|
HS Code |
458332 |
| Chemical Name | 3-Fluoro-4-Nitrophenol |
| Molecular Formula | C6H4FNO3 |
| Molecular Weight | 157.10 |
| Cas Number | 98991-39-2 |
| Appearance | Yellow solid |
| Melting Point | 98-102 °C |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
As an accredited 3-Fluoro-4-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 g, tamper-evident seal, white screw cap, hazard label displaying “3-Fluoro-4-Nitrophenol,” batch and expiry details. |
| Shipping | 3-Fluoro-4-Nitrophenol is shipped in sealed, labeled containers, protected from moisture and light. It typically requires ground transportation under standard chemical handling regulations. Ensure compliance with local and international guidelines for hazardous materials, including proper documentation. Handle with care, using appropriate personal protective equipment (PPE) during receipt and unpacking. |
| Storage | 3-Fluoro-4-nitrophenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances like strong oxidizers or bases. Avoid moisture and sources of ignition. Label clearly and handle using appropriate personal protective equipment to prevent exposure. Store in accordance with all applicable local and national regulations. |
Competitive 3-Fluoro-4-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Over two decades of dedicated synthesis and product refinement have shaped our approach to manufacturing 3-fluoro-4-nitrophenol. Tightly controlled process parameters and stringent in-house QC have given us a reliable, reproducible material that meets the real requirements of industrial research and downstream production. From the earliest years, we worked direct from phenolic feedstocks, where purification hurdles taught us to favor lines that deliver consistency and minimize batch-to-batch drift.
Identified by CAS number 403-15-6 and molecular formula C6H4FNO3, our 3-fluoro-4-nitrophenol is best described as a pale yellow crystalline solid, available in both research and production-scale quantities. Typical lots reach 99% minimum purity as verified by HPLC and NMR, with water kept below 0.2%. Each packed drum and jar has unique lot-level records, supporting full traceability from raw phenol fluorination to finished packaging.
Over the years, we have supported customers across pharmaceuticals, agrosciences, colorants, and specialty intermediates. For many, especially in life science applications, the chief value of 3-fluoro-4-nitrophenol lies in its capability as a versatile intermediate. The nitro-phenol backbone, activated with precise fluorine placement on the aromatic ring, lends itself cleanly to nucleophilic aromatic substitution and further downstream transformations.
In the early days of providing 3-fluoro-4-nitrophenol, our chemists ran pilot scale-ups for both academic labs and process development groups. Most were searching for cutting-edge fluorinated building blocks for active pharmaceutical ingredients or novel agrochemical actives. Trace impurities, especially unreacted starting materials or regioisomeric by-products, turned out to be persistent troublemakers during coupling reactions and scale-up. Quality mattered, since downstream failures always tie back to raw material variability.
One important lesson repeated constantly: introducing a single fluorine atom at the meta-position alters the electron density profile enough to drive selective reactivity in processes like nucleophilic aromatic substitution or Suzuki-Miyaura cross-coupling. Experienced process chemists know that side reactions amplify when starting material carries trace residues. Consistency in 3-fluoro-4-nitrophenol supports fewer surprises during method scale-up, saving development time and improving product yields for everyone in the chain.
Many commercial-scale customers trust direct-from-manufacturer sources for exactly this reason. Synthetic pathways involving 3-fluoro-4-nitrophenol, such as formation of fluorinated ethers and phenoxy linkages, demand confidence in the feed material. We realized early that outsourcing quality control or partial production led to more rework and higher costs. Integrated production allows us to intervene at any synthesis stage, ensuring composition and minimizing batch deviations.
Pharmaceutical research and agrochemical companies have routinely used our 3-fluoro-4-nitrophenol while developing advanced intermediates. Years ago, one major pharmaceutical group scaled up a library of substituted aniline derivatives starting from our material. They initially sourced small batches for discovery screening, but after pilot plant results established synthetic reliability, they requested multi-kilogram quantities delivered under audit control. In their campaign, minor lot-to-lot inconsistencies with a competing supplier forced multiple process deviations. Switching all future lots to our single-origin product eliminated significant lost productivity and minimized analytical troubleshooting in downstream steps.
