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HS Code |
961336 |
| Product Name | m-Bromoanisole |
| IUPAC Name | 1-bromo-3-methoxybenzene |
| CAS Number | 2398-37-0 |
| Molecular Formula | C7H7BrO |
| Molecular Weight | 187.04 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 217-219 °C |
| Melting Point | -11 °C |
| Density | 1.482 g/cm³ at 25°C |
| Refractive Index | 1.556 |
| Solubility in Water | Insoluble |
| Flash Point | 93 °C (closed cup) |
| SMILES | COc1cccc(Br)c1 |
As an accredited m-Bromoanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure screw cap, labeled "m-Bromoanisole, 99%," including hazard and safety information. |
| Shipping | m-Bromoanisole is shipped in tightly sealed containers, protected from light and moisture, and labeled with appropriate hazard warnings. During transport, it must comply with applicable regulations for hazardous chemicals, including UN 2810 (Toxic Liquid, Organic, N.O.S.), ensuring secure handling to prevent leaks, contamination, or exposure. |
| Storage | m-Bromoanisole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Proper chemical storage cabinets, ideally flameproof and labeled, are recommended to prevent accidental exposure or spillage. Always follow local regulations for hazardous chemical storage. |
Applications of m-Bromoanisole in Industrial ManufacturingAs a direct manufacturer of m-Bromoanisole, we serve a wide range of specialized downstream sectors, each requiring precise formulation, compliance, and integration into their established production workflows. Here, we detail key industrial applications, addressing real-world standards, established proportions in actual plant practice, specific process entry points, and the resulting downstream products. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers frequently use m-Bromoanisole as a crucial building block during the synthesis of advanced intermediates for active pharmaceutical ingredients (APIs), particularly in the preparation of compounds where an anisole moiety is required within the target molecule. Its reactivity under palladium-catalyzed coupling reactions and other halogen exchange processes enables the introduction of functional groups essential for antihypertensive, anti-inflammatory, and antitumor drugs. Handling and processing must adhere to strict regulations regarding trace impurities and batch traceability. The chemical enters synthesis workflow during the early or mid-stage formation of intermediates, necessitating tight control of impurities, especially in GMP environments. Final downstream manufacturing yields small molecule APIs, typically as bulk pharmaceuticals or preformulation concentrates for further tableting or encapsulation. Industry compliance standards
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2. Agrochemical Active Ingredient Manufacturingm-Bromoanisole provides a core aromatic structure for the production of certain herbicide and fungicide actives, where its substitution profile allows targeted derivatization. Agrochemical plants employ it as a substrate for Suzuki coupling or nucleophilic aromatic substitution to introduce functional groups that enhance crop protection properties. Formulators monitor incoming lot quality closely per local and international agrochemical substance regulations, especially considering residual halogenated aromatic content. The substance typically enters during the chlorination, alkoxylation, or direct coupling reaction stage in synthesis trains. The output comprises technical-grade crop protection actives, which are later formulated into EC, SC, or WG pesticide products. Industry compliance standards
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3. Liquid Crystal Monomer Production for Display PanelsElectronic chemical fabrication sites utilize m-Bromoanisole as a monomer precursor in the design of liquid crystal materials, specifically for advanced display technologies such as TFT-LCD and OLED panels. The anisole ring offers high thermal stability and specific electron distribution, important for the orientation and response properties of the final display materials. The compound is introduced early in the chemical synthesis of specialty liquid crystal molecules, frequently via Suzuki or Kumada cross-coupling for constructing biphenyl or polyphenylene structures. Manufacturers monitor raw material supply under the criteria set out for ultra-high purity, low metal content, and exclusion of ionic impurities, as electronic applications demand minimum lot-to-lot variability. Output is typically high-value liquid crystal monomers processed further into display fluids after blending and purification. Industry compliance standards
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4. Fragrance and Aroma Chemical SynthesisIn the aroma chemical field, m-Bromoanisole functions as a synthetic precursor for specific anisole-derived fragrances and flavor agents, especially for products requiring heat or UV stability. Flavor and fragrance producers employ it for controlled ring substitution, introducing alkoxy or oxygenated groups via strict catalytic processes. The raw material entry point comes during the selective bromination and subsequent etherification, where aromatic profile development is essential for final quality. Manufacturing facilities must meet IFRA-compliant production and maintain purity standards to avoid off-odors or unintended side products. Output encompasses concentrated aroma intermediates, further blended for personal care, detergents, and food flavorings. Industry compliance standards
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5. Specialty Polymer and Resin ModifierIn advanced materials manufacturing, m-Bromoanisole acts as a functional modifier during resin synthesis and specialty polymer production, such as engineering plastics and heat-resistant resins. The presence of both bromine and methoxy groups provides flexibility for later chemical transformation, facilitating the manufacture of polymers with enhanced flame retardance, dielectric properties, or UV stability. Producers integrate it at the co-monomer addition or chain extension phase, demanding exacting process control, especially where electrical or structural performance is critical. Regulatory and technical protocols ensure resin systems are fit for end-use in electronics, automotive, and high-performance coatings, with traceability and lot certification required for most applications. End products include custom-engineered resins, frequently compounded or blended in customer-specific masterbatches or formulations. Industry compliance standards
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Years spent in the lab and on the production floor have taught us to value molecules that handle repeat work with precision. m-Bromoanisole stands out among aromatic bromides for its adaptability in synthesis and its consistent track record when refining intermediates. Our company produces m-Bromoanisole in bulk, following a carefully developed route that keeps quality high and impurities low for demanding downstream chemistry.
