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3-(Trifluoromethylthio)Bromobenzene

    • Product Name 3-(Trifluoromethylthio)Bromobenzene
    • Alias 1-Bromo-3-((trifluoromethyl)thio)benzene
    • Einecs 621-341-2
    • 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

    813272

    Productname 3-(Trifluoromethylthio)Bromobenzene
    Casnumber 461-95-0
    Molecularformula C7H4BrF3S
    Molecularweight 257.07
    Appearance Colorless to pale yellow liquid
    Boilingpoint 216-218 °C
    Purity Typically ≥98%
    Density 1.64 g/cm³
    Refractiveindex 1.547
    Smiles C1=CC(=CC(=C1)Br)SC(F)(F)F
    Synonyms m-Bromophenyl trifluoromethyl sulfide
    Solubility Insoluble in water
    Shelflife 2 years (when stored properly)
    Storagecondition Store at 2-8°C, protected from light

    As an accredited 3-(Trifluoromethylthio)Bromobenzene 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, with tamper-evident cap and hazard labeling. Clearly marked: “3-(Trifluoromethylthio)Bromobenzene.”
    Shipping 3-(Trifluoromethylthio)Bromobenzene is shipped in tightly sealed containers to prevent leaks and moisture exposure. It is packaged in accordance with international regulations for hazardous chemicals, including proper labeling and documentation. Transport typically occurs via ground or air freight, ensuring temperature control and protection from light, with compliance to UN shipping standards.
    Storage 3-(Trifluoromethylthio)Bromobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat sources, ignition sources, and direct sunlight. Keep it segregated from incompatible substances such as strong oxidizing agents. Store at room temperature and ensure proper labeling. Avoid moisture and humidity. Use secondary containment to prevent spills and leaks.
    Application of 3-(Trifluoromethylthio)Bromobenzene

    Applications of 3-(Trifluoromethylthio)Bromobenzene in Industrial Manufacturing

    As an original manufacturer, we supply 3-(trifluoromethylthio)bromobenzene directly to critical downstream sectors. Our material underpins essential chemical transformations in advanced pharmaceutical synthesis, agrochemical development, specialty material production, and electronic intermediates. The following sectors illustrate specific, established applications in each field.

    1. Pharmaceutical Intermediate Synthesis

    Manufacturers use this compound predominantly in multi-step synthesis for active pharmaceutical ingredients (APIs), especially where selective trifluoromethylthio substitution is required in complex aromatic scaffolds. Its brominated moiety enables direct palladium-catalyzed cross-coupling, while the CF3S– group introduces strong electron-withdrawing character to fine-tune pharmacokinetic properties. Production lines integrate it during mid- or late-stage synthetic steps, especially in anticonvulsant, antineoplastic, and central nervous system candidate development paths.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4 GMP Guidelines
    • Chinese Pharmacopoeia – API precursor purity specifications

    Typical usage ratio

    • 0.2 to 0.8 molar equivalents, calculated against principal aromatic substrate; ratio varies in route optimization for yield versus cost.

    Downstream process integration

    • Introduced during Suzuki, Buchwald-Hartwig, or Ullmann coupling; dissolved in polar aprotic solvent with appropriate base and metal catalyst; downstream isolation often includes flash chromatography or crystallization before subsequent derivatization or deprotection steps.

    Final product types

    • Quinazoline derivatives for oncology
    • Novel benzothiazoles for CNS disorders
    • Pyridine analogs with CF3S groups for antiviral research
    • API intermediate stocks for contract drug syntheses

    2. Agrochemical Building Block

    Our raw material supports key halogenated aromatic assembly in the synthesis of modern agrochemical actives. Major pesticide and herbicide manufacturers apply it as a route to achieving high lipophilicity and metabolic stability in aryl-trifluoromethylthio compounds used in crop protection products. Its use appears in stepwise or combinatorial synthesis of novel fungicides and selective herbicides, often within research and pilot-scale settings advancing to larger production.

