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5-Bromo-4-Chloro-2-Fluorobenzoic Acid

    • Product Name 5-Bromo-4-Chloro-2-Fluorobenzoic Acid
    • Alias 5-Bromo-4-chloro-2-fluorobenzoic acid
    • Einecs 841-906-8
    • 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

    904511

    Product Name 5-Bromo-4-Chloro-2-Fluorobenzoic Acid
    Cas Number 861907-34-0
    Molecular Formula C7H3BrClFO2
    Molecular Weight 253.46
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Smiles C1=C(C=C(C(=C1Cl)Br)C(=O)O)F
    Inchi InChI=1S/C7H3BrClFO2/c8-4-2-5(10)6(9)1-3(4)7(11)12/h1-2H,(H,11,12)
    Storage Conditions Store at room temperature, tightly closed
    Synonyms 2-Fluoro-4-chloro-5-bromobenzoic acid
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract
    Application Used as an intermediate in pharmaceutical and chemical research

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

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    Application of 5-Bromo-4-Chloro-2-Fluorobenzoic Acid

    Applications of 5-Bromo-4-Chloro-2-Fluorobenzoic Acid in Industrial Manufacturing

    5-Bromo-4-Chloro-2-Fluorobenzoic Acid is a specialty aromatic intermediate manufactured to stringent quality protocols for use in advanced chemical synthesis. Its unique halogen substitution pattern positions it as a key precursor for high-value molecules across several high-precision downstream markets. Below, we outline the primary sectors utilizing this compound, focusing on real industrial use cases, processing routes, and regulatory frameworks expected by end users.

    1. Pharmaceutical Active Ingredient Intermediate Synthesis

    This compound serves as a critical advanced intermediate in the multi-step synthesis of novel fluoroaromatic pharmaceuticals, notably small-molecule kinase inhibitors and central nervous system (CNS) agents. Downstream manufacturers build upon its functionalized benzoic acid scaffold to introduce bioactive moieties essential for target-specific drug design, often via Suzuki or Buchwald-Hartwig coupling reactions. Stringent traceability and impurity control govern every production phase to satisfy new drug application (NDA) protocols.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates and APIs where applicable
    • US FDA cGMP 21 CFR Part 210/211 for bulk pharmaceutical manufacturing
    • APIC Guidance on Qualification of Intermediates

    Typical usage ratio

    • 0.5–1.2 molar equivalents relative to target core structure; process chemists adjust according to the subsequent coupling route and byproduct minimization strategies

    Downstream process integration

    • Direct charge into protected amide or amine coupling step, utilized as a halogenated aromatic precursor for further functionalization

    Final product types

    • Active pharmaceutical ingredients (APIs) for oncological, neurological, and anti-inflammatory therapies
    • Advanced pharmaceutical intermediates for patent-protected drug candidates

    2. Agrochemical Synthesis: Herbicide and Fungicide Precursors

    In the agrochemicals sector, this material finds use as a building block for synthesizing complex benzoyl-based herbicides and fungicides. After acylation or esterification, downstream producers incorporate it into proprietary molecules designed for residue control and crop-specific action. Regulatory compliance necessitates strict monitoring of trace halogen content and controlled-release compound precursors during pilot-to-production scaling.

    Industry compliance standards

    • FAO/WHO specifications for Technical Materials (including purity and impurity profiles)
    • ISO 9001:2015 for quality management
    • REACH (EC No. 1907/2006) registration for relevant downstream import/export into the EU
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 3–8% of total formulation batch by mass, optimized depending on target molecule synthesis yield and side-product control

    Downstream process integration

    • Reaction feedstock in protected acyl group attachment followed by selective chlorination or fluorination, prior to formulation and granulation for field application

    Final product types

    • Post-emergence herbicides targeting resistant weed species
    • Systemic fungicides for high-value crops such as cereals and legumes

    3. Electronic Chemicals: Liquid Crystal Intermediate

    The electronics industry leverages halogenated aromatic acids as foundation molecules in synthesizing rigid, high-fluorine content materials for advanced liquid crystal display (LCD) fluids and performance polymers. The compound enters downstream as a precursor for polymerizable mesogenic monomers tailored to precise viscosity and dielectric demands, targeting high-definition and low-energy display manufacture. Consistency of halogen placement is key for phase transition control and purity in electronic-grade applications.

