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HS Code |
839523 |
| Iupac Name | 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde |
| Molecular Formula | C13H12O3 |
| Molar Mass | 216.23 g/mol |
| Cas Number | 19151-62-9 |
| Appearance | Light yellow solid |
| Melting Point | 136-138°C |
| Boiling Point | N/A (decomposes before boiling) |
| Density | 1.23 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Structure Type | Coumarin derivative |
| Functional Groups | Aldehyde, ketone, isopropyl, aromatic |
| Pubchem Cid | 15724236 |
As an accredited 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde, labeled with chemical name, hazard symbols, and lot number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde involves securely packing drums or bags, maximizing space utilization and ensuring safe transport. |
| Shipping | 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde is shipped in tightly sealed containers under ambient or recommended temperature conditions to ensure chemical stability. Packaging complies with relevant regulatory guidelines for hazardous materials. Transport includes appropriate labeling and documentation to guarantee safe handling, minimizes risk of exposure, and meets international shipping standards for laboratory chemicals. |
| Storage | 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Avoid contact with strong oxidizing agents. Ensure the storage area is clearly labeled and has suitable spill containment. Use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde should be stored cool, dry, and airtight; shelf life typically exceeds 2 years. |
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Purity 98%: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation and increased yield. Melting Point 134°C: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde with a melting point of 134°C is used in organic synthesis reactions, where predictable phase transition improves process control. Molecular Weight 230.26 g/mol: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde at a molecular weight of 230.26 g/mol is used in medicinal chemistry research, where defined molecular profile aids compound validation. Stability Temperature 25°C: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde stable at 25°C is used in laboratory storage, where stability at room temperature reduces degradation risk. Particle Size <10 μm: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde with particle size less than 10 μm is used in formulation development, where fine particle distribution ensures homogeneous blending. Water Solubility <0.1 mg/mL: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde with water solubility below 0.1 mg/mL is used in hydrophobic compound libraries, where low solubility supports separation applications. UV Absorbance 320 nm: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde with UV absorbance at 320 nm is used in analytical calibration standards, where distinct absorbance enables precise quantification. Storage Condition: 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde stored at 2–8°C is used in long-term research sample preservation, where controlled temperature prolongs shelf life. |
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As manufacturers, we do not just work with chemicals; we know them at the molecular level, from the first raw ingredient loaded into a reactor to precise adjustments on the final purge. Among a range of coumarin derivatives we handle, 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde brings a blend of challenges and rewards that set it apart from other related intermediates. Every batch must pass rigorous tests, not only because customers count on its purity and reactivity, but because our own processes demand consistency and traceability right down to the smallest impurity profile.
In the synthesis of specialized coumarins, the substitution pattern on the chromene ring defines much of the product’s performance and downstream applications. The isopropyl group at the sixth position, paired with an aldehyde at the third and a ketone at the fourth, changes not just the molecular weight but the way this compound interacts in subsequent reactions. The aldehyde group creates a reactive center that serves as a gateway for condensation reactions, making it a starting point for complex molecule assembly, while the isopropyl group handles the subtle electronic tweaks that chemists in both research and industry require for targeted chemical properties.
Many customers ask about similarities with other chromene-carbaldehydes, especially the more basic 4-oxo-4H-chromene-3-carbaldehyde. The answer comes down to reactivity and selectivity. The isopropyl handle slightly raises the lipophilicity, fine-tunes the electronic nature of the aromatic ring, and ultimately changes the interactions with other synthetic building blocks. While it might sound like only a minor change, for researchers developing new pharmaceuticals, fragrances, or agrochemicals, those minor changes spell the difference between a successful pathway and wasted effort.
Since these molecules do not tolerate sloppy purification or inconsistent temperature profiles, we invest in both raw material vetting and process controls that catch trouble before it emerges beyond the flask stage. Each kilogram leaves our facility only after it matches our specs for melting point, residual solvents, and moisture levels. In our production suites, in-process HPLC readings give us immediate feedback, and we calibrate for side products that might look unimportant on paper but can slow down downstream reactions or require extra work from our customers.
Our experience has taught us that certain synthetic routes introduce side products with similar retention times, posing real separation challenges. Over time, we refined the steps, optimizing for minimum byproducts and maximum conversion in every run. That means we spend more time in method development for both normal-phase and reverse-phase purification, ensuring we minimize the risk of coeluting impurities. Whether this molecule serves as a pharmaceutical intermediate or a component in dyes, catalysts, or optoelectronic materials, these efforts translate directly to reliability on the end user's production lines.
