Products

Ethyl Bromoacetate

    • Product Name: Ethyl Bromoacetate
    • Alias: EBA
    • Einecs: 205-834-2
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    148986

    Cas Number 105-36-2
    Molecular Formula C4H7BrO2
    Molar Mass 167.01 g/mol
    Appearance Colorless liquid
    Boiling Point 159-161 °C
    Melting Point -51 °C
    Density 1.516 g/cm³ at 20 °C
    Refractive Index 1.445 at 20 °C
    Solubility In Water Slightly soluble
    Flash Point 61 °C (closed cup)
    Vapor Pressure 2 mmHg at 20 °C
    Odor Pungent

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

    Packing & Storage
    Packing 250 mL amber glass bottle, sealed with a plastic cap, labeled "Ethyl Bromoacetate, Reagent Grade." Includes hazard and handling information.
    Shipping Ethyl Bromoacetate is shipped as a hazardous material due to its flammability and toxicity. It must be securely packed in tightly sealed, chemical-resistant containers and labeled according to UN 1919 regulations. Transportation typically follows ground or air routes approved for hazardous chemicals, ensuring compliance with all safety and regulatory guidelines.
    Storage Ethyl Bromoacetate should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and bases. Keep the container tightly closed when not in use and store in a corrosive-resistant, clearly labeled container. Avoid exposure to light and moisture, and follow all local regulations for hazardous chemical storage.
    Application of Ethyl Bromoacetate

    Applications of Ethyl Bromoacetate in Industrial Manufacturing

    Ethyl bromoacetate serves as a key intermediate for industrial synthesis across several specialized chemical sectors. As a direct manufacturer, we maintain strict batch consistency to support downstream partners in pharmaceuticals, agrochemical active ingredient production, fine chemicals, and specialty dye manufacturing. Below we detail established industrial applications with precise compliance, formulation, and process integration data.

    1. Pharmaceutical Active Ingredient Synthesis

    Drug manufacturers use ethyl bromoacetate as an alkylating agent and reagent for constructing alpha-bromo esters, which function as central intermediates in the synthesis of barbiturates, antiepileptics, and related APIs. Its reactivity profile allows practical scale-up for nucleophilic substitution and carbon chain extension reactions under cGMP production lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF, EP, JP monographs as applicable to final APIs
    • 21 CFR Part 211 for finished dosage forms, with supplier qualification under 21 CFR Part 210
    • REACH Registration (Europe) for handling and residual trace control

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to main substrate, adjusted to minimize by-products and maximize target yield

    Downstream process integration

    • Stepwise nucleophilic substitution and alkylation reactions, typically as the first or second stage of multi-step synthetic API routes (e.g., for phenobarbital, carbamate-based drugs)

    Final product types

    • Barbiturate derivatives (e.g., phenobarbital)
    • Anticonvulsant APIs
    • Intermediates for local anesthetics

    2. Agrochemical Intermediate Manufacture

    Major agrochemical formulators rely on ethyl bromoacetate for the construction of bromoalkyl building blocks essential in synthesizing active pesticide and herbicide molecules, especially those involving haloester core substructures. Manufacturers conduct these syntheses under strict residue and impurity control as required for large-acreage crop protection products.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Evaluations
    • ISO 9001:2015 Quality Management Systems for production lines
    • REACH Compliance for intermediate registration and handling
    • Local environmental output regulations (e.g. U.S. TSCA, EU CLP for hazard communication)

    Typical usage ratio

    • 5–12% by mass in the preparation of alkylated intermediates, adjusted for target molecule structure and downstream reactivity

    Downstream process integration

    • Core alkylating step for building substituted glycine or cyclic bromoester intermediates prior to final coupling with active aromatic or heterocyclic moieties

    Final product types

    • Herbicidal API intermediates (e.g., for substituted glycine-based actives)
    • Insecticide building blocks
    • Plant growth regulator compounds

    3. Synthesis of Amino Acid Derivatives and Fine Chemicals

    Producers of specialty amino acids and fine chemicals utilize ethyl bromoacetate for synthesizing N-protected amino acid esters, chiral intermediates, and pharmaceutical excipient raw materials. This application requires highly controlled addition and thorough downstream purification to meet purity and enantiomeric excess specifications for food, pharma, and specialty segments.

