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HS Code |
594457 |
| Cas Number | 698-80-6 |
| Molecular Formula | C11H13NO2 |
| Molecular Weight | 191.23 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 91-94°C |
| Boiling Point | 348.2°C at 760 mmHg |
| Density | 1.195 g/cm3 |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Purity | Typically ≥98% |
| Synonyms | 4-(Morpholin-4-yl)benzaldehyde |
| Structure | Para-substituted benzaldehyde with morpholine ring |
| Smiles | O=Cc1ccc(N2CCOCC2)cc1 |
As an accredited 4-Morpholinobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Morpholinobenzaldehyde is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | 4-Morpholinobenzaldehyde is shipped in secure, airtight containers compliant with hazardous chemical regulations. Packaging ensures protection against moisture, light, and breakage during transit. All shipments include appropriate hazard labeling and documentation, adhering to local and international transport guidelines. Handle and store in a cool, dry place upon receipt. |
| Storage | 4-Morpholinobenzaldehyde should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a laboratory chemical storage cabinet. Protect from light and avoid exposing it to extreme temperatures. Ensure that all storage vessels are clearly labeled to prevent accidental misuse. |
Applications of 4-Morpholinobenzaldehyde in Industrial ManufacturingAs a direct manufacturer of 4-Morpholinobenzaldehyde, we serve specialized industrial sectors that require precise chemical performance and regulatory alignment. The following application scenarios reflect established use-cases in downstream industries, where our product supports formulation, processing, and end-product consistency. Each scenario details compliance standards, usage ratios, process positioning, and resulting finished goods. 1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis4-Morpholinobenzaldehyde functions as a selective building block in high-value synthesis routes for certain APIs, contributing to molecular complexity in CNS-acting compounds and oncology drugs. Pharmaceutical manufacturers rely on its reactivity and purity to support multi-step synthesis under stringent regulatory oversight, where traceability and impurity profiles remain central during process validation and scale-up. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide and Fungicide IntermediatesAgrochemical formulators employ 4-Morpholinobenzaldehyde as a core intermediate in multi-step syntheses leading to selective triazole-based fungicides and benzaldehyde-derived herbicide actives. Its application supports production of environmentally stable crop protectants with precise activity spectra, where route selectivity and minimal by-product formation determine overall cost efficiency. Industry compliance standards
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3. Fluorescent Dye and Imaging Chemical SynthesisChemical manufacturers producing advanced imaging agents and fluorescent dyes utilize 4-Morpholinobenzaldehyde as a key ring-opening or electron-donating intermediate. It supports the development of pH indicators, fluorescent stains, and biomedical tracers by enabling specific electronic transitions within the chromophore structure, crucial for detection sensitivity and imaging contrast. Industry compliance standards
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4. Specialty Polymer Modifier SynthesisIn specialty polymer and advanced resin manufacturing, formulators use 4-Morpholinobenzaldehyde as a chain-modifying co-monomer, lending selectivity in crosslink density and hydrophilicity to finished thermosets. The morpholine functionality imparts targeted changes to polymer glass transition temperature and enhances compatibility in high-performance coatings and adhesives, where precise modification is critical for downstream application conditions. Industry compliance standards
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5. Analytical Reagent and Chromatography DerivatizationProducers of analytical reagents and high-sensitivity derivatization kits select 4-Morpholinobenzaldehyde for its unique aldehydic activity in forming stable derivatives with primary and secondary amines, facilitating detection of specific analytes by HPLC or spectrophotometry. Its purity and reactivity permit consistent peak identification and quantification in regulated laboratory workflows. Industry compliance standards
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6. Fine Chemical Synthesis for Electronic and Optical MaterialsPrecision manufacturers in electronic and optical device materials leverage 4-Morpholinobenzaldehyde within synthesis steps for charge transport compounds and specialty aromatic modifiers. Its specific benzaldehyde structure optimizes carrier mobility or electromagnetic responsiveness in devices such as OLEDs, sensors, and photoconductors, where molecular tuning can significantly impact component performance. Industry compliance standards
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Supplying 4-morpholinobenzaldehyde straight from our own reactor means seeing closely how the compound behaves and what customers demand from it. Our product, known by its chemical name 4-(Morpholin-4-yl)benzaldehyde, usually appears as a pale yellow crystalline powder. Chemists in our team work directly with the raw intermediates and finished batches. The main draw for this molecule is the morpholine group, attached directly to the para-position of a benzaldehyde ring, which gives it several benefits over related benzaldehyde derivatives.
In practical synthesis, 4-morpholinobenzaldehyde stands out due to its dual reactive sites. The aldehyde function is useful as a building block in condensation reactions—such as reductive amination or the construction of more complex organic frameworks—while the morpholine group adds solubility in polar solvents and an ability to tune the reactivity in pharmaceutical intermediates. In our hands, the product routinely passes purity levels of 99% GC, with water content and heavy metals well below the widely accepted industry limits. From quality control to logistics, producing this compound ourselves means we track every step, from handling morpholine to washing and isolating the crystal.
