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4-Bromo-4'-Fluorobiphenyl

    • Product Name 4-Bromo-4'-Fluorobiphenyl
    • Alias 4-Bromo-4'-fluoro-1,1'-biphenyl
    • Einecs 629-016-2
    • 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

    281206

    Chemical Name 4-Bromo-4'-Fluorobiphenyl
    Molecular Formula C12H8BrF
    Molecular Weight 251.10 g/mol
    Cas Number 82571-54-8
    Appearance White to off-white solid
    Melting Point 73-76°C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Smiles Brc1ccc(cc1)c2ccc(F)cc2
    Inchi InChI=1S/C12H8BrF/c13-11-6-4-9(5-7-11)8-2-1-3-10(14)12(8)11/h1-7H
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 1-Bromo-4-(4-fluorophenyl)benzene

    As an accredited 4-Bromo-4'-Fluorobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5g quantity of 4-Bromo-4'-Fluorobiphenyl is provided in a sealed amber glass vial with a detailed chemical label.
    Shipping 4-Bromo-4'-Fluorobiphenyl is shipped in tightly sealed containers under ambient conditions. It is classified as a chemical substance and should be handled by trained personnel. Appropriate labeling and documentation are provided. The product may be subject to specific shipping regulations, so check local guidelines for handling, storage, and transportation requirements.
    Storage 4-Bromo-4'-Fluorobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Proper chemical storage protocols should be followed, and access should be limited to trained personnel. Always label the container clearly and appropriately.
    Application of 4-Bromo-4'-Fluorobiphenyl

    Applications of 4-Bromo-4'-Fluorobiphenyl in Industrial Manufacturing

    4-Bromo-4'-Fluorobiphenyl is a specialized intermediate for advanced synthesis, meeting strict quality standards for integration into electronic, pharmaceutical, and specialty material production. Our consistent supply ensures manufacturers achieve reliable performance during formulations and scale-up.

    1. OLED Display Material Synthesis

    Manufacturers use this intermediate in the synthesis of high-performance organic electroluminescent materials, particularly as a core building block in the construction of blue and green emitter precursors for OLED displays. The precise halogen and fluorine substitution patterns contribute to enhanced thermal stability and charge transport when incorporated into emitting layers. Introduce this component in the late-stage coupling step, where it reacts under palladium-catalyzed Suzuki or Stille coupling, forming complex conjugated systems required for active organic layers.

    Industry compliance standards

    • IEC 62341 (OLED panel performance and reliability testing)
    • REACH Registration (Europe – for precursor use)
    • RoHS Directive 2011/65/EU (limitation of hazardous elements in electronics)
    • GB/T 31467 (China – OLED panel materials inspection)

    Typical usage ratio

    • 5–15 wt% within emitter precursor synthesis, adjusted depending on target emission wavelength and end-layer composition.

    Downstream process integration

    • Enters late-stage cross-coupling reactions under inert atmosphere, following anhydrous purification and pre-formulation with catalyst and base.

    Final product types

    • AMOLED panels for smartphones
    • Flexible OLED screens for wearable devices
    • High-definition television display modules
    • Specialty lighting elements for automotive displays

    2. Pharmaceutical Intermediate for Targeted Synthesis

    High purity material supports the production of heterocyclic compounds found in various pharmaceutical research and development pipelines. Research institutes and pharmaceutical manufacturers employ the molecule as an aryl halide in cross-coupling to construct biphenyl scaffolds, which serve as key pharmacophores in kinase inhibitors and anti-inflammatory agents. It is commonly handled in GMP-compliant kilo labs, where batch reproducibility and impurity control are strictly regulated.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <797> (where applicable for intermediate handling)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, U.S.)
    • EDQM CEP (European Directorate for the Quality of Medicines Certificate of Suitability, where relevant)

    Typical usage ratio

    • 3–10 mol% as aryl halide input during biphenyl-core API synthesis, adjusted based on process route and target yield.

    Downstream process integration

    • Feeds into initial Suzuki-Miyaura cross-coupling, followed by purification and further functionalization steps under GMP controls.

