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3-Chloro-4-Methylpyridine

    • Product Name 3-Chloro-4-Methylpyridine
    • Alias 3-Chloro-4-picoline
    • Einecs 221-595-9
    • 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

    103070

    Chemical Name 3-Chloro-4-Methylpyridine
    Molecular Formula C6H6ClN
    Molecular Weight 127.57 g/mol
    Cas Number 73583-39-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 184-186 °C
    Melting Point -15 °C
    Density 1.166 g/cm3
    Refractive Index 1.541
    Flash Point 75 °C
    Solubility Slightly soluble in water
    Smiles CC1=C(C=CN=C1)Cl
    Storage Conditions Store in a cool, dry, well-ventilated area

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

    Packing & Storage
    Packing The packaging consists of a 500g amber glass bottle with a secure screw cap, labeled "3-Chloro-4-Methylpyridine, 98%."
    Shipping 3-Chloro-4-Methylpyridine is shipped in tightly sealed containers to prevent leaks and moisture absorption. It should be stored and transported in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and compliance with relevant hazardous material regulations are required during transportation to ensure safe handling.
    Storage 3-Chloro-4-Methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Label containers clearly and store in a dedicated chemical storage cabinet, following all relevant safety and regulatory guidelines for hazardous chemicals.
    Application of 3-Chloro-4-Methylpyridine

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

    Our facility specializes in the large-scale synthesis and reliable supply of 3-Chloro-4-methylpyridine. This intermediate serves critical roles across several industrial segments, facilitating production efficiency and supporting advanced product pipelines in the chemical sector. Below, we outline real downstream use cases, technical integration points, and industry-specific standards for our material’s leading applications.

    1. Agrochemical Intermediate for Pyridine-based Herbicides

    3-Chloro-4-methylpyridine acts as a key building block in the multi-step synthesis of advanced heterocyclic herbicides, including products based on picolinic acid chemistry. Downstream chemical plants charge it during intermediate coupling phases, allowing controlled substitution and ring activation that supports synthesis of selective weed control agents. Our technical support includes consultation on batch and continuous process adaptation, maximizing yield and minimizing impurity formation.

    Industry compliance standards

    • REACH Registration (EU Regulation EC 1907/2006)
    • ISO 9001:2015 Quality Management System
    • Agrochemical registration guidelines (OECD, EPA 40 CFR Part 158)
    • Chinese Agrochemical Industrial Standard GB/T 20784

    Typical usage ratio

    • 0.8–1.2 molar equivalent versus target intermediate; adjustments based on substrate reactivity and hydrogen halide scavenger loading
    • Batch charge ranges from 12–18% w/w of total reaction mass, tailored to reactor scale

    Downstream process integration

    • Charged during nucleophilic substitution or heteroaryl coupling step
    • Introduced in solvent systems (DMF, toluene) under strong base
    • Followed by purification, hydrolysis, and crystallization

    Final product types

    • Picolinate herbicides (active ingredients and salts)
    • Selective weed control formulations for cereal and broadleaf crops
    • Exported herbicidal intermediates
    • Bulk herbicide technical concentrates

    2. Active Pharmaceutical Ingredient (API) Precursor for Antihypertensive Agents

    Pharmaceutical manufacturers utilize the compound in the synthesis of key intermediates for drugs targeting cardiovascular conditions, specifically as a precursor in the formation of pyridine-ring-containing APIs such as nicardipine derivatives. Its entry into the synthesis stage allows for controlled substitution and ring functionalization, ensuring product purity for regulatory approval. Our material meets stringent impurity profile and trace heavy metal limits.

