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HS Code |
524516 |
| Cas Number | 446-82-0 |
| Molecular Formula | C7H3FN2O2 |
| Molecular Weight | 166.11 g/mol |
| Iupac Name | 4-fluoro-2-nitrobenzonitrile |
| Appearance | Yellow to brown crystalline solid |
| Melting Point | ≥ 64 °C |
| Density | 1.43 g/cm³ (estimated) |
| Purity | Typically ≥ 98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1F)N#C)[N+](=O)[O-] |
| Inchi | InChI=1S/C7H3FN2O2/c8-6-1-2-7(10(11)12)5(3-6)4-9 |
| Synonyms | 2-Nitro-4-fluorobenzonitrile |
| Storage Temperature | Store at 2-8 °C |
As an accredited 4-Fluoro-2-Nitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Fluoro-2-Nitrobenzonitrile, 25g, is supplied in a sealed amber glass bottle with hazard labeling, and safety information included. |
| Shipping | 4-Fluoro-2-Nitrobenzonitrile is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is classified for safe transport according to relevant regulations, typically requiring labeling as an irritant or hazardous material. Proper documentation, temperature control, and secure packaging are ensured to maintain product integrity during transit. |
| Storage | Store 4-Fluoro-2-nitrobenzonitrile in a tightly sealed container away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong acids, bases, and oxidizers. Use secondary containment if possible and clearly label the storage area. Ensure appropriate safety measures and spill protocols are in place. |
Applications of 4-Fluoro-2-Nitrobenzonitrile in Industrial ManufacturingAs an established chemical raw material producer, we supply 4-Fluoro-2-Nitrobenzonitrile to specialized sectors seeking high-purity intermediates for advanced chemical synthesis. Our clients rely on strict manufacturing controls to maintain batch consistency and reproducibility throughout downstream transformation processes. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers select this intermediate for multi-step organic reactions, especially aryl nitrile transformations required in the synthesis of targeted anti-infective and oncology drug candidates. The fluoro and nitro substituents play key roles during Suzuki or Buchwald–Hartwig couplings, steering regioselective transformations for subsequent functional group interconversions. Downstream, processors demand trace analytics and validated process controls to ensure the material integrates without cross-contamination, supporting adherence to cGMP production and regulatory filings in global drug markets. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide and Pesticide FormulationCrop protection compound producers use this building block when developing novel fluoroaromatic herbicide or insecticide actives. Its reactivity profile supports diazonium reactions or aromatic nucleophilic substitution, creating custom-tailored agrochemical scaffolds with enhanced pest selectivity. In this sector, raw material must meet certification for absence of persistent organic pollutants (POPs) and precision in residual solvent parameters, achieved by rigorous in-process analytical monitoring. Industry compliance standards
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3. Electronic Chemicals for Specialty Liquid Crystal and OLED PrecursorsMaterials science groups in the display industry incorporate this compound during high-precision syntheses for fluorinated aromatic precursors used in liquid crystal and organic light-emitting diode (OLED) display chemistries. Fine control of fluoro content and by-product traces is crucial to ensure display material purity, which directly impacts optical performance and device longevity. Manufacturing must include trace metal analysis and documentation for import/export within electronics supply chains. Industry compliance standards
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4. Dye and Pigment Intermediate for Fine Chemical ManufacturingProducers of specialty dyes and pigments rely on this raw material to introduce fine-tuned electron withdrawing effects into chromophore structures. It participates in nucleophilic aromatic substitution or reduction reactions, setting the stage for strong color intensity and application fastness in high-end colorant systems. Downstream, customers require analytical support for trace amine and nitro impurities to comply with consumer safety labeling and environmental discharge regulation for final applications. Industry compliance standards
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Every chemist reaching for 4-fluoro-2-nitrobenzonitrile (CAS No. 26221-06-1) wants to take confidence in their source. We don’t have to wonder about trace impurities, off-spec material, or shipment delays. We run every batch of this product ourselves, with direct oversight on everything from the supply of raw fluorobenzene through to the finished, packed solid. That’s the way we built trust with both research and bulk buyers who need the same level of certainty from start to finish.
We have learned by experience that this compound earns special attention at the intersection of fluorinated aromatic chemistry and nitration science. The single fluorine atom at the para position and a nitro group at the ortho position, flanking the nitrile, create a unique constellation of reactivity. This gives it a character distinct from simple benzonitriles, and a reactivity profile giving synthetic chemists several valuable options.
In the real world, physical form can mean the difference between a clean workflow and hours of troubleshooting. The product flows as a pale yellow crystalline powder—well-defined and sharp-melting, usually in the 85°C to 89°C range. Our clients consistently appreciate that this melting profile suits purification and makes quality assessment easy. It’s one of the reasons why buyers who know their chemistry keep coming back for our batch certificates, which match the actual production instead of the theoretical best. Residual solvents sit far below the typical detection threshold, spectral data align with authenticated samples, and HPLC traces prove the difference.
