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7-Hydroxycoumarin

    • Product Name 7-Hydroxycoumarin
    • Alias Umbelliferone
    • Einecs 202-193-8
    • 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

    572119

    Compound Name 7-Hydroxycoumarin
    Synonyms Umbelliferone
    Chemical Formula C9H6O3
    Molecular Weight 162.14 g/mol
    Cas Number 93-35-6
    Appearance White to off-white crystalline powder
    Melting Point 225-229 °C
    Solubility In Water Slightly soluble
    Flash Point 178.8 °C
    Absorption Maximum 325 nm (in ethanol)
    Density 1.489 g/cm3
    Pka 7.5
    Storage Conditions Store at room temperature, away from light

    As an accredited 7-Hydroxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 7-Hydroxycoumarin is packaged in a sealed amber glass bottle, labeled clearly, containing 25 grams of fine white to off-white powder.
    Shipping 7-Hydroxycoumarin is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. The packaging complies with international and local hazardous material regulations. Product labeling includes relevant safety and hazard information. Shipping is available for both standard and expedited delivery, ensuring temperature stability and protecting integrity during transit.
    Storage 7-Hydroxycoumarin should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Store at room temperature and follow all relevant safety guidelines for chemical storage to prevent degradation and ensure safe handling.
    Application of 7-Hydroxycoumarin

    Applications of 7-Hydroxycoumarin in Industrial Manufacturing

    7-Hydroxycoumarin (umbelliferone) proves essential across several industrial sectors, where its unique fluorescent and biochemical properties enable critical downstream manufacturing applications. The following section outlines established use cases with detailed compliance, formulation, production, and product information, directly informed by industrial practice and regulatory landscape.

    1. Fluorescent Tracers for Leak Detection and Fluid Flow Monitoring

    Industrial operators in hydrodynamics and pipeline management routinely select umbelliferone-based fluorescent agents to efficiently track leaks and monitor flow patterns in closed and open systems. The strong blue fluorescence under UV excitation ensures precise tracing, even at low concentrations, minimizing operational downtime and supporting targeted maintenance.

    Industry compliance standards

    • OECD Test Guidelines for Tracer Substances in Environmental Monitoring
    • EPA Method 9091 for Tracer Dyes in Water
    • ISO 5667-10: Water Quality – Sampling of Waste Waters
    • REACH chemical safety assessment for environmental tracers

    Typical usage ratio

    • 0.5–5 ppm (parts per million) in water systems; volume adjusted based on pipe or channel capacity, environmental dilution, and detection threshold

    Downstream process integration

    • Operators inject umbelliferone tracer solutions directly into test sections prior to flow visualization or leak integrity runs; UV or fluorometric detection equipment monitors downstream breakthrough or fluorescent dispersion following system pressurization

    Final product types

    • Fluorescent tracer kits for municipal water and wastewater systems
    • Pipeline and HVAC integrity testing reagent sets
    • Ready-to-use flow assessment kits for hydraulic testing services
    • OEM-packaged fluorescent dye concentrates for laboratory use

    2. Pharmaceutical Intermediate for Coumarin-Based Drug Synthesis

    API manufacturers utilize umbelliferone as a core building block in the synthesis of coumarin derivatives, serving as an intermediate in anticoagulant, antimicrobial, and anti-inflammatory drug programs. Quality control demands pharmaceutical-grade purity and traceability at every stage to ensure API consistency for finished formulation.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) monographs for coumarin derivatives and intermediates
    • US FDA – cGMP (21 CFR Parts 210/211) for pharmaceutical processing
    • USP General Chapters ‐ Residual Solvents Testing

    Typical usage ratio

    • Batchwise addition at 1–15% w/w of reaction input materials; exact ratio determined by target moiety, route of synthesis (e.g., etherification, acylation), and desired yield

    Downstream process integration

    • Entry point is typically the initial cyclization or condensation step for the creation of the coumarin scaffold, followed by further functionalization, isolation, and purification as API intermediates, and ongoing impurity profile monitoring per pharmacopoeia

    Final product types

    • Crystalline coumarin derivatives for use in final stage API synthesis
    • Registered drug substance intermediates for oral and topical formulations
    • Pharmaceutical reagents for R&D in small molecule drug pipelines
    • Bulk intermediates supplied to generic and branded drug manufacturing lines

    3. Analytical Reference Compound in Quality Control Laboratories

    QC laboratories across chemical, pharmaceutical, and environmental sectors adopt umbelliferone as a fluorescence calibration and quantification reference material. Its well-characterized emission profile supports trace analysis, ensuring reliable, reproducible measurements in complex matrices over repeated assay runs.

