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1-(6-Bromo-Pyridin-3-Yl)-Ethanone

    • Product Name 1-(6-Bromo-Pyridin-3-Yl)-Ethanone
    • Alias BRD-K53523902
    • Einecs 849-476-5
    • 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

    452301

    Iupac Name 1-(6-bromopyridin-3-yl)ethanone
    Molecular Formula C7H6BrNO
    Molecular Weight 200.04 g/mol
    Cas Number 237760-64-2
    Appearance Off-white to light yellow solid
    Melting Point 54-58°C
    Smiles CC(=O)C1=CN=C(C=C1)Br
    Inchi InChI=1S/C7H6BrNO/c1-5(10)6-2-3-7(8)9-4-6/h2-4H,1H3
    Solubility Soluble in DMSO, DMF, methanol
    Purity Typically >97% (assay dependent)

    As an accredited 1-(6-Bromo-Pyridin-3-Yl)-Ethanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled “1-(6-Bromo-Pyridin-3-Yl)-Ethanone, 10 grams, For laboratory use only.”
    Shipping 1-(6-Bromo-Pyridin-3-Yl)-Ethanone is shipped in tightly sealed, chemically resistant containers to prevent contamination and ensure stability. All packaging complies with international regulations for hazardous materials. Proper labeling and documentation are included, and temperature-sensitive conditions are maintained as required. Handling and transport are performed by certified personnel to ensure safety.
    Storage Store 1-(6-Bromo-pyridin-3-yl)-ethanone in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents and acids. Ensure storage temperature remains at room temperature (15–25°C). Properly label the container and follow all relevant chemical hygiene and safety protocols.
    Application of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone

    Applications of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone in Industrial Manufacturing

    As the direct manufacturer of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone, we supply this fine chemical for multiple advanced sectors. Downstream industries adapt this pyridine derivative into complex molecules through well-controlled synthesis routes. Below, we detail practical industrial use cases, compliance requirements, process stages, and typical consumer product outputs for our material.

    1. Pharmaceutical Intermediate for Antineoplastic Agents

    Leading pharmaceutical companies synthesize kinase and receptor modulators using this compound as a core intermediate. Chemists leverage its bromo-pyridyl group for Suzuki and Buchwald-Hartwig couplings when constructing heterocyclic drug candidates targeting oncology pipelines. Production runs demand consistent batch quality to meet investigational medicinal product standards. Integration occurs during advanced scaffold assembly, particularly in combinatorial libraries and lead optimization. End users formulate and test various finished small-molecule therapies for clinical development.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4, Part II for APIs
    • USP–NF for purity characterization
    • FDA 21 CFR Part 211 for pharmaceutical manufacturing

    Typical usage ratio

    • Integrated as 0.5–5 molar equivalents relative to the primary amine or boronic acid in the coupling step. Chemists adjust based on route efficiency.

    Downstream process integration

    • Charged in the intermediate step of heterocycle synthesis during structure-activity relationship studies and scale-up for pilot manufacturing lots.

    Final product types

    • Oncology small-molecule drug substances (APIs)
    • Clinical trial candidate compounds
    • Reference standards and intermediates
    • Pre-clinical screening libraries

    2. Agrochemical Research and Crop Protection Formulations

    Agrochemical innovators source this material for the synthesis of pyridine-based pesticide scaffolds. The compound provides the aromatic backbone for active molecules that undergo further functionalization—primarily for herbicide or fungicide candidates. Downstream labs perform halogenation and nucleophilic substitution, introducing this ketone within regulated pilot trials. All processes adhere to regional pesticide screening protocols and eco-toxicity assessments before final formulation or registration.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for crop protection studies
    • FAO/WHO Guidelines for Pesticide Residue Analysis
    • REACH registration for intermediates in the EU
    • ISO 9001 for quality management of process documentation

    Typical usage ratio

    • Dosed at 1–6% w/w in initial active ingredient synthetic runs, optimized per molecular pathway and downstream derivatization yield.

    Downstream process integration

    • Introduced in early-stage compound synthesis and retained through subsequent functionalization in research and upscaling for registration batches.

