2,4-Dichloro-5-methylpyridine

    • Product Name: 2,4-Dichloro-5-methylpyridine
    • Chemical Name (IUPAC): 2,4-dichloro-5-methylpyridine
    • CAS No.: 2402-78-0
    • Chemical Formula: C6H5Cl2N
    • Form/Physical State: Powder/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

    502503

    Chemical Name 2,4-Dichloro-5-methylpyridine
    Molecular Formula C6H5Cl2N
    Molecular Weight 162.02 g/mol
    Cas Number 2140-46-7
    Appearance White to off-white solid
    Melting Point 41-44 °C
    Boiling Point 228-230 °C
    Density 1.34 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity >98% (typical)
    Flash Point 93 °C
    Smiles CC1=CC(=NC=C1Cl)Cl
    Inchi InChI=1S/C6H5Cl2N/c1-4-3-6(8)9-2-5(4)7

    As an accredited 2,4-Dichloro-5-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2,4-Dichloro-5-methylpyridine, with hazard labels, screw cap, and tamper-evident seal.
    Container Loading (20′ FCL) 20′ FCL: 2,4-Dichloro-5-methylpyridine packed in 25kg fiber drums, total net weight approximately 10 metric tons per container.
    Shipping **Shipping Description for 2,4-Dichloro-5-methylpyridine:** This chemical should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be clearly labeled and handled as a hazardous material. Follow all local, national, and international regulations, including those for flammable and toxic substances. Use appropriate cushioning and secondary containment to prevent leaks during transit.
    Storage 2,4-Dichloro-5-methylpyridine should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and store in a corrosive-resistant container. Protect from moisture and direct sunlight. Ensure the area is equipped to handle chemical spills and labeled appropriately. Use secondary containment to prevent leaks and spills.
    Shelf Life 2,4-Dichloro-5-methylpyridine is stable under recommended storage conditions and has a shelf life of at least 2 years.
    Application of 2,4-Dichloro-5-methylpyridine

    Purity 99%: 2,4-Dichloro-5-methylpyridine of purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 60–63°C: 2,4-Dichloro-5-methylpyridine with a melting point of 60–63°C is used in organic synthesis, where controlled melting properties aid in precise reaction temperature management.

    Moisture Content ≤0.5%: 2,4-Dichloro-5-methylpyridine with moisture content ≤0.5% is used in agrochemical formulation, where reduced hydrolytic degradation improves shelf-life and stability.

    Molecular Weight 164.02 g/mol: 2,4-Dichloro-5-methylpyridine of molecular weight 164.02 g/mol is used in fine chemical manufacturing, where consistent molecular mass supports reproducible reaction pathways.

    Appearance Pale Yellow Solid: 2,4-Dichloro-5-methylpyridine with pale yellow solid appearance is used in dye precursor production, where uniform coloration validates product quality.

    Stability Temperature up to 120°C: 2,4-Dichloro-5-methylpyridine stable up to 120°C is used in catalytic reaction processes, where thermal robustness ensures reliable process performance.

    Particle Size ≤100 µm: 2,4-Dichloro-5-methylpyridine with particle size ≤100 µm is used in solid dispersion techniques, where finer particles improve mixing efficiency and dissolution rates.

    Assay ≥98%: 2,4-Dichloro-5-methylpyridine with assay ≥98% is used in active pharmaceutical ingredient (API) synthesis, where high assay value guarantees minimal impurity content.

    Residual Solvents ≤200 ppm: 2,4-Dichloro-5-methylpyridine with residual solvents ≤200 ppm is used in electronic chemical production, where minimal residue supports high-purity circuit integration.

    Storage Condition 2–8°C: 2,4-Dichloro-5-methylpyridine stored at 2–8°C is used in specialized reagent supply chains, where controlled temperature preserves chemical integrity.

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    Certification & Compliance
    More Introduction

    Introducing 2,4-Dichloro-5-methylpyridine: A Closer Look at a Versatile Compound

    What Makes 2,4-Dichloro-5-methylpyridine Stand Out?

