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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: Bromadiolone
    • Einecs: NA
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    369341

    Iupac Name 3-[3-(4'-Bromobiphenyl-4-yl)-1,2,3,4-tetrahydro-1-naphthyl]-4-hydroxycoumarin
    Molecular Formula C32H23BrO3
    Molecular Weight 535.43 g/mol
    Appearance Off-white to pale yellow crystalline powder
    Solubility Soluble in organic solvents such as DMSO and chloroform
    Purity Typically ≥98% (HPLC)
    Storage Temperature Store at 2-8°C, protected from light
    Chemical Class Coumarin derivative
    Structural Features Contains a brominated biphenyl group, naphthalene moiety, and a 4-hydroxycoumarin core
    Applications Research in anticoagulants, organic materials, and medicinal chemistry
    Synonyms No widely established synonyms

    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 Amber glass bottle, 1 gram, sealed with a screw cap and tamper-evident seal, labeled with chemical name and hazard information.
    Shipping This chemical is shipped in a tightly sealed, high-density polyethylene (HDPE) bottle, cushioned within certified hazardous materials packaging. It is transported under ambient temperature conditions, protected from light and moisture, and accompanied by all necessary safety documentation to comply with international shipping regulations for hazardous laboratory chemicals.
    Storage 3-[3-(4'-Bromobiphenyl-4-yl)-1,2,3,4-tetrahydro-1-naphthyl]-4-hydroxycoumarin should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Store at 2–8°C (refrigerated) and avoid prolonged exposure to air. Use appropriate protective equipment when 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 original chemical raw material manufacturer, we supply 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin for several high-value industrial applications. This specialty molecule serves critical roles in advanced sectors including pharmaceuticals, specialty chemicals, and material sciences, supporting precise process integration and stringent compliance required by leading global manufacturers.

    1. Anticoagulant Active Pharmaceutical Ingredient (API) Synthesis

    Our material functions as a core structural intermediate in the synthesis of several next-generation coumarin-based anticoagulant APIs. Pharmaceutical formulators employ this compound as a late-stage coupling agent, facilitating selective bromination and aromatic substitution. This route generates advanced oral anticoagulant candidates with targeted bioactivity. Formulators apply controlled conditions to optimize yield and minimize isomerization, supporting strict batch reproducibility critical in regulated drug manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (GMP) for APIs
    • US Pharmacopeia (USP) guidelines for anticoagulant synthesis
    • European Pharmacopoeia (Ph. Eur.) monographs referencing related coumarin derivatives
    • FDA 21 CFR Parts 210 and 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • Employed at 0.6–1.5 molar equivalents relative to final API yield, adjusted by downstream step and impurity profile management

    Downstream process integration

    • Introduced during aromatic coupling after naphthalene scaffold assembly
    • Purification follows oxidative cyclization and halogenation
    • Feedstock for subsequent sidechain modifications or salt formation
    • QC monitored by HPLC and NMR per cGMP protocols

    Final product types

    • Oral anticoagulant tablets (finished pharmaceuticals)
    • Injectable anticoagulant formulations
    • Coumarin-derivative intermediate bulks
    • Pharmaceutical reference standards

    2. Fluorescent Dye Precursors for Life Sciences

    Research reagent producers and diagnostic kit manufacturers rely on this material as a source of high-affinity coumarin dye scaffolds. The compound’s rigid, conjugated core allows specialized derivatization for stable blue to green emission. Custom syntheses convert the naphthyl and biphenyl moieties to unique labeling handles, supporting demand for robust fluorescence in high-throughput assays, cell tracing, and protein detection solutions.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic reagent manufacturing
    • REACH Registration for chemical safety in EU markets
    • OECD Guidelines for Testing of Chemicals, Section 3 for dye stability and purity
    • USP General Chapter <1040> for Analytical Reagents

    Typical usage ratio

    • Starter ratio of 5–15% by mass in dye coupling reactions, modified based on final conjugation efficiency and dye output requirements

    Downstream process integration

    • Enters as a coupling precursor during phosphoramidite or NHS-ester dye synthesis
    • Subjected to selective halogen exchange or esterification for emission tuning
    • Final purification via column chromatography or preparative HPLC
    • Packed under inert atmosphere for trace impurity control

    Final product types

    • Fluorescent labeling kits and probes
    • Diagnostic assay reagents for flow cytometry
    • DNA/RNA labeling compounds
    • Cell imaging reference standards

    3. High-Performance OLED Material Engineering

    Advanced electronics manufacturers utilize this compound for engineered host-guest OLED material systems. Its biphenyl and naphthyl functionalities impart precise electron transport and enhanced solubility in organic matrices. Material formulators implement this raw material by tuning layer composition in blue and green emitting diodes, targeting emission efficiency and device lifetime improvements for consumer displays and specialty lighting panels.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics substances
    • IEC 61249-2-21 for halogen-free electronic materials
    • JEDEC JESD22 safety and reliability standards
    • ISO 9001:2015 for quality assurance in electronics material production

