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3-Bromo-4-Chloropentafluorobutyric Acid

    • Product Name 3-Bromo-4-Chloropentafluorobutyric Acid
    • Alias 3-Bromo-4-chloro-1,1,2,2,3-pentafluorobutyric acid
    • Einecs 701-286-2
    • 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

    307410

    Productname 3-Bromo-4-Chloropentafluorobutyric Acid
    Molecularformula C4BrClF5O2
    Molecularweight 289.39 g/mol
    Casnumber 161098-32-8
    Appearance Colorless to pale yellow liquid
    Purity Typically >95%
    Solubility Soluble in organic solvents
    Smiles C(C(C(C(=O)O)(Br))(Cl))(F)(F)(F)(F)F
    Inchikey QOPUZEJNYLHUMU-UHFFFAOYSA-N

    As an accredited 3-Bromo-4-Chloropentafluorobutyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a red hazard label, tightly sealed and clearly marked: 3-Bromo-4-Chloropentafluorobutyric Acid.
    Shipping **Shipping of 3-Bromo-4-Chloropentafluorobutyric Acid:** This chemical is shipped in tightly sealed containers compliant with international transport regulations. It is labeled as hazardous, requiring handling and storage away from heat, moisture, and incompatible substances. Shipping is typically by ground or air, with appropriate documentation and compliance with relevant safety standards (e.g., IMDG, IATA).
    Storage 3-Bromo-4-Chloropentafluorobutyric acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances like strong bases and oxidizers. Protect from moisture and direct sunlight. Store at room temperature, avoiding excessive heat. Proper labeling and use of secondary containment are recommended to prevent leaks or accidental release.
    Application of 3-Bromo-4-Chloropentafluorobutyric Acid

    Applications of 3-Bromo-4-Chloropentafluorobutyric Acid in Industrial Manufacturing

    As the original manufacturer of 3-Bromo-4-Chloropentafluorobutyric Acid, we focus on actual industrial customers using this specialty fluorinated intermediate in high-value downstream production. The following sections outline authentic application scenarios—covering key formula targets, process stages, regulatory frameworks, and related finished goods—reflecting current industry practice and supply chain integration.

    1. Production of Pharmaceutical Agrochemical Intermediates

    Major agricultural and pharmaceutical synthesis enterprises utilize this compound as a core halogenated building block in the preparation of complex molecular scaffolds. The acid group and dual halogen substitution allow downstream partners to develop selective herbicide and fungicide intermediates via nucleophilic substitution under controlled laboratory or pilot plant conditions. Strict traceability, purity, and residual solvent management are required throughout.

    Industry compliance standards

    • REACH Registration (EC No. 1907/2006)
    • ISO 9001:2015 Quality Management
    • FAO/WHO Specifications for Pesticide Intermediates
    • European Pharmacopoeia (for APIs precursors)

    Typical usage ratio

    • Usage levels range from 3% to 12% in intermediate synthesis reaction mass, depending on target molecule loading and batch yield optimization.

    Downstream process integration

    • Charged during late-stage fluorination or halogen exchange, immediately prior to coupling or amidation step in pharmaceutical or crop protection active ingredient development.

    Final product types

    • Sulfonylurea herbicide intermediates
    • Pyridine and triazine fungicide precursors
    • Marketed plant growth regulator actives
    • API (active pharmaceutical ingredient) building blocks

    2. Fluorinated Specialty Polymer Synthesis

    Industrial polymer manufacturers add this compound as a functionalized monomer or chain terminator during the design of highly hydrophobic or chemically resistant fluoropolymers. The multi-halogenated structure introduces unique bonding environments, allowing customers to engineer surface properties or thermal properties in specialty resins for electronics and aerospace composites.

    Industry compliance standards

    • UL 94 Flammability for Polymer Materials
    • ASTM D543 Chemical Resistance Testing
    • RoHS Directive 2011/65/EU (electronic uses)
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • Typical dosage is 0.5%–4% of total monomer feed, adjusted to achieve target molecular weight or thermal transition properties during batch or continuous polymerization.