Manufacturers ask for m-Bromoanisole because it is a trusted choice in several industries. Its molecular formula, C7H7BrO, may look simple, but the subtle difference the methoxy group at the meta-position brings often enables cleaner transformations. Many find it essential for synthesizing fine chemicals, flavoring agents, and advanced pharmaceutical intermediates. As with every batch leaving our reactors, we confirm purity using GC methods and NMR, not just sticking to paperwork but putting our analytical team’s assumptions to the test.
Chemists sometimes conflate all bromoanisole isomers as interchangeable. That never works well in practice. The meta-substitution in m-Bromoanisole means the positioning of the bromine relative to the methoxy group distinctly shifts the electron density of the aromatic ring. This affects reactivity in cross-coupling and halogen-metal exchange. In Suzuki or Stille reactions, for instance, the meta isomer can behave differently compared to ortho or para analogues. The side products formed are often cleaner, and yields may tip higher, especially when careful temperature control mitigates side reactions seen with other isomers.
As a manufacturer, we often handle all three positions: ortho (2-Bromoanisole), meta (3-Bromoanisole), and para (4-Bromoanisole). Yet it’s the meta isomer that sees repeat orders from teams scaling complex molecule syntheses. Its reactivity profile gives a smoother route when introducing other substituents after the initial coupling step. We document feedback from chemists who need reproducible results—fluctuating outcomes with other isomers can throw off entire campaign schedules. Our records show a lower complaint rate and higher repeat order volume for m-Bromoanisole compared to its family, and that says more than a sales sheet.
Researchers and process chemists often rely on m-Bromoanisole at the convergence point of small molecule design, fragrance chemistry, and drug discovery. Every kilogram we ship enters a project where reliability in structure and function matters. The molecule acts as a pivotal intermediate in the creation of dye precursors, specialty polymers, and agrochemical actives. In one recent instance, a customer scaled up an insecticide precursor—switching to m-Bromoanisole improved crystallization consistency, saving days in purification.
In pharmaceuticals, m-Bromoanisole’s role emerges in the early steps of complex builds. After hundreds of reactions in our pilot plants and those run by our partners, a clear pattern appears: switching to m-Bromoanisole reduces the number of chromatographic passes during isolation. Less time in column means less solvent waste, a smaller environmental footprint, and a shorter lead time. These improvements browse right past academic theory, reaching practical benefits seen every day in production.
Flavor and fragrance houses also pull for m-Bromoanisole when looking for precursors with a lighter profile. The meta-substitution imparts a subtler note when further processed to anisolic derivatives. Smaller-scale perfumers have commented on reduced impurity carryover, which matters further along during blending, where small off-notes otherwise force backtracking and blending corrections.
Our facilities run mild- to large-scale batches, as most customers commission m-Bromoanisole for projects requiring hundreds of kilograms or more. The material appears as a clear, faintly yellow liquid at room temperature, with a boiling point just above 220°C. We keep water content tightly controlled—privileging dry transfer and sealed drums—because moisture shifts the reaction profiles for our users, fouling catalysts or slowing coupling reactions.
Teams have sometimes underestimated the impact of trace metals and halide byproducts on next-step reactions. Early on, we invested in improved distillation columns and polishes tailored for aryl bromides. Our m-Bromoanisole matches specification targets not just for purity (98.5% minimum by area), but also for color (APHA below 20, to avoid contamination traces in specialty products) and low residue on evaporation. Regular in-process checks and final batch analytics let us assure clients that their solvents and bases won’t stumble over unforeseen contaminants, which can be costly if caught only at a late-stage impurity panel.
Real gains in operational reliability have come from process tweaks learned over years, not just recipe following. During bromination and subsequent methylation, temperature ramps and agitation rates spell the difference between target product and a troublesome byproduct. If stir rates or the addition sequence slip out of range, alternative isomers or overbrominated species creep into the batch—affecting not just quality, but inventory planning, as rejected lots can’t be reprocessed easily.
As manufacturers, we also note subtle differences in how m-Bromoanisole behaves when stored under varying humidity and light. Unlike para isomers that show less tendency for color drift, the meta compound can develop a yellow tinge with UV exposure, hinting at phenolic byproduct trace formation. Protective packaging and rapid turnover help, but so does sharing storage advice directly with clients. One customer flagged a puzzling odorous impurity that traced back to warehouse UV lamps. Tweaking logistics, they solved the mystery and avoided similar issues across other aromatic ethers.
