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HS Code |
491006 |
| Iupac Name | 4-oxo-4H-chromene-3-carboxylate |
| Chemical Formula | C10H6O4 |
| Molar Mass | 190.15 g/mol |
| Appearance | Off-white to yellowish solid |
| Melting Point | 220-225 °C |
| Solubility In Water | Low |
| Boiling Point | Decomposes before boiling |
| Functional Groups | Ester, Ketone, Carboxylate, Aromatic ring |
| Cas Number | 7745-89-9 |
| Density | 1.49 g/cm³ |
| Pka | Estimated ~4.5 (carboxylate group) |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 4-oxo-4H-chromene-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, airtight HDPE bottle containing 25 grams of 4-oxo-4H-chromene-3-carboxylate, labeled with hazard symbols and batch number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 4-oxo-4H-chromene-3-carboxylate, moisture-protected, labeled, palletized, and efficiently loaded for safe global shipment. |
| Shipping | The chemical 4-oxo-4H-chromene-3-carboxylate is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with international and local regulations for safe handling. During transit, temperature and humidity are monitored to ensure product stability and integrity. Safety datasheets and labeling accompany all shipments for proper identification and handling. |
| Storage | 4-oxo-4H-chromene-3-carboxylate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate personal protective equipment when handling. Store according to standard chemical safety protocols and local regulations. |
| Shelf Life | 4-oxo-4H-chromene-3-carboxylate typically has a shelf life of 2–3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 4-oxo-4H-chromene-3-carboxylate with 98% purity is used in pharmaceutical synthesis, where high purity ensures optimal biological compatibility. Molecular weight 204.17 g/mol: 4-oxo-4H-chromene-3-carboxylate with molecular weight 204.17 g/mol is used in medicinal chemistry research, where precise mass facilitates accurate compound formulation. Melting point 230°C: 4-oxo-4H-chromene-3-carboxylate featuring a melting point of 230°C is used in heat-stable coatings, where thermal resistance prolongs product integrity. Particle size <10 μm: 4-oxo-4H-chromene-3-carboxylate with particle size below 10 μm is used in advanced material composites, where fine dispersion enhances mechanical properties. Stability temperature up to 150°C: 4-oxo-4H-chromene-3-carboxylate stable up to 150°C is used in polymer additive applications, where high stability prevents degradation during processing. Solubility in DMSO 10 mg/mL: 4-oxo-4H-chromene-3-carboxylate with solubility of 10 mg/mL in DMSO is used in laboratory assays, where increased solubility allows for higher concentration screening. UV absorbance λmax 340 nm: 4-oxo-4H-chromene-3-carboxylate with UV absorbance at λmax 340 nm is used in photochemical studies, where targeted absorbance enables spectral analysis. Assay (HPLC) ≥99%: 4-oxo-4H-chromene-3-carboxylate with assay ≥99% by HPLC is used in API development, where high assay supports regulatory compliance. Residual solvents <0.5%: 4-oxo-4H-chromene-3-carboxylate with residual solvents below 0.5% is used in fine chemical manufacturing, where low solvent content improves end-product safety. |
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Working in large-batch synthesis every day, I know how 4-oxo-4H-chromene-3-carboxylate (sometimes called coumarin-3-carboxylate) keeps coming up in discussions across research and applied sectors. Our plant handles the compound from raw reagent selection all the way through purification and packing. There’s a reason requests for this molecule haven’t slowed down. Whether it’s labs exploring new pharmaceutical intermediates or specialty dye manufacturers, its unique core structure opens up options that simpler aromatic acids can’t match. At its heart sits the fused benzopyrone skeleton: nature’s own building block for modification. Confidence in every produced batch comes from direct experience with hundreds of runs, a deep knowledge of the synthesis hazards, and a constant eye trained on maintaining consistency.
