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Bromodifluoroacetic Acid

    • Product Name Bromodifluoroacetic Acid
    • Alias BDFAA
    • Einecs 'EINECS 252-036-5'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    811297

    Productname Bromodifluoroacetic Acid
    Chemicalformula C2HBrF2O2
    Molecularweight 176.93 g/mol
    Casnumber 354-09-8
    Appearance Colorless to pale yellow liquid
    Boilingpoint 103-105°C (at 760 mmHg)
    Meltingpoint -28°C
    Density 2.087 g/cm3 (at 25°C)
    Purity Typically ≥98%
    Solubility Soluble in water and most organic solvents

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

    Packing & Storage
    Packing Bromodifluoroacetic Acid (25g) is supplied in a tightly sealed amber glass bottle with hazard labeling and tamper-evident cap.
    Shipping Bromodifluoroacetic acid should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport must comply with relevant hazardous material regulations, including labeling and documentation. Use suitable secondary containment for leak prevention. Avoid exposure to heat and direct sunlight. Ensure handlers use proper personal protective equipment during unloading and storage.
    Storage Bromodifluoroacetic acid should be stored in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as bases, oxidizing agents, and reducing agents. Keep the container tightly closed, preferably in a corrosive-resistant, labeled container. Handle with care, using appropriate personal protective equipment to avoid exposure. Store at room temperature and segregate from food and combustibles.
    Application of Bromodifluoroacetic Acid

    Applications of Bromodifluoroacetic Acid in Industrial Manufacturing

    Bromodifluoroacetic acid delivers value across specialized sectors where selective halogenation and fluorination properties serve as essential enablers for advanced molecular development and synthesis. As a direct manufacturer, we support production partners with detailed integration guidance and consistent supply for scale-up in regulated applications. Explore below how this intermediate supports downstream transformation in key industrial segments.

    1. Pharmaceutical Intermediate Synthesis

    Pharma manufacturers deploy bromodifluoroacetic acid as a strategic building block in the synthesis of select APIs, especially those requiring the introduction of difluoromethyl and bromine functionalities for metabolic stability and target specificity. It often functions within substitution and coupling reactions to construct complex fluorinated scaffolds, contributing critical physicochemical properties essential for final dosage forms. Typical APIs include anti-infectives and central nervous system agents approved for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Regulation No 536/2014 for clinical trials
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Chinese Pharmacopoeia specifications for raw pharmaceutical materials

    Typical usage ratio

    • 0.1–3.5 molar equivalents, depending on target structure and yield optimization in multistep syntheses; selection guided by process development batch data

    Downstream process integration

    • Fed into alkylation or acylation steps during API precursor assembly, often incorporated in the mid to late stage of multi-step, sealed reactor processes under inert atmosphere

    Final product types

    • Regulated active pharmaceutical ingredients (APIs)
    • Key advanced intermediates for further modification
    • Pharmaceutical reference standards
    • Investigational new drug (IND) compounds

    2. Agrochemical Active Ingredient Manufacturing

    Leading crop protection formulators utilize bromodifluoroacetic acid in the synthesis of difluorinated and brominated herbicides, fungicides, and insect control agents. It acts as a fluorinated precursor during the construction of active molecules tailored for improved efficacy and environmental stability. Typical use focuses on molecules listed in modern agrochemical portfolios, ensuring regulatory approval for large-scale field application.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EU Regulation 1107/2009 on plant protection products
    • US EPA 40 CFR Part 158 for pesticide registration
    • China GB/T 1600-2001 for pesticide technical material

    Typical usage ratio

    • 0.2–1.8 molar equivalents, adjusted per synthetic pathway, substrate reactivity, and target molecule registration dossier data

    Downstream process integration

    • Added during halogenation and coupling of aromatic and aliphatic compounds in batch or semi-continuous reactors under temperature- and pH-controlled conditions

