|
HS Code |
665132 |
| Chemical Name | 4-Fluoro-3-Nitrophenol |
| Molecular Formula | C6H4FNO3 |
| Molecular Weight | 157.10 |
| Cas Number | 403-51-8 |
| Appearance | Yellow crystalline powder |
| Melting Point | 102-106°C |
| Density | 1.57 g/cm3 |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 14235 |
As an accredited 4-Fluoro-3-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled “4-Fluoro-3-Nitrophenol, 25 g,” with hazard symbols, batch number, and sealed with a tamper-evident cap. |
| Shipping | 4-Fluoro-3-Nitrophenol is shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be labeled according to hazardous material regulations and handled with care to prevent leaks or spills. Shipping typically complies with international regulations for chemicals, using appropriate packaging to ensure safety during transit. |
| Storage | 4-Fluoro-3-Nitrophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from incompatible substances such as strong oxidizing agents and bases. Store at room temperature and protect from moisture. Appropriate chemical safety labeling and secondary containment are recommended to prevent accidental release or exposure. |
Competitive 4-Fluoro-3-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Years spent on factory floors and in pilot labs have shown us that every synthetic challenge carries its own set of quirks. 4-Fluoro-3-Nitrophenol (CAS 403-47-4) stands out for chemists who chase both selectivity and practicality in their routes. This specialty intermediate, labeled in our portfolio as 4F-3NP, did not earn its reputation by chance. Manufacturing it takes a carefully designed process, with controlled conditions for substitution and nitration to prevent unwanted byproducts and maintain batch-to-batch reliability. We received early feedback from the pharmaceutical sector about impurities affecting yields and spectra in final actives, which pushed us to push further. Years of improving the protocol have produced a material that customers now rely on for clean downstream transformations.
Those who spend long hours working on scale-up research know the pain that comes with variable raw materials. Shifts in melting point, minor discolorations, or varying impurity profiles can derail downstream processing. Standardization matters far more than spec sheets suggest. Our 4-Fluoro-3-Nitrophenol presents as a pale yellow solid that reflects careful handling and purification. Strict control over process temperatures, solvent systems, and real-time impurity monitoring have become a regular part of our daily routine. We hold off releasing any product until GC and HPLC readouts match the standards developed in analysis with our long-term partners. Tightness in the melting point range brings steady crystallization and good filtration for customers running multi-step sequences, especially at a pilot or commercial scale.
Chemists aiming to make complex molecules need building blocks with the right mix of activity and stability. Adding a fluoro group at the para position to a nitro group brings both new reactivity and valuable physicochemical properties. In our own process development work, we’ve seen that the fluorine atom not only tweaks electronic properties but helps mediate reactions as a directing group. The nitro group at position 3 brings additional utility, providing entryways into nucleophilic aromatic substitution, reduction to amines, and further elaboration. Those who prefer phenolic groups for late-stage diversification appreciate having this combination on hand, especially when modern synthesis pushes functional group tolerance. Unlike many simple nitrophenol analogs, our 4-Fluoro-3-Nitrophenol gives added reaction handle versatility with manageable stability, so customers spend less time troubleshooting and more time advancing their projects.
End uses for this molecule often reveal themselves through customer questions and process feedback. In medicinal chemistry, more groups pursue early-stage SAR around fluoro-nitro aromatics. Some use our 4F-3NP as a starting point to build kinase inhibitors and CNS-binding modulators, taking advantage of increased bioavailability the fluoro substituent brings. Custom peptide and heterocycle synthesis teams often use the phenolic oxygen to tether linkers or as an anchor for library diversification. Agrochemical projects favor this intermediate for its modularity, tailoring herbicide or fungicide profiles with the combined electron-withdrawing properties of both substituents. R&D teams in dye and pigment chemistry have reported using this product to tweak hue and fastness, capitalizing on the altered chromophore achieved through dual substitution. Downstream users carrying out nucleophilic substitutions or reduction-to-amino transformations regularly confirm lot-to-lot reliability after purification, giving us constant feedback on refinements and what works in practice.
The phenol derivatives available in industry may look similar in catalog listings, but hands-on work reveals hidden contrasts. We learned early not to trust “colorless” or “purity” labels until heavy analysis proved otherwise. Commercial nitrophenols without fluorination run risks of oxidation or intractable side-residues, making scale-up more stressful and potentially limiting product shelf stability. The specific substitution at 4-fluoro and 3-nitro delivers a happy medium by balancing reactivity and compatibility with modern synthetic strategies.
4-Fluoro-3-Nitrophenol resists unwanted polymerization seen in some multi-nitro phenols, thanks to optimized conditions in our synthesis that minimize overnitration and maintain strict control over the environment. Standard para or ortho-nitrophenols lack the breadth of reactivity; monofluorinated analogs without the nitro unit miss out on the versatility desired in functionalization steps. For users aiming for amine, ether, or cross-coupling derivatives, our product gives multiple synthetic entry points—without risking an unstable or excessively reactive starting material.
We support both research benchwork and commercial ambition. For those transitioning from grams to tens or hundreds of kilos, our methods have grown alongside customer demand. Over the years, we moved from manual batch methods to automated reactor control, integrating cooling and addition rates that minimize exotherms and support process safety. On a commercial line, consistent handling of corrosive fluorinating agents and nitration mixtures keeps both quality high and safety visible. Teams needing tens or even hundreds of kilos no longer wrestle with batch failures caused by uncontrolled addition or non-uniform heat flow. Documented change control and process safety checks underlie every run, informed by lessons learned during hundreds of successful campaigns.
