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2-Amino-5-Chloro-3-Nitropyridine

    • Product Name 2-Amino-5-Chloro-3-Nitropyridine
    • Alias 5-Chloro-3-nitro-2-pyridinamine
    • Einecs 636-139-6
    • 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

    211399

    Product Name 2-Amino-5-Chloro-3-Nitropyridine
    Cas Number 35390-39-1
    Molecular Formula C5H4ClN3O2
    Molecular Weight 173.56 g/mol
    Appearance Yellow to orange solid
    Melting Point 98-102°C
    Purity ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 5-Chloro-2-amino-3-nitropyridine
    Canonical Smiles NC1=NC=C(C=N1Cl)[N+](=O)[O-]
    Ec Number 609-743-2

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

    Packing & Storage
    Packing The chemical is packaged in a sealed 25-gram amber glass bottle with a hazard label, product name, batch number, and manufacturer's details.
    Shipping 2-Amino-5-Chloro-3-Nitropyridine is shipped in tightly sealed containers, protected from light and moisture. It should be handled according to standard safety protocols, including labeling and documentation. Depending on quantity and regulatory classification, shipping may require compliance with hazardous material regulations and use of appropriate packaging to prevent leaks or contamination.
    Storage **2-Amino-5-Chloro-3-Nitropyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers, acids, and bases. Protect it from light, heat, and moisture. Ensure proper labeling and keep it away from food and drink. Only trained personnel should handle its storage.
    Application of 2-Amino-5-Chloro-3-Nitropyridine

    Applications of 2-Amino-5-Chloro-3-Nitropyridine in Industrial Manufacturing

    As a manufacturer directly supplying 2-Amino-5-Chloro-3-Nitropyridine, we focus on core downstream segments where this pyridine derivative holds significant technical value. Below we provide substantiated industry pathways, specific compliance contexts, practical ratio guidance, integration details, and actual end product examples from formulation customers worldwide.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Our product plays a critical role as a heterocyclic building block in the synthesis of various pharmaceutical APIs, providing selective substitution on the pyridine ring required for specific target molecules such as kinase inhibitors and anti-infectives. Pharmaceutical manufacturers integrate this intermediate during early-stage active moiety construction to build complex molecular frameworks, with downstream steps requiring careful control of N- and Cl- positions for target specificity. End applications frequently demand tight impurity specifications and validated traceability for regulatory submission batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • EU GMP Part II for starting material suppliers
    • USP and Ph. Eur. quality requirements where designated
    • REACH Registered (as required for European manufacture)

    Typical usage ratio

    • 0.15–1.5 molar equivalents, factored relative to final API yield
    • Adjusted according to side-chain derivatization strategy

    Downstream process integration

    • Used in the initial heterocycle assembly, coupling, or nucleophilic substitution reactions
    • Charged in batch or fed in semi-continuous flow under inert conditions
    • Monitored in process QC for completeness and by-product control

    Final product types

    • Targeted kinase inhibitors (oncology APIs)
    • Novel anti-bacterial and anti-viral drugs
    • Anti-inflammatory API intermediates
    • Other custom N-heterocycle-based pharmaceutical actives

    2. Agrochemical Synthesis—Herbicide Active Ingredient Manufacturing

    The compound is directly employed by fine chemical plants engaged in the multistep synthesis of selective herbicide actives. Its unique substitution provides reactive handles for derivatizing core scaffolds needed in modern selective herbicides. Typical process routes use this intermediate in condensation or cyclization stages, demanding high reproducibility and batch consistency to ensure performance of the final crop protection product.

    Industry compliance standards

    • ISO 9001 Quality Management (for agri-inputs manufacturing)
    • FAO/WHO Specification and Evaluation of Agrochemical Products
    • REACH or local Chemical Control Regulations for environmental safety
    • GLP (Good Laboratory Practice) for product characterization studies

    Typical usage ratio

    • 0.2–0.8 molar basis, set according to synthetic route design
    • Adjustments follow pilot-scale trial results and impurity profiles

    Downstream process integration

    • Typically introduced during nucleophilic aromatic substitution stages
    • Used in batch reactors or continuous stirred tank reactors (CSTRs)
    • Controlled temperature and pH essential for minimizing chlorinated by-products

    Final product types

    • Pre-emergent and post-emergent selective herbicides
    • Sulfonylurea class actives for broadleaf weed control
    • Intermediates for pyridine-based fungicides
    • Seed treatment agents incorporating pyridine derivatives