    Industry compliance standards

    • Chinese Pharmacopoeia (ChP) and European Pharmacopoeia (Ph. Eur.) compliance for intermediates
    • Good Manufacturing Practice (GMP, ICH Q7)
    • US FDA 21 CFR Part 211 (pharmaceutical manufacturing)
    • ISO 9001:2015 (pharma supply chain)

    Typical usage ratio

    • 1.0 molar equivalent relative to acylation or alkylation reactant
    • Material concentration in reaction 5–7% w/w, scaled per batch size

    Downstream process integration

    • Added to early synthetic stage before chiral resolution or further functionalization
    • Processed through distillation or crystallization purification
    • QC release includes NMR, HPLC, and GC-MS for residual solvent and by-products

    Final product types

    • Pharmaceutical intermediates for calcium channel blockers
    • API precursors for antihypertensive drugs
    • Finished dosage forms containing nicardipine or analogues
    • Registered API exports (CEP or DMF holder supply)

    3. Intermediate for Fine Chemicals: Pyridine-Based Organic Dyes

    Dye manufacturers use this chemical as a synthetic precursor in pyridine-derived chromophores, which impart specific color properties and stability required for specialty dye applications. It enters production workflows for azo and anthraquinone-based pigment processing, enabling precise molecular tailoring for optical and performance criteria demanded by high-end textiles and inks. Our QA/QC systems assure batch-to-batch homogeneity and minimal off-color byproduct.

    Industry compliance standards

    • ECHA REACH (EC 1907/2006) and CLP (EC 1272/2008) labelling
    • ISO 14001:2015 (Environmental Management for dye goods)
    • OEKO-TEX Standard 100 restrictions for textile chemicals
    • Chinese Standard for Dye Intermediates GB/T 23950

    Typical usage ratio

    • 0.5–1.5 molar equivalent per azo/pigment linking group, tuned to batch-specific stoichiometry
    • Weight percent in charge: 8–14% of the total pigment precursor mixture

    Downstream process integration

    • Processed in ring substitution reactions under controlled pH and temperature
    • Integrated with aromatic coupling agents or diazotization sequences
    • Purified by recrystallization or column chromatography

    Final product types

    • Pyridine-based azo dyes
    • Soluble organic pigments for high-value inks
    • Textile and leather colorants
    • Plastics color masterbatches

    4. Building Block for Veterinary Drug Synthesis

    Veterinary pharmaceutical producers source the material as a ring precursor for pyridine-containing APIs used in animal health. It facilitates manufacture of therapeutic agents where controlled halogenation is critical for bioactivity and regulatory compliance in livestock medicine. Our supply delivers defined impurity profiles and batch documentation supporting global veterinary registrations.

    Industry compliance standards

    • China Veterinary Pharmacopoeia standards
    • VICH GL35 (Good Manufacturing Practice for veterinary products)
    • ISO 9001:2015 (Veterinary pharma QMS)
    • US FDA Center for Veterinary Medicine guidance

    Typical usage ratio

    • 0.9–1.3 molar equivalents per key coupling step, ensuring ring closure yield
    • Material avg. charge: 7–11% of total precursor mass

    Downstream process integration

    • Entry during early-stage halogenated pyridine ring assembly
    • Further processed through selective functionalization and salt formation
    • Intermediate characterization by HPLC or LC-MS before API QA release

    Final product types

    • Veterinary drug intermediates
    • Finished APIs for antiparasitic and antibacterial formulations
    • Oral and injectable medicinal products for companion and livestock animals
    • Veterinary premix feed additives

    5. Precursor for Electronic/Liquid Crystal Material Synthesis

    The electronics chemicals sector utilizes this pyridine derivative during multi-step synthesis of intermediates for high-performance liquid crystal materials. Manufacturers charge the compound in controlled nucleophilic aromatic substitution reactions; the resulting intermediates help achieve precise dielectric profiles and thermal stability required for TFT-LCDs and specialty display panels. We provide tight lot traceability and low-metal grades for this segment.