    Industry compliance standards

    • IEC 62474: Material Declaration for Electronic Industry
    • RoHS 3 (EU Directive 2015/863) for restriction of hazardous substances
    • ISO 14001:2015 for environmental management systems in electronics manufacturing
    • JEITA ED-7202 for management of chemical substances in electronics

    Typical usage ratio

    • 0.2–2.5% by weight in pre-polymerization mixture; adjusted based on polymer chain length and targeted TNI (clearing point)

    Downstream process integration

    • Charged to polymerization reactors for the formation of liquid crystal monomer or oligomer structures through esterification and subsequent purification

    Final product types

    • High-performance liquid crystal mixtures for TFT and OLED display panels
    • Fluorinated polyimide films for flexible electronic substrates

    4. Specialty Dye and Pigment Intermediate

    Producers of specialty dyes and high-performance pigments integrate this halogenated benzoic acid into the synthesis of highly concentrated, lightfast pigment molecules, especially for automotive, industrial coating, and synthetic fiber applications. Its electron-withdrawing groups enhance subsequent azo coupling steps, resulting in improved chromaticity and weather resistance in the final pigment product. End-use industries strictly control trace impurity carryover and batch reproducibility for regulatory and safety certifications.

    Industry compliance standards

    • DIN EN ISO 9001:2015 for pigment and dye manufacturing
    • GMP EFfCI (cosmetic pigment use)
    • ZEK 01.4-08 (German GS certification for PAH content in pigments)
    • REACH Annex XVII for dangerous substances in colorant applications

    Typical usage ratio

    • 1–5% by molar input in coupling reaction charge, tailored to achieve specific color index values and granularity targets

    Downstream process integration

    • First-stage aromatic coupling step in pigment raw synthesis, often followed by diazotization or sulfonation for subsequent derivatives

    Final product types

    • High-stability organic pigments for masterbatch plastics
    • Automotive OEM and refinish coating colorants
    • Performance dispersant dyes for synthetic fiber spinning

    5. Advanced Materials: Photoresist Resins for Semiconductor Fabrication

    Manufacturers of semiconductor-grade photoresist materials apply this raw material in the controlled synthesis of fluorinated aromatic resin precursors, targeting advancements in micro-lithography. By participating in condensation or esterification with polyfunctional cross-linkers, this compound enables fine-tuned solubility and resolution of the final resist. Process engineers uphold strict low-metal and controlled-organic impurity tolerances throughout synthesis to ensure device-grade processability.

    Industry compliance standards

    • SEMI C1: Specification for Photoresist Materials
    • ISO/TS 16949:2016 for electronic materials supplied to automotive semiconductors
    • Cleanroom ISO 14644-1: Class 5 or better for handling and packaging
    • RoHS compliance for electronics sector

    Typical usage ratio

    • 0.5–3% by solid content in pre-polymer blend; process control depends on resist type (positive or negative) and target line width accuracy

    Downstream process integration

    • Charged into condensation reaction vessel with polyhydroxyl or polyamine linkers, followed by precision blending with photoinitiators and coating onto wafers

    Final product types

    • Deep ultraviolet (DUV) and extreme ultraviolet (EUV) photoresists for IC production
    • High-resolution patterning resins for MEMS and advanced packaging
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    More Introduction

    5-Bromo-4-Chloro-2-Fluorobenzoic Acid: A Versatile Building Block in Modern Chemical Synthesis

    Introduction: Pinpointing Potential in an Evolving Field

    In the world of organic chemistry, each molecule tells a story of possibility. 5-Bromo-4-Chloro-2-Fluorobenzoic Acid rises to the challenge as an intermediate that bridges research dreams and practical breakthroughs. Countless reactions depend on reliable, well-defined building blocks. People who work in pharmaceutical labs or agrochemical development quickly see the value in a compound with a balanced combination of halogen substitutions and a carboxylic acid group. For those investing in specialty chemicals, selecting a product like this isn’t just about following formulas—it's about keeping research momentum and driving regulatory compliance at the same time.