    Industry compliance standards

    • FAO/WHO JMPR pesticide purity criteria
    • ISO 9001:2015 certified synthesis procedure records
    • REACH registration for downstream agrochemical intermediates
    • China GB2763 maximum residue limit framework (for final actives)

    Typical usage ratio

    • 0.3 to 1.0 equivalents per target arene, often depending on lab-to-pilot scale-up optimization and desired substitution pattern.

    Downstream process integration

    • Charged to coupling or nucleophilic substitution reactors as a pre-activated halogen source; sometimes converted in situ to Grignard or lithium intermediates prior to quenching with agroscience ligands; workflow includes rapid extraction and subsequent oxidation or reduction steps.

    Final product types

    • Trifluoromethylthio-substituted phenylureas
    • Aromatic sulfonylureas for selective weed control
    • Experimental broadleaf fungicides
    • Precursor stocks for seed treatment agents

    3. Specialty Polymer & Fluoropolymer Modification

    Producers of high-performance polymers employ this aromatic intermediate during the introduction of trifluoromethylthio pendant groups onto polymer backbones. The functionality imparts chemical resistance, low surface energy, and enhanced dielectric properties critical for niche engineering plastics and membrane materials. Manufacture involves co-polymerization or grafting via nucleophilic aromatic substitution on advanced monomers or oligomers, mainly as part of R&D and specialty batch production lines.

    Industry compliance standards

    • ISO 9001:2015 for traceability in specialty plastics
    • RoHS Directive 2011/65/EU for electronic materials
    • ASTM D543 for chemical resistance validation
    • UL 94 testing for flame-retardancy (if applied in electronics)

    Typical usage ratio

    • 1-6 wt% on total monomer mass; precise percentage tailored to target mechanical and dielectric properties or end-use requirements of specialty polymer.

    Downstream process integration

    • Co-introduced with monomers during key step-growth polymerization; may undergo functional group activation prior to radical or ionic polymerization setups; post-polymerization treatments may follow to achieve final property profiles.

    Final product types

    • High-performance fluorinated co-polymers
    • Membrane elements for aggressive chemical filtration
    • Low-surface-energy insulating films for electronics
    • Durable industrial coating additives

    4. Electronic & Liquid Crystal Intermediates

    Specialty electronics manufacturers utilize this compound as a pivotal intermediate in synthesizing advanced functional materials for organic electronics and liquid crystal displays. Its unique electron-withdrawing and halogenated structure facilitates preparation of custom aryl compounds that influence switching speed and charge-carrier mobility in consumer electronic devices. Most commonly, application occurs during intermediate stages of high-value ligand assembly and patternable molecular design, especially for R&D scale-up on proprietary device components.

    Industry compliance standards

    • IEC 61249-2-21 for halogen content in substrate materials
    • IPC-4101 for high performance base materials
    • IATF 16949:2016 for electronic materials supply chain
    • OEM-specific materials qualification (e.g., Samsung, LG, BOE supplier protocols)

    Typical usage ratio

    • 0.1–0.5 molar ratios based on target molecule structure, adjusted according to aromatic core assembly requirements in device patterning sequences.

    Downstream process integration

    • Fed into multi-step organic synthesis, serving as aryl halide for custom ligand attachment; followed by purification and molecular alignment optimization for solution-processing or vapor deposition processes in device manufacturing.

    Final product types

    • Liquid crystal monomers for display panels
    • Electron-transport materials for OLED/OPV
    • Precursor compounds for high-frequency device substrates
    • Functional molecular layers for photonic devices
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    Certification & Compliance
    More Introduction

    Introducing 3-(Trifluoromethylthio)Bromobenzene: A Foundation for Advanced Synthesis

    Not Just Another Halogenated Aromatic

    Our years of experience in fluorinated chemistry has shown us that the difference between ordinary and performance-driven compounds often lies in the synergy of substituents. 3-(Trifluoromethylthio)Bromobenzene has grown into a reliable asset for those seeking strong electron-withdrawing effects combined with serious functional group adaptability. At our facilities, we have fine-tuned the preparation process for this compound, and for solid reasons: structure translates directly into reactivity, and every batch impacts how smoothly a product developer or process chemist moves from raw material to end result.

