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Ethyl Bromoacetate

    • Product Name Ethyl Bromoacetate
    • Alias EBA
    • Einecs 203-696-6
    • 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

    767872

    Chemical Name Ethyl Bromoacetate
    Cas Number 105-36-2
    Molecular Formula C4H7BrO2
    Molecular Weight 167.00 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 154-156 °C
    Melting Point -51 °C
    Density 1.553 g/mL at 25 °C
    Refractive Index 1.443
    Flash Point 63 °C
    Solubility Slightly soluble in water; soluble in most organic solvents
    Purity Typically ≥98%
    Odor Pungent, fruity odor

    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 Ethyl Bromoacetate is packaged in a 500 mL amber glass bottle with a secure cap, labeled with hazard and handling instructions.
    Shipping Ethyl Bromoacetate is shipped as a hazardous chemical according to UN Number 1919. It should be securely packed in appropriate containers, with labeling for toxic and flammable liquid. Transport must comply with international regulations, including the use of safety equipment and documentation. Avoid heat, sunlight, and incompatible materials during shipping.
    Storage Ethyl Bromoacetate should be stored in a cool, dry, and well-ventilated area, away from heat and sources of ignition. Keep it in a tightly closed container made of compatible materials, and protect from moisture and direct sunlight. Store separately from strong oxidizers, acids, and bases. Use secondary containment to prevent spills, and ensure clearly labeled, dedicated storage to avoid accidental mixing.
    Application of Ethyl Bromoacetate

    Applications of Ethyl Bromoacetate in Industrial Manufacturing

    As a specialized manufacturer, we supply Ethyl Bromoacetate for diverse industrial applications where its unique reactivity and selectivity are critical to process efficiency. Below are the principal downstream scenarios utilizing our material, along with the precise industrial context for end users.

    1. Pharmaceutical Intermediates for API Synthesis

    Pharmaceutical producers integrate Ethyl Bromoacetate primarily in the synthesis of complex active pharmaceutical ingredient intermediates, such as β-amino acid derivatives, cephalosporin side chains, and antihypertensive agents. Its alkylating action is essential for introducing ethoxycarbonylmethyl groups during multi-step API build-up, supporting process yields and selectivity in cGMP-compliant environments. The ratio of Ethyl Bromoacetate depends on the target molecule and is adjusted based on molar stoichiometry and impurity profile control documented via in-process QC analytics.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, and JP monographs (as required for target APIs)
    • FDA 21 CFR Part 211 (US drug manufacturing)
    • EMA pharmaceutical quality guidelines

    Typical usage ratio

    • 0.95–1.15 molar equivalents per alkylation site, adjusted for reaction scale and target impurity limits in multi-gram to multi-ton batches

    Downstream process integration

    • Enters during nucleophilic substitution or alkylation steps, commonly after base deprotonation or enolate formation, under N2 atmosphere and temperature control

    Final product types

    • β-lactam antibiotic intermediates
    • Antihypertensive drug building blocks
    • Peptidomimetic synthesis intermediates
    • Fine chemical precursors for further pharmaceutical transformation

    2. Agrochemical Synthesis Intermediates

    Crop protection manufacturers select Ethyl Bromoacetate for constructing pyrethroid, herbicide, and fungicide scaffolds via halogenated ester introduction. Its reactivity ensures precise attachment of bromoacetyl moieties, which are key for subsequent cyclization or substitution in agrochemical active molecule creation. The integration must match both seasonal production surges and stringent regulatory residue requirements specific to local agricultural standards.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specification
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing
    • European Union Regulation (EC) No 1107/2009 (plant protection products)
    • US EPA 40 CFR Part 158 (Agrochemical registration data requirements)

    Typical usage ratio

    • 8–15% w/w relative to substrate in intermediate synthesis, varied to balance cost of goods and desired conversion efficiency

    Downstream process integration

    • Reactant in bromoalkylation or esterification stages, either batch or continuous flow, often prior to ring closure or further substitution to form the core agrochemical skeleton

    Final product types

    • Pyrethroid insecticide intermediates
    • Selective herbicide precursors
    • Triazole and imidazole fungicide side chains
    • Agrochemical screening libraries for development pipelines

    3. Specialty Fine Chemicals: Grignard and Organometallic Reagents

    Producers of custom organometallics and Grignard reagents utilize Ethyl Bromoacetate as a reliable alkyl halide source for synthesizing esters, extended carbon chains, and functionalized building blocks under controlled anhydrous conditions. The material supports high-purity requirements in electronics and specialty polymer sectors, where trace impurities affect downstream performance. Processing often entails handling in inert environments and real-time water/moisture monitoring to avoid hydrolysis or side reactions.

