Anhui Liwei Chemical Co., Limited
Products

3-Fluoro-4-Bromophenol


    • Product Name 3-Fluoro-4-Bromophenol
    • Alias 3-Fluoro-4-bromo-1-hydroxybenzene
    • Einecs 863-684-5
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    721296

    Product Name 3-Fluoro-4-Bromophenol
    Cas Number 26249-14-7
    Molecular Formula C6H4BrFO
    Molecular Weight 191.00
    Appearance White to off-white solid
    Melting Point 58-62°C
    Boiling Point 256°C
    Density 1.74 g/cm3
    Purity Typically ≥98%
    Synonyms 4-Bromo-3-fluorophenol
    Smiles C1=CC(=C(C=C1Br)F)O
    Inchi InChI=1S/C6H4BrFO/c7-5-2-1-4(9)6(8)3-5/h1-3,9H

    As an accredited 3-Fluoro-4-Bromophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled “3-Fluoro-4-Bromophenol,” hazard symbols, and batch details.
    Shipping 3-Fluoro-4-Bromophenol is shipped in tightly sealed containers made of compatible materials to prevent leaks and contamination. The package is clearly labeled following regulatory guidelines for hazardous chemicals, and includes documentation for safe handling and emergency procedures. Shipments are handled by certified carriers in compliance with local and international transport regulations.
    Storage 3-Fluoro-4-bromophenol should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Clearly label the storage area and container, and follow all relevant safety protocols for handling and storing hazardous chemicals.
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    Competitive 3-Fluoro-4-Bromophenol 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.

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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    3-Fluoro-4-Bromophenol: Advancing Chemical Innovation at the Source

    Introduction to 3-Fluoro-4-Bromophenol

    Our experience in manufacturing high-purity specialty intermediates brings out nuanced applications for compounds like 3-Fluoro-4-Bromophenol (Molecular Formula C6H4BrFO, CAS Number 774-33-0). Our reactors, engineering teams, and in-house analytical chemists have spent years honing reliable oxidation and halogenation workflows. The production approach gives us direct insight into material consistency and real-world performance—knowledge we pass to partners in pharmaceuticals, agrochemicals, and materials science.

    Unique Aspects of In-House Manufacture

    A process like para-bromination with ortho-fluorination demands careful adjustment. Exothermic reactions, trace side-products, and catalyst selection cannot be left to guesswork or batch-to-batch uncertainty. Factory staff does not just work from paper protocols—they monitor raw materials, scrutinize crystallization, and observe the end chemistry through its lifecycle. This hands-on oversight results in a consistent product with uniform melting point, color, and reactivity. Analytical sheets and batch histories stay within our own labs; archived samples come from our own lines, not repackaged barrels from elsewhere.

    Understanding Structural and Application Differences

    Some customers ask about substituting one halophenol for another, imagining that a swap from 2-fluoro-5-bromophenol to 3-fluoro-4-bromophenol will yield minor changes. In practice, we see sharp differences when the position, electronic properties, and steric effects come into play. Para and ortho effects, hydrogen bonding, and subsequent coupling reactions all respond to the ring’s substituent map. For example, in Suzuki and Buchwald-Hartwig type couplings, nucleophiles engage quite differently with 3-fluoro substitution compared to other isomers. The position of fluorine often invokes specific reactivity patterns during downstream transformations, affecting not only yields but also selectivity for key pharmaceutical or material targets. Compounds with both fluorine and bromine have become essential for synthesizing API candidates, imaging probes, and advanced polymers. Our operators and analysts consistently see performance variations during scale-ups that draw a clear line between this isomer and others circulating in the market.

    Behind the Quality: What Direct Production Means for You

    No two production campaigns look exactly the same, especially with fine chemicals where trace impurities can cascade into supply chain headaches. For 3-Fluoro-4-Bromophenol, our scale-up and regular campaigns allow immediate adjustments: reaction solvent changes, decolorization, and critical distillation tweaks. Finished product leaves the reactor only after in-house checks for elemental composition, residual solvents, and precise melting ranges. We do not farm out our QA to anonymous contractors—we rely on our own archived samples and our experienced QC staff who understand recurring fingerprint spectra. Maintaining our own line also means tighter specification windows, traceability from raw material intake to packed drum, and accountability—qualities we’ve found many users value more than a slightly lower quoted price.

    Specification Insights from Years Behind the Glass

    Chemists in custom synthesis and process development push for clarity around specification sheets. Over years of batch syntheses and pilot plant runs, we observed that true value comes from more than a guaranteed assay reading. Moisture by Karl Fischer is a key parameter; low water content influences crystallinity and prevents undesirable side reactions downstream. Particle size and color—often dismissed as cosmetic—actually provide early signals for filtration behavior or unexpected decomposition routes. Our production lines operate at scale under controlled temperature and agitation profiles, yielding a reproducible physical product that avoids problematic dust fractions or sticky residues. We have learned to call out any subtle color drift, as it often points to minor side product formation or insufficient purification, which left unchecked, can risk the performance of sensitive cross-coupling partners or bioconjugation steps.