    3. Dye and Pigment Intermediate Production

    Specialty chemical companies incorporate this pyridine derivative to introduce nitro and chloro functionalities into azo and heterocyclic dye molecules. The compound serves as a feedstock for high-purity pigment synthesis, providing colorants with enhanced resistance to light and solvent exposure. In downstream integration, the nitro group’s electron-withdrawing properties allow controlled coupling with aryl amines and diazo precursors, enabling precise tuning of shade and performance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye auxiliaries
    • German Chemicals Act (ChemG) for pigment registration
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
    • ANSI Z129.1 chemical labeling for hazardous components

    Typical usage ratio

    • 5–15% by mass of total dye batch, tailored by shade intensity target
    • Adjusted for chromatographic purity and coupling efficiency

    Downstream process integration

    • Dosed during diazotization or azo coupling operations
    • Reacted in solvent, sometimes aqueous or mixed-phase conditions
    • Specific purification and filtration steps follow to ensure batch reproducibility

    Final product types

    • High-performance yellow and red azo dyes
    • Pyridine-pigmented printing inks
    • Textile reactive dyes for cotton and polyamide fibers
    • Technical-color intermediates for paints and industrial coatings

    4. Advanced Materials—OLED and Functional Electronics Synthesis

    Manufacturers of optoelectronic materials use this compound as a precursor in developing custom ligand structures for organic light-emitting diodes and related devices. The presence of amino, nitro, and chloro groups on the pyridine ring provides critical points for functionalizing pi-conjugated systems, which are subsequently used to enhance light emission or charge mobility. Process development requires narrow impurity control and high lot-to-lot analytical reproducibility for reliable device performance.

    Industry compliance standards

    • ISO 9001 for functional electronic material production
    • RoHS (Restriction of Hazardous Substances Directive) for electronics
    • IEC 62471 safety standards for lighting components testing
    • IECQ QC 080000 for hazardous substance process management

    Typical usage ratio

    • 0.05–0.30 equivalents relative to final polymerizable unit
    • Adjusted by material formulation goals in R&D and pilot scale-up

    Downstream process integration

    • Introduced during key arylation or Suzuki–Miyaura coupling steps
    • Staged addition for high-purity ligand synthesis
    • Extensive HPLC and mass spectrometry QC applied for in-spec batches

    Final product types

    • OLED emitting layer materials
    • Electron-transporting materials for display panels
    • Conjugated polymer precursors for organic semiconductors
    • Small molecule photonic dyes used in sensor applications

    5. Specialty Chemical Catalysts and Ligand Manufacture

    Catalyst producers in the fine chemical field utilize this compound to synthesize specialty ligands and metal-chelating agents. These ligands enhance catalytic performance for cross-coupling, hydrogenation, and selective reduction processes. Looping this pyridine derivative into ligand design offers electron-rich or electron-withdrawing functionalities that support catalyst activity and selectivity, critical for high-value intermediate production.

    Industry compliance standards

    • ISO 9001 for chemical catalyst and ligand production
    • SHEQ Standards (Safety, Health, Environment, Quality)
    • Responsible Care® Management System
    • Compliance with local hazardous substance storage regulations

    Typical usage ratio

    • 0.1–2.0 equivalents, depending on ligand stoichiometry for final catalyst system
    • Ratio optimization based on required chelate stability and process scale

    Downstream process integration

    • Blended with metal salt or transition metal complexes during ligand preparation
    • Dosed in dry or inert atmosphere for air- or moisture-sensitive precursors
    • In-process controls to ensure minimal unreacted starting material

    Final product types

    • Palladium, platinum, or nickel-based coordination catalysts
    • Homogeneous catalysts for fine chemical synthesis
    • Ligand additives in specialty petrochemical processes
    • Polymerization catalysts for controlled radical processes
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    Certification & Compliance
    More Introduction

    2-Amino-5-Chloro-3-Nitropyridine: A Manufacturer’s Perspective

    Real Chemical Production, Not Just a Stock Number

    After years in chemical manufacturing, genuine value comes from attention to process, material quality, and clear communication. Many products cycle through the warehouse, but 2-Amino-5-Chloro-3-Nitropyridine stands out as one of those compounds that defines the difference between a true producer’s experience and catalog numbers. We have seen it in the raw, in the drums, in the hands of technicians and in the hands of customers who come back with real-world questions. I’ve stood in the plant as we talked through batch control and purity, smoothing out crystallization difficulties, seeing how each lot subtly shifts with upstream factors. Experience here matters, because minor impurities, moisture uptake, and handling methods—these change results downstream.

