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Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate

    • Product Name Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate
    • Alias Bromo(trifluoromethyl)ethyl fluoroacetate
    • Einecs 618-588-2
    • 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

    997105

    Productname Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate
    Molecularformula C5H5BrF4O2
    Molecularweight 254.99 g/mol
    Casnumber 751-91-7
    Appearance Colorless to pale yellow liquid
    Boilingpoint 108-112°C
    Density 1.739 g/mL at 25°C
    Refractiveindex 1.3570-1.3590
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ether and chloroform

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

    Packing & Storage
    Packing A 100g amber glass bottle, tightly sealed with a PTFE-lined cap, labeled "Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate," hazard symbols displayed.
    Shipping Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate is shipped in tightly sealed, chemically resistant containers under cool, dry conditions. Handling follows relevant regulations for hazardous chemicals. The product is packaged to minimize breakage or leakage, clearly labeled with hazard information, and usually shipped via ground or air freight according to international and local shipping guidelines.
    Storage Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and direct sunlight. Keep separate from incompatible materials such as strong bases and oxidizing agents. Store under an inert atmosphere if recommended, and clearly label the container. Follow all relevant safety and regulatory guidelines.
    Application of Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate

    Applications of Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate in Industrial Manufacturing

    Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate serves as a technically advanced intermediate in several high-value fluorochemical synthesis chains. Its defined reactivity and selectivity address specific transformation steps for downstream production, making it indispensable in specialized sectors. Below are focused scenarios demonstrating where industry practitioners integrate this material into differentiated applications.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical producers employ this compound as a key fluorinated synthon for developing next-generation herbicide and pesticide actives with improved environmental persistence and targeted activity. Utilizing its bromide function for nucleophilic substitution and its fluorinated backbone for enhanced bioavailability, formulators rely on it to introduce unique structural motifs required for patentable final molecules in the crop protection pipeline.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA Pesticide Registration (40 CFR Part 152)
    • China GB 2763 Maximum Residue Limits for Pesticides
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 0.5%–2.2% molar ratio of total synthetic batch, depending on target compound and reaction pathway
    • Dose adjusted according to active site replacement and desired fluorination degree in the end molecule

    Downstream process integration

    • Added during late-stage intermediate step via alkylation or substitution reactions under controlled anhydrous conditions
    • Directly reacts with nitrogen or oxygen nucleophiles to construct fluorinated aromatic or aliphatic segments of actives

    Final product types

    • Novel fluorinated herbicide concentrates (technical grade)
    • Active pharmaceutical equivalents for advanced insecticides
    • Pre-emergent weed control formulations
    • Field-ready crop protection liquids and microgranules

    2. Fluorinated Pharmaceutical Intermediate Manufacturing

    In specialty pharma synthesis, this raw material undergoes regiocontrolled coupling to introduce highly stable, bioavailable fluorinated groups into medicinal scaffolds. Medicinal chemists favor its specific tetrafluorinated profile for late-stage modifications, supporting development of kinase inhibitors and CNS drug leads where enhanced metabolic stability and lipophilicity are required. Its reactivity ensures precise incorporation without off-target side reactions during scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (Drug CGMP)
    • European Pharmacopoeia (Ph. Eur.) relevant monographs
    • JP PMDA GMP standards for drug substances

    Typical usage ratio

    • 0.7%–1.6% w/w vs. total intermediate weight; ratio optimized per end API fluorination site demand
    • Adjusted based on degree of halogenation needed and substitution yield in medicinal core

    Downstream process integration

    • Introduced as an electrophilic agent in Suzuki, Suzuki-Miyaura, or Buchwald coupling steps
    • Employed post-core structure build for controlled fluorine introduction, maximizing yield of the desired regioisomer

    Final product types

    • Clinical candidate kinase inhibitors (API intermediates)
    • Fluorinated benzoxazinone core fragments
    • Late-stage CNS drug intermediates
    • Next-generation antiviral precursor compounds

    3. Specialty Fluorinated Polymer Monomer Production

    Polymer manufacturers incorporate this molecule to synthesize tailored monomers for fluorinated acrylics, high-performance resins, or specialty copolymers. It acts as a functionalized building block capable of imparting both hydrophobicity and enhanced chemical resistance in engineered polymers for microelectronics, membranes, and advanced coatings. The controlled incorporation of bromo and fluorine groups allows for further post-polymerization modification and block copolymer design.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ISO 9001:2015 Quality Management Systems for polymer production
    • RoHS Directive 2011/65/EU for restricted substances
    • UL 94 Flammability Standard for plastics

