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3-Chloro-4-Cyanopyridine

    • Product Name 3-Chloro-4-Cyanopyridine
    • Alias 3-Chloro-4-pyridinecarbonitrile
    • Einecs 630-693-9
    • 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

    466416

    Productname 3-Chloro-4-Cyanopyridine
    Casnumber 63165-29-1
    Molecularformula C6H3ClN2
    Molecularweight 138.56
    Appearance White to pale yellow solid
    Meltingpoint 78-82°C
    Boilingpoint 305.5°C
    Density 1.32 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CN=CC(=C1Cl)C#N
    Inchikey OJMJUIAEMGIXNO-UHFFFAOYSA-N
    Refractiveindex 1.576 (predicted)
    Storage Store in a cool, dry, and well-ventilated place
    Hazardclass Irritant

    As an accredited 3-Chloro-4-Cyanopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 3-Chloro-4-Cyanopyridine is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 3-Chloro-4-Cyanopyridine is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material due to its toxic and irritant properties. Shipping must comply with local and international regulations (e.g., DOT, IATA), and the material is typically transported with appropriate labeling and safety documentation.
    Storage 3-Chloro-4-cyanopyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and use secondary containment if possible to prevent accidental spills or contamination. Follow all relevant safety guidelines and regulations.
    Application of 3-Chloro-4-Cyanopyridine

    Applications of 3-Chloro-4-Cyanopyridine in Industrial Manufacturing

    We specialize in the production of 3-Chloro-4-Cyanopyridine, delivering reliable quality that meets the stringent demands of advanced chemical synthesis. This intermediate plays a pivotal role in several high-value downstream applications, each governed by strict regulatory and technical criteria in global supply chains. The following sections detail major industrial use cases, specifying compliance requirements, application ratios, process stages, and typical finished goods relevant to each segment.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Medicines

    Pharmaceutical innovators employ this intermediate in the multi-step synthesis of select antineoplastic agent precursors, where precise control of reactivity and impurity profile is mandatory under cGMP conditions. The incorporation step often occurs at the heteroaromatic core-building stage, which requires validated purification protocols to meet stringent impurity thresholds dictated by major pharmacopeial monographs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Monographs for targeted oncology APIs
    • US FDA 21 CFR Parts 210/211 (cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia ChP 2025 requirements for API quality

    Typical usage ratio

    • Input level at 0.9–1.2 molar equivalents relative to pyridine core intermediates, adjusted to maximize yield while minimizing unreacted starting material and side-product formation.

    Downstream process integration

    • Added during the nucleophilic substitution stage of multi-step synthesis; batch or flow systems employ in situ reaction monitoring to control conversion and minimize residual contaminants, followed by chromatographic or crystallization-based purification.

    Final product types

    • Branded and generic small-molecule oncology APIs (e.g., kinase inhibitors containing pyridine derivatives)
    • Key intermediates for cytostatic agents

    2. Agrochemical Intermediate for Systemic Fungicides

    Major agrochemical producers utilize this material in the elaboration of pyridine-derived fungicide scaffolds. The compound enters chlorination and further functionalization steps to construct active ingredients deployed for crop protection, meeting modern agrochemical residue guidelines and performance standards across regulated markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues in Food)
    • REACH (EC 1907/2006) registration for precursor substances
    • ISO 9001 certified quality management systems for agrochemical intermediates

    Typical usage ratio

    • 0.7–1.1 molar equivalents depending on the specific fungicidal scaffold and the efficiency of the subsequent chlorination and ring functionalization stages.

    Downstream process integration

    • Introduced following initial building block assembly for further chlorination, cyclization, and coupling chemistry; intermediates are purified through solvent extraction and multi-stage filtration prior to formulation of the technical concentrate.

    Final product types

    • Technical-grade systemic fungicide actives (pyridine-based compounds)
    • Chemical intermediates for crop disease management agents

    3. Advanced Material Synthesis for Functional Polymers

    Manufacturers of specialty polymers incorporate this chlorinated cyanopyridine during monomer modification steps to introduce electron-deficient heteroaromatic rings, which enhance the chemical resistance and mechanical properties of target polymers. The integration step requires close control of impurity levels and can impact end-use properties in high-performance coatings and engineered plastics.