    Final product types

    • Small-molecule kinase inhibitor drug candidates
    • Anti-inflammatory bulk intermediates
    • Reference standards for pharma R&D
    • Pre-clinical compound libraries

    3. Liquid Crystal Material Precursor

    Leading liquid crystal manufacturers use this aryl biphenyl as a core intermediate to create terminal-substituted biphenyl compounds, which improve nematic and smectic phase stability. It is especially valued for tuning dielectric anisotropy and viscosity in display-grade LC mixtures. The material undergoes sequential coupling and substitution reactions, providing high-purity starting points for batch blending in LC formulations.

    Industry compliance standards

    • IEC 60107 (Display quality testing for LC compounds)
    • EN 60384-1 (Capacitor material composition safety)
    • RoHS 3 (Directive 2015/863 for electronic components)
    • ISO 9001:2015 (quality management for electronic materials production)

    Typical usage ratio

    • 2–7 wt% of phase-stabilizing intermediate in custom LC compound synthesis before blending into final mixtures.

    Downstream process integration

    • Enters as a primary coupling reactant for further halogenation and subsequent esterification, followed by HPLC-based purification.

    Final product types

    • Twisted nematic (TN) and super-twisted nematic (STN) LC compound blends
    • Thin film transistor (TFT) LC mixtures
    • Specialty dichroic LC materials for optical shutters
    • LC alignment layer additives

    4. Specialty Polymer Synthesis Building Block

    Polymer manufacturers utilize this functionalized biphenyl in the synthesis of high glass transition temperature materials for electronic encapsulation and specialty coatings. Its molecular geometry introduces rigidity and modulates dielectric properties in polyarylene and poly(aryl ether ketone) chains, supporting advanced material design. It often reacts in nucleophilic aromatic substitution or nickel-catalyzed coupling with bisphenols and dithiol derivatives, ensuring control over molecular weights and final properties.

    Industry compliance standards

    • ASTM D5208 (Accelerated aging for plastics)
    • UL 94 (flammability of plastic materials for parts in devices)
    • IEC 60216 (Thermal endurance properties for electrical insulating materials)
    • ISO 14001 (Environmental management for specialty plastics)

    Typical usage ratio

    • 3–8 mol% in specialty copolymer backbone construction, tailored to desired mechanical and dielectric properties.

    Downstream process integration

    • Feeds into direct aryl coupling or step-growth polymerization, preceding chain termination and pelletization or film casting.

    Final product types

    • High Tg electronic potting compounds
    • PCB substrate films with enhanced insulation
    • Protective conformal coatings for semiconductors
    • Thermal management layers for advanced electronic modules

    5. Agrochemical R&D Intermediate

    Innovators in agrochemical synthesis select this biphenyl derivative for building aryl-fluorinated scaffolds in herbicide and fungicide candidate development. Its role as a well-defined halogenated aryl fragment enables fine-tuning of bioactivity and metabolic stability, particularly when introduced early or mid-stage in synthetic routes for new active ingredients. R&D and pilot plants manage the purity and trace impurity levels in accordance with relevant agrochemical guidelines.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025 (Chemical testing and calibration for agro compounds)
    • Chinese National Standard GB 4839.1 (Agrochemical quality control)

    Typical usage ratio

    • 1–6 mol% as a structural intermediate, varying by targeted aryl substitution in lead compound structure-activity studies.

    Downstream process integration

    • Incorporated post-metalation or direct arylation, followed by purification and final functionalization steps for activity screening.

    Final product types

    • Research-stage fungicide candidates
    • Herbicide synthesis precursors
    • Active ingredient standards for field trials
    • Lead compounds for combinatorial screening platforms

    6. Fine Chemical Research and Custom Synthesis

    Contract synthesis firms and research laboratories deploy this halogenated biphenyl in the design of functionalized small molecules with custom electronic or steric properties for new material discovery, asymmetric catalysis, or as analytical derivatization agents. The material allows precise structure variation, enabling targeted property adjustments for non-routine advanced material or analytical R&D applications. Integration usually occurs in custom reaction schemes requiring strict moisture, air, and trace metal impurity control.

