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HS Code |
713817 |
| Chemical Name | p-Nitroaniline |
| Molecular Formula | C6H6N2O2 |
| Molecular Weight | 138.13 g/mol |
| Cas Number | 100-01-6 |
| Appearance | Yellow crystalline solid |
| Purity | 99% |
| Melting Point | 146-149 °C |
| Boiling Point | 332 °C |
| Solubility In Water | 1.7 g/L at 20 °C |
| Density | 1.44 g/cm³ |
| Flash Point | 235 °C |
| Refractive Index | 1.668 |
| Smiles | O2N-C6H4-NH2 |
| Iupac Name | 4-nitroaniline |
| Storage Conditions | Store in a cool, dry place |
As an accredited p-Nitroaniline (99%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 g p-Nitroaniline (99%) is supplied in a sealed amber glass bottle with a screw cap, labeled with hazard and safety information. |
| Shipping | **Shipping for p-Nitroaniline (99%):** p-Nitroaniline (99%) is shipped in tightly sealed, chemical-resistant containers to prevent moisture or contamination. It should be handled as a hazardous material, bearing appropriate hazard labels and documentation. Transport is conducted in compliance with regulations (DOT, IATA, IMDG), with care to minimize exposure to heat, shock, and incompatible substances. |
| Storage | **p-Nitroaniline (99%)** should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and strong acids. Shield the chemical from light and moisture. Properly label the container, and keep it away from food and drink. Use designated chemical storage cabinets if available. |
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Dye Intermediate: p-Nitroaniline (99%) is used in azo dye synthesis, where high purity ensures vibrant and consistent color development. Reagent: p-Nitroaniline (99%) is used in analytical chemistry, where its defined melting point (146°C) guarantees precise calibration. Pharmaceutical Intermediate: p-Nitroaniline (99%) is used in drug synthesis, where low impurity content minimizes unwanted side reactions. Polymer Additive: p-Nitroaniline (99%) is used in polymerization processes, where stable molecular structure improves thermal resistance of end products. Organic Synthesis: p-Nitroaniline (99%) is used in the preparation of nitroaniline derivatives, where controlled particle size enables efficient reaction yields. Sensor Development: p-Nitroaniline (99%) is used in fabrication of chemical sensors, where consistent stability temperature (up to 200°C) provides reliable signal output. Photographic Chemicals: p-Nitroaniline (99%) is used in photographic developer formulation, where high purity enhances image resolution and contrast. Agrochemical Synthesis: p-Nitroaniline (99%) is used in the production of pesticides, where minimized trace contaminants ensure product efficacy and safety. |
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Chemistry has built its reputation on the strength of foundational compounds, and p-Nitroaniline stands as one of those quietly crucial materials. Those who’ve spent time in a laboratory—academic, industrial, or otherwise—quickly learn which chemicals keep projects moving forward. p-Nitroaniline, with a purity of 99%, does not just check a box for standard quality; it delivers confidence to chemists aiming for consistent results. Ask anyone synthesizing dyes, pharmaceuticals, or advanced polymers—with so many outcomes relying on the purity and reliability of their starting materials, subpar ingredients often guarantee wasted time and frustration.
This particular grade of p-Nitroaniline has been refined to 99% purity, supporting dependable performance in a range of settings. Chemists routinely seek out this grade when aiming for repeatable, traceable synthesis, especially with sensitive downstream reactions. Its typical yellow crystalline appearance immediately tells anyone who’s handled lower-purity samples that they’re working with something prepared for serious applications. In my experience, batches like this—confirming melting points around 146-149°C—signal that a supplier has controlled for errors and contamination, which counts for more than just marketing. In a busy synthesis schedule, getting sent an off-color or impure sample means delays, reruns, and escalating costs.
Bringing p-Nitroaniline into a process opens doors. Its structure—a benzene ring para-substituted with nitro and amino groups—makes it ideal for building more complex aromatic compounds. Textile chemists rely on it to produce azo dyes that color fabrics vivid reds, oranges, and yellows; these are shades you’ll see in everyday clothing, not just laboratory curiosities. The compound’s role doesn’t end at color; pharmaceutical researchers build on p-Nitroaniline to reach intermediates in painkillers, antibiotics, and even malaria treatments. Speaking from the bench, it gives researchers flexibility to introduce diverse chemical groups and push their molecules closer to finished drugs.
