • Antistatic and chemically resistant coatings

    4. Advanced Electronic Chemicals Synthesis

    This sulfonyl chloride is a crucial intermediate in the bespoke synthesis of specialty fluorinated and sulfonated molecules for microelectronics and display panel manufacturing, including etchants and high-purity chemical precursors for semiconductor fabrication. Its high purity and trace-metal control support ultra-trace contaminant specifications for cleanroom chemistry.

    Industry compliance standards

    • SEMI C3-0710 (Electronic Grade Chemical Specification)
    • IEC 62474 (Material Declaration for Electronics Manufacturing)
    • USP Grade or JIS K 0557 for semiconductor chemicals
    • IATF 16949:2016 (if supplied to automotive electronics supply chain)

    Typical usage ratio

    • Used as a limiting reagent with a 1.0–1.08 molar ratio in high-purity batch synthesis
    • Adjusted based on required final purity and downstream etch rate specifications

    Downstream process integration

    • Conversion into sulfonic acid–functionalized small molecules for photolithography and etching baths
    • Introduced at early-stage organofluorine precursor synthesis in ultrapure chemical supply

    Final product types

    • Electronic-grade photoresist intermediates
    • Fluorinated sulfonic acid etchants
    • LCD and semiconductor process auxiliary chemicals
    • Microelectronics substrate cleaners

    5. Fine Chemical Custom Synthesis Services

    We supply this sulfonyl chloride as a modular building block to fine chemical contract manufacturers looking to scale specialty halogenated, fluorinated, or sulfonated entities in pilot and commercial volumes. Its distinct chemical profile supports custom molecule assembly for R&D tool compounds, reference standards, and niche high-value chemicals.

    Industry compliance standards

    • ISO 9001:2015 for project traceability
    • Responsible Care Management System®
    • GHS/CLP for labeling, storage, and handling
    • ICH Q11 (Development and Manufacture of Drug Substances) for contracted pharma projects

    Typical usage ratio

    • Ranges from 0.8–1.2 molar equivalents per customer-specified transformation
    • Usage determined by custom synthesis protocol and by-product minimization targets

    Downstream process integration

    • Stepwise introduction for scaffold sulfonation in contract multi-gram to multi-kg lots
    • Used under anhydrous or two-phase catalytic conditions depending on the route

    Final product types

    • Reference standard molecules for biotech and research labs
    • Specialty halogenated organics for material science
    • Tool compounds for industrial analytical kits
    • Niche building blocks for high-throughput screening collections
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride: From Bench to Bulk

    Our Commitment to Consistency and Purity

    Years of experience in manufacturing high-value aromatic sulfonyl chlorides have led us to constantly refine our processes for 4-Bromo-2-(trifluoromethoxy)benzene-1-sulfonyl chloride. Chemists in pharmaceutical, agricultural, and advanced materials sectors have called for a reagent offering both synthetic versatility and sharp selectivity. In our plant, the foundations of quality rest on reliable sourcing, control of moisture, and rigorous verification before the drums ever leave for your facility. By handling every critical step ourselves, from bromination to final purification, we ensure low residual solvents and a product that behaves predictably in your applications.

    Understanding 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride

    This compound combines a trifluoromethoxy group and a bromo substituent on a sulfonyl chloride-activated aromatic ring. The arrangement gives this molecule a special place among arylsulfonyl chlorides. For process chemists, the electron-withdrawing substituents improve stability and reactivity, allowing for smoother transformations even under demanding conditions. Whether developing a new kinase inhibitor or introducing a stable leaving group, this sulfonyl chloride opens up reliable downstream modifications. Our chemists have worked closely with process development teams to determine purification approaches that consistently keep trace metal contaminants low and remove potential interference in scaled coupling reactions.

    Specifications that Reflect Real Process Needs

    From pilot liters to full metric tonne lots, meeting your threshold for impurity profiles matters. We guarantee each batch with a minimum purity above 99%, confirmed by HPLC, and residual starting material below strict detection limits. Typical appearance ranges from off-white to light yellow crystalline solid. Moisture content stays below 0.2%, supported by ongoing Karl Fischer testing on every drum. Particle size control, though not as critical for many applications as in some catalysts, receives attention during crystallization. Thermal stability and melt behavior undergo stress testing during method development, capturing data on decomposition behavior to help customers tune storage and charging operations. The production process itself eliminates the need for heavy metal reagents or phosgene derivatives, reducing regulatory hazards at your site.

    Practical Use Cases in the Lab and on the Line

    Synthesizing targeted sulfonamides brings out the strengths of this molecule. Many pharmaceutical intermediates rely on mild, selective sulfonylation to build in both functional group tolerance and metabolic stability. Direct attachment of the bulky trifluoromethoxy group, in combination with the aryl bromide, creates a platform for further palladium-catalyzed cross-couplings while also enhancing bioactivity in heterocycle frameworks. Peptide chemistry groups have reported strong yields with minimized racemization, attributing performance to our careful control of acid chloride impurities. Process engineers developing new herbicides have pointed to this product as a building block for activity tuning, where the trifluoromethoxy group leads to enhanced hydrolytic resistance and tailored absorption in difficult botanical targets.