    Typical usage ratio

    • 1.0%–3.5% of total monomer input weight, adjusted for desired copolymer composition and fluorine content
    • Ratio set by target properties, e.g., water repellency or dielectric constant needs

    Downstream process integration

    • Charged into pre-polymerization feedstock under strictly monitored temperature and agitation for homogeneous copolymerization
    • Participates in free radical, cationic, or anionic polymerization steps as per chosen catalyst system

    Final product types

    • Fluorinated acrylic sheet and films for electronics
    • Resistant surface coatings for photovoltaic panels
    • High-barrier packaging polymers
    • Selective membrane materials for chemical separations

    4. Precision Fluoroalkylation Reagent in Fine Chemical Synthesis

    Fine chemical producers integrate this high-purity reagent for selective fluoroalkylation of carbon frameworks, supporting the scale-up of specialty building blocks meant for organofluorine libraries, chiral auxiliaries, and advanced research reagents. The compound’s electron-withdrawing tetrafluoropropionate structure enables reliable control over alkylation regioselectivity, yielding intermediates crucial to advanced chemical R&D and commercial batch production for synthesis-as-a-service enterprises.

    Industry compliance standards

    • ISO 17025 Laboratory Management for reagent synthesis
    • US EPA TSCA for chemical substances
    • Global Harmonized System (GHS) of Classification and Labelling
    • REACH pre-registration for R&D chemicals

    Typical usage ratio

    • 0.3%–1.8% of the limiting reactant, dependent on the complexity of the fluoroalkyl group needed and substrate reactivity
    • Ratio flexibly set per batch protocol and desired product throughput

    Downstream process integration

    • Charged to reaction flask after initial substrate activation and before final quench step
    • Heated in aprotic solvent with base/acid catalyst for regioselective C–C bond formation

    Final product types

    • Chiral fluoroalkyl intermediates for pharmaceutical research
    • Specialty ligands and organocatalysts for fine chemical catalogs
    • Multi-functional platform molecules for custom synthesis
    • Fluorinated building blocks for academic and contract research
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    Certification & Compliance
    More Introduction

    Introducing Ethyl 2-Bromo-2,3,3,3-Tetrafluoropropionate: Purpose-Built Chemistry for Innovation

    Focusing on Real-World Needs in Fluorinated Chemistry

    Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate has gained recognition as a crucial building block in the development of next-generation materials. As a manufacturer who has committed years to advancing fluorinated intermediates, our attention started shifting toward this compound as demand grew in both the agrochemical and pharmaceutical industries. Our product carries the model designation EBP-324, which distinguishes it by its consistent purity and reliable batch-to-batch performance. Over the past decade, we’ve refined our process by listening closely to users in R&D and pilot-scale labs. They repeatedly encounter bottlenecks when working with less stable or less clean analogs; we took it upon ourselves to resolve those recurring headaches.

    A Chemical with Versatile Applications

    The unique structure of Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate — featuring both a bromine atom and multiple fluorine groups anchored to a propionate backbone — unlocks several synthetic transformations unavailable through more standard alkyl bromides or simple fluorocarbon esters. Chemists who work in crop protection frequently select this molecule as a fluorine source for introducing stable CF3 or derivative groups into active ingredients. Fluorinated motifs deliver real improvements to a molecule’s environmental persistence, bioavailability, and selectivity profiles. Trying to accomplish this using non-fluorinated or mono-fluorinated esters quickly proves limiting, especially when looking to optimize metabolic stability or activity spectrum.

    Our experience supplying both kilogram and scale-up quantities to process chemists shows that reactions with EBP-324 result in higher yields with fewer troublesome byproducts compared to alternatives, such as methyl-based or non-brominated sources. In preclinical synthesis, this sharp reduction in clean-up allows project timelines to move forward with fewer delays. As pharmaceutical teams move targets through screening phases, having a fluorinated scaffold that is both straightforward to introduce and resistant to hydrolysis lets them worry less about chemical compatibility and more about final biological output.

    Specifications Rooted in Real-World Production

    Making fluorinated intermediates like this isn’t as simple as following a textbook protocol. We’ve learned firsthand that temperature ramps, pressure controls, and impurity management require constant tuning based on actual output. For our batches of EBP-324, we routinely target a purity of at least 98% (GC), verified through internal reference standards and confirmed by clients through their own analytical screens. Batches that don’t meet these requirements do not reach the packaging line. During scale-up, we found that side reactions with atmospheric moisture or organic residues threatened product quality — our plant now maintains controlled humidity and inert-gas handling throughout the entire synthesis and isolation process.

