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3'-Bromoacetophenone

    • Product Name 3'-Bromoacetophenone
    • Alias 3-Bromophenyl methyl ketone
    • Einecs 211-665-7
    • 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
    VTB
    Specifications

    HS Code

    280946

    Chemical Name 3'-Bromoacetophenone
    Other Names m-Bromoacetophenone
    Molecular Formula C8H7BrO
    Molecular Weight 199.05 g/mol
    Cas Number 2142-68-9
    Appearance White to light yellow crystalline powder
    Boiling Point 272-274°C
    Melting Point 55-59°C
    Density 1.5 g/cm³
    Purity Typically ≥98%
    Solubility In Water Slightly soluble
    Smiles CC(=O)C1=CC(=CC=C1)Br

    As an accredited 3'-Bromoacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3'-Bromoacetophenone, securely sealed, labeled with hazard warnings, and product information.
    Shipping 3'-Bromoacetophenone is shipped in secure, tightly sealed glass or plastic containers to prevent leakage and contamination. Packaging complies with relevant hazardous material regulations, and the product is labeled accordingly. It is transported in climate-controlled conditions to avoid exposure to heat, direct sunlight, or moisture. Handling instructions and safety documentation are included.
    Storage 3'-Bromoacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Store at room temperature and ensure proper labeling. Keep away from sources of ignition, heat, and direct sunlight to maintain stability and prevent degradation.
    Application of 3'-Bromoacetophenone

    Applications of 3'-Bromoacetophenone in Industrial Manufacturing

    As an established chemical raw material producer, we supply 3'-Bromoacetophenone to global industrial clients requiring high standards for traceability, compliance, and process efficiency. This intermediate serves as a key input in several advanced synthesis and transformation routes across specialty and fine chemical manufacturing.

    1. Pharmaceutical Building Blocks for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use 3'-Bromoacetophenone to construct complex heterocyclic cores in the synthesis of various APIs, including intermediates targeted at anti-inflammatory and anticancer drugs. The brominated phenyl group enables selective functionalization in cross-coupling and nucleophilic substitution processes, delivering structurally diverse molecules for further elaboration. Typically integrated at the early or mid-stage of multi-step organic synthesis, this intermediate's batch traceability and analytical profile support regulatory submissions and ensure downstream process reproducibility, from pilot scale to full cGMP batch manufacturing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) per ICH Q7
    • USP and EP standards for raw material quality
    • ICH Q3A/B Impurity Guidelines
    • FDA 21 CFR Part 210/211 for pharmaceutical intermediates

    Typical usage ratio

    • 0.95–1.10 molar equivalents in stepwise synthesis
    • Adjusted to match excess reagent or coupling partner requirements
    • Process developers optimize based on yield and purity targets

    Downstream process integration

    • Used during halogen–metal exchange, Suzuki-Miyaura, or Buchwald-Hartwig coupling reactions
    • Dosed at specific stages requiring selective aromatic bromination
    • Introduced in both batch and continuous flow synthesis setups

    Final product types

    • API intermediates for generic and branded small molecules
    • Regulatory registered pharmaceutical ingredients
    • Custom-synthesized research molecules for clinical trials
    • Fine organic building blocks for medicinal chemistry

    2. Agrochemical Synthesis: Herbicide and Pesticide Intermediates

    Leading agrochemical formulators employ 3'-Bromoacetophenone in the design of advanced herbicide and pesticide molecules. Its aromatic bromoacetyl group reacts efficiently under Friedel–Crafts acylation and other electrophilic aromatic substitution conditions, laying the groundwork for key functional motifs found in commercial crop protection products. Quality assurance demands full batch documentation and contaminant control to meet agrochemical active ingredient specifications and to pass residue screening during downstream product registration.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticide Ingredients
    • ISO 9001:2015 Quality Management System
    • REACH registration for EU chemical safety
    • EPA FIFRA compliance for US pesticide precursors

    Typical usage ratio

    • 0.85–1.15 molar equivalents based on subsequent coupling partner
    • Process scale adjusts for active ingredient yield and impurity control

    Downstream process integration

    • Enter synthetic sequence after halogenation or acylation step
    • Included in industrial reactors with precise temperature and solvent control
    • Reacts with nucleophiles or bases to introduce side chains for activity tuning