    Final product types

    • Precursor materials for selective herbicides
    • Pyridine-derived fungicide active substances
    • Synthetic reference grades for residue analysis
    • Research samples for biological screening

    3. Fine Chemical Synthesis in Specialty Resin Manufacturing

    Specialty chemical producers utilize this bromo-pyridine ketone for creating modified resins and advanced polymer additives. The compound acts as a functional monomer or modifier, reacting in controlled processes such as nucleophilic aromatic substitution or acylation. These steps occur in the presence of tailored catalysts, resulting in end polymers with altered thermal or electronic properties. Production lines emphasize traceability, solvent control, and adherence to sector-specific raw material acceptance protocols, especially in electronics and coatings industries.

    Industry compliance standards

    • ISO 14001 environmental controls for chemical plants
    • ASTM E260 for NMR spectroscopy quality tests
    • EN 13980 for process safety of explosive atmospheres
    • RoHS directives where usable in electronics resins

    Typical usage ratio

    • Employed at 0.3–2% wt of total monomer content, adapted according to design of the resin's functionality and end-use certification requirements.

    Downstream process integration

    • Charged during oligomer synthesis, often prior to crosslinking or copolymerization, to impart specific polarity or flame-retardant properties.

    Final product types

    • High-performance epoxy resins
    • Adhesive polymers for electronics
    • Specialty coatings for circuit boards
    • Heat-resistant thermosets

    4. Intermediate for Organic Light-Emitting Diode (OLED) Materials

    Electronic material developers value this compound for the construction of small-molecule OLED intermediates, especially where precise halogenated pyridine structures improve charge mobility in optoelectronic devices. The bromo-group position enables differentiated cross-coupling with aryl or heteroaryl partners during emitter or host synthesis. Stringent QC and electronics-grade handling target impurity removal and reproducibility for both display and lighting applications.

    Industry compliance standards

    • IPC-6012 for rigid printed board qualification
    • IEC 61249 for base materials in electronics
    • ISO/TS 80004-9 for nano-enabled materials
    • RoHS/REACH for limited substances in electronic devices

    Typical usage ratio

    • Used in 0.2–1.5 molar excess in cross-coupling steps depending on the efficiency required for electronic grade intermediates.

    Downstream process integration

    • Added during early-stage formation of emitter precursor structures, retained through purification, and transferred to thin-film deposition facilities.

    Final product types

    • OLED emitter components
    • Host material precursors
    • Display-grade thin-film coatings
    • Prototypes for next-generation optoelectronic devices

    5. Reagent for Academic and Industrial Research Synthesis

    Academic institutions and contract research organizations employ this ketone in SAR studies and synthetic route development for heterocyclic scaffolds. The bromo-pyridyl functionality makes it a versatile building block for advanced organic synthesis and structure probing. Material shipments require full CoA documentation and meet analytical reference standards, supporting peer-reviewed dissemination and patent filings.

    Industry compliance standards

    • GLP guidelines in research testing
    • ISO/IEC 17025 accreditation for reference material laboratories
    • National/international chemical safety codes
    • State/local R&D chemical handling protocols

    Typical usage ratio

    • Quantity varies, typically supplied in 10 mg to 10 g scale with dosing tailored to reaction stoichiometry and optimization trial size.

    Downstream process integration

    • Added to the reaction flask as the key halogenated aromatic partner in coupling, alkylation, or functional group modification experiments.

    Final product types

    • SAR libraries for drug discovery
    • Research-grade analytical standards
    • Advanced heterocyclic intermediates
    • Peer-reviewed publication compounds
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    Certification & Compliance
    More Introduction

    1-(6-Bromo-Pyridin-3-Yl)-Ethanone: Precision Chemistry in Action

    Understanding the Role of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone in Fine Chemistry

    At our manufacturing facilities, daily work with compounds like 1-(6-Bromo-Pyridin-3-Yl)-Ethanone shows us the real impact of thoughtful chemical process design. This ketone, distinct in its structure by a bromo substituent at the 6-position of a pyridine ring, doesn't merely serve as another off-the-shelf intermediate. Rather, it shapes synthesis outcomes in pharmaceutical research, crop protection development, and specialty chemical exploration. Our chemists approach every batch with their eyes set on stability, purity, and consistency, since even minor deviations in chlorination, temperature, or solvent selection during production leave visible marks on the final product’s characteristics.

