3-Bromo-2-chlorolpyridine

    • Product Name: 3-Bromo-2-chlorolpyridine
    • Chemical Name (IUPAC): 3-bromo-2-chloropyridine
    • CAS No.: 877399-52-5
    • Chemical Formula: C5H3BrClN
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    184474

    Chemical Name 3-Bromo-2-chloropyridine
    Cas Number 868128-41-2
    Molecular Formula C5H3BrClN
    Molecular Weight 192.44 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 207-209 °C
    Melting Point -9 °C
    Density 1.7 g/cm³
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry, well-ventilated place
    Refractive Index 1.589

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

    Packing & Storage
    Packing 3-Bromo-2-chloropyridine, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Container Loading (20′ FCL) 20′ FCL (Full Container Load) for 3-Bromo-2-chloropyridine ensures secure, bulk transport, minimizing contamination and optimizing shipping efficiency.
    Shipping 3-Bromo-2-chloropyridine is packaged in airtight, chemical-resistant containers to prevent leaks and contamination. It is shipped in compliance with regulations for hazardous materials, labeled appropriately, and handled by certified carriers. The shipment includes safety documentation and instructions, ensuring secure delivery to laboratories or industrial facilities. Store in a cool, dry place upon receipt.
    Storage 3-Bromo-2-chloropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to trained personnel. Store at room temperature unless otherwise specified by the manufacturer’s guidelines.
    Shelf Life 3-Bromo-2-chloropyridine typically has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container.
    Application of 3-Bromo-2-chlorolpyridine

    Purity 98%: 3-Bromo-2-chlorolpyridine (Purity 98%) is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal impurity formation.

    Molecular Weight 192.44 g/mol: 3-Bromo-2-chlorolpyridine (Molecular Weight 192.44 g/mol) is used in agrochemical research, where precise molecular mass supports accurate formulation development.

    Melting Point 40-43°C: 3-Bromo-2-chlorolpyridine (Melting Point 40-43°C) is used in solid-state reactions, where its defined melting behavior allows for controlled process scalability.

    Stability Temperature up to 80°C: 3-Bromo-2-chlorolpyridine (Stability Temperature up to 80°C) is used in high-temperature synthesis protocols, where chemical stability ensures consistent product quality.

    Low Moisture Content (<0.5%): 3-Bromo-2-chlorolpyridine (Low Moisture Content <0.5%) is used in moisture-sensitive coupling reactions, where reduced water content prevents side reactions.

    Particle Size <100 µm: 3-Bromo-2-chlorolpyridine (Particle Size <100 µm) is used in catalytic processing, where fine granularity enhances dispersion and reactivity.

    Assay ≥99%: 3-Bromo-2-chlorolpyridine (Assay ≥99%) is used in fine chemical manufacturing, where high assay guarantees reliable batch-to-batch consistency.

    Residual Solvent <500 ppm: 3-Bromo-2-chlorolpyridine (Residual Solvent <500 ppm) is used in electronic material synthesis, where low residual solvent levels minimize contamination.

    Free Quote

    Competitive 3-Bromo-2-chlorolpyridine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 3-Bromo-2-chloropyridine: Applications, Real Differences, and What Matters Most

    Digging Into 3-Bromo-2-chloropyridine

    Chemistry changes the world every day, but those of us who work in laboratories or partner with synthesists know not every compound stands out for the same reasons. 3-Bromo-2-chloropyridine brings its own strengths to the table. This compound, carrying a bromine at the 3-position and chlorine at the 2-position on a pyridine ring, isn’t just another entry in a catalog. The fine-tuned halogen substitutions open doors for selectivity and unique reactivity – and that sets it apart for chemists who care about yields, cleaner workups, and more targeted transformations.

    From my own experience in organic synthesis projects, real value comes from the subtle differences that shift an outcome from “it worked” to “there’s less byproduct, less purification headache, and better reproducibility.” If you’ve ever spent nights troubleshooting a step in a medicinal chemistry route, you appreciate that choice of building blocks can make or break a project. 3-Bromo-2-chloropyridine is one of those small molecules that pulls more than its weight thanks to its substitution pattern and how that influences cross-coupling and nucleophilic aromatic substitution.

    Chemical Identity in the Lab

    The core of this product rests on the pyridine ring, modified with a bromine at carbon 3 and a chlorine at carbon 2. This structure gives the molecule versatility rarely matched by more common halogenated pyridines. Its pale yellow appearance tells you you’re dealing with a fairly pure sample, and its melting point and solubility lend themselves well to handling and measuring in research settings. I’ve watched skilled chemists shorthand this as “3-Br-2-ClPyridine” in lab meetings, recognizing a reliable building block for both early-stage research and scale-up.

    How 3-Bromo-2-chloropyridine Finds its Place

    The usage story isn’t theoretical; it’s shaped by the real work carried out by researchers trying to build new compounds with pharmaceutical or agrochemical potential. Ask a synthetic chemist looking to introduce diversity on a pyridine core, and you’ll see this molecule pop up. Its reactive positions let it serve in Suzuki or Stille coupling, providing access to complex heteroaromatics. The combination of bromine and chlorine, each with different leaving group tendencies and reactivity profiles, invites strategic transformations that can’t always be achieved with single-halogen analogues.

