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5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine

    • Product Name 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine
    • Alias 5-Bromo-2-(1-pyrrolidinyl)pyridine
    • Einecs 629-708-2
    • 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

    484791

    Chemical Name 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine
    Cas Number 874233-63-7
    Molecular Formula C9H9BrN2O
    Molecular Weight 241.09 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in common organic solvents like DMSO and DMF
    Storage Conditions Store in a cool, dry place and away from light
    Smiles C1CC(=O)N(C1)c2ncc(Br)cc2
    Inchi InChI=1S/C9H9BrN2O/c10-7-2-3-9(11-6-7)12-5-1-4-8(12)13/h2-3,6H,1,4-5H2

    As an accredited 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine

    Applications of 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine in Industrial Manufacturing

    5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine demonstrates strong functional performance as a synthetic intermediate in select specialty chemical and pharmaceutical manufacturing workflows. As a direct manufacturer, we focus on supporting established downstream applications where its high-purity grade, batch reproducibility, and traceability directly impact quality control, formulation reliability, and final product standards.

    1. Pharmaceutical Intermediate for Anticancer API Synthesis

    Pharmaceutical synthesis protocols frequently use this compound as a key intermediate for preparing active pharmaceutical ingredients (APIs), including next-generation small-molecule kinase inhibitors and targeted anti-oncology compounds. This material enables stepwise N-heterocylic substitution in metal-catalyzed coupling reactions, significantly improving process consistency and yield for high-value APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <821> Synthesis Intermediates
    • EU EudraLex Volume 4 GMP Annex 8
    • FDA 21 CFR Part 211 (for API intermediates intended for US/EU markets)

    Typical usage ratio

    • 0.6–1.5 molar equivalents per batch, adjusted based on target API route, impurity profile control, and desired yield; optimization guided by preclinical route and regulatory filing requirements.

    Downstream process integration

    • Feeds into heterocyclic functionalization stage via Suzuki, Buchwald–Hartwig, or Negishi coupling under controlled temperature and inert atmosphere; followed by purification (chromatography/crystallization) and onward conversion to final API.

    Final product types

    • Finished oncology APIs (e.g., pyridine-derived kinase inhibitors, kinase-targeted small molecules)
    • GMP-compliant pharmaceutical intermediates for global drug manufacturers

    2. Agrochemical Active Ingredient Synthesis

    In advanced agrochemical production, this material serves as a pyridine ring-building block for the synthesis of high-value insecticide and fungicide actives. The specific brominated pyridone structure facilitates regioselective coupling and halogen exchange, supporting next-generation crop protection agents that comply with updated environmental and safety norms.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Chemical Pesticides
    • REACH Regulation (EC No 1907/2006) for pesticide intermediates
    • OECD Guidelines for Testing of Chemicals
    • ISO 17025 for batch quality control in agrochemical production

    Typical usage ratio

    • 5–20% w/w of total reactant mixture during ring functionalization steps; ratio fine-tuned based on crop protection mechanism, desired bioactivity, and downstream isolation efficiency.

    Downstream process integration

    • Introduced during selective halogenation and subsequent nucleophilic aromatic substitution; forms core scaffold prior to formulation into technical-grade agroactive ingredient and downstream formulation.

    Final product types

    • Technical concentrate and formulated fungicides/insecticides
    • Pyridone-pyridine based pesticide actives

    3. Custom Synthesis for Specialty Electronic Chemicals

    Chemical companies engaged in electronic material synthesis use this compound as a precursor to functionalized pyridine derivatives needed for OLED emitter and semiconducting polymer technologies. The structure supports cross-coupling reactions crucial for introducing electron-transport functionalities and enhancing film properties in thin-film display manufacturing.

    Industry compliance standards

    • SEMATECH Qualification Criteria for Organic Electronic Materials
    • RoHS Directive 2011/65/EU for electronic chemical raw materials
    • IEC 61249-2 for organic base materials used in PCB fabrication
    • Internal QC protocols for photophysical property validation

    Typical usage ratio

    • 2–6% by total monomer mass, set according to target emission wavelength and charge transport specification in OLED or conducting polymer designs.