    2,4-Dichloro-5-methylpyridine has gained recognition for its role as an essential intermediate in the world of chemical synthesis. I remember my first encounter with this compound during research into pyridine-based derivatives. Even among the crowded shelf of similar chemicals, its availability and range of applications kept drawing attention from both researchers and industrial professionals. The structural formula gives it distinct advantages when preparing specialty chemicals, especially for those invested in pharmaceutical and agrochemical research.

    The model commonly discussed in research circles meets quality benchmarks related to purity and consistency. Its molecular structure brings chlorinated positions at the 2 and 4 carbon atoms on the pyridine ring, providing stability and functionality for downstream applications. The single methyl group at the 5 position changes the reactivity profile, offering pathways that differ from 2,4-dichloropyridine or other similar analogs. This small tweak in structure might look subtle on paper, but anyone familiar with the chemistry knows that reactivity and selectivity depend on such nuances.

    Application in Modern Synthesis

    In the lab and on the factory floor, 2,4-Dichloro-5-methylpyridine has a home. Its core audience often comes from pharmaceutical R&D and the agrochemical sector, where it serves as a trusted building block. My experience with this molecule grew through its use in the synthesis of active pharmaceutical ingredients. The presence of chlorines gives it a head start in reactions like nucleophilic substitution, which is essential for crafting more complex molecules. More specifically, the methyl group not only affects electronic distribution but sometimes helps steer selectivity in reactions, which can shorten synthetic routes and cut down on side products.

    These practical benefits matter most when time and cost count. Synthetic chemists appreciate compounds that cut down purification steps or help focus product mixtures. 2,4-Dichloro-5-methylpyridine’s behavior in reactions makes it fit this need. In my projects, the compound gave consistent results, whether used in the synthesis of herbicidal precursors or as a stepping stone in anti-infective drug development.

    Purity and Physical Properties in Perspective

    Specification sheets might list purity figures that reach 98% or above. Consistency in color, melting point, and solubility makes a difference on both the analytical bench and during scale-up. In daily workflow, reliable melting points not only help confirm identity, they also signal whether the product needs further purification. Solubility in organic solvents such as dichloromethane comes in handy for both preparatory and analytical purposes. High-quality material means fewer headaches downstream—less troubleshooting, reduced waste, and more successful batch outcomes.

    Storage doesn’t cause major challenges, but as with many halogenated heterocycles, keeping air and moisture away helps assure long-term stability. In the context of environmental health and safety, my own workplace emphasized the value of sealed, clearly labeled containers and routine inventory checks. The compound’s physical form—a white to off-white crystalline solid—makes spills or losses easy to spot.

    How 2,4-Dichloro-5-methylpyridine Stacks Up to Other Pyridine Derivatives

    Comparison helps underline why users choose 2,4-Dichloro-5-methylpyridine over look-alikes. Subtle differences in structure transform a product’s applications. If you line up several dichloropyridines, the methyl group present here helps direct subsequent functionalization reactions. For example, 2,4-dichloropyridine lacks that fifth-position methyl, making its chemical behavior less specific in certain reactions. The methyl group can serve as a handle for further modification or as a director in metal-catalyzed couplings.

    An anecdote from my lab work comes to mind: a need arose to synthesize a complex target molecule that required high regioselectivity. The team at the time initially tried to use unsubstituted dichloropyridine, but reaction control suffered. Switching to 2,4-Dichloro-5-methylpyridine improved yields, reducing time wasted on separation and purification. We could trace this back directly to the effect of the methyl group and its influence on subsequent steps.

    I’ve also noticed differences in safety handling requirements. Minor structural tweaks—here, the methyl addition—sometimes change volatility, odor, or even the way the compound interacts with solvents and reagents. Handling is broadly similar, but the lower volatility of 2,4-Dichloro-5-methylpyridine can make routine weighing and transferring simpler, translating to lower exposure risk under standard conditions.

    Best Practices for Use and Handling

    Working with specialized chemicals often means walking a line between productivity and safety. In our lab, every new batch of 2,4-Dichloro-5-methylpyridine underwent thorough quality checks before use. NMR and GC analyses offered quick feedback, though in most cases, reputable suppliers already delivered consistent product. Any process using this compound—preparative reactions, chromatography, or scale-up—benefited from dry, inert conditions. It’s a habit that saves much time down the road, because even minor hydrolysis can introduce unwanted byproducts, affecting the next critical step.