Every time we scale up production, we pay careful attention to the byproduct matrix, so chemists avoid headaches with side-reactivity in their downstream synthesis. You can trust that halogen, nitro and cyano content all track with GC/MS and NMR benchmarks, confirming what you see is really what you get. We have invested in in-house spectrometry, chromatography, and stability testing. That’s why we stand behind our promise—these details count in critical applications, from API synthons to agricultural intermediates.
This molecule has become a backbone building block in many specialty synthesis pathways. Ask medicinal chemists working in heterocycle construction—adding a fluoro group can substantially affect both the binding affinity and metabolic stability of candidate drug molecules. Our customers in drug discovery rely on this substrate to ring-modify quinolines, pyrazoles, or triazines, with the electron-withdrawing nitro playing off the fluorine’s effects to grant regioselectivity during further functionalizations.
Researchers working on industrial dye chemistry, pigment manufacture, and advanced material science draw on this aryl nitrile as a way to shuttle electronic properties into larger chromophores or polymers. The combination of nitro and fluoro substitution provides levers for tuning color, conductivity, or reactivity in a way unmatched by unsubstituted analogues. Our batch data regularly support these applications with batch-to-batch reproducibility—no one wants to debug a scale-up failure traced back to an inconsistent starting material.
Not every benzonitrile offers the same field of application. Chlorinated, methylated, or unsubstituted benzonitriles display different polarity, reactivity, and solubility—one doesn’t substitute for another in protocols that exploit the electron-deficient aromatic system of this difunctional molecule. Fluorination, in particular, offers distinct metabolic and physicochemical properties. Where 2-nitrobenzonitrile or 4-fluorobenzonitrile show value individually, only the unique pairing here unlocks the balance of activation and blocking groups appreciated by those building more complex molecules.
From a technician’s perspective, our product has a consistently low moisture content and minimal retention of halide byproducts—something harder to achieve with chlorinated or brominated analogues. As fluorination chemistry has grown in demand across both pharma and agrochemical projects, reliable supply of pure 4-fluoro-2-nitrobenzonitrile stands out. Large-scale users appreciate that our process minimizes polymorphic forms, avoids problematic particulates, and delivers filtration-friendly powders, streamlining every handling and isolation step.
Scaling a di-functionalized aryl nitrile is a challenge not every lab or plant can take on. Whether dealing with exotherms during nitration or the sensitivity of the fluoroarene coupling, there’s a difference between a project completed on paper and a robust, reliable manufacturing process. In ramping capacity from pilot up to multiple tons, our process teams learned to govern temperature gradients, condensation rates, and purification steps tightly enough to cut impurity ladders.
Quality management cuts across every part of the supply chain. Starting materials are pre-qualified for their isomeric and halide content, since a small deviation there can throw off the entire downstream synthetic response. Our in-process monitoring bridges analytical chemistry with real production conditions. While paper specifications can look similar for any supplier, hands-on operators see real differences in material behavior—flow, consistency, and response to solvents. It all comes back to feedback from customers at the bench and the plant, telling us what works on their line, not just in an isolated flask.
Vacuum drying, material transfer, and packing all come under our direct observation. The end result: less variability for every recipient who’s expecting reproducibility day in, day out. We put our name behind every kilogram leaving the plant, since in high-stakes chemical manufacturing trust isn’t given—it’s proven per shipment.
Researchers working at the leading edge of chemical synthesis repeatedly turn to 4-fluoro-2-nitrobenzonitrile as a gateway to complexity. In cross-coupling chemistry, the ortho nitro and para fluoro pattern gives options for nucleophilic aromatic substitution (SNAr), as well as later-stage borylation or palladium-catalyzed cross linking. It’s one backbone for constructing biphenyl motifs seen in sensor technology, OLED intermediates, or photoresponsive compounds. Process chemists value its predictable substitution behavior, which limits wasted material and costly troubleshooting.
We regularly see clients use this product as a protected intermediate en route to amines, amides, or heterocycles, thanks to reliable transformability. Its dual activation—making the ring reactive at targeted positions—allows rapid diversification without excessive byproducts. Those handling kilogram quantities find that solubility in typical organic solvents assists phase separation, cutting time lost during extraction or work-up.
Drug design increasingly looks to fluorine for its power to tweak bioavailability and metabolic fate. Adding a nitro group on top opens up points of attachment for further functional groups, and the nitrile gives chemists options for cyclizations and attachments beyond the reach of more inert aromatics. Over the past decade, the demand for this aryl intermediate grew as more companies explored late-stage fluorination strategies in their pipeline compounds. That trend translated directly into increased quality scrutiny and the need for predictable supply of high-purity material.
We work with synthetic teams who use this molecule at several points along their discovery and optimization efforts. Robust purification methods, reliable supply, and characterization support are critical for every group working on next-generation kinases, GPCR ligands, or other targeted drug candidates. Failures at the material input stage cascade all the way down to the most expensive final runs; a setback in early design from a bad intermediate isn’t something anyone can afford. Those lessons shaped how we manage our production, packaging, and documentation for this product.
