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2-Bromo-3'-Chloropropiophenone

    • Product Name 2-Bromo-3'-Chloropropiophenone
    • Einecs 249-039-6
    • 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
    VTB
    Specifications

    HS Code

    845968

    Product Name 2-Bromo-3'-Chloropropiophenone
    Cas Number 34911-99-6
    Molecular Formula C9H8BrClO
    Molecular Weight 247.52 g/mol
    Appearance White to off-white solid
    Melting Point 55-59°C
    Boiling Point No data available
    Purity Typically ≥97%
    Density No data available
    Solubility Soluble in organic solvents like DMSO and ethanol
    Storage Temperature Store at 2-8°C
    Synonyms 1-(2-Bromophenyl)-3-chloro-1-propanone

    As an accredited 2-Bromo-3'-Chloropropiophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Bromo-3'-Chloropropiophenone is supplied in a sealed amber glass bottle, 25g quantity, with a tamper-evident cap and hazard label.
    Shipping 2-Bromo-3'-Chloropropiophenone is shipped in tightly sealed containers, compliant with hazardous chemical regulations. Proper labelling, cushioning, and leak-proof packaging are used to prevent spills. It is transported via approved carriers, accompanied by relevant safety data sheets and documentation, ensuring safe handling and regulatory compliance during transit.
    Storage 2-Bromo-3'-Chloropropiophenone should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep the container in a cool, dry, and well-ventilated area, ideally in a dedicated flammable chemicals cabinet. Clearly label the container, and restrict access to trained personnel only. Handle under a chemical fume hood when in use.
    Application of 2-Bromo-3'-Chloropropiophenone

    Applications of 2-Bromo-3'-Chloropropiophenone in Industrial Manufacturing

    2-Bromo-3'-Chloropropiophenone serves as a vital intermediate in specialized chemical synthesis pathways supporting the fine chemical, pharmaceutical, and agrochemical sectors. Our customer base regularly employs this material in regulated applications demanding traceable manufacturing, accurate formulation, and strict compliance with global quality standards. Below, we present verified downstream scenarios demonstrating authentic industrial consumption and production modes, grounded in specific industry practices.

    1. Pharmaceutical Intermediate for Anticonvulsant Synthesis

    Pharmaceutical manufacturers rely on 2-Bromo-3'-Chloropropiophenone during multi-step synthesis of key anticonvulsant drug classes, including derivatives used in advanced active pharmaceutical ingredient (API) production. The compound acts as a selective acylation and halogenation building block, facilitating controlled ring closure and heterocycle substitutions while meeting batch traceability requirements integral to GMP-compliant processing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) — 21 CFR Parts 210/211 (USFDA)
    • EU Guidelines for Good Manufacturing Practices for Medicinal Products (EudraLex Volume 4)
    • International Council for Harmonisation Q7 for APIs (ICH Q7)
    • USP/NF and EP monograph requirements for relevant APIs

    Typical usage ratio

    • 0.8%–5.2% by weight relative to key starting material, with batch-specific optimization based on target API yield, process scale, and impurity profile controls.

    Downstream process integration

    • Introduced in stepwise N-acylation and halogenation reactions; enters after initial condensation but before final cyclization or reduction phase; in closed QC loops to monitor residual bromine and chloride post-reaction.

    Final product types

    • Anticonvulsant API intermediates
    • Multi-ring pharmaceutical building blocks for neurological indications
    • Bulk API lots for downstream formulation of solid-dose pharmaceuticals

    2. Precursor for Specialty Agrochemical Synthesis

    Downstream manufacturers in the crop protection sector utilize this compound as a controllable halogen donor in syntheses of acylated thioether and oxime derivatives. These intermediates form the reactive centers in next-generation fungicides and selective herbicidal formulations, supporting compliant, traceable supply chains mandated by agrochemical regulation worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (JMPS)
    • ISO 9001:2015 (Quality Management Systems in Agrochemicals)
    • REACH (EC) No 1907/2006 — Registration, Evaluation, Authorisation and Restriction of Chemicals
    • OECD Good Laboratory Practice (GLP) guidelines

    Typical usage ratio

    • 1.2%–3.6% by reaction batch, ratio varies with desired halogenation degree and overall batch scale; adjustment depends on precursor substrate loading and target functional group yields.

    Downstream process integration

    • Charged at controlled addition rates into continuous stirred tank reactors (CSTRs) during synthesis of halogenated oxime intermediates; in situ quenching and phase separation steps ensure compliance with plant emissions permits.

