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4-Bromo-2,5-Difluorophenol

    • Product Name 4-Bromo-2,5-Difluorophenol
    • Alias 4-Bromo-2,5-difluoro-1-hydroxybenzene
    • Einecs 816-090-9
    • 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

    674982

    Chemical Name 4-Bromo-2,5-Difluorophenol
    Cas Number 180164-98-1
    Molecular Formula C6H3BrF2O
    Molecular Weight 208.99 g/mol
    Appearance White to off-white solid
    Melting Point 49-52°C
    Density 1.87 g/cm3 (estimated)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C1=C(C=C(C(=C1F)O)Br)F
    Inchi InChI=1S/C6H3BrF2O/c7-4-1-3(8)2-5(9)6(4)10/h1-2,10H

    As an accredited 4-Bromo-2,5-Difluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a screw cap, securely labeled “4-Bromo-2,5-Difluorophenol, ≥98%,” featuring safety and handling warnings.
    Shipping 4-Bromo-2,5-Difluorophenol is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. It is handled as a hazardous material and packaged according to international regulations. The shipment is labeled with appropriate hazard warnings and requires temperature control and secure handling to ensure safety and chemical integrity during transit.
    Storage 4-Bromo-2,5-difluorophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from sources of ignition, strong oxidizers, acids, and bases. Use appropriate chemical storage cabinets, preferably for halogenated organics. Ensure proper labeling, and store at room temperature or as recommended by the manufacturer or MSDS.
    Application of 4-Bromo-2,5-Difluorophenol

    Applications of 4-Bromo-2,5-Difluorophenol in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-2,5-Difluorophenol, we supply this intermediate to downstream industries requiring rigorous batch control, consistent purity, and traceable sourcing. Below, we outline principal industrial applications, process integration, and compliance criteria based on validated industry use cases.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient Synthesis

    API manufacturers select this compound for its reactivity in Suzuki coupling or halogen-exchange reactions to build key aromatic scaffolds, particularly fluorinated phenolic structures found in specialty antihypertensive and oncology APIs. Inline analytical systems control the introduction point to manage reactivity and byproduct formation, while batch documentation supports validation. Adherence to ICH guidelines and pharmacopeial standards governs synthesis, purification, and release to ensure traceability for regulatory submissions.

    Industry compliance standards

    • ICH Q7, Q11; EU GMP Part II
    • 21 CFR Parts 210/211 (FDA)
    • USP/NF and Ph. Eur. monograph compliance for intermediate quality
    • ICH Q3D guidance on elemental impurities

    Typical usage ratio

    • Used at 1.0–2.5 molar equivalents relative to downstream coupling partners
    • Adjustment based on desired yield and minimization of side reactions
    • Final usage ratio defined by process-specific API synthesis stage

    Downstream process integration

    • Introduced during core aromatic coupling step, either by batch addition or semi-continuous feed
    • Inline quality controls detect residual starting material post-reaction
    • Product isolation and purification require solvent extraction or crystallization prior to further derivatization

    Final product types

    • Fluorinated phenol-based APIs
    • Pharmaceutical intermediates containing difluorophenolic motifs
    • Building blocks for anticancer and central nervous system drugs

    2. Agrochemical Intermediate in Herbicide Synthesis

    Agrochemical formulators use this compound as a key constituent in synthesizing fluorinated phenolic derivatives, serving as the backbone for selective post-emergent herbicides and pest management agents. Production requires compliance with both chemical and environmental safety regulations, guided by certificate-of-analysis verification and residue control. Plant-scale synthesis adjusts the feed ratio based on targeted conversion rates and downstream bromination needs.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing consistency
    • REACH registration for manufacture/import in the EU
    • OECD GLP if used in regulated bioassay studies
    • Compliance with US EPA and EU Regulation (EC) No 1107/2009 for agrochemical active ingredients

    Typical usage ratio

    • Ranges from 0.7 to 1.5 equivalents versus the co-reactant, depending on the specific synthetic transformation
    • Usage ratio adjusted according to desired substitution pattern and minimization of off-target reactivity
    • Process evaluation via pilot-scale batch runs

