|
HS Code |
609101 |
| Name | 2'-Bromoacetophenone |
| Cas Number | 2142-69-4 |
| Molecular Formula | C8H7BrO |
| Molecular Weight | 199.05 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 51-53°C |
| Boiling Point | 275-277°C |
| Density | 1.52 g/cm3 |
| Refractive Index | 1.595 |
| Solubility In Water | Slightly soluble |
| Smiles | CC(=O)C1=CC=CC=C1Br |
| Inchi | InChI=1S/C8H7BrO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3 |
As an accredited 2'-Bromoacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "2'-Bromoacetophenone," displaying hazard warnings and chemical specifications. |
| Shipping | 2'-Bromoacetophenone is shipped in tightly sealed, chemical-resistant containers to prevent leaks and exposure. It is transported according to regulations for hazardous materials, typically under controlled temperature and away from incompatible substances. Proper labeling, documentation, and handling precautions are strictly enforced to ensure safe and compliant delivery. |
| Storage | 2'-Bromoacetophenone should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Store at room temperature, away from sources of ignition or heat. Ensure proper labeling and follow all relevant safety guidelines for handling hazardous chemicals. |
Applications of 2'-Bromoacetophenone in Industrial Manufacturing2'-Bromoacetophenone serves as a key intermediate in several advanced manufacturing sectors. Our direct production quality ensures consistency for industrial integrators and formulators who require purity and batch-to-batch traceability. The following detailed sections introduce four main downstream fields where this raw material provides critical building-block functionality. 1. Pharmaceutical Synthesis – API Intermediate ManufacturingThe pharmaceutical industry uses 2'-Bromoacetophenone in the synthesis of advanced intermediates for active pharmaceutical ingredients, particularly within CNS and anti-inflammatory drug classes. Due to its reactivity on the aromatic ring, the compound undergoes nucleophilic substitution to form complex heterocyclic cores required by several small-molecule drug substances. Formulators and process chemists leverage its selectivity during Grignard, Suzuki, or amination reactions at multi-kilogram scale for GMP manufacturing. Reaction conditions, such as solvent choice and temperature, directly affect yield and impurity profile, making raw material consistency and assay crucial for regulatory submissions and batch release. Industry compliance standards
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2. Agrochemical Active Ingredient Building BlockManufacturers in the agrochemical sector utilize this raw material as an aryl halide intermediate for herbicide, fungicide, and insecticide molecule construction. Its bromoacetyl function allows precise incorporation into complex aromatic and heterocyclic scaffolds essential for modern crop protection agents. The compound enters pesticide synthesis workflows via catalyzed cross-coupling, addition, or nucleophilic substitution reactions. Batch traceability and purity grade impact both regulatory dossier approval and SCAR assessment for environmental impact. Industry compliance standards
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3. Fine Chemical Synthesis – Organic Photoinitiator PrecursorThe UV-curable coatings and inks industry incorporates this chemical as a selective precursor for the synthesis of photoinitiators used in advanced polymerization processes. Manufacturers exploit its bromoacetyl moiety for enolate and aryl coupling to create benzoin-type and acetophenone-based photoinitiators, which offer controlled absorption maxima for tailored curing profiles. Critical control parameters include the phase-transfer reaction environment and water content, which directly influence product stability and downstream performance. Industry compliance standards
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4. Specialty Polymer Production – Monomer FunctionalizationSpecialty polymer producers employ 2'-Bromoacetophenone as a functional group donor to introduce reactivity into monomer frameworks. It enables the synthesis of customized vinyl, acrylate, or styrenic monomers with precise substitution patterns. This enables downstream creation of engineering plastics and high-performance polymers where substitution selectivity impacts final mechanical and chemical resistance properties. Raw material purity, bromide content, and moisture level critically determine the polymerization outcome, requiring validated supplier batch records for QC release. Industry compliance standards
Typical usage ratio
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Our team first synthesized 2'-Bromoacetophenone decades ago and some colleagues still remember those first small-scale batches that set our production line apart. This molecule has since woven its way into a steady rhythm in our reactors, its sharp acetophenone note and brominated backbone familiar to everyone who has ever worked here. When industries require a dependable intermediate, 2'-Bromoacetophenone is often engaged for its performance in specialty syntheses, especially across pharmaceutical and agrochemical projects. Its availability year-round matters to our partners, but beyond timing, what actually draws scientists and buyers is the repeatability they see batch after batch.
