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2-Bromo-5-Chlorobenzotrifluoride

    • Product Name 2-Bromo-5-Chlorobenzotrifluoride
    • Alias 2-Bromo-5-chloro-α,α,α-trifluorotoluene
    • Einecs 249-167-2
    • 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
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    Specifications

    HS Code

    872216

    Chemicalname 2-Bromo-5-Chlorobenzotrifluoride
    Casnumber 394-49-4
    Molecularformula C7H3BrClF3
    Molecularweight 259.45 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 199-201 °C
    Meltingpoint -6 °C
    Density 1.694 g/cm³
    Refractiveindex 1.535
    Flashpoint 82 °C
    Solubilityinwater Insoluble
    Synonyms Benzotrifluoride, 2-bromo-5-chloro-
    Smiles FC(F)(F)c1cc(Br)cc(Cl)c1
    Ecnumber 254-264-6

    As an accredited 2-Bromo-5-Chlorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dark amber glass bottle containing 100 grams of 2-Bromo-5-Chlorobenzotrifluoride, tightly sealed with a screw cap and labeled with hazard warnings.
    Shipping 2-Bromo-5-Chlorobenzotrifluoride is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical; handle with appropriate safety measures. Transport is regulated under applicable laws (e.g., DOT, IATA). Ensure proper labeling, documentation, and compatible packaging to prevent leaks, spills, or accidental contamination during transit.
    Storage 2-Bromo-5-Chlorobenzotrifluoride should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use only non-sparking tools and grounded equipment. Clearly label the container and ensure appropriate safety measures, including secondary containment to prevent spills or leaks.
    Application of 2-Bromo-5-Chlorobenzotrifluoride

    Applications of 2-Bromo-5-Chlorobenzotrifluoride in Industrial Manufacturing

    2-Bromo-5-chlorobenzotrifluoride is widely used as a key halogenated aromatic intermediate in specialty chemicals production, targeting strict sector requirements. Our manufacturing process ensures consistent purity for sensitive downstream applications. Multiple industries adopt this material as a building block or functional agent, each adopting distinct regulatory standards, process steps, and formulation strategies.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers select this compound as a targeted halogen source for active pharmaceutical ingredient (API) synthesis. Its electron-withdrawing trifluoromethyl group enables specific arylation, coupling, and substitution reactions essential for multi-step medicinal molecule construction, including anti-inflammatory and cardiovascular drug development. Consistent lot traceability and impurity control remain critical to ensure reproducible process yields and regulatory acceptance for APIs and advanced intermediates.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • EU GMP Part II
    • 21 CFR Part 211 (US FDA)
    • Chinese Pharmacopoeia (for local supply chains)

    Typical usage ratio

    • 0.1 to 1.0 molar equivalents, adjusted based on targeted API scaffold complexity and specific reaction yields

    Downstream process integration

    • Introduced during early to mid-stage coupling or halogen exchange reactions
    • Serves as a functionalized precursor for further derivatization or cyclization steps

    Final product types

    • Nonsteroidal anti-inflammatory drug (NSAID) intermediates
    • Specialty cardiovascular API precursors
    • Cancer therapeutic advanced intermediates
    • Custom small molecule contract synthesis batches

    2. Agrochemical Active Ingredient Manufacturing

    Producers in the crop protection sector utilize this halogenated benzotrifluoride for its reactivity in synthesizing selective herbicides, fungicides, and insecticide actives. The compound introduces both steric bulk and enhanced environmental stability to the molecular framework. Dedicated process controls focus on residual halide management and reduced impurity carryover, which are essential for compliance with agrochemical product registrations worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidance for Industry Data Submissions on Pesticides
    • Chinese ICAMA registration guidelines
    • REACH (EU) chemical safety requirements

    Typical usage ratio

    • 0.3–0.7 molar equivalents as a functional group donor in combined synthetic routes; adjusted per target molecule structure and desired selectivity

    Downstream process integration

    • Applied in halogen-exchange or cross-coupling stages of synthetic sequences
    • Often used before esterification, amidation, or ring-closing transformations

    Final product types

    • Trifluoromethyl-substituted herbicide actives
    • Selective cereal crop fungicides
    • Broad-spectrum insecticide precursors
    • Custom pesticide intermediate formulations

    3. Electronic Chemical Synthesis (Advanced Materials)

    Fabricators in the electronics and display industries require high-purity halogenated aromatics as intermediates for photoresist and liquid crystal monomer synthesis. This material contributes to improved electron mobility and UV resistance in specialty polymer backbones. Ultra-low residual metals, precise physical property control, and strictly documented batches are essential, supporting production of semiconductor-grade films and components under regulated manufacturing environments.

