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3-Chloro-7-Hydroxy-4-Methylcoumarin

    • Product Name 3-Chloro-7-Hydroxy-4-Methylcoumarin
    • Alias 4-Methylumbelliferone 3-chloro-7-hydroxy-
    • Einecs 'EINECS 252-429-4'
    • 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

    104915

    Product Name 3-Chloro-7-Hydroxy-4-Methylcoumarin
    Cas Number 6257-44-7
    Molecular Formula C10H7ClO3
    Molecular Weight 210.62
    Appearance Light yellow to beige powder
    Melting Point 216-218°C
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store at room temperature, away from light and moisture
    Synonyms 3-Chloro-7-hydroxy-4-methyl-2H-chromen-2-one
    Smiles CC1=C(C=CC(=C1Cl)O)C2=O

    As an accredited 3-Chloro-7-Hydroxy-4-Methylcoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 50g of 3-Chloro-7-Hydroxy-4-Methylcoumarin is securely packaged in an amber glass bottle with a tightly sealed screw cap.
    Shipping The shipping of **3-Chloro-7-Hydroxy-4-Methylcoumarin** is handled with care, ensuring the chemical is securely packaged in airtight containers to prevent moisture and contamination. It is transported in compliance with regulatory guidelines for chemicals, typically via ground or air, with appropriate hazard labeling and accompanying safety documentation.
    Storage Store **3-Chloro-7-Hydroxy-4-Methylcoumarin** in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Use appropriate chemical-resistant containers and ensure proper labeling. Avoid excessive heat, moisture, and sources of ignition. Follow safety protocols and local regulations for storage of laboratory chemicals.
    Application of 3-Chloro-7-Hydroxy-4-Methylcoumarin

    Applications of 3-Chloro-7-Hydroxy-4-Methylcoumarin in Industrial Manufacturing

    As a direct manufacturer specializing in coumarin derivatives, we supply 3-Chloro-7-Hydroxy-4-Methylcoumarin to diverse industrial sectors. Our technical support extends from formulation selection to compliance guidance, addressing specific downstream requirements established by global industry leaders.

    1. Pharmaceutical Intermediate for Anticoagulant Synthesis

    This coumarin derivative functions as a key intermediate for the synthesis of selective oral anticoagulant APIs. Downstream pharmaceutical manufacturers rely on its defined reactivity profile to construct chemically protected warfarin analogs. Our quality control ensures repeatable purity and minimal residual solvents, in alignment with stringent medicinal chemistry needs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP & EP monograph guidance for related coumarin intermediates
    • 21 CFR Part 210/211 (cGMP for Pharma Manufacturing)
    • Certificate of Analysis (CoA) batch traceability

    Typical usage ratio

    • 0.8–1.3 molar equivalents relative to active core backbone per batch
    • Adjusted by targeted conversion and desired impurity profile

    Downstream process integration

    • Introduced in the synthetic step before cyclization or halogenation
    • Blended with protected anilines and catalyst base under controlled reflux conditions
    • Subjected to subsequent hydrolysis or methylation if required by downstream structure

    Final product types

    • Warfarin sodium and related coumarin anticoagulant APIs
    • Coumarin-based blood thinner bulk powders
    • Pharmaceutical-grade intermediates for clinical trials

    2. Specialty Fluorescent Dye Intermediate

    Manufacturers of advanced fluorescent and laser dye systems select this compound for its high-yield transformation into tailored benzochromene dyes. The hydroxy and chloro groups allow precise substitution during dye synthesis, ensuring controlled quantum yield properties for specialty coatings, imaging reagents, and optical fiber components. Supply is accompanied by technical data on spectral purity and stability profiles.