Developers in both academic and corporate R&D come to us for more than steady supply. They know we adapt conditions to fit not only our plant but the realities of their later processes. Many who use this compound value its reactivity in Knoevenagel condensations or its compatibility with Wittig reactions. Getting the aldehyde functionality right, without overoxidation or ring cleavage, determines the outcome in those steps.
Anyone who has worked with highly substituted chromene derivatives recognizes their tendency to form tars and gums if not monitored closely. Over the years, our technicians have learned to use tighter temperature ramps, cleaner quenching, and no-compromise solvent recovery. The practical know-how needed to eliminate unwanted polymeric material comes through direct handling, not just reading journal articles or relying on catalog products.
A small-scale synthesis in a flask behaves differently than a hundred-liter batch, especially when handling intermediates with delicate aldehyde functionality. We track every exothermic step, and cooling rates become as important as the rate at which reactants enter the reactor. Some competitors ignore side reactions that can be tolerated in a few milligrams, but they become real issues when scaling up.
We’ve learned that the chromene core can be sensitive to both acidic and basic conditions; pH swings during workup can degrade the product, so we standardize our isolation to keep the desired molecule intact. From our plant’s perspective, that means selecting acid scavengers, solvents, and washes that actually protect the product from airborne moisture and stray ions. Not all process features appear in the finished product specification, but we see the results directly—cleaner NMR spectra, better reproducibility, and higher yields for our downstream partners.
Getting 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde into the right containers is not a small matter. This powder tends to pack and cake if exposed to humidity, so we store, dry, and pack under controlled conditions. Our packaging lines function not as afterthoughts but as extensions of our main production—each container filled under an inert nitrogen blanket, sealed tight, and accompanied by full traceability paperwork.
Transport across regions brings its own set of challenges. The aldehyde group can react with trace acids or bases in shipping containers, so we ship only after triple-checking liners and container closures. Some have tried to cut corners, resulting in messy returns or degraded product. We learned long ago that consistent moisture levels and container cleanliness alter not just the presentation, but the chemical stability of the cargo.
Our job does not end after the last drum leaves our gates. Technical questions come back to us—how does this batch perform in a particular photochemical reaction, or what purity threshold is actually necessary for a specific application? We work alongside formulation chemists and process engineers to optimize not only our materials, but the way they behave in scaled-up or pilot-scale settings.
In our own process development labs, we run the same coupling and cyclization reactions that our customers perform. This lets us pinpoint sources of failure, such as batch-to-batch variability, dust contamination, or very minor side-chain rearrangements, and stop them before they generate problems downstream. Most feedback returns directly to our process engineers—purity specs change, drying times are shortened, and packaging switches out as a result of real-world insights, not abstract product guidelines.
We routinely reevaluate our analytical methods. As new applications develop—especially in specialty dyes and advanced materials—we add new reference standards and challenge our own assumptions about what impurity levels matter. If an end user flags an unexpected result, we open our data to joint troubleshooting. Rather than simply repeating old assays, we design new ones to get to the source. These continuous process improvements separate true manufacturers from warehouse or trader operations.
Producing chromene derivatives at scale, especially with potentially reactive aldehydes, means paying close attention to environmental controls. Our facility integrates solvent recovery and up-to-standard waste management, going beyond basic compliance. We learned that untracked venting or unmonitored mother liquors can lead to real emission problems. All process steps run within closed systems, minimizing operator risk and off-plant impact.
Regulatory scrutiny continues to intensify, especially for molecules that may see use in pharmaceuticals, crop protection, or other high-profile industries. We track all raw materials for provenance, check each batch for controlled impurities, and log documentation to meet both local and international expectations. Our experience with regulatory audits shapes how we plan every process change. Even a small shift in solvent can trigger documentation reviews, so we approach every process update with both an efficiency and compliance lens.
What distinguishes our approach is seeing product quality as part of an ongoing partnership, not a one-off transaction. Some users require very high chemical purity, where even 99.5% pure batches prove inadequate; trace metals or minor aldehyde hydrates can influence outcomes in sensitive reactions. Others prefer slightly less refined product at larger scale for applications where trace impurities do not compromise the outcome. We adjust production campaigns, QC sampling rates, and batch testing based on feedback across dozens of finished products and process intermediates.
