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HS Code |
485945 |
| Productname | 7-Hydroxy-4-(Trifluoromethyl)Coumarin |
| Casnumber | 16288-06-9 |
| Molecularformula | C10H5F3O3 |
| Molecularweight | 230.14 g/mol |
| Appearance | Off-white to pale yellow solid |
| Meltingpoint | 175-178°C |
| Solubility | Soluble in DMSO, methanol, and ethanol |
| Purity | Typically ≥98% |
| Storagetemperature | 2-8°C (Refrigerated) |
| Synonyms | 7-Hydroxy-4-trifluoromethylcoumarin; 7-Hydroxy-4-(trifluoromethyl)-2H-chromen-2-one |
| Smiles | OC1=CC=C2C(=C1)C(=O)C=C(O2)C(F)(F)F |
As an accredited 7-Hydroxy-4-(Trifluoromethyl)Coumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-gram quantity of 7-Hydroxy-4-(Trifluoromethyl)Coumarin is supplied in a sealed amber glass vial with a tamper-evident cap. |
| Shipping | 7-Hydroxy-4-(Trifluoromethyl)Coumarin is shipped in tightly sealed containers to prevent moisture and light exposure. It is typically transported as a solid at ambient temperature, with appropriate labeling for laboratory chemicals. Standard chemical shipping regulations apply, ensuring safety and compliance with regional transportation guidelines for hazardous materials. |
| Storage | 7-Hydroxy-4-(Trifluoromethyl)coumarin should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong acids, and oxidizing agents. Store at room temperature or as recommended by the supplier. Use appropriate personal protective equipment when handling and always follow laboratory safety protocols. |
Applications of 7-Hydroxy-4-(Trifluoromethyl)Coumarin in Industrial ManufacturingAs a specialized manufacturer of 7-Hydroxy-4-(Trifluoromethyl)Coumarin, we supply this fluorinated coumarin derivative to leading industrial sectors recognized for their advanced chemical requirements. Below, we detail the principal downstream applications where this compound delivers practical results, supported by compliance standards, formulation data, production integration insights, and major final product outputs. 1. Laser Dye and Fluorescent Marker ManufacturingMajor photonics and optoelectronic companies incorporate this coumarin derivative as a high-performance laser dye and fluorescent tracer, valued for its distinctive emission in the blue-green spectrum and strong photostability. Precise formulation and purification are required to maintain quantum yield and longevity, and adjustments to concentration depend on the target emission intensity and matrix compatibility with solvents or polymers. Industry compliance standards
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2. Biochemical Fluorescent Probe SynthesisBiotechnology and life science reagent manufacturers use this compound as a fluorophore for labeling peptides, oligonucleotides, and proteins in molecular diagnostics. Its sharp emission profile and moderate hydrophilicity make it preferred in live-cell imaging and fluorescence resonance energy transfer (FRET) kits. Operators tune the conjugation protocol and coumarin derivative input according to project sensitivity and background requirements. Industry compliance standards
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3. Forensic and Security Ink ProductionManufacturers of security documents, identification tags, and forensic tools utilize this material for tamper-evident inks and ultraviolet detection dusts. The high-contrast, long-lived fluorescence under UV excitation supports authentication and forensic trace analysis, while formulation must ensure ink stability, compatibility with printing substrates, and environmental resistance. Industry compliance standards
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4. Analytical Chemistry Reagent FormulationProducers of analytical kits, chromatography reagents, and chemical indicators rely on this coumarin derivative for highly sensitive fluorescence-based detection of enzyme activity, metal ions, or pollutants. QC teams benefit from its predictable absorbance and emission parameters, which support accurate quantitation across spectrofluorometric workflows, with formulation concentrations tailored to the required detection limit. Industry compliance standards
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On any production day at the chemical reactors, preparation for a 7-Hydroxy-4-(Trifluoromethyl)Coumarin batch begins well before sunrise. The air fills with the hum of pumps and processors, reminding everyone of the delicate balance required to achieve a compound that remains a favorite across research and specialty industries. Our discussions always circle back to improvement, purity, and meeting the needs of customers who look for reliability in every kilogram we ship.
7-Hydroxy-4-(Trifluoromethyl)Coumarin, also known as 4-Trifluoromethylumbelliferone, has established a reputation beyond its imprint on conventional lists of fluorescent probes and synthetic intermediates. Here on site, technicians notice fluency in handling, solubility, and spectral response, which steer its selection for analytical chemistry and pharmaceutical research. This compound brings distinct advantages to labs requesting precise fluorescent markers. What makes it truly notable is its capacity for strong blue fluorescence under UV light, giving clear readability in enzyme assays, cell tracking studies, and environmental sensors with minimal background interference.