    Model and Purity: Power in Rigorous Specifications

    Let’s get specific with the variant under discussion: 5-Bromo-4-Chloro-2-Fluorobenzoic Acid, often chosen at purities of 98% or above, presents as a white to off-white crystalline powder. Having spent years in chemical R&D, I’ve found little room for error when it comes to impurities. Contaminants can ruin a batch, skew analytical outputs, and burn through precious time and resources. Analytical data like melting point and chromatographic profile provide confidence. Reliable manufacturers report tight control over batch consistency, which helps avoid headaches and enables smoother scale-up from discovery to manufacturing runs. I remember the frustration of hitting a research roadblock from off-spec material; having a trustworthy source for such a precise molecule matters more than newcomers sometimes imagine.

    Structural Highlights and What Sets It Apart

    This benzoic acid’s structural uniqueness lies in the presence of three different halogens—bromine, chlorine, and fluorine—attached to the aromatic ring. This isn’t just chemistry trivia. Each of these halogens brings distinct electronic and steric influences. Bromine, a relatively bulky group, can slow down further substitution and improves the compound’s stability towards some common degradation pathways. Chlorine at the four position contributes to electron withdrawal, which can help steer reactions through desired mechanisms. Fluorine, the smallest and most electronegative, often boosts metabolic stability and changes solubility patterns for downstream molecules.

    Comparing this acid to a simpler benzoic acid or one with only chlorine substitution, the differences become clear in laboratory settings. For example, mono-halogenated acids may miss out on the fine-tuning available when all three halogens are at play. Chemists can leverage this molecule in Suzuki couplings, amide formations, and even nucleophilic aromatic substitutions that would not proceed efficiently with less activated substrates. These details matter because developing pharmaceutical candidates with the right pharmacokinetic properties relies heavily on manipulating such fine structural points.

    Usage—Connecting Research with Application

    Talk about versatility: 5-Bromo-4-Chloro-2-Fluorobenzoic Acid stands out as a go-to substrate for constructing diverse molecular frameworks, especially in drug discovery. Think about the effort poured into lead optimization. The drive to tweak absorption, distribution, and target affinity can become a game of molecular chess, and this piece opens doors that aren’t visible with less complex acids. Process chemists frequently select it for producing substituted aromatic compounds found in advanced APIs (Active Pharmaceutical Ingredients), unique crop protection agents, or diagnostic imaging probes. I’ve been on teams where its use trimmed months off a synthesis campaign—just because it unlocked a new path to a protected core structure or allowed selective downstream modifications without excess protecting group gymnastics.

    Safety is another concern that researchers keep at the forefront. This molecule doesn’t exhibit the acute hazards seen with highly reactive organofluorines or brominated aromatics, but glove-box handling and proper ventilation should never be skipped. Solid experience tells me never to underestimate even a simple-looking acid; splashes can spoil a day, and trace byproducts from poor storage can create headaches during clean-up steps.

    Tackling the Details: Sourcing and Quality Matters

    The value of consistency rears its head every time process development scales up. One run’s impurity can haunt downstream purification, stalling regulatory progress. Reliable suppliers of 5-Bromo-4-Chloro-2-Fluorobenzoic Acid provide CoA documentation, complete with HPLC graphs, NMR spectra, and moisture content readings. Through heavy reliance on robust supply chains during my own time onboarding new synthetic routes, the lesson comes through clear: Quality saves costs by preventing batch failures and regulatory retesting. It doesn’t matter how small your operation is—cutting corners early invites stress, lost time, and, in some industries, real regulatory risk.