    Final product types

    • Safener-intermediate herbicide actives
    • Precursor to selective insecticidal agents
    • Plant growth regulator intermediates
    • Custom agrochemical pipeline development compounds

    3. Dye and Pigment Intermediate for Specialty Colorants

    Industrial dye and pigment manufacturers utilize 3'-Bromoacetophenone as a functionalized aromatic feedstock to introduce color centers, initiate coupling reactions, or facilitate halogenated chromophore structures. The compound’s selective reactivity enables controlled modifications at specific positions, supporting unique hue development and stability. Production lines benefit from the predictable melting point and purity, necessary for stringent filtration and recrystallization regimes in colorant synthesis.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile application safety
    • EN 71-3 (Toy Safety) migration limits for pigment use
    • ISO 9001:2015 and in-house color fastness protocols
    • Global Textile Standards (GOTS) for organic dye applications

    Typical usage ratio

    • 10–25% by mol in aromatic coupling stages
    • Batch size scaling aligns color intensity targets
    • Adjusted based on targeted chromophore structure and performance tests

    Downstream process integration

    • Integrated in early-stage aromatic halogenation or ketone condensation
    • Fed into continuous reactors with in-line monitoring for endpoint determination
    • Combined with diazonium salts or metallized for pigment stabilization

    Final product types

    • Specialty dyes for textile fabrics and fibers
    • High-stability pigments for industrial coatings
    • Color concentrates for plastics manufacturing
    • Inkjet and printing ink intermediates

    4. Fine Chemical Synthesis: Research and Development Intermediates

    Contract research organizations and specialty chemical labs source 3'-Bromoacetophenone as a multi-purpose starting material for molecular diversification, library synthesis, and advanced organic transformations. This intermediate finds regular use in university and industrial settings for route scouting, proof-of-concept chemistry, and the validation of scale-out potential for new chemical entities. Reliable batch consistency and full analytical profile—NMR, GC, HPLC—support research-grade requirements.

    Industry compliance standards

    • ISO/IEC 17025 testing traceability
    • GLP (Good Laboratory Practice) guidelines for analytical processes
    • Internal QA/QC protocols for research intermediates
    • Lab safety regulations: OSHA (US), EU chemical safety directives

    Typical usage ratio

    • Varies from 0.1–2.0 molar equivalents depending on target molecule complexity
    • Stoichiometry adjusted based on experimental yield optimization and substrate reactivity

    Downstream process integration

    • Used as a substrate for halogen exchange, chain extension, and cross-coupling
    • Fed into reaction vessels for custom multi-step syntheses
    • Combined with other functionalized arenes under controlled anhydrous or basic conditions

    Final product types

    • Novel organic scaffolds for SAR studies
    • Chemical probe compounds for biological research
    • Prototyping intermediates for polymerizable systems
    • Advanced functionalized aryl ketones for chemical libraries
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    Certification & Compliance
    More Introduction

    3'-Bromoacetophenone: Fine-Tuned for Modern Synthesis

    Getting to Know 3'-Bromoacetophenone

    At our manufacturing facility, we produce 3'-Bromoacetophenone with a sharp focus on purity, consistency, and compliance. Our teams have spent years refining this process. In chemical structure, 3'-Bromoacetophenone stands out with a bromine atom attached at the meta-position of acetophenone ring. This difference, though it may sound small, has driven a steady uptick in demand for this precise molecule. Researchers and formulators rely on its unique balance of reactivity and selectivity—an essential detail for industries that need exacting performance, not wildcards.

    The single largest market for 3'-Bromoacetophenone comes from pharmaceutical and agrochemical research projects. In these labs, reproducibility matters more than ever. We keep impurities out, maintain batch-to-batch consistency, and document traceability to satisfy the strictest inspection. That means reactions scale up as expected, intermediates behave predictably, and process bottlenecks don’t sap time or cash. Years of hands-on feedback from scientists tell us: stick with a stable and transparent product profile, processes move smoother. Nobody wants unexplained side products or unreliable crystallization—so we use proprietary purification and phase-conversion steps to zero in on the high assay figures expected.

    Thanks to that care, our typical 3'-Bromoacetophenone runs over 99% minimum purity by HPLC, GC, and NMR verification. Melting point sits right in the published reference window, and specific analytical signatures check out batch after batch, year after year. This level of precision matters for customers who demand the molecule not just as a curiosity, but as a reliable building block in new compound synthesis—whether chasing lead optimization or scaling to pilot batches on the road to market.

