3-Amine-2-chloropyridine

    • Product Name: 3-Amine-2-chloropyridine
    • Chemical Name (IUPAC): 3-Amino-2-chloropyridine
    • CAS No.: 372-39-4
    • Chemical Formula: C5H5ClN2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    870535

    Name 3-Amine-2-chloropyridine
    Iupac Name 2-chloropyridin-3-amine
    Molecular Formula C5H5ClN2
    Molecular Weight 128.56 g/mol
    Cas Number 87118-68-7
    Appearance Yellow to brown crystalline solid
    Melting Point 82-85°C
    Boiling Point 271°C
    Solubility In Water Slightly soluble
    Density 1.30 g/cm3
    Refractive Index 1.592
    Synonyms 3-Amino-2-chloropyridine, 2-Chloro-3-pyridinamine
    Smiles C1=CC(=NC(=C1)Cl)N
    Inchi InChI=1S/C5H5ClN2/c6-5-4(7)2-1-3-8-5/h1-3H,(H2,7,8)

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

    Packing & Storage
    Packing 250g of 3-Amino-2-chloropyridine is supplied in a sealed amber glass bottle with a secure screw cap and hazard label.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-Amino-2-chloropyridine typically involves secure drum packaging, maximizing space, ensuring safety, and preventing contamination.
    Shipping 3-Amino-2-chloropyridine is shipped in tightly sealed containers to prevent moisture and air exposure. It is transported under standard conditions, with proper labeling for hazardous materials. Packaging complies with relevant regulations, ensuring safe handling and minimizing the risk of leaks or contamination during transit. Protective equipment is recommended during unpacking.
    Storage 3-Amino-2-chloropyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture and light. Proper labeling and secondary containment are recommended to prevent accidental release and ensure safe handling. Use personal protective equipment when handling.
    Shelf Life 3-Amino-2-chloropyridine is stable under recommended storage conditions; shelf life is typically two to three years in sealed containers.
    Application of 3-Amine-2-chloropyridine

    Purity 99%: 3-Amine-2-chloropyridine with Purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Molecular Weight 130.56 g/mol: 3-Amine-2-chloropyridine with Molecular Weight 130.56 g/mol is used in agrochemical production, where it allows precise formulation and target compound compatibility.

    Melting Point 58°C: 3-Amine-2-chloropyridine with Melting Point 58°C is used in chemical research, where it enables controlled reaction conditions and repeatable crystallization.

    Stability Temperature up to 120°C: 3-Amine-2-chloropyridine with Stability Temperature up to 120°C is used in active pharmaceutical ingredient manufacturing, where it maintains chemical integrity during thermal processing.

    Particle Size ≤10 µm: 3-Amine-2-chloropyridine with Particle Size ≤10 µm is used in fine chemical synthesis, where it improves solubility and reaction uniformity.

    Viscosity Low: 3-Amine-2-chloropyridine with Low Viscosity is used in catalyst development, where it enables easy mixing and efficient catalyst-support interaction.

    Water Content ≤0.5%: 3-Amine-2-chloropyridine with Water Content ≤0.5% is used in electronic materials fabrication, where it minimizes hydrolytic side reactions and defect formation.

    Assay ≥98%: 3-Amine-2-chloropyridine with Assay ≥98% is used in dye synthesis applications, where it provides reliable chromophore formation and color stability.

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    Certification & Compliance
    More Introduction

    Introducing 3-Amino-2-chloropyridine: A Reliable Choice for Precise Chemical Synthesis

    3-Amino-2-chloropyridine isn’t the type of compound you stumble across in any old stockroom. It stands out as a specialty intermediate—its profile fits a range of synthetic needs, especially for folks and teams focusing on pharmaceuticals, agrochemicals, and advanced organic construction. Anyone who's had to juggle multiple steps in a project knows how a single, dependable reagent can save time, cost, and headaches. With its specific arrangement—a chlorine atom nested beside an amine on the pyridine ring—this compound goes beyond generic building blocks, inviting targeted reactivity that's tough to find elsewhere.

    Chemical work rarely offers the luxury of do-overs. Precision at the bench means more than good scales or careful pipetting. Back in grad school, I remember facing a project with unpredictable yields, day after day. Much of that came down to the unpredictability of intermediates. Drawing from those long nights, the value of a product like 3-amino-2-chloropyridine comes into sharp relief. The compound provides a high-purity starting point—typically at 98% or better—giving peace of mind through every step. You run reactions knowing you’ve reduced one big source of possible error.

    The specifications matter—sometimes more than buyers realize. For 3-amino-2-chloropyridine, a molecular weight of about 128.55 g/mol isn’t just a number on a label. That weight, the distinct pale yellow powder, its melting point above 65°C, signals you’re working with a specific physical identity that’s easy to recognize and track. Low moisture content protects sensitive transformations, especially nucleophilic aromatic substitution or cross-coupling reactions, which remain vital for assembling the complex scaffolds demanded by modern drug and crop-protection science.