    Industry compliance standards

    • ISO 9001 quality management for dye intermediates
    • EN 71-3 (Safety of Toys – migration of certain elements, for pigments in children’s products)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ASTM D4303 for lightfastness testing

    Typical usage ratio

    • 5–30% w/w in reaction mixture for targeted coumarin core formation
    • Adjusted depending on substituent groups and final emission wavelength requirements

    Downstream process integration

    • Dissolved in organic solvents with alkylating agents at elevated temperature
    • Reacted in presence of base and metal catalysts for coupling with aromatic amines
    • Purified by column chromatography before formulation into dye product

    Final product types

    • High-brightness laser dyes
    • Ultraviolet-activated fluorescent materials
    • Non-destructive testing indicator liquids
    • Optical brighteners for polymer films

    3. Agrochemical Synthesis—Fungicide and Herbicide Precursors

    This specialty intermediate forms part of downstream synthesis routes for coumarin-derived fungicides and select herbicides. Formulators use its methyl and chloro-functionalities to enable regioselective acylation and cyclization steps under catalytic control. Documented batch consistency supports registration with regulatory entities, enabling downstream users to streamline their compliance dossiers.

    Industry compliance standards

    • FAO/WHO Specifications for Agrochemical Active Ingredients
    • ISO 17025 for analytical testing laboratories in agrochemical QC
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • China’s Ministry of Agriculture GB 2763 MRLs

    Typical usage ratio

    • 0.2–1.5 weight ratio relative to target active ingredient
    • Adjusted per desired yield of cyclized heterocycle or ester functionality

    Downstream process integration

    • Introduced during the initial coupling reaction with methylated phenols
    • Subjected to stepwise chlorination or condensation with herbicide scaffold precursors
    • Final intermediates isolated via flash chromatography

    Final product types

    • Selective systemic fungicides for cereals and rice
    • Pre-emergent herbicide technical concentrates
    • Foliar-applied pesticide formulations
    • Coumarin analogs for biosafe crop protection

    4. UV Absorber and Stabilizer for Polymer Additives

    The coumarin scaffold enables downstream formulators to build UV absorber masterbatches for engineering plastics and coatings. The para-hydroxy substitution plays a crucial role in scavenging radical species triggered by UV exposure, while the methyl group supports melt processing compatibility. Customer-specific quality documentation includes analytical results on purity and residual solvents for compliance with polymer and electronics-grade standards.

    Industry compliance standards

    • RoHS Directive for heavy metals and halogenated substances
    • EN ISO 4892 Weathering Testing for Plastics
    • UL 94 flammability rating for polymer additives
    • FDA 21 CFR 177.1520 for indirect food contact materials (if applicable)

    Typical usage ratio

    • 0.05–0.15% w/w in polyolefin or polyester masterbatch formulation
    • Adjusted according to required UV protection factor and end-use exposure conditions

    Downstream process integration

    • Pre-dispersed into hot-melt concentrate with other light stabilizers
    • Extruded with base resin in twin-screw compounding line
    • Pelletized and QC sampled for distribution uniformity

    Final product types

    • UV-stabilized films and sheets for automotive and architectural glazing
    • Electronics-grade protective coatings
    • Masterbatch pellets for polycarbonate and polyethylene applications
    • High-durability outdoor signage and panels

    5. Analytical Reagent and Fluorescent Probe Precursor

    Leading manufacturers in clinical diagnostics and chemical analysis incorporate this molecule as a precursor for custom fluorescent probes. The hydroxy and chloro groups facilitate unified synthesis of calibration reagents for chromatographic and imaging assays, with high spectral definition and reproducibility. Supplied in analytical grade, our material undergoes additional filtration and packaging for laboratory reagent markets.

    Industry compliance standards

    • ISO 13485 for Medical Device Reagent Manufacturing (where applicable)
    • USP Reagent Grade for laboratory use
    • GLP (Good Laboratory Practice) for traceability
    • OECD guidelines for analytical validation

    Typical usage ratio

    • 0.01–0.5% by weight in probe conjugation reaction mixtures
    • Optimized according to detection sensitivity and sample matrix

    Downstream process integration

    • Coupled with linker chemistry to form target-specific probes
    • Integrated into lyophilized diagnostic reagent kits or liquid calibrators
    • Subject to spectral calibration and batch validation

    Final product types

    • Fluorescence-labeled diagnostic markers
    • Chromatography calibration solutions
    • In-vitro diagnostic (IVD) reagent components
    • Trace analysis kits for forensic and food safety testing
    Free Quote