    What Sets 3'-Bromoacetophenone Apart

    During pilot-scale development, chemists tell us that small changes in substitution patterns on the acetophenone ring have outsized impact on reactivity and downstream functionalization. 3'-Bromoacetophenone’s bromo group at the meta position delivers a completely different reactivity pattern than the para or ortho isomers. With 4'-Bromoacetophenone, for example, oxidative couplings and palladium-catalyzed cross-couplings shift toward alternative selectivity profiles. Substitution in the para position is often less sterically hindered, giving a different set of products in Buchwald-Hartwig aminations or Suzuki-Miyaura couplings.

    By focusing on the meta-position, 3'-Bromoacetophenone opens up synthetic routes not efficiently accessed by its ortho or para cousins. Medicinal chemists leveraging meta-substitution can target new analog series more efficiently. Our product’s pure profile means fewer side products in multi-step synthesis, and less time troubleshooting byproducts from unchecked side reactions. For users looking for a sharp, predictable starting material or intermediate, this precision saves labor and increases output. In agrochemical circles, fine-tuned bromoacetophenones like ours enable the development of novel herbicide and fungicide molecules not easily accessed with alternative substitution.

    Daily Manufacturing Priorities

    After decades running commercial chemical manufacturing lines, we’ve internalized that every process tweak, operator intervention, or raw material deviation can have ripple effects downstream. The synthesis of 3'-Bromoacetophenone demands strict control over temperature profiles, agitation rates, and workup procedures. Small process deviations can cause halogen scrambling or residual acetic byproducts—a headache in purification that most traders don’t see, but we tackle head-on in our own reactors. Clean reaction profiles and isolation steps keep byproduct levels low, delivering a product that doesn't interfere with later process chemistry.

    We routinely review process data from each campaign, testing reaction conditions, analyzing impurity spikes, and improving solvent recovery cycles. Early on, we switched to a closed-loop solvent recycle system and recalibrated bromine point addition to limit overbromination and improve atom economy. These manufacturing improvements don’t just boost yield—they clamp down on residual bromobenzene, acetic acid, and related side products that often slip into less strictly controlled material. The result: customers see less drift in spectral values, and more predictable downstream processing. Lower waste and environmental load benefit us too, cutting compliance headaches.

    Specs and Quality Backed By Real Output

    We never treat assay data as a numbers game to move product. Each batch of 3'-Bromoacetophenone comes with full analytical backup—proton and carbon NMR, HPLC purity checks, water content validation, and GC-MS impurity profiling. Real samples from real batches get archived for reanalysis, so a researcher can ask us for spectral overlays at any time. When teams request additional impurity cutoffs, such as extra-stringent heavy metal or halide screening, we run these as per their protocols instead of universal certificate templates.

    Users in drug discovery programs depend on fine-purity controls to keep biological tests trustworthy. Lower residual solvent, minimal halogenated benzene byproducts, and no surprises in the melting point curve eliminate time lost to failed assays. Experience tells us: even small margins in quality can mean the difference between uncovering a breakthrough and circling back to revalidate a lead due to an off-target effect caused by a contaminant. Formulators pushing into new APIs or crop protection agents have reinforced this wisdom for years. Our approach returns raw data to our customers. If a customer’s process calls for a special particle size or tailored crystalline habit, we work together to adjust recrystallization or milling settings, as long as it doesn’t degrade chemical purity. These collaborations reduce risk and accelerate timelines for our partners.

    Applications in the Lab and Beyond

    Researchers use 3'-Bromoacetophenone as a direct precursor for cross-coupling reactions, Grignard additions, and as feedstock for more elaborate carbon frameworks. Its bromo functional group offers a convenient handle for installing diverse groups and drives C–C and C–N coupling routes. In discovery chemistry, meta-substituted motifs lead to new pharmacophore architectures. Our product’s sharp meta orientation delivers different selectivity from para or ortho analogs, crucial for intellectual property or analog space exploration.

    Lab-scale users rely on predictable melting behavior and solubility, ensuring that scale-up or media exchanges happen without surprises. Production engineers see little off-gassing or fouling, thanks to our purification protocol. In chromatography-based separations, the product holds up under standard solvent systems, without leaching or ghost peaks. All these small victories in a manufacturing environment add up—minimizing time off the critical path for product development.

