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HS Code |
932955 |
| Chemicalname | 4-Fluoro-3-Nitroaniline |
| Casnumber | 54231-35-5 |
| Molecularformula | C6H5FN2O2 |
| Molecularweight | 156.12 g/mol |
| Appearance | Yellow to brown solid |
| Meltingpoint | 108-111 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | NC1=CC(F)=C(C=C1)[N+](=O)[O-] |
| Purity | Typically ≥98% |
| Density | 1.48 g/cm³ (estimated) |
| Synonyms | 1-Amino-4-fluoro-2-nitrobenzene |
As an accredited 4-Fluoro-3-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 4-Fluoro-3-Nitroaniline is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 4-Fluoro-3-Nitroaniline is typically shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It is transported as a hazardous material, following regulations for toxic and irritant chemicals. Proper labeling, documentation, and protective packaging are essential to ensure safety during transit and to comply with local and international shipping standards. |
| Storage | 4-Fluoro-3-nitroaniline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical storage cabinets and ensure proper labelling to prevent accidental exposure or contamination. Always follow standard laboratory safety protocols. |
Applications of 4-Fluoro-3-Nitroaniline in Industrial ManufacturingAs a direct manufacturer of 4-Fluoro-3-Nitroaniline, we supply this intermediate to specialized sectors that require controlled processes, quality assurance, and regulatory compliance. Our production supports key industries focused on advanced chemical synthesis, each with distinct usage formulas and process integration protocols. 1. Pharmaceutical Intermediates for Fluorinated API SynthesisLeading pharmaceutical manufacturers utilize 4-Fluoro-3-Nitroaniline as a critical intermediate during the synthesis of various fluorinated active pharmaceutical ingredients. Its nitro and fluoro functional groups allow selective transformations for advanced heterocyclic structures, especially in the development of oncology and anti-infective drugs. The compound integrates following precise GMP guidelines for impurity and residual solvent control. Customers adjust concentrations based on reaction route, solvent compatibility, and downstream purification needs. Industry compliance standards
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2. Agrochemical Synthesis of Herbicide and Fungicide IntermediatesResearch and production entities in crop protection employ 4-Fluoro-3-Nitroaniline for manufacturing key intermediates in advanced herbicide and fungicide molecules featuring fluorinated aromatic rings. This input enhances chemical stability and field performance of final actives. Strict traceability under specific agrochemical guidelines applies, including the control of aromatic nitro residues. Formulators fine-tune input ratios based on desired substitution patterns and conversion efficiency within catalytic coupling reactions. Industry compliance standards
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3. Dye and Pigment Manufacturing for Specialty ColorantsProducers of high-performance dyes and specialty pigment dispersions incorporate 4-Fluoro-3-Nitroaniline as a diazo coupling component during the synthesis of stable, lightfast azo colorants. Its controlled reactivity introduces unique spectral properties for inks, plastics, and fiber applications resistant to fading and chemical stress. Quality assurance systems monitor nitroaromatic trace limits and batch consistency. Colorant engineers select charge ratios according to targeted absorption profiles and intended dispersion media. Industry compliance standards
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4. Electronic and Specialty Resin ManufacturingIn the specialty resins sector, manufacturers depend on 4-Fluoro-3-Nitroaniline for modification of resin backbone polymers used in circuits, sensor encapsulants, and insulating coatings. The fluoro group boosts thermal and dielectric properties, while the nitro group participates in targeted crosslinking and copolymerization stages. All stages require documentation under electronics chemicals standards, with rigorous batch traceability and impurity analysis aligned to export market requirements. Industry compliance standards
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5. Fine Chemical Synthesis for Analytical ReagentsChemical producers engaged in synthesizing analytical reference reagents harness 4-Fluoro-3-Nitroaniline to create purity standards and assay components. The clear identification and trace elemental profile allow for QC routines in pharmaceutical and agricultural testing labs. Usage rates depend on the required analytical concentration, as well as compatibility with subsequent derivatization or labeling steps, under tightly controlled laboratory protocols. Industry compliance standards
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Among aromatic amine intermediates, genuine performance hinges not only on theoretical purity but also on the practical results delivered in labs and plants. From where we stand as direct manufacturers, the story of 4-Fluoro-3-Nitroaniline (CAS No. 393-39-5) begins well before it ever appears on a spot market listing. Each drum and bag represents more than a number; it reflects decisions made around reactor yields, cost profiles, and suitability for downstream chemistry.
This compound, with molecular formula C6H5FN2O2, bridges several challenging gaps for both research and production teams. Over two decades, our teams have worked with 4-Fluoro-3-Nitroaniline at a range of scales—from pilot glassware for startups tackling new dye intermediates, up to metric-ton batches for established agrochemical programs. We routinely analyze not just purity through HPLC or GC, but also actual reactivity, solubility profile under real process conditions, and the impact of micro-contaminants rarely noted in a standard certificate of analysis.
