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2-Bromo-4-Fluorophenylacetic Acid

    • Product Name 2-Bromo-4-Fluorophenylacetic Acid
    • Alias 2-Bromo-4-fluorophenylacetic acid
    • Einecs 841-746-4
    • 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

    722679

    Product Name 2-Bromo-4-Fluorophenylacetic Acid
    Cas Number 1150294-34-8
    Molecular Formula C8H6BrFO2
    Molecular Weight 233.04
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO and methanol
    Smiles C1=CC(=C(C=C1F)Br)CC(=O)O
    Inchi InChI=1S/C8H6BrFO2/c9-7-3-6(4-8(11)12)1-2-10-5-7/h1-3,5H,4H2,(H,11,12)
    Synonyms α-(2-Bromo-4-fluorophenyl)acetic acid
    Storage Temperature 2-8°C (Refrigerated)

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, white label marked “2-Bromo-4-Fluorophenylacetic Acid, 25g”, hazard symbols, batch number.
    Shipping **Shipping Description:** 2-Bromo-4-Fluorophenylacetic Acid is shipped in tightly sealed containers, protected from moisture and light. Transport complies with relevant chemical regulations (such as DOT, IATA, or IMDG). Appropriate hazard labels are used, and safety documentation accompanies the package. Handle with care, avoiding heat, sparks, and physical damage during transit.
    Storage 2-Bromo-4-Fluorophenylacetic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Protect it from moisture, direct sunlight, and ignition sources. Ensure appropriate labeling and access is limited to trained personnel. Use personal protective equipment when handling and transferring this chemical.
    Application of 2-Bromo-4-Fluorophenylacetic Acid

    Applications of 2-Bromo-4-Fluorophenylacetic Acid in Industrial Manufacturing

    2-Bromo-4-Fluorophenylacetic Acid serves as a critical intermediate in targeted chemical synthesis pathways for several high-value industries. Its reliability in reaction specificity and controllable purity profile makes it an essential raw material for demanding downstream applications.

    1. Advanced Pharmaceutical Intermediate Synthesis

    This material plays a strategic role in developing complex active pharmaceutical ingredients, especially within new-generation nonsteroidal anti-inflammatory drugs (NSAIDs) and oncology agents. Leading pharmaceutical integrators utilize it during the formation of core scaffolds, where halogen and acetic acid functionalities enable selective C–C bond formation and biaryl coupling. In regulated GMP manufacturing, precise introduction of bromo and fluoro groups enhances therapeutic molecule binding properties and metabolic stability of the final API. Both batch and continuous-flow processes require controlled addition, with careful monitoring for impurity profiles as per ICH Q7 and Q3A guidelines. This intermediate’s consistent performance supports downstream crystallization and chiral separation steps leveraged by innovators and contract manufacturers.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practices for APIs
    • USP and EP quality requirements for pharmaceutical intermediates
    • IDMP data collection for regulatory filings
    • FDA 21 CFR Part 211 (where manufactured in the US)

    Typical usage ratio

    • 0.7–1.2 molar equivalents, adjusted per synthetic route stoichiometry or desired yield in API formation

    Downstream process integration

    • Introduced after initial aromatic substitution in multi-step synthesis
    • Used in Suzuki or Buchwald coupling for side chain installation
    • Purification follows with HPLC or crystallization to pharmaceutical grade
    • Intermediate isolated or telescoped to next active compound construction

    Final product types

    • New chemical entity (NCE) APIs for inflammatory and oncology indications
    • Experimental clinical batch intermediates
    • Patented secondary intermediates in contract development projects
    • Small molecule reference standards for pharmaceutical analysis

    2. Agrochemical Building Block Manufacturing

    Crop protection companies apply this acid in precision synthesis routes for selective herbicides and fungicidal actives, where the bromo-fluoro motif enables tight selectivity and environmental persistence tuning. Process chemists utilize it to prepare key phenylacetic linkers or as a nucleophile acceptor in Grignard and cross-coupling reactions under strict REACH compliance and ISO 9001 frameworks. Careful management of residual solvents and by-products, including bromide-containing waste, aligns production with modern agri-input stewardship targets and minimizes ecological footprint in final formulated products.

