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6-Bromocoumarin-3-Carboxylic Acid

    • Product Name 6-Bromocoumarin-3-Carboxylic Acid
    • Alias 6-Bromo-2-oxo-2H-chromene-3-carboxylic acid
    • Einecs 629-216-9
    • 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

    767344

    Product Name 6-Bromocoumarin-3-Carboxylic Acid
    Cas Number 17754-47-5
    Molecular Formula C10H5BrO4
    Molecular Weight 281.05 g/mol
    Appearance Off-white to light yellow powder
    Melting Point Over 250°C (decomposes)
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in DMSO and ethanol
    Storage Temperature 2-8°C
    Smiles C1=CC2=C(C=C1Br)C(=O)C=CO2C(=O)O
    Inchi InChI=1S/C10H5BrO4/c11-5-1-2-6-8(3-5)7(10(13)14)4-15-9(6)12/h1-4H,(H,13,14)

    As an accredited 6-Bromocoumarin-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 6-Bromocoumarin-3-Carboxylic Acid, 5 grams, is supplied in an amber glass vial with a tamper-evident screw cap and labeling.
    Shipping 6-Bromocoumarin-3-Carboxylic Acid ships in securely sealed, chemical-resistant containers to prevent contamination and degradation. All packages are labeled per safety regulations and accompanied by a safety data sheet (SDS). Shipping complies with local and international hazardous materials transportation guidelines. Expedited and temperature-controlled options are available upon request.
    Storage 6-Bromocoumarin-3-carboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8 °C (refrigerator). Avoid storing with incompatible materials such as strong oxidizers or bases. Clearly label the container and follow standard chemical safety protocols to prevent contamination and ensure safe handling.
    Application of 6-Bromocoumarin-3-Carboxylic Acid

    Applications of 6-Bromocoumarin-3-Carboxylic Acid in Industrial Manufacturing

    6-Bromocoumarin-3-Carboxylic Acid serves as a precision-engineered intermediate across specific chemical synthesis sectors, with downstream applications focused on specialty pharmaceuticals, advanced dye and pigment production, agrochemical development, and specialty polymer additives. The following scenarios outline the compliant integration of this raw material in validated industrial workflows.

    1. Pharmaceutical Intermediate in Anticoagulant Synthesis

    Pharmaceutical manufacturers apply 6-Bromocoumarin-3-Carboxylic Acid as a key building block for synthesizing advanced coumarin-based anticoagulants, where its unique brominated structure enables selective modifications during synthesis of second-generation API scaffolds. Compound entry typically occurs after initial core construction, followed by stepwise functionalization and condensation reactions under controlled conditions, particularly for derivatives aiming for pharmacopoeia monograph compliance. Usage ratios remain optimized per molecular design and downstream reactivity to minimize purification challenges and support high-yield conversion, with dosage adjusted per targeted final API structure.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • United States Pharmacopeia (USP) Monographs for Coumarin Derivatives
    • European Pharmacopoeia (Ph. Eur.)
    • 21 CFR Part 211 (US FDA cGMP)

    Typical usage ratio

    • 0.3%–1.2% of total batch mass, adjusted based on stoichiometric requirements for esterification or amidation steps targeting desired anticoagulant molecules

    Downstream process integration

    • Direct addition in intermediate coupling stages after initial core ring formation; often followed by halogen exchange or carboxyl protection reactions before final drug assembly

    Final product types

    • Second-generation coumarin-based anticoagulant APIs
    • Pharmaceutical intermediates for further functionalization
    • Precursor compounds for clinical pipeline molecules

    2. Intermediate for Fluorescent Dye Manufacturing

    Producers of high-performance fluorescent dyes utilize 6-Bromocoumarin-3-Carboxylic Acid for introducing defined brominated moieties into extended π-conjugated systems, enabling fine-tuning of spectral absorption and emission properties. The material enters the selective halogenation stage, preceding condensation with electron-donating groups to create targeted fluorophores for life science imaging and analytical probes. Formulators determine the dosage based on desired chroma intensity, emission wavelength, and downstream purification efficiency to ensure optimal dye yield and batch homogeneity.

