|
HS Code |
709499 |
| Chemical Name | Ethyl α-Bromophenylacetate |
| Molecular Formula | C10H11BrO2 |
| Molecular Weight | 243.10 g/mol |
| Cas Number | 621-98-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 134-136°C at 15 mmHg |
| Density | 1.403 g/mL at 25°C |
| Refractive Index | n20/D 1.543 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Melting Point | - |
| Smiles | CCOC(=O)C(Br)C1=CC=CC=C1 |
| Storage Conditions | Keep tightly closed in a cool, dry place |
As an accredited Ethyl Α-Bromophenylacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g amber glass bottle with secure screw cap, chemical label: "Ethyl α-Bromophenylacetate," hazard symbols, batch number, and storage instructions. |
| Shipping | Ethyl α-Bromophenylacetate is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. It should be handled as hazardous material, following all relevant regulations for transport, labeling, and storage. Shipping is typically conducted by certified carriers, with accompanying safety data sheets and appropriate hazard disclosures. |
| Storage | **Ethyl α-Bromophenylacetate** should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool (2–8°C), dry, and well-ventilated area, separate from acids, bases, and oxidizing agents. Ensure secondary containment to prevent leaks, and label the container clearly. Use proper protective equipment when handling and always follow local chemical storage regulations. |
Applications of Ethyl α-Bromophenylacetate in Industrial ManufacturingAs a direct manufacturer committed to supply chain integrity and process consistency, we supply Ethyl α-Bromophenylacetate (EABPA) for a clearly defined set of precision-driven heavy chemical and pharmaceutical industry sectors. The following sections provide a technically detailed overview of EABPA integration, including regulatory compliance, recommended dosage, plant process entry points, and the corresponding finished goods for each industry where EABPA serves a critical role. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers utilize EABPA as a halogenated intermediate in the multistep synthesis of non-steroidal anti-inflammatory drugs and central nervous system agents. Its functionalized aromatic ester structure allows chemists to efficiently construct advanced phenylacetic acid derivatives, enabling high-yield transformations for active pharmaceutical ingredient (API) development under controlled GMP facilities. Large-scale users employ precise batch additions for consistent reactivity and compliance with stringent impurity profiles. Industry compliance standards
Typical usage ratio
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2. Agrochemical Active Ingredient PreparationLeading crop protection firms select EABPA for the synthesis of customized phenylacetic acid derivatives essential for several classes of selective herbicides and fungicides. Its α-bromo function delivers a reliable handle for nucleophilic displacement, allowing controlled preparation of advanced intermediates that meet international registration standards. Bulk blending follows validated protocols to achieve target dosage and reaction conversion. Industry compliance standards
Typical usage ratio
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3. Advanced Organobromine Synthesis for Specialty ChemicalsChemical production plants incorporate EABPA in the design of complex organobromine compounds for applications in flame retardancy and fine chemical manufacturing. The selective bromine atom enables tailored synthesis steps where high purity and defined reactivity are mandatory for downstream product consistency, especially for engineered resin and polymer additive segments. Quality control tracks all process parameters, with documented traceability from raw material to finished batch. Industry compliance standards
Typical usage ratio
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4. Research-Grade Building Blocks for Chemical SynthesisCustom synthesis laboratories and advanced R&D units source EABPA as a reliable building block in the rapid assembly of molecular scaffolds, structure-activity relationship libraries, and reference standards. Its defined structure ensures predictable reactivity across a range of palladium- or copper-catalyzed couplings, and documentation supports regulatory filings for investigational new entities and method validation. Each batch is accompanied by comprehensive QC documentation and COA traceability. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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In our experience as producers, Ethyl Α-Bromophenylacetate proves itself more than a string of chemical groups bonded together. With each batch, we see how the true value of this compound arises not only from purity or color but from reliability in reactions and consistency across syntheses. Our process starts with the careful selection of precursors, checking their quality at every delivery. Every operator here remembers the hard-won improvements—reducing batch-to-batch variation is not an afterthought.
Ethyl Α-Bromophenylacetate, as synthesized here, comes with a focus on the full set of functional group integrity and organoleptic properties. Its structure brings a bromine atom onto the alpha carbon next to a phenyl group, attached further to an ethyl ester. This creates a compound that offers versatile reactivity but also some specific quirks. The presence of bromine in the alpha position opens pathways that other haloesters or simple substituted phenylacetates don’t provide. When you use this compound in synthesis, you get a clear entry into further derivatization—especially useful in pharmaceuticals and fine chemical development.
Turning raw phenylacetic acid derivatives into Α-bromo esters isn’t the sort of process that tolerates shortcuts. We found that subtle changes in temperature during the bromination step can mean a shift in byproduct profile. Some operators favor slower, cleaner additions to control for minor side-chain chlorination. Over time, we’ve tested the impact of different solvents and phase-transfer catalysts, building up an internal knowledge base grounded in thousands of liters’ worth of process scale-up.
