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2-Bromo-4,5-Difluorophenol

    • Product Name 2-Bromo-4,5-Difluorophenol
    • Alias 2-Bromo-4,5-difluoro-1-hydroxybenzene
    • Einecs 'EINECS 610-010-4'
    • 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
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    Specifications

    HS Code

    989832

    Product Name 2-Bromo-4,5-Difluorophenol
    Chemical Formula C6H3BrF2O
    Molecular Weight 208.99 g/mol
    Appearance White to off-white solid
    Cas Number 57381-18-7
    Melting Point 78-82°C
    Solubility Slightly soluble in water
    Purity Typically ≥ 98%
    Smiles C1=C(C(=C(C=C1Br)F)O)F
    Storage Conditions Store at 2-8°C, keep tightly closed
    Inchi Key COWQGJXGUKHMEC-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The 2-Bromo-4,5-Difluorophenol (25g) comes in a sealed amber glass bottle with a tamper-evident screw cap and product labeling.
    Shipping 2-Bromo-4,5-Difluorophenol is shipped according to applicable chemical transport regulations. It is securely packaged in sealed containers to prevent leaks or contamination, and clearly labeled with hazard information. The shipment is handled by certified carriers, ensuring compliance with safety, environmental, and legal requirements for transport of hazardous laboratory chemicals.
    Storage 2-Bromo-4,5-Difluorophenol should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and bases. Protect from moisture and direct sunlight. Handle under inert atmosphere if possible to prevent degradation. Proper labeling and secondary containment are recommended to avoid accidental exposure or spills.
    Application of 2-Bromo-4,5-Difluorophenol

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

    As a direct manufacturer, we supply 2-Bromo-4,5-Difluorophenol to specialized downstream sectors as an advanced halogenated phenol intermediate. Below, we detail its use in major industrial segments, with clear focus on real-world regulatory, formulation, process, and end-product specifics.

    1. Pharmaceutical Intermediate Synthesis

    Several pharmaceutical manufacturers incorporate 2-Bromo-4,5-Difluorophenol in the synthesis routes of next-generation active pharmaceutical ingredients, especially in the development of kinase inhibitors and respiratory disorder drug molecules. Its unique halogenation pattern is essential for achieving precise molecular scaffolding in complex heterocyclic APIs. In these applications, its use must satisfy strict regulatory and traceability demands from regulatory bodies and customer audits. Formulators adjust dosage to reaction requirements dependent on specific pharmaceutical syntheses, with inline quality monitoring at each stage to guarantee reproducibility and purity outcomes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for related substances reporting
    • U.S. FDA 21 CFR Part 211 for finished pharmaceuticals GMP controls
    • Chinese Pharmacopoeia General Chapter 0621 (related substances in intermediates)

    Typical usage ratio

    • Intermediate integration at 0.5–1.5 molar equivalents, as defined by API route stoichiometry
    • Adjustable within 5–15% of calculated quantity, based on purity assessment and impurity profile control

    Downstream process integration

    • Initial halogenated aromatic coupling in API synthesis
    • Condensation into heterocyclic frameworks in secondary or tertiary synthesis steps
    • Inclusion in integrated flow reactors for batch or continuous manufacturing

    Final product types

    • Tyrosine kinase inhibitor pharmaceutical substances
    • Small molecule anti-inflammatory active agents
    • Respiratory disorder therapeutic compounds
    • API intermediates for preclinical and clinical supply

    2. Agrochemical Active Ingredient Development

    Producers of selective herbicides and insecticides use this compound to build complex fluorinated aromatics for crop protection products. Its reactivity profile supports the synthesis of intermediates that require both bromo-activation and difluoro substitution for targeted biological activity and environmental stability. Technical teams optimize the reactant ratio according to the precise crop protection formulation, considering molecular conversion rates and downstream product stewardship requirements.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Specification of Pesticide Products
    • REACH Registration and Substance Evaluation (for EU markets)
    • U.S. EPA 40 CFR Part 158 (Data Requirements for Pesticide Registration)
    • ISO 9001:2015 Quality Management System for chemical SOPs