    Industry compliance standards

    • ISO 9001 (General quality management for chemical research manufacturing)
    • GLP for Analytical Chemistry Labs
    • GHS (Globally Harmonized System of Classification and Labelling of Chemicals)
    • National chemical inventory reporting (where applicable, e.g., TSCA, REACH, IECSC)

    Typical usage ratio

    • 0.5–5 mmol scale per synthesis, adjusted according to required structure quantity or screening panel size. Scale-up follows specific request for targeted end-use.

    Downstream process integration

    • Introduced as core aryl moiety in coupling, derivatization, and analytic labeling processes, prior to or following chromatographic separation.

    Final product types

    • Reference standard compounds
    • Analytical derivatization reagents
    • Custom monomers for advanced polymerization trials
    • Novel small-molecule libraries for structure-property exploration
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    Certification & Compliance
    More Introduction

    4-Bromo-4'-Fluorobiphenyl: Straight from the Source

    Meet Your Next Key Intermediate

    We have spent years investing in scalable aromatic halogenation and selective fluorination processes because real performance and purity issues arise long before end-use. From the first kilo out of a glass reactor to metric ton orders piped off distillation, 4-Bromo-4'-Fluorobiphenyl lands directly in the toolkit of anyone building high-precision molecules. Our process chemists have made this compound with one goal—supporting cleaner cross-coupling and trusted batch reproducibility where the failure costs too much.

    Consistent Quality Backed by Experience

    Working with thousands of reaction hours and dozens of scale-ups, we see every impurity profile twist as a challenge to perfect the process. Our team learned early on that standard halogenated biphenyls often hide byproducts that compromise downstream reactions, especially in pharmaceutical and material workflows. We’ve eliminated those headaches with batch lot analytics and controlled atmosphere chromatography. You get tight melting point ranges, a sharp NMR spectrum, and reliably pure crystals every run.

    Understanding the Structure Makes a Difference

    The 4-bromo group at one end and the 4'-fluoro group at the opposite ring brings a rare balance of reactivity. Bromine’s reliability in palladium-catalyzed couplings meets the stabilizing effect of para-fluorine, which holds together under heat but opens possibilities for further substitutions. Chemists favor this molecule when the project demands robust Suzuki, Negishi, or Stille reactions on aromatic frameworks, with less risk of scrambling side products or isotopic confusion. Our route avoids low-yield halogen dance steps, so there’s less waste and fewer surprises in downstream chemistry.

    The Role in Advanced Synthesis

    Active pharmaceutical ingredient innovators pick 4-Bromo-4'-Fluorobiphenyl as a starting block for new heterocyclic scaffolds. Material scientists reach for it as a core monomer in electronic and electro-optical polymer chains. We’ve watched customers radically shorten their process development once reliable biphenyl blocks arrive. Our manufacturing teams talk daily with those in pilot and process development, helping them sidestep tedious rescreening steps. A flat-out pure starting intermediate saves an extraordinary amount of method optimization.

    Product Specifications Based on Real Data

    Every batch undergoes particle sizing—not just because spec sheets demand it, but because filtration and dissolution rates directly affect process time. We routinely check melting points against published literature (typically between 138°C and 142°C), but also tie those readings back to instrument calibration and humidity changes in the plant. Our FTIR plots match every peak, catching fingerprint-level differences from off-target syntheses, so you aren’t left puzzling over unexplained masses in LC-MS. High-performance liquid chromatography gives you assurance that trace biphenyls or unreacted starting materials don’t sneak in above 0.2%. This hands-on approach grows out of years fighting batch-to-batch drift in customer projects, not because “compliance” says so.

    Differentiating our 4-Bromo-4'-Fluorobiphenyl

    Every manufacturer who takes shortcuts here runs into solubility grief, sticky residues in reactors, or color bodies that darken polymers. We mapped out each side reaction in pilot scale, charting how each impurity affects Suzuki yields down the line. Our technicians use on-the-fly adjustments for batch temperature and halide equivalents to keep purity above 99%—not just on paper, but proven with repeated internal standards. Having walked alongside clients through painful process failures, we recognize when even a 0.2% unknown shows up in a chromatogram as a real bottleneck.

