|
HS Code |
994206 |
| Chemical Name | 4-Fluoro-2-nitrophenolate |
| Molecular Formula | C6H3FNO3 |
| Molecular Weight | 157.09 g/mol |
| Cas Number | 3113-99-3 |
| Appearance | Yellow crystalline solid |
| Melting Point | 98-102 °C |
| Solubility In Water | Soluble |
| Iupac Name | 4-fluoro-2-nitrophenolate |
| Smiles | C1=CC(=C(C=C1F)[O-])[N+](=O)[O-] |
| Inchi | InChI=1S/C6H3FNO3/c7-4-1-2-6(11,3-5(4)8(9)10 |
| Storage Conditions | Store in a cool, dry place |
As an accredited 4-Fluoro-2-Nitrophenolate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure cap, labeled "4-Fluoro-2-Nitrophenolate, 10g," featuring hazard symbols and handling precautions. |
| Shipping | **Shipping Description:** 4-Fluoro-2-Nitrophenolate is shipped in tightly sealed containers, protected from light and moisture. The substance should be labeled as hazardous and transported in accordance with local regulations. Use secondary containment to prevent spills, and store away from incompatible materials. Ensure proper documentation and safety data sheets accompany the shipment. |
| Storage | **4-Fluoro-2-nitrophenolate** should be stored in a tightly closed container, away from incompatible substances such as strong acids and strong oxidizing agents. Keep in a cool, dry, and well-ventilated area, protected from moisture and direct sunlight. Clearly label the container, and restrict access to authorized personnel. Follow all relevant safety guidelines and local regulations for hazardous chemical storage. |
Competitive 4-Fluoro-2-Nitrophenolate prices that fit your budget—flexible terms and customized quotes for every order.
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Our daily focus as a chemical manufacturer comes down to molecules like 4-Fluoro-2-Nitrophenolate. Behind this name sits a core tool that supports critical work in agrochemical, pharmaceutical, dye, and material science labs. We see the appreciation chemists and researchers have for this product, where reliability, consistency, and clarity matter in every batch. Our team handles 4-Fluoro-2-Nitrophenolate from raw material to finished product, ensuring the properties that make this compound valuable carry over to each user.
4-Fluoro-2-Nitrophenolate, known by its chemical structure as the fluoro-nitro analog of phenolate, sets itself apart through a unique balance of reactivity and selectivity. This compound features a nitro group at the ortho position and a fluoro group para to the oxygen atom, resulting in a molecule that provides predictable electron-withdrawing effects. In practical terms, this means that the reactivity profile is both strong and manageable, allowing for efficient coupling, aromatic substitution, and downstream synthesis without surprises.
In our facility, we produce 4-Fluoro-2-Nitrophenolate as a sodium salt in purified, free-flowing powder. We achieve this with tight process controls and constant attention to detail, both in reaction conditions and in purification steps. Water, solvent, and impurity content are monitored by a QC team. This approach means that users see clean single spots in TLC and sharp peaks in NMR, which simplifies every analysis.
Across years of manufacturing, we have seen that even small deviations in the preparation can shift outcomes for end users. So, we monitor details such as melting point, particle size, and trace contaminant levels. Typical material from our lines comes with a guaranteed purity exceeding 98%, as determined by HPLC, and with moisture content carefully held below 0.5%. This isn’t marketing—it is a direct response to what research chemists report back. When they want to scale up a route or try out a new transformation, confidence in each reagent saves time and resources.
Maintaining batch-to-batch reproducibility is just as important as single-batch purity. The sodium salt form lends itself to easier handling and dissolution in both water and polar organic solvents, making it suitable for preparative-scale or multi-step syntheses. This stability reduces degradation under typical laboratory storage, increasing shelf life and keeping workflows productive. We track stability for every lot, keeping records that reveal how the material holds up over six months, one year, and longer.
What sets this product apart from other nitrophenolates or even unsubstituted phenolates is the specific interplay between fluoro and nitro substituents. The electronically-deficient ring opens possibilities for targeted SNAr (nucleophilic aromatic substitution) reactions, which can proceed cleanly under conditions where analogs give messy or incomplete conversions. Users select this compound when they need more predictable results in substituting halides, amines, or other nucleophiles onto the aromatic core.
