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4-Benzoyl-4'-Bromobiphenyl

    • Product Name 4-Benzoyl-4'-Bromobiphenyl
    • Einecs 252-117-9
    • 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
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    Specifications

    HS Code

    284492

    Chemical Name 4-Benzoyl-4'-Bromobiphenyl
    Cas Number 56648-37-4
    Molecular Formula C19H13BrO
    Molecular Weight 337.21 g/mol
    Appearance White to off-white solid
    Melting Point 142-146°C
    Solubility Slightly soluble in organic solvents such as dichloromethane and chloroform
    Purity Typically ≥97%
    Smiles C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)Br
    Storage Conditions Store in a cool, dry place, protected from light
    Synonyms 4-Bromobiphenyl-4-yl phenyl ketone

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

    Packing & Storage
    Packing Brown glass bottle with secure cap, white label displaying "4-Benzoyl-4'-Bromobiphenyl, 5g", hazard symbols, batch number, and supplier.
    Shipping 4-Benzoyl-4'-Bromobiphenyl is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. The package is labeled according to international regulations, including hazard identification. Transport is via trusted carriers under temperature-controlled conditions, and all shipments are accompanied by a Safety Data Sheet (SDS) and proper documentation for safe handling and regulatory compliance.
    Storage 4-Benzoyl-4'-Bromobiphenyl should be stored in a tightly sealed container, away from moisture and incompatible materials, such as strong oxidizing agents. Keep the chemical in a cool, dry, and well-ventilated area, protected from direct sunlight. Avoid excessive heat and sources of ignition. Proper labeling and safety precautions are recommended to ensure safe handling and storage.
    Application of 4-Benzoyl-4'-Bromobiphenyl

    Applications of 4-Benzoyl-4'-Bromobiphenyl in Industrial Manufacturing

    4-Benzoyl-4'-Bromobiphenyl serves niche but essential functions as an advanced aromatic intermediate within multiple high-value industrial processes. The following sections detail its integration in several genuine downstream manufacturing sectors, focusing on compliance, ratio, process roles, and specific final outputs as encountered in specialty chemical production environments.

    1. Liquid Crystal Intermediate Synthesis

    Manufacturers of liquid crystals for display technologies incorporate this compound as a core structural precursor, particularly in creating complex mesogenic units. Due to its biphenyl backbone and functional substituents, it enables precise tuning of thermal and electro-optical properties in nematic and smectic liquid crystal formulations. Integration occurs post-coupling and halogen-exchange modifications, typically within multi-step routes characterized by strict impurity controls and high-yield requirements for advanced display panels.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU) on electronic chemicals
    • REACH Regulation (EC) No 1907/2006 for industrial chemical safety
    • QC protocols per ISO 9001-certified electronic chemical manufacturing
    • IEC 62977-2-1 requirements for liquid crystal display materials

    Typical usage ratio

    • Ranges from 10–35% in mesogenic core mixtures, adjusted by required dielectric anisotropy and viscosity targets

    Downstream process integration

    • Introduced after biphenyl unit formation and in pre-polymerization/conjugation steps for tailored mesogen synthesis

    Final product types

    • Nematic and smectic liquid crystal mixtures for TFT-LCD and OLED panels
    • Reactive mesogen blends for photonic device substrates

    2. Advanced Pharmaceutical Intermediate

    Pharmaceutical manufacturers rely on this substance as a key intermediate in the preparation of small-molecule kinase inhibitors and non-steroidal anti-inflammatory candidate structures. Its selective bromine functionality supports regioselective cross-coupling and subsequent functionalization, making it a valuable scaffold in preclinical pipeline compound production. The material enters GMP pilot plants where reaction control, trace analysis, and impurity isolation are conducted under validated protocols dictated by regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US cGMP for finished pharmaceuticals
    • EU GMP Part II for chemical APIs
    • Ph. Eur. and USP monographs for related chemical classes

    Typical usage ratio

    • Used at stoichiometric equivalents (1.0–1.3 molar equivalents) in targeted coupling or cyclization reactions, with adjustments based on synthesis yield targets

