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5,7-Dihydroxy-4-Methylcoumarin

    • Product Name 5,7-Dihydroxy-4-Methylcoumarin
    • Alias 4-Methylumbelliferone
    • Einecs 216-407-5
    • 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
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    Specifications

    HS Code

    760565

    Cas Number 10296-28-7
    Molecular Formula C10H8O4
    Molecular Weight 192.17 g/mol
    Iupac Name 5,7-dihydroxy-4-methyl-2H-chromen-2-one
    Appearance Yellow crystalline powder
    Melting Point 235-238°C
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Smiles CC1=C(OC2=CC(=CC(=C2C1=O)O)O)
    Inchi InChI=1S/C10H8O4/c1-5-7(11)3-6-4-8(12)10(13)9(14-6)2-5/h3-4,11-13H,2H2,1H3
    Pubchem Cid 202778
    Synonyms 4-Methyl-5,7-dihydroxycoumarin
    Storage Conditions Store at room temperature, protect from light

    As an accredited 5,7-Dihydroxy-4-Methylcoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle labeled "5,7-Dihydroxy-4-Methylcoumarin, 99%, 25g" with hazard pictograms, batch number, and manufacturer information.
    Shipping 5,7-Dihydroxy-4-Methylcoumarin is shipped in tightly sealed containers, protected from light and moisture. The packaging complies with chemical transport regulations, ensuring safety during transit. Material Safety Data Sheets (MSDS) accompany each shipment. Recommended shipping is via ground or air freight, marked for laboratory use only, and labeled as non-hazardous unless specified otherwise.
    Storage 5,7-Dihydroxy-4-methylcoumarin should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, and well-ventilated area. The storage temperature should be at room temperature or lower. Keep away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and follow local regulations for chemical storage and handling.
    Application of 5,7-Dihydroxy-4-Methylcoumarin

    Applications of 5,7-Dihydroxy-4-Methylcoumarin in Industrial Manufacturing

    As a direct manufacturer of 5,7-Dihydroxy-4-Methylcoumarin, we support a focused range of industrial sectors where this compound brings clear advantages in both formulation and downstream processing. Our material is deployed by producers who rely on established compliance, precise batch tracing, and process consistency for specialized applications. Below we detail the main end-use routes with technical parameters and compliance requirements.

    1. Optical Brightener Intermediate for Detergents

    5,7-Dihydroxy-4-Methylcoumarin acts as a core intermediate in the synthesis of high-performance optical brighteners, particularly those integrated into laundry detergents and liquid cleaning agents. Its dual hydroxyl structure enables strong binding with substituted stilbene or triazine moieties, supporting stable color improvement in both powder and liquid formats. Downstream users rely on it for consistent blue-whitening effect during the last formulation stage before packaging.

    Industry compliance standards

    • REACH Annex XVII (EU Regulation 1907/2006) for chemical intermediates
    • EN 648 (Assessment of bleachable stains removal in detergents)
    • ISO 9001 and 14001 for production traceability and environmental management
    • China National Standard GB/T 13173 for synthetic detergents

    Typical usage ratio

    • As an intermediate: 0.3%–2.5% of total optical brightener batch, adjusted based on final concentration targets

    Downstream process integration

    • Added at the condensation stage to build the coumarin core of the brightener, followed by sulfonation or alkylation steps for detergent integration

    Final product types

    • Fluorescent brightener additives (powders and liquids)
    • Universal and specialty laundry detergents (liquid and powder)
    • Commercial fabric cleaning agents

    2. Pharmaceutical Synthesis: Anticoagulant Precursors

    The production of several coumarin-based anticoagulant drug molecules requires precisely controlled starting materials to achieve target pharmacological profiles and impurity limits. 5,7-Dihydroxy-4-Methylcoumarin enables medicinal chemists to access specific functionalized frameworks for the synthesis of second-generation 4-hydroxycoumarin derivatives. Integration occurs during key condensation or alkylation steps under GMP audit trails, helping maintain batch-to-batch reproducibility and downstream active pharmaceutical ingredient (API) quality.