    Typical usage ratio

    • 5–30% based on total mass of synthetic reaction mixture for intermediate formation
    • Higher concentration at 20–35% for direct halogen exchange or cross-coupling reactions

    Downstream process integration

    • Precursor input in Suzuki-Miyaura cross-coupling for herbicide scaffold construction
    • Stepwise functionalization to introduce tailored biologically active groups
    • Purification via crystallization prior to downstream formulation blending

    Final product types

    • Fluorinated phenoxy herbicide intermediates
    • Insecticide ring structures for new actives
    • Plant growth regulator ingredient precursors
    • Multi-mode action agrochemical libraries

    3. Advanced Material Coatings And Polymers

    Manufacturing of specialty polymers and high-performance coatings integrates this material at critical steps for introducing halogenated and fluorinated functional groups. R&D and plant chemists utilize it to impart unique characteristics such as thermal stability, hydrophobicity, and chemical resistance to cured resin and engineered polymer architectures. Process engineers carefully monitor the input ratio to secure batch uniformity and to comply with downstream safety and emission standards, especially during large-scale continuous production.

    Industry compliance standards

    • ISO 14001 Environmental Management in chemical manufacturing
    • ASTM D256 for testing impact properties of plastic specimens
    • EU RoHS Directives (for electronic and electrical device coatings)
    • ISO 10993-5 for biocompatibility of materials used in certain applications

    Typical usage ratio

    • Incorporation at 1–5% by weight in monomer mixture for specialty resin synthesis
    • Up to 10% for high-value niche polymer modifications, as dictated by functional property targets

    Downstream process integration

    • Chain initiation in copolymer reactions
    • Side group insertion during polycondensation or polyaddition
    • Reactive diluent in thermal curing cycles for protective coating formation

    Final product types

    • Fluorinated thermoset resins
    • UV-resistant industrial coatings for electronics
    • Surface protective layers for automotive components
    • Dielectric polymer films for advanced circuitry

    4. Electronic Chemical Synthesis

    Producers of specialty electronic chemicals incorporate this intermediate in the synthesis of functional materials for microelectronics and optoelectronic devices. Its dual halogenation enables the production of highly pure, low-defect materials required for high-frequency circuitry and thin-film transistor technologies. Laboratory and pilot plant chemists carefully balance stoichiometry to optimize final electronic properties, working within stringent contamination and purity management frameworks set by semiconductor industry requirements.

    Industry compliance standards

    • SEMI C44 – Specification for Grade 4 Electronic Chemicals
    • IEC 62474 for material declaration in electronic products
    • JIS-K 0126 (Japanese Industrial Standards for electronic-grade reagents)
    • ISO 9001:2015 traceability and batch record controls

    Typical usage ratio

    • 0.5–3 molar equivalents per step, tightly controlled for device specification
    • Variations within ±0.25 equivalents based on feedback from materials testing and electrical properties assessment

    Downstream process integration

    • Precursor functionalization in molecular electronics material synthesis
    • Coupling into extended ring systems during OLED and TFT material production
    • Final purification before deposition or film application steps

    Final product types

    • Organic semiconductors for TFT and OLED displays
    • Advanced dielectric materials for multilayer circuit boards
    • Photoresist sensitizers for lithography processes
    • Thin-film optoelectronic functional layers
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    Certification & Compliance
    More Introduction

    2-Bromo-4,5-Difluorophenol: From the Manufacturer’s Perspective

    The chemical business rewards accuracy and trust. Our team has invested years refining the production of 2-Bromo-4,5-Difluorophenol, a compound that supports innovation in pharmaceuticals, materials science, and agrochemicals. Any manufacturer knows the challenges that come with handling halogenated phenolic intermediates. Getting these molecules right demands knowledge about organic chemistry, strict quality control, and a shared sense of responsibility for what goes downstream. Over the years, understanding the subtleties of this particular compound has given us a real appreciation for what precise synthesis brings to the industry.

