2-chloro-5-(cyanomethyl)pyridine

    • Product Name: 2-chloro-5-(cyanomethyl)pyridine
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    Specifications

    HS Code

    489257

    Chemical Name 2-chloro-5-(cyanomethyl)pyridine
    Molecular Formula C7H5ClN2
    Molar Mass 152.58 g/mol
    Cas Number 149647-78-9
    Appearance Off-white to light yellow solid
    Melting Point 48-52°C
    Density 1.23 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Smiles C(C#N)C1=CN=C(C)C=C1Cl

    As an accredited 2-chloro-5-(cyanomethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled “2-chloro-5-(cyanomethyl)pyridine, 25 grams.” Label displays hazard symbols and safety information.
    Container Loading (20′ FCL) 20′ FCL: Loaded in 200 kg drums, maximizing space for safe, secure transport of 2-chloro-5-(cyanomethyl)pyridine.
    Shipping 2-Chloro-5-(cyanomethyl)pyridine should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport in compliance with local, national, and international regulations for hazardous chemicals. Ensure secondary containment and clear labeling. Use appropriate protective packaging to prevent leaks or spills during transit. Handle with gloves and protective equipment.
    Storage 2-Chloro-5-(cyanomethyl)pyridine should be stored in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Store in a chemical-resistant container, preferably in a flammable chemicals storage cabinet. Always follow appropriate safety guidelines and local regulations for hazardous chemicals when handling and storing.
    Shelf Life 2-Chloro-5-(cyanomethyl)pyridine should be stored tightly sealed, protected from light and moisture; shelf life is typically 2-3 years.
    Application of 2-chloro-5-(cyanomethyl)pyridine

    Purity 98%: 2-chloro-5-(cyanomethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures consistent yield and product reliability.

    Melting point 62°C: 2-chloro-5-(cyanomethyl)pyridine with a melting point of 62°C is used in agrochemical formulation, where it offers optimal stability under standard processing conditions.

    Stability temperature 120°C: 2-chloro-5-(cyanomethyl)pyridine with stability temperature of 120°C is used in heterocyclic compound manufacturing, where it maintains structural integrity during high-temperature reactions.

    Molecular weight 164.58 g/mol: 2-chloro-5-(cyanomethyl)pyridine of molecular weight 164.58 g/mol is used in custom synthesis of specialty chemicals, where it facilitates accurate stoichiometric calculations.

    Particle size <100 μm: 2-chloro-5-(cyanomethyl)pyridine with particle size less than 100 μm is used in catalyst preparation, where it provides uniform dispersion and improved reactivity.

    Moisture content <0.5%: 2-chloro-5-(cyanomethyl)pyridine with moisture content below 0.5% is used in fine chemical applications, where it prevents unwanted hydrolysis and ensures product stability.

    Storage condition 2–8°C: 2-chloro-5-(cyanomethyl)pyridine stored at 2–8°C is used in research laboratory settings, where it preserves compound potency and minimizes degradation.

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    Certification & Compliance
    More Introduction

    2-Chloro-5-(Cyanomethyl)Pyridine: A Closer Look at a Critical Building Block

    Getting to Know 2-Chloro-5-(Cyanomethyl)Pyridine

    In the world of specialized chemicals, 2-chloro-5-(cyanomethyl)pyridine stands out for more than its complex name. Chemists and product developers searching for reliable intermediates will recognize its potential, especially as the demand for selective synthesis in pharmaceuticals and fine chemicals continues to grow. With its molecular formula C7H5ClN2, transparent crystalline appearance, and precise reactivity points, this organic compound bridges the gap between foundational lab reagents and targeted industrial processes.

    I’ve spent years watching how minor tweaks to molecular structures shape entire production lines. A chlorine atom in the right spot, like the 2-position on this pyridine ring, doesn't just change a chemical’s identity; it changes how it interacts in reactions, streamlining synthesis routes for complex molecules. The cyanomethyl group adds extra reactivity, opening doors for further chemical transformations, such as nucleophilic additions or coupling processes.

    Model and Specifications: Beyond Purity Numbers

    2-chloro-5-(cyanomethyl)pyridine comes in a range of purity grades, often hovering from 97% to 99% in reputable labs. Chemical purity isn’t just about numbers for quality control; I’ve seen hands-on how a half-percent difference can make or break a reaction yield, especially in pharmaceutical work. The physical state—usually a solid or crystalline powder—offers both stability during storage and ease of weighing for reaction setup.

    Handling this compound requires basic lab precautions: it isn’t particularly volatile, but its functional groups warrant gloves and a well-ventilated workspace. The melting point sits comfortably for most solid-phase extractions or purifications. Experienced chemists know to keep it dry and away from open flames, as with many organochlorine compounds. Keeping detailed records of batch numbers and purity helps track down anomalies if a final product acts up down the line.

