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5-Amino-2,3-Dichloropyridine

    • Product Name 5-Amino-2,3-Dichloropyridine
    • Alias 5-Amino-2,3-dichloro-pyridine
    • Einecs 635-910-3
    • 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

    928456

    Chemicalname 5-Amino-2,3-Dichloropyridine
    Casnumber 156781-95-8
    Molecularformula C5H4Cl2N2
    Molecularweight 163.01 g/mol
    Appearance Off-white to yellow solid
    Meltingpoint 120-124°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 2,3-Dichloropyridin-5-amine
    Smiles NC1=CN=C(Cl)C(Cl)=C1
    Inchikey ABJZTIRXCCJAKI-UHFFFAOYSA-N
    Storagetemperature Store at 2-8°C

    As an accredited 5-Amino-2,3-Dichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 5-Amino-2,3-Dichloropyridine (25g) is a sealed amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping 5-Amino-2,3-Dichloropyridine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be labeled as a hazardous chemical, handled with appropriate safety precautions, and transported according to local, national, and international regulations for hazardous materials, ideally via ground transport to prevent exposure to extreme conditions.
    Storage 5-Amino-2,3-dichloropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from direct sunlight, moisture, and sources of ignition. Handle under an inert atmosphere if sensitive to air. Label containers clearly and follow all relevant safety and regulatory guidelines for hazardous chemicals.
    Application of 5-Amino-2,3-Dichloropyridine

    Applications of 5-Amino-2,3-Dichloropyridine in Industrial Manufacturing

    5-Amino-2,3-Dichloropyridine functions as a critical intermediate across several industrial verticals requiring high-purity heterocyclic compounds. Our facility supports global manufacturers in sectors where precise synthetic pathways and compliance documentation are essential. Below, we outline its main application scenarios with in-depth integration and regulatory details.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical firms integrate this intermediate during the multi-step synthesis of specific anti-infective APIs, where pyridine ring modification is a core requirement. The compound’s stable amino and dichlorinated structure enables selective substitution or cross-coupling in patented drug development, especially within cephalosporin and kinase inhibitor projects. Batch records require meticulous inclusion and traceability due to stringent regulatory audits. Our production supports process validation with lot-specific CoA and complies with pharmacopoeial impurity limits essential for finished actives.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • EU GMP Volume 4, Annex 8 (Sourcing and supply chain traceability)
    • USP-NF/EP/JP limits on residual solvents and heavy metals in intermediates
    • WHO Prequalification Programme for APIs

    Typical usage ratio

    • Concentration typically between 0.05–0.25 molar equivalent relative to main active scaffold depending on the target API structure and synthetic scheme; scaled to gram–kilogram levels per batch.

    Downstream process integration

    • Introduced at the step of nucleophilic aromatic substitution, Suzuki coupling, or amidation in continuous or batch reactors before subsequent purification and API crystallization.

    Final product types

    • Cephalosporin derivatives
    • Small-molecule kinase inhibitors
    • Intermediate API pyridine derivatives
    • Anti-infective actives

    2. Agrochemical Synthesis (Herbicides and Fungicides)

    In the crop protection industry, manufacturers employ this material as a pyridine fragment donor, forming part of the synthetic backbone for select herbicidal and fungicidal agents. Chlorinated pyridine intermediates prove vital in constructing bioactive molecules with targeted field activity and environmental persistence. Our facility offers validated, reproducible quality under agro-GMP protocols, supporting customers’ registration dossiers with documented impurity profiles and batch traceability.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for quality management in agrochemical manufacturing
    • REACH Annex VIII data requirements for active ingredient intermediates
    • China ICAMA registration technical standard for pesticide actives and intermediates

    Typical usage ratio

    • Ranges from 0.08–0.2 molar equivalent relative to the target pyridine-based agrochemical; adjusted based on crop-specific formulation requirements and target yield per campaign.

    Downstream process integration

    • Dosed into the base-catalyzed coupling or cyclization steps when constructing the heterocyclic core of the herbicidal agent, prior to further functional group additions and formulation into technical concentrates.

    Final product types

    • Pyridine-based herbicide actives
    • Systemic fungicide active ingredients
    • Intermediate technical concentrates for agricultural application

    3. Dye Intermediate Manufacturing (Specialized Pigments)

    Producers of pigment and specialty dye intermediates incorporate this compound for synthesizing dichloropyridine-structured colorants, used where chromatographic purity and batch color stability are critical for application in plastics and fibers. Technical advantages include improved bonding in azo and quinoline dye scaffolds, offering manufacturers high reproducibility and minimal by-product formation during condensation reactions. Our batch tracking and impurity documentation enable reliable pigment standardization.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for dyes in textiles and apparel)
    • EN 71-3:2019 (Toy Safety—Migration of certain elements, relevant for dyed plastics/toys)
    • Zhejiang Provincial Dye Product Quality Standard (for dye intermediates in China)
    • ISO 9001:2015 for dye intermediate production

    Typical usage ratio

    • Added at 0.1–0.4 mole per mole of primary phenolic substrate, with the exact ratio adjusted per final color intensity and intended product batch size.