    Downstream process integration

    • Supplied as an advanced intermediate in late-stage batch processes, entering at the coupling or halogen-exchange phase in heterocycle construction

    Final product types

    • Targeted kinase inhibitor clinical candidates
    • Experimental anti-inflammatory drug substances in early development

    3. Specialty Polymer Additive Manufacturing

    Producers of high-performance engineering polymers, particularly for electronic encapsulants and optoelectronic films, apply this raw material as a functional comonomer or cross-linking agent. The aromatic bromide and carbonyl functionalities provide thermal stability and tunable refractive indices in specialty polyesters and epoxies. It is charged into controlled reactive extrusion or solution polymerization steps, with batch documentation and in-process quality checks mandatory for downstream use in high-reliability devices.

    Industry compliance standards

    • UL 94 flammability standards for plastic parts
    • ISO 14001 environmental management standards in polymer processing
    • IEC 61249-2-21 for base materials in printed circuit boards
    • RoHS Directive compliance for end-use qualifying applications

    Typical usage ratio

    • Typically 3–8% by weight in engineering polymer formulations, varied by required cross-link density and thermal stability

    Downstream process integration

    • Added during pre-polymer dosimetry or directly fed to the polymerizing vessel during backbone functionalization steps

    Final product types

    • High-temperature optical films for microelectronic use
    • Encapsulant matrices for LED and sensor modules

    4. Organic Photoinitiator Synthesis

    Chemical manufacturers in the UV-curable coatings and inks segment use this compound as a strategic photoinitiator intermediate. The benzoyl and biphenyl moieties are functionalized further via acylation, etherification, or cross-coupling to produce bespoke photoinitiator molecules. These final products undergo rigorous spectrophotometric and chromatographic release testing, and strict adherence to environmental and worker safety standards governs all stages of downstream integration.

    Industry compliance standards

    • Regulation (EC) No 1272/2008 (CLP) for classification, labeling, and packaging of chemicals
    • ISO 17025 laboratory accreditation for QC analysis
    • EN 71-3:2019 for safety of photoinitiators in toys/applicable coatings
    • Oeko-Tex® Standard 100 for restricted substances in textile inks

    Typical usage ratio

    • Employed at 5–15% equivalence in precursor batches for photoinitiator formation, monitoring process yield to meet UV absorption performance goals

    Downstream process integration

    • Introduced at the pre-final condensation or arylation step during synthesis of substituted benzophenone or diaryl ketone photoinitiators

    Final product types

    • Custom photoinitiators for UV-cured acrylate inks and overprint varnishes
    • Radical-type initiators for optically clear adhesives and coatings

    5. Fine Chemical Dye Intermediate

    Manufacturers specializing in high-value specialty dyes draw on this raw material for the synthesis of biphenyl-based chromophores required in color filter and dye-sensitized solar cell applications. Using Suzuki couplings or Friedel–Crafts acylations, production chemists build extended conjugation systems essential for specific absorption and fastness characteristics. Material is delivered in purity grades suitable for dye house certification, and endpoints are stringently validated via spectroscopy and chromatographic analysis.

    Industry compliance standards

    • EN 71-9 for organic colorant materials in consumer products
    • REACH Annex XVII for colorant safety and consumer exposure
    • ISO 9001 for quality management in dye chemical production
    • ZDHC (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List

    Typical usage ratio

    • Supplied at 8–20% molar ratio in dye synthesis streams, controlled relative to chromophore length and target coloration

    Downstream process integration

    • Enters the initial aryl coupling stage or serves as a branching point in construction of core dye scaffolds

    Final product types

    • Color filter precursors for display manufacturing
    • Dye-sensitized solar cell (DSSC) absorbent compounds

    6. Functional Materials for Organic Semiconductors

    In the production of advanced organic semiconductors, R&D and pilot plants employ this compound as a building block for π-conjugated oligomers and polymers. Its unique electronic properties contribute to high charge-carrier mobility and defined energy levels in fabricated transistor and photodetector devices. The compound is introduced during precision coupling reactions, with molecular weight and purity tightly controlled in accordance with performance standards for optoelectronic integration.