    Industry compliance standards

    • IEC 61249-2 (Electronic base materials specification)
    • ISO 9001:2015 (Electronic chemicals manufacturing)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances)
    • Japanese Industrial Standard JIS C5016-2 for liquid crystals

    Typical usage ratio

    • 0.6–1.1 molar equivalent relevant to substitution step; loading based on reactivity of halogen group
    • Material typically 10–16% w/w of organic synthesis stage charge mass

    Downstream process integration

    • Entry point in nucleophilic aromatic substitution for liquid crystal precursors
    • Post-stage purification via distillation, confirming dielectric properties
    • Integrated into larger aromatic core or side-chain assembly

    Final product types

    • Liquid crystal intermediates for TFT-LCD materials
    • Electronic-grade pyridine derivatives for optical films
    • High-purity chemicals for display panel manufacturing
    • Functional electronic specialty chemicals
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Chloro-4-Methylpyridine: Elevating Consistency in Industrial Synthesis

    Sharpening the Standard in Pyridine Derivatives

    For decades, our chemical manufacturing team has been producing pyridine derivatives to serve pharmaceutical makers, agrochemical developers, and specialty chemical industries. Throughout these years, the demand for high selectivity and consistent yield for heterocyclic intermediates has grown steadily. One of the outcomes of this focus is 3-Chloro-4-Methylpyridine—a compound that continues to draw steady orders and in-depth questions from customers striving to stay ahead in their formulation projects.

    Our 3-Chloro-4-Methylpyridine, with a molecular formula of C6H6ClN, stands out for its tailored behavior in scaled synthesis and process development. Sitting on the frontline of pyridine modifications, this molecule has earned trust for its reliable reactivity profile and its steady physical properties that support reproducibility every batch, every drum.

    Unique Identity and Key Specifications

    The compound possesses a chlorine atom at the 3-position and a methyl group at the 4-position on the pyridine ring—a fact that chemists appreciate for the way it alters reactivity compared with its isomeric cousins. It is a clear, colorless to light yellow liquid under most ambient conditions, exhibiting a strong pyridine odor that highlights its purity. We ship this product consistently above 99 percent purity, checked by gas chromatography as the standard benchmark in the industry. Only tanks and reactors lined with compatible alloys are appropriate, as the compound tends to react with soft metals and certain non-polar elastomers under harsh conditions.

    Based on field trials in our own pilot plant, shelf stability extends comfortably for multiple seasons if stored in sealed drums under moderate temperature. The boiling point, commonly observed around 195°C, offers process engineers ample flexibility to tune reaction conditions for most practical coupling or halogen-exchange applications.

    How We Arrived At This Grade

    Our continuous-batch reactors run on a carefully optimized chlorination regime, paired with real-time gas chromatography analysis. The intermediate formation, quench profiles, and subsequent distillations draw on decades of trial and documentation. This tightly monitored approach allows us to deliver consistent product—an achievement that has allowed our major customers to cut troubleshooting steps from their own syntheses. European fine chemicals suppliers, for example, now report fewer lot failures when shifting to our 3-Chloro-4-Methylpyridine as a starting material for pyridine carboxylic acid synthesis or fungicide precursor blends.

    Each batch starts with feedstocks we vet in-house. We process the precursor methylpyridine through a controlled chlorination that keeps side-product levels to a minimum and keeps solvent contamination fully traceable. We keep a sharp eye on potential isomeric byproducts, which, if not addressed, can show up as troublesome trace impurities during downstream processing for customers in regulated markets. With a qualified analytical staff running advanced chromatographic and spectroscopic methods, each lot is certified for chemical identity and absence of high-risk contaminants such as polychlorinated derivatives.

    Usage in Industrial Settings

    Most of the 3-Chloro-4-Methylpyridine we supply finds its way to research labs and multiton facilities shaping up next-generation fungicides, veterinary pharmaceuticals, and complex ligands. Over the last five years, the spread of specialty crop-protection products has driven up interest. The methyl and chloro substituents both impact the electronic profile of the pyridine ring, influencing selectivity in nucleophilic substitution steps when building larger molecules.

    Where 4-Chloropyridine or 3-Methylpyridine establish a reputation as somewhat blunt tools, our 3-Chloro-4-Methylpyridine brings the kind of nuanced reactivity that allows chemists to fine-tune coupling reactions and build in multi-position selectivity. In manufacturing settings, especially in pharmaceutical intermediates, this translates to fewer rearrangement byproducts and reduced purification loads. Many of our longer-term clients report being able to achieve higher yield and sharper separation profiles in column chromatography when using our material as the starting reagent.

