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HS Code |
441256 |
| Chemical Name | 4-(Morpholine-4-Sulfonyl)-Phenylamine |
| Molecular Formula | C10H14N2O3S |
| Molecular Weight | 242.29 g/mol |
| Cas Number | 61648-56-4 |
| Appearance | White to off-white solid |
| Melting Point | Approximately 180-185°C |
| Solubility | Soluble in DMSO, ethanol; slightly soluble in water |
| Synonyms | 4-Aminophenyl morpholine-4-sulfonate |
As an accredited 4-(Morpholine-4-Sulfonyl)-Phenylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 4-(Morpholine-4-Sulfonyl)-Phenylamine, securely sealed in a labeled amber glass bottle, packaged within a protective carton. |
| Shipping | 4-(Morpholine-4-Sulfonyl)-Phenylamine is shipped in secure, leak-proof containers compliant with chemical safety regulations. Packaging ensures protection from moisture, heat, and light. The shipment includes proper hazard labeling and documentation, with transportation by certified carriers. Handling instructions and safety data sheets accompany all deliveries to ensure safe and compliant transit. |
| Storage | 4-(Morpholine-4-sulfonyl)-phenylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and restrict access to authorized personnel. Wear suitable protective equipment when handling to prevent skin and eye contact. |
Applications of 4-(Morpholine-4-Sulfonyl)-Phenylamine in Industrial ManufacturingAs a dedicated producer of 4-(Morpholine-4-Sulfonyl)-Phenylamine, we supply this specialty intermediate to established downstream industries where it delivers precise technical and regulatory benefits. Our deep process knowledge supports the integration of this raw material across multiple value chains, meeting stringent commercialization and quality benchmarks. 1. Synthesis of Sulfonamide Pharmaceutical IntermediatesPharmaceutical manufacturers rely on 4-(Morpholine-4-Sulfonyl)-Phenylamine as a sulfonamide-building block in the production of active pharmaceutical ingredient intermediates. It enters sulfonation and coupling stages in multi-step syntheses for anti-infective and anti-inflammatory compounds, offering high selectivity in nitrogen–sulfonyl modification. Technical teams adjust input ratios based on target molecule design, molecular weight, and downstream hydrogenation requirements. Quality control protocols focus on trace-level impurity suppression and reproducible batch-to-batch reactivity for final medicinal purity profiles. Industry compliance standards
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2. Production of Advanced Polymer StabilizersPolymer compounders and additive manufacturers use this compound as a functional group donor in specialty stabilizer blends for engineered plastics, including polyamides, ABS, and polycarbonates. The amine-sulfonyl group offers oxidative stability and UV protection in melt compounding lines. Formulators determine dosing by resin grade and expected service life, closely monitoring interaction with base resin and pigment systems. Material enters polymer extrusion or reactive blending, followed by QC testing for migration and compatibility before shipment as masterbatch or direct additive. Industry compliance standards
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3. Specialty Dye and Pigment Intermediate ManufacturingColorant producers use our material as a precursor for sulfonamide-based azo and anthraquinone dye intermediates. It provides a key nitrogen source in diazotization and coupling reactions, supporting high chroma and enhanced solubility for premium textile, leather, and ink dyes. The input ratio varies with chromophore complexity and desired fastness performance. Downstream processors implement precise pH and temperature controls to maximize yield and reproducibility during colorant synthesis and crystallization. Industry compliance standards
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4. Advanced Agrochemical Intermediate ApplicationsLeading agrochemical formulators source this chemical for targeted use as an intermediate in the synthesis of selective sulfonylurea and sulfonamide herbicides. Its structure facilitates efficient coupling onto pyrimidine and triazine rings during active ingredient assembly, allowing precise modulation of biological activity and soil mobility. Ratio determination depends on target molecule substitution patterns, regulatory residue limits, and downstream purification strategies. Producers maintain compliance with national and global agronomic standards by controlling batch impurities and validating input traceability. Industry compliance standards
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At our production facility, we work with hundreds of aromatic amines and sulfonyl derivatives every year. Among them, 4-(Morpholine-4-Sulfonyl)-Phenylamine always draws recurring attention from our collaborating partners in pharmaceutical, agrochemical, and specialty chemical sectors. Its distinct molecular structure, blending the stability of a morpholine ring with a sulfonyl phenylamine anchor, enables applications that routine anilines or standard sulfonyl groups simply cannot support. From the earliest days of bench-scale synthesis, we learned that this compound opens up pathways to new analogues that preserve reactivity profiles while minimizing volatility and minimizing hazardous decomposition found in similar nitro-based amines.