    Downstream process integration

    • Feeds into oxidative or nucleophilic aromatic substitution stages
    • Integrated reagent metering to manage exothermicity and avoid runaways
    • Waste management aligns with local chemical disposal requirements

    Final product types

    • Selective herbicides with difluoroaryl groups
    • Pre-emergence and post-emergence agrochemicals
    • Intermediates for insecticide synthesis

    3. Electronic Material Intermediate for Liquid Crystal Production

    Manufacturers of advanced liquid crystals and display materials use this compound to introduce specific halogen and fluorine positioning into aromatic rings, supporting the synthesis of high-efficiency LC mixtures. Pure, microcontaminant-free lots allow incorporation into multi-step syntheses, with trace analysis performed at each step to ensure final LC phase performance and compliance with electronics-grade purity guidelines.

    Industry compliance standards

    • RoHS 2011/65/EU restrictions for hazardous substances
    • IEC 62474 declarable substances standards
    • ISO 9001:2015 for batch validation
    • Customer-specific impurity and trace-metal specs (sub-ppm levels)

    Typical usage ratio

    • Usually 0.8 to 1.2 molar equivalents, tailored for stepwise functionalization
    • Optimized based on desired liquid crystal isomer yield and purity targets

    Downstream process integration

    • Introduced in coupling or substitution steps for custom LC core production
    • Monitored via HPLC or GC-MS for low residual levels
    • Integrated with continuous flow or batch microreactor systems

    Final product types

    • Liquid crystal intermediates for TFT/LCD devices
    • Specialty electronic films for mobile and display panels
    • Aromatic core reagents for advanced display technologies

    4. Monomer Segment in Fluorinated Polymer Manufacture

    Producers of high-performance polymers incorporate this compound as a monomeric building block to create specialty fluoropolymers with tailored solubility and electronic resistance. Precision measurements ensure compatibility with other monomers, and batch records document every phase of material transformation for QC and regulatory review. Processing operations often require custom solvent systems to maintain product integrity during high-temperature polymerization.

    Industry compliance standards

    • ISO 14001 for environmental controls
    • ISO 9001 for polymer production traceability
    • Material Declaration per IEC 62474 when used in electronics
    • Restricted Substance List (RSL) compliance for downstream electronics or medical use

    Typical usage ratio

    • Injected at 2%–10% weight/weight of total monomer blend, tailored for end-use performance
    • Adjustment based on target mechanical and chemical resistance of finished polymer

    Downstream process integration

    • Added during co-polymerization or block polymerization stages
    • Requires monitoring for homopolymer vs. copolymer ratio control
    • Residue analysis ensures removal of unreacted starting material

    Final product types

    • Fluorinated specialty polymers for chemical-resistant coatings
    • Printed circuit board dielectrics
    • Performance films for automotive and aerospace electronics

    5. Fine Chemical Intermediate for Aroma Chemical Formulation

    Specialty fine chemical and perfumery manufacturers utilize this compound sparingly as a precursor in trace-level synthesis of highly fluorinated aroma molecules. Such intermediates require sophisticated synthetic handling and thorough QC, as even trace impurities affect fragrance performance. The unique substitution pattern enables novel olfactory properties in response to market demands for specialized aroma notes.

    Industry compliance standards

    • IFRA code of practice for aroma raw materials
    • EU Cosmetic Directive (EC) No. 1223/2009 for substance purity
    • REACH registration for classified substances
    • ISO 22716 for manufacturing consistency

    Typical usage ratio

    • Often 0.1–0.5 equivalents as trace intermediates relative to downstream core
    • Adjustment ensures regulatory limits on component levels

    Downstream process integration

    • Enters aromatic substitution or etherification stage in aroma synthesis sequence
    • Trace level introduction monitored to prevent regulatory exceedance of fluorinated residues
    • Final purification via fractional distillation or chromatography

    Final product types

    • Fluorinated tonal aroma molecules
    • High-end perfumery compounds
    • Food and cosmetic fragrance enhancers (subject to allowable limits)
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2,5-Difluorophenol: Behind the Chemistry

    Everyday at our manufacturing plant, we work with a wide variety of aromatic intermediates. Among them, 4-Bromo-2,5-Difluorophenol stands out for its uncompromising potential in specialty synthesis. As chemical manufacturers, we understand the tangible value of streamlined production, precise data, and consistent quality—nothing substitutes for hands-on experience with molecules like this.