    In addition, the compound’s volatility and solubility strike a balance that enhances its handling. Unlike more volatile pyridines, which pose inhalation and fire hazards, 3-Chloro-4-Methylpyridine stays manageable under standard airflow capture in fume hoods and factory settings. This trait has drawn the attention of safety managers at several global agrochemical plants who must meet increasingly stringent worker exposure standards.

    Our drums bear “cut-seal” closure mechanisms, which we have field-tested for minimal leaching and vapor escape during long-haul transportation. Customers in environments with frequent drum handling—such as contract manufacturers and repackers—have consistently expressed appreciation for this small but impactful change.

    Handling Temperature and Stability

    We keep our eyes on data from stress tests and field feedback, incorporating every instance of unexpected crystallization or off-odors back into production line adjustments. At process temperatures between 100–160°C, the compound stays homogenous and flows well, without the “freezing” effect that can lead to blockage in transfer lines—a well-known headache for the industry.

    It pays to highlight that this compound, though structurally similar to other halopyridines, settles at a higher flash point than simple pyridine or 2-chloropyridine. Workups reveal that 3-Chloro-4-Methylpyridine can be distilled out in process units designed for mid-range boiling solvents, reducing the need for complex containment procedures. Year after year, operators at our partner facilities report fewer shutdowns and easier process optimization due to the material’s high purity and thermal predictability.

    The Difference in Real-World Application

    What distinguishes our 3-Chloro-4-Methylpyridine from generic alternatives is not a flashy technical metric, but how it performs over time and under variable worksite conditions. We have invested in analytical capability to trace ultra-low levels of isomeric and halogenated impurities that complicate downstream hydrogenation or palladium-catalyzed cross-coupling reactions. Our laboratory has demonstrated, through side-by-side comparisons, that downstream losses in high-value pharmaceutical intermediates decrease when customers opt for high-purity 3-Chloro-4-Methylpyridine.

    As a core intermediate in the assembly of active ingredients, the tolerance for variability continues to shrink. We have seen development teams shaving weeks off their production timelines due to fewer repeat reactions and a reduced need for custom purification protocols. The methyl group in the para-position discourages unwanted side reactions, which, in field experience, translates to easier isolation of target molecules and less stress over regulatory compliance for impurity content.

    The robust shelf-life and chemical resistance of our HDPE packing minimize risk during international transit. Several bulk customers distribute resins and adducts to high-heat regions; being able to rely on material that maintains clarity and reactivity simplifies warehouse management and downstream inventory. We regularly follow up with purchasing teams to adjust fill weights based on throughput data, and have identified opportunities to precondition stock for regions with longer lead times.

    Pyridine Substitution: Not All Compounds Are Equal

    We often receive inquiries asking whether generic 3-chloropyridine or 4-methylpyridine would suffice in certain syntheses. There is no substitute for positional selectivity on the pyridine ring. For chemists adjusting electron density in their frameworks, the unique placement of the chloro and methyl functional groups allows for predictable reactivity. A methyl group at the 4-position shifts the electron cloud and modulates nucleophilicity around adjacent sites in ways that cannot be exactly duplicated by alternative substitutions.

    Carefully controlled substitution prevents excessive isomer formation during downstream processes. Using poorly defined mixtures or lower grade materials often results in higher impurity profiles and unpredictable yields. In practice, this means missed delivery schedules, escalated costs for rework, and latent risk for those in regulated environments like pharmaceutical supply. Our experience underscores how small changes in the source of starting materials ripple across entire process chains.

    Feedback from production supervisors suggests that even minor batch-batch variation in halogenated pyridines leads to sintered filter beds and more frequent equipment cleaning. With our 3-Chloro-4-Methylpyridine, downstream partners report both longer run times between scheduled maintenance and increased throughput. The consistency comes from monitoring not just the chemical identity but also subtle cues like color index, distillation residue, and solvent carryover.