    Competitive 3-Chloro-7-Hydroxy-4-Methylcoumarin prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Chloro-7-Hydroxy-4-Methylcoumarin: A Focus on Quality and Practical Use

    Our Experience Manufacturing 3-Chloro-7-Hydroxy-4-Methylcoumarin

    At our chemical plant, we have spent years synthesizing and handling coumarins for both domestic and international partners. 3-Chloro-7-Hydroxy-4-Methylcoumarin stands out among its peers for a few solid reasons: consistent reactivity, high purity after recrystallization, and a manageable profile during scale-up from lab to tonnage batches. The product’s appearance may not catch the eye—a pale yellow or off-white crystalline solid with a slight aromatic note—but there’s a real sense of accomplishment that comes with every batch meeting the high standards that pharmaceutical and specialty chemical applications demand.

    We aren’t working with an abstract white powder; every shipment gets the personal touch—small-batch inspection, heel samples for traceability, HPLC tests to verify purity, and frequent spot-checking with NMR for structural consistency. Over time, our crew has fine-tuned the conditions for chlorination at the 3-position to maximize selectivity while minimizing byproduct formation. Mishaps in temperature control—or using a low-grade solvent—can trigger impurity profiles that sabotage downstream coupling or condensation steps. Once you have worked a full shift troubleshooting off-spec material, you learn how small decisions in process management impact the lives of those running the next reaction, whether in research or kilo-lab production.

    Understanding Specifications and Model Differentiation

    3-Chloro-7-Hydroxy-4-Methylcoumarin, with its CAS number 2491-78-5 and molecular formula C10H7ClO3, is more than just a collection of atoms in a row. Batches from our reactor generally fall between 98% and 99.5% HPLC purity. That might seem like splitting hairs for those used to bulk commodity chemicals, but every fraction of a percent can influence the crystallization behavior or the UV absorption profile.

    We control particle size through filtration and drying, since fine powders can trigger dust hazards or suffer from static buildup in the packaging line. Many of our customers request a tighter cut on moisture content, below 0.3%, which doesn’t happen by accident—especially in high-humidity months. Small improvements in our tray dryers’ airflow and the addition of clean room protocols have paid off in customer feedback and repeat orders.

    Unlike basic coumarin derivatives, 3-Chloro-7-Hydroxy-4-Methylcoumarin requires special attention at the chlorination and hydrolysis stages. The presence of both hydroxyl and chloro functional groups gives this molecule a dual edge: improved reactivity in Suzuki or Buchwald-Hartwig cross-coupling, and better solubility in polar organic solvents. Compared with 7-hydroxy-4-methylcoumarin (without the halogen), you’ll notice a shift in NMR spectra and improved leaving group behavior, especially for applications that require further substitution at the 3-position.

    Why Synthetic Consistency Matters in Real-World Production

    Our manufacturing team knows that this coumarin derivative usually finds its way into pharmaceutical research, notably as building blocks for kinase inhibitors, antimicrobial scaffolds, and advanced fluorescent probes. Quality can’t be separated from end-use. We get calls from synthetic chemists and R&D directors who already have a procedure in mind, and even slight batch irregularities can force them to rethink purification. More than once, a purified kilogram has been reworked because the starting material failed a simple color spot test or TLC check. That kind of feedback stings, but it sticks with you. We have since tightened our final filtration to remove persistent colored impurities—traces that would otherwise escape routine UV detection.

    This isn’t just about meeting a check-box on a spec sheet. Pharmaceutical developers care about trace contamination, polymorph formation, and the quirks of solvent residue—all factors that don’t just slow their progress, but spike costs and delay timelines. By providing a coumarin intermediate that’s robust batch-to-batch, you foster a working relationship rather than a transactional sale. Part of the job is anticipating downstream synthetic requirements: Is the product stable under light? Will a particular counter-ion from purification interfere with a catalyst later? Our experience has forced us to approach every batch as a collaborative effort with the chemists who depend on us.