    Supporting Reliable Performance for Diverse Industries

    From direct conversations with R&D groups, we know 3-Fluoro-4-Bromophenol serves a dual role: key intermediate and functionalized building block. In pharmaceuticals, teams deploy it for synthesis of fluoroaromatic scaffolds, which then undergo further derivatization to create complex small molecules, kinase inhibitors, or metabolites for in-vitro studies. At the preclinical stage, avoiding carryover impurities becomes critical—not only for regulatory compliance but also for clarity in ADME, toxicity, or binding assays. If the starting phenol introduces halide contaminants, or fluorine migrates to unintended positions, downstream validations and approvals quickly derail. In agroscience applications, customers use fluorinated bromophenol for herbicide or fungicide lead candidates, where electron-withdrawing substituents modulate biological target affinity. Specialty materials and polymer researchers appreciate the unique properties of aromatic fluorine-bromine motifs, where thermal stability and resistance to degradation persist under challenging fabrication conditions. Our ability to pinpoint subtle differences in by-products and physical profile allows users across sectors to develop more robust protocols, even when application specifics diverge strongly from one field to the next.

    No Shortcuts in Handling or Packaging

    Material handling poses another layer of transparency. Our teams pack 3-Fluoro-4-Bromophenol under strict conditions to prevent exposure to light, ambient moisture, or cross-contaminants. Because onsite staff manage drum and bottle filling under real-time supervision, we catch and resolve issues before they reach the shipping floor. In our experience, inappropriate packaging for compounds with halogens or phenolic functionality can accelerate sublimation, discoloration, and stuck caps—not just cosmetic concerns, but practical headaches for bench chemists with tight timelines. Our packaging staff know the impact of even slight deviations—spilled powder, sticky residues in liners, or staticky materials that stick to tools—affect every hour spent on sample preparation. We see this feedback in every returned drum or special request, and we integrate those lessons into our SOPs, whether it takes an extra drying round or re-testing an aging lot.

    Real-World Challenges and Solutions in Custom Synthesis

    Contract customers often approach us with specialized needs for fluorinated or brominated phenols, pushing traditional routes beyond the limits. Onsite technical staff spend considerable time solving problems that sound simple on paper but reveal complexity at scale. For example, solvent extractions and phase separations stop being textbook when kilograms of semi-crystalline fluoro-bromophenol need isolation at high yield. We work closely within our own teams to troubleshoot yield loss, batch consistency, or even minor color differences. In one recent campaign, a slight adjustment in reaction time and base addition improved purity from 97% to over 99.5%, dramatically reducing the downstream work-up. This level of flexibility is only possible for staff working directly on the lines, observing daily equipment cycles and feedstock quality—something hard to replicate in outside supply chains.

    Why Position and Electronic Effects Shape Outcomes

    Comparisons with other phenol derivatives always invite questions about substitution pattern effects. Our chemists study not only what’s on paper, but also what happens in real reaction vessels. 3-Fluoro-4-Bromophenol differs significantly from 2-fluoro, 2-bromo, or non-halogenated analogs. Placing fluorine in the meta position influences oxidative stability and reactivity with a variety of coupling partners. Bromine in the para position enables higher conversion rates in palladium or copper-catalyzed arylation while minimizing undesired dehalogenation. The precise alignment of substituents matters even more during multistep syntheses, where cumulative electronic effects impact not just structure but also color, volatility, and storage stability. Customers report sharper signals in NMR, improved yields, and fewer side-products for downstream chemistries, especially those requiring orthogonal protecting group manipulation. Our role as manufacturer helps us accumulate not just analytical results but practical anecdotes: yields and crystallization profiles often diverge widely based on which isomer is fed to a multistep campaign.

    Direct Manufacturer Insight: Accountability from Reactor to Lab Bench

    For us, accountability runs from the raw fluorobenzene feedstock all the way to sealed glass bottles in our warehouse. Each lot of 3-Fluoro-4-Bromophenol carries a documented history—operator shifts, detailed yield records, solvent batches, and analytical batch certificates. This creates a practical advantage for buyers who value origin, consistency, and traceability. Technical discussions are not abstract; if a customer faces solubility challenges or product drift during storage, our technical staff can reference their own archives, sometimes pulling previous batches for direct comparison. We do not rely on foreign brokers to bridge knowledge gaps or provide half-complete technical support. Instead, our teams take responsibility, whether by offering repeat analyses, carefully investigating shipping issues, or providing bench-scale feedback.

    Continuous Improvement Based on Field Experience

    Feedback from R&D partners and production chemists directly shapes our internal processes. Each complaint or compliment influences future production runs. Teams responsible for halogenation learn not just from standard deviations in laboratory analytics but also from actual user experience: reaction behavior at scale, solubility across solvent systems, and performance in downstream chemistries feed back into updated batch protocols. We maintain open communication with QA staff, synthesizing both standard and specialty lots as required by customer projects. Suppliers who see only reselling or buy-and-ship cycles miss out on this improvement feedback loop, and we see proof of that in rejected lots from outside sources—discoloration, unanticipated side-products, or unreliable melting points. Years of meeting specialized requests, troubleshooting on the fly, and adapting to new downstream needs yield a better, more reliable intermediate.