    Competing “off-the-shelf” material often arrives with broader melting point spans and dull, off-white tint—clear indicators of incomplete conversion or mishandling. That ambiguity puts your cyclization chemistry or device fabrication workflow in jeopardy. We lock down every production run with in-process QA, hand-checking against last month’s spectral fingerprints and running reference standards. There are no off-resin solvents or ambiguous supplier marks to complicate downstream validations. Everything comes direct from our own reactors.

    Worker and Environmental Safety in Manufacture

    Industrial-scale halogenation of biphenyl rings creates both workplace safety and environmental discharge risks. Our facility uses closed systems and local exhaust to prevent fugitive emissions of bromine and fluorinating reagents. Waste streams from purification undergo multi-stage neutralization and scrubbing, so off-gas and aqueous residues are below national reporting thresholds. Employees across the line wear full-face shielding and carry online monitors linked to our main control room. We hold open workshops for every new operator, so no one ignores “routine” maintenance or workaround hazards in pursuit of yield.

    Our waste profile for 4-Bromo-4'-Fluorobiphenyl synthesis shows a lower halide burden due to our engineering tweaks—shifting from classical halogen sources to solution-phase brominations with strict stoichiometry. The result: cleaner water discharges, less equipment corrosion, and lower operator exposure. All our solvent recovery metrics and environmental controls stay available for on-site audits because we believe transparency builds genuine trust.

    Real-World Applications Shaped by Direct Feedback

    Our customers teach us the most about how this product performs under real manufacturing stresses. A leading OLED material developer gave us feedback on residual blue tint affecting thin-film clarity. We modified filtration protocols to address the subtle traces of off-path isomers, boosting device yields by 4%. In pharma settings, process engineers traced a catalyst deactivation traceable to nano-level bromine impurities. After several plant visits and side-by-side lab comparisons, our technical team tightened reactor flush routines and extended post-synthesis holds to eliminate the culprit. The issue disappeared in the first new batch.

    Years of technical service experience make plain that no process stands still. Polymers and drug candidates evolve, so every foundational intermediate gets called on to meet higher standards. Researchers in aromatic chemistry run increasingly sensitive functionalizations—often using unique ligands, microwave heating, or pressure reactors. By providing trackable, thoroughly characterized batches of 4-Bromo-4'-Fluorobiphenyl, we help keep research and production projects from stalling out over avoidable starting material inconsistencies.

    Advantages over Other Halogenated Biphenyls

    Classic biphenyl intermediates often come substituted at only one ring, or with crowded ortho positions that cause unpredictable reactivity and poor yield in high-value couplings. With the bromo and fluoro groups placed para across the biphenyl framework, our compound stands apart. The unique geometry ensures selectivity in Pd-catalyzed reactions and clean cleavage steps. Downstream oxidation or amination steps move faster and return sharper HPLC peaks. Users report higher recovery in both preparative and analytical methods, with fewer issues from sticky side reactions.

    Compared with unsubstituted biphenyl or single-halogen variants, 4-Bromo-4'-Fluorobiphenyl brings a combination of activation and stability. The bromine acts as a coupling handle, while the fluorine tunes the electronic landscape for greater resistance to degradation. We find customers using this compound as a gateway to advanced ligands, custom monomers, and drug-like fragments. Our unique control over isomeric purity and halide substitution supports its use where downstream transformations are sensitive to even minor deviations in substrate structure.

    Supply Chain Reality: Manufacturing, Not Middleman

    We have learned what supply interruptions and inconsistent intermediate stocks do to pilot plants and commercial campaigns racing deadlines. As the direct manufacturer, we control every input. We screen all starting biphenyl, halide sources, and reagents in-house. Third-party distributors simply cannot guarantee the same transparency or depth of analytical tracking. We can trace every drum, every spectral shift, every yield anomaly back through years of lab records and operator logs.