    Industry compliance standards

    • ISO/IEC 17025: General requirements for competence of testing and calibration laboratories
    • USP <825> Reference Standards Requirements
    • GLP-compliant documentation under OECD Principles
    • EN 17034: General requirements for the competence of reference material producers

    Typical usage ratio

    • Typically prepared in standard solution sets ranging from 0.1–10 µg/mL for calibration curve generation; quantity adjusted according to assay limits of detection and matrix

    Downstream process integration

    • QC personnel weigh, dissolve, and dilute batch-certified umbelliferone standards for daily instrument verification, calibration curve creation, and cross-method validation of fluorometric, HPLC-FLD, and environmental analysis platforms

    Final product types

    • Certified reference solutions for laboratory calibration
    • Analytical standards for pharmaceutical composition verification
    • Ready-packed setpoints for environmental tracer quantification
    • Control tablets and calibration blends for field analyzers

    4. Active Ingredient in Optical Brightening Agents for Detergents

    Detergent and cleaning product manufacturers leverage umbelliferone’s optical brightening effect to improve the visual appearance of laundered textiles and hard surfaces. The molecule absorbs ultraviolet light and re-emits visible blue fluorescence, neutralizing yellowing and increasing perceived brightness in end-user applications.

    Industry compliance standards

    • Regulation (EC) No 648/2004 on Detergents (EU)
    • EN ISO 22716: Cosmetics – Good Manufacturing Practices (sanitizing products)
    • AISE (International Association for Soaps, Detergents and Maintenance Products) ingredient guidelines
    • REACH registration for surfactant and additive substances

    Typical usage ratio

    • 0.01–0.2% w/w in powder or liquid detergent base; dosage corrected based on surfactant matrix and desired whitening strength, while ensuring washfastness and safety

    Downstream process integration

    • Blenders introduce umbelliferone at the liquid slurry homogenization or final perfume/additive blending stage, with controlled dispersion and stability checks throughout bulk mixing and packaging sequences

    Final product types

    • Laundry detergents for retail and institutional clients
    • Surface cleaning agents with “brightening” label claims
    • Textile pre-treatment additives for garment manufacturers
    • Dishwashing powders with built-in optical brighteners

    5. Plant Physiology Research Reagents

    Plant science laboratories and agrobiotech companies employ umbelliferone as an indicator and probe in enzymatic assays, particularly for monitoring glucosidase and esterase activities in plant extracts. These research tools aid in mapping metabolic pathways, optimizing crop phenotypes, and developing new agricultural inputs.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) Principles
    • FAO/WHO Guidelines on the Quality Control of Pesticides for Laboratory Use
    • ISO 17025 for Competence of Testing Laboratories
    • CropLife International stewardship and safety protocols

    Typical usage ratio

    • Standard working concentrations typically 20–200 µM in assay wells, adjusted by enzyme activity and tissue type to ensure measurable hydrolysis and reliable kinetics data

    Downstream process integration

    • Researchers introduce umbelliferone substrate during the enzyme assay incubation phase, monitor reaction progress by fluorescence, and collect kinetic profiles to characterize plant enzyme function or screen agrochemical candidates

    Final product types

    • Enzyme assay kits for academic and corporate research
    • Custom plant metabolism workflow reagents
    • Standard reference substrates in agricultural biotechnology labs
    • Screening panels for breeding and GMO trait validation
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    Certification & Compliance
    More Introduction

    7-Hydroxycoumarin: Experience from the Manufacturing Floor

    Walking Through Real Production—Not Just Data Sheets

    Years on the production line have proven that choosing the right chemical can change an entire process. 7-Hydroxycoumarin, which some recognize as umbelliferone, stands out the moment it leaves our reactor. The fine, bright powder signals purity, not just by what’s on a technical spec, but by how evenly it moves through feeders and mixers used in research labs and processing plants. Bright blue fluorescence under UV light—this is what customers use to assess quality by eye, and what our testing team uses to confirm a finished batch turning out exactly as required.

    From Laboratory Curiosity to Manufacturing Staple

    This molecule began as a lab curiosity, known for its place in plant science. In hands-on manufacturing, 7-hydroxycoumarin has grown into a backbone for a wide range of industries. Years ago, researchers first valued it for its fluorescence, finding it could be traced easily in chemical and biological systems. Now, every batch we blend responds predictably under calibration lamps. Chemists in pharmaceuticals tap 7-hydroxycoumarin as a marker in enzyme assays and metabolic studies, where tracking and quantification matters more than ever. Its reliable signal outperforms many of the generic alternatives that sometimes arrive with inconsistent results, affecting downstream research at best and invalidating data at worst.