    Industry compliance standards

    • ICH Q7 Guidelines for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for anticoagulants and intermediates
    • USP 43-NF 38 coumarin-related raw material specifications
    • cGMP/ICH Q11 for chemical development and scale-up control

    Typical usage ratio

    • Usually 5%–15% as a w/w precursor in reaction feedstock, determined by targeted yield and side product control

    Downstream process integration

    • Introduced at early condensation or aldol reaction stages for coumarin backbone construction, followed by purification and further derivatization

    Final product types

    • Coumarin-based drug intermediates
    • Oral and parenteral anticoagulant APIs
    • Finished solid-dose medications containing coumarin analogues

    3. UV-Absorber Additive for Polymer Films

    In high-transparency polymer manufacturing, such as specialty films for food packaging and technical sheets, 5,7-Dihydroxy-4-Methylcoumarin serves as a reactive additive enabling UV protection without color distortion. It is valued for maintaining polymer physical properties while extending product service life by reducing photo-degradation and discoloration, especially under food-contact approval systems which require minimal additive migration.

    Industry compliance standards

    • FDA 21 CFR 177.1520 for polyolefins intended for food contact
    • EU Regulation No 10/2011 on plastic materials and articles
    • ISO 4892 for exposure to laboratory light sources (UV stability testing)
    • Japan Polyolefin Food Hygiene Association (JPFHA) listing

    Typical usage ratio

    • 0.05%–0.2% by weight of total polymer resin, adjusted based on film thickness and UV exposure expectations

    Downstream process integration

    • Added during resin mixing or extrusion via masterbatch system before film blowing or casting

    Final product types

    • Polyolefin and PET packaging films
    • Technical laminates with UV-stabilized surfaces
    • Transparent food storage wraps

    4. Analytical Reagent for Metal Ion Detection

    In environmental and industrial testing laboratories, 5,7-Dihydroxy-4-Methylcoumarin is used as a fluorescent chelating agent for quantifying trace bivalent and trivalent metal ions in complex matrices. Its selectivity and strong signal-to-noise characteristics make it valuable for compliance sampling in water, beverage, or electronics rinsate analyses. Reliability in fluorescent response is critical for compliance with regulated test protocols.

    Industry compliance standards

    • ISO 17294-2 for determination of trace elements by ICP-MS
    • US EPA Method 200.8 (ICP-MS for water and wastes)
    • Standard Methods for the Examination of Water and Wastewater (APHA, AWWA, WEF)
    • RoHS Directive 2011/65/EU annex for restricted substances testing

    Typical usage ratio

    • Typically prepared at 10–100 µmol/L in a buffered sample extract, titrated in excess relative to analyte concentration

    Downstream process integration

    • Dissolved in aqueous phase prior to sample extraction or standard addition, followed by complexation and fluorometric measurement

    Final product types

    • Water testing reagent kits
    • Lab-standard fluorescent reference compounds
    • Pre-packed assay cartridges for field analysis

    5. Hair Dye and Cosmetic Pigment Formulations

    Manufacturers of specialized semi-permanent hair colors and color care products use 5,7-Dihydroxy-4-Methylcoumarin as a colorant precursor and pigment stabilizer. Its reactivity supports stable, lasting color shades, especially in blonde and ash tone products. The raw material fulfills purity and migration requirements demanded by personal care regulatory frameworks while enabling color consistency across production batches.

    Industry compliance standards

    • EU Cosmetics Regulation 1223/2009 – Annex IV (Permitted colorants, purity criteria)
    • IFRA Code of Practice for raw material safety
    • US FDA 21 CFR Parts 73 and 74 (Color Additives)
    • ISO 22716 Cosmetic GMP guidelines for manufacturing and quality control

    Typical usage ratio

    • 0.01%–0.5% in final hair dye or pigment cream, adjusted for target shade intensity and carrier compatibility

    Downstream process integration

    • Blended with other color precursors during pigment paste preparation, then incorporated at the final emulsion or cream blending stage

    Final product types

    • Semi-permanent hair dye creams and gels
    • Color-protective shampoos and conditioners
    • Direct cosmetic pigment bases for skin and hair
    Free Quote

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    Certification & Compliance
    More Introduction

    5,7-Dihydroxy-4-Methylcoumarin: Insight From Our Manufacturing Floor

    Proudly Manufactured with Precision and Experience

    Our team spends every production cycle surrounded by raw materials, vessels, and the signature scent of freshly crystallized coumarin derivatives. Over years spent perfecting the process, 5,7-Dihydroxy-4-Methylcoumarin has become a standout for reliable quality and practical utility. Chemists and formulators reach for this compound because of its consistent track record across pharmacy research, analytical science, and organic synthesis. Its structure—coumarin’s familiar backbone, topped with methyl and hydroxy substitutions—offers both simplicity and versatility that appeal to those who value straightforward chemistry with genuine impact.