In synthetic dye and pigment research, the way our product crystallizes, its particle size, and its color intensity under various lighting conditions—from daylight to UV—matter in ways that most standard catalogs ignore. Similarly, pharmaceutical researchers require certificates of analysis that include not only HPLC purity but residual solvent content, loss on drying, and packaging methods that guarantee shelf-life performance.
We work with customers who specify the product as a reference standard, so our internal standardization matches industry-recognized benchmarks. Even within families of coumarin aldehydes, the specific substitution dictates which applications the molecule best serves. While some prefer precursors with different alkyl or aryl substituents, our long experience handling isopropyl substitution gives us clarity in troubleshooting crystallization behavior, long-term storage, and the effect of temperature and humidity on stability.
Chromene chemistry presents well-documented issues around shelf-life and product handling, especially when introducing bulky or electron-donating substituents. The isopropyl at the sixth position adds physical bulk, but its electronic pushing effect also means even minute traces of incompatible stabilizers or cleaning agents can introduce quality concerns. Instead of defaulting to standard purification routines, our chemists screen every step, from solvent selection to drying temperatures, for its specific impact.
Maintaining color consistency poses its own set of difficulties. The product, as a pale yellow crystalline powder, can absorb trace contaminants that shift appearance. For applications in pigments or optical films, even slight color changes demand investigation. Our colorimeters, not just subjective inspection, track batches over time, and we adjust isolation protocols when deviations emerge.
Some application chemists worry about the compound’s susceptibility to slow polymerization during storage, especially if exposed to light or oxygen. We approached this with repeated stability trials, varying storage temperatures and atmosphere, and using real-life packaging samples rather than theoretical containers. Our real-world storage reports guide our customers in their own handling, contributing to longer shelf-lives and more consistent results.
Plenty of users evaluate our 6-isopropyl-substituted chromene carbaldehyde against more common analogs like methyl- and ethyl-substituted derivatives. The differences go beyond simple melting point or spectral data. Isopropyl’s steric effect alters downstream reactivity in cross-coupling and cyclization steps, so researchers often see higher selectivity in forming specific isomers or greater resistance to side reactions that might plague smaller substituents.
Unlike some competitors who blend several chromene intermediates in a single facility, we run each on a separate dedicated line, reducing cross-contamination risks. Internal studies on cross-reactivity, inadvertent co-crystallization, and solvent retention have proven that investment pays off with stronger batch-to-batch consistency. Customers chasing novel scaffolds or unusual structure-activity relationships appreciate the attention to both chemical and physical purity streams.
Aldehyde chemistry means users sometimes swap related carbocyclic or heterocyclic building blocks when searching for new lead compounds. Our process team has exchanged data with others working on related lactone and coumarin syntheses, revealing subtle but essential divergences in the chemistry. Hydrogenation, halogenation, and C-H activation routes give very different results when the isopropyl group starts interfering, making tight production control not just helpful but critical.
At the end of the day, manufacturing 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde and similar compounds is as much about expertise and responsiveness as it is about reactors and quality systems. Our production crew, from plant operators to process chemists, bring skills honed by years standing beside the very equipment, not just reading about it. Changes to raw material sources, temperature profiles, or isolation methods get flagged early, not as afterthought but as frontline experience.
Proficiency here means acting on pattern recognition—spotting drifting spectra or subtle handling issues before they affect the final product. Everyone in the value chain, from those charging the reactor to those performing the last QC check, knows their work shows up in the customer’s results. We build this compound for labs pushing the boundaries of chemistry and for production shops seeking reliability batch after batch.
Each run, we listen. Feedback leads to upgrades, new process controls, or changes in analytical standards. The finished product reflects more than technical compliance; it embodies years of direct-facing problem solving, real-world storage challenges, and continuous learning from both triumphs and setbacks.
Markets continue to widen, and curiosity about advanced coumarin derivatives keeps growing. As both applications and regulatory expectations shift, we stand ready to evolve. Our technical reporting, upstream sourcing, and downstream guidance all respond dynamically to science’s pace. Our chemical process is more than tradition or routine—it’s the day-to-day result of putting real experience into every intermediate that leaves our doors, including 6-Isopropyl-4-oxo-4H-chromene-3-carbaldehyde. That is what keeps us advancing—listening, learning, and producing with a craftsman’s touch.