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Ethyl 2-Chloronicotinate

    • Product Name Ethyl 2-Chloronicotinate
    • Alias Ethyl 2-chloropyridine-3-carboxylate
    • Einecs EINECS 401-110-0
    • 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

    520164

    Chemicalname Ethyl 2-Chloronicotinate
    Casnumber 13360-45-7
    Molecularformula C8H8ClNO2
    Molecularweight 185.61
    Appearance Colorless to light yellow liquid
    Boilingpoint 261-263°C
    Density 1.258 g/cm3
    Purity Typically >98%
    Refractiveindex 1.513
    Solubility Slightly soluble in water; soluble in organic solvents
    Synonyms 2-Chloronicotinic acid ethyl ester
    Smiles CCOC(=O)C1=NC=CC(Cl)=C1
    Storagetemperature Store at 2-8°C
    Flashpoint >110°C

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

    Packing & Storage
    Packing The 25g Ethyl 2-Chloronicotinate is packaged in a sealed amber glass bottle with a secure, chemical-resistant screw cap and labeling.
    Shipping Ethyl 2-Chloronicotinate is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. Packages are clearly labeled according to hazardous material regulations. During transit, it is kept away from incompatible substances, heat, and moisture. Shipping complies with local and international safety standards to ensure safe delivery and handling.
    Storage Ethyl 2-Chloronicotinate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. The storage area should be clearly labeled, and unauthorized personnel should have limited access. Avoid contact with moisture and store at room temperature unless otherwise specified by the manufacturer.
    Application of Ethyl 2-Chloronicotinate

    Applications of Ethyl 2-Chloronicotinate in Industrial Manufacturing

    We manufacture Ethyl 2-Chloronicotinate, a key intermediate with proven downstream adoption across high-value chemical sectors. Below we present substantiated industrial application scenarios, providing critical formulation, compliance, and process integration details to support B2B technical and procurement teams.

    1. Agrochemical Synthesis: Advanced Pyridine-Based Herbicides

    Formulators in the crop protection industry adopt Ethyl 2-Chloronicotinate as a core building-block for synthesizing substituted nicotinic acid derivatives, notably within the production of selective post-emergent herbicides. This step advances molecular frameworks with activity against resistant broadleaf weeds. Downstream operators require tight compliance with agrochemical purity standards, as regulated markets demand traceability and residue control from intermediate to finished formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (authorisation of plant protection products)
    • ISO 9001:2015 quality management for agrochemical intermediates
    • REACH registration (EU) or TSCA compliance (US), depending on geography

    Typical usage ratio

    • 5–30% w/w relative to the total precursor batch; exact inclusion rate set by downstream route selectivity, fouling control, and final herbicide target loading

    Downstream process integration

    • Intermediate fed into condensation or amide/esterification stages following nitration or halogenation of the base pyridine ring
    • Utilized in temperature-controlled closed systems to achieve high crude yield and minimize side products impacting purity
    • Post-reaction, passes through multiple crystallization or distillation refinements for downstream blend uniformity

    Final product types

    • Nicotinate-based selective herbicides (e.g., analogues of nicosulfuron, pyridinecarboxylic acid herbicides)
    • Herbicide technical concentrates, EC and SC formulations for commercial agriculture

    2. Pharmaceutical Intermediate: Niacin-Related API Precursors

    Active pharmaceutical ingredient manufacturers employ Ethyl 2-Chloronicotinate in the elaboration of modified nicotinate scaffolds, particularly for heterocyclic skeletal expansion in specialty APIs targeting cardiovascular and metabolic indications. The compound’s reactivity supports efficient construction of multi-substituted pyridine derivatives, vital for high-value generic and originator drug pipelines. GMP oversight dictates scrupulous batch tracking and extensive impurity profiling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines
    • Ph. Eur. and USP monographs for related APIs and intermediates
    • 21 CFR Part 210/211 for finished pharmaceutical producers (FDA USA)
    • Trace metal and residual solvent control per ICH Q3D and Q3C

    Typical usage ratio

    • 0.1–2.5 molar equivalents based on specific step in synthetic sequence; adjusted by reaction scale and desired API output

    Downstream process integration

    • Charged at defined points in multi-stage synthesis, notably during nucleophilic aromatic substitution or amidation reactions
    • Careful solvent selection and real-time impurity monitoring to meet regulatory impurity thresholds
    • Followed by re-crystallization and multi-stage HPLC purification

    Final product types

    • Nicotinic acid analogues as API or pharmaceutical intermediates
    • Finished tablets, capsules, and parenteral formulations containing expanded pyridine derivatives