    Industry compliance standards

    • REACH (EC 1907/2006) compliance for chemical safety
    • ISO 9001:2015 Quality Management for Specialty Chemicals
    • EN 71-3 (if intended for laboratory dyes in diagnostics with relevant toy safety standards)
    • Chemical purity traceability in accordance with GLP when destined for laboratory research reagents

    Typical usage ratio

    • 0.5%–2.0% by weight of the total chromophore synthesis mix; dosage optimized per fluorescence yield and molar extinction coefficient targets

    Downstream process integration

    • Introduced post-coumarin core assembly, immediately prior to arylation or amidation that extends the conjugated system; typically followed by solvent crystallization and filtration stages

    Final product types

    • Laboratory-grade fluorescent dyes for cell labeling
    • Laser dye compounds
    • Spectroscopic reagents used in HPLC and fluorescence detection systems

    3. Precursor for Specialty Agrochemical Synthesis

    Agrochemical formulators leverage the brominated carboxylic acid structure as a gateway for preparing advanced coumarin-based herbicide and fungicide molecules. Entry occurs during the early-stage construction of active ingredient scaffolds, where selective bromine substitution facilitates improved bioavailability or enhances soil persistence. Operators fine-tune the usage level by referencing targeted field trial data and environmental fate evaluations, coordinating precise integration into multistep synthesis routes to achieve high conversion rates and batch reproducibility.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Toxicity, Biodegradability)
    • ISO 9001:2015 for Agrochemical Manufacturing
    • FAO/WHO specifications for pesticide active ingredients
    • REACH registration for intermediates used in plant protection products

    Typical usage ratio

    • 0.2%–1.5% of total synthesis input, varied per active ingredient yield and pathway selectivity in pilot and scale-up batches

    Downstream process integration

    • Added at the bromination or carboxyl activation step following initial aromatic substitution; commonly followed by cyclization or chlorination to finalize crop protection agent structure

    Final product types

    • Selective herbicide actives containing brominated coumarin scaffolds
    • Protective fungicide intermediates
    • Soil treatment precursors

    4. Additive for High-Performance Polymeric Materials

    Specialty polymer manufacturers introduce the brominated carboxylic acid in controlled amounts for synthesizing advanced functional monomers, particularly where improved flame retardance, photostability, or tunable surface chemistry is required. Material feed occurs during functional monomerization via ester or amide formation, subsequently entering co-polymerization or crosslinking stages. Process engineers calibrate the additive ratio based on the target performance properties, resin compatibility, and regulatory constraints for final finished goods intended for high-specification industrial, optical, or coatings applications.

    Industry compliance standards

    • UL 94 (Flame Retardancy Standard for Plastics Components)
    • ISO 10993 (for biocompatible resins in certain optical or medical uses)
    • RoHS Directive 2011/65/EU (for restricting hazardous substances in electrical/electronic equipment)
    • ISO 14001 (Environmental Management System for Chemical Manufacturing)

    Typical usage ratio

    • 0.1%–0.8% by weight in functional monomer feeds; dosing adjusted per polymer matrix compatibility and targeted end-use property enhancements

    Downstream process integration

    • Charged during monomer functionalization prior to bulk polymerization, with post-reaction purification and blending steps for compound resin masterbatch production

    Final product types

    • Flame-retardant engineering polymers
    • Photoactive coatings and films
    • Precision optical-grade resins
    • Specialty composite materials
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    Certification & Compliance
    More Introduction

    6-Bromocoumarin-3-Carboxylic Acid: Experience from the Bench

    Knowledge Gained Through Hands-On Chemical Craftsmanship

    In our production labs, 6-Bromocoumarin-3-Carboxylic Acid has become a trusted specialty intermediate, supporting a range of research and manufacturing projects. Over years of refining the synthesis, patterns have emerged that separate this compound from other coumarin derivatives on our shelves. Our team has spent many hours adjusting reaction conditions to achieve a balance of reproducible purity and scalable yield, specifically tuning multiple reactors to support batches large enough for industrial projects, but clean enough for the demands of analytical and preparative chemists as well.