    Overview and Chemical Profile

    Chemists looking at our 2-Bromo-4,5-Difluorophenol will recognize its structural intrigue. With both bromine and two fluorine atoms on the ring, along with a phenolic hydroxyl, it shows significant differences from simpler halophenols. The presence of the difluoro and bromo substituents changes not just the reactivity, but also downstream application options. It is more than just a building block; its electronic and steric contributions shape subsequent reactions.

    Our standard product comes as a white to faintly off-white crystalline solid. Purity tests usually show a GC level above 98%, although liquid chromatography often reveals even fewer trace impurities. Synthesis routes have evolved with pressure from industry regulators and customer needs—moving away from older, less efficient halogenation approaches to greener, more selective processes. This ensures a reliable batch every time, with trace metals and residual solvents kept low. Water solubility remains limited, which makes it necessary to handle with solvents compatible with customers’ processes, usually in organic media.

    Why Commit to 2-Bromo-4,5-Difluorophenol?

    You only keep making a specialty chemical for years if it genuinely answers a need. This molecule answers several: For pharmaceutical innovators, it acts as a versatile core for synthesizing fluorinated scaffolds, which often show improved metabolic stability and receptor affinity. In crop protection, the double-fluorination helps modulate bioactivity and persistence, while the bromine opens routes for Suzki, Heck, or other transition metal-catalyzed couplings. The phenol group enables further derivatization—ether, ester, or other protective group strategies work effectively.

    We have seen clients use it in small-molecule drug research, aiming for selective kinase inhibitors or novel antibacterial agents, where ring substitutions can dictate the path of SAR. The precise arrangement of halogens matters; mono-halogenated and mixed halo compounds don’t provide the same reactivity, nor do they yield the same downstream results in coupling reactions. For those developing OLED materials or advanced polymers, the compound’s unique substitution pattern creates opportunities for both doping and backbone modifications, leading to materials with different electronic or thermal properties.

    Quality, Consistency, and Traceability

    Reputation grows from reliability. Each kilogram leaving our facility has clear batch traceability, rigorous analytical records, and reproducibility built in. We rely on both in-house GC-MS and third-party NMR testing, ensuring matching data from different sources. It's not just about hitting a purity spec. Years of handling sensitive “exotic” halophenols have taught us that customers notice small things—how a batch crystallizes, subtle impurities that don’t show up at first glance, and changes in color or melting point when the process slips. Everything gets checked, from reagent sourcing (down to the lot) to packaging in approved anti-static, moisture-resistant drums.

    One technical issue that keeps coming back is the risk of oxidative decomposition, mainly during storage or shipment—especially in moist or warm conditions. We’ve designed closed-loop filling lines, nitrogen blankets, and advanced packaging to minimize air and water ingress. For high-purity grades designed for pharmaceutical use, we keep additional process steps for in-line filtration and secondary purification. Internal lot codes allow us to retrieve every data point if a question or complaint arises. Integrity and transparency are not negotiable: these standards mean our clients’ work never takes an unexpected turn due to material variability.

    Common Applications and End-Uses

    The world of halogenated phenols keeps getting bigger as researchers build new families of molecules, but not all starting points are created equal. Our focus has always been on supporting advanced research and commercially viable syntheses. In drug discovery, fluorine substitution can transform bioactivity, often turning a good lead into a clinical candidate. Our 2-Bromo-4,5-Difluorophenol has played a quiet but vital role as a core in medicinal chemistry pipelines, enabling the elaboration of libraries for in vitro screening.

