|
HS Code |
928787 |
| Chemical Name | Phenol, 2-Fluoro-3-Nitro- |
| Molecular Formula | C6H4FNO3 |
| Molecular Weight | 157.10 g/mol |
| Cas Number | 320-41-2 |
| Appearance | Yellow solid |
| Melting Point | 62-64°C |
| Boiling Point | 270°C (estimated) |
| Density | 1.53 g/cm3 (at 20°C, estimated) |
| Solubility In Water | Slightly soluble |
| Flash Point | 136°C |
| Smiles | C1=CC(=C(C(=C1O)F)[N+](=O)[O-]) |
| Pubchem Cid | 215403 |
| Inchikey | DOOVSCKWIJSNNO-UHFFFAOYSA-N |
As an accredited Phenol, 2-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, 2-Fluoro-3-Nitro-" is packaged in a 25g amber glass bottle with a secure, tamper-evident screw cap. |
| Shipping | **Shipping Description for Phenol, 2-Fluoro-3-Nitro-:** Ship Phenol, 2-Fluoro-3-Nitro- in tightly sealed, chemically compatible containers, protected from light and moisture. Label according to hazardous chemical regulations. Store and transport at ambient temperature, complying with local, national, and international regulations for hazardous organic chemicals. Ensure appropriate documentation and emergency procedures are in place during shipping. |
| Storage | Store Phenol, 2-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 light and moisture. Clearly label storage containers and ensure restricted access to trained personnel. Follow all relevant chemical safety regulations and guidelines. |
Competitive Phenol, 2-Fluoro-3-Nitro- prices that fit your budget—flexible terms and customized quotes for every order.
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In nearly three decades behind reactors and glassware, I've watched innovators in pharmaceuticals, crop protection, advanced polymers, and dyes look for raw materials that add value and reliability to their synthesis pipelines. The road to steady production always begins with inputs that deliver precision and repeatability even as market pressures and regulations shift. If there’s one molecule that captures the sweet spot between unique reactivity and manageable handling, it’s Phenol, 2-Fluoro-3-Nitro-. We call it by its CAS number here as shorthand, but those familiar red and yellow drums in our warehouse have been an anchor for specialty projects both at bench and commercial scale.
Every run of this phenolic intermediate comes from a controlled batch setup, not continual commodity streams. Many customers ask why that matters. Take the nitro group at the 3-position — it introduces electron-withdrawing character that’s essential for directed ortho-metalation, improving regioselectivity in Suzuki and Buchwald couplings. Meanwhile, the fluorine substituent at position 2 not only enhances metabolic stability for downstream pharma synthesis, but also resists harsh conditions in agrochemical formulations. Chemists have learned to count on the selectivity, while process engineers value the product’s robust physical form, with minimal dust and consistent particle size. Reliable melting and boiling points support both high-throughput and experimental-scale needs.
It’s easy to lump fluoro-nitrophenols together without thinking about subtle differences in reactivity. At the manufacturing level, small shifts in temperature profile or stoichiometry can introduce trace impurities — sometimes as little as 0.1% — that complicate downstream purification, polymerization, or crystallization. That’s why we maintain control over every step, from the initial fluorination to the final recrystallization and filtration. Each batch gets GC and HPLC checks tailored to end-use, with certificates detailing impurity profiles down to parts-per-million. If a batch falls short of specs, it’s reworked or rejected. That’s non-negotiable, because one off-spec drum can ruin months of customer work or ongoing production runs. Decades of customer feedback informed the critical thresholds around moisture, color, and by-products, directly integrated into our release protocols.
As a phenolic intermediate, 2-Fluoro-3-Nitro-Phenol shows marked differences from isomers and analogues. Replace the fluoro with a chloro at the 2-position, and downstream halogen exchange processes slow down. Swap the nitro group to the 4-position, and you lose the orthogonal reactivity that makes this molecule so suitable for constructing heteroaromatics and benzoxazoles. Production chemists notice the subtle volatility improvements here too: the presence of the ortho-fluorine lowers the boiling point in a way that eases separations via distillation, compared to traditional non-fluorinated phenols.
