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4'-Bromobutyrophenone

    • Product Name 4'-Bromobutyrophenone
    • Einecs 212-104-9
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    183125

    Product Name 4'-Bromobutyrophenone
    Cas Number 5067-64-1
    Molecular Formula C10H11BrO
    Molecular Weight 227.10 g/mol
    Iupac Name 1-(4-Bromophenyl)butan-1-one
    Appearance White to off-white crystalline powder
    Melting Point 58-62°C
    Boiling Point 315.5°C at 760 mmHg
    Density 1.418 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CCCC(=O)C1=CC=C(C=C1)Br
    Synonyms 4-Bromobutyrophenone; p-Bromobutyrophenone

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

    Packing & Storage
    Packing 4'-Bromobutyrophenone is packaged in a 25g amber glass bottle with a secure screw cap, featuring clear hazard labeling.
    Shipping 4'-Bromobutyrophenone should be shipped in tightly sealed containers, clearly labeled, and packed with appropriate cushioning materials. It must be transported according to local and international chemical safety regulations, preferably by ground in compliance with hazardous materials guidelines. Avoid exposure to extreme temperatures, moisture, and direct sunlight during transit.
    Storage 4'-Bromobutyrophenone should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Ensure storage is in a designated chemical storage cabinet, ideally flammable-proof, and clearly labeled. Keep away from direct heat sources and ignition points to ensure safe handling.
    Application of 4'-Bromobutyrophenone

    Applications of 4'-Bromobutyrophenone in Industrial Manufacturing

    4'-Bromobutyrophenone serves as a critical chemical intermediate for several sectors that require precision synthesis. As a direct manufacturer, we supply this raw material for dedicated downstream uses, where controlled formulation and compliance with specific industry standards are mandatory.

    1. Pharmaceutical Intermediates Production

    Our clients utilize 4'-Bromobutyrophenone primarily in the multi-step synthesis of active pharmaceutical ingredients, particularly for the preparation of certain substituted phenylbutyrophenone derivatives. In regulatory-compliant pharma lines, its bromine functionality enables targeted structural modification, supporting the formation of psychoactive and antipsychotic compound scaffolds within cGMP batch reactors. Customers rely on precise feeding of the raw material during the condensation and cyclization stages, integrating in validated process maps where strict change controls apply.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • EU Regulation (EC) No 1223/2009 for chemical contaminants in pharma manufacture
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) requirements for API intermediates

    Typical usage ratio

    • 5–20 mol% relative to final API precursor, adjusted by reaction scale, reactor charge, and required yield of substituted phenyl skeletons

    Downstream process integration

    • Direct addition into batch synthesis after initial aryl halide activation
    • Precursor in Grignard or ketone functionalization steps for multi-step organic syntheses
    • QC-confirmed for purity before entry into regulated API production lines
    • Used in dry, low-moisture environments due to brominated structure’s sensitivity

    Final product types

    • Pharmaceutical API building blocks (e.g., butyrophenone-type antipsychotics)
    • Specialty psychiatric medications (post further synthesis and formulation)
    • Research-grade small molecule intermediates
    • Reference substances for pharmaceutical screening

    2. Agrochemical Intermediate Manufacturing

    Our material functions as a precursor in agrochemical pipelines, where its brominated aromatic group allows efficient construction of selective herbicide and pesticide molecules. The compound is favored for its high reactivity with nucleophiles in custom synthesis projects, supporting the tailored modification of base molecules in synthesis reactors commonly found in advanced crop protection facilities. The controlled delivery of this intermediate ensures tightly regulated batch traceability and minimizes residual brominated contaminants in outgoing formulations.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation, and Restriction of Chemicals (EC No 1907/2006)
    • ISO 9001 certified process management for agrochemical synthesis
    • OECD Principles of Good Laboratory Practice (GLP) for pesticide intermediate testing
    • China National Standard GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 3–12% by mass in active molecule synthesis, dependent on target molecule complexity and downstream derivatization

    Downstream process integration

    • Input during the arylation or halogen exchange steps in herbicide and insecticide synthesis
    • Batch-dosed under nitrogen to mitigate undesired side reactions
    • Inline purity monitoring during high throughput synthesis
    • Waste minimization procedures for residual brominated organic substances

    Final product types

    • Selective post-emergence herbicides
    • Novel synthetic insecticides
    • Crop protection intermediate concentrates
    • Technical grade agrochemical actives (for further formulation)

    3. Fine Chemical Synthesis for Fragrance and Flavor Precursors

    This material enters fine chemical plants as a reactant for complex aryl ketone synthesis, which is essential for producing high-purity intermediates in the flavor and fragrance sector. Its aromatic ketone core supports Friedel-Crafts acylation steps, crucial for generating aldehydes and musky aromatic bases, deployed by major fragrance ingredient suppliers. Downstream users benefit from batch-specific documentation to ensure compliance with regulatory expectations, particularly where residual brominated compounds must be minimized in output fractions.

