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Ethyl 4-Bromobenzoate

    • Product Name Ethyl 4-Bromobenzoate
    • Alias Ethyl p-bromobenzoate
    • Einecs 211-528-0
    • 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

    888738

    Cas Number 54048-10-3
    Molecular Formula C9H9BrO2
    Molecular Weight 229.07 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 294°C
    Density 1.473 g/cm³
    Refractive Index 1.552
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited Ethyl 4-Bromobenzoate 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 with a red cap, labeled "Ethyl 4-Bromobenzoate, 99%". Includes hazard symbols and handling instructions.
    Shipping Ethyl 4-Bromobenzoate is typically shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition, heat, and incompatible substances. Appropriate labeling and documentation are required to comply with regulatory transport standards for hazardous materials.
    Storage Ethyl 4-bromobenzoate should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet. Avoid storing with incompatible materials such as strong oxidizers or acids. Proper labeling and secondary containment are recommended to prevent spills and ensure safe handling.
    Application of Ethyl 4-Bromobenzoate

    Applications of Ethyl 4-Bromobenzoate in Industrial Manufacturing

    Ethyl 4-Bromobenzoate serves as an essential intermediate across multiple high-value sectors in advanced chemical manufacturing. Every application scenario below focuses on established, evidence-based industrial usage of this compound, with emphasis on process integration and regulatory requirements observed by our downstream partners.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Ethyl 4-Bromobenzoate plays a pivotal role as a building block in the synthesis of complex heterocyclic scaffolds used for advanced pharmaceutical compounds. Its functional bromide position enables selective Suzuki and Stille coupling reactions in multi-step medicinal chemistry pathways. Pharma manufacturers apply it in key palladium-catalyzed transformations to attach aromatic moieties in their proprietary molecules, often for anti-inflammatory, anti-bacterial, or anticancer drug candidates. The high purity specification delivered by direct manufacturers supports stringent regulatory filings, while our product batch traceability meets end-to-end compliance requirements in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (U.S. FDA cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4 Part II (GMP for APIs)
    • Relevant Pharmacopoeias (USP, EP depending on downstream product)

    Typical usage ratio

    • 0.2–0.8 molar equivalents relative to core substrate in multi-step syntheses. Proportion may adjust based on reaction yield and desired batch volume.

    Downstream process integration

    • Introduced during aromatic coupling reaction sequences by GMP-certified pharmaceutical manufacturers, followed by purification and chemical transformation stages prior to API crystallization or isolation.

    Final product types

    • Small-molecule active pharmaceutical ingredients targeting infectious diseases, oncology, or CNS disorders
    • Pharmaceutical intermediates registered in DMFs/CTDs

    2. Agricultural Agrochemical Intermediate Production

    Ethyl 4-Bromobenzoate supports agrochemical companies in developing new-generation fungicides, herbicides, and insecticides. Its structural features allow for the introduction of substituted benzoyl units in targeted crop protection agents. Agrochemical synthesis teams apply it during the elaboration of active ingredients that provide improved spectrum and targeted field performance, utilizing the bromide group for further functionalization with amine or heterocyclic groups as required by specific mode-of-action chemistries.

    Industry compliance standards

    • FAO/WHO Guidelines on Pesticide Specifications
    • ISO 9001:2015 Certified Production Processes
    • REACH registration (EU chemical safety)
    • China ICAMA product licensing for pesticide technicals

    Typical usage ratio

    • 10–25% by weight in target intermediate synthesis steps. Ratio adjusted for specific chain length and substituent requirements in finished formulation.

    Downstream process integration

    • Charged into early-stage acylation or coupling procedures at dedicated synthesis workshops preceding large-scale technical-grade agrochemical production.

    Final product types

    • Technical-grade crop protection active substances (fungicide, herbicide, insecticide bases)
    • Formulated agrochemical concentrates for commercial agricultural use

    3. Specialty Dye Intermediate Manufacturing

    In the colorant and specialty dye sector, Ethyl 4-Bromobenzoate functions as a core intermediate in developing benzoyl-containing dyes with high lightfastness and improved substrate affinity. Downstream users leverage its structure during Friedel-Crafts acylation or nucleophilic substitution to install aromatic frameworks essential for robust fabric dyes and technical pigment dispersions. Quality and purity parameters customized by manufacturers ensure end-use stability and compatibility within batch dyeing or print pastes.

    Industry compliance standards

    • OEKO-TEX 100 Restricted Substances List for Dyestuffs
    • ISO 9001:2015 Quality Certification
    • EU REACH Annex XVII (for azo dye restrictions)
    • ZDHC MRSL for dye input management

    Typical usage ratio

    • 12–18% by weight relative to total dye intermediate mass, depending on shade intensity and molecular design.