Our internal comparisons against standard 2-nitrophenol showed that the fluoro group tightens the melting range by several degrees, trims the by-product list in most reduction reactions, and improves storage stability under ambient conditions. Many in the pharma community see this as a practical advantage, especially when synthesizing intermediates that must travel through cold chain logistics without degrading. Long-term stability tests, using our in-house protocols, found that tightly sealed material held up well against hydrolysis and photodegradation, cutting overall waste and minimizing re-processing costs.
Sourcing raw materials always brings the same requests: keep the lot-to-lot color light, minimize dust during weighing, and package so the compound arrives intact — not caked or compressed into brick. Having refined the last mile of drying, our 2-Fluoro-3-Nitro-Phenol consistently falls into a fine, flowable crystalline powder. It scoops easily and dissolves rapidly in common organic solvents, speeding up batch charging. Handling this compound requires fewer interventions for clumping, allowing automated feeders to operate at design throughput. Customers working with automated liquid handlers in medchem labs have told us how dependable this powdery form is for microplate dispensing.
Any chemical operation running bulk material needs to anticipate regulatory, waste, and hazard mitigation. 2-Fluoro-3-Nitro-Phenol, by virtue of the substituent pattern, presents a marginally lower dust explosion risk than its more volatile peers, and our packaging further minimizes exposure. Moisture pick-up stays below 0.1% in sealed drums. Unlike some higher-nitrated compounds, it stores securely at ambient temperatures with no significant color development over months. Additives and stabilizers become unnecessary, avoiding unintended side reactions during critical syntheses.
Choosing an intermediate isn’t just about molecular structure. In pharmaceutical R&D campaigns, even trace metal contamination or off-odor can mean weeks of costly troubleshooting. Our plant layout keeps clean and dirty flows separated at every stage. That infrastructure investment pays off where it counts: QA results reveal that iron, copper, and heavy metal contaminants never rise above allowable thresholds, and odor is consistently neutral. These factors often escape mention on data sheets but matter deeply in high-stakes or high-throughput environments.
Feedback from a customer scaling an API synthesis led to tweaks in drying profiles and particle size controls. They reported higher yields and shorter filtration times, which, in tight development timelines, made a significant difference. Working side-by-side with formulators and process engineers, especially during method transfers from lab to kilo scale, drives small but meaningful changes in operational protocols. Sometimes it’s a change in packaging liner material to reduce static charging, other times a slight tweak to the final milling step to guarantee a narrower PSD. That constant back-and-forth dialogue, aided by field visits and shared troubleshooting sessions, keeps our specs aligned with actual production conditions — not just regulatory paperwork.
Comparing 2-Fluoro-3-Nitro-Phenol to its siblings on the benzenoid ring opens up a story about selectivity and process adaptability. Isomers and derivatives exist with substituent switches — for example, 4-Fluoro-2-Nitrophenol or 3-Fluoro-2-Nitrophenol — but none match the balance of electron density and reactivity found in our compound. These subtle electronic differences show up in yields during condensation and coupling reactions, with many synthetic chemists noting higher throughput and cleaner conversion profiles from the 2,3 pattern. Documentation collected from our customers over the years highlights that troublesome dimerization and oxidative by-product formation stays lower with this scaffold, sparing downstream reprocessing and chromatographic clean-up.
Passing a sample between QC labs repeatedly brings up the issue of consistency. Our historical data shows tighter standard deviation in melting ranges and assay purities compared with materials imported from third-party brokers. Internal stress-testing under forced degradation, such as exposure to controlled humidity and light, demonstrates superior stability — customers working in early-stage development see lower loss factors after six months of storage, which justifies their premium on fresh material direct from source, rather than rolling the dice with reprocessed or warehoused stock.
Plant operators and EHS managers raise issues about transport, spillage, and exposure risk on a regular basis. Strictly adhering to tested protocols for packaging, labeling, and shipping, each outgoing batch reflects the growing scrutiny from regulatory bodies worldwide. We keep compatibility documentation up-to-date with the latest global transport and hazard regulations, and the lot documentation includes a clear footprint of each process and test point. Environmental audits over the years pushed us to upgrade our dust collection and solvent recycling systems. The downstream result benefits not only our operation, but also our customers who receive cleaner product with a smaller carbon footprint.
