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HS Code |
236861 |
| Product Name | 2-Bromo-5-Methoxybenzoic Acid |
| Cas Number | 40305-12-8 |
| Molecular Formula | C8H7BrO3 |
| Molecular Weight | 231.05 |
| Appearance | White to off-white solid |
| Melting Point | 157-160°C |
| Boiling Point | No data available (decomposes) |
| Purity | Typically ≥98% |
| Solubility In Water | Slightly soluble |
| Storage Condition | Store at room temperature, keep container tightly closed |
| Smiles | COC1=CC(=C(C=C1)Br)C(=O)O |
| Inchi | InChI=1S/C8H7BrO3/c1-12-6-3-2-5(8(10)11)4-7(6)9/h2-4H,1H3,(H,10,11) |
| Synonyms | 2-Bromo-5-methoxybenzenecarboxylic acid |
| Density | No data available |
| Refractive Index | No data available |
As an accredited 2-Bromo-5-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle with a secure screw cap and detailed labeling, including safety information. |
| Shipping | 2-Bromo-5-Methoxybenzoic Acid is securely packaged in sealed, chemical-resistant containers to prevent leaks or contamination. It is shipped in compliance with relevant hazardous material regulations, including appropriate labeling and documentation. Transport is typically via ground or air freight, depending on destination, ensuring safe and timely delivery to authorized recipients. |
| Storage | 2-Bromo-5-Methoxybenzoic Acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong acids, bases, or oxidizing agents. Avoid moisture and excessive heat. Proper labeling and secure shelving are essential to prevent accidental spills and ensure safe long-term storage. Always follow local safety regulations. |
Applications of 2-Bromo-5-Methoxybenzoic Acid in Industrial ManufacturingAs a specialized manufacturer, we supply 2-Bromo-5-Methoxybenzoic Acid primarily for use in high-value fine chemical synthesis. Our material serves as a key building block in several advanced industrial processes, notably in pharmaceutical intermediates, agrochemical intermediates, specialty dyes and pigments, and electronic chemical materials. Below, we outline major real-world application routes that integrate our product into downstream industrial manufacturing. 1. Pharmaceutical Intermediate for Antihypertensive Sartan SynthesisPharmaceutical manufacturers incorporate our product as a critical starting reagent for the synthesis of specific antihypertensive drugs in the sartan class, such as Olmesartan medoxomil and Azilsartan medoxomil. During multi-step organic synthesis, our high-purity material is subjected to controlled halogen-metal exchange and subsequent coupling, ensuring batch consistency and compliance with stringent regulatory requirements in active pharmaceutical ingredient (API) production. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide EngineeringThe agrochemical sector utilizes our compound for the targeted synthesis of molecular fragments in new-generation selective herbicides. During scale-up manufacturing, downstream blenders rely on our precise specification control, particularly for aromatic substitution reactions that shape the bioactivity of the final active ingredient in weed control products. Industry compliance standards
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3. Precursor in Specialty Dyes & Pigments ManufacturingManufacturers of high-performance organics pigments and specialty dyes use this ingredient as a functionalized intermediate in synthesis routes where control over aromatic bromination and methoxy protection is critical. In dye chemistry, the controlled incorporation of our material enables fine-tuning of chromophore structure, leading to improved tinting strength and chemical fastness for demanding industrial coloration applications. Industry compliance standards
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4. Functional Material in Electronic ChemicalsOur material finds application among manufacturers of organic electronic and optoelectronic functional materials, where its electron-donating methoxy and bromine functional groups play a role in the construction of advanced conjugated molecules. Process engineers utilize controlled grades of the acid to introduce specific halogenated aromatic units into molecules for organic semiconductors and advanced display components, where electrical and thermal stability is paramount. Industry compliance standards
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Competitive 2-Bromo-5-Methoxybenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
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As a direct manufacturer with over twenty years of dedication to benzoic acid derivatives, I’ve learned that consistency in chemical behavior shapes the future results for our clients. 2-Bromo-5-Methoxybenzoic Acid, known by its CAS number 28965-14-6, serves as a cornerstone in the portfolio of building blocks favored by researchers and synthesis specialists. This compound emerges from the growing need for functionalized intermediates with precise reactivity patterns. Plants such as ours are not simply reacting starting materials—we design each batch to reach a reproducible purity and to deliver reliable performance, batch after batch.