    Industry compliance standards

    • IPC-4101 specification for base materials used in semiconductors
    • RoHS lead and halogen content limitations for electronic chemicals
    • ISO 14644-1 for controlled manufacturing environments
    • SEMATECH process material guidelines for organic electronics

    Typical usage ratio

    • Used at loading levels of 6–15% in monomer/oligomer precursor mixes, tailored to electrical mobility and crystallinity parameters

    Downstream process integration

    • Charged during early monomer synthesis and cross-coupling steps, guiding polymer backbone structure

    Final product types

    • Organic thin-film transistors (OTFTs)
    • Photodetectors and flexible sensor arrays
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    Certification & Compliance
    More Introduction

    4-Benzoyl-4'-Bromobiphenyl: Practical Experience Shaping Better Chemistry

    Quality Shaped by Precision in Synthesis

    Over our years in chemical production, certain raw materials have stood out for their impact on process reliability and consistent downstream results. 4-Benzoyl-4'-Bromobiphenyl has become a mainstay in our inventory not out of sheer convenience but due to a combination of purity, reliable performance, and ease of handling in real industrial settings. Our current batch, synthesized under carefully controlled temperature and pressure, reflects lessons learned through repeated pilot runs and full-scale manufacturing cycles. The molecular structure (C19H13BrO, CAS No. 16158-39-7) places a bromine atom and a benzoyl group on the biphenyl framework—features that open doors to a host of functional transformations.

    Most who work with advanced aromatics learn that even small variances in substituent placements or trace contaminants tilt the odds of process deviations. High-performance liquid chromatography and NMR analysis screens every lot for structure and trace by-products, as in-house chemists know that downstream vendors value certainty in input quality. Maintaining a bromine substitution at the para position, alongside a benzoyl group, sets a defined stage for cross-coupling, cyclization, or further substitution—none of which tolerate unpredictability. Each lot gets a certificate with assay, moisture, and impurity profile because theory loses value if not matched with verifiable, repeatable results in the tank.

    From Laboratory Curiosity to Industrial Confidence

    Early on, 4-Benzoyl-4'-Bromobiphenyl started as a candidate for academic research and proof-of-concept syntheses. As demand rose, its actual worth became clear in industrial-scale production. The compound’s reactivity owes a lot to both the electron-withdrawing benzoyl and the halogen, which can drive selective Grignard reactions, form carbon-carbon bonds through Suzuki coupling, or foster new heterocycles for specialty intermediates. Applications range from performance polymers and specialty plastics to ligands for catalysis, photo-responsive materials, and precursor roles in pharmaceutical intermediates.

    Scaling such a compound means rethinking typical lab procedures. Solvent ratios get recalculated for reactor charging rates, agitated vessel geometry influences mixing efficiency, and controlled quench after bromination prevents unwanted side formations. Generating kilogram or metric-ton batches introduces complexities unseen in flask-scale work—heat loads, phase separation, and filtration throughput dictate the rhythm of the process. Our technical team adapts protocols in-house, avoiding disruption to planned production runs or downstream users.

    Usage Realities: Value Beyond Paper Specifications

    Lab-scale data looks crisp, yet plant operations judge chemical value by practicality. 4-Benzoyl-4'-Bromobiphenyl holds up under this lens. Purity above 99% (HPLC), low residual solvents, and minimal trace halides matter more than theoretical melting points or catalog claims. During repeated production campaigns for our clients, we observe how this intermediate saves time in post-reaction cleanups, reduces the need for excess reagents, and fits right into automated or semi-continuous process lines.

    Ease of handling, from bulk transfer to weighing at the bench, remains consistent. Flow behavior ensures no bottlenecks at the reactor charge step or during filtration. Shelf stability minimizes loss due to degradation or color changes. Our technical documentation backs up each claim with historical batch analysis, trace impurity logs, and end-user feedback, not just standard COA data. Few customers ever ask about the synthetic route, yet our years optimizing this process pay dividends each time a new lot gets shipped—unexplained residues, inconsistent flow, or batch-to-batch variance are problems our regulars simply don’t face.

