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3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin

    • Product Name 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin
    • Alias Brodifacoum
    • Einecs NA
    • 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

    510062

    Chemical Name 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin
    Molecular Formula C34H25BrO3
    Molecular Weight 561.47 g/mol
    Appearance Powder or crystalline solid
    Solubility DMSO, chloroform, and other organic solvents
    Purity Typically ≥98% (when commercially available)
    Storage Temperature 2-8°C (refrigerated)
    Iupac Name 4-hydroxy-3-[3-(4'-bromobiphenyl-4-yl)-1,2,3,4-tetrahydronaphthalen-1-yl]-2H-chromen-2-one

    As an accredited 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 10 g amber glass bottle, sealed, labeled with name, CAS number, purity, and safety precautions.
    Shipping Shipping of 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin is conducted in accordance with applicable chemical safety regulations. The compound is securely packaged in sealed, labeled containers with appropriate hazard documentation. Temperature and light protection are ensured to maintain sample integrity during transit. Shipping complies with relevant international and local guidelines.
    Storage Store 3-[3-(4'-Bromobiphenyl-4-yl)-1,2,3,4-tetrahydro-1-naphthyl]-4-hydroxycoumarin in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerator temperature). Keep away from incompatible materials such as strong acids, bases, and oxidizing agents. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety and chemical hygiene protocols during storage and handling.
    Application of 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin

    Applications of 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin in Industrial Manufacturing

    As an experienced manufacturer in advanced fine chemical synthesis, we support downstream industries with high-purity 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin. Our clients rely on its defined molecular structure and consistent batch quality for specific applications spanning high-performance coatings, pharmaceutical intermediates, OLED emitter development, and specialty analytical reagents. Below, we detail the principal industrial segments deploying this raw material, outlining compliance, dosage, process integration, and end product output for each use.

    1. Pharmaceutical Intermediate for Anticoagulant Synthesis

    In the pharmaceutical sector, this compound acts as a key active building block for the synthesis of highly selective 4-hydroxycoumarin anticoagulant derivatives. Dedicated process streams utilize its unique aromatic structure to achieve desired binding characteristics. The inclusion of the bromobiphenyl moiety allows for late-stage functionalization in medicinal chemistry workflows.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monograph 01/2024:1175 and associated impurity thresholds
    • US FDA 21 CFR part 211 Drug Manufacturing standards
    • ChP (Chinese Pharmacopoeia) requirements for synthesis and assay

    Typical usage ratio

    • Employed at 0.8–1.2 molar equivalents, determined by route-specific stoichiometry for intermediate coupling reactions. Adjustments occur based on batch scale and purity profile of other reactants.

    Downstream process integration

    • Introduced during second-stage condensation or cyclization steps, following the initial benzylation of coumarin ring. Maintains molecular integrity through purification and proceeds into final API crystallization or salt formation units.

    Final product types

    • Oral anticoagulant active ingredients for regulated generic and patented drugs
    • API intermediates for contract manufacturing organizations
    • Reference standards for clinical product release

    2. Specialty Dye Intermediate for Fluorescent Pigments

    Advanced pigment and dye producers utilize this coumarin structure in synthesizing high-intensity fluorescent materials, leveraging its extended pi-conjugation for specific emission spectra required in forensic, textile coloration, and security ink markets. The presence of the 4'-bromobiphenyl unit further enables precise halogenation modifications in downstream organic synthesis.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile dyes
    • ISO 9001:2015 Quality Management for pigment production
    • REACH (EC 1907/2006) chemical registration
    • DIN EN 71-3 for heavy metal and migration tests on toy inks

    Typical usage ratio

    • Blended at 0.2–0.5% w/w in concentrated dye formulations, with precise calibration based on target color fastness, brightness index, and solvent system compatibility.

    Downstream process integration

    • Inserted into the core condensation phase for pigment precursor synthesis, typically after initial nitration and reduction. Follow-up steps involve sulfonation or halogenation for desired dye characteristics.

