|
HS Code |
155005 |
| Productname | 4-(4-Morpholino)-3-Nitrobenzaldehyde |
| Molecularformula | C11H12N2O4 |
| Molecularweight | 236.23 g/mol |
| Casnumber | 213298-94-2 |
| Appearance | Yellow to orange crystalline powder |
| Meltingpoint | 123-127°C |
| Purity | ≥98% |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Boilingpoint | No data available |
| Density | No data available |
| Storagetemperature | 2-8°C (Refrigerated) |
| Smiles | O=Cc1ccc(N2CCOCC2)cc1[N+](=O)[O-] |
| Synonyms | 4-Morpholino-3-nitrobenzaldehyde |
| Hazardstatements | May cause eye and skin irritation |
| Refractiveindex | No data available |
As an accredited 4-(4-Morpholino)-3-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 4-(4-Morpholino)-3-Nitrobenzaldehyde, labeled with safety and identification details. |
| Shipping | 4-(4-Morpholino)-3-Nitrobenzaldehyde is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with regulations for handling chemicals, ensuring safety and integrity during transit. Appropriate hazard labeling and documentation accompany the shipment, and transport is typically via ground or air, in accordance with local and international chemical transport guidelines. |
| Storage | 4-(4-Morpholino)-3-nitrobenzaldehyde should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Use appropriate chemical storage cabinets and label clearly. Ensure access is restricted to trained personnel and follow standard laboratory chemical safety protocols. |
Applications of 4-(4-Morpholino)-3-Nitrobenzaldehyde in Industrial Manufacturing4-(4-Morpholino)-3-Nitrobenzaldehyde serves as a specialty intermediate in several industrial value chains, valued by downstream manufacturers for its unique reactivity profile in target synthesis routes. The following application sections outline established market-verified scenarios where this molecule contributes to final product performance, process efficiency, and regulatory compliance. 1. Pharmaceutical Intermediate for Piperazine-Based Antitumor AgentsAs a key aldehyde fragment in the synthesis of certain heterocyclic anti-cancer molecules, 4-(4-Morpholino)-3-Nitrobenzaldehyde supports the construction of pharmacologically active scaffolds containing both morpholine and nitrobenzene moieties. Its introduction at the specific condensation stage maximizes selectivity and yield during active pharmaceutical ingredient (API) build-up, aiming for stringent purity and impurity control standards required in parenteral or oral dosage forms. Process chemists favor its use for consistent lot-to-lot reproducibility and compliance with international pharmacopeia standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Dye Intermediate in High-Fastness Disperse Dye ProductionThis compound enables the design of specialized chromophore building blocks for disperse dyes that must withstand repeated washing, light exposure, and mechanical stress in polyester and acetate fiber coloration. Its nitro and morpholino group positioning permits colorists to tailor shade intensity and fastness through controlled diazotization and coupling reactions. Commercial dye synthesis runs integrate this intermediate specifically to achieve compliance with demanding environmental regulations on dye purity and by-product minimization. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Building Block in Agrochemical Synthesis (Herbicide R&D)Research and process development teams in the agrochemical sector apply this intermediate when constructing morpholine-substituted heterocyclic cores for herbicide discovery or scale-up. Its aldehyde function serves as a versatile platform for condensation with a range of amines, enabling structure-activity relationship (SAR) exploration to improve selectivity and environmental profiles. Regulatory regimes require complete traceability for each lot, and handlers incorporate robust quality documentation at this input stage to facilitate regulatory submissions for trial and pre-commercial herbicide candidates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Electronic Chemical Synthesis (Photoresist Additives)In the microelectronics chemical supply chain, this aldehyde derivative provides a rigid aromatic core with electron-withdrawing and morpholine substituents critical for tuning the solubility and developer resistance of novolak-type photoresists. Leading fabs and photoresist formulators integrate this specialty block at defined synthetic stages to meet line width control and defectivity requirements essential in semiconductor lithography. End-users demand documentary evidence of lot traceability, impurity specification, and total metal content, each tracked back to the point of entry of this intermediate. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Chemical Probe Manufacturing for Biological ResearchBiotechnologists and chemical biology tool providers utilize this aldehyde as a core building block to construct small-molecule probes for protein labeling and mechanistic pathway studies. Its structure allows conjugation with various nucleophilic residues, facilitating preparation of tagged or fluorescent derivatives. High-purity lots are mandatory, and protocol-driven QC ensures the finalized reagents comply with current best practices in laboratory safety, analytical documentation, and material traceability for cellular and molecular biology labs worldwide. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-(4-Morpholino)-3-Nitrobenzaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In our chemical production lines, 4-(4-Morpholino)-3-Nitrobenzaldehyde is a familiar companion. We have watched it run through stainless reactors, examined the color as the reaction forms the desired aldehyde group, smelled its distinct character during batch releases, and fielded calls from researchers who rely on this compound to push their work ahead. This compound, with a molecular formula of C11H12N2O4 and a yellowish solid form, has carved itself a niche among intermediates for advanced material synthesis and medicinal chemistry.
