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4'-Bromo-3'-Nitroacetophenone

    • Product Name 4'-Bromo-3'-Nitroacetophenone
    • Einecs 421-900-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    412957

    Productname 4'-Bromo-3'-Nitroacetophenone
    Casnumber 5471-87-6
    Molecularformula C8H6BrNO3
    Molecularweight 244.04 g/mol
    Appearance Yellow crystalline powder
    Meltingpoint 114-117°C
    Boilingpoint No data available
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.76 g/cm³ (approximate)
    Purity Typically ≥98%
    Synonyms 4-Bromo-3-nitroacetophenone
    Smiles CC(=O)C1=CC(=C(C=C1)Br)[N+](=O)[O-]
    Inchikey HHKHGCPQIOVHLR-UHFFFAOYSA-N
    Storageconditions Store at room temperature, keep container tightly closed, protect from light
    Hazardclass Irritant

    As an accredited 4'-Bromo-3'-Nitroacetophenone 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 4'-Bromo-3'-Nitroacetophenone, labeled with chemical name, formula, hazard symbols, and batch number.
    Shipping 4'-Bromo-3'-Nitroacetophenone is shipped in secure, chemically-resistant packaging, labeled according to hazardous materials regulations. It is transported under controlled conditions, avoiding extreme temperatures and moisture. Compliance with local and international shipping regulations is maintained, and all necessary safety data and documentation are provided to ensure safe and legal transit of the substance.
    Storage Store **4'-Bromo-3'-Nitroacetophenone** in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers or bases. Keep the container tightly closed and clearly labeled. Avoid exposure to moisture and ignition sources. Use secondary containment to prevent spillage and store in a designated chemical storage cabinet, preferably for hazardous or toxic organics.
    Application of 4'-Bromo-3'-Nitroacetophenone

    Applications of 4'-Bromo-3'-Nitroacetophenone in Industrial Manufacturing

    As the direct manufacturer of 4'-Bromo-3'-Nitroacetophenone, we specialize in producing high-purity material for critical sectors across fine chemicals and advanced intermediates. Below, we outline strategically validated industrial application fields where our product delivers reliable performance, compliance, and technical integration.

    1. Pharmaceutical Intermediate for Quinolone Antibiotics

    Manufacturers use this compound as a key building block in the synthesis of advanced quinolone pharmaceutical intermediates, such as those destined for fluoroquinolone antibiotics. Its controlled bromine and nitro substitution pattern ensures high regioselectivity in nucleophilic aromatic substitution and cyclization reactions. This enables production of essential intermediates under strict regulatory requirements for purity and traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) guidelines (FDA 21 CFR Part 210/211)
    • European Pharmacopoeia monographs on API process controls
    • US FDA Drug Master File (DMF) referencing for intermediates

    Typical usage ratio

    • Utilization ranges from 0.9 to 1.2 molar equivalents in condensation steps, adjusted according to downstream route optimization and impurity control studies.

    Downstream process integration

    • Introduced during early stage aromatic ketone activation, followed by nucleophilic attack and subsequent cyclization to yield quinolone scaffold precursors.

    Final product types

    • Fluoroquinolone antibiotic active pharmaceutical ingredients
    • Intermediates for proprietary antibacterial compounds
    • Key blocks for generic antibacterial APIs

    2. Agrochemical Intermediate for Herbicide Synthesis

    This raw material is a direct precursor in the manufacture of selective herbicide intermediates, particularly those requiring aryl ketone frameworks with electron-withdrawing substituents. The structural reactivity of the nitro and bromo groups supports precision modifications in multi-step agrochemical syntheses that demand batch reproducibility and robust impurity analysis, especially at pilot and large scale.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical production
    • EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) requirements
    • US EPA 40 CFR Part 169: Production regulations for pesticide chemicals
    • OECD Guidelines for the Testing of Chemicals for environmental safety

    Typical usage ratio

    • Standard input at 1.0 to 1.1 mol equivalents per target arylation/coupling reaction; tuning based on activity studies and targeted final product yield.

    Downstream process integration

    • Fed into arylation steps, often followed by reduction, coupling, and cyclization to form final herbicidal actives.

    Final product types

    • Nitroaromatic herbicide actives
    • Precursor molecules for broad-spectrum weed control formulations
    • Custom intermediates for innovative agrochemical molecules

    3. Dye and Pigment Intermediate for Specialty Colorants

    Producers of specialty dyes employ this ingredient for synthesizing nitro- and bromo-containing aromatic ketones central to azo dye and pigment manufacture. Its controlled substitution pattern offers tunable chromophore properties and ensures stability under subsequent coupling, diazotization, and reduction processes, supporting the colorfastness and purity demands of advanced pigment manufacturers.

