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HS Code |
859741 |
| Chemical Name | Methyl 4-Bromo-3-Methylbenzoate |
| Cas Number | 57311-78-7 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 |
| Appearance | White to off-white solid |
| Melting Point | 54-58°C |
| Boiling Point | 289.6°C at 760 mmHg |
| Density | 1.49 g/cm3 |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=C(C=CC(=C1)Br)C(=O)OC |
| Refractive Index | 1.557 |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
As an accredited Methyl 4-Bromo-3-Methylbenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White crystalline solid in a sealed amber glass bottle, labeled "Methyl 4-Bromo-3-Methylbenzoate, 25g," with hazard and safety information. |
| Shipping | **Shipping Description:** Methyl 4-Bromo-3-Methylbenzoate is typically shipped in sealed, chemically resistant containers, protected from moisture and direct sunlight. The package should comply with relevant transport regulations, clearly labeled with hazard information. Handle with appropriate safety measures, including use of gloves and goggles. Store in a cool, dry, and ventilated area during transit. |
| Storage | **Methyl 4-Bromo-3-Methylbenzoate** should be stored in a tightly closed container, kept in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from light, moisture, and heat. Always label the container clearly and avoid sources of ignition. Use in a chemical fume hood and keep out of reach of unauthorized personnel. |
Applications of Methyl 4-Bromo-3-Methylbenzoate in Industrial ManufacturingMethyl 4-Bromo-3-Methylbenzoate serves as a strategic intermediate in advanced chemical synthesis, providing reliable performance for specialty downstream industries. As a direct manufacturer, we supply this raw material in strict alignment with regulatory and customer-specific requirements. The following application scenarios illustrate its primary industrial integrations, with dedicated information on compliance, formulation, manufacturing process and final product forms. 1. Active Pharmaceutical Ingredient Building BlockPharmaceutical manufacturers utilize this compound in multi-step syntheses for small molecule drug development, where its aromatic substitution pattern enables selective reactions critical in complex API intermediates. The purity profile supports stringent regulatory demands and tight residual solvent controls. Process chemists introduce the ester within early-stage synthetic routes to construct key frameworks subsequently elaborated into anti-inflammatory, CNS, and oncological therapeutic classes. Industry compliance standards
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2. Agrochemical Active Ingredient IntermediateThe ester finds application as a synthesis intermediate in the production cycles of next-generation crop protection agents. Agrochemical R&D teams integrate it into bench-scale and commercial batches due to its reliable halogenation and methylation pattern, which serves as a precursor for constructing selective herbicides and fungicides. Efficient downstream functionalization supports cost-effective route scouting in industrial settings where traceability and contaminant control are essential. Industry compliance standards
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3. Fine Chemical Synthesis for OLED and Electronic MaterialsProducers of organic materials for advanced electronics deploy this methyl ester as an aryl bromide source in synthesizing specialty monomers, where electronic and steric features are critical for achieving consistent electronic transport properties. It functions as a platform molecule in palladium-catalyzed cross-coupling reactions, enabling formation of extended conjugated systems for light-emitting and charge-transport layers used in OLED displays and organic transistors. Industry compliance standards
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4. Custom Synthesis for Specialty Research and Reference StandardsUniversities, contract research organizations, and analytical labs choose this material as a reliable arylated building block when developing reference standards or synthesizing labeled compounds for trace analysis. Its well-defined functional groups permit high-fidelity isotopic or structural modification, supporting rigorous analytical validation studies and regulatory submission data packages. Labs benefit from manufacturer-supplied documentation for method validation and full chain of custody. Industry compliance standards
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Methyl 4-Bromo-3-Methylbenzoate draws attention in chemical synthesis because of its direct structure and reactivity. As a manufacturer working hands-on with aromatic compounds, we recognize certain unique qualities that come with this ester. With the bromo group on the para position and a methyl on the meta, the compound takes on a personality that’s not easily confused with simple methylbenzoate or other halogenated esters. The controlled introduction of bromine into aromatic esters isn’t just about ticking a box; it’s about achieving a targeted mix of reactivity and stability. Numerous customers in the pharmaceutical, agrochemical, and fine chemical industries rely on this approach for precise synthetic routes.
During production, we work with carefully sourced raw materials and rigorously managed conditions. Our batch records show that a clean methyl ester formation requires precise temperature control during the esterification step. If temperatures drift, the byproduct stakes rise and the purification challenges follow. Each run gets HPLC, GC-MS, and NMR scrutiny before any packs leave the cleanroom. What sounds routine in paperwork turns into hours of direct handling and troubleshooting, keeping these standards part of every shipment.