    Traditional building blocks often bring predictable behavior. This compound, with its electron-withdrawing bromine atom placed precisely where seasoned medicinal chemists want it, reacts in a way that allows specific downstream transformations. Acylation at the ethanone side, cross-coupling on the pyridyl bromide, and modified nucleophilic substitutions—all occur with a higher degree of selectivity than similar pyridinyl ethanones lacking the halide. The difference shows up in the lab. When we produce related compounds without the bromine, the regioselectivity of intended reactions starts to drop. That translates to more impurities and higher costs in isolation steps.

    Specifications That Reflect Daily Realities

    Over years of manufacturing, our specifications for 1-(6-Bromo-Pyridin-3-Yl)-Ethanone have evolved with customer feedback and internal quality audits. Analytical results matter when researchers face tight project deadlines. Our typical material appears as an off-white to pale yellow solid, stemming from fine control of crystallization and solvent evaporation. Chemically, we test each lot with both HPLC and NMR to verify a minimum purity exceeding 98 percent, as even minor impurity signatures can disrupt sensitive syntheses. Our team understands that color changes, trace solvent residues, or byproducts from incomplete bromination hint at problems upstream—in reaction parameters or workup protocols.

    Those parameters aren’t arbitrary. They come from hundreds of iterative pilot runs and weeks of troubleshooting. Trace moisture from an improperly dried filtrate may encourage degradation in long-term storage, so we monitor water content as part of release checks. The melting point range (typically between 56-60 degrees Celsius for a well-prepared batch) provides another quick gauge of integrity. If that number drifts, our staff investigates root causes, from heat-source accuracy to vessel contamination. All this shows in a consistent, reliable material, batch after batch.

    Going Beyond Off-the-Shelf: Where Our Approach Makes a Difference

    Lab bench and production line never look the same. Scale finds its own way of amplifying minor nuisances from R&D batches into operational headaches. We don't just copy published procedures—we run dozens of trial reactions at bench scale to capture reproducible optimizations. Consider crystallization: a subtle tweak to cooling gradients and agitation speed in the final hour can separate process success from a sticky filtration nightmare. We develop these steps in-house, tracking performance with statistical controls, not assumptions.

    Our teams often discuss how marketplace offers for 1-(6-Bromo-Pyridin-3-Yl)-Ethanone overlook practical issues: shipping stability, caking in transit, packaging safety, even dust hazard. By producing compounds in controlled environments designed for fine moisture and airborne contaminant management, we reduce risks for downstream users. Custom packaging—foil or coated polyethylene, depending on anticipated shelf life—matches real customer environments, not just warehouse needs.

    Supporting Innovation in Pharmaceutical and Agrochemical Applications

    A decade of field feedback tells us how our compound moves from the drum to pharmaceutical R&D benches or crop-protection R&D plants. Our partners in medicinal chemistry prefer our material for Suzuki-Miyaura couplings or Buchwald-Hartwig aminations because halogen placement influences reactivity. Repeated side-by-side trials show that bromo substitutes at the 6-position on pyridine rings offer cleaner reactivity than their 2- or 4-substituted cousins under palladium catalysis. The ethanone group then allows straightforward elaboration—think imines, oximes, or reductive aminations—facilitating combinatorial library efforts for discovery programs.

    In agricultural innovation, the strong leaving group effect of our bromine atom speeds up certain functionalizations crucial for optimizing molecule potency. Our clients have reported higher yields of target fungicidal or herbicidal actives from their pilot plants, highlighting reduced formation of unwanted byproducts and simplified downstream purification.

    We listen to those outcomes in regular technical support calls and site visits. If a researcher struggles with reaction workup downstream or notes unusual instability, our manufacturing specialists don’t refer them to a generic FAQ—they dig into analytical records, sharing details from recent production runs and helping troubleshoot the process on a molecular level. This sets our chemical manufacturing apart from resellers detached from both recipe and reaction kettle.