    Industry compliance standards

    • FSSC 22000 or ISO 22000 (food and pharma fine chemicals)
    • USP for pharmaceutical excipients
    • Chemical safety compliance with OSHA/CLP for facility handling
    • REACH for substance lifecycle management

    Typical usage ratio

    • 1.1–1.3 mole equivalents based on amino or alcohol functional group of substrate, with fine-tuning for enantiopurity

    Downstream process integration

    • Direct alkylation or esterification step for masking carboxylic acids or introducing bromoacetate side chains; feeds into chiral resolution, enzymatic modification, or downstream deprotection/hydrolysis

    Final product types

    • Boc-protected amino acid esters
    • Chiral building blocks for peptide synthesis
    • Excipient intermediates for pharmaceutical and nutraceutical use

    4. Dyes and Pigments Intermediate Production

    Manufacturers in the dyes and pigments sector utilize ethyl bromoacetate to introduce bromoacetyl groups into aromatic bases, forming intermediates for specialty dyes including azo, anthraquinone, and triarylmethane types. The material’s controlled reactivity ensures precise functionalization within multistep syntheses conducted under strict emissions and workplace safety regimes.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for emission control
    • OHSAS 18001 / ISO 45001 Occupational Health and Safety Management Systems
    • REACH Annex VII-VIII for large-volume industrial processing
    • European Commission Regulation EU 2019/1021 (POPs regulation for persistent organic pollutant avoidance)

    Typical usage ratio

    • 3–8 wt% in batch processes when functionalizing aromatic amines or phenols, with specific ratio depending on dye structure and process yield optimization

    Downstream process integration

    • Bromoacetylation stage for aromatic or heterocyclic precursors, usually as an early step prior to azo coupling or other color-forming transformations

    Final product types

    • Azo dye intermediates (e.g., for textile and leather dyes)
    • Triarylmethane pigment precursors
    • Anthraquinone-based dye intermediates

    5. Synthesis of Flavors and Fragrance Intermediates

    Producers of flavor and fragrance compounds adopt ethyl bromoacetate for constructing esters and lactones with defined aroma profiles. This application requires rigorous control of trace residues and adherence to food safety standards, as the compound enters key positions within cyclic or linear aroma chemicals.

    Industry compliance standards

    • FCC (Food Chemicals Codex) specification for intermediates
    • IFRA (International Fragrance Association) Standards where relevant
    • GMP for the Production of Food Additives and Flavorings (China GB 31638)
    • REACH compliance for fragrance materials

    Typical usage ratio

    • 0.5–2.5 molar equivalents in aroma intermediate synthesis, with tight control to avoid over-functionalization or off-odor formation in final formulation

    Downstream process integration

    • Initial alkylation or esterification step for forming key lactones or functionalized esters; feeds directly into further cyclization or hydrolysis reactions

    Final product types

    • Lactone aroma intermediates (e.g., for coconut, peach, or creamy notes)
    • Aliphatic ester-based fragrance precursors
    • Fine chemical intermediates for compounded flavors
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    Certification & Compliance
    More Introduction

    Ethyl Bromoacetate: Reliable Reagent for Synthesis

    Introducing Our Ethyl Bromoacetate

    Ethyl bromoacetate stands out as a dependable building block for synthetic chemists and industrial manufacturers who look for clean, straightforward chemistry. In our facility, we produce ethyl bromoacetate through a tightly controlled process that monitors each phase for consistent purity. Our typical offering meets the demands of those seeking analytical-grade standards, and we routinely supply batches with 98% or higher purity. You get a transparent, colorless to slightly yellowish liquid that fits right into established lab routines without fuss. CAS number 105-36-2 and the molecular formula C4H7BrO2 give you the shorthand to compare with prior supplies.

    What Makes Our Ethyl Bromoacetate Different

    Over the years, we have learned the difference between technical convenience and practical value. In real research, what matters is not just the listed purity but the absence of unknowns — we focus on low water content, tightly managed bromide byproducts, and attention to proper packaging. You won’t find precipitate issues due to oversights in drying or filtration. We ship our ethyl bromoacetate only in glass or industry-approved fluorinated polymer bottles to avoid leaching or reactivity, guaranteeing product integrity for trusted upstream and downstream reactions.

    Some might think all ethyl bromoacetate is alike. In our experience, lab bottlenecks often trace to subtle differences in storage stability or how a supplier approaches distillation. When you buy from a manufacturer who does the synthesis, not only the repackaging, you skip risk-laden relabeling and get traceability back to the batch. That sense of control matters much more than most realize. We back each lot with a certificate of analysis covering major and minor impurities, moisture content, and the clean boiling range monitored during vacuum distillation.

