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HS Code |
342892 |
| Chemical Name | Methyl 2-bromobenzoate |
| Molecular Formula | C8H7BrO2 |
| Molecular Weight | 215.05 g/mol |
| Cas Number | 610-94-6 |
| Appearance | Colorless to pale yellow liquid or solid |
| Boiling Point | 263-265°C |
| Melting Point | 20-24°C |
| Density | 1.54 g/cm3 |
| Refractive Index | 1.570 |
| Smiles | COC(=O)C1=CC=CC=C1Br |
| Pubchem Cid | 11720 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
As an accredited Methyl 2-Bromobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 2-Bromobenzoate (100g) is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | Methyl 2-Bromobenzoate is shipped in tightly sealed containers, protected from light and moisture. It should be handled and transported according to local regulations for hazardous chemicals, typically labeled as harmful or irritant. Shipping must ensure prevention of leaks or spills, with proper documentation and compliance with international chemical transport guidelines. |
| Storage | Methyl 2-Bromobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Ensure proper labeling and keep away from food and drink. Use appropriate personal protective equipment when handling the container to prevent exposure. |
Applications of Methyl 2-Bromobenzoate in Industrial ManufacturingOur methyl 2-bromobenzoate integrates into multiple high-value downstream industries, serving as a functional intermediate with significant utility in complex synthesis routes. The following sections outline its established industrial applications, detailing critical compliance standards, processing practices, and end-use product categories. 1. Pharmaceutical Intermediate SynthesisIn pharmaceutical manufacturing, methyl 2-bromobenzoate is an essential starting material for the synthesis of active pharmaceutical ingredient (API) precursors such as antihypertensive agents and non-steroidal anti-inflammatory drugs. Downstream formulators rely on its controlled halogenation and ester functionality to build structurally complex molecules through targeted coupling reactions. Its purity and traceability are strictly monitored to meet regulatory submission dossiers and audit requirements for human medicinal use. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)Chemical formulators in the crop protection sector utilize methyl 2-bromobenzoate as a specialty aryl building block for synthesizing benzoic acid-derived herbicides and broad-spectrum fungicide actives. The raw material’s reactivity enables efficient ring substitution and molecular coupling, meeting batch yield requirements and impurity thresholds. Batch records and audits focus on the traceability of each synthesis step to maintain agroeconomic and regulatory compliance. Industry compliance standards
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3. Specialty Chemical and Dye ManufacturingSpecialty chemical producers incorporate methyl 2-bromobenzoate as a strategic intermediate in the fabrication of custom aromatic compounds and high-performance dyes. The brominated benzoate structure supports tailoring of optical and physicochemical properties for advanced pigment systems and chromophore modifications. Trace residuals and degradation profiles must comply with colorant purity standards, critical for both industrial and regulatory audits in this sector. Industry compliance standards
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4. Synthesis of Liquid Crystal MaterialsWith growing demand for high-definition displays, liquid crystal manufacturers select methyl 2-bromobenzoate for constructing custom benzoate and cyano-substituted aromatic cores vital to nematic and smectic phase LCD compounds. The synthetic routes require careful handling and rigorous purity control due to the strict optical and electrical specifications of final materials. Manufacturing audit trails and analytical reports must document compliance throughout every conversion step. Industry compliance standards
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5. Fine Chemical Synthesis for Fragrance PrecursorsPerfume and aroma chemical manufacturers use methyl 2-bromobenzoate as an ester moiety source to synthesize select benzoic acid-derived aromatic aldehydes and alcohols. It allows for controlled introduction of fragrance-carrying functional groups, supporting batch-to-batch consistency in complex aroma blends. Trace analysis and allergen screening must meet internal QC as well as industry-wide safety norms for human exposure. Industry compliance standards
Typical usage ratio
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As a manufacturer specializing in fine organic chemicals, we know firsthand how critical purity and reliability are for our clients across industries. Through years on the production line and in quality testing labs, we’ve worked with methyl esters in varied forms. Among these, methyl 2-bromobenzoate has carved out its place for chemists seeking a high-performing intermediate. The feedback we receive from small research outfits, multinational pharma, and specialty material producers tells the story: consistent quality and process efficiency with methyl 2-bromobenzoate makes a marked difference, especially as global quality standards continue to tighten.
At our facility, methyl 2-bromobenzoate often starts as a white to faintly yellow crystalline powder, possessing the typical faint aroma characteristic of methyl esters. Its molecular structure, a straightforward benzoic acid methyl ester substituted with bromine at the ortho position, brings reactivity and selectivity that few analogues can match. The CAS number 606-36-2 links researchers and commercial buyers to a decades-deep literature and regulatory backbone. We routinely prepare this compound at 99% minimum GC purity, with water content tightly controlled below 0.5%, to minimize side-reactions for sensitive syntheses.
Batch-to-batch consistency matters more than most appreciate, and we achieve this by controlling every step of the process—from raw material selection and bromination conditions to careful purification with fractional distillation and crystallization. This deliberate attention reduces the risk of producing off-spec product, which in downstream reactions can mean lost time, wasted reagents, and failed batches.
