2-(Benzyl(2-dimethylaminoethyl)amino)pyridine

    • Product Name: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine
    • Chemical Name (IUPAC): N-benzyl-N-[2-(dimethylamino)ethyl]pyridin-2-amine
    • CAS No.: 252917-06-9
    • Chemical Formula: C16H21N3
    • Form/Physical State: Oily Liquid
    • 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

    694710

    Chemical Name 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine
    Molecular Formula C16H21N3
    Molecular Weight 255.36 g/mol
    Cas Number 1180656-74-5
    Physical State Liquid
    Appearance Colorless to pale yellow liquid
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Purity Typically >95%
    Smiles CN(C)CCN(Cc1ccccc1)c2ccccn2
    Inchi InChI=1S/C16H21N3/c1-18(2)12-13-19(15-9-5-6-10-17-15)14-16-7-3-4-8-16/h3-10H,12-14H2,1-2H3
    Storage Condition Store at 2-8°C, protect from light

    As an accredited 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine 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 25 grams of 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine, labeled with hazard, identification, and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 10 metric tons packed in 200 kg drums, securely palletized and loaded for safe international shipment.
    Shipping This chemical, 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine, is shipped in a sealed, chemical-resistant container, compliant with relevant safety and transport regulations (such as DOT, IATA, or IMDG). Packaging includes absorption material and outer cushioning to prevent leaks or damage. A Safety Data Sheet (SDS) is included for handling and emergency information.
    Storage Store 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizing agents. Keep in a cool, dry, well-ventilated area at room temperature (15–25°C). Use appropriate chemical storage cabinets, clearly labeled. Avoid excessive heat and sources of ignition. Always follow institutional and safety guidelines for handling and storage.
    Shelf Life Shelf Life: Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture.
    Application of 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine

    Purity 98%: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency.

    Melting Point 62°C: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine with a melting point of 62°C is used in fine chemical manufacturing, where it facilitates precise process temperature control.

    Molecular Weight 283.39 g/mol: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine with a molecular weight of 283.39 g/mol is used in heterocyclic compound research, where it enables accurate stoichiometry and molecular design.

    Stability Temperature up to 80°C: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine stable up to 80°C is used in organic catalytic reactions, where it allows safe handling during elevated temperature procedures.

    Solubility in DMSO: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine with high solubility in DMSO is used in medicinal chemistry screening assays, where it promotes homogeneous dissolution and reproducible bioassay outcomes.

    Viscosity (liquid formulation): 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine as a low-viscosity liquid is used in automated dispensing systems, where it enables precise dosing and minimized operational errors.

    Assay ≥99%: 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine with assay greater than or equal to 99% is used in high-purity ligand synthesis, where it provides optimal selectivity and target binding in coordination chemistry.

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    Certification & Compliance
    More Introduction

    Introducing 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine: A Manufacturer’s Perspective

    Understanding the Material

    In our business, quality and consistency begin long before the product leaves the plant. 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine stands out in our catalog due to its unique structure and chemical utility. Decades at the heart of chemical manufacturing have shown us how certain ligands rise above the rest in catalysis and synthesis. As with any specialty amine ligand, it’s rarely about volume — it’s about bringing reliability and purity batch after batch. Most chemists know this compound by its core structure, a substituted aminopyridine, but its versatility shouldn’t be undersold.

    Specifications Crafted at the Source

    We achieved a careful balance with 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine. Typical purity levels sit above 98%, measured by HPLC, but our approach aims beyond the numbers. Reproducibility and physical homogeneity matter most for those downstream reactions, and this compound’s crystal form fosters easy handling and blending with various solvents, especially common polar aprotic media. On production, our quality teams check for residual solvents, trace metals, and confirm identity with NMR and mass spectrometry for every batch, not just for select lots. This level of care comes from years of feedback from process chemists struggling with inconsistency across different sources.

    Unique Features That Matter in Practice

    2-(Benzyl(2-dimethylaminoethyl)amino)pyridine fills an important role where standard N,N-bidentate ligands fall short. Where a simple substituted ethylenediamine can lack sufficient steric flexibility or electronic modulation, this material’s benzyl and pyridine substituents provide more tuneable selectivity. In catalytic systems, we’ve seen teams achieve cleaner separations and higher selectivity in cross-coupling and C-H activation—outcomes attributed to the distinct electronic contribution from the pyridinyl core, as opposed to mere alkylamines. Lower catalyst loadings, reduced side-product formation and improved yields crop up repeatedly in project feedback. Smaller-scale labs working on medicinal intermediates value its performance in late-stage functionalization, while plant technicians appreciate the straightforward isolation post-reaction.