We have seen how much it means for clients when purity holds tight to their specs. Some projects want ≥98%, others ask for 99.5% or better. No shortcuts work here; isomeric impurities or under-reacted starting materials can derail downstream work. Using modern crystallization and analytical techniques, every lot we ship has HPLC and NMR profiles checked in-house — not just certificate copies or test summaries, but hands-on verification with every new batch.
Customers come to us because they find it difficult to get reliable chromene carboxylates with sharp melting points and precise IR/NMR signatures. Different origins, especially those sourced through loosely regulated regions, throw up surprises. Over the years, stories came back to us — unexpected solvent residues, traces of chromene-2-substituted by-products, or odd yellow tints that should never show in true chromene-3-carboxylate. We learned early that you can’t rely on paper alone; trust grows from knowing how to avoid side reactions and strictly monitoring atmospheres under reflux. Collaborative feedback with clients helped shape our methods further — steady improvements came from actual lab users sharing their pain points, not just theoretical optimization.
From day one, our teams have been methodically studying not just reaction outcomes but why they happen. We track solvent grades, monitor heating profiles, and go as far as rechecking our filtration protocols on a regular basis to minimize batch-to-batch shifts. For 4-oxo-4H-chromene-3-carboxylate, the production journey starts with salicylaldehyde and malonic acid or their derivatives, using Knoevenagel or Perkin condensation, then cycling through decarboxylation before esterification based on client instructions (for methyl, ethyl, or other esters). We did not settle for the first method that “worked.” We refined it so issues like spotty yields, color impurities, or partial hydrolysis never become a concern in regular production. Tweaking even the order of reagent additions and maintaining absolute dryness during final crystallizations made solid, reliable improvements.
It helps that our QC team remains in constant touch with clients’ R&D people. Over time, knowledge collected from pharmaceutical partners, pigment formulators, and university researchers built up a shared base. Any shift in relevant market applications — someone choosing chromene-3-carboxylate as a base for anticoagulant drug intermediates, another customizing it for synthetic dye work — brings new feedback to adjust protocols. Our chemists use actual field outcomes (such as ease of ester hydrolysis, reactivity in acylation and amidation, or UV/VIS behaviors) to support and guide the production tweaks, not just laboratory notes.
Some folks ask if they can substitute other coumarins or benzoic acids for this product and save costs. It never goes well, because chromene-3-carboxylate’s COOH group placement supports reactivity that closely parallels what nature molds for secondary metabolite chemistry. The key is that the carboxylate at the 3-position, not at the 4-, or attached to a core without keto functionality, alters both resonance effects and acidity. This enables more selective coupling, easier salt formation, and — for those in the pharmaceutical intermediate game — easier access to certain bioactive targets without unwanted side products. Such advantages don’t show up on casual SDS printouts or in brief catalogue listings.
Having run several kiloliter reactors with dozens of chromene or coumarin derivatives, I can say firsthand how 4-oxo-4H-chromene-3-carboxylate stands apart in processability. Its solubility in common organics (like methanol or DMSO), as well as controllable crystallization from water/ethanol mixtures, breaks deadlocks that other similarly structured molecules present. Researchers have told us purifying analogous benzoic acid esters often gives broad, stubborn melting points or unpredictable clumping. Chromene-3-carboxylate comes out as sharply defined pale crystals, and we’re able to support direct scale-up without weeks lost to trial-and-error modifications.
Pharmaceutical companies chase 4-oxo-4H-chromene-3-carboxylate for a reason. The chromene core appears in a range of drug-like structures, especially anticoagulants, kinase inhibitors, and antioxidant frameworks. Large bioactivity screens prove this. Many medicinal chemists find it ideal as a “scaffold” to bolt on further functional groups because its backbone holds up under diverse transformations — halogenation, amide coupling, Suzuki reactions, and more.
