|
HS Code |
628999 |
| Chemical Name | 4-Nitro-3-Phenylphenol |
| Cas Number | 2113-58-8 |
| Molecular Formula | C12H9NO3 |
| Molecular Weight | 215.21 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 148-150 °C |
| Boiling Point | No data available |
| Solubility In Water | Slightly soluble |
| Density | No data available |
| Synonyms | p-Nitro-m-phenylphenol |
| Pubchem Id | 148957 |
| Structure | Biphenyl ring substituted with nitro and hydroxyl groups |
| Smiles | C1=CC=C(C(=C1)C2=CC=CC=C2)[N+](=O)[O-] |
| Inchi | InChI=1S/C12H9NO3/c14-12-8-7-10(9-4-2-1-3-5-9)6-11(12)13(15)16/h1-8,14H |
| Refractive Index | No data available |
As an accredited 4-Nitro-3-Phenylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle labeled "4-Nitro-3-Phenylphenol, 25g" with hazard symbols, lot number, expiry date, and secure screw cap. |
| Shipping | 4-Nitro-3-Phenylphenol is shipped as a solid in tightly sealed, chemically resistant containers to prevent contamination and moisture exposure. It must be labeled as a hazardous material, shipped in compliance with local and international regulations, and accompanied by appropriate safety data sheets. Handle with care to avoid inhalation or skin contact. |
| Storage | 4-Nitro-3-Phenylphenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Store it away from direct sunlight and moisture. Ensure proper labeling and use secondary containment to prevent spills or contamination. Access should be limited to trained personnel. |
Competitive 4-Nitro-3-Phenylphenol prices that fit your budget—flexible terms and customized quotes for every order.
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The chemical industry rarely rests. Every day, clients, researchers, and production managers reach for new solutions to streamline synthesis, strengthen end products, or pioneer applications. Manufacturing 4-Nitro-3-Phenylphenol is not just about supplying another molecule to the market; it’s about ensuring predictability, purity, consistency, and alignment with the demands of actual working labs and factories.
4-Nitro-3-Phenylphenol, commonly known in the industry by its CAS number 2587-11-5, stands out due to its specific substitution pattern: a nitro group at the para position relative to the phenol moiety, and a phenyl group at the meta position. This molecular architecture gives it a particular reactivity profile valued by fine chemical producers, research labs, and specialty manufacturers who build upon its framework to create more complex molecules.
Direct experience with custom chemical synthesis teaches the value of building blocks that balance chemical stability with selective reactivity. 4-Nitro-3-Phenylphenol possesses unique features among substituted phenols. The nitro and phenyl groups fine-tune electron distribution in the benzene ring, affecting both reactivity and solubility. During manufacturing, our technicians control process parameters precisely: subtle changes in reaction temperature or purification methods can tilt the product toward unwanted isomers, or reduce overall yield. Years of refining this process have enabled us to deliver material with high assay standards, low impurity levels, and minimal trace moisture.
Users of 4-Nitro-3-Phenylphenol want reliability. This molecule often serves as a key intermediate in the manufacture of dyes, pharmaceuticals, and performance chemicals. For example, research-scale and manufacturing-scale syntheses of certain azo dyes or specialty antioxidants rely on the selectivity provided by the nitro and phenyl substitutions. The compound’s profile allows further modifications, such as reduction to amines or coupling with active alkylating agents, without risking unwanted side reactions at the phenolic site.
From one batch to the next, consistency remains a top concern—especially for partners implementing strict quality management systems or regulatory controls. Our production batches of 4-Nitro-3-Phenylphenol routinely show assay levels above 99.0% by HPLC, minimal inorganic residue, and tight particle size range following post-synthesis milling and sieving. Controlling trace metal contamination and moisture content forms a non-negotiable part of each production run; deviations disrupt downstream processes, lead to colored impurities in finished products, and cause failures in sensitive catalytic applications. Feedback loops from actual user complaints, not generic specifications, drive our focus here.
Experience also reminds us about the significance of physical form and packaging. Researchers handle small volumes inside a fume hood; large manufacturers demand tens or hundreds of kilograms that flow easily and resist clumping. For such quantities, electrostatic charging and cross-contamination become real risks. Controlled grinding, anti-static liners, and continuous monitoring of packing conditions solve problems before they leave our loading dock. That is the difference between making a product to spec and making it ready for the actual demands of production chemists and operators.
