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2-Amino-5-Chloropyridine

    • Product Name 2-Amino-5-Chloropyridine
    • Alias 5-Chloro-2-aminopyridine
    • Einecs 219-508-3
    • 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

    835964

    Chemical Name 2-Amino-5-Chloropyridine
    Molecular Formula C5H5ClN2
    Molar Mass 128.56 g/mol
    Cas Number 1072-98-6
    Appearance Light yellow to beige crystalline powder
    Melting Point 108-112°C
    Boiling Point 271°C (estimated)
    Solubility In Water Slightly soluble
    Density 1.267 g/cm³
    Purity Typically ≥98%

    As an accredited 2-Amino-5-Chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g 2-Amino-5-Chloropyridine arrives sealed in a white, chemical-resistant HDPE bottle with hazard labeling and lot information.
    Shipping 2-Amino-5-Chloropyridine is shipped in tightly sealed containers, protected from moisture and light. It should be stored and transported at room temperature, in compliance with local hazardous material regulations. Appropriate labeling and documentation are required, and the package must be handled by trained personnel wearing suitable protective equipment.
    Storage 2-Amino-5-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 it from moisture and direct sunlight. Label the container clearly, and store away from food and drink. Always follow appropriate safety protocols, including the use of personal protective equipment when handling.
    Application of 2-Amino-5-Chloropyridine

    Applications of 2-Amino-5-Chloropyridine in Industrial Manufacturing

    2-Amino-5-Chloropyridine serves as an essential intermediate in several highly regulated chemical value chains. As a manufacturer specializing in this raw material, we ensure quality and traceability to facilitate consistent downstream performance. Below, we present the most established industrial application scenarios, highlighting technical specifics for B2B procurement teams and process engineers.

    1. Pharmaceutical Intermediates – Synthesis of Antiviral Agents

    Major pharmaceutical companies use 2-Amino-5-Chloropyridine as a building block during multi-step syntheses for specific antiviral drug substances. Its chloro-substituted pyridine ring enhances molecular reactivity, which enables site-selective amination, N-alkylation, or ring closure reactions, pivotal in producing active pharmaceutical ingredients (APIs) for innovative and generic antiviral compounds. Downstream formulation incorporates it via API routes requiring stringent QC to comply with global medicinal standards. Our controlled supply ensures trace impurity management critical to final drug safety.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 U.S. FDA cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP) references for APIs
    • Chinese Pharmacopoeia (ChP) monographs and relevant local Drug Master Files (DMFs)

    Typical usage ratio

    • 5–15% of total intermediate mass in multistep synthetic sequences, varying with API structure and process yield requirements; adjusted according to stoichiometry and scalability in pilot-to-commercial production.

    Downstream process integration

    • Introduced at early or mid-stage condensation or cyclization steps within API synthesis; batch or semi-continuous reactor charging based on reaction kinetics and impurity profile targeting.

    Final product types

    • Finished antiviral API powders and granules (e.g., nucleoside analogues)
    • Direct-compressed antiviral tablets
    • Oral suspension formulations
    • Further-processed combination antiviral regimens

    2. Agrochemical Intermediates – Crop Protection Synthesis

    Agrochemical manufacturers utilize 2-Amino-5-Chloropyridine extensively for synthesizing systemic and contact herbicides, fungicides, and insecticide molecules. It serves as an essential scaffold for heterocyclic derivatives, imparting enhanced selectivity against target pests. Production lines require precise dosing within proprietary formulations to optimize crop safety and environmental loading. Each batch must comply with regulatory residue thresholds and traceability documented across the entire supply chain.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • ISO 9001:2015 quality system for crop chemical manufacture
    • EU Regulation (EC) 1107/2009 on plant protection product approval
    • EPA 40 CFR Part 158 guidelines for active ingredient registration and data reporting

    Typical usage ratio

    • 2–8% of total input mass depending on target molecule and synthetic complexity; ratio optimized per reaction sequence and purification yield in seasonal production cycles.

    Downstream process integration

    • Charged as a core starting material or coupling reactant in condensation or selective N-arylation during active ingredient assembly; remains in closed reactor systems to prevent occupational exposure.

