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HS Code |
854251 |
| Product Name | 2-Bromo-4'-Methoxyacetophenone |
| Cas Number | 92871-48-0 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 63-65°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Density | 1.53 g/cm³ (approximate) |
| Smiles | COC1=CC=C(C=C1)C(=O)CCBr |
| Inchi | InChI=1S/C9H9BrO2/c1-12-8-3-2-6(4-7(8)5-10)9(11)5-7/h2-4H,5H2,1H3 |
| Storage Conditions | Store at room temperature, protect from light and moisture |
As an accredited 2-Bromo-4'-Methoxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-4'-Methoxyacetophenone, sealed with a screw cap and labeled with hazard warnings. |
| Shipping | 2-Bromo-4'-Methoxyacetophenone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and must be transported according to applicable regulations, typically via ground or air freight. Appropriate documentation and labeling are required to ensure safe handling and compliance during transit. |
| Storage | Store 2-Bromo-4'-Methoxyacetophenone in a cool, dry, and well-ventilated area, away from heat and ignition sources. Keep the container tightly closed and protected from direct sunlight and moisture. Store separately from incompatible substances such as strong oxidizing agents. Use with appropriate ventilation and avoid prolonged exposure. Ensure proper chemical labeling and restrict access to authorized personnel. |
Applications of 2-Bromo-4'-Methoxyacetophenone in Industrial Manufacturing2-Bromo-4'-Methoxyacetophenone serves as a crucial intermediate in advanced organic synthesis across several specialized manufacturing segments. Its chemical properties support the creation of high-value downstream molecules with stringent process and regulatory demands, especially where halogenated acetophenones are required. As a direct manufacturer, we address the distinct needs of each industrial route by supplying consistently pure material and supporting customer formulation integration. 1. Pharmaceutical Intermediate Synthesis (API Building Blocks)In pharmaceutical manufacturing, this compound enters as a halogenated acetophenone unit to construct advanced intermediates for active pharmaceutical ingredient (API) synthesis, particularly in creating molecules with specific aromatic substitution patterns. Production teams often value its contribution to regioselective reactions during multistep synthesis for anti-inflammatory agents or CNS drugs. Its controlled reactivity aids in minimizing byproduct formation and maintaining pharmaceutical grade compliance throughout regulated environments. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide and Fungicide SynthesisAgrochemical producers employ this compound to form core structures of selective herbicides and fungicides. Its reactivity with azoles or triazines makes it indispensable for crafting target compounds that demand precise aromatic substitution patterns. Production units utilize it where high bromine selectivity under moderate conditions is essential for maintaining downstream product purity, while raw material traceability must align with agro sector requirements. Industry compliance standards
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3. Fine Chemicals for UV Absorber Additive ProductionManufacturers of UV absorber additives use this compound to assemble benzophenone or benzotriazole derivatives, supporting the protection of polymers and coatings against photodegradation. Its structure enables precise placement of bromine on the aromatic core, significantly impacting downstream additive efficiency and stability. Production lines require tight process controls to integrate this material at the precursor stage of high-purity UV absorber synthesis for plastics, paints, or fiber applications. Industry compliance standards
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4. Specialty Dye and Pigment Intermediate SynthesisProducers in the specialty dye and pigment industry depend on this material for constructing methoxy- and bromine-substituted aromatic frameworks, supporting colorant molecules that demand high photostability and color intensity. During pigment synthesis, its bromine and methoxy functionalities permit tailored spectral properties, while downstream integration requires precise addition timing to achieve uniform chromophore formation and to meet color matching specifications for textile or coating end-uses. Industry compliance standards
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2-Bromo-4'-Methoxyacetophenone stands out as a reliable building block for pharmaceutical, agrochemical, and specialty chemical synthesis. We produce this fine chemical on-site in our own facilities, drawing on extensive experience with halogenated acetophenones and related compounds. Our model for this intermediate follows a refined synthesis route ensuring consistent purity and batch-to-batch continuity. The molecule’s structure, with a bromine atom at the ortho position and a methoxy group on the para position relative to the carbonyl, gives it a specific reactivity profile not easily mimicked by other substituted acetophenones. Chemists value the unique balance of electron-withdrawing and electron-donating groups, which shapes downstream transformations and coupling reactions.
Our experience with this compound reaches back over a decade. As manufacturers who run kilo- to ton-scale batches, we have followed the ways this molecule gets chosen for advanced synthesis, especially in medicinal chemistry projects searching for new active pharmaceutical ingredients. The bromine substituent on the aromatic ring assists with selective cross-coupling or further derivatization, often with robust yields when standard protocols fail for other aromatic halides. The methoxy group on the para position brings electronic tuning, which can enhance or redirect selectivity in subsequent transformations, setting it apart from unsubstituted 2-bromoacetophenone.