    Downstream process integration

    • Fed into the reaction vessel just before polymerization initiation, often as a co-monomer or end-cap agent, followed by high-temperature, solvent-based chain propagation and extrusion.

    Final product types

    • High-performance fluorinated resins
    • Specialty cable coatings
    • Electronics encapsulants
    • Membranes for chemical processing

    3. Synthesis of Fluorinated Surfactant Precursors

    Advanced surfactant producers in textile, electronics, and fire safety industries incorporate this raw material when building chain-extended fluorinated acids and salts used in low-surface-energy wetting agents and specialty emulsifiers. The unique structure enables downstream blending into performance-critical additives while supporting tight compositional specifications.

    Industry compliance standards

    • OECD PFAS Risk Management Guidelines
    • Directive (EU) 2019/1021 on Persistent Organic Pollutants (POP)
    • ISO 14040/44 Life Cycle Assessment (for environmental claims)
    • U.S. EPA TSCA Inventory Listing (if imported/used in the USA)

    Typical usage ratio

    • 1%–9% w/w relative to total fluorosurfactant precursor batch, fine-tuned according to branching degree and required chain length for target emulsification potential.

    Downstream process integration

    • Reacted via stepwise fluorination, sulfonation, or amidation, before neutralization and purification above 99% purity, followed by downstream blending into commercial surfactant concentrates.

    Final product types

    • Textile repellency agents
    • Fire-fighting foam additives
    • Semiconductor rinse surfactants
    • Industrial cleaning formulations

    4. Electronics-Grade Chemical Synthesis

    Downstream users in the electronics chemicals sector leverage this fluorinated acid as a precision precursor during the creation of wet-etching agents, photoresist developers, and surface treatment reagents. The presence of both bromo and chloro substituents can be exploited in tailoring etching selectivity and process purity, meeting stringent industry requirements for trace contaminant control.

    Industry compliance standards

    • SEMI C93/C94 (High-Purity Specialty Chemicals for Semiconductor Manufacturing)
    • ANSI/ESD S20.20 (Electrostatic Controls)
    • IEC 61340 for Antistatic Packaging
    • ISO 9001:2015 for Electronics Quality Management

    Typical usage ratio

    • 0.2%–2% in high-purity chemical blends, defined per process wafer load and bath dynamic; trace-checked post-mix to prevent ionic contamination.

    Downstream process integration

    • Dosed into pre-mix or inline blending systems as functional group donor, followed by microfiltration and point-of-use filtration in cleanroom-grade filling and packaging zones.

    Final product types

    • Photoresist developers
    • Semiconductor wet etchants
    • Plasma ashing and strip chemicals
    • Microelectronic interconnect treatment liquids

    5. Reference Material for Analytical Chemistry Validation

    Certified laboratories and chemical standards manufacturers utilize this high-purity acid salt as a reference compound in the calibration of LC-MS and GC-MS methods specific to environmental or workplace monitoring of halogenated fluorinated acidic species. Traceable impurities and isotopic purity support method validation and regulatory compliance in analytical applications.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Competence
    • EPA Method 537.1 for Perfluorinated Chemicals
    • EN 17034 Certified Reference Materials
    • USP General Chapter <1225> Validation of Compendial Procedures

    Typical usage ratio

    • Preparation in standard solutions between 1 ppb and 1000 ppm, depending on the detection range and instrument sensitivity for validation or calibration runs.

    Downstream process integration

    • Dissolved and diluted under gravimetric or volumetric control, further processed through isotopic enrichment or purity verification by NMR or mass spectrometry, then dispensed into ampoules for distribution.