Some competitors push for higher throughput by ramping up reaction rates with aggressive conditions. We have learned how over-ambitious heating triples the risk of undesired alpha,alpha’-dibrominated species, which impacts the usefulness of the end product. At our facility, acid-washed glassware and rigorous nitrogen sweeps are the rule, not the exception. These details make the difference: odor, color, and the assay results all reflect the care that went into the process long before packaging.
Specifications on our Ethyl Α-Bromophenylacetate speak most in the lab, not just on a datasheet. We understand clients look for a clear pale yellow liquid, with GC purity consistently above 98%. Moisture or hydrolysis during storage can quickly drop its value, so we keep water content well below 0.2% through deep vacuum packing and the use of inert gas blanketing.
For those who seek more than a routine alpha-bromo ester, our batches undergo chiral GC analysis to check selectivity, even when not explicitly required. Over the years, we’ve fielded numerous requests to adjust specification ranges—one batch destined for a crop protection research program, another for peptide coupling experiments. It’s rare that a single spec fits all fields, so our team remains flexible, always reviewing the requests one synthesis at a time.
Having produced multiple haloacetates and phenyl-substituted esters ourselves, we constantly compare Ethyl Α-Bromophenylacetate with its chemical siblings. In work-ups, this ester’s balance of reactivity and boiling point makes it superior to methyl analogues for researchers who want manageable volatility. Larger alkyl esters tend toward excessive viscosity and slower reactivity, complicating their use in multi-step synthesis.
What sets our Ethyl Α-Bromophenylacetate apart, especially under harsh or unforgiving conditions, is its controlled purity and predictable yield in downstream processes. We learned from direct customer feedback—one client noted that switching away from less optimized suppliers immediately reduced their byproduct removal steps by two full rounds of extraction. Another mentioned how our product ran cleaner on NMR, making purification less wasteful.
As producers, we often see Ethyl Α-Bromophenylacetate heading out for vastly different end uses, from pharmaceutical intermediates to building blocks for agrochemical molecules. Medicinal chemists appreciate how the alpha-bromo function handles Suzuki and other cross-couplings more readily than some unactivated bromides. The ester group tolerates a range of conditions, weathering common bases and nucleophiles without premature hydrolysis when handled with standard care.
Some customers in smaller, high-value markets use the compound to build custom peptides and other sensitive structures, where side-reactions would taint the entire project. They need a product without excessive residual acid or trace metal content, since these interfere with catalysts or reduce downstream yields. In scaling up, we stay in close contact, gathering client feedback and folding their lab data back into our own improvement cycle.
Production at scale has shown that even minor differences in synthetic routes can reflect downstream in customer results. Over years, different research groups told us how minor impurities from certain suppliers actually change results in bioassays or lead to regulatory holdups. We’ve responded by refining both the main route and the purification steps, including live GC monitoring and periodic third-party validation.
The difference between a reliable supply of high-grade Ethyl Α-Bromophenylacetate and a source prone to variability often becomes clear under scale-up or real-world manufacturing conditions. Our facility maintains a dedicated reactor line for these sensitive alpha-halo esters, including redundant filtering and drying equipment. The scheduling team tracks demand spikes or major research campaigns in real time, which the lab group uses as an opportunity to reinforce best practices and avoid cross-contamination.
For many, the compound meets a critical need in both new molecule design and manufacturing. Its balance between reactivity and stability streamlines work in both bench and pilot scale. Chemists trust it for arylation, alkylation, or further halogenation steps. We listen carefully when clients run into bottlenecks—such as a recent group working on optically active derivatives, who flagged an issue with hydrolytic stability during extended storage. We revamped our packaging and began offering dedicated low-moisture lots, seeing a quick improvement in customer outcomes.
We’ve sat with teams designing continuous flow operations who need a grade free of non-volatile residues. Their syntheses proved more reliable once we shared our direct GC and Karl Fischer measurements, and set up automatic lot-by-lot analytical reporting. Down the hallway, our QA team keeps detailed records—when research institutions request trace impurity profiles, they’re not left waiting.
Years in production have taught us that safe handling is as much about clean process control as it is about worker training. Every shift here drills on solvent handling and emergency response tailored to reactive alpha-bromo compounds. Proper PPE, strict control on open vessel use, and an airtight material track from drums to reactor all reduce the risk of unwanted exposures. Even decades in, we never treat this as routine.
Regulatory shifts in emerging markets, as well as tighter guidelines in mature industries, can affect the acceptability of specific synthetic reagents like alpha-halo esters. By working closely with compliance teams and staying ahead of changes in permitted trace impurity levels, especially residual bromides and heavy metals, we help ensure our customers avoid wasted batches or last-minute delays due to shifting requirements. Documentation leaves nothing to chance—audits regularly confirm alignment with both local and international purity benchmarks.