Researchers often ask about the quality difference they see with our 7-Hydroxy-4-(Trifluoromethyl)Coumarin. Years of hands-on synthesis taught us that purity levels above 99% matter, not just for compliance but for accurate, reproducible measurements. Each batch passes through a rigorous sequence of crystallization and chromatography steps, overseen by experienced specialists aware of how minor residue can upset entire research programs. Our decision to use high-performance liquid chromatography (HPLC) and NMR for every lot came after seeing the inconsistency that minimal variance brings to end-user results.
On the other side of the production floor, discussions with visiting scientists reveal a mix of excitement and need for new coumarin derivatives. 7-Hydroxy-4-(Trifluoromethyl)Coumarin proves attractive across several disciplines not just for its brightness, but also for how it interacts with enzymes and reactive species. Our own lab’s experience with enzymatic assays highlights how its unique trifluoromethyl group helps reduce cross-reactivity and non-specific binding. The consequences are simple—a cleaner signal, lower false positives, and less troubleshooting on expensive equipment.
It stands out in pharmaceutical and diagnostic assay development. When screening for candidate drugs, minor spectral shifts caused by impurities or solvent traces can mean the difference between discovery and wasted funds. Our process eliminates these risks, giving pharmaceutical researchers a practical advantage—less time spent recalibrating and more attention on real findings. Fluorescent labeling of biomolecules, especially proteins and peptides, owes much of its success rate to the strong selectivity and photostability shown by coumarins like this one.
Having met researchers from environmental science teams, we see its popularity in the tracing of biological and pollutant flows in water samples. Its blue emission makes it possible to conduct field tests without advanced equipment—portable UV lamps reveal its presence instantly, increasing the pace of on-site monitoring. We’ve received feedback from users in remote locations reporting how even small variations in purity made a difference in detection limits and reliability.
In our production experience, not all coumarins behave the same during purification or application. Substitution at the 4-position with a trifluoromethyl group delivers more than improved fluorescence. It adds metabolic stability, a factor not always visible on spec sheets but immediately obvious to researchers measuring compound longevity in biological systems. This stability stems from the electron-withdrawing nature of the trifluoromethyl group, making the entire scaffold less prone to degradation or unwanted side reactions encountered in real assays.
A range of coumarin derivatives pass through our reactors. Compared to variants lacking the hydroxy group at the 7-position, 7-Hydroxy-4-(Trifluoromethyl)Coumarin handles conjugation and functionalization with greater efficiency. The hydroxy group acts as a handle for custom labeling, covalent attachments, or glycosylation steps, a point routinely raised by synthetic chemists we supply. Our technical support team often works directly with client teams optimizing this compound for next-generation antibody-drug conjugates and enzyme sensors.
The handling properties matter too. Its powder form flows without clumping, stores safely in moisture-free containers, and remains stable across reasonable temperature ranges. Manufacturing teams value these features because they streamline logistics, reduce wastage, and keep downstream processes on schedule. Lab managers frequently mention fewer clogs in HPLC columns and smoother weighing for multi-milligram runs, thanks to our consistency in particle sizing and dryness.
Selecting reliable raw materials builds the integrity of every batch we make. After years of witnessing market swings and supply interruptions, our procurement prioritizes trusted upstream partners who understand the strict criteria required for specialty organics. We maintain a traceable supply chain for each ingredient entering our reactors, including specialized trifluoromethylating reagents and resorcinol analogs. By sticking to these practices, we safeguard each synthesis from variability. This traceability proves crucial for academic collaborators submitting regulatory paperwork, especially when working in strict environments like LDT or cGMP facilities.
Product safety plays an equally important role. Our in-house safety engineers, informed by years of incident analysis, set standards for dust management, fume extraction, and worker protection that match both regional and international regulations. Staff receive training refreshers at regular intervals, keeping the focus on hazards unique to fluorinated materials and organic powders. Our certification efforts extend not just to end users but to everyone involved along the path from synthesis through packaging and distribution.
Shipping to customers in more than 25 countries, we build every outgoing lot based on stability studies drawn from years of temperature, light, and humidity data. Customized packaging options, including amber vials or inert gas flushing, reflect actual feedback from industrial and academic users encountering harsh climate or logistical conditions. Our logistics team keeps detailed records to help reproduce this protection, creating a consistent experience whether the material goes across a city or halfway around the globe.
Collaboration drives our improvements. Routine conversations with scientists often point to the challenge of maintaining low backgrounds and long signal windows in fluorescence microscopy. Our solution draws from both synthetic strategy and hands-on purification—minimizing photo-bleachable impurities, controlling particle size for even dispersion, and verifying emission spectra for lot-to-lot uniformity. This iterative approach speeds up discovery cycles for researchers, who pass on problem reports that feed directly back to our quality control protocols.