    Industry compliance standards

    • EU REACH regulations and SVHC compliance for dye intermediates
    • ISO 9001 chemical manufacturing standards
    • Oeko-Tex Standard 100 criteria for eco-toxicological safety (if pigment is for textiles)
    • ZDHC MRSL requirements when targeting apparel dyeing

    Typical usage ratio

    • Typical charge is 0.8–1.4 molar equivalents per pigment unit operation, with ratio fine-tuned for targeted shade and process loss minimization.

    Downstream process integration

    • Added as primary aryl donor in dye coupling steps, especially in the manufacture of complex azo and anthraquinone pigment precursors.

    Final product types

    • Specialty azo and anthraquinone dyes for plastics/textiles
    • Organic pigment intermediates
    • Colorant additives for specialty coatings and printing inks

    4. Fine Chemical Intermediate for Heterocyclic Compound Synthesis

    Specialty fine chemical producers rely on this raw material during heterocycle construction processes where bromo and nitro substitution is critical for regioselective cyclization, functional group interconversion, or nucleophilic aromatic substitution. This enhances the synthesis of pharmacologically active intermediates and custom ligands for advanced research and industrial catalyst programs.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical synthesis
    • GHS hazard classification and safe handling documentation
    • Chemical control compliance under local hazardous substance regulations (e.g., German Chemikaliengesetz)
    • Internal quality release protocols matching downstream customer QC requirements

    Typical usage ratio

    • Range is 1.0–1.3 molar equivalents, with lab-to-plant transfer studies used to optimize batch sizes and impurity profiles.

    Downstream process integration

    • Charged in initial nucleophilic aromatic substitution, followed by closure into heterocyclic rings through multistep synthetic schemes.

    Final product types

    • Intermediate scaffolds for small molecule libraries
    • Pharmacologically relevant heterocycles
    • Ligands for asymmetric catalysis in industrial processes
    Free Quote

    Competitive 4'-Bromo-3'-Nitroacetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding 4'-Bromo-3'-Nitroacetophenone: Practical Insights from the Manufacturer

    Direct Experience with 4'-Bromo-3'-Nitroacetophenone

    Working every day in our reactors and labs, we've learned that making pure and consistent 4'-Bromo-3'-Nitroacetophenone (also identified by its CAS number for those who need quick cross-references) demands a careful hand and reliable controls. We don’t just read datasheets—we have seen how trace impurities or less thoughtful process choices can affect an entire production lot, sending productivity off-track for our partners who count on us for each delivery. Every batch teaches us something new about quality and handling.

    Our direct production approach means we see both the strengths and challenges this compound brings. It’s not a warehouse leftover or a shipped bottle from a mystery source. What leaves our facility has gone through targeted steps for separation, crystallization, and drying. Having spent years scaling and optimizing these phases, we understand what our customers care about most: batch-to-batch predictability, minimal waste, and safety during storage and use.

    Key Characteristics of Our 4'-Bromo-3'-Nitroacetophenone

    This compound draws interest because of its unique combination of a bromine atom and a nitro group on the acetophenone backbone. That substitution pattern—para bromo and meta nitro—makes for different physical and chemical behavior than similar molecules. Compared to a less substituted acetophenone, we’ve observed that this molecule’s electron-withdrawing groups can tune reactivity, which suits downstream transformations in pharmaceuticals or specialty chemicals. This isn’t theory to us; these details shape the process design and ultimately, how well customers turn our raw material into their finished products.

    Our clients use this material in various synthetic routes, especially for pharmaceutical intermediate development. We’ve seen its value where a specific orientation of functional groups improves selectivity or yield in their next reaction step. For years, research chemists have turned to our offering during scale-ups and pilot runs, reporting better control during aromatic substitutions and coupling reactions compared to less pure imports or generic stocks. Close contact with their bench results has prompted us to refine our washing and filtration steps to meet ever-tightening impurity cutoffs. Those aren’t just marketing claims—we’ve set up our in-process checks with HPLC and NMR to spot trace byproducts before they become a headache for someone else later in the supply chain.

