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HS Code |
154235 |
| Name | 2-Bromo-6-Methylbenzoic Acid |
| Cas Number | 4949-29-7 |
| Molecular Formula | C8H7BrO2 |
| Molecular Weight | 215.05 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 194-198°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Density | 1.678 g/cm³ |
| Smiles | CC1=C(C=CC=C1Br)C(=O)O |
| Inchi | InChI=1S/C8H7BrO2/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4H,1H3,(H,10,11) |
As an accredited 2-Bromo-6-Methylbenzoic Acid 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-6-Methylbenzoic Acid, sealed, labeled with hazard warnings and chemical details. |
| Shipping | 2-Bromo-6-Methylbenzoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. It is transported as a non-hazardous solid under ambient conditions, with clear labeling per regulatory standards. Proper documentation accompanies each shipment to ensure safe handling and compliance during transit and storage. |
| Storage | 2-Bromo-6-Methylbenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizing agents. Ensure proper labeling and avoid moisture contact. Store at room temperature and protect from physical damage to maintain chemical stability and purity. |
Applications of 2-Bromo-6-Methylbenzoic Acid in Industrial Manufacturing2-Bromo-6-Methylbenzoic Acid serves as a key intermediate for several specialized chemical sectors worldwide. As a direct manufacturer, we supply this compound to downstream producers who incorporate it into advanced synthesis processes for added value. Each application segment on this page outlines real industrial scenarios where this raw material integrates into well-defined products under specific regulatory frameworks. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Many pharmaceutical synthesis routes employ this material as a critical starting point for the construction of complex molecular scaffolds, especially in the production of APIs for non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive agents. The downstream process leverages its brominated aromatic core to facilitate halogen-metal exchange and coupling reactions, forming vital intermediates. Application recipes adjust ratios based on target impurity profiles and regulatory monographs, requiring thorough control in reaction steps and analytical verification for GMP compliance. Industry compliance standards
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2. Agrochemical Intermediate for Advanced Herbicide SynthesisProducers of novel pyridine- and benzoic acid-based herbicides rely on this compound as a halogenated precursor for selective field-use actives. It enters the process at early transformation stages to introduce steric and electronic effects required for target-specific binding. The addition level follows proprietary formulation rubrics to achieve clean conversion, and plant records must meet agrochemical regulatory requirements for traceability and quality assurance. Industry compliance standards
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3. Fine Chemical Intermediate for Specialty Dye SynthesisDownstream dye producers select this raw material as a brominated nucleus in the synthesis of high-performance colorants, including azo and anthraquinone-based dyes for advanced textile applications. Manufacturers benefit from its precise halogen position, which influences chromophore reactivity and final pigment stability. Each batch uses strict feed ratios for shade consistency and to stay within industry-allowed limits for residual aromatic impurities. Industry compliance standards
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4. Organic Synthesis Building Block for Functional PolymersExpert polymer modification specialists incorporate this acid into step-growth or post-polymerization functionalization strategies to create halogen-functional copolymers and specialty resins. Its molecular structure offers a reactive handle for substitution, enabling production of polymers with custom properties for barrier coatings, adhesives, and engineered plastics. The consumption rate and polymer feed are adjusted to achieve desired degree of functionalization without exceeding toxicity thresholds set by industrial health regulations. Industry compliance standards
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5. Advanced Material Synthesis for Electronic ChemicalsProducers of specialty electronic materials use this compound as a building block for synthesizing halogen-modified small molecules and liquid crystalline materials required in display technologies. The ortho-bromo and methyl configuration supports targeted reactivity for formation of custom mesogens and high-purity electronic intermediates. Precise dosing is governed by the structure-property relationships of the final material and strict quality control traceability to meet downstream electronics manufacturing standards. Industry compliance standards
Typical usage ratio
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In our work as chemical manufacturers, we come across no shortage of specialty compounds, but 2-Bromo-6-Methylbenzoic Acid often stands apart in the portfolio. We produce it in-house, scaling from gram to ton quantities, and every batch comes with its share of challenges and lessons. It is easy for those outside the factory to see it as just another halogenated benzoic acid, but those who have handled the process know that this molecule ties up a rich combination of selectivity, yield, and downstream application. The combination of the bromo group at the 2-position and the methyl substituent at the 6-position gives the material a unique chemical balance that has many advantages and quirks compared to more typical benzoic acid derivatives.
Our team tracks feedback and trends across the industry. Over the last decade, customers from pharmaceutical, agrochemical, and material science sectors have given us a real picture of where this product matters. Standard benzoic acids can be too unreactive for cross-coupling or specialty functionalizations. The introduction of a bromine atom provides a powerful handle, while the methyl group adds both steric and electronic effects that can steer reactions or tailor end-product solubility and stability. These details shape the role of 2-Bromo-6-Methylbenzoic Acid in research, pilot-scale development, and production environments.