    Industry compliance standards

    • SEMI C3 standard for electronic chemical purity
    • JEITA (Japan Electronics and Information Technology Industries Association) chemical guidelines
    • UL94 flammability ratings for downstream polymers
    • RoHS Directive (EU) for hazardous substance restrictions

    Typical usage ratio

    • 2–10% by weight in electronic formulation batches, with adjustments based on required molecular architecture and end-use certification testing

    Downstream process integration

    • Enters polymer precursor syntheses for polyarylene ether, high-performance polyimides, and LCD monomer units
    • Used in controlled aryl coupling or fluorinated block assembly processes

    Final product types

    • Advanced photoresist formulations
    • OLED and LCD intermediate monomers
    • Dielectric polymer resins
    • Microelectronic component encapsulants

    4. Specialty Dye and Pigment Intermediate Production

    Manufacturers of industrial and specialty dyes employ this compound for its capacity to introduce both halogen and trifluoromethyl groups into azo and anthraquinone core structures. Its application enables development of high-stability pigment molecules with tailored solubility and strong colorfastness for plastics, inks, or coatings. Controlled integration ensures minimization of byproduct formation and compliance with modern environmental and end-user toxicity standards.

    Industry compliance standards

    • GHS classification and labelling for dye chemicals
    • Oeko-Tex Standard 100 (for textile dyes)
    • REACH Dye Substance Registration
    • EN 71-3 (Safety of Toys – migration of dye-related elements for toy inks and coatings)

    Typical usage ratio

    • 0.5–1.5 equivalents in halogenation or coupling steps, varying by pigment structure and targeted fastness standards

    Downstream process integration

    • Used during dye intermediate formation prior to diazotization or coupling with chromophores
    • Enters as a halogenated aryl unit in multistep pigment build-up reactions

    Final product types

    • Lightfast plastic dyes
    • Inkjet pigment intermediates
    • Specialized automotive and polymer colorants
    • High-solubility textile dyes

    5. Fluorinated Building Block Supply for Polymers

    Producers of specialty fluoropolymers and high-performance plastics incorporate this compound as a trifluoromethyl-bearing aromatic unit for chain growth, backbone modification, and tuning of physicochemical properties such as hydrophobicity, chemical resistance, and dielectric performance. The material enters process steps demanding robust temperature and solvent performance, with full quality control for molecular structure, homogeneity, and trace byproduct management.

    Industry compliance standards

    • ASTM D471 (Rubber and polymer chemical resistance testing)
    • UL 746A (Polymers for electrical equipment)
    • ISO 10993 (for polymer components in medical devices, where applicable)
    • REACH for polymeric intermediates

    Typical usage ratio

    • 1–8 mol% in fluorinated polymerization reactions, scaling by desired property balance in finished resin or copolymer

    Downstream process integration

    • Added in early-stage aromatic polymerization or copolymer modification cycles
    • Incorporated prior to curing/crosslinking or extrusion steps for bulk plastic production

    Final product types

    • Chemical-resistant coatings
    • High-purity fluoropolymers for electronics
    • Membranes for fuel cell and battery systems
    • Dielectric films for advanced insulation

    6. Fine Chemical Contract Manufacturing

    Toll and contract manufacturing organizations rely on this halogenated intermediate for diverse custom molecule assembly, including performance additives, specialty solvents, and niche organic compounds. Order specifications dictate purity, moisture content, and analytical profile, ensuring seamless integration into client-controlled downstream syntheses. Batch control and documentation align with client-specific ISO and customer audit requirements.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical manufacturing)
    • Chemical Facility Anti-Terrorism Standards (U.S. DHS for regulated sites)
    • Client-specified analytical release criteria (HPLC, GC-MS, NMR)
    • Material transport (UN Recommendations for Chemicals)