    Downstream process integration

    • Utilized in core coupling or substitution reactions carried out in dye intermediate synthesis plants before blending and formulation into final colorant batches.

    Final product types

    • Acid, disperse, and reactive dye intermediates for textile and paper coloration
    • High-performance pigments for digital and specialty inks

    4. Fine Chemical Synthesis for Polymer Additives

    The fine chemicals industry integrates Ethyl 4-Bromobenzoate as a precursor when engineering polymer performance additives, especially those used in high-heat or UV-resistant engineering plastics. The compound’s aromatic bromide enables precision-blocking and crosslinking reactions that impart thermal stability and flame retardancy. It forms part of rigid segment backbones within advanced co-monomers, influencing mechanical properties in downstream formulated polymers.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for Chemical Manufacturing
    • RoHS Directive (EU limits on brominated compounds in electronics)
    • UL 94 Flame Rating Certification for Plastics
    • REACH registration for plastic additives

    Typical usage ratio

    • 0.5–2.0% by weight in additive masterbatch production lines, adjusted for targeted flame retardancy or mechanical strength requirements.

    Downstream process integration

    • Charged into additive synthesis reactors as part of polymer precursor modification, followed by compounding into pelletized or liquid masterbatches for plastic processors.

    Final product types

    • Flame-retardant additive masterbatches
    • Engineered resin compounds for electronics, automotive, and building materials

    5. Laboratory Research Reagents for Material Science

    Advanced material science research units source Ethyl 4-Bromobenzoate as a specialized starting material for synthesizing functional polymers, liquid crystals, and surface modification agents. Custom research protocols utilize its structure to achieve targeted chemical modifications on laboratory scale, supporting exploratory investigations in electronics, nanomaterials, and surface engineering. Consistent spectral profiles and impurity controls from primary manufacturers ensure integrity in reproducible experiments and pilot lines.

    Industry compliance standards

    • GLP (Good Laboratory Practice) guidelines for reagent use in research
    • ISO 17025 for testing and calibration laboratories
    • Internal QA/QC protocols in academic and industrial research environments

    Typical usage ratio

    • 0.05–0.2 molar equivalents relative to target synthesis batch depending on experimental design and substitution pattern pursued.

    Downstream process integration

    • Added during initial reagent setup for coupling, substitution, or polymerization assays in R&D laboratories, with monitoring for side reaction minimization.

    Final product types

    • Proprietary functionalized polymers for coatings, membranes, or sensors
    • Small-molecule building blocks for advanced materials screening
    • Analytical reference standards in material validation studies
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    Certification & Compliance
    More Introduction

    Ethyl 4-Bromobenzoate: Reliable Intermediate for Modern Synthesis

    Expert Insights from a Chemical Manufacturer

    In the field of chemical manufacturing, Ethyl 4-Bromobenzoate plays a significant role as an intermediate known for its consistency and adaptability in organic synthesis. Drawing from years of hands-on experience in production and downstream applications, our team has learned that subtle differences in manufacturing control impact both yield and usability. Ethyl 4-Bromobenzoate, with CAS number 99-08-1 and the structure built around a brominated aromatic ring, provides a solid starting point for building more complex molecules. This reliable compound supports a range of industries, including pharmaceuticals, agrochemicals, and advanced materials.

    Understanding the Product

    Most users recognize Ethyl 4-Bromobenzoate by its appearance as a colorless to pale yellow liquid. It carries a molecular formula of C9H9BrO2 and usually falls within a purity range of over 99% after fractional distillation and rigorous QC procedures. As a manufacturer, attention always turns toward batch consistency and rigorous impurity removal. The compound's stability is high under typical storage conditions – an advantage for long-haul transportation and shelf-life concerns, frequently cited by our global partners.

    Common applications rely on the reactivity of its para-bromo group and its ethyl ester functionality. Pharmaceutical companies often seek this compound for preparing more complex aromatic esters, exploiting its bromine substituent in cross-coupling reactions such as Suzuki or Stille coupling. In agricultural R&D, customers convert Ethyl 4-Bromobenzoate into active ingredients for crop protection. Fine-chemical producers value its reactivity during stepwise synthesis, especially when substituting at the para position to avoid side reactions typical in multi-step processes.

    Comparison with Similar Substances

    Manufacturers frequently discuss the differences between Ethyl 4-Bromobenzoate and other brominated esters or isomeric benzoates. For instance, the ortho and meta isomers occasionally crop up in request lists, though para derivatives, like this one, generally offer fewer positional ambiguities during downstream halogenation or metal-catalyzed coupling. Those seeking 4-bromobenzoic acid esters often debate between methyl and ethyl variants – the ethyl group provides a slightly higher boiling point and a less volatile ester bond, making it more manageable during solvent removal and purification steps at scale.

