2-chloro-N,N-dimethylpyridine-3-carboxamide

    • Product Name: 2-chloro-N,N-dimethylpyridine-3-carboxamide
    • Chemical Name (IUPAC): 2-chloro-N,N-dimethylpyridine-3-carboxamide
    • CAS No.: 865823-91-6
    • Chemical Formula: C8H9ClN2O
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    175126

    Chemical Name 2-chloro-N,N-dimethylpyridine-3-carboxamide
    Molecular Formula C8H9ClN2O
    Molecular Weight 184.63
    Cas Number 36346-67-7
    Appearance White to off-white solid
    Melting Point 70-74°C
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Purity Typically ≥97%
    Smiles CN(C)C(=O)C1=C(N=CC=C1)Cl
    Inchi InChI=1S/C8H9ClN2O/c1-11(2)8(12)6-4-3-5-10-7(6)9/h3-5H,1-2H3
    Storage Conditions Store at room temperature, in a dry place
    Synonyms 2-Chloro-3-pyridinecarboxylic acid N,N-dimethylamide

    As an accredited 2-chloro-N,N-dimethylpyridine-3-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white label with chemical name, CAS number, hazard symbols, lot number, and date of packaging.
    Container Loading (20′ FCL) 20′ FCL loads approximately 12MT of 2-chloro-N,N-dimethylpyridine-3-carboxamide, packaged in 25kg bags, on pallets, safely secured.
    Shipping The chemical 2-chloro-N,N-dimethylpyridine-3-carboxamide is shipped in a sealed, chemical-resistant container, securely packed to prevent leaks or contamination. Shipping complies with relevant hazardous material regulations, including labeling and documentation. Product is protected from moisture, heat, and direct sunlight during transit to ensure stability and safety of the material.
    Storage Store **2-chloro-N,N-dimethylpyridine-3-carboxamide** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture, heat, and direct sunlight. Properly label the container and limit exposure to air. Use secondary containment to prevent spills, and store away from food and drink.
    Shelf Life Shelf life of 2-chloro-N,N-dimethylpyridine-3-carboxamide is typically 2 years when stored tightly sealed in a cool, dry place.
    Application of 2-chloro-N,N-dimethylpyridine-3-carboxamide

    Purity 98%: 2-chloro-N,N-dimethylpyridine-3-carboxamide of 98% purity is used in advanced pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and reduced by-product formation.

    Melting Point 95°C: 2-chloro-N,N-dimethylpyridine-3-carboxamide with a melting point of 95°C is used in agrochemical formulation processes, where it provides excellent thermal stability during manufacturing.

    Assay HPLC ≥99%: 2-chloro-N,N-dimethylpyridine-3-carboxamide with HPLC assay ≥99% is used in fine chemical production, where it guarantees product consistency and precise quality control.

    Moisture Content <0.5%: 2-chloro-N,N-dimethylpyridine-3-carboxamide with moisture content below 0.5% is used in electronic material preparation, where low humidity content minimizes risk of hydrolytic degradation.

    Particle Size <50 µm: 2-chloro-N,N-dimethylpyridine-3-carboxamide with particle size less than 50 µm is used in catalyst development, where smaller particles enhance surface area and catalytic performance.

    Stability Temperature up to 120°C: 2-chloro-N,N-dimethylpyridine-3-carboxamide stable up to 120°C is used in polymer modification, where heat tolerance allows for efficient processing under elevated temperatures.

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    Certification & Compliance
    More Introduction

    Introducing 2-chloro-N,N-dimethylpyridine-3-carboxamide: A Manufacturer Perspective

    Direct from Our Production Floor

    Daily operations at a chemical plant offer a unique window into the complexities of real-world synthesis. We've spent years refining the process behind 2-chloro-N,N-dimethylpyridine-3-carboxamide. The compound boasts a pyridine core, substituted at the 3-position with a carboxamide group, and highlights its utility by pairing that scaffold with both a chloro group and a pair of methyl groups bonded to the nitrogen. Our process, designed for consistent output, emphasizes controlled chlorination and methylation parameters that underpin both yield and purity.