Chemists and procurement professionals often ask about assay levels, moisture, and impurity profiles with a focus that reflects the cost of failure in actual syntheses. Over hundreds of in-plant runs, typical material comes off our lines at ≥99% purity by HPLC—though meeting a number means little if unexpected byproducts disrupt the yield or crystallization downstream. That's why our technical staff routinely revisits every batch’s TLC resemblance, color shade, and even filterability. While most traders report basic chemical parameters, in our experience it’s the subtle variances in melting point range, mechanical conveyance, and true batch-to-batch odor profile that determines if a scale-up run will stay on-spec or lead to troubleshooting.
Particle size and color hue shift slightly with process variables, which in turn affect ease of dissolution or suspension in diverse solvent systems. Our practical take: what works for a low-volume custom synthesis may clog a line when scaled up unless every input, especially finely milled amines like 4-Fluoro-3-Nitroaniline, comes as specified and repeatable. Having seen operators wrestle with feed hoppers and vacuum lines, we prioritize practical characteristics no specification sheet alone can cover.
4-Fluoro-3-Nitroaniline plays an increasingly pivotal role in modern dye, pigment, pharmaceutical, and crop protection synthesis. In the dye sector, fluorinated intermediates open doors to brighter, more lightfast colors—especially for specialty textiles and inks where industry standards keep climbing. Synthetic chemists frequently select our 4-Fluoro-3-Nitroaniline for its reactivity at the amino and nitro sites, lending itself readily to diverse downstream coupling and ring-closing transformations. Laboratories pushing towards new generation herbicides and fungicides have noted more selective activity when starting from a fluorine-containing aromatic framework.
Over the years, we’ve received feedback from process chemists at pilot plants who’ve confirmed a marked difference in final product stability linked directly to the position of the fluoro and nitro groups on the aromatic ring. The unique electron-withdrawing nature of the para-fluoro, ortho-nitro arrangement appears to foster enhanced substrate specificity for coupling with diazonium salts and in selective reduction steps. These characteristics have led innovative pharmaceutical companies to use our material in restricted-access APIs, where predictable purity determines regulatory approval on final batches.
Suppliers with limited technical background may bundle all aminonitrobenzenes together, but years of hands-on manufacturing and lab troubleshooting draw out the real distinctions. Take 3-Fluoro-4-Nitroaniline as a comparator—the isomer switch alone shifts both reactivity patterns and toxicological assessments. We’ve worked closely with end users on GC-MS impurity fingerprinting, which revealed that trace isomeric content from neighboring products, even below 0.5%, can impact the color intensity in dye manufacture or the pharmacokinetic profile of a new molecule.
Physical properties aren’t trivial—finer milled powders tend to dust more, while denser crystalline stock holds up better in pneumatic conveying. Experience with truck and rail delivery confirms that poor selection of packaging or grind size leads to caking or segregation, especially in humid environments with long overland storage. This has a knock-on impact on time-to-dissolve, yield, and even health-and-safety at blending facilities.
For chemists aiming at straightforward SNAr substitution—using the fluoro as a leaving group—this product’s particular substitution pattern boosts electrophilicity, making it the preferred starting point for preparing aryl ethers or amides under mild conditions. We’ve seen academic research teams regularly demonstrate higher conversions with our material than with 2-fluoro-4-nitroaniline, for example, due to the altered resonance and inductive effects that come with each substitution pattern on the aromatic ring.
Having seen the pitfalls of inconsistent upstream feedstock, our keepers maintain strict controls over nitrobenzene and fluorination intermediates; one off-spec input and the resulting batch may carry forward colored impurities or changes in IR spectrum. Our process avoids repetitive contamination cycles by proactive equipment rotation, advanced vent scrubbing, and frequent titration of system solvents. Some buyers overlook these details, but experienced manufacturers know consistency hinges on continuous vigilance at each production stage.
Global supply chain crunches have taught us to re-examine every aspect of sourcing and finished-goods handling. We keep buffer inventories within plant, not just at third-party warehouses, ensuring controlled environmental storage for chemically sensitive materials. Our plant team logs not only shipping weights, but also humidity and temperature every hour during packaging. With 4-Fluoro-3-Nitroaniline, these small steps matter—damp conditions over a cross-continent journey can change everything from free-flow properties to UV-stability in the final product.
Being direct producers, we partner regularly with industrial users who want real solutions to practical issues—whether those relate to scale-up, regulatory compliance, or waste stream management. Our regular technical exchanges with end users—at the bench and on the shop floor—have helped prevent filter fouling, adjust pH drift, and reduce time spent hunting for off-odor contamination.
Direct regulatory compliance forms part of our process and not merely an afterthought. As environmental scrutiny increases across global markets, the need for cleaner waste management during 4-Fluoro-3-Nitroaniline synthesis has prompted upgrades in our nitration sections and post-synthesis basification. Wastewater signatures now feature reduced COD and lower organic halide residuals—hard-won outcomes from iterative investment in abatement tech rather than theoretical planning. We’ve shared these improvement models with downstream blenders and encouraged further closed-loop handling.