    Industry compliance standards

    • ISO 9001: Quality management in the chemical industry
    • IEC 60695-2-11 (for polymer combustion resistance where applicable)
    • RoHS Directive (EU) 2015/863 for restricting hazardous substances in end-use electronics applications
    • REACH (EC 1907/2006) for polymer precursors registration

    Typical usage ratio

    • 0.3–0.8% by weight as a comonomer or functional group donor, with the actual proportion fine-tuned based on targeted polymer type and property profile.

    Downstream process integration

    • Fed directly into monomer tank during step-growth or chain-growth polymerization; the aromatic building block reacts via nucleophilic aromatic substitution or addition linkage, then final polymers are isolated by precipitation and washed for downstream formulation.

    Final product types

    • Functionalized engineering polymers for electronics casings
    • High-performance coatings and paints for industrial use

    4. Fine Chemical Intermediate in Heterocyclic Compound Synthesis

    Custom synthesis enterprises and research-based chemical companies require this intermediate for constructing complex heterocyclic scaffolds, particularly in the development of novel ligands and advanced specialty chemicals. Usage typically targets high-purity requirements under multi-step reaction controls, with downstream purification assuring specified quality grades for research or pilot-scale applications.

    Industry compliance standards

    • ISO 17025:2017 (testing and quality standards for laboratory chemical synthesis)
    • REACH (EC 1907/2006) for laboratory and specialty use substances
    • GLP (Good Laboratory Practice) for traceability in custom synthesis
    • Internal analytical specifications agreed with downstream customers

    Typical usage ratio

    • 0.5–1.2 molar equivalents, adaptable per target heterocycle’s synthetic pathway and desired conversion rate in lab/pilot scale operations.

    Downstream process integration

    • Used as the initial coupling agent or electrophile in palladium-catalyzed cross-coupling, aromatic nucleophilic substitution, or condensation reactions; work-ups include silica gel chromatography and solvent exchange for high-purity product isolation.

    Final product types

    • Custom-developed heterocyclic intermediates
    • Specialty ligands for chemical research and material science
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    Certification & Compliance
    More Introduction

    Getting to Know 3-Chloro-4-Cyanopyridine: A Closer Look from a Chemical Manufacturer's Perspective

    As a chemical manufacturer with experience producing heterocyclic intermediates, we see daily how 3-Chloro-4-Cyanopyridine shapes projects across the pharmaceutical and agrochemical sectors. Many years of hands-on synthesis and quality control have taught us what makes this pyridine derivative stand out and why our customers keep coming back for it. Here, we share our observations—not just as producers, but as partners committed to the entire life cycle of the molecule.

    The Fundamentals: What is 3-Chloro-4-Cyanopyridine?

    3-Chloro-4-Cyanopyridine, also known by its structure as 3-chloro-4-pyridinecarbonitrile, belongs to the family of substituted pyridines. This compound has a chlorinated atom at the 3-position and a cyano group at the 4-position on the pyridine ring. Each batch we craft relies on precision: the synthesis always demands keen attention to moisture levels, temperature profiles, and strict prevention of cross-contamination. Over time, we have fine-tuned our process to reduce residual moisture and maintain consistent particle size, both of which affect downstream reactions for our customers.

    The typical chemical specification centers around the molecular formula C6H3ClN2 and a molecular weight of 138.56. Our output targets a purity of at least 99.5% by HPLC, which keeps side reactions to a minimum when clients use this compound further down their synthesis chain. Using precision glassware and well-maintained reactors, we keep metallic impurities below 10 ppm—considerably stricter than what many generic suppliers promise. Impurity data has shown that even trace levels of metal ions can lead to difficulties when using coupling reagents or catalysts; maintaining purity remains a daily concern for us.

    Why Accuracy in Specifications Matters

    We have worked with hundreds of development teams—chemist to chemist—and time and again, the message is consistent: consistent quality outcomes depend on reliable specifications throughout multiple lots of a key intermediate. If one batch of 3-Chloro-4-Cyanopyridine deviates by just half a percent in purity, that can force weeks of method revalidation or require extra purification, particularly for customers who operate at a multikilogram scale. It’s not just a piece of paperwork—these numbers become real cost and time factors. By standardizing our output and openly sharing batch-level CoAs, we simplify scale-up and validation for our partners.

