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Ethyl 4-Bromophenylacetate

    • Product Name Ethyl 4-Bromophenylacetate
    • Alias ethyl 2-(4-bromophenyl)acetate
    • Einecs EINECS 412-110-5
    • 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

    890329

    Chemical Name Ethyl 4-Bromophenylacetate
    Molecular Formula C10H11BrO2
    Molecular Weight 243.10 g/mol
    Cas Number 54030-38-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 290 °C
    Density 1.41 g/cm3
    Purity Typically >98%
    Solubility Insoluble in water, soluble in organic solvents
    Refractive Index 1.541
    Storage Conditions Store at room temperature, keep container tightly closed
    Smiles CCOC(=O)CC1=CC=C(C=C1)Br
    Synonyms Ethyl 2-(4-bromophenyl)acetate
    Flash Point 140 °C

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

    Packing & Storage
    Packing 250g of Ethyl 4-Bromophenylacetate is packaged in a sealed amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping Ethyl 4-Bromophenylacetate is shipped in tightly sealed containers to prevent leaks and contamination. It is packaged according to international regulations for chemical transport, typically under dry and cool conditions. Proper labeling, handling precautions, and documentation are ensured to comply with safety and environmental standards during shipping.
    Storage Ethyl 4-bromophenylacetate should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Separate from strong oxidizing agents or acids. Proper labeling and secure storage help prevent accidental exposure or spillage. Always follow institutional or manufacturer safety guidelines.
    Application of Ethyl 4-Bromophenylacetate

    Applications of Ethyl 4-Bromophenylacetate in Industrial Manufacturing

    Ethyl 4-Bromophenylacetate serves as a key building block in specialized industrial sectors, supporting value chain innovation across pharmaceutical, agrochemical, and fine chemical production. Our vertically integrated manufacturing ensures consistent quality and supply traceability, directly supporting customers’ advanced synthesis routes and formulation objectives. Below are the core downstream application scenarios for this material, with detailed technical specifics on standards, dosage, process integration, and end product forms.

    1. Pharmaceutical Intermediates for Anti-inflammatory API Synthesis

    This compound acts as a critical intermediate in the synthesis pathways of selective COX-2 inhibitors and other non-steroidal anti-inflammatory drug (NSAID) active pharmaceutical ingredients, where the 4-bromophenyl moiety forms an essential pharmacophore. Its structural attributes enable precise halogenation patterns during later-stage coupling and cyclization steps in high-value API production lines.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP-ICH Q7)
    • EDQM CEP (European Directorate for the Quality of Medicines Certificate)
    • USP/NF and European Pharmacopoeia monograph conformance (for intermediates destined for regulated APIs)
    • FDA DMF registration (where used in US-bound drug supply chains)

    Typical usage ratio

    • Ranges between 0.8 to 1.2 molar equivalents per synthesis batch, adjusted to stoichiometry of downstream condensation step and target yield. Actual quantity determined by desired product purity and scale-up reaction efficiency.

    Downstream process integration

    • Added at the intermediate stage of multi-step organic synthesis, commonly via ester condensation followed by halogen-metal exchange and Suzuki or Heck cross-coupling for final API assembly.

    Final product types

    • Selective COX-2 inhibitor APIs (e.g., analogs of celecoxib derivatives)
    • Other custom pharmaceutical intermediates featuring bromophenylacetate scaffolds
    • Fine chemical reference standards for R&D and analytical purposes

    2. Agrochemical Intermediate for Herbicide Synthesis

    In the crop protection sector, this material enters the value chain as a precursor in synthesizing certain brominated phenyl-based herbicides and plant growth regulators. The aromatic bromine atom allows precise subsequent substitution, facilitating downstream synthesis of biologically active compounds with high selectivity indexes in weed management products.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems (for chemical synthesis)
    • FAO/WHO pesticide specifications (where applicable)
    • China National Standards (GB/T 19001) and EU REACH registration for export
    • Hazardous Chemical Registration (if handled under PRC regulations or equivalent in export destinations)

    Typical usage ratio

    • Incorporated at 0.5 to 0.9 molar ratio depending on the specific herbicide’s synthetic route and target selectivity. Ratio is determined in relation to the ensuing halogen substitution or ester hydrolysis requirements.

