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2'-Bromo-4'-Fluoroacetophenone

    • Product Name 2'-Bromo-4'-Fluoroacetophenone
    • Einecs 252-037-1
    • 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

    841218

    Product Name 2'-Bromo-4'-Fluoroacetophenone
    Molecular Formula C8H6BrFO
    Molecular Weight 217.04 g/mol
    Cas Number 64872-34-6
    Appearance White to off-white solid
    Melting Point 56-60°C
    Boiling Point No data available
    Density No data available
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like DMSO and methanol
    Smiles CC(=O)C1=CC(=C(C=C1)F)Br
    Inchi InChI=1S/C8H6BrFO/c1-5(11)6-2-3-8(10)7(9)4-6/h2-4H,1H3
    Refractive Index No data available
    Storage Conditions Store at 2-8°C, keep container tightly closed

    As an accredited 2'-Bromo-4'-Fluoroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of 2'-Bromo-4'-Fluoroacetophenone is packaged in a sealed amber glass bottle with a printed hazard label for chemical safety.
    Shipping **Shipping Description:** 2'-Bromo-4'-Fluoroacetophenone is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous material, following all DOT, IATA, or IMDG regulations. Package with appropriate labeling and documentation. Store and transport under cool, dry conditions, and ensure compliance with local and international chemical shipping requirements.
    Storage 2'-Bromo-4'-Fluoroacetophenone should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Proper labeling and handling procedures must be followed to prevent accidental exposure or chemical reactions.
    Application of 2'-Bromo-4'-Fluoroacetophenone

    Applications of 2'-Bromo-4'-Fluoroacetophenone in Industrial Manufacturing

    As a direct manufacturer of 2'-Bromo-4'-Fluoroacetophenone, we supply this specialized aromatic haloketone intermediate to global industry leaders engaged in pharmaceutical synthesis, agrochemical research, and advanced material development. The following sections outline actual use scenarios, industry standards, and processing details from our clients’ production environments.

    1. Pharmaceutical Intermediate for API Synthesis

    This compound finds targeted application in the synthesis of kinase inhibitor APIs, particularly as a building block for fluorinated benzylated structures used in oncology drug pipelines. Major pharmaceutical manufacturers introduce it during heterocyclic core assembly, where the bromo-fluoro functionality enables regioselective coupling with aminopyridines and pyrazoles. QC departments reference monograph guidance to control residuals within established limits.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF General Chapters & Individual API monographs
    • EMA Guideline on Setting Health Based Exposure Limits
    • REACH registration for intermediate status

    Typical usage ratio

    • Mol ratio depends on the API target route; typically used at 1.0–1.2 eq relative to the coupling partner in the core-forming step
    • Adjustment required to minimize excess starting material in process validation

    Downstream process integration

    • Employed in the mid-stage of the multistep API synthesis, specifically after initial core assembly and before N-alkylation or Suzuki-Miyaura coupling
    • Used under controlled batch or flow protocols, with integration monitored by HPLC for purity thresholds

    Final product types

    • Small-molecule kinase inhibitor APIs (oncology indications)
    • Investigational new drug (IND) candidates featuring fluorinated aromatic cores
    • Pharmaceutical intermediates for further amination or cross-coupling

    2. Agrochemical Discovery: Herbicide Lead Optimization

    A number of agrochemical research organizations use this raw material as an essential intermediate in the design of new-generation herbicide candidates, leveraging its bifunctional aromatic structure for rapid SAR (structure-activity relationship) exploration. Regulatory teams ensure compliance with applicable crop chemical substance registrations prior to field trials in the synthesis of 3-aryl substituted triazines.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Synthesis and Characterization Sections)
    • ISO 1750: Pesticides and other agrochemicals–Common names
    • Regulation (EC) No 1107/2009 on Plant Protection Products
    • GLP compliance stipulated by national agrochemical regulatory agencies (e.g., EPA, EFSA)

    Typical usage ratio

    • Added at 0.9–1.1 eq relative to nucleophilic partner, optimized per SAR campaign to minimize purification burden
    • Formulation scientists may amend stoichiometry to accommodate high-throughput lead screening

    Downstream process integration

    • Inserted following the installation of the key aromatic scaffold, prior to heterocycle formation
    • Integrated via halogen-metal exchange or direct cross-coupling for rapid analog synthesis

    Final product types

    • Lead triazine herbicides (pre-commercialization)
    • Experimental agrochemical classes containing fluoro-aryl substituents
    • Reference compounds for field efficacy testing in regulated GLP trials

    3. Fine Chemical Intermediate for OLED Material Synthesis

    Producers of organic semiconductors and display materials apply this halogenated acetophenone in the construction of electron-transport and emissive layer molecules for OLED display devices. The high electron-withdrawing nature of the substituents enables precise design of π-conjugated monomers, supporting tight control in downstream polymerization processes. All synthesis processes observe stringent impurity control aligned with optical application standards.

