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HS Code |
672375 |
| Chemical Name | 4-Phenylmorpholine |
| Cas Number | 104-07-6 |
| Molecular Formula | C10H13NO |
| Molecular Weight | 163.22 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 6-8°C |
| Boiling Point | 116-117°C at 10 mmHg |
| Density | 1.08 g/cm³ |
| Solubility | Soluble in water and organic solvents |
| Smiles | C1COCCN1C2=CC=CC=C2 |
| Refractive Index | 1.551 |
| Flash Point | 117°C |
| Synonyms | N-Phenylmorpholine |
As an accredited 4-Phenylmorpholine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 4-Phenylmorpholine, tightly sealed with a screw cap, labeled with hazard and identity information. |
| Shipping | 4-Phenylmorpholine is shipped in tightly sealed containers to prevent contamination and moisture ingress. It is packaged according to international regulations for chemical transport, often as a liquid or solid, labeled with hazard information. During shipping, temperature and handling precautions are strictly followed due to its classification as a hazardous substance. |
| Storage | 4-Phenylmorpholine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the storage area free from ignition sources and limit exposure to air and moisture. Appropriate labeling and secondary containment are recommended to prevent accidental release or contamination. |
Applications of 4-Phenylmorpholine in Industrial Manufacturing4-Phenylmorpholine serves as a crucial intermediate and functional auxiliary in several specialized industrial value chains. Owing to its unique structural features, it finds targeted use in selected high-value sectors where strict regulatory oversight, customized formulation control, and advanced process requirements matter. The following sections detail verified core applications supported by current industrial practices. 1. Pharmaceutical API Intermediate SynthesisResearchers and industrial producers utilize 4-Phenylmorpholine as an intermediate during active pharmaceutical ingredient (API) synthesis for select neuroactive compounds and antihistamine drugs. The molecule is introduced during specific condensation or alkylation steps, allowing precise structural modifications. Production plants rigorously validate purity and consistent batch performance throughout scale-up. Downstream customers focus on traceability and regulatory trace compliance during procurement and technical transfer of this intermediate to finished pharmaceutical product lines. Industry compliance standards
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2. Fine Chemical Synthesis for Specialty DyesChemical manufacturers apply 4-Phenylmorpholine as a precursor or functionalizing agent within advanced dye manufacturing, specifically targeting mordant and acid dye classes. Its introduction modifies chromophore properties and enhances solubility profiles relevant to demanding textile and printing applications. Process engineers tightly control addition rates and reaction atmospheres to ensure the desired shade intensity and reproducibility across industrial dye lots. Industry compliance standards
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3. Organic Corrosion Inhibitor ProductionThe formulation industry incorporates 4-Phenylmorpholine into custom corrosion inhibitor blends tailored for industrial water treatment, metalworking fluids, and petroleum refinery applications. The compound acts as an effective nitrogen donor, imparting passivation properties to steel and copper surfaces under harsh process or environmental exposures. Optimizing dosage protects critical assets without interfering with dispersion, de-emulsification, or other formulated additive functions in the finished product. Industry compliance standards
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4. Agrochemical Active Ingredient DevelopmentSelected agrochemical synthesis routes utilize 4-Phenylmorpholine as a ring system builder or substituent donor for specialty herbicide and fungicide active molecules. Agrochemical formulators rely on its chemical stability and controlled reactivity to construct key intermediates, leading to actives with targeted bioactivity, environmental persistence, and resistance management features. Large-scale operations monitor phase purity using NMR and LC-MS, securing batch-to-batch uniformity for regulatory dossiers and field trial requirements. Industry compliance standards
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5. Polyurethane Catalyst ManufacturingAdvanced polyurethane foam and elastomer plants utilize 4-Phenylmorpholine as a tertiary amine catalyst component. Its unique morpholine structure modulates reaction kinetics, affecting foam rise time, cell structure, and final hardness in automotive, construction, and insulation applications. Manufacturers carefully balance the addition to meet exacting requirements for volatile amine content, odor, and regulatory limits on catalyst residue in end products. Process optimization ensures safe handling and minimal byproduct formation. Industry compliance standards
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On the production floor, 4-Phenylmorpholine stands out as a specialty compound that keeps turning up in important applications. As someone who’s worked with this substance through the synthesis and quality control stages, it’s become clear that there’s more to it than a simple line on a product list. Our chemists respect the value it brings to pharmaceutical intermediates, pesticides, and specialty polymers. Ask any synthetic chemist who’s had to choose a morpholine-derived scaffold—they’ll tell you it comes down to reactivity, reliability, and how it fits into both legacy and new methods.
4-Phenylmorpholine carries a six-membered morpholine ring, where a phenyl group connects at the fourth position. Formula: C10H13NO. Plenty of specialty amines show up in catalogs, but the phenyl group confers extra stability and lipophilicity that influence both partition coefficients and downstream reactivity. In our reactors, this translates into consistent batch yields and reproducible outcomes during purification—customers who formulate active pharmaceutical ingredients often mention this feature.
