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2-Cyano-3-Nitropyridine

    • Product Name 2-Cyano-3-Nitropyridine
    • Alias 2-Cyano-3-nitropyridine
    • Einecs 244-333-9
    • 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

    409141

    Chemical Name 2-Cyano-3-nitropyridine
    Molecular Formula C6H3N3O2
    Molecular Weight 149.11 g/mol
    Cas Number 13525-54-7
    Appearance Yellow crystalline solid
    Melting Point 104-106°C
    Solubility In Water Slightly soluble
    Smiles C1=CC(=C(N=C1)C#N)[N+](=O)[O-]
    Inchi InChI=1S/C6H3N3O2/c7-4-5-2-1-3-8-6(5)9(10)11/h1-3H
    Storage Conditions Store in a cool, dry place away from incompatible materials
    Purity Typically >97%
    Synonyms 2-Cyano-3-nitro-pyridine
    Hazard Statements Harmful if swallowed; may cause respiratory irritation

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

    Packing & Storage
    Packing A 25-gram amber glass bottle, labeled "2-Cyano-3-Nitropyridine," features hazard warnings, lot number, and manufacturer information. Sealed for safety.
    Shipping 2-Cyano-3-nitropyridine is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored in a cool, dry, well-ventilated area, away from incompatible substances. During shipping, regulatory guidelines for hazardous chemicals must be followed, and relevant labeling, documentation, and protective packaging are essential to ensure safe transport.
    Storage Store 2-Cyano-3-Nitropyridine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances like strong oxidizers and reducing agents. Ensure the storage area is free from moisture and ignition sources. Properly label the container, and restrict access to authorized personnel. Use secondary containment to prevent spills.
    Application of 2-Cyano-3-Nitropyridine

    Applications of 2-Cyano-3-Nitropyridine in Industrial Manufacturing

    2-Cyano-3-Nitropyridine serves as a vital intermediate for advanced synthesis in key sectors including pharmaceuticals, agrochemicals, fine chemicals, and specialty dye manufacturing. Its unique functional profile and reactivity enable manufacturers to develop high-value end products meeting stringent international regulatory demands and production specifications.

    1. Pharmaceutical API Intermediate for Pyridine-Derived Drugs

    Pharmaceutical companies employ 2-Cyano-3-Nitropyridine as a key building block in the synthesis of pyridine-based active pharmaceutical ingredients (APIs), particularly for the production of anti-infective, anti-diabetic, and central nervous system (CNS) actives. It enters the process through nucleophilic substitution, paving the way for downstream transformations such as amination or reduction according to the specific API route. The precise addition amount depends on the desired molecular target and stoichiometric requirements in multi-step syntheses.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • cGMP (21 CFR Parts 210/211, FDA)
    • European Pharmacopoeia Monographs for Pyridine Derivatives
    • USP General Chapters: Synthesis Process Validation

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target intermediate, adjusted to route-specific yield and conversion rates

    Downstream process integration

    • Added during early or intermediate API construction steps in closed reactor systems, followed by solvent controls, chromatographic purification, and downstream finishing (crystallization or isolation of API)

    Final product types

    • Pyridine-derived APIs for anti-infective therapies
    • Diabetes management actives
    • CNS modulator pharmaceuticals
    • API intermediates supplied to global formulation sites

    2. Agrochemical Synthesis for Heterocyclic Herbicide and Fungicide Precursors

    Large-scale agrochemical synthesis uses 2-Cyano-3-Nitropyridine as a precursor for heterocyclic compounds with systemic herbicidal and fungicidal effects. Manufacturers integrate the material in multi-stage production processes involving cyclization and nitro group modification, targeting agroactives with high plant systemicity and environmental stability. Dosage calibration is based on conversion efficiencies and impurity control for registration standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems for Agrochemical Raw Material Manufacturing
    • REACH (EC 1907/2006) for Chemical Substances Registration in the EU
    • OECD Principles of Good Laboratory Practice (GLP) for Toxicological Testing

    Typical usage ratio

    • 10–30% by weight in the initial batch, adjusted by desired conversion of pyridine ring in target herbicide or fungicide molecules

    Downstream process integration

    • Charged at the ring formation or nitro reduction step, followed by alkylation, formulation with surfactants, and granulation of finished agroactives

    Final product types

    • Heterocyclic herbicide technical concentrates
    • Precursor intermediates for triazolopyridine fungicides
    • Granular and emulsion-concentrate crop protection formulations
    • Bulk intermediates sold to global agrochemical formulators

    3. Dye and Pigment Intermediate for Pyridine-Based Colorants

    Manufacturers in the specialty dyes sector select 2-Cyano-3-Nitropyridine for the synthesis of pyridine-containing azo and nitro dyes used in high-performance inks, technical textiles, and color masterbatches. The material is combined in batch or continuous flow with coupling agents during chromophore construction. The precise incorporation level is determined by target color index and thermal/light fastness profiles required by end applications.