Other nitrophenolates lack the same degree of tuning, as the absence of the fluoro group reduces their ability to support selective reactivity. Meanwhile, simple phenolates don’t deliver the nitro group’s electron-withdrawing influence. In comparative screening, our customers often report that reactions featuring 4-Fluoro-2-Nitrophenolate give improved regioselectivity and reduced by-product formation. For those synthesizing building blocks or active intermediates in a regulated or time-sensitive environment, these differences aren’t subtle—they affect yields, waste generation, and downstream purification burdens.
Pharmaceutical companies, contract research organizations, agrochemical innovators, and dye manufacturers have all found a place for this chemical in their toolkits. Medicinal chemistry teams lean heavily into the electron-poor nature of the ring to unlock selective scaffolding routes or to prepare derivatives that resist oxidative degradation. In agrochemical development, it’s valued for the way it helps introduce substituents that improve biological compatibility and environmental safety.
Our technical team often fields pre-purchase questions about scaling from grams to kilograms. We’ve put years of effort into maintaining consistent reaction conditions at both R&D and pilot scales. For larger orders, we document every upstream decision—starting material lot selection, reaction monitoring, filtration, and isolated yield optimization. Our feedback loops come directly from customer experience and our own process analytics, not generic trade reports or secondary sources.
Many of our regular customers use 4-Fluoro-2-Nitrophenolate as a platform to test new ligands, catalysts, or protective group strategies. The molecule’s clean background and well-understood reactivity removes a source of experimental “noise” that often costs weeks or months in project timelines. We’ve been approached to troubleshoot cases where previous suppliers introduced trace metal contaminants or supplied material that degraded on standing. We share chromatograms and spectral data to highlight the purity side-by-side with historical supplies. Side-by-side testing under real lab procedures, not just written-out specs, drive our improvements.
Sometimes purchasers need to push the boundaries—late-stage functionalization, microwave-assisted processes, or non-conventional solvents. Our plant’s flexibility supports custom drying, particle size control, or alternative counter-ion preparation. We have adjusted process parameters to help customers develop easier filtration, lower residual sodium, or better compatibility with automation equipment. The feedback loop runs both ways—if a formulation or application exposes a limit, we adapt with upstream modifications rather than offering workarounds or band-aid solutions.
Each shipment of 4-Fluoro-2-Nitrophenolate undergoes compliance screening for restricted impurities. Our facility tracks emerging regulations in key destinations, not just by reading but by direct collaboration with safety assessors and regulators. When new analytical methods emerge for trace contaminants or persistent by-products, our labs re-validate test suites so buyers in every region get defensible documentation. We build compliance into the daily routine, making it easier for users to clear regulatory audits and keep projects moving.
Waste minimization is a growing concern. We focus on solvent recovery, recycling, and yield improvement throughout manufacturing—efforts that cut down not just hazardous waste, but also cost and turnaround time. While some makers tout a green label, we invest in process changes that show up on waste manifests sent to local authorities. The chemistry beneath 4-Fluoro-2-Nitrophenolate lends itself to clean synthesis, but years of incremental refinement have lowered water and solvent input while raising isolated yields.
Inside the plant, we treat this compound with a mindset shaped by repeated experience. The crystalline sodium salt handles without dusting, pours evenly, and stores with little tendency to cake or absorb moisture. This consistency pays off when labs work under time pressure or in shared spaces. Each drum leaves our site with seals and tamper-evident packaging—a step that sounds basic, but one repeatedly requested by major clients who have encountered counterfeiting or mix-ups.
Buffering moisture control during production minimizes hydrolysis, ensuring the shelf-life measured in years, not months. Some partners request smaller packaging or inert-atmosphere filling, and we have set up lines to make this practical without slowing down normal output. We see fewer customer returns or deviations when these packaging instructions are matched to precise real-world use cases—high-humidity labs, variable temperature controls, or field use for on-site application development.
One of the clearest signals from our user base has involved ease of integration. Typical customer feedback highlights reduced impurity carryover into post-reaction workups when using our product versus competitors’ analogs. For researchers aiming at patent filings or regulatory dossiers, low impurity profiles translate to accelerated filings and lower risk of repeat synthesis. Recent advances in purification technology have let us drop organic solvents from the final wash, reducing possible trace contamination further. These aren't just process tweaks—they arise directly from hands-on chemists confronting practical challenges.
