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HS Code |
230591 |
| Chemical Name | Ethyl 2-Oxo-2H-Chromene-3-Carboxylate |
| Molecular Formula | C12H10O4 |
| Molecular Weight | 218.21 g/mol |
| Cas Number | 26247-13-6 |
| Appearance | White to off-white solid |
| Melting Point | 110-113 °C |
| Solubility | Soluble in organic solvents such as DMSO, ethanol, methanol |
| Purity | Typically ≥98% |
| Smiles | CCOC(=O)C1=CC2=CC=CC=C2OC1=O |
| Storage Conditions | Store at room temperature, protected from light and moisture |
| Iupac Name | Ethyl 2-oxo-2H-chromene-3-carboxylate |
As an accredited Ethyl 2-Oxo-2H-Chromene-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of Ethyl 2-Oxo-2H-Chromene-3-Carboxylate, labeled with hazard warnings and product details. |
| Container Loading (20′ FCL) | 20′ FCL loading: 10MT on pallets, 25kg fiber drums, securely packed and shrink-wrapped, ensuring safe transportation of Ethyl 2-Oxo-2H-Chromene-3-Carboxylate. |
| Shipping | Ethyl 2-Oxo-2H-Chromene-3-Carboxylate is shipped in tightly sealed containers under dry, cool conditions. The packaging complies with chemical safety standards to prevent leaks or contamination. Proper labeling and documentation are included, and the shipment may require handling as a potentially hazardous material according to local and international regulations. |
| Storage | Ethyl 2-Oxo-2H-Chromene-3-Carboxylate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Ensure proper labeling and store at room temperature or as directed by the manufacturer’s guidelines for chemical stability and safety. |
| Shelf Life | Ethyl 2-Oxo-2H-Chromene-3-Carboxylate typically has a shelf life of 2–3 years when stored in a cool, dry place. |
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Purity 98%: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Melting Point 118°C: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with a melting point of 118°C is used in organic synthesis, where consistent melting enhances process repeatability. Particle Size 10 µm: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with particle size 10 µm is used in fine chemical production, where rapid dissolution accelerates reaction rates. Molecular Weight 232.22 g/mol: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with molecular weight 232.22 g/mol is used in heterocyclic compound development, where precise stoichiometry improves formulation accuracy. Stability Temperature 60°C: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with stability at 60°C is used in agrochemical formulations, where thermal stability ensures shelf-life extension. Viscosity Grade Low: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with low viscosity grade is used in liquid dye manufacturing, where enhanced flow properties enable uniform dispersion. Solubility in Methanol ≥20 mg/mL: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with solubility in methanol ≥20 mg/mL is used in analytical chemistry protocols, where high solubility facilitates sample preparation. Assay ≥99%: Ethyl 2-Oxo-2H-Chromene-3-Carboxylate with assay ≥99% is used in reference standard preparation, where high assay guarantees analytical reliability. |
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In our manufacturing halls, every batch of Ethyl 2-Oxo-2H-Chromene-3-Carboxylate tells a story that goes beyond routine synthesis. We begin each production cycle by selecting high-grade raw materials, free from unwanted byproducts and moisture. Our teams track each variable throughout the process—temperature, stirring rate, solvent quality—to secure reliable crystalline purity for every lot.
Over years of experience with the coumarin series, we've learned the value of precision. This compound, often referred to as an ethyl ester of a coumarin carboxylate, bridges the gap between basic chromene structures and more advanced pharmaceutical intermediates. Chemists searching for predictable reactivity often turn to this molecule. In the glass reactor, the esterified carboxyl group on position 3 doesn’t complicate downstream reactions. The free keto group at position 2 remains accessible, opening up routes for acylations, alkylations, and hydrolysis. Such versatility allows our customers to move quickly from development to larger-scale projects.
Reliable synthesis serves no one without consistent purity. Our supervisors establish production parameters that reduce side products, especially those that could trace back to oligomerization or hydrolysis at the sensitive 3-position. We filter each batch with vacuum techniques, not just to speed up work but to lower contamination risks. Thin Layer Chromatography and HPLC analyses take place in-house, every time, with documented trends kept on file for reference.
Trace levels of residual solvents sometimes cause headaches in labs not focused on careful solvent removal. Our approach lowers ethyl acetate, dichloromethane, and other process solvents to below industry-standard thresholds. We run Karl Fischer titrations in wet seasons, looking for water content that might skew melting points or cause batch-to-batch variability. For every consignment, we include a data packet showing HPLC, NMR, and FTIR results, not just a basic certificate of analysis.