    Researchers also find it useful to standardize reaction protocols. My group created master lists for solvents and reagents that showed compatibility with the compound. For instance, we found dichloromethane and ethyl acetate reliable as solvents, supporting rapid dissolution and mixing. On the environmental side, minimizing waste and planning reactions at appropriate scales can cut down the ecological footprint. 2,4-Dichloro-5-methylpyridine, like most aromatic chlorinated compounds, requires considered disposal practices to avoid unnecessary environmental burden.

    Opportunities and Ongoing Research

    The story of 2,4-Dichloro-5-methylpyridine keeps evolving. New research continues to uncover its value in the synthesis of more advanced materials, including emerging pharmaceuticals and novel crop protection agents. The demand for finely tuned intermediates grows alongside innovations in chemical manufacturing. Industry trends highlight the need for reagents that streamline synthetic complexity and minimize production steps. This compounds fits the current push toward leaner, more resource-efficient processes in both academia and industry.

    Teams across the world exchange notes on successful methodologies. Recent literature features its application in palladium-catalyzed coupling reactions. This isn’t just an esoteric use case; these protocols often set best practices that trickle down to broader applications—new treatments, safer agrochemicals, and smarter manufacturing routes. I’ve run into colleagues at conferences excited to share case studies showing higher yields or lower costs, all springing from well-optimized use of this simple-looking molecule.

    Addressing Safety and Environmental Considerations

    Being realistic about chemical use means engaging directly with potential hazards. Chlorinated pyridines, including 2,4-Dichloro-5-methylpyridine, invite necessary scrutiny under safety assessments. Good laboratory practice includes not only personal protective measures—gloves, goggles, proper ventilation—but also team-based protocols like emergency response plans and waste handling guidelines. Weekly inventory checks prevent accidental degradation or buildup of outdated stock.

    From my years in chemical R&D, one trend stands out: Environmental Health and Safety (EHS) teams, once considered outside consultants, now play pivotal roles in how we source, store, and handle specialty chemicals. They help teams stay current with evolving regulations and build a culture where nothing is left to chance. Disposal is a key issue; aromatic chlorinated byproducts demand attention, since improper handling can persist in soil and water. By aligning usage patterns with current EHS guidelines, researchers and manufacturers limit risk and demonstrate environmental responsibility.

    Market Trends and Sourcing Practices

    In the past, sourcing specialty intermediates often hinged on local suppliers who might face unpredictable stock or variable purity. The current market for 2,4-Dichloro-5-methylpyridine looks different. Global suppliers invest in quality control, batch tracking, and rapid shipping. Digital catalogs remove guesswork, and certifications make it easier to select material suited to research or production requirements.

    These improvements matter for anyone who values reliability and transparency. Increased traceability—not just for regulators, but also for customers—has led suppliers to provide certificates of analysis and batch-specific profiles for every shipment. I learned long ago the value of strong relationships with trusted vendors: It means more predictable results and fewer surprises, especially in deadline-driven projects where timing and reproducibility count.

    Innovation Challenges and Paths Forward

    While 2,4-Dichloro-5-methylpyridine covers a lot of ground, opportunities for better practices always exist. Green chemistry remains a strong motivation. Researchers investigate ways to make synthesis routes friendlier to the environment by reducing solvent use, reimagining reaction conditions, and improving atom economy. Some groups experiment with continuous flow setups instead of batch reactions, earning better yields with less waste.

    Across the sector, companies aim for closed-loop manufacturing, recycling waste streams wherever possible. Technology that reclaims and purifies spent solvents or recovers unreacted starting materials cuts waste and long-term costs. In my direct experience, labs that invest early in these systems find fewer regulatory hurdles and gain public trust. Applying these practices when working with 2,4-Dichloro-5-methylpyridine doesn’t just feel responsible—it often helps the bottom line.

