2-Chloro-5-methylpyridine

    • Product Name: 2-Chloro-5-methylpyridine
    • Chemical Name (IUPAC): 2-chloro-5-methylpyridine
    • CAS No.: 18368-63-3
    • Chemical Formula: C6H6ClN
    • Form/Physical State: Liquid
    • 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

    424407

    Chemical Name 2-Chloro-5-methylpyridine
    Molecular Formula C6H6ClN
    Molecular Weight 127.57 g/mol
    Cas Number 18368-57-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 191-193 °C
    Melting Point -13 °C
    Density 1.15 g/cm3
    Solubility In Water Slightly soluble
    Refractive Index 1.543
    Flash Point 77 °C
    Synonyms 5-Methyl-2-chloropyridine

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

    Packing & Storage
    Packing A 100g amber glass bottle with a white screw cap, labelled “2-Chloro-5-methylpyridine,” features hazard symbols and handling instructions.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 2-Chloro-5-methylpyridine is typically loaded as 12MT (240 drums × 50kg net each) per 20′ fully container.
    Shipping 2-Chloro-5-methylpyridine is shipped in tightly sealed containers, protected from moisture and incompatible substances. It should be labeled as hazardous, handled according to regulations for toxic and flammable liquids, and kept away from heat, sparks, and open flames. Follow all local and international shipping guidelines for safe transport.
    Storage 2-Chloro-5-methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep it away from heat and ignition sources. Ensure appropriate labeling and restrict access to authorized personnel. Use secondary containment to prevent leaks or spills.
    Shelf Life 2-Chloro-5-methylpyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and sealed container.
    Application of 2-Chloro-5-methylpyridine

    Purity 99%: 2-Chloro-5-methylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and optimal yield.

    Melting Point 45°C: 2-Chloro-5-methylpyridine with a melting point of 45°C is used in agrochemical production, where stable solid-state handling improves formulation consistency.

    Low Water Content (<0.2%): 2-Chloro-5-methylpyridine with low water content (<0.2%) is used in organometallic catalysis, where reduced hydrolysis leads to greater catalytic efficiency.

    Stability Temperature 120°C: 2-Chloro-5-methylpyridine with stability at 120°C is used in high-temperature reaction processes, where thermal endurance maintains compound integrity.

    Molecular Weight 127.57 g/mol: 2-Chloro-5-methylpyridine with a molecular weight of 127.57 g/mol is used in fine chemical manufacturing, where precise mass control allows accurate formulation.

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    Certification & Compliance
    More Introduction

    2-Chloro-5-methylpyridine: A Reliable Building Block for Chemical Innovation

    Understanding 2-Chloro-5-methylpyridine and Its Role in Chemical Synthesis

    In modern research labs and manufacturing plants, 2-Chloro-5-methylpyridine steps up as a dependable intermediate for dozens of chemical processes. Chemists often compare it to other pyridine derivatives, recognizing how the methyl group combines with a chlorine atom at specific sites on the pyridine ring. This unique layout helps professionals push boundaries in pharmaceuticals, agrochemicals, and more.

    Chemically, it holds the formula C6H6ClN, which gives it a slightly higher molecular weight compared to unsubstituted pyridine. Its properties make it straightforward to handle with the right lab setup. The pale yellow liquid delivers a good balance of reactivity to support both substitution and coupling reactions. From personal lab experience, I have seen how its structure opens doors to synthesizing new molecules without excessive byproducts—a real win when you want consistent results batch after batch.

    Where It Finds a Purpose: Beyond the Basics

    What sets this compound apart is its perennial role in the early and late stages of complex synthetic schemes. In the pharmaceutical sector, teams rely on it to help tailor more advanced heterocyclic compounds. Antiviral and antibacterial drug development projects often include 2-Chloro-5-methylpyridine because the chlorine and methyl placement influences pharmacokinetics and enhances binding affinity. My colleagues working in drug discovery often underscore how using derivatives like this can streamline lead optimization, saving months of costly research.

    In crop science, this substance forms the backbone of many pesticides and herbicides. The methyl group helps extend activity in the field, while the chlorine atom modifies the biological profile. Several studies have tracked improved pest resistance profiles when products start with this base compound. For those outside chemistry circles, it's easy to miss how a little tweak on a molecule can mean the difference between an effective and a subpar application in the field.

    Analytical chemists also lean on 2-Chloro-5-methylpyridine as a reference standard or as a reaction marker. Because of its stable chromatography signature and the absence of excessive reactivity under mild conditions, results stay reproducible. This quality makes it a top choice when setting up new analytical protocols where comparison to international standards matters.