From the manufacturer’s perspective, the synthesis and isolation of 2-Bromo-6-Methylbenzoic Acid is more than a protocol—it's a story of refinement. The aromatic bromination at the ortho position is sensitive to temperature, addition rate, and choice of solvent. Early on, we encountered issues with regioisomeric by-products or incomplete reactions, especially when scaling up. Chromatographic purification can be tedious unless the batch is tuned for clean conversion. Over time, optimization isn’t just about cutting costs; it’s about learning how to minimize side products and improve recovery without introducing corrosion or excessive waste. This knowledge, accrued through repetition and careful note-taking, gives the customer a product that is consistent and reliable—attributes that supply chain professionals do not take for granted.
Solid samples of 2-Bromo-6-Methylbenzoic Acid leave our factory as white to off-white powders, and we provide purity data alongside, typically above 98% by HPLC. Some buyers request additional data: melting point, trace metal analysis, or residue on ignition. Analytical teams collect this data not because of regulatory box-checking, but because downstream reactions can respond quite differently to minor impurities. Experienced synthetic chemists think about batch-to-batch variation in product color, texture, or even particle size. These physical attributes do not just affect appearance—they sometimes help indicate changes in synthesis, crystallization, or storage that could impact reactivity down the line.
You see the real difference with 2-Bromo-6-Methylbenzoic Acid once it is used as a raw material for the next synthetic step. Medicinal chemists appreciate its versatility as a coupling partner in Suzuki, Buchwald-Hartwig, or carbonylation reactions. The bromo group at the 2- position is both reactive enough to allow smooth transition metal catalysis and selective enough to avoid uncontrolled poly-substitutions. The methyl group at the 6-position brings subtle influence. For instance, in Suzuki couplings, it limits ortho reactivity and can nudge selectivity toward single substitutions. Sometimes, it deflects unwanted side reactions or enhances the stability of intermediate products during long, multi-step syntheses.
The real-world implications are concrete. In the agricultural chemistry field, we’ve seen customers use this product as a starting block for herbicides or seed-coating actives that require tailored absorption and degradation rates. The methyl substituent is not just a passenger; it shifts the degradation profile, sometimes allowing for a product that persists long enough for reliable activity but still breaks down in soil conditions as required by regulatory drivers. Even outside pharma or agrochemistry, in polymer or specialty material fields, researchers prefer this benzoic acid for pre-functionalized aromatic monomers. The downstream properties of materials—color, glass transition temperature, or even weathering response—change simply due to that initial methyl and bromo arrangement.
The buzz in the catalog world often centers around classic benzoic acid, 4-bromobenzoic acid, or 3,5-dimethylbenzoic acid. Many are used as reference points for comparison. 2-Bromo-6-Methylbenzoic Acid distinguishes itself both by structure and by function. Compared to para-bromo analogs, the ortho-bromo configuration is less common but more valuable in certain syntheses. The adjacent methyl group significantly affects both the reactivity pattern and solubility profile. Anyone who has struggled with poorly soluble intermediates knows how a methyl group can tip the scale, especially in organic solvents during high-throughput screens or scale-ups.
One of the details that often gets missed in other types of content is the way stereo effects come into play. We see it often when customers run aromatic substitutions: the methyl group introduces a steric shield adjacent to the carboxylic acid, which can suppress undesired side reactions or decarboxylation. The impact carries through purification stages as well—some crystallization solvent systems work well for one isomer, but not for another, and our technical support field these questions regularly.
Some buyers who switch from unsubstituted or meta-substituted benzoic acids to 2-Bromo-6-Methylbenzoic Acid gain significant increases in coupling yields or product lifespan. We follow up with these teams and gather real feedback; they report time savings, reductions in purification effort, or finding new reactivity windows that simply weren’t accessible with other analogs.
Practical field use has shown us that protecting the material during storage is nearly as important as the initial synthesis. Even with robust packaging, exposure to heat or light can impact color and reactivity. Moisture can aggravate hydrolysis at the carboxyl position, so dry conditions make a big difference for stability. Every batch comes double-bagged with desiccant during transport, and warehouses routinely monitor humidity.
Quality doesn’t stop with the final analytical report. In our facility, we’ve caught batches that checked every box on the standard data sheet but failed customer applications because of micro-traces of side products only evident by NMR or titration. We’ve learned to apply targeted tests based on the customer segment—one team needs detailed halide titration, another tracks methyl group oxidation, and yet another requests kinetic solubility measurements in their preferred solvent. Our experience on the ground delivering not just product but technical support makes the difference, especially for customers running time-sensitive projects or scale-ups.
Production teams enjoy it when researchers tell them how 2-Bromo-6-Methylbenzoic Acid enabled a new reaction or product line. Recently, one materials scientist told us about a new light-absorbing polymer that only worked because our substituted acid allowed selective cross-linking. These lab stories travel back to the plant floor, where process engineers see first-hand how even small tweaks in the molecule or the process can unlock larger results. Innovation drives us as much as quality assurance.
Discovery chemistry relies on these kinds of robust intermediates. In the world of pharmaceuticals, time-sensitive campaigns for new drug candidates depend on steady supply and known reactivity. One project stands out: a team of medicinal chemists used our acid as an intermediate for a library of kinase inhibitors. Their cycle times shortened from months to weeks because the key Suzuki couplings ran reliably with fewer purification steps. The learning here isn’t theoretical; it translates to real savings and more product delivered into preclinical testing.