Our process produces 2-Bromo-5-Methoxybenzoic Acid as a white to off-white crystalline powder, with an HPLC assay consistently at or above 98%. We set the melting point between 151°C and 154°C. Impurities in trace amounts get flagged and eliminated before packing. I can point to specific instances in process control where slight over-bromination or incomplete methylation caused out-of-spec products elsewhere in the industry, so we take additional measures in each quality check. Every kilogram released passes through checks for moisture content, heavy metals, and residual solvents. Our routine goes beyond lab jogging—we run pilot batches to ensure that bulk scale reflects our small-scale analytics.
Storage can sound like a dull topic, yet mistakes here spell trouble in a chemical warehouse. We rely on airtight, light-resistant drums to keep every batch stable. Even in damp monsoon seasons, we confirm the absence of caking. Each lot comes with an in-house testing report that details crystal form, particle size, and organic purity—results you can trust whether you’re using this substance in pilot or production lines.
Chemists in pharmaceutical, agrochemical, and specialty chemical labs lean on 2-Bromo-5-Methoxybenzoic Acid for coupling reactions and cross-coupling applications, especially in Suzuki and Buchwald-Hartwig routes. The bromine at position 2 makes this compound a favorite for selective reactivity—not only for its predictability in halogen substitution, but also for its leaving group properties in forming carbon-carbon or carbon-nitrogen bonds. In-house, we have collaborated on scale-ups aiming for next-generation fungicides and kinase inhibitors. In these pathways, the methoxy moiety at the 5-position acts as a stability enhancer under tough reaction conditions. Downstream users have remarked to us that the predictable reactivity of this compound saves weeks in R&D versus similar isomers. In use, even a minute difference in substituent positions can create hurdles; here, our product’s structure keeps pathways open for targeted syntheses.
Years ago, specialty chemical buyers struggled with batch variability and unclear impurity profiles from intermediates bought through fragmented channels. Sourcing directly from our plant, customers get more than material on paper: our commitment to sourcing high-purity raw materials, maintaining reactant stoichiometry within strict windows, and providing full IR and NMR traceability means you always start with a foundation of reliability. Our feedback loop with customers doesn’t stop at the dock—we stay in contact through the full production stream, whether resolving scale-up bottlenecks or fine-tuning crystalline form for formulation compatibility.
Feedback loops sharpen our product. For instance, in a recent feedback cycle from a pharmaceutical partner, our QC pinpointed a minor retention time impurity, traced it to a rare batch of methylating agent, and corrected future lots before dispatch. This closes the gap between bench chemistry and bench-top quality, so you lose less material in purification steps and avoid unwelcome surprises during process optimization.
Working hands-on with reaction optimization, I’ve seen where generic bromo-methoxybenzoic acids go off-script. Isomers such as 4-bromo-3-methoxybenzoic acid or 4-bromo-2-methoxybenzoic acid diverge in reactivity due to positional effects. The difference goes beyond a CAS number—downstream transformations (such as amidations or biaryl couplings) respond differently to steric and electronic influences on the ring. Our 2-Bromo-5-Methoxybenzoic Acid offers a methyl ether at position 5, which helps reduce side reactions in nucleophilic substitution or Pd-catalyzed couplings. The bromine at position 2 prevents over-coupling or branching seen with meta-substituted analogues. Clients told us of failed library syntheses due to vendor-mixed isomers; we respond by tightly controlling positional purity, confirmed by both 1H and 13C NMR, alongside HPLC and MS scans.