    Industry compliance standards

    • REACH Annex IX (precursor registration and use tracking)
    • ISO 9001:2015 (quality management in agrochemical manufacturing)
    • OECD GLP for analytical data supporting regulatory dossiers
    • Directive 2009/128/EC (EU Sustainable Use of Pesticides)

    Typical usage ratio

    • 1.0–1.3 equivalents versus aryl halides or boronic acids in key step
    • Tuned based on required herbicide/fungicide scaffold substitution pattern

    Downstream process integration

    • Enter at chain-extension or coupling stage in multistep synthesis
    • Undergoes halogen exchange or oxidative coupling for active-site insertion
    • Typically followed by esterification or amide linkage reactions
    • Formulation and encapsulation of actives for market-ready products

    Final product types

    • Halogenated phenylacetic-acid derived herbicides
    • Selective triazole fungicides
    • Intermediates for next-generation crop protection active synthesis
    • Analytical standards for environmental residue monitoring

    3. Specialty Chemical Synthesis for Liquid Crystal Materials

    The electronics sector sources this compound as a highly controlled intermediate for manufacturing liquid crystal monomers and specialized display additives. Its unique aromatic pattern supports mesogen tuning in nematic and smectic phases, critical for display panel switching speed and color rendering accuracy. Major panel and material manufacturers carefully dose it in key coupling reactions, such as Kumada and Heck, under ISO 14001 certification for reduced process emissions. Downstream protocols enforce ultra-high purity isolation without ionic contaminants, to meet stringent Japanese Electronic Industry Development Association (JEIDA) purity thresholds for electronic consumer end-use.

    Industry compliance standards

    • JEIDA purity specifications for liquid crystal materials
    • ISO 14001:2015 Environmental Management in electronic raw material use
    • IEC 62474 for material composition reporting
    • RoHS Directive for lead/bromine/fluorine content limits in finished goods

    Typical usage ratio

    • 0.8–1.0 equivalents, precise ratio determined by monomer design and phase transition characteristics required in downstream LC host synthesis

    Downstream process integration

    • Incorporated in cross-coupling steps to attach terminal group to LC mesogen precursor
    • Purification by repeated column chromatography or preparative HPLC
    • Material further functionalized to tune alignment and thermal stability
    • Strict final QC for metal ion and halide residue

    Final product types

    • Nematic and smectic liquid crystal monomers for TFT-LCD production
    • Alignment layer additives for display glass
    • Specialty photonic crystal compounds
    • Advanced OLED intermediate mixtures

    4. Fine Chemical Intermediate for Organic Dyes and Pigments

    Producers of specialty dyes and pigments select this acid to introduce precision halogenation in polycyclic aromatic rings, supporting high-performance coatings and inkjet dispersions. Through staged bromination and acylation, manufacturers target colorfast intermediates and molecular structures resistant to UV and solvent attack. Formulators adjust acid usage to balance hue strength and particle size in the final pigment. In high purity pigment lines, the process follows ISO 17025 analytical verification for batch-to-batch consistency and complies with requirements of the Global Textile Standard (GOTS) and Oeko-Tex for absence of restricted aromatic amines in textile applications.

    Industry compliance standards

    • ISO 17025 for test laboratory verification of purity and identity
    • Global Organic Textile Standard (GOTS) for textile-use dyes
    • Oeko-Tex Standard 100 for restricted substance content
    • EN 71-3 for pigments in toy coatings

    Typical usage ratio

    • 0.5–1.2 equivalents depending on required halogen density and coupling step in pigment/dye molecule assembly

    Downstream process integration

    • Feeds into halogenation or Friedel–Crafts acylation for ring substitution
    • Post-functionalization for pigment nucleation or dye solubility
    • Final purification conducted with solvent extraction and filtration
    • Colorant blended for physical and spectral property testing

    Final product types

    • High-performance organic pigments for automotive and aerospace coatings
    • Textile-reactive dyes with controlled halogen profiles
    • UV-stable inkjet printer colorants
    • Hypoallergenic pigment components for sensitive application lines
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-4-Fluorophenylacetic Acid: A Manufacturer's Perspective

    Every day in our production plant begins before sunrise. The hum of reactors and scent of fresh solvents greet us, a reminder that chemistry never stands still. From our earliest days in specialty aromatic acids, we established a reputation for reliability and clarity. Among our highly engineered products, 2-Bromo-4-Fluorophenylacetic Acid stands out as a core molecule that has powered so many research and development breakthroughs in pharmaceutical and agrochemical labs.

