|
HS Code |
175491 |
| Cas Number | 403-15-6 |
| Molecular Formula | C6H4FNO3 |
| Molecular Weight | 157.10 |
| Iupac Name | 4-fluoro-3-nitrophenol |
| Appearance | Yellow crystalline solid |
| Melting Point | 61-65 °C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=C(C=C1F)O)[N+](=O)[O-] |
| Inchi | InChI=1S/C6H4FNO3/c7-4-1-2-5(8(10)11)6(9)3-4/h1-3,9H |
| Pubchem Cid | 107483 |
As an accredited Phenol, 4-Fluoro-3-Nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical "Phenol, 4-Fluoro-3-Nitro-" is packaged in a sealed 25-gram amber glass bottle with a secure screw cap. |
| Shipping | Phenol, 4-Fluoro-3-Nitro- should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be labeled as hazardous, handled with proper personal protective equipment (PPE), and transported according to local, national, and international regulations for chemicals—preferably as a limited quantity or in specialized hazardous material packaging. |
| Storage | Store **Phenol, 4-Fluoro-3-Nitro-** in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. Protect from direct sunlight and moisture. Ensure proper labeling and restrict access to trained personnel. Use suitable corrosion-resistant shelving or cabinets if required due to its potentially hazardous nature. |
Competitive Phenol, 4-Fluoro-3-Nitro- 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!
Speaking with practical experience in chemical synthesis, we see Phenol, 4-Fluoro-3-Nitro-, also called 4-fluoro-3-nitrophenol, as a clear example of how specialty chemistry flexes to meet research and industrial demand. The product does not fall under the umbrella of everyday phenols. Instead, this compound stands out with its fluoro and nitro functional groups. Production brings a range of technical challenges, but addressing these directly creates a consistent supply with reliable purity—for chemists and process engineers who insist on precision.
The path from raw materials to the final product is exacting. We do not view production simply as a reaction to market requirements, but as a technical exercise that leaves no room for shortcuts. At every batch, tight controls on synthesis temperature and pressure, followed by multi-stage purification, pull impurities below detection limits. HPLC analysis confirms product purity exceeding 99%. The demand for this level of quality never arises from administrative pressure—it stems from real-world failures when off-spec intermediates enter complex processes. We have seen the headaches poor purity causes: lost yields, runaway side reactions, unexpected color formation. Stepping up QC minimizes repeat problems in our own plant and downstream operations.
Shrinking variables makes a direct impact on outcome. Our standard output presents as a pale yellow solid with a melting point falling consistently between 75-78°C. Moisture, even trace levels, invites problems in scale-up so we drive residual water below 0.5% by Karl Fischer analysis. Because the fluoro group’s reactivity is sensitive to both acid and base, our team ensures minimal ionic contamination. Heavy metal checks are not an afterthought—they sidestep catalyst poisoning and corrosion observed by our process engineers in the past. Each batch is characterized fully: melting range, IR fingerprint, NMR confirmation, HPLC chromatogram, and if client protocols require, LC-MS submission. Process transparency does not complicate; it reduces troubleshooting and builds confidence among chemists who look for more than a claims sheet.
Chemically, swapping a hydrogen for a fluorine changes behavior radically. In simple phenols, substitution at the para position means greater electron withdrawal, which influences acidity and the pathways open for downstream modification. Adding a nitro group at the meta position further shifts properties—boosting electrophilic activity, and transforming applications beyond brown bottles and bench-top stock solutions. Many ask about the difference between 4-Fluoro-3-Nitro-phenol and other fluoro- or nitro-phenols. Experience shows that the specific positioning on the ring governs reactivity in cross-coupling reactions and influence on biological assays. Product designers and medicinal chemists have flagged the meta-nitro arrangement as a key intermediate when building more complex structures. Having supplied to both pharmaceutical and pigment research, we understand these are not simple molecules for off-the-shelf use, but require trusted sourcing to maintain process flow.
This compound moves through pipelines mostly as an intermediate. We ship to manufacturers of active pharmaceutical ingredients, specialty agrochemicals, and companies focused on dye research. The main attraction: both fluoro and nitro groups open routes for further transformation, such as nucleophilic aromatic substitution, reduction to amines, or cross-coupling to construct unusual aromatic systems. Chemical engineers value rapid conversion rates and selectivity; we leverage our firsthand knowledge of failed reactions to highlight the necessity of narrow impurity profiles. Several partners—developing new kinase inhibitors and agrochemical actives—have pointed to bottlenecks when their phenol feedstocks arrive with residual ortho isomers. Our control over positional purity, evidenced through batch-by-batch analytical reporting, guarantees the downstream chemistry works as designed.
Over years of hands-on handling, we have witnessed unprotected storage or casual packing negatively impact both shelf life and reactivity. Tightly sealed, low-humidity storage avoids hydrolysis and undesirable polymerization. Mild moisture can disrupt separation of fluoro-nitro-phenols, leading to the loss of batch or the need for secondary processing. Both technical and business losses result. We use aluminum-lined containers, filled and sealed under nitrogen, rather than standard PE bags, a change implemented after early shipping trials let in trace humidity and led to client complaints. Temperature-controlled warehousing, plus real-time humidity tracking, has made the difference between repeat successful deliveries and replacement orders. Safety, too, owes much to proper packing; dust mishandling can result in minor mucous membrane irritation. Industrial users rely on our Material Safety Data for their own training but knowing the nuances of this molecule’s hazard profile comes from years of direct plant experience—not theoretical desk work.