For university labs and manufacturing plants alike, one solid batch of 99% p-Nitroaniline may go on to create dozens of products. In our lab, it has often served as a foundation for coupling reactions, particularly the diazotization process—transforming the amino group into a diazonium salt that unlocks a whole palette of follow-up chemistry. Even folks outside the traditional chemistry space—think agriculture, photography, or pigment specialists—turn to it because other starting materials might lack the same reactivity or cost-effectiveness.
Anyone who’s sorted through catalogs or called around suppliers can tell you, not all p-Nitroaniline is equal. Lower grades, sometimes labeled as technical or laboratory grade, seldom guarantee the kind of purity a research chemist or pharmaceutical manufacturer depends on. Contaminants, even at fractions of a percent, can introduce false readings in analytical tests or shut down a reaction midstream. I remember one project where a batch with unidentified contaminants required days of troubleshooting, wasted reagents, and repeat synthesis—all avoidable with a higher-purity product.
Compared to ortho- or meta-nitroaniline isomers, the para form’s predictable reactivity streamlines planning. This consistency simplifies downstream chemistry and aligns with textbook protocols that steer clear from isomeric unpredictability. Another difference emerges in solubility; p-Nitroaniline dissolves well in organic solvents but resists water, letting chemists separate their products faster and with less mess. These differences become obvious in scale-up scenarios, where process engineers value reductions in waste and quicker purification cycles.
People new to chemical purchasing might wonder whether it matters where p-Nitroaniline comes from. The honest truth is, reliable sourcing matters almost as much as the chemistry itself. Good manufacturers document their processes, publishing certificates of analysis with every shipment. Not every supplier puts the same effort into purity verification or invests in modern equipment that prevents contamination. The best labs pick partners who’ve built trust over time, who stay transparent and responsive if problems arise. I’ve learned this the hard way; a bargain purchase looks attractive until an unexpected impurity derails a critical synthesis, underscoring the adage: “You get what you pay for.”
Proper handling of p-Nitroaniline in the lab deserves equal attention. Its crystalline form reduces dust but can still pose risks if mishandled during weighing or transfer. Training matters here—spills, inhalation, or contact with skin all have health consequences, especially with aromatic amines containing nitro groups. Many labs—mine included—audit their workflows, checking that fume hoods, gloves, and proper storage protocols keep everyone safe. Students and technicians learn the ropes early, recognizing signs of exposure and understanding emergency washing procedures. No academic pursuit or product launch justifies a shortcut here.
Purity is not just a bureaucratic benchmark or a line on paperwork; it’s something researchers experience day after day. With each experiment, small uncertainties compound. More impurities mean less predictive behavior, lower yields, and costlier troubleshooting. I have seen seasoned chemists groan at minor yet persistent contaminants—from slight color differences to strange odors—recognizing the headaches those introduce later in the synthetic pathway. For anyone who’s ever tried scaling a reaction from milligrams to kilograms, small inconsistencies at the start grow into massive operational hurdles. Investing in reliable, high-purity 99% p-Nitroaniline is often the cheapest insurance you can buy.
Beyond lab benches, regulatory agencies have begun requiring cleaner, traceable materials. Pharmaceutical developers juggle strict quality-control regimes, and nothing stops a drug application like unexplainable variances in starting materials. Users in textile or pigment manufacturing face similar regulatory landscapes, where consumer safety and product consistency both come under scrutiny. While there are cheaper options on the market, cost-saving here too often leads to larger exposures down the line—both financial and reputational.
Chemicals like p-Nitroaniline sometimes appear generic because their names crop up in undergraduate textbooks and product guides. In truth, behind every "-aniline" lies a web of industrial know-how. Not all material marked “99%” is functionally equivalent. Miniscule differences in synthetic pathways or purification steps may result in batches that look fine to the eye but behave unpredictably with sensitive reactants. Good labs keep records of a material’s lot number, storage conditions, and supplier—forming a paper trail that saves projects from frustrating holdups.