    Downstream process integration

    • Acts as a regioselective coupling substrate during C–N or C–C bond formation, typically introduced in the synthesis of π-conjugated segments prior to purification and downstream device grade material conversion.

    Final product types

    • EML (Emissive Layer) materials for OLEDs
    • Hole transport and electron transport intermediates for display modules
    • Functional small molecule dopants for organic semiconductors

    4. Fine Chemical Intermediate for Analytical Reagents

    Research reagent and diagnostic kit manufacturers use this compound as a high-purity intermediate for the preparation of tailored pyridine-modified ligands and fluorescent probes. Its controlled reactivity and specific substitution patterns allow precise modification for spectroscopic, bioanalytical, or chromatographic end uses.

    Industry compliance standards

    • ISO 9001:2015 for reagent manufacturing quality management
    • ACS Reagent Grade Specifications
    • USP General Notices for Analytical Reagents
    • OECD Principles of Good Laboratory Practice (GLP) for test kits

    Typical usage ratio

    • 0.1–0.5 molar equivalents, calculated based on coupling efficiency, chromophore loading targets, and downstream purification requirements of the analytical reagent protocol.

    Downstream process integration

    • Enters as an initial scaffold reagent in custom ligand/probe synthesis via metal-catalyzed or activated ester coupling; subsequently purified before integration into analytical kit formulation or sensor device assembly.

    Final product types

    • Pyridine-tagged fluorescent or colorimetric reagents for analytical assays
    • Chromatography derivatization kits for laboratory and industrial QC use
    • Molecular probe components in diagnostic systems
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    More Introduction

    5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine: Unpacking the Value Behind a Trusted Chemical

    In labs all over the world, chemists count on certain building blocks for their research, and 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine has earned a place among them. You may not recognize the name unless you spend time poring over chemical catalogs, but talk to a synthetic organic chemist and odds are this compound has crossed their bench. More than just another name in a list, this molecule carves out value through both its structure and its performance, giving researchers an option that stands apart from cousin chemicals.

    Understanding 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine’s Appeal

    A lot of the excitement around this substance comes right down to how chemists can use it. If you picture a toolbox, some wrenches fit dozens of bolts, some fit only one. This compound works much the same way when it comes to molecular construction. Whether it’s used as an intermediate in drug discovery or involved in new material design, the presence of both the bromine atom and the pyrrolidone-1-yl group on the pyridine ring lets scientists branch out in several directions. Few other pyridines let you combine both electrophilic and nucleophilic substitution potential in a way that scientists find genuinely practical.

    There’s a reason chemists gravitate toward certain models. Take this compound’s chemical backbone: the attachment of a bromine at position 5 and a pyrrolidone-1-yl group at position 2 on the pyridine ring is intentionally designed. During cross-coupling reactions like Suzuki or Buchwald–Hartwig, this arrangement gives rise to opportunities for arylation or amination where other similar molecules might hit a wall. Over the years, as research needs have shifted from bulk synthesis toward targeted, high-value modifications, this dual-functionalized pyridine has stepped up.

    Why Specifications Matter

    For anyone who’s ordered chemicals on a tight research timeline, the importance of knowing exactly what you’re getting can’t be overstated. Purity matters most. Impurities can slow down a project or confuse results, and nobody wants to chase a ghost peak in their NMR spectra. Reliable suppliers publish typical purity levels for 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, often reaching 98 percent or higher. Appearance gives another clue; batches arrive as off-white to beige powder, which tells researchers something about how the batch handled both synthesis and purification.

    Hygroscopicity becomes relevant, especially in labs that lack advanced storage. Because this compound holds its structure well under ambient conditions—assuming you keep the lid on tight and the bottle dry—researchers avoid the headaches associated with frequent weighing errors or chemical degradation. In my own experience, running reactions for medicinal chemistry teams, I could always count on this molecule to arrive fresh and ready for use, not clumped from moisture or altered by air exposure. These qualities mean less troubleshooting and more progress—especially valuable when time runs short.

