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2-Bromo-3-Fluorophenol

    • Product Name 2-Bromo-3-Fluorophenol
    • Alias 2-Bromo-3-fluoro-1-hydroxybenzene
    • Einecs 628-903-1
    • 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

    252437

    Chemicalname 2-Bromo-3-Fluorophenol
    Molecularformula C6H4BrFO
    Molecularweight 191.00 g/mol
    Casnumber 261714-41-2
    Appearance White to light beige solid
    Meltingpoint 70-74°C
    Purity Typically ≥ 97%
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Smiles C1=CC(=C(C(=C1)O)Br)F
    Inchi InChI=1S/C6H4BrFO/c7-5-3-1-2-4(9)6(5)8
    Storagecondition Store at 2-8°C, protected from light

    As an accredited 2-Bromo-3-Fluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Bromo-3-fluorophenol, tightly sealed with a screw cap and labeled with safety information.
    Shipping 2-Bromo-3-Fluorophenol is shipped in securely sealed containers, compliant with chemical safety regulations. It is packed with cushioning material to prevent breakage, labeled as a hazardous material, and accompanied by appropriate documentation. Temperature conditions are maintained as recommended, and shipping is handled by certified carriers experienced in transporting laboratory chemicals.
    Storage 2-Bromo-3-Fluorophenol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, direct sunlight, and incompatible substances such as strong oxidizers. Protect from moisture. Use appropriate personal protective equipment when handling. Store at room temperature and keep the chemical clearly labeled and out of reach of unauthorized personnel.
    Application of 2-Bromo-3-Fluorophenol

    Applications of 2-Bromo-3-Fluorophenol in Industrial Manufacturing

    As a specialized chemical raw material producer, we supply 2-Bromo-3-Fluorophenol for several precisely defined downstream manufacturing scenarios. Utilized for its halogenated phenol structure, this intermediate plays a key role in synthesis workflows across regulated fine chemical, pharmaceutical, and material sectors. Below, we detail real-world industrial applications, compliance benchmarks, formulation guidance, core process points, and resulting end-products.

    1. Agrochemical Active Ingredient Synthesis

    Agrochemical formulators incorporate this compound as a crucial building block for selective herbicide and insecticide APIs, especially fluorinated and brominated aromatic intermediates. Its position as an ortho-bromo, meta-fluoro substituent allows for directed synthetic transformations under controlled catalyst loading, facilitating production of high-purity actives. Stringent quality management and batch traceability support consistent performance in approved crop protection compounds.

    Industry compliance standards

    • REACH Annex XVII–direct API precursor use
    • ISO 9001:2015 process validation for agro intermediates
    • GLP (Good Laboratory Practice) batch release for regulated actives
    • Chinese GB/T 19001 system for exported agrochemicals

    Typical usage ratio

    • 0.10–0.28 molar equivalents per target molecule, dependent on final API structure
    • Adjusted per stepwise conversion efficiency in multi-stage synthesis

    Downstream process integration

    • Integrated in step 2 or 3 of condensation or halogen exchange reactions
    • Introduced before ring closure or amine derivatization in active compound production
    • Time, temperature, and solvent control critical for selectivity
    • Followed by phase separation and QC for residual halides

    Final product types

    • Pre-emergence and post-emergence herbicide active ingredients
    • Selective insecticide APIs for seed treatment
    • Fungicidal building blocks in advanced formulations

    2. Pharmaceutical Intermediate for CNS Drug Synthesis

    Pharmaceutical manufacturers utilize this compound as an aromatic intermediate in the synthesis pathway for central nervous system (CNS) drug molecules, such as selective serotonin reuptake inhibitors (SSRIs) and related benzofuran analogs. Its halogen pattern supports ortho-lithiation, facilitating efficient coupling and controlled fluorine incorporation, required by pharmacopoeial purity standards. Strict QC, trace level impurity monitoring, and production record retention apply for regulated API supply chains.

    Industry compliance standards

    • ICH Q7 GMP for API intermediate production
    • USP and EP monograph impurity profile review
    • FDA cGMP 21 CFR 210/211 compliance
    • China Drug Master File (DMF) registration where required

    Typical usage ratio

    • 1.0 equivalent per API backbone in coupling reactions
    • Ratio may be reduced (down to 0.6) for high-yield batch conversion

    Downstream process integration

    • Used after halogen-lithium exchange in aromatic ring functionalization
    • Typically enters the reaction spreadsheet after deprotonation step
    • Processed under inert atmosphere, with temperature monitoring for active-site protection
    • Followed by direct coupling or cyclization for target CNS compounds

    Final product types

    • Active pharmaceutical ingredient for CNS disorder medications
    • Benzofuran and benzothiophene pharmaceuticals
    • Registered serotonergic drugs (raw API and formulated product)

    3. Liquid Crystal Display (LCD) Monomer Synthesis

    Specialty electronics industry utilizes this halogenated phenol for synthesizing rigid-core monomers in advanced liquid crystal display materials. Its dual halogen functional groups enable highly selective etherification and cross-coupling polymerizations, supporting manufacture of high-contrast nematic and smectic LCD mixtures. Stringent handling and material compatibility checks ensure defect-free monomer integration into proprietary liquid crystal systems.

