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HS Code |
869854 |
| Cas Number | 23056-36-2 |
| Molecular Formula | C10H9BrO2 |
| Molecular Weight | 241.08 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 47-50°C |
| Density | 1.44 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol, chloroform) |
| Smiles | CCOC(=O)C1=CC=C(C=C1)CBr |
| Inchi | InChI=1S/C10H9BrO2/c1-2-13-10(12)8-3-5-9(6-4-8)7-11/h3-6H,2,7H2,1H3 |
| Synonyms | 4-(Bromomethyl)benzoic acid ethyl ester |
| Storage Temperature | Store at 2-8°C |
| Hazard Statements | Irritant; Harmful if swallowed and in contact with skin |
As an accredited Ethyl 4-(Bromomethyl)Benzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of Ethyl 4-(Bromomethyl)benzoate is supplied in a tightly-sealed amber glass bottle, labeled with hazard and identification information. |
| Shipping | Ethyl 4-(Bromomethyl)benzoate is shipped in tightly sealed containers, protected from light and moisture. It should be transported according to local, national, and international regulations for hazardous chemicals, often as "Dangerous Goods." Proper labeling, safety documentation (SDS), and temperature control are required for safe and compliant shipping of this compound. |
| Storage | Ethyl 4-(Bromomethyl)benzoate should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and store at room temperature or as otherwise specified by the manufacturer. Ensure proper chemical labeling and keep out of reach of unauthorized personnel. |
Applications of Ethyl 4-(Bromomethyl)Benzoate in Industrial ManufacturingAs a direct manufacturer of Ethyl 4-(Bromomethyl)benzoate, we support multiple performance-driven sectors where this fine chemical enables targeted molecular modifications. Below, we present sector-specific applications made possible by our strict production and quality management standards, focusing on industries with established downstream usage. These scenarios highlight actual industrial integration, from compliance to process flow and final goods. 1. Pharmaceutical Intermediate SynthesisMany advanced pharmaceutical manufacturers utilize Ethyl 4-(Bromomethyl)benzoate as a key benzylic bromide intermediate during the assembly of specialty APIs and complex therapeutic molecules. Its reactive moiety enables efficient benzylation, alkylation, and functional group attachment steps essential for building blocks such as antihypertensive or anticancer drugs. Careful regulation of molar ratios during batch and flow chemistry ensures consistent yields and high-purity intermediates required by the final dosage form. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionProducers of crop protection agents and advanced agrochemicals employ Ethyl 4-(Bromomethyl)benzoate to enable key alkylation or esterification steps. Its specific molecular structure supports the modification of aromatic scaffolds, facilitating synthesis of potent herbicide, fungicide, and insecticide active ingredients. Accurate ingredient metering ensures strict adherence to activity and residue specifications set for regulated markets. Industry compliance standards
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3. Advanced Material Monomer DevelopmentIn high-performance polymer and specialty resin manufacturing, Ethyl 4-(Bromomethyl)benzoate functions as an essential functionalized monomer or co-monomer for branching aromatic chains. Producers exploit its benzylic bromide for controlled radical or step-growth polymerizations, designing custom-engineered polymers for microelectronics, OLEDs, and liquid crystal panels. Precise ratio management is required to regulate chain propagation and film-forming properties. Industry compliance standards
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4. Specialty Fine Chemical SynthesisProducers in the specialty and custom synthesis sector apply Ethyl 4-(Bromomethyl)benzoate as a structured source of benzylic bromide for downstream halide-to-amine or thioether transformations. The compound supports route scouting and library construction of benzoate-based derivatives, with close control over reaction conditions and stoichiometry to minimize impurities and facilitate targeted molecular design for academic, flavor, fragrance, and advanced coating markets. Industry compliance standards
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Experience in chemical manufacturing changes the way you look at a product like ethyl 4-(bromomethyl)benzoate. After years in synthesis, every small decision in the plant shapes how this compound ends up being used in labs and industry. Unlike more generic benzoates or standard methyl substituents, the bromomethyl group at the para position gives this molecule distinct character, and a lot of care goes into keeping it pure, consistent, and free from the little surprises that can ruin a batch downstream.
The CAS number for ethyl 4-(bromomethyl)benzoate reflects a precise molecule: a benzoate ester linked to ethyl and para-substituted with a bromomethyl group. Its structure directs its behavior—creating opportunities, but also setting boundaries chemists need to keep in mind. Production environments never let us forget how reactive the bromine can be. Bromination likes to stray, so the plant hinges on airtight control from start to finish. From raw material checks to the choice of solvent, every tech running the reactors knows what sloppiness brings: colored byproducts, tricky filtrations, or odors that send up alarm bells. Final inspection always pulls samples to track trace organics and halide content, well beyond the basics each market requires.
