3,5-Dichloro-2-CYANOPYRIDINE

    • Product Name: 3,5-Dichloro-2-CYANOPYRIDINE
    • Chemical Name (IUPAC): 3,5-dichloropyridine-2-carbonitrile
    • CAS No.: 65167-89-7
    • Chemical Formula: C6H2Cl2N2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    538365

    Productname 3,5-Dichloro-2-cyanopyridine
    Casnumber 60134-13-2
    Molecularformula C6H2Cl2N2
    Molecularweight 173.00
    Appearance Off-white to light yellow solid
    Meltingpoint 90-94°C
    Density 1.47 g/cm3 (estimated)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents like acetone
    Smiles C1=C(C=NC(=C1Cl)C#N)Cl
    Inchi InChI=1S/C6H2Cl2N2/c7-4-1-5(8)10-3-6(4)2-9
    Synonyms 2-Cyano-3,5-dichloropyridine
    Storagetemperature 2-8°C (cool, dry place)

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

    Packing & Storage
    Packing 250g of 3,5-Dichloro-2-cyanopyridine is supplied in a tightly sealed amber glass bottle with a printed hazard label.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 14 metric tons, packed in 280 drums (each 50 kg) for 3,5-Dichloro-2-cyanopyridine.
    Shipping 3,5-Dichloro-2-cyanopyridine is shipped in tightly sealed containers under ambient conditions. Containers should be labeled clearly and handled by trained personnel. The chemical must be protected from moisture, direct sunlight, and incompatible substances. Proper documentation and compliance with local, national, and international regulations for chemical transport are required.
    Storage 3,5-Dichloro-2-cyanopyridine should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong acids, bases, and oxidizers. Keep the container tightly closed and clearly labeled. Protect from moisture and light. Use appropriate chemical storage cabinets and ensure spill containment measures are in place to prevent environmental contamination.
    Shelf Life 3,5-Dichloro-2-cyanopyridine is stable under recommended storage conditions; shelf life is typically 2-3 years in a cool, dry place.
    Application of 3,5-Dichloro-2-CYANOPYRIDINE

    Purity 99%: 3,5-Dichloro-2-CYANOPYRIDINE with purity 99% is used in agrochemical intermediate synthesis, where it ensures high-yield conversion rates.

    Molecular weight 173.02 g/mol: 3,5-Dichloro-2-CYANOPYRIDINE with molecular weight 173.02 g/mol is used in pharmaceutical research, where consistent molecular composition enhances reproducibility in drug discovery.

    Melting point 65-68°C: 3,5-Dichloro-2-CYANOPYRIDINE with melting point 65-68°C is used in fine chemical manufacturing, where controlled solid-to-liquid transitions support process efficiency.

    Stability temperature up to 120°C: 3,5-Dichloro-2-CYANOPYRIDINE with stability temperature up to 120°C is used in high-temperature reaction systems, where it maintains structural integrity during synthesis.

    Particle size <50 µm: 3,5-Dichloro-2-CYANOPYRIDINE with particle size <50 µm is used in formulation of specialty coatings, where uniform dispersion improves product homogeneity.

    Moisture content ≤0.2%: 3,5-Dichloro-2-CYANOPYRIDINE with moisture content ≤0.2% is used in electronics chemical processing, where minimized water content prevents hydrolytic degradation.

    HPLC assay ≥98%: 3,5-Dichloro-2-CYANOPYRIDINE with HPLC assay ≥98% is used in laboratory-scale syntheses, where high assay values guarantee analytical accuracy.

    Residual solvent <500 ppm: 3,5-Dichloro-2-CYANOPYRIDINE with residual solvent <500 ppm is used in active pharmaceutical ingredient development, where low solvent levels enhance final product safety.

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    Certification & Compliance
    More Introduction

    3,5-Dichloro-2-CYANOPYRIDINE: Expanding Possibilities for Chemical Synthesis

    Looking Closely at 3,5-Dichloro-2-CYANOPYRIDINE

    Most people outside of chemical research rarely hear about substances like 3,5-Dichloro-2-CYANOPYRIDINE, yet this compound quietly supports a surprising range of laboratory and manufacturing progress. Its chemical structure—a pyridine ring decorated with chlorine atoms at the 3 and 5 positions and a cyano group sitting at the 2 position—gives chemists a springboard for building much more complex molecules. The demand for precision in fine chemicals and pharmaceuticals keeps this material in demand, not because it is universally applicable, but because it does a handful of things extremely well.