Another agriculture client used our material for fluorinated phenoxy herbicide synthesis. Late-stage process validation identified halide contamination in a separately sourced product, which led to excessive by-product formation during O-alkylation. By shifting to our strictly isolated and purified 3-fluoro-4-nitrophenol, their downstream crystallization yields improved by over 8%, reducing waste volumes and saving thousands in post-processing labor months later.
Both clients valued consistent melting point, guaranteed purity, and batch-to-batch homogeneity. Beyond those numbers, what matters most is transparency—real technical support direct from chemists who actually work with the material, not intermediaries with no process details.
Our expertise isn’t limited to a single substituted phenol; we manufacture a range of fluorinated aromatic nitro compounds and have seen the subtle impact each substitution brings. Some customers compare 3-fluoro-4-nitrophenol to its close relatives, like 4-fluoro-3-nitrophenol or 2-fluoro-4-nitrophenol. Chemically speaking, shifting the fluorine from the para to the meta or ortho position alters resonance and inductive withdrawal effects. This changes both reactivity and downstream transformation efficacy.
In coupling and nucleophilic reactions, our chemists have found that the meta-fluorine of 3-fluoro-4-nitrophenol selectively activates the aromatic system while suppressing side reactions that trouble more symmetrical isomers. We regularly analyze isomeric purity using GC-MS and NMR to qualify every lot before shipment. This attention to chemical detail pays off in fewer downstream filtration and purification headaches.
Some applications, particularly in medicinal chemistry, deliberately seek the unique pharmacophoric effects conferred by a 3-fluoro substitution rather than the alternatives. Fluorine’s presence at this site can block metabolic hydroxylation or direct bioisosteric properties, impacting both the metabolic stability and receptor binding profile of new drug candidates. Our own collaborations with medicinal chemists have confirmed that even small changes in substitution pattern can make or break an entire compound class.
In our production facilities, we start with safer, controlled fluorination of selected phenolic precursors. Temperature, solvent, and timing must remain tightly managed—anything less produces side isomers or incomplete conversion, which spells problems for the next user. Our technical teams long ago settled on a two-stage purification setup, initially extracting with phase-separation and solvent distillation, then running column chromatography with precisely adjusted eluents. Each lot receives analytical checks before and after drying, using both HPLC and detailed NMR analysis.
We don’t rely on a single purity metric. Our standard reports include full spectral data, chromatograms, and impurity profiling with cutoff triggers for known side products such as 2-fluoro-4-nitrophenol and unreacted nitrophenol. Material departing the plant receives batch-sequenced packaging seals, which allows downstream users to track issues back far more precisely than with aggregated distributor stock.
Waste reduction remains a top priority. We have incrementally shifted solvents over the years to favor recyclability and operator safety. Recycling nearly 80% of solvents and reprocessing off-spec side fractions helps to keep both our costs and environmental impact under tighter control.
Customers often ask about the true advantages of direct-from-source chemical manufacturing. Buying 3-fluoro-4-nitrophenol from a non-manufacturer leaves too much in the dark—original origin can get lost, storage conditions may drift, and lot-level deviations become harder to troubleshoot. As a manufacturer, every container shipped bears our own record of production and inspection, backed by a technical team able to respond with synthesis, purification, and application-specific knowledge.
Some labs, frustrated by delays from third parties, turned to us for direct response in handling complaint batches. Full root cause analysis—often extending back to raw material lots, filtration conditions, or storage temperature logging—became possible only with tight vertical integration. For scale-up projects facing regulatory audits, traceability isn’t just a quality point; it’s a business-critical need. We hold years’ worth of batch histories for every intermediate, allowing us to respond to requests for retrospective documentation that many trading intermediaries struggle to provide.
Bulk users sometimes push for cost savings by testing multiple suppliers, only to find that minor impurity drifts crash harder in multi-ton production lines. We’ve seen cGMP and ISO audit teams quickly pick up on missing documentation chains, leading to serious delays during pharmaceutical registration. For each drum and jar leaving our site, the full documentation follows, so there are no black holes in the supply history.