We see the product heading out the door in multi-kilo drums, bound for different hands, each with a slightly different goal. Pharmaceutical teams might reach for ethyl 4-(bromomethyl)benzoate as a key piece in building substituted phenyl compounds—an intermediate that opens new aromatic structures. Research chemists press those boundaries, exploiting the para-bromomethyl as a site for nucleophilic substitution, Suzuki reaction, or ester hydrolysis. In polymer work, we have customers who manipulate the ester and halide to grow custom materials, always pushing for new combinations that need this specific molecular geometry.
This product gets its start in reactors balanced for both temperature and stoichiometry. Operators focus on controlling exotherms, so the bromination stops right at the methyl group—never drifting onto the ring, avoiding unwanted isomers. Conditions vary by batch size, but the essentials are always the same: careful addition, close monitoring of progress, and timely quenching. Impurity profiles frustrate newcomers until they see how small changes in reflux rate or addition points can water down quality. Over years of cycles, our team developed fine-tuned methods for extraction and purification that favor the target compound's stability, stripping away side-products before they build up in storage. Consistency takes repeated validation—no one trusts a batch until it passes both classic spectrometric checks and some hands-on bench analysis. Real feedback always comes from synthetic chemists themselves; even traces of overbrominated byproducts can ruin a route, and we see their notes come back if we slip.
Some clients ask why ethyl 4-(bromomethyl)benzoate matters versus using other benzoate derivatives. The answer sits right in its reactivity and precision. Other benzoate esters lack the reliable handle that the bromomethyl group brings. Substitute at the ortho or meta position, and the patterns change—yield drops, step counts rise, or protecting groups become a headache. The para position allows for a clean entry into downstream functionalizations, and in practice, this saves a lot of headaches. Chloromethyl and iodinated versions appear in literature, but the bromine often gives the best combination of leaving group ability and manageable downstream safety. We see that reflected in the feedback and the repeat orders from groups tuning their own unique processes. It's not the only way to build substituted benzoic acid derivatives, but it often stands out for being predictable under standard conditions, with most nucleophiles handling the bromine without fuss.
Compared to more common esters like methyl or propyl benzoate, the addition of the bromomethyl function makes this much more than a flavor compound or mild synthetic intermediate. Handle it correctly, and it opens up synthetic doors quickly. The ethyl ester brings a balance of hydrolytic stability and solubility—faster than methyl for some saponifications but less volatile, easier to recover, and less likely to complicate downstream purification. Over time, clients pick up on these small differences, tailoring their syntheses so cycles run faster or waste is trimmed. From the plant floor, we’ve watched development cycles drop by weeks once a process switches over to bromomethyl benzoates instead of multi-step aryl bromination. Every production manager keeps these stories in mind when a chemist calls in about switching up a route.
Plenty of spec sheets and certificates get printed, but the truth is, specifications only mean something when they actually line up with the real output. Our experience says purity matters most. For ethyl 4-(bromomethyl)benzoate, purity above 98% isn’t just a sticker—it changes how much time teams spend in recrystallization or chromatography later. Water traces, unreacted starting materials, and especially dibromomethyl or brominated ring products drive users to curse a batch. Our QC lab reviews every drum, scanning for even subtle shifts in melting point, color, or GC trace that can tell us about minor contaminants. We target clear, white to light yellow crystalline yields. Even a hint of persistent odor or off-white tint prompts a deeper look because someone downstream will notice what slipped through. Chemical manufacturing is unforgiving like that.
The handling experience counts, too. We ship it in HDPE drums with vapor-tight seals—not just for regulatory compliance but because bromomethyl benzoates like to pick up moisture and can start to degrade if left open to the air too long. Teams using automated dispensers or robotic samplers request intact seals, so these get checked before a drum leaves the building. From long-term storage, we keep everything cool, dry, and out of light to maintain shelf life. Over years of shipping and storage, customers relying on old stocks report reliable performance as long as those environmental basics stay in check.
Most chemists ordering this product have already run their own lab-scale tests before coming to us for large quantities. They need exact specifications—consistent melting points, sharp NMR signals, no ghosts in the IR profile. But chemistry rarely stays on paper. We see our product used in run-of-the-mill SN2 nucleophilic substitutions, leveraging the bromomethyl group to hook functional amines or thiols onto the ring. Recent years brought a spike in demand from groups building ligands for organometallics, where every extra impurity can knock down catalytic turnover. Some academic partners dig into more creative cross-couplings—using Suzuki or Heck conditions to bring entirely new rings or functional groups onto the core. In pharmaceutical development, we see the ester hydrolyzed after initial derivatization, then the acid gets plugged right into lead compounds heading for clinical evaluation.
