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3-(2-Bromoacetyl)Pyridine Hydrobromide

    • Product Name 3-(2-Bromoacetyl)Pyridine Hydrobromide
    • Alias 3-(2-Bromoacetyl)pyridine HBr
    • Einecs 259-908-6
    • 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

    652049

    Productname 3-(2-Bromoacetyl)Pyridine Hydrobromide
    Casnumber 848133-35-5
    Molecularformula C7H7Br2NO
    Molecularweight 296.95
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint 153-157°C
    Solubility Soluble in water and polar organic solvents
    Storagetemperature 2-8°C
    Synonyms 2-Bromo-1-(3-pyridyl)ethanone hydrobromide
    Hazardclass Irritant
    Chemicalstructure BrCH2COC5H4N•HBr
    Hscode 29333999

    As an accredited 3-(2-Bromoacetyl)Pyridine Hydrobromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical 3-(2-Bromoacetyl)Pyridine Hydrobromide (5g) is packaged in a tightly sealed amber glass bottle with detailed labeling.
    Shipping 3-(2-Bromoacetyl)Pyridine Hydrobromide is shipped in secure, sealed packaging compliant with international hazardous material regulations. It is protected from light and moisture, with necessary documentation included. Refrigeration or additional temperature controls may be applied depending on specific requirements. Handle only by trained personnel with appropriate personal protective equipment (PPE).
    Storage Store **3-(2-Bromoacetyl)pyridine hydrobromide** in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong bases or oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerated). Ensure the storage area is clearly labeled and compliant with chemical safety regulations. Avoid sources of heat and ignition.
    Application of 3-(2-Bromoacetyl)Pyridine Hydrobromide

    Applications of 3-(2-Bromoacetyl)Pyridine Hydrobromide in Industrial Manufacturing

    As an established producer of 3-(2-Bromoacetyl)Pyridine Hydrobromide, we support advanced manufacturing sectors by supplying a compound integral to specialized organic synthesis. Below, we outline authentic industrial scenarios where our material enters production streams, strictly highlighting regulated, real-world uses driving end-product performance and safety.

    1. Pharmaceutical Intermediate Synthesis

    Our material functions as a key intermediate precursor in the synthesis of active pharmaceutical ingredients (APIs) for targeted therapeutic classes. Due to the compound’s nucleophilic and electrophilic functional sites, it enables efficient construction of pyridine-based scaffolds found in various drugs. Formulators select this intermediate in the assembly of substance moieties for both generic and original molecule medicines, requiring strictly controlled addition and compliance with drug master file submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.) standards for API synthesis
    • US FDA 21 CFR Part 210/211 for Finished Pharmaceuticals
    • China National Medical Products Administration (NMPA) DMF requirements

    Typical usage ratio

    • Stoichiometric ratios from 0.90 to 1.05 molar equivalents, adjusted based on desired yield and impurity profile of target API intermediate

    Downstream process integration

    • Used during stepwise assembly of heterocyclic precursors following halogenation reaction sequences; typically added after initial coupling reactions to introduce bromoacetyl functional groups

    Final product types

    • Synthetic intermediates for quinoline and pyridine-derived APIs
    • Analgesic, anti-inflammatory, and antiviral drug substances
    • Research-grade pharmaceutical intermediates for clinical development
    • Key impurity reference standards for QC release testing

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    Manufacturers in the crop protection sector apply the material to generate pyridine-based moieties present in selective herbicides and systemic fungicides. The functionalized pyridine nucleus introduced via our chemical enables construction of bioactive agrochemical backbones with precise substitution patterns. Processing teams carefully control concentration and reaction times to ensure compliance with residue and impurity requirements stipulated by global agrochemical regulators.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides and Intermediates
    • ISO 9001-based quality management for agrochemical manufacture
    • EU Regulation (EC) No. 1107/2009 on Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for testing

    Typical usage ratio

    • 0.95–1.15 molar equivalents relative to the aryl or heteroaryl core, adjusted according to the specific chlorination or acylation step