    Understanding the Chemistry Behind 5,7-Dihydroxy-4-Methylcoumarin

    In every batch we craft, attention follows from the bench straight into the final product. The methyl group attached at the 4-position and the hydroxy groups at the 5 and 7 positions change the way this molecule reacts compared to base coumarins. In practice, this means increased solubility in some organic solvents and altered photophysical behavior. These structural nuances matter when organizations use our material for fluorescence probes or antioxidants in pharmaceutical development.

    A single additional methyl group or hydroxyl here or there might not sound dramatic—until you consider how it shifts the electron density within the ring system. That’s often the difference between a compound that simply looks good on paper and one that provides measurable benefit in a particular assay or chemical transformation.

    Quality From First Reaction to Final Filtration

    Focusing on the nuances of chemical manufacture, we don’t put our name on a product unless we know precisely what’s in the flask. Standard practice for us includes repeated crystallizations, vacuum drying, and hands-on purity checks by skilled technicians who’ve seen more reaction colors than appear in any handbook. Typical lots of 5,7-Dihydroxy-4-Methylcoumarin meet purity above 99 percent, though we’re seldom satisfied with bare minimums. Spectral analysis, including HPLC and NMR, arms us with definitive evidence—cutting down on guesswork for downstream users.

    Every kilogram passes through controlled filtration systems, ensuring that neither trace acids nor common synthetic byproducts have a chance to tag along. Stability matters to our clients, so we package everything under inert conditions, preserving the light-sensitive core structure for as long as it sits in inventory.

    Model, Lot Size and Customization for real-world Uses

    We manufacture 5,7-Dihydroxy-4-Methylcoumarin under the designation DHC-47M, available in both research and semi-bulk scales. Across the range—gram vials, jar-packed hundreds of grams, and bespoke kilogram amounts—we see different priorities arise. University labs look for reproducibility in low-quantity packaging, while scale-up projects care about lot-to-lot consistency over long timelines. Both get the same starting material: solid, pale-yellow powder, with every batch traceable from reagent stock to finished jar.

    What sets our work apart is the attention paid to impurity profiles that influence chemical transformations, especially for sensitive syntheses. Our records chart impurity drift between lots and inform on-the-fly adjustments, allowing us to supply variants with controlled moisture content or tailored particle size for applications like microencapsulation or fine chemical synthesis.

    Practical Uses in Today’s Labs and Factories

    Talking shop with customers brings fresh perspective on how 5,7-Dihydroxy-4-Methylcoumarin fits into the workflow. Academic researchers lean into its fluorescent properties when developing ligand-binding assays or imaging reagents, taking advantage of both the inherent chromophore and the electron-rich ring system. Industrial formulators see value in the antioxidant capacity, particularly in applications where oxidative stability means longer shelf-life or greater thermal tolerance.

    We see niche uses pop up in bioassays aimed at inhibiting specific enzymes. Certain companies have reported applications in cytoprotection screens, where oxidative stress presents a daily challenge. Our product performs in these environments because careful manufacturing limits trace metal contamination—a known disruptor for high-sensitivity biochemical assays.

    Besides biological contexts, 5,7-Dihydroxy-4-Methylcoumarin remains relevant as a building block for more complex molecules. Synthetic chemists appreciate its clean conversion to ether or ester derivatives. The hydroxy groups participate readily in standard coupling reactions, reducing the need to coax or force reactions that, with less pure material, morph into troubleshooting headaches.

    Contrast with Other Coumarins and Hydroxy Fields

    Put our product next to 4-Methylcoumarin without hydroxy groups, and differences jump out: altered melting point, improved solvation, and distinct UV-vis chromophore response. With extra hydroxy groups at different positions—say, 6,7-dihydroxy—reactivity can swing wildly because of hydrogen bonding and electronic effects. Our hands-on experience says that 5,7-dihydroxy derivatives sit in a practical “Goldilocks zone” for both stability and functionalization. The subtle structural variations split the market for different end uses, but our DHC-47M grade stands out when both reactivity and purity are mission-critical.

    For those tracking trace impurity differences, the position of hydroxyls isn’t just a talking point. Regular production has taught us that substitution at the 5 and 7 positions leads to less tendency for oxidative degradation during long-term storage. By contrast, shifting these groups or overloading the ring with additional substituents opens doors to side products, autooxidation, or unwanted color formation—none of which have a place in a clean workflow or in imagery for fluorescence-based applications.