    During my years in industry, research budgets were always tight. The nature of the job meant searching for compounds that performed reliably, again and again. 3-Amino-2-chloropyridine has found a permanent place on project lists, not just for its function but for its manageable handling. In the storeroom or on the bench, its composition stays stable in the original sealed packaging, with minimal tendency to cake or degrade over reasonable timescales. This stability translates into fewer wasted experiments and less need for repeat orders—small efficiency gains that add up over time, especially in larger R&D facilities.

    Benefits for Precision Synthetic Routes

    3-Amino-2-chloropyridine isn’t another simple amine or generic chloropyridine. Its unique structure lets chemists access a territory closed off to other, less-selective reagents. The amine works as a key nucleophilic center, opening reactive doors for classic transformations—think acylation, sulfonylation, or even urea formation—while the chloride at the 2-position gears up the ring for Suzuki, Buchwald-Hartwig, or other modern coupling reactions. Having seen more than a few disappointed faces after a failed multi-step run, I’ve come to respect intermediates that pull their weight across different mechanisms.

    Pharmaceutical chemists, especially those running structure-activity relationship (SAR) studies on heterocyclic cores, appreciate how this compound helps diversify libraries quickly. Since regulatory submission deadlines rarely show mercy, a reliable intermediate allows teams to build candidate molecules without last-minute surprises. Regulatory filings and audit trails depend on the quality and traceability of such intermediates. Missing out on the right compound at this crucial stage can derail timelines and budgets.

    In agricultural chemistry, too, rapid shifts in regulatory policies and pest resistance prompt the need for scalable, adaptable synthesis. The ease of derivatizing both the amine and the chloro positions feeds growing demand for new leads. 3-Amino-2-chloropyridine carries just the right combination of electronic and steric properties to open doors for both direct and stepwise elaboration—a distinct edge over simpler pyridines, which often lack the necessary functionality or selectivity for certain routes.

    Difference from Other Products: Real-World Advantages

    A lot of buyers end up asking if there’s any real difference among similar-looking intermediates. After testing both 3-amino-4-chloropyridine and 2-chloro-5-aminopyridine in assorted routes, the answer comes quickly: small structural shifts can make or break a scheme. With 3-amino-2-chloropyridine, the adjacency of the two groups makes new bonds possible in ways that aren’t accessible with isomers, especially where subtle electronic effects dictate the fate of a reaction. It's easy to overlook the value until a reaction gives a surprise product, forcing someone to trace the mistake back to their starting material.

    Suppliers play into this too. Over the years, I’ve watched projects struggle with inconsistent batches—impurity spikes, particle size shifts, unexplained color changes. 3-Amino-2-chloropyridine’s typical sourcing routes offer far greater reproducibility because established synthetic methods—often rooted in robust Chichibabin protocols or direct amination—have been honed for industrial reliability. A secure, documented provenance keeps things above board for compliance and downstream trading.

    The handling profile brings extra confidence as well. The solid, crystalline nature is less prone to dust issues—plenty of us still shudder at the memory of inhaling volatile amines during scale-ups. Simple containment works, and thanks to its specific moisture content and thermal properties, it resists sticking together or turning into a mess under reasonable storage conditions. That makes it friendly not just for analytical staff, but also for operators unfamiliar with exotic heterocycles.

    Field Experience: Problems Solved by Reliable Intermediates

    Some years ago, our lab got tasked with building a series of kinase inhibitors—each cycle brought pressure to cut synthesis time. Early on, our first-choice starting material arrived with poor documentation and strange off-white chunks. We lost days, even weeks, cleaning up samples and running additional analytics. Switching to a reputable batch of 3-amino-2-chloropyridine—backed by real, verifiable assay reports and clear melt profiles—practically cut those headaches out. The difference showed up in yields and purity, but more than that, it restored trust in the process. Project managers like to focus on milestones; chemists stress about real-world surprises. Both groups sleep better once the starting materials actually perform as advertised.

    As for students or early-career staff, consistent intermediates mean less wasted time troubleshooting unexplained variances. The biggest payoff comes over the long haul: smaller error bars, faster optimization, and clear documentation for every regulatory audit. Choosing the right compound at the outset rarely grabs headlines, yet those decisions shape the full arc of discovery and development.

    Going Beyond One Reaction: Scale, Health and Safety

    Any chemist working at larger scale pays attention to more than just reaction yields. Occupational safety and environmental impact matter more as quantity increases. 3-Amino-2-chloropyridine’s relatively low volatility and consistent particle form reduce airborne exposure. Handling the powder under a fume hood, rather than risking splashing of concentrated acids or obscure dichlorides, keeps procedures direct. Reliable safety data from established testing (such as published LD50 references and compatibility lists) allows supervisors to design clear risk protocols. In my experience, familiarity with a reagent reduces accidents. Knowing how 3-amino-2-chloropyridine behaves in humid or warm conditions lets staff store and handle it with confidence, instead of wasting time learning from minor spills or inconsistent off-gassing.

    On waste minimization, the compound responds relatively well to standard destruction techniques; chlorinated heterocycles can be a pain in terms of environmental handling, but published data confirm simple, cost-effective strategies for most facilities. If management wants lower EHS costs, this matters. I’ve seen projects hit brick walls with more troublesome precursors, especially where local waste contractors balk at handling unknowns. Here, traceability and routine practices make disposal smoother, and audited trails keep compliance officers satisfied without endless piles of paperwork.

