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HS Code |
488285 |
| Chemical Name | 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde |
| Molecular Formula | C14H19NO2 |
| Molecular Weight | 233.31 g/mol |
| Cas Number | 56961-19-4 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in common organic solvents such as DMSO and methanol |
| Storage Temperature | Store at 2-8°C, keep container tightly closed |
| Smiles | O=Cc1ccc(OCCN2CCCCC2)cc1 |
| Inchi Key | XNZDSHMAKMUYJK-UHFFFAOYSA-N |
As an accredited 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap, labeled with chemical name, hazard information, and lot number. |
| Shipping | 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde is shipped in a tightly sealed container, protected from moisture and light. Packaging complies with chemical safety regulations, including proper labeling and cushioning materials to prevent breakage or leakage. Transport may require temperature control and adherence to local, national, and international shipping guidelines for specialty chemicals. |
| Storage | 4-[2-(1-Piperidinyl)ethoxy]benzaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Store at room temperature and ensure proper labeling. Use appropriate personal protective equipment (PPE) when handling. Keep out of reach of unauthorized personnel. |
Applications of 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde in Industrial Manufacturing4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde serves as a specialized intermediate in advanced chemical synthesis. As the direct manufacturer, we supply this material to several high-value chemical production chains where precise formulation and regulatory compliance are mandatory. The following sections outline key downstream applications, each with detailed compliance, use, processing, and product outcome information. 1. Pharmaceutical API Intermediate for Antipsychotic CompoundsOur material enters as a core building block in the synthesis of certain atypical antipsychotic active pharmaceutical ingredients such as iloperidone and related analogues. Customers in the pharmaceutical sector need consistent purity for multi-step syntheses that require controlled oxidation and reductive amination. The intermediate supports route customization based on target molecule complexity and regulatory registration batch needs. Industry compliance standards
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2. Advanced Agrochemical Active Ingredient SynthesisLeading agrochemical formulators employ this compound as a key intermediate for producing selective herbicides and plant growth regulators. The raw material participates in targeted reactions for molecular modification, aiding in the creation of bioactive benzyl derivatives. Precision in integration steps ensures downstream residue analysis meets national and international regulatory limits, supporting both pilot and commercial production. Industry compliance standards
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3. Specialty Organic Electronic Materials PrecursorManufacturers of organic semiconductors and advanced electronic functional materials use this raw material to generate highly specific benzaldehyde-based monomers, which are further modified for OLED emitters and organic photovoltaic layers. The compound’s reactivity provides a fine-tuned structure for downstream ring-closure, polymerization, or substitution—supporting strict purity demands to prevent defect occurrence in thin film deposition. Industry compliance standards
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4. Chemical Research and Development for CNS Ligand LibrariesContract research organizations and medicinal chemistry labs integrate the material into small-molecule libraries aimed at central nervous system (CNS) targets. The functionalized benzaldehyde group serves as a point of diversification in library design for ligand binding and SAR studies. High batch consistency allows direct registration in electronic notebook systems and controlled compound archives, supporting preclinical neuroscience investigations. Industry compliance standards
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5. Fine Chemical Intermediate for Fragrance and Flavor SynthesisAuthorized fine chemical producers utilize this intermediate in patent-disclosed aldehyde modifications to produce complex aroma compounds. Its role focuses on ether-bound aromatic aldehyde formation, promoting delicate olfactory profiles for luxury fragrances and specialty flavors. Process integration maintains batch blending under inert conditions to protect sensitive groups, while ensuring downstream compliance with international flavor and fragrance safety standards. Industry compliance standards
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In our years handling specialty chemicals, certain compounds come up time and again for their reliability and adaptability. 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde is one of those compounds that keeps earning attention. On the production line, it stands out thanks to its unique piperidinyl ethoxy side chain linked to a benzaldehyde core. This feature opens doors for diverse chemical transformations. Every day spent in our synthesis lab confirms a simple truth: structure matters, and this aldehyde’s design increases its reactivity profile in ways traditional benzaldehydes just don’t offer.
As a manufacturer, getting to this molecule isn’t just about mixing some reagents and hoping for the best. Our process draws on years of refining reaction steps, solvent choices, and purification strategies. Each batch starts with carefully sourced basic piperidine and ethylene oxide derivatives, followed by a controlled connection to the benzaldehyde backbone. We tightly manage temperature and pH, as these affect yield and isomer formation. For customers used to inconsistent supply or variable purities, the difference in a factory where every step is hands-on – with real eyes on the crystallization tank and not just remote automation – makes a practical difference.
