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HS Code |
817451 |
| Name | 4-N-Decyloxybenzaldehyde |
| Cas Number | 21329-16-0 |
| Molecular Formula | C17H26O2 |
| Molecular Weight | 262.39 |
| Appearance | White to off-white solid |
| Melting Point | 37-39°C |
| Boiling Point | 218°C at 3 mmHg |
| Solubility | Insoluble in water, soluble in organic solvents |
| Density | 1.01 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | CCCCCCCCCCOC1=CC=C(C=C1)C=O |
| Synonyms | 4-Decyloxybenzaldehyde |
| Refractive Index | 1.520 at 20°C |
As an accredited 4-N-Decyloxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-N-Decyloxybenzaldehyde, 25g, is packaged in an amber glass bottle with a screw cap, labeled with chemical details and hazard warnings. |
| Shipping | 4-N-Decyloxybenzaldehyde is shipped in tightly sealed containers, protected from light and moisture to ensure stability. Standard shipping is via ground or air as per regulations, with appropriate labeling for chemical substances. Ensure compliance with local and international transport and handling requirements for laboratory chemicals during shipping and storage. |
| Storage | 4-N-Decyloxybenzaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep it separate from strong oxidizing agents and acids. Proper labeling and protection from physical damage are essential. Use appropriate personal protective equipment when handling and ensure storage in accordance with local regulations. |
Applications of 4-N-Decyloxybenzaldehyde in Industrial Manufacturing4-N-Decyloxybenzaldehyde provides essential functionality in specialized organic synthesis routes, advanced material manufacturing, and optoelectronic production. The following application segments illustrate its integration into critical industrial processes, based on direct manufacturing usage and end-user requirements. 1. Liquid Crystal Intermediate for Display TechnologyManufacturers of liquid crystal materials for advanced LCD panels rely on this compound as a key intermediate. It enables specific mesogenic behaviors when preparing esters and Schiff base systems required in nematic and smectic phases. Quality assurance teams focus on consistent high purity to control optical anisotropy and electrical response in final display assemblies. Industry compliance standards
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2. Organic Synthesis of Aromatic Aldehyde Derivatives for Polymer AdditivesChemical engineers direct the use of 4-N-Decyloxybenzaldehyde to synthesize functionalized monomers and additives for specialty polymers. These derivatives enhance the processability, flexibility, and weather resistance of engineering plastics and elastomers used in automotive and electrical applications. Synthetic steps require precise temperature and pH control to retain the integrity of the alkoxy substituent. Industry compliance standards
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3. Intermediate for Organic Light-Emitting Diode (OLED) MaterialsProcess engineers exploit this compound’s long alkoxy chain and aldehyde group to prepare light-emitting and hole-transport intermediates critical for OLED construction. Its controlled reactivity in Suzuki and Wittig coupling reactions yields molecules with tuned bandgaps, influencing device brightness and color purity in consumer electronics and technical lighting. Industry compliance standards
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4. Synthesis of Schiff Bases for Analytical Chemistry ReagentsAnalytical reagent producers use 4-N-Decyloxybenzaldehyde as a key aldehyde in the preparation of specialized Schiff base ligands. These ligands serve as chelating agents in transition metal complexation, enabling precise trace metal detection and extraction in environmental and pharmaceutical analytics. The process optimizes purity and moisture control to guarantee consistent reagent performance in downstream labs. Industry compliance standards
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5. Building Block for Specialty Aromatic Esters in Fragrance FormulationFine chemical facilities utilize this aldehyde to synthesize niche aromatic esters and acetal derivatives sought after in fragrance bases. These intermediates provide long-lasting scent notes and increased volatility control. Production strictly controls reaction conditions and trace impurity profiles to comply with end-use safety and environmental regulations demanded by the personal care sector. Industry compliance standards
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On the production floor, every batch tells a story. Each molecule represents hours of engineering, stringent quality checks, and real-world problem-solving. 4-N-Decyloxybenzaldehyde, model C17H26O2, has secured its place in our reactors for more than a decade now. Colleagues in our R&D group and those who monitor the reactors down the line all agree: reliability stems from both the purity and the process behind this compound.
We manufacture 4-N-Decyloxybenzaldehyde to rigorous standards. Purity levels consistently hover above 99%. The compound shows up as a white to off-white crystalline solid. Melting point measures reliably between 44°C and 46°C. Solubility sets it apart—readily mixes with most organic solvents, particularly ethanol and chloroform. In our QC records, spectroscopic signatures always match the baseline, confirming the structural integrity batch after batch.
This isn’t your typical benzaldehyde derivative. The decyloxy side chain imparts greater hydrophobicity than shorter alkoxy series (such as butyloxy or hexyloxy). In the laboratory, staff notice a clear difference in how this product responds in mixed solvent systems. The longer carbon tail adds both mass and an altered reactivity profile. Our process technicians make it a point to log even the minor variations in crystal size and shape, knowing such details affect downstream processing.
