Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

6-Bromo-4-Hydroxycoumarin

    • Product Name 6-Bromo-4-Hydroxycoumarin
    • Alias 6-Bromo-4-hydroxy-2H-1-benzopyran-2-one
    • Einecs 249-972-7
    • 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

    434353

    Chemicalname 6-Bromo-4-Hydroxycoumarin
    Casnumber 2522-71-6
    Molecularformula C9H5BrO3
    Molecularweight 241.04 g/mol
    Appearance Off-white to light yellow crystalline powder
    Meltingpoint 221-225 °C
    Solubility Slightly soluble in water, soluble in organic solvents like ethanol and DMSO
    Purity Typically ≥98% (HPLC or GC)
    Structure A coumarin derivative with bromine at position 6 and hydroxyl at position 4
    Synonyms 6-Bromo-4-hydroxy-2H-chromen-2-one
    Storageconditions Store at room temperature, protected from light and moisture

    As an accredited 6-Bromo-4-Hydroxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 6-Bromo-4-Hydroxycoumarin, 5g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with product and hazard details.
    Shipping 6-Bromo-4-Hydroxycoumarin is shipped in tightly sealed, chemically resistant containers to prevent contamination and degradation. Packages are clearly labeled in accordance with relevant regulations, and protected from light and moisture. Shipping follows all safety and hazardous material guidelines, with documentation provided for tracking and compliance during domestic or international transport.
    Storage 6-Bromo-4-Hydroxycoumarin should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from light and incompatible materials such as strong oxidizing agents. Protect the compound from moisture and store at room temperature unless otherwise specified by the manufacturer’s guidelines. Always use proper personal protective equipment when handling and storing this chemical.
    Application of 6-Bromo-4-Hydroxycoumarin

    Applications of 6-Bromo-4-Hydroxycoumarin in Industrial Manufacturing

    6-Bromo-4-hydroxycoumarin serves as a specialized intermediate in regulated downstream industries. Our production targets demanding sectors where high-purity standards and controlled integration govern the application of this compound. Below, we detail leading industrial scenarios with verified market demand and compliance direction.

    1. Pharmaceutical Synthesis: Anticoagulant Drug Intermediates

    Pharmaceutical manufacturers employ this coumarin derivative primarily in the synthesis of oral anticoagulant agents within the 4-hydroxycoumarin class, including warfarin and related actives. Its brominated structure provides essential chemical handles for regioselective substitution and controlled condensation during the production of APIs. Product integration occurs under validated cGMP regimes, with critical purity benchmarks set by pharmacopoeial references. Manufacturers adjust coupling process parameters to optimize yield and minimize unwanted byproducts, ensuring material traceability from intermediate to finished dosage form.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <795>, <797>, <800> for compounding and hazardous drugs
    • European Pharmacopoeia monographs for coumarin-derived actives
    • 21 CFR Part 211 U.S. cGMP for finished pharmaceuticals

    Typical usage ratio

    • Used at 0.3–0.7 molar equivalents versus aldehyde partner during condensation step; variation depends on target molecule
    • Adjust for purity (>98%) and process impurity profile

    Downstream process integration

    • Enters at the first or second synthetic stage for active API chain elongation
    • Subjected to base-promoted cyclization and subsequent functionalization
    • Tightly controlled under validated SOPs and monitored for trace residuals

    Final product types

    • Warfarin tablets and injectables
    • Phenprocoumon bulk API
    • Acenocoumarol finished formulations
    • Medicinal research standards for preclinical assay

    2. Fine Chemical Building Blocks for Dye Manufacturing

    The dye and pigment sector applies this coumarin compound in the synthesis of specialized fluorescent dyes and colorfast pigments for industrial and analytical applications. Brominated coumarin nuclei introduce chromophoric properties essential for high-brightness finished goods and improved stability against photo-degradation. Batch adjustments account for downstream halogenation and sulfonation stages, with purification steps linked to color index benchmarks and REACH registration.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • OEKO-TEX Standard 100 for textile dyes
    • ISO 9001:2015 for chemical quality management
    • Specific migration limits (SML) for food-contact colorants (EU 10/2011)