For smaller operations, the temptation to buy lower-priced batches arises regularly. My involvement in both research and small-scale manufacturing has shown that up-front savings almost always get eaten up by decreased reliability, reruns, and customer complaints. Those with real-world deadlines or funding pressures grow to appreciate materials that remove uncertainty, even at a premium, because those save money and reputations in the end.
Environmental responsibility sits near the top of most research agendas today. Modern p-Nitroaniline production increasingly adopts greener practices: using more efficient syntheses, reducing hazardous byproducts, and improving recovery of spent solvents. With regulatory bodies pushing for stricter controls on emissions and waste, suppliers who’ve modernized their plants can provide cleaner, safer products with a lower environmental footprint.
From watching this transition firsthand, the best suppliers remain proactive—investing in new waste-handling technologies, reformulating production recipes, and seeking out greener paths that don’t compromise on quality. End-users who ask tough questions about production practices signal to the market that green chemistry is a competitive advantage. Responsible purchasing supports suppliers who value worker safety and sustainability alongside product performance. For those of us in chemistry, it’s encouraging to see progress here. As large buyers and university labs adjust their purchasing criteria, the industry as a whole moves forward.
Long workdays in the lab teach plenty of lessons not always spelled out in textbooks. For newcomers, here are a few hard-earned tips about working with substances like p-Nitroaniline:
While some compounds quietly do their job in the background, p-Nitroaniline sparks real innovation in chemistry. By enabling targeted modifications to aromatic rings, it has shaped research from cancer therapies to novel sensors. Commercial enterprises producing specialty dyes or functional intermediates often depend on its predictable performance; new businesses emerge when foundational materials allow for confidence in experimentation.
I recall a project focused on developing antimicrobial coatings. The entire workflow relied on coupling p-Nitroaniline to other aromatic groups. Early attempts with a lower-grade sample led to inconsistent activity and a raft of negative results. Switching to a higher-purity material, the product not only met our internal targets, but also passed the more stringent toxicology exams required for regulatory approval. Time and again, this theme repeats; materials that give consistent, high yields support faster patent filings, easier technology transfer, and fewer obstacles during commercialization.
Globalization continues to transform how chemicals travel from factory to test tube. Markets in Asia, for instance, have surged with both local consumption for textiles and export demand for pharmaceuticals. Large-scale projects depend on reliability at every stage; interruptions over questionable quality or documentation create significant downstream risks. It’s not only the largest companies that benefit from higher standards—universities, niche manufacturers, even third-party testing labs all see better outcomes from materials vetted by modern protocols and robust supply chains.
I’ve seen firsthand how investment in infrastructure—new warehouses, temperature-controlled shipments, trained logistics managers—elevates an entire ecosystem. Competitive suppliers quickly learn that getting purity right increases customer retention and builds brand trust. In a fiercely competitive market, these advantages shape who succeeds in the long run.
Chemical safety regulations change quickly. In some parts of the world, authorities now ask for traceability at every step of a drug or dye’s life cycle—from p-Nitroaniline’s production through conversion into a finished product. These regulatory shifts increase demand for better batch records, tighter chain-of-custody controls, and advanced impurity profiling. For users, staying informed means joining professional organizations, attending workshops, and participating in networks where best practices get shared. I once participated in a panel on chemical safety, where experiences—from minor near-misses to serious regulatory warnings—helped shape more robust institutional systems.
Keeping up with compliance isn’t just about fear of penalties; it’s about making sure teams go home safe and products meet the expectations of regulators and end-users alike. Companies who foster a culture of learning, ask for feedback, and regularly update protocols tend to outperform more static, cost-driven competitors.
New directions for p-Nitroaniline will likely come from shifts in consumer demand and technological advancement. Some research groups are probing its use in advanced materials for electronics and energy storage, hoping to take advantage of its stable aromatic backbone. Others focus on refining its reactivity to deliver even more precise chemical transformations. Developments in machine learning and analytics let chemists design and optimize new reactions faster, but those technologies only deliver full value when built on reliable, known ingredients.
High-purity p-Nitroaniline, well-documented and efficiently handled, has the potential to remain a mainstay in the chemical world for a long time. It rewards careful buyers and disciplined practitioners, reduces risk, and expands the possibilities for innovation across industries. For anybody looking to make breakthroughs, it pays to begin with the kind of materials that have been proven, batch after batch, to hold up under scrutiny.