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HS Code |
536447 |
| Chemical Name | Tetrahydropyran-4-carbaldehyde |
| Molecular Formula | C6H10O2 |
| Molecular Weight | 114.14 g/mol |
| Cas Number | 872-59-3 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 88-90°C at 16 mmHg |
| Density | 1.077 g/cm3 at 25°C |
| Melting Point | -32°C |
| Refractive Index | 1.450-1.453 |
| Flash Point | 82°C |
| Smiles | C1COCCC1C=O |
| Solubility | Soluble in common organic solvents |
As an accredited Tetrahydropyran-4-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a screw cap, labeled with chemical name, formula, safety symbols, and handling precautions. |
| Shipping | Tetrahydropyran-4-Carbaldehyde is shipped in tightly sealed containers, protected from moisture and air, under cool, dry conditions. The containers are clearly labeled with hazard information. Transport complies with relevant chemical safety and regulatory guidelines to prevent leaks or exposure, ensuring both chemical integrity and environmental safety during transit. |
| Storage | Tetrahydropyran-4-carbaldehyde should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and store it under inert atmosphere if possible, such as nitrogen or argon, to prevent oxidation. Ensure it is kept away from strong oxidizing agents, acids, and bases. Store at recommended temperatures specified by the manufacturer. |
Applications of Tetrahydropyran-4-Carbaldehyde in Industrial ManufacturingTetrahydropyran-4-Carbaldehyde serves as a specialized intermediate in advanced organic synthesis. Its use remains concentrated in select downstream industrial sectors, each with defined compliance and process parameters. As a direct producer, we enable precise integration into customer manufacturing flows, supporting product innovation and regulatory adherence. 1. Pharmaceutical Intermediate for Piperidine-Based APIsProcess chemists employ Tetrahydropyran-4-Carbaldehyde in manufacturing piperidine-ring systems foundational to CNS, anti-infective, and cardiovascular active pharmaceutical ingredients. The compound participates in condensation and reductive amination routes, facilitating efficient synthesis of heterocyclic intermediates. Customers optimize input ratios based on target molecule yield, impurity profile, and solvent selection, with GMP documentation supporting full traceability across batch records. Industry compliance standards
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2. Synthesis of Flavors and Fragrances: Pyran-Derived Aroma CompoundsFormulators in aroma chemical plants utilize Tetrahydropyran-4-Carbaldehyde as a building block for pyran-based aldehydes and acetals, which impart fresh, green, and fruity notes. The compound participates in acetalization and oxime conversions under controlled temperature and acidity to meet IFRA and FEMA guidelines. Ingredient use balancing and quality documentation remain essential to preserve batch reproducibility and compliance with export or regional flavor regulations. Industry compliance standards
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3. Agrochemical Synthesis: Building Block for Heterocyclic Crop Protection AgentsAgrochemical synthesis units employ this raw material as a key intermediate for constructing nitrogenated heterocycles present in modern insecticides and fungicides. The aldehyde facilitates nucleophilic substitutions and cyclizations, enabling efficient scale-up of pyran-pyridine hybrid scaffolds. Accurate dosing and reaction monitoring ensure end-use compliance with crop protection approvals and regulatory residue thresholds. Industry compliance standards
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4. Advanced Polymer Synthesis: Functional Group Crosslinker in Polymeric MaterialsIn specialty polymer production, Tetrahydropyran-4-Carbaldehyde introduces pendant aldehyde groups allowing for post-polymerization crosslinking. Industrial users select it to modify polyols and vinyl polymers, establishing reactive sites for further functionalization or improved physicochemical properties. Careful adjustment of molar ratios and curing temperatures determines final network structure, with analytical verification ensuring batch-to-batch homogeneity for demanding resin or adhesive markets. Industry compliance standards
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In our manufacturing halls, Tetrahydropyran-4-Carbaldehyde (4-Formyltetrahydropyran) is more than a compound with a systematic name. Over years of scaling up production, refining process controls, and solving practical challenges, this molecule has shown itself as a core building block for advanced synthesis in pharmaceutical, agricultural, and material science sectors. As chemists and process engineers, we see much more behind its six-membered oxygen heterocycle than what catalog descriptions can convey.
On the production line, we start from the ground up — aiming for a product that delivers both chemical reliability and operational consistency. We standardize our Tetrahydropyran-4-Carbaldehyde to reach a purity exceeding 98% by GC, making sure each batch brings clean, clear peaks and a well-defined NMR spectrum. The melting point range often hovers between 26°C and 30°C, and both physical state and color fall within tightly monitored limits: a faint, pale liquid, sometimes appearing as a low-melting solid under cool storage. Moisture content never exceeds 0.3%, thanks to regular Karl Fischer checks and scheduled vacuum drying that keep water ingress under control during both packaging and storage.
Packing is not an afterthought for us. We choose HDPE bottles and steel drums lined with inert polymer, based on order scale and planned storage time. This limits contamination and loss of material by sticking or sublimation, both of which pose real headaches in practical distribution. Shelf-life stability checks over the past years have pointed out that this aldehyde performs robustly if kept cool and dry, even through fluctuating warehouse conditions that cannot always be avoided in global logistics chains.