    Industry compliance standards

    • EN 71-3: Safety of Toys – Migration of Certain Elements (Colorant Use in Toys)
    • OEKO-TEX® Standard 100: Chemical Safety for Textile Inputs
    • ISO 9001:2015/QC inspection protocols for dye intermediate production
    • REACH Compliance for Dyes & Pigments in Europe

    Typical usage ratio

    • 5–15% of total dye intermediate mass in chromophore assembly, fine-tuned for shade depth and migration requirements

    Downstream process integration

    • Fed into the dye-reactive aromatic ring formation reactor, followed by diazotization, coupling, filtration, and concentration steps

    Final product types

    • Pyridine-based azo liquid and powder dyes
    • Technical textile colorants
    • Printing and solvent-base ink colorants
    • Color masterbatched plastics for automotive and electronics

    4. Fine Chemicals for Advanced Materials and Specialty Building Blocks

    In fine chemical manufacturing, 2-Cyano-3-Nitropyridine enables the assembly of functionalized pyridine rings incorporated into specialty ligands, advanced electronic materials, and catalysts. Processing engineers add precise quantities during nucleophilic aromatic substitution or condensation reactions, based on desired reactivity for the downstream applications. Ratio decisions rely on the targeted output and conversion kinetics in the specific chemical transformation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (Fine Chemicals)
    • ISO 14001:2015 Environmental Management for Fine Chemical Sites
    • RoHS Directive (for electronic component intermediates in the EU)
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) compliance

    Typical usage ratio

    • 2–25% by mass, depending on molecular complexity and downstream synthetic sequence

    Downstream process integration

    • Added to catalytic batch reactors or flow reactors at the cyclization or substitution stage, subsequently isolated via distillation or chromatography

    Final product types

    • Specialized bidentate ligands for catalysis
    • Pyridine-containing monomers for advanced polymers
    • Organic intermediates for optoelectronic and sensor materials
    • Small molecule research compounds for advanced material applications
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    Certification & Compliance
    More Introduction

    Introducing 2-Cyano-3-Nitropyridine: Reliable Quality from the Factory Floor

    Experience in the Production of 2-Cyano-3-Nitropyridine

    Navigating the world of pyridine derivatives presents a list of challenges every chemist knows too well. 2-Cyano-3-Nitropyridine ranks among the more specialized compounds in this space. At our manufacturing site, chemical handling and protocol compliance remain fundamental, not just to secure product quality, but to honor the high expectations our clients bring to each order. This material, often appearing as a pale yellow powder, occupies a unique position in the toolbox of pharmaceutical research and other synthesis-driven industries.

    From experience on the shop floor, the nitro group at the 3-position lends the molecule distinctive reactivity. It interacts with nucleophiles in a highly selective way. On the other end, the cyano group opens the door to a range of further modifications. Our operators and chemists have seen research partners use 2-Cyano-3-Nitropyridine not only as a building block for more complex active pharmaceutical ingredients, but as a key intermediate paving the way to nitrogen-rich heterocyclic systems, including those in agrochemical and dye synthesis.

    In every batch, monitoring purity and isomeric control ranks among the highest priorities. We deliver material at no less than 98 percent purity, which comes directly from careful selection of starting materials and process monitoring at each reaction checkpoint. Unlike off-the-shelf intermediates or bulk commodity chemicals, 2-Cyano-3-Nitropyridine demands custom technique. Years in the industry have shown that inconsistent input quality or suboptimal crystallization can lead to trace impurities. These matter. Even at sub-percentage levels, impurities can complicate downstream steps, affecting catalyst activity or introducing color in later reactions.

    Understanding the Model and Specifications That Matter

    Our experience reflects that a model description for 2-Cyano-3-Nitropyridine does not end with a catalog number. Though catalogs use identifiers such as C6H3N3O2 and CAS 5470-18-8, researchers and process scale buyers routinely ask more pointed questions. Does this material fit our existing HPLC calibration? Can we trust the melting point range not to creep up from batch to batch?

    Quality manifests in subtle ways. Tight melting point control, normally between 140°C and 143°C, signals that crystallization has gone well and solvent inclusion remains minimal. Our team relies on direct, on-the-bench monitoring using both HPLC and NMR. Purity is not left to a single test. It takes teamwork between production and QC labs to eliminate residual solvents, fines, and off-target isomer formation. Wetness, usually below 0.5 percent by Karl Fischer titration, protects downstream processes from side reactions often initiated by traces of water.