    Industry compliance standards

    • REACH Regulation (EU) 1907/2006 (Substance traceability & SVHC controls)
    • ISO 14001:2015 (Environmental Management for chemical synthesis)
    • Internal QC protocols (metal impurity and halide residue testing)
    • National Fire Protection Association (NFPA) Chemical Storage Guidelines

    Typical usage ratio

    • 1.05–1.20 molar equivalents versus the organometallic reactant, modulated to optimize yield in kilo- to multi-ton scale syntheses

    Downstream process integration

    • Charged directly into Grignard or metal-catalyzed coupling reactors, in jacketed vessels under controlled exothermic conditions and inert gas protection

    Final product types

    • Functionalized Grignard intermediates for further carbon chain extensions
    • Organometallic additives for specialty polymer modification
    • Building blocks for advanced electronic materials
    • Custom reagents for contract synthesis R&D

    4. Fragrance and Flavor Ester Intermediates

    Industrial fragrance and flavor manufacturers specify Ethyl Bromoacetate as a precursor for synthesizing key aromatic esters and flavor enhancers. Its selective bromoester function enables straightforward transesterification and subsequent reduction or substitution reactions to generate high-purity molecules, fulfilling rigorous safety and sensory quality profiles. Material tracing and residue management remain critical due to direct application in food-contact or cosmetic-grade products.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • EU Regulation (EC) No 1334/2008 (Flavorings and certain food ingredients)
    • ISO 22000:2018 (Food safety management for ingredient processing)

    Typical usage ratio

    • 3–8% w/w in batch transesterification setups; precise ratio set by desired ester concentration and ring closure efficiency for downstream product

    Downstream process integration

    • Fed into esterification or aromatic modification lines, with phase separation and purification conducted prior to final blending with neutral carriers or diluents

    Final product types

    • Fruit aroma esters for beverages
    • Synthesized musk and ambergris replacements
    • Flavor intermediate compounds for bakery and confectionery
    • Perfume additive bases for mass-market personal care

    5. Dye and Pigment Intermediate Synthesis

    Leading dye and pigment manufacturers deploy Ethyl Bromoacetate for the targeted synthesis of reactive dyes, specialty colorants, and pigment molecule linkers. The bromoacetate function readily supports nucleophilic substitution to graft chromophoric fragments under controlled pH and temperature protocols, ensuring both coloration intensity and dispersibility as required by end-use substrate or fiber type. Material handling systems are adapted to fully recover any volatile organobromine residues in compliance with green chemistry targets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) requirements
    • ISO 9001:2015 Quality Management in colorant manufacturing
    • EU REACH and GHS (Globally Harmonized System of Classification)

    Typical usage ratio

    • 4–12% w/w in dye intermediate preparation lines, ratio optimized by absorption spectrum and substrate compatibility requirements

    Downstream process integration

    • Inserted during late-stage chromogen functionalization or linker formation, with real-time UV-Vis monitoring to match shade reproducibility targets

    Final product types

    • Reactive dyes for cotton and synthetic fibers
    • Specialty pigments for plastics and inks
    • High-performance optical brighteners
    • Colorant intermediates for hair and textile dye blends
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    Certification & Compliance
    More Introduction

    Ethyl Bromoacetate: Chemistry Backed by Generations of Expertise

    More Than Just a Chemical: Our Commitment to Precision and Quality

    Making ethyl bromoacetate isn’t a simple matter of mixing a few reagents in a tank. It calls for deep respect for chemical reactions, an eye for detail, and decades of knowledge working with sensitive halogenated organics. In our facility, every batch of ethyl bromoacetate gets careful attention. We watch temperature, moisture, and purity at every step, because impurities can cause trouble downstream during synthesis. Our approach has always been hands-on. We test, analyze, and refine until the clear, colorless liquid we bottle meets tight standards. The aim is to give chemists a product they can trust, batch after batch, whatever their application demands.

    Model and Typical Specifications

    Our ethyl bromoacetate carries a molecular formula of C4H7BrO2, offering a molar mass of 167.01 g/mol. You’ll find it as a colorless to pale yellow liquid with a sharp, sweet odor. Purity levels remain consistently above 99%. Density hovers around 1.46 g/cm3 at 20°C, and boiling point sits at approximately 158°C. Water solubility stays low, so phase separation during work-up rarely gives trouble. Most reactions benefit from minimized water content, so our product contains less than 0.05% moisture, proven by Karl Fischer titration in our on-site labs. Chloride and cyanide impurity levels hardly register, well below industry thresholds.