Chemists and production planners alike know the difference between a general-purpose aldehyde and a cyclic variant. Tetrahydropyran-4-Carbaldehyde brings unique reactivity, not simply because of its carbonyl, but due to the ring system’s conformational rigidity and its oxygen atom’s gentle electron-withdrawing character. In our own laboratories and as reported by partners, this feature makes nucleophilic addition and condensation reactions more selective. The neighboring ether oxygen subtly tunes electron density, letting you coax greater regioselectivity or improved yields in several setups, particularly in forming C-C bonds and in heterocycle expansions.
Compared to the much more common linear aldehydes, or even other cyclic analogs like tetrahydrofurfural or glutaraldehyde, this product rarely brings surprises during workup. Its boiling range sits well above ambient, sparing technicians from the constant re-condensation and loss that can plague lower-molecular-weight members of the aldehyde family. This characteristic alone has streamlined cleanup, giving students and operators alike more forgiving windows during preparative work.
In multi-step drug development, raw materials must match the selectivity demands of modern routes. Tetrahydropyran-4-Carbaldehyde repeatedly finds its way into the hands of medicinal chemists working on new intermediates, such as those leading to advanced heterocycles and protected sugars. One of our own team’s favorite results came from an iterative Grignard addition, which relied on the aldehyde’s moderate reactivity — lively enough for dearomatization but tame enough to avoid runaway side reactions. We continue to hear from contract partners who use the same lot for both small-molecule and polymer modification, with limited need for re-purification before running pilot-scale transformations.
Beyond pharmaceutical trials, this molecule grows in popularity among developers of specialty agrochemicals. In one collaborative effort, the oxygenated ring offered a point of differentiation from typical chain aldehydes, leading to a more stable active against environmental hydrolysis. It has edge in protecting labile functional groups, especially under basic or mildly acidic conditions, thanks to the ring’s snug geometry and resistance to open-chain rearrangement.
Our plant staff have seen that Tetrahydropyran-4-Carbaldehyde tolerates routine shipping agitation and repackaging steps better than many aldehydes of similar molecular mass. Bulk containers often arrive at customer docks showing minimal residue or product volatilization. We attribute this partly to the hydrogen-bond acceptor properties of the cyclic ether, which lessen self-association and the corresponding pressure swings seen in linear or aromatic aldehydes. This means less evaporative loss, fewer fumes during transfer, and easier compliance with VOC limits in enclosed manufacturing suites — issues that hit hard for anyone running 500-liter reactors across a twenty-shift week.
No aldehyde is risk-free, and those who run pilot or commercial plants must always respect its reactivity profile. Exposure routes matter: laboratory-scale spills bring a sharp, characteristic odor, but wider releases can mean challenging air handling. We have spent time optimizing vented closures, rapid transfer tubes, and effective local exhaust. This investment pays off: technicians at our site report little downtime or unscheduled maintenance due to residual buildup, corrosion, or over-limit headspace concentrations.
Tetrahydropyran-4-Carbaldehyde is not a high-volume mass-market aldehyde, nor do we treat it like a disposable bulk commodity. Each time we scale up a fresh reactor charge, feedback from development colleagues feeds process adjustments. In our team’s experience, such feedback matters more than any guarantee on a datasheet. Several years ago, for instance, a customer sought tighter control on trace acetal by-products. Our shift to in-line GC monitoring — operated by technicians with hands-on reactor experience — slashed those levels and improved overall batch reproducibility. This kind of incremental, at-the-source improvement cannot be matched by repackers or traders who lack eyes on the process itself.
Supply networks in this segment involve long lead times and demanding purity constraints. A gap in ingredient quality or a minor contaminant has serious costs: reaction stalling, wasted man-hours, rejected final batches. Being the direct producer, our reputation, inventory turnover, and daily workflow all ride on the product entering — and leaving — our facility free of the usual headaches that trail loosely controlled intermediates.
Some customers try to sub-in similar-sounding compounds, hoping for quick fixes. Yet our experience says the six-membered ring, with its tetrahydropyran oxygen, brings differences in reaction mechanics compared to open-chain alternatives or aromatic relatives. Analytical teams downstream quickly report where these shortcuts fail: unexpected impurity formation, color drift, variable crystallization, or off-odors in extracted product. The source-matched, tightly controlled Tetrahydropyran-4-Carbaldehyde always proves its worth in fewer deviations and easier troubleshooting.
Our manufacturing process for Tetrahydropyran-4-Carbaldehyde evolved from classical oxidation techniques, but over the last decade we have pushed to limit heavy-metal wastes and solvent usage. Today’s workflow leverages recyclable oxidants over classical chromium-based routes, with in-process recovery loops for solvents. We chose these paths not for marketing, but because we have watched first-hand the savings in downstream effluent load and the practical avoidance of regulatory headaches. Such choices also cut operator exposure and make plant hygiene maintenance easier, reducing risk not just for our staff, but for anyone handling drums at the customer’s site.