    3. Fine Chemical Synthesis: Specialty Dye and Pigment Intermediates

    Industrial dye and pigment producers utilize Ethyl 2-Chloronicotinate as a precursor in the synthesis of high-fastness pyridine ring-containing colorants. This compound enables targeted modification of chromophore structures, delivering improved lightfastness and wash resistance for specialty textile and digital-ink applications. Manufacturers must rigorously control off-target halogenation and batch color consistency to satisfy final product quality requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • EN 71-3 (safety of toy colorants, for relevant pigment types)
    • ISO 9001:2015 certified QC systems for colorant intermediates
    • REACH Substance Evaluation (EU)

    Typical usage ratio

    • 10–18% by mass within the chromophore precursor batch; optimized for desired hue and process efficiency

    Downstream process integration

    • Introduced during the coupling or halogen-exchange reaction stage for pyridine ring incorporation
    • Reaction vessels equipped with color and pH control sensors for reproducibility
    • Successive isolation steps include aqueous workup, drying, and microfiltering to ensure pure colorant output

    Final product types

    • Pyridine-based dyes for technical textiles (polyester, nylon, acetate)
    • High-stability digital inkjet pigment dispersions

    4. Electronic Chemical Manufacturing: Conductive Polymer Additives

    Producers of specialty conductive polymers in the electronics industry adopt Ethyl 2-Chloronicotinate as a targeted modifier to introduce heteroatomic nitrogen centers for enhanced charge carrier properties. The material fits into advanced copolymer synthesis routes, allowing for fine-tuned band gap and surface interaction control crucial to OLED and thin-film transistor customers. Downstream workflows require strict solvent residue management and conformance with electronic grade impurity cutoffs.

    Industry compliance standards

    • JEITA (Japan Electronics and Information Technology Industries Association) purity specifications
    • IEC 61249 (base material for printed circuits, halogen content)
    • RoHS 3 (EU, hazardous substance restrictions)
    • ISO 14644 (cleanroom management for electronic chemical processing)

    Typical usage ratio

    • 0.5–3.5% w/w in pre-polymer feed blend; precise dosage set by required electronic conductivity attributes

    Downstream process integration

    • Fed into reactor during conjugated polymer backbone growth, using anhydrous process conditions
    • Batchwise or continuous operation with online conductivity and viscosity tracking
    • Post-polymerization purification by membrane filtration and fractional precipitation

    Final product types

    • Pyridine-modified polythiophene or polyfluorene conductive polymers
    • Electronic-grade films and coatings for OLED displays, printed sensors, and semiconductor encapsulation

    5. Veterinary Drug Intermediate: Chloronicotinate-Based Antiparasitics

    Veterinary medicine companies employ Ethyl 2-Chloronicotinate as a controlled reactant for producing advanced pyridine-based antiparasitic agents targeting livestock and companion animal markets. Accurate ratio and impurity control remain essential to achieve pharmacopoeia compliance, reduce environmental persistence, and avoid adverse metabolite formation during finished product synthesis. Manufacturers operate under animal health-specific regulatory frameworks requiring traceability through each process stage.

    Industry compliance standards

    • VICH GL 34 (GMP for veterinary pharmaceutical ingredients)
    • Ph. Eur. and Japanese Pharmacopoeia animal health monographs
    • FDA Guidance for Industry: Veterinary Drug Residue Tolerances
    • ISO 22442 (animal tissue traceability, where applicable)

    Typical usage ratio

    • 1–7% by mass in the target reaction step; dosage refined per antiparasitic moiety and downstream purification efficiency

    Downstream process integration

    • Enters early-stage coupling or halogen-exchange reaction vessels, in closed-loop containment to prevent cross-contamination
    • Product isolated by phase extraction, recrystallization, and fine-tuned drying to meet vet drug-grade specification
    • Full batch traceability encoded with QC checkpoints for each stage

    Final product types

    • Active ingredients for oral, pour-on, and injectable antiparasitic formulations (imidacloprid-type)
    • Premix veterinary active concentrates for further formulation
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    Certification & Compliance
    More Introduction

    Ethyl 2-Chloronicotinate: A Manufacturer’s Perspective on Production and Uses

    Our Drive to Manufacture Ethyl 2-Chloronicotinate

    Stepping into the world of fine chemicals over two decades ago, we built our business by focusing on specialty intermediates that play an essential role in modern synthesis. Ethyl 2-Chloronicotinate has earned a place among our most requested products, especially by teams engaged in pharmaceutical research and advanced crop science. The molecule's value becomes more apparent the deeper you go into development pipelines, where subtle structural choices can mean the difference between breakthrough and bottleneck. Based on years working with both seasoned process chemists and newcomers, we recognize the real-world needs and challenges surrounding such a versatile compound.