Production teams often face requests for a family of coumarin-related intermediates—some in the methyl, propyl, or benzyl ester forms. In our workflow, the ethyl ester consistently provides the best balance of hydrolytic stability and manageable reactivity. Methyl esters react faster to acid/base hydrolysis but may introduce volatility in high-temperature steps. Benzyl esters add bulk, which can hinder some transformations. The ethyl group in this ester avoids both extremes. Separation, crystallization, and washing all proceed with fewer complications, and most downstream users report excellent yields when switching over from other esters.
We field questions about how our material differs from 3-hydroxy- or 4-carboxyl analogues. In side-by-side syntheses, the 3-ester form enables selective functionalization which is harder with the 4-carboxyl versions, where steric crowding near the lactone ring upsets reaction consistency. Our product’s reactivity profile remains predictable, and unwanted by-products rarely appear above trace levels.
From order to shipment, we dedicate space for dry and dark storage. Personnel monitor large lots for any sign of hydrolysis or discoloration before packing. Routine shelf-life checks prove our batches resist decomposition under ambient storage—often surpassing the 12-month mark if kept dry. Technical teams clean all glass and stainless steel lines with solvents that completely flush previous residues. We’ve logged years without cross-contamination between different chromene derivatives.
On the production floor, we practice closed transfer and minimize open-air exposure. Some trial batches under high humidity revealed early on that even slight moisture can affect product quality, so we established sealed container protocols early in our manufacturing program. Our experience shows that other esterified coumarins don’t always stand up to storage; some yellow rapidly or develop hydrolytic odors. Ethyl 2-Oxo-2H-Chromene-3-Carboxylate remains stable and crystalline, holding up to transit in most climates.
Universities and research labs request this coumarin intermediate to develop pharmaceuticals, UV-sensitive dyes, and even some agrochemical prototypes. Pharmaceutical researchers appreciate its clean NMR profile when screening for active compounds. We’ve seen uptake in fine chemical manufacturing, where it serves as a precursor for anticonvulsant candidates, anti-inflammatory scaffolds, and enzyme inhibitors. In some dye chemistry programs, its core structure gets modified to extend fluorescence or provide photo-reactivity.
Compared to less refined coumarin substrates, our product allows users to pursue diverse syntheses with confidence that off-flavors, residual acids, or unknown tars won’t interfere. Chemists regularly contact us after switching from more basic material sources, reporting cleaner reaction baselines and higher isolation yields.
Each production cycle, we implement layered hazard controls and waste management. Our operators wear splash-resistant gear, especially during solvent handling and acid neutralization. Automated pumps and nitrogen blanketing minimize vapor emissions in the factory bay. Waste streams head directly into our in-house collection tanks before final neutralization and disposal.
During scale-up, unexpected exotherms present real hazards for esterification reactions. We monitor these with in-reaction temperature probes, shutting down heating if temperature drifts outside a safe zone. Our management insists on using sealed, jacketed reactors so we avoid open boils and worker exposure. For every ten batches, we collect sample residues and send them for third-party analysis. Such checks assure customers—and our own quality control team—that no persistent contamination lingers from previous lots.
Disposal matters as much as synthesis. We neutralize acidic washings and distillation residues before transfer to municipal waste treatment. Over time, procedural adjustments have brought solvent recycling up to 70 percent for our largest lines. An active fume hood system captures off-gassing and keeps working conditions healthy. Regular staff training means everyone handles reagents and product with the same care, batch after batch.
Feedback from our partners guides our product refinements. Early on, some customers noticed micro-particles remained in the crystalline mass after solution crystallization. We adapted filtration routines, sometimes running twin filters where only one sufficed before. Our team tunes the cooling rate and solvent batch purity to ensure granular products with no clumping. Several labs noted improved spectral clarity in their own analytics—from UV through IR.
Years of batch records provide trendlines for impurity formation and allow us to refine our processes in real time. If a customer flags an unexpected by-product, our technical staff trace it back—not just to the current batch, but to process modifications or changing raw material vendors. Each adjustment gets recorded and benchmarked against subsequent runs. The margin for error shrinks with every cycle, cutting out the variability that frustrates downstream research.