    Final product types

    • Pre-formulated technical-grade herbicide intermediates
    • Active ingredient concentrates for broadleaf crop applications
    • Base materials for granule and suspension agrochemical formulations

    3. Synthesis Intermediate for Dye and Pigment Manufacture

    Specialty chemical producers employ 2-Bromo-3'-Chloropropiophenone as a selective halogenation and acylation intermediate in the production of complex aromatic dye precursors. The material’s high-purity profile and controlled halide content suit regulatory expectations for commercial dyestuff synthesis, enabling precise color consistency and regulatory traceability in final textile and leather applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemical safety)
    • REACH Annex XVII restricted substance lists
    • ZDHC (Zero Discharge of Hazardous Chemicals) standards for dye manufacturing
    • ISO 14001:2015 (Environmental Management System)

    Typical usage ratio

    • 0.7%–2.4% by reaction mass, depending on chromophore scaffold; adjustment based on dye shade depth, substitution pattern complexity, and downstream purification efficiencies.

    Downstream process integration

    • Meticulously dosed to aromatic backbone precursor during mid-stage coupling reactions; subsequent acid/base extractions and crystallizations cater to standardized pigment grade requirements and compliance audits.

    Final product types

    • Sulfonated and halogenated dye intermediates
    • Color-stable pigment dispersions for textile printing
    • Specialty dyes for high-fastness leather finishing

    4. Intermediate in Advanced Photochemical Material Synthesis

    Producers of photoinitiators and photoresist compounds use this molecule as a targeted halogen source to build specialty aromatic backbones for use in regulated semiconductor and advanced imaging applications. Its controlled reactivity enables efficient functional group installation with minimal byproduct formation, critical to ensuring high yields of materials for photolithographic processes in microelectronics fabrication.

    Industry compliance standards

    • SEMI C3 — Specifications for High-Purity Chemicals (Semiconductor Equipment and Materials International)
    • ISO 9001:2015 for electronic chemical manufacturing
    • RoHS Directive 2011/65/EU for hazardous substances restriction
    • IEC 62474 — Material Declaration for Products of and for the Electrotechnical Industry

    Typical usage ratio

    • 0.4%–1.5% by feedstock weight, ratio adjusted to photoinitiator scaffold and desired spectral absorption properties; dial-in based on lithographic process needs and required purity grade.

    Downstream process integration

    • Introduced during aromatic substitution cycles in photoactive resin precursor production; strictly controlled addition sequence to limit side reaction and guarantee high photoinitiator activity in final blend.

    Final product types

    • Photoresist intermediates for semiconductor wafer processing
    • High-solid photoinitiator compounds for UV-cured coatings
    • Aromatic resin blends for micro-patterning technologies
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-3'-Chloropropiophenone: From the Manufacturer’s Perspective

    Proven Chemistry Backed by Real Industry Experience

    In the chemical business, you build a real relationship with your products over years of production and problem-solving. 2-Bromo-3'-Chloropropiophenone stands out in our broad lineup as a cornerstone compound for many downstream transformations in both lab and industry settings. We have handled this chemical’s synthesis at scale, adjusted purification processes to fit client expectations, and listened carefully to what chemists require on the ground.

    Getting to Know the Model and Characteristics

    2-Bromo-3'-Chloropropiophenone—sometimes simply spoken about in shorthand on the shop floor—has a clear identity thanks to its bromo and chloro functional groups attached to the aromatic ring and propiophenone backbone. This isn’t a commodity product bagged by the ton and tossed into storage; it’s made in controlled runs that respect the sensitivity of both halogen groups. We control moisture content, particle size, and purity not by following generic guidelines, but through regular feedback from customers who need reliable performance every time.

    Our standard model emphasizes high-purity content, which matters deeply to researchers and specialty manufacturers. Purity checks run beyond basic HPLC and GC measurements; we scrutinize for trace salts and look at the color and odor since even minor anomalies signal possible byproducts that can throw downstream synthesis off course. Over years of hands-on production, we’ve noticed dry environments and controlled atmosphere storage help prevent hydrolysis and keep the material stable over long periods. This knowledge does not come from textbooks but from watching batches mature and listening to experienced chemists troubleshoot with us.

    Usage Patterns Across Industries

    2-Bromo-3'-Chloropropiophenone occupies a somewhat niche but critical spot in fine chemical and pharmaceutical pipelines. Most of our larger orders stem from either intermediates production for pharmaceuticals or as a step in various organic syntheses—particularly those building on the aromatic ketone structure. Contract manufacturers order this compound for modification reactions like nucleophilic substitution or for coupling into more complex heterocyclic compounds.

    On the lab scale, academic groups use it for its strong reactivity at both halo positions, enabling selective modifications with bases, metals, or nucleophiles. Our regular dialogue with research chemists shapes how we optimize packaging—sometimes small ampoules with minimal headspace for rapid benchwork, sometimes larger drums for semi-bulk syntheses, always with anti-caking and desiccant support. This close collaboration smooths later steps and cuts surprises when material arrives for time-sensitive reactions.