With a molecular weight of 163.22 g/mol, the compound’s moderate polarity and aromatic character support both nucleophilic and electrophilic substitutions in subsequent reactions. Chemical engineers have commented, standing by the reactors, about how certain impurities rarely persist due to the steric and electronic properties of this scaffold. Morpholine by itself often ends up too hydrophilic for some applications, while 4-Phenylmorpholine provides an accessible balance due to the aromatic substitution.
As a manufacturer, we prepare and handle various morpholine analogs: N-alkyl, N-aryl, even those with substitutions at 2 and 3 positions. 4-Phenylmorpholine brings something distinct in the way the phenyl group at carbon 4 adjusts the basicity and decreases water solubility. That subtle shift matters to formulation chemists who deal with precipitation, solubility, and crystallization in multi-step synthesis.
4-Phenylmorpholine does not act as a straightforward morpholine surrogate in every reaction designed for its simpler cousin. Medicinal chemists who need a non-basic, lipophilic moiety for drug-like molecule scaffolding choose this compound to avoid the excessive water solubility and protonation issues that morpholine itself can create in finished drugs. It offers a steady option for building blocks, especially where aniline-based alternatives introduce harsh activation energies or excessive side reactions.
Real production experience shapes every kilogram of 4-Phenylmorpholine released from our lines. The process involves aniline, ethylene oxide, and a controlled environment where moisture and air exposure must remain limited. The aromatic substitution presents certain challenges on scale-up—the increased boiling point compared to unsubstituted morpholine often calls for custom distillation columns and glass-lined reactor vessels. Operators comment about the sweet, faint amine odor, distinct from the harsher notes of unadorned morpholine.
Analytical chemists in our labs verify quality at every stage, watching for residual aniline and by-products like 2-phenylmorpholine. Thin-layer chromatography and gas chromatography keep yields high and impurities low, which suits pharmaceutical partners well, since they trust the chain of custody and analytical transparency. Failure to control variables during cyclization can lead to isomeric mixtures—in those batches, we apply extra purification steps and track impurity profiles to protect downstream synthesis reliability.
The phenyl-substituted structure unlocks functional possibilities. Formulators and process chemists have found that it works as a ligand for homogeneous catalysis—its steric footprint enables sufficient binding with transition metals, without the side reactions typical of less hindered analogs. Engineers working on pilot lines have set up runs where 4-Phenylmorpholine jumpstarts cyclization reactions or acts as a nucleophile in coupling strategies, reducing the occurrence of unwanted salt by-products.
Over decades, fine chemical development teams have reported that 4-Phenylmorpholine provides unique value in pharmaceutical intermediate synthesis, especially for molecules aimed at CNS (central nervous system) targets. Its presence in active moieties enhances blood-brain barrier permeability, while avoiding some of the cytotoxicity issues present in more basic morpholine scaffolds. Medical chemists return to it because the aromatic ring subtly shifts electronic distribution, enabling higher selectivity in late-stage cross-coupling and amide bond formation.
In the agrochemical sector, 4-Phenylmorpholine features in synthetic routes for specific insecticides and herbicides. The aromatic morpholine motif lends itself to formulations with improved substrate adhesion and metabolic stability. As pesticide actives require tighter regulatory scrutiny, formulators favor intermediates with established toxicological profiles—production under current Good Manufacturing Practices uses validated cleaning protocols, with exhaustive residual solvent testing for each lot.
We supply 4-Phenylmorpholine primarily as a clear to pale yellow liquid, with purity upwards of 99%. Our standard offering suits both kilo lab and production scale, delivered in steel drums with inert gas headspace for shelf life. Chemists interested in formulation stress the importance of moisture content—typically kept under 0.2%—since water traces can complicate subsequent nucleophilic substitutions or cause amine carbonylation. The boiling point averages around 270–280 °C, while flash point approaches 123 °C, requiring flameproof handling on the production floor.
Shipping teams highlight the value of sturdy, lined containers and clarity in labeling, given its role as a controlled intermediate in some jurisdictions. Reactivity and handling guidelines surface in each batch record, but feedback cycles from customers often shape packaging improvements. For those who require specific isomer ratios or lot-based COAs (Certificates of Analysis), direct communication with our technical representatives streamlines the path from order to bench or reactor.
4-Phenylmorpholine enters the market with a recognized profile. Operators and environmental officers keep air exposure controlled, using local exhaust ventilation. Its vapor pressure supports open handling in ventilated spaces, but process teams gear up with personal protective equipment during bulk transfer, to protect against skin and respiratory contact. Over time, seasoned handlers learn to distinguish between acute exposure symptoms associated with phenyl amines versus more volatile nitrile analogs.
Waste management, especially when residues enter water streams, raises regulatory scrutiny. We install activated carbon scrubbing and batch-based emission capture on site, to address environmental compliance and uphold community trust. The presence of the phenyl group means it degrades more slowly than unsubstituted morpholine; wastewater treatment teams monitor effluent.