    Typical usage ratio

    • Ranges from 0.1–3% weight in the active organic stack, tailored by host-guest configuration and emission color spectrum requirements

    Downstream process integration

    • Solubilized in organic solvent blends before spin-coating or vacuum deposition
    • Co-evaporation with host matrix in emissive layer formation
    • Thermal annealing to achieve uniform molecular dispersion
    • Inline spectroscopic verification for emission characteristics

    Final product types

    • OLED display panels for consumer devices
    • High-resolution lighting diodes
    • Wearable electronics displays
    • Rigid and flexible OLED substrate modules

    4. Synthetic Intermediates in Agrochemical Development

    Major crop protection producers turn to this material as a late-stage precursor in the research and scale-up of selective coumarin-based herbicides and fungicides. By incorporating the bromobiphenyl-naphthyl scaffold, formulators achieve tailored activity against target weeds and pathogens. Careful reaction monitoring allows consistent halogen incorporation, improving field stability and persistence required for effective modern agricultural inputs.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • US EPA 40 CFR Part 180 (Tolerance regulation for pesticide chemicals)
    • ISO 17025 for analytical lab verification
    • Good Laboratory Practice (GLP) per OECD Principles

    Typical usage ratio

    • Reactant input at 0.7–2.0 equivalents dependent on downstream crop selectivity tuning and side reaction minimization

    Downstream process integration

    • Key intermediate introduced post-coumarin ring functionalization
    • Undergoes targeted halogen exchange chemistry
    • Purified by liquid-liquid extraction or column chromatography
    • Batch split for further alkylation or formulation into EC/SC products

    Final product types

    • Selective herbicide technical concentrates
    • Water-dispersible fungicide solids
    • Ready-to-use crop protection formulations
    • Research reference standards for regulatory filings

    5. Advanced Photoinitiator Synthesis in Industrial Coatings

    Industrial formulators in UV-curable coatings and ink sectors use this molecule as a tailored base for high-performance photoinitiators. Coumarin derivatives built from this intermediate provide rapid, controlled crosslinking under UV exposure with minimal yellowing. Process engineers incorporate it by fine-tuning the biphenyl-naphthyl arrangement to optimize photoreactivity, supporting demand for rapid curing and low volatile emissions in protective and decorative coatings.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty chemical production
    • ISO 17025 for performance testing of coatings
    • REACH (EC 1907/2006) chemical registration covering photoinitiator usage
    • ASTM D7767-11 for emission and VOC limits in surface coatings

    Typical usage ratio

    • Loading levels at 1–4% by mass in UV-curable resin systems, adjusted to lamp wavelength and resin formulation

    Downstream process integration

    • Blended into acrylate/methacrylate prepolymers
    • Processed via reactive extrusion or solvent casting
    • Applied in thin films, then photopolymerized with custom UV sources
    • QC evaluation for cure depth and yellow index

    Final product types

    • Industrial protective coatings
    • UV-cured printing inks
    • Decorative automotive topcoats
    • Performance adhesives for electronics assembly
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    Certification & Compliance
    More Introduction

    Introducing 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin: Direct from the Manufacturer’s Bench

    Experience from the Lab Floor

    In the world of specialty organic synthesis, not many compounds get a team excited quite like 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin. Our chemists have watched the complexity of this molecule come to life on the workbench, and every batch that comes out carries with it the care, discipline, and insight that can only come from direct hands-on manufacturing. We handle everything from sourcing raw materials to purification, so we know every nuance that might affect performance and quality. As actual makers, we scrutinize every synthesis step because we expect our customers will put this specialty intermediate through equally demanding applications, whether in advanced research, formulation, or final product testing.

    Diving into the Chemistry

    This compound stands out not only because of its mouthful of a name. It features a coumarin core, a group that has become a building block for anticoagulants and fluorescent probes, but we build on this classic structure with a unique fusion: a tetrahydronaphthyl ring fused to a bromobiphenyl system. The combination gives researchers and developers access to electronic effects and geometries no simple coumarin can offer.

    Our in-house synthetic route skips the detours and shortcuts you’ll find in less-stringent operations. We don’t stop at controlling reaction time and temperature—we directly monitor solvent quality, purity at each stage, and deal with by-products before they reach the final drum. By opting for this level of diligence, we maintain a reproducible high-purity standard. Typical batches achieve purity greater than 98% by HPLC, and we run NMR and IR as routine checks rather than as one-off spot checks.

    Chemists and formulators benefit from this diligence in a very real way. Lower traces of synthetic by-products mean experimental variability drops. Every batch aligns with documented spectra, avoiding surprises in downstream research. When customers send feedback about consistency, they are speaking to habits grounded in our commitment to make one compound right the first time, every time.