Environmental and regulatory oversight keeps moving higher. Our site audits now range as much for emission controls as they do for product analytics. m-Bromoanisole escapes easy classification in some regions, but our teams have learned to anticipate restrictions on aryl bromides and ether-release thresholds. Installing regenerative thermal oxidizers has trimmed fugitive losses nearly to zero; we also recycle solvents at high efficiency and reclaim side fractions from distillation for use in non-critical blends.
Strict handling protocols reframe the safe use and disposal of aromatic bromides. Worker training focuses on exposure control—ventilated process bays, sealed lines, and regular exposure monitoring. Our safety team monitors short-term and chronic exposure data, well aware that long-term studies on aryl bromides are limited. Offering full transparency to customers about test results and regulatory compliance ensures buyers can trust in origin, purity, and safe handling advice, which is no longer a backend issue but part of responsible sourcing.
Our forward planning draws on feedback from users scaling up production of new pharmaceuticals, agrochemicals, and niche flavors. Price pressures and purity standards continue to sharpen. More clients now request green synthesis routes with catalyst reuse and solvent minimization. We have invested into process intensification, using flow chemistry to keep exotherms in check and reduce residence time. Early results show yields rising, and we expect new process patents to build on the back of molecular work done with m-Bromoanisole as a core intermediate.
Some customers experiment with next-generation coupling techniques—photoredox methods, milder palladium sources, or bio-based ligands. m-Bromoanisole’s stability under varied conditions helps facilitate adaptation to these newer protocols. Our technical support team often shares application notes and process war stories, helping clients shift from legacy batch reactions to more efficient, cleaner modern steps. End users now frequently invite us for troubleshooting during early development phases, recognizing that tweaks in intermediate quality have an outsized impact on downstream yield and regulatory alignment.
Being the actual manufacturer, we log every drum and batch at every transfer point—scratching out errors at the source instead of letting cumulative mistakes cost everyone later. Finished batch certificates detail every analytic: GC profiles, impurity peaks, water content by Karl Fischer, and color index. We keep back samples for up to five years, enabling root-cause analysis if clients ever flag out-of-trend results. This focus on traceability reassures buyers that their supply will not miss critical documentation, a requirement that auditors increasingly watch for.
Our customers often pass regulatory scrutiny for imported intermediates, especially for active pharmaceutical use, and traceability across the line shortens batch release time. Each kilogram produced crosses multiple checkpoints, not just for quality but for compliance with evolving international norms, such as European REACH or US TSCA. Our digital tracking system, paired with actual hands-on inspections, matches every unit with source documentation. This reliability lets our clients meet rising due diligence expectations laid out by regulators and end buyers.
Every longtime manufacturing customer shapes our standards. The questions they ask prod us into new QA methods, hybrid production schedules, and supply chain reconfiguration. Firms looking to scale a new agrochemical sometimes find their trial batches behave oddly with bromoanisole sourced elsewhere but stabilize quickly with our m-isomer. In some cases, fine-tuning the reactor charge or adapting the order of addition—lessons earned batch by batch—has helped teams avoid late-stage scrapping of material.
Direct feedback from manufacturing partners pushes us to look for greener, safer alternatives to legacy reagents. Together we’ve run pilots using milder solvents and lower temperature regimes, preserving product quality without causing drift in yield or purity. A recent run for a pharmaceutical client replaced legacy chlorinated solvents with dimethyl carbonate, an outcome few predicted a decade back. m-Bromoanisole’s performance in that setting reminded us how manufacturing innovation often travels in step with customer trust and willingness to pilot newer routes.
Bulk users know that subtle details in shipping and storage can make the difference between a reliable intermediate and a bottleneck. Our drums leave the factory sealed under nitrogen, and we time shipments to reduce transfer steps, because even minor contamination or delays can prompt hydrolysis or color drift. Partnering with specialty haulers with experience in handling temperature-sensitive aromatic bromides prevents incident reports; onsite checks ensure product arrives in specification, regardless of distance or season.
On request, we provide full documentation, not just product analysis but summaries of method development and root-cause reports for any deviation. Open communication has become a baseline expectation, especially as more of our clients integrate m-Bromoanisole into high-value supply chains. Any product recall or late-stage production hitch for our clients could ripple through global lines, highlighting the importance of consistency, support, and shared accountability.
Through years of producing m-Bromoanisole at scale, we have seen how every choice—from raw material sourcing, process setup, to supply chain partnership—impacts the performance of downstream products. As regulatory and market standards tighten, reliable chemistry paired with full transparency allows both us and our clients to focus on value creation rather than troubleshooting. m-Bromoanisole’s unique reactivity and stability, paired with rigorous manufacturing discipline, have kept it a mainstay in countless laboratory and industrial campaigns. With ongoing investment in greener routes and smarter quality controls, we expect its value in synthesis to expand further, bringing cleaner reactions, better yields, and safer workplaces for years ahead.