    Understanding the Model and Main Specifications

    Our team produces 2-Bromo-4-Fluorophenylacetic Acid with great care and technical rigor. Each batch passes several checkpoints, from crystallization to final drying, before we approve it for shipment. What sets our manufacturing process apart is our consistent batch purity, usually above 98%, and close control over moisture and residual solvent. We manage particle size distribution to avoid dusting, making handling in synthesis suites safer and more predictable.

    The molecular formula for this compound is C8H6BrFO2, with a molecular weight of about 233.04 g/mol. We routinely verify the structure by NMR and chromatographic methods after synthesis. Over the years, we learned that even subtle variances in halogen content or byproduct profile can disrupt downstream reactions. Through persistent optimization, we diminished trace halide contaminants, which translates to fewer headaches for technicians running multi-step syntheses. Physical properties, such as melting point and bulk density, come with every shipment so process chemists can plug our data directly into their workflow documentation.

    How Our Customers Use It

    Our clients work across medicinal chemistry, fine chemical research, and material science. Some integrate 2-Bromo-4-Fluorophenylacetic Acid as an intermediate in the design of pharmaceutical candidates, especially where selective halogenation opens new routes for further substitution. Specific therapies in CNS, oncology, and anti-infectives often benefit from structures derived from this building block. In many laboratories, chemists report the acid group and halogen arrangement allow for diverse transformation pathways like amide formation, Suzuki coupling, and other cross-coupling reactions.

    We field technical questions weekly about reaction conditions and solubility. From experience, this compound dissolves cleanly in polar aprotic solvents: dimethylformamide, acetonitrile, and N-methyl-2-pyrrolidone perform reliably. With careful pH adjustment, the carboxyl group activates for high-yield conversions. Catalytic methods, either palladium or copper mediated, often proceed without excessive byproduct formation, as verified by repeat HPLC and GC-MS analysis in our facility.

    Learning from Real-World Production Challenges

    When we first scaled up production of 2-Bromo-4-Fluorophenylacetic Acid over a decade ago, supply chain upheavals posed headaches. The demand curve for halogenated aromatic acids often outpaces bromine supply, especially during years with tight raw material constraints. Early on, we faced seasonal constraints with bromine drums and fluorinated benzene sourcing. The team adapted by switching to a modular synthesis route and strengthening key supplier relationships. These changes trimmed lead times and stabilized costs, ensuring our partners could plan reliably.

    Shipping regulations for halogenated aromatic acids shift as international agencies release new standards. Years of experience navigating UN packing requirements shaped our packaging strategy. All outgoing shipments use certified high-density polyethylene containers, sealed with tamper-proof rings. Pallets finish with stretch wrap and weather-resistant labeling. Our logistics crew posts photos of every pallet to the customer portal to double check compliance before dispatch.

    How It Compares to Similar Products

    We produce a family of halogenated phenylacetic acids. Each possesses its own behavioral thumbprint in organic synthesis. Take 2-bromo-phenylacetic acid—lacking the fluorine, it reacts more sluggishly in nucleophilic substitution. 2-Fluorophenylacetic acid, on the other hand, resists oxidative halogenation, which limits utility for those working with more aggressive electrophiles.

    Adding a bromine atom at the ortho position, alongside a fluorine at the para spot, changes reactivity in ways our synthetic chemists learned through real-world tests. The bromine activates the ring for palladium-catalyzed coupling, while the fluorine increases metabolic stability in target molecules. This unique pairing reduces side reactions, and in our routine NMR and HPLC screens, achieves cleaner product profiles versus mono-substituted analogs. Customers consistently report fewer purification cycles and higher isolated yields, especially in stepwise drug synthesis campaigns.

    Passing on Technical Improvements to Customers

    New chemistries keep pushing boundaries. We continually refine our own process. Last year, we transitioned to greener oxidants, cutting down waste-water halide content by 60%. Our analytical staff test not only for chemical purity but also for residual halide contaminants and heavy metals, as required by leading pharmaceutical companies in Europe and North America. We publish impurity profiles and residual solvent data for every lot, because many partners conduct stringent risk assessments for genotoxic or mutagenic impurities.