It’s not only the pharmaceutical industry investing in new uses for 4-fluoro-2-nitrobenzonitrile. Electronic materials producers pursue aromatic fluoro compounds for high-performance polymer backbones and tailored electronic functions. In OLED or organic photovoltaic devices, the right aryl precursor unlocks electronic pathways inaccessible to unsubstituted or methylated analogues. Here, batch quality can spell the difference between target conductivity or color response and a failed device.
We know from customer feedback in advanced materials that contaminants or inconsistent particle size can lead to inhomogeneous films—costing countless hours in R&D. Our focus on reproducible grinding and sieving enables downstream users to get exactly what they expect on the first attempt. This reduces resource draw in electronic or sensor prototyping, turning what could be project delays into fast results. Serving across industries, we share best practices and gather data from users to tune every run for both main and emerging applications.
With strict global oversight on hazardous synthesis, choosing a manufacturer committed to safety and stewardship is no idle concern. Our processing lines incorporate closed-loop solvent handling and integrated waste minimization. All operators train for careful management of energetic nitro compounds—our site records account for hundreds of safe batch completions without incident. Managing the nitro and cyanide functional groups throughout synthesis and packing reduces long-term risk for both workers and customers.
We don’t leave compliance as an afterthought: our production logs, raw material traceability, and emissions control join analytical records to support customer and auditor requirements. For markets with heightened regulatory oversight—particularly those handling active pharmaceutical ingredients in Europe, North America, or Japan—we supply detailed batch histories and support documentation. Sharing environmental performance and safety track records with customers builds confidence, not just for regulators but for downstream users who value continuous quality.
Years of in-house chemistry went into tightening up yield, reducing impurities, and cutting waste on this molecule. Purification cycles experienced continuous adjustment, upgrading crystallization steps to raise throughput and material purity. Investment in new reactor designs let us fine-tune heat transfer and agitation, which limited the formation of oily or off-color byproducts frequently encountered by less-controlled processes.
No two campaign runs look identical; sometimes raw material lots introduce variations that must be caught early. Our plant chemists work with on-site analytics to respond in real time. These lessons carry forward as we make cycle improvements—from tweaks in solvent composition to implementation of new drying technology that limit exposure and product degradation. Every change cycles through validation with input from ongoing feedback.
A good chemical packed poorly can waste days: caking, moisture ingress, or static buildup create problems at every handling step. From early shipments in basic glass bottles, we shifted to specialized drums and lined containers that block light, moisture, and avoid scuff contamination. Our loading teams operate enclosed feeds, minimizing air exposure and particulate contamination. For sensitive end-users, we offer advanced degassing and inert packing options; for the rest, reliable powder flow means less downtime and easier measuring.
International clients have strict import standards and want assurance on compliance with packaging and labeling. We send samples and full batch code documentation not only for regulatory reasons but because it reflects our commitment to transparency. Each logistic detail gets triple-checked so receivers get material unchanged from our site to their bench.
Every supply disruption, every off-spec shipment taught us that building direct relationships delivers value beyond price. Our staff answer technical queries about reactivity, impurity profiles, or processing compatibilities because we oversee each step and carry the real process data. No question gets deferred to a distant “supplier of record” with only abstract guarantees. We record every batch, every adjustment, and maintain sample retentions to assist with any technical review.
That also means supporting scale-up advice when clients move from grams to kilograms—or pivot from pharma research to pilot agrochemical leads. Product support does not end at the point of sale. Our analytical lab shares spectral data, method development support, and troubleshooting to give clients complete assurance in project-critical steps.
Global chemical supply chains have grown more unpredictable. Rising demand for fluorinated aromatics in specialized sectors increases competitive pressure for consistent supply of critical intermediates like 4-fluoro-2-nitrobenzonitrile. Buyers want more than batch-to-batch reproducibility—they need partners invested in process resilience.
To sustain that, we’ve worked to diversify raw material sources, invest in local purification options, and introduce risk assessments for all major synthetic steps. Automation plays a larger role in both the analytical and production labs to cut the impact of workforce shortages or supply crunches. Knowing which points in the process most affect impurity profiles and reactivity directs investments where they yield the best impact.
We continue to upgrade analytical instrumentation and log reporting, ensuring tighter quality thresholds and faster out-of-spec detection. Sharing data openly with our partners, both up- and downstream, keeps everyone alert to rising standards and emergent risks. The result: a supply of high-quality 4-fluoro-2-nitrobenzonitrile that delivers certainty in a shifting market.
Four-fluoro-2-nitrobenzonitrile stands as a key intermediate only as strong as its manufacturing pedigree. We’ve built years of operational experience into every lot, focusing on the daily discipline that produces chemical precision and reliability. Our direct control over the route, analytics, and packing provides our customers with the certainty needed for confident scale-up, troubleshooting, and innovation.
Every batch record, analytical readout, and customer feedback loop improves the process and builds the experience that sets manufacturing-led suppliers apart from simple distributors. With us, buyers get more than a product; they get the surety of craftsmanship, transparency, and direct expertise—all reflected in the performance and consistency of their key benzonitrile building block.