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4-Bromo-2,6-Difluorophenol

    • Product Name 4-Bromo-2,6-Difluorophenol
    • Alias 4-Bromo-2,6-difluorophenol
    • Einecs 'EINECS 405-060-5'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    838569

    Chemical Name 4-Bromo-2,6-Difluorophenol
    Cas Number 179324-73-5
    Molecular Formula C6H3BrF2O
    Molecular Weight 207.99 g/mol
    Appearance White to off-white solid
    Melting Point 69-71°C
    Smiles C1=C(C=C(C(=C1F)O)F)Br
    Inchi InChI=1S/C6H3BrF2O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H
    Solubility Slightly soluble in water, soluble in organic solvents

    As an accredited 4-Bromo-2,6-Difluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Bromo-2,6-Difluorophenol (5g) is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 4-Bromo-2,6-Difluorophenol is shipped in tightly sealed, chemically compatible containers to prevent leaks and contamination. It is transported as a hazardous chemical, complying with relevant regulations (such as DOT and IATA). Proper labeling, documentation, and handling protocols are observed to ensure safe delivery and protection for handlers and the environment.
    Storage 4-Bromo-2,6-Difluorophenol should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature and clearly label the container. Follow all relevant chemical storage regulations and safety guidelines to prevent accidental exposure or contamination.
    Application of 4-Bromo-2,6-Difluorophenol

    Applications of 4-Bromo-2,6-Difluorophenol in Industrial Manufacturing

    4-Bromo-2,6-Difluorophenol is a precision halogenated aromatic compound manufactured to support advanced synthesis in the pharmaceutical, agrochemical, specialty polymer, and liquid crystal sectors. Comprehensive understanding of its downstream integration guarantees efficient adoption in targeted processes with strict compliance requirements.

    1. Pharmaceutical Intermediate for Anti-Infective Synthesis

    Manufacturers use 4-Bromo-2,6-Difluorophenol as a controlled intermediate during scale-up production of specific anti-infective and respiratory system drug substances. Its unique halogen substitution pattern enhances reactivity in Suzuki and Buchwald–Hartwig cross-coupling steps. Formulators introduce it directly in the early-stage heterocycle assembly and molecular backbone functionalization, ensuring high chemical yield critical for API batch consistency. Maximum traceability and impurity control remain essential from kilo lab to ton-scale routes.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) raw material monograph requirements
    • FDA 21 CFR Part 211 – Requirements for the Preparation of Drug Substances
    • REACH Registration (EC 1907/2006) for substance traceability

    Typical usage ratio

    • 0.8–1.5 molar equivalents per functional group in synthetic sequence
    • Adjustment based on reactivity and desired yield during optimization

    Downstream process integration

    • Charged into stirred vessel under inert atmosphere to minimize undesired side reactions
    • Engaged during Pd-catalyzed coupling, chlorination, or acylation step
    • Final workup ensures regulatory-acceptable residual levels in API intermediates

    Final product types

    • Respiratory tract infection APIs (e.g., fluoroquinolone class molecules)
    • Cephalosporin precursor intermediates
    • Anti-bacterial fine chemicals for formulated generics
    • Chemical research standards for in vitro pharmacology

    2. Agrochemical Synthesis: Selective Herbicide Building Block

    Chemical manufacturers incorporate this raw material to create fluorinated aromatic cores of selective herbicides. Its electron-withdrawing substituents increase chemical stability under field UV and soil conditions. Manufacturers implement this building block during the halogen substitution and coupling stages to form robust phenoxy or aryloxyacetic acid herbicide actives, maintaining strict batch homogeneity required by multinational crop science firms.

    Industry compliance standards

    • FAO Specification for Pesticide Active Ingredients
    • ISO 9001:2015 certified manufacturing and traceability protocols
    • European Union Regulation (EC) No 1107/2009 on crop protection products
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 0.7–1.3 molar equivalents in initial coupling reactions
    • Reactivity adjustments according to seed scale-up and pilot studies

    Downstream process integration

    • Fed into batch reactors at the halophenol activation stage
    • Combined during nucleophilic aromatic substitution to introduce difluorophenol moiety
    • Integrated as aryl source in metal-catalyzed oxidation, under strictly controlled temperature

    Final product types

    • Selective broadleaf herbicide actives
    • Phenoxy herbicide intermediates
    • Agrochemical R&D libraries for resistance testing
    • Seed coating additives with enhanced environmental stability

    3. Advanced Liquid Crystal Monomer Manufacturing

    Producers of specialty display and optics chemicals utilize 4-Bromo-2,6-Difluorophenol during the preparation of high-performance liquid crystal monomers. The ortho-difluorinated structure allows for fine-tuned dipole moments in mesogenic units, supporting unique electro-optical properties required in panel and display manufacturing. Production relies on this component during the monomer formation and side chain derivatization to ensure tight physical property windows for device performance.