    What Sets Ethyl 2-Chloronicotinate Apart

    This particular ester, with the structure defined by a nicotinic acid core chlorinated at the 2-position and an ethyl ester functional group, has an edge over many related intermediates. Technical specifications are important, but actual experience tells a more nuanced story. Unlike its methyl or isopropyl relatives, the ethyl group glides through saponification and transesterification processes without introducing unnecessary volatility or loss. For chemists troubleshooting reaction issues, the extra carbon in the ethyl group offers balance: less prone to unwanted side reactions during scale-up and downstream purification compared to the methyl derivative, but without the steric hindrance that appears in longer chains like propyl or butyl esters.

    Manufacturing Challenges and Insights Gained Through Experience

    Scaling production of Ethyl 2-Chloronicotinate isn’t just about tweaking temperatures or pressures. Even though the reaction to introduce chlorine at the 2-position seems straightforward on a whiteboard, implementing high selectivity across hundreds of kilograms can turn into its own research project. Batch consistency often stumbles on subtle factors—trace water, acid content, or even which supplier’s base solvent comes through the door. The purification stage is where the real art unfolds, mainly because trace impurities at parts-per-million levels can snowball into problems in catalytic cycles or when intermediates move further down the chain toward actives.

    Early in our manufacturing history, we ran into persistent color impurity issues despite seeming compliance with analytical specs. Over several campaigns, process engineers realized that slight differences in the grade of chlorination reagent led to formation of colored byproducts. After in-depth investigations, we shifted to a proprietary controlled-addition protocol and saw both yield and color purity levels surpass internal benchmarks. Practical lessons like these can’t be gleaned from literature alone, and we now provide guidance and application support for users struggling with similar batch and color consistency issues.

    Specifications: Delivering Real-World Performance

    With Ethyl 2-Chloronicotinate, end-users rarely ask about theoretical assay values. Their concerns tend to revolve around reproducibility in multi-step syntheses. Most of our current offerings target a minimum assay above 98%, as determined by GC and HPLC, but we’ve also learned that unspecified micro-impurities control the success of downstream steps. Stabilizing the moisture content below 0.5% has proven critical in nucleophilic aromatic substitutions, improving not only yields but crystallinity of later-stage intermediates such as pyridine-derived actives.

    Particle size is another overlooked but important factor. Though this compound is usually handled as a liquid (boiling gently around 250°C under reduced pressure), small quantities occasionally precipitate if storage conditions fluctuate. By testing different batches stored at varied humidity and temperature profiles, we built an internal protocol for quick redissolution, helping labs restart stalled reactions without scrapping stock.

    Applications: Why Customers Trust Ethyl 2-Chloronicotinate

    The molecule’s versatility gives it a distinct place in both the pharmaceutical and agricultural sectors. In active pharmaceutical ingredient (API) research, chemists use it as a building block for pyridine-containing scaffolds, which form the backbone of drugs ranging from anti-infectives to CNS agents. The ethyl functionality provides a smooth entrance into hydrolysis or further ester modifications, while the 2-chloro group enables stepwise building of more complex nitrogen heterocycles. Early on, some customers wrestled with byproduct formation during amination reactions; our collaboration to optimize starting material quality and suggested tweaks to base strength and temperature led to measurable improvements in product profiles.

    Agrochemical innovators find particular value in using Ethyl 2-Chloronicotinate as a key intermediate in the synthesis of potent herbicide and fungicide candidates. Unlike certain monohalogenated analogues, the compound balances reactivity and selectivity, making it especially popular in SAR (structure-activity relationship) campaigns. Several multinational groups working in crop protection feeder pipelines have reported higher conversion rates and more manageable purification workflows compared to less well-defined precursor esters.

    Comparisons with Related Compounds in Practice

    Looking at other commonly used nicotinic acid derivatives, differences start to surface right at the bench. Methyl 2-chloronicotinate, while cheaper, tends to hydrolyze too readily under routine conditions, complicating precise control of downstream steps. Longer-chain esters, such as butyl or isobutyl, sometimes bring solubility perks in non-polar solvents, but require harsher conditions to cleave, risking partial breakdown or higher impurity carryover. The ethyl ester finds its niche—not just because it is the “middle ground,” but due to a well-established balance between chemical stability and reactivity.

    For large-scale API manufacturing, reliability matters even more than price per kilo. Our direct feedback suggests that transition metal catalysis, which features heavily in modern heterocycle synthesis, proceeds with fewer setbacks when starting from ethyl 2-chloronicotinate of pharmaceutical-grade purity. Patents and batch records from several global companies underline that improved reproducibility got them over regulatory hurdles more smoothly.

    Supplying Ethyl 2-Chloronicotinate Safely and Responsibly

    Dealing with this compound involves more than just a drum and a datasheet. Years in the field taught us that safe handling shapes the long-term health and efficiency of every operation, from bench to bulk. Because the chloro group can generate corrosive fumes if mishandled, we offer practical training and, if needed, site visits to walk through real risk points in day-to-day transfers, filtration, and waste processing. Upgraded drum liners and cold storage support delivered clear drops in localized vapor events during unloading at customer plants.

