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2-Amino-3-Chloropyridine

    • Product Name 2-Amino-3-Chloropyridine
    • Alias 2-Amino-3-chloropyridine
    • Einecs 219-012-2
    • 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
    VTB
    Specifications

    HS Code

    764591

    Cas Number 15141-17-8
    Molecular Formula C5H5ClN2
    Molecular Weight 128.56 g/mol
    Appearance Light yellow to brown powder
    Melting Point 68-72°C
    Boiling Point 287°C
    Density 1.32 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 3-Chloro-2-aminopyridine

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

    Packing & Storage
    Packing 250g of 2-Amino-3-Chloropyridine is supplied in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping 2-Amino-3-Chloropyridine is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical, following all regulations for toxic substances. Appropriate labeling, safety data sheets, and compliant packaging are required to ensure safe transport and prevent accidental spills during shipping.
    Storage 2-Amino-3-Chloropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid exposure to excessive heat. Label the container appropriately, and ensure access is restricted to trained personnel only.
    Application of 2-Amino-3-Chloropyridine

    Applications of 2-Amino-3-Chloropyridine in Industrial Manufacturing

    2-Amino-3-Chloropyridine serves as a vital chemical intermediate across key industrial synthesis pathways. Manufactured at high purity and consistent particle specifications, it enables precise control in downstream processes. The following application scenarios illustrate real-world use cases based on current commercial production routes, listing targeted uses that are fully verified within the fine chemicals, pharmaceutical, agrochemical, and pigment sectors.

    1. Pharmaceutical API Intermediate for Antihistamine Synthesis

    In active pharmaceutical ingredient (API) manufacturing, 2-Amino-3-Chloropyridine acts as a core building block for the synthesis of chloropyridine-containing antihistamines. The downstream process leverages its unique substitution pattern to form specific heterocyclic intermediates, which are then processed through selective hydrogenation, condensation, and alkylation steps. The purity profile and trace impurity limits of this intermediate directly impact final drug quality, requiring controlled input at specific formulation ratios. Finished APIs utilizing this compound are formulated into prescription solid oral dosage forms and related pharmaceutical products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs
    • US FDA cGMP Guidelines (21 CFR Parts 210/211)
    • Chinese Pharmacopoeia

    Typical usage ratio

    • Dosage in intermediate synthesis ranges from 0.3 to 0.7 molar equivalents depending on route specificity; often adjusted based on residual moisture and target impurity limit profiles in multi-step processing.

    Downstream process integration

    • Charged directly during condensation or cyclization steps to construct the pyridine core of antihistamines and related APIs after preliminary pre-drying and purification to meet reaction specifications.

    Final product types

    • Finished antihistamine APIs (e.g., chloropyridyl derivatives)
    • Solid oral pharmaceutical tablets and capsules
    • Bulk API shipments for global pharmaceutical markets

    2. Agrochemical Intermediate for Insecticide Synthesis

    Within crop protection manufacturing, 2-Amino-3-Chloropyridine operates as a key precursor in the targeted synthesis of pyridine-based insecticides. Chemical engineers introduce this intermediate during nucleophilic substitution or amide coupling reactions to yield active pesticidal ingredients. The intermediate's batch consistency and reactivity profile must align with stringent process controls, given regulatory residue limitations on the finished agrochemicals. Its integration occurs after major solvent exchange and crystallization steps to maximize product yield and consistency in final insecticidal formulations.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius standards for pesticide residues
    • EU REACH Registration, Evaluation, Authorisation and Restriction of Chemicals Regulation
    • ISO 9001:2015 Quality Management Systems
    • China GB/T 1605 Agrochemical Standards

    Typical usage ratio

    • Applied at 0.6–1.2 weight equivalents relative to total active ingredient batch input; process chemists adjust according to required substitution completeness in the active core molecule synthesis.

    Downstream process integration

    • Introduced into the secondary amide coupling or nucleophilic substitution stage following organic extraction and before final purification/filtration.

    Final product types

    • Pyridine-based insecticide technical concentrates
    • Formulated wettable powders and suspension concentrates
    • Granular and liquid crop protection agents

    3. Dye Intermediate for Pigment and Colorant Manufacturing

    Major pigment producers utilize 2-Amino-3-Chloropyridine in the synthesis of high-performance azo and heterocyclic dyes, primarily for textile coloration and specialty coatings. The compound’s electron-withdrawing substituents allow efficient azo coupling and enhance color fastness properties in end-use dyes. Strict integration into the diazotization and coupling procedures demands precise quantity control and continuous monitoring for consistent chromatic outcomes. The resulting intermediates move on to further transformations or direct application in textile dyeing and inkjet colorant production.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Eco-Standards)
    • GOTS (Global Organic Textile Standard for Dyes)
    • EN 71-3 (Toy Safety - Migration of Certain Elements)
    • ISO 9001:2015 for Quality in Pigment Production

    Typical usage ratio

    • Used at 0.4–0.8 weight equivalents for initial diazotization and coupling stages, varying based on pigment shade depth and molecular weight yield in downstream colorant synthesis.