    Managing Purity and Traceability at Scale

    Modern project requirements—and regulatory reviews—push for detailed traceability. Regular feedback from our customers about the use of this compound in regulated settings has shaped our supply chain management. Raw material selection starts with verifiable sources and full batch histories. We audit our upstream suppliers of both pyridine building blocks and brominating agents. In-house, our team manages batch records that document each step, from filtration rate to exact drying conditions.

    Customers working under good manufacturing practice (GMP) conditions ask about cross-contamination and residual solvent risk. We answer not with generalities, but tracked, batch-specific impurity profiles. Over the years, we’ve reduced levels of problematic impurities such as dibromo byproducts and chlorinated degradation products to well below customer-specified limits, much of this progress coming from direct consultations with development teams using our reagents in their own facilities.

    Trace metal analysis forms another core part of our quality regimen. Even low ppms of palladium, iron, or copper—carryovers from catalysts and metalware in synthesis—alter biological results in research or product approval phases. Continuous investment in atomic absorption equipment and clean-processing protocols keeps these levels minimal. If a customer requires a specific trace analysis—say, confirmatory ICP-MS data for regulatory filing—we retain enough batch material to run extra analyses on demand.

    Differences that Matter: How Our 1-(6-Bromo-Pyridin-3-Yl)-Ethanone Stands Out

    Chemists who know the nuances of pyridinyl chemistry realize that not all batches or manufacturers approach this compound in the same way. Material from generic traders sometimes exhibits wide melting point ranges, variable coloration, even sulfur or nitro contamination. Catastrophic for sensitive reactions, this uncertainty lengthens development cycles and undermines confidence. Our in-house controls prevent these problems before a single kilogram leaves the plant. In our facility, every run triggers analytical review—the team tracks both consistency and anomalies. If a trend appears between lots—say, a spike in a minor impurity—we trace it to machine, operator, or feedstock, tighten the process, and record full investigative details for downstream users.

    Many market offerings source materials from several subcontractors, blending multiple lots with little control over intermediary handling. Our chemists handle every reaction in one vertically integrated production line, ensuring seamless handoff from batch reactor to final packaging. Documentation follows every step, and users requesting regulatory files for clinical or environmental review receive not a vague certificate, but a data-packed dossier, reflecting true batch-specific values.

    Routine feedback from our clients consistently mentions fewer failed runs, clearer spectra, and less risk of unreactive or incompatible material than they have experienced with low-cost alternatives. Staff on our quality line recognize the role of seemingly minor production details—like whether reactor glass or stainless steel is used for a given step—in minimising background impurities.

    Safety and Handling: Practical Experience Informs Every Step

    Our work with 1-(6-Bromo-Pyridin-3-Yl)-Ethanone has taught us that handling risks remain best minimized through attention to fine detail, both in production and customer transport. Laboratory teams find that the compound emits a faint, characteristic odor, reminiscent of related halopyridines, which acts as an early warning for spills. Our manufacturing crews use nitrogen-purged transfer vessels and low-dust transfer protocols, since even minor inhaled quantities can cause significant respiratory irritation. We help users set up receiving docks with proper exhaust ventilation and PPE recommendations based on real workplace experience, not generic MSDS documents.

    Packing operations always occur in controlled, low-humidity environments to avoid product cake formation or premature degradation, especially crucial for customers planning long-term storage. Drums sealed with tamper-evident closures and batch-specific barcoding accompany every outgoing shipment, addressing traceability needs from the outset. These steps do not come from theory, but from months of practical feedback and recurrent audits, both company-run and third-party.

    Sustainability and Continuous Improvement in Our Operations

    In a market increasingly attentive to environmental impact, chemical manufacturing must balance process efficiency with a commitment to sustainability. Our production of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone has benefited from targeted investments in waste-stream management. For instance, reclamation of bromination residues and recycling of pyridine solvents avoid both operational waste and downstream disposal liabilities.

    Continuous process improvements shave resource use without sacrificing product reliability. Recent upgrades have cut overall solvent consumption per batch by over 20 percent, thanks to improved distillation protocols and automation at bottleneck unit operations. As regulations evolve, we adapt both raw material sourcing and in-plant safety practices, bringing our operational footprint below evolving guidelines for emissions and hazardous waste.