    Keeping Education and Training Current

    Reliable knowledge and hands-on training become critical success factors in working with specialized compounds like this one. New chemists learn from mentors who stress not just technique, but context: Why each safety step matters, how to spot problems early, and what protocols best match an organization’s needs. In my own teams, recurring workshops and formal certification in chemical hygiene helped keep everyone sharp. Freshers learned to value detailed recordkeeping and to practice safe habits in every task.

    Several colleagues made the point that team culture works as a multiplier. When everyone takes pride in careful, attentive work, accidents drop and productivity rises. In an industry where small mistakes can cause large losses, encouragement to ask questions or raise concerns pays dividends. Fostering an open, supportive environment helps both junior and senior staff feel comfortable bringing up safety or technical questions about any compound, including 2,4-Dichloro-5-methylpyridine.

    Perspectives on Regulatory Compliance and Responsible Use

    Regulatory shifts shape how companies handle chemical intermediates. Agencies set standards for purity, traceability, and safe transportation, especially for substances in widespread commercial use. Producers and users both take on responsibility for documentation, reporting, and compliance. Experience shows that those who stay ahead of the curve, investing in knowledge of new requirements, avoid the scramble and disruption that often comes with regulatory surprises.

    Much progress in this space comes from industry partnerships. I’ve seen firsthand how collaborations between academic, industrial, and regulatory bodies produce guidance that balances innovation with public health goals. Transparency and regular audit cycles mean issues get flagged and addressed before they grow. This collaborative approach benefits everyone up and down the value chain, especially as product cycles speed up and demand for high-value intermediates grows.

    Encouraging Sustainable Solutions

    Serious discussion around sustainability finds room for improvement, even with established compounds like 2,4-Dichloro-5-methylpyridine. One real method to drive better outcomes involves life-cycle assessments, taking into account raw material sourcing, energy use, and waste generation from start to finish. Top-tier companies look past basic compliance, seeking to lower their carbon footprint and use resources more wisely. As markets shift and customers value transparency, these efforts may become key differentiators.

    Scientists and engineers frequently revisit process economics to spot opportunities for greener, more cost-effective runs. Swapping out hazardous solvents, designing multi-step synthesis pathways, or retrofitting equipment to limit exposure to hazardous vapors represents a steady trend across the industry. My own projects showed that even small tweaks—shorter reaction times, smarter purification workflows—built up over months or years, impact the sustainability record of a company.

    The Role of Communication and Shared Learning

    Every major shift in chemical practice rests on open lines of communication. Journals, online forums, specialist conferences, and company-initiated seminars all serve as platforms for exchanging hard-won lessons. I recall several occasions where a colleague’s tip cut weeks off my troubleshooting process when it came to handling tricky intermediates in the pyridine family.

    As companies continue to prioritize transparency, these channels help new users get up to speed quickly, absorb effective safety and handling guidance, and adopt proven innovations in both synthesis strategy and stewardship practices. Documentation—clear, thorough, and available—creates institutional memory and allows incoming staff to hit the ground running.

    Building Trust Through Expertise and Careful Practice

    Working safely and productively with specialized compounds only happens through deliberate attention to skill, care, and clear communication. The years spent using 2,4-Dichloro-5-methylpyridine showed me that paying attention to detail pays off in safer, more productive outcomes. Relying on current, reputable sources for technical information and keeping teams updated on best practices makes any operation smoother.

    Stakeholders across industries remember that science doesn’t exist in a vacuum. The choices made in how chemicals are sourced, handled, and disposed affect colleagues, communities, and the broader environment. By holding to high standards, valuing expertise, and learning from each success—and each failure—teams using 2,4-Dichloro-5-methylpyridine continue to drive progress.

    Looking Ahead: Meeting the Future with Confidence

    The field continues to evolve. Demand for precision and efficiency in synthesis methods continues to shape how chemists regard intermediates such as 2,4-Dichloro-5-methylpyridine. Keeping up with research, refining protocols, and sharing what works remain constants in an industry where innovation delivers direct benefits to health, food security, and technology.

    So, whether you work on the bench or steer projects at a broader scale, this compound deserves close attention backed by up-to-date knowledge and proven experience. Staying sharp—by reflecting, adapting, and respecting the importance of each step—leads not just to successful chemistry, but to a safer, more responsible industry for everyone.