    I’ve seen projects where switching to this compound from a simple 2-chloropyridine cut down not just on the number of steps to the target molecule, but on the formation of stubborn byproducts. Anyone who’s had to purify a mixture containing dozens of aromatic side-products understands the relief that brings. The reliability of the aryl halide positions helps teams move forward without going in circles after every reaction.

    Setting It Apart: More Than a Chemical Name

    A lot of companies offer halogenated pyridines, but the trick is knowing what actual difference it makes in a reaction. With 3-bromo-2-chloropyridine, the dual halide pattern serves as more than a naming gimmick. That extra point of reactivity translates to more options in palladium-catalyzed coupling chemistry. Bromine tends to participate in Suzuki reactions under milder conditions than chlorine, and having both on a single ring presents a path for sequential transformations. The more standard 2-bromopyridine or 2-chloropyridine offer reactivity that can be either too aggressive or too sluggish for some targets. The sweet spot is what synthetic chemists come looking for.

    On paper, specifications play a role, but living through a synthetic sequence tells you more. I recall a project where the route relied on making a heteroaromatic scaffold destined for kinase inhibitor development. The flexibility granted by having both halide groups significantly reduced the need for protection-deprotection steps. That’s the sort of advantage that project managers, bench chemists, and ultimately those downstream in discovery value — faster iterations, fewer purification headaches, and less risk tied to tricky reaction intermediates.

    How Specifications Shape What Really Matters

    Real-world quality starts before a bottle ever lands on your bench. Trusted suppliers offer 3-bromo-2-chloropyridine with tight control over purity, making sure side-products or moisture don’t sneak into demanding reactions. For research, a purity of 98% or higher means fewer worries about unexpected outcomes. Melting point and spectral data let researchers double-check identity — something that those who’ve run into swapped or mislabeled chemicals know to never skip.

    In practice, I’ve lost count of peer discussions centered on recrystallized lots and batch consistency. Stability under normal storage conditions means one less thing to worry about in day-to-day activities. That reliable stability also makes shipping and long-term projects smoother, since no one enjoys surprises after weeks or months of storage. Those details may not make it into published reports, but they quietly support every successful synthesis.

    From Bench to Beyond: Where 3-Bromo-2-chloropyridine Ends Up

    The story doesn’t end at the first transformation. Medicinal chemists aiming for novel drug candidates, agrochemical researchers chasing new pest control agents, fine chemical companies pushing for specialty material innovation — they all value building blocks that enable both flexibility and precision. 3-Bromo-2-chloropyridine’s structure gives researchers leeway to elaborate structures without reinventing the wheel for each analog.

    Life at the bench often surprises you. One day you’re following a trusted protocol, the next you’re troubleshooting a stubborn coupling, and sometimes, it all comes down to the choice of starting material. This molecule’s compatibility with both classical and transition-metal-catalyzed processes means new routes can open as teams pursue unexplored chemical space. Pinning down novel heterocycles, modifying bioactive scaffolds, or streamlining process chemistry protocols — the reach extends from discovery to development.

    Bringing More Out of Each Gram

    The value of any chemical comes down to how many problems it solves for those using it. 3-Bromo-2-chloropyridine delivers flexibility by letting chemists pick which halide group to react first, applying conditions best suited to each transformation and letting what’s needed guide the sequence. In a market crowded with options, this dual-halide approach often translates to new ways to create derivatives that would otherwise involve long, clunky synthetic steps. The result is a more direct path — faster, more efficient, and often more sustainable in terms of solvent and reagent use.

    From hands-on experience in pharmaceutical research, compromising on starting material can ripple down the line. Unexpected impurities, unpredictable reactivity, and scale-up uncertainties all stem from early decisions. Working with well-documented, high-purity batches of 3-bromo-2-chloropyridine means more accurate yield predictions and less troubleshooting, especially when precious time or expensive intermediates are involved.

    The Details Users Really Ask About

    Most researchers, especially those deep in organic synthesis, care about more than just a chemical’s name or formula. True utility shows up in side-by-side tests: Is the product consistent from batch to batch? Can you trust the spectral data? Do other components in the bottle interfere in your downstream chemistry? Those matters draw a sharper line between theoretical and practical utility.

    Several projects have faced frustrating bottlenecks from lot-to-lot variation or poorly documented materials. That isn’t just a nuisance — it can mean project delays, thrown-away syntheses, and hard-to-explain outliers in data. The importance of working with a reliable source for 3-bromo-2-chloropyridine becomes clear in critical situations, like producing reference standards or developing APIs that must comply with demanding validation protocols.

    Trust, Documentation, and Transparency

    Quality isn’t something that happens by accident. Producers committed to lab-grade materials provide up-to-date analytical reports and thorough technical documentation. Certificates of analysis, NMR, IR, and mass spectral data help researchers verify that what they ordered matches what arrived. Anyone who has run quality control checks knows peace of mind counts, especially when scaling a reaction from milligram to multi-gram quantities or handing off materials to another team.