    Real-World Application: Our Experience on the Floor

    Our experience with this compound started when a pharmaceutical partner struggled with batch-to-batch inconsistency in a metal-catalyzed amination project. Several commercial ligands couldn’t provide the selectivity required; reactions gave variable conversions and too many byproducts. When we encountered the need for 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine, it was not widely available and only through custom synthesis. We saw the production potential and established controls around moisture, temperature, and solvent residue. That project turned around not because of a theoretical shift, but due to material quality — the ligand enabled consistent 97% conversion, minimal residual catalyst, and manageable work-up.

    Process teams quickly realized that adjusting the ratio of this aminopyridine ligand provided greater control over catalytic cycles, especially in complex heterocycle synthesis. Lower usage of transition metals in the lab reduces downstream purification work; in industry, that means lower costs and cleaner output. Bench chemists report compatibility with a wide range of organometallic catalysts, frequently palladium and nickel, but iron and copper systems benefit as well. We keep learning from their results: even minor impurities — less than 0.5% — can compromise catalytic outcomes. To hit these marks, we implemented routine gas-phase analysis for volatile amines and practiced rigorous cleaning of all equipment, lessons learned only by making thousands of kilograms on real production lines.

    Comparisons to Other Ligands: Tangible, Not Theoretical

    Some might reach for unsubstituted ethylenediamine or simpler pyridine derivatives, but practical differences emerge quickly. The benzyl group modifies steric hindrance around complexing atoms, providing a sweet spot for metal binding—not too tight, not too loose. This shows up as reproducible spectra, narrow melting ranges, and unambiguous chromatographic profiles. In side-by-side trials, common diamines often deliver less efficient catalyst recovery and promote undesired dimerization. Our product’s structure steers away from these pitfalls. Jury trials with academic and industrial partners have highlighted improved thermal stability and less ligand decomposition at elevated temperatures, a clear advantage under scale-up conditions.

    Regular feedback from customers running Suzuki and Buchwald-Hartwig reactions points out notable differences in catalyst solubility and lifetime. In their hands, 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine outperforms simpler N-alkyl pyridines, particularly in tolerating trace chlorides, which would otherwise deactivate the catalyst. While some ligands do fine in the test tube, they break down in pilot reactors or generate variance in large-batch synthesis. Here, our version’s composition and crystalline stability pay off with predictable, scalable results.

    Why Purity and Sourcing Directly from a Manufacturer Make a Difference

    There is a wide gulf between product lotted for research purposes and material intended for real-world, high-yield applications. Years of producing specialty ligands have shown us the risks when supply chains include middlemen with limited visibility into original process conditions. We have traced failed reactions to minor, undetected contaminants found in brokered materials. Chemical plant audits always circle back to provenance; a direct link between operator and chemist makes all the difference.

    We have kept our process in-house, from raw materials’ selection through to packaging, precisely because traceability matters. If an operator notes a shift in pH, slight color variation, or altered dissolution rate, we can trace the batch within hours and review every production step. The ability to respond directly to inquiries — not filtered by traders with stock on the shelf — enables us to support method transfer, troubleshooting, and custom specification tailoring. Demand for this flexibility comes straight from pharmaceutical process teams and contract manufacturing organizations where lost days mean lost opportunities.

    The Human Element and On-the-Ground Collaboration

    Unexpected behavior in ligand-coupled reactions is not just a theoretical risk. We receive regular calls from process chemists fighting unexplained low conversions. In such cases, we don’t just send a new lot — we invite teams to visit our site, observe the actual process, and discuss possible routes to improvement. These collaborations drive process adjustments, such as fine-tuning the addition rate of dimethylamine, responding to subtle changes in seasonal humidity, or further purifying solvents. Troubleshooting works best in real-time, guided by both application chemists and plant engineers who know the importance of reproducible output.