    From my time in academic labs and brushing shoulders with process chemists in industrial setups, I’ve come to appreciate the subtle but key differences that set 3,5-Dichloro-2-CYANOPYRIDINE apart from its cousins. Chemists always seek tools that offer reliability, reactivity, and a manageable safety profile. Not all pyridines offer these traits in equal measure. This compound manages to strike a balance, offering predictability in reactions and a manageable set of handling procedures for trained professionals. These advantages draw out its full value—not just for one niche use, but as a partner in many different reaction schemes.

    Specifications Matter: Purity, Quality, and Physical Form

    The chemical’s value starts with its make-up: a molecular formula of C6H2Cl2N2 and a molecular weight around 187. The importance of purity cannot be overstated—small traces of moisture or other contaminants force reactions off course. Labs and production lines choosing 3,5-Dichloro-2-CYANOPYRIDINE expect specifications like purity above 98%, minimal water content, and a predictable melting point. Some manufacturers offer this product as an off-white or almost pale yellow powder, which hints at the consistency in production and care taken in packaging and storage.

    There’s a lot of talk about analytical data in procurement meetings—NMR spectra, HPLC purity readings, GC-MS scans—but behind all of these numbers lies a simple truth: success in a synthetic step often depends on the batch quality of just one building block. Once, working with a team scaling up a cross-coupling reaction, I saw an unexpected impurity in a starting material throw off the whole downstream process. Thankfully, reliable suppliers of high-quality 3,5-Dichloro-2-CYANOPYRIDINE help chemists avoid these pitfalls.

    Where 3,5-Dichloro-2-CYANOPYRIDINE Delivers the Most Value

    This compound’s strengths sit squarely in the fields of pharmaceutical intermediates, agrochemicals exploration, and specialty chemicals research. Its unique substitution pattern both activates the ring and provides convenient handles for further transformation—chemists can carry out substitutions, couplings, or reductions with some predictability. In pharmaceutical research, the push for new treatments means sifting through huge libraries of candidate molecules. Rapid access to varied cyanopyridines, especially those with halogens in strategic spots, makes a real difference in timelines.

    On the crop protection side, several classes of modern agrochemical molecules draw heavily from substituted pyridine cores. The electron-withdrawing nature of the cyano and chloro groups can radically tune biological properties—sometimes making a new product more selective, metabolically stable, or potent at lower doses. As someone who has seen agricultural field trials struggle to balance innovation and regulation, I recognize how key these starting blocks can be.

    Specialty chemicals companies take a different approach, diving into the reactivity soup that dichloro (and sometimes cyano) functionalities bring. Using 3,5-Dichloro-2-CYANOPYRIDINE as a precursor unlocks advanced materials: liquid crystals, dyes, functional polymers, and even environmental remediation agents. In these markets, reliability and the ability to customize reaction conditions remain vital.

    How It Stands Apart from Other Pyridine Derivatives

    Not every pyridine pulls its weight the same way. For example, the 2,6-dichloro-3-cyanopyridine variant reacts in a distinctly different way because of how the groups play off each other around the ring. The position and number of halogens impact both reactivity and selectivity in downstream chemistry. Laboratories with a focus on diversity-oriented synthesis gravitate to 3,5-Dichloro-2-CYANOPYRIDINE for this very reason: it creates opportunities while avoiding some of the pitfalls associated with other isomers.

    Another frequent question in industrial chemistry involves cost-to-benefit analysis. Some alternatives offer lower upfront costs or easier synthesis, but they don’t always provide the precise combination of activation and stability that the 3,5 version does. The cyano group acts like a beacon for further reaction—especially in nucleophilic aromatic substitution—while the dichloro pattern resists unwanted side reactions. In practice, I have seen research teams struggle to select the best building block, sometimes cycling through multiple candidates before landing on this one for the right fit. Its versatility often tips the balance, especially for projects where success depends on careful orchestration of function and safety.