    Packing and storage loom large. The nitro and cyano groups each add layers of sensitivity to this compound. Operators pack in light-tight, moisture-resistant liner bags, sealed under inert gas. These methods reflect direct feedback from customers who reported material dulling or discoloration after only a few weeks using older packaging approaches. We shifted to smaller volume packs for high-purity batches, knowing well that smaller inventory size helps avoid ambient exposure—even in busy pilot labs where humidity control may be imperfect.

    Key Chemistry Features and Application Potential

    Several features set 2-Cyano-3-Nitropyridine apart from routine pyridine derivatives. The conjugation of its nitro and cyano functionalities allows for streamlined substitution and condensation reactions. In pharmaceutical R&D, this means medicinal chemists save steps when building scaffold cores for new compound libraries. Aromatic nitration often brings broad reactivity, but placing a cyano group ortho to a nitro provides a selective site for metal catalyzed transformations or amination reactions without sacrificing stability.

    In the agrochemicals sector, intermediate chemists recognize its value in constructing custom pyridinecarboxamide or pyridinecarboxylic acid derivatives. Its structure resolves common bottlenecks that emerge with single-functionality pyridine compounds, reducing the need for workarounds or protection-deprotection cycles. Our batch records document how this precise isomer achieves high selectivity, preventing the formation of unwanted isomeric byproducts during sequential reaction steps.

    The pigment and dyestuff sector likewise benefits from its dual functionality. By enabling the introduction of both electron-withdrawing and electron-donating substituents in later steps, 2-Cyano-3-Nitropyridine acts as a crossroads molecule—critical for building color-stable systems or photoactive heterocycles. Application chemists we work with highlight how careful control of nitro/cyano orientation improves not just reactivity but also the long-term stability of end-products under challenging storage or use conditions.

    From Laboratory to Large-Scale—Unique Considerations

    Scaling up production involves real risks. Small-batch methods occasionally perform differently than those in reactors pitching hundreds of kilograms per week. One lesson has stayed clear: direct translation from literature procedures almost always ends in frustration. Laboratory-scale protocols convince on paper, but ignore heat management, crystallization kinetics, and the subtleties of solvent removal. Many times, overlooked exotherms during the nitration step have led to runaway reactions or charred intermediates. We have responded by deploying continuous monitoring, focusing on temperature gradient control and staged addition rates for nitrating agents.

    Crystallization—so straightforward in a 250 ml flask—poses unique questions in a 2,500 liter reactor. Agglomeration and uncontrolled nucleation can trap impurities, reduce yield, or force costly reprocessing. The best operators learn to adjust agitation and seed crystal size mid-batch. This has paid off, reducing average downtime and improving bed filtration times. Losing even a single shift to a filtrate gone cloudy or a vacuum line blocked with fines reinforces the hard truth that process knowledge and real-world experience count for more than any flowchart or SOP binder.

    As an original manufacturer, we maintain direct accountability for in-process management. Years of internal audits have underscored the need for redundant checks—not just before drums head to shipping, but at every intermediate sampling point. High-resolution analytical runs help catch issues early, allowing real-time corrections rather than deferred troubleshooting at the end of a campaign.

    Comparison with Other Pyridine Intermediates

    From a chemist’s view, 2-Cyano-3-Nitropyridine pulls double duty, acting as both an electrophile and a nucleophile in well-controlled conditions. Its close cousin, 3-Nitropyridine, handles nucleophilic substitution well, but lacks the cyano group’s reactivity boost when forming C–C or C–N bonds. On the other side, 2-Cyanopyridine offers the cyano functionality, but the absence of the nitro group limits later transformations, especially where electron density modulation is critical.

    We have seen research partners experiment with both analogs. Their feedback remains consistent: using 2-Cyano-3-Nitropyridine simplifies multi-stage synthesis, skipping separate nitration or cyanation cycles. This translates to less handling of hazardous reagents and energy input, fewer waste streams, and, significantly, lower likelihood of problematic impurity formation. Direct side-by-side trials in pilot plants affirm what bench results suggest. The added synthesis flexibility translates to shorter overall project timelines and better reproducibility.

    From a manufacturer’s standpoint, supplying this compound requires specialized equipment compared to simpler pyridines. We engineer containment and waste capture systems to handle the nitro group’s potential decomposition products and ensure no cross-contamination risks with cyanide derivatives elsewhere in the plant. Years of handling these materials reinforce the wisdom of dedicated reactor lines, both for operator safety and to guarantee clients’ regulatory filings clear the scrutiny of routine and forensic audits.