    Final product types

    • Technical-grade pesticide actives (powders, solutions)
    • Suspension concentrates for foliar application
    • Granular and water-dispersible herbicide blends
    • Microencapsulated insecticidal formulations

    3. Dye and Pigment Manufacture

    Specialty dye works and pigment producers employ this ingredient as a key intermediate to create pyridine-based coloring agents, essential for textile, paper, and specialty coatings sectors. Its aminated structure allows coupling with diazonium salts, resulting in highly stable, vivid chromophores. The chemical’s purity directly influences color intensity, batch-to-batch uniformity, and application fastness, making reliable sourcing vital for global dye houses offering advanced pigment portfolios meeting sector-specific compliance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile chemical components safety)
    • REACH Annex XVII compliance (EU chemical registration, evaluation, restriction)
    • ZDHC Manufacturing Restricted Substances List (MRSL) for finished goods
    • ISO 13320 quality control for pigment particle size

    Typical usage ratio

    • 3–12% of initial pigment synthesis batch mass, fine-tuned based on chromophore target structure, substrate compatibility, and post-treatment requirements.

    Downstream process integration

    • Dosed during primary coupling stages in batch or continuous syntheses; integrated into aqueous or solvent-phase reactions, followed by filtration and drying steps for pigment finalization.

    Final product types

    • Textile direct and reactive dyes
    • High-performance printing inks
    • Pyridine-derived plastic colorants
    • Industrial pigment powders for paint and specialty coatings

    4. Chemical Synthesis of Veterinary Pharmaceuticals

    Producers of veterinary medications rely on the compound’s reactivity within the assembly of active molecules intended for livestock and companion animal health. Incorporation must respect local and international regulations on residue levels in animal-derived food products. The controlled use supports synthesis of new-generation antimicrobials and antiparasitic agents, with process records maintained for every batch to facilitate veterinary product registration and post-market traceability audits.

    Industry compliance standards

    • VICH GLs (International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products)
    • European Medicines Agency (EMA) Guidelines on quality of veterinary pharmaceuticals
    • 21 CFR Part 514 (FDA New Animal Drug Applications)
    • Good Agricultural and Collection Practices (GACP) for animal health products

    Typical usage ratio

    • 4–10% input by weight in target molecule synthesis; variations depend on end-use pharmacophore and purification protocol to manage veterinary drug safety profiles.

    Downstream process integration

    • Added at intermediate formation stages via ring-closure condensation or amination; output then processed through crystallization and phase purification before formulation into veterinary actives.

    Final product types

    • Oral and injectable veterinary drug APIs
    • Medicated premixes for animal feed
    • Antiparasitic tablet and suspension products
    • Veterinary topical formulations
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    Certification & Compliance
    More Introduction

    2-Amino-5-Chloropyridine: Insight from the Manufacturer’s Bench

    Understanding the Core of Reliable Pyridine Chemistry

    Long days in the plant tend to create a different relationship with each compound, and 2-Amino-5-Chloropyridine is one that sits on our production lines often. Its chemical formula, C5H5ClN2, creates a backbone that bridges fine chemicals with intermediate manufacturing every week. In practical terms, we approach this material by recognizing what our technicians handle daily: clean crystalline solid, off-white in color, sharp aromatic trace that lingers at the inspection hoods.

    In our factory, the model produced most heavily is of technical grade with an assay typically above 99%. Our lots show moisture sensitive behavior — even small deviations in storage lead to noticeable clumping, so we reinforce the importance of properly sealed containers. This extra vigilance has grown into a habit for anyone on night shift, whether they are moving drums or weighing out fractions for downstream blends. We see stability and low impurity levels as non-negotiable; our QA lab checks Impurity A and B, always aiming to keep actual impurity much lower than commonly tolerated thresholds.

    Temperature conditions during synthesis can impact consistency. Temperatures above 250°C often increase unwanted byproduct formation, so our reactors never stray from a controlled window, which keeps each batch in line with the last. Direct steam inlets help us maintain this sweet spot, and the operators know when to adjust based on subtle differences in reflux time and exotherm profiles — better control leads to less rework and higher customer trust.

    Why 2-Amino-5-Chloropyridine Matters in Practice

    Our production stories link directly to the range of uses our customers bring to the table. Feedback from formulators, especially in pharmaceuticals and agrochemical synthesis, keeps this material in demand. The molecule’s arrangement, with its amino and chloro positions, makes it an irreplaceable building block for compounds like antihistamines, fungicides, and dye intermediates. Synthetic complexity in the lab finds a shortcut when this core fragment is present; several pharmaceuticals in regulatory submission today depend on it for their success.