    Final product types

    • Fluorescent inks for official document security printing
    • Special effect dyes for textile and thread manufacturing
    • Forensic marker solutions and UV-detectable coatings

    3. OLED Emitter Synthesis for Display and Lighting Applications

    Material R&D teams in the optoelectronics sector employ this advanced coumarin derivative as a molecular precursor for small-molecule OLED emitters, utilizing its rigid aromatic core for charge transport layers and tunable emission in blue-green spectra. Its unique tetrahydronaphthyl ring assists in controlling aggregation and device longevity.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances
    • JEITA ED-7307 for electronic material traceability
    • IEC 62321 for chemical material testing in electronics
    • ISO 14001:2015 for environmental management in display supply chains

    Typical usage ratio

    • Used at 1.5–2.5% molar content within emitter and host blend layers, adjusted based on quantum yield and device efficiency targets, further refined via spin-coating or vapor deposition protocols.

    Downstream process integration

    • Introduced into organometallic complex formation or directly into physical vapor deposition feedstocks before layer stacking onto ITO glass substrates. Post-integration, annealing ensures charge mobility uniformity.

    Final product types

    • AMOLED panels for high-definition mobile devices
    • Solid-state lighting emitters with high CRI (Color Rendering Index)
    • OLED-based security display elements

    4. Analytical Reagent for Biochemical Detection Kits

    Producers of high-precision diagnostic and analytical test kits employ this compound as a sensitive reagent in coumarin-based fluorescence and chromogenic assays. Its structure allows selective labeling and detection reactions, necessary for bioanalytical quantification platforms and environmental monitoring systems.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management for diagnostic reagents
    • CLSI (Clinical and Laboratory Standards Institute) GP44 for reagent verification
    • EU In Vitro Diagnostic Regulation (IVDR) 2017/746
    • FDA 21 CFR 809 for in vitro diagnostic products

    Typical usage ratio

    • Standardized at 0.01–0.2% w/v in final detection solutions, titrated based on assay response threshold and required detection limits in fluorescence microplate or HPLC platforms.

    Downstream process integration

    • Introduced post-buffer formulation during coupling to target analytes or enzyme-linked conjugates, followed by freeze-drying or lyophilization to stabilize the finished reagent kit components.

    Final product types

    • Fluorescence-based ELISA kits
    • Chromogenic substrates for clinical biochemistry analyzers
    • Trace pollutant detection strips for environmental monitoring
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    Certification & Compliance
    More Introduction

    3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin: Reflections from the Manufacturing Floor

    Our Direct Experience with 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin

    Every product coming out of a chemical reactor tells a story about the process, the technicians behind the controls, and the clients waiting for it to show up in their R&D pipeline. 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin, which some in the lab shorten to “Bromo-biphenyl-naphthyl coumarin,” represents countless hours of method development, insights gained from practical setbacks, and a steady refining of our procedures to meet sharply defined standards.

    In the early days, the conversation about this compound often came up as if it was just another custom intermediate. Quite a few in the field met the request with skepticism. Handling a biphenyl-brominated core with a naphthyl bridge, capped by a hydroxycoumarin, took more than skill with the glassware. It meant choosing the right grade of every starting material, running TLC checks after every step, and optimizing column load so that every gram of product cleared the required tests for purity. We have gone through enough iterations to learn the quirks of recrystallization, washing, drying, and packaging that get this compound off the line without unnecessary degradation or contamination.

    From Bench to Scale: Manufacturing Insights

    Scaling a synth like this pushes the team to look for solid, repeatable results. The best process on paper doesn’t always hold up when the solution volume shifts from 50 ml in the hood to 10 liters on the shop floor. Specific to this molecule, solubility in different solvents, reaction kinetics, and byproduct formation have to be monitored through each batch. During chromatography, it’s easy for tailing peaks to crowd the main product. During isolation, humidity and even the temperature of the filtration glassware factor into yields, occasionally swinging by several percentage points if someone skips a step.

    The product runs off with a strong yellow-brown hue. Analysis by NMR, HPLC, and elemental techniques consistently tells us about the real chemical story inside, letting the technical crew spot polymorphic forms and minor impurities. These analytical repetitions have driven us to invest in more precise metering pumps, automated temperature control for sensitive coumarin cyclization steps, and custom drying techniques that rip out traces of solvent, so the shipped batch matches its stated specification. Every production run records batch numbers, raw material origins, and operator signatures to leave a defensible trail—an important point when customers run their own independent verifications.