    Industry compliance standards

    • EU Regulation (EC) No 1334/2008 for Flavourings
    • IFRA (International Fragrance Association) Standards for chemical inputs
    • ISO 22716 (Cosmetic Good Manufacturing Practices)
    • JCIC (Japan Cosmetic Industry Association) import controls

    Typical usage ratio

    • 1–8% based on batch formula, adjusted for yield control and end product purity goals

    Downstream process integration

    • Charged during acylation or aromatic modification for intermediate aroma synthesis
    • Real-time process analytics to monitor bromine removal or conversion
    • Packed column distillation for ketone intermediate isolation
    • Batch-to-batch documentation for traceability and customer audits

    Final product types

    • Musky aromatic ketone intermediates
    • Specialty aldehydes for fragrance compound blending
    • Custom aroma chemical bases for consumer scent formulations
    • Process-tested flavor synthesis intermediates

    4. Specialty Polymer and Resin Synthesis

    We supply this raw material to polymerization plants as a chain-initiating aryl ketone, particularly for specialty resins and engineering thermoset matrix applications. Its structure enables highly controlled radical polymerization, such as in the creation of custom crosslinked polymers for electronics encapsulation and advanced coatings. Downstream operators utilize our lot-specific COAs to document bromine content and monitor conversion through dynamic thermal and chemical processing steps, complying with both material safety and performance standards.

    Industry compliance standards

    • ISO 9001 and ISO 14001 (Environmental) for materials conversion
    • Restriction of Hazardous Substances Directive (RoHS) for electronic polymers (EU 2011/65/EU)
    • UL 94 flame retardance testing for brominated intermediates in resins
    • ASTM D638 for thermoset tensile strength

    Typical usage ratio

    • 1–10 phr (parts per hundred resin) in prepolymer stage, modified based on specified crosslink density and target mechanical performance

    Downstream process integration

    • Fed during prepolymer mixing and initiation in reactors for thermosets
    • Thermally monitored batch runs for bromine tracking and elimination verification
    • Post-cure quality checks for free bromide content
    • Documentation with each production lot for compliance traceability

    Final product types

    • Custom flame-retardant thermosetting resins
    • Encapsulation matrices for microelectronics
    • Specialty printed circuit board polymers
    • High-performance coating resins
    Free Quote

    Competitive 4'-Bromobutyrophenone 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

    4'-Bromobutyrophenone: A Manufacturer’s Perspective

    Looking at 4'-Bromobutyrophenone in Daily Plant Life

    Every day in the lab, the quiet shine of crystalline 4'-Bromobutyrophenone catches my eye before I put on gloves. Here, we know its scent, its heft, the subtle flecks it leaves behind. Each step of its creation reflects years of refining both technique and understanding. There are faster ways to make molecules, but care delivers consistency—the kind that reaches the customer as promised.

    Many see 4'-Bromobutyrophenone only as a CAS number, but under our roof, it’s more than that. You find it referenced as 4-Bromo-4-phenylbutan-2-one or 1-(4-Bromophenyl)-1-butanone. In our work, the name matters less than its performance: an off-white solid, showing sharp melting at about 52–54°C, dissolving well in most organic solvents, offering a stable midpoint for building complex molecules.

    Real Stories From Real Batches

    I remember the first time we scaled from grams to multi-kilo runs. Small glassware made way for heavier reactors. The exotherm, once a mild warmth in a flask, could become a rush of heat in a steel vessel three feet across. Every tweak in dropping speed, every pass of the agitator blade, every fraction of a degree in temperature made a difference. Those hard-won details let us give chemists what they count on: 4'-Bromobutyrophenone that looks the same, reacts the same, holds the same structure from drum to drum.

    Behind every lot, our technicians run thin-layer chromatography, NMR, GC-MS. They’ve looked at enough data to spot a stray impurity before an instrument sounds. Our batches run at HPLC purity levels above 98% because we keep the process in-house, watching the reaction from bromination through to crystallization. Real control means less batch-to-batch variation and fewer surprises for synthesis teams down the line.