    Final product types

    • Herbicide technical materials
    • Fungicide intermediates
    • Registered pesticide active ingredients
    • Microbial growth inhibitors for crop protection

    3. Fluorinated Material Monomer Production

    Producers of specialty fluoropolymers and fluorinated elastomers source bromodifluoroacetic acid as a chain transfer agent and co-monomer modifier. Its unique functional groups introduce controlled branching and halogen content within resin structures, critical for applications requiring low surface energy, chemical resistance, and thermal stability—such as membrane components and engineered fluoroplastic parts.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for synthetic resin manufacturing
    • ASTM D2116 for fluoroplastic materials
    • REACH Regulation (EC) No 1907/2006 for monomer registration in the EU
    • GB/T 2790–2013 for fluororesins in China

    Typical usage ratio

    • 0.3–2.5 wt% relative to total monomer charge, optimized based on mechanical property targets and fluorination requirements

    Downstream process integration

    • Introduced at the polymerization feed stage in bulk, emulsion, or suspension reactors, typically under nitrogen atmosphere and elevated pressure to control propagation steps

    Final product types

    • Modified fluoropolymer granules
    • High-performance fluorinated coatings
    • Engineered elastomeric membranes
    • Fluorinated wire and cable insulation compounds

    4. Specialty Fine Chemical Synthesis

    Chemical manufacturers leverage bromodifluoroacetic acid as a targeted reagent for the construction of advanced intermediates and specialty molecules in custom synthesis projects. Its dual halogen and fluorine profile offers selective reactivity in nucleophilic substitution, coupling, and cyclization reactions where precise insertion of difluoromethyl and bromo groups is mandatory for experimental compounds and analytical reference standards.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for fine chemicals
    • GMP guidelines for non-pharma specialty chemicals
    • European Chemicals Agency (ECHA) safe handling directives
    • Local environmental impact assessment (EIA) protocols

    Typical usage ratio

    • 0.5–2.0 mole equivalents per target molecule, detailed by reaction scale, target substitution, and reactivity profiling

    Downstream process integration

    • Employed as an active halogenating and fluorinating agent at dedicated transformation steps in pilot and kilo-lab reactors—often within inert solvent systems or under dry conditions to avoid side reactions

    Final product types

    • Reference analytical standards
    • Laboratory-scale intermediates for research
    • Non-commercialized specialty fluorinated compounds
    • Synthesis precursors for further chemical modification
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    Certification & Compliance
    More Introduction

    Bromodifluoroacetic Acid: A Reliable Choice for Modern Chemical Synthesis

    Expertise in Fluorinated Carboxylic Acid Production

    Over the past two decades, we have invested energy and resources into developing high-purity, innovative fluorinated intermediates. Among them, Bromodifluoroacetic Acid (CAS 354-15-4) stands out in our specialty acids portfolio. This compound combines a distinctive bromine atom and difluoromethyl group, giving it reactivity and selectivity that standard carboxylic acids rarely match. Years of working at the bench, analyzing process results, and scaling up under production demands ensure every batch consistently meets strict quality standards.

    Model, Purity, and Physical Specifications

    Our process yields Bromodifluoroacetic Acid with a purity typically greater than 98%. The acid appears as a colorless to pale yellow liquid at room temperature and offers a sharp, distinctive odor that experienced operators recognize quickly. Each shipment comes with a detailed batch analysis, displaying the water content, acid value, and precise assay by GC or NMR as appropriate. Within our operations, in-process controls track potential impurities—especially halogenated byproducts—so the final product aligns with customer process windows.

    Bromodifluoroacetic Acid has a molecular formula of C2HBrF2O2, and a molecular weight of 176.93 g/mol. Its boiling point falls around 93–95°C at reduced pressure, which makes distillation manageable in most laboratory and production settings. Storage in tightly sealed containers reduces hydrolysis and limits decomposition over shelf life. Every lot leaves our facility only after passing stability and purity checks—a practice adopted from repeated feedback from field users and in-house chemists.