Much of the global demand for 4-morpholinobenzaldehyde comes from the pharmaceutical and specialty chemical sectors. API manufacturers want reliability and traceability, because this molecule often features at early or midway points in complex organic syntheses. Our main customers are looking to form new C–N or C–C bonds, where a morpholine ring brings desired pharmacological effects or solubility enhancements in drug candidates.
Producing this aldehyde involves using specific routes—typically Vilsmeier-Haack or Duff formylation, followed by purification and crystallization. Handling the process in-house, we prevent contamination from trace byproducts that can trouble downstream applications. Every batch comes off the line after passing analytical methods such as NMR, HPLC, GC-MS, and melting point screening. By producing and analyzing the product ourselves, we pick up subtle differences in crystal habit, particle size, and batch-to-batch color, all of which may matter for a customer’s outcome in scale-up runs.
Trying to assemble active compounds in bulk or at bench-scale depends on getting the main aldehyde in reliable condition. Out of factory, our 4-morpholinobenzaldehyde fits a melting point of 81–84°C and a molecular weight of 191.22. Most requests settle on custom pack sizes in sealed drums or bottles, filled and tested under nitrogen protection, as the aldehyde function does not like excess air or moisture during long storage. High-purity material ensures that super-stoichiometric reactants do not build up dangerous aldehyde impurities in a finished API or advanced intermediate.
Handling it daily, our staff routinely observe how even minor contaminants (like N-oxide or trace metallics) disrupt downstream hydrogenations or oxidations. Many resellers and traders do not track the origin, and in that case, unexpected side-products sometimes appear, especially in amine condensation steps. By making the aldehyde ourselves and controlling the whole route, we cut out this uncertainty. Finished material always includes a certificate analyzed against a library of reference spectra, not just a typical COA with a pass/fail line for purity.
Organic chemists often compare this product with related benzaldehyde derivatives—such as the unsubstituted benzaldehyde, 4-methoxybenzaldehyde, or the similarly structured 4-piperidinylbenzaldehyde. Each brings its own set of solubility, reactivity, and toxicity profiles. The morpholine ring at the para-position brings both a less harsh nitrogen, due to the ether oxygen in the heterocycle, and higher solubility with polar solvents like ethanol, methanol, or DMF.
From a synthetic perspective, this added ring softens conditions in reactions involving nucleophilic attack or Lewis acid catalysis. In our reactions, the morpholine group tends to be more stable to basic hydrolysis and less prone to unwanted rearrangement than piperidine or dimethylamino groups at the same position. Large-scale users report fewer side products and lower levels of unwanted tars when running Mannich, reductive amination, or Chichibabin reactions from our product. Less time lost to purification means higher throughput and more predictable trial synthesis on the R&D side.
Scaling this synthesis from kilograms to tons meant developing practical solutions for solvent use, waste streams, and in-process analysis. To keep aldehyde content high and formation of unwanted by-products low, we optimized temperatures, nitrogen blanketing, and in-line filtration. Troubles in early runs—such as color impurities or resin formation—taught us to use buffered workups and food-grade filtration media, rather than cruder methods common with low-cost suppliers.
By isolating the solid in a way that avoids contact with iron or copper, we keep heavy metal readings below 5 ppm. Many global companies rely on this to pass the stricter regulatory regimes in pharma, such as EU GMP and US FDA standards for drug precursors. Shipping the product cross-border requires strict adherence to local customs and environmental protocols, so we document trace solvents, residuals, and compliance with the latest RoHS and REACH guidance.
Packing and handling protocols also matter for end users. Aldehydes generally absorb oxygen, turning yellow or brown if exposed. Real-world experience suggests that resealable, light-blocking packaging works better than simple clear containers, especially in humid or warm regions. We field dozens of customer inquiries a year tied to storage or shelf-life. Our staff regularly check retention samples under varying temperatures so we can offer real support to anyone running into discoloration or melting issues.
Many of our customers do not just use 4-morpholinobenzaldehyde as a simple reactant—they incorporate it as a core motif in new drug candidates, imaging agents, or performance polymers. This compound’s structure makes it a favorite for building up piperazine, morpholine, or other nitrogen-containing scaffolds with pendant aldehyde groups.
Our technical team has worked with process chemists to adjust the particle size and purity depending on application—whether for solution-phase synthesis, batch reactions, or flow chemistry setups. In one case, producing custom-milled batches allowed a multinational research group to speed up reaction rates and avoid filter clogging, a time-saving major enough to justify a change in procurement policy. Collaborations like this, grounded in day-to-day factory work, deliver stronger outcomes for R&D and plant scale-up.
