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HS Code |
206405 |
| Cas Number | 65743-19-9 |
| Molecular Formula | C12H13BrO2 |
| Molecular Weight | 269.14 g/mol |
| Iupac Name | Ethyl (E)-3-(4-bromomethylphenyl)prop-2-enoate |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 148-152°C at 4 mmHg |
| Density | 1.379 g/cm³ |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, ethanol) |
| Purity | Typically >98% |
| Smiles | CCOC(=O)C=CC1=CC=C(C=C1)CBr |
| Refractive Index | 1.565 (at 20°C) |
As an accredited Ethyl 4-Bromomethylcinnamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl 4-Bromomethylcinnamate is packaged in a 25g amber glass bottle with a secure screw cap and detailed chemical labeling. |
| Shipping | **Ethyl 4-Bromomethylcinnamate** is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. Packaging complies with international regulations for hazardous materials. The product is stored under cool, dry conditions and clearly labeled. Transportation is handled by certified carriers, ensuring compliance with safety requirements for chemicals. |
| Storage | Ethyl 4-Bromomethylcinnamate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, preferably at 2-8°C (refrigerator). Ensure the chemical is clearly labeled and kept away from incompatible substances such as strong oxidizers. Follow all relevant safety guidelines and local regulations for chemical storage. |
Applications of Ethyl 4-Bromomethylcinnamate in Industrial ManufacturingEthyl 4-Bromomethylcinnamate serves as a specialty intermediate for advanced synthesis in multiple chemical sectors. We supply this material directly from our plant, supporting precision formulation and scale-up manufacturing in downstream industries where reliability, traceability, and documented performance are required. 1. Pharmaceutical Intermediate for API SynthesisDownstream pharmaceutical manufacturers utilize this chemical as a building block for targeted synthesis of specialty Active Pharmaceutical Ingredients, notably in the production of derivatives incorporating cinnamoyl or brominated moieties. During scale-up, our material enters multi-step synthesis under documented conditions, with full traceability from batch to batch, as required by regulatory inspected facilities. Product quality conforms to rigorous control at each stage, ensuring safety and purity through the reaction pathway. Industry compliance standards
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2. Fragrance Intermediate for Aroma CompoundsLeading fragrance compound manufacturers use Ethyl 4-Bromomethylcinnamate as a unique intermediate to synthesize complex aromatic esters and aldehydes. The chemical structure enables downstream alkylation or reduction, delivering target notes for use in perfumery, scented oils, and high-value aroma product lines. Quality controls address both purity and olfactory profiling, as set by specific industry standards for safe fragrance composition. Industry compliance standards
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3. Fine Chemical Synthesis for Agrochemical IntermediatesMajor agrochemical manufacturers select Ethyl 4-Bromomethylcinnamate as an intermediate for the synthesis of brominated cinnamate-based herbicide and fungicide actives. Its reactivity suits targeted introduction of bromine to bioactive frameworks, following validated industrial routes with strict process controls. Documentation supports full supply chain traceability and compliance with agricultural chemical regulations. Industry compliance standards
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4. Specialty Polymer Monomer in Functional MaterialsManufacturers of specialty polymers leverage Ethyl 4-Bromomethylcinnamate as a functional monomer in advanced copolymerization. Its molecular structure allows site-selective incorporation into macromolecular chains, imparting tailored mechanical, optical, or reactive properties. All batches undergo rigorous QC to match downstream polymerization requirements, especially where consistency and reactivity control are paramount. Industry compliance standards
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5. Intermediate for Photoinitiator Manufacture in UV-Curable SystemsManufacturers of photoinitiators for UV-curable coating and ink systems utilize Ethyl 4-Bromomethylcinnamate as a precursor in the synthesis of benzoin- or cinnamate-type photoinitiator molecules. The material supports controlled linker introduction for desired absorbance and reactivity profiles, with all lot data fully validated for manufacturing traceability, especially for industrial-grade coating applications. Industry compliance standards
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6. Fine Organic Synthesis in Research and Development LaboratoriesChemical synthesis laboratories and R&D divisions in fine chemical companies apply Ethyl 4-Bromomethylcinnamate as a precursor for custom synthesis of novel organic molecules, often under high-purity or analytical standards. Documentation and CoA/QC package allow direct integration into controlled experiments, total-synthesis projects, or proof-of-concept molecule development, supporting patentable innovation in molecular design. Industry compliance standards
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Every manufacturer that’s ever worked with challenging organic frameworks recognizes the value of a clean, reliable halogenated intermediate. Our Ethyl 4-Bromomethylcinnamate fits right into that toolkit. From our first small-batch synthesis on the pilot line to current scaled-up manufacturing, each run reflects careful attention—no shortcuts in process consistency, purity, or batch documentation. We understand where this compound goes and what’s expected downstream, so we treat every order as if we’re filling our own shelves, not just shipping to another stop in the chain.