    Typical usage ratio

    • Defined case-by-case, typically 0.2–2.0 molar equivalents per step as dictated by end-customer synthesis or process protocol

    Downstream process integration

    • Supplied for integration at initial aryl halide substitution or advanced functionalization steps
    • Loaded into custom reactors per campaign with closed system handling

    Final product types

    • Specialty organic intermediates
    • Niche performance additives for industrial fluids
    • Contract-developed solvent components
    • Fluorinated processing aids
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    Competitive 2-Bromo-5-Chlorobenzotrifluoride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Bromo-5-Chlorobenzotrifluoride: Practical Chemistry for Real-World Results

    Introduction: Decades of Experience Distilled in a Versatile Intermediate

    Stepping into our lab early every morning, I see more than just rows of drums and chrome-lined reactors. Each container tells a story of countless experiments, scale-ups, and raw trial and error. Among them, the 2-Bromo-5-Chlorobenzotrifluoride stands out—not because of marketing hype, but because countless formulations and chemical syntheses depend on its precision, reliability, and chemical strength. Crafting this compound day in, day out, means learning lessons from spills, runaway temperatures, and the evolving needs of our partners in pharmaceuticals, agrichemicals, and materials science. The importance of molecular building blocks like this one only grows as process chemistry races forward.

    About the Product

    The molecular structure of 2-Bromo-5-Chlorobenzotrifluoride (model: BCBTF-61369-DO, CAS Number: 401-78-5) reflects a simple yet powerful substitution pattern: a benzene ring dressed with both chloro and bromo substituents and the three-fold punch of a trifluoromethyl group. This design brings balancing act between reactivity and stability. Over years of manufacturing, we’ve refined our process to keep the purity above 99%, keeping water and other halogen impurities below industry benchmarks. Appearance remains an important visual check—clear, colorless to pale yellow liquid, density just above 1.6 g/cm³, and boiling range clustered tight for reproducibility across batches.

    Why 2-Bromo-5-Chlorobenzotrifluoride Catches Synthetic Chemists’ Attention

    Most chemists who turn to us have combed through catalogs searching for a functionalized aromatic that doesn’t just tick boxes, but actually performs. The appeal here centers on the electron-withdrawing character of the trifluoromethyl group. This seems abstract at first, but in practice, reactions that rely on controlled aromatic substitution see both selectivity and yield lift when using this molecule as a substrate or intermediate. The bromine and chlorine enable fine-tuned cross-coupling steps (such as Suzuki or Ullmann reactions), where reliable reactivity in production-scale runs can mean the difference between meeting a shipment schedule or missing a launch window.

    Our team often receives feedback from process chemists—sometimes the scaling challenge comes down to the starting material, not downstream purification. In particular, the presence of both bromo and chloro substituents lets chemists pick and choose follow-up reactions: bromine for palladium-catalyzed couplings, chlorine left untouched for later derivatization, and the strong fluorinated group locking the aromatic ring’s properties in place. Conventional benzotrifluorides without dual halogen functionalization just don’t offer the same strategic flexibility.

    Specification Nuances that Matter on the Plant Floor

    Composition in the fine chemicals world becomes a make-or-break factor in downstream synthesis. For our BCBTF-61369-DO batch, careful fractionation eliminates persistent impurities that often slip past routine quality control elsewhere. We routinely see queries about off-odors and color shifts encountered with lower-purity imports or “trader-labeled” stock. In our experience, these small problems snowball in hydrogenation or arylation steps. There’s nothing like running a multi-kilo transformation and discovering discoloration at the workup stage, only to trace it back to a fraction of a percent of halide leftover.

    We religiously log every little tweak in our process—from column switching to the precise grade of base used in washing stages. Data logs from our past three years show less than 0.2% deviation in halide content lot-to-lot, translating into fewer false starts for formulation scientists or analytical headaches for the quality team. The weight of repeatable purity beats the promise of a single analytic certificate every single time. Downstream, the specification matters just as much at the bottom of a process reactor as it does on paper.