    Industry compliance standards

    • RoHS Directive for restricted chemical substances in electronics
    • EN IEC 63000 for material documentation in displays
    • JIS C 0950 environmental performance for Japan market
    • Sony SS-00259 Green Partner program for supplier qualification

    Typical usage ratio

    • 5–15% by mass in core monomer batch for LCD blend pre-polymer
    • Optimized based on targeted birefringence and dielectric threshold of final LCD material

    Downstream process integration

    • Added at initial monomer loading in closed-system polymerization
    • Reacted via aromatic etherification/C–C coupling as core structure
    • Purified by repeated crystallization and phase extraction before blending
    • Batch verified by optical and electrical property QC

    Final product types

    • Nematic liquid crystal monomers
    • Specialty optical switching compounds
    • Custom LCD blends for high-performance electronic display panels

    4. Fluorinated Polyarylether Resin Manufacturing

    High-performance materials manufacturers leverage this phenolic as a reactive monomer in engineering thermoplastic production, especially for fluorinated polyarylether (PAE) and polyaryletherketone (PAEK) resins. The compound’s unique halogen orientation delivers precise control during nucleophilic aromatic substitution reactions, enabling synthesis of polymers with elevated chemical resistance and processability, critical for demanding industrial applications. Material handlers apply full chain-of-custody documentation and environmental compliance tracking.

    Industry compliance standards

    • ISO 14001 environmental control in polymer processing
    • ASTM D6262 for PAEK material characterization
    • REACH Regulation for polymer ingredients in the EU
    • UL 94 V-0 flame retardancy standard for end-use material

    Typical usage ratio

    • 3–12% by weight relative to comonomers in polymer backbone formulation
    • Adjusted according to target fluorine content and thermal properties

    Downstream process integration

    • Introduced at co-monomer charging step of batch reactor
    • Undergoes nucleophilic aromatic substitution to form ether linkage
    • Polymerization under elevated temperature and vacuum to drive conversion
    • Subsequent granulation and compounding for downstream molding

    Final product types

    • High-purity PAE and PAEK engineering resins
    • Composite pellets for chemical-resistant components
    • Injection-molded parts for automotive, aerospace, and electronic applications
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    Certification & Compliance
    More Introduction

    2-Bromo-3-Fluorophenol: Experience from the Production Floor

    Direct Insights from the Manufacturing Plant

    Over years in the chemical industry, it has become clear that every substitution on an aromatic ring brings new challenges and possibilities. The story of 2-Bromo-3-Fluorophenol illustrates what happens when production leans on technical skill, real-world observation, and systematic refinement. As a manufacturer, every batch tells its own story — not just of molecular arrangement, but of all the small choices that shape the final result.

    This compound shows up where careful selectivity matters. Working day in and day out with halogenated phenols, I have seen how the different substituents behave during synthesis, purification, and handling. The addition of a bromine at the second position and a fluorine at the third creates a molecule that stands apart from more common phenols.

    A Close Look at the Structure

    On paper, the skeleton of 2-Bromo-3-Fluorophenol looks straightforward — a benzene ring with a hydroxy group (phenol), a bromine atom at the ortho position, and a fluorine atom at the meta. This combination isn’t just a curiosity; it shapes everything from reactivity to physical handling. As a manufacturer, controlling halogenation reactions calls for both reliable equipment and deep attention to reaction kinetics.

    Typical phenols behave one way when they move through a reactor. Bromination at the second position brings more weight and changes the electron distribution, making subsequent fluorination less predictable. Once fluorine enters the mix at the meta position, it sharpens selectivity yet can cause issues with volatility and byproduct formation.

    Working hands-on with these molecules, I have learned to respect the unpredictability of aromatic substitution, especially with highly reactive reagents. This product is not a run-of-the-mill phenol or even a generic bromophenol. It demands a specific approach from start to finish.

    Specifications from Years of Refinement

    Bringing consistency batch after batch does not come from luck. Each parameter — from melting point to color, from impurity profile to crystalline texture — reflects a process tuned over repeated production cycles. Typical technical indicators derived from careful runs show a melting range around 53–57°C and a tendency to form pale crystals under controlled cooling.

    The team regularly checks for residual halides, ensures the absence of unwanted heavy metals, and confirms structural integrity through NMR and GC-MS once every set. This focus on analytical depth means surprises remain rare by delivery time.