Many clients originally ask for plain 2-bromoacetophenone but switch to our 4’-methoxy substituted version after testing routes that require fine-tuning electronic effects. The changes in solubility and crystallization behavior, brought about by the methoxy group, help technicians and researchers purify and isolate intermediates with fewer side products. When used in applications targeting large, functionalized molecules, failure to select the right aromatic substitution sometimes results in diminished yields or laborious downstream purifications. Our technical support frequently helps customers switch to the 4’-methoxy product when other bromoacetophenones fail to perform.
In the modern chemical industry, consistency means as much as cost. Our team doesn’t just blend and repackage. We control every step, from the selection of brominating agents to the treatment of mother liquors and recovery of solvents for ecological and economic value. Experience has taught us that chlorinated solvents, while useful, often introduce impurities, so we developed routes that minimize or omit these—slashing both unwanted byproducts and downstream handling risk. Every batch undergoes verification by HPLC, GC-MS, and NMR to ensure the assayed content exceeds stringent benchmarks, reaching purities that fit the most demanding synthesis routes. Fully-characterized material supports documentation needs for process transfer or regulatory submissions, when relevant.
One of the trickier aspects in producing high-purity 2-Bromo-4'-Methoxyacetophenone involves washing out trace isomers and unreacted precursors. These require careful pH control and selective solvent washes. Our process utilizes years of in-plant data to reliably separate off-target bromination byproducts, giving our downstream partners a cleaner starting point for their chemistry. We direct attention to minimizing discoloration or the formation of high-boiling impurities, which can gum up reactors or cause unexpected test results. What looks like a fine white powder in the jar often hides these hidden headaches. We design our workflow with these practical realities in mind, because we handle and process the same intermediates ourselves.
2-Bromo-4'-Methoxyacetophenone presents meaningful advantages in applications where electron density on the aromatic ring shapes outcomes in palladium-catalyzed couplings or radical chemistry. Plain 2-bromoacetophenone, lacking the methoxy, generally proves less efficient in Suzuki or Heck reactions, and sometimes fails entirely in routes that require strong push-pull effects. The para-methoxy confers not only higher reactivity for nucleophilic aromatic substitution, but also shifts physical properties in subtle ways—such as a lowered melting point and easier handling in crystallization. Conventionally, 4-bromoacetophenone variants do not provide this balance of properties, so users wanting to streamline multi-step syntheses favor the 2-bromo-4’-methoxy arrangement.
In scaling up, solvent compatibility and phase separation play everyday roles. Products lacking methoxy groups can precipitate rapidly under normal crystallization conditions, sometimes leading to occluded impurities that resist removal. Our methoxy-modified molecule gives a slower, more controlled crystal growth, aiding isolation. For manufacturing teams, this reduces labor and uncertainty around acceptable material for API synthesis. Regular communication with pharmaceutical contract manufacturing partners has taught us that erratic crystallization behavior can threaten an entire project timeline, so these small differences matter out of proportion to their apparent simplicity.
Our 2-Bromo-4'-Methoxyacetophenone often finds its way into synthesis workflows making advanced benzene derivatives, either as coupling precursors, ketone-selective intermediates, or seed molecules for heterocycle formation. The pharmaceutical sector relies on this material as a scaffold for introducing biologically active fragments, especially where selective bromo substitution provides a convenient handle. Developers of agrochemicals and photovoltaic small molecules also source this compound when building up libraries of functionalized aromatics. Custom synthesis routes routinely require hundreds of grams to multiple kilograms, so we design packaging and documentation to anticipate efficient lab or pilot-plant transfers.
Most process chemists value products that can cut steps or boost clean yield, and 2-Bromo-4'-Methoxyacetophenone regularly exceeds expectations on both fronts. In work with contract research labs, we have seen teams switch from less-substituted acetophenones after suffering through late-stage purification bottlenecks. Even slight impurities in the halide or inconsistency between batches can translate into months of delays for projects under tight regulatory review. Our tight batch reproducibility and traceability give customers the peace of mind they look for when investing in new processes.
Over the years, specialty polymer developers and electronic material manufacturers have also adopted our product for its predictable solubility and compatibility with polar and semi-polar solvents. These features derive from the combined chemical influence of bromo and methoxy groups on the core aromatic structure. Consistency in melting range and particle size distribution, verified in QC, supports automated dosing and blending equipment, saving valuable technician time. When R&D teams push processes toward scale-up, even these practical details shape their choice in supplier.
Unlike those who simply move drums, we monitor reaction progress, troubleshoot bottlenecks, and invest capital in plant upgrades that make critical intermediates more accessible to chemists downstream. Knowledge gained from handling not only this product but also a suite of related aryl ketones helps us anticipate end user requirements, cutoff points for impurity control, and the subtle factors that affect commercial-scale reliability. Internal feedback from our own chemists, who use the product in developmental scouting and scale-up, reach the production floor directly.