Product consistency starts on the production floor. Industry requests for Methyl 4-Bromo-3-Methylbenzoate often focus on certain purity levels—95% may be comfortable for some intermediates, but our pharma partners consistently look for purity above 98.5%. This isn’t just a selling point; it prevents downstream process headaches. Trace halogenated impurities or unreacted methylbenzoic acid can halt a multi-step synthesis halfway, wasting precious time and substrate.
We standardize a white to very pale yellow crystalline powder, typically melting between 62-65°C. Packaging leaves no room for cross-contamination. Every drum or bottle leaves vacuum-sealed, with a certificate that goes beyond a simple purity value and covers moisture, residual solvents, and heavy metal traces. Each customer sees a transparent summary rather than generic statements, and every batch lot gets traceability from raw material to finished product in our plant software.
The value in this compound comes from its adaptability in synthesis—something that only emerges from repeated, hands-on reaction work. Methyl 4-Bromo-3-Methylbenzoate slips into a variety of cross-coupling protocols. We see it used as a substrate in Suzuki–Miyaura or Stille coupling, where the bromo group stands ready for palladium-catalyzed substitutions. Over years of supplying to contract research labs, most feedback involves these substitution routes. Chemists value the way this ester backbone resists hydrolysis under mild coupling conditions, giving more freedom with catalyst and solvent choices.
We have seen research teams request this product intending to cleave the methyl ester downstream, or to introduce diverse aryl groups at the bromo position. What they report matches our own screening: the methyl group in the meta position relaxes electron density enough to moderate the reactivity without over-activating the ring, making this compound a smart entry point for elaborate molecule construction. If asked how this compares to para-methyl or ortho-bromo analogues, the consensus from scale-up batches and bench work points to higher isolated yields and easier purification with the 4-bromo-3-methyl format.
Many clients starting out confuse this compound with Methyl 3-Bromo-4-Methylbenzoate or the non-methylated methyl 4-bromobenzoate. After running dozens of comparative reactions, we notice tangible operational differences. The bromo at the para position reacts more cleanly in cross-coupling reactions, and the extra methyl at the meta site can suppress certain side reactions, especially oxidative dimerization. Analytical feedback from partner labs, confirmed in our QC, shows distinct NMR peaks—this isn’t a trivial matter for routine method development. The chemical community sometimes asks why not just start from the easier, single-substituted aromatic esters. Lab experience over time answers this: missing that methyl group changes yields, and sometimes alters the pharmacophore landscape in discovery projects. One missing group costs weeks of pathway validation.
The social aspect of supply chains supports this product’s popularity. Distribution partners found that even modestly impure batches from certain sources led to recurring complaints of inconsistent reactivity. We run side-by-side kinetics with samples from various countries—ours consistently triggers clean conversion above 98%. That reduces late-night troubleshooting at the client bench, and earns us direct feedback.
Diversification in demand keeps us sharp on quality control. Medicinal chemists, the first adopters of this product, teach us a lot through feedback loops. Even though kilogram-scale production rarely enters their routine, milligram and gram-scale work directly influences our larger processes. One customer’s trouble with dimethyl impurities forced a plant upgrade. Later, partners in agricultural chemistry pressed us to supply ton-level quantities, expecting the same consistent cleanliness without extra cost. Our reaction protocol evolved—switching solvents, upgrading crystallization, tying up fewer downstream resources in post-synthesis cleanup.
Production volumes may have increased, but standards hold. Analytical data gathered over hundreds of campaign batches gets revisited annually, resulting in marginal improvements with each year. The market for Methyl 4-Bromo-3-Methylbenzoate keeps shifting as new synthetic routes, particularly biocatalytic and direct arylations, nudge traditional chemistry to adapt. We track those changes and adjust workflows—not just waiting for commercial orders to define plant behavior, but shaping protocols in response to new reaction demands as soon as credible academic or patent literature points toward a fresh technique.
A manufacturer’s job includes wrestling with practicalities, not just lab notebooks. Methyl 4-Bromo-3-Methylbenzoate holds up well under dry storage. Still, extended exposure to moisture leads to slow hydrolysis—an observation borne out by real batch mishaps and not just theoretical hazard sheets. We stress this point to customers looking to store product for half a year or more. Our packaging gets updated if a pattern emerges in feedback, shifting toward multilayer barriers as soon as increased hygroscopicity appears in climate-controlled stockrooms.
Even though the compound stays stable in shipment, factory teams remain cautious near open-packed intermediates. A mild but unpleasant aroma escapes if handled carelessly; this matches the predicted behavior for methyl esters with brominated rings. Regular air sampling in our facility records no significant vapor risk, but operators stay masked to avoid irritation. These lessons reflect not just regulatory compliance but a low tolerance for workplace complaints—a key ingredient in training new staff.
