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2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile

    • Product Name 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile
    • Alias TFEO-BR
    • 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

    392361

    Chemical Name 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile
    Cas Number 156117-41-4
    Molecular Formula C12H6BrF6NO2
    Molecular Weight 410.08
    Appearance White to off-white solid
    Purity Typically >= 98%
    Melting Point 52-55°C
    Solubility Insoluble in water; soluble in organic solvents such as DMSO and DMF
    Smiles N#Cc1c(Br)cccc1(OCC(F)(F)F)OCC(F)(F)F
    Inchi InChI=1S/C12H6BrF6NO2/c13-8-5-4-7(9(6-8)21-3-11(14,15)16)22-10(17,18)19-2-1-20
    Storage Conditions Store at 2-8°C, protect from light and moisture

    As an accredited 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 5-gram amber glass vial with a secure screw cap, labeled with compound name, purity, quantity, and hazard warnings.
    Shipping 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile is shipped in tightly sealed, chemical-resistant containers under ambient temperature conditions. Packaging complies with all relevant safety and regulatory requirements, ensuring protection from moisture and light. Appropriate hazard labels and documentation are included to facilitate safe transport and handling. Shipping is conducted via certified carriers for chemical substances.
    Storage 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances. Protect from moisture and direct sunlight. Store under inert atmosphere if sensitive to air or moisture. Label clearly, and keep away from strong acids, bases, oxidizers, and reducing agents.
    Application of 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile

    Applications of 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile in Industrial Manufacturing

    2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile serves as a critical intermediate for fluorinated aromatic compound synthesis in multiple specialized chemical industries. As the original manufacturer, our production supports strictly validated, high-purity supply for customers’ advanced applications across downstream sectors. The following scenarios illustrate precisely how industrial clients utilize this material, highlighting relevant regulations, precise formulation roles, integration into process lines, and typical end-products found in the market.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies employ this molecule as a building block in the production of advanced APIs where fluorinated aromatics boost metabolic stability and target bioactivity. The bromonitrile group allows for selective late-stage derivatization, often through palladium-catalyzed coupling or nucleophilic substitution reactions. These processes require tight impurity control to meet regulatory standards for new drug substances and their intermediates. Integrators typically optimize batch quantities in response to route-of-synthesis scale-up and impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Guidelines for Excipients and Intermediates in APIs
    • USP General Chapter <1086> Impurities in Drug Substances
    • FDA 21 CFR Part 211: Finished Pharmaceuticals cGMP

    Typical usage ratio

    • 10–25 mol% relative to overall API batch charge; exact ratio depends on specific API side-chain attachment and yield optimization.

    Downstream process integration

    • Charged during the late-stage coupling, etherification, or cyanation step in API intermediate synthesis, typically at the kilo- to multi-ton scale in reactor trains.

    Final product types

    • Pharmaceutical intermediates for fluorinated oncology drugs, CNS modulators, and anti-infective agents.

    2. Fluorinated Agrochemical Synthesis

    Crop protection manufacturers rely on the compound for the synthesis of selective herbicide and fungicide actives containing fluorinated aromatic rings, which enhance field persistence and rainfastness. Its high electron-withdrawing effect serves in tuning molecular reactivity for downstream halogen-metal exchange, Suzuki coupling, or functional group elaboration in pre-final intermediates. Usage is monitored for compliance with food crop and environmental legislation in major agricultural markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals—Agrochemical active ingredients
    • REACH Regulation EC 1907/2006 (EU)
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) Registration Procedures

    Typical usage ratio

    • 5–15% (wt/wt) of synthetic sequence feedstock, actual input dependent on target molecule’s fluorine content and manufacturing route selection.

    Downstream process integration

    • Introduced at the key aromatic functionalization phase or ring closure operation within pilot and large-scale agrochemical synthesis trains.

    Final product types

    • Selective herbicide actives (e.g., for cereal crops), systemic fungicide precursors, and pre-emergence weed control compounds.