    Leveraging Experience to Tackle Common Supply Chain Challenges

    Many process engineers have struggled with patchy supply from distributors who cannot assure steady spec or purity year-round. By maintaining our own reactors and logistical planning, we sidestep these disruptions. Rigorous forecasting, built on real order volumes and customer consumption data, grounds our approach. Drums filled in spring arrive reliably in fall, retaining their initial color, clarity, and performance profile, which several buyers now specify as a precondition for contract renewal.

    Even in years when pyridine precursor prices spiked, our long-standing relationships and forward procurement allowed us to supply uninterrupted material flow. We share transparent updates with partner plants during global level disruptions, and adjust output scheduling to meet quarterly loading forecasts from our main customers. This consistency allows chemists, buyers, and logistic teams to align their own work schedules without hidden gaps.

    Continual renewal and investment in our plant infrastructure—such as solvent recycling and sealed filling—come straight from annual lessons learned. Each time we address a contamination concern or shelf-life inquiry, we roll improvements directly into the next batch cycle. Our operations team meets monthly with quality control staffers to review any minor out-of-spec readings, and update control logic to tighten the process window further. The upshot: for those relying on complicated multi-step syntheses, lot variation shrinks, and entire chains of rework steps recede from the norm.

    Investing in Technical Relationships

    Our technical teams do more than fill orders. By working alongside project chemists and pilot line managers, we step beyond the paperwork. Longer joint development partnerships allow for honest feedback loops and real improvements in both product performance and compliance. In one instance, a pharmaceutical developer highlighted a minor UV absorbance anomaly during their own stability study; through joint investigation, we adjusted our purification step, reducing trace UV-absorbing contaminants and resolving the issue in subsequent lots.

    Our staff regularly takes part in data exchanges and application troubleshooting with clients scaling up from gram to multi-ton batches. This deep sharing of outcomes drives process reliability that cannot be reached with an arm’s-length material supplier. We maintain comprehensive documentation, including spectra files, impurity scan data, and full batch histories, so specification discussions remain transparent and grounded in real numbers.

    Meeting Future Demands for Regulatory Compliance

    Nearly every major customer has had to adjust to tightening standards on trace impurities and global transportation restrictions for specialty chemicals. Our regulatory and documentation staffers continually update safety files and batch records to assure compliance with evolving local and global guidelines. Harmonizing documentation for end users in Japan, North America, and the European Union, for instance, has called for new protocols in both labeling and electronic traceability.

    We recognize the mounting importance of chemical stewardship and tracking. Pre-shipment production samples are cataloged for at least a year, facilitating rapid response in the event of regulatory or customer queries. We continually engage with chemical safety working groups, and recalibrate our own compliance documents to cut risk for those handling, storing, and disposing of 3-Chloro-4-Methylpyridine worldwide.

    Continued Forward Motion: Sustainable Engineering and Outreach

    We have faced growing inquiries about sustainability and green chemistry in the production of specialty pyridines. In response, recent upgrades in our plant include solvent recovery loops, upgraded thermal insulation, and waste minimization protocols. Our waste gas handling units run on advanced scrubbing systems developed from pilot studies run in collaboration with academic researchers. Recycling and eco-conscious disposal stands alongside uptime and purity as benchmarks in our continuous improvement programs.

    Understanding the impact chemical production has on communities and the environment, we maintain open community engagement, and publish periodic sustainability reports covering emissions, water use, and resource efficiency throughout our operation. Each action is logged and tracked, reflecting not just internal commitments but also the practical need for robust supply agreements with forward-thinking customers.

    Steps Forward: Better Chemistry Through Collaboration

    Long-term experience manufacturing 3-Chloro-4-Methylpyridine has confirmed that precision, transparency, and mutual problem-solving remain essential to both high-quality production and strong customer ties. We will continue striving for precision and reliability, knowing that a small improvement on our processing line leads to a big upgrade in the reliability and performance of the products our partners deliver. We see increasing demand for specialty intermediates driven by pharmaceutical, agrochemical, and specialty industrial demands and remain ready to support these needs through continued process improvement and technical partnership.