    The Role of Bromodifluoroacetic Acid in Custom Synthesis

    Demand for specialized fluorinated building blocks has grown steadily. Pharmaceutical research and agrochemical development rely on unique reactivities from halogenated carboxylic acids. Bromodifluoroacetic Acid holds an important place due to its ability to transfer the difluoromethyl group together with a reactive bromine site. In nucleophilic substitution reactions, this compound opens doors for attaching CF2 groups onto aromatic or heterocyclic scaffolds. The difluoromethyl motif often increases metabolic stability or modulates biological activity, which medicinal chemists exploit in drug discovery.

    In our own production labs, we observe how a carefully controlled introduction of Bromodifluoroacetic Acid leads to clean conversion rates and predictable product profiles. Reaction engineers overseeing pilot programs have remarked on the reagent’s crisp stoichiometry—results reflect calculations without significant side formation, which cuts down on purifications and batch corrections. From routine fluorination to complex carbon coupling, the acid integrates well into existing workflows, particularly where a direct source of CF2 is needed.

    Differences from Traditional Carboxylic Acids and Brominated Compounds

    Working with simple carboxylic acids, you expect certain reactivity patterns: acid-base behavior, decarboxylation, and mild nucleophilicity. Add bromine, and electrophilicity increases—but most brominated acids lack the electronic complexity of a difluorinated analog. Bromodifluoroacetic Acid delivers both. Our experience with similar molecules, such as chloro- or trifluorinated acids, proves that adding fluorine atoms often amplifies the acidity and affects how molecules interact in multi-step synthesis. The difluoromethyl group in this compound pulls electron density through both inductive and resonance effects, which creates unique possibilities for controlling reaction selectivity.

    Chemists using only bromoacetic acid sometimes find themselves limited by unwanted byproducts, variable yields, and moderate product stabilities. Our data over repeat runs shows that the difluorinated version corners side reactions, especially in coupling or substitution. It holds up better under strong bases and resists random oxidation, so multi-step sequences can push further without excessive monitoring. In our plant’s test labs, we’ve replaced legacy intermediates with Bromodifluoroacetic Acid when cleaner transitions, higher pot yields, or novel fluorinated targets are on the table.

    Meeting Research and Industrial Needs

    Chemical research rides on reproducibility. Nothing stalls a project more than unreliable intermediates or inconsistent reactivity. In launching our Bromodifluoroacetic Acid production, our technical teams worked with leading pharma groups to run kilo-scale custom reactions. Analytical groups checked every step using high-sensitivity NMR and titration systems. This cooperative approach taught us to adapt drying, storage, and transfer conditions so the acid arrives in prime form, minimizing internal degradation and water uptake.

    Laboratory requests sometimes call for fresh acids in glass or fluoropolymer—our logistics team ensures careful decanting and packaging. For plant-scale customers, bulk drums require confirmed inert atmospheres and leak-resistant fittings, which we arrange through specially sourced drums and container linings. Because the product’s acidity and corrosiveness can strain standard valves and joints, we’ve standardized fluoropolymer joint seals in our filling stations—learned from field maintenance reports after early, minor leaks in steel-based lines.

    Reliable Sourcing and Process Consistency

    In-house production brings advantages: tighter quality control, greater traceability, and responsiveness to unforeseen supply chain hiccups. By managing every production phase—small-batch QC, main reactor campaigns, and final packaging—we can guarantee both the physical integrity and chemical authenticity of Bromodifluoroacetic Acid. Customers needing repeat shipments benefit from the same source of raw fluorine, consistent bromine streams, and analytic records—no drift between batches. Our team records temperature deviations, pressure adjustments, and calibration logs for every production sequence. Years of real-world troubleshooting, from pilot glitches to full-batch root cause analysis, have sharpened procedures—one reason process engineers in the field stop buying from speculative brokers after switching to a manufacturer with measured procedures and history.