    How We Solve for Real-World Usage

    Since this compound turns up in research on anticoagulant analogues, advanced material science, and fluorescence tagging, questions around solubility, stability, and compatibility come up routinely. What surprised us—when we started making this at scale—is that its bulky naphthyl-bromobiphenyl region doesn’t hinder solubility as much as theory suggests. Yes, its preferred solvents tend toward the apolar: toluene, chloroform, and ethyl acetate show reliable dissolution. Aqueous systems need a co-solvent bump, and our technical team has collated data and shared solvent regimes with several research houses navigating formulation hurdles.

    Storage deserves its own mention. While coumarins often demand light protection, our data shows this compound benefits from cool, inert storage but exhibits stable handling under lab lighting over routine work periods. Consistent vacuum packing before shipping shaves down the risk from humidity and airborne contaminants. We switched to layered barrier packaging last year after trial runs demonstrated reduced off-odors and longer shelf lives in side-by-side tests.

    We keep a close hand on logistics, too. No third-party warehousing or untracked drop-shipping. The chain of custody remains closed, and it traces from kettle to your lab, because we take pride in our product doing for you what it does for us.

    What Sets This Molecule Apart

    Having watched this project go from gram-scale curiosity to a regular fixture in our campaign runs, the most striking difference from straightforward coumarin derivatives emerges in the solid-state properties and reactivity. Most suppliers out there dabble in ordinary hydroxycoumarins; those lack the structurally rigid, electron-rich biphenyl moiety, and they certainly do not carry a bromine “handle” for cross-coupling.

    The tetrahydronaphthalene ring in our structure increases bulk and rotational constraint, which in turn reduces some photodegradation seen in planar analogues. Working with actual samples confirms this: We see reduced UV-yellowing compared to standard hydroxycoumarins over weeks of exposure, giving film manufacturers and photoactive formulators more confidence in shelf life. If you dig into the literature, the benefit shows up as a tighter bandgap in spectroscopic assays and increased photostability in preliminary materials testing.

    For those interested in further derivatization, the para-bromobiphenyl segment delivers a ready entry point for Suzuki-Miyaura and other palladium-catalyzed coupling reactions. Unlike non-halogenated products, you can build up libraries of analogues or branched chains directly—useful for custom probes, pharmaceutical intermediates, or functional materials. We’ve learned the value of this versatility from customers who want to walk their ideas directly from chemical concept to scalable candidate in a handful of steps.

    One of the challenges with halogenated biphenyl systems often comes down to stability and halide lability under basic or strongly reducing conditions. Through close process control we suppress side reactions, and our in-process GC tracking shows residual bromide remains at less than 0.2% in all ship-ready batches. In practical terms, that means smoother downstream chemistry and fewer surprises in scale-up studies.

    Specifications and What They Mean in Practice

    Factory data sheets and certificates can tell you about melting point, purity, and assay results, but those numbers have context only when the team generating them takes pride in real-world repeatability. Our regular output shows melting ranges between 187°C and 194°C, reflecting a narrow window tied to minimal impurities. Color always registers white to very pale yellow, never the “off-white” seen with minor contamination or thermal degradation during large-scale filtration.

    Moisture control always proves critical for hydroxycoumarins, which can pick up environmental water during crystallization. We reduce this risk by stepwise vacuum drying and fast transfer into non-permeable liners, so Karl Fischer titration clocks in below 0.2% H2O. Packing staff uses IR and endpoint titration instead of simply relying on weight loss at drying stations—direct analysis stands as the only way to avoid false confidence.

    Particle size in finished form usually falls into a consistent range—no unwelcome clumps or fines that complicate handling or reproducibility. We pass each lot through sieves as part of post-crystallization checks, and laboratory notes track pourability and recoverability for pharma customers who care about more than what shows up on a printout.

    Every finished container ships with reference spectra, including 1H NMR, 13C NMR, and mass spec, so that labs on the receiving end match our fingerprints to their own. If discrepancies crop up, we address them from the actual kettle, not from a back-office script or third-party warehouse inventory.

    Customer Projects: Direct Feedback Matters

    Early on, we sent several test lots to academic groups probing the fluorescent properties of extended coumarins. Their bench chemists noticed red-shifted emission compared with classic 4-hydroxycoumarins, which turned out useful for high-background biological media. Post-run communications let us refine our purification scheme, isolating a minor impurity that suppressed fluorescence in some batches, and this fix became standard. That story sticks with our production staff, proving feedback cycles directly improve both the compound and our work habits.

    Another customer, pursuing novel anticoagulants, needed lots where transition-metal residues fell far below standard thresholds. Our team built in a routine scavenger phase during the work-up, shaving palladium and copper traces well below regulatory guidance limits. These changes did not come from a process manual; they came from troubleshooting with the same hands running reactor, column, and drying screens and reporting results peer-to-peer.