    Many customers initially expect something akin to generic coumarin derivatives. The real difference starts to show when processes run at scale. Our 7-hydroxycoumarin has found a place in medical diagnostic kits, in formulation of optical brightening agents, and in serving as a reference standard for analytical equipment. Reproducibility from drum to drum matters here—not just for shelf-life, but for every run of a batch process that relies on steady performance. Our internal tests run spectra matching and purity checks every time yield is finalized, ensuring no batch leaves the floor without matching its reference file. Chemists, even the most skeptical, come to appreciate that this consistency does not happen by chance or solely because an MSDS says so, but because each lot passes eyes and hands trained over years spent guarding the boundary between acceptable and superior.

    Why Consistency Means More Than Purity Numbers

    There is more to chemistry than purity on paper. True, we hold to a minimum of 99% assay, verified by both HPLC and UV methods. Yet, any seasoned producer knows—minute shifts in crystal habit, residual solvents, or trace impurities can mean the difference between a downstream process moving smoothly or grinding to a halt. Our technicians spot-check not only the bulk powder, but also the flow characteristics, odor, and even static buildup in different humidity conditions. A few years ago, a trial lot with slightly altered drying rates taught us that even subtle changes can affect how 7-hydroxycoumarin interacts in solution, changing filtering times and yield for one major pharma client. This real-world feedback cycle drives us to focus not just on purity, but on particle size and ease of dissolution every time jars roll off the line.

    Clients in analytical chemistry have explained that, with other suppliers, batch-to-batch shifts in fluorescence can force recalibration of equipment, burning days off productive research. Our daily QC workflow includes matching against an internal fluorescence reference. This test takes only minutes but pays huge dividends for labs downstream, whose workflow can count on steady intensity, blanking out unpredictable spikes or drop-offs.

    The Edge Over Related Products

    Some ask why 7-hydroxycoumarin remains the product of choice instead of using more modified coumarins or other benzo-heterocycles. The answer plays out on manufacturing floors where reliability and predictability rule. Modified analogs often bring extra side chains, complicating purification and introducing variability batch-to-batch. Their synthesis runs longer, and extra steps invite more points of potential contamination. The nature of the 7-hydroxyl group, positioned for slightly lower electron density, gives a unique emission band in fluorescence—sharp and clear, as opposed to the smeared spectrums of some derivatives.

    We collaborate closely with scientists who troubleshoot obscure separation issues. Their reports confirm that our 7-hydroxycoumarin, with its high assay and clean spectral profile, reduces variables in HPLC and fluorescence detection, where small differences in chemical structure cause headaches with solvent shifts or retention times. Many have tried swapping in other fluorophores like resorufin or 4-methylumbelliferone but returned to our product, citing its sharp separation in analytical runs and low background interference, critical when chasing low-abundance metabolites in complex biological systems.

    Building Trust Through Transparent Manufacturing

    In this business, trust gets built batch by batch. We pride ourselves on opening our production line to regular customer audits, an offer taken up by more than a dozen partners in the past year alone. Visitors see how manual checks on color, powder texture, and melt point back up our chromatogram sheets. Our lab workers document every deviation, no matter how minor, and communicate concerns directly to clients if batches need adjustments. This approach means production schedules might run a little longer, but what ships matches every expectation set from a scientist’s protocol or a production validation study.

    Some competitors cut corners, particularly when demand fluctuates. We faced a surge from the diagnostics industry during the last influenza season. Instead of pushing output at the expense of inspection, our team ran overtime, carefully ramping up capacity while reallocating our most trusted analysts to spot check blending, drying, and packaging. A single mislabeled lot can disrupt months of work in downstream applications, especially where regulatory scrutiny enters the picture for diagnostic kits or pharmaceutical R&D.

    Scaling up for new markets also brings challenges. Exporting 7-hydroxycoumarin for international partners introduced logistics and compliance complications—from import customs to compliance with pharmacopoeia monographs. Our quality and regulatory team tackled these head-on, updating documentation and responding to requests for extended impurity profiling. Unlike typical commodity exports, we treat every inquiry with the same rigor we reserve for our largest domestic contracts, no exceptions for lot number traceability or supply chain transparency.

    Application Diversity—All From a Single Core

    Every production cycle shows us new practical uses outside the standard catalog descriptions. Food safety labs rely on our batches to serve as internal standards when running residue analyses. Plant physiologists measure enzyme kinetics, tapping the fluorescence signature to peer into real-time plant metabolism. Cosmetic manufacturers approach us seeking high-purity coumarins, driven by demand for safer, transparent ingredients in skin-brightening formulations. Our 7-hydroxycoumarin, with its well-characterized profile, gives them a reliable building block that won’t surprise during scale-up production or final regulatory review.

