|
HS Code |
569002 |
| Chemicalname | p-Aminophenol |
| Iupacname | 4-aminophenol |
| Molecularformula | C6H7NO |
| Molarmass | 109.13 g/mol |
| Casnumber | 123-30-8 |
| Appearance | White to light purple crystalline solid |
| Meltingpoint | 184-187°C |
| Boilingpoint | N/A (decomposes) |
| Solubilityinwater | Moderately soluble |
| Density | 1.293 g/cm³ |
| Odor | Slightly phenolic |
| Ph | Slightly acidic (aqueous solution) |
| Storagetemperature | Store below 30°C |
| Refractiveindex | 1.636 (20°C) |
| Synonyms | 4-Aminophenol, p-Hydroxyaniline |
As an accredited P-Aminophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | P-Aminophenol is packaged in a 500g amber glass bottle with a secure screw cap, labeled with hazard warnings and product details. |
| Shipping | P-Aminophenol should be shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and requires proper labeling and documentation. Transportation must comply with local, national, and international regulations, ensuring the package is handled with care to prevent spills, contamination, or exposure. |
| Storage | P-Aminophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizing agents. It must be protected from light and moisture, as it is sensitive to both. Use secondary containment to prevent spills and keep away from heat sources or ignition. Proper labeling and access control are essential. |
Competitive P-Aminophenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
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Tel: +8615380400285
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Producing P-Aminophenol has always demanded careful control of every reaction variable. We have focused on meeting the requirements of downstream users, whether they are in dyes, pharmaceuticals, or rubber antioxidants. This product, which we make in a variety of grades, plays a critical role in shaping the quality and reliability of end products across different sectors.
Making P-Aminophenol calls for a combination of high-purity raw materials and equipment that can keep up with the exothermic profile of the reduction stage. Our reactors and filtration setups have evolved over the years, with changes prompted by firsthand process feedback. Our operators, drawing on years of practice, follow the reaction kinetics closely, as minor deviations create higher levels of undesired byproducts like ortho-isomers or excess aniline. Chemical processing is not just a task to us; it’s a craft built on careful monitoring and chemistry knowledge.
We manufacture different grades by adjusting process parameters and purification steps, using either catalytic hydrogenation or reduction with iron and acid. We see clear performance distinctions between these methods. The catalytic route tends to deliver a paler, finer crystalline material with lower levels of heavy metals, while the iron reduction method can leave more trace impurities. When a client asks for a product fit for pharmaceutical synthesis of paracetamol, we steer toward the hydrogenation route — it avoids metal residues that interfere with stringent regulatory audits.
Analytical testing is an everyday part of our routine. HPLC, melting point analysis, and heavy metal content tests all tell us what the batch contains, not just what we intended. A recent switch to a more sensitive HPLC method uncovered trace impurities that would otherwise slip past classical chromatography. Managing this level of detail allows us to offer products that line up with current good manufacturing practices, especially when clients seek P-Aminophenol for APIs.
Various industries have developed their own benchmarks, and our onsite lab adapts methods to suit. For the photographic industry, which demands virtually colorless P-Aminophenol, we control iron and copper levels at low ppm, since even trace levels distort color development. In the dye sector, deeper color is less sensitive, but insoluble matter is monitored strictly, as users report filter clogging and uneven blending with inferior lots. The test data from our own bedsides gives us a real sense of how far to go based on each customer’s use case.
Crystallinity, moisture content, and particle size hit the common questions we receive. A few years ago, batches produced in summer months showed clumping — we learned to dry under nitrogen and optimize the final filtration temperature to prevent caking. A product is only as good as its stability and consistency, and this lesson stays with our team.
P-Aminophenol finds its most recognized use in the production of paracetamol. Our pharmaceutical customers come to us for a grade where we certify low heavy metals and controlled acidity. The implications of even small levels of 4-chloroaniline or unreacted aniline reach well into downstream safety reviews. Knowing which impurity matters most, and why, comes from working side-by-side with chemists troubleshooting their own reactors.
In the dye industry, users demand product in bulk packaging, often in 25 or 50 kilogram drums, for large-batch coloring. Consistency matters more than theoretical purity, since off-color or off-odor batches lead to rejected drums or reprocessing. In photographic development, the stakes rise. The finished material has to maintain sharp color developing properties, so we measure reducing substances and iron content to ensure no “fogging” or color drift.
Rubber antioxidants form another market, and users often request coarser or more granular forms. Here, dust suppression matters — our post-filtration process reduces airborne fines. This is less of a concern in pharma, but in rubber, a high-dust product makes the compounding environment harsher for workers and leads to handling complaints.
Practically, chemicals like ortho-aminophenol and meta-aminophenol share a family resemblance but show distinct coloration, solubility, and reactivity in actual applications. We keep P-Aminophenol (para isomer) production lines dedicated and avoid cross-contamination from ortho/ meta lines, particularly since ortho-aminophenol creates unwanted dye hues and introduces toxicity concerns in pharma.
Buyers sometimes expect “aminophenol” to be interchangeable, but isomer performance differs sharply. Para-aminophenol delivers clear, strong nucleophilicity at the para position, favoring selective acetylation for API synthesis. Meta and ortho alternatives create side products that tie up expensive solvents or fail to react as intended. We train sales and technical staff to communicate these risks, relying on customer feedback as our main teacher.
