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HS Code |
956570 |
| Cas Number | 1741-12-0 |
| Iupac Name | 1-(4-aminophenyl)propan-1-one |
| Molecular Formula | C9H11NO |
| Molecular Weight | 149.19 g/mol |
| Appearance | Pale yellow to white crystalline powder |
| Melting Point | 63-65 °C |
| Boiling Point | 332.6 °C at 760 mmHg |
| Solubility In Water | Moderate |
| Density | 1.109 g/cm³ |
| Pubchem Cid | 14412 |
As an accredited 4'-Aminopropiophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4'-Aminopropiophenone is supplied in a 100-gram amber glass bottle, clearly labeled with hazard symbols and relevant safety information. |
| Shipping | 4'-Aminopropiophenone is shipped in tightly sealed containers to prevent contamination and moisture exposure. The package is clearly labeled with hazard and handling information in accordance with regulatory guidelines. It is transported under strict temperature and safety controls, ensuring compliance during storage and transit to authorized recipients only. |
| Storage | Store 4'-Aminopropiophenone in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Ensure proper labeling and restrict access to authorized personnel. Follow all relevant chemical hygiene and safety guidelines for storage. |
Applications of 4'-Aminopropiophenone in Industrial ManufacturingAs a direct manufacturer of 4'-Aminopropiophenone, we support a range of specialized industrial sectors. Below we outline detailed applications, focusing on real-world usage and integration within downstream chemical processes, including essential compliance criteria, formulation guidelines, process stages, and final product categories. 1. Pharmaceutical Intermediate – Synthesis of Local Anesthetics4'-Aminopropiophenone serves as an essential intermediate in the synthesis of active pharmaceutical ingredients (APIs) for local anesthetics, particularly within the production of drugs such as lidocaine and related analogues. The compound participates in reductive amination and acylation steps that form key structures of target APIs. Manufacturers require strict process verification, multi-step purification, and batch traceability. This application demands high-purity raw material compliant with pharmaceutical regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate – Synthesis of Pyridine-Based Crop Protection AgentsDownstream agrochemical plants use 4'-Aminopropiophenone to introduce amino-functional moieties essential for constructing pyridine-derived pest control agents. The compound is processed via amination or cyclization, enabling efficient creation of structures used for fungicides and herbicide actives. Integration requires validated handling procedures to reduce cross-contamination, along with compliance to agrochemical intermediate traceability systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Chemical Synthesis – Photoinitiator Component ManufacturingChemical companies utilize this compound to synthesize advanced photoinitiator molecules used in free-radical polymerization for UV-cured paints, inks, and adhesives. 4'-Aminopropiophenone undergoes controlled substitution and condensation reactions to produce tailor-made photoinitiator precursors. Downstream manufacturers demand precise specification controls, particularly regarding residual amine and impurity profile, with batch certification required for regulatory audits. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Flavors and Fragrance IntermediateThe aroma chemicals sector uses 4'-Aminopropiophenone to build intermediate structures for musk aroma agents and other functional fragrance bases. The compound’s reactivity supports efficient coupling and cyclization reactions, enabling production of intermediates with tightly-controlled olfactory properties. Compliance includes batch-wise documentation, impurity profiling by GC-MS, and declaration under the International Fragrance Association (IFRA) standards for ingredient traceability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Dye Intermediate for Technical and Industrial ColorantsTechnical dye manufacturers employ this compound in synthesizing amino-aromatic structures for specialty azo and anthraquinone dyes, widely used in plastics, textiles, and coatings. The chemical participates in diazotization and coupling operations, contributing to color stable and heat-resistant dye molecules. Downstream users require chain-of-custody documentation and batch-level color strength validation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Producing 4'-Aminopropiophenone, also recognized by its chemical identity as 1-(4-aminophenyl)-1-propanone, has brought us up close to the nuts and bolts of what true reliability means in specialty intermediate manufacturing. In our daily operations, we’ve seen how choices in precursor chemistry ripple through the performance and ease of use for downstream customers. Unlike third-party sellers who report information secondhand, we carry out the synthesis step by step, watching how raw material quality, reaction control parameters, and purification levels bear directly on output consistency.
Looking back on hundreds of batches, our own observations show that the nature of the 4'-amino group in this molecule delivers more than just another functional aromatic amine to the marketplace. Unlike some standard aniline derivatives, this compound grants greater versatility for downstream chemical synthesis. By maintaining a steady focus on impurity limits, particle size distribution, and water content, we’re able to support projects where a highly selective amination or reduction process is required. The feedback loop we maintain with end-users has taught us this product’s strengths and limitations more thoroughly than anything learned from literature alone.
Standard catalog descriptions rarely tell the full story. In producing 4'-Aminopropiophenone, we’ve learned many factors influence both suitability and outcome for a given project. Chemists often look for a white to off-white crystalline powder when they order, but what they’re really buying is control over their synthesis. Purity above 99% is typical, but there’s more to performance than a number on a certificate.