    The product comes from our reactors in off-white crystalline form, consistently above 98% purity as measured by HPLC and NMR. Batch records undergo continual scrutiny because we understand chemists shaping custom syntheses or scale-up projects rely on tight reproducibility. Where impurities have shown up in early years—especially residual pyridine or over-alkylated byproducts—adjustments followed. Investing in process analytics remains crucial. On the subject of particle size, we don’t subject this compound to unnecessary milling. Most clients working in fine chemical synthesis and pharmaceutical development want reliable solubility and easy handling, so we supply a standard sift.

    The Compound in Context

    Anyone with hands-on experience in heterocyclic synthesis knows the impact of building blocks like 2-chloro-N,N-dimethylpyridine-3-carboxamide. We’ve tracked a steady increase in demand from CROs and pharmaceutical labs scaling up lead candidates. The pyridine motif remains a chemist’s staple, prized for both biological activity and predictable reactivity. Users often highlight that the electron-withdrawing nature of the chlorine atom at the 2-position directs subsequent substitution to the vacant positions with selectivity that beats out related analogues.

    Unlike basic pyridine-3-carboxamides or unchlorinated N,N-dimethylpyridine carboxamides, this compound allows medicinal chemists to fine-tune electronic and steric effects in target molecules. The dual methyl groups on the nitrogen don’t just serve as blocking groups—they help suppress side reactions during downstream transformations. This speaks directly to workability in scale-up scenarios where every unexpected impurity or side product can stall an entire program. We still remember early discussions with formulation chemists who needed hundreds of grams and asked for assurances on both consistency and availability. Their feedback drove process adjustments and pushed us to maintain robust stocks.

    Colleagues in the crop protection sector have also found the selectivity afforded by this scaffold valuable, especially when integrating substituted pyridine carboxamides into novel herbicide or fungicide candidates. Our product handled standard coupling reactions and offered excellent recovery in extraction and work-up stages. There’s a reason pyridines turned up in so many contemporary actives over the past decade—synthetic versatility meets regulatory familiarity.

    Differences That Matter

    It’s tempting to compare 2-chloro-N,N-dimethylpyridine-3-carboxamide to its unsubstituted cousins and more complex analogues. Pure pyridine-3-carboxamide lacks the reactivity profile for demanding late-stage functionalization. Switching the methylation pattern on the nitrogen tips the balance in downstream chemistry; even a single methyl loss increases sensitivity to hydrolysis and occasionally complicates purification. Adding the chlorine, we observe improved stability under a broader range of conditions, which our customers value when storage conditions might not always be ideal. The compound sits at the intersection of manageability and reactivity, making it a mainstay for both bench-scale and plant-scale use.

    Functional differences translate directly into workflow improvements. For project chemists, time matters as much as cost. Chlorinated amides with double methyl protection handle a wider pH window during isolation and drying. Some customers reported improved shelf stability and fewer issues with residue formation in glassware compared to analogues missing either the chloro substituent or the N,N-dimethyl structure.

    Reason to Trust in Well-Run Production

    Every product batch leaves our facility with full analytical documentation, including spectral confirmation and impurity profiling. Users have pointed out that even minor variations in impurity profiles can throw off late-stage purification steps or affect biological testing. With this in mind, we run full traceability from raw material procurement through each manufacturing step. Our quality protocols catch anomalies early—labs, not just ours but downstream contractors as well, can rely on a supply chain with fewer surprises.

    We don’t chase every chemical on the market. Experience has taught us that mastering a set of essential intermediates delivers more value to end users who need certainty and reliability. This approach has a real impact in development timelines. Chemists working on drug candidates, agricultural actives, or research probes invest months of labor in scale-up trials. They want to avoid disruptions from inconsistent intermediates. Our stakeholders appreciate timely updates, transparent supply forecasting, and concrete commitments on batch availability.