Our model of 2'-Bromoacetophenone follows the IUPAC designation and traditional molecular structure: a bromine atom at the ortho position relative to the acetyl group on the benzene ring, with formula C8H7BrO. Chemically, the positioning of that bromine atom is more than academic. It marks a true difference in reactivity patterns during downstream functionalization. Many routes depend on that “2’” – other brominated isomers, like p-bromo or m-bromo, show less utility for acylation or nucleophilic substitution steps. Working with it up close, the crystalline powder displays a slightly off-white to pale yellow color. Experienced chemists can gauge purity visually, but batch analytics are always conducted: routine HPLC and NMR checks guarantee clarity, because our customers rely on consistent >98% purity for reliable conversions.
During packing, product consistency depends on avoiding gradual moisture uptake or self-decomposition. Years back, certain suppliers supplied material that clumped before use, costing involved teams precious hours to redissolve and filter out particulates. Our packaging protocols draw from real-world experience: nitrogen-flushed, sealed containers, desiccated storage, and short dwell times under ambient air minimize any risk of hydrolysis or discoloration. Bulk lots can run up to a metric ton per year, but we treat each drum with the same attention as the smallest lab sample, because quality losses slide downstream into every single step a buyer takes.
A number of industries find 2'-Bromoacetophenone’s chemical behavior ideal for introducing both a reactive bromo-site and a stable phenyl group in one step. Its typical role is as a raw material in the synthesis of fine chemicals—especially for the preparation of building blocks needed in pharmaceutical research. Chemists can use it for alkylation, condensation, and halogen-metal exchange. Medicinal chemistry units appreciate that ortho-substitution offers a handy starting point for the production of heterocyclic motifs, including indoles, benzofurans, and other scaffolds valuable in drug discovery programs. There’s a reason it’s seen in patent filings across antihypertensive, antimicrobial, or anticancer development pipelines.
Historically, our 2'-Bromoacetophenone has also supported agrochemical clients. They seek it for the same reason drug firms do: selective reactivity and efficiency. The ortho position allows for rapid cyclization, enabling cost-effective synthesis of crop protection molecules that reach regulatory registration. Chemical researchers in academic settings keep finding new transformations as well. Some recent routes to insecticides arose after trials using our material, providing shortened process timelines that reduced overall waste and improved selectivity. By controlling side reactions at scale, we’ve helped research groups move from a handful of milligrams to full kilogram demonstrations, ensuring their intellectual property reaches market-ready status safely.
Manufacturing this compound over the years, we have seen how minor process changes affect not just the chemical yield, but also the broader impact on downstream chemistry. One year, impurities crept in from a feedstock supplier change. The shift in impurity profile caused sulfonation steps in two customers’ plants to produce a stubborn side product, halting their scale-up campaign. Post-mortem analysis tracked the culprit back to the source. Ever since, we have maintained strict traceability for every metric ton—the sort of documentation auditors appreciate. We learned quality assurance requires not just instruments but human vigilance and solid lines of communication between floor workers, QC personnel, and end-users. This vigilance makes a difference for users scaling bench chemistry into full commercial reality.
People outside chemical manufacturing sometimes overlook the logistical side. One recent surge in global demand briefly created a raw material squeeze, prompting calls from regular partners who couldn’t afford production downtimes. Thanks to our close relationship with upstream bromine suppliers, we balanced orders and provided priority shipping for mission-critical applications. This wasn’t luck—it followed from years spent building trust and always favoring transparent communication over short-term profit. Clients recognized that commitment and, once the supply chain returned to normal, continued sourcing here out of appreciation for that extra effort.