    Regulatory, Safety, and Handling Experience

    Fluorinated acids demand respect and planning in production and use. Bromodifluoroacetic Acid, while less hazardous than some industrial fluorine-based materials, still reacts with metals and many organic bases if careless. We use corrosion-resistant vessels and fit vented lines on storage tanks, after learning the hard way that even tiny leaks can cause localized pressure build-up, especially in humid conditions. Vent scrubbers neutralize acidic vapors to protect both workers and equipment bays. We keep inventory logs for regulatory compliance and issue detailed transport manifests—practices born from regional site audits and years spent adapting to new global safety standards.

    In R&D and pilot plants, experienced chemists avoid casual skin or eye contact. Local extraction, gloves, and goggles shield operators during filling and weighing. Spilled acid seldom causes catastrophic outcomes, but early absorption and neutralization with basic wash solutions prevent lingering residues on benches and floors. We share standard protocols with every client and listen to in-house safety teams—many best practices come straight from customer feedback after field incidents or close calls. The acid’s volatility at raised temperatures encourages tight handling procedures in scale-up; automated feeder systems and sealed reactors are now standard in our partner plants.

    The Importance of Analytical Validation in Application

    Our own analysts have built a catalog of spectral and chromatographic data across dozens of runs. Confirming structure and purity is central not just to our lab, but to downstream users—especially where the acid becomes a key fragment of an API or an advanced agrochemical intermediate. Over time, subtle impurities—mono- or polyfluoro-bromoacetic variants—showed up in some production trials until we tightened temperature ramps and modified raw material chemistry. This experience put extra emphasis on validating every mother liquor and each distillation fraction. Samples ordered by pharma customers for preclinical series now receive NMR, GC-MS, and micro-elemental analysis reports straight from batch records.

    Part of production expertise comes from learning where contaminants can enter, how batch histories differ, and why structures look right but still fail downstream purity screens. We draw on process-development partnerships, working directly with client chemists to optimize melting points, remove residual water, or separate unrelated halogenated byproducts. Combining our chemical knowledge with open benchmarking ensures that Bromodifluoroacetic Acid performs each time—whether as a short-step intermediate or the structural core of a next-generation product.

    Supply Chain Confidence and Responsiveness

    Market volatility, weather impacts, and transport limits have become a daily reality. By operating as a primary manufacturer, we insulate our customers from stock-outs and price spikes. Bromine and fluorine sourcing runs deep into our supply agreements—planned years ahead—so even during global disruptions, we keep regular stock of Bromodifluoroacetic Acid. Bulk buyers and small R&D groups both benefit when the source responds quickly, shares tracking, and supports batch re-testing if needed.

    Our warehouse supervisors run periodic stability pulls and photo-age samples to confirm shelf life, feeding results back to change or update inventories. During supply chain audits, customers routinely send their technical teams to tour our reactors and packaging lines. These visits spark further process improvements—from pump upgrades to revised paperwork workflows—that ensure every container matches original batch specs. Sourcing directly from the manufacturer grants confidence and leverages years of in-house adjustments and real talk about what works, what doesn’t, and where next steps in scale-up can turn risky if the supply goes off-spec.

    Customization and Process Flexibility

    Every new application brings up special requirements. Project chemists sometimes look for minor specification tweaks, such as tighter water content, limits on halide byproducts, or different solvent blends for easy reaction staging. In-house synthesis lets us adapt: distillation ranges can adjust; packaging changes on request. Over several large custom contracts, we’ve designed single-use filling lines, modified venting for extreme destination climates, and invested in new analytical equipment to scan for trace impurities never tracked ten years ago.

    Clients scaling up syntheses benefit from prompt technical discussion with chemists and production staff—not just generic sales support. This direct approach solves problems quickly, especially where research teams uncover bottlenecks during gram-to-kilogram conversions. We’ve advised innovators commercializing new fluorinated amides, swapped in Bromodifluoroacetic Acid for unreliable older intermediates, and tracked real-time pH curves and reaction endpoints to ensure target product formation. Technical input from plant operators and QC chemists, based on hundreds of runs, gives practical, reliable solutions—not just theoretical advice.