    Comparing Real-World Impact

    Chemistry as a field always juggles fundamentals and application. It’s easy to get lost in catalog numbers or piles of technical data, missing the bigger picture of how one compound can shape entire projects. With 3,5-Dichloro-2-CYANOPYRIDINE, the impact emerges through improved efficiency and broader access to unique molecular frameworks. From a project manager’s viewpoint, shaving a week or two off a synthesis pipeline can mean the difference between a published paper or a failed grant. For companies, the compound’s track record backs up claims of reliable performance, while chemists find that its predictable reactivity means fewer surprises and wasted materials.

    In my experience collaborating with interdisciplinary teams, I saw that clear communication about quality and sourcing matters as much as technical ability. A robust supply of 3,5-Dichloro-2-CYANOPYRIDINE supports this, letting chemists focus on invention instead of supply headaches. Trusted suppliers who stake their reputations on batch consistency tackle a huge part of this challenge.

    Supporting Responsible Sourcing and Handling

    Once you dive into the world of industrial chemicals, questions of safety and environmental responsibility come up quickly. Handling 3,5-Dichloro-2-CYANOPYRIDINE calls for personal protective equipment, trained staff, and strict protocols—not only to stay on the right side of regulatory oversight, but to keep workplaces safe. The presence of halogens and a cyano group means the compound carries moderate risks if mishandled, though experience shows that accidents remain rare with proper lab culture.

    Over recent years, the chemical industry has responded to stricter controls and public scrutiny. Companies now document their chain of custody, demonstrate safe disposal practices, and often use green chemistry approaches to minimize waste. As a former member of a chemical safety committee, I helped design protocols for cyanopyridine handling and containment. These steps aren’t optional—they wind up shaping trust between suppliers, researchers, and the wider public.

    Trends Toward Sustainability With Specialty Pyridines

    As demand grows for chemicals like 3,5-Dichloro-2-CYANOPYRIDINE, attention shifts toward sustainable manufacturing. Synthesizing halogenated and nitrile-containing aromatics once relied almost entirely on harsh reagents and energy-intensive conditions. Newer routes—catalysis, continuous flow processing, and atom-efficient steps—now allow producers to limit hazardous byproducts and improve energy management.

    Green chemistry thinking doesn’t just benefit regulatory compliance. These advances matter for long-term business resilience, too. Companies that invest in cleaner and smarter methods find themselves positioned ahead of the curve. I’ve watched smaller firms leapfrog bigger competitors by pushing new synthetic routes that cut waste, win over regulatory agencies, and impress large customers asking for documentation on responsible sourcing.

    Challenges: Cost Control, Supply Chain Stability, and R&D Constraints

    Every chemical market throws up its own hurdles. For 3,5-Dichloro-2-CYANOPYRIDINE, controlling production costs can be tough, with fluctuations in raw material pricing and regional variations in environmental fees. When global supply chains fray, lead times stretch out and prices spike, affecting project budgets and even causing production delays. Strong networks with multiple approved suppliers help, but there’s always a need for ongoing risk management.

    On the research side, developing new applications or improved derivatives calls for persistent investment. Companies that rely on this pyridine derivative can’t afford to rest on existing products. Investment in new reactions, smarter processes, and downstream products opens up more opportunities and defends against commodity market risks.

    Applications Across Drug Discovery, Agrochemicals, and Beyond

    The clearest impact of 3,5-Dichloro-2-CYANOPYRIDINE shows up in drug discovery pipelines. Medicinal chemists use it for introducing both halogen and nitrile groups at well-defined positions in a single synthetic move. This shortens routes to potential drug candidates and helps with rapid analog design, crucial for assembling lead compound libraries.

    Agrochemical companies tap into the same capabilities, often in parallel with pharmaceutical research. The goals overlap: fine-tuning bioactivity, shaping physical properties, and ensuring environmental stability. Working alongside agronomists and regulatory affairs teams, chemists often push the boundary of what these building blocks can do for plant health, pest resistance, and selective weed control. These practical wins help put food on tables and keep land productive.