    We see the most specialized requests from synthetic chemists, who leverage its hydroxyl functionality as a stepping stone in multi-stage syntheses. The purity of the parent material streamlines subsequent reactions, especially where minute impurities would propagate down a chain synthesis, complicating downstream purification. It has even found a role in environmental science, where its presence serves as a minute tracer in groundwater migration studies. These cross-disciplinary uses reinforce our commitment to not just meeting, but anticipating, next-wave demands that require close attention at every step from reactor to package.

    Facing and Fixing Real Manufacturing Challenges

    In practice, meeting changing industry needs means more than tweaking reagent input. Production-scale chemistry throws curveballs—temperature swings, seasonal humidity, and shifts in raw material quality. Sourcing the precursors for 7-hydroxycoumarin once suffered from a shortage in ortho-hydroxybenzaldehyde. Instead of searching for faster shortcuts, we invested in co-developing supplier verification, guaranteeing traceability and consistently high input quality. Our chemists adapted solvent ratios and temperatures, flagging minute variations that could lead to off-flavors in processed powders—a real concern in end uses for cosmetics or flavors.

    Safety is another front rarely visible from data sheets. Handling large quantities requires dust mitigation and off-gas scrubbing—exposure controls that we adjust seasonally to guard against static discharges and inhalation risk. Our investment in site-specific ventilation design, paired with mandatory safety reviews, stems directly from incidents logged years back. Each change—no matter how incremental—originates in someone’s boots-on-the-floor experience and lessons learned the hard way.

    Standing Apart in a Crowded Field

    The chemical market holds no shortage of coumarin-based products, many promising the same outcomes at lower cost. Through cycles of shortages, changing regulatory demands, and supply chain interruptions, our pace has never faltered. Our 7-hydroxycoumarin does not cut corners. By sticking to high-purity synthesis, focused quality tracking, and relentless customer interaction, we maintain our own production standards and those of the scientists and manufacturers relying on our product. Every bottle leaving our facility represents a chain of skilled work, reviewed and tested in-house, not outsourced to faceless third-parties or converted from bulk intermediates designed for different end-uses.

    In feedback sessions, users praise not just purity but the tactile signs of quality. The way the powder handles, the sharpness of its melting transition, the UV fluorescence uniformity—these are properties built through cumulative expertise, not lucky accidents. Our years of involvement in every step, from procurement through final packaging, mean we recognize and act quickly when even minor shifts appear. These day-to-day lessons have led us to introduce in-line monitoring that ties directly to our PLC systems, capturing data points and raising alarms at the moment a batch deviates from historical targets.

    No Substitute for Technical Engagement

    Reliable manufacturing means keeping conversations open. Our technical team works directly with R&D partners developing new diagnostic panels and with downstream producers scaling from pilot plant to tonnage batches. Differences between 7-hydroxycoumarin and other available coumarin derivatives often surface only then—in extraction losses, changes in solvent compatibility, or shifts in expected performance. We keep a line open with every customer willing to share their results, whether triumph or unexpected challenge. These partnerships have honed our approach, driving improvements not just for routine output, but for rare or high-stakes orders—such as large runs requiring custom particle size or extended impurity profiling for regulated industries.

    Working as a chemical manufacturer does not leave room for partial engagement. Each drum, each bottle, carries the weight of our own reputation, but more importantly, the trust and expectation of those who depend on quality not in the abstract, but in measurable results. Different users measure value in different ways. A researcher values the sharpness and reliability of fluorescence, a formulator needs predictable mixing, a cosmetics chemist counts on low background and high purity. Our aim is to meet all these benchmarks, not in theory, but borne out through years of practical feedback—adjustments made, problems solved, and relationships built around whatever science demands next.

    Looking Forward—Continuous Adaptation

    Chemical manufacturing, especially for specialty products like 7-hydroxycoumarin, never truly ends at a finished batch. Each succession of runs teaches us something new—about sources of variability, user expectations, and the persistent drive toward even higher standards. The markets for analyte detection, next-generation optical brighteners, and bespoke intermediates in organic synthesis show no sign of slowing, but the winners will be those who combine technical expertise with willingness to listen and adapt. Success here grows from hands-on engagement, openness to scrutiny, and a resilience built, not on shortcuts, but on attention to thousands of small details.

    From the plant floor to the laboratory bench, 7-hydroxycoumarin continues to shape what modern science and industry can expect. Our commitment brings not just chemical product, but the added value of know-how accumulated over years—an advantage no generic material or resold commodity can match, and one that continues to earn its place drum by drum.