    Working directly at the source of synthesis provides practical insights not always captured in standard product lists. For us, each kilogram of 6-Bromocoumarin-3-Carboxylic Acid tells its story of meticulous halogenation, careful separation, and hard-won quality control. We operate under the lens of spectroscopic and chromatographic scrutiny, and the decisions we make at each synthesis step reflect a sense of stewardship for every downstream application, whether it goes into advanced pharmaceuticals, pigment development, or high-level academic research.

    How Model Choices Shape Chemistry

    Most inquiries we receive ask about the practical footprint of our 6-Bromocoumarin-3-Carboxylic Acid in ongoing projects—what sets it apart from other coumarin acids and their halogenated relatives? The answer begins with our process, tuned not only for finished purity but also for chemical friendliness. The product usually takes the form of a pale, crystalline solid, consistent from batch to batch, with HPLC purity routinely monitored above 98%—a benchmark we hold tightly through both in-process checks and final verification.

    Our standard bulk offering weighs in at upwards of several kilograms per lot. We never treat this as a side product or cheap commodity, because the structural demands of introducing bromine to the coumarin core require precision at each phase. Side reactions lurk in uncontrolled environments, imparting color, changing melting points, and ruining usefulness for synthesis downstream. Over time, we found the right combination of solvent, temperature, and purification techniques to minimize such issues, part of the “know-how” that comes from living with a compound through every stage of its evolution.

    What Makes 6-Bromocoumarin-3-Carboxylic Acid Unique on the Bench

    6-Bromocoumarin-3-Carboxylic Acid starts with coumarin’s familiar bicyclic ring but swaps the usual hydrogen at the sixth position for a reactive bromine, while the carboxyl group sits at the third carbon. This structural arrangement sets a reliable platform for downstream customization, especially suited for Suzuki or Heck couplings and other C–C bond-forming protocols heavily used to make modern medicinal chemistry libraries. The electron-withdrawing effect of bromine not only directs subsequent reactivity but also introduces new photophysical possibilities for developers interested in fluorescent probes or specialty dyes.

    In practice, colleagues across pharmaceutical development often cite this molecule’s balance: reactive enough to serve as a versatile synthetic partner, yet robust enough for storage, weighing, and transfer without the fuss often seen with less stable brominated organics. Our product does not clump, degrade, or give inconsistent assay values—results backed by repeated FTIR, NMR, and melting point studies. Each lot travels with its analytic fingerprint from production to customer, supporting GMP and non-GMP workflows alike.

    A Closer Look at Specifications and Integrity

    We believe technical information should always be rooted in direct production experience. Here, the melting point serves as a dependable indicator of both identity and purity for 6-Bromocoumarin-3-Carboxylic Acid; for us, it offers a reality check beyond the routine certificate. We also track moisture by Karl Fischer titration and use LC-MS confirmation to reassure project chemists handling downstream coupling reactions.

    Beyond these numbers, our teams learned to monitor the “smaller signals”—trace impurities, color changes, and physical consistency that sometimes only emerge after extended shelf-life studies. In identical storage conditions, batches produced from alternative raw material sources or using shortcuts in bromination tend to discolor or produce off-smells. We have made the conscious decision to limit throughput in exchange for repeatability in every drum or bottle shipped. This commitment often leads to longer lead times, but recurring feedback from industrial partners highlights the stability and reproducibility our process delivers year after year.