    Why This Product Matters

    A small difference in the halogen arrangement can have huge effects. Most who have spent years at a reactor know the pain of inconsistent batches. The bromo group, more reactive than the chloro, gives access to specific transformations unavailable with mono-chlorinated or mono-brominated analogs. The ortho-position of the chloro atom to the phenyl ring blocks some routes, forcing chemists to get inventive—in both synthesis planning and impurity control. Each time we field questions about side products, we revisit our own batch records, learn from unexpected analytical results, and tweak process steps accordingly.

    Real-world projects have revealed the value of this distinct substitution pattern. For example, catalytic cross-coupling chemistries can take advantage of the differing reactivities of the bromo versus the chloro. In some customer pilot plants, selective activation of the bromo lets researchers introduce new functional groups, then return to the chloro position for a second functionalization without risking overreaction or waste. Our own staff have gone into partnering facilities, tweaked temperature ramps, and shared details on solubility handling, because we know that seeming trivialities—crystal color or melting onset—tell skilled operators a whole story about batch performance.

    What Sets Our Material Apart

    Many in this industry have learned the hard way that not all 2-Bromo-3'-Chloropropiophenone is created equal. Some batches from less attentive factories arrive greyed or malodorous, plagued by unreacted starting material, odd halide ratios, or traces of water from slapdash drying. We have seen firsthand how even seemingly minor contaminants can derail an entire project, forcing expensive rework and delays. That experience led us to double down on repetitive purification and rigorous batch tracing. We monitor not just for formal purity numbers, but for batch-to-batch consistency, solubility in key solvents, and shelf stability under practical storage conditions.

    Repeated collaboration with process chemists shaped our approach down to details like powder flow and packaging resistivity. If the product attracts static in dry climates, we switch packaging or offer alternate anti-static liners. Finer particle grades support cold reactions or quick dissolutions; larger granules allow easier handling for those preferring slower addition. Honest feedback from field users, not speculative trends, shape our continuous improvements.

    Differences from Similar Products

    Chemists regularly ask us about alternatives—plain 2-bromopropiophenone, 3’-chloropropiophenone, even mono-halogenated propiophenones. Comparisons seem obvious on paper but behave differently under real lab pressure. Mono-halogenated analogs lack the specific activation and blocking possibilities required in multi-step syntheses. The unique pattern of halogens on this molecule provides a flexible platform for diverse chemical modification and more selective functional group interchanges. Many first-time users report easier purification steps after switching from mono-halogenated versions, especially in high-pressure hydrogenation or aqueous workups.

    We also note that 2-Bromo-3'-Chloropropiophenone often decreases the number of steps required in complex syntheses compared to starting from plainer compounds. Advanced manufacturing groups save on both reagents and time, and they openly share these savings in their post-project reviews with us. Others point out that the intermediate’s reactivity profile aligns better with standard transition-metal catalyzed couplings, which reduces costly troubleshooting in both research and scale-up phases.

    Safety, Handling, and Lessons Learned

    Over years of production, safety protocols have moved from simple checklists to built-in reflexes that guide every batch. 2-Bromo-3'-Chloropropiophenone doesn’t come with the severe danger profile of some regulated substances but does require respect for its halogenated nature. Every person on our team, from refinery technician to load-out operator, approaches each blend-up with an understanding of the compound’s volatility and necessary containment.

    Regular safety training and ventilation upgrades form our foundation, backed by real alerts from on-site incidents or returns from clients who encountered an off-gas incident. Attention to these warnings moved us to reinforce PPE guidelines and switch up our vapor containment systems. Our facility doesn’t view spills or exposure with complacency—we keep audits tight, share findings directly with our partners, and fold every lesson back into how we run new batches.

    Environmental Commitment Rooted in Real-World Practice

    Sustainability talk grows louder every year, but in chemical manufacturing, real improvement means meaningful action. 2-Bromo-3'-Chloropropiophenone synthesis produces halogenated byproducts, and our responsibility does not end at the door of our facility. Over the years, we replaced legacy solvents with greener alternatives and set up solvent recovery loops that cut hazardous waste by half in certain quarters.

    We coordinate with downstream users—especially those scaling up—to map safe disposal of any spent material or offcuts. Our technical staff are available for consultation, which helps avoid unsafe dumps and environmental noncompliance. While we keep pushing for lower-impact syntheses, the lessons from field experience show no single fix solves all: steady, collaborative improvement delivers the surest progress.

    Adapting to Evolving Regulations

    Each time regulatory agencies release a new circular covering halogenated intermediates, our compliance teams work directly with process engineers to verify that every tank, drum, and line trace meets or surpasses expectations. That can mean tighter documentation, stricter origin checks, or new testing protocols for trace impurities. Experience taught us that delays in documentation on items like 2-Bromo-3'-Chloropropiophenone never end well for anyone; we stay ahead by keeping internal systems up to date and actively contacting authorities when unclear items come up.