    From our point of view, real differences emerge in the hands-on workflow. Batch crystallization, filtration rates, and solvent selection are all influenced by the ester group and the position of the bromine substituent. During chiral synthesis routes, chemists value the predictability of the para-bromo configuration. Meanwhile, the ethyl ester group strikes a practical balance: not as labile as methyl, not as hydrophobic as longer-chain esters. Ease of hydrolysis back to the parent acid also tips the scale in favor of ethyl for many users looking to convert esters post-functionalization.

    Production Technique and Quality Control

    Our production of Ethyl 4-Bromobenzoate depends on a finely tuned process that leverages direct bromination, careful temperature regulation, and controlled esterification steps. Unlike many commercial sources, direct oversight allows tight control over trace impurities. Even minor differences in solvent grade or reaction pH influence the presence of byproducts, so periodic batch validation has become second nature. Purity readings consistently top 99%, and this isn’t an abstract achievement—it often translates to more efficient cross-coupling outcomes and reduced side product formation, real advantages observed with repeated customer feedback.

    Quality metrics extend past just the assay value. Moisture content, residual acidity, and specific refractive index are measured routinely. Variability in any of these factors may not show up immediately on a spec sheet but can shorten shelf life or complicate scale-up efforts in downstream synthesis. Our QC laboratory uses both gas chromatography and proton NMR to confirm product integrity. It’s this process—end-to-end visibility and a feedback loop with users—that leads to continuous optimization. In our experience, the impact of a bad batch can ripple through multiple projects, which underscores the need for rigorous checks at every step.

    Handling, Storage, and Environmental Responsibility

    Experience teaches that even straightforward compounds can introduce surprises if mishandled. Ethyl 4-Bromobenzoate remains robust under dry atmospheric conditions, best stored in sealed containers and away from direct sunlight. Deliberate packaging selection prevents contamination and reaction with moisture. Spills involving this compound respond well to conventional containment and clean-up procedures, thanks to its stable ester group. Laboratory teams have learned the value of methodical storage—temperature swings and open air can introduce hydrolysis, shifting the balance toward 4-bromobenzoic acid or unintended side products. Such outcomes create headaches in both analytics and reaction reproducibility.

    Responsible manufacturing extends beyond just safe packaging. Our onsite wastewater management captures and removes brominated organics before any discharge, an investment aligned with stricter regulatory expectations worldwide. This has required not just routine monitoring, but also investments in closed-system handling and solvent recovery to reduce environmental impact. Chemical manufacturing gains trust not only from product reliability, but also from sustainable and transparent practices—something customers increasingly demand and something we have built into our workflow.

    Market Demands and User Needs

    Changes in downstream demand shape both production schedules and purity targets. A sudden uptick in pharmaceutical R&D or a new agrochemical discovery can drive rapid adjustments. Research feedback over the past several years has flagged several recurring priorities. Users want reproducible purity from lot to lot, and easy access to both technical support and full COA documentation. Academic labs want reliable lead time and competitive pricing, but pharmaceutical teams are laser-focused on minimizing variable impurities that can throw off bioassay data.

    Direct conversations with users have revealed pain points: occasional delays around customs clearance, requests for custom batch sizes to meet pilot plant or kilo-lab projects, and concerns about long-term supply continuity. In response, the logistics team works closely with both global distributors and direct customers to fine-tune shipping, anticipate regulatory documentation (especially for new market regions), and deliver reliable technical support.

    Industry Trends Impacting Ethyl 4-Bromobenzoate

    Industry shifts influence not only demand, but also the methods of production. Automation has helped in delivering tighter process controls and stronger batch records, both valuable when establishing traceability. Tighter environmental controls, especially around emissions, have fostered innovation in solvent recycling and energy-efficient reactor design. As new synthetic methods, like photoredox cross-coupling and metal-free coupling reactions, gain wider adoption, the need for ever-purer starting materials grows. Feedback from customers shows that even minor impurities can inhibit high-throughput screens or skew catalyst activity.

    Regulatory trends cannot get overlooked. Global updates around brominated organics and evolving REACH registration norms in the EU have pushed many manufacturers to tighten their process audits. Tracking the full lifecycle of Ethyl 4-Bromobenzoate, ensuring compliance with all current and upcoming regulatory filings, has become an expected part of partner relationships. More organizations ask pointed questions about supply chain responsibility, especially around source transparency and the use of conflict-free raw materials.

    Collaboration with Customers and Continuous Improvement

    The feedback loop with customers drives meaningful improvements. Real stories from the synthesis bench add value—one pharmaceutical client traced a recurring chromatography issue to trace p-toluidine contamination, which our team addressed by doubling the scrubbing capacity prior to esterification. Over several months, both stakeholders shared process control updates and monitoring protocols, ultimately leading to a cleaner final product for all partners.

