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HS Code |
666024 |
| Name | 4-Bromophenylacetyl Bromide |
| Cas Number | 5053-73-4 |
| Molecular Formula | C8H6Br2O |
| Molecular Weight | 293.94 g/mol |
| Appearance | White to off-white crystalline solid |
| Boiling Point | 313.9 °C at 760 mmHg |
| Melting Point | 60-63 °C |
| Density | 1.842 g/cm³ |
| Solubility In Water | Decomposes |
| Purity | Typically >98% |
| Refractive Index | 1.609 |
| Smiles | Brc1ccc(cc1)CC(Br)=O |
As an accredited 4-Bromophenylacetyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Bromophenylacetyl Bromide is supplied in a 25g amber glass bottle, sealed with a Teflon-lined cap for safe storage and transport. |
| Shipping | **Shipping Description:** 4-Bromophenylacetyl Bromide should be shipped in tightly sealed, chemical-resistant containers, protected from moisture and physical damage. It must be clearly labeled as a hazardous material, and transported according to applicable regulations for corrosive and toxic substances. Ensure handling by trained personnel with appropriate safety documentation and emergency procedures in place. |
| Storage | 4-Bromophenylacetyl bromide should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon. Keep it in a cool, well-ventilated area away from moisture, heat sources, and incompatible substances like strong bases and oxidizers. Store in a designated corrosives cabinet and clearly label the container to prevent accidental misuse or exposure. |
Applications of 4-Bromophenylacetyl Bromide in Industrial ManufacturingAs an experienced chemical manufacturer, we provide 4-Bromophenylacetyl Bromide for key industrial sectors where specificity, purity, and reproducibility are critical. Our technical team supports customers in maximizing production consistency and addressing compliance in highly regulated markets. Below we outline major applications with technical and compliance information for each sector. 1. Pharmaceutical Intermediate for Atypical Antipsychotic SynthesisPharmaceutical manufacturers use 4-Bromophenylacetyl Bromide as a core acylation agent during the synthesis of several advanced intermediates for atypical antipsychotic APIs, including those related to arylacetamide frameworks. In multi-step organic synthesis, this compound is introduced during the targeted coupling stage to provide the bromo-phenylacetyl group essential for downstream transformations. Process controls focus on impurity limits, trace bromide content, and controlled reaction conditions. Production batches require strict batch-to-batch reproducibility and analytical traceability. Industry compliance standards
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2. Agrochemical Intermediate for Selective HerbicidesLeading agrochemical producers employ 4-Bromophenylacetyl Bromide when manufacturing specific classes of pre-emergence herbicide and soil treatment agents. The compound forms a pivotal coupling agent to introduce the electron-rich bromo-arylacetyl fragment, often in the formation of new amide bonds during active ingredient synthesis. Reaction conditions must minimize residual bromide levels in compliance with food chain safety and integrate robust in-process controls for large-scale multi-ton batches. Industry compliance standards
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3. Fine Chemical Intermediate in Liquid Crystal Component SynthesisSpecialty electronic and optical material manufacturers use 4-Bromophenylacetyl Bromide as a precursor when synthesizing advanced intermediates for non-linear optical (NLO) and liquid crystal display (LCD) compounds. The compound participates in Friedel-Crafts and acylation steps to generate tailored bromo-aryl structures, required for unique electronic characteristics and phase transition performance of the final liquid crystal products. Customers carry out tight analytical monitoring of residuals and purity profiles. Industry compliance standards
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4. Active Intermediate for Pharmaceutical Imaging Agents4-Bromophenylacetyl Bromide is harnessed in the chemical synthesis of radiolabelled and MRI-active imaging agents. The compound’s bromo component is often exploited for subsequent radiolabel insertion or further halogen exchange. Manufacturers in this sector operate under specialized low-volume, high-purity constraints. Rigorous quality assurance is implemented throughout the process, especially where patient-contact FDA and EU standards apply. Documentation systems emphasize total traceability from raw material lot to finished diagnostic intermediate. Industry compliance standards
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5. Synthesis Precursor for Specialty Dyes and PigmentsManufacturers in the colorant industry incorporate 4-Bromophenylacetyl Bromide in the design of high-performance bromo-aryl dye intermediates. The bromophenyl group enables the manufacture of colorants with improved stability and chromatic properties for plastics, polymer coatings, and textile inks. Formulation chemists control addition based on color strength and desired tint. Products undergo final purification to remove residual bromide and ensure heavy metal compliance. Industry compliance standards
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Producing specialty building blocks like 4-Bromophenylacetyl Bromide gives unique insights into the raw chemistry at work on an industrial scale. Not many companies tackle halogenated acetyl bromides at scale, due to the technical challenge and environmental expectations. Our team deals with these challenges every production run, so it’s worth sharing what sets this compound apart, and why it remains a trusted intermediate in fine chemical synthesis — particularly in the pharmaceutical and agrochemical sectors, where no corner can be cut.