Chemicals trace their journey from benzene and toluene derivatives through each reaction, isolation, and purification step—each with challenges that only hands-on process chemists really appreciate. We begin with pharmaceutical-grade salicylic acid, protecting the carboxyl group before introducing the methoxy and bromo-substituents through selective halogenation and methylation steps. We use clean, controlled crystallization to limit inclusion of reaction byproducts—solvent residues, inorganic salts, and over-reacted products are all tracked for removal through each stage.
After handling thousands of kilograms yearly, we know well how moisture and oxygen exposure degrade product over storage months. Our process features triple nitrogen blanketing, in-line moisture detectors, and vacuum-sealed packaging, to cut down degradation. Long experience tells me customer complaints often arise from products stored in less-controlled environments or shipped via generic containers—these shortcuts don’t belong in a serious synthesis operation. Direct dispatch enables full accountability, and each shipment leaves with samples archived for traceability.
We don’t walk away after a truck leaves our gate. Trouble sometimes starts with a change in solvent for a pilot run, or with a modification in protocol on the user end. Our in-house technical team fields requests for process optimization, providing analytical data and guidance on expected side products under various reaction conditions, saving downstream users both labor and material. Whether developing a new library for medicinal chemistry or shifting a process from gram to ton scale, we stand ready to share not just our product, but our hard-won expertise.
Plenty of distributors promise a product; few can answer for it with process notes and off-spec troubleshooting. As a manufacturer, we’ve seen patterns emerge: less-resourced suppliers cut costs by running lower purity methyl iodide for methylation, introducing trace contaminants that disrupt downstream reactions. We rely on high-purity methylation agents and in-process testing at every step. Chloride and sulfate traces, common culprits in failed couplings, get reduced through repeated washing and vacuum drying. In contrast to off-the-shelf offerings from trading houses, every batch gets fingerprinted by FTIR, 1H NMR, and LC-MS, so surprises stay out of the customer’s flask.
We’ve tuned our process to keep byproducts out of the way—not just for the main product, but for any potential derivatives formed in subsequent reactions. Chemists working on active pharmaceutical ingredients, crop protection molecules, or material science building blocks cannot afford time lost in re-purification or ambiguous analytical results. As process engineers, we see the real cost of “low price, high impurity” chemicals, paid for in wasted solvent, lost process time, or even batch rejection at the QC stage. Reputable end-users value documentation, origin transparency, and technical backup—in a crowded marketplace, this is the clearest difference we bring by standing behind our molecules.
Safety officers and plant engineers often bring up chemical hazards in intermediate production. We pay close attention to industrial hygiene throughout every batch. Application of closed-system halogenation, local extraction around reaction vessels, and solvent recovery in methylation steps help to protect workers and reduce environmental impact. Our history reflects a record of clean audits, driven by in-house lab work showing trace residual bromine and volatile organics well below regulated thresholds. We also design our manufacturing lines for minimal solvent waste, running distillation and recycling wherever possible. Disposal of spent mother liquors runs through an authorized waste partner, with regular sampling to meet compliance targets.
Manufacturing intermediates like 2-Bromo-5-Methoxybenzoic Acid brings responsibilities that reach far beyond the factory fence. Near-miss incidents drive facility upgrades. We participate actively in staff training, on-site monitoring, and documentation for every process variable. Community and regulatory transparency matter—a history of openness with local agencies, periodic stack sampling, and emergency response planning safeguard both our workers and our neighborhood. Years of incident-free operations come from this foundation, not luck or happenstance.
New trends and regulations—whether in occupational safety, product registration, or import customs—keep evolving, and staying ahead means maintaining lines of communication with our clients. Researchers often face changing requirements for trace impurities or documentation credentials as part of their drug master files or agricultural registration packages. We respond by keeping analytical archives and updated method validation folders accessible to customers, not hidden behind bureaucracy.
Some of our clients run tight project deadlines, with pressing needs for batch-specific documentation. Since the pandemic years, requests for digital records, video batch reports, and flexible shipment sizes have ticked upwards. We accommodate these challenges, running custom reaction scales and accelerated testing protocols to meet compressed timelines. At the same time, we work in the background to anticipate changes in global substance lists, ensuring our product satisfies both present and emerging requirements.