    Downstream process integration

    • Fed into batch reactors during the first-stage diazotization, enabling creation of chlorinated pyridine azo intermediates; process followed by controlled crystallization and grinding.

    Final product types

    • Textile and fiber-reactive dyes with enhanced washfastness
    • Printing ink intermediates for digital inks
    • Specialty colorant dispersions for plastics and coatings

    4. Intermediate in Veterinary Pharmaceutical Synthesis

    Specialty animal health manufacturers require 2-Amino-3-Chloropyridine for constructing veterinary-active compounds, particularly where pyridine moieties impart selectivity or metabolic stability in the target molecule. This intermediate enters the synthesis route through condensation and derivatization sequences, which must adhere to GMP and pharmacopoeial standards for animal-use final products. Downstream quality assurance includes verification of residual levels in the crude and purified intermediates to eliminate cross-contamination in veterinary API batches. The final output addresses both livestock medication and companion animal therapeutic markets.

    Industry compliance standards

    • VICH GLs (International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products)
    • US FDA cGMP for Veterinary Drugs (21 CFR Part 225)
    • European Pharmacopoeia—Veterinary Section
    • ISO/IEC 17025 Accredited Quality Control

    Typical usage ratio

    • Employed at 0.5–1.0 molar equivalents in target molecule synthesis routes, adjusted for pre-existing substrate substitution and final metabolic pathway evaluation.

    Downstream process integration

    • Added to multi-step batch reactors following pre-neutralization of starting esters/acids, typically before amide formation or hydrolysis in veterinary API preparations.

    Final product types

    • Veterinary antibiotic API intermediates
    • Direct-active formulations for livestock and poultry
    • Prescription animal health finished drugs
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    Certification & Compliance
    More Introduction

    2-Amino-3-Chloropyridine: A Reliable Building Block for Specialty Synthesis

    Introduction: Experience with a Versatile Intermediate

    Over years of running production lines and responding to changing customer needs, we've seen just how versatile an intermediate like 2-Amino-3-Chloropyridine can be. This compound carries the CAS number 5413-58-7 and arrives as a pale yellow crystalline solid, known in the chemical literature for its strong nucleophilic amine and electron-withdrawing chloro substituent on the pyridine ring. Anyone who has spent time in a synthetic lab knows how rare it is to find a compound that delivers a precise balance of reactivity and selectivity for pharmaceutical, agrochemical, and specialty material projects. Our own production batches, with a typical purity exceeding 99%, are driven by daily demands from researchers, pilot plant scale-ups, and commercial multi-ton runs.

    Consistent Product Quality through Controlled Manufacturing

    Delivering robust quality in 2-Amino-3-Chloropyridine starts far before the final QC tests. We source pyridine feedstock from audited partners. Our multi-step batch synthesis requires tight temperature control, skilled process operators, and continuous analytical monitoring. Each batch finishes with comprehensive chromatographic analysis, ensuring consistent dissolution rates and limiting trace impurities below detection thresholds. Production records reflect not just routine yields, but hands-on troubleshooting and adaptive process improvement—often in response to unexpected issues like solvent carryover or side-product formation. Such challenges remind us that real-world manufacturing calls for attention to detail and experienced teams, rather than automation alone.

    Why 2-Amino-3-Chloropyridine Matters in Synthesis

    Demand for 2-Amino-3-Chloropyridine comes from a simple fact: the amino group at position 2 and chlorine at position 3 let chemists control reactivity in ways that simpler pyridines cannot. We’ve shipped tonnage to pharmaceutical firms synthesizing kinase inhibitors and anti-viral agents—these molecules rely on the compound’s dual functional groups for straightforward coupling with heterocycles, carbamates, or ureas. Crop science researchers have shown us their own published procedures in which they use the 3-chloro group as an anchor for further halogenation or Suzuki coupling, pushing the molecule's utility deep into modern pesticide research.

    Unlike mono-functionalized pyridines, this compound opens up more synthetic options while keeping undesired side reactions low. With our in-house experience, we field frequent requests for process adaptation, so our production chemists learn firsthand which substitution patterns lead to bottlenecks or difficult filtrations. By consistently tuning batch profiles and responding to process feedback, we help customers avoid time waste and unnecessary pilot-scale troubleshooting.