The chemical community often discusses innovation in aromatic sulfonamides and aminoaromatics, but progress happens quietly on the factory floor. Our own hands-on involvement with 4-(Morpholine-4-Sulfonyl)-Phenylamine made this clear. A few years back, demand for selective and stable sulfonamide linkers soared with new projects in kinase inhibitor development and peptide coupling. Teams required a consistent supply of sulfonyl-protected phenylamines that could be easily introduced under mild conditions without excessive degradation. Many early candidates failed due to poor solubility in key organic solvents or excessive reactivity that complicated purification. Here, our formulation held its promise. The morpholine ring, known for its moderate polarity and basicity, grants more process flexibility and consistently reproducible yields.
4-(Morpholine-4-Sulfonyl)-Phenylamine that leaves our facility meets a precise specification driven by repeated QC reality checks. Each lot streams through UV-Vis, HPLC, and NMR walkthroughs. Only material with high purity—98% and above—proceeds into the final packing rooms. We keep moisture content and trace ion contamination consistently low, a priority when manufacturing advanced intermediates used in sensitive reactions. Product typically appears as an off-white to light beige solid, reflecting the purity but also a practical recognition that absolute chromatic perfection does not always correlate with chemical cleanliness, especially for aromatic sulfonyl compounds.
Our plant uses glass-lined and stainless steel reactors for the synthesis, shifting batch volumes based on real-time project demand. Temperature and pressure controls, often manually adjusted by seasoned technicians, help avoid runaway exotherms. The morpholine-sulfonyl substitution proves less prone to hazardous byproducts than many chloro- or nitro-substituted cousins, which keeps facility downtime low and supply lines more reliable. We see fewer batch reworks, which passes savings and peace of mind along to formulators and researchers further down the supply chain.
Professionals familiar with standard anilines, simple sulfonamides, or even p-toluenesulfonamide derivatives often ask about the differences. The answer is clear once the material is used at process scale. Standard p-toluenesulfonamides lack the morpholine moiety, missing out on the extra hydrophilicity and secondary amine sensitivity. They show rapid deactivation in many transition metal-catalyzed couplings and poorly dissolve in many polar solvents. Our 4-(Morpholine-4-Sulfonyl)-Phenylamine demonstrates cleaner coupling with aromatic halides and far better tolerance to oxidation, with high shelf stability that translates to confident stockpiling and predictable performance.
Generic sulfonyl anilines leave active sites too exposed and react prematurely in multi-step syntheses. Formulating with the morpholine ring brings bulk and slight electron-withdrawing character, tempering unwanted side reactions in peptide, heterocycle, and urea formation. Customers who substituted this material for lower-cost anilines repeatedly report that overall yields increase, with fewer chromatographic bottlenecks. We see less tar formation in reaction vessels and faster workup protocols, particularly when large volumes are in play.
The daily work of our team brings us into contact with a surprising array of chemists and process engineers. Whether the end use is a pharmaceutical intermediate or a building block for next-generation material science, 4-(Morpholine-4-Sulfonyl)-Phenylamine joins syntheses as a robust link between aromatic cores and polar, reactive sidechains. Both the pharmaceutical sectors and custom fine chemical manufacturers have moved steadily toward more selective, less hazardous transformations. This compound, with its reliable reaction profile and high tolerance to common scale-up solvents like DMF, DMSO, and acetonitrile, remains a dependable choice for bottleneck applications.