    Practical Uses in the Real World

    5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine hasn’t reached household status, but step into labs focused on pharmaceutical research, specialty materials, or advanced electronics and its fingerprint appears frequently. Medicinal chemists working in early-stage drug discovery lean on it during lead optimization. The pyrrolidone ring can mimic motifs found in biologically active compounds, making this molecule a flexible piece on the chessboard. When library synthesis calls for rapid analog construction, the bromine atom opens doors for swift halogen-metal exchange or cross-coupling to introduce diversity across a series of scaffolds.

    Polymer scientists test its potential as a functional monomer or linker, drawing on both the rigidity of the pyridine ring and the solubility boost from the pyrrolidone. Some colleagues working in optoelectronic materials highlight its utility in crafting new ligands and templates for metal coordination. At the bench, what stands out is how cleanly this molecule supports transformations—even under a range of catalyst loads and temperature regimes—making it fight above its weight in both academic and industrial research.

    What Sets It Apart From Other Substituted Pyridines?

    To appreciate what makes 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine distinct, it helps to compare it to close relatives, like simple 2-bromopyridine or 5-bromo-2-aminopyridine. Basic pyridines with only halogen substitution can undergo coupling, but they rarely deliver the extra dimension that the pyrrolidone group brings. Adding the lactam ring at position two shifts both the electronic character and 3D shape of the molecule, which may improve solubility, change reactivity, or even impact how well a new compound interacts with its intended target.

    From the synthetic side, installing both substituents in just the right place can be a challenge; the fact that this product is now readily available saves researchers hours spent troubleshooting routes or purifying complex mixtures. Over time, I have seen plenty of projects rescued simply because a dual-functional intermediate like this was at hand. In a climate where every resource counts, ease of use and reliability carry real weight.

    Considering Quality and Supply Chain

    Trust builds over time. Several years ago, during a fast-moving collaboration, I ran into supply chain delays with a different pyridine derivative. Sourcing 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine ended up saving the project because the supplier stood by their lead times and ensured quality checks each time. For organizations governed by strict regulatory and scientific standards, details like batch-level certificates of analysis and transparent purity claims become key.

    While product datasheets provide numbers, the real measure comes from reproducibility. There’s no faster way to lose trust with a team than submitting inconsistent results. This compound, sourced from reputable vendors, rarely disappoints in that regard. Analytical data from industry and academic labs back up claims of stability, batch-to-batch uniformity, and clear compositional reporting.

    Applications That Push Boundaries

    Drug discovery isn’t the only arena where this compound earns its keep. In material science, subtle changes in a molecule’s layout can affect properties like conductivity, optical absorption, or catalytic activity. Colleagues in research institutions have used the pyrrolidone-1-yl group to attach metal ions or polymers, leveraging its chelating potential and hydrogen bonding ability. In high-performance coatings and specialty polymers, the combination of a brominated aromatic and a heterocycle opens the door to application spaces that simple pyridines just don’t reach.

    Students learning organic synthesis value hands-on experience with compounds offering multiple transformation points. This particular molecule features in published procedures on C–N bond formation, palladium-catalyzed cross-couplings, and regioselective functionalization. Experienced chemists know the frustration when an academic synthesis falls apart at scale; access to intermediates like 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, with reliable purity, simplifies the troubleshooting process and brings more predictable results.

    Safety, Transparency, and Responsible Handling

    Safe handling always takes center stage, no matter how routine a reagent seems. Based on structure and available data, researchers expect brominated pyridines to demand the usual gloves, goggles, and fume hood care. With 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, teams appreciate clear, accessible safety data and transparent hazard communication. As more labs revisit their sustainability and safety policies, clear documentation and traceable production practices keep this compound within reach, even in settings committed to adopting green chemistry principles.