Production runs sometimes expose us to issues that standard literature glosses over. Transport in humid seasons used to lead to cakes of intergrown P-Aminophenol crystals. Complaints arrived about “welded” lumps that would not dissolve properly. In house, we tried dryers and inert atmospheres, but the transport chain proved tougher than factory conditions. Packing under dry nitrogen, adding extra desiccant, and modifying drum liners improved stability.
Other times, regulatory scrutiny tightens due to the critical role P-Aminophenol plays in medicine and dye safety. Industry audits dive into nitrosamine formation risk, calling for better tracking of precursor inventories and reaction byproducts. Thanks to daily test records, we support client filings and provide chain-of-custody evidence that every lot is traceable.
Heavy metal control, especially with the older iron reduction process, caused headaches. Wells delivering process water came with swings in iron content. Sampling by well and using newer filtration media solved recurring spikes. Customers gave us feedback on discoloration and metallic taste in end-products which led us to review whole water management policies. Practical challenges motivate us — customer claims and regulatory visibility both matter, so adjustments happen in real time.
We invest in pilot equipment and trial annual upgrades before scaling. A few years ago, a customer required a particle size range that cut dust and improved dispersal in their process. We ran a multi-month granulation optimization, switching between spray-drying and wet granulation — at the bench, results from spray drying seemed perfect, but scaled results delivered a finer dust than expected and clogged their feed hoppers. Only by inviting the customer’s technical staff to side-by-side trials in our plant did we settle on the current granule form. Adjusting filtration speeds, drying temperature, and anti-caking protocols created a better batch, one we now standardize for all similar customers.
Taking feedback directly from end-users improved product review cycles. Teams in our plant meet quarterly to review claims data, even for markets as far-flung as West Africa or South America. Users tell us what worked, what fell short, and what they wish our product did. “No surprises in the drum” is a phrase we hear — it means a lot to those blending 10 drums into a reactor and not discovering lumps or off-colors at the last minute.
Handling toxic nitrobenzene and managing hydrogenation conditions involves real laboratory hazards. Over the years, safety training has sharpened, and our plant layout moved to containment areas where spill risk lands far from drains. Waste streams from reduction still carry reactive residues, so we treat and monitor effluents specifically for nitrophenol and aniline breakdown. Neighbors and inspectors ask questions, and rightfully so. Our compliance record helps us maintain community trust and access to export markets.
Reducing environmental impact means investing in continuous improvement. Using catalytic hydrogenation creates fewer inorganic byproducts than iron reductions, making treatment less costly and reducing sludge. Efforts to cut fugitive emissions, both in plant and in trucking, address local air and water standards. Employees also take part in safety and environment committees, tracking tasks such as routine drum inspections and site walkabouts. Solving one batch issue after another means less material ends up in the wrong place.
Direct communication with users, be they large pharma firms, dye houses, or photographic compounders, saves everyone time. Our staff fields questions about solubility curves, blending properties, and regulatory compliance, drawing on past trouble tickets and first-hand testing. More often, customers bring in their technical contacts to our factory to see batches in real time. These visits created trust and led to collaborative improvements — sometimes as simple as adjusting drum colors so warehouses could spot P-Aminophenol at a glance.
Transparency around process changes helps users plan. Upstream raw material issues, such as nitrobenzene supply, affect pricing and delivery. Providing advance notice on lead time swings lets buyers plan their inventory more reliably. This is more than a courtesy; it’s the result of learning, sometimes the hard way, that slow or incomplete information costs both sides in the end.
We see real impact when users source from manufacturers who know their process inside out. Questions about shelf life, blending, and trace impurities find quick answers when the technical team behind the product knows why and how a change matters. Third-party traders cannot respond as well to shipments that show up with excess fines or an off-odor, and end-users get stuck waiting for answers. As manufacturers, we answer for each batch we produce, with test reports and process details ready.
Pressure for lower residual solvents and fewer impurities grows each year, and buyers value working with suppliers who keep up with evolving standards. A process improvement last year cut acetone carryover by one third, and customers — often under their own regulatory deadlines — sent positive notes as a result. Each improvement in the plant ends up reflected in customer satisfaction, even if it starts in a QC lab or reactor setup deep in the factory floor.
The field of P-Aminophenol production never stands still. Everything from process equipment to regulatory filings changes with new standards and best practices. Our team reviews scientific journals, supplier bulletins, and client feedback to stay current. In-house pilot runs and open communication with both suppliers and clients give us early notice of what’s coming, whether in dye formulation trends or new pharmaceutical regulations.
Providing P-Aminophenol that meets functional and regulatory needs takes ongoing commitment and the flexibility to adjust. We build relationships with customers based on trust and a common goal — a product that performs as expected, with documentation and technical backing that holds up to scrutiny. Every lot shipped represents a shared investment in compliance, function, and long-term reliability.
Direct manufacturing gives us the experience to deliver P-Aminophenol that meets specific user demands. We adapt by learning from the real-world problems our users bring, and by investing in process improvements that create value for every application: medicine, dyes, photography, and rubber industries included. No two years are quite the same, and each batch tells its own story. Continual improvement — be it in quality control, drum design, or analytical technique — helps us provide a better product today than we did last year.
We draw from daily plant operations, customer conversations, and field feedback rather than relying on abstract promises. In the world of industrial chemicals, direct experience counts. Our goal stays consistent: a reliable, pure, and application-ready P-Aminophenol each time, made possible by people on both sides of the supply chain dedicated to quality.