Some innovative applications include its engagement as a protecting group withstanding both acid and base hydrolysis. We regularly field requests from peptide chemists seeking protection strategies that outlast aggressive hydrogenation or extended acidolysis. Conventional benzenesulfonyl and tosyl groups often fail in such conditions, but the 4-(Morpholine-4-Sulfonyl) motif persists, later deprotected with minimal loss of the target structure. Medicinal chemists cite the material’s capacity for selective activation: the electron distribution around the morpholine ring tunes downstream N-alkylation and acylation, lending tighter control over fragment-based lead optimization.
Agrochemical researchers apply the same features to the design of bioactive analogues, aiming for increased hydrophilicity and environmental stability. Classic arylamines oxidize or hydrolyze too easily under field conditions, but the morpholine-sulfonyl group delays decomposition, stretching product shelf life and application windows. Handling requirements remain straightforward: standard PPE, containment for fine powders, gentle ventilation, and most importantly, no special inert-atmosphere protocols for everyday weighing and transfer.
Manufacturers rarely share the hidden grind behind producing specialty aromatic amines, but here the details matter. Our 4-(Morpholine-4-Sulfonyl)-Phenylamine runs involve constant troubleshooting, from batch crystallization to solvent exchange in purifications. Temperature gradients, glassware fouling, and raw material trace impurities challenge even experienced teams. Through in-house modifications—fine-tuning crystallization rates, screening anti-solvents, calibrating column media—we cut cycle time and push recovery rates. Repeat customers pick up on these differences: greater batch-to-batch consistency shaves weeks off analytical qualification and regulatory approval steps.
At commercial scale, performance demands become stark. Downstream partners expect not only high purity but also physical properties compatible with feeds to reactors and formulation vessels. Particle size distribution affects feeding rates, and poor powder flow complicates large-scale blending. Early years saw us rework several tons of product each quarter because of caking or excessive fines. Experience taught us to target a balance: just enough milling and fine screening so the compound moves smoothly through standard powder hoppers, but not so aggressively as to introduce excessive dust handling challenges.
Our clients in the pharmaceutical sector tend to focus on trace contaminant control, for both safety assessment and regulatory clearance. Here the sulfonyl-morpholine hybrid structure helps: it produces fewer easily-oxidized species during storage, reducing the formation of colored impurities and unwanted low-level sulfonic acids over time. This translates to simplified purification for their downstream intermediates, cutting out several rework or reprocessing cycles that add to overall cost.
Although not regulated as a high-hazard chemical, proper handling remains essential. Our operators receive ongoing training on safe powder transfer, preventing fine dust inhalation and avoiding static build-up in storage bins. In the rare event of a material spill, standard neutralizing and clean-up protocols suffice. Disposal routes through incineration meet both local and international compliance marks for aromatic sulfonamides.
Environmental impact remains an ongoing topic in every production review. Alternative anilines and common sulfonyl intermediates discharge more halogenated waste and chlorinated byproducts during their manufacture. Our morpholine-4-sulfonyl route sidesteps this, functioning without chlorinated solvents in the main transformation. Fewer washings and simpler filtrates ease downstream effluent treatment. Customers engaged in green chemistry initiatives or stricter compliance prefer this cleaner route, and audits frequently acknowledge the tangible reduction in chemical oxygen demand (COD) across the process stream, compared to old-school sulfonylation methods.
The global supply of synthetic intermediates swings each year. A few seasons back, constraints on basic morpholine and aromatic starting materials prompted volatility. Our longstanding partnerships with primary producers, together with investments in secured raw material storage, helped guard against these shocks. Even as upstream markets tightened, we maintained supply timelines, giving our partners plenty of warning and an honest assessment instead of making risky delivery promises. This trust, built over decades, allows our chemical to stay in research and production pipelines, minimizing costly line stops and failed product launches.
Quality process design also plays a part in logistical reliability. We bulk-pack under controlled, low-humidity conditions in anti-static lined containers. Each batch undergoes documented, traceable lot release not because of regulatory pressure but due to direct observations on the factory floor: just a few careless baggings under damp weather will ruin a shipment’s flowability, sapping value for everyone in the chain.