    Practical Applications: From Discovery to Bulk Synthesis

    Most people tracing a product’s story from lab bench to palletized drums don’t see the dramas that unfold in the scale-up suite. Take pharmaceuticals, for instance: a new candidate drug might hinge on a halogenated aromatic that translates through several intermediates before final formulation. Our 2-Bromo-5-Chlorobenzotrifluoride finds itself right in these crossroads, providing a launchpad for introducing fluorinated moieties onto core scaffolds. Medicinal chemists leverage its cross-coupling activity to stitch together complicated molecules, making use of the differential reactivity between bromo and chloro groups.

    Agrochemical firms turn to this molecule for similar reasons. Contact with actual formulation teams taught us that resistant pests, regulatory trends, and cost pressures often push product developers to compact lead times and fine-tune compound libraries quickly. Here again, flexibility matters: selective activation of bromine or chlorine lets chemists build in new bioactive fragments without a long chain of protection and deprotection steps.

    Material science applications continue to surprise even seasoned chemists. The electron-rich, fluorinated backbone influences both polarity and solubility, lending itself to specialty coatings, dyes, and high-performance polymers. As specs on dielectric strength or hydrophobicity tighten, the difference between a subpar intermediate and one made with true process discipline becomes blindingly clear.

    What Sets Our Material Apart from Common Bench Stock

    Plenty of suppliers describe products in generic terms, focusing on the chemical name alone. I’ve sampled plenty from other sources, driven by curiosity or in response to customer testing requests. Usually the difference shows up not in the first run, but in the fifth or tenth. Fine particles, inconsistent color, or an unexpected odor hint at problems from crude production or poor purification. In larger reactors, contamination snowballs—leading to foaming, unexpected side reactions, or costly shutdowns.

    We avoid these pitfalls by obsessing over every feedstock and every stage. Our experience led to a robust routine: analytical checkpoints at incoming raw material, in situ sampling at key stages, and GC/LC-MS confirmation of purity before product sealing. Our best batch records show orders processed and shipped with end-to-end traceability, which experienced buyers often call to verify after working with brokers or non-manufacturing label brands. The truest sign is repeated business from process engineers and laboratory directors who’ve run production with competitive products and switched back for the sake of smoother downstream operations.

    Safety, Handling, and Logistics: More than Just Numbers

    No chemical story is complete without hard truths about transport, storage, and daily handling. 2-Bromo-5-Chlorobenzotrifluoride has a profile that strikes a good balance: it keeps a manageable boiling point (around 215°C) and doesn’t readily hydrolyze under ambient storage. We work with customers to forecast raw material intake and finished goods shipping patterns, since volatility and halogen content require steady environmental control to prevent off-gassing or container degradation over seasons in transit.

    A common operational hurdle can be static build-up during pumping or splashing. We’ve engineered our filling and transfer lines with static-dissipative features, based on near misses reported during plant scale-up. In daily operations, every drum arranged for long-term storage is flushed with inert atmosphere—no dramatics, just measures learned from decades of real-world troubleshooting. Safety officers report fewer odor complaints and hazardous vapor alarms since we overhauled our transfer packaging and added triple gasketing at drum heads.

    Regulatory Pressure and Traceability: Playing the Long Game

    We operate in a world where short-term fixes no longer cut it. Regulatory bodies scrutinize everything from benzotrifluoride emissions to waste halide management during derivatization runs. Being the primary manufacturer, not just a pass-through vendor, means we stand squarely behind every lot we release. Regular audits from buyers as well as compliance agencies have sharpened our tracking protocols. It’s become standard practice to supply full batch analytical histories, extended impurity profiles, and supply chain documentation. This approach not only reassures downstream partners, it helps us flag potential process improvements before non-conformance ever creeps into finished lots.

    We noticed years ago that non-manufacturing brokers often fall behind on paperwork, especially for regulated markets or REACH registrations. Our history shows that overdelivering on traceability and regulatory readiness reduces headaches—fewer import holdups, more predictable batch qualification, and a smoother ride from customs entry to factory gate.

    Comparing with Related Halogenated Intermediates

    Plenty of halogenated aromatics crowd vendor listings and chemical catalogs. So why focus on the 2-Bromo-5-Chlorobenzotrifluoride structure? Simply put, most alternatives offer either high reactivity or high stability—not the two together. For instance, 4-chlorobenzotrifluoride or its brominated analog lacks the dual substituent flexibility offered by the 2-bromo-5-chloro motif. This dual handle lets chemists orchestrate complex syntheses with fewer steps and greater control over side reactions.