With experience running hundreds of batches, we see how certain physical properties offer practical advantages. The compound’s melting point (46-49°C) allows safe storage at room temperature and easy handling, neither hygroscopic nor prone to clumping under ordinary conditions. Its solubility profile proves convenient as it dissolves well in typical organic solvents—ethyl acetate, DCM, hexanes—without creating excessive residues or precipitating out during processing. These features support its role as a reliable intermediate for large-scale and laboratory use alike.
We have found that the ortho-bromo substituent brings a unique dimension for synthetic chemists. The bromine atom activates the aromatic ring for further functionalization in a controlled manner, making it more reactive than para or meta analogues for certain cross-coupling reactions. Because of the steric and electronic effects, users report higher selectivity with palladium or copper-catalyzed reactions, such as Suzuki, Stille, or Ullmann couplings, when compared with their experience using unsubstituted methyl benzoate or other halogenated esters.
Feedback from customers continually confirms that methyl 2-bromobenzoate is far more than a generic benzoate ester with a halogen tag. Major demand comes from pharmaceutical and agrochemical projects, especially those pivoting toward diversification via aromatic functionalization. In our experience, methyl 2-bromobenzoate serves as a robust intermediate for synthesizing fine chemicals such as 2-substituted benzoic acids, biaryl derivatives, and benzofused heterocycles.
Several customers engaged in active pharmaceutical ingredient (API) pathways appreciate the clean conversion and high yield achievable from brominated intermediates. For example, its role as a precursor to 2-aminobenzoic acid derivatives or as a starting point for further Grignard or lithium-halogen exchange chemistry has surfaced repeatedly in joint development projects and technical troubleshooting discussions. Agrochemical formulation teams have raised the issue of competing byproducts during halogen exchange, but purity at our benchmark minimizes these concerns and simplifies downstream purification—a difference that’s reflected in their bottom line.
In our plant’s technical meetings, chemists working with biaryl-pyridine syntheses often point to the performance edge offered by methyl 2-bromobenzoate over methyl 2-chlorobenzoate. The bromine's greater reactivity typically allows the use of milder reaction conditions and less forcing catalyst systems, reducing costs for smaller-scale pharmaceutical research and making scaling up smoother when projects head for commercialization. There’s also growing use in specialty polymer projects: our partners in the electronics sector have used methyl 2-bromobenzoate as a monomer precursor for functional polyesters or liquid crystal intermediates, capitalizing on the aromatic rigidity and ortho-position selectivity.
Those new to our sector often ask why a manufacturer would commit resources to methyl 2-bromobenzoate over seemingly similar compounds. Here, direct production experience illustrates several clear distinctions. While methyl benzoate and methyl 2-chlorobenzoate are significant building blocks, the switch to bromination provides a noticeable boost in reactivity. For example, methyl 2-chlorobenzoate requires harsher or more active catalytic conditions in cross-coupling and nucleophilic substitution reactions. This translates to greater energy consumption, longer batch cycles, and sometimes a higher rejection rate due to incomplete conversion or side-products.
We can cite cases where end users shifted their process from methyl 2-chlorobenzoate to methyl 2-bromobenzoate for these reasons, ultimately reporting shorter reaction times and improved yields. Similar feedback applies to the comparison with methyl 2-iodobenzoate: although the iodo variant is even more reactive, it is much less stable, costlier to produce and store, and generally not suited for bulk use due to safety concerns around decomposition. Methyl 2-bromobenzoate balances performance and cost better than either alternative.
Some azeotropic esters, like ethyl or propyl 2-bromobenzoate, remain on the periphery for specialized uses. We have pursued pilot runs and technical trials with these derivatives, but our analysis, supported by customer trials, reveals little benefit over the methyl ester in most large-scale scenarios. The methyl ester’s manageable boiling range, established toxicology profile, and ready availability of feedstock routes anchor its status as the mainstay option for most of our customers.
Raw material handling often separates reliable suppliers from unreliable ones. We source benzoic acid and brominating agents only from trusted global suppliers audited for compliance with environmental and labor standards. Consistent supply contracts mean less downtime, and our in-line monitoring assures us that impurities and byproducts rarely pass initial separations. Our facility routinely analyzes incoming raw bromine for halide and sulfur contaminants, since even parts-per-million differences can ultimately influence the performance of the final ester in sensitive electronic or pharmaceutical applications.
The synthesis workflow at our site features stainless steel reactors capable of precise heat exchange, enabling us to tightly control exothermic bromination. Improvements in reactor design allow uniform temperature and pressure conditions throughout the batch, reducing local hot spots and uneven substitution that can otherwise lead to unreacted starting material or undesired dibromo side-products. We operate solvent recovery and distillation lines that recycle process streams, both for cost efficiency and to limit environmental footprint—key as downstream regulators increasingly expect green chemistry protocols.