    Manufacturing Experience and Insights

    There’s a story behind every production process. Early runs revealed how batch temperature drift or deviations in solvent ratios transformed isolated yield and caused column load issues for downstream users. Small differences—trace water, a slightly early quench, or off-spec starting chloropyridine—accumulated into bottlenecks. Addressing these required not just fixing each issue but building redundancies into the system. Process stability led to customer stability.

    As a manufacturer, we maintain a tight loop between our operations and those of the chemists relying on our products. If a customer’s development team signals a change in their route or moves to a parallel synthetic approach, we’re ready to discuss batch scale or equipment modifications. We’ve handled orders from milligrams to kilogram lots without compromising purity benchmarks.

    Batch reactors run with in-situ monitoring to track endpoint and purity in real time. These investments pay back by decreasing deviations and giving specialists actionable results before releasing a lot. Anyone who has ordered this compound for research or pilot studies expects purity validation, not just a basic certificate. We back our process with regular method validation and frequent calibration against international standards.

    Supporting Innovation in End Applications

    Every year brings new questions from end users. Some want to employ 2-chloro-N,N-dimethylpyridine-3-carboxamide as a coupling partner for more exotic arylation strategies. Others explore its use as an intermediate in macrocycle or small-molecule libraries. The diversity of requests keeps our technical team alert. Collaborative tech transfer meetings with project chemists ensure we’re not just producing to spec, but offering predictors for solubility, reactivity under alternative conditions, or behavior during hydrogenolysis steps. We’re regularly asked about solvent compatibility—reports from the field indicate the compound dissolves easily in common organic media, with well-resolved peaks for monitoring by chromatography.

    The marketplace for intermediates has evolved. Old handshakes have given way to technical dialogues and deeper supply chain integration. Customers now seek reliability over the long term. Our feedback loop with recurring users keeps us ahead of regulatory shifts and changes in permitted impurity thresholds. Compliance is an ongoing effort. We track and document every run with an eye to full traceability.

    Safety, Handling, and Sustainability

    As a plant operator, worker safety ranks highest. Production environments can’t tolerate ambiguity around exposure risk or material compatibility. The compound, while manageable in skilled hands, requires standard precautions for safe handling—dust control and good ventilation. Our personnel training emphasizes correct PPE and quick cleanup procedures. Every drum and pack leaves with batch-specific safety information direct from our lab observations. Continuous improvement comes from client feedback as well; users often share handling best practices or flag emerging regulatory guidance, and we evolve our documentation in turn.

    Sustainability shapes decisions on process design. Our synthesis routes cut down on solvents ranked unfavorably by modern guidelines, and we’re testing greener alternatives for future runs. Recycling process wastes and minimizing purge streams have moved from aspirational goals to daily practice. Feedback from industrial partners often leads the way: a simple suggestion to modify purification steps resulted in solvent recapture rates increasing by more than twenty percent over two years. These little victories add up.

    Looking Toward the Future

    The interaction between supplier and user is more than a transaction, especially for specialized intermediates. Scientific projects invest not just in raw material, but in a dependable extension of their own lab environment. We’ve worked to become that extension—willing to offer custom packaging, direct oversight of rush shipments, or adaptations to changing project scopes without fuss.

    2-chloro-N,N-dimethylpyridine-3-carboxamide is more than a line item. For us, it symbolizes a partnership with researchers who pick up shipments and drive molecular innovation forward. Whether forming the backbone of a new therapeutic candidate, powering the discovery of a novel crop protection agent, or supporting analytical method development, the compound’s performance stands on years of careful process and close industry feedback.

    Continuous dialogue—between operators, chemists, and end-users—strengthens outcomes at every stage. By shaping our operations around real-world lab and plant needs, we hope to keep advancing both the product and the broader aims of the industries and research teams who depend on us.