    We field requests from R&D chemists seeking to replace single-halogen derivatives for improved selectivity in late-stage functionalization. Direct side-by-side pilot trials have shown higher yields and cleaner reactions when the chlorine substituent is in the fifth position, allowing for precision targeting during aryl coupling or halide exchange steps. In polymer applications, our compound’s resistance to unwanted side reactions means fewer batch failures and less troubleshooting on the final product line. These aren’t just theoretical differences—they play out over weeks and months of process development, influencing costs, timelines, and ultimately, finished product quality.

    Challenges We’ve Solved, and Ongoing Innovation

    Chemistry never sits still. Production challenges that seemed insurmountable a decade ago—catalyst fouling, trace metal contamination, inconsistent particle size—now get resolved with daily discipline, incremental upgrades, and a bit of hard-earned luck. We’ve worked hand-in-glove with equipment engineers and process chemists to adjust reactor headspace designs, tighten up distillation steps, and swap out critical reagents for higher-purity alternatives compatible with our sustainability strategies.

    Once, shifting a batch from pilot to full-scale revealed impurities untraceable by standard batch analytics. Years ago, we invested heavily in inline monitoring, which now alerts us to spikes in exotherm or rare impurity formation before a lot ever moves to storage tanks. This willingness to adopt and adapt hard and soft instrumentation has helped us catch quality concerns early and keep our output among the cleanest in the industry.

    Listening to Customers: From the Development Lab to the Loading Dock

    No one-size-fits-all story describes how chemists actually deploy 2-Bromo-5-Chlorobenzotrifluoride. Whether it’s a process development group racing to commercial-quantity API intermediates, or a specialty materials producer fine-tuning the halogen content in a new polymer backbone, we learn most by getting honest feedback. We keep communication lines wide open, offering on-site technical support and remote troubleshooting when ramping up new processes. Sometimes our best insights come from observing a purification step in action, or redesigning a delivery schedule to align with a customer’s campaign run.

    Our experience led us to design flexible packaging—ranging from small glass lab bottles to moisture-proof, corrosion-resistant drums—so receiving departments don’t have to scramble adapting bulk chemical transfers to incompatible gear. We routinely co-develop custom specs, matching purity to highly specific process needs, and take pride in adjusting specifications to suit a process route or unusual analytical method. All of these adjustments draw on real feedback from the field, never just sales metrics or industry averages.

    Anticipating the Future: Sustainability and Process Efficiency

    The chemical landscape keeps shifting, shaped by new environmental rules, shifting customer priorities, and a renewed focus on green manufacturing. Our plant team keeps one eye on process intensification—each kilogram of 2-Bromo-5-Chlorobenzotrifluoride must justify its resource footprint. Solvent recovery now reclaims over 80% of process solvents, and energy management protocols schedule runs to maximize waste heat recycling. We stage regular internal audits to track metrics on carbon emissions, water consumption, and waste halide disposal. These changes don’t happen overnight, but they start with telling the truth about what’s working, and what isn’t.

    Feedback from buyers often circles back to sustainability: requests for detailed carbon tracing, interest in renewable feedstocks, and tighter control on waste byproducts. We take these conversations seriously, collaborating with green chemistry groups to keep finding cleaner synthetic routes, alternate solvents, and improved purification methods. Real change builds on practical, measurable steps—backed by the hard data that responsible manufacturing demands.

    In Sum: Chemical Manufacturing with Accountability

    Years of experience in synthesizing, purifying, and shipping 2-Bromo-5-Chlorobenzotrifluoride taught us that every drum reflects both chemistry and trust. Subtle differences in production, purification, and logistics ultimately transform a basic reagent into a cornerstone intermediate for pharmaceuticals, agrochemicals, and advanced materials. Ongoing investment in quality control, regulatory readiness, customer communication, and sustainable practices keeps our product and partnership at real-world standards. No shortcuts, no abstraction—just the continuous, hands-on evolution of chemistry in action.