For those developing downstream products such as pharmaceuticals, the established safety profile for this intermediate enables more straightforward regulatory documentation compared to less familiar new chemical entities. Toxicological studies suggest modest acute oral and dermal toxicity, with data sets supporting decision-making in workplace hygiene and risk assessment protocols.
Every batch of 4-Phenylmorpholine moves through a dedicated quality control loop. Our laboratory teams run FTIR, NMR, GC-MS, and Karl Fischer titration on every lot. Purity data and impurity profiling integrate with documentation requirements for regulated industries. We store reference spectra and chromatograms for client audits, ensuring a transparent paper trail for critical materials.
Process teams also track yield losses and impurity formation in real time, informing both our continuous improvement projects and rapid troubleshooting steps, so customers benefit directly from manufacturing feedback. Trace isomer formation never escapes notice; the process group keeps rigorous records and adjusts reactor dwell times and temperature ramps as new data emerges from lab and pilot-scale improvements. It’s a cycle of feedback on structure–activity, not just a rote QC protocol.
Collaborations with pharmaceutical developers show 4-Phenylmorpholine in action at the bench. They use it for ligand design, heterocycle synthesis, and scaffold hopping. Feedback from synthetic teams reveals the clear advantages in late-stage functionalization, especially where mild Lewis acids or transition-metal catalysis take place. It never surprises us when proprietary CNS drug scaffolds trace their origins to phenylmorpholine moieties sourced from these very lines.
Process chemists working in contract manufacturing connect with our technical team to tackle bottlenecks in sequence chemistry. Having worked both on the synthesis floor and with method development labs, I’ve seen 4-Phenylmorpholine streamline routes where more traditional amines would otherwise require harsher conditions or extra purification cycles. This means finished actives reach customers faster and with less environmental burden from side product disposal.
Performance in coatings applications emerges less frequently, but materials scientists continue exploring this compound as a potential amine hardener or phase transfer catalyst. Direct experience with polymer trials shows the phenyl-morpholine linkage confers both hydrophobicity and some thermal stability, opening doors to hybrid thermoset compositions not readily available from aliphatic morpholines.
Every producer faces the stubborn disagreement between keeping purity high and costs reasonable. For 4-Phenylmorpholine, minimizing side reactions requires precise control of reagent ratios and a solid understanding of the template effect of the phenyl ring. Operators and engineers collaborate each shift to achieve target yields, not through guesswork, but by combining raw data from process analytics and tried-and-true experience from the plant floor.
Handling demands care with solvent selection. During production, we favor aromatic-free solvents to prevent competitive side reactions; our teams learned through practical setbacks that using cheap toluene can complicate workups, especially on larger scales. Contamination by related morpholine isomers sometimes occurs, particularly if cyclization doesn’t run to completion—over several product cycle iterations, the team devised incremental improvements, including modified pressure vessels and staged additions of ethylene oxide.
As regulations evolve and downstream requirements shift, we invest in scalable containment and process upgrades. Feedback loops from customers, cheminformatics screening, and continuous dialogue help us maintain the reliability that downstream innovators expect.
Production of 4-Phenylmorpholine at scale demands more than a simple knowledge of bench-top chemistry. Since we control the entire process, from raw materials to packaging, we hold responsibility for every impurity, omission, and adjustment. Our operators invest attention in everything from order shipping to reactor cleaning, knowing how small differences ripple through to finished products. Sourcing only high-grade aniline, maintaining real-time monitoring of ethylene oxide additions, and keeping analytical documents ready for audit define the daily routine.
We share results—both successes and batch deviations—directly with partners. The relationship extends beyond mere supply; regular exchanges and site visits with customers foster stronger networks of practice, allowing us to anticipate needs rather than react to them. Our technical support teams speak with formulation chemists, not just sales agents, keeping dialogue grounded in lab experience rather than abstract promises.
Markets and regulatory landscapes keep changing, but the reliable supply of foundational intermediates remains essential. For 4-Phenylmorpholine, tighter restrictions on chemical transport and increasingly detailed client requirements drive us to expand both analytical capabilities and logistics planning. Recent investments in closed-transfer systems and bulk packaging suit larger batch users looking to cut down on waste, while smaller scale labs appreciate the flexibility in container sizing and turnaround times.
Our operational philosophy comes from being both a producer and a scientific collaborator. On any given day, our control room teams talk with development chemists about optimizing yield, while engineers on the line suggest new reactor maintenance schedules to improve long-term uptime. The feedback isn’t just welcomed; it’s required to deliver not only a product but a partnership. It’s a shared effort—driven by our team’s practical knowledge and informed by steady feedback from the industries we serve.
After years of hands-on production, detailed quality assessment, and direct conversations with partners, our approach to 4-Phenylmorpholine is shaped by more than molecular diagrams or specification sheets. The difference shows up in the reliability of supply, the openness of technical conversations, and the flexibility in adapting to each customer’s challenge. No manufactured molecule stands alone; every variant reflects lessons learned from reactors, shifts, client demands, and the steady accumulation of insight. By providing more than a raw ingredient—by offering knowledge, transparency, and genuine support—we see projects completed faster, with better control, and a foundation built on trust and mutual expertise.