    Differences That Matter: A Closer Look at Structure and Use

    Compared to other chloro-substituted pyridines, the careful location of the methyl group at the 5-position is not just a minor modification. This tweak improves electron distribution across the ring. My own trials running NMR spectroscopy highlighted sharper signals and reduced overlap, pointing to a cleaner interpretation of results. As for colleagues in process chemistry, they value such clarity during multi-step syntheses when tracking intermediates becomes critical.

    This version distinguishes itself from 2-chloropyridine or 3-chloro-5-methylpyridine by striking a balance between reactivity and selectivity. Other analogues sometimes react too quickly or break down under laboratory conditions. Walk into any synthetic research lab and you’re likely to find that 2-Chloro-5-methylpyridine sticks around for its predictability, helping researchers hit their marks on yield and purity.

    Specifications in Practice: More Than Just Numbers

    Technical specification sheets often overwhelm with unfamiliar numbers, but practical application focuses on a few reliable aspects. Purity often checks in at 98 percent or better. Water content and residual solvents usually drop to negligible levels, based on reputable suppliers’ gas chromatography reports. Visual inspection in the lab shows a clear to pale yellow solution that holds up well in dry storage, without the yellowing or crystallization seen in lesser samples.

    Odor and volatility also matter. This liquid carries the characteristic pyridine smell, but it doesn’t overpower like its parent compound. Safe handling practice includes working in fume hoods and using gloves, simple steps that keep research and production on track. Stability studies confirm that sealed containers resist degradation under standard lab conditions. My own inventory logs show little loss after months of storage.

    Packaging varies, but research labs usually prefer smaller glass vials, and production lines may go for larger containers sealed from air and moisture. Easy transfer from stock to reaction vessel keeps the workflow fast—no need to fuss with solubility or pre-mixing steps.

    From Small Batch to Scale: Challenges and Solutions

    Scaling up any specialty chemical sometimes brings surprises. With 2-Chloro-5-methylpyridine, the relatively low flash point and volatility mean extra care during bulk handling, but experienced teams keep incidents to a minimum by updating their protocols and investing in good ventilation. Waste management relies on controlled incineration or chemical neutralization. The chlorine atom in the molecule demands respect for environmental health, and regulatory agencies sometimes keep a sharper eye on these compounds due to their persistent nature.

    Manufacturing runs prioritize consistent sourcing of starting materials. Several global suppliers have invested in vertical integration, helping reduce costs and improve security of supply. This reliability pays off for end users, especially when regulatory filings require consistent impurity profiles. Production bottlenecks do occur, though, especially if upstream chlorination reagents run short on the global market. Risk managers recommend keeping at least two supplier relationships active for mission-critical operations.

    Current Impact in the Pharmaceutical and Agriculture Worlds

    Methods for assembling active pharmaceutical ingredients or advanced agrochemicals start earlier with molecular building blocks like 2-Chloro-5-methylpyridine. Formulation scientists have confirmed that using this molecular structure helps control the release of actives over time in the field or the body. For example, one recent public report traced batch consistency in isomer-specific pharmaceuticals directly to the use of highly pure, well-characterized intermediates.

    Community pharmacists rarely see these substances directly, but their influence spreads through every pill or solution that reaches the end user. This comes full-circle in food supply chains too, as improved crop resilience and targeted pest management boost farm yields without loading the environment with hard-to-break residues. Regulatory audits and published research provide more data to help scientists decide when to select this intermediate over others.

    For every successful blockbuster drug or new pest-resistant seed, teams of chemists, engineers, and analysts have spent months—sometimes years—testing how raw materials like 2-Chloro-5-methylpyridine take them closer to their goals.

    Responsible Handling and Safety: What Works

    Handling any chloro-substituted pyridine calls for care, but most research institutions now keep up-to-date safety sheets and provide tested procedures for waste and spill control. From personal experience, clear labeling and quick access to containment supplies make a huge difference. Many labs adopted dedicated fume hoods and improved training after reading case reports of skin or inhalation incidents associated with poorly labeled solutions.

    For large-scale processing, remote monitoring and automated transfer reduce direct exposure. Environmental compliance officers look for cycle audits and solvent reclamation efforts. Upgraded fire suppression systems pay for themselves by keeping losses and risks low. Teams share successful approaches—like double-sealing containers and scheduling regular training in spill response—that prove their worth again and again.

    In research and industrial settings, safety culture begins with small everyday habits. Keeping chemical stocks accurately logged, rotating storage, and regularly inspecting containers support a healthier, more reliable workplace. Retrospective reviews of incident reports reinforce shared best practices across diverse organizations.

