|
HS Code |
137804 |
| Chemical Name | 7-Dimethoxycoumarin |
| Cas Number | 2035-29-6 |
| Molecular Formula | C11H10O4 |
| Molecular Weight | 206.20 g/mol |
| Iupac Name | 7,8-Dimethoxy-2H-chromen-2-one |
| Appearance | White to off-white crystalline powder |
| Melting Point | 141-144°C |
| Solubility | Slightly soluble in water, soluble in organic solvents like ethanol and DMSO |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 7,8-Dimethoxycoumarin, Isofraxidin |
| Pubchem Id | 68075 |
| Smiles | COC1=CC2=C(C=CC(=O)O2)C(=C1)OC |
As an accredited 7-Dimethoxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 7-Dimethoxycoumarin is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled for laboratory use. |
| Shipping | **Shipping Description for 7-Dimethoxycoumarin:** 7-Dimethoxycoumarin is shipped in tightly sealed containers, protected from light and moisture. It is typically dispatched via ground or air transport compliant with chemical safety regulations. Packaging ensures stability during transit, and includes labeling for chemical identification and hazard information. Handling instructions and safety datasheets accompany each shipment. |
| Storage | 7-Dimethoxycoumarin should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible materials such as strong oxidizing agents. Store at room temperature and label the container clearly. Follow all applicable safety guidelines and regulations when handling and storing this chemical. |
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Chemistry rewards care and attention. In the lab, every gram of 7-Dimethoxycoumarin represents more than a simple compound. Behind the white crystal stands seasoned chemists, years of practical research, and a honed process that fuses reliability with reproducibility. Our team tracks every variable: solvent purity, stirring speed, reaction temperature, product stability. The goal is always the same—deliver a consistent, high-grade product batch after batch.
Let’s talk about 7-Dimethoxycoumarin, sometimes known by its molecular formula C11H10O4. Its structure offers a classic coumarin backbone, made more adaptable by two methoxy groups located at positions 7 and 3. These small modifications make a big difference for researchers and formulators. Our particular lot typically comes with a purity above 98 percent by HPLC, free-flowing and reliably stable at room temperature.
The route to pure 7-Dimethoxycoumarin isn’t guesswork, especially if your work demands certainty. Many years ago, we handled batch scale-ups from beaker to kilogram-scale glass reactors, learning where the pitfalls hide. Methoxylation conditions have a narrow window—off by a degree, and by-products creep in. Routine thin-layer chromatography in the early stages gives us snapshots of the reaction, but we’ve learned not to lean on just one technique. Once crystallized and washed, every batch faces a multi-step purification protocol, including column chromatography if we notice any signal drift. The feedback loop between production and QC teams remains short; any fluctuation in melting point or spectral readout gets immediate review before a batch leaves the plant.
Many of our clients rely on this process discipline because even modest impurities can skew their downstream results. Whether it’s for probe studies in fluorescence or as a precursor for more complex molecules, there’s no shortcut. Everything—reagent freshness, glassware choice, agitation rate—finds its way into the end product.
Working with coumarin derivatives, you quickly realize subtle molecular tweaks result in real-world differences. Customers sometimes ask why choose a dimethoxy variant over a plain coumarin, or why not settle for a 3,4-dimethoxy isomer. The answer depends on the interaction they’re engineering. Those two methoxy groups improve solubility in organic solvents—a shift noticeable even in simple mixing and solubility tests. Perhaps more important for some, their presence shifts the compound’s electronic absorption band, making it a more effective fluorophore for certain applications.
Take a standard coumarin scaffold. It’s useful, but lacks the fine-tuning photophysicists crave. Substituting a methoxy at position 7 offers increased quantum yield and a bathochromic (red) shift in the emission spectrum; add a second at position 3 and the behavior enhances further. For those developing fluorescent probes or trace markers, this tuning makes their work more reliable. If you’ve wrestled with signal-to-noise issues using 7-hydroxycoumarin, you’ll notice the difference the moment you switch to the dimethoxy analog.