As a physical solid, 2'-Bromoacetophenone can be handled with routine care; operators avoid exposure, because its lachrymatory tendencies lead to eye and respiratory irritation. Our staff wear full PPE when sampling or repacking, and downstream users should do the same. Acetophenones as a class are reactive, so spills need prompt action and good ventilation during weighing. One engineer described how an early shift spilled a bag’s worth onto an uncovered bench, forcing them to halt workflow and flush lines to remove traces. It reminded us that the cost of a lost hour far outweighs the modest savings from shortcuts—safety investments always pay off in the long run.
Worker safety and environmental control remain front-line concerns for us. Our emissions protocols aim well below local regulations; we contain dust and vapors through both process design and automated monitoring. We treat all liquid waste and off-spec product through approved chemical destruction—our compliance record speaks for itself after years without a single reportable incident. We also trace every outbound package, providing full shipment documentation with delivered lots. This keeps regulatory compliance in order and helps clients address their own local obligations with ease, without facing gaps caused by documentation lapses or inconsistent supply.
Several isomeric forms exist in the brominated acetophenone family, but the ortho version’s chemistry stands apart in real-world labs. For example, 2'-Bromoacetophenone supports regioselective coupling not possible with p-bromo or m-bromo alternatives. We have seen some buyers try to substitute p-bromoacetophenone due to inventory mismatches, only to find key reaction steps either slow or fail outright. Such missteps cost both material and time—both in short supply across research and commercial settings. The difference traces directly to substitution patterns on the ring, making selection of the right isomer more than academic.
Among brominated acetophenones, ours stands on proven reproducibility and strict impurity controls. Competitors sometimes introduce traces of other halogenated byproducts by using lower-purity starting bromine or non-optimized synthesis steps. Our in-process monitoring and careful workup reduce these contaminants below chromatographic detection limits, especially for demanding pharmaceutical and agrochemical applications. Customer feedback sometimes flags new impurities not expected in traditional literature; if necessary, we adapt our purification regime and inform clients with updated spec sheets and COAs. That kind of responsive support builds lasting partnerships that outlast the ups and downs of procurement trends.
Chemists searching for 2'-Bromoacetophenone often face pressure between exploring novel reactions in the lab and guaranteeing scalable processes for production. We have produced quantities suitable for milligrams-to-tons transitions, and our production line adapts based on project profiles. Academic groups appreciate the ability to order a single bottle; global pharmaceutical firms contract metric tons to feed continuous flow reactors. Each order passes through the same in-house QC—every batch gets its chromatogram and spectral check, and every order ship-out is tracked by our logistics team who understand how late delivery can cost days or even weeks.
Some suppliers claim high throughput, but struggle without feedback from customers pushing their capabilities to real limits. Several years ago, an agrochemical partner needed a special variant for asymmetric hydrogenation research. By sharing analytical results and on-site inspection, we adapted our process, delivering the desired chirality level and resolving their synthesis stalling point. These customizations don’t come from bulk commodity processes; direct communication, open data sharing, and team-to-team dialogue turn hurdles into growth opportunities for both sides. In this sense, 2'-Bromoacetophenone isn’t just another chemical—it’s a point where real innovation happens across the sector.
Drug discovery and new pesticide development depend on reliable access to key intermediates like 2'-Bromoacetophenone. Its adaptability endures rigorous use: one season, it serves for sulfonamide formation; another, it anchors a fresh synthetic route for kinase inhibitors. That range defines its value beyond just technical specifications. Feedback from R&D labs sharpens how we propose solutions—for example, by producing batches with tighter impurity profiles or with pre-weighed aliquots to support automated high-throughput screening. Sometimes, our production team even collaborates with select clients through non-disclosure to experiment with co-processing options or new synthetic transformations.