    Ground-Level Applications: Lessons from the Factory Floor

    Most end-users come to us with clearly defined synthesis goals. 6-Bromocoumarin-3-Carboxylic Acid serves as a prized building block, trusted for its power in cross-coupling chemistry. Feedback from direct partnerships with pilot-scale synthesis teams gave us new respect for just how demanding downstream transformations can be. The unique blend of strong bromine reactivity and carboxyl group offers hooks for both carbon-carbon and amide bond creation. In catalyst-rich cross-coupling, it provides reliable turnover without unexpected side reactions, bridging the gap between bench-scale trials and multi-kilo campaigns.

    Academic labs have also pushed the limits of this material, building richer dye and probe collections for bioimaging and environmental monitoring. Coumarin’s photophysical core, when combined with the tuned electronic effects of bromine, yields absorption and emission profiles that unlock new analytical possibilities. We’ve watched teams run detailed photostability assays on our material—information they often choose to share, allowing us to further tweak parameters at the factory level.

    How It Stands Apart from Other Coumarin Derivatives

    Compared with parent coumarin-3-carboxylic acid or simple brominated coumarins at other positions, our 6-bromo variation shows a unique intersection of ease of functionalization, excellent shelf-life, and minimal batch-to-batch drift. Some substitutions in other positions disrupt solubility or decrease reactivity without adding value. Halogen substitution at the sixth position boosts both the synthetic range and practical benchtop stability. For the teams working on structure-activity relationship libraries, that means more options and fewer stalled syntheses.

    Certain alternatives, such as 7-bromocoumarin-3-carboxylic acid, display different reactivity patterns under palladium-catalyzed procedures; some competitors’ products struggle to match the reliability we see from our tightly monitored processes. The origin of key raw materials and the care in purification pay off in later uses; this feedback came directly through sustained customer relationships, not marketing surveys.

    Safety Informed by Years of Real Handling

    Safety always grows from a base of daily project work, not from paperwork. With repetitive and direct handling at the scale of kilograms, our crew learned through routine exposure that 6-Bromocoumarin-3-Carboxylic Acid, though generally easy to manage, should be kept sealed, dry, and away from open heat due to its light-sensitivity and reactivity typical of many activated aromatic systems. Our procedures reflect not only regulatory frameworks but the rhythm of production staff working buckets, not vials; real accidents spark changes to protocols quicker than office memos. Material management always respects the reactivity of the bromine atom, and our facilities favor enclosed transfers, slow additions, and prudent air filtration.

    Direct feedback from our workers prompted improvements to PPE standards and encouraged regular air quality checks, limiting chronic exposure risks found with similar halogenated materials. Real-life production and packaging experience forms the backbone of our material safety education, giving us confidence in the consistency and safety of the product we ship.

    Supporting a Versatile Pathway for Researchers and Industrial Chemists

    Every delivered batch of 6-Bromocoumarin-3-Carboxylic Acid illustrates what careful production means at the coalface of chemical manufacturing. Work doesn’t end with reaction completion or purification; it extends all the way to the hands that measure, analyze, and react the compound on their own benches and reactors. Our long-standing relationships with project chemists allow us to integrate real laboratory feedback directly into small adjustments in our processing, closing the loop and tightening specifications.

    Recommendations from large-scale users have driven us to improve both product consistency and packaging. Using vigilant quality controls, we avoid glass fiber contamination and particle size variability that plagued earlier runs; tighter sieving and improved drum liners keep the material free-flowing and manageable at all ambient temperatures. Storage tests across varying humidity and temperature regimes—modeled after both warehouse and laboratory environments—demonstrate that, under optimal storage, samples stay stable for extended periods, supporting just-in-time demands. That’s tested performance, not just a claim.

    Addressing Common Pain Points for Partners

    Friction often arises not from molecular performance itself, but from the transitions between stages—sampling, scaling, or process handoff. In our experience, poor documentation or gap-ridden Certificates of Analysis can derail a production project after substantial investment. Over time, we’ve invested equally in post-synthesis documentation as in the chemical work itself, capturing minor changes in aroma, color, and melting point alongside batch numbers and analytical runs. This level of transparency lets end-users spot deviations before they affect synthesis—an ecosystem built by chemists for chemists, tuned by real setbacks, and refined by lived experience.