    Specialists on our production line keep daily logs. If a batch drifts from spec, they troubleshoot cause—incomplete crystallization, bottlenecks with excess washing, or temperature gradient fluctuations—before releasing a new run. We share best practices in downstream documentation too, so R&D chemists save time identifying sources of impurities, foaming, or filter clogging. These one-percent changes in workflow, learned over countless cycles, help us deliver product with fewer surprises.

    Why Source Directly from the Manufacturer?

    Working face-to-face with the end-user brings a level of insight not easily matched by intermediaries. One research group needed custom packaging in inert atmosphere due to air sensitivity of the downstream intermediate—our plant team filled the request without disrupting production. Over years of direct shipment, feedback from customers shaped our packaging, technical sheets, and even prompted multi-kilogram scale batches with lot-specific certificates of analysis for regulatory filings.

    A production bottleneck in fine chemicals hurts everyone downstream. By controlling every step, from raw input to final pack-out, we prevent surprises. We do not blend third-party batches or substitute unverified lots, as this compromises process validation for the pharmaceutical industry. Each run is documented, traceable, and repeatable—this makes troubleshooting possible should an end-user encounter an unanticipated result.

    Regulatory Awareness and Standards Compliance

    Our familiarity with global regulatory standards spans a decade and hundreds of batch submissions. Regulatory expectations for aromatic intermediates in life-science applications have risen. Audits now require heavy-metal screening, residual organic solvent testing, and proof of absence of persistent organic pollutants.

    We built our lab team’s proficiency for ICH Q3A/B/ICH Q7 relevant to pharmaceutical starting materials. This includes validated HPLC, GC, ICP-MS, and titration work, plus secondary screening as required. Transparency builds trust: every partner receives full certificates of analysis and full documentation outlining trace element analysis and batch processing history. Some customers request data packs for method validation to support their filings, which we supply directly. Years of collaboration with their regulatory affairs teams means we have firsthand experience supporting method transfers and GLP documentation reviews.

    Moving the Industry Forward: Environmental and Safety Commitments

    Sustainability changes start inside the plant. We invested in closed-loop solvent recovery, which dropped our VOC emissions and reduced need for off-site incineration. Energy management in the reactor hall shifted from basic heat exchange to full digitization, saving power and improving batch timing. We also switched plant lighting and ventilation systems to run on timers and motion sensors, reflecting not just cost savings, but a company ethic to mind the durable impact of chemical manufacturing.

    Hazard controls on the production floor now include continuous exposure monitoring, double-gloving for caustic steps, and fire suppression redundancies. New staff complete hands-on training on bromine and fluorinated intermediate handling, led by our senior chemists. A near-miss incident several years ago triggered a plant-wide review and a culture of constant vigilance—practical changes like additional local exhaust and routine PPE audits sharply reduced reportable incidents.

    Supporting Research, Innovation, and Collaboration

    We learned the most from collaborating with academic labs, contract research organizations, and in-house process chemists at large pharma. These customers often share their custom synthesis results, feedback on impurity triggers, and requests for alternative grades or chiral analogs. Our technical team holds quarterly reviews to discuss how new use-cases and performance data shape potential improvements, either in purity specs or supply logistics.

    Research teams sometimes request tailored solvents, unusual shipping timelines, or ultra-pure material grades—not available through distribution channels. By acting on these requests, we deepen relationships, save our partners development time, and build shared knowledge. Our site visits to customer pilot plants and R&D suites also inform future product improvements and packaging.

    We are not simply fabricating another molecule for a catalogue. Our work connects directly with scientists striving to design new therapies, explore novel reaction space, or bring more sustainable chemistry to market. The feedback loop of problem-solving and solution-sharing continues to sharpen our skills.

    The Path to Tomorrow

    The role of a specialty chemicals manufacturer means more than making compounds to spec. It means listening to evolving needs in the market, anticipating supply chain wrinkles, and keeping open lines of technical communication. Every month brings new requests—whether for detailed impurity data, process optimization tips, or tailored packaging solutions. The trust built on decades of performance and direct problem-solving has become our strongest asset.

    Every batch of 2-Bromo-4-Fluorophenylacetic Acid leaves our facility as the combined effort of skilled hands, technical insight, and genuine interest in moving chemical innovation forward, one reaction at a time.