    Industry compliance standards

    • RoHS 2 (2011/65/EU) for hazardous material restrictions in electronics
    • ISO 9001:2015 for chemical materials used in optical devices
    • UL 94 flame classification for display device components
    • Restriction of PAHs and heavy metals (Chinese Standard GB/T 26572-2011)

    Typical usage ratio

    • 5–15% by mass in custom monomer synthesis batches
    • Modulated according to target dielectric and viscosity specification

    Downstream process integration

    • Incorporated during the formation of the aromatic core of LC monomers
    • Used in esterification to attach functionalized alkyl chains, controlling miscibility
    • Purification via gradient distillation to semiconductor standards

    Final product types

    • Twisted nematic (TN) and in-plane switching (IPS) LC mixtures
    • High-temperature-resistant liquid crystal panels
    • Laminated optical films for televisions and smartphones
    • Advanced touch panel substrates

    4. Fluorinated Specialty Polymer Additive Synthesis

    Producers of performance polymers select 4-Bromo-2,6-Difluorophenol as a precursor for integrating aromatic fluorine content in polymer chains. This approach imparts critical non-stick, heat-resistant, and solvent-resistant characteristics to the end materials. Process engineers employ it during chain-terminating or branching reactions, optimizing final polymer architecture for technical rubber, wire insulation, and industrial coatings markets.

    Industry compliance standards

    • UL 746C polymer materials requirements for electrical applications
    • ASTM D5208 (Accelerated Weathering of Polymeric Materials)
    • RoHS 2 Directive limits for chemicals in electronics
    • ISO 14001 for sustainable polymer production processes

    Typical usage ratio

    • 2–8% by weight as a functional comonomer or chain modifier
    • Adjustment according to dielectric and mechanical performance testing

    Downstream process integration

    • Dosed into autoclave reactors with polycondensation precursors
    • Functionalized with polyether or amide segments via direct coupling
    • Employed during melt blending step for uniform dispersal in engineering plastics

    Final product types

    • Fluoropolymer-based technical films
    • Automotive wire and cable insulation
    • High-performance elastomers for chemical processing equipment
    • Protective coatings for metal substrates
    Free Quote

    Competitive 4-Bromo-2,6-Difluorophenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Bromo-2,6-Difluorophenol: An Insider’s Perspective from the Manufacturer

    Getting Closer to What Makes a Robust Intermediate

    Direct from our production floor, 4-Bromo-2,6-Difluorophenol carries a reputation among chemists that stems from more than just its formula. We have invested years refining its synthesis route to craft a crystalline powder with a hallmark purity level that supports today’s increasingly complex molecular engineering. Producers who work hands-on with aromatic compounds recognize that the margin for impurity becomes thin as end applications demand higher levels of consistency, especially when feeding into pharmaceutical syntheses and specialty chemical processes. At our facility, every batch walks through a series of quality checks targeting precisely those volatile fingerprints—residual solvents, trace metals, unintended isomer formation.

    The core of 4-Bromo-2,6-Difluorophenol’s value lies in its structure—a phenolic skeleton with bromine and fluorine atoms controlling reactivity at the 2 and 6 positions. This balance turns it into a precision tool for demanding coupling and substitution reactions. A few years back, we found that even slight shifts in our halogenation phase, particularly the timing and temperature of fluorine introduction, could swing the content of by-products like 2,4- or 3,5-disubstituted isomers. Customers in the agrochemical arena flagged increased batch-to-batch discrepancy, prompting our R&D team to fine-tune reagent dosing protocols. After tweaking our reactor design and pivoting to an in-situ monitoring approach, we shrank impurity profiles to less than 0.5%, translating to near-seamless integration into downstream syntheses.

    Realities of Scale: Specifications and Handling

    Daily production brings unique challenges, especially as kilogram-lot demand transitions into pilot and full-scale manufacturing. The minimum purity for our 4-Bromo-2,6-Difluorophenol clocks in at ≥99%, but in practice, it routinely reaches beyond this figure. Moisture content remains low—well below 0.2%—since the presence of water not only alters reactivity but also fosters clumping or caking during storage. Granule size matters, too: excess fines clog filters, while oversized crystals slow dissolution or downstream transformations. Every new lot undergoes a sieve analysis to keep the distribution within set bounds.