    What Ethyl Bromoacetate Does Better

    Organic synthesis always puts pressure on reagents to perform, especially when yield, purity, and downstream performance matter. Ethyl bromoacetate often steps in when alkylation, esterification, and pharmaceutical intermediate preparation require certainty in both reactivity and the absence of contaminants. Since bromine atoms activate the methylene group, the compound works best for introducing ethoxycarbonyl and bromoethyl groups. Its balance of volatility and chemical stability lets researchers control rate and selectivity in the lab and at scale.

    Some chemists might reach for methyl bromoacetate as a close cousin, but the ethyl analog brings better control in certain transesterification and nucleophilic substitution reactions. Ethyl esters hydrolyze a bit slower than methyl esters, which matters when selective cleavage is needed down the line. In contrast, isopropyl or tert-butyl bromoacetates show much more steric hindrance, complicating SN2 reactions and cutting yields. Our product’s unimposing structure and consistent reactivity let custom syntheses run without repeated troubleshooting.

    Applications Rooted in Practical Laboratory Experience

    As direct manufacturers, we’ve seen ethyl bromoacetate deployed across medicinal chemistry, agrochemical research, and advanced material science. In our customers’ hands, reaction protocols draw on the reagent’s clean response with nucleophiles. Peptide synthesis techniques rely on ethyl bromoacetate as a mild alkylating agent for protecting group strategies. Custom API synthesis often involves ethyl bromoacetate to make esters that can be converted into building blocks no other bromoacetate can yield as efficiently. It proves essential among researchers developing beta-amino acid derivatives and new heterocycle frameworks.

    On the crop science front, the compound often appears during active ingredient scale-ups, enabling alkylation steps that demand both selectivity and reliable availability. Having west-coast and midwestern customers with unique process requirements has taught us to adjust specifications for trace impurities to fit new project standards, so scale-up teams don’t lose time on unexpected byproducts. This back-and-forth with researchers and in-house chemists continues to drive refinements in our purification protocols, so the product they get is ready for the demands of today’s custom chemistry.

    Production Realities and Safety

    Making ethyl bromoacetate involves more than glassware and vacuum pumps. We use well-maintained reactors with corrosion-resistant linings and automated dosing to minimize side reactions and waste streams. Each operator knows not only the procedure but the warning signs of any deviation, because small errors can magnify fast. Careful separation and purification steps eliminate unreacted starting materials, hydrolyzed side-products, and color bodies that can interfere with later chemistry.

    Anybody who has worked up an alkylating reaction knows the importance of handling bromine intermediates with respect. We fit our plant with high-volume scrubbers and vented hoods, and everybody on the floor wears protective clothing. Regular safety drills and environmental monitoring keep our process safe for the crew and the community outside our walls. Safe packaging is non-negotiable; we use strong amber bottles and custom liners that stand up to solvents and fluctuations in temperature, so transport stays safe whether the shipment travels across town or around the globe.

    What Sets This Ethyl Bromoacetate Apart from Others in the Market?

    Not all ethyl bromoacetate comes from producers who understand the headaches a bad batch causes. Some rival products, especially those routed through multiple intermediaries or repackers, pick up water, acetic acid, or other halide contaminants on the journey. These can spell disaster in sensitive applications. The product we make has earned loyalty in demanding pharma and fine chemical labs. We always monitor for bromide, chloride, unreacted ethanol, and even trace byproducts from side reactions, so nobody is left with surprises.

    Feedback from our partners and clients often points to consistent color, purity, and chemical behavior under varied reaction conditions. Analytical support sits just a call away, helping troubleshoot or confirm performance. Some imported materials promise purity but arrive with inconsistent water content or a yellow tint that points to breakdown or poor storage. We pride ourselves on prompt delivery of fresh stock, backed by regular revalidation and real-world use data. Our teams care about usability — no sulfide or halide smells, low residue in evaporators, and full, clear labeling on every container.

    Supporting Green Chemistry and Sustainability

    Waste handling remains central to our production philosophy. The synthesis route has evolved from traditional batch chlorination to greener, solvent-recycling approaches. We limit halogenated waste through in-line recovery, and off-gasses pass through advanced treatment before ever reaching the environment. Partnerships with solvent recovery firms have enabled circular practices that cut new resource use and disposal costs. Precursor selection leans on high purity, short transport paths, and documented chain of custody.