    Downstream process integration

    • Fed during the condensation step for azo or condensation coupling syntheses, ahead of metallization or diazotization in the pigment/dye production sequence.

    Final product types

    • Metallized azo dyes for polymer fibers
    • Dichloro-pyridine based pigments for plastics
    • Textile colorant intermediates

    4. Electronic Chemical Intermediate (OLED and Display Materials)

    Manufacturers in the electronic materials sector use this molecule for the preparation of pyridine-based intermediates tailored to OLED emitter or electron transport layer construction. The dichloro and amino functional groups offer versatile positions for further halogenation or cross-coupling, supporting rigorous chemical purity and batch-to-batch consistency demanded by display engineering. Quality assurance focuses on metal trace analysis and low residual moisture to avoid downstream device defects.

    Industry compliance standards

    • IEC 61249-2-21 (halogen content limits for printed wiring boards and electronic assemblies)
    • RoHS Directive (2011/65/EU, restriction of hazardous substances)
    • IECQ QC 080000 (Hazardous Substance Process Management System)
    • ISO 14644-1 (Cleanroom manufacturing for electronic intermediates)

    Typical usage ratio

    • Introduced at 0.1–0.3 mole per mole of target aryl halide substrate; optimized for each electronic material precursor based on stoichiometry and electronic performance requirements.

    Downstream process integration

    • Used in Suzuki or Buchwald–Hartwig cross-coupling during the stepwise assembly of electron-transport materials, prior to layer purification and formulation for OLED deposition.

    Final product types

    • OLED emitter intermediates
    • Pyridine-engineered electron transport layers
    • Display material intermediates for flexible screens

    5. Veterinary Drug Intermediate Synthesis

    Animal health product manufacturers utilize this substance in the multi-step synthesis of advanced veterinary drugs where heterocyclic modification enhances efficacy and absorption. The dichlorinated pyridine ring system provides a key synthon for introducing selectivity in anthelmintic or parasiticide drug development, with process verification supported by DMF (Drug Master File) data and batch impurity tracking.

    Industry compliance standards

    • VICH GL40 (Good Manufacturing Practice for APIs used in veterinary products)
    • US FDA CVM Guidance 2015 (Veterinary drug intermediates)
    • European Pharmacopoeia (Ph. Eur) monographs for veterinary actives
    • China Veterinary Drug Administration (MOA) registration requirements for intermediates

    Typical usage ratio

    • Typical dose level is 0.06–0.12 equivalent per mol of main veterinary API precursor; adjustments based on desired synthetic route and in-process impurity control.

    Downstream process integration

    • Charged during pyridinylation or cross-coupling phase in multi-step API assembly before chromatographic purification and formulation into veterinary dosages.

    Final product types

    • Anthelmintic drug actives
    • Veterinary parasiticide intermediates
    • Modified pyridine veterinary pharmaceuticals
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    Certification & Compliance
    More Introduction

    5-Amino-2,3-Dichloropyridine: Insights from the Manufacturer’s Bench

    A Closer Look at 5-Amino-2,3-Dichloropyridine

    In the chemical business, small details often decide the fate of large projects. Out of our diverse range of pyridine derivatives, 5-Amino-2,3-Dichloropyridine stands out for those who work at the frontiers of pharmaceutical synthesis and complex agrochemical design. Over two decades of experience in heterocycle chemistry lay behind the production of this particular compound on our shop floor.

    Many in our industry recognize the importance of pyridine compounds for fine chemical intermediates, but few have handled the practical side of their synthesis and scaling. 5-Amino-2,3-Dichloropyridine belongs to a distinctive niche: its unique arrangement of halogen and amino substituents opens synthetic options that strict isomers or less reactive analogues simply cannot match. With each batch, our crew deals with sensitive reaction conditions, solvent choices, and purification steps, refining the process to ensure consistent crystalline material for demanding downstream customers.

    Our Production Approach and Why It Matters

    Real stories from our line start with raw material procurement. Chloropyridines and aminating agents are sourced for reagent stability and traceability, as experience has shown quality issues often start here. Early on, we saw how variations in input purity tracked with yield loss and colormetric shift during recrystallization: no shortcut pays off here. Technicians continually monitor each stage, using titration, TLC, and HPLC — practices we refined after seeing how missed impurities can poison catalytic cycles or introduce side-products into client syntheses.