    What We Implement and Why

    The compound itself features a bromine atom and a trifluoromethylthio group in the meta positions on the benzene ring. That seems straightforward, but it changes things in practice. Adding bromine to an aromatic system offers a handle for cross-coupling. The trifluoromethylthio group delivers substantial lipophilicity and a triple pack of electron-withdrawing power, meaning it controls distribution in organic phases and can tamp down or shift rates in target reactions. Physically, we prepare this product as a light, nearly colorless liquid in the lab, with a purity designed for the exacting needs of pharmaceutical intermediates and materials scientists. We've measured consistent boiling ranges under reduced pressure, and every drum we ship leaves our plant with a GC profile confirming low levels of residual impurities and controlled moisture.

    Engineering Consistency for Your Workflow

    Labs and pilot facilities order 3-(Trifluoromethylthio)Bromobenzene for a wide range of synthetic applications. Some are looking for the robust leaving group properties of bromine to drive Suzuki, Negishi, or Buchwald–Hartwig couplings. Others value the stability the SCF3 group contributes in medicinal chemistry scaffolds, pushing through late-stage functionalizations without unwanted hydrolysis or side reactions. We learned early on that reaction scale and yield are always under the microscope; a clean, reproducible starting material is an absolute must. Variations in product quality show up as variable reactivity, fouling, or costly purification steps. Every change in raw material impacts not just an isolated yield figure but the downstream economy of an entire project.

    Specifications that Support Experimentation

    We manufacture 3-(Trifluoromethylthio)Bromobenzene with molecular formula C7H4BrF3S and a molecular weight of about 257.07 g/mol. The product comes in standard drum and bottle packaging, each clearly labeled to allow easy tracing through your own workflow. We rely on gas chromatography and NMR for every lot, as we’ve learned firsthand how traces of related benzyl or brominated byproducts create headaches during scale-up or regulatory filings. Moisture content is monitored using Karl Fischer titration; residues above specified limits slow alkylations and have even stalled progress on larger campaigns at customer sites in the past. Our supply chain includes a cold storage protocol specifically for this product, we moved to this step after fielding feedback about volatility and component degradation in overseas transit.

    Why 3-(Trifluoromethylthio)Bromobenzene Matters for Innovation

    Fluorinated and brominated aromatics keep earning attention as building blocks because they consistently unlock new chemical space. In our direct collaboration with researchers in both agrochemical development and clinical candidate scale-up, this product stood out for its versatility. We’ve watched teams use it to anchor structure-activity relationship studies, building libraries by selectively swapping out the bromine. At the same time, the SCF3 group resists metabolic degradation, lending extra in vivo stability to candidate molecules. We experienced cases where this stability turned a borderline in vivo performer into a viable lead in antitumor screens. The lipophilic tail, thanks to the trifluoromethylthio group, proved irreplaceable in designing molecules for deeper tissue or blood-brain barrier penetration.

    Component Differences that Shape Synthesis

    We see buyers carefully comparing 3-(Trifluoromethylthio)Bromobenzene to its trifluoromethyl (CF3) and methylthio (SCH3) analogs. The SCF3 group sits in an unusual middle zone, exerting stronger electron withdrawal than CF3, while still offering greater chemical stability than SCH3. In practice, we’ve seen its resistance to oxidation in basic or thermal conditions. Process chemists at our client firms report fewer byproducts in halogen-metal exchange or transition-metal-catalyzed reactions. For coupling-based library synthesis, the ortho-para directing influence of bromine (over iodide or chloride analogs) produces cleaner products, helping reduce purification times.

    Practical Use Cases from the Bench

    Ralating real use back to process chemistry, one project involved rapid optimization of a phenyl-based fungicide. Standard bromobenzenes failed to deliver candidate molecules with required metabolic stability. Only the SCF3 substituted version generated active compounds with an acceptable half-life in plant assays. In scale-up for fluorinated specialty monomers, higher volatility of some halogen alternatives caused loss during distillation, but our product retained integrity at process-relevant temperatures. Our materials delivered tighter product specs, which meant that a multinational client could reduce solvent usage and lower waste in their own syntheses of advanced intermediates.