    Industry compliance standards

    • RoHS 3 (EU Directive 2015/863) for restricted substances in electronics
    • ISO 9001-certified QMS for specialty chemicals production
    • IEC 62321 screening for halogenated aromatic compounds in electronics
    • Producer specifications for OLED grade materials (impurity ppm level)

    Typical usage ratio

    • Varies by target motif: commonly 1.0 eq in Suzuki, Stille, or Heck coupling reactions for intermediate formation
    • Material scientists may modulate loading between 0.8–1.2 eq for batch/reactor scale-up stability

    Downstream process integration

    • Imported as a core monomer for initial aromatic backbone assembly
    • Reacted with boronic acid or stannane derivatives to yield OLED-application intermediates

    Final product types

    • Electron transport layer (ETL) and hole blocking layer molecules for OLED displays
    • Light-emitting molecular materials for flexible/mobile screen technology
    • Intermediate building blocks for functionalized aryl-heteroaryl hybrids

    4. Custom Synthesis of Specialty Research Reagents

    Several advanced fine chemical laboratories procure this compound for the preparation of fluorinated aryl carbonyl reagents used in analytical chemistry and exploratory synthesis. The controlled introduction of the bromo and fluoro groups is leveraged in isotope labeling projects and mechanistic probe construction, subject to documented analytical validation procedures.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory testing and calibration
    • OECD Principles of Good Laboratory Practice
    • National/institutional research chemical registration (as applicable)
    • Transport and use protocols under UN 3077 (Environmentally hazardous substances)

    Typical usage ratio

    • Used from 0.5 to 1.5 eq based on synthetic objective, particularly for multi-step labeling or probe synthesis
    • Adjusted for scale-up and isotopic dilution as required by analytical teams

    Downstream process integration

    • Applied at the penultimate step in reagent assembly or as the starting point for further halogen exchange or cross-coupling
    • Subjected to purification by column chromatography or preparative HPLC prior to downstream R&D use

    Final product types

    • Fluorine-labeled aryl research-grade probes
    • Custom analytical reference standards for spectroscopy
    • Laboratory-scale specialty reagents for chemical research
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    Certification & Compliance
    More Introduction

    2'-Bromo-4'-Fluoroacetophenone: An Inside Look from the Manufacturing Floor

    The Evolution of Halogenated Acetophenones

    On our production line, life never stands still. Over the last decade, chemists and engineers have watched the growth of halogenated aromatic compounds, with acetophenones serving as reliable building blocks for innovation. Among these, 2'-Bromo-4'-Fluoroacetophenone stands out. Every kilogram leaving our reactors brings new possibilities for pharmaceutical synthesis, agrochemical research, and advanced material development.

    Our Experience with 2'-Bromo-4'-Fluoroacetophenone

    In the lab, the fine white to off-white crystalline powder of 2'-Bromo-4'-Fluoroacetophenone quickly becomes familiar. From the careful weighing to the final packaging, the compound resists caking even after long storage times. Through direct observation, we notice a distinct clean scent similar to other fluoroaromatics—an early sign of purity that rarely fails.

    Our chemists handle hundreds of similar molecules every year, but the behavior of this compound guides process decisions right down to the filter choice. Some might expect trouble with moisture, but this acetophenone handles ambient conditions with less fuss. The compound’s melting range lands solidly within expectations for similar molecular weight ketones, leaving few surprises during synthesis.

    Key Specifications Aligned with Real Needs

    Onsite HPLC and NMR analysis show batch purities exceeding 98.5% without the need for extensive post-purification. Impurities—like trace dibromo or difluorinated analogs—can rise when synthesis conditions drift, but frequent instrument checks help us catch these early. Labs using the material in downstream coupling reactions depend on this reliability, since even minor variants complicate separation and decrease yields.

    Each drum is filled with dense crystals, average particle size in the lower micron range, which stirs and dissolves fast in most organic solvents. Industrial partners who need hundreds of kilos in a month guide our drying and grinding steps. By listening to user feedback, we avoid over-grinding, since a powder too fine raises dust and can be hard to handle.