We’ve been supplying 4-N-Decyloxybenzaldehyde to a range of specialty materials manufacturers. Most common applications involve its use as a key intermediate in the preparation of liquid crystal compounds. Research partners and industry clients alike often describe the selection of the decyloxy chain as a tactical choice—long enough to impact phase behavior, yet short enough to avoid unwanted aggregation or waxy by-product formation.
Our customer feedback regularly highlights how this compound performs in mesogenic core development. In particular, users aiming to fine-tune transition temperatures and maintain robust electro-optical properties report a preference for the decyloxy variant over shorter or longer analogs. Whether for conceptual design in the academic laboratory or scaled-up synthesis for device manufacturing, users value the predictability this product brings to the table.
Technicians at our facility have run direct side-by-side syntheses with 4-N-Butyloxybenzaldehyde, 4-N-Hexyloxybenzaldehyde, and 4-N-Dodecyloxybenzaldehyde. Yields for 4-N-Decyloxybenzaldehyde remain stable across batches larger than 100 kilograms. Our monitoring team observes consistent melting behavior across each production run, even when shifting from pilot reactors to the largest kettles. This consistency becomes essential where downstream polymerizations are sensitive to aldehyde content and by-product levels.
Compared to shorter chain analogs, this molecule offers improved solubility with a range of aromatic and aliphatic solvents—an advantage for customers preparing intermediate or final products that require precise dissolution rates. Against longer alkoxybenzaldehydes, we’ve noted better handling properties. Dodecyloxy derivatives tend to produce waxier textures, complicating both transportation and formulation. More than one customer who previously integrated dodecyloxy grades in their own synthesis found clumping and segregation in bulk containers. Shipping and storage costs remain lower for the decyloxy analog because of these improved flow characteristics.
On the production side, operators pick up on subtle but meaningful differences during the reaction sequence. 4-N-Decyloxybenzaldehyde forms with less by-product retention than the longer chain ethers. In daily operations, this means less downtime for cleaning and lower consumption of solvents during purification. These details may sound routine, but over hundreds of batches, the savings in both time and resources add up. Our environmental management team tracks the reduced solvent load and acknowledges both the lower carbon footprint and lower water use compared to manufacturing some closely related derivatives.
Reactor operators notice a manageable exotherm during the etherification step, which gives additional control over crystallization and filtration. From the earliest days of scale-up, batch consistency remained a focus. Technicians monitored yields and impurity profiles across different scales and equipment. They reported that decyloxy-functionalization leads to a more controllable solidification process. That feeds back into less processing time downstream, translating to more consistent ship dates for customers.
Several years ago, a liquid crystal display materials firm faced frequent quality deviations from an imported batch of a similar product sourced elsewhere. They brought residual solvent complaints and inconsistent melting points to our team. Our technical support group pulled chromatography data, melting point data, and even impurity spectra from both their material and our in-house standards. Applying the synthetic procedures honed in our own laboratories, we quickly delivered a fresh lot of 4-N-Decyloxybenzaldehyde. Our customer reported sharper thermal transitions and fewer issues during alignment layer polymerizations. From initial complaint to final supply, the turnaround time dropped by over a week—a direct result of having manufacturing, quality inspection, and technical service under one roof.
Our environmental team remains mindful of the resources needed for every production run. Solvent recovery and recycle rates have climbed steadily. In the processing of 4-N-Decyloxybenzaldehyde, operators implemented a solvent stripping sequence that cut waste by a measurable percentage, improving overall yield and reducing both disposal costs and environmental impact. This is possible thanks to the compound’s physical robustness, which stands up during recovery stages without significant degradation.
By integrating vapor recovery technology, we reclaim most of the reactive solvent. Operators record energy reduction at each stage. The waste treatment staff compiles annualized data so we can set new, more ambitious targets each year. These steps translate into a lower overall footprint not just in our own operation but in the value chain—from supplier to customer.
Raw materials dictate so much about a finished batch. Our purchasing group sources only high-grade starting aldehydes and alkyl halides from vetted partners. Incoming shipments undergo spectroscopic and chromatographic analysis before entering inventory. Down the line, every batch of 4-N-Decyloxybenzaldehyde passes multiple lab checkpoints. Our staff regularly measures purity by HPLC and records batch-specific spectra in a central database. Drum handlers and logistics staff coordinate closely to ensure every lot moves out in moisture-tight containers, with packaging tailored for transit stability.
Replicable results matter to every user. Whether the application focuses on high-value electronics, specialty resins, or novel materials development, users look for that batch-to-batch reliability. We log how even subtle shifts in color or melting point are reported and tracked, so end-users face no surprises when their shipment arrives. Over time, we’ve learned to treat every output not just as a chemical, but as an assurance of performance.