    Supply Chain and Traceability in the Modern Marketplace

    Supply chain disruptions have hit chemical projects hard. The difference between a trusted, pure intermediate and a variable, little-documented product can run into lost weeks—sometimes lost grant cycles. 3-Amino-2-chloropyridine has the advantage of being available from major distributors globally, usually accompanied by a COA and robust batch records. In practical terms, sourcing teams waste less time and fewer dollars hunting down rare compounds. For any therapeutic or high-value crop project, supply chain resilience underpins almost every timeline. What’s more, consistent batch identities simplify recordkeeping and regulatory readiness, shrinking the admin load for quality management teams.

    Remote work and tighter project cycles over the past few years put even more pressure on compound selection. More labs run lean—sometimes just a handful of scientists doing the work that teams twice their size used to handle. Reducing the risk introduced by unreliable intermediates protects both talent and capital.

    Solutions for Project Headaches: Practical Suggestions

    Over the decades, I’ve seen teams benefit most from three simple practices:

    The broader chemical landscape rewards this diligence. Teams that consistently secure high-quality intermediates move faster, waste less, and publish with greater confidence. For 3-amino-2-chloropyridine, these habits guard against the kind of low-level risks—contamination, degradation, last-minute substitutions—that can ruin innovation’s momentum.

    Maintaining Trust and Expertise for Better Outcomes

    Decisions at the bench ripple up and out. Every researcher depends on their materials to perform as described—no hidden moisture, no mystery polymorphs, no silent impurities gumming up the works. The reputation of 3-amino-2-chloropyridine within the synthetic community rests not only on data sheets, but on the lived experience of chemists, who test each claim and pay the price for shortcuts. Whether in a teaching lab, a startup, or a large multinational, trust in an intermediate forms the backbone of productive work.

    Publication and regulatory submission cycles have only tightened since my early years in the field. Preclinical deadlines arrive fast; missed targets don’t wait for materials to catch up. Teams that standardize on well-documented, high-purity intermediates face fewer stumbling blocks later—project overviews for investors, application forms for agencies, and even everyday discussions with collaborators feel less stressful when one variable, at least, stays fixed.

    Transparency drives these advantages home. A COA with real testing data smooths communication with external auditors. Reliable labeling and batch traceability tie every experiment back to a material reality, protecting IP portfolios and enabling rapid troubleshooting when problems arise. Over dozens of projects, I’ve watched trust in materials turn into new therapies, greener crop controls, and more efficient labs. Each starts with smart purchases and careful verification at the intermediate stage.

    Comparing Precedents: Small Choices, Big Outcomes

    Colleagues often debate whether it’s worth the premium for a particular intermediate. The answer comes down to experience—the hidden costs that bubble up only after failed syntheses, missed readings, or mystery machine downtime trace back to suspect inputs. Time and again, specific intermediates like 3-amino-2-chloropyridine limit those headaches by making each subsequent step easier to debug and scale.

    Those who have worked with less-predictable materials know the frustration and expense of cleaning up after-the-fact. Solvent waste climbs, yields slide, and time ticks away on the project calendar. With high-quality intermediates, the focus shifts to the chemistry itself—novel transformations, streamlined purifications, bolder structure designs. In the balance between up-front cost and downstream reliability, the latter wins out once you’ve managed a few tight timelines or run up against unexpected regulatory hurdles.

    Responsible Sourcing in a Changing World

    As chemical sourcing grows more global, responsibility matters. The international reach of 3-amino-2-chloropyridine reflects both the product’s importance and the growing need for compliance across regions. Labs working across borders need consistent identities, unambiguous inventory, and trusted logistics to avoid legal or practical snags. Projects that start with the right intermediate handle future developments—patent filings, revalidations, tech transfers—with fewer headaches. Reliable intermediates reduce the urge to cut corners, maintain scientific integrity, and reinforce best practices in every transaction.

    From personal experience, projects that skimp on these fundamentals lose more than just money. Scientific culture, staff morale, and institutional memory all take a hit when an unreliable batch stalls momentum or introduces invisible risk. 3-amino-2-chloropyridine, sourced and managed by teams who understand these risks, ends up supporting not just good chemistry, but also good science—timely results, credible papers, and safe, healthy working environments.

    The Future of Intermediates and Their Expanding Role

    Innovations in drug discovery, crop improvement, and material science will keep pushing the demands placed on building-block reagents. Today’s workflows rely more than ever on intermediates that anticipate new types of chemistry—the need for fine-tuned reactivity, compliance with stricter safety standards, and easy adaptation to automation. 3-amino-2-chloropyridine carries a structure that fits current methodologies while offering enough flexibility to handle tomorrow’s advances. Its value echoes through the research chain, from ideation to real-world application.

    Smart organizations invest in reliable sourcing not just for immediate gains, but to protect the future of their science. Choosing 3-amino-2-chloropyridine isn’t about a one-time transaction; it’s about laying groundwork for discoveries that matter, while serving the needs of the next generation of innovators. That should mean safer labs, faster learning, and results the whole community can trust.