    Many customers select 2-Amino-5-Chloropyridine because it enables efficient coupling reactions and allows for selective substitution. Conventional pyridine intermediates lack the dual reactivity given by the amino and chloro groups in the 2 and 5 positions. If one tried to use 2-Aminopyridine or 5-Chloropyridine singly, extra synthetic steps would usually need to be added, creating more waste and lower yield. In the factory, we’ve seen process chemists reduce overall cycle times by over 20% just by switching to this compound, avoiding entire protection and deprotection cascades in the route.

    Direct feedback from both R&D and industrial scale partners shows that the product’s performance can influence overall project timelines. There’s less troubleshooting around impurities — high-purity lots, with low residual solvents and ash content, translate to cleaner downstream chemistry and fewer surprises in final API or formulation analysis. By keeping close tabs on the water content and avoiding trace metals, we see less risk of regulatory flags further down the supply chain.

    Working With the True Material: Practical Insights and Lessons Learned

    Years of filling, packing, and sampling 2-Amino-5-Chloropyridine have convinced our crew there’s no substitute for hands-on familiarity. Too many complaints in the market relate not to the compound itself but to mishandling. It’s sensitive to moisture and contamination, so we keep our production under strictly inert atmospheres — nitrogen lines, triple-walled drums, desiccant packs with each outgoing shipment. Even small lapses show up as brownish tint or clumped crystals that slow down downstream feeding. This level of vigilance helps our buyers avoid frustrating downtime at their own lines, and the feedback we receive drives improvements in each quarterly SOP update.

    In the past, we have helped several partners troubleshoot solubility and filtration questions. Not everyone expects its moderate solubility profile in ethanol or N,N-dimethylformamide, and some facilities see plugging of lines or filters when crystallization kinetics aren’t managed right. Sharing real lab data on solvent choice, heating rates, and cooling profiles has, for more than one customer, meant the difference between a stalled batch and a smooth campaign. There are not many days that go by without a discussion at the plant about solvent compatibility, preferred stir rates, or the right filter grades — all driven by our own production experiences.

    Packing teams log results for every outgoing batch, staying alert for changes in particle size distribution, which shifts subtly with even minor tweaks in crystallization conditions. Particle size can influence handling in automated systems; free-flowing microcrystalline powders have much less risk of bridging during transfer than coarser granules, especially in high-humidity climates. Practical experience taught us that a single incorrect packing temperature spike can lead to cakes that resist scooping and slightly reduced recovery rates.

    What Sets 2-Amino-5-Chloropyridine Apart From Related Pyridine Compounds

    Enough time on a manufacturing floor shows the distinctions between closely related chemicals are rarely academic. 2-Amino-5-Chloropyridine shares many properties with other aminopyridines and chloropyridines but stands out through its unique reactivity. The combination of amino and chloro substituents on the pyridine ring positions the molecule for diverse synthetic applications, especially where selectivity and efficiency are critical.

    Compared to 2-Chloropyridine, which lacks the nucleophilic amino group, our product opens up access to broader coupling chemistries. Reactions that would stall or require harsher conditions find better yields and higher regioselectivity using 2-Amino-5-Chloropyridine. In comparison to 2-Aminopyridine, the chloro group on the fifth carbon increases options for cross-coupling and downstream substitution, helping chemists streamline multi-step syntheses.

    In the eyes of process development teams, this means fewer reaction steps and often a safer profile during intermediate stage production — the less you need to play with aggressive halogenation or amination sequences, the fewer handling hazards appear. Our safety team pays attention to incident logs in the industry; recent years have shown that using this molecule directly has cut process hazard reports in several customer plants, mostly by eliminating the need for on-site chlorination with all its associated risks.

    Seeing Real-World Outcomes — Beyond Technical Data

    A manufacturer learns to look at verdicts not just from the lab or QA sheet but from downstream performance. Our material goes into hundreds of research and production lines each quarter, but we remember details from specific feedback: shortened timelines for regulatory submissions, solid clarification in pilot plant operations, and reductions in overall chemical waste output. When plants growing crops hundreds of miles away start using a new fungicide built on this molecule, supply chains tighten up, and logistics teams breathe a little easier.

    Across the world, regulatory standards for purity and trace metals have ratcheted up. We meet these standards not just for compliance but because strict batch records and validated production routes save time later. The pressure-tested method, tested on our own floor, feeds directly into what we ship out. We keep residual solvents below 500 ppm, a standard set after one particularly problematic incident several audit cycles ago when cross-contamination with n-butanol delayed an entire shipment. Cost, performance, and reliability drive every update to our batch protocols.