Supply chain interruptions have shown that buying from anonymous distributors adds risk to business. A few years back, customs policy shifts stranded dozens of shipments of benzoic acid intermediates at port because of missing certificates from origin manufacturers. Our clients who sourced directly from us avoided week-long disruptions thanks to pre-arranged documentation and verification archives available on demand. Direct lines of communication allow us to identify and fix problems before they grow, often intervening mid-shipment or with customs brokers when needed.
The global trend towards sustainable, traceable chemistry places extra scrutiny on upstream raw materials and environmental records. Our sourcing policies for all key reagents—including salicylic acid, methyl iodide, and bromine—center on documented, sustainable suppliers. Our internal guidelines exclude sources that repeatedly fail to meet standards, because we see too clearly the cost of cutting corners. Quality and compliance reflect day-to-day decisions made by production staff, procurement officers, and technical teams—all working together, not apart.
Many users ask why not substitute with a structurally similar product in their synthesis. Synthetic planning depends on more than a name or a functional group. For example, 2-Bromo-5-Methoxybenzoic Acid resists over-reactive decomposition in typical Suzuki couplings, standing up to harsh bases or ligands that might crack open a less protected ring. Its solubility profile supports efficient uptake in coupling or amidation steps, limiting losses during work-up stages. Alternates like 4-bromo-2-methoxybenzoic acid tend to drift into competitive couplings or hydrolysis under similar conditions, a real issue for scale-up chemists pacing plant equipment for throughput and reliability.
I remember a project where our client switched mid-stream to an alternative isomer sourced through a trader, to save cost. The result—a cascade of side reactions, reduced yield, followed by a week of purification headaches and process revalidation. The feedback cycle between process chemists on our floor and customer R&D redirected the project, restoring both schedule and confidence. Steps like these don’t appear in data sheets, but they build relationships and raise downstream value. Structure matters, not only on paper, but in the lived outcomes of real projects.
Our feedback system covers more than complaints—it ranges from requests for larger drum packaging, specialty labeling for cold-chain transit, to questions about alternative solvents or filtration recommendations. One recurring story: a customer running 2-Bromo-5-Methoxybenzoic Acid into an amide coupling needed to cut down filtration time. Our technical team shared best practices for pre-wetting filters, tweaking solvent polarity, and using activated carbon steps developed over many batches. With feedback, we continually improve our handling guidelines, based on firsthand operational experience, rather than just literature sources.
Over the years, synthesis teams working with us became accustomed to getting answers within hours, not days. We see follow-up requests whenever a process runs into unexpected haze, discoloration, or incomplete reaction. In every case, a dedicated technical contact closes the gap quickly, checking both our lot data and reaction variables with the end user, not pushing a generic solution. We measure our value not by product volume, but by reduction in reactive troubleshooting on the user side.
Our approach grows out of real-world experience, not committee-driven standards. The handoff from plant to bench means more than ticking off a list of moieties and melting points. Here, it’s a question of trust built up over deliveries, emergency shipments, process hiccups, and the shared ambition to make better molecules, faster. 2-Bromo-5-Methoxybenzoic Acid remains one of our most referenced intermediates, not because it’s trendy, but because its behavior lets researchers drive projects forward without slowdowns. Controlled environments, reliable analytics, and a refusal to paper over problems place our offering apart from generic intermediates purchased on a price sheet.
Decades of manufacturing and collaboration have shaped every kilogram that leaves our operation. Teams from research, process engineering, QC, regulatory, and logistics talk over every improvement, challenge, or anomaly until the story adds up. Every delivered batch reflects direct experience—not just a series of numbers on a COA, but the accumulation of solution-focused work. For chemists and innovators counting on 2-Bromo-5-Methoxybenzoic Acid, that’s the real source of confidence—chemistry informed by expertise, transparency, and a long view of performance in the field.