    Downstream process integration

    • Part of heterocycle functionalization stages, following initial backbone construction; introduced via controlled addition, typically under reflux, to form N-substituted pyridine intermediates within multi-step syntheses

    Final product types

    • Active intermediates for triazole-based fungicides
    • N-heterocyclic building blocks used in selective herbicides
    • Regulated precursor substances for proprietary crop protection agents
    • Reference standards for pesticide formulation analysis

    3. Fine Chemical Production: Pyridine-Derivative Synthesis

    Producers of advanced fine chemicals use our compound as a brominated acylating agent in the development of pyridine-derivative molecules required for electronic materials, specialty catalysts, and functional molecular probes. The reactivity profile allows for tailored functionalization, providing custom syntheses with narrow impurity profiles and high batch reproducibility. Manufacturing controls ensure integration at rates optimized based on substrate reactivity and downstream purification steps.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for chemical substances
    • ISO 9001:2015 certified process management
    • Specialty Chemical Manufacturers Association (SOCMA) guidelines
    • Internal raw material traceability and batch validation protocols

    Typical usage ratio

    • 1.00–1.20 eq, dependent on specific nucleophile used and target conversion; optimization performed via in-situ monitoring and HPLC assessment

    Downstream process integration

    • Introduced after primary substrate activation in functional group interconversion processes, often followed by rapid work-up and chromatographic purification for high-purity fine chemicals

    Final product types

    • Pyridine-based specialty ligands for electronic and photonic applications
    • Chemical intermediates for research and laboratory reagents
    • Tailor-made precursors for organometallic catalysts
    • Reference materials for advanced analytical laboratories

    4. Chemical Research & Development (Heterocyclic Compound Synthesis)

    R&D departments and contract manufacturing organizations purchase our compound for targeted heterocycle assembly and molecular scaffold exploration within medicinal chemistry, material sciences, and analytical standard production. Due to its reactivity, researchers employ it in proof-of-concept and process optimization projects, where strictly documented protocols and quality controls must support each use. Adjustment of ratios and introduction stage depends on project-specific objectives.

    Industry compliance standards

    • GLP compliance for laboratory and preclinical studies
    • ISO/IEC 17025 for laboratory accreditation
    • Institutional safe chemical handling protocols
    • Internal chain of custody and sample tracking procedures

    Typical usage ratio

    • Variable: 0.5–2.0 eq according to research protocol requirements and exploratory stage, determined through trial runs and LC-MS confirmation

    Downstream process integration

    • Reactant or modulator in method development studies; usually charged into refluxing solution or stepwise dosing alongside other building blocks to probe cyclization or side-chain introduction

    Final product types

    • Novel heterocyclic compound libraries for drug discovery
    • Model compounds for structure-activity relationship studies
    • Analytical reference materials for impurity profiling
    • Prototypes for specialty functional materials
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    Certification & Compliance
    More Introduction

    3-(2-Bromoacetyl)Pyridine Hydrobromide: An Insider’s Look at the Manufacturing Bench

    The chemical we’re talking about—3-(2-Bromoacetyl)Pyridine Hydrobromide—doesn’t make the headlines outside of synthesis labs, but it matters where people work on the frontier of pharmaceutical and specialty chemical innovation. This compound earns its keep as an essential intermediate for a range of projects involving heterocyclic chemistry. Here at the manufacturing site, where the smell of solvent and hum of overhead fans never really fade, everyone respects what it takes to produce it consistently and cleanly. Day in and day out, we’ve learned how critical reliability and precise characterization can be, because this is where research projects and large-scale developments intersect.

    Model and Specifications: What We Build and How We Know It’s Right

    We produce our 3-(2-Bromoacetyl)Pyridine Hydrobromide according to a model that’s shaped by direct collaboration with end-users over the years. Chemists looking to streamline their synthetic routes often choose this compound for its ability to introduce a bromoacetyl group without common contaminants like unreacted pyridine or excess brominating agents. Every shipment leaves with an assay our analytical team stands behind—GC-MS, NMR, and HPLC verification, with purity standards that usually go north of 98%. Particle size, water content, and residual solvent levels reflect what the application actually demands, not just a generic spec. Bulk batches run in reactors tailored for halogenation ensure consistency whether someone needs a few hundred grams or multiple kilos.