    Adoption in electronics chemistry continues to grow, particularly in functionalizing liquid crystal precursors and OLED intermediates. The bromo substituent lends itself to clean Suzuki or Stille coupling, while the sulfonyl chloride function provides a gateway to robust, additional derivatization. For certain dyes and specialty polymers, the direct introduction of a trifluoromethoxy group combines strong electronegativity with desirable lipophilicity. Material scientists report improved performance traits in final products, owing in part to the controlled trace impurity content our processes achieve.

    Comparison with Other Sulfonyl Chlorides

    As the family of arylsulfonyl chlorides has expanded, subtle structural shifts can lead to dramatic shifts in chemical behavior. The coupling of both bromo and trifluoromethoxy groups, as seen in this product, achieves an interplay that sets it apart from the more common methyl, chloro, or simple phenyl analogs. In actual synthetic sequences, the trifluoromethoxy group imparts both electron-withdrawing power and increased molecular volume, helping suppress side reactions and boosting selectivity in most coupling strategies. The bromo group naturally unlocks site-specific arylation or amination by standard Pd-catalyzed methods. We have seen direct feedback from customers that impurity profiles differ substantially from classical tolyl or chlorophenyl sulfonyl chlorides that can leave problematic residues in final downstream products.

    Simple arylsulfonyl chlorides fall short in applications requiring highly fluorinated motifs or demanding moisture sensitivity profiles. The increased lipophilicity of our product translates to cleaner separation steps and crisp, low-odor profiles post-reaction. Additionally, the thermal handling benefits—demonstrated through DSC and TGA studies—remove bottlenecks in both scale-up and purification, reducing operational downtime and limiting equipment corrosion compared to more aggressive sulfonyl chlorides. Not all manufacturing techniques are equal. Our synthesis minimizes problematic trace impurities such as ortho-bromo or bis-sulfonated byproducts, producing an easier-to-handle compound for high-purity, regulated industries.

    Backed by Decades in Chemical Synthesis

    The journey of arylsulfonyl chlorides has been shaped by ongoing feedback from research labs, regulatory bodies, and customer process development teams. We have run stability trials under diverse climate conditions and built in excess packaging protection for extended storage and long-haul shipping. Chemists with direct handling experience have seen that some batches from non-integrated producers bring unwelcome surprises, ranging from excess solvent carryover to variable melting points and batch-to-batch odor fluctuations. Our team’s hands-on approach, supported by a robust in-process analytics lab, has allowed us to catch and correct these issues long before the product reaches end users.

    Traceability remains a cornerstone. Every drum carries comprehensive documentation, including current HPLC, GC, and titration results, so users have clear, actionable quality data tailored to their actual process requirements. Instead of relying heavily on brokers or middlemen, we keep tight control over material flows, responding directly to customer questions about lot-to-lot variation, reactivity notes, or shipment timelines. Changes in upstream regulatory guidance or raw material supply receive immediate internal review, minimizing risk for buyers needing business continuity assurance.

    Sustainability and Safety as Everyday Practice

    The specialty chemicals field faces mounting pressure around environmental practices and worker safety. In our district, regulation covers everything from source emissions to packaging closure types. We have responded by installing continuous emissions monitoring, improving solvent recycling, and investing in real-time environmental reporting technology. Crystalline arylsulfonyl chlorides present well-understood hazards, but our protocols around containment, dust abatement, and PPE use stem from first-hand experience—an approach that remains grounded in tireless risk reduction and open worker feedback.

    Safe handling of this compound means more than standard protocols. Each shift, our operators monitor reaction containment and work with engineering teams to adjust controls when venting patterns change or container geometry introduces mixing risks. We share these learnings with customer safety leads and help align handling SOPs with evolving site requirements. Spill abatement plans, alongside tailored fire-fighting recommendations based on unique compound properties, come from years spent designing and commissioning aromatic halide production lines under real-world constraints.

    Outside industry walls, regulatory pathways increasingly scrutinize persistent fluorine-containing molecules. Our manufacturing choices have shifted to less persistent solvents where possible and reforms to downstream waste treatment. Customer audits, inbound and outbound, inspect not just product output but steps taken to minimize environmental and human risk for every kilogram shipped out.

    Supporting Innovation: Beyond the Drum

    The needs of synthetic chemists keep evolving. No two downstream pipelines look quite alike, and our experience supplying sulfonyl chlorides underpins more than routine batch supply. Pilot orders often seek responsiveness: modifications in particle size, alternative packaging, or documentation to address regulatory filings. Our technical team reviews all change controls with a view toward safety, compatibility, and integrity of final use. Analysts in our quality center replicate end use environments to anticipate issues with solubility, cloud point, or stability in reaction solvents. In feedback sessions, research partners have rated our sampling flexibility and ongoing technical dialogue as critical supports for shifting project priorities.