    3. Specialty Liquid Crystal Intermediate Production

    Manufacturers of high-performance LCD and OLED display chemicals use the raw material as a fluorinated precursor for niche biphenyl and terphenyl liquid crystal intermediates. These structures impart high dielectric anisotropy and low viscosity needed for fast-response displays. Material addition rates are defined by targeted mesogen homologues and the electro-optical parameter map for the application genre.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances, EU 2011/65/EU)
    • Japanese JIS C61202 for liquid crystal chemicals
    • IEC/TC47 Requirements for Electronic Chemicals
    • REACH Regulation Annex XVII (EU) for substances in electronic materials

    Typical usage ratio

    • 3–12 mol% per mesogenic ester synthesis, adjusted per molecular design for TN or IPS mode displays.

    Downstream process integration

    • Added at the halogenated aromatic etherification or Grignard coupling step within mesogen core assembly.

    Final product types

    • Liquid crystal compounds for TFT-LCD alignment layers, OLED prepolymers for display emitters, and display-grade mesogen blends.

    4. High-Performance Fluoropolymer Modifier Production

    Producers of custom fluoropolymer compounds apply this intermediate in the synthesis of trifluoroethoxy-modified monomers. These monomers are then integrated into backbone structures to impart chemical resistance and hydrophobicity in engineering plastics and elastomers. The selection and proportion of the nitrile bromide derivative influence copolymer flexibility and free volume, dictated by application profiles in aggressive media or electronic encapsulation.

    Industry compliance standards

    • ASTM D543 Chemical Resistance of Plastics
    • ISO 9001 Quality Management for Polymer Manufacturing
    • UL 94 Flammability for Plastics Materials
    • RoHS/REACH for Polymer Raw Materials

    Typical usage ratio

    • 0.5–3% by mass in total copolymerization feed, differing by resin design and target performance criteria for chemical barrier or insulation.

    Downstream process integration

    • Feeds directly into solution or emulsion copolymerization steps for high-performance resin synthesis, pre-blending as a reactive monomer component.

    Final product types

    • Engineered fluoropolymer sheets, specialty films for automotive gaskets, electronic potting compounds, and high-purity fluoroplastic linings.
    Free Quote

    Competitive 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile: Direct from Our Factory Floor

    Getting to the Heart of Modern Fluorinated Benzo­nitrile Chemistry

    Our work as a chemical manufacturer doesn’t come down to badges or certifications alone—it’s about grit, precision, and commitment to quality. When we talk about 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile, we’re talking about a product that’s shaped by decades at the intersection of advanced organic synthesis and industrial scale-up. This compound, with its formula C11H5BrF6NO2, holds a distinct place among benzonitrile derivatives. Manufacturing such a chemical isn’t a matter of filling drums and sticking on a label. The bromine at the 3-position, coupled with two trifluoroethoxy substituents at the 2 and 6 positions, isn’t just an arbitrary arrangement. Each batch rolls off our line benefiting from in-house know-how about selective substitution, byproduct reduction, and rigorous purification.

    What Sets This Molecule Apart

    The backbone of the molecule—an aromatic ring with carefully chosen electron-withdrawing and donating groups—lets it stand out in downstream syntheses. The cyano group attached to the ring opens avenues in specialty chemical applications, delivering reactivity without compromising stability during transportation or storage. We’ve worked to optimize yields not just for the sake of efficiency, but because consistent batch performance is vital to our downstream partners. Analytical tracking during production, especially NMR and GC-MS at multiple in-process stages, allows us to control isomer ratios, track purity, and meet narrowing impurity thresholds. 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile emerges as a white to off-white crystalline solid under ambient conditions, with a melting point typically around 59-65°C, which fits well with automated dosing systems in modern synthetic labs.

    What End Users Accomplish with It

    This isn’t a vanity molecule. The pharmaceutical and agrochemical developers we supply rely on the plug-and-play nature of our product, especially in the design of new active ingredients that need both hydrophobic shielding and electronic fine-tuning. What does that mean for users? When researchers want to build molecules with high metabolic stability, the trifluoroethoxy substituents break up predictable decomposition patterns. The brominated aromatic core offers a clean handle for forming new C–C or C–N bonds through Suzuki or Buchwald-Hartwig couplings. We deliberately avoid residual moisture and non-aromatic halides to prevent downstream artifact formation. From bench to pilot plant, our batches run with narrow lot-to-lot performance, providing synthetic results that chemists can trust when scaling up, or validating with their own NMR and HPLC data.

