|
HS Code |
718559 |
| Chemicalname | 2-Fluoro-4-Nitrophenol |
| Molecularformula | C6H4FNO3 |
| Molecularweight | 157.10 g/mol |
| Casnumber | 700-37-8 |
| Appearance | Yellow solid |
| Meltingpoint | 106-109°C |
| Density | 1.56 g/cm³ (estimated) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1O)F)[N+](=O)[O-] |
| Inchi | InChI=1S/C6H4FNO3/c7-5-2-1-4(9)3-6(5)8(10)11/h1-3,9H |
As an accredited 2-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 grams, tightly sealed with screw cap. Label displays chemical name, hazard warnings, supplier details, and batch number. |
| Shipping | **2-Fluoro-4-Nitrophenol** is shipped in sealed, chemical-resistant containers, clearly labeled with hazard information. It is transported according to regulations for hazardous materials, typically under ambient conditions, and with proper documentation. Precautions are taken to prevent exposure to heat, moisture, and physical damage during transit, ensuring safe handling and delivery. |
| Storage | 2-Fluoro-4-nitrophenol should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, well-ventilated area, separate from incompatible materials such as strong oxidizers or bases. Use appropriate chemical storage cabinets and ensure the area is clearly labeled. Always follow safety precautions and regulatory guidelines for hazardous chemical storage. |
Competitive 2-Fluoro-4-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Producing specialty chemicals demands more than technical formulas; it draws on proven methods, close process oversight, and an understanding of what our customers need on the ground. 2-Fluoro-4-nitrophenol (CAS 403-15-6), as a unique aromatic intermediate, requires such attention from the moment raw materials arrive through each step of synthesis and purification.
Our 2-fluoro-4-nitrophenol is synthesized through a controlled nitration of fluorophenols, followed by precise purification and systematic testing after crystallization. The finished product consistently appears as a yellow crystalline powder, reflective of its high purity. Purity levels, batch after batch, are measured by modern chromatographic techniques, reaching not less than 98% GC area, often surpassing this due to attention during the last steps. Moisture and volatile content remain under 0.5% as measured by Karl Fischer titration, supporting storability and reliability in downstream applications.
Melting point falls in the 75-79°C range, and this thermal behavior matters for users planning scale-up into downstream coupling, etherification, or protection steps. Particle size is monitored but not heavily modified at our site, because most requests in catalogs and custom batches ask for naturally occurring crystal habit, rather than micronized or granulated forms.
2-Fluoro-4-nitrophenol occupies a critical place in the toolbox for synthesizing more complex molecules. It serves in the construction of fluoro-substituted aromatic compounds, advanced agrochemical intermediates, and pharmaceutical scaffolds. In our experience, consistent product quality directly affects coupling reactions, such as those using palladium catalysts. Incomplete purification or irregular byproduct content causes problems in complex step-up synthesis—customers who push for high-yield batch reactions verify this in pre-purchase evaluations. Our control over each stage of production, including trace metal analysis, reflects feedback from formulators who report issues linked to catalyst poisoning by trace iron or copper.
Over the years, research institutions and process chemists have selected this intermediate for developing structure-activity relationship libraries and for installing specific functional groups at the 4-position to modulate pharmaceutical properties. Granularity and ease-of-handling are reported less frequently as obstacles than the ultimate freedom from halogenated or unconverted phenol isomers.
Not all sources produce the same 2-fluoro-4-nitrophenol. Our entire process was refined to prevent ortho/para isomer contamination, which is a known side-effect when reaction temperatures drift or catalyst charges vary. Some competitors blend material from several sources, causing batch-to-batch variation that undermines reproducibility. We built traceability into each drum, linking process data back to starting lots and QC records. The result is low-level impurity profiles that actually matter to end users: fewer methylated phenol residues, little to no halogen scrambling, and recordable run-to-run purity, even as annual volumes have increased.