Other uses benefit from this structure, too. Pharmaceutical researchers often pick the 7-dimethoxy version as a core scaffold, counting on its improved reactivity pattern in specific substitutions or coupling reactions. In crop protection research, certain plant pathologists have caught on that this molecule’s altered hydrophobicity helps screen candidate molecules for transport studies. In our experience, laboratories that initially tried less-substituted coumarins shift to the dimethoxy variant and rarely look back, once they’ve seen its cleaner spectra and easier handling.
The specification sheets seldom tell the full story. It’s easy to find ‘reagent grade’ or ‘analytical grade’ 7-Dimethoxycoumarin, but not every source truly delivers on those claims. Several years ago, we benchmarked our process against bulk suppliers. Head-to-head in NMR and mass spectra, odd peaks crept into commercial samples from bulk resellers—sometimes because of incomplete purification, sometimes due to careless solvent removal. These invisible flaws compound in sensitive downstream applications.
By contrast, running a full suite of analytical checks—NMR, HPLC, UV-Vis absorption, IR spectroscopy—we spot and remove stubborn contaminants. Three lots a year, we also make the extra effort and test for trace metals, even though the odds say we shouldn’t expect any. The batch history for each lot tracks back to raw material purchase dates, synthesis logs, and storage conditions, so any abnormal reading sparks a thorough check and rapid response. That’s what true in-house control looks like, and why experienced chemists prefer negotiating directly with manufacturers.
Not all applications demand the same purity or physical form, but researchers deserve to know what actually works in practice. Through conversations with our customers and hands-on troubleshooting, we’ve seen where 7-Dimethoxycoumarin stands out. In fluorescence-based DNA quantitation, background signals from impurities cripple results—our material regularly yields a cleaner baseline, letting even low copy-number amplifications shine through. Its light absorption properties also make it a strong choice for calibrating spectroscopic equipment, especially where a predictable extinction coefficient streamlines calculations.
Synthetic chemists have approached us for multi-gram lots, seeking a starting material that doesn’t introduce difficult-byproducts. It performs well in Friedel-Crafts reactions, Suzuki couplings, and Mannich condensations. Recently, our technical support team worked with a polymer scientist struggling with residual base impurities in their dye-loaded films; switching to a higher-purity 7-Dimethoxycoumarin batch cleared up polymerization issues and eliminated fluorescent ‘ghosting’ in their final product.
One exploration in environmental chemistry deserves mention: a water analysis lab discovered that the dimethoxy groups gave the molecule improved stability against hydrolysis under mildly acidic conditions. Their new extraction protocol, built on this property, simplified labor-intensive pH adjustments.
Research and development teams count on reliable reactivity for synthesizing novel drug candidates. We monitor feedback loops constantly, integrating end-user discoveries into process tweaks. This cycle—batch manufacture, real-world use, then process refinement—keeps the bar high.
We don’t just hand over the product but share practical advice rooted in repeated field-testing. For small or meso-scale research, most teams find our 7-Dimethoxycoumarin remains stable at room temperature under dry conditions. Exposing it to high humidity or open air for long periods can trigger slow decomposition or color change, signaling the start of breakdown. Our batches ship in amber glass with heat-sealed sachets for a reason.
For those running parallel reactions, gentle heating in an inert atmosphere reproducibly dissolves the powder in organic solvents like DMSO or dichloromethane. Quick tip: always degas your solvent before introduction, and set up a nitrogen blanket if you plan on leaving reaction mixtures overnight. During scale-up, some end-users underestimate how subtle heat gradients in larger vessels influence dissolution rates. Running a simple test on a smaller scale before full batch production can uncover this. Practical experience with coupling and acylation reactions has also shown that using anhydrous conditions prevents side reactions—an hour spent prepping your system saves days in troubleshooting.
The practical difference between high-purity material and what’s passable could cost a week’s delay or a clean result—the choice matters day-to-day.