Our supply chain remains transparent. We trace incoming chemicals from original suppliers, checking for documentation on purity and contaminant levels. Key inputs pass through secondary purification steps before use. We run spot GC analysis on every significant drum and bag. By dusting off raw material before transfer and pre-rinsing all storage tanks, we reduce possible contributions to end-batch residues.
Every container of Ethyl 2-Oxo-2H-Chromene-3-Carboxylate ships with a unique batch code. Users in the lab or manufacturing line can request production records tied directly to that code, from reaction log to final moisture check. This level of tracking doesn’t just satisfy regulatory or audit requirements—it provides peace of mind for any process that builds upon our chemistry.
Research clients value flexibility—they run pilot studies, scale syntheses, and sometimes pivot mid-project. We set up our operations to accommodate both kilo-scale and ton-scale orders. Small lots come in moisture-resistant, double-sealed jars for bench-top use. Large-scale shipments head out in drums, packed under dry nitrogen with layered liners to prevent condensation and static buildup.
Flexible logistics mean our partners never wait long for replenishment. We maintain rolling reserves and monitor demand for seasonal spikes. With every outgoing shipment, our logistics manager checks lot numbers, packaging integrity, and shipment documentation. Customer labs sometimes share storage tips for long-haul or humid environments, and we incorporate their advice wherever site conditions differ significantly from ours.
Dye chemists favor the coumarin core for its spectral properties. Plant scientists explore its effects in growth modulation. Medicinal chemists use our product as the pivotal intermediate for synthesizing trial inhibitors, anti-cancer leads, and anti-thrombotic agents. Each application puts different demands on purity and reactive potential. The ethyl ester’s reactivity supports late-stage diversification even where less stable esters might decompose or vaporize.
Our facility can tune specifications when customers require anhydrous product, particularly for moisture-sensitive alkylation or cyclization reactions. Several clients experimenting with photoreactive derivatives contact us for product lots processed under red light or under stricter environmental controls. We provide post-crystallization drying and inert packaging upon request, tracking every deviation as part of our quality management system.
All our process adjustments and operational protocols came from hands-on troubleshooting. Production teams respond rapidly if a chromatogram shows new peaks, or if a supervisor spots discoloration in a flask. The lab team maintains an in-house reference archive of every batch going back several years, ensuring new production never falls below historical standards.
We leverage long relationships with raw material vendors and keep redundant suppliers for core chemicals. Dry air, piped nitrogen, and filtered water enter every stage in synthesis and post-reactor processing. Our technical leads participate in regional workshops and technical forums where we compare process yields and impurity trends with other producers. Each challenge leads to a close review and a new opportunity for tighter control and reduced environmental impact.
We work alongside our customers, not above or apart from them. Our chemists answer synthesis questions directly and respond to application feedback with concrete proposals. If a research group wants to integrate our product in new photophysical testing or as a protein label precursor, we provide as much batch documentation and process detail as needed.
Because our roots lie in process chemistry, we never outsource key synthesis steps. Quality, compliance, and traceability stem from real-time involvement, not distant oversight. With every consignment, we stay available for technical support—by phone, video, or direct site visits. Many of the refinements that set our product apart have come directly from open conversations with scientists and engineers facing day-to-day project hurdles.
Chemical regulations shift across markets, requiring ongoing attention. Over the last decade, we adapted our analyses and reporting to satisfy evolving rules on pesticide residues, solvent retention, and trace heavy metals for export. Our laboratory regularly updates reference standards for spectroscopic identification. Documentation packs now include expanded elemental analysis, supporting both pharmaceutical registration and industrial specifications.
For customers entering new markets or regulatory environments, we offer detailed impurity profiles and third-party validation reports. Transparency stays at the core of our business model—customers see not just batch numbers, but the data and reasoning behind our QC release decisions.
Reliable supply of Ethyl 2-Oxo-2H-Chromene-3-Carboxylate matters every day in research and production labs. From its chemical stability in storage to its ease of handling on the bench, the compound supports ambitious synthetic work and industry-scale production alike. Over time, direct feedback, open technical collaboration, and methodical documentation have shaped our process. Every container we ship, no matter the destination, stands as the result of years of hands-on experience, technical learning, and consistent customer engagement.
Our team remains ready to guide you through any application or purity demand your project might bring. We believe in supporting advancement not only by meeting technical specifications, but also by remaining transparent, responsive, and accountable from synthesis to delivery. Through dedication to quality, safety, and clear communication, we continue to build the foundations for the chemistry of tomorrow.