    Handling, Packaging, and Storage: Views from the Workshop

    We never treat safety and handling as afterthoughts. Each container, whether glass or fluoropolymer-lined steel, gets sealed under nitrogen. Our own warehouse team flags the compound as sensitive to light and moisture. While it retains bulk stability under standard warehouse conditions, open-top storage isn’t on the table. We move material from sealed reactors to dedicated packaging stations, and never allow cross-contamination with similar brominated or fluorinated intermediates. This process, managed by hands-on technicians who track each lot from reactor to drum, sits at the core of our batch-integrity philosophy. Long-term partner labs repeatedly report low backgrounds on their analytical runs, a direct result of our internal packaging and environmental controls.

    The Why and How of Industrial Batch Production

    There’s an art to synthesizing substituted benzonitriles at scale. The reagents we use—including protected ethylene glycol derivatives, brominating agents, and dehydration catalysts—reflect practical constraints and real-world demands for purity. Selection comes out of repeated bench trials and kilo-scale test batches, where we rigorously compare not just the reaction yields, but side-product spectra and downstream reaction suitability. We’ve adjusted the sequence of introducing bromine and trifluoroethoxy groups over time, based on feedback from our own plant chemists and external partners chasing niche intermediates for fluorinated APIs. Routine analytical feedback loops, including Karl Fischer titration for trace moisture and high-resolution mass spectrometry, mean the product leaving our production line doesn’t need pre-cleanup at our customers’ sites.

    Technical Features Born Out of Manufacturing Experience

    We learned early in our production runs that product performance isn’t all about numbers in a spec sheet. High fluorine content often translates into unique handling issues, such as static buildup or caking in low humidity environments. Our engineers adjusted not only packaging methods but grinding protocols, moving from glass-mortar grinding to nitrogen ball-milling to avoid trace metal pick-up. By integrating in-line IR analysis, we ensure the characteristic aromatic C≡N stretch and F–C bands remain clear batch after batch. Extended stability studies, set up in our own facility, point to shelf lives that satisfy shipping risks to continents with variable regulatory climates.

    Comparing with Peer Products: Why Make This One?

    Some might ask why we bother producing this specific benzonitrile instead of more routine ones. Plenty of benzonitriles include fluorine or bromine, but few offer such clean access to multi-functional substitution without cross-reactivity headaches. Lower-fluorinated analogs sometimes fall short in stability or biological relevance. Benzonitriles lacking bromine close off straightforward access to further cross-coupling partners. Multi-step pharmaceutical syntheses rarely tolerate upstream variability; inconsistent material means lost time and failed QC. We hear from R&D teams who tried sourcing similar intermediates through traders, only to see uncontrolled impurity spikes or unpredictable isomer mixes. Sourcing direct from a manufacturer, with documentation for each synthetic stage and real-time analytical data, makes tighter control over final product quality a reality.

    Supporting Sustainable Chemical Production

    Modern chemical production throws up challenges beyond yield or purity. Environmental impact and compliance carry weight. Our main plant’s environmental team designed a solvent-recovery regime for the major high-boiling ethers in our process, cutting down not only on raw material usage, but also reducing disposal costs and regulatory risks. Post-reaction processing diverts spent materials to approved recycling contractors. We track each lot from raw material barrel to the finished product that heads out of our gates, offering full traceability for downstream audits. Water-management, including on-site testing of effluents, ensures that trifluorinated side-products do not slip into the local ecosystem. Such controls are not optional extras—they’ve become necessary for regulatory compliance and future-proofing our site’s operating license.