    Environmental Stewardship and Regulatory Practice

    Chemical manufacturing, especially with halogenated reagents, places obligations on suppliers to minimize emissions and manage waste responsibly. Over years of operating, we’ve converted legacy vent systems, doubled up scrubber units, and adopted waste acid recovery—steps that moved our environmental impact below statutory benchmarks. Our water treatment units dissect and separate halogenated waste streams. Even minor process adjustments, like switching transfer lines or reusing feedstock containers, trim waste and shrink the carbon footprint of Bromodifluoroacetic Acid production.

    Regulatory authorities demand extensive documentation for fluorinated intermediates, and our compliance staff routinely submits REACH, TSCA, and national inventory dossiers. Every batch trace runs back to raw materials, with process data archived and ready for inspection. Customers aiming for their own registrations or process filings receive comprehensive support: batch histories, analytic results, and full performance validation, as learned from hands-on experience with previous regulatory reviews. Open dialogue with both auditors and downstream users advances our reputation as a straightforward, reliable supplier.

    Direct Support and Customer Partnership

    Partnership means more than transactions. Lab and purchasing teams want answers about lead times, purity grades, and technical suitability. Our experience tells us that email or phone correspondence only goes so far—many questions demand direct input from people who actually make the product. By connecting lab chemists to production teams, and inviting client feedback, both sides learn about batch-to-batch variations, latent issues, or optimization possibilities. This commitment developed out of frustration with unclear communication chains years ago, which slowed down key R&D projects and complicated troubleshooting.

    We arrange site visits for larger users, share samples for pilot reactions, and open up process analytics as long as confidentiality stays respected. Our technical service doesn’t stop after delivery—follow-up calls and on-site consultations uncover improvements in packaging, dispensing, or transport. Plant engineers who receive regular training and updates report fewer handling incidents and higher satisfaction with received product. Listening closely to those who use and depend on Bromodifluoroacetic Acid keeps our improvements grounded in real, everyday workflows.

    Comparisons: Why Choose Our Bromodifluoroacetic Acid Over Alternatives?

    Having handled and compared Bromodifluoroacetic Acid to trifluoroacetic acid, bromoacetic acid, and other difluorinated analogs, we see practical differences that matter. The twin influence of bromine and difluoromethyl creates a chemical profile with stronger acidity, greater selectivity in coupling, and more robust resistance to hydrolysis than simpler carboxylic acids. Labs switching from bromoacetic acid to our product often report improved reaction yields, less formation of side products, and easier downstream purification. Compared to trifluoroacetic or monochloro-difluoroacetates, our acid shows more predictable reactivity, particularly when attaching to aryl or heteroatom systems.

    Peer manufacturers may offer similar goods at first glance, but verification runs and user feedback tell the full story. Technical support, delivery reliability, and consistent analysis separate experienced chemical manufacturers from under-resourced or batch-inconsistent suppliers. Labs that previously sourced through distributors often note shipment mix-ups, missing analysis, or unclear origin data—issues not found when sourcing direct from the original producer. Our business model, experience, and routine attention to detail make our Bromodifluoroacetic Acid a practical choice for research, production, and custom synthesis alike.

    Seamless Project Integration and Long-Term Vision

    Our drive grows out of working next to synthesis chemists, pilot engineers, and safety officers who handle these intermediates each day. Success depends on steady supply, responsive support, and a willingness to adapt process for new and old applications. The years spent refining each step of Bromodifluoroacetic Acid production, alongside trusted technical partners, ensure reliable results and open channels for collaboration. Our goal aligns with those of creative chemists and industrial innovators who see the need for new, high-value fluorinated acyl sources delivered with real-world reliability and straightforward technical backup.