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HS Code |
118030 |
| Chemicalname | N-(4-Chlorophenyl)-2-Nitrobenzenamine |
| Molecularformula | C12H9ClN2O2 |
| Molarmass | 264.67 g/mol |
| Casnumber | 6358-13-4 |
| Appearance | Yellow crystalline solid |
| Meltingpoint | 137-140°C |
| Solubility | Slightly soluble in organic solvents |
| Density | 1.38 g/cm³ (approximate) |
| Synonyms | 4-Chlorophenyl-(2-nitrophenyl)amine |
| Smiles | C1=CC=C(C=C1)NC2=CC=CC=C2[N+](=O)[O-] |
| Inchi | InChI=1S/C12H9ClN2O2/c13-10-6-8-3-4-9(5-7-10)15-12-2-1-11(14(16)17)5-7-12/h1-8,15H |
As an accredited N-(4-Chlorophenyl)-2-Nitrobenzenamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of N-(4-Chlorophenyl)-2-Nitrobenzenamine, securely sealed in an amber glass bottle, labeled with safety, batch, and hazard information. |
| Shipping | N-(4-Chlorophenyl)-2-Nitrobenzenamine should be shipped in tightly sealed containers, protected from light and moisture. Transport must comply with local, national, and international regulations for hazardous chemicals. Use appropriate labeling indicating its chemical hazards. Ensure packaging prevents leaks and exposure during transit, and provide relevant safety data sheets (SDS) with the shipment. |
| Storage | N-(4-Chlorophenyl)-2-nitrobenzenamine should be stored in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Store it in a chemical-resistant container and protect it from moisture and direct sunlight. Follow all relevant safety guidelines and local regulations for storage. |
Applications of N-(4-Chlorophenyl)-2-Nitrobenzenamine in Industrial ManufacturingAs an original chemical manufacturer, we supply N-(4-Chlorophenyl)-2-Nitrobenzenamine for controlled, specialized industrial applications. This compound is primarily used in the synthesis of high-value specialty chemicals. Below, we detail real-world downstream sectors and their compliance, usage, integration, and final product data. 1. Intermediate for Agricultural Chemical SynthesisAgricultural chemical producers incorporate this material as a functional aromatic amine intermediate to build new-generation herbicides and selective fungicides. Manufacturers employ tight batch process control to meet regulatory purity mandates and prevent contamination. The amine structure ensures compatibility with halogenation and reduction routes, facilitating precise molecular customization required in active agrochemical ingredients. Industry compliance standards
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2. Synthesis of Advanced Dye IntermediatesThe compounds’ electron-withdrawing nitro group and para-chloro substitution allow azo and anthraquinone dye manufacturers to construct high-stability colorants for specialty textile and plastic masterbatch applications. Our customers use this amine to enhance UV stability and chromatic intensity in colorant synthesis. Industry compliance standards
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3. Pharmaceutical Intermediate for API SynthesisPharmaceutical manufacturers employ this material as an upstream building block in multi-step synthesis of certain active pharmaceutical ingredients (APIs), particularly those requiring aromatic amine scaffolds with electron density modulation. Its halogen and nitro substitutions enable specific reactivity in ring substitution and acylation, crucial for the assembly of pharmacophore backbones. Industry compliance standards
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4. Raw Material for High-Performance Polymer AdditivesPolymer compounders use N-(4-Chlorophenyl)-2-Nitrobenzenamine as a precursor to high-end chain-extending agents, antioxidants, and UV absorbers. The dual substituent structure supports stability against oxidative aging and photo degradation, key in producing specialty plastics for electronics and automotive. Industry compliance standards
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As a chemical manufacturer involved in the daily realities of process operations, production quality, and customer feedback, we approach every synthesis batch of N-(4-Chlorophenyl)-2-Nitrobenzenamine with an understanding of its practical value. This compound, commonly recognized for its unique structure, stands out in specialty synthesis, especially within the fields of pharmaceuticals, dyes, and advanced intermediates. Machinery, raw materials, and strict temperature controls form the backbone of each production cycle, but it’s the outcome—the consistent molecular configuration—that earns the trust of R&D chemists and plant formulators.
Each model of N-(4-Chlorophenyl)-2-Nitrobenzenamine steps off our reactor line accompanied by authenticated batch records and rigorous pre-release testing. This substance, with the formula C12H9ClN2O2, showcases its distinguishing nitro and chloro groups directly on the benzene rings. In our experience, these functional groups bring a set of chemical behaviors unmatched by similar aniline-based intermediates. Actual production data often guide our small process adjustments, so product reliability remains tightly controlled from lot to lot.