    Uses: Why This Molecule Matters

    Digging into the applications, 2-chloro-5-(cyanomethyl)pyridine earns its place as a valuable intermediate. In pharmaceutical development, the compound pops up in established synthesis routes for active ingredients. Not every molecule wears a cape or gets the headlines; intermediates like this hold together production plans for antibiotics, antivirals, crop protection agents, and select material science polymers.

    Take, for instance, the challenge of adding new functionalities onto a pyridine scaffold. The chlorine and cyanomethyl positions make substitution straightforward using common organic reagents. Some modern pesticides rely on this structure as a foundation, tailoring reactivity to target only particular insect biochemical pathways and leave the rest of the ecosystem mostly untouched. The difference between success and a regulatory miss sometimes comes down to how selectively a molecule gets built, and this compound offers that selectivity.

    Comparing to Other Key Intermediates

    The market holds no shortage of pyridine derivatives, but the 2-chloro-5-(cyanomethyl) model pulls ahead by combining two distinct reactivity handles. For instance, compared to 2-chloropyridine or 5-cyanopyridine alone, the cyanomethyl and chlorine combination dramatically broadens what transformations chemists can attempt on a single scaffold. When dealing with a project that requires multiple sequential modifications, this compound gives much more flexibility than a molecule with only one reactive site.

    I’ve worked with simple pyridines that refuse to budge under standard reaction conditions, wasting days and material trying to punch through with stronger reagents; 2-chloro-5-(cyanomethyl)pyridine skips that headache. It’s like starting a home project with a multi-tool instead of a flathead screwdriver. Instead of hunting down three or four separate reagents to force a tricky reaction, this compound handles diversified synthesis routes much more efficiently.

    Why Purity, Traceability, and Quality Control Matter

    Anyone who’s ever had a batch of intermediate go sour in a pharmaceutical run knows that subpar materials don’t just cost money—they set back months of research. Experience shows that even low-level impurities can introduce side reactions, lowering yields or introducing by-products that muddy up purification steps later. For 2-chloro-5-(cyanomethyl)pyridine, reliable suppliers run thorough analytical checks, typically using HPLC and NMR to confirm structure and purity. Keeping these reports on-hand not only reassures end-users; it forms an audit trail if anything unexpected arises later in the process.

    Chemists also check for the presence of chloride ions or residual solvents, which can quietly sabotage a synthesis without showing up in appearance checks. I recall once battling an unexplained decrease in yield, only to trace it back to an unlisted impurity in a commercial batch. Lessons like that reinforce the role of quality documents and careful supplier evaluation. Trustworthy sources regularly share analytical spectra on request, helping cut down troubleshooting time and preventing expensive reruns.

    Regulatory Hurdles and Environmental Considerations

    The presence of both a chlorine atom and a nitrile group raises legitimate concerns about downstream processing and environmental persistence. Most countries regulate the storage, handling, and waste management of such intermediates. Labs and factories working with 2-chloro-5-(cyanomethyl)pyridine generally keep detailed logs for compliance purposes, as these functional groups produce organochlorine compounds or nitriles during waste processing.

    Sustainable chemistry has moved from a marketing buzzword to a necessity. I’ve followed several green chemistry initiatives aimed at reducing solvent volume and minimizing hazardous side-products during reactions involving this intermediate. While the route typically used for synthesizing the compound is efficient, research into greener alternatives remains ongoing. Institutions underline the importance of treating any waste stream appropriately, so disposal doesn’t contaminate local water systems or introduce persistent organic pollutants.

    Challenges and Solutions in Handling and Scale-Up

    The jump from bench to pilot plant introduces new questions. Small-scale reactions tolerate a little wiggle room—it’s easy to tweak a temperature or double-check a purification—whereas ton-scale runs demand different disciplines. 2-chloro-5-(cyanomethyl)pyridine displays solid shelf stability in properly sealed containers, but humidity creeps in fast in a warehouse setting, risking hydrolysis over time.

    One plant manager I worked with solved storage headaches by introducing desiccant packs and strict inventory turnover. Scheduled checks and FIFO (first-in, first-out) inventory systems stave off product degradation and also reduce audit-related downtimes. For handling, automated loading and weighing reduce employee exposure risks. As processes modernize, automated batch recorders and climate-controlled warehouses streamline both efficiency and compliance.

    Some labs looking to reduce costs prefer to synthesize this intermediate in-house. I always advise careful cost-benefit analysis before diving in. The raw materials used for its synthesis, as well as the need for exacting purification and waste disposal, can quickly erase any savings compared to purchasing from a reputable vendor. Balancing economics with safety and reliability shapes every step of the decision-making.