Our daily involvement with the synthesis of various substituted phenols provides bottom-up insight into small differences in molecular structure and the outsized effects they deliver. Generic para-nitrophenol or unsubstituted phenol can appear similar on paper, but real-world behavior diverges quickly. Substitute a phenyl group in the right position, as in 4-Nitro-3-Phenylphenol, and the resulting molecule exhibits distinct solubility profiles, altered UV-Vis absorption, and modified chemical reactivity. For chemists seeking targeted selectivity, these properties cannot be replaced by cheaper or simpler alternatives.
Comparisons often come up with compounds like 4-nitrophenol or 3-phenylphenol. In practical synthesis, 4-nitrophenol provides a stronger activating effect on the aromatic ring but falls short in structural versatility: the lack of a phenyl ring at the 3 position narrows the range of transformations available afterward. Meanwhile, 3-phenylphenol lacks the electron-withdrawing push from the nitro group, leading to reduced functionalization efficiency where a strong activating or deactivating influence is required. Those who switch between such molecules for cost or convenience end up contending with reduced yields and unexpected byproducts. Only the dual-substituted 4-Nitro-3-Phenylphenol fits a particular synthetic path where both electron-withdrawing and steric influences are needed in harmony.
Down on the plant floor or inside the R&D lab, the reality behind every product application looks different from the scenario painted by marketing brochures. 4-Nitro-3-Phenylphenol’s strong electron-deficient core makes it ideal for nucleophilic aromatic substitutions and selective reductions. Its use as an intermediate in crafting certain pharmaceuticals and advanced materials brings tangible benefits: reproducibility, predictable downstream reactivity, and few side reactions.
Many customers in the dye industry use this compound both as a coupling component and as a precursor for further elaborations. Years working with pigment manufacturers exposed us to multiple case studies where incorrect phenol selection sabotaged overall project yields. Aromatic substitutions can create impurities that carry through to the final pigment, especially if the phenol is not suitably protected or if the nitro group is not positioned correctly. With 4-Nitro-3-Phenylphenol, manufacturers consistently feedback higher purity in the final dye product and less need for costly secondary purification.
Pharmaceutical researchers value the stability under standard lab conditions and the clarity of NMR and HPLC spectra when tracing subtle reaction intermediates. One recurring challenge, especially in early-stage drug development, involves scaling up selectively substituted phenols from grams to kilograms. Results hinge on having tight control of trace-level contaminants since regulatory filings demand not only purity by standard techniques but also a full accounting for potential process-related impurities. Every production run of 4-Nitro-3-Phenylphenol meets these increasingly stringent standards, drawing on insights gained from customer audits and international compliance requirements.
QC is not a mere formality. Every lot gets sampled and analyzed using HPLC, GC-MS, and NMR in our lab. We learned that simple melting point readings or thin layer chromatography do not tell the full story; they miss isomeric impurities, oxidation products, or trace byproducts from side reactions. The production process continually evolves, drawing from real batch results rather than theoretical targets. Whenever a batch fails to hit our standard, it’s isolated—no recycling, no blending, no “making it right by dilution.” Too many horror stories from buyers who received off-spec material after such corrective attempts. We design our quality assurance for honest results, not for the ease of passing a spec sheet.
We also document everything digitally for full traceability. If a customer flags an issue, we do not just send a replacement. We trace the entire production trail, right down to raw materials, operator notes, and reagent lots. Over the years, managing traceability at this granularity has saved major customers weeks of troubleshooting. They value this diligence, not just for audit requirements but for uninterrupted operation.
It’s tempting to treat chemical packaging as an afterthought—simply fill a drum, seal it, and ship it. Our experience says otherwise. For 4-Nitro-3-Phenylphenol, especially in quantities above 20 kg, powder caking and electrostatic build-up can waste hours of a technician’s time or contaminate a reactor charge. We shifted to double-layer inner bags, static-resistant liners, and drums jacketed to prevent condensation shifts during overseas shipping. Each drum comes labelled with actual fill date, batch number, and analytical results for that batch. Too many “bad batches” in the market trace back not to the synthesis itself, but to mishaps during transit.
Feedback from our logistics team and clients led us to schedule routine checks on long-haul and ocean shipments. We deploy shock sensors, carry temperature data loggers inside bulk consignments, and audit third-party warehousing sites for ambient control. The compound tolerates standard storage conditions but shows sensitivity if left in environments with high humidity or exposed to direct sunlight for extended periods. Time and again, well-designed packaging and proper transport protocols avert customer complaints and ensure on-receipt purity.
Producing, handling, and shipping phenolic compounds textured with nitro groups demand respect for occupational and environmental guidelines. Every staff member who handles solid or solutions of 4-Nitro-3-Phenylphenol receives hands-on safety training. Experience underlines that knowledge and respect for chemical reactivity, rather than overreliance on labels and paperwork, provide real accident prevention. We maintain ventilation, splash protection, and tracked access in all production and packaging zones. This approach goes beyond compliance—it protects our team, reduces insurance claims, and minimizes downtime from avoidable accidents.