    Where 4'-Bromobutyrophenone Goes

    From the factory floor, we see packages bound for pharma labs, agrochemical startups, and academic groups. Most commonly, 4'-Bromobutyrophenone takes a role as an intermediate. Its aryl bromide handles make it a sturdy starting point for Suzuki and Heck couplings. If you’re building a new drug candidate and need to tack on complexity at the para position, this is the stuff that gets you there. The phenone structure sets it up to join ring systems or form the backbone for heterocycles with biological activity.

    The molecule doesn’t just work because it has a bromide—anyone could throw a bromine on a benzene ring. What matters lies in the stability of the ketone and the placement of that bromide within reach of a coupling partner. We see success stories: researchers have used our product in CNS-active scaffolds, even in ligands bound for enzyme inhibition studies. In every case, the molecule’s performance ties back to purity, consistency, and the absence of contaminants that can ruin a synthesis or cloud biological tests.

    Understanding What Sets It Apart

    People sometimes ask if there’s an easy substitute for 4'-Bromobutyrophenone. Structurally, one could look at other aryl bromides of similar chain length—maybe 4-bromopropiophenone or the related iodide. Plenty of catalog suppliers shift between them without much thought. Here, we see the practical differences. Not every brominated ketone behaves well during storage; moisture uptake or slow decomposition can cause yield headaches or extra work at the workbench. Our protocols stress dry, well-sealed containers, nitrogen atmosphere, and cool storage to extend shelf life and keep product loss to a minimum.

    The chain length and substituent position matter, too. Compared to its cousins, 4'-Bromobutyrophenone has the four-carbon backbone. That extra methylene group shifts reactivity in predictable ways, making it less prone to certain side reactions that trip up shorter ketones. It gives more flexibility for downstream functionalization—a big reason why pharma screens latches onto this compound when simpler ketones come up short.

    Manufactured right, the end result comes free of colored byproducts or halide impurities. Side reactions during bromination—unwanted dibromides or over-oxidation—can creep in when reaction conditions aren’t closely managed. With constant batch monitoring, we spot these outliers early, so clients don’t discover surprises halfway through a critical synthesis.

    Day-to-Day Challenges in Synthesis and Handling

    Producing 4'-Bromobutyrophenone at scale never runs on autopilot. Each reaction relies on a delicate balance: enough agitation to dissolve everything, controlled bromination rates to prevent excess heat, and careful timing of quenching. Staff experience turns theory into reality—years on the line teach patience, since a rushed process invites byproducts and caked reactor walls.

    On the downstream side, long crystallization takes patience. Filtering under nitrogen limits exposure, bringing out bright, dry product ready for packing. Spill a little, and you’ll see just how tenacious fine powder can be until contained correctly. Experienced hands know the little tricks: grounding lines to dissipate static, smoothing out cake surfaces for best drying, running bottles fast to the vacuum oven for the last trace of solvent.

    Safety and Sustainability: Hard Decisions and Practical Steps

    Every brominated intermediate raises real safety questions, especially as the world looks harder at green chemistry principles. We take worker safety and compliance beyond checklists. In our facility, every bromination step runs under fume hoods or closed reactor loops. Emergency scrubbers stand ready, always maintained. Every staff member walks through response training, not because regulators insist, but because bromine doesn’t forgive mistakes.

    We commit resources to closed-loop solvent recovery and careful waste handling. Less contamination out means a cleaner environment and, often, lower disposal costs. Over the years, we’ve trimmed solvent waste by rethinking steps where pure product can crystallize out, leaving more reusable solvent behind. In truth, production barely resembles its earlier, more wasteful forms.

    Many intermediates today come under regulatory scrutiny, so we work closely with government agencies to meet evolving safety and shipping rules. Border paperwork grows more complex each year. Internally, batch history can document every step—raw materials tracked, spectra archived, packaging logs reviewed before anything leaves the dock.

    Feedback from Laboratories and Lessons Learned

    We learn most from the bench chemists who use our compounds. Sometimes a phone call comes in: a reaction stalled, a solvent switch necessary, unwanted fluorescence traced back to an impurity. Solving these puzzles together makes better molecules and cements trust between supplier and chemist. By sharing technical notes and refining specs, our customers get higher yields, less troubleshooting, and more reproducible science.

    One time, a university lab chased down a crystallization problem, finally pinning it to rare byproducts present in a competitor’s batch. Their troubleshooting? Run the same sequence with our lot. This is how real-world testing often validates the details we stress—proper purification, consistent NMR peaks, and filtration that doesn’t leave fines behind. Success at the customer’s bench often depends on these behind-the-scenes choices.