    We produce 5-Amino-2,3-Dichloropyridine in standard lots that range from pilot-level tens of kilograms to commercial metric tons, depending on client and project need. Each process iteration has taught us about the “hidden” variables that textbooks gloss over — not just temperature and solvent polarity, but the impact of stirring regime and trace metal contamination, especially in the chlorination and subsequent amination. We engineer our process setups to limit worker exposure, as pyridine derivatives cause obvious irritation and require strict fume handling.

    Batch logs reveal the difference between a high-purity output and a re-worked batch often boils down to what can seem like a minor valve error or a mis-timed addition of sodium amide. We designed backup monitoring — not just for cGMP, but born out of lessons from hard-won process scale-ups. Often, it takes hands-on persistence to keep bottlenecks from swelling into costly delays.

    Physical and Chemical Features

    As a solid, 5-Amino-2,3-Dichloropyridine appears at ambient temperature as off-white to pale yellow crystals, the color reflecting minute variations in precursor handling and storage. Over years, we standardized our drying steps to ensure moisture content never sneaks above 0.3%, as higher water traces show up in NMR and reduce shelf stability in clients’ storage. Melting point checks cross-verified with DSC give us reliable markers, since product crossing certain purity thresholds will shift this number by as much as half a degree.

    Chemically, our clients value this molecule for the electronic activation conferred by both amino and dichloro substitution. The 2,3-dichloro pattern, coupled with the nucleophilicity of the 5-amino, lets customers pursue coupling and substitution pathways not open to simpler dichloropyridines. Our process keeps the product free from over-chlorinated or mono-chloro byproducts, as we saw long ago that such impurities poison Pd, Ni, and Cu catalysts used by some end users. This level of control set us apart from the more generic offerings on the market, especially from repackers or commodity traders with looser quality accountability.

    Differences from Other Compounds and Why They Matter

    In the pyridine series, subtle changes in substitution patterns equate to enormous differences in downstream reaction utility. 5-Amino-2-Chloropyridine or 5-Amino-3-Chloropyridine, for example, don’t deliver the same electronic push for certain Suzuki or Buchwald–Hartwig couplings, nor do they direct regioselective substitutions with the same ease. Our chemists have tested these reactions and seen yields and selectivity drop when the substitution map changes. Some clients request side-by-side comparisons for process route scoping; our samples have shown that the 2,3-dichloro variant accelerates reactions requiring electron-withdrawing activation adjacent to the nitrogen ring site.

    The difunctional nature — chlorine at both positions 2 and 3, amino at 5 — has also allowed pharmaceutical groups to assemble densely functionalized intermediates without extensive protection-deprotection cycles, narrowing process windows and reducing step count. This fundamentally cuts development risk and costs, a fact we’ve been told directly by client project leads seeking faster clinical trial entry.

    In contrast, more common derivatives like 2,6-Dichloropyridine lack the amino trigger, which limits amide bond formation and reduces the scope for direct arylation. Earlier in our company’s history, we offered these more conventional products, but industry demand for more versatile scaffolds pushed us toward mastering synthesis routes for molecules like 5-Amino-2,3-Dichloropyridine. The switch paid off, unlocking more collaborative projects, since researchers trust our handling and insight into both the known and hidden challenges of pyridine chemistry.

    Refining and Scaling — The Human Side

    Long production runs don’t succeed through equipment alone. Our staff put in serious hours tuning feed rates, monitoring exotherms, and logging deviations. Training new operators means more than reading out SOPs; it means knowing how to judge the “look and feel” of a batch, years before more advanced in-line sensors arrive. A young process tech recently caught a small but critical shift in product hue following a condenser clean-out. That early intervention kept us from a significant yield loss and taught the entire team about the importance of hands-on vigilance. No paperwork replaces the instinct formed from direct work with real product, day-after-day.

    Facility upgrades only go so far. We invested in better filtration and solid handling, but also learned the value of real dialogue between R&D and production. When a former bench chemist joined our shift team, scrap rates fell — a practical illustration of why manufacturer-side experience delivers better product to the customer than a mere distributing intermediary. We back up these process gains with documented batch histories, open to client audits. Engineers can discuss the real-world steps we take since no reseller or aggregator brings that ground-level perspective.

    Meeting Industry Needs — and Anticipating Change

    New projects keep rolling in from pharmaceutical, crop science, and material science innovators. Their scale requirements shift constantly. Many times, we receive short-notice requests for both kilogram samples and sudden scale-up batches. Our customers trust us to deliver not just because we “have product,” but because our expertise spans lab synthesis, pilot conversion, and commercial transfer — all on a process we built from scratch. We’ve spent years demystifying route complexities, adjusting work-up and crystallization for optimal loading and throughput.