As more companies investigate fluorinated phenolic compounds for specialized applications, demands grow stricter. Pharmaceutical projects no longer accept vague reference standards—they expect carefully validated spectra, impurity profiles, and stability data. Customers in Europe ask for complete REACH registration details, impurity breakdowns, and supply chain risk mapping. Responding to those requirements, we continually update our in-house testing protocols, collaborate with client QA teams, and adapt packaging to the needs of long-distance transport or sensitive handling.
Open discussion with researchers and process engineers influences the way we improve 3-fluoro-4-nitrophenol production. New reaction sequences in bioactive molecule development require trace moisture content below 0.10%. Some customized lots now come under argon or nitrogen blanket packaging, preventing degradation before formulation labs access the compound.
We’ve encountered growing interest from material scientists pushing for fluorinated precursors in OLEDs, specialty polymers, and electronics coatings. Their requirements call for new analytical proxies—trace chloride and sodium content, specific particle size distributions, and extreme long-term stability. Where those needs match our purification and quality control infrastructure, we already deliver. In unusual cases, we tinker with the process route or carry out contract-based custom manufacturing runs.
Scaling up 3-fluoro-4-nitrophenol manufacturing brings learning opportunities. Early on, we encountered issues such as tool corrosion from aggressive fluorinating agents or unexpected exotherm during the nitration step. Modernization of reactors, installation of controlled feeding systems, and round-the-clock environmental monitoring have greatly reduced batch deviations and personal risk. The best process remains flexible enough to change as new purity or regulatory hurdles arrive.
Looking back, we see value in the trials and troubleshooting that came from direct manufacturing experience. As regulatory oversight tightened on both product quality and environmental management, we made the choice to bring more analytical capacity in-house. Now, qualification steps for every lot include GC-MS for trace impurity detection and ICP-MS for metals analysis. This level of direct oversight grows from hard experience with both regulatory and end-user demands.
Genuine commitment to continuous improvement shapes every aspect of our 3-fluoro-4-nitrophenol offering. Process teams share findings with downstream users, work with external labs to benchmark product performance, and actively solicit on-site audits.
Practical handling knowledge also matters. Our technical staff provides guidance on safe manipulation, packaging, and storage—knowledge rooted in real-world experience handling bulk and small-lot shipments. Years of shipping to varied climates and conditions around the globe taught us to anticipate issues like moisture ingress or contamination from improper warehousing. We offer tight-seal, moisture-resistant HDPE jars for lab quantities and metal-lined drums for industrial consignments.
Technical consultations often begin even before an order. Compound compatibility, shelf-life concerns, application-specific purity, or request for retained reference samples all get addressed by chemists with hands-on synthesis and purification background. We keep backup retain samples from every lot produced, supporting both customer audit needs and troubleshooting in long-term projects.
Shipping logistics receive the same attention to detail as synthesis. Temperature controls, customs documentation, danger goods declarations, and even labeling formats are constantly reviewed to meet rapidly changing destination country requirements. Every metric and observation arising during batch production, filling, and dispatch is logged and retrievable.
Fluorinated aromatic compounds deserve special attention in both manufacturing and downstream use. Our site invests steadily in air and liquid waste capture, solvent recovery, and operator safety. As demand grew, we moved beyond baseline local requirements to pursue broader environmental impact reviews, including life cycle analysis for our main starting materials.
Customer audits examining exposure controls, fugitive emissions, and off-site recycling options welcomed transparent documentation and repeatable procedures. For critical customers in pharmaceuticals and advanced materials, this scrutiny often provides a deciding factor in long-term partnership.
Internal training and robust protocols around handling nitrogen dioxide and related reagents keep our team safe and ensure confidence from users concerned about both workplace and final product safety.
Choosing 3-fluoro-4-nitrophenol from a direct manufacturer with deep experience brings advantages in both technical performance and peace of mind. Every year, customer queries introduce us to new reaction systems, emerging applications, and unexpected synthesis challenges. Many of our best process improvements and analytical simplifications came from shared problem-solving with users facing tight project timelines or escalating analytical requirements.
We avoid jargon and deliver honest, direct technical answers. Our feedback cycle between production staff, analytical chemists, and customers brings to life the value of hands-on experience that no amount of catalog browsing or distributor-led purchasing substitutes. 3-fluoro-4-nitrophenol production, rooted in decades of focused process development, stands as an example of what careful, manufacturer-driven chemical supply can achieve.