    Model, Form, and Reliable Delivery

    Our product typically comes as a crystalline powder, with color and particle size varying slightly depending on slight lot-to-lot changes in crystallization temperature and solvent choice. We’ve invested years in finding solvents that give a high yield and a stable, low-dust crystal. Instead of pushing every reaction through a “one size fits all” routine, our technical staff routinely adjusts for environmental conditions or raw material shifts, aiming for consistent appearance and easy weighing and transfer. Trying to cut corners on downstream drying or milling only leads to clumping issues and customer complaints, so we go the stubborn route and finish each run with proper screening.

    Handling and packaging have taught us more than any experiment could. We’ve learned to avoid wide-mouth containers to keep ambient humidity at bay, and we always check that seals hold up during longer storage or shipping delays. These decisions come straight from years of customer conversations about sudden clumping during a rainy season or finding an unexpected off-odor after weeks in customs. Every new detail gets pulled into our process tweaks.

    Comparing with Other Aromatic Acetophenones

    A chemist looking for something akin to 4'-Bromo-3'-Nitroacetophenone quickly runs into options like mono-substituted bromoacetophenones or nitroacetophenones, as well as other di-substituted patterns. Our years of bench and plant practice have made the unique character clear. The dual electron-withdrawing groups not only affect how this compound behaves in a given reaction—they also change physical handling. Single nitroacetophenones, for example, often show broader melting points and sometimes handle moisture differently, leading to more variable weighing for the same quantity. On the shelf or in process, our compound remains stable longer, a direct result of its specific substitution pattern.

    Customers diving into coupling reactions or seeking specific aromatic substitutions often report sharper product formation and easier purification using our di-substituted product. Trying to chase the same end product with a mono-substituted intermediate usually means more side products and heavier purification loads, ramping up time and cost. We don’t need a theoretical model to show this—our own workup notes and customer feedback files stack with reports of expedited reaction times and predictable color changes at the bench. We’ve re-optimized reactions together, cutting hours from downstream column chromatography steps.

    Why Details in Preparation Matter

    It’s easy to overlook the production details behind what appears to be a simple powder. Consistent product doesn’t just arise from following a textbook synthesis. Our engineers track every run’s temperature, agitation, and addition rates, and they never assume a shortcut on solvent recovery won’t show up later in solubility or filterability troubles. Over the years, we’ve swapped out pump designs, swapped in better reactor linings to cut down on trace metal contamination, and trained our staff to spot color shifts at the earliest stage. These measures came straight from lost batches and costly redos in the past.

    Failures—sometimes from trying to push for faster cooling, other times from buying slightly cheaper reagents—have taught us that a steady hand matters more than chasing every last penny on the bill of materials. Any chemist who’s had to explain low assay results downstream learns quickly that upstream quality matters. That’s why our QA and production leadership walk the shop floor every week, talking with operators about subtle changes in solid appearance and odor long before a problem shows up in a certificate of analysis.

    Usage in Advanced Chemicals and Pharmaceutical Research

    We’ve supplied 4'-Bromo-3'-Nitroacetophenone into dozens of pilot programs for advanced chemicals and pharmaceutical intermediates. One pattern stands out: researchers use our material as a scaffold for more complex molecules. The reliability of reactivity—thanks to the para and meta substituents—has become a staple for making heterocycles or as a starting point for further functionalization. We often see projects progressing from gram-quantities to multi-kilo campaigns, and our technical team stays ready to tackle scale-up questions.

    Scale-up requires real-world tweaks. Customers have pointed out that changing the grade or moisture content—something easy to overlook—can yield different results on yield and reaction profile. Our experience in tweaking crystallization solvents to reduce carryover, or grinding to avoid dust, pays off directly in consistent pilot and production runs out in the field. If a customer suddenly reports that filterability or color has shifted, we retrace our steps and revise our process to bring things back in line.

    Pharmaceutical projects lean on our ability to flag impurities early. An unplanned by-product can tank a synthetic pathway; we keep a library of batch data, developing an eye for patterns that suggest something might be off based on subtle changes. No high-value intermediate survives carelessness at the source. Experience has shown us the value in redundant QC checks—checking not just the final assay, but also tracking process water, pH, residual solvents, and even shipping conditions.

    Batch Consistency and Repeat Orders

    Repeat customers have made clear that consistency matters more than heroic one-time purity. Our regular production of 4'-Bromo-3'-Nitroacetophenone gives us experience in tracking not just the big-picture specs, but also those finer grains—unexpected color shifts, micro traces of related impurities, or changes in bulk density with subtle batch-to-batch variations. Failing to record or respond to these minor differences can lead to serious headaches for anyone running long syntheses or planning regulatory filings.