    Downstream process integration

    • Introduced in early-stage esterification, followed by hydrolysis and electrophilic substitution, often involving stepwise chlorination or amination in active ingredient assembly lines.

    Final product types

    • Brominated phenyl herbicide technical materials
    • Active ingredient concentrates for crop protection formulations
    • Agrochemical R&D analytical standards

    3. Intermediate for Synthesis of Liquid Crystal Monomers

    This compound delivers distinct value as a halogenated aromatic starting material for specialty esters and biphenyl compounds found in advanced liquid crystal monomer formulations. Its well-defined bromine position and ester group enable precise further functionalization, supporting downstream integration within display and optical material manufacturing.

    Industry compliance standards

    • ISO 9001 and ISO 14001 (for liquid crystal material supply chains)
    • RoHS Directive (2011/65/EU) for hazardous substance limits in electronics
    • Technical requirements from downstream display panel OEMs
    • REACH regulations for manufacture and use in the EU

    Typical usage ratio

    • Used at 1.0–1.4 molar equivalents depending on liquid crystal monomer target, modulated by the structure and chain length of core aromatic units in final application.

    Downstream process integration

    • Processed through nucleophilic substitution or ester-exchange reactions with specific diols or alcohols to formulate monomer blends used in LCD manufacturing. Integration timing controlled by desired optical anisotropy and viscosity parameters.

    Final product types

    • Nematic and smectic liquid crystal monomers
    • Optically active esters for display panel production
    • Intermediate compounds for specialty optical coatings

    4. Fine Chemical Building Block for Fragrance Synthesis

    This ester, owing to its aromaticity and controlled halogenation, is adopted by fine chemical producers as a core intermediate in creating musky, balsamic, or woody aroma components. The compound’s structure allows targeted transformation into aldehydes, alcohols, or aromatic acids with fragrance relevance, supporting downstream ingredient manufacturers in the perfumery sector.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice compliance for downstream products
    • ISO 22716:2007 Good Manufacturing Practices for cosmetics ingredients
    • Purity and impurity profiling as per in-house QC protocols
    • Relevant SDS labeling for transport in bulk chemical form

    Typical usage ratio

    • Implemented at 1.0–1.3 equivalents in fragrance intermediate synthesis depending on the intensity of aroma profile targeted, and downstream derivatization process design.

    Downstream process integration

    • Inserted during ester hydrolysis and subsequent controlled oxidation or reduction as part of aroma molecule assembly, prior to blending and purification for perfumery use.

    Final product types

    • Aromatic aldehyde and alcohol intermediates for fragrances
    • Fine chemical components for musky and woody scents in luxury perfumes
    • High-purity specialty aroma chemicals for cosmetic formulations

    5. Starting Material for Advanced Dye and Pigment Manufacture

    This compound provides a halogenated phenylacetate group ideal for synthesizing specialty dyes and colorant precursors used in plastics and textile industries, especially where controlled chromophore substitution is needed for high color stability and fastness. The molecular structure offers process engineers an efficient entry point for creating azo or anthraquinone dye frameworks through further derivatization steps.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile and leather applications downstream)
    • EU REACH Annex XVII for hazardous chemical restrictions in colorants
    • Chemicals Management Plan (Canada) for pigment precursors
    • Heavy Metals and Aromatic Amine content controls per EN 71-3 (toys pigments)

    Typical usage ratio

    • Employs 0.7–1.0 molar equivalents per chromophore unit, with precise dosing guided by desired intensity, solubility, and process limitations in the end-use formulation.

    Downstream process integration

    • Reacted initially through aromatic substitution, nitration, or diazotization followed by coupling reactions, integrated into the pigment or dye intermediate assembly sequence ahead of final crystallization and blending.