    Moisture content needs strict control, since even a hint of water alters downstream reactions. Over time, we learned the hard way that phenolic hydroxy groups attract atmospheric moisture, especially during cooling and packaging. Maintaining a dry-house environment and using moisture-proof liners stopped spoilage and gave more reliable shelf life.

    Handling, Storage, and Practical Realities

    Handling 2-Bromo-3-Fluorophenol isn’t just about paperwork or standard-glove guidelines. The sharp, slightly medicinal odor signals phenol activity — distinct, but not as biting as unsubstituted variants. Workers in the plant quickly recognize it in the air, which keeps everyone alert to spills long before alarms or sensors activate.

    Brominated compounds can cause skin and respiratory discomfort if left unchecked. As part of ongoing training, plant operators use well-ventilated enclosures and work with open vessels only when absolutely necessary. Over years of trial, we moved away from glass containers, which suffered thermal shock, in favor of polymer-lined drums for bulk quantities.

    The temperature stability sits in a comfortable range for shipping across most temperate regions. Long-term storage at room temperature preserves both purity and appearance, but unexpected heat spells, such as those that hit southern warehouses one summer, expose a tendency to discoloration if exposure exceeds safe bounds. Adding real-time temperature trackers in shipping containers stopped this source of waste.

    Applications: Lessons from Customer Feedback

    Field experience remains the best teacher. Feedback from formulators in pharmaceuticals, crop protection, and material science circles back to the plant floor regularly. The hydroxy group, together with two different halogens, makes this compound attractive where both electron density and reactivity need tailoring.

    In medicinal chemistry, for example, the molecule acts as a bridge to larger, more complex targets that need precise placement of functional groups. Nucleophilic substitutions proceed more predictably thanks to how bromine and fluorine interact—users mention improved yields with lower side reactions in some coupling steps.

    Agrochemical research teams contact us about the clean halogenation pattern, which helps them avoid unwanted metabolic breakdown products when screening new fungicides or herbicides. Small variations in halogen position and choice have outsized impacts on environmental fate; the meta-fluorine slows microbial degradation, buying crucial time for field effects.

    On the material science side, adding this intermediate feeds into specialty polymers or customized monomer chains. Not every phenol derivative transfers desired thermal or chemical resistance, but the unique halogen pairing here raises both attributes in finished materials if properly used in the synthetic route.

    Why Not Swap for Another Phenol?

    A question heard often: couldn’t a simpler bromophenol or plain fluorophenol do the same job? Side-by-side, their differences show up quickly in lab results and plant experience.

    A sole bromine at the ortho position increases molecular weight but slows certain cross-couplings, often due to steric hindrance. Products with just a fluorine lack the same bond disruptiveness that bromine gives—especially in nucleophilic aromatic substitution. Dual halogenation opens synthetic windows shut to either alone. Where metabolite patterns matter, the meta-fluorine shifts both polarity and bioavailability, giving structures that behave differently through a biological system.

    Processability shifts too. Some phenol derivatives show sticky melts or become unexpectedly volatile during rotary evaporation. Employees remember years where off-spec material formed oily residues in the filters, traced back to small tweaks in substitution pattern. This dual halogen combination resists that tendency, giving more predictable, manageable solid forms by the time it hits final packaging.

    Health, Safety, and Continuing Improvements

    Overseeing a production line doesn’t allow shortcuts — not when handling potentially toxic or reactive intermediates. Exposure limits for brominated aromatics differ between countries, but the company standard has always aimed for stricter containment than regulations demand. Employees rotate jobs to reduce contact risks and every workstation integrates full local exhaust, even during maintenance shutdowns.

    PPE isn’t just a box-ticking formality. Before every large campaign, shift leaders review the incident logs and stage live training runs with simulated spills and evacuations. “Near misses” carry as much weight as actual spills; if one container leaks, all units get reviewed, and process tweaks make it less likely to recur.

    This compound’s reactivity finds use in the lab, but it means extra respect on the floor. Bromine-vapor detectors, spill kits, and regular scrubber checks are standard. Employees flag any off-color or off-odor material for reanalysis—in past years, such vigilance revealed early signs of side-reactions that small-scale analytical work simply missed.

    Environmental Responsibility: Action, not Just Policy

    Waste doesn’t disappear just because it’s bagged and drummed out. Over several production cycles, the plant moved to closed-loop solvent recovery for halogenated waste streams. Dual containment trenches limit run-off risks, and the R&D team enforces random audits on effluent quality.

    Routine inspection caught higher-than-expected bromide traces once, linked back to a faulty valve. Management met with frontline staff to troubleshoot, leading to a new valve maintenance schedule and a staff incentive for spotting root causes early.