    Logistics also make a difference. During transport, certain analogs of this compound degrade, releasing unwanted byproducts with a pungent odor. After evaluating different container liners and seal types, we adopted fluoropolymer-capped bottles. This practice prevented decomposition and preserved material integrity on arrival, as confirmed by customer feedback loops. Shelf life concerns matter most when supply chains stretch across continents. We run stability trials under simulated transit conditions, checking not just for remaining bromide, but for the subtle shift in fluoride resonance that signals the earliest onset of hydrolysis. Based on this, the recommended storage conditions and maximum holding times stem from actual data instead of a theoretical best guess.

    Direct Comparisons: What Sets EBP-324 Apart

    Over the years, we have trialed and tested a wide range of fluorinated esters and brominated analogs under bench and pilot plant scenarios. EBP-324 stands apart from non-fluorinated propionates by offering a much greater chemical stability, particularly during high-temperature reactions or longer-duration refluxes. Many labs turn to methyl 2-bromo-2,3,3,3-tetrafluoropropionate or its iso-propyl cousin as alternatives, but those introduce a higher risk of side ester cleavage or uncontrolled polymerization. In a typical alkylation or substitution, our ethyl-based version delivers a predictable pattern of selectivity, confirmed by NMR and supported by both academic and industrial case studies.

    Some practitioners ask about the differences compared to other halogenated esters, especially those featuring chlorine or iodine instead of bromine. We’ve found that the bromine atom in EBP-324 offers a strong leaving group for nucleophilic substitution — better than chloride, less prone to side elimination than iodide in most common conditions. In catalytic cycles aimed at introducing perfluoroalkyl chains, the combination of bromine and high fluorine content allows transformations to proceed in a cleaner, faster, more controllable fashion, reducing waste and downstream purification steps. This is not always obvious from vendor brochures but becomes quickly evident when scale grows to multi-kg lots.

    Cost factors enter discussions with process engineers, who want predictable and straightforward pricing models. Unwanted breakdown during storage or shipping leads to re-ordering, extra expense, and waste disposal headaches. EBP-324’s resistance to spontaneous decomposition has measurably lowered these hidden costs for a growing group of our customers.

    Reflections from Production: Supporting Responsible Chemistry

    We don’t view this molecule as just another line item in a catalog. The reality of industrial-scale chemical manufacturing is that every intermediate we supply affects downstream safety, environmental footprint, and the ultimate viability of the customer’s process. Fluorination brings real benefits — sometimes essential breakthroughs — but also introduces challenges around waste handling and regulatory compliance. Our facilities adopt vapour monitoring, solvent treatment, and waste minimization at every stage. Early on, we discovered that common batch reactors produced volatile organics during the bromination stage; after repeated testing, jacketed vessels with fully enclosed condensation loops eliminated releases at the source. It’s not only about meeting a compliance checklist. Worker safety and product reliability stay front-of-mind on every shift.

    End-users increasingly ask about the lifecycle impact of fluorinated intermediates. We collect real-world feedback from customers about both upstream waste and downstream byproducts. With this input, our team has tailored our reaction sequences to minimize halogenated effluent and to capture not just the easily measured gases, but also the hard-to-detect trace byproducts that regulators now target. Whenever a new shipment leaves our facility, our QC team tracks both standard purity and the extended fingerprint of minor byproducts, prepared to offer full analytical transparency on request.

    This has helped several large clients pass regulatory inspections in Europe and Asia, where uploading detailed impurity profiles and batch records to regulatory bodies now forms part of normal business. We treat these requirements as an opportunity to push our own standards higher and to preempt future compliance headaches for our customers.

    Working Directly With Formulators and Process Chemists

    One of the most rewarding parts of this job comes from collaboration with the chemists and process engineers using our materials. Nearly every major improvement we have implemented came from frank discussions with users who stress-tested EBP-324 under real project conditions. Typical requests focus on minimizing impurity carry-over from precursor steps or controlling pH drift downstream of process addition. Even the capping rate of the ethyl group itself has been optimized based on hard numbers, after a pilot customer documented improved separation during a critical cyclization stage by using our material rather than an off-brand competitor’s.