    Final product types

    • Functional dye intermediates for engineering plastics and fibers
    • Specialty pigments for paints, inks, and high-stability coatings
    • Colorant additives for automotive and architectural applications
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    More Introduction

    Ethyl 4-Bromophenylacetate: A Manufacturer’s Perspective

    Looking Closely at Ethyl 4-Bromophenylacetate in Chemical Synthesis

    Ethyl 4-Bromophenylacetate lands itself on the workbenches of many pharmaceutical research teams and fine chemical manufacturers. Its clean acetate group and the bromine atom on the para position of the phenyl ring give it a character well-suited for unlocking new chemical possibilities. In our own production lines, we can hear the raw solvents mixing, and smell the strict protocols that ensure the air stays clear as we synthesize each batch. Unlike some intermediates that seem plain or stubborn to react, this compound opens new doors.

    Model, Purity, and Consistency Drive Quality

    Every gram leaving our plant matches what researchers expect: a clear, pale yellow liquid, with a purity above 99%. Batch records show actual numbers, not just target specs. Our facilities focus on the CAS number 6740-85-8, and that isn’t just record keeping; it’s the difference between reproducibility and uncertainty. From experience, researchers don’t have patience for contaminants or sloppy isomer mixtures. No one wants an NMR spectrum carrying surprise aromatic signals. Each vessel, glass-lined or metal, gets meticulous attention to temperature control and agitation, especially when working up the product after bromination. We sample, analyze, and confirm the absence of residual starting material by GC and HPLC. Any sign of excess acidity or stray halide brings production to a halt for troubleshooting. From my years walking the plant floor, outcomes remain predictable when every run begins with the right raw phenylacetic acid and n-Butanol, and the bromination only proceeds once solvents pass Karl Fischer dryness checks.

    Usage: Where Synthesis Harnesses Its Power

    Across the globe, R&D teams lean on Ethyl 4-Bromophenylacetate as a solid starting block for making statins, anti-inflammatory agents, and imaging compounds. Medicinal chemistry throws curveballs at routine manufacturing, but this compound steps up where others don’t. The para-bromo group allows direct coupling with Suzuki and Heck reactions, letting our customers build complex ring systems efficiently, especially when trying new molecular scaffolds. Several API process chemists have told us they value the mild ester hydrolysis—there’s no fight to get the parent acid for further amide coupling, and little risk of overreacting side chains.

    Some intermediates seem sticky or volatile under similar handling, complicating scale-up. Ethyl 4-Bromophenylacetate pours well, leaves cleanly during extractions, and distills with a crisp cut. In kilo-scale reactors, this predictability saves hours, not just minutes. For photographic and pigment work, it finds use where electron-donating groups might destabilize color; the bromo handles UV stable, synthetic intermediates without degrading.

    Behind the Scenes: From Plant to Lab

    Routine doesn’t always look glamorous on the outside, but it makes custom chemistry possible. My earliest memories of joining this field involve long shifts understanding not just how molecules fit together during a reaction, but also how trace water, inconsistent temperatures, and poor raw material selection ruin batch quality. Our equipment—vacuum stills, jacketed kettles, and inline filtration—faces more scrutiny under the watchful eyes of process chemists than any spreadsheet could convey. Each batch analyzed means another lesson learned, tweaked, and retested as we target minimal batch-to-batch variation.

    By choosing high-quality starting materials and continuous monitoring, the plant limits the need for downstream purification. We’ve seen how a single shortcut, such as using recycled bromine without strict quality checks, produces trace byproducts detectable by savvy customer labs. Repeat business usually rests on a record of consistency, and we’ve experienced both the sting and satisfaction that come with customer feedback.

    What Makes It Stand Apart?

    Many manufacturers offer phenylacetate derivatives—some with nitro or methyl substituents—yet few deliver the same versatility and reactivity for cross-coupling seen with the para-bromo group. Our teams chose this molecule because it delivers a predictable leaving group for palladium-catalyzed couplings, opens pathways toward high-value APIs, and keeps protecting group chemistry simple. In contrast, ortho- or meta-brominated analogues introduce steric crowding that slows down the same reactions and builds up unwanted byproducts. Para-chloro versions, on the other hand, lack the same ease of purification—chloro derivatives usually linger as traces in final products due to reduced reactivity in certain coupling systems.