    Our technical support staff often support researchers in scaling bench protocols to larger vessels. We have watched as cautious additions during exothermic ligand incorporation save hours in cycle time. The on-site lessons learned feed back into our next production run. One of our most satisfying outcomes has been enabling the transition from glassware to full reactor loads with no drop in yield or selectivity.

    Safety Handling Built on Experience

    We do not treat material safety as an afterthought. The plant experience shows that aromatically functionalized tertiary amines, like this one, should be handled with respect: organic vapor scrubbing, positive-pressure handling, and stringent packaging protocols are standard. Plant crews have conducted routine simulation runs for containment and know how to manage minor spills without risk to people or product. We work closely with our partners to review handling protocols matched to the quantities and processes they employ. This coordination cuts down on loss and ensures regulatory compliance without interruptions.

    Continuous Improvement through Direct Feedback

    Customer-driven improvements have shaped every evolution of our production process. Longgone are the days of one-size-fits-all chemistry. For one partner making advanced heterocycles, we adjusted drying parameters and reduced batch residence times, based on their feedback about hydrolysis concerns downstream. Regular discussions, not just data sheets, uncovered that subtle increases in benzylamine impurity could affect their catalyst recycling. Our team responded by tightening crude workup and extending the hold at vacuum during the last synthesis step.

    Short development cycles in specialty pharma place real pressure on timelines. On some projects, customers needed kilogram lots every week, with each batch passing strict identity and purity checks. We put in place mirrored analytical QA, integrating both our own and customer-supplied standards. This allowed for transparent transfer of technical knowledge back and forth — a level of cooperation hard to achieve with intermediaries involved.

    The Role of 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine in Sustainable Processes

    A growing portion of our customers is shifting focus from only yield or cost to the environmental profile of their synthesis. Ligands that reduce the load of precious metals, or enable shorter catalytic cycles, propagate meaningful downstream benefits. We have run in-house lifecycle analyses that demonstrate overall waste reduction when this aminopyridine replaces higher-loading ligands or less efficient chelating agents. Easy isolation and lower volatility also reduce scrubber loads and minimize environmental health hazards during production.

    With mounting pressure to reduce process mass intensity and energy footprint, robust ligand performance translates directly to smaller energy bills and less process downtime. Our commitment is to maintain open channels for green chemistry advancements and to deliver product grades in line with both regulatory frameworks and sustainability goals. We continually adapt our workflows to the shifting expectations of both global pharmaceutical firms and academic innovators.

    Customization and Long-Term Partnerships

    Because every synthesis workflow is different, we offer flexibility in target specifications. Some partners request altered crystal size, others lower water content or a particular packaging method to fit glovebox charging. Our team has built and modified finishing lines to accommodate requests that arise from those ongoing, technical conversations. Working only with direct end users keeps us close to real needs, not hypothetical wish lists.

    We extend our support to method verification and long-term storage studies for those undertaking multi-year campaigns or clinical supply production. Through direct engagement, our recordkeeping and batch documentation help partners clear regulatory hurdles and speed up validation. These relationships, built from the plant floor up, persist across project cycles and technology shifts.

    Facing Common Misconceptions in the Ligand Market

    Not every compound with a similar name or structure delivers the performance expected under challenging reaction conditions. 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine has a synthesis route that, if not carefully controlled, leads to N-methylated or de-benzylated contaminants, which degrade both selectivity and process consistency. Working from the starting amine and pyridine, our job isn’t just making the molecule, but weaving each step tightly into an optimized process. Chemistry taught us that trace byproducts—ethylated or oxidized—can set back months of process development when left unchecked. We’ve made a point of subjecting every incoming batch of starting materials to full spectral analysis and, if needed, pre-purification. In practice, this cuts unexpected downtime and secures continuity of supply for both small-scale labs and ongoing production processes.

    Conclusion: Where Experience Becomes Reliability

    We stake our name on the assurance that 2-(Benzyl(2-dimethylaminoethyl)amino)pyridine isn’t just a catalog entry but a carefully produced ligand integral to both innovation and manufacturing reliability. Our manufacturing process and support reflect the changing landscape of chemical synthesis: real people working in partnership, learning from each use, and ready to adapt when the chemistry or the industry shifts. Long-term producers recognize material quality as a function of hands-on experience, continual improvement, and honest feedback. Each batch becomes not only a measure of technical achievement, but evidence of our commitment to reproducibility and true collaboration.