    How 2'-Bromo-4'-Fluoroacetophenone Stands Out

    Our process team has spent years perfecting the halogen exchange reaction that allows one position to accept a precise fluoro group while the other bears a bromo. Many alternatives offer different substitution patterns, but the 2'-bromo, 4'-fluoro structure hits a sweet spot for certain cross-coupling and carbonyl functionalization work.

    Chemists often compare it against the more common 4-bromo-2-fluoroacetophenone or mono-halogenated versions. In our hands, the 2'-bromo position opens up selective reactivity compared to the 4' isomers, allowing for Suzuki-Miyaura and Buchwald-Hartwig couplings under milder conditions. Our QC labs stress-test each lot in both palladium and copper catalyzed reactions to make sure unwanted side-products remain below detection thresholds.

    Synthetic drug units work with dozens of aromatic ketones, but few combine the right balance of electron withdrawing and steric properties. The 4'-fluoro substitution brings a push-pull effect that has improved selectivity in at least three of our customers’ focused library syntheses. Farmers relying on new herbicide candidates come back to this intermediate year after year because downstream reactivity saves steps in the process.

    Real Uses and the Feedback Loop from Customers

    From pharma to fine chemicals, requests arrive weekly for input on custom modifications or scale adaptation. Several research partners share published reaction data that use 2'-Bromo-4'-Fluoroacetophenone for introducing structural diversity into drug candidate libraries. One medicinal chemistry group found that modifications at the 2’-bromo position led to higher metabolic stability in lead compounds.

    Others in polymer research value the clean, predictable fragmentation pattern the compound shows in mass spec—an important point for tracking during process development. A major crop science firm pointed to reduced by-product formation in selectivity screens, which helps cut unnecessary purification runs.

    With each shipment, users send back questions—could a larger particle size reduce static in their feeders, or could we provide more detail on minor by-products? These practical questions drive change at our site. Over two years, we switched from a basic drum to high-barrier polyethylene liners after receiving concerns about storage under humid conditions in tropical labs.

    Comparing 2'-Bromo-4'-Fluoroacetophenone with Related Intermediates

    Most aromatic ketone manufacturers offer the basics: mono-bromo or mono-fluoro acetophenones, and sometimes di- or tri-substituted versions. Traditional 4-bromoacetophenone remains popular due to its ready availability and lower cost. But for chemists needing orthogonal reactivity, the dihalo combination in this compound often means shorter synthetic sequences and less waste.

    Fluoro-only analogs lack the selectivity inherent to the 2'-bromo group, forcing extra protection and deprotection steps. The overall cost per reaction tips in favor of our compound where functional group tolerance matters. In the materials field, our partners achieved higher yields in the synthesis of novel polyarylethers because fluorinated positions resisted unwanted side reactions at elevated temperatures.

    We see requests for custom ratios as users explore structure-activity relationships. Some now realize that switching to our product reduces environmental impact—less need for hazardous solvents and cutbacks in distillation cycles. Large pharma is always chasing efficiencies, and rapid access to high-purity, dihalogenated acetophenones opens more efficient routes to targets.

    Manufacturing Practice & Quality as a Culture

    Our floor staff and QC chemists track changes in raw material sources directly. Years ago, an impurity from a new supplier nearly derailed a scale-up, but in-house controls and batch records caught the problem fast. This taught us to lock down critical supply chains and to verify every lot before it reaches the reactors. Solvent quality and reaction temperature tracking are logged hour by hour. The team understands that if a compound veers even a few tenths of a percent in purity, customer procedures can fail downstream.

    Process controls don’t end with the reaction. Vacuum drying parameters help avoid color changes and odor shifts. During the last inspection cycle, a sharp-eyed mixer noticed a faint rose-tint—a sure sign that a batch sat too long at one temperature. Instead of shipping, the lot got recycled, saving everyone future headaches.

    Regulatory Observations and Safe Handling

    Every bottle and drum we fill passes through experienced hands that know these chemicals carry risks. Local regulations don’t allow cutting corners with shipments or hazard labelling. Our facility sits inside a zone tightly regulated by national authorities, which means compliance checks and documentation become second nature. Plant workers run regular drills, not just the minimum required. PPE use and clear labeling cut down incidents; no one wants setbacks traced to avoidable accidents.

    We encourage partners and users to share their experiences with packaging, storage, and transportation incidents since those details rarely make the literature headlines. Learning from small mishaps helps us update protocols, especially as new markets bring in requests from different climates or infrastructure realities.

    Process Innovation Drives Progress

    Several years ago, production yields stalled around the mid-80% range due to side reactions with trace water. After months of trial and error, process engineers devised a staged addition protocol using in-line Karl Fischer titration that stabilized the bromination step. Feedback from real-world use led to tighter specification of water content, boosting yields and cutting total synthesis costs.