    What Makes This Coumarin Derivative Unique

    Our clients look for a handful of coumarin-based molecules, but this particular one stands out because of its molecular backbone. The rigid biphenyl-bromide moiety offers a reliable platform for further transformations, while the hydroxycoumarin end gives it promise as a building block for bioactive compounds. Clients in medicinal chemistry point to its potential for interacting selectively with protein active sites, thanks to the shape and electron distribution of the coumarin unit.

    We often compare its behavior to simpler coumarins or unmodified biphenyl derivatives. In those molecules, functionalization sometimes happens too early or in the wrong place. With this structure, the bromide’s position allows smooth entry points for Suzuki, Stille, or Buchwald cross-coupling, letting researchers build out larger conjugates without dealing with wild side reactions. The naphthyl segment rounds out molecular rigidity, stabilizing the desired orientation of the entire framework. When chemists look for a heavy-atom coumarin core with precise anchoring, this molecule lands near the top of the list.

    Physical handling differs, too. The crystalline solid requires specific moisture controls during packaging. Inadvertent exposure to ambient humidity over a weekend can turn an easily flowable powder into a stubborn cake, causing lost time and costly repackaging efforts. Our production notes stress careful management of desiccator protocols and immediate vacuum-sealing after final QC.

    Application Trends: What the Cropped White Coats Are Doing with It

    The biggest users of this molecule come in from medicinal or organic opto-electronics research. On the medicinal chemistry side, the compound serves as an advanced intermediate. It fits projects driven by the search for novel anticoagulants, though final applications branch out into enzyme inhibitors, anti-inflammatory leads, and fluorescent tagging scaffolds for bioimaging. The naphthyl-enhanced rigidity improves selectivity, and more chemical developers ask after this type of molecular shape as they chase patentable structures that dodge the existing thicket of protected pharmaceutically active compounds.

    Other labs working in material science have requested this product for use in new types of fluorescent films or light-responsive polymers. The combination of heavy atom (bromine), conjugated pi-systems, and a polar hydroxy makes it useful in testing energy transfer, charge mobility, or as a dopant in organic light-emitting diodes. Our newer clients bring up interest in two-photon absorption efficiency, hoping the structural features translate into superior performance for their optical or sensor projects.

    Traditional derivatives, often featuring simpler aromatics or lacking a bromine anchor, do not provide the same cross-coupling flexibility. Without this, a series of expensive and time-consuming protection-deprotection steps creeps into their syntheses, raising costs and risks of low yield for the next molecular step. We've fielded requests from contract synthesis groups who tried making this compound themselves, only to discover that inconsistent starting materials and subtle process factors led to product batches that failed on both HPLC purity and biological activity.

    Challenges in Quality and Process Integrity

    On the scale-up side, the greatest hurdle with this molecule reveals itself during crystallization and filtration. The sticky, resinous mother liquor can trap significant amounts of the product, frustrating attempts to achieve target yields. Our troubleshooting teams worked through combinations of temperature cycling, varying solvent mixes, and agitation speed to land on a protocol that frees up more product from sticky residues.

    Each time we adjust a control parameter, production records reflect both immediate yield changes and impact over several subsequent batches. It takes a willingness to experiment and adjust based on frontline operator feedback, not just following the established literature. Few publications capture all the nuances of actual shop floor conditions: ambient air shifts, batch-to-batch raw material differences, or microvariations in glassware cleanliness. Cleanroom protocols, tight scheduling, and team communication help keep every reaction on its rails.

    Quality holds meaning beyond the sheet showing purity percentages or melting points. Overdrying can fracture crystals, making blending and transfer more difficult. Underdrying can lead to agglomeration in bulk containers during shipping. Some of our manufacturing refinements have pared back unnecessary solvent steps, not only for cost reduction but to minimize residual solvent traces that prompt flags at the receiving end. Consistency in particle size and bulk density, monitored during each batch, supports uniform dissolution behavior, predicted by our own in-house analytics and verified by customer feedback.

    Certainty in Supply: Building Trust through Manufacturing Experience

    Every batch produced stands on the foundation of collected experience. Trust with clients grows out of transparency—documented deviations, corrected in real-time, and shared across batches. Many customer complaints stem not from pure missing shipments, but from differences between pilot-scale and bulk quantities. A single chemical’s behavior shifts as equipment size, room temperature, or operator technique adjusts with scale. We track and adapt to these factors, avoiding cookie-cutter answers about process stability. Over time, repeated shipments of this complex coumarin have shown that investing in stable raw material suppliers and technical training for staff pays back in the consistency that researchers and production chemists demand.