    Comparing 4'-Bromobutyrophenone to Related Building Blocks

    On paper, you’ll see dozens of aryl bromides and aryl ketones. The catalog numbers blur into each other, tempting some to pick based only on price or quick shipping. But functionally, 4'-Bromobutyrophenone’s structure puts it in a distinct class. The para-bromide opens cross-coupling chemistry to a wide set of conditions—phosphine ligands, Pd or Ni catalysis, bases mild and strong. Its direct neighbors, ortho or meta bromides, often give lower yields in the same conditions or introduce steric bulk that demands workflow changes.

    Against its shorter-chain analogs, 4'-Bromobutyrophenone gives a balance between reactivity and stability. Yet for some applications, that longer chain would miss the mark—electronic effects, leaving groups, or metabolic fate can dictate the final choice. In drug discovery, following a lead into metabolic stability often guides chemists toward this motif. The extra carbon confers blockage against unwanted oxidation or allows subtle tuning of physical properties, like solubility in a final tablet blend.

    Some users have tried flipping to halogenated acetophenones for cost or perceived simplicity. In our testing and customer anecdotes, the acetophenone core can lead to clogging or unhelpful dimerization under coupling—problems that 4'-Bromobutyrophenone skillfully avoids. These chemical fine points often mean the difference between weeks of troubleshooting and a direct route to the goal compound.

    If you’re working in combinatorial chemistry, the traceability and predictability we manage at the factory become critical. Small substitutions may look trivial on a blackboard, but across dozens of runs, impurities or reactivity shifts cost real time and real money.

    Scaling Up Without Compromising Quality

    Bringing a novel building block like 4'-Bromobutyrophenone from concept to market takes courage to invest in new hardware, reformulate old processes, and train staff in real-time. We don’t shy away from the fact that each jump in scale creates new complexity: heat flow in big tanks is not the same as in a flask, and crystal growth takes on a life of its own with larger volumes and longer cooling times.

    Achieving high yields isn’t enough; product purity, reproducibility, and safety come to the front. Over the years, we phased in more real-time analytics—inline HPLC, temperature logging, computer controls on dosing. Old-fashioned vigilance still matters, though. Laboratory notebooks from a decade ago still sit on our shelves, not for nostalgia, but as proof of hard-won wisdom. Those pages show where problems could arise and how the best operators learn to predict and prevent issues before they reach the customer.

    Most clients never see these decisions, but in the finished bottle, every long shift, every carefully monitored process, and every recalibrated instrument matters. As a manufacturer, integrity is visible in small details—a consistent melting point, uniform crystals, clean spectra—that the chemist on the receiving end relies on for everything downstream.

    Transparency, Trust, and Questions Welcomed

    In a field where cutting corners can damage reputations and slow research, our policy favors openness. We invite requests: batch spectra, chromatograms, stability data beyond the minimum spec sheet. If something unexpected happens—even a minor change in appearance or packaging—we alert users quickly and work to find the cause before shipments resume. Over time, this transparency builds not just business, but actual working relationships with our end users.

    Readiness to discuss process controls, sustainability efforts, or safety improvements isn’t just a sales pitch. Our team puts a face behind each drum of 4'-Bromobutyrophenone that leaves the warehouse. We’ve answered hundreds of technical questions, walked clients through troubleshooting, and shared both successes and mistakes. This real-world, lived experience finds its way into every batch report and shipping label.

    Future Possibilities With 4'-Bromobutyrophenone

    The field continues to evolve. New synthetic tools—photoredox, electrochemistry, greener bromine sources—look promising for future cost and safety improvements. We invest resources back into bench trials, exploring routes that cut out hazardous steps or open up fresh derivatives. The feedback loop between manufacturing and research remains tight. As the chemical industry shifts toward more sustainable methods and stricter regulatory standards, our production lines adapt proactively.

    With experience as a guide, we remain confident in 4'-Bromobutyrophenone’s value. Its utility as a building block persists, not just for its chemical makeup but for the reliability and support we continue to provide. On this foundation, customers can find the confidence and consistency needed to build the next generation of pharmaceuticals, advanced materials, and agrochemicals.

    The story of 4'-Bromobutyrophenone isn’t just one of molecules; it’s one of the people and care behind them. In every lot shipped, we see years of trust, hands-on knowledge, and daily decision-making that enables progress in so many labs beyond our walls.