    Handling fine chemicals like 3-Chloro-4-Cyanopyridine goes beyond the numbers printed on the spec sheet. Over the years, we've learned optimal storage involves low humidity and cool environments in tightly sealed drums. Exposure to light and air during sampling or repackaging can impact shelf life and reaction yields, so our facilities use nitrogen-packed containers right from filtration through shipping. Our warehouse team logs temperature and humidity daily—the extra effort translates directly to increased chemical stability for customers on the receiving end.

    Understanding Its Place in Synthesis

    Having shipped this compound to R&D and production clients for over a decade, we've tracked how demand shifts alongside advances in medicinal chemistry and crop-protection fields. Most projects utilize 3-Chloro-4-Cyanopyridine as a building block during heteroaromatic substitution and palladium-catalyzed coupling reactions. Medicinal researchers prefer the molecule because it allows quick access to disubstituted pyridine frameworks, important for scaffolds in kinase inhibitors and antiviral agents.

    We have supported scale-ups where a reliable 3-Chloro-4-Cyanopyridine supply has shortened the entire project timeline. Developers can attach functional groups at the para nitrile or ortho chloro position, creating chemical diversity in their lead series. Many who switch to higher-purity grades report improved selectivity and reduced byproducts in their Suzuki, Buchwald-Hartwig, and nucleophilic substitution reactions.

    Since the cyano substituent activates the pyridine ring toward nucleophilic aromatic substitution, some customers use it to access 3-amino-4-cyanopyridines or 3-substituted-4-aminopyridine derivatives. Agrochemical innovators rely on this route to develop herbicidal compounds and pest-control agents. We've even talked clients through process bottlenecks, offering insights from our own synthetic route to help optimize yields and reduce off-target halogen exchange.

    Differentiating Our Product: Not All Pyridines Are Equal

    We see a range of pyridine derivatives on the market—each with its own profile. Comparing 3-Chloro-4-Cyanopyridine to 2-chloropyridine, for example, reveals why scientists gravitate toward one over the other in specific applications. The electron-withdrawing cyano group at the 4-position not only stabilizes the ring but also changes the reactivity and selectivity of further chemical transformations. Customers working in nitrogen heterocycle synthesis have found that our 3-chloro variant reacts with milder conditions than unsubstituted analogs, resulting in less thermal degradation and clearer product profiles.

    We also field requests for analogs such as 3-Bromo-4-Cyanopyridine or multi-cyano substituted pyridines. Feedback from chemists tells us the chloro derivative hits the sweet spot between reactivity and commercial viability: its production remains less costly and more scalable with current catalytic routes than the bromo analog, and fewer safety restrictions surround its handling and transport. Shipment logistics benefit from fewer restrictions due to a lower GHS rating compared to analogous dibromo or fluorinated pyridines—our logistics team tracks regulatory shifts to keep customers informed about shipping and customs documentation.

    For end-users, ease of purification also factors in. Analytical chemists confirm that intermediate products derived from our 3-Chloro-4-Cyanopyridine consistently show tighter NMR and LCMS profiles compared to products of other chlorinated pyridines. In practice, this saves time during prep and leads to simpler workups, which has ripple effects on waste generation and batch throughput.

    Safety and Handling: Practical Lessons from the Production Floor

    Our staff has clocked thousands of hours in the plant—every shift brings lessons in process safety. Despite its solid form, 3-Chloro-4-Cyanopyridine can irritate skin and eyes; over the years, we've refined our loading and packing techniques to minimize exposure. SOPs always call for double-layer PPE, mobile evacuation units, and improved air filtration. Regular health and safety reviews led to one innovation: we now use vacuum transfer during drum filling, reducing airborne particulates and improving plant safety.

    Waste minimization plays a role throughout each campaign. Solvent recovery units reclaim over 80% of process media—both to lower operating costs and cut environmental impact. Starting with well-characterized cyanopyridine intermediates allowed us to adopt waste-driven improvements faster. Each near-miss or incident gets fed directly into our continuous safety training, informed by real-life scenarios, not just textbook warnings.

    Focusing on Quality Control and Technical Support

    QC teams in our facility test for over a dozen parameters in every lot of 3-Chloro-4-Cyanopyridine. Chromatography and spectral analysis make up the backbone of our verification process. Recent investments in mass spectrometry and automated titration let us pinpoint batch-to-batch consistency with even tighter tolerances. Real data from our labs shows that stable particle size distribution helps control the reactivity in coupling reactions, which our customers appreciate for reproducible results.

