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HS Code |
434614 |
| Chemical Name | 3-Cyanocoumarin |
| Cas Number | 4487-51-0 |
| Molecular Formula | C10H5NO2 |
| Molecular Weight | 171.15 g/mol |
| Appearance | Light yellow to beige powder |
| Melting Point | 195-198°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 3-Oxo-2-benzopyrancarbonitrile |
| Smiles | C1=CC2=C(C(=O)OC2=CC1)C#N |
| Inchi | InChI=1S/C10H5NO2/c12-10-5-7-3-1-2-4-8(7)6-9(13-10)11/h1-5H |
| Storage Temperature | Store at 2-8°C |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 3-Cyanocoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 3-Cyanocoumarin contains 5 grams of fine powder, sealed in a labeled amber glass bottle for light protection. |
| Shipping | 3-Cyanocoumarin is shipped in tightly sealed containers, protected from light and moisture. It is transported as a non-hazardous solid, following standard chemical packaging protocols. Ensure it is kept away from incompatible substances and extreme temperatures during transit. All shipments comply with relevant local, national, and international chemical shipping regulations. |
| Storage | 3-Cyanocoumarin should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store in a chemical storage cabinet, preferably in a tightly sealed glass or plastic container, and clearly label the storage area for hazardous chemicals. |
Applications of 3-Cyanocoumarin in Industrial Manufacturing3-Cyanocoumarin serves as a high-purity intermediate in multiple industrial settings, particularly where specialized photochemical, agrochemical, and fine chemical syntheses occur. As an original manufacturer, we ensure consistent quality and reliable supply to integrate seamlessly with specific formulations and downstream processing steps. 1. Fluorescent Dye IntermediatesFluorescent dye producers use 3-Cyanocoumarin in condensation and substitution reactions to synthesize specialty fluorescent markers, including coumarin-based laser dyes and photo-stable tracers. This material enters during the core aldehyde or phenol coupling stage, where high purity and defined particle size ensure efficient conversion and minimal byproducts. Downstream blending with solvents and co-reactants follows stringent purity control to support stable dye molecular structures, later formulated for bio-imaging, security inks, or analytical sensors. Industry compliance standards
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2. Pharmaceutical Intermediate Synthesis3-Cyanocoumarin functions as a privileged scaffold for various pharmaceutical active ingredients, especially in the synthesis of anticoagulants or electron-rich heterocycles. Medicinal chemistry teams introduce it during Suzuki coupling or nucleophilic substitution, typically under inert atmosphere and catalytic conditions, ensuring selectivity for cyano- and coumarin-bearing core structures. Its handling and quality comply with trace impurity control, facilitating GMP-compliant downstream operations and reliable scale-up for pilot to bulk production. Industry compliance standards
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3. Agrochemical Active Ingredient Building BlockChemical synthesis teams for agrochemicals exploit the cyano-functionalized coumarin for constructing selective herbicides, fungicides, and pesticide intermediates. The material typically integrates during ring-closing steps when assembling complex heterocycles, facilitating effective bioactive compound formation with high selectivity. Stringent QC for heavy metal and aromatic impurity thresholds is critical, assuring environment-related compliance on exported and domestic products for field applications. Industry compliance standards
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4. Specialty Polymer and Resin SynthesisAdvanced materials manufacturers utilize 3-Cyanocoumarin as a functional monomer or matrix modifier in optical-grade resins, photostable plastics, and specialty coatings that require UV-detection or enhanced fluorescence. It is reactive in free-radical or polycondensation polymerization, forming covalently-bound units within the material backbone. Precise quality control for residual solvents and thermal stability parameters are enforced to support high-performance optical and electronic applications. Industry compliance standards
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5. Chemical Sensor and Analytical Reagent PreparationProducers of chemical detection kits and environmental assays integrate 3-Cyanocoumarin in the formulation of sensor elements, particularly where selective UV or fluorescence response is essential. The raw material undergoes solution blending or microencapsulation with indicator agents, followed by immobilization onto test strips or optical surfaces. Purity level and solubility profile directly affect sensor sensitivity, driving adherence to strict analytical standards and traceability requirements for device calibration and certified assay kits. Industry compliance standards
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As a manufacturer deeply embedded in the landscape of organic compounds, we have learned that the practical value of a molecule only becomes visible through daily use, consistent analysis, and honest conversation with our customers. 3-Cyanocoumarin, with the CAS number 1077-28-7, has secured its spot in our inventory not just for its molecular beauty but for its reliability and merit in real applications. The key here isn’t just purity or physical data, but genuine on-the-ground performance and versatility. Years of production experience have taught us the nuances that elevate this compound beyond its basic formula.