Industrial chemistry chases efficiency, and our compound represents a small but important shift toward more manageable sulfonamide chemistry. Continued customer feedback helps drive incremental changes—optimizing drying cycles for improved solubility profiles, reformulating batch solvents to reduce cross-contamination risk, trialing new analytics for early impurity detection. The move to continuous flow processes in some specialty applications required us to adapt the particle size and solubility characteristics, ensuring the compound remains compatible with high-throughput reactor inlets and microfluidic transfer systems.
The pharmaceutical and fine chemical industries push harder for process intensification, lower waste, and greater reaction yields with each project. Our work connecting directly with process chemists, scale-up engineers, and bench scientists helps us spot emerging needs before they disrupt schedules or budgets. As potent kinase and protease inhibitors continue to shape drug discovery, the specific reactivity and protection characteristics of 4-(Morpholine-4-Sulfonyl)-Phenylamine keep it in the arsenal. Field studies and symposia still spark requests for custom analogues and new functional group variations; our R&D team regularly modifies the morpholine ring and phenyl backbone to tailor electronic properties or increase selectivity under demanding coupling conditions.
First-time users encounter a learning curve similar to any specialty intermediate. Moisture pick-up, occasional caking, and handling ultrafine fractions challenge even seasoned technicians. Newer process teams, eager to economize, sometimes rush scale-up without pilot trials. Here, our technical support stresses blending protocols, storage in sealed, low-humidity environments, and staged solvent introductions during dissolution. These end up more effective than any off-the-shelf troubleshooting kit.
Raw material purity upstream continues to pose risk across the industry. Morpholine derivatives suffer from trace amine and aldehyde contaminants if sourced from volatile markets. We pre-screen every batch on arrival using validated chromatographic methods, rejecting out-of-spec feedstock before it can cascade failures down the line. Even skilled chemists rarely guess at the exact source of a production hiccup until troubleshooting with the raw numbers in hand. Committing to real-time, ongoing raw material assessment costs more at first but shields everyone down the value chain from expensive and unpredictable disruptions.
Our experience tells us that quality goes hand-in-hand with transparency and process mindfulness, not just technical specification sheets. Customers return and new partnerships begin because real-world results—reaction success, cleaner separations, and dependable project timelines—speak far louder than any marketing copy or abstract data set. Whether a process chemist or formulator, the difference comes through on the bench every time.
As regulatory discussions grow sharper about trace impurities in pharmaceuticals and crop protectants, the subtleties of process chemistry create new hurdles. 4-(Morpholine-4-Sulfonyl)-Phenylamine, developed and handled under tight, documented controls, offers consistent physical and chemical characteristics. Labs and factories using our material gain an advantage moving from research use to scale-up and commercial manufacturing. Teams save time and resources on unnecessary extensive requalification, freeing up schedules and budgets for actual innovation and development.
Our facility, staffed with experienced crews familiar with sulfonamide chemistry, continues to upgrade processes in line with customer feedback and regulatory evolution. The day-to-day realities on the factory floor shape what we deliver: only batches that truly meet the standard leave our doors, because we understand that our reputation—and the end product's success—rest on the smallest of details in every shipment. We keep an open line with every customer, knowing challenges can arise, and quick, honest communication outpaces any half-promise or speculation.
Industry dialogue focuses on speed, cost, and compliance, but behind each campaign lies the intricate work of transforming raw chemistry into a material that adapts to new project requirements, withstands process variations, and responds to the changing face of global demand. Our hands-on approach to 4-(Morpholine-4-Sulfonyl)-Phenylamine production, from lot validation to final package, results from decades of cumulative problem-solving. The journey from synthetic planning to industrial delivery draws on hard-won lessons—batch after batch, adjustment after adjustment—always guided by the needs and suggestions of those who actually use the material, never just a set of commercial values or short-term targets.
Every new project brings differences in scale, application, and downstream formulation methods, so we maintain flexibility without sacrificing reliability or openness. Our work with 4-(Morpholine-4-Sulfonyl)-Phenylamine demonstrates what can happen when authentic manufacturing perspective meets consistent customer dialogue and unyielding quality control: a specialty product that not only solves emerging technical challenges but also stays rooted in the realities of modern industrial chemistry.