    Agrochemical development also benefits. Biological endpoints can shift dramatically with seemingly small changes: two fluorines on adjacent ring positions change the balance of hydrophilicity and lipophilicity, affecting uptake, systemic movement, and breakdown by plant enzymes. The bromo position makes the molecule easy to build onto heterocycles or aliphatic chains, using Pd-catalyzed cross-coupling. Typical transformations include aromatic etherifications, O-alkylations, or selective deprotection, all of which respond consistently due to the stable, well-defined structure of our batches.

    Materials scientists have found uses as well. The dual electron-withdrawing effects from bromine and fluorine shift the phenol’s reactivity, which can be harnessed when making high-performance molecules for electronics. The fluorinated phenotype alters crystal packing and increases resistance to oxidation; this proves useful for formulations exposed to light or heat. Our own customers have reported success synthesizing dye intermediates, photoinitiators, and modified resins that require shelf-stable phenolic precursors.

    Comparisons: How Does it Differ from Other Halophenols?

    A question that often reaches our team concerns the difference between our 2-Bromo-4,5-Difluorophenol and more common alternatives like 2-Bromophenol, 4-Bromophenol, or even difluorinated phenols lacking bromine. The most direct distinction comes from the electronic map that the substituents create: two fluorines at 4 and 5 lower electron density on the ring, making the molecule less reactive to electrophilic substitution but more receptive to certain coupling strategies. The bromine site remains an ideal leaving group for metal-catalyzed cross-couplings, with less chance for regioisomer formation in downstream synthesis.

    Mono-fluorinated phenols don’t offer the same level of control in introducing polar or lipophilic character, and they rarely match the balance of chemical stability and transformation potential. Even multi-bromo compounds carry higher environmental risks (due to brominated byproduct toxicity) and can form mixed isomers more readily. For those running larger campaigns or pilot projects, using fully defined, high-purity 2-Bromo-4,5-Difluorophenol means less batch-to-batch frustration, and faster process optimization.

    We’ve found that new customers sometimes experiment with more available or “cheaper” materials, only to turn to our product once the need for selectivity, reproducibility, or regulatory acceptance becomes non-negotiable. Some try other isomeric halophenols but struggle when impurities or side reactions compromise synthesis. The difference lies not only in the structure but in the way we produce and document every lot. This comes from decades spent working closely with users, troubleshooting problems during scale-up, and handling strict quality checks.

    Safety, Environmental Footprint, and Handling

    Manufacturers stand at the interface of chemistry and stewardship. The presence of both bromine and fluorine atoms in the molecule means special care at the bench and throughout logistics. Our operations have moved to closed processing and strict waste gas capture, ensuring emissions never leave regulatory compliance. You can’t shortcut safe handling of halogenated materials. All packaging passes certification for transport of hazardous substances, with material compatibility and persistent traceability.

    On a practical level, we find that most customers run reactions in well-ventilated labs, with gloves and eye protection standard. The low vapor pressure helps, but spills and dust can present challenges. Our drums and containers include clear labeling, batch numbers, and recommended storage instructions. Experience has shown that temperature stability is robust—goods withstand normal warehouse cycles—but extended exposure to air or damp conditions should be avoided. We ship with desiccants and gas-barrier inner liners for longer transit.

    Supporting Clients and Future Directions

    There’s a growing move towards greener chemistry and reduced environmental impact. Suppliers everywhere claim eco-friendliness, but the proof always comes through third-party audits and how much hazardous waste is minimized. We have invested in recovery systems for solvents and byproducts. Reaction optimization has reduced reagent input by more than twenty percent over the last decade, thanks to better catalyst design and refined temperature control. We recycle spent solvents where possible, and segregate halogen waste for proper destruction.

    Supply chain disruptions over the last several years have tested every chemical manufacturer. Regular communication with our raw material suppliers and backup vendor options have kept delays minimal. We track emerging regulations concerning persistent organic pollutants, and work with outside labs to monitor effluent streams—no one can afford surprises from evolving safety rules. Our customers have their own compliance burdens to meet, so timely, thoroughly documented shipments matter from the gram scale up to drum lots.