The structure of 3-Cyanocoumarin—comprising the coumarin core fused with a cyano group at the third position—directly affects its photophysical and chemical properties. Achieving consistency batch after batch means paying close attention to synthesis routes, reagent quality, and temperature controls. Over the years, we have refined a protocol that limits by-product contamination, reduces need for post-processing, and leads to a product that is trusted by both research chemists and those scaling up for commercial applications.
Through hands-on experience, we’ve come to realize that reproducibility is not an abstract goal but an outcome of persistent scrutiny. Regular feedback loops between synthesis, quality control, and customer satisfaction teams have allowed us to fine-tune not just purity but also factors like particle morphology, solubility, and color characteristics. Our standard offering remains a crystalline solid with verified HPLC and NMR data, but we track more than numbers: visual checks, dryness, and handling properties all matter to our warehouse teams and eventually to end-users.
Aside from melting points and assay values, the usability of 3-Cyanocoumarin rests on predictable handling and compatibility with solvents and reaction media. In the lab, the compound dissolves readily in solvents such as acetonitrile, DMSO, and dichloromethane—solvents that chemists turn to for their versatility and capacity to support various coupling reactions or photophysical studies. Our customers regularly report that our material minimizes background noise in fluorescence studies, thanks to limited extraneous impurities, and supports reproducible yields in fine chemical syntheses.
Among our production teams, there’s an appreciation for details that might get lost in academic literature—the way the compound responds to humidity, packaging that prevents clumping, storage that keeps it free-flowing even after months on the shelf. Over time, our packaging protocols have moved away from general-purpose containers to barrier bags with silica packs, drastically reducing caking and streamlining subsequent weighing or transfer steps.
The conversation about 3-Cyanocoumarin often centers on its role as a building block in synthetic chemistry and advanced materials. Its cyano functional group opens the door for further functionalization in a variety of reaction pathways, including nucleophilic addition, palladium-catalyzed coupling, and more specialized transformations. This flexibility has made it a regular feature in R&D departments where time and budgetary constraints require reagents that work predictably and don’t cause delays through unexpected impurities or stability issues.
For those in the photophysics community, 3-Cyanocoumarin makes frequent appearances as a fluorophore or as a scaffold for labeling applications. Our close collaboration with research partners has shed light on practical matters, like minimizing photobleaching and maximizing quantum yield, both of which are heavily influenced by solvent and matrix purity—not just the nominal assay of the coumarin itself. We utilize batch testing protocols that reflect the real-world photostability needs of our customers, not just textbook purity data.
Organic synthesis is a field that values ruggedness as much as innovation. The cyano group on 3-Cyanocoumarin remains inert under a broad range of conditions, allowing stepwise functionalization without unwanted side-reactions. Over time, we’ve received questions from customers about compatibility with strong bases, acids, or oxidants. Our in-house testing regimen, developed through years of troubleshooting and direct feedback, means our customers adopt 3-Cyanocoumarin with a clear understanding of where it shines and where it is best used in combination with other reagents.
In areas such as pharmaceuticals and advanced materials, where trace impurities can derail months of downstream work, we provide detailed impurity profiles and encourage batch reservations for projects requiring absolute consistency. The direct lines of communication between production managers and our scientific support teams allow for rapid sharing of analytical findings and tweaks in process parameters, based on customer feedback from real projects, not hypothetical use-cases.
Each coumarin derivative has its own story to tell. 3-Cyanocoumarin distinguishes itself from its close relatives—like 7-amino or 4-methyl substitutions—by providing a handle for further cyanation chemistry and supporting a slightly different absorption and emission profile. For those working in fluorescence detection or tracer molecule synthesis, that subtle shift in emission wavelength can make the difference between signal and noise, between a publishable result and an inconclusive one.
Through side-by-side trials, both in our labs and in collaboration with industry colleagues, some differences emerge sharply. Derivatives with electron-donating groups display altered chemical stability and sometimes higher background in analytical assays, particularly when exposed to light or oxygen. 3-Cyanocoumarin’s electron-withdrawing cyano group delivers greater chemical resilience and unique reactivity, valuable in fields that depend on controlled, modular synthesis. Those making substitutions at other positions, such as 4- or 7-, often face incompatibilities or less reliable scale-up, especially in large-batch manufacturing.