    The Details that Set Our Product Apart

    Producing 3-(Trifluoromethylthio)Bromobenzene in consistently pure form means controlling every variable, from starting material selection to packing atmosphere. We stopped using lesser brominated benzene grades after tests showed off-odors and yellowing on storage. Weekly in-house batch monitoring flagged moisture as a quick culprit for hydrolysis, so we revamped our drying and sealing protocol. Crucially, we dedicate reactors and purification lines to this synthesis, rather than switching from other sulfur- or nitrogen-containing intermediates. That move cut cross-contamination risk and eliminated the inconsistent GC peaks we used to see when alternating product lines.

    Regulatory and Handling Perspective

    Over time, we’ve learned that regulatory scrutiny hangs over halogenated and fluorinated compounds, especially those with potential environmental persistence. We maintain tight documentation for every lot. Customers working under cGMP or custom synthesis agreements expect a full chain of custody and impurity profile. We keep those records on hand, and our analytical staff responds directly to customer inquiries about impurity carryover, elemental contamination, or trace solvent residues. We’ve coordinated directly with logistics partners to avoid unintentional warming or freezing in transit—seemingly small, but this keeps product in spec at the customer’s dock. Proper PPE, indirect venting, and careful inventory management are issues baked into daily operations, not afterthoughts.

    Crafting for Compatibility

    Simply put, compatibility in modern synthesis means more than matching a chemical’s phosphorylation or halogen-reactivity. We developed 3-(Trifluoromethylthio)Bromobenzene so that it works across various catalyst systems. Our feedback loop with process R&D teams revealed that some brominated aromatics can accelerate ligand decomposition or catalyst fouling during scaling. For our compound, we adjusted purification to bring metal contaminants to sub-ppm levels. Coordination complex formation with metals (Pd, Ni, Cu) during reaction is less pronounced in our experience, and this means less downtime and less handholding during pilot-scale runs. Direct discussions with end users pushed us to document these improvements, which we now include in our technical support notes on request.

    Downstream Impact on Cost and Sustainability

    Even as tight margins and ESG demands move upstream in chemical manufacturing, a product’s life cycle carries real consequences for sustainability. We examined the decomposition routes for several trifluoromethylthio-armed benzenes, and found that ours generates lower quantities of persistent fluoro-organic fragments during both use and disposal. Consistently pure product helps customers reduce solvent and energy use in their own operations, since less reprocessing or column work is required. Supporting greener chemistry isn’t a matter of marketing: the waste management bills, regulatory filings, and factory audits tell the true story.

    Why Pharmaceutical and Agrochemical Innovators Rely on Our Product

    Collaborating directly with pharmaceutical project teams, we’ve supported the synthesis of kinase inhibitors and CNS-active small molecules. Teams pursuing SAR expansion reach for SCF3-bearing rings for their distinctive polar lipophilicity, and the bromine handles unlock parallel functionalization. In the agrochemical space, we've observed that shifting from CF3 to SCF3 often enhances foliar absorption and durability, especially under weathering conditions. Years of supplying these sectors taught us that agreement between analytical spec and benchtop reproducibility is what attracts repeat orders. Our in-process sampling helps avoid the batch-to-batch ‘surprises’ that disrupt filings or process validations.

    Learning from User Feedback: Continuing to Improve

    Direct, honest feedback from our buyers shaped our quality improvements. Customers spoke bluntly about prior suppliers providing inconsistent or yellowed product batches. In response, we scheduled more frequent organoleptic testing and launched an NMR-based screening step before shipment. Suggestions from process chemists using the product for metal-catalyzed reactions led us to screen solvents and test product miscibility in arylation reactions before launching bulk production lots. We no longer accept ‘close enough’ performance; data drives every release.