    Traditionally, larger molecules with “exotic” frameworks sometimes transfer poorly from flask to plant. We faced early clumping and yield loss during filtration, so we retooled our crystallization step: temperature-gradient cooling and anti-solvent allocation improve yield and aid uniform collection. We get better product flow, and customers get fewer hands-on headaches during weighing and charging.

    Regulatory and Compliance: What Being a Manufacturer Means

    Rules around chemical intermediates can change fast, especially for compounds with potential bioactivity or downstream drug applications. As the actual manufacturer, we document every step, from raw material identity to batch traceability, tying real names and instruments to every process run. We address questions about compliance with the voice of someone who ran the synthesis, managed the solvents, and watched the QC instruments tick.

    Meeting compliance does not happen by accident or through paperwork alone. We run internal training on hazard recognition, waste controls, and process validation because we trust our staff to stop a line if anything feels off. This confidence transfers to our clients, who sometimes need evidence for their own audits or regulatory submissions. What we offer—authentic manufacturing history and direct answers—is a form of partnership not typically found with intermediaries or repackagers.

    Comparisons with Other Products

    The research market overflows with hydroxycoumarins and biphenyl-containing molecules. What differentiates this compound in practice comes down to the interplay among structural rigidity, electronic richness, and functional diversity. Typical commercial coumarins offer very little in terms of downstream functionalization—once you buy a finished structure, you are bound by what is on the bottle. Here, the presence of the bromobiphenyl group makes creative synthetic work possible in-house or on the fly.

    The market’s simpler biphenyl intermediates often forgo any coumarin moiety, and none we’ve seen match the combination of facile halogen coupling, extended conjugation, and solid-state consistency. Film-makers, polymer chemists, and developers searching for tunable photoproperties have reached out to us after running into glass transition issues or brittleness with linear coumarins. Our compound offers both a broader absorption edge and a more forgiving mechanical profile—features not obvious on paper, but entirely evident at the bench.

    Direct from the factory, we provide not just shipped material, but genuine technical background. You’ll get details on how our compound performs across a range of media and what to expect in terms of shelf life, reactivity, and purification. This depth of experience—from actual process runs to customer feedback—simply does not appear in standard catalog listings or third-party distributor blurbs.

    Navigating Challenges and Solutions

    Scaling up specialty compounds always involves hard lessons, and 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin was no exception. Our crystal engineering team fought early issues with solvate retention, which led to seasonal variations in melting point and color. By overhauling our final solvent selection and implementing staged drying, we now keep batch consistency tight all year round.

    Handling brominated compounds demands respect, especially as residual halides threaten to trigger side reactions in late-stage transformations. In pilot runs we ran a battery of scavenging experiments, tuning our workup to minimize interference and keep halide levels predictable. Developers with strict impurity requirements get a product that adapts to their standards, not the other way around.

    On the logistical front, our experience showed many end users struggle with delays from detached warehouses or foreign re-packers. By shipping directly from our plant and tying every batch back to its synthesis data, we prevent mislabeling and storage mishaps that can plague compounds with specialized stability requirements. Our facility’s real-time tracking and on-site inventory give clients peace of mind—and if a problem does arise, it’s our staff, the ones who actually made the product, who answer the call.

    This wider view—from hands-on synthesis and quality control, through direct customer feedback, to regulatory hurdles—shapes not only our approach to this compound, but the way we see the business of specialty manufacturing. Customers do not just need a standard compound off a gallery of catalog pages—they need an engaged partner who anticipates the pitfalls and opportunities unique to each batch and each scenario.

    What You Get With Our Approach

    Direct manufacturing means every label, every specification serves as an invitation to ask more, probe deeper, and push boundaries. We craft this compound not only to meet technical specs, but to perform consistently across platforms—whether you are pushing fluorescence limits, blending into advanced functional polymers, or designing new pharmacological leads. The backing comes not just from automated equipment but from a team of chemists who carries lessons from every synthesis run, every purity challenge, and every shared breakthrough.

    The development of 3-[3-(4'-Bromobiphenyl-4-Yl)-1,2,3,4-Tetrahydro-1-Naphthyl]-4-Hydroxycoumarin inside our facility has been more than a product launch; it has been a test of everything we know about real-world, bench-to-scale organic chemistry. From raw materials to direct support, every phase reflects choices honed through practice rather than product templates. We take customer challenges as cues for improvement, and we see every lot as an opportunity to prove what true manufacturing experience means.

    Partnering with actual manufacturers guarantees not just technical answers, but solutions rooted in deep familiarity. From quality to logistics to regulatory support, those who work with our team get more than just a compound—their projects benefit from everything our staff has learned in practice, and every improvement we continue to make to keep quality and consistency at the benchmark level.

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