    Typical usage ratio

    • Ranges from 2–5% by weight in dye synthesis reaction mixture
    • Final amount varies with target fluorescence intensity and downstream coupling partner

    Downstream process integration

    • Added during initial ring substitution phase, followed by sulfonation or azo-coupling
    • Refined through chromatographic separation and crystallization
    • QC checks for emission spectra and purity

    Final product types

    • Laser dyes for scientific instrumentation
    • Textile dyes with improved wash fastness
    • Fluorescent markers for biochemical assays
    • Industrial pigments in specialty coatings

    3. Agrochemical Intermediate: Synthesis of Plant Protection Compounds

    Leading agrochemical formulators require this intermediate for the development of specific coumarin-based herbicides and fungicides. Its brominated core offers high reactivity for further functionalization, which downstream R&D teams exploit to optimize bioactivity or environmental stability. Material loading is guided by greenhouse residue studies and international MRL requirements, with robust batch records ensuring field-to-lab traceability. Emphasis rests on selectivity and breakdown profile validation, mapped to crop safety benchmarks.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide residue limits
    • EU Regulation (EC) No 1107/2009 for plant protection product approval
    • ISO 17025 laboratory accreditation for QC testing
    • GLP (Good Laboratory Practice) for environmental studies

    Typical usage ratio

    • 0.5–1.5 molar equivalents introduced per batch; optimization based on conversion rate and downstream halogenation needs
    • Pilot batches determine practical ceilings for formulation

    Downstream process integration

    • Forms core scaffold in early synthesis steps for coumarin-based actives
    • Advanced through halogenation, alkylation, and esterification
    • Final actives isolated after chromatographic purification

    Final product types

    • Selective herbicide actives (field crops, rice paddies)
    • Systemic fungicides with extended residual activity
    • Pre-emergent weed control granules
    • Seed treatment formulations

    4. Specialty Chemical Synthesis: Fluorescent Probe and Sensor Modules

    Producers of advanced sensor and detection solutions use this coumarin derivative for fabricating modular fluorescent probes, benefiting from the molecule’s inherent luminescence and substituent-reactivity. Integration targets responsive dyes for optical biosensors and chromatography detection modules. Strict batch-to-batch uniformity supports regulatory filing for diagnostics and analytical kits. Downstream reactions adapt the core to varied wavelength outputs and substrate reactivities, with comprehensive chemical registration for end-device safety assessment.

    Industry compliance standards

    • ISO 13485:2016 for medical device component manufacturing
    • FDA 21 CFR Part 820 Quality System Regulation
    • OECD Good Manufacturing Practice for analytical reagents
    • EU CLP Regulation (EC No 1272/2008) for labeling and hazard communication

    Typical usage ratio

    • 1–3% weight to total probe mass, with adjustment per target detection limit
    • Fine-tuning by photophysical screening in post-synthesis qualification

    Downstream process integration

    • First introduced during sensor conjugation step or direct chemical immobilization
    • Subsequently modified through click chemistry or azide-alkyne cycloaddition
    • QC validation for emission wavelength and Stokes shift

    Final product types

    • Medical diagnostic fluorescence test kits
    • Chromatography column markers
    • Environmental sensor chemical modules
    • Protein tracking dyes in molecular biology
    Free Quote

    Competitive 6-Bromo-4-Hydroxycoumarin prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    6-Bromo-4-Hydroxycoumarin: Insights from Direct Manufacturing

    Introduction to 6-Bromo-4-Hydroxycoumarin

    Our journey with 6-Bromo-4-Hydroxycoumarin starts with hands-on research and pilot-scale reaction development. This compound’s popularity among research groups and downstream manufacturers didn’t happen by chance. Coumarin derivatives, especially bromo-substituted analogs, drew focus in organic synthesis labs for their versatility. When our team scaled up synthesis, we relied on a mix of classic techniques and modern instrumentation to refine quality and batch consistency.