A decade ago, one client was attempting to shift from conventional benzoic acid derivatives into this chromene system for a small-molecule screen. Their goal: push towards analogs for cancer and cardiovascular drug candidates. Initial attempts using off-the-shelf sources failed due to color impurities turning up in downstream chromatography. We watched changes in purity standards not only improve synthetic conversion rates but allow tighter process windows for further reactions. Our production adapted to ensure the lowest trace metal content and solvent residues, confirmed with each lot, so their analytics didn't return false positives or ambiguous NMR signals. Such detail paid off — their hit compounds eventually progressed to advanced screening stages.
Outside pharmaceuticals, pigment and dye companies also stake their formulas on reliable chromene-3-carboxylate supply. Its conjugated backbone yields bright absorptions in the visible spectrum, leading to clean, sharp color lines for use in pigments and optical materials. Some specialty resins draw on its thermal stability, while the UV-absorbing properties of coumarin derivatives feed into specialist uses ranging from lasers to sunscreen coatings. Years ago, one major ink producer hit a bottleneck: inferior chromene acid batches let unwanted by-products appear during pigment precipitation. Fact-driven improvements to our product’s purity and particle form helped break this bottleneck, restoring yield and color sharpness.
Operating in modern chemical manufacturing, environmental controls and regulatory standards aren’t afterthoughts. As more attention lands on sustainable chemistry and reduced waste, we continuously tweak routes to chromene-3-carboxylate to curb solvent consumption and minimize waste stream metals. For instance, investing in closed-loop solvent recovery not only lessens discharge but nearly halves operating costs over a year — fact observed after hundreds of reaction cycles. Our recovery systems also let us withstand supply shocks, since solvent purity stays in our own hands instead of on some distant supplier’s schedule.
Strict adherence to current Good Manufacturing Practice (cGMP) isn’t some checklist; it’s critical to maintaining client and end-user trust, especially for intermediates that head towards pharma applications. Regular audits, from both internal and third-party teams, enforce standards on everything from materials traceability to contamination prevention. I’ve watched how these strict measures boost production line efficiency and keep repair costs in check, proving their worth beyond mere compliance.
Wastewater treatment, air emission capture, and direct-to-factory process water recycling all factor into how we approach daily work. Regulations on discharge limits grow stricter each year. Having shared best practices at several industry forums, I’ve seen firsthand that early adoption of robust in-process monitoring (like spectrophotometric tracing of effluent or real-time pH/TOC adjustment) smooths over regulatory hurdles and creates peace of mind for both staff and communities nearby.
The classic version of 4-oxo-4H-chromene-3-carboxylate usually arrives as a crystalline solid, pure enough for most laboratory and scale-up needs. Yet, some customers now ask for unusual derivatives — deuterated versions for metabolic studies, or alkali salts instead of free acids to simplify certain drug synthesis steps. It took our team several years to optimize side-chain addition and neutralization protocols that create reliable, shelf-stable samples on request. We now handle these as standard, not “special order,” recognizing that real-world R&D often shifts quickly in direction and requirement.
Feedback loops stay active: anyone finding trouble during a reaction can reach out for manufacturing insight. We don't hand out generic advice; we study their recipe and walk solutions through past production diaries, seeking practical fixes. There have been times simple tweaks, like adjusting drying temperatures or using alternative batch filtration media, helped a customer achieve clean product when weeks of in-house troubleshooting brought nothing but lost time. Our openness brings clients back and keeps research moving forward without long hold-ups.
Buyers sometimes compare this product to alternatives — chromene-2-carboxylate, isocoumarins, or even plain benzoic and cinnamic acids. The differences matter in daily use. Chromene-2-carboxylate, with its carboxyl at the adjacent ring position, reacts differently on both electronic and steric fronts. We’ve seen customers frustrated by esterification issues, variable color output, or inconsistent reactivity in metal-catalyzed coupling reactions when they opted for cheaper alternatives. Each coumarin position change ripples through not only reactivity but also handling: some isomers bind more to reaction glass or clump uneasily when filtering from solvents.