    Getting each lot right means walking through reactions carefully. Our process control team watches the profile change in real time, running in-line monitoring and routinely pulling spot samples that chemists review right on the shopfloor. We’ve seen the pitfalls—trace side-products that can gum up downstream synthesis, solubility quirks that make filtration tricky, and hydrobromide salt formation that swings with small changes in temperature or agitation. Over the years, we’ve focused on getting each step robust. For example, we use only high-purity solvents and store our starting pyridine stocks under nitrogen to prevent moisture drift. These details don’t get noticed in a catalog, but they show up in yield and downstream reproducibility. This is what we talk about at production meetings and what we reference when someone calls in and wants to troubleshoot a reaction gone awry.

    Usage: Bridging R&D and Production Scale Realities

    3-(2-Bromoacetyl)Pyridine Hydrobromide stands out for its compatibility with a wide range of coupling and cyclization reactions. Organic chemists in drug discovery appreciate how the bromoacetyl moiety engages nucleophiles—amines, thiols, and enolates tend to perform reliably in both small vials and round-bottom flasks loaded up for preparative runs. Many groups working on kinase inhibitors have asked for scale-up support, because their building blocks need to be both pure and ready to react. In these cases, only a well-controlled hydrobromide salt delivers the correct reactivity profile without unpredictable side reactions. The difference between a solid crystalline batch and a slightly sticky, over-humidified sample is night and day during tricky formation of heterocycles or extended conjugated systems.

    Some customers deploy this intermediate straight into their routes for agrochemical or specialty ligand synthesis, leveraging the reactivity window the bromoacetyl group brings. We know from long experience that this is a sensitive spot in many synthetic sequences. There’s often no room for extra water or for undetected halide impurities, as these can cause a domino effect in subsequent steps. We listen when process chemists describe an unexpected color change or drop in yield. That feedback comes right back to our plant team, prompting us to keep improving washing, drying, and packaging methods. Dry ice packs and special polymer linings in our shipping drums are not window dressing—they protect the salt’s shelf life as it travels from our door to a customer’s.

    What Sets 3-(2-Bromoacetyl)Pyridine Hydrobromide Apart From Related Intermediates

    Over the years, we’ve worked closely with teams who compare this molecule to similar alpha-haloketones and pyridinyl derivatives. Feedback from the field underscores how the hydrobromide salt version addresses points that free-base or hydrochloride alternatives don’t fully solve. For example, storage and handling on real-world benches is far easier with the hydrobromide salt: hygroscopicity drops, packaging integrity improves, and the shelf life extends even if room temperatures fluctuate. In ongoing projects that stretch out over months, these seemingly small changes matter—especially in resource-limited or high-throughput screening environments.

    We’ve fielded questions about alternatives, such as 3-(2-chloroacetyl)pyridine or free bromoacetylpyridine, and put them to the test side-by-side. The hydrobromide salt’s crystalline form streamlines filtration and measurement, reducing operational headaches for the actual users. At the bench, this means fewer discrepancies batch-to-batch. Researchers working with analogous carbamoyl or methyl ketones often find reactivity less predictable, and the downstream purification tougher. Years of batch records show better kinetic control and higher isolated yields when the process starts with our hydrobromide salt. That built-in reliability trims waste and cuts down on post-reaction troubleshooting, freeing up resources for what chemists care most about: moving projects forward.

    The difference comes down to performance over time. Many academic teams working with model compounds comment on the predictability cycle after cycle, whereas teams in process development prize the suppressed formation of unwanted byproducts. We’ve seen large pharmaceutical groups repeatedly opt for this specific hydrobromide salt once their pilot-scale processes kick off, even after initial rounds may have compared several closely related compounds. They value both consistency and support—attributes that stem from how we run our own reactors and validate every batch, not just from a line on a technical datasheet. Our granular tracking, from raw material lots to calibration logs, prevents drift in quality. Ultimately, researchers trust what they get from us, and that shows up in their speed to result.