    In specialty chemical and material science sectors, 3,5-Dichloro-2-CYANOPYRIDINE opens doors to advanced coatings, electronics materials, and dyes. Our modern world depends on such innovations, yet these products rarely earn wide recognition. They underpin improved durability, faster electronics, and better environmental protections through clever chemistry grounded in these niche intermediates.

    Quality Assurance, Regulation, and the Evolving Marketplace

    Laboratories and manufacturers increasingly face global scrutiny over purity standards, traceability, and compliance. Regulatory authorities like the US FDA and the European Chemicals Agency both set high bars for documentation. Consistent supply of legitimate, high-purity 3,5-Dichloro-2-CYANOPYRIDINE builds trust and helps research teams pass audits or move substances through pre-clinical phases. I’ve seen firsthand how tight record-keeping and third-party testing smooth the path for scaling up a once-lab-scale procedure.

    Digital marketplaces now connect buyers and sellers worldwide. This dynamic helps keep prices competitive, but it also raises the risk of fake or adulterated goods. Astute procurement teams rely not only on price or delivery speed but prioritize proven track records for quality. Well-established labs share supplier lists, cross-check COAs, and run independent analytical verifications. Such vigilance shields organizations from regulatory headaches, wasted effort, and even ethical risks in product development.

    Throughout the markets that rely on 3,5-Dichloro-2-CYANOPYRIDINE, confidence stems not from marketing but from continual validation—whether by direct experience, published data, or peer recommendations.

    Tackling Industrial-Scale Challenges

    Manufacturing at scale brings a unique set of challenges for 3,5-Dichloro-2-CYANOPYRIDINE. Scaling up reactions without losing material efficiency or compromising environmental controls means constant tinkering and process optimization. I’ve witnessed pilot plant teams face snags, fixing batch-to-batch variability or improving recovery from highly engineered reaction setups. These real-world adjustments separate journal success from industrial viability.

    Collaborations between chemical engineers, QC staff, and R&D chemists drive breakthroughs here. Small improvements—a new filtration technique or a gentler purification step—can trim production timelines and cut costs, while still maintaining high-purity output. The learning curve can be steep, but each fix translates to more reliable products down the line.

    With demand tightening, especially from pharmaceutical and specialty chemical segments, the pressure remains on to deliver both quality and consistency. Industry insiders recognize that prompt troubleshooting of supply interruptions and commitment to single-batch traceability keeps buyers coming back.

    Supporting Ethical and Effective Use

    Chemists and management teams alike hold a responsibility: to use powerful reagents like 3,5-Dichloro-2-CYANOPYRIDINE for advances that benefit society, without sacrificing safety or ethics. Training, open communication, and continual learning go hand-in-hand with technical skill. Ethical review panels, safety audits, and open forums now play bigger roles in fostering a culture where responsible handling is part of daily operations.

    For those preparing the next generation of chemists, standardizing best practices around hazardous intermediates includes everything from reagent substitution during training programs to running real-world scenario drills. These investments pay off in safer labs and safer workplaces when newcomers step into commercial settings.

    None of these practices take away from the potential locked inside this one compound. Instead, safety and responsibility augment its usefulness, helping keep doors open for wider application and public trust.

    Forward Paths: Innovation and Adaptation

    Continual progress in organic synthesis and material science spotlights intermediates like 3,5-Dichloro-2-CYANOPYRIDINE as essential enablers of discovery. Industry and academic efforts coalesce when tackling difficult problems—whether that means deploying catalyst technologies, tuning selectivity for novel compounds, or developing lower-impact manufacturing.

    Keeping pace with global trends, suppliers and customers alike match step with new digital tools for quality control, automated process monitoring, and supply chain transparency. Integration of these advances cements future growth, lowering risks and creating more adaptable organizations.

    Having watched the chemical field shift so fast over the past decade, I’m encouraged by the willingness to challenge old assumptions and push for smarter, safer, and more sustainable standards. For 3,5-Dichloro-2-CYANOPYRIDINE, this translates to its continued relevance across sectors and into the hands of creative scientists ready to tackle tomorrow’s challenges.