We thrive on feedback. Over the years, we’ve seen laboratories run split tests between our 7-Dimethoxycoumarin and off-the-shelf options from catalog vendors. Teams share data with us—chromatograms, fluorescence plots, crystallization photographs. If a sample doesn’t meet expectations for a specific assay or reaction route, we roll findings into our process improvement log.
Every product batch carries a unique lot number, logged against raw material and QC findings. If a client flags an unexpected by-product, we pull retained samples from our controlled archive and re-run comparison tests. Once, a long-standing customer in a commercial formulation plant noticed an unfamiliar mass signal; our rapid review identified a change in their own solvent system, not the 7-Dimethoxycoumarin. The open channel saves time and cuts out guesswork.
When the data suggests a new impurity profile, we re-examine both incoming raw materials and our own purification steps for drift. Staff training keeps pace with process evolution. Yearly reviews expand our range of integrity checks—a pure compound this year might call for adjusted threshold levels next year as instrumentation sensitivity inches upward.
Long-term reliability doesn’t come from chance. Direct dialogue with the production team always trumps generic catalog buying. When purchasing 7-Dimethoxycoumarin, the communication line remains open—technical questions, batch customization, and expedited shipments bypass unnecessary delays. Direct access grants more than a COA; it opens a window into production notes, deviation logs, and process adjustments made for similar applications.
We know the history of every batch. From our synthesis reactor logs to the HPLC and NMR traces archived with each finished shipment, there is no black box. Our chemists frequently work beside R&D clients to troubleshoot rare solvent interactions or help interpret batch-specific quirks. Having this flexibility and access to expertise benefits the science and the bottom line. Research moves faster with fewer unknowns.
Source changes, even minor ones, introduce real risks. Years ago, a customer running kinetic studies on anticoagulant analogs swapped suppliers based on price. Chromatograms shifted subtly, and by year’s end, several months of work unraveled—impurities from poor upstream purification threw off yield calculations and forced a do-over. A few cents per gram saved led to much costlier delays. Consistency at the source makes all the difference.
Years in chemical manufacturing taught us the market never sleeps. Demand for quality 7-Dimethoxycoumarin now comes from more corners: organic electronics, medical imaging, agrochemical discovery, forensic science. As technical requirements grow stricter and more diverse, manufacturers who understand the needs of end-users adapt more quickly. This has practical consequences in the lab—refining isolation techniques, tightening analytical cut-offs, and exploring greener synthesis to minimize waste.
Green chemistry isn’t a buzzword in our plant. Reducing hazardous solvent consumption per kilogram produced not only lowers cost but lessens environmental impact. Trials with catalytic, less energy-intensive syntheses advance every year. The pursuit isn’t just regulatory—our lab staff prefer cleaner, safer conditions and the customers see benefit from fewer impurities carried over. Last year, introducing a solvent recovery loop trimmed input costs and shrank the plant’s waste output for 7-Dimethoxycoumarin by nearly 20 percent. Lessons go on: better yield, cleaner air, improved worker safety.
Looking forward, we’re exploring process intensification—moving from batch to flow chemistry for certain syntheses. Early prototypes suggest a real drop in by-products, a streamlined purification stage, and more affordable scale-ups. The feedback cycle continues: new process forms, tighter analytic standards, and immediate end-user testing.
Owning the manufacturing process for 7-Dimethoxycoumarin commits us to more than pure chemistry. It means we answer for every step, respond to real-world lab challenges, and watch how one minor detail can ripple through a year’s worth of work. It means sharing practical experience, acting on user feedback, and keeping standards high even as project requirements shift.
All the unseen care behind every bottle—each night spent troubleshooting crystallization, every investment in analytical upgrades—culminates in a product that works in practice, not just on paper. 7-Dimethoxycoumarin finds its worth in chemists’ hands and real-world results. As manufacturing professionals, we find satisfaction when researchers return with better data, easier workflows, and stories of discovery. Every advance we make as producers helps fuel the next leap in science.