Beyond pharma, sectors like agrochemicals and specialty polymers increasingly adopt this molecule. In crop protection, it can serve as a precursor to selective herbicide candidates, while polymer researchers explore its use in polyfunctional crosslinkers or in molecular electronics. Demand for larger, impurity-free batches has risen in the last five years, especially from contract manufacturing organizations (CMOs) that supply to multiple global brands.
Our plant-level documentation reflects this shift. For each batch, we retain synthesis notes, analytic data, and storage logs, so any customer can trace the origin back to the exact reactor run and analytical signature. Unlike distributors or third parties, we carry the risk and responsibility for errors, and we fix issues directly. If an end-user in Europe requests a specific impurity profile to comply with EMA guidelines, or a US biotech wants radiopurity for labeled precursors, we provide samples from retained stock or fresh production.
Peer review in chemistry means sharing not just the assay but the details: what solvents were used, which filtration aids, which lot of morpholine, and even the purity data for those. Over years of supplying this product, we have seen that advanced users perform NMR fingerprinting rather than rely only on HPLC. We share our spectra, analyze for residual solvents beyond standard specs, and routinely update our methods to match changing industry guidelines. In this field, details count.
Producing chemical intermediates in volume brings inevitable questions about process safety and environmental impact. For 4-morpholinobenzaldehyde, the main process risks involve handling formaldehyde sources, chlorinated formylating agents, and the resulting organic residues. In scaling up, we engineered closed-loop solvent recycling and VOC abatement, using in-plant scrubbers and continuous emission monitoring. Protecting our operators means using PPE and scrubbers even in open transfer steps, with regular monitoring of volatile organic concentrations.
The plant follows international and local safety standards, but hands-on learning has taught us the importance of short transfer lines, inert gas blankets, and real-time temperature probes. Our leadership reviews each safety incident and upgrades the process, piping layout, or alarm systems as real cases dictate. Waste streams from morpholine-containing syntheses are neutralized in on-site plants, and solid wastes end up only in licensed incineration sites.
We view sustainability as an evolving target. For example, in recent years, we switched from chlorinated to less hazardous formylation reagents for in-house runs destined for eco-sensitive European customers. Annual audits include not just paper compliance but real on-the-spot walkthroughs and air/water monitoring. The environmental performance has boosted our status with multinational API partners who carry out their own on-site verifications.
Purchasers occasionally ask what sets our factory-made 4-morpholinobenzaldehyde apart from products circulating from resellers or other makers. The big differences appear in side-by-side analytics. It is easy to measure melting point depression or note a yellow tint in a crude sample, but problems usually reveal themselves in subsequent chemistry: incomplete conversion, foul odors, or reaction mixtures that require extra purification.
Several years ago, customers receiving material from generic supply houses reported more batch-to-batch inconsistency in yield and side-product content. Synthesis teams found themselves discarding entire test runs due to a lack of reproducibility. By comparing mass spectra, NMR, and impurity profiles from direct and indirect sources, our clients started tracking improvements in their production metrics. Fewer failures translated to less wasted time in formulation, QA release, and scale-up batches.
These real-world outcomes reinforce our choice to keep manufacturing in-house, tightly control supply chain inputs, and reinvest in process improvements rather than low-cost outsourcing. This decided difference matters even more for customers making high-purity intermediates or pilot batches for regulated industries.
Producing specialty aldehydes invites ongoing challenges. Once, a major pharmaceutical client flagged a subtle impurity in their GC trace. Instead of deflecting blame or passing the complaint along, we re-examined both processes and intermediates. We traced the contaminant to a morpholine feedstock supplier, and our technical team reformulated procedures to purchase only from approved vendors with up-to-date audit trails. By staying close to raw material producers, we’ve reduced similar surprises.
Not every batch runs perfectly, and equipment fouling sometimes threatens timelines. Our engineers responded by installing in-line cameras and new filtration systems. This vigilance results in a lower rejection rate and tighter feedback for both production teams and customers. Over a decade supplying 4-morpholinobenzaldehyde, continued dialogue with scientists, purchasing managers, and end-users shapes our data-driven improvements to process and analytics.
Chemicals like 4-morpholinobenzaldehyde do not just represent a single transaction. Our team views every order as a starting point for longer partnership. End-users trust us to provide more than just a product—they expect sound data, flexible logistics, and ongoing technical support, especially when regulatory hurdles get stricter every year.
Manufacturing chemical intermediates comes with direct responsibility for quality, safety, and downstream impact. Staff in our plant see the effects of decisions made every day in purchasing, maintenance, storage, and shipping. These practical lessons translate into greater reliability for those who use our 4-morpholinobenzaldehyde, in research labs or full-scale production alike.