    In time-critical launches, such as in agrochemical scale-up or process validation for a new drug candidate, direct communication means faster troubleshooting. Custom documentation, compliance records, and retained reference samples lay the groundwork for high-trust partnerships. Scaling from grams to tonnes can reveal bottlenecks or interaction effects not seen in benchtop runs, so our support does not end with dispatch. We have navigated seasonal temperature swings, unexpected logistical holds, and customer feedback on unexpected filtration outcomes, adapting packaging and shipment logistics as needed.

    The Future Role of 4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride

    Emerging areas such as targeted molecular imaging, custom polymers, and next-generation crop protection agents demand unique arylsulfonyl building blocks. Chemists continue to expand the application space for halogenated, fluorinated sulfonyl chlorides, drawing on sophisticated reactivity and property enhancement. Our direct involvement in method scouting and pilot demonstration places us in a strong position to serve synthetic challenges that require tight controls—be those around trace metals, allergen exclusion, or differential solubility among downstream intermediates.

    New instrument platforms and reaction design are changing how chemists approach functionalization. As applications push toward more selective functional group modifications in complex scaffolds, tight batch consistency becomes non-negotiable. The structure of this product facilitates selective coupling and robust transformation across a spread of modern catalytic methods. In areas like photoredox or electrochemical cross-coupling, researchers have found that careful selection of arylsulfonyl chloride substrates improves turnover and selectivity rates. This opens further avenues in controlled polymer synthesis, sophisticated ligand design, and new approaches to fluorinated material surfaces.

    Industry requirements remain dynamic, with regulatory standards around trace environmental contamination and downstream material handling growing stricter. Our long-term perspective focuses on optimizing every step of production, not just for immediate procurement but with a clear view to sustainability and regulatory alignment for years ahead.

    Direct Dialogue with Scientific Users

    As a specialized provider, we keep our technical and commercial teams in direct dialog with users—no information siloes, no third-party games of telephone. Chemists on both ends have traded data on everything from batch reactivity trends to packing density shifts under humid transport. Our long-standing relationships with researchers and production engineers have helped shape improvements to everything from lot release protocols to how we advise on bulk storage at low ambient humidity. Updates on regulatory trends, upcoming warning changes, and market pressures come directly from our engagement in multistakeholder chemical forums and industry roundtables.

    Supply resilience counts, especially for projects running on knife-edge timelines or requiring one-off production campaigns. By owning every step—reactor design, work-up, packaging, and compliance—we cut out delays and clarify ordering transparency. Upstream supply disruptions, unexpected new regulatory filings, or shifts in global logistics receive same-day attention from our production and logistics leads. Customer supply chain managers relay positive feedback about our proactive attitude toward critical timing and flexible fulfillment, based on direct, continuing listening to what process owners say about their realities on the ground.

    Continuous Quality: A Shared Priority

    Customers measure supplier trust by how predictably product performs batch after batch, year after year. Our teams log every deviation, every shift anomaly, and every root-cause fix into real-time production records. Inspection teams accept only drums that clear our established threshold for water, key residuals, and functional group density. Field complaint rates trend well below industry averages, evidence of a quality mindset that places customer experience at the center of the production effort.

    We revisit manufacturing methods with every process change, including workflow optimizations, revised moisture control setups, or resin bed technology advances. In cases where the global supply chain for critical fluorinated raw materials tightens, our purchasing group finds alternative partners and arranges split-shipment validation for key customer projects. As customer compliance expectations evolve—whether for genotoxic impurity controls, allergen exclusion, or export restrictions—our documentation and QC infrastructure adapts proactively.

    Feedback Drives the Future

    Direct, detailed technical feedback has steered our decision making over the years. It shapes product handling, packaging resilience, logistics approaches, and customer education measures. In practical terms, this could mean reinforcing container liners to survive rougher cross-border truck runs or refining user documentation to clarify best practices for first-time receivers in emerging markets. Chemical manufacturing is never static. Every decision around process, packaging, and practice draws directly from user stories, complaints, and the need to fix every process pain point customers experience.

    For 4-Bromo-2-(trifluoromethoxy)benzene-1-sulfonyl chloride, we treat every kilogram shipped as a reflection of our accumulated know-how, adaptation, and shared interest in seeing high-value reactions run safely and efficiently. The ideas and advice of working chemists, shipped with every drum, carry real weight—guiding every upgrade, risk review, and continuous improvement effort inside our facilities. We look forward to the challenges and opportunities ahead, always in direct partnership with the hands that turn ideas into products on factory floors and in research labs worldwide.