    Batch-level traceability supports these efforts, from source material intake through finished product shipment. A real benefit we see is the speed with which this approach solves sourcing questions or expedites site inspections. Success rests on quick, factual records, not just compliance statements. Auditors sent by large pharma partners routinely ask for chain-of-custody detail or historical QC data; our readiness here shortens their visits and cements ongoing trust.

    Direct Feedback Loops Shape Real Progress

    In our facility, improvement does not happen only in the lab or boardroom. It grows out of unfiltered conversations with end users—researchers tracking unexplained chromatogram spikes, production managers looking to tweak loading times, or maintenance crews noting batch residue in pipes. These lines of communication cut through the fog of abstraction and help define concrete change.

    Sometimes, adapting drying protocols brings the biggest stability gain. Sometimes, it’s a packaging tweak or deeper raw material screening after a customer points to persistent trace metal pickup. In each case, practical insights drive our team to rethink the process, always with a focus on real-world performance rather than isolated metrics. Our plant operators talk straight with the receiving chemists—whether it’s a new lot consistency concern or solubility differences showing up mid-process—so issues are handled before they become problems.

    Openness to Customization

    Customization is no slogan for us; it’s an ongoing solution for recurring problems. Over years, we have adjusted batch sizes, dryness, levels of micronization, and solvent residues to meet concrete user needs. Where one customer’s process favors a fluffier grade, another’s might seize unless we package in inert gas. These adaptations arise out of real production runs, not theory. We gain much by visiting client facilities and observing the chemistry as it unfolds rather than assuming uniform methods solve every challenge.

    Driver requests from repeat customers have led us to develop special handling lines with extra inerting or low-temperature controls. In the rare event of recall or field complaint, a full technical team stands ready to track issues backward and make batch-specific amendments. This is not about selling to everyone; real impact comes from crafting 2-Bromo-3'-Chloropropiophenone to fit the environments and applications out there today.

    Collaboration With Research and Academia

    Academic partnerships bring an often-overlooked edge in manufacturing specialty chemicals. Groups exploring cutting-edge catalysis or complex downstream syntheses constantly probe the boundaries of available intermediates. In responding to these needs, flexibility and openness become our strongest tools. Graduate researchers run tests with unconventional solvents or heating rates, and their candid reports let us spot previously unnoticed impurities or stability quirks. These collaborations drive routine process upgrades and even influence core equipment changes in the plant.

    We benefit from seeing how 2-Bromo-3'-Chloropropiophenone reacts under unusual conditions. In shared projects, academic labs sometimes reveal unexpected strengths or incompatibilities, prompting a process rethink on our end. The resulting feedback loop does not stop at formal project closure but rolls forward, building trust and elevating product standards across the board.

    Field Challenges and Ongoing Solutions

    Each year brings its operational puzzles in chemical manufacture. The shift to new raw materials introduces flux in reactivity profiles; transport disruptions force us to plan and buffer inventory with more care. 2-Bromo-3'-Chloropropiophenone, with its reactivity and environmental demands, forces focus on fail-safes. Drum sealing upgrades, temperature-controlled storage, and well-trained shipping partners emerged out of real transport pains—spoiled or caked intermediates, shipment delays, or rejected lots at delivery.

    By writing up and openly discussing every near-miss or field return, our operational team reduces repeat mistakes and tightens standard practices. This ongoing critique—shared with both customers and supplier partners—forms a living manual of production and delivery that constantly evolves with the realities of manufacturing and regulation.

    Looking Ahead: Continuous Refinement

    Over the decades in this business, we have learned that compounds like 2-Bromo-3'-Chloropropiophenone don’t stand still. Synthesis costs shift, regulations change, and new catalytic cycles emerge in both academic and industrial settings. Each change presses us to review how we produce, test, and support this critical intermediate for its users. By building feedback loops right into every operation and pulling lessons out of both success and failure, we deliver a higher standard of reliability and value.

    Future developments may shift some reaction paradigms or invite greener alternatives, and we aim to adapt production so that environmental impact drops further with each iteration. Regular review periods keep us nimble, and the strong bonds with both the largest buyers and the smallest labs anchor decision-making in day-to-day business rather than distant theory.

    Final Thoughts From the Plant Floor

    2-Bromo-3'-Chloropropiophenone does not sit apart from its users or applications. Every year, new stories come back from the lab bench, the pilot plant, or the packaging dock, adding depth to our understanding of how form, function, and quality truly drive progress. By valuing real customer feedback and never stepping away from direct engagement, we ensure that every lot reflects years of hard-earned skills, lessons from the field, and an unwavering commitment to both safety and innovation. Our team believes that the compound’s impact comes not only from its molecular structure, but from the hands, minds, and voices of those who use and make it, every day.