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HS Code |
396854 |
| Chemicalname | 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid |
| Casnumber | 29066-91-5 |
| Molecularformula | C10H9BrO4 |
| Molecularweight | 273.08 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 235-240 °C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in ethanol and DMSO |
| Storagetemperature | Store at 2-8 °C |
| Synonyms | 3-Bromo-4-hydroxy-5-methoxycinnamic acid, Bromohydroxy methoxycinnamic acid |
| Boilingpoint | No data available |
As an accredited 3-Bromo-4-Hydroxy-5-Methoxycinnamic 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 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid, sealed with screw cap, labeled for laboratory use. |
| Shipping | 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid is shipped in tightly sealed, chemical-resistant containers, typically under ambient temperature, and protected from light and moisture. Handling complies with relevant safety and regulatory guidelines, including appropriate labeling and documentation. Transport by air or ground follows all chemical safety and hazard regulations to ensure safe delivery. |
| Storage | 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid should be stored in a tightly closed container, protected from moisture, light, and incompatible substances. Keep it in a cool, dry, well-ventilated area, ideally at room temperature or as specified by the manufacturer. Avoid heat and sources of ignition. Clearly label the container and restrict access to trained personnel. |
Applications of 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid in Industrial ManufacturingAs an established manufacturer with deep formulation and process insight, we supply 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid to specialized sectors where its unique molecular structure meets demanding industry productivity and quality requirements. The following real-world application scenarios provide detailed, differentiated information for supply chain professionals and downstream production managers. 1. Pharmaceutical Intermediate for Targeted Oncology APIsLeading pharmaceutical firms use this compound as a highly selective intermediate in developing active pharmaceutical ingredients (APIs) for next-generation anticancer drugs, notably those targeting kinase or epigenetic pathways. It is chosen for its consistent acid bromide reactivity and low impurity background, enabling reliable synthesis routes for late-stage intermediates. Chemists integrate it at a precise stage of molecular assembly to achieve the necessary aromatic substitution and maintain stringent safety, traceability, and impurity controls according to regulatory requirements. Industry compliance standards
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2. UV-Absorbing Monomer Synthesis for Specialty PolymersProducers of high-performance polymers select this material for its cinnamic backbone in the manufacture of UV-stable specialty resins. Its structure delivers potent absorption in the UVA and UVB spectra, essential for fabricating weather-resistant coatings and optical plastic components. Materials scientists employ it as a functional monomer or comonomer, blending it during polymerization to introduce photoprotective properties into copolymer chains, thus reducing photo-degradation risk in critical outdoor, automotive, and optical applications. Industry compliance standards
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3. Chemical Probe Synthesis in Biomedical ResearchResearch institutions and custom chemistry labs utilize this compound as a scaffold in the synthesis of molecular probes for signal pathway analysis and protein labeling studies. Its electron-rich aromatic system supports high reactivity for the selective tagging of biomolecules, allowing for efficient bioconjugation or fluorescent tag addition. Researchers typically employ this intermediate at a strategic synthetic step to introduce distinctive chemical handles for downstream probe modification, supporting robust analytical characterization and reproducibility under regulated laboratory conditions. Industry compliance standards
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4. Fine Chemical Synthesis for Agrochemical DiscoveryAgrochemical R&D groups incorporate this raw material into discovery-phase synthesis programs to construct novel lead candidates for crop protection. Its brominated cinnamate framework offers a customizable platform for assembling analogs with selective herbicidal or fungicidal profiles, particularly for structure–activity relationship (SAR) studies. It participates in key step reactions such as hybridization with heterocyclic moieties, enabling controlled introduction of bioactive functionalities while maintaining production batch records compliant with agricultural sector validation protocols. Industry compliance standards
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5. Photocurable Resin Additive in Electronic EncapsulantsElectronics encapsulation manufacturers use this component as a UV-absorbing and stability-enhancing additive in photocurable resins for protective electronic packaging materials. The acid’s molecular configuration provides tailored photoreactivity, supporting dimensional stability and extended service life under intense UV exposure conditions typical of high-power LED arrays and sensor modules. QC teams validate the integration stage to assure homogeneity and performance across encapsulant lots designed for rapidly-evolving electronics applications. Industry compliance standards
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Competitive 3-Bromo-4-Hydroxy-5-Methoxycinnamic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid that leaves our facility reflects years of close attention to detail, rigorous quality management, and a dedication to real-world usability. As a manufacturer, we judge ourselves by reproducibility and trust. Researchers, pharmaceutical developers, and specialty chemical teams have come to rely on us because we never shortcut on grade or accountability.