    We transitioned to green solvents in certain steps after customers raised concerns over residuals in downstream pharmaceuticals. Dimethyl carbonate replaced less favorable alternatives, and by shifting the workflow, we knocked half a day off the total cycle time. Each improvement sprang from continuous dialogue with labs and plants on the receiving end, not from isolated R&D planning.

    Downstream Transformations and Performance

    Aromatic ketones like ours live and die by their ease in cross-coupling. Several users in academic synthesis circles point out that ortho-bromo substitution increases the range of boronic acids or amines they can introduce, especially when aiming for complexity. One pilot plant observed improved separation of products and unreacted starting material thanks to subtle solubility tweaks from the fluorine atom.

    Material scientists also praise the clean bond formation and stable reactivity of this intermediate. In their specialty, stability under UV and mild acids matter more than the ultimate pharmacology. This compound outperformed several single-halogen benchmarks over multiple accelerated-aging studies, holding up to harsh conditions.

    Repeat requests from fragrance intermediates manufacturers surprise even our old hands. The unique substitution pattern brings out novel scent profiles, and industrial perfumers tweak their products with pinpoint changes that depend on this specific intermediate’s availability and consistency.

    Waste Management and Environmental Impact

    Responsible production stretches from raw material sourcing to effluent management. Halogenated intermediates call for extra attention in both solid and liquid waste streams. Our plant captures and recycles solvents on-site instead of venting. When spent material heads offsite, we track destruction or recovery down to the batch number. Third-party audits keep this process real.

    Pushback from downstream users helped kill off certain catalysts that left hard-to-remove residues. Local water authority checks add another safety net, so both city and country laws get satisfied. Each improvement isn’t perfect, but input from environmental officers and onsite chemical engineers has cut waste sent to landfill by half over three years.

    Collaborative Development and Customization

    Not all users need the same form of 2'-Bromo-4'-Fluoroacetophenone. One medicinal chemistry client working at sub-gram levels needed ultra-dry, sub-500 micron particles for automated synthesizers. Others, ordering in drums, asked for anti-caking agents or smaller containers due to frequent scale-up runs. Each request feeds a feedback loop that shapes new SOPs.

    We tweak drying protocols, add documentation on batch-to-batch moisture levels, and ship trial lots for pilot batches. Corporate partners often report new regulatory demands halfway through long projects, forcing more transparency on impurities and trace element profiles. Each added requirement ends up strengthening our technical base rather than slowing progress.

    Open communication helps everyone win. Downstream losses or headaches in end-use disappear before they start, and both sides keep ahead of regulatory shifts that inevitably come.

    Supply Chain Reliability in an Uncertain World

    The last few years have brought unforeseen challenges to global chemical logistics: export restrictions, supply shortages, demand surges, and silk road bottlenecks. Our operations team tracks global raw material markets daily. Having backup agreements with secondary halogen and fluorine suppliers proved essential as the industry watched prices swing wildly during post-pandemic recovery.

    Inventory management now rests on real consumption rather than yearly averages. Some months, requests outstrip usual forecasts, with new fields—like specialty pigment synthesis or electronics—driving rapid spikes. We built safety stocks without sacrificing shelf life by monitoring shelf stability through ongoing lab analysis. Our production rhythm adapts with actual demand, not outdated projections, so users get fresh product every cycle.

    The Importance of Transparency and Traceability

    Chemists and buyers ask detailed questions that deserve direct, practical answers. Each drum leaves with a full analytical certificate, including GC-MS and moisture results. We respond to sample requests by shipping material from the actual production lots rather than “representative” batches stored for years. Batch records stay live for regulatory review, providing a detailed chain of custody from raw ingredients through to shipment.

    Our team learned long ago that trust grows fastest when data moves freely. Sharing primary test results and opening the plant to technical audits mean customers make informed choices, not gamble on hidden flaws. As synthesis work grows more demanding every year, small differences in trace metals, halogen content, or stability make or break whole programs.

    Looking Forward: Supporting the Next Wave of Chemistry

    Behind each bottle of 2'-Bromo-4'-Fluoroacetophenone lies a blend of years of manufacturing know-how, lab experimentation, user feedback, and regulatory adaptation. Producers like us balance efficiency, cost, and safety by listening to end users who reshape guidelines and demand transparency.

    By keeping connections open between plant and lab bench, by prioritizing calls for innovation and accountability, we expand the range and reliability of what this compound can achieve—across drug discovery, agricultural innovation, advanced materials, and beyond.