    Why Analytical Transparency Matters

    Our experience proves that researchers and industrial users care about the data behind every drum, not just the COA attached on paperwork. To that end, we release real chromatograms and spectroscopic profiles with each lot, showing actual impurity peaks and baseline resolution. Our customers have commented that this openness turns sourcing into a partnership, not just a transaction. Analytical transparency ripples out in practical ways. For example, knowing that certain isomeric impurities won’t disrupt a targeted Heck or cross-coupling step means process chemists can design with certainty. We get direct feedback after shipments, which helps us tweak not only our QA/QC protocols, but also our synthesis and purification recipes in future campaigns.

    Regulatory and Documentation Backed by Experience

    Shipping fluorinated, brominated aromatics is no simple task. Our document management team prepares the required transport papers and regulatory filings. Each shipment goes out with batch-specific documentation including synthesis route, in-lab analytical signatures, and residual solvent profiles down into the ppm range. We don’t stop at what’s written down; if our partners need clarification or supporting documentation for global filings, our in-house regulatory chemists get involved, drawing on a working library of previous shipping records and in-process observations. This operational continuity closes the gap between documentation and real product handling, a benefit that intermediaries seldom offer.

    Industry Trends and Future Directions

    As benzonitrile derivatives gain ground in pharmaceutical and agrochemical pipelines, we see specifications tightening year after year. No longer do end users accept “good enough” when it comes to batch quality, odor, or reactivity. With pressures rising to speed up discovery without sacrificing batch consistency, reliable supply matters more than ever. Our approach centers on listening to what downstream innovators actually need, running small-scale validation trials in partnership, and updating our procedures as new data and regulatory demands surface. As green chemistry pushes manufacturers like us to adopt smarter, cleaner production routes, we test alternative reagents and solvents—balancing ease of manufacturing with sharper environmental performance, without leaving users to shoulder the risks.

    Connecting the Laboratory and the Production Plant

    Unlike many suppliers, our story starts in the research lab and continues on the scale-up floor. From process development chemists to packaging and logistics, each team contributes to making this benzonitrile derivative work for its final users. No batch gets released until QC, safety, and product stewardship specialists sign off together. Our thorough documentation and internal training mean that whether a shipment is leaving for a CRO in Europe or a pharma site in North America, the product profile, analytical support, and technical advice remain consistent. Our familiarity with specific applications, from lead compound development to specialty polymer synthesis, shapes each run’s parameters, reducing the risk of failed campaigns or unnecessary troubleshooting in the field.

    Feedback from End Users and Continuous Improvement

    Direct manufacturer-to-user feedback cycles serve as a foundation for improvements. End users regularly share results from their own reaction trials, flagging points where our material meets or exceeds thresholds or suggesting tweaks for higher performance in new transformations. We don’t just log feedback—we set aside in-house time to run side-by-side comparisons, analyze return data, and adjust our specs if repeated issues emerge. Our production’s flexibility grows with every feedback loop; by managing every step ourselves, we don’t face third-party bottlenecks when user specifications evolve.

    Stepping Beyond the Bench: Real-World Impact

    It’s easy to glance at a chemical name and see only a list of atoms. At our factory, the story behind 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile stretches out over hundreds of liters, multiple weeks, and intertwined teams. We understand the processing risks inherent in every organofluorine or brominated aromatic we supply—like controlling for decomposition during purification, or minimizing residual halide carry-over. Each container carries more than just product; it contains the sum of many small improvements born from real production floors, not from supply-chain theory or trading desks.

    The Path Ahead for Advanced Benzonitriles

    Production of complex aromatic intermediates keeps evolving under the combined demands of scale, safety, and specificity. With each batch of 2,6-Bis(2,2,2-Trifluoroethoxy)-3-Bromobenzonitrile, our experienced hands and eyes work toward raised expectations from global customers. We build partnerships that last, rooted in direct communication—where feedback doesn’t need to travel through layers of resellers. This directness shapes technical choices, documentation, environmental programs, and above all, a commitment to letting our product tell its own story in labs and plants worldwide. For users demanding both precision and dependability, our manufacturing team stands as a resource, sounding board, and responsible supplier, ready to shape the future of advanced benzonitrile chemistry, one shipment at a time.