Global shifts in bromine pricing often sway the economics of supplying this compound. When regional feedstock supplies tighten, it puts pressure on both availability and cost. Rather than leave customers in the lurch, we maintain in-house bromination capacity using legacy reaction vessels—periodically modernized to keep up with emissions and process efficiency. Having this infrastructure gives us direct control over lead times. No dependency on distant or unvetted bromine supply chains keeps our batches arriving stable, and buyers don’t have to wait out market swings.
Sudden regulatory changes for organobromine compounds across Europe and North America once threatened to pinch operations. We tackled these updates head-on, validating every process against current and anticipated guidelines. Rather than scramble after non-compliance complaints, we get ahead: routine external audits, regular staff compliance reviews, and prompt adjustment to product documentation keep us aligned with expectations. This investment gets paid back through steady business, as new customers trust the experience we bring to every negotiation.
Daily factory life for us revolves around attention to detail and a willingness to adapt. Supplier feedback uncovers subtle blind spots—one client’s impurity complaint set off a full review of our crystallization process, leading to new equipment installation and better yields. Industry colleagues occasionally reach out with ideas for co-development, sometimes pitching reformulations that fit their unique requirements. Although not every request makes it into our main catalog, this active back-and-forth builds shared knowledge that shapes both our technology and our approach to customer service.
In recent years, we noticed a growing industry need for analytical transparency. Formerly, a basic certificate of analysis covered the basics. Now, detailed NMR, IR, and MS data are standard requests. Clients want full clarity on polymorphs, trace solvents, and possible non-aromatic byproducts. We respond with complete digital packs for every lot, integrating LIMS-driven tracking with secure delivery of raw analytical data. Our customers know what they’re getting, and we field fewer uncertainty calls.
Chemical purchasing agents often hold samples of alternative methylbenzoates and ask about performance differences head-on. Through years of factory and lab work, we’ve clocked meaningful, practical takeaways. Aromatic esters lacking the 4-bromo group tend to show reduced reactivity in standard coupling chemistry. Skipping the 3-methyl group occasionally shifts key physical properties—altered melting points, different solubility in reaction solvents—which throws off planned protocols.
Methyl 3-Bromo-4-Methylbenzoate, while a positional isomer, behaves noticeably differently in several conditions. The reactivity, solubility in DMF and THF, and even color stability as dry powder sometimes shift just enough to introduce uncertainty. Customers running parallel synthesis campaigns with both compounds have shared yield tables with our team. Over time, the clear feedback points to superior process smoothness with our 4-bromo-3-methyl variant—reduced tar byproduct, narrower melting range, and more predictable NMR spectra, helping streamline both research and manufacturing scale-up.
Working daily with specialty aromatics means learning from experience—the mistakes and the small wins. With Methyl 4-Bromo-3-Methylbenzoate, half the job becomes sharing what we’ve picked up: how aging sample batches evolve, which process tweaks save time, how a barely noticeable impurity peak can trip up a whole business unit. We keep records not just to comply, but to spot trends before they cut into productivity. Everything from color grading to trace storage odors plays a role in real-world logistics, and our staff carries the collective memory of hundreds of runs. This hands-on knowledge seasons every transaction.
Chemical manufacturing doesn’t stay locked in the lab. We track each order to see what customers invent next. Sometimes batches end up in life science tools, sometimes in dyes, sometimes in academic studies a world away from industrial routine. We answer tech questions directly, help troubleshoot failed scale-ups, and pass along solutions that work for us. If one customer cracks a workaround for solubility or crystallization, we’re quick to add it to our own training and share the advice if asked.
Practical plant life circles back to troubleshooting: moisture ingress, variable yields, or customer requests for greener processes. Sometimes material arrives at a client’s lab showing an unusual off-tone or trace solvent content above specification. Rather than dismiss these as one-offs, we set up root cause analysis teams and respond with workflow and storage adjustments. That builds a culture of continuous improvement, keeping us competitive and keeping customers loyal.
Our team has also experimented with greener solvents and lower temperature protocols to reduce overhead and emissions. Advances in continuous flow chemistry, informed by on-the-ground feedback from both our plant and customer pilot lines, move these ingredients closer to being safer and more sustainable. We see industry trends shifting away from heavy metals in catalysis, and our supply chain adapts—integrating new purification steps that match customer preferences for minimal residuals. Each tweak to handling or quality control holds real-world impact, cutting down on waste and improving working conditions.
Manufacturing a specialty compound like Methyl 4-Bromo-3-Methylbenzoate teaches one lesson above all: success stands on repeatable excellence, clear communication, and respect for the experience behind each reaction. Reliable supply, direct feedback, and hard-won process control build the real story behind every kilogram that leaves our shop floor. Our collective experience—factory staff, analysts, reaction engineers, sales, and customer-facing scientists—shapes not just how we produce, but how we help our partners solve their unique challenges.