Preparing any sensitive aromatic aldehyde takes care, but introducing both morpholino and nitro groups brings a new layer of complexity. Our team found that direct nitration doesn’t yield clean products, so we use a stepwise approach to first protect, then nitrate, then form the morpholine ring. This gives a crisp, reproducible product every time. The aldehyde’s purity directly influences downstream success, so each lot undergoes HPLC, NMR, and mass spectral analysis. A typical batch yields a melting point near 105–109°C. Trace moisture and by-products are common culprits for failed syntheses; our team invests the time in careful drying and filtration to get consistent, low-impurity results. Laboratories and production groups alike testify to the difference between a bench-made rough product and the carefully manufactured batches we create daily.
Beyond standardized lots, we answer specific requests for micro-scale research quantities and kilo-scale process runs. A university team once called us to discuss switching their synthetic route to our aldehyde because their own pilot batches lacked reproducibility; their project lead couldn’t get a consistent yield in subsequent reactions. We listened closely, checked their purification steps together, and then shipped two preparation scales so their group could compare performance. The difference showed up in the form of cleaner NMR baselines and bright yellow crystals, visible even to the student’s benchmate. This experience is not unusual, since researchers notice that small differences in how a key building block is made reach into every following step.
Hospitals and research centers use this compound for very concrete purposes. Synthetic chemists reach for it when building up complex molecules for pharmaceuticals, such as anti-infectives or CNS drugs, because the morpholine ring imparts metabolic stability and solubility, while the nitro group activates aromatic substitutions and other reactions. Our own quality managers have walked customers through shipment records, checking lot numbers, purity, and stability, because they know researchers can’t afford surprises between columns and reactions. In process chemistry, even small changes in an input batch influence downstream crystallization and impurity profiles, so our repeat buyers always ask about lot repeatability and documentation, not just a certificate of analysis.
A biotech startup approached us with a question about scale-up; they needed 100 grams for preclinical candidates, but had run into bottlenecks purifying bench-made aldehydes. Our synthetic route, with a focus on stepwise purification and robust work-up, meant they saw improved chromatography and fewer side products—the difference showed sharply on their LC-MS traces. A contract research organization using our aldehyde reported that downstream reduction to the corresponding alcohol worked with over 90% yield and no need for additional purification. Consistency like this emerges from a hands-on manufacturing approach.
We speak every week with researchers who run synthesis optimization or are launching fresh projects. Ecology test labs tap into this aldehyde for dye intermediate studies. Custom polymer labs turn to it for specialty crosslinking experiments, facilitated by the balance of reactive nitro and aldehyde groups. Every engineer who unpacks a drum or a bottle from our site wants to see batch records, spectral data, and shelf-life test results. This direct line between our reactors and our customers’ benchtops has sharpened our understanding of the diverse ways this single compound shapes new chemical matter.
For those who ask why 4-(4-Morpholino)-3-Nitrobenzaldehyde outperforms more conventional aromatic aldehydes, experience provides a clear answer: The morpholino group combines with the nitro ring to bring a unique reactivity profile. Benzaldehydes lacking the morpholine ring don’t have the same solubility in polar aprotic solvents and show more side reactions in amination protocols. Those stripped of the nitro group fail to activate the aromatic core, so coupling partners need harsher conditions. Technical leaders at customer firms have noted their pilot reactions run more cleanly, and post-reaction work-up is simpler, when using this compound as opposed to unsubstituted analogs or chlorinated alternatives, which often produce greater waste and more difficult separation.
Problems rarely show up in textbooks, but they show up in plant records; product caking during long-term storage, bottle discoloration due to excess light or air, fines complicating transfer between drums. Our team tracks every notification, whether it comes from QA, regulatory affairs, or right from a customer’s shipment unboxing. As a manufacturer, we keep logs of temperature swings during storage and transport, and we log calls describing off-color samples. Routine stability testing lets us compare product from day zero to one-year and two-year marks, with confirmed findings that color and melting point hold steady under dry, controlled conditions. We have adjusted our packaging over time, adding foil lining or inert gas purges for large lots, and respond quickly when researchers request smaller vials to prevent repeated exposure to atmospheric moisture.
Operating day by day on an industrial site offers a perspective that’s different from what appears in standard data sheets. We see what happens during accidental spills or cleaning work between batch runs. The compound emits a faint odor—noticeable but not overpowering. Inhalation is rarely the issue that worries our site team; the risk comes from skin contact or the fine yellow powders that become airborne if handled carelessly. Gloves and dust masks stay standard equipment for every technician. During large-scale drum filling or transfers to customer containers, our process engineers designed workspaces to minimize powder dispersion with local LEV and smart airflow planning.