    Researchers working in more regulated environments, such as pharmaceutical GMP settings, must look for statements on ICH Q7 compliance from their suppliers and demand traceability to the original batch. Having read through FDA warning letters focused on ambiguous or missing data, the importance of proper documentation is more than a regulatory box-check—it’s an insurance policy for future business continuity and the reputation of any organization handling these specialty chemicals.

    Why the Substitution Pattern Holds Value

    Let’s take a closer look at why three halogens in these exact positions matter. In medicinal chemistry, introducing bromine, chlorine, and fluorine profoundly changes a benzoic acid’s interplay with metabolic enzymes and protein targets. Fluorine’s reputation for increasing bioavailability and metabolic resistance proves invaluable—small shifts in oxidative stability can decide whether a drug candidate makes it into clinical trials or goes back to the drawing board. My own experience assisting a team on CNS ligand synthesis showed clearly how adding a fluorine to the benzene ring reduced unwanted metabolism, stretching plasma half-lives enough to keep candidates in the game. Bromine, far from being a mere spectator, also offers a convenient site for further derivatization, especially via palladium-catalyzed cross-couplings.

    Compared to benzoic acids that only pack chlorine substitutions, this molecule opens up more downstream chemistry. Chlorine alone doesn’t offer much flexibility for high-yielding Suzuki coupling or Buchwald-Hartwig amination. A bromo substituent at the five position is reactive enough yet doesn’t lead to constant scrambling or loss through hydrolysis. Research shows this multi-halogen strategy keeps options open for lead diversification—something medicinal chemists chasing new patent territory are likely to appreciate.

    Routes to Derivatives and Custom Applications

    Synthesizing specialty derivatives from 5-Bromo-4-Chloro-2-Fluorobenzoic Acid often feels like working with a flexible foundation. The acid’s halogen pattern sets the stage for tailored transformations, such as nucleophilic aromatic substitutions or Suzuki coupling with boronic acids. Cross-coupling at the bromo position enables rapid branching out to biaryl systems, which play a role in anti-cancer and anti-infective development. Substitution at chlorine opens another toolbox for generation of tailored analogs with diverse physical properties.

    Process chemists aiming for high product throughput appreciate the clean, reproducible reactions stemming from a well-defined substrate. By handling multi-step syntheses where one poorly characterized impurity can halt progress, they develop a respect for the hidden backstory behind every bottle on the shelf. It isn’t just about saving labor or cost; in regulated environments, solid intermediates with ample batch history and chain-of-custody records mean fewer questions from inspectors and more robust downstream validation.

    Common Pitfalls and How to Avoid Them

    Practical experience reveals common mistakes that surface during the use of benzoic acid derivatives like this one. Moisture sensitivity can spoil a well-planned purification. Chemicals that linger exposed to ambient air may pick up water, leading to difficulties in crystallization or chromatography. I recall a failed scale-up that traced back to a batch stored open in a humid lab—luckily, extra purification rescued the yield but added unwanted delays and costs.

    Quality control also comes into play during reactions involving transition metal catalysis. Trace metals remaining from ill-defined stock can poison expensive catalysts, turning what should have been a routine step into a troubleshooting nightmare. Working with suppliers willing to share details about residual metal content and recent environmental monitoring reports can save labs hours of lost productivity.

    Navigating Discrepancies with Other Substituted Benzoic Acids

    Not every benzoic acid delivers the performance required for high-stakes synthesis. Comparing this compound with ortho- or meta-halogenated analogs, researchers quickly spot the experiential differences in reactivity, stability, and downstream versatility. Fluorine’s role in tuning pKa values gives chemists finer control over selectivity during derivatization steps. Recently, peers in academia noted how a single positional shift can create a domino effect through a multi-step synthesis, sometimes complicating scale-up or changing product crystallinity in ways that catch even experienced hands by surprise.