    Why Ethyl Bromoacetate Remains Essential

    Our customers use ethyl bromoacetate for multiple reasons. The most common is as an alkylating agent — people in pharma and biochemistry settings know its efficiency for introducing ethyl ester groups onto a molecule. In industrial-scale production, especially in multi-step syntheses, it’s not just about price or grade. They want reproducibility and scalable process reliability. For nucleophilic substitution, ethyl bromoacetate provides a clean, efficient path to new carbon bonds, whether you are assembling simple compounds or starting a complex molecule. The high reactivity of the bromine atom lets chemists use milder conditions, reducing unwanted side-products compared to chloro analogs.

    Outside pharma, we see use in friction modifiers, pesticides, dyes, and certain specialty coatings. Students and researchers often share feedback about our standard packaging format — we offer 250 mL, 500 mL, and 1 L bottles because these volumes minimize repeated air exposure, keeping the reagent active and cutting waste.

    Handling, Safety, and Practical Experience

    No chemical synthesis proceeds without respect for hazards. Ethyl bromoacetate has a sharp, pungent odor and vapor exposure can irritate mucous membranes. As a manufacturer, we invest in proper fume extraction and handling controls so the product never leaves our site without a full safety briefing. Our staff perform outgoing QC in ventilated enclosures. On the customer side, users rightly ask about shipping and storage. We recommend keeping containers tightly sealed in a cool, well-ventilated place, away from sources of ignition, acids, and alkali. Spills present a dual challenge: skin and respiratory hazards and environmental toxicity. We suggest those working with it understand its properties and keep proper PPE on hand. Good communication between supplier and user helps limit missteps — as a factory, we emphasize transparency from label to delivery.

    Common Alternatives and Technical Differences

    Ethyl bromoacetate (EBA) occupies a specific role in the broader family of haloacetates. You can find ethyl chloroacetate, methyl bromoacetate, or even isopropyl bromoacetate, each with its merits. We often get asked why customers choose EBA over ethyl chloroacetate. The main reason: reactivity. Bromine leaves more readily in nucleophilic substitutions, making reactions smoother and sometimes shortening reaction times. In cases where methylation could trigger undesired side products or where steric hindrance plays a part, ethyl bromoacetate hits the sweet spot for chain extension and ring closure steps.

    For low-temperature work or where high yields are essential, EBA consistently outpaces the chloro version, especially with weak nucleophiles. Yet, due to the higher cost of bromine, those on tight budgets sometimes prefer chloroacetates; we believe results, not raw material cost alone, shape smart choices. For methyl bromoacetate, the smaller alkyl chain can change reaction outcomes, especially with sensitive substrates. EBA delivers less volatility and more control in distillation and separation — a benefit that matters when scale-up enters the picture.

    Our experience with academic labs and industry partners suggests that storage stability makes a real practical difference. As EBA hydrolyzes upon prolonged exposure to moisture, we focus on minimizing headspace and encourage users to keep bottles tightly capped and use aliquots in gloveboxes or inert atmosphere setups if precision is critical.

    Applications We Encounter Most Often

    The stories we hear from customers often teach us as much as our own testing. In organic chemistry, ethyl bromoacetate is central to malonic ester synthesis, one of the classic routes to carboxylic acids, ketones, and more complex frameworks. A number of our regular clients run multi-kilo runs aimed at producing pharmaceutical intermediates, specifically for beta-amino acid building blocks. They value the tight margins of error our consistent quality allows. Researchers in crop science favor EBA for its role in constructing new herbicide actives, where chain extension, selectivity, and reproducible reactions matter.

    Dye manufacturers like the versatility: ethyl bromoacetate enables alkylation of specific aromatic structures, influencing color strength and fastness. In recent years, several startups have explored its use in specialty polymerization initiators — we support them by offering smaller bottle lots and frequent lot analysis updates. Our technical team answers questions about solubility, reactivity, and typical boiling points, and we regularly offer advice based on direct experience, not just book figures.

    Lessons From Decades of Production

    Manufacturing EBA teaches a company patience and rigor. From raw material selection to complete purification, it’s important to control every variable. One recurring challenge comes from bromination: excess heat or trace water can produce unwanted byproducts, or worse, batch instability. Our approach involves slow addition, in-line moisture capture, and carefully staged distillation. Quality assurance for us isn’t paperwork; it’s repeatedly retesting stored samples six, twelve, even twenty-four months after production.

    We see that customers who worked with unreliable sources in the past often suffered unexplained side reactions or decomposition during storage. This is why we invest in long-term shelf-life studies and frequent feedback loops with actual practitioners. Instead of focusing simply on passing regulatory standards, we want the working chemist to finish their project successfully, without problems due to a supplier’s shortcuts or unreported impurities. Experienced users who switch to manufacturer-direct supplies often remark on greater batch-to-batch trust. To us that means as much as any inspection certificate.