We make 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid for labs and businesses that need certainty. We synthesize and purify this compound using techniques shaped by group expertise, process refinement, and honest feedback from partners who use it every day. What sets this product apart isn’t simply its specifications—those are just the foundation. The difference comes from people who watch every step, check every variable, and solve bottlenecks before they move downstream into your workflow.
Our typical lot analysis lands between 98% and 99.5% purity by HPLC, and we confirm structure with NMR and mass spectrometry. Appearance, melting range, and elemental analysis stay consistent across lots, matched from initiation to packaging by technicians who can distinguish subtle variances long before a sample ever reaches your bench. We don’t just follow a checklist; we document, verify, and challenge our processes with each cycle, focused on what matters during scale up or exploratory screening.
For molecular researchers and drug discovery teams, 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid offers a rare combination of a selectively substituted aromatic ring and cinnamate backbone. Our process minimizes side products that complicate downstream functionalization—less risk of halogen migration, methylation artifacts, and phenol instability which can otherwise trip up syntheses at larger scales. Unlike off-the-shelf intermediates that sometimes display questionable reproducibility or mismatched analytical spectra, we send an actual sample from every batch for independent third-party verification.
We produce 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid because medicinal chemists, biologists, and agrochemical innovators ask for it by name. This molecule often turns up in screening libraries for enzyme inhibition, oxidative stability tests, and as a functional handle in synthetic programs looking to build novel amides, esters, or ethers. We have seen clients use it for kinase target validation, fluorescent probe development, and structure-activity relationship (SAR) studies, where predictable performance in multistep reactions makes long-term planning possible.
Conversations with partners have shown us that small differences in reactivity, color, or micro-impurities can set back months of work. Synthetic libraries that rely on uniform halogenation or require further derivatization benefit from our material’s absence of aromatic over-bromination or O-demethylation byproducts. Some customers told us about timelines blown by failed coupling reactions traced to a competitor’s inconsistent product. Experiences like these remind us that incremental improvements in purification aren’t minor—they’re the reason projects stay on track or hit bottlenecks.
Dose-response studies and receptor binding assays benefit from our strict batch-to-batch analytical standards. Many of our clients—academic, corporate, and startup—share data with us on performance in solid-phase synthesis or fragment-based drug discovery. That dialogue gives us real-world insight into what helps or hinders innovation, and we pour that knowledge back into improved workflow control and open documentation standards.
We owe our reputation as a chemical manufacturer to our transparency and relentless troubleshooting at the bench. Our knowledge started on scales smaller than a single gram, and we continue to question each new scale-up to root out unanticipated byproducts or inefficiencies. Years of running parallel chromatographic purifications, adjusting reaction atmospheres, and fending off moisture ingress taught us that purity is never the only goal—predictable handling and reproducibility matter just as much, especially when scaling for process validation or new product launch.
Pharmaceutical development often requires quick adaptation based on pilot results. With this acid, we offer documentation with full analytical spectra. Buyers told us they value clear traceability—knowing where, how, and when reagents entered the cycle. That means fewer surprises at QA review and greater confidence during regulatory submissions. It means when your team receives material from us, you’re gaining access to the story behind each batch, not just a label and lot number.
Several major research groups shared that reaction yield, downstream coupling success, and bioassays hinge not only on overall grade, but also on the right impurity profile. They worked with competitors who centered on price, only to discover chromatographic inconsistencies and hidden batch differences. Our ability to control for even small process variants makes our withstanding performance possible. Direct input from users in the field gives us a picture of the compound’s unique strengths in biological stability and synthetic accessibility compared with other halogenated cinnamates or structurally similar phenolic acids.
Chemists often ask what separates this molecule from related derivatives like para-methoxy, meta-bromo, or plain hydroxycinnamic acids. Every functional group on the aromatic ring influences reactivity, solubility, and downstream application. For instance, a different regioisomer may demand harsher conditions for further coupling. We have compared parallel syntheses using 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid and its isomers, and observed smoother esterification and greater photostability with the bromo at the 3-position. The methoxy group slows oxidation and helps mitigate handling risks for heat-sensitive downstream reactions—a detail flagged by both academic and production partners in their process notes.
Across common uses, the position of the bromine distinguishes our product from meta- or para-bromo cinnamic acids. This subtlety affects both chemical reactivity and safety handling. We focus tightly on ring substitution because customers using the compound for SAR suite building, peptide tagging, or azide-alkyne click chemistry report dramatically different outcomes depending on where halogenation occurs. The collaborative work we have done to optimize extraction, minimize light-driven decomposition, and support lyophilization for those working with small quantity protocols pays off in feedback—teams cite our batch stability and predictability as unique among suppliers.