Internally, we store the compound sealed, with humidity monitoring and clear lot segregation to prevent cross-contamination with closely related nitroaromatics. We replace paper labels with solvent-resistant prints after customers showed how ethanol wipes during inventory checks sometimes blurred critical text. Practical lessons like these shape every aspect of our manufacturing and shipping protocols.
Volume requirements differ widely across customers, from microgram samples for synthetic route scouting to several kilograms for preclinical API production. We invested in high-pressure reactors, liquid-transfer pumps, and automated crystallization controls for this very reason; scale-up brings unique challenges, and the purity constraints only grow tighter as the lot size increases. Our skilled plant team adjusts reaction time, temperature profile, and solvent ratios batch-wise, logging any deviation from SOPs. The focus is always product integrity, not just quantity—a perspective best appreciated if you’ve watched an entire week’s run trashed by a half-degree deviation or incautious phase separation.
Big volume customers—whether they’re pharma companies prepping early-stage candidates or academic groups pooling orders—depend on us for firm delivery timelines. We keep backup stocks of critical starting materials, and plan overlapping production schedules to handle surges, because the best route is no use if the product doesn’t show up when the lab needs it.
Our laboratory team approaches quality control with hands-on determination. New equipment comes to life only after side-by-side comparison with trusted reference standards and repeated calibration using actual production material, not just commercial samples. Liquid chromatography offers purity data, but long experience shows that visual changes or subtle changes in odor can signal issues as clearly as any instrument. Each batch gets retained samples, tested not only at release but also at annual checkpoints; any drift over months can flag shipment or storage conditions needing improvement.
We offer customers full access to lot data, impurity profiles, spectral overlays, and documented retest intervals. This transparency didn’t happen overnight, and it grows with every technical inquiry received—whether it comes from an industry veteran or a graduate student working through summer. We watch customer feedback translate into fresh QC protocols every quarter, reshaping internal training and test documentation.
Manufacturing specialty nitroaromatics and morpholine derivatives raises relevant environmental and safety challenges. We’ve responded by installing in-line scrubbers and upgrading our waste treatment trains to handle nitro-containing effluents. Regular audits and investment in closed-system transfers reduce worker exposure and minimize community risks. Every run draws from lots of operational and regulatory experience, especially as regional controls on nitro-based compounds tighten.
We take responsibility for cradle-to-gate emissions: solvents get recycled wherever technically feasible, and residual wastes see proper neutralization before discharge. Our facility tracks every production run against both local laws and globally recognized standards, out of respect for the community we work in and the research teams that rely on us to deliver not just quality, but accountability.
The manufacture of 4-(4-Morpholino)-3-Nitrobenzaldehyde doesn’t stand still. We collaborate with academic partners and industrial teams seeking better yields, fewer by-products, or novel applications for this building block. Feedback loops between the shop floor and the customer’s R&D bench have led to new purification routes, improved recrystallization solvents, and innovative approaches to particle size control. More than once, an email from a researcher about an unexpected impurity after storage pushed us to rethink stability testing protocols or even swap out packaging materials.
Our tech support team—drawn from production chemists and engineers—fields application questions week in and week out. Sometimes it’s troubleshooting a Friedel–Crafts reaction that isn’t working; other times it’s about regulatory documents or batch certs needed for grant applications. We treat every inquiry as a partnership opportunity, knowing that a successful reaction outcome is only as good as the attention paid to every production detail along the way.
Day after day, the performance of 4-(4-Morpholino)-3-Nitrobenzaldehyde in syntheses across the globe reaffirms the importance of disciplined manufacturing. Customers return for lot-matched batches and detailed records not because of advertising but because their results depend on it. We evaluate manufacturing not just as an exercise in chemistry but as a service to those advancing science. As practical issues crop up—ingredient shortages, transportation delays, packaging leaks—we bring them into our internal reviews and adjust accordingly, often inside the same quarter, to prevent the same issue recurring for any downstream customer.
Inside the factory, each team member sees how their choices about temperature hold times or raw material insertion rates show up in the product vials scientists open months later. We maintain that link, factory to bench, through every aspect of our quality system.
The path from raw ingredients to a ready-to-ship lot of 4-(4-Morpholino)-3-Nitrobenzaldehyde runs deeper than laboratory notes or procedural diagrams can capture. It’s shaped by years of hands-on manufacturing, continuous feedback from users blending reactions or purifying targets, and the lessons learned from every hiccup, delay, or customer discovery. We have grown alongside evolving applications, adapting purification steps and refining logistics, keeping an eye on both technological improvements and regulatory expectations.
Researchers, formulators, and QA leaders recognize the difference a reliable source makes—from fewer failed reactions to straightforward downstream processing and clarity in every analytical result. Our experience as manufacturers stays inseparable from each gram or kilogram we ship: honest communication with our customers, transparent documentation, and a willingness to improve on every run. By grounding each production cycle in feedback, evidence, and shared goals, we turn a nuanced, challenging compound into a robust tool for the world’s innovators—one lot at a time.