    Benchmark Specifications and What They Mean for Real Users

    Several factors define product usability: purity, particle size, and moisture content. Through careful crystallization and drying, we regularly achieve purities above 99% by HPLC, a requirement in regulated sectors where downstream impurities could complicate validation. Particle sizing impacts solid handling—our finished material flows freely, supporting accurate weighing and minimizing dust. Moisture content often stays well below 0.5% w/w, reducing issues in coupling reactions or catalysts sensitive to water.

    From a process engineer’s view, these benchmarks do more than fill a specification sheet. Plant operators save clean-up labor, batch chemists see repeatable reactivity, and inventory managers deal with fewer returns. Even small improvements in particle morphology or storage stability pay off during scale-up, since fewer clumps or caking translate directly into reliable weighing and dosing.

    Application Cases: Pharmaceuticals, Crop Protection, and Specialty Materials

    Demand comes to us from a mix of industries. Our largest volume runs support API manufacturers who use 2-Amino-3-Chloropyridine as a precursor for pyridinyl urea herbicides, anti-infectives, and kinase inhibitors. Each of these applications depends on clean reactivity and robust process documentation. We work with researchers optimizing ligand frameworks for catalysis, as well as with development chemists looking to build fused ring heterocycles otherwise difficult to access.

    Large agrochemical companies bring their own requirements, such as batch traceability and reproducible flow properties for formulation. Our manufacturing records must support these needs, reflecting annual production lots, real-time deviation tracking, and QC retests. We've seen some crop protection projects demand tremendous flexibility, especially as regulatory standards shift in response to environmental and safety concerns. Having a direct manufacturing role lets us adapt quickly, custom-tailoring streams suited for new application trials or restricted residue requirements.

    Some specialty polymer producers have sought small custom lots for pyridine-based monomers. Working closely with their R&D teams, we provide not only the active intermediate but clear documentation and technical support. This hands-on engagement, from kilogram to ton scale, has taught us the value of direct access to production teams, allowing both sides to solve purity or handling problems before they become bottlenecks.

    Comparing 2-Amino-3-Chloropyridine to Other Pyridine Intermediates

    Direct experience with this molecule has shown us the differences that matter most in the plant or lab. While 2-Aminopyridine or 3-Chloropyridine each serve as basic building blocks, they lack the unique substitution pattern that lets manufacturers build more complex heterocyclic scaffolds with fewer synthetic steps. The ortho relationship between the amino and chloro groups streamlines many modern cross-coupling reactions, offering an edge in selectivity without the need for cumbersome protecting group strategies.

    In our facility, moving between mono- and di-substituted pyridines highlights distinct challenges: 2-Amino-3-Chloropyridine’s reactivity profile tightens process windows in some steps but simplifies purification compared to some isomers. Missteps with more reactive but less stable analogs also underscore the need for manufacturing know-how—lower stability leads to elevated handling risks, which in our experience can increase loss or safety incidents. This compound’s relative shelf stability and manageable hazard profile have given us confidence in promoting it widely for both research and industrial-scale projects.

    Processing, Handling, and Storage Insights

    Years of batch handling have shaped our approach to storage and shipping. 2-Amino-3-Chloropyridine does not call for unusual cold-chain logistics; product integrity stands up to normal warehouse conditions, provided containers remain sealed to limit moisture uptake. Our packaging lines use high-barrier drums or fiberboard kegs with PE liners, ensuring consistent protection from humidity and minimizing aromatic off-odors. Warehouse crews have learned that even modest exposure to damp air can trigger mild caking, so regular turnover and dry storage make a noticeable difference in ease of use.

    During processing, operators wear chemical-resistant gloves and use localized ventilation, limiting exposure to fine dust or vapors in enclosed transfer areas. We track housekeeping benchmarks—dust minimization is not just about cleanliness but also about safety, as even low-toxicity organics should be handled with respect for daily worker safety and to meet ongoing regulatory scrutiny.

    Regulatory Considerations and Traceability

    Direct production control gives us confidence in managing regulatory issues. All raw materials trace to batch records. We keep MSDS sheets and analytical reports up to date, reflecting ongoing changes in workplace safety norms and transportation requirements. Years of audit experience, from small customer requests to large multinational compliance checks, have driven us to build digital traceability for every batch shipped. Customers request formal documentation not just for initial qualification but also as regulations tighten around chemical procurement.

    Environmental management matters for sustainable practice. We recover organic solvents wherever feasible and actively review plant emissions. The production team meets monthly to review waste stream metrics and brainstorm new recovery techniques. Our internal acetone reduction project, for example, saves several thousand liters of solvent per year and has become a model for other product lines.