Polymer researchers tell us about incorporating ethyl 4-(bromomethyl)benzoate to introduce pendant functional groups along polymer backbones, acting as key handles for further modification. Peptide chemists use the bromomethyl as a linker, giving them room for downstream cyclizations or scrupulously controlled conjugations in imaging research. Sometimes, a biologist calls in to double-check the residual solvent content—they want watertight information before introducing any new reagent into a bioassay. The more information we return, the less downtime or confusion they face later.
No chemical process rolls forward without bumps. For this product, the biggest headaches come from controlling the bromination step and keeping the product stable through handling and distribution. Bromine-based synthesis always brings risk—corrosive reagents, vigorous exotherms, and product streams that need regular TLC. At scale, the plant team braces for sudden temperature rises, float switches getting stuck, or unexpected color changes in intermediate samples. These aren’t theoretical problems; they mean cleanup, downtime, and paperwork that nobody likes. It pays to keep extra trained eyes on each step, not just the final output.
Over the years, in response to growing demand for ultra-pure material, we invested in additional purification columns and trained our teams to spot the subtle signs of overreaction or poor separation. Analytical chemists learned to anticipate seasonal shifts in product appearance depending on feedstock origin, tuning extraction solvents to get predictably clean outcomes. One memorable year, a subtle solvent trace from a supplier nearly derailed a pharmaceutical customer’s reactor run. Careful analysis and tighter supply chain controls prevented a repeat, teaching us not to relax even when things run smoothly. Every mistake draws sharp lessons, and we bank these into stricter SOPs for every batch that comes afterward.
Many users ask about environmental and workplace safety issues around brominated chemicals. It’s a real concern when you work next to these materials every day. All our bromine handling runs in contained hoods and sealed lines—no room for improvisation. Employees get outfitted with full PPE, continuous training, and active ventilation, and spills get managed before they become stories told in accident reports. Waste handling takes priority, since no one wants regulatory headaches or community pushback over halogenated organics entering the waste stream. With each inspection or audit, we field questions from customers and authorities, always showing transparent logs of inventories, exposure tracking, and incident logs. It’s not just box-checking; a mistake here matters to real people.
On the industry end, safety data and proper labeling get reviewed at least twice before shipping. We quickly share full batch composition details on request, especially for those with strict regulatory or GLP needs. That relationship keeps doors open; customers need to trust that the product matches its paperwork, every single time, especially for pharmaceuticals or medical research. Over the years, we’ve never regretted prioritizing oversight and transparency over speed when filling the order book.
The chemical world moves in cycles, and ethyl 4-(bromomethyl)benzoate now sees rising attention as research into advanced building blocks and smart polymers accelerates. Integration with green chemistry protocols emerges, so requests come in for more information on byproduct treatment, energy usage, and opportunities for recycling spent solvents and waste streams. Internal development now aims at minimizing off-gassing, reducing bromine use, and recovering solvent through closed loops—less about publicity, more about long-term sustainability for the business and people on the factory floor.
On the customer side, we hear more calls for tailored batch sizes and on-demand delivery. Small research labs rarely want bulk, but pilot lines demand steady supply at consistent quality throughout the year. We coordinate closely with our shipping partners, investing in smarter packaging and staggered delivery schedules to meet peaks in R&D demand, all the while ensuring that quality assurance doesn't get sacrificed under tight timelines. Experience tells us that saving a few days on delivery means nothing if the material doesn't pass muster upon arrival. Each failed batch hammers home the need for reliable logistics networks and firm tracking from factory floor to the end user's bench.
At the end of the day, manufacturing ethyl 4-(bromomethyl)benzoate is a test of discipline and pride for every team member. From QA techs taking a last-minute GC run to shipping clerks confirming correct documentation, dedication to precision defines the outcome. Our process learned from years of both errors and triumphs—a single missed impurity or sloppy reaction run can mean hours of rework and sleepless nights for everyone in the chain. That shared history colors the ongoing commitment to improvement, whether troubleshooting new batch reactors, implementing tighter environmental controls, or responding to unexpected customer questions.
Real-world feedback forms the backbone of incremental change. As customers develop new applications, our technical support keeps pace, updating standard work instructions, investing in better training, and tweaking plant scheduling to handle specialty runs with minimum hassle. Our operators trace each pound of product, knowing that reliability, not just compliance, dictates whether customers return. Each lot shipped out the door underlines the practical, grounded reality that consistent, dependable manufacturing delivers advantage in today’s crowded specialty chemical market.
For those seeking a reliable halogenated aromatic building block, ethyl 4-(bromomethyl)benzoate represents a crossroads of reactivity and stability, shaped by years of tested plant routines and tight standards. Our work behind the scenes carries through the supply chain, coloring everything from the first gram handled in the lab to the final stage in advanced manufacturing. In making sure those grams meet the highest expectations every time, we put the manufacturer’s experience into every drum, yielding real, tangible value for every chemist, researcher, and production manager who trusts us with their next breakthrough.