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HS Code |
692830 |
| Cas Number | 2113-58-8 |
| Molecular Formula | C12H9NO2 |
| Molecular Weight | 199.21 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 93-97°C |
| Boiling Point | 378.8°C |
| Density | 1.256 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 195°C |
| Purity | Typically ≥98% |
| Refractive Index | 1.660 |
| Pubchem Cid | 13705 |
As an accredited 3-Nitrobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, labeled "3-Nitrobiphenyl, 25g". Includes hazard symbols, product code, and manufacturer's details. |
| Shipping | 3-Nitrobiphenyl is shipped in tightly sealed containers, clearly labeled with hazard warnings. It must be transported according to applicable regulations for hazardous chemicals (UN 2811, Class 6.1, Toxic Solid, Organic). The product should be kept away from sources of ignition and handled by trained personnel using appropriate personal protective equipment. |
| Storage | 3-Nitrobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. It should be kept out of direct sunlight and protected from moisture. Proper chemical storage facilities should be used to minimize the risk of exposure or environmental contamination. |
Applications of 3-Nitrobiphenyl in Industrial Manufacturing3-Nitrobiphenyl is an essential aromatic intermediate deployed across multiple advanced industrial fields. As the direct manufacturer, we ensure detailed application alignment, rigorous compliance, and precise technical adaptation according to each downstream sector's requirements. Below, we outline core application scenarios, each reflecting actual industry demand and established regulatory frameworks. 1. Agrochemical Synthesis for Selective Herbicides3-Nitrobiphenyl serves as a crucial precursor in synthesizing key heterocyclic structures for selective herbicide active ingredients, particularly within diphenyl ether-based herbicide classes. Technical teams use it during the coupling and ring-closing stages, where its specific reactivity and chemical stability enable controlled functional group modification. Close monitoring of impurity levels and adherence to strict specifications are mandatory to meet regulatory submissions in international markets. Industry compliance standards
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2. Specialty Dye and Pigment ManufacturingAromatic nitro compounds like 3-Nitrobiphenyl form the core of many high-performance azo and anthraquinone dyes. Colorant manufacturers rely on this raw material during azo coupling and diazotization steps, where precise stoichiometry and low metal content preserve end product brightness and stability. Strict compliance with European Union and US environmental directives governs each phase of manufacture, from raw material storage through final blending, especially for textile and plastics coloration. Industry compliance standards
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3. Pharmaceutical Intermediate for Antineoplastic CompoundsWithin the pharmaceutical sector, 3-Nitrobiphenyl functions as a controlled intermediate in synthesizing aromatic structures for certain antineoplastic and investigational drug candidates. It enters targeted reduction and amination sequences—requiring GMP-level traceability, validated cleaning protocols, and comprehensive impurity tracking throughout kilo-lab to commercial scale-up. All material batches undergo release tests for identity, purity, and residual solvent content aligned with ICH Q7 guidelines. Industry compliance standards
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4. Polymer Additive and High-Temperature Resin ProductionThe compound acts as a specialty modifier in producing high-temperature biphenyl-based resins and advanced polymers. Specialty resin manufacturers utilize its nitro functionality to increase glass transition temperature (Tg), enhance mechanical strength, and impart flame resistance. Recipe engineers must ensure nitro group conversion meets target downstream performance, with QA teams conducting DSC and TGA analysis on each batch to certify performance under elevated thermal stress. Industry compliance standards
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5. Electronic Materials and Organic Semiconductor SynthesisAdvanced electronics industries use 3-Nitrobiphenyl to build complex, conjugated molecules for organic semiconductors and layered electronic materials. Its electronic delocalization properties support uniform charge transfer essential for device performance. Precise reagent addition, impurity profile control (especially halide and heavy metal traces), and compliance with specialty electronic-grade material specs are strictly enforced throughout pilot and commercial syntheses. Industry compliance standards
Typical usage ratio
Downstream process integration
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In the business of chemical manufacturing, every process step matters, and every product plays its own role in building reliable supply chains. Our focus on 3-nitrobiphenyl, recognized by its molecular formula C12H9NO2 and CAS number 2150-38-1, reflects years of refining production methods and responding directly to industrial user feedback. This compound stands out in our line-up for solid, practical reasons. Our chemists have spent decades focusing on biphenyl derivatives and their nitro-substituted forms. 3-nitrobiphenyl is produced through electrophilic aromatic nitration, resulting in a golden-yellow crystal with light sensitivity. In our own facilities, we run this reaction under controlled temperature and pH, using clean feedstock and rigorously filtered reagents. These choices all trace back to the same need: deliver a consistent product that works for demanding applications downstream.