2-Bromo-4'-Methoxyacetophenone never exists in a vacuum in our facilities. Our close monitoring of precursor quality, batch tracking, and scheduling minimizes cross-contamination. We established a single-stream workflow for managing raw materials and effluent, reducing both costs and environmental load. Customers tell us this approach translates into easier documentation at the point of use. We produce the product in continuous and batch modes, responding to market demand and long-term projects, so lead times rarely slip.
For downstream users pursuing regulated routes, the paperwork often weighs as much as the drums. All product leaves our plant with a complete analytical record, supported by spectra and chromatograms when requested. Our facilities operate under documented quality programs, logging each lot’s critical process points and results. Instead of leaving quality assurance for later, or simply passing reins to resellers, production and QC teams work together before intermediate batches are dispatched. On-site labs validate identity and assay every shipment, using reference material retained from every campaign for comparison and trend analysis.
Special regulatory requirements often insist on impurity profiling, polymorphism checks, and solvent residue analysis. We anticipate these hurdles and upgrade our process documentation accordingly. Several clients have run full synthetic validation for API registration using our 2-Bromo-4'-Methoxyacetophenone, and we readily supply historical records or custom data packages that align with their regulatory frameworks. Experience in international shipment and cross-border compliance supports timely delivery and use, without regulatory snags or documentation gaps. Since we track markets and customer trends, we routinely prepare documentation banks for repeat customers, shortening the turnaround on repeated purchases.
Long-term involvement with aromatic bromination means we have optimized conditions to control both regioselectivity and conversion rates. Our chemists have tested a range of brominating agents, tuning temperature and pH to avoid overbromination or unreacted substrate. By favoring certain solvent systems, we improve isolation of the product and lower the incidence of corrosive byproducts. Continuous improvement cycles address feedback from our own technical trials, so process changes reflect both lab and production-scale realities.
Worker safety and environmental considerations always play large roles in fine chemical production. Over years of handling halogenated aromatic compounds, we developed protocols for ventilation, containment, and waste neutralization. In the earliest days, management of bromine offgas and aqueous waste required significant investment in scrubbing systems and monitoring. Today’s process reflects hard-won lessons from unanticipated pressure excursions or minor leaks; plant operators carry out detailed, regular inspections at every shift change, and safety engineers review product risk assessments based on on-the-ground usage, not theory. These practical safeguards increase not only actual safety but also the comfort level of plant staff who make the product day in, day out.
As original producers, not middlemen, our approach always places application and process reliability at the forefront. Each batch matches the specifications and performance chemists recognize from analytical references, reducing surprises in route scouting. Batch numbers, certificates of analysis, and storage conditions reflect field realities and upcoming project demands. Risk of downtime—either in production or during external audits—gets minimized thanks to digital inventory tracking and robust communication between lab and shipping.
Supply chain resilience earned even more attention in recent years. Periodic supply interruptions of brominating agents or precursor acetophenones made us reinforce relationships with upstream partners, qualifying secondary sources after round-robin validation in our reactors. Our procurement team shares a floor with the technical staff to quickly address any issue—whether an unexpected impurity spike or a packaging dent. Instead of deflecting, we manage such events directly, with transparency and commitment to correction.
Long experience also means advanced warning for users about ideal storage or transport. We recommend storage at agreed-upon temperatures and protection from moisture. Over time, this guidance sharply cut incidents of caking or slow decomposition, saving users both money and frustration. Unlike resellers, our technical team responds with detailed usage advice tailored to intended application, drawn from hands-on trials rather than distant reference.
Veteran chemists in process development remember the frustration of unreliable raw materials. Projects stall, costs rise, and confidence wanes when shipments land with out-of-spec products or paperwork missing key analysis. Our commitment as the original producer of 2-Bromo-4'-Methoxyacetophenone comes from troubleshooting these same problems in our own labs. That’s why beyond the molecule itself, we supply responsive service, open dialogue on technical problems, and willingness to adapt documentation or packaging to project needs. It’s routine for our staff to join joint calls with customers, walking through spectral analyses to resolve ambiguities or troubleshoot reactivity.
Knowledge built up through daily plant operation supports informed problem-solving for customers scaling from vial to drum. Real-world trials and failures feed back into process improvement, not only for this intermediate, but for related compounds produced in-house. Since most of our customers use halogenated acetophenones as part of broader R&D or manufacturing efforts, we frequently troubleshoot application-specific problems together, identifying whether a hiccup lies with the starting material or a downstream transformation.
In the ever-changing landscape of specialty chemicals, robust products from responsible manufacturers matter. We design our production and documentation around actual user needs, informed by years of direct feedback and project participation. Those who choose our 2-Bromo-4'-Methoxyacetophenone gain access to more than just a molecule—they tap into a body of accumulated knowledge, structured documentation, and an experienced team that assists from first inquiry through to repeat project execution.