Technical support doesn't stop at the point of sale. Our product development chemists field regular questions about purification, analytical fingerprinting, and outgassing during solid formulation. We’ve helped customers optimize crystallization to reduce product loss, suggesting solvent systems that keep yield up and labor hours down. This only happens by carrying knowledge forward from our own manufacturing floor—details like optimal shelf conditions or best filtration methods.
The impact of specialty chemical production goes beyond product yields. Over time, stricter environmental and safety regulations changed how we handled energy balance, effluent, and reagent recovery. 4-Fluoro-3-Nitrophenol production presents the usual challenges: handling hazardous starting materials, containing nitration byproducts, and managing fluorinated wastes. We addressed these realities by tightening process controls, introducing closed-system operations, and capturing emissions into properly engineered scrubbers. Regular audits and process hazard reviews keep our teams accountable and support compliance with both local and international guidelines.
As end users face their own compliance hurdles—RoHS, REACH, or custom in-house green chemistry rules—our experience smoothing regulatory approval paths for more complex actives proves an asset. Product traceability extends from sourcing of raw materials to lot-specific batch records, so every delivery comes with an auditable history. Customers often ask about lifecycle impacts; ongoing process optimizations target solvent reduction and re-use, driving down waste and cost for everyone in the chain. Our commitment to reducing hazardous discharges and improving energy efficiency runs through our production decisions, not just our marketing.
Every production campaign brings its own set of headaches. Shifts in raw material availability, subtle changes in reagent quality, or temperature swings in shipping can make or break product integrity. We’ve seen lots show up at customer sites with minor discolorations or off-odors if shipping and storage conditions weren’t nailed down. Early on, we discarded subpar batches and revised transit packaging to keep out moisture or oxygen, which could trigger slow degradation for sensitive phenols.
More importantly, maintaining customer trust means quick and honest responses to out-of-spec situations. We document the details of every deviation and communicate fast to downstream users about what happened and how we corrected process errors. It’s easy to claim “no batch failures,” but real-world production produces the occasional issue. Transparent exchange and fast replacement prevent lost time at the client end. Over years of operation, these details build a track record that enables clients to rely on our 4-Fluoro-3-Nitrophenol and plan their research with confidence.
The real work doesn't stop with a high-purity drum at the loading dock. Our technical team supports scale-up scientists with practical data: solubility in common solvents, stability under light and heat, and compatibility with downstream reagents. Customers producing grams for lead optimization often ask about solvent purification, air sensitivity, or long-term storage. Users at the plant level want strategies for process integration or waste minimization. Our answers come directly from what worked—and didn’t—on our own lines, which saves others from repeating avoidable missteps.
For some, 4-Fluoro-3-Nitrophenol simply opens up a usable synthetic window; for others, it means shortening their pathway or improving the efficiency of their transformations. We regularly partner with research and process teams exploring new reactivity, supplying custom analytical results or even alternate lot samples tailored to their application. When customers seek deeper engagement, we provide recommendations for protective equipment, secondary containment, or in-process monitoring, all based on our factory experience. This technical backbone, more than any catalog claim, holds together our long-term partnerships.
Much of what sets this product apart has come from listening. Real-life case studies end up shaping our process improvements and final product attributes. Years ago, one customer struggled with poor crystal growth, reporting processing delays. Together, we found a solution with a subtle tweak to crystallization solvent, giving better recovery and batch-to-batch appearance. Feedback on solubility profiles or preferred particle size distributions guided our switch to gentle drying and sieving, helping avoid fines or oversized chunks that clog feed lines on commercial reactors. Practical challenges—clumping in high-humidity environments, incomplete transfer in filters, or off-gassing during formulation—are never theoretical in our factory.
By working alongside R&D and production teams, we learn about emerging needs for materials with specific impurity thresholds, or formats suitable for continuous feed systems. This close technical connection keeps our 4-Fluoro-3-Nitrophenol more than just a line on a catalog; it forms a foundation for robust and agile process chemistry in many sectors.
Customers often see their needs change over the course of a multi-year relationship. Market conditions, new regulatory hurdles, or shifts in global supply can force a sudden transition. Our philosophy centers on candid technical discussion, prompt response to any incident, and willingness to adapt our offerings to solve real challenges. By sharing timely data on process changes or anticipated lead times, we help clients plan their own logistics and project milestones. Missteps get addressed directly, and product improvement plans reflect both internal continuous improvement and the evolving realities of our users worldwide.
Every lot leaving our plant reflects a commitment to scientific rigor and operational responsibility. We do not hide behind polished brochures or empty claims. By surfacing both the strengths and limitations of our product in real language, we build the kind of confidence that keeps our 4-Fluoro-3-Nitrophenol integral to critical projects, large and small.
Success in making superior 4-Fluoro-3-Nitrophenol owes far more to daily problem-solving than to any fixed recipe. We see this molecule continuing to support new synthetic methods, as chemists ask more from their building blocks—better functional group compatibility, cleaner transformations, less environmental and safety overhead. The pressure to innovate will only grow alongside stricter rules for waste and emission controls, from our factory site to our customers' plants.
Our investment in cross-functional teams ensures that feedback loops from real applications constantly patch back into manufacturing. Product passports, live inventory tracking, and advanced analytics let us share vital information on shelf life, solubility, or degradation pathways instantly. Upgrading process controls, introducing real-time monitoring, and collaborating on greener chemistries are all integral to pushing the limits of what advanced intermediates can provide.
Working as a chemical manufacturer brings daily exposure to evolving needs for reliability, compliance, and performance. These demands, more than any sales talk, drive how we make and deliver our 4-Fluoro-3-Nitrophenol. The shared goal—giving scientists and process teams worldwide a dependable, usable intermediate for the next breakthrough—keeps us in constant motion, pushing for solutions that transform synthetic chemistry from the bench to the plant.