    Questions from clients don’t just land with a support team—they reach chemists directly on the manufacturing floor. This dialogue helps us align process improvements with actual user needs in real time. Not every customer operates at the same scale, and a pharma developer’s feedback on solubility or analytical challenges often triggers refinements in our own plant. We document every tweak, large or small, and share process insights so users understand how our latest lot compares with those made years before.

    Continual training and skill development among our operators ensures that our skill set matches the evolving needs of this specialty compound. Plant chemists handle regular inter-lab exchanges and technical troubleshooting, which helps us address application-centric issues that arise as researchers push the limits of complex organometallic reactions or design new process routes using unconventional solvents.

    Looking Ahead: New Challenges, New Solutions

    Sourcing raw materials for 3-Chloro-4-Cyanopyridine hasn't always been straightforward. Shifts in the commodity market, issues with supply chain interruptions, and periodic regulatory changes challenge the manufacturing process. We’ve solved these by integrating dual sourcing and taking initiatives to pre-qualify substitute vendors for critical upstream chemicals. Our purchasing department runs regular audits and samples every incoming lot, using a traceability system that goes from supplier’s dock all the way to finished-product warehouse.

    As downstream users request narrower impurity profiles or larger batch sizes, we adapt by expanding capacity and introducing more advanced purification steps. Typical solvent extraction and crystallization get augmented with column purification, which some clients in regulated pharmaceutical markets now require for API synthesis. We draw on our hands-on know-how to maintain throughput without compromising on batch quality—a lesson learned from manufacturing high-purity intermediates for GMP applications.

    For teams scaling up from gram to ton production, logistical and documentation support makes a difference. We run small pilot lots in parallel with commercial production, so custom specifications or unique packaging needs can be worked out ahead of the main campaign. Our documentation team manages full trace analytical reports, helping regulatory affairs teams downstream. We see this as a partnership that extends beyond the factory gate.

    Environmental Responsibility: Progress Not Promises

    Runoff and emissions management forms part of our daily operations. Reactions that generate inorganic chloride waste get routed to neutralization and recovery units. Eco-audits have helped us swap out higher-impact solvents when better substitutes become available. Managing a chemical facility comes with a responsibility, not just for shelf-stable product but for every side-stream and effluent.

    Every year we review our emissions and water usage, tying improvements directly to shop-floor decisions. Process innovations like continuous flow chemistry have allowed us to trim batch time, cut solvent use, and limit operator contact with intermediates. There’s no shortcut to genuine sustainability—each improvement must earn its place through real reductions and practical adoption by our operators.

    Bridging Scale and Service: What Our Practice Brings

    Customers value predictability, especially when a project scales from lab bench to full pilot plant. Over the years, we've shared practical tips, like optimum dissolving protocols or filtration hacks that address the quirks of 3-Chloro-4-Cyanopyridine's solubility. Our packaging recommendations, from nitrogen purged drums to vacuum-sealed liners, grew out of hard lessons from disrupted batches and feedback loops with site chemists. Each shipment aims to arrive with reactivity and bulk characteristics unchanged from the day we packed it.

    Chemists developing new molecular entities or optimizing crop protection agents look for more than just a material with high assay value—they need support that matches their project pace. The reality is, some projects pivot overnight, with developers shifting focus to a different salt form or route. Fast, open communication and flexibility across our plant teams help bridge these gaps, saving both sides precious time and avoiding costly project stalls.

    Long-Term Experience Matters

    Our years on the production and technical side grant perspective that can’t be replaced with a spec sheet or datasheet. Real expertise comes from tackling process upsets and adjusting conditions to fit the unpredictable world of specialty chemical manufacturing. Fluctuating moisture content, vendor changes, or sudden spikes in demand each require boots-on-the-ground responses and a willingness to share lessons from both successes and setbacks.

    Ultimately, 3-Chloro-4-Cyanopyridine continues to serve as a reliable cornerstone for innovation, thanks both to its chemical structure and to the effort put in by everyone who handles the product, from raw material sourcing teams to shift supervisors to analytical chemists. Each improvement, each challenge met, feeds back into a cycle of continuous advancement—not just for today’s batch, but for every future project. Our customers know they can rely on a genuine partnership built on demonstrated competence and transparency, every step of the way.