    Another common request involves small-scale custom modification on Ethyl 4-Bromobenzoate, such as offering it pre-packed in inert atmosphere drums for moisture-sensitive downstream uses. As a producer, quick pivots like these are possible without major process disruption. Open dialogue about performance, packaging, and shipping has led to a much deeper understanding of practical end-use concerns. Combined with regular plant audits and investment in analytical upgrades, this approach reduces error and delivers real value back to users.

    Why Quality Matters: Downstream Impact

    Having worked through many customer pilot runs and scale-up experiments, it’s clear that Ethyl 4-Bromobenzoate often defines the trajectory of a project. Poorly controlled batches can derail expensive catalyst screens, generate inconsistent assay results, or lengthen development timelines. In some instances, downstream users have returned partially used lots, flagging unanticipated volatility or unwanted byproducts. Tracing these back through our internal batch records—thanks to robust, centralized data tracking—has made problem-solving swifter and prevents future headaches.

    A fine chemical isn’t just a commodity; it’s a critical link in a cascade of synthetic decisions. Manufacturing teams see this every day. For example, a process uptrend—targeting a higher throughput in Suzuki coupling—demanded slightly tighter control on trace halides in the starting ester, leading to a targeted review of both bromination and washing steps. Adjustments in both upstream and downstream processing have quadrupled batch reliability since then. Quality, therefore, isn’t just a marketing claim; it affects the physical results achieved by chemists worldwide.

    Opportunities for Further Optimization

    The pressure to refine synthetic intermediates remains high as the chemical industry intensifies its move towards greener, more efficient processes. Our own efforts to cut down on hazardous solvent use has led to the adoption of softer washing systems, reducing both material costs and environmental impact over several production cycles. Projects on process intensification and alternative bromination methods show real promise for increasing both yield and selectivity, especially as demand for custom derivatives swells.

    Users have also called for dual-purpose packaging—suitable for both manual bench feeds and automated dosing, particularly within pilot plant settings. Integrating these needs involved not just packaging adjustments, but also changes to in-house labeling, batch tracking, and direct digital access to lot certificates. These tweaks, though incremental at first glance, add up to real-world savings and improved lab efficiency. In several cases, customer process engineers now interact directly with our technical advisors during both onboarding and troubleshooting, reducing cycle times and aligning standards faster than ever before.

    Supporting Research and Development

    We have also seen increased use of Ethyl 4-Bromobenzoate in high-value material science and specialty polymer fields. Its reactivity profile allows for efficient construction of functionalized polymers, where the presence of a single bromine or ester group can define physical attributes like solubility or filterability. Many start-ups and research groups come to us for insight on how the compound’s characteristics will influence not just initial coupling, but also downstream manipulation in multi-step syntheses or composite formation.

    Some groups pursue custom isotopic labeling, or require more stringent metal content controls for sensitive electronic applications. These requests push our teams to further dial in analytical precision on each lot. The fact remains—every application brings a unique set of purity, stability, or handling concerns, each informing a new tweak in our workflow. The result is not just incremental technical progress, but a steady building up of institutional know-how.

    Looking Forward: Adapting to a Changing Market

    With supply chains under constant strain, the need for a responsive, transparent manufacturing partner has only grown. Lead times, cost predictability, and consistency sit at the top of customer checklists during pre-purchase discussions. In response, our team invests in local warehousing and improves demand forecasting using analytics tied back to order history and market trend analysis. Any adjustment in feedstock pricing or global regulatory status flows directly to our projection models, helping us buffer against sudden disruptions.

    As end users adopt Lean manufacturing, Six Sigma, and other continuous improvement methodologies, supplier relationships bend toward greater data transparency. Batch documentation, digital traceability, and lot-specific certificates are now expected, not just ‘nice-to-haves.’ Our focus on digital transformation—linking QC records with shipping and customer service interfaces—reflects this evolving expectation. The result is reduced lag between inquiry and fulfillment, fewer mistakes, and greater confidence both ways.

    Conclusion: Building Trust through Direct Manufacturing

    Decades of experience in chemical manufacturing have shaped our approach to Ethyl 4-Bromobenzoate production. This compound isn’t just a line item; it serves as a foundation for new research, better medicines, safer agricultural products, and innovative materials. The true difference lies in direct control over synthesis, tailored batch-level optimization, rapid troubleshooting, and honest partnership with customers. As new applications emerge and old ones scale to new heights, this hands-on, data-supported approach keeps quality high and risks low. It’s a cycle that benefits researchers and industrial users alike, shaping not just individual projects, but the future of chemical innovation itself.