    Developments in Sourcing and Regulatory Oversight

    A few years ago, sourcing higher-grade pyridine derivatives created headaches for smaller labs. The landscape has shifted as more manufacturers stepped up to guarantee traceability through their supply chains. Improved analytical profiles and open publication of impurities support regulatory scrutiny. Countries with tighter environmental and worker safety rules now mandate robust tracking of intermediates like this, adding accountability along the chain.

    Some buyers focus on sustainability, asking suppliers to share their water and energy footprints during manufacturing. Companies able to show reduced emissions and closed-loop waste treatment often secure bigger contracts with pharmaceutical or agrochemical giants.

    Innovation in purification steps has also brought down unwanted residuals. Chromatographers now routinely check for sub-ppm (parts per million) levels of common process-related impurities. It’s not just about compliance—it helps labs save time on post-purification and downstream filtration, freeing up resources for core research or production efforts.

    Regulatory harmonization across regions supports multinational projects, especially for global clinical trials or agricultural launches. Teams spend less time adapting to minor procedural differences and more time focusing on outcomes that matter.

    The Environmental Equation

    Concerns about environmental impact never leave the agenda. The presence of chlorine atoms prompts agencies to ask tougher questions about degradation and by-product control. Several chemical plants successfully piloted improved scrubbing and multi-stage waste treatment, cutting hazardous releases dramatically. Published field data backs up these improvements with measurable drops in surface water residues. Farmers and local residents see real progress in lowering chemical footprints while maintaining productivity.

    Academic-industrial partnerships take center stage in solving persistent challenges. For instance, researchers testing biocatalytic paths to the same core molecule found energy savings and less reliance on heavy metals. These pilot programs may scale up soon, offering a cleaner route to essential intermediates like 2-Chloro-5-methylpyridine.

    Progress still takes time—especially in retrofitting older plants or aligning competing business priorities—but the tide keeps shifting as the sector responds to stricter standards and community expectation.

    Supporting the Next Generation of Research and Products

    Young scientists entering the field often meet 2-Chloro-5-methylpyridine as one of their first hands-on projects. Its robust characteristics offer enough challenge to teach best practices, but not so much that errors spiral out of control. University labs sometimes share stories about creative new transformations built around this core structure, inspiring students to see both the foundational science and its everyday application.

    Mentorship programs pair experienced process chemists with trainees to teach real-world troubleshooting: how to spot trace impurity drift or how to plan for solvent compatibility. These lessons hold value whether you’re running a small research group or operating a big manufacturing line. Over the years, I watched several teams develop confidence with this intermediate before stepping up to more sensitive, less forgiving molecules.

    Not surprisingly, cross-field collaboration grows in value. Analytical chemists working alongside organic synthesis experts tackle purification and structure confirmation. Environmental monitors and safety officers provide essential feedback loops, closing the gap between innovation and responsible stewardship.

    Pushing for Continuous Improvement: Tools, Methods, and Mindset

    No matter the field, continual tinkering and method upgrades help companies and institutions stay ahead of process and safety risks. Data from real-world users matter more than promotional claims, making community-led feedback loops central to steady improvement. Researchers publish new findings that help trim energy use, cut down on solvent waste, or improve shelf-life.

    Quality control teams regularly update testing protocols based on international trends in impurity detection. For example, wider adoption of high-resolution mass spectrometry revealed trace compounds missed by earlier tools, prompting new supplier standards. Each fix—sometimes small, sometimes sweeping—keeps the pipeline of pharmaceutical or crop science innovation moving.

    Openness to incremental change remains a hallmark of organizations that succeed over the long term with compounds like 2-Chloro-5-methylpyridine. Companies that encourage peer review, ongoing training, and shared problem-solving reach their production and safety targets faster and with fewer surprises.

    Looking Forward: Future Uses and Responsible Innovation

    There’s always pressure to find the “next best” intermediate, but the ongoing relevance of 2-Chloro-5-methylpyridine grows out of its reliability and adaptability. Ongoing trends in green chemistry might soon bring new synthesis pathways, improving atom economy and managing waste better than older routes. Researchers exploring new reactions look for ways to adjust methyl and chloro group placements, spurring innovation across drug and agricultural product lines.

    Markets may fluctuate, and regulatory rules shift, but teams that routinely re-examine their processes stay ahead. Collaborative projects between public and private labs keep introducing safer, faster, and more eco-friendly ways to make and use specialty chemicals. Industry groups increasingly publish open data on manufacturing improvements—helping rival institutions and the wider scientific community learn from each other’s advances.

    A richer understanding of molecules like 2-Chloro-5-methylpyridine lays the groundwork for safer, more effective products that benefit society at large. Knowledge-sharing and hands-on commitment to environmental and workplace safety will keep shaping the responsible use of this compound as research and industry move forward together.