    It’s not just theory. Over the past five years, customer surveys and external audits showed projects using this intermediate saw average throughput increases above 15%. In the world of large volume pharma and agrochemical synthesis, that means more product to market and less stress from regulatory rework. We invest in process control and real-time batch analytics; success means the rare batch that falls outside of spec gets caught before a truck ever leaves our gate.

    Troubleshooting and Improvement: Experience on the Production Floor

    Ongoing production brings with it the benefits of a hundred small lessons. Process safety incidents linked to poor handling of pyridine derivatives have decreased on our lines through regular hazard training and equipment upgrades. We learned that corrosion at valve seats, where vapor phase chlorinated compounds concentrate, needed more attention — stainless or glass-lined solutions reduced maintenance downtime and increased batch consistency.

    Production engineers noticed improvements after cooling curves were tweaked during crystallization. By slowing the temperature drop from 60°C to 20°C over hours instead of minutes, we saw smoother powders and fewer oversized particles. These operational details turn into more predictable performance at the blending or formulation stage. Technicians share these tips during shift turnover, and the on-site process notebook keeps every lesson alive for each new worker.

    In one example, a pharma client reported elevated ash content in production feed. We reviewed our upstream solvent recovery setup and discovered overlooked process water recycling lines were leaking trace sodium contamination. Installing secondary ion-exchange packs solved the issue, and product lots over the following quarter showed a 30% reduction in ash — not just an academic figure, but a real aid in keeping customer synthesis clear and regulator-friendly.

    Hazardous waste handling streams have always been a point of pride in well-run chemical manufacturing. We revamped our filtration units and solvent reuse strategies last year, dropping total waste output without sacrificing lot quality. Less solvent loss presents not just environmental benefit but long-term cost reductions that we pass on through improved contract pricing. Staff training on containment, spill control, and reactive residue management all comes from real-life incidents logged as learning opportunities, not just audit points.

    Solutions Born from Day-to-Day Manufacturing Challenges

    Solving real-world manufacturing issues often means going beyond the textbook. Direct customer calls taught us flexible bulk packaging options matter. Drum or intermediate bulk container? Each plant is different. Some bulk customers want double lined drums sealed under inert atmosphere; others prefer smaller airtight bags so they can meter out smaller daily amounts with less risk of moisture pickup. Our logistics team accommodates, because once you’ve swept up clumped product in summer heat you never forget the value of the right packaging solution.

    Shipping delays, especially for export orders, used to cause headaches with seasonal demand. By investing in buffer stock and holding safety inventory ahead of peak months, we keep orders moving regardless of port congestion or transportation bottlenecks. This cuts down lead times and makes for steadier supply to customer warehouses.

    Communicating real process data has also cut surprises for new users. We share actual solubility, melting point, and impurity data — straight from the last batch, not just from historic CoAs. Customers appreciate upfront knowledge of limitations, such as the compound’s partial solubility in cool DMF or lower volatility compared to other chlorinated pyridines.

    Supporting chemists through technical data only works with honesty. Sometimes the desired process just won’t work the way a formulation chemist hopes based on literature, so we connect them with technicians and process development teams who help optimize conditions. Sharing relaxation times, agitation rates, and filtration tips, our plant managers help projects stay on course.

    Looking Forward: Responsible Production and Ongoing Refinement

    Modern chemical manufacturing cannot ignore evolving regulations or the environmental footprint linked to specialty intermediates. We meet regional expectations for safety, emissions, and waste, but there’s always more to do. Our approach now includes process mapping to minimize emissions, tighter controls for routine air sampling at vent stacks, and investment in sustainable energy for plant utilities. R&D projects under development target greener routes, with the aim of reducing both reaction energy input and overall byproduct streams.

    Over the long term, reducing the environmental and safety burden of all pyridine manufacturing means integrating feedback from plant operators, lab teams, and end users alike. The next batch shipped rolls out with half a dozen lessons baked in from the last one. Every production record, batch log, and customer ticket adds another layer of refinement to our material and service.

    Technical knowledge, a dedicated team, and respect for detail combine in each shipment of 2-Amino-5-Chloropyridine. The invisible links between worker practices, process tweaks, and customer feedback drive quality higher and shape a different kind of reliability. For those who depend on specialty intermediates to keep production lines active and regulatory risks low, those invisible investments at the factory level mean a lot more than a clean spec sheet. They shape how science finds its way into the everyday world.