    The global push toward less hazardous chemistry means end-users demand higher-purity inputs with smaller footprints. We keep documentation up to date, including full traceability, REACH compliance, and details for green chemistry auditors. Some clients have asked for custom packaging to further reduce plastic waste, and we’ve responded by trialing steel drums and returnable totes for local customers.

    How Traceability and Consistency Pay Off in Research and Manufacturing

    Every reputable chemist knows the frustration when a reaction stops working from one batch to the next. Reliable ethyl bromoacetate closes that gap. All stock comes from monitored processes and carries full batch documentation. If a problem surfaces, it gets tracked back and addressed right at the source. New projects often ride on the certainty that each bottle behaves the same. Academic labs and pilot plants alike have sent us reports of improved yields and fewer troublespots from starting a sequence with our material.

    Some competitors offer product “off the shelf,” but can’t answer questions about origin, handling, or subtle impurities. Our focus on analytical transparency and production records keeps projects on track and spares everyone costly repeats. Whether customers run a kilo lab or manage metric ton production, the same level of attention goes into every shipment. We report not just COA numbers but supporting chromatograms, moisture analysis, and even retention time references for key byproducts.

    Real Feedback from Chemists at the Bench

    Our customer service line isn’t just for orders; it serves as a feedback loop with real-world users. Process chemists often report how switching to our product cut reaction times or lifted yields, thanks to cleaner starting points. One pharmaceutical partner shared how a single failed batch — traced to off-spec ethyl bromoacetate from an outside supplier — cost weeks in troubleshooting. Material from our plant restored their synthesis and kept development on its timeline. Small scale-up teams thank us for advance notice if any analytical reading shifts, so their formulations never run into avoidable setbacks.

    University teams send us detailed reports on exploratory methodology, confirming reactivity in a range of alkylation strategies. Data from these collaborations has fed refinements back into process controls and user documentation. We believe in honest exchange; when our partners notice issues, the concern gets routed straight back to the plant floor for solutions. Samples from every new batch run through duplicate analysis both in-house and by outside labs, building mutual trust with the scientists counting on our products.

    Why Quality Control Can’t Be an Afterthought

    Some suppliers treat quality as a box-ticking exercise, but we know every step from synthesis to packaging has a direct impact in the field. Gas and liquid chromatography, NMR, and titration form our day-to-day toolkit — not occasional checks. Turnover in QC labs runs low because we invest in training and recognize the direct impact their skills have on our product’s reputation. We always aim to find issues upstream, adjust before release, and only ever ship stock we’d use in our own research.

    Years spent responding to customer queries have taught us this: A single percentage point change in moisture or acetic acid content can change a reaction’s path entirely. The quality lab staff are always on watch for unexpected trends. Documentation isn’t buried in a filing cabinet — it’s ready for anyone who asks, from lead researchers to warehouse staff. We post real-time batch analysis online for trusted partners facing regulatory audits or rapid scale-up, cutting time lost tracking paperwork.

    Looking Forward: Responding to New Demands and Regulations

    Chemical manufacturing never stands still, and neither do regulatory expectations. Brominated esters like ethyl bromoacetate fall under increasing scrutiny for emissions, handling, and worker exposure. We keep abreast of all regulatory developments, whether domestic or from abroad, tailoring safety sheets and transport documents to the requirements of each country. Operators receive ongoing updating in best practices, so our team’s knowledge base grows along with shifting demands.

    We’re responding to market calls for even more transparent sourcing and logistics. Inspection from major end-users drives us to share every step of our chemical stewardship process, offering supporting evidence from raw input to final shipment. Near-term upgrades in plant digitalization will further cut error rates and improve batch traceability.

    Product Integrity and Partnership: The Foundation of Our Ethyl Bromoacetate

    Years of experience have convinced our team of one simple fact: Process improvement is pointless if it doesn’t translate into a better experience for working chemists. Each customer and partner has helped shape not just the purity profile but the entire supply approach. Ethyl bromoacetate stands as more than a reagent in our eyes — it’s an assurance that every stage of a laboratory or production process can proceed with greater certainty. Trust takes years to build in fine chemicals, and one misstep can unravel it overnight. We know consistency isn’t a marketing line, but a reality forged in every batch, every analysis, and every on-time delivery.

    We welcome chemists who value thorough support, clear communication, and openness to share both challenges and successes. Our commitment remains to the principles that have made our plant a mainstay among those who ask more from their chemicals: reliability, transparency, and a relentless drive to improve. Ethyl bromoacetate from our hands isn’t just another catalog listing — it represents our ongoing investment in chemical progress, environmental responsibility, and the scientific relationships that have shaped our growth from day one.