We do not approach chemicals like an inventory—every batch ties back to real use cases and feedback from customers in colorant, agrochemical, and pharmaceutical fields. End users seek out 3-nitrobiphenyl specifically as a precursor for synthesis, not just “another nitro compound.” Our technical team has observed that subtle differences in impurity profiles or moisture content can crash entire downstream reactions or increase filtration time. So while other manufacturers might consider a small residual moisture level or a trace biphenyl content acceptable, our practical experience says otherwise. Over years, customer complaints about filter clogging or byproduct formation during hydrogenation have guided us on where to tighten quality parameters and where to loosen them for cost efficiency.
With a melting point typically near 82–84°C, 3-nitrobiphenyl demands careful storage—exposure to light and humidity can degrade it, leading to inefficiencies that only surface many steps downstream. In our warehouse, we wrap packages in light-blocking liners, checking the bulk periodically for any sign of physical change. Analytical chemistry backs our processes: each lot leaves the plant with HPLC and gas chromatography data, showing both the major peak and side products all chemists dread. Over the years, users have told us that off-site sources sometimes show yellow-brown residues or a bitter, acrid odor, scars of incomplete purification or careless packaging. We keep our finished product free from these issues through a combination of extra vacuum drying and vigilant control over crystallization rates. If the color slides too far toward brown, we know to rework the lot rather than ship substandard material.
In conversations with end users, specifications emerge from actual hurdles, not from theoretical book values. For example, we keep iron content below 5 ppm—not because it looks good on a certificate, but because iron-catalyzed decomposition can wreck complex Suzuki couplings. Some clients care about chloride residues, others follow their own test scripts, but universal concerns always include color, solubility, and ease of weighing. Over time, detail after detail accumulates into a hard-won standard: 3-nitrobiphenyl that behaves predictably, whether it’s headed for a small-batch organic synthesis or a massive dye manufacturing line.
The majority of our output goes to midstream producers—groups that make azo dyes, specialty organic pigments, or advanced intermediates for pharmaceutical R&D. We’ve learned from hands-on contact that downstream processes don’t tolerate surprise. For example, hydrogenation of 3-nitrobiphenyl to 3-aminobiphenyl is a sensitive reaction, susceptible to catalyst poisoning from poorly controlled sulfur or phosphorus traces. Years ago, one multi-ton order went awry at a pigment customer's plant because of unintended catalyst fouling. That incident led us to overhaul our own supply chain, increasing scrutiny on every upstream material, especially nitric acid and biphenyl purity.
For dye manufacturing, conversion to 3-aminobiphenyl matters most. This amine activates coupling to diazonium salts, laying the groundwork for lightfast azo dyestuffs used in textiles and plastics. Substituted biphenyls often find their place in high-value colorants, thanks to their stability and intense color yield. Our clients run continuous processes, and any deviation in bulk chemical behavior—like a sticky cake, an unusual color change, or uncharacteristically long filtration—means hours lost and money burned. Through direct site visits and sample exchanges, we get a front-line look at what works and what must be improved. Reliability builds only through repeated problem-solving, and every technical adjustment in our plant has real-world roots at the customer’s reactor.