    Where phenylacetate itself may serve as an idle building block, the 4-bromo version steps up. Its bromo group participates directly in further functionalization. One of the largest wins we’ve seen comes from researchers using it to cut steps from old multi-stage syntheses—introducing the bromo at the right time rather than later through direct halogenation minimizes potential for poly-bromination and waste. More than once, new customers have come to us complaining they tried off-brand sources or synthetically crowded analogues, only to meet inconsistency or isolation headaches. Purity impacts more than yields; impurities can tie up catalysts, poison downstream steps, or require expensive cleanups.

    Manufacturing Realities: Scaling Challenges and Experience

    Scaling Ethyl 4-Bromophenylacetate takes more than chemistry know-how; it calls for strict process discipline. Reactors filled with kilogram quantities act differently than glassware on the lab bench. Reaction exotherms grow swift and sharp. We allocate double containment and remote temperature watchdogs for bromination, limiting risk. Even small process changes—like solvent ratios or stirring speeds—alter outcomes and trace impurity profiles. Old facility logs still carry lessons from unexpected purity drops tied to a faulty cooling loop or an overused batch of catalyst.

    Each shipment heads out with a full analytical panel—GC, NMR, water content, residual solvents, and halogen content included. In our experience, promising new synthetic steps means little if the raw material supplier cuts corners. Batch records not only inform customers but highlight small improvements we make, like switching to better agitation or using newer filtration membranes. Over the years, we saw customers try sourcing from non-specialist brokers, only to face crystallization issues and inconsistent methyl group contamination. Every snafu upstream can create chaos downstream; tight quality control in the first step shortens the path to API approval and onboarding.

    Responsible Handling and Long-Term Supply Commitments

    Ethyl 4-Bromophenylacetate requires careful attention even after it changes hands. Drum storage calls for temperature control because high ambient heat increases decomposition rates. Surplus stock in warehouses held too long turns sticky or darkens, a sure sign of hydrolysis. We advise direct shipping from our climate-controlled storage to customer sites and always double-check shelf life before dispatch. Teams performing scale-up or kilo-lab synthesis appreciate getting product that hasn’t sat neglected; that detail translates to actual working hours saved during each campaign.

    Chemical security and responsible handling count as much for safety as for purity. Our on-site staff undergo regular training specific to halogenated aromatics, and we run drills covering everything from bromine exposure to environmental containment. Our approach isn’t just box-ticking—lost time to accidents or contamination costs more than robust training. Transparency around our sourcing, production, and shipping assures customers they see a real manufacturer, not a virtual storefront or packaging warehouse. Our batch traceability can retrace shipments going back years, a direct answer to regulatory and customer audit requests.

    Standing by Our Track Record

    Markets constantly change, and each year brings new regulatory pressures or supply chain hiccups. Through firsthand challenges—port slowdowns, raw material shortages, sudden jumps in energy prices—long-term relationships with reliable suppliers matter more than ever. One of our biggest strengths stems from investing in continuous process improvements and listening closely to technical customer feedback. Many research organizations, small and large, stay with us across generations of product development, citing not only cost but reliability and open communication.

    Sometimes, customers face daunting requirements or novel regulatory compliance steps, and we help with submission dossiers or trace impurity discussions. Our team doesn’t hesitate to open historical data sets or provide extra sample panels. We know how critical it is for early-stage pharmaceutical projects to trust what sits in a drum or bottle, especially when reviews focus on consistent impurity profiles across dozens of batches.

    Looking Forward: Innovation and Sustainability

    Manufacturing Ethyl 4-Bromophenylacetate cleanly means paying attention not only to output, but also to the environment. We’re no strangers to the challenge of bromine recovery and waste minimization. Our on-site treatment systems tackle organohalide waste streams, scrubbing exhaust and neutralizing residues before disposal. Solvent recycling and catalyst reuse programs, born of real-world cost and regulatory pressure, also cut waste and carbon output, lending direct environmental and commercial benefits.

    A few years back, we piloted continuous-flow processes for key steps, cutting cycle times and enabling greater reaction selectivity—results weren’t immediate, but with persistence, we reduced side-product generation and boosted safety. Teams in our R&D division feed input from customer labs back into process engineering. This loop between application chemists and production specialists builds more robust, more flexible manufacturing approaches that don’t just chase technical advancement but also answer sustainability head-on.