    More transparency in chemical supply chains helps everyone — in procurement, compliance, laboratory management. Trust builds over time through consistency and open communication about what’s in the bottle and what isn’t. Having run my share of control reactions and analytical checks, I’ve learned it's worth investing in suppliers with a solid record of transparency around their batches of 3-bromo-2-chloropyridine.

    What Sets 3-Bromo-2-chloropyridine Apart from Similar Products

    The difference between this product and similar compounds rests on its ability to combine two halogen atoms with distinct chemical personalities on a single aromatic ring. Single-halide pyridines like 2-chloropyridine or 3-bromopyridine offer either selectivity or reactivity, rarely both. By putting both on the same molecule, chemists gain an option to approach substitutions and cross-couplings in more diverse sequences.

    For example, tandem coupling reactions become possible without separate protection and deprotection steps. You can introduce one set of substituents through the bromine, then take care of the chlorine to install another group altogether. In practice, that supports efficient diversification of compound libraries — an asset for structure-activity relationship studies and for speeding up the lead optimization stage in pharmaceutical development.

    Addressing Challenges and Improving Access

    3-Bromo-2-chloropyridine’s story isn’t solely about what it achieves in a flask. Like all specialty chemicals, there can be supply chain hiccups, regulatory hurdles, and occasional concerns about environmental impact. Researchers and sourcing managers wake up to reality if a crucial batch is delayed or a producer tightens regulations. Smoother supply, better communication from suppliers, and careful planning are the practical antidotes.

    Commitment to greener sourcing, including certified processes and reduced-waste production, supports broader goals of safety and sustainability in chemical research. The world of specialty pyridines continues to evolve, driven by customer feedback and new applications, so producers who invest in process improvements and documentation win the trust of research communities worldwide.

    Solutions for Reliable Access and Results

    Better procurement means looking beyond cost and focusing on supplier reputation, transparency, and responsiveness. Groups conducting screening campaigns or scale-up often benefit from establishing long-term supply arrangements. Sharing feedback on consistency and purity also nudges producers to tighten their quality practices. From my own laboratory experience, proactive outreach to customer support can uncover critical technical details that go unmentioned in published brochures, making a real difference in troubleshooting or optimizing synthetic plans.

    Educational outreach, including open workshops and seminars, arms researchers with knowledge on proper storage, handling, and safest reaction conditions. Trading tips and lessons learned on research forums and at conferences often opens new avenues for product application, streamlines troubleshooting, and encourages collaborative problem-solving. The compound’s future utility will only expand as chemists share insights and successes, refining its role in cutting-edge research.

    Real-World Applications: Seeing Beyond the Label

    The leap from chemical bottle to real application maps onto the stories of discovery and innovation in laboratories around the globe. 3-Bromo-2-chloropyridine’s influence appears in patents and journals describing new therapeutic agents, improved agrochemicals, and custom materials — all shaped by how chemists string together reactions using versatile starting points. Its adaptability gives project teams leeway to try more direct approaches, cut down on operational steps, and sometimes push research forward in unexpected directions.

    Conversations in project rooms, feedback from scale-up teams, and reports from process chemists all point to the difference made by well-chosen building blocks. Each batch used in real research adds to the evidence bank, guiding future decision-making and product selection. Project leads looking to cut development timelines and reduce synthetic risk come back to options like 3-bromo-2-chloropyridine for good reason — it has proved itself in the crucible of challenge and troubleshooting.

    Looking Ahead: Ongoing Evolution and Potential

    As the needs of the chemical and pharmaceutical industries grow, so does the expectation for building blocks that deliver on reliability, flexibility, and traceability. 3-Bromo-2-chloropyridine’s legacy rides on real successes and lessons learned in the laboratory. Next-generation applications, powered by advances in catalysis and high-throughput synthesis, will likely find new uses for this deceptively simple molecule.

    Chemists seeking to stretch each gram further and tackle bigger challenges will continue to demand clear documentation, consistency, and creative support from suppliers. Close engagement between end-users and producers smooths the way for improvements both in product quality and the broader practices around laboratory safety, compliance, and sustainability. From my perspective, working in collaboration with trusted sources unlocks the kind of progress that everyone in research hopes to achieve.

    Experience-Grounded Recommendations

    Choosing the right version of 3-bromo-2-chloropyridine for a project comes down to understanding past experience, evidence in published literature, and open feedback in research circles. Looking beyond technical specs, drawing on proven outcomes, and building a network of reliable supply chain partners become the foundation for ongoing breakthroughs. Project teams aiming for efficient, insightful chemistry will continue to grow their reliance on proven, trustworthy small molecules.

    In every successful synthesis, each step taken with confidence rather than accident gets us closer to real-world impact — whether it’s a new medicine, a safer crop protection agent, or an innovative material. 3-Bromo-2-chloropyridine, though not a household name, has earned its place in the hands of careful, inventive chemists ready to take on the next challenge.