Our analytical chemists maintain validated HPLC and GC-MS methods, developed specifically for this product. We support clients with impurity mapping, updating certificates to track shifts in byproduct content or volatility. Product support keeps a file of typical and outlier batches, so we can discuss sources of minor shifts with longstanding partners.
Packaging is as critical as synthesis in protecting product integrity. Standard practice at our plant involves sealing the material in HDPE bottles or lined drums, followed by nitrogen-purged secondary containment if extended transport outside temperate zones is expected. Our warehouse approach avoids exposure to direct sunlight, unnecessary temperature swings, and moisture in order to maintain crystal quality and dissolve risk. Some competitors shortcut drying or allow product to sit unprotected awaiting packaging; even slight atmospheric pickup influences melting behavior, and this creates headaches in scaling chemical reactions.
Onsite, we monitor warehouse ambient humidity and temperature, guided by routine checks. Packs are made only after orders are confirmed, a practice that has reduced customer complaints regarding caking or inconsistent flow properties. Drum and interior bagging choices have developed in response to genuine feedback, notably from export clients who experience extended sea or rail journeys.
We’ve watched trends in demand as fluorinated intermediates find greater roles in pharmaceuticals and agrochemical programs. Through hundreds of customer interactions, we hear that consistent purity, real-time traceability, and responsive documentation carry more weight than superficial product specifications. End users emphasize how even minor isomeric or unreacted byproduct problems can escalate into expensive downstream purification or rejected projects.
We focus on selective fluoro-nitration, guided by thorough upstream purification and continuous recycling of unreacted material. This approach not only helps constrain costs, but also reduces environmental burdens from spent acid and solvents. Operators and QC teams work closely to troubleshoot any drift in impurity load, and corrective action happens before material ever leaves site. Site audits from customers reinforce the need to sustain this discipline.
2-Fluoro-4-nitrophenol stands apart from closely related nitrophenols such as 4-fluoronitrobenzene or 4-nitrophenol, largely due to the simultaneous presence of a fluoro substituent and the nitro group in the right places on the aromatic ring. This pairing changes not only reactivity during cross-coupling, but also endows unique electronic properties at the ring system level—important for those constructing more elaborate molecules. While 4-nitrophenol is recognized for its use in dye intermediates and analytical chemistry, the replacement of a hydrogen with fluorine especially at the ortho position creates a clear distinction in behavior under most coupling and protection protocols.
In conversation with application chemists, we’ve seen that small differences in halogen type and position guide the selection of solvents, catalysts, and even temperature profiles during key reactions. Much effort behind the scenes goes into preventing cross-contamination with other substituted phenols, some of which are regulated separately or pose different handling hazards. Product stewardship extends to clearly labeling, segregating, and documenting each batch to help clients track and trace usage from lab trial to production scale.
Handling nitrophenolic intermediates in a modern chemical plant involves sound process controls, robust personal protection programs, and diligent environmental controls. Our facility runs closed reactors, multistage scrubbers, and effluent neutralization steps to protect workers and reduce environmental load. We maintain compliance with applicable local and international handling and shipping conventions, including REACH and pertinent transport codes.
Waste minimization matters. Distilled solvent streams are recycled, process waters are monitored for nitroaromatic content, and off-spec or filtered dusts are safely blended into incineration cycles. Our operations avoid batch venting or open transfer at critical stages. Employees are trained on both the hazards and best practices with nitro aromatics, down to cleaning and changeover between lots.
In recent years, we scaled up from pilot reactors to full-scale glass-lined production, responding to global shifts in fine chemical procurement and cost pressures on active pharmaceutical ingredient manufacturers. This move involved automating charging and workup steps, investing in real-time remote monitoring, and substantially increasing documentation transparency. Upstream, we source fluorinated and nitrated feedstocks from audited suppliers, many of whom have moved toward greener synthesis and improved lot certification. Customers who visited our site during scale-up commented that upgrading analytics and integrating digital records helped ease their own regulatory submissions.