Fielding technical questions from clients gives us constant reason to improve process standards. Early batches often showed small but sometimes process-altering aromatic side products. By directly comparing client HPLC results against our production logs, we pinpointed catalyst sources and modified our reaction vessels’ surface coatings. Our R&D line spends as much time working on detection limits and stability improvements as scaling up output. We do not treat feedback as a suggestion box, but as actionable data. One particular client R&D center approached us about bioassay interference tied to isomeric contamination—our shift to more frequent in-process controls eliminated this concern. The lack of downtime and batch rejection since then matches our own bottom-line aims but aligns with customer value equally.
Demands for REACH or other compliance push manufacturers to document every transfer and storage step. But strict traceability avoids more than paperwork. Tracking starting materials, reaction conditions, and each lot’s analytical result allows swift recall in case of incident, but more importantly, it lets process chemists at customer sites anticipate variability and optimize conditions. Our chain-of-custody protocols were developed after an incident where an upstream change in one reagent led to out-of-spec side byproduct formation—our process logs let the client’s QA and our own team isolate and resolve the issue, minimizing business disruption. The result: buyers know they will not navigate blind corners when new regulatory questions come up.
Scaling production while maintaining high purity represents ongoing challenges. Fluctuations in raw material supply, or minor Tweaks to purification, change the game for downstream partners. Our technical leads meet monthly to review deviations and feedback. Where requests arrive for increased scale, we look to pilot line feedback rather than theoretical runs only. This hands-on mentality keeps the product consistent whether the order is 100 grams for a research customer, or 100 kilograms for a major synthesis campaign. Clients who dealt with inconsistent supply elsewhere have reported missed project milestones. Building and holding a reputation for batch-to-batch consistency matters long after initial delivery.
Calls for green manufacturing shift the focus to both process solvents and waste. Our past operations used more hazardous solvents, and treatment costs spiked, alongside safety risk. Gradual adjustment—without sacrificing purity or recovery—required adopting less toxic options, closed-loop solvent recovery, as well as reducing emissions and byproducts during nitro group introduction steps. Industry-wide, the tension exists between traditional low-cost methods and new regulatory standards. Direct measurement and stepwise change prove more reliable than sweeping overhauls. Our guiding aim: balance chemical performance with real cost and environmental safety, always reporting progress and setbacks with transparency to our customer base.
The demand curve for 4-Fluoro-3-Nitro-phenol ties closely to ongoing innovation in pharmaceuticals and crop science. This is not a generic, always-in-demand product. When particular patent filings or new biological targets emerge, demand spikes—sometimes unpredictably. Our history tells us that only agile production—with the ability to quickly scale up and back down—keeps both the production floor and client projects running smoothly. Attempting to stockpile this chemical, given its sensitivity, leads to increased spoilage and financial losses. Careful alignment of production with real usage rates—guided by ongoing dialogue with buyers—reduces wastage and maintains supply consistency.
All specialty chemicals carry inherent risk from unstable supply chains. The process of sourcing reliable, consistently pure starting materials demands global relationship building. Sudden export restrictions or shifts in freight capacity hit the specialty phenol market as hard as any. We confront these risks through diversified sourcing, backup suppliers, and ongoing validation of incoming raw materials. The cost of a missed lot, should one supplier falter, is much higher than modest spreadsheet savings. This strategy goes beyond our own interests—it feeds directly into project team stability for each partner depending on us for on-time delivery. Every new geopolitical event sharpens our approach; we've shifted raw source partnerships actively in response to prior disruptions, aiming always for steady, predictable flows.
Working with Phenol, 4-Fluoro-3-Nitro-, we've learned that each new application—be it bioactive molecule discovery, pigment intermediate synthesis, or fine-tuned electronic materials development—exposes gaps in general practice and reveals new ways we can strengthen both product and service. What appears as a simple aromatic intermediate on paper turns, in reality, into a high-stakes component for specialized chemistries. Over the course of years, direct engagement with users—hearing pain points, chasing analytical discrepancies, and sandpapering rough spots in production—has shaped our approach to every product run.
It's routine for us to answer direct technical queries from laboratory scientists, field engineers, and process supervisors. These conversations challenge our process assumptions, pushing us to refine every control and analytical checkpoint. We don't view our product as anonymous white powder or a CAS number—it's a working tool for chemists and engineers taking on challenging synthesis problems or building complex molecular structures. Each improvement we deliver—lower trace metals, higher reproducibility, tighter control on isomeric purity—reflects thousands of conversations and hundreds of root-cause investigations from earlier supply runs.
In specialty chemical manufacturing, the story of 4-Fluoro-3-Nitro-phenol highlights the impact of hands-on experience over abstract process charts. What matters most is the working partnership between producer and end user—a relationship underpinned by direct communication, transparent reporting, and prompt, effective adjustment to problems as they arise. Our plant staff, QA chemists, and supply managers invest in each improvement not as a box-ticking exercise, but because a misstep in production or supply would disrupt high-stakes research, production, and innovation across every industry niche this compound touches. This direct, experience-driven approach keeps us moving forward, shaping better processes, tighter products, and closer partnerships with every new batch we bring to market.