    Uses and Applications—Insights from the Manufacturer

    Like many aromatic lactones, this product started attracting attention for its versatility. Research groups and commercial enterprises approach us for three main reasons. The primary use falls in pharmaceutical synthesis. Medicinal chemists chase scaffolds that blend hydrophobic and hydrophilic features, and the combination of hydroxy and chloro groups on the coumarin backbone enables both ester formation for prodrugs and cross-coupling for rapid analog development. Where other coumarin intermediates fall short, this one helps open new routes to fluorinated, alkylated, or amino-modified analogs that wouldn’t be accessible by direct substitution.

    Another common use is in fluorescence chemistry. The extra chloro substituent at the 3-position modifies the photophysical properties, shifting excitation or emission profiles and opening the door to new analytical probes for molecular biology. Early on, we fielded calls from researchers who struggled with batch-to-batch variability in absorption wavelength—a signal that purity and the control of minor impurities (not just main component) truly matter for photonics applications.

    There is also a niche pull for specialty fragrance and agrochemical research, though in our experience, those are smaller volumes. A few partners have asked about alternative solubility profiles for encapsulation systems, particularly in controlled-release agricultural setups. The dual oxygenation (lactone and hydroxy) keeps doors open for functional modification, from sulfonation to etherification, without triggering significant decomposition or discoloration.

    We see projects that take this intermediate in surprising directions. Some clients are pushing it for custom dye development and as a precursor for UV-blocking co-polymers in specialty coatings. The nature of this molecule allows for tunable derivatization—clients can branch off into sulfonate, alkoxy, or amino-modified products with predictable yields, and that wasn’t always possible with simpler coumarins. The real deciding factor: how carefully your batch controls trace halogen content, water, and residual starting materials.

    How We Address Differences from Other Products

    Our competitors often offer simple hydroxycoumarins or non-halogenated analogs. These work fine for textbook reactions. Yet at production scale, the presence of the 3-chloro group saves time in halogen exchange reactions and speeds up Suzuki and Buchwald-Hartwig couplings. Anyone running a large combinatorial library knows halogen introduction adds steps, wastes starting material, and requires harsher conditions—so having it built into the molecule smooths the path for both discovery and manufacturing.

    Chloro/hydroxy combinations on a methylcoumarin backbone aren’t easy to isolate without some skill. Side products from over-chlorination or incomplete hydrolysis can cloud up the purity and complicate process validation. Over the years, we have fielded calls from process engineers who spotted cloudiness or precipitate during their own recrystallizations, only to trace it back to starting material shortfalls. Our team continues to invest in process adjustments—updated quenching protocols, trace metal removal, and vapor phase drying—which have trimmed down batch rejection rates and won more loyal customers in the fine chemicals sector.

    Some products sold on the open market cut costs by skipping steps in final purification. By sticking with more labor-intensive isolation and chromatography, we maintain a low impurity profile, which benefits the next operator’s synthetic campaign. Recently, a customer pointed out that switching providers resulted in problematic downstream N,N-dialkylation side reactions. Upon testing, the culprit was a residual dichloro byproduct. Technical details like that don’t show up in general market summaries, but make all the difference on a scale where every kilo counts.

    Temperature- and light-sensitivity can also distinguish lots of 3-Chloro-7-Hydroxy-4-Methylcoumarin. Uncontrolled exposure will prompt slow degradation or even batch spoilage. Our facility invested in amber glass-lined storage and double-bagged secondary containment. By tailoring storage and freight conditions, we keep the active content and appearance stable—all while minimizing formal quality disputes.

    Even something as basic as melting point range (the typical value sits around 184–186 °C in our best lots) cues repeat buyers to genuine manufacturing consistency. Tiny shifts in this range signal small changes in microstructure or crystal hydration, and buyers who track these with us over repeat orders gain trust that we aren’t swapping sources or reverting to alternative synthetic routes to trim costs.

    Addressing Customer Issues and Looking to the Future

    Chemists using our 3-Chloro-7-Hydroxy-4-Methylcoumarin typically raise two main issues: solubility in unusual solvents, and batch-to-batch reactivity. We have worked with customers who require large volumes dissolved in polar aprotic solvents for continuous flow synthesis. Factors like humidity during drying can throw off exact solubility, so our drying room logbook is now checked at every shift change. Moisture pick-up isn’t just a cosmetic flaw; it directly alters downstream yields in organometallic desks.