The material offers a unique niche. Similar to the more common cinnamate esters, Ethyl 4-Bromomethylcinnamate invites selective transformations at the bromomethyl group. What sets ours apart starts with the raw inputs—every inbound drum, every solvent, every source is traced and checked not only for stock purity but for authenticity. The result shows in the product: a clear, light yellow crystalline solid, typically packaged at >98% GC purity. Most competing intermediates in this chemical family (phenylpropenoates, for instance) lack the same combination of conjugated system and reactive benzylic halide. Our process ensures low residual chloride or other alkylating halides, which translates to fewer surprises when multi-step syntheses reach scale.
We crystallize every lot of Ethyl 4-Bromomethylcinnamate in-house. The compound’s melting range falls close to 60–64°C, with a faintly sweet odor—subtle but distinct, which long-timers in the lab often note as a sign of both purity and fresh processing. Each drum moves through vacuum drying and a final sieving before it leaves our facility. Moisture content routinely tests below 0.2%. This extra effort matters for anyone who’s run a condensation or coupling and waited for stray water to finally stop interfering. Since we keep our reagents under nitrogen until packing, customers can expect stable shelf-life without premature decomposition or color change.
Throughout production, TLC and HPLC analytics offer a running record. We keep heavy record books, not just batch numbers. If something veers off spec, it gets flagged, not ignored. The focus: maintain tight control on by-products, particularly those that could co-elute with the intended product during isolation. Some suppliers treat a faint baseline haze in the chromatogram as acceptable—our philosophy says dig deeper and avoid any pattern that might show up during scale-up, when minor ghosts become major headaches. That’s not theoretical. Small-scale screening and kilogram-scale processing rarely behave the same; we keep our own scale-up runs on hand for both reference and troubleshooting.
Pharmaceutical synthesis anchors most inquiries about Ethyl 4-Bromomethylcinnamate. Our feedback loops with process chemists sharpen that focus. In both early discovery and process development, the bromomethyl handle opens doors for nucleophilic substitutions, Suzuki couplings, and other Pd-catalyzed transformations. We see direct interest from teams assembling diaryl frameworks and heterocycle side chains that need a resilient, bench-stable bromide. This isn’t just about providing a building block; it’s about providing a track record that’s been validated across dozens of bench and pilot-plant campaigns.
Polymer and specialty material labs have found ways to tune the backbone functionality of their projects using this compound. The ester group not only improves solubility in polar solvents but also behaves predictably during hydrolysis and transesterification. For anyone running analog searches or screening reaction conditions, the bromomethyl group acts without dragging unexpected side reactivity from the aromatic core. That difference—confidence in reactivity site selectivity—keeps waste streams clean and simplifies purification work later.
We’ve lost count of the number of times an R&D customer thanked us for a product that didn’t force a column chromatography rescue run due to shadow impurities. It may sound trivial, but every hour spent chasing down side products skews both the project timeline and costs. Direct feedback shaped our overhead filtration and packing operations. What sounds like a simple process—crystallize, filter, dry—requires experience and patience to get repeatable results on a real-world, scalable basis. We teach our production team these trade-offs, not just the steps but the “why” behind them.
Ethyl 4-Bromomethylcinnamate’s behavior under heat, light, and long storage sometimes gets overlooked outside the manufacturing plant. From the supplier’s vantage, those questions matter; failures or process drift rarely show up brightly in a single analysis. Experience taught us that reactivity tests—batch to batch, over multiple seasons—offer more insight than any single certificate of analysis. We keep both short-term accelerated aging studies and multi-month shelf-life samples under multiple conditions: cool, ambient, and elevated to simulate shipping environments. It’s the only way we trust the drum that leaves our gate mirrors the one we sampled after synthesis.
Clients have come to appreciate our willingness to share these findings. We don’t just recite a number for decomposition onset. Interested in how the product looks after six months sealed in the original packaging, or after cycling through docks in monsoon conditions? We open the records. Collaboration comes first; if a downstream process runs better at a slightly higher moisture target, or requests for a larger crystalline fraction roll in, we adjust at source, not just at the documentation stage. This attitude stems from years in the plant, not from a marketing desk.
Each drum tracks back to full batch records. Raw materials trace not just to supplier code but to actual delivery dates, lot numbers, and analytical receipts. In each monthly quality meeting, our team reviews flagged deviations, not only for compliance but for lessons and opportunities. In the odd—but inevitable—instance where a parameter missed target, we trace the dominoes right back to lab records or a vendor invoice. Real trust grows when problem-solving happens openly and upstream.
Most halogenated aromatic esters currently on the market cluster toward either chlorides or less-substituted domains, limiting synthetic options when seeking to vary functionality at the benzylic position. Ethyl 4-Bromomethylcinnamate breaks the mold. Not only does the para-bromomethyl group bring higher selectivity in substitution reactions, but it also provides a cleaner route for transition metal-mediated cross-couplings. Technicians who have spent weeks tuning conditions for mono- versus di-substitution know the frustration of halogen-label ambiguity—ours is analytically confirmed to minimize such cross-loading, particularly on the aromatic ring. Low-level homologue contamination, especially with 3- or 2-position substitutions, can sabotage scale-up runs, a pitfall we track with detailed NMR and mass spectra for every batch.
