|
HS Code |
546252 |
| Chemical Name | 1-Bromo-4-Fluoro-2-Nitrobenzene |
| Cas Number | 446-21-1 |
| Molecular Formula | C6H3BrFNO2 |
| Molecular Weight | 220.00 |
| Appearance | Yellow solid |
| Melting Point | 60-64°C |
| Boiling Point | 265°C |
| Density | 1.806 g/cm3 |
| Purity | ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1F)[N+](=O)[O-])Br |
| Inchi | InChI=1S/C6H3BrFNO2/c7-5-2-1-4(8)3-6(5)9(10)11/h1-3H |
| Refractive Index | 1.608 |
| Hazard Class | Irritant |
| Storage Conditions | Store at room temperature, in a dry, well-ventilated place |
As an accredited 1-Bromo-4-Fluoro-2-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, sealed with a red cap and chemical-resistant label displaying hazard symbols, compound name, and lot number. |
| Shipping | 1-Bromo-4-Fluoro-2-Nitrobenzene is shipped as a hazardous chemical, typically in tightly sealed containers to prevent leaks. It must comply with regulations for toxic and environmentally hazardous substances, including appropriate labeling and documentation. Shipments should be protected from heat, moisture, and incompatible materials, and handled by trained personnel using suitable safety precautions. |
| Storage | **1-Bromo-4-Fluoro-2-Nitrobenzene** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, or open flame. Keep away from incompatible materials such as strong reducing agents and bases. Store at room temperature, protected from moisture and direct sunlight. Properly label all storage containers and follow relevant safety and regulatory requirements. |
| Purity 99%: 1-Bromo-4-Fluoro-2-Nitrobenzene with a purity of 99% is used in active pharmaceutical ingredient synthesis, where it ensures high product yield and reduced impurities.Melting Point 59°C: 1-Bromo-4-Fluoro-2-Nitrobenzene with a melting point of 59°C is used in organic intermediate production, where it allows efficient processing at moderate temperatures.Molecular Weight 220.99 g/mol: 1-Bromo-4-Fluoro-2-Nitrobenzene at 220.99 g/mol is used in agrochemical research, where defined molecular mass facilitates accurate stoichiometry in reactions.Stability Temperature 120°C: 1-Bromo-4-Fluoro-2-Nitrobenzene with stability up to 120°C is used in high-temperature coupling reactions, where it maintains structural integrity without decomposition.Particle Size <20 μm: 1-Bromo-4-Fluoro-2-Nitrobenzene with particle size less than 20 μm is used in catalyst preparation, where it promotes uniform dispersion and enhanced catalytic activity.Low Moisture ≤0.5%: 1-Bromo-4-Fluoro-2-Nitrobenzene with moisture content ≤0.5% is used in moisture-sensitive syntheses, where it prevents undesirable hydrolysis and improves reaction efficiency. |
Competitive 1-Bromo-4-Fluoro-2-Nitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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Our work starts right at the reactor. As a chemical manufacturer, we spend each week surrounded by hundreds of substituted aromatics. Among them, 1-Bromo-4-Fluoro-2-Nitrobenzene stands out in both utility and demand. This compound, with the molecular formula C6H3BrFNO2 and CAS number 446-07-1, serves as a reliable starting material for building more elaborate chemistries. It finds its way into everything from pharmaceutical intermediates to fine chemical syntheses. Its unique blend of bromo, fluoro, and nitro groups gives it a reactivity profile rare among similar ingredients, meaning it solves particular synthetic challenges that other monohalogenated or mono-substituted variants just can’t touch.
Every batch we produce shows the consistency and purity that professional chemists insist on. We target high purity—typically above 99% by GC—because any less invites trouble downstream during scale-up or research. Impurities complicate purification steps, ruin yields, and slow timelines, and no one wants to run five columns to clean up a cheap input. By investing in precise chlorination and careful control of reactant ratios during nitration, we avoid problematic byproducts—including dangerous dinitro or dibromo readings that would otherwise appear in poorly managed reactions. We watch for o,p-isomer contamination as well, since properties can change with even minor structural shifts.
Over two decades, requests for 1-Bromo-4-Fluoro-2-Nitrobenzene haven’t wavered. Downstream teams chasing complex targets in both medicinal chemistry and specialty materials return to this molecule for its versatility. The electrophilic ring allows for selective cross-coupling reactions, opening up routes that alternative precursors close off. For large multi-step syntheses, having a product that doesn't scramble under basic or acidic reaction conditions saves serious rework. The presence of a strong electron-withdrawing nitro group influences reaction rates in subtle but valuable ways—controlling ortho/para selectivity and reducing unwanted side reactions.