By keeping lines open with labs specializing in combinatorial chemistry, photodynamic therapeutics, and natural product mimics, our manufacturing team hears firsthand which differences support efficiency at the bench. That real-world conversation can’t come from reading certificates alone—it only comes from building, breaking, and re-building synthetic methods together, then documenting which steps consistently deliver on yield and reproducibility.
We invest in QC not out of routine, but from collective experience troubleshooting failed syntheses and mischaracterized intermediates. Our technologists talk openly with the chemists who depend on this grade. They know that each new batch isn’t just about checks on an assay form, but about keeping margins of error razor-thin for teams who plan months ahead. Batches pass through hands-on chromatography, in-process audit trails, solvent log monitoring, and fine-scale drying protocols. Teams remembered how an undetected moisture band in a comparable product from elsewhere delayed whole project milestones. It reinforced our commitment to routine Karl Fischer titration as a standard practice—not to mention real-time digital tracking of individual lot storage, packaging, and shipment conditions.
Our R&D group keeps a running archive of spectral data, not just for compliance but to resolve trace questions long after product shipment. Real stories from customers who flagged minor peak shifts or asked for alternate analytical runs—sometimes for regulatory review, sometimes for process validation—drive us to keep primary data and methodological transparency as ongoing priorities. That culture comes from our background in both academic and industrial labs, where everyone understands that even minor changes in a profile can have major downstream effects.
Sourcing raw materials for this compound means digging deeper than the usual vendor lists. Our procurement team chases not just price, but supply chain traceability, solvent background, and environmental impact from basic starting materials through to final waste disposal. That process often uncovers unexpected variables—a slightly different brominating agent, a regional disparity in methoxy group suppliers—each of which risks subtle impurities or unanticipated reaction inefficiencies. We document the impact of each shift, from filtration method changes to on-site storage impacts, and let customers know what to expect up front.
Environmental health and worker safety influence our day-to-day synthesis. Our facility has moved toward closed handling systems, minimal operator exposure to volatile agents, and routine in-process checks for byproduct volatilization. We have reduced solvent use by process innovation and taken steps to recover, recycle, or safely neutralize waste streams associated with bromination. The drive for purity and stability in this product goes hand-in-hand with lowering the broader ecological impact—a goal our technicians and partners both see as shared responsibility.
Our team never assumes that existing best practices suit every new user. Project teams often approach us with questions about solvent compatibility, scale-up planning, or unexpected issues unique to their workflow. Some partners perform derivatization, others run long-duration biological assays; both groups need confidence the product will behave as expected. Whether adjusting particle size by custom grinding or guiding prep for lyophilization, our production chemists work directly with collaborators, troubleshooting not just for purity, but for practicality during their own runs.
One example arose from a team building a combinatorial kinase inhibitor library—they noted that minor pH shifts in their stock prep could alter spectral features, so we customized drying conditions to keep water content low and batch stability high. Our collaborative approach, developed over years working side-by-side with direct users, brings value that a generic supplier model cannot offer. We share operative details, real spectra and run logs, empowering partners to optimize their experiments, not just adapt to generic products.
Teams developing new screening assays require reliable building blocks, especially as scientific questions grow more complex. Developers working with 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid have integrated it into metabolic targets and photoactive signaling molecule research. The compound’s flexible reactivity opens possibilities in enzyme immobilization, esterification, and both traditional and green synthetic chemistry. Each use case loops back to us, offering stories of success and areas for improvement. We treat these engagements as chances to expand both our chemical know-how and our sense of shared stewardship with those forging ahead in biomedical discovery, materials research, and specialty manufacturing.
Our purpose-driven process means our staff never stops looking for small technical improvements that can translate into outsized impact at the bench. Whether through cleaner crystallization, optimization around hazardous intermediates, or deeper end-use collaboration, we continue to shape and refine every lot we create. Security in the details—batch after batch—builds the foundation for bold new work in medical science, chemical engineering, and research progress worldwide.
The ongoing partnership between production chemists and our customers animates the way we see quality. It’s not just about molecules traded in the abstract, but about the concrete reliability that underpins experiment, innovation, and business alike. By manufacturing 3-Bromo-4-Hydroxy-5-Methoxycinnamic acid with an ear to the ground—listening, tweaking, refining—we enable teams to focus on challenges that matter, knowing their core building blocks won’t let them down. That is the value of manufacturing with purpose, and the benchmark we aim to set for every lot shipped, every time.