    We produce 4-Bromo-2,5-Difluorophenol with careful control over each reaction parameter, because minor variations can ripple into later stages for our clients. Its structure—featuring a bromo group at the para-position and fluorine atoms at the ortho–para positions—shapes both its reactivity and selectivity. Over years of manufacturing, we’ve found that phenolic intermediates bearing multiple halogens play a crucial role in preparing advanced pharmaceuticals, agrochemicals, and specialty materials. Selecting a compound with both bromine and fluorine atoms opens a window to transformations that neither mono-halogenated nor non-halogenated phenols can achieve.

    Molecular Characteristics Shaped by Hands-On Production

    Our batches of 4-Bromo-2,5-Difluorophenol are formulated to a minimum purity of 98%, and we control crystallinity and moisture content to safeguard reactivity. The compound’s CAS reference—a detail our staff track through every batch—marks each shipment, but what truly concerns us is the molecule’s behavior across various steps in a customer’s lab or plant. Unlike broader blend-type phenols, this compound delivers consistent melting profiles and reliable solubility in common solvents at industrial scales. This reliability, forged through our own continual process monitoring and analytic refinement, matters more than the generic numbers printed on a spec sheet.

    Working directly with the synthesis, we’ve observed that 4-Bromo-2,5-Difluorophenol offers a notable contrast to more common difluorophenols or single-halogen counterparts. The bromo group, in particular, serves as a handle for palladium-catalyzed coupling, while the fluorine atoms temper the phenol’s reactivity and affect the compound’s electron distribution. This balance extends shelf life and improves downstream transformation yields—less waste, more robust outcomes, and fewer headaches in scale-up routines.

    Applications Driven by Real-World Problems

    High-value pharmaceutical work increasingly depends on late-stage functionalization, and this compound slots neatly into that workflow. We’ve supplied the compound to research divisions where its halogen pattern allows for targeted cross-coupling or nucleophilic substitutions, essential for building drug scaffolds with improved potency or selectivity. Our team has worked with scientists designing new kinase inhibitors, where aromatic halogens dictate biological activity. In those projects, access to a reliably manufactured phenol can mean the difference between a year’s worth of progress or a stalled campaign.

    Agricultural chemistry clients find 4-Bromo-2,5-Difluorophenol indispensable for constructing herbicidal and fungicidal agents. Our manufacturing adjustments for impurity profiles directly help these users avoid unwanted byproducts that sometimes compromise late-stage chlorination or ring closure. In the materials sector, development chemists often look for aromatic building blocks where fluorination confers unique dielectric or stability properties; the dual halogenation in this molecule addresses that demand and broadens polymer design portfolios. We keep our lines of communication with formulators open, so improvements in selectivity or handling often come straight from factory floors and R&D benches—there’s no substitute for listening to people who use what we make.

    Pursuing Consistency from Lab Scale to Full-Scale Production

    Scaling up the production of 4-Bromo-2,5-Difluorophenol tested our team’s skills in both safe reaction design and efficient purification. The process integrates batch and continuous-flow steps where reaction exotherms are tightly managed. We invested in both analytical instrumentation and skilled staff who understand how to spot minute impurities and structural isomers—details that might never show up on a mass-market spec sheet, but which matter in downstream transformations.

    Recrystallization solvents and drying protocols that work fine in a lab can introduce headaches at multi-kilo scale, so much of our optimization work focused on practical realities: filterability, dust control, solubility limits, and byproduct suppression. We learned the hard way that selecting the wrong crystallization solvent can trap unreacted precursors or lead to too rapid nucleation, making purification expensive and inconsistent. Tweaks came from real production runs—replacing a commonly used alcohol solvent with a less polar alternative improved both overall yield and the purity of the isolated compound. For our customers, these improvements mean a more reliable supply, lot after lot, no matter where their own scale-up process lands.