    The Substance at the Core

    This molecule, 2-Amino-5-Chloro-3-Nitropyridine, has a simple sounding name, yet it sits at the crossroads of several key synthetic pathways. Its composition gives it the reliable reactivity profile, without introducing a raft of tricky functional groups. Over time, we refined our own method to limit trace impurities—especially chlorinated byproducts. The product arrives as a faint yellow to pale brown crystalline powder, showing proper identity by consistent melting point and clean NMR spectra each batch, backed by HPLC area percentages above 98%.

    Manufacturing Realities: Experience Over Numbers

    People who only buy and sell chemicals on a spreadsheet rarely understand the practical variables that show up in plant-scale operations. In synthesis, the real test comes with temperature control, pressure settings, the life of the columns doing the final purifications. We’ve learned to keep the nitration step cool and steady to avoid over-nitrated material—burned batches can throw off final color and leave persistent off-odors. This isn’t details for the sake of detail. The downstream effects can include batch-to-batch differences that matter for reliability in pharmaceutical or agrochemical applications.

    Pyridine Chemistry and Application Context

    This compound first caught attention decades ago in pharmaceutical and fine chemical industries. The pyridine backbone allows versatility in ring modifications, so chemists quickly saw it as a useful scaffold. The amino group at the 2-position and the nitro group at the 3-position each unlock a path to further synthetic elaboration. The chlorine atom in the 5-position suppresses side reactivity, especially in more demanding halogenation or metalation steps. We commonly see it serve as an intermediate for anti-tumor and anti-infective programs, but recent inquiries come from specialty pigment manufacturers and some emerging electronics polymers. That kind of persistent demand speaks to reliability and adaptability.

    Purity, Moisture, and Storage—What We Have Learned

    Buyers ask about moisture content. In real production work, every hour in an open drum matters. Exposed too long, especially on humid days, and you start to see caking along the rim—moisture present can catalyze decomposition if the storage environment is warm or unventilated. Dry rooms help, but bagging technique counts for a lot. We had one run shipped to a customer overseas that sat on a dock for a week in the monsoon season—the analysis upon arrival showed a drop in assay to 96%. These are the lessons you only truly learn from repeated real-world handling.

    Comparing to Other Pyridine Derivatives

    Some customers ask for similar functionality but with methyl, fluoro, or different nitro-positioned compounds. For those who never stepped foot in a chemical plant, all these derivatives look similarly granular and yellow. But the substitution pattern impacts more than a line-item on an assay. The 2-amino, 5-chloro, and 3-nitro configuration grants a blend of reactivity and stability. Anyone who’s handled 3-amino versions, or those missing the chloro group, knows how easily side reactions take over when running downstream processes—in particular during cross-coupling or amidation sequences. Several times, customers working with generic 3-nitropyridine tried substituting in our material. Reproducibility and yield shifted; they switched to ours for better control.

    Scaling Up: Not Just More of the Same

    Small-scale chemistry does not always translate easily up to plant runs. The batch sizes, mixing times, cooling rates, and even the finish on the steel tanks all matter. A few years back, a colleague at a neighboring firm tried to push their kilo-lab process to full scale in one shot, relying on simple temperature control and off-the-shelf crystallization equipment. Outcome: low yield, significant byproduct, hard-to-filter sludge, and lost time. We’ve tuned our own reactor charging sequence to produce crystallized intermediates free-flowing enough to avoid filter blinding. Quality here starts at the source, with no room for shortcuts.

    Analytical Controls—Beyond a Checkmark

    Plenty of suppliers consider an HPLC certificate or a melting point chart as proof of product quality. Those definitely have their place, but I’ve seen occasional issues where similar peaks or melting points hide trace levels of isomers or solvents. Our team looks for more than that: the way the powder looks under a lamp, the physical flow between gloved fingers, and even subtle discoloration on filter papers. Over the years, this approach picked up early warning signs that would otherwise slip by, saving replacement shipments and reputation headaches.

    Interfacing with End Users

    Our customers—often chemists, engineers, or process developers—call us to discuss more than just price or delivery times. They want to talk process troubleshooting, long-term supply agreements, and what happens if their current route changes. That kind of communication helps everyone win, because substitutions on the fly can send a project in the wrong direction, delay campaigns, or waste months of effort. One pharmaceutical team wrote back to say their initial 60% yield off a generic sample improved to 88% yield with our material, simply due to tighter color and moisture control. That story repeats itself: when customers share end-use challenges, we respond with advice drawn from live production, not just a PDF data sheet.

