|
HS Code |
483317 |
| Iupac Name | 3-(Phenylamino)phenol |
| Molecular Formula | C12H11NO |
| Molar Mass | 185.23 g/mol |
| Appearance | Off-white to light brown solid |
| Cas Number | 5693-16-7 |
| Melting Point | 126-130°C |
| Solubility In Water | Slightly soluble |
| Density | 1.21 g/cm3 (estimated) |
| Structure Type | Aromatic amine, Phenol compound |
| Pubchem Cid | 68261 |
| Smiles | C1=CC=CC=C1NC2=CC(=CC=C2)O |
As an accredited 3-(Phenylamino)-Phenol 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 3-(Phenylamino)-Phenol, labeled with product details, hazard symbols, and safety information. |
| Shipping | 3-(Phenylamino)-Phenol is shipped in tightly sealed containers, compliant with chemical safety regulations. Packaging prevents moisture and light exposure, ensuring product stability. It is labeled according to hazardous material guidelines, including hazard warnings and handling instructions. Shipping follows all relevant local, national, and international transportation rules for laboratory chemicals. |
| Storage | Store **3-(Phenylamino)-phenol** in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and light. Use only in designated chemical storage areas, and label containers appropriately. Wear appropriate personal protective equipment (PPE) when handling to avoid inhalation, ingestion, or skin contact. |
Competitive 3-(Phenylamino)-Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615380400285
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Every batch of 3-(Phenylamino)-Phenol holds a certain story. In our factory, the sights and sounds of glass-lined kettles and the rigorous routine in quality control labs become the backbone of what you see in a single drum of this compound. Over the years, we have come to know this product not only as a chemical structure — C12H11NO — but as a pivotal ingredient that directly supports practical innovation in various sectors.
Our manufacturing process begins with access to high-quality aniline and phenol, reacting through electrophilic substitution. This route ensures the final output displays a pale to slightly brown solid, with purity that consistently meets demanding technical and research standards. Precision stays at the core here; experience shows that even a small deviation in reaction temperature or a subtle impurity in the raw feed can show up later. Chemists in our plant closely inspect each step, washing and recrystallizing until the target specifications are reached.
The final outcome is clear: users receive a solid form, generally supplied in 25 kg fiber drums to protect against contamination and moisture. Internal lots typically fall within a melting range specific to 3-(Phenylamino)-Phenol, which, as operators in the plant can attest, signals completion and stability. Water content and trace metals stay tightly monitored. We have seen that when these figures stray, it tells us either something went off in the purification or a valve seal isn’t up to the mark.
The value of 3-(Phenylamino)-Phenol becomes obvious if you walk through research institutions or specialty chemical units using this compound. One mainstay use lies in the synthesis of advanced dyes and colorants, where the molecule’s unique structure — an aromatic amine linked to a phenol group — creates chromophores with high color intensity and stability.
Further downstream, pharmaceutical researchers prize this compound as a core building block for more complex heterocyclic scaffolds. Our customers in this sector send us feedback that the product’s consistent melting point and solubility play a decisive role. They do not work in the abstract; trials and reactions often fail if the intermediate comes with unwanted isomers or trace metals. Direct conversations with bench chemists and process scale-up engineers guided changes in our filtration protocols and moisture control procedures.
Over time, the market for specialty polymers and adhesives began tapping this molecule for its phenolic oxidative potential and thermal resilience. We did not simply learn about this from textbooks; customers showed us their finished goods — resin panels, flexible films, anti-corrosion additives — and the connection with our product’s batch-to-batch reliability became obvious. They look for a clean aromatic backbone and a well-balanced amine/phenol substitution because these properties feed directly into polymer crosslinking and long-term material performance.
New buyers often ask: how does 3-(Phenylamino)-Phenol differ from similar aniline derivatives or related phenolic intermediates? From hands-on production and customer troubleshooting, several differences stand out.
Typical aminophenol compounds, such as 2-aminophenol or 4-aminophenol, offer single-ring substitution; their reactivity can be quite sharp, and the resulting products tend to show high oxidation potential but lack the conjugated system provided by the extra aromatic ring in 3-(Phenylamino)-Phenol. With our product, chemists find extra resonance stabilization, making it suitable for applications requiring both electron-rich and slightly hindered functional groups. That slight electronic modification matters in specialty pigment formation and pharmaceutical synthesis, affecting shade, solubility, or even toxicity profile.
Our process differs from generic suppliers who often focus on 4-aminodiphenyl ether or other diaryl compounds. Through years of refining crystallization and purification, we control side-products like bis-phenyl derivatives and tarry polymeric by-products that tend to haunt less-experienced manufacturers. Our reaction engineers make constant adjustments to the timing of quenching, pH adjustments, or how quickly we transfer from the reaction kettle to the filtration stage. As a result, the finished 3-(Phenylamino)-Phenol serves as a cleaner, more reliable intermediate, not just a generic bulk chemical.
In practical use, the extra ring and amine group in this molecule enable unique substitution chemistry in azo and diazo derivatives, useful for making richer, more lightfast dyes. This multifunctionality sets it apart from simpler phenol or aniline intermediates. Our colleagues on the production floor understand that each nuance in synthesis impacts not only purity but the final product, whether destined for inkjet cartridge makers or a pharmaceutical pilot plant.