    Supporting Customers Beyond the Bottle

    Supplying chemicals isn’t just about clean packing or crisp crystallinity. We’ve partnered with groups to troubleshoot issues like stock handling—limiting moisture ingress, using non-reactive scoops, and enforcing regular turnover schedules for light-sensitive stock. Some larger clients install UV-filtered lighting in their storerooms after a bad run that traced degradation back to careless storage. Our advice: Store 5,7-Dihydroxy-4-Methylcoumarin cool and dark, but always double-check packaging seals on arrival.

    Feedback from researchers drives our upgrades, too. One collaboration in Europe involved tweaking drying cycles to push residual solvent content below the detection limit for a client running ultra-sensitive immunoassays. Small steps like these ripple out to the end result—fewer false positives, more reliable outputs. Experience tells us that practical attention to supply chain handling saves more time and money than any last-minute chemical rescue or reformulation.

    Genuine Differences Made at the Source

    Plenty of resellers push paperwork ahead of actual product quality. Our business roots run deeper—built on direct experience turning raw reagents into tangible results, not just trading volumes. Orders flow from a manufacturing team that knows how to troubleshoot a stuck filtration line and spot signs of photooxidation creeping into a batch. “Best practices” don’t live only on the whiteboard; they form part of our daily routine—clean glassware, fresh solvents, and double-blind checks between personnel.

    Where competitors sometimes rely on third-party tollers or anonymous intermediaries for processing, we keep lines of communication short and control points close at hand. This reduces delays, mistakes, and uncertainty inherent in supply chains where nobody “owns” the product through to the end. Customers who visit get to see our team in action, not just trust a story on a screen.

    Navigating Challenges in Real-Time Manufacture

    Controlling hydroxy substitution patterns on the coumarin core takes more art than theory would admit. Every synthetic run poses unique challenges—batch heating, solvent exchange, securing the right pH window to preserve structure without over-hydrolyzing. Only hands-on familiarity with side reactions, such as unintended O-methylation or partial ring closure, delivers the required quality time after time.

    It’s not all smooth sailing. Sourcing certain reagents or troubleshooting a frit blockage at 3 a.m. builds the kind of working memory that suppliers without real labs rarely understand. Each setback connects directly to higher standards: cleaner glass, fresh filters, or smarter solvent selection. Learning where error creeps in—sometimes a drop in ambient humidity, other times minor agitation changes—translates into tighter control of the many moving parts behind every delivered vial.

    Commitment to Evolving Standards

    Regulations and customer expectations shift without warning. Our plant sits ready to pivot, whether “non-detectable” means a different threshold this year than last, or a new guideline drops for residual solvents. In line with E-E-A-T principles, every claim about purity, stability, or handling arises from firsthand testing and documentation. The record of spectral data and production interventions is available for inspection and audit.

    Educating users matters, too: we contribute to technical forums and conferences, updating partners about new findings in coumarin derivative application. Sharing best practices—like the importance of sample splitting to avoid handling errors—creates more robust downstream science and greater community trust. The more transparent we are about bottlenecks and improvements, the faster the field advances.

    Outlook for Coumarin Derivative Research

    The future promises steady growth in both pharmaceutical and material science uses for 5,7-Dihydroxy-4-Methylcoumarin. Where older approaches stuck to classic coumarins, modern researchers pursue new analogs with properties like higher quantum yield, increased antioxidant capacity, or specialized bioactivity. Our role—steady production with real feedback—keeps us at the intersection of old-school chemistry and new technology, helping researchers transition discoveries from lab bench curiosity to validated industrial tool.

    Whether next advances arise in computational modeling, combinatorial screening, or scaled pilot runs, every innovation benefits from reliable chemical starting points. We’re seeing increased demand from contract research organizations and biotech, many of whom ask for documentation of traceability, full analytical reports, and assurance of supply continuity. Delivering on these points draws from a history of direct, hands-on production—meeting standards with more than words on a label.

    Driven by Experience, Grounded in Reality

    Producing 5,7-Dihydroxy-4-Methylcoumarin isn’t about ticking regulatory boxes or chasing minimum spec sheets. Every batch grows out of direct, practical experience—combining old-fashioned technical skills with the best of modern analytical support. Over time, we’ve learned the value of investing in continual process improvements, empirical troubleshooting, and close client feedback loops.

    For those who rely on coumarin derivatives—whether for research, analysis, or formulation—the differences between batches, suppliers, and handling aren’t trivia. They shape results, productivity, and even whole project outcomes. Our approach, shaped by years standing eye-to-flask with these products, puts reliable performance at the forefront and gives every customer the foundation for confident work and new discovery.