    Beyond synthetic ease, downstream purification steps deliver additional separation power when using a mix of halogen substituents. Techniques such as preparative HPLC benefit from the varied hydrophobic and electronic properties brought by each halogen. It’s not just a matter of luck; extra attention to the interplay between structure and purification can make the difference between a single pass and repeated cycles that chew up columns and solvents.

    Environmental and Regulatory Realities

    The growing strictness of environmental regulations casts a spotlight on automated waste management and responsible sourcing. Each halogen, especially bromine and chlorine, commands attention during waste disposal. Industries must comply with EPA and European REACH guidelines on the responsible handling and reporting of halogenated byproducts. In my role evaluating site preparedness, I have seen the consequences for non-compliance—lost permits, regulatory investigations, and black marks on supplier records that hurt business down the line. Adopting thorough documentation, segregated disposal, and third-party auditing provides a layer of protection that far outweighs any upfront cost savings from lax oversight.

    Downstream customers, particularly pharmaceutical companies, increasingly demand proof of consumer and environmental safety with each shipment. Having suppliers that issue full audit trails for their benzoic acid derivatives helps users stay ahead of both internal audits and global regulatory swings. The days of unverified stock moving through supply chains without scrutiny have faded. Companies that understand this landscape and align with best practices in environmental stewardship position themselves as long-term partners, not just commodity vendors.

    Practical Solutions for Real-World Challenges

    On the front lines of applied chemistry, real-world challenges surface every day. Cost pressures, new regulatory hurdles, and unpredictable market swings drive buyers to cut deals that sometimes backfire. Investing in high-quality benzoic acid derivatives means reducing the risk of recalls, failed audits, or newsworthy mishaps. Allocating budget to cover third-party verification at key points in the supply chain can save multiples in lost product or legal fees down the road. From my experience, a team that takes the time to vet new suppliers finds their workflow smoother and their troubleshooting load lighter.

    Process innovation can also address common bottlenecks. Many companies now integrate inline monitoring to detect trace degradants or moisture content during storage and transfer. While such continuous quality assurance once appeared resource-intensive, widespread use of digital tools has made rapid detection and documentation more accessible and less costly. Early adopters tend to report fewer product withdrawals, more predictable yields, and happier clients—whether they’re internal R&D teams or external customers.

    Outlook: Meeting Modern Demands with Science and Diligence

    The demand for thoughtful chemical synthesis keeps expanding as industries pursue targeted therapies, greener pesticides, and smarter materials. 5-Bromo-4-Chloro-2-Fluorobenzoic Acid won’t appear on magazine covers or attract big headlines, but its story sits at the crossroads of innovation and reliability. For those invested in building safer and more sustainable product lines, choices made at the molecular level influence not just the bench-top success of tomorrow’s drug or coating, but also the stability and reputation of the organizations developing them.

    After working both in the lab and on the regulatory side, I have seen firsthand how a simple decision—like sourcing a robust, well-documented benzoic acid intermediate—spares years of headaches. Strong supply relationships, unwavering attention to quality, and adapting to shifting regulatory expectations can transform a basic bottle of powder into the backbone of a thriving product line. For scientists, managers, and buyers alike, investing in the right building block pays dividends that only become clear years down the road, in the form of fewer failures, regulatory green lights, and a steady path to market.

    Conclusion: Unseen but Essential

    5-Bromo-4-Chloro-2-Fluorobenzoic Acid seldom gets celebrated publicly, but those with years in research, process scale-up, or compliance understand what steady supply and robust documentation really mean. Chemists who care about more than just yield—who keep an eye on worker safety, regulatory responsibility, and downstream impact—know precisely why sourcing decisions for specialized intermediates matter so much. As demands in pharmaceuticals, agriculture, and advanced material science keep growing, this building block stands out not for its appearance or public profile, but for the results it quietly empowers in the hands of careful, conscientious teams.