Material prepared through our optimized reduction system avoids troublesome side-products found in less carefully made aminoketones. It makes a difference down the line, especially for those heading into API or fine chemical development. The trace metals, residual solvents, and minor aromatic byproducts—these cause headaches that laboratory screening can uncover only after wasting time and money. Real-world experience tells us that minimizing these origins of downstream contamination often makes or breaks a synthesis route.
Physical handling shouldn't complicate production schedules. In our labs, ensuring free-flowing, non-hygroscopic product has reduced customer downtime during scale-up or pilot production. Years of feedback have shown that, if the material tends to cake, bridging in feeders or inconsistent dosing follows. To us, those are not just theoretical issues; we've listened to operators struggle through them before adjusting our drying and packaging processes. Now, with bulk polyethylene liners and moisture-barrier packaging, we’ve taken concrete steps to eliminate this risk point.
Synthetic chemists reach for this intermediate in several pharmaceutical, agrochemical, and pigment applications, but far too many overlook how cutting corners in the sourcing stage affects final yield and purity. Through countless conversations and technical support requests from customers, we know well the kinds of obstacles teams have faced after using inconsistent batches.
The ketone functionality offers tremendous value for condensation and reductive amination reactions. Projects that demand diamine or substituted phenylpropyl backbones have benefited from the selectivity of this starting material. In one instance, a customer looking to prepare active pharmaceutical ingredients shared that subpar control of the amino group’s placement in isomeric mixtures wrecked their downstream chromatography, costing them considerable labor hours and columns. Our experience with tailored hydrogenation pressures and purification steps has produced single-digit ppm impurity levels, meeting the specifications major pharmas need for strict DMF or regulatory filings.
Performance as a crystallization building block also comes into play for pigment and dye manufacturers. In several projects, adjusting solvent systems and cooling profiles during isolation allowed us to supply material with optimal granular form. This direct feedback loop improves not only our process control but helps end-users avoid unnecessary workflow bottlenecks in their own plants.
Every market segment brings its own challenges. To meet varying scale requirements, we focus on flexible batch sizes—from kilogram samples for research to multi-ton containers for production. Frequent discussions with purchasing and R&D departments clarify trends in usage patterns. The expectation for continuous reliability is not abstract for us; it’s the standard by which returning customers gauge our worth.
From specification to application, we see requests that go well beyond a simple purity number. Customers might ask us to profile specific impurities by GC-MS, ensure controlled micron sizing for better dispersibility or even share residue-on-ignition data. Only by running these checks in-house do we really safeguard downstream product safety and regulatory compliance. These details matter, particularly for clients filing regulatory documents who require complete traceability. Over time, handling full documentation and providing tailored analytical data for each lot has shown us how critical transparency can be—not only for risk management but also for building industry trust.
Comparing 4'-Aminopropiophenone to other aminoaromatic ketones, the difference rests in the balance of reactivity and stability. Some clients have traditionally relied on para-aminoacetophenone or other ring-substituted aminoketones, only to encounter issues in subsequent functionalization. Our product’s backbone, with the phenyl group positioned for both selectivity and reduced side-reactions, provides a way to tune chemical behavior.
Process development chemists have pointed out that the propanone side chain enables an extended palette of condensation reactions compared to simple acetophenones. The three-carbon chain widens the choice of nucleophiles for Michael addition, imine formation, or nucleophilic substitution. After consistently solving problems that arise with shorter-chain analogues—such as too-rapid over-reduction or reduced crystallinity—our production team has come to appreciate subtle but important differences in how 4'-Aminopropiophenone slots into both established and novel synthesis routes.
Several projects in the fine chemicals field requested that we custom-tailor crystal size or moisture content to avoid problems downstream. This kind of hands-on interaction underscored for us that customer priorities go well beyond price. As a manufacturer, tweaking process flow to suit a congested product pipeline, or helping a customer resolve stability issues during column chromatography, makes a real difference in time-to-market and resource planning.
Downstream manufacturers, particularly in regulated industries, have ever-tightening demands on traceability, documentation, and safety. Regulatory audits, especially in pharma synthesis, look for robust supplier controls on both product purity and information traceability. From our years in chemical production, we’ve implemented full lot tracking and in-house validated analytical testing—not just for peace of mind, but because the regulatory frameworks demand such rigor.
Authorities worldwide, such as those enforcing REACH and other chemical safety standards, ask manufacturers to guarantee that no controlled impurities or cross-contaminants occur. By building continuous internal quality checks and running certificate of analysis documentation for every lot, we ensure our materials support customer needs through extended compliance processes. Many users may not realize until a late-stage pilot run just how much these preventive measures save in future regulatory headaches. Years of dealing with these realities as a direct manufacturer, not as a simple repackager or trader, have sharpened our processes and deepened our commitment to reliability.
Our facility once witnessed a problem: shipment delays and clumped material caused by inadequate packaging from a previous supplier. This setback taught us not to underestimate basic operational factors like moisture ingress prevention and robust secondary containment. We now triple-check all seal points and guarantee that packaging resists tears or environmental fluctuations. End users working in semi-automated dispensing notice the difference as fewer production stoppages translate to smoother, more predictable workflows.