Like any specialty chemical, 3-Cyanocoumarin presents its share of production and logistic obstacles. Our early days saw batch-to-batch variability tied to raw material sources, which prompted long-term partnerships with upstream suppliers that prioritize traceability and quality. One lesson stands out: a manufacturer cannot solve problems reactively or rely solely on certificates provided by others. We invested in in-house analytical capabilities and adopted sampling protocols that review not just the finished product but intermediates as well.
Transporting 3-Cyanocoumarin exposed us to challenges involving temperature swings, vibration, and even minor container abrasion over long hauls. We realized standard packaging couldn’t prevent micro-contamination during summer heat waves, so we developed double-sealed approaches and started logging storage conditions in real-time. These adjustments paid off, reducing customer complaints and improving our own confidence in delivered material. Several process edges came directly from customer observations—real-world details that never make it into published product summaries but that matter to working chemists and engineers.
Assuring integrity in specialty organic molecules requires vigilance at every step. We operate in a field where the practical difference between 98% and 99% purity goes beyond marketing claims—it decides which products a manufacturer trusts for high-sensitivity applications. Routine testing involving HPLC, NMR, MS, and moisture analysis forms our baseline, but the real checks come through lab trials, accelerated stability studies, and open dialogue with those who use our materials every day.
Feedback loops sometimes identify subtle issues—banding in chromatographic analysis, minor color shifts, or changes in melting point after months in storage. Rather than ignore or explain away these signals, our approach involves root-cause analysis, and we close every batch review with actionable steps for future improvement. Sometimes it means adjusting filtration rates, other times it calls for changing the grade or origin of solvents. The willingness to make real changes sets production teams apart from distributors and resellers.
Years spent manufacturing chemicals at scale reveal that safe handling and environmental stewardship don’t come down to checklists. Working with 3-Cyanocoumarin means understanding not just material compatibility and storage temperature, but also efficient workflows that prevent wastage, exposure, or contamination. Proper PPE, local ventilation, and a culture of open reporting lead to fewer incidents—not just compliance with paperwork.
Our team reviews real-world incidents (minor spills, near-misses, shipping delays) and holds training refreshers grounded in our own experience, not just regulatory scripts. This culture leads workers at every station to look out for warning signs, such as changes in crystal appearance or odd odors, before minor issues become reportable events. Our environmental policies—not tacked on for public relations but born from hands-on necessity—prioritize recycling solvents, minimizing off-spec product, and proper neutralization of residues.
One of the most rewarding aspects of manufacturing 3-Cyanocoumarin has been seeing our partners take it from bench-scale reactions to complex product launches. Many of today’s new materials, diagnostic tools, and imaging agents start with exploratory reactions—often with small, high-purity batches that must behave exactly as advertised. Through steady supply of reproducible lots, technical support that responds to real requests, and the occasional after-hours phone call to troubleshoot a stubborn experiment, we have maintained long-lasting relationships across disciplines.
Our team regularly participates in downstream evaluations to see how small process tweaks upstream (like purification solvent switches or alternative crystallization conditions) impact end-use or downstream chemistry. We share analytical data beyond what is typically requested, sometimes surprising a project manager with detail on polymorph distribution or trace metal content. These exchanges remind us that good manufacturing isn’t just delivering a box—it’s a chain of choices that help or hinder R&D productivity.
Chemical manufacturing rarely provides a finish line. For each kilogram produced, testing demands increase, regulatory frameworks shift, and end-user requirements grow ever more specific. For 3-Cyanocoumarin, the challenge is not only to meet but to anticipate what our partners need next—whether a larger drum size for scale-up, COA details that support regulatory filings, or simply a more convenient package for precise aliquoting in the lab. We get there by listening carefully, tracking real-world outcomes, and refusing to settle for the status quo just because previous batches were approved.
Working with a molecule like this, you come to appreciate the texture of the job: the satisfaction of a beautiful crystalline batch, the frustration of a process hiccup, the communal pride when a collaborative project succeeds. Chemical manufacturing, at its best, offers an interplay between technical rigor and the curiosity to explore upgrades that matter—not just on paper but at the moment a chemist opens a new container and gets right to work.