Discussions about 3-nitrobiphenyl usually invite comparisons—not just with its isomers (2-nitrobiphenyl and 4-nitrobiphenyl), but also with standard nitrobenzenes and nitrotoluenes. Each has its place, but 3-nitrobiphenyl performs in a niche where substitution pattern directly controls downstream reactivity. The para-isomer (4-nitrobiphenyl) sometimes turns up as an impurity, especially if nitration conditions run too hot or uncontrolled. Years of tweaking our process have driven this impurity below 0.1%, not for the sake of chasing numbers on a report, but because even a trace complicates separation and can change color quality in end applications. Nitrobiphenyls generally meander through multi-step reactions before their final use, and each isomer carries its own quirks—the m-position in 3-nitrobiphenyl proves essential for certain pharmaceuticals, such as development-stage kinase inhibitors and targeted dyes.
Contrast this with regular nitrobenzene or dinitrotoluene: those broad-use workhorses serve in bulk explosives or resin precursors, but won't meet the needs for biphenyl-based high-performance molecules used in OLEDs or specialty pigments. Trying to replace 3-nitrobiphenyl with cheaper analogs sounds tempting, but customers return to quality because process yields drop or unwanted byproducts climb. As a manufacturer, we have fielded requests to “blend down” this product, mixing off-spec batches to cut costs. Experience shows this tactic leads only to headaches for all involved. Our policy: deliver single-lot, single-origin product, so downstream analysis matches upstream input—no mystery performance slips.
Today’s industrial users don’t ask for generic chemicals—they demand substances that clear specific hurdles. In synthesizing advanced pharmaceuticals or specialty dyes, a pure starting point avoids weeks of rework, rerunning flash columns, or coping with intractable residues. The demand for green chemistry methods has changed the landscape as well. End users look for suppliers who keep hazardous byproducts to a minimum and who actively manage energy and waste. We have transitioned our own 3-nitrobiphenyl process through several iterations, shifting to less wasteful nitration conditions, reclaiming excess acid, and reducing offgas with regenerative scrubbing.
Our internal teams worked closely with process engineers at dye and pharma facilities, tuning our protocol so bulk orders arrive at the right crystal size and free-flowing nature. Particle size, density, and dustiness all factor into how easily plant operators can transfer the chemical without loss or health risks. For those in pilot plant settings, weighing accuracy and easy dispersibility turns into one less source of error during development. That’s why we pack under inert gas in sealed drums or double polyethylene liners, each marked with unique barcodes tied back to our batch records. We don’t simply hand off a package and disconnect—tech service follows each shipment into use, working through questions about solubility, thermal stability, or rare reactivity.
Chemical manufacturing rarely follows a straight line. Batch quality, upstream raw material swings, and even shifts in global regulations ripple through supply and require real adaptation. Some years bring easy access to high-purity biphenyl at low cost; others, market constraints or trade disruptions force a hard look at process design and logistics. We keep multi-year contracts for our core raw materials and cross-test suppliers to manage risk. In tough times—like during regional raw material shortages—our role as a producer, not just a reseller, lets us buffer customers from the worst shocks. Our plant can flex production volumes and adapt schedules when far-off market crises threaten a customer’s lead time. That flexibility is only possible by maintaining both in-house reaction engineering and good relationships with technical vendors, not just commodity traders.
Listening to user feedback remains the most effective force for progress. Some improvements only surface after a user encounters a problem nobody predicted. For example, at one specialty dye manufacturer, we saw an odd case: a recurring haze in pigment dispersions traced back to sub-micron particle fragments. This feedback spurred us to add a new filtration step, refining our isolation protocol so that the next batch delivered fully transparent, high-gloss product. Such stories reinforce that practical chemistry is never static—each real flaw teaches a lesson that no textbook captures. Problems met in a quiet research lab, a bustling chemical plant, or an artisan dye workshop feed directly into what goes back into the next day’s manufacturing change log.