We see variances in the physical profile from batch to batch largely eliminated by optimized crystallization and drying steps. Particle size distribution counts for reproducibility in downstream processing, and customers engaged in solid formulation frequently comment on the tight distribution range maintained from our facility. Within our shop floor discussions, purity levels—frequently exceeding 98% by HPLC—are referenced more as a statement of pride than mere compliance.
No two production campaigns for specialty amines look exactly the same; issues like solvent carryover, intricate filtration requirements, and precise nitro group placement demand an experienced hand. Laboratory teams on our end focus not just on meeting, but sustaining, critical thresholds for purity (ensuring no persistent isomeric impurities), residual solvents (commonly methanol or ethanol), and moisture content. We don't treat these values as boxes to check; they represent the foundation for our customers’ success in downstream reactions.
Moisture, for instance, can influence reactivity and shelf-life, so our warehouse and packaging staff monitor ambient humidity and seal product drums securely without shortcuts. The distinct yellow-tan crystalline form, with occasional ivory hues, signals a clean, stable run, and experienced chemists in our company can often predict performance in coupling reactions or reductions just by reviewing appearance and melting point consistency.
In application, N-(4-Chlorophenyl)-2-Nitrobenzenamine delivers a stable, reliable starting point for the synthesis of active pharmaceutical ingredients and certain agricultural molecules. We have watched small pharma and crop-protection companies leverage this intermediate in nitro reduction, azo coupling, and acylation reactions. Output from our reactors heads directly to some of the world’s most demanding pilot plants; process engineers there often share feedback on solubility in polar aprotic solvents and reaction kinetics that shape their yields. They aren’t shy about reporting clumping, filterability, or issues with anti-caking agents—and we listen closely, taking those lessons to heart in every campaign.
Some clients work at the gram scale for lead optimization, while others push tons through continuous reactors. Each group needs confidence that the core material remains unchanged, so process validation and repeat analytical checks remain central to our operation. We track and review real-life customer outcomes, not just textbook reactions, and use those insights to guide our own process improvements.
Manufacturing teams often get tasked with explaining what sets N-(4-Chlorophenyl)-2-Nitrobenzenamine apart from other nitroanilines or chlorinated amines. To us the differences go beyond simple molecular comparisons. The placement of the nitro group at the 2-position in relation to the amino linkage, and the specific 4-chloro substitution on the phenyl ring, combine to give this molecule distinct reactivity.
For those who wrestle with synthetic routes, these details matter. Nitroanilines lacking the chloro substituent tend to show widely different solubility and coupling behavior, sometimes bringing increased by-product profiles in multistep synthesis. Simpler anilines, or variations where the nitro or chloro is para or meta, often trigger alternate reaction pathways or demand costly purification. Our teams have run side-by-side tests with those analogs and consistently observed more predictable, smoother reactions using N-(4-Chlorophenyl)-2-Nitrobenzenamine, especially in metal-catalyzed hydrogenations and nucleophilic aromatic substitutions.
Some customers ask about replacing this compound with others to trim costs or adapt to regional sourcing restrictions. In practice, substituting even a single functional group often leads to diminished yields or undesired color formation in final products. Product development teams in pharma often double-check with us before a switch, as even seemingly minor alterations in ortho/para substitution can destroy the tight structure-activity relationship needed in follow-on chemistry.
Maintaining a steady output of N-(4-Chlorophenyl)-2-Nitrobenzenamine calls for constant vigilance, both in supplier relationships and internal process oversight. Raw material markets for chlorinated and nitroaromatic compounds seldom present smooth sailing. We have faced sudden shortages of starting anilines or required halogenating agents, driven by regulatory changes in exporting countries or fuel supply disruptions. Not every supplier meets the standards we expect, so procurement works closely with QC to prequalify every source.
Batch-to-batch reproducibility stays high when our teams keep close tabs on incoming raw materials. Process chemists run small-scale pilot tests with each lot of critical feeds. By anticipating shifts in solvent quality or trace impurity levels, we prevent batch failures or delays downstream. Inside the plant, instrumentation—NMR, GC-MS, moisture analysis—is kept well-calibrated; our maintenance schedule remains as regular as clockwork, which reduces the odds of off-spec material slipping through.
We do sweat the details: even marginally increased thermal loads or filtration backpressure can shift impurity profiles. Our operators, some of whom have been with us for decades, develop a sense for the sounds, smells, and visual cues that signal a smooth versus problematic run. Management supports frequent training and open communication between shifts, since these invisible handoffs keep on-time deliveries up and reprocessing costs down.
Producing nitro and chloro organics brings inherent risks; our own safety engineers engage deeply not just to meet legal codes but to avoid the very real dangers of runaway reaction or hazardous off-gas exposure. The plant’s investment in closed systems, solvent recovery, and robust off-gas scrubbing came not just from auditor recommendations, but from years of hands-on experience. Our shift supervisors remember earlier decades, when rudimentary controls produced occasional near misses with uncontrolled pressure rises. That history reinforces our current standards.