A unique aspect of our supply is willingness to custom-tailor certain characteristics if justified by end-use. For example, we’ve trialed milled forms for customers with automated dosing but also preserved bulk crystal structure for those working with manual charge. This measure of flexibility has helped process engineers solve real-world handling issues, not just theoretical ones reported on datasheets.
Supply chains for specialty aromatics can show volatility tied to shifts in base chemical pricing, regulatory constraints on precursors, or downstream demand blips. We keep regular contact with major purchasing partners to anticipate surge needs or supply gaps, sharing what to expect from our operations in terms of lead-times and planned batch schedules. Buffers in inventory and process availability help mitigate spikes and dips; limited overstock protects against slow-moving lots degrading in storage. Clarity about natural process variations—color shifts due to minor oxidation, for instance—lets users adapt their QC sampling or pre-consumption blending.
Users sometimes struggle with broader availability of related products, such as multi-halogenated phenols or those built from alternate synthetic routes, especially in regions where restrictions on nitroaromatics are tightening. We work to maintain consistent access and transparent records that help customers navigate shipping or customs requirements, staying tuned to any shifts in regulations or labeling needs.
We partner with academic groups and industrial R&D labs exploring new uses or optimizing reactions involving 2-fluoro-4-nitrophenol. Supplying gram to multi-kilo pilot orders, we offer not only bulk product but also technical information about side-reaction suppression, solvent choices, and stabilization during shipping and storage. Project reviews often uncover small improvements, such as adjusting batch drying or recommending inert atmosphere storage, that ultimately increase yields and cut troubleshooting in high-value synthesis.
By remaining in conversation with researchers, we’ve seen new application frontiers open, including selective functionalization for diagnostic compounds and the preparation of organofluorine building blocks used in bioactive screening libraries.
A common concern among users of specialty nitroaromatics involves contamination risk—residual metals, other halogens, or even process solvents showing up at ppm level. Years of production history have revealed that what’s “fit for purpose” is not static. Our response includes routine spectral scans for each lot, documentation of all cleaning and storage procedures, and openness to third-party inspection and lot validation.
Some users with stricter requirements request additional purification steps and solvent changes. We view this not as extra work but as an investment in long-term relationships. Sometimes, products destined for high-sensitivity applications require extended drying or blending to homogenize trace impurity levels; we track these through the entire process. Any report of altered behavior in final use — changed color, melting behavior, unexpected TLC bands — triggers a root-cause analysis, helping both us and the client to resolve process blips quickly and prevent recurrence.
Staying current with advances in aromatic fluorination, nitration, and purification methods shapes how we manage production. Participating in technical conferences, reading process chemistry literature, and pilot testing ideas from process development groups at our site all feed into ongoing optimization. Internally, we encourage operators and technicians to propose improvements or flag anomalies in real time. All changes, whether prompted by new regulations, customer requests, or internal testing, are logged and available for periodic audit.
We choose not to make unsupported claims or mask batch variation behind generic guarantees. Instead, we provide data, explain sources of minor differences, and invite clients to participate in specification changes. This lets us maintain trust and reduce surprises on both sides — one of the main reasons customers stay with us across multiple product lines and changing project priorities.
The landscape for fine chemical manufacturing continues to evolve quickly, shaped by new regulatory limits, emerging markets, and shifting end-use requirements. In supplying 2-fluoro-4-nitrophenol, staying ahead means more than running reactors; it includes active engagement with users, ongoing process and analytical improvement, and a strong commitment to environmental stewardship.
Companies relying on our intermediates face cost and technical pressures from their own customers, needing intermediates that don’t just meet basic assay requirements but also ensure process reliability and regulatory readiness. Our best practices in documentation, traceability, and batch support call on years of accumulated production experience, personal interaction, and real-world troubleshooting. Since every kilogram delivered reflects both our technical standards and understanding of downstream challenges, we keep pushing to support better science and more robust supply partnerships, driven by honest feedback and practical knowhow.