Our workhorse product, often recognized by CAS number 2114-00-3, stands as a white to pale yellow crystalline mass. Typical purity hovers above 98% by GC analysis, and moisture must be kept very low — less than 0.25% — due to the reactivity of the acyl bromide group. Most competitors either buy from resellers or outsource. Instead, we oversee the entire process, and this gives total control in crystallization, purification, and packing. Real-world purity reflects not just the reported analysis but also the absence of non-volatile side fractions picked up in routine extractions. The product is typically bottled in glass with PTFE lining, with standard batch sizes from one kg up to a few hundred kilograms. We’ve found that every lot needs to be swiftly protected from light and moisture exposure from filtration to packing, or else nasty polymerization and color changes will set in.
What’s often missed in lab descriptions is how hard it is to scale this compound without thermal runaway or byproduct tars. We have designed jacketed vessels, not standard glassware, with staged additions and in-line bromine scavenging. The end result is a product that consistently passes the application hurdle in both lab and process setups — crystallinity, color, and immediate reactivity without excess “free bromine.”
Many manufacturers advertise substituted acetyl bromides, but careful scrutiny is worthwhile. 4-Bromophenylacetyl Bromide offers a blend of halogen reactivity and phenyl stability, so it’s ideal as a coupling partner for stepwise introduction of complexity into heterocyclic systems. Other acyl bromides — say, phenylacetyl bromide or 4-chlorophenylacetyl bromide — differ in both reactivity and toxicity handling. The para-bromo version offers optimal balance: enough resonance for reasonable shelf life, but high reactivity for subsequent nucleophilic attack or Friedel–Crafts reactions. Small changes in the aromatic ring make big differences downstream. The 4-bromo label indicates selective reactivity (minimizing pesky ortho/para isomer confusion) and cleaner transformations to both amides and esters.
Some buyers assume 4-bromo is “just another halide.” Reality looks very different in synthesis. Unlike the more wet, volatile acetyl chlorides, or the more stable phenyl analogs, 4-Bromophenylacetyl Bromide feeds certain key reactions where the bromo group serves as both a leaving group and a handle for further functionalization via palladium cross-coupling or nucleophilic displacement. This reactivity series can’t be fully replicated by other acetyl bromides. Over the years, researchers have leveraged this property in anti-infective, CNS, and herbicide discovery pipelines, so we emphasize this distinction to project chemists. Limiting side-product formation and allowing the desired aryl-bromide to persist into the final API structure often saves weeks of route scouting.
It sounds simple in a catalog to list out a “clear, shelf-stable” intermediate. Production tells another story. If drying steps are rushed, residual acid or water shortens lifetime and compromises yields. During the bromination and acylation stages, uncontrolled temperature spikes lead to tarry byproduct, which no amount of filtering later will fix. On an industrial floor, every percent of efficiency and cleanliness counts. We’ve picked up some scars along the way: learning that fugitive vapor control during transfer, and in-line drying right before bottling, separates high-grade batches from “almost there.” Technicians track the process not by manuals, but by the honest smell, appearance, and thin layer chromatography finger-prints that come with hands-on experience.
Transport also changes the risks. The acyl bromide group is no friend to humidity or temperature swings. During hot months, we rely on cooled trucks and warning indicators. Even a few grams of stray moisture in a drum can spell disaster — pressure buildup and corrosion of linings. It’s not the sort of product that should ride overseas in bare plastic, as we learned years back from a batch that vented in transit and had to be reprocessed. We recommend breaking down large shipments into manageable lot sizes, marked with real-time manufacture dates, never “stock-piled” from a mysterious overseas broker.
There are a dozen stories packed into every kilogram that leaves the plant. Drug discovery teams look for 4-Bromophenylacetyl Bromide as a key aryl building block. Medicinal chemistry campaigns commonly use it to build amide or ester linkages with strong electron-withdrawing behavior, tailoring binding affinity in the final molecule. It isn’t just a stepping stone — the bromo handle enables rapid diversification for SAR (structure–activity relationship) studies, especially where further halogenation, Suzuki, or Sonogashira coupling is on the table.
In the agricultural sector, its value shines in lead optimization for herbicides and fungicides. The bromo group survives through multiple transformation steps, making it possible to introduce further substitutions or effect selective reduction. Chemists are often forced to build reactivity into every step, and this compound often serves as the fork in the road for both simple and advanced scaffolds. It doesn’t have the volatility or spontaneous polymerization issues seen in pure acetyl bromides lacking the aromatic ring.
There’s also a role in dyes and specialty material science, where the goal shifts: here, handling and purity closely affect yield and color stability. Not all intermediates translate from bench to plant scale smoothly. 4-Bromophenylacetyl Bromide, prepared with careful, contamination-free workflow, keeps impurity carryover to a minimum, which is vital when end products carry regulatory scrutiny to the part-per-million level.
One lesson has become clear: relying on textbook procedures only goes so far. Scaling halogenated intermediates means relentless attention at every step. Choosing solvent for bromination, deciding on purification method, managing exotherm: these all play into final purity and batch-to-batch reliability. We select raw materials from trusted local producers — no hidden fillers, no cutting corners. Each solvent run is double-certified for purity and checked for reliability, since even low-level contaminants can complicate acylation yields or trigger undesirable color formation.