    This vertical control allows us to offer just-in-time production scaling, with fast turnaround between sample trials and multi-tonne shipments. Regulatory and documentation teams receive results straight from our analytical chemists—never from generic supplier libraries or consolidated “certificates” stripped of lot-level detail. That way your own QA and regulatory filings can trust that every figure comes from freshly measured data, not copy-pasted templates.

    Reliable Packaging and Logistics

    All our shipments use moisture-barrier lined containers and secondary shock protection. Operators check fill weights on calibrated balances and seal every drum with serialized tamper collars. With each order, our logistics specialists review transit routes for extreme temperature or mechanical shock risk. For international shipments, we pre-clear all paperwork, so customs officers see clear origin and chemical identity—not a rebranded lot floating across continents.

    After fielding too many customer complaints about broken liners and powder caking, we invested in static-controlled cleanrooms for all 4-Bromo-4'-Fluorobiphenyl loading operations. No powder leaves our site without passing both moisture content and particle flowability checks within hours of dispatch. We learned from experience that a little extra time in packaging saves days of troubleshooting for material handlers down the road.

    Regulatory Footprint and Documentation

    Every regional authority—from REACH to TSCA to Asian market agencies—demands robust traceability for each batch of aromatic intermediates. Our compliance records reflect direct synthesis parameters and supply chain documents. We retain detailed batch data, including operators, instrument calibration schedules, and storage environment records for each lot. In regulatory audits, we share actual raw data and instrument logs. Quality assurance personnel from biotechnology and electronics customers frequently review our documentation firsthand during plant visits.

    Having worked directly with inspectors and multi-national regulatory teams, our team keeps well ahead of reporting changes and evolving substance lists. We use internal audits modeled on the strictest international standards, updating protocols after feedback from both public authorities and customer quality teams. Every certificate and dossier—whether for customs, safety, or environmental review—draws from exact measurements and live trace files, not generic templates. This hands-on regulatory support cuts time from submission to approval, so customers face fewer bottlenecks while scaling with new partners.

    Continued Innovation and Customer Collaboration

    Sourcing feedback from customers has shaped both our product line and our approach to manufacturing. The growing trend toward green chemistry, harsher downstream process conditions, and high-throughput experimentation puts legacy aromatic intermediates to the test. We see research projects demanding smarter reactivity, tighter impurity specs, and scalable supply chains. By hosting open forums with R&D and process teams at customer facilities, we spot bottlenecks and engineer solutions together.

    One recent example: a customer scaling a specialty polymer needed a way to minimize static charge buildup during powder handling. By modifying particle size distribution and adding microcrystalline anti-caking steps, we helped them cut losses and boost throughput on the production floor. These cycles of shared troubleshooting extend right into our own plant operations, so our production methods adapt to real-world process problems—not just theoretical purity targets.

    Building Trust with Direct Communication

    Customers rarely accept “good enough” in critical applications. We answer technical questions with data and raw spectra. If a researcher needs support troubleshooting a new catalyst batch or resolving an analytical ambiguity, our chemists go straight to the source. Direct access to our R&D and scale-up teams means product discussion stays on the technical level, not buried under sales scripts. Problems turn up in every large-scale chemical process—our team’s role is to bring solutions rooted in direct manufacturing know-how.

    We make it a point to invite customer QC and process experts to site audits and virtual walk-throughs. We don’t sidestep tough questions or gloss over supply chain disruptions. The more you know about our real-world manufacturing, the more confident you’ll be in adopting 4-Bromo-4'-Fluorobiphenyl for high-value chemistry.

    Conclusion: Backed by Hands-On Manufacturing

    Every step in 4-Bromo-4'-Fluorobiphenyl production—reaction design, quality testing, packaging, logistics, compliance—builds on years of hard-won plant experience. We provide this compound not just as a catalog item, but as a result of active collaboration across process engineering, technical support, and customer development. The difference shows up in more reliable scale-ups, sharper yields, and fewer downstream surprises. When you work with a manufacturer who owns every step of the process, you gain a partner ready to troubleshoot, optimize, and deliver on every order. That’s why our 4-Bromo-4'-Fluorobiphenyl stands apart for every high-stakes application where purity and reliability decide project success.