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2'-Bromoacetophenone

    • Product Name 2'-Bromoacetophenone
    • Einecs 205-521-6
    • 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

    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 & Storage
    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.
    Application of 2'-Bromoacetophenone

    Applications of 2'-Bromoacetophenone in Industrial Manufacturing

    2'-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 Manufacturing

    The 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

    • ICH Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 U.S. FDA cGMP for Finished Pharmaceuticals
    • EU EudraLex Volume 4 GMP Guidelines for Intermediates
    • Relevant monograph controls for residual solvents and heavy metals (USP, EP)

    Typical usage ratio

    • 1.0 to 1.3 mole equivalents per target API synthesis step, adjusted for process yield and reactant stoichiometry

    Downstream process integration

    • Reaction sequence entry after initial aromatic substitutions and prior to coupling or cyclization
    • Purification by crystallization or chromatography before further transformation
    • QC release based on HPLC and NMR identification, residual solvent compliance, and specification check

    Final product types

    • Certified pharmaceutical API intermediates (e.g., substituted benzodiazepines, triazoles)
    • Finished drug substances following downstream synthesis routes

    2. Agrochemical Active Ingredient Building Block

    Manufacturers 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

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for test item preparation
    • REACH Regulation (EC) No 1907/2006 – Substance Registration and Safety Data
    • ISO 9001:2015 for manufacturer quality management systems

    Typical usage ratio

    • 0.95 to 1.10 mole equivalents per synthetic crop protection molecule, scaled based on target yield and impurity profile

    Downstream process integration

    • Introduced post-first benzene ring functionalization, before heterocycle construction or sidechain addition
    • Processed by chlorination, methylation, or condensation according to product-specific synthesis protocol

    Final product types

    • Pesticide actives, such as triazole and pyrazole-based herbicides and fungicides
    • Technical grade active ingredient concentrates for formulation companies

    3. Fine Chemical Synthesis – Organic Photoinitiator Precursor

    The 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

    • ISO 22007-2:2015 Plastics – Determination of Thermal Conductivity (relevant for end-use coatings)
    • EN 71-3 Safety of Toys – Migration of certain elements (for photoinitiators in child-use products)
    • GHS/CLP Regulation (EC) No 1272/2008 labeling requirements for raw material handling

    Typical usage ratio

    • 0.95 to 1.05 mole equivalents for photoinitiator backbone creation, fine-tuned for target molecular structure and absorption properties

    Downstream process integration

    • Added as the bromoacetyl donor in step one of photoinitiator assembly
    • Processed by nucleophilic substitution or Friedel–Crafts acylation depending on product family
    • Purified to high assay for direct downstream utility

    Final product types

    • Photoinitiator actives (e.g., benzoin derivatives, acylphosphine oxides) for inks, adhesives, and ophthalmic device manufacturing
    • UV-curable resin systems used in electronics and fiber optics

    4. Specialty Polymer Production – Monomer Functionalization

    Specialty 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

    • ISO 9001:2015 Quality Management for specialty chemical production
    • RoHS Directive 2011/65/EU for restricted hazardous substances in electronics-use plastics
    • ASTM D5630-13 Standard Test Method for Ash Content in Thermoplastics

    Typical usage ratio

    • 0.8 to 1.2 mole equivalents per main-stage monomer functionalization, aligned with desired substitution density and product application

    Downstream process integration

    • Added during monomer modification phase before main-stage polymerization
    • Integrated in pre-polymer reactors for sidechain installation or crosslink site introduction
    • Monitored for unreacted residuals to limit downstream polymer defects

    Final product types

    • Advanced engineering polymers, such as functionalized polystyrene and polyacrylates
    • Specialty copolymers for electronic, medical device, and automotive applications
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    Certification & Compliance
    More Introduction

    2'-Bromoacetophenone: An Experienced Producer’s Perspective

    Honest Introduction from the Laboratory Floor

    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.

    What Our 2'-Bromoacetophenone Offers

    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.

    Reactant Role and Real Uses

    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.

    Lessons Learned Along the Way

    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.

    Performance and Handling: What Actually Matters

    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.

    Comparing 2'-Bromoacetophenone: Specificity Matters

    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.

    Flexibility for Scale and Application

    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.

    Supporting Research and Innovation

    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.

    Supply Chain Resilience and Collaboration

    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.

    Upholding Ethical and Regulatory Standards

    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.

    Knowledge Feedback Loops: Improving Through Use

    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.

    Conclusion: Why 2'-Bromoacetophenone Still Matters

    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.