Waste minimization forms a pillar of our operation. Residual mother liquor and washings pass through a solvent recovery process and ultimately get neutralized and filtered at our on-site effluent treatment plant. This avoids the uncontrolled discharge events that have led to regulatory crackdowns in parts of the world with less rigorous oversight. Engineers adapt reactor cleaning and waste treatment based on periodic reviews and new legislative requirements. Many years in this sector taught us the cost of treating EH&S like a checkbox rather than an ongoing project.
Any chemical business feels the impact of supply chain shocks, feedstock shortages, or regulatory changes. 4-Nitro-3-Phenylphenol buyers experienced supply interruptions during global logistics bottlenecks. Long-term partnerships, longstanding agreements with reliable upstream vendors, and a robust raw material inventory grant us responsiveness, not just resilience. We forward purchase sensitive raw materials, invest in buffer inventory, and keep a running dialogue with key clients about volume projections. This proactive approach smooths out price volatility and delays, compared to traders who hunt for spot market opportunities.
We resist the urge to chase short-term pricing swings. Sustained quality relies on predictable sourcing: same grade, same supplier, same verification. Sudden changes, even for small cost savings, disrupt qualification protocols, provoke revalidation, and risk cascading quality incidents. Direct experience with urgent substitution requests during past supply disruptions shaped this philosophy. As manufacturers of 4-Nitro-3-Phenylphenol, we know that even small raw material differences can change the impurity profile and cause unexpected downstream issues.
Factories are not static places. Process tweaks, new regulatory pressures, and feedback loops from customer labs push real manufacturers toward continuous improvement. Our R&D group reviews historical lot data, customer comments, and market signals—not just assumptions about how buyers use our product. That is how we refined drying protocols, reduced trace chlorinated impurities, and tuned our milling set-up for better bulk material flow.
We respect the reality that no process achieves final perfection. End users keep discovering quirks or evolving needs. Recent feedback pointed to improved panel labeling for easier batch tracking at the dock. Plant engineers wanted expanded options for drum sizes and flexible shipment terms for faster deployment. We adjusted. These changes grow from dialogue, not from internal guesses or consultant playbooks. The wider the scope of real-world feedback, the stronger the final product.
Many industries that depend on 4-Nitro-3-Phenylphenol operate under heavy regulatory scrutiny. Pharmaceutical and specialty chemical customers demand traceable records, validated analytical methods, and documented supply chains. We develop and supply the supporting certificates—analytical reports, impurity profiles, historical trend analyses—directly from our internal database, built up over years of manufacturing and quality assurance cycles.
Auditors who visit our site see manufacturing in action, not staged test runs. Every reaction, analysis, and packaging step follows documented SOPs written by those who do the work, not a distant compliance office. Any client can trace their specific batch all the way from raw materials intake to packaged goods. Problems found “downstream” receive clear, direct answers about origin—no stonewalling, deflection, or vague explanations. Real-world audits reward this level of integrity and transparency.
The world of fine intermediates pushes for greener processes, reduced energy consumption, and minimized waste. 4-Nitro-3-Phenylphenol manufacturing shares this pressure. We have already retooled some reaction steps to reduce solvent dependency and investigated catalytic versus stoichiometric options in nitration. These adjustments flow from demand—not just internal targets but user guidelines, investor pressures, and anticipation of incoming regulations around organic pollutant release.
We work with customers to prototype greener alternatives or to optimize downstream processing that relies on our phenol. Our technical support group collaborates with research partners who are testing catalytic hydrogenation, direct photoredox transformations, and alternate purification methods to improve overall process sustainability. Not every initiative works right away, but real insight emerges from transparent exchanges of data and ideas.
Downstream trends in personalized medicine, high-performance pigments, and smart materials all turn attention toward more selective and reliable intermediates. By integrating client feedback, academic research, and plant-floor observations, we adjust our production and quality systems to deliver what the next generation of chemical manufacturing demands from 4-Nitro-3-Phenylphenol.
Supplying 4-Nitro-3-Phenylphenol is not a matter of simply matching a specification or filling a drum. Every day, experience in synthesis, quality control, logistics, and compliance combines to deliver a compound that works for real-world users. The molecule’s structure offers distinct advantages over simpler phenols, answering specific needs in synthesis, dyes, and pharmaceuticals. By sharing our direct manufacturing insight and responding actively to true customer feedback, we strengthen both product and partnership. That’s what genuine chemical manufacturing means—working closely, learning constantly, and delivering more than just a batch number.