We’ve compared our process with generic suppliers in both domestic and overseas markets. In side-by-side reactions—acylation, Grignard addition, and catalytic hydrogenation—the consistency of our product means fewer unreacted starting material peaks and less drag-down in yields. Customers often share HPLC traces back after piloting our material, confirming the minimized tailing and shoulder peaks seen with lesser-purified competitors. With regulatory filings for pharma ingredients hanging in the balance, nobody wants to troubleshoot unexplained side peaks from the intermediate stage. This reflects what we see: discerning chemists are paying closer attention to the sources of their building blocks, moving away from bulk traders and toward dedicated chemical manufacturers who demonstrate repeatable quality over cycles of project work.
No chemical is immune to practical headaches, and Ethyl 4-Bromomethylcinnamate is no exception. Some customers, eager to cut process costs, attempted to work with recycled or partially downgraded bromomethyl intermediates—leading to sluggish reactions, repeated crystallizations, or even outright failed steps downstream. We’ve documented enough salvage campaigns to caution: starting with off-grade intermediates almost always costs more than the initial savings. Instead, we’ve developed a consultative support approach. Our own chemists can review customer reaction schemes, suggest work-up tweaks, and—if needed—adjust our purification protocol to hit new thresholds customers are after, not just historical targets.
Working side-by-side with production managers, we’ve tuned particle size distribution, filtered out troublesome fines, and adjusted solvent washes for specific customer needs. Not every situation demands further purification—many projects actually see higher throughputs and cleaner isolations from a slightly broader crystallization cut, compared to the brittle “ultra-pure” fraction some specs might suggest. We know this from real world, not just theory. Our plant operators work closely with our R&D team; every shift logs not only the obvious test outcomes but also “feel” notes—grind texture, bulk flow, sample color—which help interpret subtle changes even before formal analysis returns.
Shipping presents its own set of hurdles. Ethyl 4-Bromomethylcinnamate remains fairly robust for an ester, but prolonged exposure to sunlight or poorly vented containers shows up as color shifts and clumping that would never pass our own internal QC for re-packing. To avoid these situations, we designed packaging with thick, opaque liners and batch-labeled drums. In some cases, we use pre-chilled shipping for sensitive overseas orders approaching the end of our recommended shelf-life window. Most bulk handlers overlook this step, but it saves headache for users relying on just-in-time delivery in high-throughput manufacturing plants.
Project managers in pharma and material science report significant benefits from a single-source, transparent relationship with their intermediate supplier. We hear it over and over: reliable access and open communication with our technical team help them avoid costly surprises mid-campaign. We’ve built a library of process tips and troubleshooting notes—not generic user guides but real histories developed in collaboration with customers who ran into scale-up obstacles. Sometimes a minor drying tweak or an extra wash step prevents an entire lot from being scrapped. Our years in process troubleshooting go directly back into production improvements—the best training often comes from fixing something that went sideways, not just following a protocol by rote.
When we compare chromatographic traces between historical runs or troubleshoot a stalled reaction in concert with a customer’s lead chemist, we learn together. These joint efforts improve overall process design, not just the application of Ethyl 4-Bromomethylcinnamate. Over time, small changes—adjusted column solvent, re-optimized base choice, better sampling—add up to workflows that run smoother. Our willingness to document, share, and adjust methods with partners stands as proof of our role as a genuine manufacturer, not just a repackager or broker.
As our downstream clients push for more sustainable chemistry, Ethyl 4-Bromomethylcinnamate’s reactivity profile offers new flexibility in reducing hazardous reagents and fine-tuning functional group manipulations. Early-stage work shows promise for more direct, one-pot transformations in both pharmaceutical and specialty coatings markets. Collaborating on green chemistry routes, we’ve trialed solvent swaps and lower-energy isolation steps without trading away product integrity. Our R&D team works alongside customers developing flow-chemistry solutions that shrink solvent volumes and save energy during coupling steps using this intermediate.
Not every experiment works on the first attempt, but sharing setbacks as well as successes means the learning is real, not just surface-level. We write up each process modification and circulate lessons within our plant and to key customers, building trust and transparency along the way. Going forward, we encourage process chemists and sourcing managers to propose novel use cases or ask for tailored process variables. The best innovations often come from pushing the boundaries of standard practice—and as the original manufacturer, we can respond quickly, providing both product and process flexibility not available from generic sources.
Ethyl 4-Bromomethylcinnamate stands out not simply as another product on our line but as a direct outcome of our manufacturing philosophy. We believe that reliability, openness, and process understanding make the difference between a costly experiment and a successful production run. Every kilogram that leaves our plant carries years of experience, hands-on learning, and a willingness to help solve chemistry’s real-world puzzles. For those who care about where their materials come from and what happens when challenges arise, we welcome your questions, your feedback, and your toughest process problems. Manufacturing this compound is as much about partnership as it is about chemistry—and we look forward to setting new standards together.