    Prioritizing Safety and Compliance from the Source

    Every chemical journey involves consideration for safety, regulatory compliance, and reliable logistics. By keeping all production, analytics, and shipment preparation in-house, we gain full visibility. QC analysts maintain up-to-date files—spectra, COAs, and records of every lot are cross-checked according to site-specific guidelines. Storage follows protocols developed from real accident histories. Operators have seen how a small change in humidity or handling can introduce unwanted hazards or degrade delicate aromatic halides. Our safety managers educate on-site staff and adapt packaging or process steps based on trends in safety reports, not just regulatory mandates. Because we do not separate manufacturing from safety, questions of process discharge, vapor management, and worker protection all play into our day-to-day decisions. This translates into better reliability for customers who care about GxP compliance, safe handling, and predictable shelf life.

    Key Differences Marked by Direct Control

    3-Fluoro-4-Bromophenol stands apart from many similar phenolic compounds due to its dual halogen pattern. Our years of manufacturing reveal that dual halogenation consistently alters reaction rates in catalytic couplings and nucleophilic substitutions. From seed crystal formation to large-kilogram batch behavior, the product’s distinct fingerprint reduces the kinds of troubleshooting headaches process chemists encounter with less carefully crafted intermediates. We take direct control over each step: reagent selection, tank cleaning cycles, temperature profiles, and analytical sign-off. In an industry where product substitution can lead to delays or hard-to-correct downstream failures, the lines we operate serve as a check against unwanted substitutions, incomplete conversions, or hidden process changes. Researchers dealing with complex synthetic routes, pharmaceutical validation, or scale-dependent conditions depend on these differences not as theoretical benefits, but as practical, time-saving realities.

    Listening to Customers as a Basis for Future Development

    A good manufacturer listens for both emerging needs and nagging pain points. Our technical team works directly with pilot program managers and process chemistry leaders to adapt manufacture when new coupling reactions or regulatory guidelines appear. Over time, our processes for 3-Fluoro-4-Bromophenol have evolved: changes in feedstock purity, new drying techniques, and modifications in reactor agitation—all originating from customer experience rather than random innovation. If a material doesn’t perform in some new imaging probe or API intermediate, the responsible chemist and production lead sit down together to work through the issue, usually armed with both analytic and experiential data. Staff in direct contact with the material catch sources of micro-contaminants, monitor for unwanted polymorphs, and flag subtle inconsistencies, ensuring development efforts translate back into improved finished product. Our willingness to open archives, repeat syntheses, and experiment with improved protocols means each batch reflects a long chain of learning built up across hundreds of production cycles.

    Sustainability in Practice, Not Just on Paper

    Environmental questions increasingly frame how chemicals reach the market, particularly those containing halogens. We recognize that sustainability is more than a regulatory checkbox. By controlling site operations, material throughput, and waste streams, our teams achieve targeted solvent recovery and actively lower the carbon footprint associated with 3-Fluoro-4-Bromophenol. Process improvements proposed by on-site engineers find fast implementation alongside routine batch operations—cycling solvents, optimizing energy draws, and reducing unnecessary transportation loops. Because we do not rely on reshipping or cross-border warehouse hopping, every batch reflects opportunities for waste minimization and environmental controls. Over time, this direct engagement supports both compliance and the larger drive for responsible chemical manufacture, impacting greenhouse gas emissions and long-term site viability.

    Providing Consistency That Enables Innovation

    Research teams and scale-up manufacturers do not have time to redo failed reactions or recycle subpar intermediates due to differences in feedstock. Our experience producing 3-Fluoro-4-Bromophenol in-house means partners know what to expect: consistent assay, reproducible melting point, defined particle characteristics, and minimal batch-to-batch drift. This reduces troubleshooting, validation time, and unexpected material requalification, letting researchers focus on developing better pharmaceuticals and advanced materials. Operating as the manufacturer, we see clearly how trace contaminants or unclear provenance can disrupt entire synthesis campaigns, particularly as demands for faster, more agile R&D grow worldwide. By protecting every step from feedstock to final package, our staff builds trust that cannot be replicated by traders or disconnected distributors.

    Conclusion: More Than a Molecule, a Real Manufacturing Partnership

    3-Fluoro-4-Bromophenol offers unique performance thanks to its chemical structure and electronic character. True value emerges through our direct involvement—factories, technical teams, warehouses, and QA labs all woven together to ensure a dependable supply. Over time, lessons learned from unscheduled breakdowns, pilot-scale hiccups, and rapid customer feedback loops have shaped not only our workflow, but also our understanding of how careful manufacture improves outcomes up and down the value chain. For technical buyers seeking real accountability, product assurance, and a voice in future improvements, working directly with the manufacturer of 3-Fluoro-4-Bromophenol brings efficiency, reliability, and genuine transparency few intermediates on the market can match.