    Final product types

    • Secondary reference standards
    • Certified calibration solutions
    • Quality control check standards
    • Lab proficiency testing kits
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    Certification & Compliance
    More Introduction

    3-Bromo-4-Chloropentafluorobutyric Acid: An Insider’s Perspective on Manufacturing and Industrial Value

    Our Experience with 3-Bromo-4-Chloropentafluorobutyric Acid

    Working daily with 3-Bromo-4-Chloropentafluorobutyric Acid, known in our production facility as Model BCPFB-01, brings a real awareness of what this substance means in modern chemical development. The fluorinated carboxylic acid profile makes it a specialty product by any standard. Containing both bromine and chlorine together with five fluorines bonded to its butyric acid backbone, this material isn’t just another entry in a catalog. We manufacture BCPFB-01 in lot quantities ranging from single-kilogram pilot runs to multi-metric-ton batches, each requiring high-precision control in every synthetic stage. Handling this compound drives home the value of consistent process chemistry, not just for purity, but for downstream reliability in advanced applications.

    Understanding the Unique Structure and Its Implications

    The heart of BCPFB-01's story lies in its structure—a butyric acid chain carrying bromine and chlorine atoms at key positions, with a pentafluoroalkyl tail delivering a strong electron-withdrawing effect. This unique combination shifts reactivity in meaningful ways. The acid’s melting and boiling points, solubility in polar and nonpolar solvents, and interaction with classic nucleophiles all stem from the heavy halogenation. For a manufacturer, this means heating and pressure profiles diverge from standards set by simple haloacids or perfluorinated acids.

    In production, we approach BCPFB-01 as both a challenge and an opportunity. Safety measures demand thoughtful ventilation and containment due to volatility and the reactive nature of its halogens. The acid’s tendency toward hydrolytic stability—compared with non-fluorinated analogs—gives our customers a material that shows less decomposition under harsh processing, such as in organofluorine coupling reactions.

    Quality assurance includes HPLC and NMR verification, measuring both halogen content and purity to trace-impurity levels. We draw on more than a decade’s experience in fluoro-haloalkyl syntheses to troubleshoot issues. We have found that 3-Bromo-4-Chloropentafluorobutyric Acid offers an output consistency well above what traditional mono-halogenated acids can support.

    How 3-Bromo-4-Chloropentafluorobutyric Acid Drives Applications

    Let’s talk about the actual role this acid plays outside our doors. Customers value it as a critical building block for high-performance materials, especially in agrochemical and pharmaceutical development. The power of fluorination—combined with heavy halogen substitution—draws strong interest from process chemists seeking site-selective activation or deactivation in complex syntheses.

    We’ve seen this compound selected for custom molecule design, taking advantage of the pentafluoro moiety’s ability to resist metabolic breakdown in bioactive candidates. Bromine and chlorine substituents unlock more options for stepwise derivatization. This is not hypothetical; we have supported lab-scale and pilot expansion work where the stability of BCPFB-01 carried sensitive intermediates through multiple reaction environments—acid, base, oxidative, and reductive—where lesser acids would degrade or change character.

    The acid group at one end enables attachment to varied functional handles. Some advanced polymer backbones incorporate BCPFB-01 to introduce both hydrophobic and reactive sites along their chain, changing surface energy or thermal response. The difference shows in applications, not just in laboratory measurements, but in the sustained shelf life and reproducibility of formulations.

    Comparing BCPFB-01 with Other Halogenated Acids

    Anybody producing or using metric tons of haloacids notices the differences in behavior across the spectrum. Take trifluoroacetic acid, for example—a classic in life sciences. Its light weight, volatility, and lack of heavier halogen atoms put limits on downstream reactivity. Tetrafluorobutyric acid tries to extend the carbon chain but still falls short when selective halogen coupling is needed.

    When we compare BCPFB-01 to 3-bromopentafluorobutyric acid or 3-chloropentafluorobutyric acid—both produced in house as well—the dual halogen substitution stands out. Dual functionalization means more control during late-stage manufacturing. The bromine atom supports palladium-catalyzed cross-couplings not accessible with only chlorine. Conversely, the chlorine supports cost-effective nucleophilic substitution for rapid addition or alteration of existing chains. We see our industrial partners exploit this by sequencing reactions to make pharmaceutical intermediates, eliminating purification bottlenecks that come with less selectively substituted acids.