Feedback from end users regularly guides our strategy. For instance, consistent requests for higher batch sizes led us to scale up our reactors, but not at the expense of the small-batch purity standards valued in R&D settings. Customization options—whether it’s size, form, or spectral tuning—stem from lessons learned during scale-up. Synthetic chemists on our staff test every change before releasing it widely, reducing surprises downstream. By listening first, we deliver what labs actually require, not simply what the catalog lists.
Regulatory compliance has never been optional for specialty chemicals, and 7-Hydroxy-4-(Trifluoromethyl)Coumarin presents distinctive challenges. Export regulations covering fluorinated organics, especially for medical or agricultural research, grow stricter every year. Our internal compliance team keeps up with evolving rules on shipment, waste, and handling, ensuring our documentation matches customer needs. Experience has taught us that proactive transparency with regulatory agencies prevents unwanted shipment delays and supports global users in timely project execution.
Trace impurities matter, particularly for advanced photochemical applications. For those developing photoresists and optoelectronics, we employ additional purification protocols to remove background absorbance and residual metals. Analytical data remains open to clients on request, letting industrial users fit us into their critical process controls. Over time, the reduction in rejected lots and customer complaints speaks to the attention our staff pays during every stage—something that can’t be achieved by distributors lacking direct control over synthesis and packaging.
Stability across shipping and storage environments counts for more than shelf life. In the field, materials see real sunlight, variable humidity, and temperature swings. Our product’s record for minimal photodegradation and resistance to hydrolysis stands as a product of real-world testing. Environmental consultants and diagnostics developers share stories of using our coumarin successfully in South American rainforests, Middle Eastern summers, and temperate university laboratories alike.
Comparing 7-Hydroxy-4-(Trifluoromethyl)Coumarin to related molecules, several features emerge from practical manufacturing. Adding a hydroxy group at the 7-position not only provides greater flexibility for downstream coupling but also boosts its water solubility, a notable ask from researchers working in biological or environmental settings. The trifluoromethyl group at the 4-position increases both metabolic stability and electron density, influencing both the emission wavelength and compatibility with diverse assay conditions.
Where other coumarins may show drift in spectral features due to environmental factors, such as pH or ionic strength, this version maintains signal intensity under a broader range of conditions. In our own testing, run by staff biochemists and chromatographers, this translates into fewer experimental repeats and more robust datasets. Those working with classic umbelliferone derivatives may encounter lower photostability and a need for tighter storage controls; our product alleviates those pain points, based on clear evidence shared by repeat users and firsthand analyses.
Handling differences also matter in scale-up. During pilot production runs, powder fouling and inconsistent density plagued attempts at automated filling with inferior coumarins. Through granular process control, using particle engineering learned from decades on the line, we deliver a reproducible material that supports both bulk manufacturing and precise research workflows. Consistency in bulk density, pourability, and dispersion make this material a practical upgrade from older variants, as our facility teams frequently demonstrate for new clients during technical visits.
The pace of change in specialty chemicals drives us to constant adaptation. New areas, such as real-time cellular imaging and wearable sensors, demand materials that exceed purity and performance levels once thought satisfactory. Our technical team maintains an open channel with research institutions, learning about upcoming assay formats and novel labeling chemistries. We dedicate a portion of production capacity to experimental variants and accept feedback on custom specifications, recognizing that tomorrow’s breakthroughs depend on flexible, inventive partnerships.
Sustainability figures deeply in our operation. Manufacturing fluorinated compounds raises both environmental concern and technical challenge. We continually refine solvent recovery, energy use, and waste treatment methods. Participation in responsible care programs holds us to a higher standard for emissions and waste, with year-on-year reductions in resource use. These efforts offer peace of mind not just to corporate partners but to laboratory users requesting documentation of responsible sourcing and production.
We engage directly with scientific groups and standards committees setting guidelines for fluorescent markers and photostable probes. Sharing knowledge across industries helps foster responsible adoption and informs our ongoing safety and handling recommendations. Staff chemists sit on advisory boards and contribute insights from both failed and successful production campaigns—these stories help avoid missteps with new compound families.
From the point of view of our manufacturing team, 7-Hydroxy-4-(Trifluoromethyl)Coumarin stands out as more than a premium specialty chemical. Its advantages take root in real decisions made during sourcing, synthetic planning, purification, and technical support. Daily interactions with users and R&D partners shape improvements in quality, logistics, and documentation. Where science pushes the need for reliable fluorescent markers, our team answers with solutions drawn from decades of hands-on work and honest conversations about what makes a batch succeed.
We measure success not by volume sold, but by the confidence of researchers relying on our coumarin in the lab, in the field, or in the hands of a technician halfway around the globe. Manufacturing at this level means learning constantly—adapting to new analytical requirements, field conditions, and regulatory changes. Every kilogram shipped carries a story of persistence, precision, and the everyday skill of teams committed to chemical excellence.