It’s easy for a manufacturer to lose sight of the “why” behind the certificates. We see it in moments where an unexpected audit request pops up or a regulatory update triggers a packaging or transport review. Staying transparent and accessible to customer compliance teams changed our approach, driving process improvements and new documentation standards. We regularly incorporate feedback about document formatting, SDS layout, and traceability to make adoption quicker for procurement and regulatory review teams working inside both large enterprises and agile startups.
As global supply chains turned brittle across industries, securing consistent source material became less about price and more about certainty. We have always maintained redundant raw material sources, with active relationships across fluorination and nitration upstreams. Our equipment can pivot from batch to semi-continuous operations quickly when demand spikes. The ability to flex production lines and hold stable reserves of both intermediates and finished goods has made us a favored source in years when global chemical supply faces turbulence.
Some of our long-term partners started requesting real-time tracking and more precise projections as a result of market volatility. Upgrades in warehouse management and batch tracking systems let us deliver up-to-date inventory and order timelines. A reliable advance notice means our customers avoid emergency spot buys or costly process delays. Sharing on-hand and pipeline stock updates openly helped build trust through some difficult periods, cementing relationships that last through both lean and busy cycles.
Many projects start with small-bottle R&D samples. Our technical service teams, made up of career chemists and engineers, are in regular touch to help interpret NMR, MS, or elemental analysis data for customers troubleshooting syntheses. Years of method development experience go into each interaction. As customers scale up, pilot drum shipments provide a clear link to production scale reliability, with full batch traceability and impurity tracking. APIs, specialty monomers, and dye intermediates made using our 2-Fluoro-3-Nitro-Phenol have reached commercial synthesis, not just lab validation, and feedback from those users continues to shape our process control.
A pharmaceutical partner who struggled with metal-catalyzed hydroxylation found run-to-run consistency improved after we implemented tighter reactor cleaning routines and standardized cargo seal protocols. Crop science firms tell us the fluorine-phased intermediate stands out during field validation — batch performance stays high even after storage and transport through tough logistics. Problems flagged by real-world users drive changes faster than any theoretical lab projection alone. Our people often work elbows-deep with partners during tech transfers, rooting out issues in filtration, handling, or trace impurity isolation to ensure what we send is ready for the reality of industrial synthesis.
Advances in green chemistry and safer processing influence our plant each year. We invested in solvent recovery systems and chose process conditions that reduce hazardous waste while maintaining product quality. These changes pay dividends in cleaner material for our customers and safer environments for our staff. We share best practices openly with researchers, reporting both successes and setbacks in conferences and trade forums so the broader community benefits. This philosophy of transparency has helped us fine-tune everything from screening protocols for residual solvents to optimizing crystallization, setting benchmarks in both purity and process efficiency.
Process chemistry doesn’t stop at the plant gate. Our team keeps up with published literature and faces customers who test every assumption. We take feedback seriously when a new downstream transformation or solvent system changes product requirements. In some cases, we have manufactured custom grades with reduced residual solvent, tailored PSD, or even modified packaging — each change documented and validated before approval. These partnerships emphasize practicality, not just technical specification. The aim stays clear: materials that arrive on-time, ready for integration, with no surprises.
Much of the value in specialty intermediates like 2-Fluoro-3-Nitro-Phenol comes from unseen work: weeks spent validating process windows, updating instrumentation, or refining QA protocols after late-night shift discoveries. By maintaining direct dialogue with end users — plant chemists, EHS staff, production engineers, and lab managers — we keep our standards grounded in the practical realities faced on the warehouse floor, reactor vessel, and packaging line each day. The difference shows up over time: more reproducible batches, fewer plant shutdowns, and streamlined regulatory clearance.
No compound is “just” a chemical to us. In making 2-Fluoro-3-Nitro-Phenol, decades of hands-on effort, supplier vetting, and user input result in materials that stand up to real-world pressure. We leverage our experience not only to deliver a specialty molecule, but to share ways it can best support production, development, and innovation across industries. The true judgment for any manufacturer comes from customers who depend on that next truckload or small-batch delivery. Each shipment reflects not just what’s possible in synthesis, but what’s sustainable, scalable, and worthy of trust, from one expert team to another.