    Real-World Differences: What Sets This Compound Apart

    Among the broad bench of biphenyl derivatives, 4-Benzoyl-4'-Bromobiphenyl distinguishes itself by the unique dual function of its substituents. Bromine at the 4' position facilitates targeted halogen-metal exchange or palladium-catalyzed couplings, while the benzoyl group bolsters stability and dictates electronic character. Many analogs lack such balance; those with extra halogenation often yield too much instability or spur on unwanted cross-reactivity, while fewer functional groups limit downstream derivatization.

    Comparisons with unsubstituted biphenyl or fully halogenated species highlight why users return to this material: selectivity and manageable reactivity. Too little substituent activity and reactions drag; too much and side-products pile up—our product falls in a sweet spot engineered for confidence and yield. Even during scale-up for pilot trials or commercial manufacturing campaigns, customers note lower by-product formation and cleaner phase separations compared to earlier stand-ins.

    Industry Insights: Meeting the Unwritten Demands

    Many in chemical manufacturing know the real battle is fought after basic procurement. Materials that seem equivalent on paper can diverge quickly in performance. Over the last decade, we monitored how subtle supplier changes—whether from local plant upgrades or the global supply chain—ripple down to pharmacists, coating developers, and electronics engineers. Only direct manufacturing experience equips a supplier to spot the problems and course-correct before final delivery.

    Our experience with 4-Benzoyl-4'-Bromobiphenyl reveals customers expect more than purity—they need speed of dissolution, stability over months, and absence of catalyst poisons. Tight control over raw input quality (for both biphenyl and benzoyl reagents) ensures we keep metal and halide impurities far below usual industry norms. This proactive stance stems from problems we encountered early: batch failures due to unnoticed trace metals—a headache that only factory floor experience could resolve, not textbook best practices.

    Continuous Improvement and Responding to Feedback

    Chemical supply does not run on static achievements. Alongside each major order, technical exchanges with formulators prompt tweaks—from alternate drying methods to packing in anti-static, moisture-barrier bags. In several cases, our own staff trialed the intermediate in-house to replicate end-user conditions, pinpointing bottlenecks invisible at the synthesis or isolation stage but obvious under real production rates.

    Most feedback points to reliability, but now and then a new market requirement appears. Semi-conductor industry partners needed even tighter particulate controls and absence of photoinitiator impurities. In pharmaceuticals, a single ppm of residual bromide caused issues for API synthesis. Our analytical setup (GC, ICP-MS, Karl Fischer) stays tuned to these needs, matching not only current, but also anticipated regulatory and functional expectations. Internal traceability protocols mean old issues never reappear, no matter the volume or shipping method.

    Commitment to Transparency and Track Record

    No manufacturing claim matters without a trail. Our staff archives CLP documentation, impurity breakdowns, and third-party audits in accessible databases, so producers from research to ton-scale operations know what to expect from each barrel or bag. Transparency also shapes our collaborative approach to regulatory compliance—helping early-stage R&D teams decipher evolving international transport legislation, or guiding bulk buyers on the best storage and handling setup for their region.

    Drawing from failures and successes, we sometimes advise buyers against ill-suited applications—such as those requiring higher halogen loading or needing functionalized biphenyls incompatible with the benzoyl moiety—saving others from dead ends our own chemists confronted before. Openness here seeds mutual growth, not just short-term transactions.

    Sustainability: Adapting to a Greener World

    Greener approaches to aromatic halide synthesis have drawn increasing attention. Pressure grows from customers and regulators to streamline energy use, cut hazardous waste, and improve lifecycle assessments. In response, our team invested in solvent recycling, smart process control for bromination steps, and optimized workups that curb halogen and acid by-products. Years spent adjusting protocols means fewer reactor cleanings, reduced utility consumption, and lower airborne emissions.