Our customers, from major pharmaceutical research operations to emerging start-ups, recognized these practical advantages right away. They saw how the molecule works as a bridge between easy-to-source halobenzenes and much rarer, hard-to-make difunctionalised aromatic compounds. It serves not just for target molecule construction but also as a platform for library developments. Medicinal chemists value how the nitro and fluoro groups can be transformed with mild reagents, generating an array of amine or hydroxylated products. Material scientists benefit from the compound’s influence on electronic properties, finding reliable results batch after batch. The bromo substituent, in particular, acts as a handy leaving group under palladium-catalyzed coupling reactions, improving yields in key steps where other aryl bromides or fluorobenzenes let them down.
Out on the plant floor, our standard workflow puts safety and repeatability at the top of the agenda. Dense, acrid fumes from bromo and nitro intermediates show why we never compromise on containment, ventilation, and careful addition rates. We keep the reaction exotherms under firm control, using jacketed reactors and slow addition of nitrating acids—any slip can trigger side-product formation, lower yield, and put workers at risk. Monitors for nitrogen oxides and hydrogen bromide run continuously, and we keep close logs of all reactant sources.
Every barrel we ship comes from a lot that’s been tracked from raw material intake to finished packaging. We run HPLC and GC-MS on every run, looking for evidence of side reactions or incomplete conversions. This level of traceability wasn’t always the industry norm, but we learned early that even a tiny process drift can show up weeks later in a customer’s delayed delivery or product recall. For us, the process audit trail and NDAs with major buyers go hand in hand—no shortcuts, just transparent chemistry and honest reporting.
No two labs have the same tolerance for trace contaminants. Some large-scale agricultural chemistries accept technical-grade material so long as it stays within regulatory impurity specs. Others, particularly custom pharma contracts, stick to analytical or pharmaceutical grade, rejecting even minor above-threshold halogenated byproducts. We maintain distinct production lines for each, separating technical and high-purity batches right from the weigh-in.
It's not just about purity numbers. Moisture content matters for storage stability; residual acid from workup impacts safety in handling. Some buyers specifically request low-metal levels due to downstream catalyst poisoning risk—common in Suzuki or Buchwald-Hartwig reactions where palladium black formation ruins entire production batches. We pull samples at every key step for both organic and inorganic residue checks, not just after filtration. This policy reduces rework and unwanted surprises mid-process like unexpected exotherms or filter clogging.
Anyone familiar with halogenated nitrobenzenes quickly learns the differences between structural isomers. 1-Bromo-4-Fluoro-2-Nitrobenzene’s substitution pattern creates a chemical “fork in the road” for further derivatization, allowing selectivity not available from meta-positioned analogues. Chemists looking at 3-bromo or 5-fluoro substitutions run into regioisomer separation challenges after each transformation. By contrast, the para and ortho ring positions in our compound make downstream protection-deprotection sequences much cleaner.
Standard 2-nitrofluorobenzene, for instance, reacts differently in nucleophilic aromatic substitutions—the bromine increases activation at the 4-position, offering more reliable outcomes in stepwise synthesis. Some customers used to work with unfunctionalized mononitrobenzenes but switched to this difunctional version, reducing the need for post-reaction purification, which eats up time and resources. Even standard bromonitrobenzenes miss out on the electronic effects deployed by the fluorine para to the nitro group—subtle but important when chasing certain SAR studies in drug discovery.
We worked with teams who wasted months trying to pin down yields with singly substituted nitrobenzenes from other suppliers. Switches to 1-Bromo-4-Fluoro-2-Nitrobenzene halved their synthetic steps and gave project managers a clearer view of cost and timeline. Overdosing catalysts, troubleshooting side product formation, and guessing which impurity is interfering with analysis—these headaches drop off when the core substrate is predictable and pure. For anyone new to halogenated aromatic intermediates, the learning curve smooths out quickly with transparent, reliable supply.
Shipping chemicals like this comes with practical considerations. The compound arrives as a yellow crystalline powder, easily handled in standard packaging. It travels best in HDPE drums lined with moisture barriers to avoid caking or hydrolysis. We train all logistics partners in safe handling—keeping the containers sealed tightly, avoiding exposure to strong bases or acids during transport, and flagging any sign of envelope compromise so recipients see only clean, dry product.
Onsite, stability at ambient temperatures means users rarely encounter color changes, clumping, or loss in reactivity unless they leave product open to air and light for extended periods. We include moisture indicators in shipments on request, and customers with long-term storage needs often refrigerate or keep stocks under argon, though this isn’t always strictly required for short projects. Documentation goes out with every pallet, listing both lot numbers and the quality assurance results, so every team knows exactly what they’re getting.
Questions about sourcing, sustainability, and regulatory compliance never slow down. We answer them every week as new customers expand into global markets. Brominated and nitrated aromatics attract regulatory scrutiny, so we document the origin and traceability of every raw material. Our bromo source comes from fully audited refineries, never from conflict regions. Nitric acid inputs meet Responsible Care standards.