In labs and pilot plants, our engineers compare the carbon footprint and total emissions of each batch, versus published benchmarks. These measurements are not marketing luxuries. Poorly controlled synthetic steps elsewhere often result in wide emission swings or disproportionate solvent waste. By directly overseeing production and investing in engineering improvements, we achieve consistent performance on both environmental and economic axes.
Taking end user reports seriously has shaped every modification we have made to our Tetrahydropyran-4-Carbaldehyde line. Process engineers who run intensive kilo labs bring problems to us — from solubility quirks in water-miscible solvents, to troublesome atmospheres when drumming out during humid months. No third party can replicate this direct communication. In the last round of scale-ups, a pharma partner’s project leader shared concerns about low-temp storage stability. Our QC team learned from this to adopt an alternate stabilization strategy, switching out trace antioxidant choices and revisiting drum liner materials. This input resulted in a demonstrable drop in peroxides and batch returns.
Many of the upgrades to our isolation and packing approach flow straight from customer trial runs and not just internal brainstorming. In this ongoing, two-way process, unfiltered operator feedback shapes which process bottlenecks we address, and which headaches get fixed at the root level.
Tetrahydropyran-4-Carbaldehyde tolerates typical warehouse conditions well, but, like any aldehyde, can show sensitivity to heat and oxidants over time. Storage tests in climate-variable depots have underscored that keeping ambient temperature under 30°C extends product life and color stability. Our packaging method — tight-seal HDPE plus inert lining — has reduced yellowing, peroxide buildup, and off-odors, which can spell hassle for users in sensitive process environments. Those running long-haul shipments or holding stock for multiple projects have reported lower rejection and less material lost to “aging out.”
Over the years we learned that while many intermediates arrive planning for a just-in-time inventory flow, real-world projects drift or run late. Stock resilience, resistance to air ingress, and surviving months of shelf time set practical limits on how much “specification creep” causes batch failures. For this product, repeat rounds of simulation and QA sampling mean our confidence is grounded in repeated experience, not just isolated data pulls or wishful thinking.
Structural diversity in fine chemicals serves a larger cause in research and industrial innovation. Tetrahydropyran-4-Carbaldehyde’s specific ring system and aldehydic function distinguish it from more run-of-the-mill electrophiles. In specialty synthesis, the molecule steps into roles where five-membered rings or open-chain alternatives cannot. Diverse applications call for the ability to deliver a neutral, stable, and well-characterized aldehyde that resists side reactions like self-condensation or oligomerization under stored or working conditions. We designed our manufacturing platform with these demands at the forefront, because our own in-house use has shown where process weaknesses show up — not hypothetically, but in kilos lost, or shipments bounced, or pilot runs stalled by an uncharacterized impurity.
End users often cite issues with aromatic aldehydes creating color or causing instability during downstream hydrogenation. Here, our six-membered oxygen heterocycle resists polymerization better and brings a less aggressive profile in typical reduction reactions. Scale-up teams report that predictable, moderate reactivity means smoother process cycles and less off-baseline troubleshooting. Our chemists, who have spent years running these same intermediates, back up these observations with hands-on results — not marketing gloss, but logged process times, batch output figures, and independent QC data from multiple consecutive runs.
Continuous improvement is not a buzzword in chemical manufacturing. For Tetrahydropyran-4-Carbaldehyde, every adjustment — whether shrinking residual moisture, tightening color spec, or improving lot tracking — grows from real lessons learned on our own plants. Peaks in demand, swings in raw material prices, and unplanned process delays all test how much control we have over day-to-day execution. By directly controlling both synthesis and packaging, we can see every variable that affects the finished product, whether it is how slow cooling crystallizes material on a humid day, or how a trace by-product appears due to a minor temperature drift in the oxidation reactor.
There remain challenges. Even the most carefully produced intermediate faces transport risks, equipment fouling, and regulator-driven constraints on aldehydes as a chemical class. Our view, sharpened by years of shipping every size from drum to vessel-load, is that tight process control and open communication with end users matter more than ever. We keep pressing for better analytical tools in-line, smarter packaging options, and back-and-forth with application chemists who notice subtle but important differences long before a distant reseller would. Each effort aims for the practical goal: ensuring that our product fits seamlessly into evolving process needs — not just today’s, but for the next generation of fine chemical innovation.
Day after day, we see Tetrahydropyran-4-Carbaldehyde bridge the gap between laboratory promise and factory-scale delivery. Its value extends beyond its immediate function in forming new bonds or cycles. Our work, both as direct producers and regular users, grounds each improvement in lived experience, measured performance, and regular user input, not superficial descriptors or generic claims. Delivering this molecule to spec, on time, and reliably batch after batch draws on more than process diagrams or regulatory compliance. It grows from long-term factory familiarity and mutual trust with the groups who rely on us to help them reach the next milestone in synthesis and product development.