    Packaging improvements—lighter composite drums, returnable containers—help shrink transport impact. Production staff receive quarterly training on waste minimization, and each improvement gets passed on in updated technical bulletins. Embracing these efforts means long-term supply resilience amid shifting global regulatory climates and mounting scrutiny of specialty chemicals across sectors.

    Integrating Knowledge from Experience

    Industry-wide guidebooks rarely reflect the thousand small choices behind successful intermediate manufacture. Each season, new synthetic needs surface—from faster-reacting photo-initiators for 3D printing, to stringent demand for solvent compatibility in medical device coatings. The journey of 4-Benzoyl-4'-Bromobiphenyl production reflects decisions built on hands-on plant trials, lessons from failed test batches, and process tweaks inspired by customer feedback. This personal investment fosters relationships: researchers, technical officers, and operators come to us—not just for product, but for knowledge that boosts their operational reliability.

    The collective history of plant engineers, analytical chemists, and process operators shapes the material as much as the chemical formula itself. Equipment selection took months of trial and error, learning that tight thermal control at the bromination stage pays off through cleaner downstream crystallization. Adjusting grinding procedures led to optimum bulk density and dust suppression—improvements only realized through persistence and shared commitment across teams.

    Supporting Emerging Applications and Collaborative R&D

    Beyond traditional specialties, recent years saw 4-Benzoyl-4'-Bromobiphenyl crossing into emerging research in OLED materials and specialty photoreactive polymers. Even as some sectors plateau, demand rises among device developers for intermediates that balance performance with manufacturability. Our approach to these opportunities stems from offering small R&D lots alongside bulk material, combined with detailed impurity fingerprints to support precise end-use characterization.

    Collaborative development does not just mean sending samples. Open dialogue with technical partners alerts us to new purification requirements, while shared pilot data brings process innovations back into our own production cycles. The cycle of improvement broadens the scope of this intermediate year after year.

    Mitigating and Addressing Challenges in Production

    Every specialty intermediate faces production challenges that shift with market forces, technology changes, or regulatory tightening. Fluctuating costs for bromine or biphenyl feedstocks have, at times, threatened pricing stability and availability. Our long-term contracts, supply diversification, and periodic inventory reviews shield regular purchasers from these swings. Plant maintenance cycles and operator training maintain output consistency, and proactive spare parts stocking prevents unscheduled shutdowns.

    Handling potentially hazardous chemicals, such as brominating agents, sets safety as a top priority. Regular risk audits guide ventilation upgrades, advanced PPE protocols, and automated feed systems that safeguard both staff and product. Incidents across the industry underline the need for continuous process hazard analysis and readiness to adapt to regulatory or practical shifts.

    Trust Built on Long-Term Relationships

    Reliability in the eyes of formulators and purchasing managers comes from more than any certificate or technical data sheet. It grows with each successive delivery that matches, or exceeds, established expectations. Through repeat orders, transparent troubleshooting, and willingness to adapt internal processes for special requests, our commitment is proven in the field, not in promotional material.

    Many of our customers approach us precisely because our plant staff respond from direct manufacturing experience, sharing what worked (or didn’t) across hundreds of syntheses and scale-up campaigns. This foundation curbs mishaps, speeds troubleshooting, and forges confidence rooted in practice. Pathways for improvement—suggested by those who actually use the material at scale—get prioritized, tested, and folded into each process run.

    Looking Forward: Future-Proofing Specialty Aromatics

    The experience cultivated here goes toward anticipating tomorrow’s needs. Industry observers note regulatory and market pressures rarely let up. Analytical requirements grow more demanding, supply chains tighten, and downstream users expect transparent support from their suppliers in adapting to new regulations or performance standards. We continue to invest in instrumentation, batch traceability, and greener process adaptations to ensure that our 4-Benzoyl-4'-Bromobiphenyl—no matter the application—remains a trustworthy, practical solution in both current and emerging fields.

    Achieving this means keeping an ear to the ground across the industries we serve, ensuring the story of this compound never gets set in stone but keeps evolving alongside real-world needs. This blend of technical foundation, operational rigor, and a constant drive for better chemistry keeps our product and reputation strong in a world where every detail counts.