Benzaldehydes as a class have dozens of well-known uses. What distinguishes this material is the substituent's impact on activity and compatibility. In and out of research circles, people keep asking for ways to introduce piperidine without harsh conditions. This compound lets you bolt on the piperidinyl group with fewer side reactions compared to traditional N-alkylation steps. That means smoother progress, fewer wasted runs, and tighter batch-to-batch consistency. Process development chemists, especially, notice the chromatogram stays cleaner and downstream derivatization requires less fuss.
Once synthesized, the main challenge isn’t just purity—it’s stability. Our storage rooms show the lessons of experience. This aldehyde tolerates short periods at ambient temperatures for handling; longer term, we keep it tightly sealed away from light and moisture. Aldehydes tend to react with atmospheric oxygen or trace water, leading to degradation. Investing in low-moisture environments and amber glass pays off by preserving color and reactivity longer. Years of real-world results drive our own in-house guidelines, so our partners avoid surprises after delivery.
Demand comes from several places: pharmaceutical intermediates, fine chemical synthesis, and specialty agrochemical building blocks. Over the past two decades, we’ve found that this compound reduces synthetic steps for drug candidates featuring cyclic amines. That isn’t just theoretical—colleagues in process R&D report step-count reductions and improved route flexibility. For those moving to pilot scale, the ease of integrating this building block makes scaling up less stressful.
Outside pharma, we see requests from teams developing new polymers and resin modifiers. The piperidine ring serves as a robust electron donor, and the ethoxy linkage delivers flexibility. Those pursuing light-stable polymers notice better shelf life and product integrity with this compound, compared to standard aryl aldehydes that fall short under UV exposure.
Structure–activity relationships seldom lie, and plant operators quickly spot the differences between 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde and its simpler relatives. Take unsubstituted benzaldehyde—a workhorse, but far less selective when heading into Mannich or reductive amination protocols. The piperidinyl ethoxy side chain in our product boosts solubility in polar and semi-polar solvents, giving process chemists options for greener reaction conditions. That means reduced reliance on chlorinated solvents.
Another relative, 4-ethoxybenzaldehyde, looks similar at first glance but misses the piperidinyl punch, resulting in less functional group diversity for downstream steps. We routinely field questions from researchers frustrated with the static reactivity of simpler benzaldehydes. The feedback loop from lab to plant and back shows clear preference for our molecule when reactivity tuning and step reduction matter.
Year after year, chromatography remains our best friend. Every batch runs through high-resolution HPLC and GC to monitor purity, with NMR providing confirmation of the desired structural isomer. Routine checks like these aren’t just about checking boxes for a certificate—they catch trace byproducts before they leave our facility. Customers who have switched from other sources notice the difference instantly on their own quality control tests. Inconsistent suppliers often skip these verification steps, leaving users to discover unstable or impure lots at the worst time—during critical synthesis runs.
Few things derail a production run like unanticipated polymerization or inconsistent reactivity. Over the past decade, some clients have shared stories of botched reactions due to off-spec aldehyde. We’ve learned that trace metal contamination—barely detectable with handheld analyzers—plays havoc with sensitive reactions. Addressing these issues means investing in higher grade starting materials and regularly cleaning reactor internals. Quality is a matter of daily discipline, not just paperwork.
Transferring a few hundred grams to multi-kilogram lots never goes exactly as planned. Heat transfer, agitation, and even the type of seals on process lines affect product isolation and reproducibility. Our site teams keep detailed records of every adjustment, and open communication with pilot plant chemists saves time and raw materials. For 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde, the main challenge is controlling side reactions at scale; batch splitting, continuous removal of side products, and pressure filtration have all made measurable improvements.
Clients interested in kilogram or larger quantities often bring up consistency issues between lots. It's not enough just to meet analytical thresholds—we look at factors like color, smell, and how easily the aldehyde incorporates into the next synthetic step. After seeing too many cases where small, unnoticed changes in process water or reagents created headaches downstream, we built extra analytical checks into our workflow. This approach has cut costly rework and minimized unplanned downtime.
Meeting purity and documentation requirements means keeping up with shifting regulations, especially in pharmaceutical and specialty chemical applications. Auditors always want detailed batch records, and we've seen how pre-emptive transparency shortens review timelines. Certification doesn't just happen on paper—every deviation or out-of-specification event is tracked in real time, giving us a true history of every lot shipped.
Clients working in regulated markets appreciate full traceability: knowing which technician oversaw each batch, what instruments logged the QC results, and how storage conditions matched stated guidelines. We go beyond minimum requirements for documentation, helping end-users respond to regulatory scrutiny before issues arise.