Our sector faces mounting pressure to reduce waste, minimize hazardous by-products, and use green chemistry principles. With 2-Bromo-6-Methylbenzoic Acid, the balance between process efficiency and environmental footprint becomes a major point of focus. Where possible, we push towards streamlined one-pot syntheses, lower solvent usage, and more efficient purification protocols. By investing in better process controls and waste recovery, we’re helping our buyers meet the regulatory standards set by authorities in North America, Europe, and Asia-Pacific.
Much of our information flow comes from customers who operate under strict compliance standards. One agrochemical developer flagged trace brominated by-products as a concern, so we responded by tightening our wash protocols and introducing batch-level by-product screening. This approach saves our partners downstream product rejets, reduces regulatory headaches, and cuts overall costs across the value chain. The industry’s move toward more sustainable production isn’t just about marketing; it directly influences how we stack up against commodity-grade suppliers and holds us to a higher standard expected of an actual manufacturer.
Surprising as it may seem, much of our process refinement comes from user feedback and careful observation. We keep an archive of customer trials, highlighting both successes and occasional mishaps. One recurring request relates to particle size control. For some high-throughput syntheses, users ask for a specific mesh range or slurry grade to optimize dispersion and reaction kinetics. While our plant’s baseline targets mid-range sizes, we developed both finer and coarser variants for those running solid-phase syntheses or requiring rapid dissolution. This collaborative model, grounded in actual production experience, keeps our manufacturing environment responsive and technically sound.
Another lesson relates to storage solutions. Factories with flexible scheduling sometimes store intermediates longer than planned, bringing stability and shelf-life into sharper focus. We share validated storage recommendations and, when possible, provide extended-stability data drawn from our own inventory records. If a customer needs to hold inventory through plant shutdowns or transit delays, this data makes the difference between a smooth resume and a costly loss.
We rarely see two identical projects from different customers. Some labs push for maximum reactivity; others need tailored purification approaches to match strict product profiles. Our team maintains open channels with R&D chemists working at the bench, managers under pressure for cost control, and logistics leads focused on continuous supply. If an unexpected issue crops up during a reaction—color change, off-gas, or a lower yield than expected—having access to the actual manufacturer, not just a warehouse or order desk, makes all the difference. We have the process and analytical know-how to suggest tweaks: adjusting pH, modulating work-up temperature, or switching to a fresh batch with proven lot data.
Sometimes issues require more hands-on support. Several buyers have looked for unique salt forms or custom-packaged variants that streamline their own process. Our technical leads work directly with their production teams to design these solutions, based on our accumulated production experience. Having a feedback loop running from our plant floor directly into customer labs helps us catch problems, validate changes, and ship product both faster and with more confidence.
Modern chemical manufacturing sits in a landscape shaped by global supply challenges, regulatory shifts, and increasing focus on provenance. Buyers care where their specialty intermediates come from, and we respond with direct transparency on sourcing, process changes, and batch histories. In the case of 2-Bromo-6-Methylbenzoic Acid, we document our supply trail and can provide full traceability of raw materials and process intermediates. Supply interruptions are rare, and by keeping critical steps in-house, we sidestep the risks that come from relying on resellers or third-party processors.
This approach also keeps us nimble. If a raw material supply chain is threatened—such as sudden restrictions on specific precursors or supply crunches after geopolitical disruptions—we can pivot in near real time. Our regular internal audits and backward integration with select precursor manufacturers ensure a resilient supply, minimizing knock-on effects for our end users.
Many buyers new to 2-Bromo-6-Methylbenzoic Acid ask where it aligns or diverges from similar halogenated or methylated benzoic acids. The core distinction lies in both electronic and steric properties. The placement of bromine next to the carboxylic acid directs reactivity and can suppress non-selective halogenation or unwanted secondary modifications in aromatic couplings. The methyl at the 6-position fine-tunes solubility and interface with solvents or downstream substrates, granting more control over both reaction yield and finished product stability.
This blend of features supports efficient, high-yielding reactions in medicinal chemistry, better environmental fate in agrochemical products, and enables advanced polymer design. Customers searching for a single raw material to deliver reliable, predictable results often settle on this compound after running parallel tests with similar products and encountering fewer downstream headaches. The manufacturer’s perspective highlights hard-won insights—careful optimization, analytical vigilance, and a technical support approach rooted in daily production, not just catalog sales.
Trust in specialty chemicals rests not only on purity or price, but on consistency, technical support, and supply reliability. Our experience with 2-Bromo-6-Methylbenzoic Acid underscores this point. We know the implications of every decision in synthesis, storage, and shipment, and we engage in a two-way conversation with users from lab bench to commercial scale. Long-term buyers value our commitment to documentation, quick troubleshooting, and willingness to refine the product to meet evolving project needs.
By focusing on real-world outcomes and building an adaptable, responsive manufacturing environment, we serve not only as a material supplier but as a partner in innovation and process development. Our team brings a manufacturer’s discipline, attention to detail, and technical depth to every shipment of 2-Bromo-6-Methylbenzoic Acid, and we see that reflected in the success of our customers’ applications, from early-stage research to commercial market launch.