Waste management traces back to process design. Strong internal reuse of solvents and stripping of halogenated residues for safe incineration or specialist disposal limits our environmental footprint. Regular training on PPE, chemical storage, and first response procedures is non-negotiable—most of our staff have seen real-world incidents and bring a practical, lived understanding of why these standards matter.
Many formulation scientists and research groups approach us seeking not just a product but a manufacturing partner who appreciates the real world of deadlines, yield optimization, and regulatory submissions. We maintain a dialogue with those developing new processes who often wish to push the boundaries of cost, throughput, or reaction diversity. Having direct access to the manufacturing process, R&D teams at our facility sometimes collaborate side-by-side with external researchers to tweak key parameters—trying alternate solvents, adjusting reactant loading, or running stress tests across scale-up volumes.
Our production history shows how even minor technical modifications—refined agitation, staged addition of chlorinating agents, tightly controlled nitro group introduction—can drive more robust outcomes. Research feedback loops right into real-world practice; we regularly take pilot-scale learnings and invest them in full-scale plant modifications. This responsiveness sets us apart from traders or generic suppliers, since we live and breathe the process, making continuous improvements in lockstep with industrial need.
Our days rarely pass without time spent pouring over chromatograms, spectra, and trend charts. Real purity—the lack of structurally similar contaminants or process by-products—translates to fewer surprises for our customers’ QC labs. Retention times, peak ratios, and impurity profiles matter, but so does the capacity to reproduce every result. Over years, we’ve learned which analytical techniques flag subtle degradation or highlight process drift early enough to correct it.
Long-term buyers expect more than just a printed certificate; they require honest dialogue about analytical improvements or unexpected findings. Our people treat these questions not as complaints but as catalysts for operational improvement. When reports surface about off-odors or slight color shifts, technical teams waste no time investigating root causes—adjustments to filtration, choice of antisolvents, or altered drum lining materials provide real solutions.
Shipping and storing N-(4-Chlorophenyl)-2-Nitrobenzenamine present their own set of headaches, ranging from clumping in humid climates to subtle color shifts under warehouse lighting. Our packaging line doesn’t settle for generic bags or drums; instead, our material arrives in tight-seal, light-resistant containers, sized for easy access in both lab and plant settings. Each container line receives traceability stamps right at the filling station, ensuring any rare problems can be traced back directly to their source.
We see how direct exposure to moisture, heat, or strong sunlight accelerates breakdown or lumps formation, so warehouse managers keep stocks off the floor and well away from exterior doors. Rotational stock control stems from practical experience—no one wants to deal with cake formation or slow dissolution just because containers sat too long near a warehouse vent.
Clients often demand precise documentation for regulatory filings, and our documentation team acts on a policy of full transparency. Full batch histories, process modifications, nonconformance reports, and detailed COAs remain available to qualified customers. Regulatory traceability goes beyond a paperwork task; it forms part of the fabric of our operational discipline.
We keep a close eye on emerging changes in chemical control laws and dangerous goods shipping rules. Documentation adapts as best practices evolve, and our teams stay in regular contact with external auditors, regulatory authorities, and industry working groups. On more than one occasion, proactive process-change documentation saved partner companies from late-stage headaches at the regulatory filing step.
Our journey with N-(4-Chlorophenyl)-2-Nitrobenzenamine hasn’t followed a straight, unbroken line. Technical issues have prompted unplanned downtime, staff have experimented with agitation rates or antisolvent blends, and supply chain hiccups have sometimes tested our resilience. The team learns by direct engagement, through production reviews and out-of-spec event analyses. Peer-to-peer training, process mapping, and retrospectives are part of our regular routine.
Competitive pressures, pricing shifts, and shifting end-market demands push us to innovate in practical ways, not simply in theory. Chemists and process engineers collaborate, test, and improve—sometimes in ways external observers would never guess by reading a simple product data sheet. We persist because every batch that finds its way to a research bench or production line represents our commitment, not just a line in a sales document.
Putting a product like N-(4-Chlorophenyl)-2-Nitrobenzenamine into the hands of customers involves more than running standard reactions and filling drums. Every process variable, every feedback loop from users, and every technical innovation shapes the compound’s value in actual use. Downstream differences in reactivity, color, and contaminant profiles trace right back to decisions made at the reactor or filter press.
It’s this direct involvement that gives us confidence today and motivation for ongoing improvement. We view each batch as a partnership grounded in shared technical goals and the knowledge that expertise and hands-on discipline at the point of manufacture remain the real drivers of customer success.