    Differences That Resonate in Real Applications

    The presence of two fluorine atoms next to a phenolic hydroxyl group and a para-position bromine makes this molecule much more than just a halogenated phenol. We’ve watched several clients compare this compound directly with monosubstituted phenols or compounds with only a single electron-withdrawing group. In practical reactions, the electron-withdrawing combination increases the acidity of the hydroxyl, modifies transition states, and often decreases unwanted side reactions. Traditional phenol or 2,4-difluorophenol often lead to lower conversion or extra purification steps when used in certain Suzuki or Buchwald–Hartwig couplings. By contrast, our product delivers sharper, more predictable reaction endpoints and easier workups.

    Pharmaceutical and agrochemical developers notice the difference in both crystallization kinetics and finished product stability. The dual halogen pattern increases compatibility with metal-mediated cross-couplings, reduces rates of undesired oxidative decomposition, and offers greater control in protecting or modifying the phenolic oxygen.

    Unlike generic phenolic intermediates, our process delivers a consistent impurity profile and keeps trace contaminants (like residual acid catalysts or isomeric by-products) at levels below the thresholds that would impact health, safety, or downstream reaction outcomes. We use high-pressure liquid chromatography to validate every lot, leveraging years of method development specific to this molecule; we don’t just default to generic analytics. That difference shows up in the performance of our clients’ syntheses, where yields are boosted and troubleshooting calls drop off sharply.

    Safety, Handling, and Storage Practices from the Manufacturing Floor

    Direct experience with large-scale handling informs every procedure we implement. As a moderately hazardous halogenated phenol, this compound requires careful control of personal protective equipment and forced ventilation in all handling areas. Even at high purity, solid 4-Bromo-2,5-Difluorophenol gives off a faint but pungent odor; experienced plant operators work efficiently to shield it from prolonged exposure to open air.

    Over the years, we reduced waste in filtration and packaging by changing over to vapor-barrier pouches and introducing reusable screw-cap bottles for large-scale users. Extra care goes to batch traceability, so every drum and every bottle reflects the manufacturing date, lot number, and full impurity profile—our own plant’s recordkeeping enables better inventory management and safer workplace practices for customers.

    Building Trust by Accountable Practices—and Fixing Issues on the Fly

    In chemical manufacturing, errors become lessons. We have encountered and tackled problems with raw material sourcing, changes in regulatory expectations, or sudden shifts in demand. We take special note of how our solvents and brominating agents are sourced under responsible purchasing practices. Our suppliers undergo routine audits similar to those in pharmaceutical production. We have phased out chlorinated solvents to cut down on environmental impact and switched to more sustainable halogen donors.

    On the rare occasion that a shipment does not meet its intended specification, quick communication matters more than paperwork. With one pharmaceutical client, a variation in melting point appeared due to atmospheric moisture. Our plant team immediately ran additional Karl Fischer titrations, isolated the source, changed the drying regime, and revalidated the batch—all within three days—from start to reshipment. This agility, built on practical knowledge, keeps trust intact.

    Quality: More Than Just a Number

    For a complex intermediate like 4-Bromo-2,5-Difluorophenol, quality cannot be reduced to a certificate of analysis. Our chemists carry out routine GC-MS and NMR checks, not only for expected impurities, but also for trace hydrolysable groups that might arise during handling or storage. Stability studies in-house simulate temperature cycling, and we watch for color, solubility, or crystallinity drift. Only through continual feedback—across years of supply and batch-to-batch evaluation—do we feel confident in what we ship.

    Customers notice when large-scale batches mirror pilot-scale samples in every way, saving time in revalidation and process transfer. In one collaboration with an agrochemical company, they reported an unexpected crystallization failure using product from a different manufacturer. Our lot, made with a tailored finishing step, resolved the issue, saving our partner weeks of delay and significant cost. These moments reaffirm our belief that attention to manufacturing makes a difference.