    The regulatory picture also plays a significant role, especially for global customers. Several partners have faced scrutiny due to trace contaminants like nitrogenous byproducts, which can elude basic QC. Building on shared experiences, we implemented batch-specific tracking and issue joint certificates of analysis upon request, tailored to the needs of both regulated pharmaceutical operations and more nimble R&D groups. These efforts reduced customer down-time and assured compliance in audits.

    Real-World Problem Solving and Partnership Stories

    Working directly with chemists as both manufacturer and technical partner, we often hear about the practical struggles rather than just price or paperwork. One South Asian customer aimed to switch from methyl to ethyl 2-chloronicotinate for a late-stage intermediate, only to face filtration blockages and cloudy crystallizations. Joint troubleshooting surfaced an instability in the work-up phase, traced back to minor differences in local water mineral content affecting the ester’s precipitation profile. We proposed incremental adjustments to the extraction pH and suggested a staged drying protocol, which successfully restored clarity and yield.

    In another case, a European CDMO sought to reduce their environmental footprint while increasing batch output. They initially saw the heavy use of chlorinated solvents as a blocker. Our R&D group piloted a greener process using non-chlorinated extractants and implemented a closed-loop solvent recovery system. As a result, waste was slashed by over 30%, and downstream purification became more straightforward, since less residual chlorinated byproducts persisted in the product.

    These examples underscore that expertise in manufacturing goes hand-in-hand with ongoing conversation; our work doesn’t end the moment the drum leaves the factory. Continued feedback pushes us to improve yield, color, purity, and process safety so our partners can innovate and deliver breakthrough products of their own.

    Improving Industry Standards with Continuous Feedback

    As demand grows for both specialty and bulk lots, we have witnessed changes in expectations around quality consistency and documentation. Large generics houses scrutinize every batch for micro-level impurities, pushing manufacturers like us to rethink not just batch testing protocols but also entire production design. This isn’t bureaucratic overreach; it reflects years of real-world scrutiny that better aligns fine chemical production with the evolving needs of regulated industries.

    To keep pace, we’ve started to employ automated in-process analytic checks, integrating multi-point data tracking during chlorination and esterification steps, which has helped nip problems in the bud. These investments have brought our out-of-spec batch rate below 0.3% in the last year, paving the way for larger partnerships with global innovators who need just-in-time supply for pilot and commercial campaigns.

    Opportunities for Innovation and Future Trends

    Looking forward, we see an expanding role for Ethyl 2-Chloronicotinate in both known and emerging application spaces. With artificial intelligence-assisted drug design uncovering new pyridine-based frameworks, the versatility of this intermediate stands to touch even more discovery pipelines. Agriscience developers have begun targeting “smart” herbicidal agents, and fine-tuning halogenated pyridines for slower breakdown in field conditions.

    Sustainability conversations across the sector impact every choice we make as a manufacturer. Our own shift toward lower-energy synthesis routes and solvent minimization not only aligns with best practices but cuts back waste produced per batch. Some customers have asked about fully bio-based raw materials—not just greener solvents but renewably sourced reagents. While such shifts take time, our product teams work closely with suppliers to pioneer experimental lots, aiming for the same batch quality but with reduced environmental overhead.

    Building Lasting Relationships: Service Beyond Supply

    Although producing high-purity Ethyl 2-Chloronicotinate at scale will always form the backbone of our work, lasting success comes from the relationships we form and the lessons we share. By inviting feedback, running joint development efforts, and supporting process optimization after the point of sale, we try to shape a real partnership rather than a one-off supply transaction. Success for our customers—whether measured in a robust new API, better crop protection for farmers, or smoother regulatory inspection—makes our work worthwhile.

    Industry changes never happen in isolation. Adjusting a synthetic route or tightening an impurity threshold in our facility can ripple outward, enabling global partners to achieve goals that once seemed out of reach. As more applications arise and standards climb, we see Ethyl 2-Chloronicotinate playing a growing role as both a workhorse intermediate and a test bed for the next generation of manufacturing best practices.

    Conclusion

    Experience in manufacturing has taught us that no product exists in a vacuum. Every batch shipped, every improvement piloted, and every phone call from a customer shapes the direction of our business and the wider industry. Ethyl 2-Chloronicotinate may look simple on a molecular diagram, but in the hands of skilled chemists, it becomes a crucial tool for discovery and progress. By embracing feedback and sharing expertise, we continue to earn the trust and respect of those pushing the limits of what’s possible in pharmaceuticals, agriscience, and beyond.