    Choosing Materials: What End Users Tell Us

    Feedback from long-term partners tells its own story. Many report failed reactions when switching to materials sourced through traders or mixed-origin suppliers. Subtle differences in isomer ratios and the presence of micro-impurities—often not declared in a datasheet—can derail catalyst efficiency or impact crystallization endpoints. Direct sourcing from dedicated manufacturers eliminates guesswork about composition and shelf life. We maintain batch traceability and keep retention samples for years, ready for retesting or regulatory trace-back requests.

    Tooling and formulation teams appreciate the transparency our process allows. Upfront communication around current stock, incoming production lots, and actual analysis results builds trust. End users rarely benefit from generic answers; instead, they value insights into process tweak history and the option to request custom specifications for color, particle size, or wetness.

    Long-standing projects have taught us that partnerships with process development chemists work best when both sides speak plainly. No one benefits from glossing over complexities like off-odor drift or trace mineral contamination. As a result, customers reward suppliers who invest in real dialogue and back up claims with hard analytical data from batch records. The proof does not rest inside a marketing brochure but in the way each order performs when transfer lines clear and chemistry runs at scale.

    Meeting Challenges in a Changing Regulatory Landscape

    Regulations on specialty chemicals and key intermediates continue evolving, sometimes unpredictably. End users deserve assurances that material provenance, handling, and record-keeping meet the highest global standards. We take every update from international agencies seriously and adapt quality documentation to meet updated expectations. This diligence encompasses REACH, FDA DMF filings, and multi-region import-export clearances.

    After years navigating inspection cycles, we have learned that early engagement with compliance bodies smooths the way forward. Trace contaminants like heavy metals or residual solvents cannot be left to chance. They draw direct scrutiny in every batch, both for human health and environmental stewardship. We use validated, externally calibrated analytical instruments and maintain detailed SOPs for documentation. These practices did not come from executive directives; they emerged through hard-won experience after watching batches recalled, or delayed at customs, due to minor paperwork gaps or ambiguous certificates.

    Storage and shipping further complicate compliance. Moisture absorption or accidental overexposure to light during transit can shift assay results. We have invested in specialized containers, robust labeling, and logistics partners who sign off on every transfer step. This hands-on approach protects products and reputations alike—ours as well as our customers'.

    Driving Innovation through Close Collaboration

    Continuous improvement has become more than a slogan. Each campaign offers new learning—sometimes frustrating, sometimes surprising. A failed batch analysis may point the way to better solvent recovery, improved catalyst choices, or safer ways to control exothermic steps. We maintain open lines with formulation and R&D partners, urging two-way feedback on unexpected issues. In a recent cycle, customer pressure to lower HPLC-detectable trace nitroaniline led us to examine filter media compatibility and tweak drying parameters mid-run. This kind of agile response simply does not happen in organizations that view production through a distant lens.

    Direct feedback about downstream process bottlenecks, storage failures, or delayed instrument calibration cycles builds resilience. Manufacturing remains an applied science, and those standing too far from daily operations rarely catch the details that separate merely functional product from material that inspires loyalty. Our success has been built batch by batch—not on marketing promises, but on the results that show up at customers’ hoods and reactors.

    From the start, product knowledge grows in context. Direct experience handling nitro and cyano intermediates has improved our safety, reduced batch waste, and created a culture of careful documentation. Each successful shipment reflects not abstract commitment, but hands-on knowledge transferred from line operator to lab analyst, from plant engineer to account manager.

    The Path Forward for 2-Cyano-3-Nitropyridine Users

    Users across sectors—pharmaceuticals, agrochemicals, pigment, and beyond—bring unique demands to the purchase and application of 2-Cyano-3-Nitropyridine. Where some look for methodical batch-to-batch consistency, others focus on regulatory status or cost containment for pilot work. Providing direct access to process data, not just generic COA sheets, gives buyers confidence to plan and execute novel synthesis. We stand ready to discuss process variables, application hurdles, or custom requirements as projects shift from discovery to scale-up.

    The line between commodity product and specialty intermediate narrows when customers encounter unanticipated roadblocks. We draw on long experience to anticipate complications in handling, shipping, reworking, or reformulation. A phone call from a production chemist about clogging in filtration or off-hue powder prompts immediate action, often troubleshooting right alongside clients instead of simply issuing a replacement batch. Those relationships build over years of successful collaborations and shared problem-solving, not through the anonymity of global supply chains.

    Ultimately, 2-Cyano-3-Nitropyridine demands mindful handling, robust process control, and honest communication at every step. We see the difference attentive manufacturing makes, in both routine success and in the fact that our customers come back with new challenges. The lessons earned on the factory floor shape each campaign, pointing toward smarter, safer, and more efficient production methods—so that when the next synthesis cycle begins, every gram packed reflects not just chemical formula, but the sum of all our shared experience.