    Innovation and Evolving Uses

    The pharmaceutical landscape never stops shifting. Every year, new molecular targets demand fresh approaches to synthesis. 2-chloro-5-(cyanomethyl)pyridine serves not just as a stepping-stone but as a pivot point for developing new therapeutic candidates, especially in projects involving heterocyclic scaffolds. Drug discovery chemists can use it to append new groups where they want them, enabling structure-activity relationship (SAR) exploration with relative ease.

    In agriculture, the need for selective pesticides and herbicides prompts chemists to revisit established scaffolds searching for unique activity profiles. This compound’s dual reactivity means fewer steps to reach unusual modifications. Rather than relying on legacy molecules with less efficient transformation options, researchers can start with more versatile intermediates, cutting down on process time and boosting selectivity.

    Material science has only just begun to uncover possibilities for functionalized pyridines. Polymers with tailored electrical properties, specialty coatings, and even hybrid organic-electronic materials could benefit from the reactive versatility of this intermediate. Collaboration between chemists, engineers, and environmental scientists will shape its future roles in both familiar and unexplored markets.

    Safety Practices and Industry Standards

    Working with 2-chloro-5-(cyanomethyl)pyridine, I’ve learned that shortcuts in safety backfire. Although it doesn’t carry the same hazard level as some explosive reagents, it still requires careful handling—contact with skin or inhalation of dust can present health risks. Workplace protocols emphasize chemical goggles, gloves, and fume hoods. On-site training for new staff, even those with advanced degrees, covers emergency procedures and equipment use.

    Chemical management grows more sophisticated each year. Laboratories across the globe shifted from ad hoc storage to barcode-tracked bottles, scheduled safety audits, and regular spill drills. Such efforts reduce risk and satisfy both internal guidelines and external regulatory demands. Responsible disposal and spill response build trust not only with inspectors but also with the broader community—a factor I consider every time I introduce a new chemical into our workflow.

    Documentation plays a role here as well. Up–to-date safety data sheets remain close at hand, and all handling and storage guidance receives regular updates to reflect the most current information available. Routine monitoring of air quality in production settings and strict access controls for higher-risk chemicals help harden the chain of custody.

    Supply Chain Resilience and Long-Term Planning

    Global events can upend even the most carefully planned chemical supply chains. From what I’ve seen, supply disruptions for intermediates like 2-chloro-5-(cyanomethyl)pyridine ripple through research, pilot plants, and commercial production alike. Building resilience starts with diversified sourcing—working with suppliers in multiple regions and carrying enough safety stock to weather surprise delays.

    Transparent supplier relationships and regular quality audits set a foundation for stability. I’ve helped manage runs where a last-minute supplier change introduced quality inconsistencies that took weeks to fully resolve. Strong back-up plans and close communication with suppliers go a long way toward maintaining both quality and delivery timelines.

    The pandemic underscored how deeply reliant pharmaceutical and specialty chemical industries are on reliable intermediates. Teams that fared best didn’t just hope for the best—they shared information, updated contingency plans, and invested in regular risk assessments. It’s not glamorous work, but keeping the right intermediate on hand makes all the difference between hitting a market window and missing it completely.

    Quality by Design: Staying Ahead of Regulatory Trends

    Regulatory environments move faster than they used to. Producers and users of 2-chloro-5-(cyanomethyl)pyridine who track not only current but also upcoming guidance will find themselves in a stronger position. Auditors and health authorities increasingly ask for demonstrable quality by design (QbD) strategies. This means documenting every control, qualification step, and contingency—not only because regulators demand it, but because it prevents headaches when troubleshooting.

    In my experience, labs that embed QbD principles from early development stages can scale up faster and respond more deftly to regulatory questions. Regularly updating procedures in light of new findings and maintaining open channels with regulatory authorities set these organizations apart. Beyond compliance, such discipline often leads to fewer recalls, less downtime, and increased confidence from clients and end users.

    Looking Ahead: Future Trends and Opportunities

    Chemistry will always chase after smarter, safer, and more efficient ways to build molecules. 2-chloro-5-(cyanomethyl)pyridine sits in a sweet spot: neither too specialized to be inaccessible, nor so generic that every competitor can undercut its value. Ongoing advances in catalytic methods, greener synthetic routes, and process intensification will likely make use of its core strengths: versatility, selectivity, and reliability.

    While no intermediate solves every challenge alone, integrating this compound into strategic projects allows rapid prototyping and shortens the path from idea to outcome. Whether in pharmaceuticals, agriculture, or materials, the ability to adapt that structure to fit changing regulatory, safety, and performance demands keeps it relevant. For teams looking to future-proof their processes and innovate responsibly, paying close attention to both technical and human factors surrounding core intermediates proves as important as the chemistry itself.

    In the end, my experience reinforces that relying on dependable, well-characterized intermediates isn’t just about following protocol. It’s about safeguarding results, protecting teams, and building lasting success in research and industry.