We comply with EU REACH and US TSCA guidelines, sharing documentation on restricted or declarable substances as part of every compliance file. Years back, a major client pushed us to adopt stricter separation of hazardous and non-hazardous plant streams. Implementing real-time inventory tracking improved both regulatory reporting and batch traceability. We retain samples for every lot, supporting stability studies or customer-driven retesting long after delivery.
Handling of effluent and byproduct gases also matters. Older plants sometimes vent halogenated exhaust or ignore water discharge limits, but we upgraded all our scrubbers, and invest in closed-loop water recycling—local regulators no longer give the benefit of the doubt to manufacturers who treat environmental controls like afterthoughts. Qualitative and quantitative test results from third-party labs back up every environmental claim.
Every producer faces inevitable challenges: inconsistencies in raw material deliveries, process drift in extreme weather, or equipment calibration slips. These problems don’t disappear with scale, and they show up quickly when deadlines approach. We learned through experience to schedule process runs around local weather spikes—dry, stable days produce better, lower-moisture lots, reducing the need for post-production drying.
We work directly with reagent producers so acetone, dichloromethane, and other solvents meet strict in-house specs—out-of-spec solvent leads to incomplete dissolutions, temperature spikes, or unpredictable isolations downstream. Every kilogram of 1-Bromo-4-Fluoro-2-Nitrobenzene represents dozens of iterative improvements. Close feedback loops with customers reveal even minor differences batch-to-batch—trace differences in crystal morphology, melting point, or shelf life.
A few years back, a surge in demand from a pharmaceutical client prompted process upgrades. Their feedback highlighted color variability in non-refrigerated shipments, driving us to winterize our crystallization protocols and add secondary drying steps. These changes improved stability and made rework almost obsolete for all clients—an example of direct collaboration translating into measurable process improvements.
Most of our regular customers stick with us not just for supply reliability, but for transparent problem-solving. Chemical research rarely follows a straight line. Changes in final compound targets, updates in regulatory filings, or raw material shortages upend even the most organized synthesis. By opening our process logs and sharing real-world results from our own R&D, we help partners adapt syntheses without costly downtime.
In the early years, partnership meant regular emails and annual visits. As global regulations and supply chains tightened, customers turned increasingly to suppliers who kept honest records and shared real data—not just marketing claims. We’ve hosted visiting scientists to witness our batch processing and quality checks firsthand, resulting in faster approvals and stronger trust on both sides. Long-term clients join our feedback sessions, reviewing both complaint resolutions and proposed upgrades to handling, packaging, or documentation.
Our in-house chemists keep up with literature—journals, patent filings, and regulatory revisions—so we know when major research projects might need new specifications or documentation. Customer collaborations led us to integrate alternative packing formats, like smaller foil-lined tubs in place of drumful lots, reducing risks of moisture uptake and improving usability at the benchtop. These aren’t just process tweaks—they directly affect R&D success rates, speedup manufacturing, and lower costs for everyone in the chain.
Global events regularly influence both feedstock pricing and product demand. Disruptions in bromine or fluorine production—political instability, export controls, force majeure at major facilities—send shockwaves through the specialty aromatic markets. Rather than wait for shortages, we hold buffer inventories of both precursor chemicals and drum stocks. Demand spikes driven by expansion in electronic materials or clinical development cycles can push lead times up, but we plan annual production forecasting based on customer forecasts and rolling stock levels.
We align with downstream schedules where possible, shipping on a just-in-time basis to reduce warehousing costs both for us and buyers. Adjusting to unplanned demand often reveals weaknesses in either sourcing or plant capacity, but tight feedback with regulars gives us more time to adapt. As interest in fluorine-containing and nitroaromatic pharmaceuticals increases, we commit resources to expand not just plant size, but also quality oversight and technological upgrading.
Experienced chemists ask pointed questions about structural confirmation, batch data, and impurity profiles. We encourage this scrutiny—it shows buyers understand that “spec compliance” only goes so far. By sharing full spectra, chromatograms, and even small-scale process deviations, we build trust and avoid hidden surprises. Some teams ask for method validation files, especially when their target molecules enter clinical development and face strict regulatory review. Sharing every available detail is the fastest way to keep projects on schedule and budgets on track.
We also acknowledge the learning curve for teams new to this molecule. Our support team often walks first-time buyers through solvent selection, temperature management, and safe isolation steps, especially when scale moves up from lab to kilo quantities. Users appreciate that this advice comes not from reseller scripts, but from firsthand production experience—and it pays off when customers avoid waste or delays.
We stand by every kilogram of 1-Bromo-4-Fluoro-2-Nitrobenzene that leaves our site. For users who prioritize consistent reactivity, low impurity profiles, and open communication, the difference between direct manufacturing supply and an anonymous catalogue becomes clear over time. Our customer base includes universities, start-ups, and major research centers looking for a supplier committed to both quality and honesty. Modern chemistry depends on both technical mastery and partnership, and we focus our work on delivering both every day.