    Process scale-up brings its own set of headaches. A reaction that works beautifully in a 250-milliliter flask does not always behave in a 200-liter reactor. Problems like variable exotherm or inconsistent color formation prompted changes in our quench step and post-reaction washing. Through dozens of scale-up runs, we refined the sequence, improving both yield and process predictability, while keeping worker safety tight. To ensure that pilot projects don’t come to a standstill, we maintain a stock of both standard and custom grades, complete with in-process certificates. The reliability of our intermediate allows our partners to focus on the more creative aspects of formulation rather than spend energy troubleshooting basic raw material variances.

    A Commitment to Transparent Communication and Ongoing Support

    As producers, we believe in staying accountable through clear and documented communication. Every lot of EBP-324 ships with its own full certificate, but the paperwork only tells part of the story. Our internal logs track not just basic physical constants, but also a running history of customer-reported outcomes: reaction yields, impurity signatures, stability under various conditions, and feedback on ease of use. This open style keeps us honest and helps push further process upgrades. When questions arise about process substitution, compatibility with other fluorinated or non-fluorinated reagents, or downstream purification, our experienced technical team stands ready with real examples, not theoretical responses. Data drawn from previous runs and shared customer experiences add to the collective knowledge base.

    Occasionally, a shipment finds its way into a challenging application — perhaps a new fluorinated pesticide or a proprietary medical chemistry program. In those cases, we coordinate sampling and analytical support built around the specific project goals, not generic one-size-fits-all answers. This kind of service may sound old-fashioned, but transparent partnership has consistently delivered better results for both sides.

    Documentation from previous lots, along with batch-to-batch stability reports, is always kept on file, allowing researchers or quality officers to see how the material has performed over time and under different storage regimes. This helps reduce surprises down the line and empowers process scale-up teams to plan with better foresight and confidence.

    Improving Synthesis and Downstream Performance

    One significant reason customers continue choosing EBP-324 involves its behavior during downstream synthetic transformations. In SN2 reactions, the compound consistently demonstrates clean conversion, leaving minimal unreacted starting material or halogenated side products. For pharmaceutical discovery or specialty crop protection programs, this minimizes rework. Through tight control over initial purity and careful bottle sealing, our product sees little decline in reactivity even after several months on the customer’s shelf. Chemists who have attempted similar reactions with other suppliers’ bromo-fluoropropionates often see more rapid decomposition and unwanted residue formation, which leads to frustration, delays, and the risk of project derailment.

    The combination of ethyl ester backbone and tetrafluoro substitution creates a perfect balance between reactivity and stability. While more heavily fluorinated compounds can resist desired reactivity, and less-substituted esters can fall prey to hydrolysis or over-reduction, this specific molecule has shown dependable results across a range of solvent and temperature conditions. These aren’t theoretical gains — feedback from pilot runs and multi-kilo manufacturing campaigns back up the performance gap.

    Not long ago, a partner working on a custom fluorinated coupling agent provided a side-by-side performance log of our EBP-324 versus another commercial source. Their process shifted from repeated post-reaction scrapings and product loss, to a stable workflow with greatly increased batch success rates. Cost savings, lower waste, and fewer troubleshooting cycles followed. Supporting project timelines and reducing waste has always been more persuasive than any advertising pitch.

    Looking to the Future: Responsiveness Drives Progress

    Molecules like Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate are at the frontier of several new industrial and medicinal syntheses. As applications grow more advanced and regulatory demands tighten, the specifics of production and delivery matter ever more. Our team continues investing in both people and equipment to spot issues early, communicate findings openly, and implement real-world solutions rather than quick fixes. Listening directly to user reports of side reactions, stability hiccups, or process-induced color shifts improves not only our own batch records but often influences upgrades at the end-user's site as well.

    To keep pace with rapid industry change, we partner with leading analysts, maintain participation in round-robin inter-lab purity checks, and share anonymized trends among project teams to build collective expertise. At all times, we aim for decisions based on evidence and consistent customer experiences, rather than sales literature or untested claims. This means regularly reevaluating how we make and supply this compound, including the adoption of new analytical techniques as they emerge.

    Ultimately, chemical manufacturing is a joint venture between producer and user. In our experience, real improvements happen where transparent feedback, traceable documentation, and practical support co-exist. Ethyl 2-Bromo-2,3,3,3-tetrafluoropropionate has already unlocked new synthetic possibilities across far-ranging industries. As teams discover even more demanding uses, our foundation remains unchanged: reliable quality, clear communication, and a willingness to solve problems hand-in-hand with our partners.