    This product stands out largely due to the bromo group on the 6-position, opening pathways for subsequent substitution while retaining the biological and photochemical activity coumarins are known for. In our reactors, we start with resorcinol and ethyl bromoacetate, harnessing precise conditions to avoid polybromination and degradation—factors sometimes seen in non-specialized operations.

    CAS Number, Appearance, and Core Specifications

    Every batch of 6-Bromo-4-Hydroxycoumarin arrives at our QC lab with a white-to-off-white crystalline appearance, underscoring high purity. Specifications routinely hit a minimum assay of 98% by HPLC, with melting points controlled between 245–249°C. Residual solvents, halogen contamination, and trace byproducts sit below detection thresholds set by both industrial standards and our process benchmarks. Over years, we have adapted analytics to catch subtle shifts that can affect downstream reactions.

    Instead of distributing only a powder, we support custom micronization on direct request. Some groups prefer smaller particle size for rapid dissolution in DMF, DMSO, or other organic systems. By heavy investment in air-jet milling, we adjust particle profiles without risking thermal decomposition or unwanted halogenation.

    Intended Usage: Research and Industrial Applications

    Direct users employ 6-Bromo-4-Hydroxycoumarin as a scaffold and coupling partner across diverse segments. Chemists working on heterocyclic synthesis rely on this compound for Suzuki, Sonogashira, and Buchwald-Hartwig couplings. Academics dig into photophysical research: the compound absorbs UV and blue light, opening avenues for sensor and dye development. Our partners in agrochemicals have explored brominated coumarins as precursors to fungicides and growth regulators.

    We’ve seen large-volume projects where this material supports synthesis of anti-inflammatory drug intermediates or functional materials for environmental monitoring. Some downstream groups convert the bromo position, tailoring the coumarin ring for library synthesis and lead optimization. Feedback from process chemists led us to minimize metal impurities and adapt packaging to suit both glassware-based and pilot-plant scale reactions.

    Key Differences from Other Coumarin Derivatives

    Working as producers rather than pure resellers, we notice real-time pain points end-users face with generic bromocoumarins. The placement of the bromo group makes all the difference. At the 6-position, the compound preserves electronic distribution patterns ideal for nucleophilic aromatic substitution. By contrast, brominations at positions 3 or 7 change reactivity and solubility, often leading to process setbacks or product loss.

    Commercially, the market sees low-purity alternatives, sometimes cut with unreacted coumarin and multibrominated byproducts. We’ve invested heavily in both reaction optimization and multi-stage filtration to guarantee assay and control polymorphism. Through close partnerships with chromatographers and scale-up managers, every drum carries a traceability report, linking batches to their origin on our reactor logs.

    Process Integrity and Quality Control Insights

    As a manufacturer, we face the direct consequences of synthetic errors and reactor drift. Rather than rely on post-hoc remediation, our team rebuilt the workup and purification sequence two years ago, slashing yield losses and minimizing waste solvent production. Defining the right loading of Lewis acid catalysts, monitoring temperature ramps, and tracking bromoacetyl group uptake ensured each lot behaved identically on NMR, HPLC, and MS analysis.

    We maintain a full material characterization profile. Carbon/hydrogen/halogen analysis, UV-vis absorption, and crystallinity all feature in our regular checks. This drives confidence for users who need lot-to-lot reproducibility. Even storage conditions factor in. Because this compound can take up atmospheric moisture and degrade at elevated temperature, all drums exit our warehouse with internal liners and low-humidity warning tags.

    Practical Experience with Application Development

    Real feedback comes from colleagues translating 6-Bromo-4-Hydroxycoumarin into new chemical entities. Pharmaceutical R&D groups appreciate the absence of polyhalogenated contaminants, which interfere with bioassays and structure-activity studies. Our partners in analytical chemistry use the compound as a standard for fluorescence calibration due to predictable emission peaks.