    As a specialty manufacturer, we watch the response to pentafluoropropionic acids too. These shorter chains bring volatility and less steric hindrance but drop reactivity in macrocycle or polymer syntheses. BCPFB-01’s butyric acid tail achieves a balance—high electronegativity influence, decent chain length, robust behavior in both solution and melt conditions. That flexibility supports modern chemical design, from adhesives to specialty coatings, to targets in next-generation insecticides.

    Quality Control Philosophy and Real-World Problem Solving

    Room for error vanishes quickly when crafting high-halogen, multi-fluorinated acids. Unstable intermediates, persistent byproducts, or batch-scale deviations invite downstream headaches. Early on in our scaling journey, we ran into issues with trace halide contamination causing unexpected reactivity. Standard distillation or aqueous extraction can leave too much behind. We introduced high-vacuum stripping and spent real time measuring lot-to-lot stability. Tracking performance over seasons, employee hands, and equipment cycles underpins the value we see in every kilogram shipped.

    Our technical team doesn’t wait for client complaints—we study the behavior of BCPFB-01 under various storage and shipping conditions. We document moisture uptake, acid value drift, and color changes. Some clients report surprising resistance to decomposition under light or high-humidity, which matches our own accelerated aging tests. Experience also shows that high purity—>99 percent confirmed by quantitative NMR—reduces need for in-house pre-processing. Not every synthetic acid holds up this way, and the lessons travel into our other fluorinated offerings.

    Meeting Regulatory Expectations—and Going Further

    As the original manufacturer, we work from the first day to ensure BCPFB-01 meets current environmental and safety guidelines. The industry-wide shift toward transparency and risk assessment is shaping how we record process inputs and track byproducts. Take the concern over persistent organofluorines. We monitor effluent streams, collect samples for internal analysis, and tune our process windows to minimize environmental impact each time we tune up a reactor.

    Regulatory pressure increases every year for halogenated intermediates, partly due to the complex environmental fate of both the acid and its uses. Our process team regularly reviews analytical reports for perfluorinated byproducts and updates our production documentation in cooperation with end users seeking cleaner profiles for their proprietary formulations. What started as an internal safety effort now supplies direct benefits to users facing tighter import/export and RoHS regimes.

    Supporting Custom Development and Scale-Up

    A small order lets a customer define a bench-scale process; a large order supports a shift up to semi-works or full-on production. We invest in custom solutions for each customer, not just out of pride, but because real innovation grows from direct technical dialogue. Our engineers help troubleshoot problems that crop up: isomer population drift, apparent solubility incompatibilities, co-solvent effects, and batch consistency. We work hand-in-hand with process chemists to fine-tune reactivity, offering data from our own batch logs so users understand what to expect.

    With BCPFB-01, we provide authenticated control samples matched to main shipment material for traceability across the product lifecycle. Few manufacturers extend technical support past routine documentation. We make the case that real-world application feedback leads to measurable improvement. When one customer saw unanticipated crystallization during storage, we collaborated to modify their stabilizer profile and conduct parallel storage stability trials in our own lab. The results improved not just their process but what we deliver to every customer since.

    Facts That Matter in Industrial Use

    3-Bromo-4-Chloropentafluorobutyric Acid’s density and corrosivity reinforce the need for equipment made from compatible fluoropolymers or glass-lined steel. Reaction scale-up reveals operational detail; the acid’s exothermicity with common bases or nucleophiles requires continuous monitoring and immediate adjustment when deviations appear. This same energy profile makes BCPFB-01 a candidate for aggressive derivatization in chemical synthesis, speeding reactions that ordinarily need days at reflux.

    On the environmental side, halogenated intermediates often invite concern, but BCPFB-01’s relatively high stability slows breakdown, providing an economic advantage for long-term storage and extended processing cycles. Drum storage in our own warehouse offers an example, with a shelf life measured in years—not months—when proper containment and temperature management are maintained.