The details of daily work define product quality. At our site, operators endure the odor of warm aniline long after a shift ends, while laboratory staff remember tense moments after a run yields off-target melting points. Through this, we have realized that reliability stems less from grand process innovations and more from steady repetition, routine cleaning, and rigid adherence to standard operating procedures.
Quality is checked not once or twice but at several stages. Every shipment undergoes in-house HPLC and GC trace analysis. We use data not as a regulatory checkbox but as a running log that guides the next week of production. If a batch falls outside historical trend lines — perhaps a minor impurity shows up at 200 ppm instead of the routine 30 ppm — plant management calls an all-hands meeting to root out the cause. Our maintenance teams stay ahead of equipment fouling or gasket leaks, understanding that even a minor episode can translate into off-target product weeks later.
From firsthand experience, we see how returning customers value shipment-to-shipment consistency. One global ink manufacturer once notified us that a minor drift in polymorphic content disrupted their formulation. Resolving this took looking deep into our drying protocol, eventually leading us to adopt a new vacuum drying step and retrain our operators. Relationships form not through smooth-talking sales, but on the reliability and personal touch in how we approach process control.
As regulatory frameworks around chemical supply tighten, direct manufacturers take notice. Documentation, trace batch numbering, and controlled sampling are not theoretical for us; they are demanded by partner audits and global customs offices. We keep every analytical certificate tied directly to its lot drum. Questions about residual solvents, trace heavy metals content, or GHS labeling come into play with each international shipment. We learned early on that regulators respond not just to paperwork but to a track record of real compliance and open communication about incidents. Our staff prepare for every audit by walking through physical stockrooms and checking label condition, not by shuffling forms behind a desk.
Our experience shows that environmental responsibility starts at the plant gate. Wastewater treatment, solvent recovery, and energy balance audits run in the background, affecting choices in raw materials and reaction conditions. We work with high-concentration acid scavengers that avoid introducing halides or heavy metals into the waste chain. Employees take pride in seeing environmental inspectors remark on the crisp air inside the plant. For us, traceability and environmental compliance are stitched into daily routines, not a one-off annual report.
Running a production line for 3-(Phenylamino)-Phenol brings real-world challenges. Changes in aniline or phenol prices often squeeze our margins overnight. Dealing with inconsistent raw material supply, especially in volatile markets, forces experienced purchasing teams to hedge and warehouse critical feedstocks months in advance. In slow periods, excess inventory ties up capital, while sudden surges mean overtime shifts and occasional outsourcing of non-core steps.
Unlike bulk commodity molecules, specialty intermediates like this one do not move in neat, predictable patterns. Demand jumps when a large buyer lands a new dye or polymer contract, and it drops just as fast when global trends swing. We plan cautiously, staying updated on both technological shifts and downstream market changes. Our close contact with R&D teams at partner companies gives us early warnings about product trials or qualification runs, which lets us scale up in a matter of days, not weeks.
The constant maintenance of reactor vessels, safety checks, and raw material vetting is intense. Unexpected failures, such as a cooling loop rupture or a membrane filter clog, threaten to disrupt output schedules. Chemical manufacturing rewards vigilance, quick thinking, and a willingness to learn from every unplanned event.
Direct discussions with scientists and product formulators shape much of what we do. Over the years, our technical service chemists have visited customer labs to unravel issues: a shift in melting point causing downstream yield loss, or a slight yellow tint in a product critical for pure white polymer preparations. These practical issues rarely have one-size-fits-all solutions. They involve tweaks in drying conditions, new anti-static packaging, or additive-free lots.
Customers have helped us discover new uses. In one project, a collaborator demonstrated that minor aniline content in 3-(Phenylamino)-Phenol improved solubility in glycol-based inks for textile printing. The insight led us to develop an optional variant with a tight specification for controlled residual aniline. Situations like this confirm the ongoing importance of direct user feedback and hands-on experimentation over theoretical forecasts.
Sometimes users request certificates beyond the standard: requests for full LC-MS spectra, extractables testing, or documentation on PAH content. Our technicians have adapted by building a library of analytical records, not just relying on basic assays. As commercial users grow more sophisticated, product support becomes less about paperwork and more about open, credible answers grounded in real manufacturing know-how.
Thinking about future needs, it becomes clear that successful chemical manufacturing demands steady investment, continuous training, and a willingness to re-examine past habits. Several years ago, a trial with a catalytic dechlorination step reduced trace halogen impurities that once seemed inevitable. Feedback from customers in electronics and photonics showed cleaner chromophores and improved device stability. Many improvements come not from massive re-tooling projects but from a worker’s observation or a night-shift engineer’s clever piping redesign.
Looking ahead, we watch shifting regulations, evolving green chemistry standards, and new opportunities in domains such as organic electronics or biocompatible polymers. Responding well takes more than adding compliance paperwork. It calls for learning new synthesis pathways and maintaining robust dialogue with forward-thinking users. Our relationships evolve not just through specification sheets but through visits, product trial batches, and shared problems solved on both sides of the supply chain.
Every 25 kg of 3-(Phenylamino)-Phenol tells a story of meticulous production, hands-on troubleshooting, and a partnership with the broader community of innovators. The compound’s status in dyes, polymers, and research is bolstered by reliability developed from long-term industrial practice. By responding quickly to shifts in market and technology, and by keeping production closely linked with user feedback, we move beyond being simply a supplier. Instead, we work as an ongoing partner in the journey from reaction flask to finished product.