    Partnerships with downstream customers often inform our R&D agenda for process improvements. Real-world suggestions about reagent compatibility with green chemistry workflows or requests for specific impurity fingerprints find a receptive audience in our process engineers. Where possible, we tailor purification steps or train plant operators accordingly. This practical, two-way channel accelerates our response to regulatory or market-driven process revisions.

    Insights from the Manufacturer’s Perspective

    Unlike resellers, our perspective on 1-(6-Bromo-Pyridin-3-Yl)-Ethanone comes with hands-on knowledge of its quirks and latent hazards, from raw material logistics through plant equipment dynamics. We see firsthand how seemingly small deviations—a damp filter cake, inconsistent heat gradients, unstable precursor lots—reverberate throughout production and later, in customer hands. Our operators acknowledge the compound not as a mere SKU, but as a complex chemical entity whose real-world behavior depends on more than theoretical purity values.

    Crafting this compound involves more than preparing a standard package or quoting a specification sheet. Over the years, we’ve learned to audit every critical point. From the earliest days, occasionally losing a drum to ambient moisture or temperature spikes, our crew has instituted practical redundancies. Batch tracking starts at the nuclear magnetic resonance scanner and runs through the final warehouse scan. Our technical sales team keeps communication channels open even after delivery, ready to trace a single spectroscopic blip back to the kettle or filtration bay that spawned it.

    The compound’s position as a favored intermediate didn’t grow overnight. Many hours of process troubleshooting, modification of reaction vessel internals, and handoffs between synthetic, analytical, and safety teams have shaped its current place in custom synthesis projects. Each success story—with a client’s successful scale-up or a rapid impurity resolution—pushes our teams to look for the next efficiency gain or risk minimization approach.

    Shaping Value Through Technical Expertise and Transparency

    Researchers and process chemists seek reliability and technical expertise, not just an attractive price per kilogram. Our role as an actual manufacturer gives us control over every facet—something that numbs the sting of unplanned deviations in customer research or pilot production. As new synthetic protocols emerge, often accelerating discovery timelines in fast-moving industries, we invest in characterization technologies to validate our material’s suitability. The chain from raw material to end-user remains direct, with no unexplained gaps or hidden processing steps.

    Conversations about supply or technical questions always involve our chemists, not call-centre intermediaries. We believe this transparency, from batch genealogy to impurity tracking, supports innovation, not just compliance. When market standards rise, our team pushes process controls further, minimizing risk and maximizing product performance in practical settings.

    Meeting and Exceeding Changing Demands

    The journey of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone in our production line mirrors changes in the industries it serves. As medicinal chemists push for faster turnaround, more detailed impurity profiles, and support for combinatorial chemistry, our facilities adapt, fine-tuning everything from reaction monitoring tools to customized documentation. Agrochemical discovery programs push us on both yield and sustainability, demanding a closer partnership between development and technical teams.

    We see the difference first-hand in customer project outcomes. Cleaner syntheses, reduced side-product formation, and improved scalability feedback strengthen our in-house processes. The drive for even greater purity, faster turnaround, and greener practices never lets up, and with each challenge our production staff and engineers discover new ways to refine every batch of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone.

    Responsibility to Customers, Colleagues, and the Environment

    Our responsibility as a manufacturer extends well beyond compliance or routine fulfillment. Every operator, chemist, and engineer in our plant feels the impact of their work not only in product quality but in its downstream effects—on researcher productivity, on workplace safety, and on the environment. Our approach combines pride in technical achievement with a practical understanding of scale, long-term storage hazards, and the realities of industrial chemistry.

    As industries evolve, so does the critical role of 1-(6-Bromo-Pyridin-3-Yl)-Ethanone. Whether entering a new pharmaceutical screening cascade or serving as a foundation for a novel crop-protection compound, its performance and reliability reflect decisions made long before it arrives on the customer’s workbench. For us, this means a steady focus on deep technical support, continual process refinement, and a commitment to both customer and environmental needs.