It’s common for clients to share their process details once they’ve run preliminary reactions. Some come in looking for bulk drums and realize mid-project that they require a particular enantiomer or lower boiling fraction. Our team has overhauled initial processes at least twice in the past year to match such evolving needs. We see these requests not as disruptions but as part of the living process of specialty chemical manufacturing. Appraising impurity fingerprints or shifting reaction quench times, we roll lessons from every partnership forward into greater consistency and traceability.
On the production floor, operators relay stories of trouble-shooting crystallization bottlenecks before final filtration. Every operator, from reactor technician to mid-level supervisor, knows the importance of documenting anomalies—no shortcut passed on from shift to shift. In this way, when a client’s analyst asks about a faint trace in their LCMS, we pull up production deviations or chromatogram archives in minutes.
Supply chains in chemicals rarely behave predictably. Raw material fluctuations, transport bottlenecks, or sudden spikes in specialty demand create headaches for both producers and customers. We have kept operations flowing by diversifying upstream sources for phenylacetic acid and selectively pre-stocking brominating agents. In times of volatile global logistics, we hold buffer stocks so researchers and manufacturers keep production going.
Sometimes, a university group or startup will only discover a supply gap after publishing their preliminary work using commercial samples. We try to work with both transparency and empathy, giving honest lead times and realistic delivery commitments rather than painting an overly optimistic picture. Our technical and sales teams meet weekly, not just to process orders, but to spot pain points emerging from clients’ insights.
We have always worked to minimize the environmental footprint of our processes. Modern upgrades in solvent recovery, reduction in off-gas emissions, and safer handling of byproduct streams were not simple investments—they represent years of tuning both batch and continuous equipment. By improving recovery and cut-point efficiency, we support cleaner production. We often field questions from partners about lifecycle impacts, and we are forthright on our solvent use, waste treatment, and energy initiatives.
Many of our long-term clients are now under pressure to decarbonize their own supply chains. They request batch data, not just analysis sheets. In response, we supply detailed process emissions summaries and voluntarily pursue audits based on green chemistry principles. By building open-book partnerships around verification and accountability, we all help push the field forward.
We remember the early projects where a skilled medicinal chemist called late to discuss a failed coupling step. Tracing the issue, we found their lab had switched between two lots of α-bromo esters: one made in-house, one sourced from us. Our batch’s high selectivity and narrow impurity range meant their reactions performed as expected, while locally-prepared material, made under different conditions, introduced unpredictable byproducts. From then on, we collaborated directly, exchanging HPLC traces and discussing timing for future reorders so they would never risk interruption.
Today, students and senior chemists alike call our technical team for advice on scale-up, compatibility, and mechanistic questions. Many have shared drafts of publications or patent applications with us under confidentiality, trusting that our experience makes their work more robust. We help them interpret data—such as unexplained peaks in NMR or odd color shifts. A real-world understanding, honed by years of direct chemical production, deepens this trust.
Clients have shown us the real-world value and the avoidable difficulties when a chemical like Ethyl Α-Bromophenylacetate falls short on consistency. A research group once shared their raw LC traces, revealing how small increases in color bodies forced extra chromatography steps. After reviewing our own logs, we changed one filtration protocol, resulting in clearer product and more satisfied clients. Another customer, frustrated by odd odor spikes in competitor’s materials, found ours not only purer but more stable across shipments. Such feedback informs every incremental improvement.
Every order leaving our facility reflects the practicalities learned from years of experience and dozens of production cycles. As other firms adjust to trending “just in time” supply paradigms, we keep local buffer stocks and redundant quality controls. Our deliveries consistently arrive as ordered because we know every day lost on a failed batch or a delayed shipment undercuts trust built over years.
Not every producer has walked the floors at midnight, checking on crystallization controls or opening up storage drums by hand to check for discoloration or condensation. We built our approach on these hands-on moments—learning that chemical production hinges on control, communication, and the humility to adapt under pressure. Our commitment to quality and process is grounded not in policy, but in decisions made every day by people who have run, tested, and handled Ethyl Α-Bromophenylacetate under real-world conditions.
Those who rely on Ethyl Α-Bromophenylacetate for their synthesis or production work want more than a label or generic data sheet. They need assurance drawn from the experience of people who have solved the same challenges themselves. Customers from research to full-scale manufacturing have trusted us because they see the results in every reaction run, every cleaner product line, and every transparent conversation around technical hurdles. Each improvement comes not from abstract strategy, but from tackling the issues that matter: reliable chemistry, honest partnership, and an open-eyed view of the path ahead.