    Following product through its entire lifecycle — from incoming raw material all the way to the finished drum — has shown that seemingly minor process tweaks prevent unplanned environmental releases. Anyone who stands on the waste dock at midnight in midwinter sees firsthand the value of these details.

    Work with recycling partners helps reincorporate halogen-containing side streams into secondary processes rather than disposal. The future points towards further reducing extractive sourcing of bromine and fluorine, instead leaning on circular chemistry whenever consistent quality is achieved.

    Traceability and Regulatory Demands: More Than a Checkbox

    No business operates in a vacuum, especially not with specialized aromatic compounds. The team tracks all regulatory updates across target markets. Analysts prepare dossiers for every consignment, showing chain of custody from raw material arrival, through synthesis and purification, to shipment.

    Problems sometimes show up in the paperwork, such as discrepancies in apparent purity after shipping delays. Every time, the root is traced back to unforeseen interactions during transit, not just lab oversight. Over the years, working closely with downstream users and regulators helped build best practices that serve both parties.

    Guaranteeing exact structural placement is more than a matter of trust. Technologies like 1H/19F NMR and high-resolution mass spectrometry act as proof points. On the factory floor, each request for additional documentation builds a muscle memory for compliance—no lot leaves the plant without full traceability.

    Lessons from the Production Line

    Working on the production floor shows that not all chemicals with similar-sounding names behave the same way during synthesis or use. Small structural changes in aromatic compounds mean new hazards, altered reactivity, and different end uses. 2-Bromo-3-Fluorophenol stands as an example of a compound that rewards close attention to detail. Each tweak in reactor temperature, solvent ratio, or drying method adjusts not just yield, but the character of the final product.

    Operators remember which extraction method preserves the best crystal texture; lab staff recall how a slightly longer drying step before grinding holds purity higher after shipping. Customers who rely on consistent melting or reliable color value become trusted sources of feedback, sending test results back that feed process adjustment.

    No two manufacturing campaigns produce precisely the same challenges. Sometimes, a seasonal change in humidity throws off crystal habit. Other times, a subtle impurity requires re-tuning the purification column. Learning from each run builds an institutional memory, letting us pass hard-won know-how on to the next generation of operators.

    Transport, Lab Use, and User Experience

    Shipping is not a mere afterthought. Overseas customers raise concerns every year about customs delays, temperature extremes in transit, or damage to packaging. Based on decades of export experience, upgrades to packaging and embedded temperature monitors in long-haul containers now prevent many common hassles.

    Chemists using 2-Bromo-3-Fluorophenol in synthesis need reliability — not just on paper, but on the bench and in the reactor. A difference of even half a degree in melting point or trace residues from upstream processes leads to headaches when scaling from grams to kilograms. Processes are regularly reviewed against customer-side performance data, tightening tolerances gradually as new combinations crop up in research.

    Lab requests for smaller lots or alternate pack sizes come up regularly. By aligning production runs with customer order patterns, waste from partial drums dropped. Over the years, investing in smaller-scale, automated filling equipment prevented contamination across orders and kept nimbleness possible even for medium volume demand.

    Future Outlook: Building on Experience

    Running a chemical manufacturing plant isn’t just about output — it’s about durability, relationship, and readiness to change. The market for aromatic halogenated phenols continues to evolve as new technologies open up and regulatory frameworks shift. Key to staying relevant is not just hitting purity benchmarks but listening to customer needs, regulatory signals, and front-line expertise.

    As new synthesis techniques emerge or as sustainability takes an ever-larger share of discussion, there’s an ongoing push to improve every aspect of production. Ongoing investment in process safety, emissions control, and staff training keeps the team ready for fresh demands. Plant managers meet monthly with the R&D team to review both old problems and new ideas for higher-yield, lower-waste reactors, aiming for cleaner and safer batches.

    Customer formulations become ever more sophisticated, and demand for custom modifications rises. Flexible batch reactions, robust purification techniques, and sturdy plant equipment allow for shifts, whether to accommodate a more reactive fluorination step or a tighter impurity profile. Continued direct dialogue with users helps steer process innovation, rather than reacting to problems once they’re baked in.

    Summary Through Practical Experience

    The story of 2-Bromo-3-Fluorophenol comes not from catalogs or sales brochures, but from thousands of hours spent in plant halls and quality labs. Each technical challenge, spilled drum, or satisfied customer adds a piece to the company memory bank. The difference between this compound and similar-sounding ones goes beyond academic structure or regulatory number: it lives in the daily choices, constant feedback, and shared goals of everyone from operator to end user.

    Bringing forward a robust supply of this specialty intermediate grows from lessons learned: on reaction setups, tightly managed QA checks, customer dialogues, and responsible stewardship. The work never stops — every batch, every drum, every piece of user feedback guides the next improvement. That is what it means to manufacture 2-Bromo-3-Fluorophenol, day in and day out.