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4-(4-Morpholino)-3-Nitrobenzaldehyde

    • Product Name 4-(4-Morpholino)-3-Nitrobenzaldehyde
    • Alias MNBA
    • Einecs 629-917-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 4-(4-Morpholino)-3-Nitrobenzaldehyde

    Applications of 4-(4-Morpholino)-3-Nitrobenzaldehyde in Industrial Manufacturing

    4-(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 Agents

    As 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

    • Good Manufacturing Practice (GMP, ICH Q7)
    • United States Pharmacopeia (USP) Monographs for APIs
    • European Pharmacopoeia (Ph. Eur.) requirements for pharmaceutical intermediates
    • ICH Q3A/B (Impurities in New Drug Substances and Products)

    Typical usage ratio

    • Stoichiometric ratios of 0.98–1.05 equivalents relative to nucleophilic core reagent, with optimization per batch based on target molecular yield and purity profile

    Downstream process integration

    • Direct addition during condensation or reductive amination step in multi-step synthesis of piperazine or morpholine-containing APIs

    Final product types

    • Antitumor drug substances (e.g., selective kinase inhibitors)
    • Advanced intermediates for oncology drug candidates
    • Crystalline API bulk for formulation into oral and injectable medicines

    2. Dye Intermediate in High-Fastness Disperse Dye Production

    This 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

    • Oeko-Tex® Standard 100 (Textile Safety Requirements)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Annex XVII for aromatic amines and dye toxicity
    • ISO 105-C06 (Textiles—Tests for Colour Fastness—Part C06: Colour Fastness to Domestic and Commercial Laundering)

    Typical usage ratio

    • Intermediate charge of 0.6–1.2 mole per mole of coupling base, level depending on specific shade and chromophore target

    Downstream process integration

    • Charged to diazotization/coupling kettle for formation of azo or anthraquinone dye intermediates; fully reacts prior to isolation and purification steps

    Final product types

    • High-fastness disperse dyes for synthetic fiber textiles
    • Colorants for plastic and fiber blends
    • Specialized industrial textile inks

    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

    • OECD Principles of Good Laboratory Practice (GLP) for field trial actives
    • ISO 9001:2015 (Quality Management Systems for synthesis operations)
    • Regulation (EC) No 1107/2009 (EU plant protection product regulation)
    • US EPA Pesticide Registration requirements for new actives

    Typical usage ratio

    • Introduced at 0.85–1.2 equivalents relative to the co-reactant in condensation or cyclization, adjusted to balance reactivity against downstream purification loads

    Downstream process integration

    • Added during initial condensation or ring closure to form herbicidal core, followed by purification and formulation for biological trials

    Final product types

    • Small-molecule herbicide R&D candidates
    • Advanced agrochemical intermediates for large-scale field testing
    • Screening samples for selectivity and environmental studies

    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

    • SEMI C94-0321 (Photoresist and Ancillary Chemicals for Semiconductor Manufacturing)
    • ISO 9001:2015 (Quality Management System—Specialty Chemicals for Electronics)
    • RoHS Directive (2011/65/EU) for electronic grade chemicals
    • Internal foundry process specifications for impurity and metal limits

    Typical usage ratio

    • Reactant charge of 0.95–1.1 equivalents in polymer modification reactions, adjusted by desired resist feature size and cross-linking density

    Downstream process integration

    • Enter as a functional monomer during resin backbone modification or advanced additive blending, prior to photoresist formulation, filtration, and packaging

    Final product types

    • Photoresist polymers for semiconductor production
    • Advanced additive packages for micro-pattern etching
    • Electronics-grade coating materials

    5. Chemical Probe Manufacturing for Biological Research

    Biotechnologists 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

    • ISO/IEC 17025 for laboratory reagent quality
    • OECD Good Laboratory Practice Guidelines for tool compound production
    • REACH registration (when crossing EU/EEA borders for research chemicals)
    • US NIH guidelines for lab chemical safety documentation

    Typical usage ratio

    • 0.9–1.05 equivalents relative to labeling group in final condensation, modulated by desired probe purity and functional group density

    Downstream process integration

    • Reacted in last-step derivatization to introduce reporter tags or affinity handles, followed by preparative chromatography and analytical QC release

    Final product types

    • Covalent protein-labeling probes
    • Fluorescent molecular tags
    • Small-molecule affinity reagents for target validation studies
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    Certification & Compliance
    More Introduction

    Introducing 4-(4-Morpholino)-3-Nitrobenzaldehyde: Experience Straight From the Manufacturer

    From Our Reactor to Your Lab Bench

    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.

    Getting to the Core: What Makes This Benzaldehyde Stand Out

    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.

    Crafting to Meet Customer Needs

    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.

    How 4-(4-Morpholino)-3-Nitrobenzaldehyde Powers Projects

    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.

    Practical Use Cases From Real Labs

    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.

    Real Differences Compared to Other Aldehyde Intermediates

    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.

    Troubleshooting and Support: Direct From the Manufacturing Floor

    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.

    Handling and Safety: Manufacturer Insights Beyond Labels

    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.

    Material Availability and Batch Scalability

    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.

    Controlling Quality: From Each Batch to Every Drum

    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.

    Environmental Responsibility and Compliance

    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.

    Ongoing Research and Collaboration

    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.

    Commitment to Consistency and Service

    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.

    Conclusion: Manufacturer’s Perspective on Reliability and Innovation

    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.