    Differences That Matter: Comparing With Other Esters and Halides

    It’s one thing to list a row of chemical intermediates on a chart; it’s another to see how they perform where it counts—in scaled coupling reactions, reliability under pressure, and customer audit trails. Compared with methyl, isopropyl, or tert-butyl phenylacetate derivatives, the ethyl ester balances volatility and hydrolysis perfectly for large-scale operations. Too volatile, and products vanish during work-up. Too stable, and chemists struggle to open the ester link without harsh reagents. Over time, process feedback proved the ethyl group as a sweet spot—reactive, yet manageable.

    The bromine in the para position isn’t just a decorative badge. It confers specificity to subsequent transformations. With ortho- or meta-brominated analogues, steric bulk frustrates coupling, slows reaction kinetics, and forces extra purification. Para-chloro analogues, though sometimes touted as cost-saving substitutes, often resist reaction conditions needed for certain C–C bond formations. We’ve worked with clients who tested chloro and iodo variants; iodine acts with extreme reactivity, but supply volatility and high cost keep it out of most commercial routes. Our experience with the bromo offers both reactivity and affordability—making it the practical choice across many syntheses.

    Practical Considerations in the Lab and Plant

    Routine doesn’t guarantee success. Each new project challenges us to revisit old assumptions. Some customers send back feedback about unexpected crystallization, hinting at solvent residues or trace impurities. Our analytical teams jump in; sometimes the culprit ties back to a minor raw material source change upstream. Open reporting culture means these lessons improve the next batch, not just for us, but for the end-user.

    Product-handling tips sometimes seem trivial until issues arise. Chemists working quickly on benchtop projects might miss the importance of tightly sealed storage or the need for anhydrous solvent when opening the ester group. For kiloscale syntheses, differences between drum-packed and smaller bottles show up in recovery rates. Even the shape of the container, the quality of the liner, and the logistics of temperature during shipping add up to real costs out of pocket and time lost during project milestones.

    Commitment to Compliance and Long-Term Supply

    Regulatory ceilings keep rising, especially in the pharmaceutical and specialty chemical sectors. Our QA and regulatory affairs teams collaborate with auditors and customer scientists alike, producing traceable certificates of analysis, impurity profiles, and documentation tailored to specific project needs. Year on year, these efforts grow more complex—not as a result of new bureaucracy, but because downstream product approvals in regulated industries hinge on documented reliability. Ethyl 4-Bromophenylacetate’s chain of custody means something, as we stand by every lot number down to the shift that ran the reactor and the date each analytical test was performed.

    No batch leaves our warehouse without sign-off from staff who track deviations, production notes, and ongoing customer feedback. We’ve seen supply disruptions hit the industry—routine as they feel in recent years—but we keep a strategic buffer and nurture relationships with raw material suppliers to weather most upsets. Open, honest forecasting with clients lets us adjust, prioritize, and scale production slots to fit both long-range partnerships and urgent requests.

    Customer Service: Real Answers, Not Automated Replies

    One critical aspect sets direct manufacturers apart: our technical teams answer queries with hands-on knowledge. No call centers or script-reading responses—just process chemists, analytical specialists, and plant engineers who’ve been there, handled the compound, resolved the issues, and updated procedures based on experience. Troubleshooting sometimes takes as much follow-up as original manufacturing; assay drift, shipping delays, or new project specs often need actual people, not just tracking numbers. This responsive, down-to-earth approach keeps most of our long-term partnerships running smoothly, and often leads to new collaborations as word spreads between R&D groups.

    Conclusion: Real Value Built on Expertise and Integrity

    To sum up, Ethyl 4-Bromophenylacetate is not just another chemical intermediate crowding the market. Its value comes from hands-on expertise, production consistency, careful attention to detail, and deep commitment to both quality and transparency. Year after year, its adaptability in synthesis, reliability at scale, and clear communication set genuine manufacturers apart from resellers or drop-shippers. We’ve held to these standards not because regulations demand it, but because our experience says it’s the only way to build real, lasting value for all who depend on our product.