Supporting research means more than providing a commodity. It means understanding intellectual property constraints, speed-to-market needs, and the scramble to hit milestones before grant funding runs thin. By sharing application notes and troubleshooting observations, we help academic groups and corporate teams maximize return on every gram delivered. If unexpected reactivity emerges during a scale-up, our chemists confer directly rather than route issues through a customer-service filter. The industry demands both speed and reliability; those who can offer both end up as trusted partners throughout product development cycles.
Recent disruptions—ranging from logistics slowdowns to export controls—proved just how connected the fate of chemical research and manufacture is to stable supply. Our track record in navigating these shocks owes credit to the relationships built across decades, both upstream with raw material providers and downstream with formulators and synthetic chemists. There’s no quick shortcut here; only consistent transparency and a long view deliver the flexibility researchers need to keep moving no matter what shakes up the market. During shortages, we prioritize legacy partners who, in turn, offer valuable long-term forecasts and process insights, creating a virtuous feedback loop.
Some manufacturers treat every sale as an isolated event, but experience has shown us that the true value of chemical manufacturing is measured not per kilogram but per project milestone achieved across many years. We treat each inquiry as the start of a long-term relationship; it pays dividends for both sides when priorities realign or new regulatory requirements emerge. Open channels ensure rapid adaptation—feedback travels from the bench in a university lab to corporate process teams and straight back to our own R&D chemists, closing the loop in both quality and innovation.
Complying with both international and local regulations represents a core value across our operations. The status of 2'-Bromoacetophenone has changed in some jurisdictions due to its potential as a precursor for CS agents or restricted pharmaceuticals. We proactively monitor regulatory developments and enforce rigorous internal controls, screening every order not only for proper permitting but for risk indicators flagged across industry databases. Our compliance team receives annual training; we routinely update due diligence forms and provide up-to-date documentation to all clients as part of our shipping documentation.
To ensure products serve only legitimate research or manufacturing objectives, every shipment is backed by traceable records and partner screening, reducing the risk of diversion to unapproved uses. We participate in relevant chemical manufacturer networks and working groups, sharing process improvements and lessons learned to raise the bar for responsible handling of controlled substances. Compliance isn’t paperwork for us—it’s an active, everyday practice that ensures researchers, innovators, and operators work within rules protecting both worker safety and community security.
Every gram shipped becomes part of a worldwide experiment. Whether a laboratory teams uses our material to discover a new synthetic step or a factory technician finds a bottleneck during large-scale conversion, feedback always works its way back to us. This ongoing exchange, built through direct reporting and long-form field discussions, shapes our ongoing process improvements. If an odor profile indicates nuanced impurities during pilot plant runs, one phone call triggers an investigation by our analytical team. These “soft signs” matter as much as formal data—they translate into refinements at the margins, where real-world outcomes are shaped by more than numbers.
Beyond technical innovation, this feedback builds trust, fostering a network of scientists and engineers who rely on a consistent, honest supplier rather than just a source for bulk chemicals. Over time, these networks grow, enabling both sides to experiment boldly. For us, being able to say “we know this compound from bench to tonne” means we accept responsibility not just for manufacture, but for enabling progress across the field as a whole.
2'-Bromoacetophenone keeps proving its worth. This isn’t down to abstract technical advantages, but because the molecule keeps earning its stripes in the hands of real chemists, scale-up engineers, and process designers around the world. It brings both predictable reactivity and ready adaptability for both established and next-generation synthesis. Anyone working in demanding research or production environments knows how much a single inconsistency can cost in time, resources, or reputation. Decades producing and delivering this compound have shown us the value of diligence, direct communication, and the patience to solve hard problems with partners searching for real-world results.
We remain committed to improving not just our processes but our ability to anticipate new uses, tighter regulatory requirements, and the creative inventions of our customers. That is how high-quality manufacture of 2'-Bromoacetophenone moves forward: through collective knowledge, trust built on performance, and absolute dedication to supporting critical work in research and development across every industry touched by organic synthesis.