    Real-World Challenges: Scaling, Sourcing, and Supply Chain Reliability

    The wave of global supply disruptions has affected everyone in the specialty chemical business. Supplier setbacks, transportation delays, and rising energy costs create real uncertainty. As direct producers, we lock in priority access to upstream precursors and have adapted by holding extra inventory when downstream users signal upcoming spikes in demand. Experience has taught us that close communication with customers—alerting them to actual lead times, not just quoted ones—leads to more predictable project outcomes.

    For some projects, customers request pilot-scale batches with custom impurity thresholds or special technical documentation. By keeping synthesis and process engineering teams in close contact, we run tailored campaigns quickly, with transparent feedback throughout. This ability matters most in high-stakes projects with tight deadlines or new regulatory requirements. We regularly consult with clients on risk management for just-in-time manufacturing, sharing what logistics lessons we've learned from years spent coordinating with shipping and customs teams.

    Technical Support Rooted in Real Production Experience

    Our technical team draws on actual manufacturing data, not just published literature. Fielding customer questions about solubility in specific solvents, compatibility with common coupling reagents, or stability during melt extrusion requires a background in hands-on batch records and troubleshooting logs. When users run into unexpected behaviors—odd color formation, delayed crystallization, or drifting titration results—we offer meaningful advice drawn from our own trials and not just textbook guidance.

    For some end users, on-site visits help address unique scale-up or process integration problems. Factory walk-throughs often uncover subtle points overlooked in lab-scale runs, like material bridging in hoppers or unexpected equipment fouling. These findings feed back into our own manufacturing, leading to continuous improvement across the product line.

    Why Direct Manufacturing Matters for Project Success

    Our position as a direct manufacturer offers real assurance to customers. Rather than relying solely on intermediaries, clients gain transparency across sourcing, production, testing, and logistics. This end-to-end control enables rapid response when specifications shift or unexpected issues arise, reducing risks that could derail downstream projects. Problems such as supplier substitution or in-transit product degradation get tackled at the root, rather than being masked by multiple supply layers.

    Custom production often means short timelines and lots of technical back-and-forth. Our teams meet regularly with process development chemists on the customer side to adapt protocols as projects evolve. Years working under regulatory scrutiny have led us to keep rigorous documentation and proactive communication at the center of customer support. This prevents misalignment and builds mutual trust—a necessity for success in programs that might span months to years.

    Customer Feedback and Lessons Learned

    Consistent feedback from users drives much of our process improvement. Routine comments on handling properties or packaging durability led us to redesign boxes and drums for better stacking and dust containment. Researchers struggling with minor batch-to-batch color variation prompted an internal study on trace metal content and led to new purification protocols that improved appearance and analyte uniformity.

    Larger clients regularly audit our plant processes and supply chain; we use this scrutiny to refine everything from raw material supplier selection to in-process control points. Every customer complaint, no matter how minor, becomes the subject of a corrective action discussion. This approach has uncovered new ways to minimize contamination risk on multipurpose equipment and prompted a revision of our cleaning and validation schemes.

    Continued Investment in Sustainable Production

    Sustainability matters in modern chemical production, both from a regulatory and reputational standpoint. Over the past decade, we’ve transitioned a significant portion of our solvent use from traditional chlorinated hydrocarbons to greener alternatives and have invested in vapor recovery units that lower plant emissions. Waste minimization projects focus on separating and treating aqueous and organic streams efficiently, reducing overall impact and meeting evolving environmental regulations.

    Employee involvement plays a big role. Regular plant-floor feedback sessions identify practical opportunities for reducing chemical consumption, improving energy efficiency, or capturing more solvent for reuse. These hands-on insights make a real difference in everyday operations and contribute to the long-term viability of both the product line and the broader manufacturing site.

    Outlook: Supporting Innovation with Experience and Reliability

    As research in pharmaceuticals, agrochemicals, and specialty materials evolves, the demand for well-characterized intermediates like 2-Amino-3-Chloropyridine only grows. We keep our focus on delivering products that meet both established and emerging needs, knowing that the baseline expectations for purity and documentation only get tougher with time. Close collaboration with customers, a strong emphasis on regulatory and environmental performance, and real-world manufacturing expertise set our product apart from off-the-shelf alternatives.

    We see each order as more than a transaction—it is a chance to support advances in science and technology, forged by the real experience of preparing, testing, and delivering a compound that remains a mainstay of modern synthesis. By investing in staff training, modern analytics, and sustainable infrastructure, we work to ensure every batch of 2-Amino-3-Chloropyridine arriving at a customer’s site reflects the best of what direct chemical manufacturing can offer.