No synthetic workflow comes without hurdles. Sometimes, customers adapting recipes from lower alkoxy derivatives run into solubility limits they hadn’t anticipated. The decyloxy analog dissolves well in mid-chain alcohols and aromatic solvents, but oversaturating solutions can lead to unexpected precipitation if temperature control drops. Our application specialists counseled several customers on adjusting temperatures and mixing techniques to sidestep these issues. In response, formulation chemists modified dosing rates and mixing orders; those who adapted their approach found their issues disappeared.
Static charge build-up during powder handling, particularly in low-humidity packaging environments, has caught operators off guard. In a few documented cases, packaging line changes to antistatic drums eliminated issues. Our shipping specialist remains in close contact with formulators who face such environmental variables, ensuring feedback cycles reach engineering and production teams quickly.
Operators in our warehouse rarely face product degradation thanks to a focus on airtight packaging and minimized exposure to light and moisture. Sampling rooms stay humidity-controlled, and only fresh tools touch the stock. When a customer reports a long storage time before use, we recommend storage below the melting point and in well-sealed vessels. Warehouse staff record conditions for every drum as part of routine tracking—identified by barcode, with timestamps from fill-through to shipping dock.
Experience has shown that substandard containers, or opening and closing multiple times, lead to clumping or minor loss of purity. By implementing strict container opening protocols and moving to single-use liner technology, we’ve seen a drop in such complaints. Our own staff uses the same product in downstream blends; no better way exists to find vulnerabilities than direct use in our own formulations.
Chemists appreciate that the decyloxy chain offers a reliable platform for further substitution on the aromatic ring. Researchers investigating new analogs for electronic applications highlight that the decyloxy variant maintains high reactivity while limiting side-reactions common with shorter chains. Analytical staff note the ease with which this product integrates into standard workups—extraction and purification protocols parallel those developed for other large-volume benzaldehyde ethers.
Feedback also shows that inconsistency in chain length distribution, a problem with some outside producers, never disrupts work here. By investing in reliable alkylation sources and batch monitoring, we control narrow chain length distributions in every lot. That hands-on care enables end-users to set recipes and QC targets without worries about input drift from shipment to shipment.
Driven by collaboration with both academic and industrial labs, we’ve provided custom-sized lots of 4-N-Decyloxybenzaldehyde for those pushing the frontier of mesogenic material design. In argument after argument, the balance of polarity and hydrophobicity from the decyloxy group tips the scale toward improved alignment properties. Researchers cite that this compound's presence in the central core lowers viscosity and enables faster switching times in tested prototype devices. Field-reporting engineers demonstrate, in both small and pilot-scale device fabrication, that the decyloxy chain supports better homogeneity in phase-separated systems.
Materials scientists who test a range of benzaldehyde intermediates have shown, through peer-reviewed data, improved voltage holding and clearer color expression when using the decyloxy form. These differences stem from real, observable chemical behavior, not just statistical fluctuations.
Behind every drum sits paperwork: analytical certificates, regulatory files, and compliance documents maintained in a central database. Our team updates regulatory dossiers to meet evolving regional, state, and international chemical management rules. Product stewardship leads at the site train operators to recognize changes in hazard classification or labeling mandates. Each batch ships with document packets specific to local expectations. Dedicated compliance staff gather feedback from inspectors and safety professionals so that nothing gets missed between production and final receipt by the customer.
Whenever regulatory agencies advise changes in reporting or record-keeping, our staff reviews documentation and updates storage practices in real time. Our environmental health and safety coordinators regularly visit shop floors, gathering observations from both logistics and production personnel. They treat these inputs as valuable direct data on how the compound moves and is stored throughout its lifetime.
Production teams use data from each completed lot to push process improvements. Technicians discuss ways to both boost yield and minimize impurities. Meetings bring together operators, R&D staff, logistics professionals, and customer-facing engineers to review experiences with real customer applications. Successes and problems feed into process adjustments that further hone the quality of each batch. Our culture of direct communication across departments supports a low-defect, high-reliability product.
Each yearly review leads to new targets for solvent use, recycling, and yield. Batch records analyze outlier data, tracking any temperature excursions or materials deviation in real time. Operators view continuous documentation not as bureaucracy but as a hedge against possible quality erosion down the line.
Customers regularly bring us both straightforward and complex formulation issues. Some want minor chain length modifications; others need detailed performance trials at scale. Our willingness to adjust production parameters, and to ship both large volumes and research quantities, gives us a unique view into emerging requirements from both classic and next-generation formulation scientists. Several of our most critical process changes in the past decade came directly from customer-driven requests.
Over time, customers have come to trust that the 4-N-Decyloxybenzaldehyde they receive from our site shows up as ordered, performs consistently, and adapts to their evolving targets. This grounded approach to both product and partnership forms the core of our approach to chemical manufacturing.