    Requests for custom particle size drive us to update our filtration technology annually. Finer cuts suit rapid dissolution, but they bring higher risk of dust and operator exposure. Our line crew weighs in with practical feedback—on one occasion, a change in filter paper grade stopped both nuisance fines and prevented machine blockages. These updates, born from day-to-day operator experience, trickle back into product consistency.

    Long-term, our plant intends to further automate both analytical verification and recipe scale-up. Customers increasingly submit detailed requests for electronic QC records, which we supply. Traceability isn’t just a buzzword, so we archive both analytical spectra and video logs of each batch drawdown. Teams in process development appreciate this transparency, especially venture-backed or regulatory-focused startups who can’t afford to troubleshoot unknown starting materials.

    Final packaging is another make-or-break point. We pack in HDPE drums lined with moisture-absorbent sachets and tamper-proof seals. Early in our production, leftover odors from cleaning solvents once flagged our lots to QA inspectors—simple fixes to our cleaning schedule stemmed complaints and nudged customer loyalty upward.

    We’re realistic about the scope and demands of our customer base. The rise of AI-driven synthesis robots and machine-learning retrosynthesis means that ingredient consistency and digitized QC will only grow more crucial. Our goal is to guide our process teams to stay a step ahead, tweaking recrystallization protocols, purging lines more aggressively, and logging every change—not for bureaucratic neatness, but because those details keep chemists at the bench one step ahead in their own timelines.

    Continuous Improvement, Backed by Hands-On Experience

    Our experience producing 3-Chloro-7-Hydroxy-4-Methylcoumarin taught us respect for the cumulative impact of small process changes. The strictest analytical regime sometimes misses what a careful inspector will spot—a slight color cast, a skewed melting point, or a crystallization issue on a humid day. This kind of tactile familiarity with the product ensures we don’t become complacent as volumes ramp up or client requirements evolve.

    Raw materials present one of the deepest sources of variability. A new batch of coumarin, a minor grade shift in anhydrous solvents, or a supply-chain-driven switch in chlorinating agent—all can create headaches downstream, sometimes only showing up as slightly shifted chromatograms in end-use. Our procurement strategy now links raw material batch IDs through every stage. This change stems from real-world challenges, not regulatory pressure, and gives our partners confidence that the supply is only as consistent as our attention to detail.

    As regulatory scrutiny increases, especially in pharmaceutical and biotechnological applications, our analytical portfolio continues to grow. We now confirm trace heavy metals, halogen content, and conduct advanced photostability assays to make sure every lot entering the supply chain performs as intended. Customers pursuing green chemistry ask about solvent recovery and energy use; our answers don’t come from a marketing sheet, but from process logs and energy audit figures.

    Looking Ahead: Supporting Next-Generation Chemistry

    3-Chloro-7-Hydroxy-4-Methylcoumarin is carving out new territory in specialty fine chemicals, diagnostics, and advanced materials. The teams who work to make every lot match the last know firsthand that consistency matters more than chasing the lowest price. Feedback from researchers, production chemists, and QA departments all helps us refine batch parameters and flag quirks before they reach a pilot plant or a glass column.

    We make no pretense about solving every synthetic challenge with a ready-made answer. Still, daily experience on the production floor—watching the color change during chlorination, logging humidity swings on sticky days, double-checking each final HPLC chromatogram—builds practices that are harder to codify, but mean better results for the people counting on us. Strong relationships throughout the supply chain, transparent dialogue on every batch variance, and the occasional course correction have helped us build a product that punches above its weight in quality and reliability.

    In short, the work doesn’t stop at synthesizing a molecule and checking a box. The ongoing challenge is seeing how every process tweak, every material swap, and every close call with an off-spec reaction shapes the quality and utility of 3-Chloro-7-Hydroxy-4-Methylcoumarin. Hands-on experience—listening to partners, testing every lot, and remembering where setbacks first taught us care—continue to inform how we make, and remake, this versatile intermediate for chemists everywhere.