    Exploring Limitations And Responsible Use

    We do not hide limitations. Ethyl bromoacetate’s harsh odor, toxicity, and strong alkylating capacity demand thoughtful storage and careful use. Poor ventilation or lack of basic protocols can invite operator risk. Decomposition, particularly in the presence of strong base or prolonged heat, occasionally causes local pressure build-up – anyone scaling production should install appropriate venting and failsafes. Waste management is another real-world factor. We advise partners to neutralize residues in-line before discharge, using dedicated systems to prevent unintentional halogen release into wastewater or air.

    From a regulatory perspective, bromo-organic compounds increasingly face scrutiny for environmental persistence. Over the years, we have collaborated with waste engineers and university researchers, working to identify safer byproducts, lower-impact process alternatives, and greener purification routes. While the underlying chemistry remains robust, sustainability pressures keep us searching for incremental improvements. This is another area where direct manufacturer experience adds value beyond what a catalog specifier can provide.

    Field Solutions & Ongoing Development

    On larger production lines, teams sometimes encounter clogging or instability during storage. In response, we developed custom bottle inserts to minimize vapor phase formation and container sweating, especially when shipments move between different climate zones. We modified our shipping protocols based on feedback from customers in South Asia and South America, as tropical climates can increase the risk of hydrolysis or local container pressure. We also offer technical support for adjusting dosing and handling setups depending on machine type or reaction scale.

    Smaller labs expressed concern about unavoidable leftovers after dispensing, due to the narrow bottle necks. We heard them. Our latest bottles have modified pour spouts for smoother transfer and to limit air influx, cutting down on reagent loss and keeping material fresh for longer. As a manufacturer, we see connections in user experience that no third-party trader catches, and we put that knowledge back into our designs.

    Why Choose Manufacturer Direct Over Reseller Stock

    Manufacturing gives us direct oversight. Resellers often change containers, relabel stock, or mix old and fresh lots. When you buy from the manufacturer, you get documented origin, batch control, and answers to technical questions straight from the chemists responsible for each drum or bottle. We do not dilute, blend, or repack based on outside inventory pressures. If a particular reaction or application requires extra-low water content, or you need a certain analytical certificate, you can request that before the product leaves our site.

    Communication flows more efficiently. If your end use changes or a project shifts direction, we work to modify production parameters for your next order. Industry feedback guides how we set up delivery, with tracking and real-time updates to limit transit exposure. For urgent deliveries, we can sometimes pull from in-process stock without waiting for next-quarter bulk shipments.

    Supply chain disruptions, raw material shortages, or regulatory changes don’t get lost in translation. Direct lines between production chemist and end user mean responses are accurate, fast, and tuned to the realities of your operation, not some generic catalog number.

    Research, Responsibility, and Looking Ahead

    As chemical makers, we stay focused not just on process efficiency, but on growth — ours and yours. We see more demand for sustainably made ethyl bromoacetate, especially in the pharmaceutical and crop science sectors. Projects exploring new anti-infective molecules or next-generation colorants push us to refine our processes further, with a focus on cleaner effluent streams, waste reduction, and increased yields.

    Newer analytical techniques like GC-MS and NMR have raised the bar. We use these not just for in-house QC but also to support application troubleshooting in the field. If a user faces reactivity drops or byproduct spikes, we can compare batch spectra and track down root causes. This closes the loop from plant to bench and back again.

    Every year we review upstream sourcing to ensure bromine and base alcohols come from reputable, transparent suppliers. Not all products on the market take this same approach, and cases of mislabeling or adulteration still occur. We offer open documentation on request, detailed trace reports, and direct communication with the chemists who made and checked your batch.

    The Manufacturer’s Perspective

    Being at the origin gives us the broadest view — from incoming raw inventory, through day-to-day plant operations, into the realities of global logistics. We work closely with end users to adjust product spec, adapt packaging, and offer technical guidance so that the product matches what really works in synthetic organic labs and in scale-up settings.

    For us, ethyl bromoacetate is not simply a commodity reagent. We treat its safe, reliable handling and delivery as a partnership. That means responding to real feedback, solving practical challenges, and supporting you not with boilerplate answers but with the full history and lived expertise of actual chemical manufacturing. The next time you reach for this trusty reagent, you can have confidence it was made — and supported — by those who understand the importance of every last drop.

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