    Manufacturing Realities: What Decades on the Production Floor Teach Us

    Chemicals like 3-(2-Bromoacetyl)Pyridine Hydrobromide demand more than a recipe out of a textbook. Every production cycle involves thousands of decision points: temperature ramps, mixing speeds, solvent swaps, and timing all need close attention. There’s a temptation in the industry to treat organic intermediates as commodities, but anyone who spends time on the R&D/production interface knows better. Minor deviations during the bromination step, oxygen sneaking into the reactor headspace, or even a slightly out-of-spec solvent drum can set off a chain of complications that ripple out to the customer: difficult crystallizations, unpredictable color changes, or higher assay rejects. We keep an archive of case studies where rapid troubleshooting and old-fashioned know-how saved the day. Some of these fixes come from a midnight call with a customer in another time zone, others from years of testing containment for corrosive fumes or scaling out a batch that behaved unpredictably in summer weather.

    Lab protocols sometimes miss details that manufacturing realities bring to the front. Scale matters—reactions behave differently with a hundredfold upsize, and mixing geometry in a kilo-scale kettle doesn’t mimic a flask easily. In our experience, details like nitrogen purging, staged reagent additions, and extended holding times for complete conversion can mean the difference between a clean, bright batch and a problematic one. Careful attention to workup and salt formation step keeps the product’s physical properties in the optimal range and keeps the release process efficient. We test not only assay and purity, but also bulk density and flow, since those impact how preparation techs at our customers’ sites measure and dispense batches. That feedback loop—plant to customer and back—drives the incremental changes that keep our product a step ahead in reliability.

    Why Purity and Traceability Can't Be Compromised

    Any chemist who’s tried to drive a multi-step synthesis forward with subpar intermediates knows the cost of compromise—in time, effort, and missed milestones. Purity here means more than just a nice HPLC peak; it’s about absence of problematic minor components and total bromide balance. We subscribe to a mindset that goes past minimum compliance. Each production run gets logged and archived for traceability, so if a question turns up months later, we can fetch the exact sampling data and in-process records on demand. We own the process, so there’s no finger-pointing or gaps in the chain of responsibility.

    We’ve had conversations with chemists dealing with last-minute surprises—an unexpected side reaction, a stuck filtration, or a color change that hints at trace ionic impurities. Providing a rapid turnaround on analytical support as part of the product experience keeps projects on schedule. We’ve made it a practice to run not just final-release QC, but also stability and compatibility tests in the context of real-world applications. Storing reference samples under simulated shipping stresses and checking for transformation or decomposition sets a higher bar. These investments have paid off through reduced returns and repeat orders from groups who once struggled with inconsistent intermediates. Such reliability doesn’t show up in specs alone; it comes from a culture of accountability and direct experience with both the molecule and the science behind it.

    Shipping, Handling, and Supporting Success Beyond the Factory Gate

    Materials like 3-(2-Bromoacetyl)Pyridine Hydrobromide can degrade if handled or stored wrong. Moisture, light, and temperature fluctuations create headaches for logistics unless handled by knowledgeable teams right from packaging. Early on, we learned not to rely on generic bulk shipping solutions. Dedicated barrier-lined containers and silica desiccant packs in each drum became our norm after customer feedback from export shipments flagged subtle changes on the receiving end. We track not just internal quality but also monitor shipping routes and warehouse practices, flagging hot spots where climate swings could impair stability. By ghost shipping test batches and analyzing arrival samples, we prevent surprises—an advantage that caught the attention of regulated industries monitoring data integrity all the way to the point of use.

    On arrival, we advise handling in a dry box or under controlled conditions, but we also design for situations where ideal facilities may not exist. Explaining these nuances face-to-face with manufacturing or lab teams, rather than sending a boilerplate storage memo, fosters the kind of trust that forms lasting partnerships. We see the results when the same R&D group comes back to us, project after project, knowing the material will perform the same, batch after batch. Long-term customers have integrated feedback from our technical team into their handling SOPs. This approach extends beyond simple customer service—it reflects a manufacturer’s investment in their product’s role in the customer’s success.