    Resource Investment and R&D Expansion

    In our operations, commitment to this compound starts at procurement. We source rings and thiolating agents only from audited, traceable sources. Each lot’s analytical data expands our hard-won in-house database, so patterns in stability and reactivity are tracked over time. Bringing product to industry-leading standards prompted investment in dedicated distillation and filtration rigs, ensuring metal levels and residual solvents never creep up untracked. Our R&D division tests each batch in a handful of core cross-coupling and electrophilic aromatic substitution model reactions, and we publish the anonymized data trends for customer review.

    Bridging Scale and Laboratory Results

    Pilot facilities and gram-to-kilogram research settings face very different challenges, but a consistent, high-spec product is the best hedge against headaches later. We realized long ago that downstream processes infrequently adjust to variable input purity; process engineers want ‘clockwork’ response. By standardizing key physical constants, we help scale-up chemists anticipate handling characteristics and plan for plant-scale couplings or substitutions. We provide real, current melting point, boiling range, and density data, so no one is left guessing during a rushed campaign. Our product matches the keen expectations researchers set after running a single clean trial at milligram scale.

    Staying Ahead in a Rapidly Evolving Chemical Landscape

    The surge in demand for fluorinated intermediates hasn’t led us to compromise. Every year, more synthetic routes demand halogenated triggers or challenging electronic effects in precisely controlled molecular environments. Our plant teams train on and enforce strict cleaning, cross-checks, and multi-stage filtration. We log every process tweak, audit supply side quality, and support customers who run into difficult scale-ups or synthesis blockades. Some competitors might cut corners, but our longevity in the sector is built on evidence-driven consistency and technical transparency. Our team, from operators to analytical scientists, owns our shared commitment to clean fluorinated outputs.

    Sharing the Knowledge: Transparency and Support

    We take our role as a manufacturer seriously, understanding that synthetic chemistry is not just about product delivery, but also about reliable, honest technical partnership. We field questions from research chemists, process engineers, analysts, and regulatory managers. Each inquiry—whether about hygroscopicity, shelf life, or melt crystallization challenges—is treated as a prompt to either supply hard data or design a test to address the concern. Sometimes, this creates extra work on our end, but these investments shape more robust projects for our customers and improve our own operations. Feedback and support arrangements have led us to directly troubleshoot pilot plant hiccups, from strange coloration during storage to stubborn traces of starting benzene. Documentation, analytical data, and support grow together.

    How Real-World Demands Molded Our Approach

    We don’t just ship chemicals; we support a deep community of scientists, engineers, and planners who keep pushing boundaries. For end users hoping to move from 'feasibility' to repeatable production, product traceability and batch honesty matter as much as the technical performance itself. In supporting critical projects across pharmaceuticals and agrochemicals, we’ve brought our compound to tighter tolerances, adapted packaging to field restrictions, and responded in real time to usage reports. Our history, built up through thousands of kilograms shipped to destinations worldwide, stands alongside each bottle we send to a customer. Every ask from a client, whether it’s “can you lower impurities below 0.05%?” or “has anyone solved solubility in t-butyl methyl ether?”, is taken as a new challenge. We roll up our sleeves and test, rather than guessing or hedging.

    Choosing Solutions Over Promises

    Raw material cost swings, logistical barriers, and regulatory pressures all bear on the final step—delivering the right building block for applications demanding reliability. We never rest on templated assurances or hypothetical advantages. Material from our reactor earns its place at the bench or plant, batch after batch, because we listen, iterate, and keep analytical data open to review. Over twenty years of chemical production, we discovered that the tools and processes supporting critical reactions—from solid-liquid separation to impurity spot tests—are as much a resource as the product itself. Direct engagement with R&D customers revealed time and again where value accumulates: not just in the structure, but in the work and care invested every step of the way.

    Future Outlook

    Markets for advanced halogenated and fluorinated intermediates demand ongoing learning, investment, and an honest appraisal of risk and reward. As environmental, economic, and regulatory expectations rise, our commitment remains. We will keep improving both substance and service, always grounded in the real-world outcomes demanded by chemists and engineers. We see each order for 3-(Trifluoromethylthio)Bromobenzene not merely as a transaction, but as a trust in our process, our standards, and our people. These expectations define our work every day.