    Unwanted contamination or unexpected variance in bromine content caused wasted hours in several early customer campaigns. We adopted fast cycle chemical and analytical updates; every run that doesn’t pass tight internal control gets a full breakdown and, if necessary, repeated with tighter in-process checks. Sharing these updates with partners—sometimes in the middle of an urgent production run—builds long-term trust, the sort that grows stronger with each challenge tackled together.

    Potential Paths for Further Collaboration

    Our role doesn’t end at bulk shipment or lab delivery. By maintaining direct technical conversations with research leads and production managers, we explore custom batch sizes, alternate purification strategies, and unique packaging requests. Open feedback encourages iterative improvement. We invite process chemists to review not only our product, but also our underlying processes. This two-way street of information-sharing made our product lineup stronger season after season and built a network of real-world chemistry support that can address unforeseen process bottlenecks as they emerge.

    Some partners ask for specific dissipation profiles for their special synthesis steps; others push for alternative forms—pre-dissolved in solvent, micronized, or in combination with co-reactants for more direct addition. Over years of these requests, we built a library of formulated options, always guided by stability and chemical compatibility. We hold back on expanding this list until a real need arises—flexibility, in our framework, means practical deliverability, not just extra SKUs.

    Why Reliability Comes from Direct Manufacturer Engagement

    In this market, information often stays stuck at the distributor or catalog level. We break that model by inviting regular visits from research collaborators, industrial scale users, and auditing chemists. Our manufacturing protocols grew more robust thanks to such scrutiny. We don’t hide behind brokers or anonymous sales offices; real technical experience at the bench supports each batch that leaves our site.

    This direct connection shapes how we train our staff, apply process analytics, and respond to every quality concern, no matter how small. Our lab doors stay open to feedback, and we collect both compliments and complaints with the same interest. In the end, the reliability of 6-Bromocoumarin-3-Carboxylic Acid comes from this daily discipline—a transparent chain linking initial raw material sourcing, careful process monitoring, and hands-on testing, right through to final dispatch. This engagement forges a level of product confidence that pushes beyond faceless sourcing, creating a quality curve that rises over time.

    The Evidence for a Best-in-Category Building Block

    Consistency in yield, assay, and impurity profiles forms the backbone of our material’s solid reputation. Our analytics division draws directly from pilot plant experience, knowing which peaks and troughs in chromatograms really matter. Rather than chasing the lowest cost, we prioritize meeting and sustaining high-purity cutoffs, because that’s what our user base has shown it values after years of incremental improvement. Analytical results don’t live just on paper—they echo through each stage of a project, affecting rates of reaction, purity of final targets, and, ultimately, team morale.

    Packages arrive with clear documentation, careful labeling, and, when required, extra analytical data. This commitment to clarity, forged through daily practice and real feedback, keeps confusion and rework at bay. Our partners recognize this difference—not because of marketing, but because failed batches, discontinued analogs, or delayed shipments have real and predictable costs in their operations.

    Moving Forward: Commitment Rooted in Practice

    Each batch of 6-Bromocoumarin-3-Carboxylic Acid we produce reflects the lived practice of synthesis, listening, adjustment, and delivery. Modern chemical manufacturing rests on this unglamorous foundation—countless cycles of planning, execution, and validation, powered just as much by practical experience as by raw data. Materials aren’t just measured in kilograms, but in successful runs, trouble-free couplings, and quiet nights in the pilot plant office after months of work come together in a single reliable product.

    As our partners continue to tackle new chemical challenges, we draw daily inspiration from their practical needs. Our front-line focus remains steady: keeping 6-Bromocoumarin-3-Carboxylic Acid a dependable, high-quality building block, nurtured by hands-on chemical experience, informed by frank conversations, and shaped by the lessons that only come with time, repetition, and genuine collaboration.