Environmental stewardship now shapes decisions nearly as much as cost or timeline. We review every step for opportunities to cut waste, prevent leaks, and reclaim leftover acids and solvents. This approach does not emerge from pressure to tick regulatory boxes, but from honest accounting: less waste means both lower cost and more goodwill. We keep close tabs on all emissions, from stack gases to wastewater. In fact, a recent process redesign cut our water consumption by nearly 18 percent. We also harness solvent recovery in our crystal washing, contributing to both our own sustainability targets and the risk assessments downstream users must complete for their own certifications.
Chemists in the field care about what happens in their flasks, not how a commodity chemical looks on paper. They want a product that doesn’t gum up pumps, settle out of solution, or build static charges in pneumatic conveyors. Our experience with 3-nitrobiphenyl reaches beyond analytical data—direct conversations with production line chemists reveal what truly matters. For example, one client developing a new pigment for automotive coatings reported grainy unfiltered masses, traced back to subtle shifts in the cooling curve during crystallization. Our team visited on site, adjusted our own plant equipment, and cut the bulk filtration time for that customer in half on their next order. This rapid, direct response stands as the standard for building confidence, not just delivering another drum to the loading dock.
In interactions with pharmaceutical researchers, a common request revolves around maximizing reactivity and minimizing side reactions in cross-coupling sequences. They want reliable, chromatographically clean 3-nitrobiphenyl to streamline libraries of test molecules—one misbehaving spot on a TLC plate costs days or weeks of research. Synthetic accessibility, purity, and safety data come up again and again, and we share our own long-term stability profiles, shelf-life recommendations, and storage best practices. Some customers need frequent sampling, others batch certifications for internal audits; our team adapts, not just because regulators demand it, but because users’ success traces directly to our product’s performance.
Downstream users rarely operate in isolation, either—regulatory compliance, workplace exposure risk, and transport safety all circle into the planning conversation. We back every batch with up-to-date documentation, offering both full MSDS and typical application notes gathered across hundreds of experiments and dozens of customer projects. This data-driven transparency streamlines customs clearance and safety reviews, supporting both stable operations and occupational health.
3-nitrobiphenyl is not a high-profile specialty, but for the users banking on stable performance in dye, pigment, or pharmaceutical lines, sourcing from a true manufacturer makes a tangible difference. Hybrid traders source and resell for margin alone, rarely engaging with the nuts and bolts—the scraped reactor, the fine dust, the need to re-house a batch due to temperature swings. In contrast, we wake up to lab reports, maintenance logs, and phone calls from the floor asking, “Can you tweak this for us next time?”
We have seen substitution experiments: clients try to save a few percent per kilo, only to switch back upon meeting unexpected hurdles. Our survival doesn’t rest on price cuts or bulk deals, but on days when a senior chemist calls to say, “This batch helped us cut three steps,” or, “Filtration ran smooth all week.” The overtime hours, the investment in tighter controls, and the direct shipment tracking all point back to a guiding principle: the right material in the right form, made by people who have seen the process end to end.
As regulations evolve, especially regarding nitro derivatives’ transport and labeling, we stay a step ahead—flagging upcoming changes and updating procedures before problems arise. This comes through close reading of international GHS guidelines, annual staff retraining, and frequent outside audits from both global and domestic authorities. These efforts, though less glamorous than touting spec sheets, shape the quiet confidence that keeps downstream operations risk-free and productive.
The choice of where to source 3-nitrobiphenyl cannot rest on numbers alone. The best chemical starts with the best process, the tightest feedback loop, and a readiness to improve. Every kilogram that leaves our plant bears the marks of continuous learning and real problem-solving. Our years in the nitroaromatics sector have taught an unambiguous lesson: chemicals, more than any abstract commodity, depend on the hands and eyes behind the product. What matters most is not just functional groups and purity, but the reliability of people and process—a quietly delivered promise in every shipment that reaches the hands of a working chemist or industrial blender. That’s the story and substance behind the 3-nitrobiphenyl we make, backed by experience, not marketing.