    Stability and Shelf Life—Concrete Experience

    We do not rely on manufacturer’s typical shelf lives as gospel. Relying only on literature values can backfire—actual shelf life changes with climate, storage vessel, and transport conditions. Months in southern shipping ports will test stability far more than a sealed container in a climate-controlled warehouse. We have pulled three-year-old samples from our retention library and run full analyses—most show the same purity and handling behavior as day one, provided they were sealed and kept out of direct sunlight. Opened drums left in humid warehouses, though, regularly see slight degradation or caking, so we always recommend resealing after each use. This comes not from manuals but from direct loss investigations and hard-won customer trust.

    Reactivity in the Real World: Downstream Challenges

    This compound must behave consistently in scale-up pharmaceutical or agricultural processes. If reaction rates swing with small differences in impurity profile, whole campaigns can stumble. We once supported a customer running a Suzuki coupling, where trace metal content tripped a downstream failure. After reviewing our process, tightening the filtration step, and running additional ICP-MS screens, those issues disappeared. This kind of troubleshooting always takes learning, not speculation, and relies on candid discussions both ways.

    Sourcing Strategy: Price, But with Context

    We never claim to be the cheapest bidder. There’s a temptation to treat chemicals like commodity pork bellies, but experience says otherwise. Many times, we have watched companies buy bargain samples from traders, only to watch their project budgets bleed out fixing downstream failures. Price counts, but so do documented traceability records, consistent storage, and real process histories. When someone returns year after year, asking for the same lot control and batch release support, it’s clear that price never tells the whole story.

    Innovation by Increment: How Production Advances Happen

    Innovation in chemical manufacturing often comes as a series of fine step improvements. Our team initiated a change a few years ago by adjusting post-reaction quench timing. This might sound minor on paper, but it improved the purity from 96% to 98.5%, eliminating a stubborn orange tint. Adjustments like this start with a QC report and a conversation between production and R&D—not a headline, just a change that delivers cleaner, better product for increasingly demanding applications.

    Product Handling: Practical Insights from the Floor

    Our operators have learned to trust their eyes and noses as much as any instrument. Some see product color drifting, others notice filtering speed drops, or batch aroma shifts. We encourage these feedback loops, tracing issues to steps in the process. One example: an operator caught the trend that powder sticking to bag seams predicted off-spec moisture content, leading to a procedural update on drum filling and resealing. Those kinds of interventions don’t come from third-party audits—they come from daily practice, cycles of observation, learning, and adjustment.

    Waste and Byproducts—Managing Real-World Outcomes

    In environmental matters, manufacturing is never just about outputs. Disposal of waste from the nitro group installation or chlorination steps needs careful handling, shaped by a close reading of local and international regulations. Our local experience shows wastewater and organic solvent residues must always be neutralized and tracked, both to meet regulations and to avoid operational headaches in future runs. A few years ago, changing a single filtration solvent fixed a recurring environmental permit concern and even cut disposal costs. These aren’t academic changes; they happen through diligence and feedback.

    Market Trends—Watching Beyond the Lab Bench

    The global market for substituted pyridines keeps expanding. Pharmaceutical teams continue to find new pathways for the scaffold, especially when looking for more selective kinase inhibitors or anti-infectives less prone to resistance. Over the past decade, some pigment makers have pivoted towards higher-chlorine, lower-nitro variants, yet demand for 2-Amino-5-Chloro-3-Nitropyridine remains steady because of its balance of cost, reactivity, and process safety. Evolving REACH and EPA guidelines drive continual review, especially around trace impurity declarations and product histories. Keeping current means engaging in the regulatory process, not treating it as a paperwork burden.

    Trust and Endurance Over Time

    Years in the field shows single-batch performance matters, but so does the ability to keep delivering identically over hundreds of runs. Customers remember missed shipments and color drifts. They also remember the operator or manager who took their call and solved problems without hiding behind generic emails or unnecessary intermediaries. That reliability, from raw input to final drum, cannot be faked or rushed. Every complaint, compliment, or question has sharpened the way we handle product, documentation, and people.

    Lessons Learned, Solutions Going Forward

    Every challenge—caking powder, scale-up hiccups, analytical surprises, or customs delays—teaches lessons that feed directly back into the process. No process is perfect, and every improvement comes from honest recognition of what happens after drums leave the loading dock. Best results come from blending attention to raw material quality, upstream supplier vetting, in-plant process knowledge, and open customer communication. For anyone considering switching to, or working with, 2-Amino-5-Chloro-3-Nitropyridine, looking to the manufacturing source and their real-world experience pays off. The incremental stories from the plant, the lab, and the customer together drive the persistent reliability that makes a difference. That’s what sets well-made product apart in the world of fine chemicals.