    We field regular questions about volatility, odor, and potential for off-gassing during process integration. Enhanced ventilation and careful temperature ramping address these points. Past experiments with less carefully handled acids led to corrosion or contamination, so our handling staff work under rigorously reviewed protocols, logging sample draws, and watching for process drift that could degrade material value.

    Pursuing Cleaner Synthesis and Waste Management Improvements

    Every halogenated acid demands responsible stewardship, but for high-value products like BCPFB-01, waste minimization pays off. Downstream purification benefits immediately from reduced side reactions and impurity carryover. We continue to refine unit operations, swap out traditional solvents for less hazardous alternatives, and invest in improved distillation processes. Our engineering team uses online monitoring for release of airborne halides and collects condensate streams for recycling, which reduces both cost and environmental liability.

    Whenever possible, we direct excess waste flows through a closed-loop treatment unit, capturing residual fluorinated species and preventing them from entering municipal waste streams. We don’t just rely on vendor-certification for waste collectors—our own staff analyze effluent streams for trace halogen and organic load before release, setting a higher benchmark than regional regulation alone. Improvements in containment and waste treatment often flow into parallel product lines, but the lessons from BCPFB-01’s process build awareness for the whole team.

    Seeing the Product in the Broader Market

    Experience tells us the chemical market rewards consistency, but researchers and processors want more. BCPFB-01 answers those needs: high reactivity without significant side product risk, wide range of functionalization, and compatibility with both large-scale industrial platforms and laboratory setup. Feedback from formulators in specialty polymers and agrochemical precursors pushes us to continue batch-to-batch optimization.

    Unlike high-volume commodity acids, BCPFB-01 does not lend itself to trivial substitution; its reactivity and selectivity come from a carefully controlled manufacturing route, blending halogen introduction, fluorination, and purification within narrow margins. Customers using analogs with fewer halogen substitutions often see reduced yield or more impurities, losing efficiency during scaling or failing critical product benchmarks. By focusing on upstream quality—right from raw feedstock selection and real-time monitoring—we give each kilogram of acid a direct impact on manufacturing economics and finished material specifications.

    Supply chain impact rises in importance during tight markets. Our team maintains a reserve of critical precursors and implements dual-sourcing on sensitive inputs, ensuring reliable delivery. When delays hit organic fluorination supplies, we leverage alternate synthetic routes validated in small pilot campaigns. Our in-house testing validates physical property data, meaning spec sheets reflect real production, not just generic expectations from external labs.

    Looking Ahead: Honest Appraisal and Industry Collaboration

    As the chemical industry faces tighter restrictions on organofluorine and multi-halogen intermediates, we treat BCPFB-01 as more than a line item. It represents years of refinement, adaptation, and trust between manufacturing staff and downstream users. Each request for a new impurity profile, storage format, or support document adds another layer to our knowledge base.

    Close cooperation with researchers working on environmental fate and remediation gives us insights not widely shared among disconnected suppliers. We use these findings to redesign process controls, select safer alternatives for cleaning and transfer, and build robust documentation for audits. The return for industry is a safer, harder-working ingredient that supports complex synthesis without unnecessary risk. Responsible handling pays off both commercially and ethically, bringing peace of mind to everyone along the value chain.

    In our view, 3-Bromo-4-Chloropentafluorobutyric Acid brings together what manufacturers and applied scientists really look for: purity, reactive versatility, process safety, and a track record of reliable delivery at every scale. The acid’s unique structure—both a challenge and a tool—lets industry partners achieve outcomes that push the limits of what current chemistry allows. Facing regulatory evolution, greater transparency, and higher expectations from end markets, we see value in continuing to sharpen the edge of BCPFB-01. By placing production knowledge and joint troubleshooting at the center of what we do, we aim to support not only existing demand, but also new application development grounded in real-world experience.