    Recent collaborations have shown new frontiers with this compound in material science. The 4-hydroxy group directs metal binding, allowing users to prepare coordination polymers for light-harvesting applications. Selective substitution at the bromo position yields custom-tuned fluorophores and enzyme inhibitors, confirmed by both bench-scale tests and gram-scale pilot projects within our own facility.

    Some biotechnologists utilize this compound as a launching point for synthesizing sensors sensitive to ionic heavy metals. Synthetic routes benefit from our high-purity benchmark: every downstream transformation carries fewer side-products, resulting in higher isolated yields and cleaner analytical traces.

    Waste Handling and Environmental Responsibility

    Producing halogenated intermediates involves real environmental risk. Our reactors run on closed-loop solvent recovery systems, and waste bromo-organics move through catalytic incineration, not landfill. We’ve learned that vigilance with bromine balances both plant safety and compliance with regional regulations. Each lot receives a profile through our LIMS for full chemical accountability, reducing surprises in user-side waste streams.

    Internal efforts at solvent optimization and catalyst recovery did not just shrink our environmental footprint—they helped us stabilize input costs for customers dealing with narrow project budgets. No end-user wants to navigate hidden halogen disposal expenses after purchase. Those details matter in daily operations, side-by-side with chemical purity.

    Packaging, Stability, and Handling Insights

    From packing line to bench, a good chemical distinguishes itself by its reliability over time. We standardized on aluminum-laminated bags with a puncture-proof secondary container, which shut down common complaints about moisture ingress and caking. Finished goods age in climate-controlled storage, and our outgoing QA samples face accelerated stability testing at 40°C and 75% RH. This process uncovered a rare off-coloration in a series that we traced back to a mislabeled solvent batch, a lesson that pushed us to tighten supplier audits.

    Researchers who buy in multi-kilo volumes request custom repackaging, sometimes down to 10 g vials for convenience during screening projects. Direct engagement with lab managers led us to switch anti-static liners and adjust label adhesives, reducing shed particulate contamination. Everything connects to actual daily use, whether for analytical development or multi-step synthesis.

    Regulatory and Documentation Clarity

    End-to-end documentation can frustrate both producers and users. Years spent dealing with varied client requests mean that, beyond the usual CoA, we bundle NMR, MS, and lot-specific impurity profiles as standard. Local workplace safety codes ask for transparent storage and disposal recommendations. We integrate hazard labeling systems on-pack and within all digital material, including advice on PPE based on direct lessons learned from our plant team.

    We take an open-book stance with regulatory audits. Coumarin derivatives attract attention due to potential biological effects, especially in pharma and fine chemicals. Our quality files retain backlogged production and waste treatment records, easing due diligence for research partners, especially in international collaborations.

    Challenges We Have Solved and What Remains

    Our early runs presented issues—overbromination, stability concerns, inconsistent color. Simple tweaks did not suffice. We revised the oxidation stage, tuned impurity stripping cycles, and invested in new analytical runs after every plant change. Hand-in-glove feedback between operations and QC shrunk failure rates from double digits down to rare, isolated outliers.

    The challenge that remains centers on balancing demand bursts with continuous batch reproducibility. Sometimes, sudden orders for sizable academic or industrial lots strain plant schedules. To respond, we keep raw material buffers and mature a rolling forecast system. User groups with specific customization requests—particle size or packaging—may face a short wait, reflecting our insistence on not sacrificing batch quality for speed.

    Reflections and Moving Forward

    The story of this compound weaves through real lab benches, not just spreadsheets. We follow reactions through all-day plant shifts and rush-hour chromatogram meetings, always aiming for predictability and genuine improvement. Each feedback loop, contract, and follow-up call adds new experience to the playbook. The reality of producing fine chemicals never reaches perfection, but with 6-Bromo-4-Hydroxycoumarin, we found reliability stems from both technical precision and a willingness to adapt to each customer’s process workflow.

    Ultimately, our perspective stays rooted in production experience, pragmatic adaptation, and direct user feedback. Every drum reflects that reality, built from small incremental insights over years of manufacturing, optimization, and partnership with end users. The chemical itself stays the same; the craft grows with each batch and new application brought to our door.