    Technical support never stops at the point of sale. Our chemists frequently help interpret data, review proposed transformations, or suggest troubleshooting options when clients encounter unexpected byproducts. Synthetic chemistry still throws curveballs, especially when scaling up or exploring new coupling conditions. Our expertise grew from years in the industry—not just from textbooks or papers, but from the trial-and-error that comes with scaling up for real-world commercial needs. Frankly, if manufacturers stay behind a desk, they miss the hands-on reality of running reactions, facing equipment issues, and shipping to places with harsh climates or unpredictable transit times.

    Key Lessons From Years of Manufacturing

    It’s easy to underestimate the value of a reliable specialty chemical until a process grinds to a halt. From day one, focusing on consistency—of both the physical chemical and the documentation—has been the backbone of trust with our customers. We make no secret that our best process improvements come from direct client feedback rather than internal ideas alone. Simple tweaks, like adjusting drying times or storage conditions, have solved raw material headaches in partner labs.

    Take purity for example. A client developing kinase inhibitors reported uneven results using halophenols sourced elsewhere, until we helped them identify trace metal contamination and a persistent byproduct from incomplete halogenation. Our ability to trace each processing step and offer samples for independent verification meant they quickly switched to our material, successfully progressing their candidate down the pipeline. Small things—like stabilizing agents or packaging protocols—make all the difference over years of shipments. As manufacturers, responding quickly, taking responsibility, and not blaming the end user for chemistry setbacks, turns one-off buyers into loyal partners.

    Another recurring lesson is that innovation does not stand still. Regulatory requirements and end-user expectations ratchet up every few years. What set the standard in 2015 sometimes misses the bar in recent audits. We keep our teams involved with national and international standards organizations—no point ignoring benchmarks that influence future business. Audits and paperwork can be a headache, but they force continuous improvement and safer practice.

    Future Developments and Industry Challenges

    Looking forward, specialty molecules like 2-Bromo-4,5-Difluorophenol will play larger roles in next-generation therapeutics and materials. Process intensification, automation, and digital tracking have all entered daily production. Our automated synthesis and in-line analytical tools now monitor every key parameter, generating real-time run data and flagging anomalies for operator review. This reduces the potential for human error, catching trends long before a product ever reaches a customer.

    Logistics have become trickier. Recent shipping restrictions on halogenated materials and bottlenecks in sea freight challenged the old assumptions about lead times and costs. Our answer has been flexible packaging sizes, qualified secondary shippers, and investment in regional storage. Having inventory closer to key markets has cut weeks off delivery. Transitioning to more sustainable packaging—reducing plastics, increasing recycling—is now a core design principle for new product launches.

    Recycling of halogenated organic waste draws mounting scrutiny. We maintain open channels with regulators and have built relationships with compliant waste handlers to ensure destruction meets both legal and ethical standards. Customers increasingly want to know the fate of what’s not used, and we support transparent certificates of destruction for materials returned unused or as part of off-spec lots.

    Building Trust Through Experience

    If there's one thing years in the field have proven, it's that expertise flows from practice, repetition, and real-world troubleshooting. Making 2-Bromo-4,5-Difluorophenol isn’t just a technical challenge, it’s about accountability—ownership of decisions made at every stage. From raw materials through to the final kilogram shipped, the product carries the signature of every person who worked on it.

    What sets us apart isn’t just synthetic know-how or process control. It's the conversations with a client at midnight, trying to track down the cause of a crystallization problem; it’s the willingness to rerun a batch after an out-of-spec analytical result, and follow the paperwork trail until the issue’s root cause is clear. Those experiences build confidence—not just in this product, but in every molecule carrying our label.

    Across the industry, buyers and project leaders gravitate to manufacturers who pick up the phone, answer technical questions clearly, and see themselves as full partners rather than simple vendors. That’s how we’ve built our approach to 2-Bromo-4,5-Difluorophenol: not as a commodity, but as the product of shared expectations, high standards, and the respect that only experience earns.