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Ethyl 4-Bromomethylcinnamate

    • Product Name Ethyl 4-Bromomethylcinnamate
    • Alias Ethyl (E)-4-(bromomethyl)cinnamate
    • Einecs 632-391-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Ethyl 4-Bromomethylcinnamate

    Applications of Ethyl 4-Bromomethylcinnamate in Industrial Manufacturing

    Ethyl 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 Synthesis

    Downstream 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 211 Current Good Manufacturing Practice
    • Ph. Eur. (European Pharmacopoeia) monographs relevant to intermediates
    • ISO 9001:2015 certified quality management system

    Typical usage ratio

    • 0.8–1.2 mole equivalent in condensation or substitution step, adjusted based on the molecular stoichiometry of the target API

    Downstream process integration

    • Charged during the intermediate synthesis stage, followed by selective catalysis or further halogenation, depending on the target molecule
    • Residuals monitored in multi-stage purification and crystallization

    Final product types

    • Brominated API precursors
    • Active pharmaceutical salts
    • Fine chemical intermediates for further modification

    2. Fragrance Intermediate for Aroma Compounds

    Leading 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

    • IFRA (International Fragrance Association) safety standards
    • EU REACH Regulation for chemical registrations
    • ISO 9235 Natural aromatic raw materials requirements (if blended with naturals)
    • Good Manufacturing Practice as per ISO 22716

    Typical usage ratio

    • 2–6% of total synthetic intermediate pool in batch formulas, subject to desired aromatic profile

    Downstream process integration

    • Enters as a substrate for reductive alkylation steps or further esterification, depending on the end aroma molecule design
    • Processed under monitored thermal and pH-controlled conditions to ensure profile consistency

    Final product types

    • Aromatic aldehyde bases for perfumery
    • Complex esters used in flavor and fragrance blends
    • Custom aroma compounds for premium consumer products

    3. Fine Chemical Synthesis for Agrochemical Intermediates

    Major 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

    • OECD Principles of Good Laboratory Practice (GLP) for synthesis validation
    • FAO/WHO recommendations for pesticide quality
    • EC Regulation 1107/2009 for plant protection product approval (EU)
    • ISO 9001:2015 quality assurance for agrochemical precursors

    Typical usage ratio

    • 0.95–1.15 mole ratio for bromination/esterification steps, depending on the target active ingredient structure

    Downstream process integration

    • Used in initial coupling or halogen-exchange step; end-point analysis ensures conversion before further derivatization
    • Material balance and impurity profiles archived to meet safety dossier requirements

    Final product types

    • Brominated cinnamate herbicides
    • Precursor esters for fungicidal agents
    • Synthesis intermediates for pest management formulations

    4. Specialty Polymer Monomer in Functional Materials

    Manufacturers 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

    • ISO 9001:2015-certified processes
    • RoHS Directive 2011/65/EU for chemical content in end-use electronics or consumer goods
    • REACH registration for specialty monomers (EU)
    • ASTM D256 for polymer impact resistance, where relevant

    Typical usage ratio

    • 1–5% monomer incorporation by weight, adjusted based on desired copolymer functionality and application end-use

    Downstream process integration

    • Fed into bulk, solution, or emulsion polymerization reactions as a co-monomer or chain-modifier
    • Real-time monitoring of conversion rate and residuals during the polymer build process

    Final product types

    • UV-curable resins
    • Specialty copolymers with enhanced chemical resistance
    • Advanced materials for coatings or microelectronics

    5. Intermediate for Photoinitiator Manufacture in UV-Curable Systems

    Manufacturers 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

    • ISO 14001 environmental management for chemical plants
    • REACH compliance for polymer and coating chemicals
    • OECD GLP for process validation in photoinitiator development
    • ASTM D7767-11 for UV-cured coating application testing

    Typical usage ratio

    • 0.8–1.3 equivalents in the photoinitiator’s synthetic coupling step, adjusted for UV absorbance specification targets

    Downstream process integration

    • Engaged in esterification or alkylation step before final photoinitiator molecule assembly
    • QC ensures absence of residual intermediates and consistent photoactivation performance

    Final product types

    • Benzoin-structure photoinitiators for inks
    • UV-curable coating photoinitiator blends
    • Cinnamate-derived initiators for lacquer and overprint varnishes

    6. Fine Organic Synthesis in Research and Development Laboratories

    Chemical 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

    • ISO 17025 accreditation for R&D analytical chemistry
    • OECD GLP for chemical research protocols
    • Material Safety Data Sheet (MSDS) and full traceability documentation
    • Journal-referenced characterization standards (NMR, HPLC, MS)

    Typical usage ratio

    • 0.05–1.0 mole-scale trials, adjusted for preparative or analytical-scale synthetic requirements

    Downstream process integration

    • Added as a key intermediate in stepwise synthetic routes, often via controlled bromination or ester-functionalization
    • Purified post-reaction to meet tight analytical specs for experimental uses

    Final product types

    • Reference standards
    • Synthetic intermediates for patent applications
    • Novel organic compounds for academic or industrial R&D
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    Certification & Compliance
    More Introduction

    Ethyl 4-Bromomethylcinnamate: Our Approach to Purposeful Chemical Manufacturing

    Standing Out in the Field of Specialty Intermediates

    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.

    Physical Properties and Batch Qualities That Matter in Synthesis

    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.

    Usages Driven by Real Process Demands

    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.

    Process Reliability and Traceability: Beyond Just Purity Specs

    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.

    How This Product Differs From Other Halogenated Aromatic Esters

    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.

    Tough Lessons from the Field: What We’ve Learned with Customers

    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.

    Supporting Projects that Rely on Consistent Outcomes

    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.

    Looking Ahead: New Developments and Customer-Led Innovations

    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.

    Commitment Without Compromise

    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.