Quality control extends beyond in-process checks. Each lot undergoes full characterization using gas chromatography, high-performance liquid chromatography, and proton NMR before being released. In the past, we’ve dealt with products from outside contractors where purity or spectral fingerprints failed to match our standards, so our team cross-references every certificate of analysis against in-house benchmarks. This approach catches problems long before they reach customers and supports the reproducibility on which research teams rely.
Heightened environmental regulation in recent years has reshaped our practices in several ways. Waste minimization always features prominently in our operation reviews. Bromination processes tend to raise concern due to formation of inorganic salts and potential halogenated organic byproducts. Our scrubber systems and waste water treatment protocols address these issues by neutralizing and collecting waste streams for regulated disposal and, where possible, reusing solvents internally.
Our compliance team interacts with agencies globally, staying current on emerging standards around hazardous material handling, emissions, and EHS (environmental, health, and safety) management. Having been directly involved in registration dossiers and technical file preparation for REACH and other international chemical safety programs, we know how importers and end users benefit from documented traceability. Customers in Europe and North America often request detailed impurity profiles, and we supply supporting data readily because we build analytics into every batch campaign. This transparency consistently leads to smoother import/export transactions and fewer holdups at border checks.
Through dialogue with university researchers and R&D heads at large pharma, we see that easy reactivity, high purity, and minimized lot-to-lot variation drive loyalty. Too often, off-spec material from secondary traders leads to failed experiments, delayed process qualification, or loss of regulatory compliance. Sourcing direct from manufacturer means customers get documentation that matches reality, not overlooked or missing impurity data.
Feedback loops with our clients have led to several improvements in recent years, including new packaging options for minimizing moisture uptake during long shipping, optimized delivery schedules supporting just-in-time inventory, and offering smaller pilot-lot shipments for early-phase trials. We train our own shipping staff and partner carriers to handle regulated chemicals in compliance with global transit standards so that users receive their goods unmixed, unadulterated, and within safe exposure limits.
End users value prompt, evidence-based technical support. Our technical staff return calls about synthetic troubleshooting, chromatography quirks, or compatibility with downstream solvents every month. Partnering in this way has shown measurable cost savings for both sides: less material lost, improved project timelines, and stronger project documentation, critical for QA audits or patent filings.
Handling brominated aromatics like methyl 2-bromobenzoate involves certain challenges. While toxicity concerns are moderate compared to many industrial intermediates, exposure precautions—protective gear, closed systems—remain essential at all facility scales to prevent skin and respiratory contact. Controlled ventilation and double-sealed storage drums prevent workplace exposure, and we collaborate with downstream users to improve their local storage, reducing risk of contamination and loss through volatilization.
Many of our medium- and large-sized customers come to us for recommendations on integrating methyl 2-bromobenzoate into scale-up protocols. Reaction exotherms can become significant at larger volumes, and the choice of solvent or catalyst can alter heat transfer and run times dramatically. We share our own process models and batch records with customers under confidentiality, supporting faster technology transfer to new sites or scaling from kilo to metric ton runs. This degree of technical sharing distinguishes a manufacturer from a mere trading agent.
Occasional bottlenecks emerge when users seek to push yields higher by using excess reactants or by reducing catalyst load, sometimes resulting in lower selectivity or unwanted residues. Drawing from our own pilot and production experience, we counsel users to reformulate for trade-offs in throughput versus purity, usually recommending extra in-line purification over simple scale-up. Our investment in pilot plant facilities enables joint development and shared learning, in contrast to bulk producers concerned only with volume and cost.
Recent years have seen growing interest in greener chemistry and renewable resource inputs. Innovation teams within our company are piloting alternative brominating agents derived from less hazardous sources, as well as solvent systems with lower VOC emissions. We maintain close ties with raw material innovators, giving us a head start on emerging trends and positioning us to serve clients committed to sustainable practices. As industry standards shift toward full life-cycle analysis and increasingly stringent EHS reporting, we remain ahead of the curve, both for regulatory compliance and for customer needs.
Global supply chains have gained complexity as demand for brominated aromatics, including methyl 2-bromobenzoate, grows in emerging specialty chemical markets. Our approach incorporates local production options in Asia and North America, reducing freight risk and allowing us to buffer unexpected spikes in regional demand. Stockpiling intermediates, working closely with trusted logistics partners, and staying agile in scheduling help us provide reliable supply continuity in a sometimes turbulent market.
An ongoing challenge all manufacturers face is the temptation to cut cost at the expense of traceability or environmental responsibility. Our experience shows that the long-term value of investment in compliant systems, ethical sourcing, and technical collaboration with customers pays far greater dividends—both for business continuity and for the trust we build with users around the world.
Through years spent perfecting our product, collecting feedback from users, and investing in technical infrastructure, we’ve seen methyl 2-bromobenzoate become a mainstay intermediate for chemists needing performance, reliability, and traceability. From laboratory bench to large-scale plant, our commitment to quality and direct accountability benefits our users, and our focus on sustainability keeps us aligned with evolving regulatory and market expectations. Our door remains open to technical collaboration and shared improvement, because experience has proven that better chemistry comes through partnership—not just product delivery.