    Outside the laboratory, companies anchor new manufacturing campaigns on a reliable bromoacetophenone source. Our experience with long-term shipments, bulk packaging stability, and cold-chain compliance ensures that each drum arrives unscathed. For companies qualifying alternative suppliers, we open our production records and quality data, so procurement and quality teams get clarity before making a switch. If a customer voices a concern or flags a spec drift, our technical managers walk with them step by step, rather than shuffling paperwork. Over years, this open accountability wins us repeat partners who tire of commodity traders and look for real expertise behind every drum or pallet.

    Staying Ahead by Listening and Solving Problems

    Manufacturing reality teaches the crucial lessons—predictable supply, consistent composition, and the ability to adapt when an application uncovers a sticking point. In the early 2010s, we responded to a surge in fine-chemical customers who wanted lower endotoxin burden for their semi-prep campaigns. By redesigning our workup to minimize bio-burden and optimizing storage protocols, we kept batches inside the narrowest microbial specifications. Another industry push came from the need for halide control in microelectronics, as meta-bromoacetophenone can appear as a trace impurity in complex functional materials. We built in extra analytics at our customer’s request, and batch adjusted to tighter output windows.

    The lesson is clear: only constant attention, rooted in real-world application, keeps the product at the quality bar our customers set. We don’t treat 3'-Bromoacetophenone as a nameless commodity. In the past, a few off-patent suppliers relaxed their standards and dumped poor quality onto the market. That only caused frustration for technical managers, led to more plant trials, and even forced plant shutdowns as byproduct profiles drifted away from customer specs. By keeping close tabs on feedback and making upgrades when needed, we’ve maintained a two-way street with experienced users, not just new buyers.

    If a biologist or materials chemist flags an odd spectral anomaly, our technical staff investigates until they can trace the root cause—rarely do we hear the old excuse to just “buy another lot.” This rigorous back-and-forth built our analytical playbook, not to mention a few fascinating process tweaks along the way.

    Environmental Care in Chemical Production

    Regulators and innovators set the pace for cleaner, safer chemical processes. In 3'-Bromoacetophenone manufacture, we’re challenged to reduce both solvent use and halide emissions without sacrificing yield or purity. Several years ago, we engineered a multi-effect distillation system allowing us to recover and recycle halogenated solvents, cutting waste and improving the lifecycle impact. Though the up-front investment stung, the long-term cost and compliance savings keep our facility within the latest benchmarks. That approach—treating every kilogram as a stewardship challenge, not just inventory—protects our team as well as the communities nearby.

    Our scrubber plant operates all year, handling both routine vent streams and batch shut-downs. Trace emissions of bromine or acid gases don’t just vanish—they’re scrubbed and monitored, with third-party audits validating our environmental numbers. Wastewater from cleaning and process wash-down undergoes batch treatment before release. We withhold operational shortcuts, even when raw costs pinch, because regulators and local partners watch these details closely. In return, we keep operating thresholds high, and never dodge compliance costs onto someone down the road.

    Customers who now factor supply chain ESG standards into their sourcing see these efforts not as window dressing, but as foundational. Our technical product data includes environmental certifications on handling, raw material sourcing, and downstream traceability. For partners tuning their own green chemistry initiatives, direct access to our process and compliance heads means they get honest answers about where improvements pay off, versus where legacy chemistry just can’t yet provide a magic bullet.

    Technological Upgrades and Continuous Process Improvement

    In chemical manufacturing, knowledge advances in increments, not leaps. We didn’t upgrade our dry recovery stage until a year of lab trials convinced us it doubled throughput with no effect on final product quality. Other new hardware, such as distributed control systems for better real-time monitoring, directly reduced batch rejection by over 25% one year, proving that operational discipline carries through to product consistency. For contracting partners, these steady improvements mean fewer delays from batch recalls or reruns.

    We apply the same evidence-guided decision making to raw material sourcing. We test incoming aryl precursors and bromine stocks with every delivery, qualifying each lot before use. This vigilance insulates us from global fluctuations in purity or supply. Customers facing last-minute regulatory upgrades or quality audits receive transparent documentation showing the supply chain end-to-end. If industry innovation pushes an alternative greener synthesis or less hazardous brominating agent, we’re ready to pilot new workflows until the chemistry makes sense at industrial scale.