We also see increased demand for transparent, up-to-date documentation. As producers, the work isn’t over after providing the first COA. We stand by each batch right through user validation—not just for the core specifications but any analytical retests and required pharmacopoeia documentation updates. Clients benefit from our on-site analytical facilities, which keep supplies validated even while meeting increasingly complex regulatory disclosure requirements in the US, Europe, and Asia.
One point worth highlighting: chemical solutions are only as good as the support that stands behind them. Technical assistance is more than a quarterly site visit; it’s a steady channel for real-time troubleshooting and process improvement. We’ve supported R&D teams having difficulty achieving phase separations during multi-step syntheses and advised on minor process upgrades to boost yields based on direct knowledge from our batch histories.
There’s persistent feedback about stock consistency. We respond not just with improved storage and packaging but also with real adjustments in particle engineering and impurity control. Some customers initiated independent benchmarking programs, and in most cases, our batches maintained color and solubility uniformity across split-year orders. We use this data as a feedback loop to make adjustments, avoiding the errors that can arise from reliance on static or outdated data sheets.
A leading pigment manufacturer faced unplanned downtime due to an unusually sticky batch sourced externally. By tracing the issue to both residual solvent content and trace metal contamination, we adapted the purification process for their application. After implementing tailored post-synthesis filtration, the next shipments ran clean, and their downtime dropped significantly.
Custom pharmaceutical projects often hinge on subtle differences in precursor quality. A customer scaling up to clinical trial production encountered crystallization fouling. Joint testing revealed a previously unaccounted for impurity, present at under 0.2%. By providing a tighter fractionated intermediate cut, we preserved desired particle size and improved product yield. These real-world cases only become clear because of open technical exchanges from both sides—a benefit of working directly with plants as the origin, not as a middleman.
Producing and delivering 4-Fluoro-3-Nitroaniline entails more than reaction monitoring. We’ve encountered the practical realities of scale-up and large-volume filtration that lab protocols alone fail to reveal. With milled powders, static charge can be a significant but overlooked hazard; grounding and humidity control safeguards the process, protecting operators. On the user’s end, we’ve shared blending and slurry formation tips based on first-hand experience of how varying base quality impacts final dissolution times, especially in high-shear systems.
Disposal and waste streams remain a persistent issue for downstream processors. Feedback loops between our team and user EHS departments led to the adoption of more robust neutralization protocols and solvent recovery systems, directly reducing field complaints and compliance headaches. Manufacturers understand that unplanned downtime or environmental surcharges hit the bottom line, making process resilience more than a compliance task—it’s a core operational benefit and a brand differentiator.
The most valuable process improvements come through hands-on continuous iteration, not from textbook optimization. Recent investments in real-time reaction monitoring (NIR and automated titration) allow us to adjust batch parameters on-the-fly, giving each new run a head start against unknowns that have snared earlier generations of manufacturing. Our team’s insights, drawn directly from day-to-day problem-solving, are now integrated into standard operating procedures throughout the site.
In the realm of sustainability, we address hazardous waste minimization through distillation column upgrades and thorough process mapping. It’s common for outsiders to focus on single-metric improvements, but longer-term reductions in hazardous byproducts have emerged through active dialogue between plant staff and outside partners. Our philosophy remains rooted in pragmatic problem-solving—buffering both supply and day-to-day operations against surprises, while reinforcing trust with our industry partners.
We believe in direct technical support—in plain language. We regularly help researchers adapt lab-scale isolation and purification techniques to plant-scale flow, recognizing that what works in a glass beaker often needs retooling for a multi-ton batch. Our in-house analytics lab stands ready to troubleshoot new process bottlenecks, optimizing for both purity and throughput. For scale-up chemists, it’s not about pushing paperwork but about sustained support that keeps workflows reliable at every stage.
We track evolving needs: in the pharmaceutical sector where 4-Fluoro-3-Nitroaniline serves as a key building block, and in colorant and fine chemical sectors where tighter stewardship of chemical footprint matters. End-users comment on consistency over quarterly cycles, not just over single sample lots—and our approach to manufacturing continues adapting in response.
Modern industrial chemistry demands more than passing technical data along a chain; confidence and reliability flow from producers with hands-on experience of both synthesis and downstream implementation. Our partnership model centers on the recognition that every batch of 4-Fluoro-3-Nitroaniline moves industry forward through both tested performance and practiced technical feedback.
Real-world differences between a commodity amine and a precisely made, robustly supported batch of 4-Fluoro-3-Nitroaniline show up in every downstream process, be it a pharmaceutical synthesis run or a pigment line blending. As we look ahead, our goal remains clear: deliver both consistent product and actionable expertise, working hand-in-hand with researchers, engineers, and manufacturing teams who demand the most out of every drum we ship.