It has been a long journey to minimize operator exposure and eliminate repetitive handling. Dedicated fume extraction, local scrubbers, and strict PPE rules protect both team and product integrity. Our operators undergo annual retraining to keep skills current, because small errors in bromine handling cause reliability problems and costly batch downgrades. IT and process automation have given us better tracking and real-time control, but we believe the operator’s eye is still irreplaceable for issues automation can’t predict — like subtle changes in crystal texture or onset of phase separation.
We hear buyers say, “Is there much difference between 4-Bromophenylacetyl Bromide and other aromatic acyl bromides?” There is, and we’ve seen it play out over years of supply. Compared to 4-chloro derivatives, the bromo is more forgiving in cross-coupling and more stable against hydrolysis, which helps in longer, multi-step synthesis. Compared to analogous fluorinated versions, it remains more reactive under standard conditions, without requiring exotic activation. Against unsubstituted phenylacetyl bromide, it allows further functionalization through the aromatic bromo, opening doors for more robust synthetic exploration.
Switching from batch-to-batch on our floor, it’s clear each handle creates its own quirks in the reactor: 4-bromo products usually have a higher melting point and more robust shelf stability. Also, downstream waste and byproduct management is easier since bromo-containing waste is better tracked and treated compared to chlorinated or mixed halide streams. This becomes very relevant for clients with ISO14001 or similar environmental targets. Also, purification by recrystallization tends to go more smoothly: the product comes out as crisp white plates rather than yellow oils, which makes quality assurance more straightforward.
Consistent supply forms the backbone of any serious research project. We treat this chemical as a collaborative tool, not just a catalog entry. Our technical team supports end-users with advice on solvent selection, drying, and reagent compatibility. Years ago, in a complicated step-up synthesis, a project team ran into repeated batch contamination using lower-cost acetyl bromides. Working together, we modified filtration and packing, tracked down an invisible source of contamination, and got their yields up. Having the manufacturer on hand for such problem solving means more than any specification sheet or standard analysis can provide; it’s about track record and accountability.
We also encourage feedback once batches hit the research bench or pilot suite. Surprises sometimes arise, even in well-studied chemistry; our experience confirms that small changes in dryness, impurity loading, or exposure before use make big differences. End-users are encouraged to store all brominated acetyl products in tightly closed amber bottles, under inert gas, and use them within six months of receipt for critical work. Those who pay attention to these handling subtleties see more success and often push the compound into successful preclinical or even scaled manufacturing campaigns.
Many overlook disposal and emission issues with heavily brominated intermediates. We’ve made real investments in scrubber systems and closed transfer lines to contain and neutralize vapors. Years of regulatory compliance, from local environmental permits to national dangerous goods codes, have taught us that it’s rarely worth the risk to cut costs at the expense of safety and documentation. Drift from “good enough” standards doesn’t survive a real audit, or worse, an accident. We have moved towards greener byproduct management practices — reusing bromine-containing wash water for neutralization, and documenting chain-of-custody for all waste.
A lot has changed in recent years. End-users now expect full traceability, allergen and contaminant statements, and direct access to the quality control lab for unusual questions or advanced spectra. Only producers who run their own development and scale-up can support these requests meaningfully. Teams in QA and process development interact directly with plant operators to troubleshoot any outliers. Aggressive third-party brokers without any production infrastructure can’t provide the real-world context of a plant-floor team, and their products often fall short on non-standard tests or customized batch requests.
Price volatility and sporadic lead times create real headaches for buyers of 4-Bromophenylacetyl Bromide. We’ve established a supplier network and long-term bromine sourcing contracts to insulate against supply shocks. Buffer stocks aren’t enough in this industry — transparency with delivery schedules and a “no-surprise” policy are more valuable than cut-rate deals. Our on-site analytical capabilities, including NMR and GC-MS validation, keep rejections low at the receiving dock, which matters most on pilot and scale-up campaigns where every batch affects end timelines.
Process optimization never stops. We remain committed to lowering waste, reducing shipment delays, and training the next generation of plant operators and chemists. Industry feedback has led us to periodic review of our techniques and raw material qualifications; technical staff keep a logbook of issues encountered and lessons learned, especially when handling sensitive brominated batches. We stand ready to collaborate on tailored grade requests — pharmaceutical, agricultural, or custom research — as guided by user demand and specification.
The work that goes into 4-Bromophenylacetyl Bromide production offers critical lessons on marrying chemistry with real-world logistics, safety, and honest partnership. As the landscape rapidly evolves, end-users deserve a supply chain that recognizes the actual stakes of failed batches, compliance audits, and regulatory oversight — not just a faceless list of specifications. Creating a safe, consistent, and transparent pipeline for advanced chemicals unlocks discovery, but also demands a commitment to standards that go beyond simple product claims. We continue striving to strengthen that commitment each day, keeping quality at the center of everything — so the researchers and teams relying on our materials can keep pushing boundaries with full confidence in every batch.