In rare cases, users report higher-than-expected reactivity with especially potent nucleophiles. We collaborate to map possible countermeasures, from modifying the addition sequence to adjusting pH or switching solvents. Our teams treat each anomaly as unique instead of giving canned responses, a strategy that wins repeat business and builds real trust. This cycle of problem-solving shapes every improvement made to our process.
Manufacturers and lab managers often ask how 4-Fluoro-2-Nitrophenolate stacks up against compounds such as 4-Nitrophenolate or 2-Fluorophenolate. Both have served their place in synthesis, but our feedback shows users face challenges with lower selectivity and batch inconsistency. The presence of both fluoro and nitro substituents stabilizes the anion, improving control in substitution reactions. This stability reduces side product formation, where mono- or unsubstituted phenolates lead to broader impurity profiles.
Industries with extensive regulatory oversight, such as pharma and crop protection, show preference for more predictable results and reduced analytical troubleshooting. Techniques such as LC-MS and qNMR make even small differences in impurity levels visible. We have benchmarked side-by-side reactions—same conditions, same scale, different phenolate salts. The reaction using 4-Fluoro-2-Nitrophenolate routinely comes in with higher isolated yields, sharper melting points, and easier workups, shaving hours or days off development time.
Material science groups, particularly those designing functional dyes or pigments, value the chromophore modifications made possible by this compound compared to basic phenolates. The inserted fluoro and nitro functionalities enhance color fastness and resist photooxidation. These aren’t just features—they allow new applications, from electronics to printable coatings, where product reliability carries a premium.
Markets never sit still, and neither do the demands on intermediates like 4-Fluoro-2-Nitrophenolate. Researchers continue exploring new coupling partners, greener solvent systems, and safer downstream processing. We’re investing in analytics—routine checks with high-resolution mass spectrometry, expanded impurity libraries, and periodic cross-checking with external labs. This helps us flag issues early, before customers see even small deviations in their workflows.
Requests for custom grades have increased. Sometimes a project calls for different particle sizes or alternate counter-ions. Some teams want more detailed characterization, beyond what appears on an ordinary CoA. We have built protocols for custom requests, relying on the robust baseline process and dedicated technical support. The extra steps—from recrystallization to spectral confirmation—aren't glossed over as "special" but incorporated into a living process map used for continuous learning.
We share summaries of key findings with purchasing and technical stakeholders, both successes and occasional setbacks. Challenges that crop up across customer projects often point to new opportunities. For example, a spike in demand for high-purity intermediates in bioconjugation pushed us to refine our final filtration method. Feedback loops like these create improvements that become the new standard, not just a one-off fix.
We operate with the attitude that every insight—from users, technical staff, or regulators—drives how we make, qualify, and deliver 4-Fluoro-2-Nitrophenolate. The close relationship between bench chemistry and plant operation cements quality at a granular level. Each modification, whether driven by equipment upgrades or new analytical checks, feeds directly into a process log shared by every member of the production chain.
We believe the best results come from direct manufacturer engagement. Not only do we supply high-grade 4-Fluoro-2-Nitrophenolate, we track how evolving chemical challenges prompt process improvements. Longevity in supply relationships lets buyers plan projects in confidence, knowing last year’s lot matches this year’s—and any changes reflect new value, not hidden risks.
From first inquiry to follow-up questions months later, our team commits to straightforward, transparent guidance. Issues around substitution chemistry, purification logistics, or raw material changes aren’t kicked down the line or answered with boilerplate. Instead, we resolve them through face-to-face technical conversations, sharing chromatographic and spectral details openly. The follow-through keeps customers coming back not only for product, but for partnership.
In summary, 4-Fluoro-2-Nitrophenolate stands as a workhorse for researchers and process chemists tackling difficult synthetic challenges. This product represents the best of what large-scale chemical manufacturing can deliver—batch consistency, predictable reactivity, and user-driven evolution. We appreciate the trust our clients place in us and return it with every drum, package, and document we ship.
Production never stands still. Each new question, trend, or challenge refines our understanding and improves our output. We remain focused on providing 4-Fluoro-2-Nitrophenolate at a standard that matches the ambition and precision of our customers, ready to solve today’s problems and anticipate tomorrow’s needs.