    Years of production have taught us: never trust that a well-performing process can run on autopilot. We keep frontline teams in the communication loop and regularly move development chemists onto production shifts to close the gap between R&D and plant-floor execution. This cycle roots out process inefficiencies early and keeps theoretical adjustments grounded in operational reality. We treat new standard operating procedures as living documents, updating them after serious review and field trial, not as bureaucratic hurdles. The product stays sharp—meeting shifting industry targets and reducing backlogs from unexpected technical obstacles.

    Setting Standards by Real-World Practice

    We don’t pitch 3'-Bromoacetophenone as an indistinguishable widget. Our customers benefit from hundreds of person-years refining, scaling, and troubleshooting every detail of how it’s produced and shipped. By running our own reactors, handling our solvent recovery, and fielding every support question directly, we align our output with what bench scientists, process engineers, and regulatory auditors expect. Each analytical report, shipment, and technical consultation returns one message: attention to manufacturing detail and user experience outpaces commodity trading any day of the week.

    If you chase new compounds, demand robust supply, or must scale up from gram to multi-ton production, 3'-Bromoacetophenone from our line brings the confidence that comes only from skilled manufacturing. Through steady investments, real dialogue with users, and an unwavering focus on regulatory and environmental compliance, we aim to turn a fundamental building block into an advantage rather than a bottleneck. In this line of work, that means a lot more progress in a lot less time.

    Differences Compared to Similar Compounds: Why the Meta Matters

    Chemists sometimes ask why they shouldn’t opt for 2'- or 4'-bromoacetophenone instead. The debate usually boils down to molecular geometry and practical reactivity. The meta-bromo arrangement in 3'-Bromoacetophenone projects different characteristics than ortho (2') or para (4') isomers regarding electronic influence and steric accessibility. For palladium-catalyzed couplings or directed ortho metalation, the meta isomer opens up synthetic space that other isomers choke off. Medicinal chemistry teams in particular value the altered electron density and cross-coupling profiles, which directly influence structure-activity relationships and can protect new patents.

    We’ve produced all three isomers upon request and tracked purity, ease of handling, and downstream reaction profiles. Out of these, 3'-Bromoacetophenone consistently offers lower side-product generation during Suzuki coupling and nucleophilic substitution reactions. Vendors distributing all three interchangeable isomers miss the subtle but crucial gains in API or advanced intermediate synthesis. Analytical data validates those gains: NMR, HPLC, and GC traces show fewer contaminants and sharper main peaks with our meta product, cutting post-reaction purification times.

    Down the supply chain, end users told us tales of batch-to-batch drift and product variability when using mass-market grades of bromoacetophenones. Variable reactivity, hidden residuals, and off-color lots bring headaches to busy labs and plant lines. Rather than treating bromoacetophenones as fungible, our manufacturing philosophy recognizes the non-negotiable need for the right isomer in the right spec for the right synthesis. That philosophy keeps both large and small users loyal year after year.

    Future-Focused Manufacturing: Meeting Tomorrow’s Standards

    As regulations and user requirements tighten, we expect the market for high-fidelity intermediates like 3'-Bromoacetophenone to grow more demanding. Tighter impurity controls, better documentation, more sustainable processing—these are not future challenges, but daily practice at our plant. New applications in electronics, advanced pharmaceuticals, and agricultural chemistries drive our teams to forecast evolving technical needs. Working closely with leading users isn’t just a business plan; it’s a laboratory for better, smarter, and safer production.

    We keep an open technical feedback channel, adjust process and quality specs, and never mail in our commitment to transparency. In every batch we release, careful hands-on work ensures the product meets or exceeds user expectations. That tradition sets 3'-Bromoacetophenone from our plant apart from bulk-traded lots with uncertain provenance or unknown process histories.

    Years in, we recognize that great chemistry comes from tight process fixtures, strong teamwork, and continuous learning from every user who challenges us to deliver better. For 3'-Bromoacetophenone, that means a product built for today’s toughest requirements, with tomorrow’s solutions always under consideration. We produce it not just by formula, but by pride in the work—and that difference shows, whether in a start-up’s flask or a multinational’s reactor train.