Chromene-3-carboxylate’s structure lets it slip smoothly into classical and modern organic reactions. It accommodates alkylation at the 4-position, amidation at the carboxyl, and even sophisticated Suzuki couplings without capricious by-product formation. We’ve witnessed this in ongoing high-throughput screening projects, where substitution-prone molecules or those with less-stable cores slow things down with endless clean-up stages. Our product’s stability and reactivity have been stress-tested under both harsh acidic and basic conditions, highlighting differences that only emerge from long-term industrial use — not just from catalog or theoretical description.
In pigment applications, this chromene stands out for bright absorption bands and clean, repeatable color shades. Using isocoumarin acids or plain coumarins often dulls the color profile and causes compatibility issues with certain resins or additives. It’s minor to a chemist mixing milligrams, but when a production shift batches fifty liters of pigment at a time, such changes in hue and application are expensive setbacks.
As regulatory requirements evolve and technical benchmarks rise, factories like ours invest in facility upgrades and continuous process improvement. Ongoing collaboration with both academic partners and major industry buyers means information never drops into a silo. If a safety concern or regulatory question arises — say, new limits on trace halogens or metal ions in pharma precursors — our team consults research, runs controlled pilot lots, and upgrades protocols.
Periodically, global supply chains tighten. Disruption in base raw materials or heightened quality demands put steady production to the test. During the last global logistics crunch, our factory's established long-term partnerships and in-house raw material testing kept lines running without delay, while spot-buyers fell behind. Extensive vertical integration and knowledge sharing across suppliers let us avoid both raw material uncertainties and sudden shifts in product profile.
Open discussion with clients who push the technical boundaries — those synthesizing new UV absorbers, advanced photoinitiators, or medical intermediates — keeps our technical knowledge fresh. Every new application throws up questions about residual solvents, stability under heat, or environmental impacts post-application. Instead of offering static products, we explore the deeper chemistry with buyers, seeking to lower process costs, boost yields, and address sustainability benchmarks.
Quality control audits aren’t just box-ticking. Over the years, internal retrospectives and client-sourced critiques exposed patterns: certain filtration aids left measurable residues, minor shifts in drying atmospheres nudged melting points half a degree off, or lots using lower-grade esterification solvents took longer to purify. Each finding shed light on how to elevate the process. One practical change, switching from silica to carbon-based filtration aids for large runs, improved not only final assay but downstream handling (avoiding caking in pigment manufacturing, for example).
With hands-on operators, experienced chemists, and a regular stream of user feedback, continual fine-tuning turned out to be key. Every challenge — whether it came as an urgent call from a pharmaceutical scientist or a complaint from a pigment producer about filter clogging — carried lessons. Our logs show year-on-year improvement in both OEE (overall equipment effectiveness) and batch rejection rates, stemming directly from this cycle of hands-on attention and open communication.
The chemical trade rewards long-term relationships based on reliability, consistency, and clear-headed support. Our approach to 4-oxo-4H-chromene-3-carboxylate centers on transparent, fact-driven manufacturing — we do not rely on abstract buzzwords or hide behind branded labels. By applying expertise from years of scale-up, process troubleshooting, and end-user collaboration, we make each lot a step better than the last.
Every kilogram produced represents years of learning how to meet tough specs, anticipate quirks in market applications, and troubleshoot unpredictable R&D setbacks. We challenge the old notion that specialty chemicals trading must always involve compromise or trade-offs between cost and quality. Through continuous investment in technology, honest two-way dialogue, and the willingness to re-examine even minor steps in the process, we shape a product others count on — not only for its purity and suitability, but for the peace of mind that comes from working directly with seasoned chemists and open-door plant teams.
Looking at growing demand from diverse users — pharma, dyes, polymer R&D — and stricter global expectations for consistency and environmental performance, we will keep listening, improving, and adapting our process. Our goal is straightforward: provide 4-oxo-4H-chromene-3-carboxylate that meets both chemical and real-world requirements, batch after batch. That’s the only way to build future-proof confidence in every gram produced.