    Many manufacturing facilities focus on common or commodity-grade coumarins, producing them at larger scale. In contrast, our team focuses on advanced intermediates like this brominated coumarin-naphthyl hybrid, handling limited volumes but placing more weight on traceability and reproducibility. This chemical never sees open-bid auctions, site brokers, or unsupervised repackaging. Each request for this compound cycles through our technical team, who review process notes before every run and stick closely to signed-off batch sheets. We define our production runs by product identity, analytical profile, and by feedback loops to customer labs, not by unstated “industry standard” grades.

    Industry Regulation and Responsible Production

    Oversight from regulatory authorities, environmental standards, and health and safety agencies shapes each piece of this compound’s production. The bromide content, potential for naphthyl-origin byproducts, and reactivity of coumarin-based molecules each bring their own monitoring requirements. Waste streams route through established destruction, not simply down the drain, and each drum reflects the work that goes into safe, compliant handling.

    Process changes, from updating a solvent to tuning a pH level, receive pre-review, often involving multiple rounds of safety checks and risk assessments. The manufacturing crew takes the training protocols seriously because missed steps cost more than just numbers on a spreadsheet—they ripple out to packaging returns, lab rework, and broken trust. Each gram of product that ships out reflects not just reaction efficiency but a background of personal responsibility in the handling of hazardous materials.

    Staying Ahead in a Rapidly Shifting Chemical Landscape

    Research demand spikes unpredictably. As more universities, life science companies, and technology startups chase new lead compounds, the specificity of intermediates like this one rises. Many of the big catalog suppliers promise every structure under the sun but treat complex molecules as afterthoughts. We make our living not by speculating on price swings or chasing marketplace trends, but by learning every variable in our process and updating with customer needs. Last batch caught a new impurity on the NMR? It goes straight into the process update for the next run, archived for anyone who needs to replicate the batch next quarter or next year.

    Some labs attempt in-house synthesis, and their feedback keeps us sharp. Hearing about struggles with incomplete coupling, polymerization, or persistent traces of starting biphenyl helps us build detailed technical documentation and troubleshoot shared problems. Direct feedback has driven us to create custom sample sizes for early-stage screenings, so researchers waste less time on stock solutions that may not survive more than a few days in the fridge.

    Competitive products lack the combination of ease in cross-coupling and final crystallinity. Others carry more problematic byproducts, resulting from faster, cheaper processes using higher-temperature steps that risk rearranged coumarin backbones. By producing and purifying in-house without outsourcing, we retain immediate control over each parameter, responding to process observations rapidly and minimizing lag between discovery and solution.

    Supporting Next-Generation Science

    This product’s journey doesn’t stop at our warehouse. Finished molecules land in screeners for enzyme assays, go through patenting stages with major pharmaceutical applicants, or end up in device prototypes on the material science end. The team takes satisfaction tracking published outcomes; our clients occasionally share spectra, patent numbers, or thanks for the reliable deliveries that let them focus on discovery, not resupply.

    The generation of data that tracks from our records through customer labs into published results matters for everyone in the pipeline. The discovery that starts in our reactor glass might show up down the line as a key step in next-generation antibiotics, high-performance electronics, or new fluorescence tags for live cell imaging. Knowing our process stays robust—backed by cross-checked certificates of analysis, traceable batch numbers, and responsive technical dialogue—strengthens the field as a whole.

    Final Thoughts from the Manufacturer's Perspective

    Batches of 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin do not simply roll off the end of a generic production line. Making this complex coumarin derivative demands investment in equipment, technical skills, and shared knowledge—not just among management or senior chemists, but by every operator weighing out powders or tracking fill times on drying ovens. Where others see just a long name or a complicated molecular diagram, we see the sum of hands-on trial, error, and learning translated into reliable results for outside researchers.

    Our commitment runs through every step, from selecting the right raw materials, protecting the finished product from moisture or oxygen, and responding to customer feedback with real improvements to the next batch. Every gram tells a story that links our technical team with the wider world of innovation, supporting science with concrete results from our own experience, not just what’s written in the literature. This approach, rooted in practical know-how and commitment to the researcher’s needs, continues to push quality and reliability forward—one batch, one molecule, at a time.