Another practical lesson has been the importance of handling knowledge. We train our operators in safe unloading, inerting, and waste management. Customers have shared stories of spills or cross-contamination incidents due to unfamiliar bulk powder distribution techniques. Sharing what works—down to the detail of auger speeds or glovebox purging—has become a valued extension of our technical support.
Chemists and purchasing agents reach out every month seeking fault analysis and solutions to technical bottlenecks. Instead of letting problems fester, we host regular knowledge-sharing sessions—where our manufacturing staff talks directly with end users about both the strong points and risks of this compound. In fields where large-scale synthesis counts every kilogram of input and every hour on reaction time, it pays for us to help troubleshoot at the source.
For clients scaling up pilot lines, the availability of consistent, on-spec batches backed by complete documentation has enabled smarter decision-making about production planning. Some needed advice on solvent swaps for improved environmental metrics; others required support adapting to a different reactor type. Our ongoing partnerships have shown us that readiness to adapt and technical responsiveness keeps both our operation and customer projects running smoothly.
There’s no shortage of lower-cost alternatives from places where batch tracking and process validation take a back seat. Through years of dealing with rejected shipments and failed audit trails from such sources, we’ve become convinced the industry must look past short-term savings. Traceability is not an afterthought for us—every step, from raw material receipt to final lot labeling and shipping, anchors our reputation for reliability. It’s more than just a badge of honor; it’s the insurance that helps downstream firms avoid unforeseen quality control failures, production shutdowns, or even product recalls.
Full in-process recordkeeping, reference sample archiving, and rigorous lot release testing are not just legal requirements. These practices ensure incoming complaints disappear and client relationships strengthen. By maintaining a stable, qualified raw material supply chain, our operation has drastically reduced disruptions caused by upstream volatility. For us, transparency builds trust, and only manufacturers who follow through on this commitment earn long-term repeat business.
Each problem or question that lands in our inbox becomes the fuel for process improvement. Over the years, open customer feedback about filtration problems, color stability issues, or inconsistent flow properties has pointed us directly toward areas in need of adjustment. We invest in better filtration, test alternative drying schemes, and upgrade filling lines based on real end-user data, not just what laboratory trials suggest.
One particular case—where a pigment manufacturer reported sporadic color residues due to a side reaction byproduct—drove us to rerun development studies and overhaul that synthesis step. Collaborating closely with their technical specialists, we isolated the issue and adjusted reactivity protocols until the problem disappeared. Lessons like these stick with a manufacturing team and inform the next round of continuous improvement, making every future delivery more reliable.
Modern markets measure suppliers not just by their ability to meet a specification, but also by their adherence to ethical and sustainable production. As a producer, we’ve watched environmental and safety expectations rise quickly over the last decade. Our facilities implement solvent-recovery units, minimize emissions, and closely monitor waste stream composition in line with both local and international guidelines. Where possible, we’ve reduced hazardous process steps through greener alternatives—switching reaction conditions, modifying quenching methods, and supporting our customers’ own compliance targets.
We know a chemical’s lifecycle doesn’t end when it leaves our warehouse. Supporting safe transport, spill readiness, and material stewardship ties directly to our credibility in the wider industry. Customers increasingly ask us for sustainability documentation, lifecycle analysis, and details on carbon footprint. It’s not enough to print a certificate; practical, measurable progress on process sustainability helps us build stronger, forward-looking partnerships.
Choosing a consistent supply partner for 4'-Aminopropiophenone shapes downstream production efficiency, project success rates, and even overall business reputation. Over time, users have shared how on-time, predictable shipments have sped up timelines for medicine rollouts, new product launches, or regulatory filings. Material quality affects not just reaction yields, but ease of handling, environmental compliance, and ongoing cost of quality controls.
For those selecting this compound for new syntheses, it pays to consider not only published specification sheets but also the practical experience and accountability of the production partner. In our view, every batch tells a story—one that starts with controlled sourcing and ends with real-world performance. This belief has shaped the way we do business, how we respond to client challenges, and the discipline we bring into our manufacturing hall.
The conversation around 4'-Aminopropiophenone must move past generic purity claims and into the domain where practical performance, consistent supply, and ethical responsibility meet. Over years navigating the evolving landscape of chemical production, we’ve learned that substance beats marketing every time. The best material is one that not only meets the technical requirements for a synthesis step, but also arrives safely, performs predictably, and holds up under scrutiny—whether by auditors or chemists.
Our hands-on approach and direct experience as a genuine manufacturer have shaped our views on reliability, transparency, and real-world value. Looking ahead, we’re committed to building strong, informed relationships with every client—not by promising what can’t be delivered, but by focusing on the measurable, practical outcomes that matter most. Through open communication, technical support, and unyielding attention to quality, we continue to make 4'-Aminopropiophenone a dependable foundation for the industries it empowers.