    Continual Process Improvement: Learning From Every Batch

    Years of running back-to-back campaigns with 3-(2-Bromoacetyl)Pyridine Hydrobromide revealed something simple: every batch offers an opportunity to close the gap between theory and practice. The manufacturing crew invests in process tweaks based on real outcomes, not just isolated lab data. We might shift order of reagent additions, upgrade condenser capacity to tackle stubborn volatiles, or experiment with antisolvents to optimize crystal form. Keeping close communication with chemists who actually use the product uncovers subtle challenges—like ease of weighing in gloveboxes, compatibility with high-throughput robotics, or the way dust generation affects sensitive analytical platforms.

    No improvement is too small. For every major process upgrade, there’s a dozen small, nearly invisible tweaks—like relabeling drums to include scannable trace codes, improving fiber drum seal integrity to reduce exposure risk, or customizing batch sizes in response to unpredictable supply chain conditions. Every member of the team—from reactor operators to warehouse techs—feels accountable for the batch’s journey from vessel to vial. This approach pays dividends in resilience and reliability that standardized, one-size-fits-all protocols rarely match.

    Real-World Outcomes and the Value of Direct Manufacturer Relationships

    Where we see the biggest difference from being a direct manufacturer, not just a supplier, is in the relationship with the users of 3-(2-Bromoacetyl)Pyridine Hydrobromide. Projects live or die by lead time, traceability, and honest answers about problem-solving. Customers want more than a box of chemicals—they want insight, assistance, and a sense that the people they source from will pick up the phone and bring practical input when the going gets tough. Our senior process chemists and technical support staff put in the work to really understand customer projects and help troubleshoot unexpected developments. This goes both ways; the feedback we receive arms us with knowledge that benefits future clients, keeping our production protocols evolving rather than stagnant.

    We stay ahead by prioritizing information flow. Detailed batch documentation, sharing best practices on handling, and offering insights from our own troubleshooting archives have become standard. The value of a transparent, responsive supply chain makes itself clear every time a customer calls with a timeline crunch or a regulatory question. Being able to pull a full suite of analytical and process data at a moment’s notice—as direct manufacturers and stewards of the process—sets us apart from organizations further removed from the source. This closeness to both the product and the people using it means that performance in real-world syntheses, rather than just test-tube conditions, remains at the heart of how we define quality.

    The Ever-Changing Landscape: Remaining Attuned to Industry Shifts

    The field of heterocyclic intermediates and bromoacetylation chemistry doesn’t stand still. Regulatory frameworks tighten, environmental controls on processing equipment evolve, and green chemistry principles place new constraints on traditional routes. We’re not bystanders to these changes. Ongoing investment in process safety—reducer emissions, improved waste handling, and in-process recycling—aligns both with our own values and with what our partners expect. We track regulatory changes that affect global shipping, managing compliance documentation and ensuring labeling practices reflect evolving standards. Staying tuned to industry changes means running regular reviews and continuous training, both in the lab and on the production floor.

    Technology shifts have brought automation and advanced in-line sensors to our reactors, raising the repeatability and reducing human error. We track these metrics with the same seriousness as older generation process logs; mixing tradition and modernity in the plant is not a slogan but how we work. Discussions with customers often include how newer process needs—such as support for continuous flow chemistry or adaptability for automated screening workflows—are shaping the way intermediates like 3-(2-Bromoacetyl)Pyridine Hydrobromide are specified and delivered. We adapt, not by rote, but by maintaining an engineering and problem-solving mindset rooted in real production experience.

    Conclusion: More Than a Molecule—A Partnership Across the Project Lifecycle

    Manufacturing 3-(2-Bromoacetyl)Pyridine Hydrobromide means more than getting the molecule in a drum. It’s about understanding how chemists at the cutting edge of research and production depend on consistent, reliable supply, honest answers, and a partner who listens and responds. The years at the bench, in the control room, and on the phone with project teams shape every batch we deliver. We’ve learned that success rides on details others might overlook, and that the value of a direct relationship with the manufacturer carries over in real terms: in purity, in performance, and in peace of mind. Every challenge faced and improvement made, from the reactor to the receiver’s bench, defines who we are and what our product brings to the table.