    We have spent years refining our in-process controls to catch potential drifts. Powder flow, solubility, and even taste (described mainly for safety) serve as practical batch identifiers. Customer feedback has shaped our protocols: if a material looks, pours, or smells even slightly off, we lock down the batch until we identify the source.

    Direct Support and Feedback Loop

    Our relationship with research labs and production teams brings a steady stream of direct feedback. Many requests for alternate particle sizes, different packaging styles (such as smaller bottles or lined drums for moisture resistance), and expedited analyses have prompted us to adapt in ways that remote suppliers often miss. We share spectral data and batch records openly, inviting critical review and third-party confirmation when needed.

    Few things matter more than fast, open communication on product behavior in the field. Our approach encourages customers to call or message with unexpected results—be it a new reaction outcome or a physical change in the solid—so we can trace each concern to process or storage parameters. Many of our process improvements began from these calls.

    Environmental and Safety Considerations

    Years working directly with substances like 4'-Bromo-3'-Nitroacetophenone have made environmental controls second nature to us—not as marketing tools, but as essentials for long-term stability and good neighbor practices. We routinely monitor effluents and air releases, keeping halogen and nitroaromatic loss well within strict internal limits. We recycle solvents wherever technical feasibility allows without risk to batch purity, a shift that took years of small, steady investment.

    Anyone who’s actually handled this compound in kilo-scale reactors knows the challenges with dust and occasional odor associated with brominated and nitrated aromatics. We run local ventilation and train all staff on direct handling, keeping safety data front and center. There’s no glossing over the fire, inhalation, and skin contact risks, so our production area stays equipped for quick cleanup, and all new operators pass detailed hands-on training with supervisors. We revise and update SOPs as soon as new incident reports come in—experience continually feeds back into safety.

    Real Solutions to Supply and Quality Challenges

    The global chemical market throws curveballs each year—fluctuating raw material availability, shipping slowdowns, and emerging regulatory expectations. We’ve stayed ahead through direct sourcing for raw bromo and nitro reagents, developing alternate qualified suppliers and maintaining buffer stocks. By handling synthesis, drying, and packaging in-house, we can keep supply flowing consistently even as outside markets shift.

    We have helped customers avoid production shutdowns by supporting rapid batch releases, sharing real-time stock levels, and keeping open lines through every time zone. Many times, our technical staff has worked overnight or through weekends to validate test results and arrange emergency shipments. Experience has taught us the value of over-communicating both progress and problems—waiting until a customer notices a delay only sours the relationship. We’ve built our recommendations for alternate grades or analogs based on both specs and firsthand lab results, not just a brochure or secondary source.

    Industry Advancement and Future Focus

    Our ongoing investment in process improvement, analytical validation, and direct dialogue with research and production chemists has made our 4'-Bromo-3'-Nitroacetophenone a reliable choice for growth fields. We keep current on legislation—tracking hazardous substances protocols and country-by-country requirements—so customers avoid surprises with imports or new application filings.

    As downstream chemistry shifts, we stay alert to new approaches, from greener synthesis to micro-scale pilot batches for emerging therapeutics. We’ve routinely altered plant schedules to run pilot-scale test batches, using customer input to refine our process and keep contaminants low.

    Close contact with researchers, regulatory specialists, and logistics teams ensures our feedback loop runs both ways. This approach keeps our team alert and responsive: we welcome new challenges, troubleshoot by digging deep into root causes, and keep our sights set on both day-to-day performance and long-term, sustainable growth.

    Why Our Manufacturing Ethic Delivers Value

    Over the years, we’ve moved past the idea that product quality is a one-time achievement. It’s a constant process—a steady stream of practical trials, honest feedback, and adaptive improvements driven by real-world results. As a manufacturer, our focus remains on delivering not only a high-purity 4'-Bromo-3'-Nitroacetophenone, but the kind of day-in, day-out reliability that lets our partners innovate, scale, and meet regulatory needs without interruption.

    Direct experience sets our product apart—knowing the process details, fielding every technical call firsthand, and learning from every batch, both the wins and the lessons. Each shipment reflects the combined knowledge and commitment of a team that expects problems to arise, tackles them before they leave the building, and stands ready to support users long after delivery. We believe this grounded, focused ethic delivers lasting value to every research and production partner relying on our 4'-Bromo-3'-Nitroacetophenone.