    During my own stints in academic teaching labs, timely provision of clear safety protocols along with every new reagent gained students’ buy-in far more than generic warnings ever could. As regulatory expectations for hazardous materials evolve, suppliers who pair their product with well-maintained documentation help protect both researchers and downstream environments. This level of attention to detail strengthens confidence in adopting new research tools.

    What Could Be Improved?

    The best products aren’t those that stay static, but those that adapt to new scientific demands. As high-throughput screening accelerates in many chemical research fields, there’s growing interest in packaging sizes that serve both large-scale campaign and rapid-hit exploratory work. Researchers working with 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine have voiced a preference for available multi-gram and small milligram options, allowing fine-tuned control without excess waste.

    Another area for improvement involves transparency around the environmental footprint of synthesis routes. The chemical industry faces rising pressure to reduce solvent waste, energy consumption, and hazardous byproducts. Drawing on my own experience, labs increasingly ask for supplier data on green synthesis protocols and responsible sourcing—not just performance specifications. By forming partnerships with chemical manufacturers who invest in sustainable production, the research community can align day-to-day lab practices with global sustainability targets.

    At the same time, rapid communication channels between researchers and suppliers allow emerging needs to be met. Whether it’s feedback on batch consistency or requests for alternative container types, the vendors most committed to supporting scientific progress stand out for their willingness to engage and evolve.

    Potential for the Future

    Chemistry marches ahead by building on proven tools and pushing beyond them. 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine looks set to stay relevant as research priorities change. In the medicine of tomorrow—where treatments grow more targeted and molecules more complex—there will be a place for flexible, dual-functional intermediates. Material scientists seeking next-generation displays, sensors, or catalysts rely on innovation not just in concepts, but in the fundamental reagents available to them.

    Staying connected with those on the frontlines of research, whether in university labs, startups, or global pharmaceutical organizations, helps both sides gain clarity on what works, what needs to change, and how new ideas can take root. This process, driven by both curiosity and practical need, shapes the way everyday chemicals like this one lead to remarkable discoveries—often out of the limelight, but with real impact.

    When I look back on projects where progress came swiftly and safely, it’s clear that reliable access to complex intermediates did far more than save a few steps. It gave teams the confidence to try new things and follow promising leads. As chemistry keeps evolving, it’s the products that bridge gaps between old and new, simple and advanced, that will keep scientists coming back. 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, through its thoughtful design and proven performance, fits the bill.

    Focus on Evidence and Expertise

    Building trust in any chemical product—especially one crossing from academic studies into industrial production—relies on evidence. Published research, supplier validation, and peer-to-peer recommendations all factor in. Over time, published literature has mapped out the functional space for 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, highlighting both the breadth and specificity of its use. Companies and universities choose to keep this intermediate stocked not just for one-off reactions but because it repeatedly solves common challenges. Reports in respected journals point to its versatility in forming carbon–nitrogen and carbon–carbon bonds, its role in building heterocyclic compounds, and its participation in structure-activity relationship studies.

    Drawing from my years in both bench chemistry and project management, the number one request from colleagues remains straightforward: reduce surprises, deliver what’s promised, and share what’s learned. This chemical, by answering those requests, offers both a lesson and a model for what makes a research product genuinely valued.

    Summary of Key Considerations

    5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine stands as more than a product code or an obscure catalog entry. By pairing precise functional groups on a reliable scaffold, it brings something valuable to a crowded field—enabling new chemistry, supporting breakthrough ideas, and reducing friction in everyday research. The edges where its behavior differs from standard pyridine derivatives appear in cleaner transformations, better yield reliability, and the expanded reach for medicinal, materials, and analytical discoveries.

    Quality, transparency, and responsiveness to evolving research goals keep this compound relevant. The more researchers, suppliers, and educators focus on these principles, the better the outcomes across the field. My own experience echoes what many have found: the right chemical tool, well-made and well-documented, can be the difference between stalled ideas and real progress. 5-Bromo-2-(Pyrrolidone-1-Yl)Pyridine, in practical use and in practice, brings these ideals within reach.