    Our facility operates under validated, documented systems aligning with recognized international standards. Frequent random sampling from the production line, cross-referenced with finished inventory, prevents lot discrepancies that disrupt supply chains. On a typical day, lab techs run thin-layer chromatography, NMR, and GC-MS spectrometry on samples. Only those meeting tight thresholds for identity and chemical integrity move forward.

    We store the product under nitrogen with humidity strictly controlled. Over time, exposure to air can cause color shifts or reduced shelf life. Although its melting point sits comfortably above ambient lab conditions, sudden temperature swings push some batches towards slight pink discoloration—a sign of slow oxidation. Our site’s climate-controlled warehouse, monitored by both human and automated checks, sidesteps these pitfalls. This hands-on vigilance saves clients from delayed processes once their own QC teams inspect incoming materials.

    Usage from the Lab Bench to Commercial Synthesis

    On the user end, this compound rarely goes straight into finished goods. Most often, it functions as a pivotal intermediate in the stepwise construction of larger, more complex molecules. Medicinal chemistry teams draw on its electron-rich core when aiming for targeted nucleophilic or palladium-catalyzed couplings. The unique substitution pattern blocks other reactive sites, ensuring selectivity during subsequent functionalizations. In contrast to more fully halogenated phenols, 4-Bromo-2,6-Difluorophenol offers the right combination of activity and protection. A chemist can leverage the bromo group for Suzuki or Stille couplings, while the fluorines increase metabolic stability and modulate electronic effects—a feature highly sought after in drug and agrochemical scaffolds.

    Early on, our customers puzzled over side reactions lowering yields during aromatic substitution. After collaborating with several leading pharma partners, we identified that trace iron or copper from unrefined routes can sabotage key metal-catalyzed couplings. By ramping up our pre-purification step and tightening process controls, we largely eliminated catalyst poisoners. The result: higher, more predictable conversion rates with less downstream purification work.

    Scale-up also forced a rethink about solvent compatibility. While small-lot work often sticks to DMSO or DMF, we found that larger-volume users benefit from cleaner, lower-toxicity options. We responded by developing a robust purification method to deliver material that dissolves cleanly in less polar solvents, shrinking the eco-footprint of subsequent steps. For clients under pressure to meet green chemistry mandates, this made a measurable difference.

    Comparison Points: Differentiators from Nearby Analogs

    The world of phenolic intermediates spans a wide variety of halogen patterns. 4-Bromo-2,6-Difluorophenol draws comparisons to siblings like 2,6-difluorophenol, 2,4-difluorophenol, or 2,6-dichlorophenol, but its unique bromine-plus-fluorine framework adjusts both reactivity and downstream fate. Compared with 2,6-difluorophenol, the bromine enables richer cross-coupling chemistry. In contrast to 2,6-dichlorophenol, the bromo group reacts much more readily under palladium catalysis, easing scale-up and reducing side reactions. The balance of low-to-moderate electron withdrawal gives medicinal chemists better control over regioselectivity and activation energies, streamlining lead compound generation with fewer synthetic detours.

    Some competitors offer higher-halogenated versions or alternative substitution patterns. Our direct feedback from clients consistently points to cleaner conversions and fewer unmanageable by-products with 4-Bromo-2,6-Difluorophenol. Its mid-range melting point and moderate volatility add further convenience to both storage and shipping—important for partners running multi-site operations across varying climates. Cost-versus-performance balance also wins favor, especially when compared to fully fluorinated precursors that push budgets without measurable gains in reactivity or downstream flexibility.

    Lessons Learned Through Hands-On Production

    Producing 4-Bromo-2,6-Difluorophenol at scale isn’t just about hitting technical specs on a sheet. Each production run refines our understanding of reaction dynamics, impurity sources, and handling constraints. Several years back, an unexpected solvent shortage upended our schedule. By working closely with our logistics and supplier teams, we pivoted to an alternative solvent system, running side-by-side pilot batches to chart the effects on isomer distribution and residual impurity profiles. The outcome wasn’t always ideal—some batches required rework—but the long-term takeaway was a more resilient, flexible process that now safeguards us (and our clients) against upstream volatility.

    We also invest heavily in waste stream management. Halogenated by-products and spent solvents demand careful, responsible handling. Our facility operates its own on-site waste treatment, backed by partnerships with leading recyclers. Much of what we produce goes into advanced pharmaceutical intermediates or crop protection agents, so we keep sustainability and regulatory compliance at the center. Our environmental and quality teams run continuous risk assessments and periodic audits so that as regulations shift, our product and by-products stand up to scrutiny.