Handling organic solvents, reactive intermediates, and exothermic reactions day in and day out teaches respect for safe operations. Disposal of waste streams containing aldehydes and piperidines follows strict guidelines. Our plant moved to fully enclosed solvent systems to reduce fugitive emissions and implemented catalytic oxidizers where needed. Continuous feedback from plant staff and inspectors drives improvements, and we prioritize changes that protect both workers and surrounding communities.
Several years ago, we switched from older, open-batch reactors to closed systems with real-time monitoring of VOCs. This cut emissions and reduced the risk of accidents involving volatile aldehydes. Sustainability isn’t just a corporate goal—it’s built into our plant layout and maintenance routines. We work with regional authorities to audit waste treatment processes and refine them based on test outcomes, keeping environmental stewardship front and center.
Supply chain pressures challenge every manufacturer. Raw material volatility, logistical disruptions, and shifting demand from client sectors mean our ordering and stocking system needs constant adjustment. In tight markets, buyers looking for 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde value suppliers who don’t cut corners under pressure. Experience counts here—our extended relationships with upstream chemical producers let us maintain inventory even during global supply shocks.
There are no shortcuts to dependable delivery. We coordinate with reliable hauliers, pack products in custom-lined containers, and trace lots from tank to end-user. Delayed or spoiled shipments create direct costs for both supplier and user. Our plant’s investment in on-site warehousing and local fulfillment cuts risk and keeps lead times short.
Users’ expectations keep changing. Med chem teams now look for more than simple reactivity—they want building blocks that enable new ring systems, bioisosteres, and scaffold modifications. 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde fits into several emerging synthesis routes, appearing in patents for CNS-active targets and new ligands.
Polymer and resin developers have started blending piperidinyl-functionalized aromatics to boost photostability and enhance pigment compatibility. In response, we’ve made process tweaks for tighter specification controls on trace water and peroxide content. Getting these traces down means fewer surprises for end-users, especially in light-sensitive or moisture-sensitive applications.
Another trend: greener chemistry. Researchers seek to replace halogenated solvents with safer alternatives. Our experience shows this benzaldehyde’s solubility favors such transitions, without the reactivity penalties sometimes seen with other building blocks. Where others face solvation issues, our customers’ reactions go through cleanly.
Feedback from those at the bench matters to us. Clients processing hundreds of grams, not just milligrams, share insights into blending, solution stability, and filterability. They tell us reaction times often shorten, and isolation becomes less tedious than with bulkier or less reactive aldehydes. Technical consultations sometimes reveal improved color stability in dyed polymers, or faster clean-up in continuous reactors. Success at scale points directly to our investment in manufacturing rigor and product consistency.
Customers who tried switching back to lower-spec competitors during temporary shortages often return. Their own experience shows lower impurity profiles translate into easier downstream purification, higher yields, and, in regulated spaces, fewer regulatory headaches. Our engineering and QC teams stay in regular touch with users—not just sales teams—because this is how nuanced improvements come to light.
Every plant has room for improvement. Small adjustments in solvent grade, temperature ramp rates, and agitation routinely lead to better yields or cleaner products. We track each tweak, build them into batch records, and share results across the team to avoid repeating mistakes. Our internal lab delivers feedback within hours, not days, so adjustments can go straight into the next synthesis run.
No finished process stays locked in forever. We’ve rebuilt certain steps after users reported elevated peroxide levels—something most QC routines would have missed but which appeared in sensitive downstream assays. This culture of active listening ensures the product arriving at a customer’s dock today improves on last year’s batch.
Real success with 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde comes from partnerships, not just transactions. We host technical workshops, provide samples for scale-up studies, and walk customers through unexpected troubleshooting. Open exchanges yield shared solutions, whether it’s handling quirks, documentation needs, or logistics questions.
Some of our longest-standing clients began with a single inquiry about impurity tracking in their own synthetic line. Joint investigations led us to alter washing protocols and tweak post-synthesis filtration, creating wins for both sides. Ongoing discussions about safety, batch record transparency, and innovation pipelines ensure we aren’t left behind as market demands shift.
Moving ahead, investment in automation, digital batch tracking, and tighter environmental controls will play a bigger role in refining both product quality and workplace safety. Technology enables more granular tracking of reaction parameters, delivering even tighter control over product consistency.
Shaping the future means adapting to customers’ evolving demands and industry shifts toward greener, smarter processes. The lessons learned in our plant—where process discipline, open communication, and adaptation are daily realities—drive us to keep 4-[2-(1-Piperidinyl)Ethoxy]Benzaldehyde at the forefront of specialty chemical manufacturing. Our commitment isn’t just to supply a chemical but to enable the next breakthroughs for our partners around the world.