    Supporting Data: Facts That Matter in Real-World Use

    Through years of production, we’ve accrued performance and safety data for 4-Bromo-2,5-Difluorophenol that informs both our protocols and our customers’ downstream development. Flash points are measured by closed-cup methods; dust suppression protocols are updated after every rare spill or event. During our most recent five-year period, on-site incident rates linked to this compound were lower than for other halogenated phenols produced in the same facility. This safety record comes not from luck, but from concrete investments in training and process redesign.

    We log all incidents, track trending reports, and review hazard data in light of evolving global and local regulations. We aim to communicate transparently about all known hazards: skin and respiratory irritation from direct contact and dust inhalation, environmental persistence, and best practices for handling.

    Challenges and Pathways for Improvement

    Manufacturing 4-Bromo-2,5-Difluorophenol at scale has challenged us in sourcing, process safety, and environmental impact. Sourcing high-purity fluorinated precursors traditionally depends on a small pool of suppliers, some of whom face geopolitical or regulatory uncertainties. To address this, we have diversified our purchase contracts and developed in-house purification methods for key starting materials, reducing vulnerability to global supply chain shocks.

    In reaction safety, early protocols leaned heavily on solvent extraction and aqueous workups. Over the years, feedback from operators and environmental officers drove a shift to solvent minimization and more contained batch reactors, reducing both operator exposure and waste streams by nearly 30%. Routine safety drills and process hazard reviews form the backbone of our ongoing effort to improve.

    We face persistent challenges in refining crystal sizing, because the flow properties of this compound affect automated weighing and dosing systems. Engineering staff work closely with lab chemists to monitor particle size distribution, enabling users downstream to reduce time spent breaking clumps or resolving dosing errors.

    We regularly connect with customer process chemists, exploring ways to further curb solvent use, lower waste, and improve downstream workups. Tracking those requests sharpens our focus on what real users struggle with—not what marketers imagine. This efficient feedback loop, built on honest dialogue, steadily makes our product and our processes better.

    Commitment to Knowledge Sharing and Continuous Learning

    In manufacturing, every day brings up new questions. We train technical sales and support teams to understand the compound’s quirks, but we also invest in bringing clients’ feedback straight back to the reactor. Our chemists regularly contribute to peer-reviewed process journals and industrial symposia, advocating for best practices in halogenated phenol production and safety. These efforts anchor us in the broader technical community and foster relationships that help solve problems as soon as they arise.

    We share case studies with customers where changes in handling or reaction setup led to improvements at their own facilities: better yield, safer handling, reduced rework. Data collected on our production floor underpins these recommendations, and no recommendation goes to print or email unless we’ve validated it in our own plant. We see ourselves as partners in advanced synthesis, not just as suppliers. Every insight, from the pump operator or the QC chemist, strengthens our collective ability to deliver safer and better chemicals.

    Looking Ahead: The Role of 4-Bromo-2,5-Difluorophenol in Advanced Synthesis

    Demand for highly functionalized aromatic compounds continues to climb in both pharmaceuticals and advanced materials. Our direct work with 4-Bromo-2,5-Difluorophenol has shown us that investing in the quality, safety, and reliability of specialty intermediates brings downstream benefits few can measure on a spreadsheet. Those benefits are felt in faster R&D cycles, more robust regulatory submissions, safer workplaces, and ultimately in the innovative products launched by our customers.

    As regulatory expectations evolve and markets shift, we remain committed to open technical dialog, continuous improvement in production, and transparency in every step. Years spent working every detail of this compound’s production—from procurement and reaction to packaging and shipment—anchor our commitment to everyone who works with or builds on what we make.

    In the end, it’s not the molecular structure printed on a label or the spec limits on a data sheet that define a truly valuable product, but the collective effort of chemists, engineers, operators, and clients working together. Our long history with 4-Bromo-2,5-Difluorophenol means we recognize and solve problems before they ever become an issue on your bench or your factory floor—and that, more than any marketing claim, is the true standard of reliability in chemical manufacturing.