    Feedback runs both ways. Early clients noticed dust formation during repackaging, leading to losses and handling headaches. We adapted by modifying our packaging design, moving from simple polyethylene liners to multi-layer, anti-static bags. The inside of each drum now meets a stricter surface finish standard to avoid abrasion. Over time, breakage rates and off-spec returns dropped by more than half, supporting a leaner operation at both our end and the user’s facility.

    Supporting New Applications and R&D Approaches

    R&D teams count on reliable intermediates to fuel innovation. We field regular requests for custom grades—higher purity, low-metal content, or alternative particle specifications. Each order opens a conversation about outcome requirements, analytical protocols, and process fine points. Our chemists not only manufacture but also collaborate: providing application notes, troubleshooting problematic reactions, or recommending best practices for scale-up. We tracked one project in which an emerging biotech used our 4-Bromo-2,6-Difluorophenol as a springboard to a new fluorinated lead compound. Through direct support and process tweaks, we cut weeks from their development timeline and ensured they cleared their preclinical submission gate without purity or impurity issues.

    Regulations continue to evolve, especially for compounds with halogen atoms given their environmental persistence. We actively partner with industry groups, regulatory advisors, and client safety teams to keep documentation, traceability, and analytical data up to date. For export shipments, our documentation crosses regional and international thresholds, reflecting the material’s composition, residual solvent analysis, and compliance with transport and handling guidelines. Our investment in transparent, data-backed documentation has kept clients on safer ground through regulatory reviews and audits.

    The broader adoption of process analytical technology (PAT) tools spurred us to share our own in-line monitoring data with clients. Real-time visibility into key process steps equips everyone downstream to spot problems before they escalate. Clients using PAT with our product report higher confidence in their own finished goods, reducing downtime and scrap rates.

    Moving Forward: Challenges and Solutions on the Horizon

    Markets keep pushing for greater speed and tighter specifications. Supply chain disruptions—raw material shortfalls, regulatory shifts, or transport hurdles—can ripple through production timelines. One key strategy that has worked for us lies in maintaining a diverse network of upstream suppliers, including multiple qualified vendors for each critical raw input. This spread of sourcing minimises risk, keeping finished product availability robust even in unpredictable conditions.

    Digital transformation is reshaping plant operations. We’ve implemented real-time monitoring dashboards and predictive maintenance schedules on our reactors, which helps head off batch deviations. Area supervisors can review up-to-date data on product quality, safety incidents, and equipment status, which has improved first-pass yield and employee safety. This direct connection from operator to product keeps everyone informed, creating a culture of accountability and quick response rather than waiting for a weekly review.

    We continue to work with downstream partners toward greener synthesis. Some clients are switching from traditional halogenated solvents to safer alternatives, or searching for routes that generate less waste. Our R&D arm feeds back findings from these joint projects into our own plant, shortening process cycle times and cutting the environmental impact of each kilogram manufactured.

    The next generation of 4-Bromo-2,6-Difluorophenol applications will likely move beyond pharmaceuticals and crop protection. We see increasing inquiry from electronics, pigments, and high-performance materials sectors. Here, the physical and chemical profile of our compound—specifically its melting range, volatility control, and resistance to photodegradation—draws in R&D teams hunting for materials that outperform conventional aromatic building blocks without escalating regulatory risk.

    Listening, Learning, and Adapting

    Manufacturing 4-Bromo-2,6-Difluorophenol has connected us to a global customer base ranging from established multinationals to fast-moving start-ups. Each brings unique expectations, timelines, and compliance hurdles. Our experience producing and shipping this compound across continents keeps us focused on agility. We learn from client feedback and on-the-floor challenges, adapting processes and packaging to fit real-world demands.

    If there’s a single lesson our team draws from years in this industry, it’s that reliable supply underpinned by technical expertise builds lasting trust. End users judge us not on marketing claims, but on delivered quality, conformance to specification, and responsiveness to unforeseen obstacles. We see our 4-Bromo-2,6-Difluorophenol as the result of that ongoing commitment—optimized through hands-on production, informed by feedback, and improved by a culture of transparency and problem-solving.

    Looking ahead, the challenges won’t slow down—markets grow more demanding, and regulations keep tightening. Our promise holds: to manufacture every batch with care, supported by technical depth and practical experience, and to support our partners far beyond the point of delivery. That’s the foundation behind every kilogram we ship.