    We’ve also adapted to the shifting regulatory landscape. Authorities have become more diligent about precursor tracking and compliance in response to greater proprietary interest in pyridine derivatives. Our teams audit raw material flows and maintain documentation required by regulatory frameworks. This rigor is built-in, not added on — a lesson from projects where rushed documentation delayed shipments at customs or led to rejected lots. Every kilogram we ship stands backed by traceable inventories and operator logs.

    Environmental responsibility also entered center stage for us. Many halogenated compounds run afoul of waste management challenges. We tackled this head-on, designing solvent and wash cycles for minimal impact and manageable emissions. Solvent recovery rates now exceed 93% on average batch volume, a statistic we only achieved after sustained investment in modern distillation units and well-trained plant operators. These practices keep our operation sustainable, but they also reassure customers who want product traceability and eco-conscious manufacturing.

    Pain Points and Solutions: Lessons from Real Projects

    The biggest surprises rarely come from what’s in a sales spec. Early in our production history, a multinational client flagged a problem: minute residues of by-products nearly shut down their catalyst process mid-stream. The lesson? Downtime and rework often originate in seemingly minor batch-to-batch differences. We didn’t just refund the order; as manufacturers, we set about re-engineering the synthesis with new intermediate cleans, additional NMR tracking, and cross-site QC. Full transparency delivered a positive turnaround and turned a near-miss into a partnership that continues today.

    With 5-Amino-2,3-Dichloropyridine, users care about batch reproducibility. Labs working on scale-up, especially for regulatory filings, see huge downstream costs if their lead chemical has a shifting impurity profile. We set out to guarantee that every batch falls within the narrowest analytical spread available, using multistep analytics that third-party vendors often find cost-prohibitive to maintain.

    Customer support means direct manufacturer engagement. Traders and stockists can’t answer “why did this lot crystallize slower?” or “how does moisture content affect API synthesis downstream?” Our personnel work directly with R&D leads on customer sites, troubleshooting batch quirks and unexpected reactivity. This collaboration often reveals the subtle real-world variables — glassware contamination, atmospheric variability in vacant storage, differences in dryer cycle validation — affecting final outcome. By guiding clients through these gray areas, we help them avoid costly re-do or regulatory hold-ups.

    Market Feedback and the Continuous Improvement Cycle

    Customers offer invaluable feedback, from Fortune 100 procurement specialists to start-up bioorganic chemists. Specific requests inform our ongoing process adjustments. A series of inquiries about residue levels from European labs led us to implement additional purification and introduce more sensitive LC-MS protocols — a costly upgrade, but one that cut finished product rejection rates by a noticeable margin. This has contributed more than any price decrease or faster shipment in retaining larger, longer-term projects.

    Unlike common warehouse stock, 5-Amino-2,3-Dichloropyridine benefits from a “feedback loop” of constant process monitoring and process data-sharing. The more detail we can get — spectral, physical, or anecdotal from the bench — the better we tweak subsequent runs. Where many non-manufacturer sellers operate on “ship and forget,” our operation tracks every outbound lot and logs field reports. We learn from these, using onsite expertise and historical batch data to improve customer outcomes on the next cycle.

    Why End-Users Rely on Direct Manufacturers

    Scientists and purchasing managers often face a basic question: source material from integrators, or insist on direct-from-manufacturer traceability? Over our history, direct customer partnership has translated to faster scale-up, easier regulatory clearance, and overall lower risk. Scientists gain access to real experts — not call center intermediaries — and can tap into technical details that go deeper than surface-level product commentary. This matters most on challenging projects, where unexpected chemistry throws up new questions mid-campaign.

    Third-party traders rarely bring first-hand insight about process bottlenecks or variables that affect reproducibility — areas direct manufacturers live and breathe. From sharing batch-level impurity data to joining technical troubleshooting calls, we see our role not as box shippers but as collaborative partners to the labs and factories building tomorrow’s medicines and agrochemical solutions. The lessons we learn from the floor — and from the field — constantly reshape the way we produce and deliver our products.

    Looking Ahead for 5-Amino-2,3-Dichloropyridine

    Demand for complex building blocks won’t slow down. As clients push for shorter, cleaner synthetic routes — and regulators demand stricter traceability — we see a growing role for niche heterocyclic compounds. Years of experience producing 5-Amino-2,3-Dichloropyridine have taught us to stay agile. Chemistry, after all, remains more than recipe-following; it’s a craft built on persistence, open communication, and constant honing of process details.

    Any innovation in the marketplace depends on foundational partners who understand the weight of consistency and reliability. Those rare moments when chemists unlock new reactivity or see a better yield, they often come back to a well-made starting material, built by teams who treat each lot with the same care as the first. That’s the perspective we bring — not just as chemical suppliers, but as manufacturers grounded in hands-on practice and a deep respect for the challenges and opportunities our customers face every day.