2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine

    • Product Name: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine
    • Chemical Name (IUPAC): 2,6-bis[1-(2-tert-butylphenyl)iminoethyl]pyridine
    • CAS No.: 857850-66-7
    • Chemical Formula: C33H39N3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    220112

    Chemical Name 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine
    Molecular Formula C31H37N3
    Molecular Weight 451.65 g/mol
    Appearance Yellow to orange solid
    Melting Point 185-188°C
    Solubility Soluble in chloroform, dichloromethane, and toluene
    Cas Number 131139-08-5
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place away from light
    Application Ligand for transition metal complexes
    Synonyms 2,6-Bis[1-(2-tert-butylphenylimino)ethyl]pyridine
    Smiles CC(C)(C)c1ccccc1N=C(C)c2cccc(N=C(C)c3ccccc3C(C)(C)C)n2

    As an accredited 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 50 grams of 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine supplied in a sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Ships 5.5–6.5 MT packed in 25 kg fiber drums, maximizing capacity while ensuring product safety and compliance.
    Shipping The chemical **2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine** should be shipped in a tightly sealed container, protected from moisture and light. It must be labeled appropriately with hazard warnings and handled according to standard chemical shipping regulations. Transport should occur under ambient conditions, following all relevant safety and regulatory guidelines for organic compounds.
    Storage 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine should be stored in a tightly sealed container, protected from moisture and air. Keep the chemical in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong acids and oxidizing agents. Proper labeling and handling according to standard laboratory safety protocols are recommended.
    Shelf Life 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine is stable for at least two years when stored under inert atmosphere in a cool, dry place.
    Application of 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine

    Purity 98%: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with purity 98% is used in homogeneous catalysis applications, where it ensures high catalytic efficiency and selectivity in olefin polymerization reactions.

    Melting Point 178°C: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with a melting point of 178°C is used in ligand design for coordination chemistry, where it imparts excellent thermal stability to metal complexes.

    Molecular Weight 526.77 g/mol: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine at a molecular weight of 526.77 g/mol is used in synthesizing transition metal complexes, where it provides enhanced molecular architecture for improved complexation.

    Stability Temperature up to 220°C: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with stability up to 220°C is used in high-temperature catalytic processes, where it maintains strong ligand field strength under demanding reaction conditions.

    Particle Size <10 µm: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with particle size below 10 µm is used in advanced material synthesis, where it promotes homogeneous dispersion in polymer matrices.

    Solubility in Toluene: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with high solubility in toluene is used in solution-phase synthesis, where it facilitates optimal reactant mixing and product yield.

    NMR Purity >99%: 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine with NMR purity greater than 99% is used in precision catalyst development, where it minimizes impurities that could inhibit catalyst activity.

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    Certification & Compliance
    More Introduction

    2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine: Driving Selectivity and Performance in Modern Catalysis

    Our Commitment to Quality Manufacturing

    Years of refining our manufacturing techniques have taught us the value of precision and consistency, especially when it comes to specialty ligands like 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine. Every batch comes from a controlled process at our production facility, designed to meet strict industry standards. Our technical teams actively oversee synthesis from the preparation of starting materials to the final product isolation. By prioritizing analytical purity, we produce a ligand appreciated by research laboratories and industrial teams worldwide.

    Molecular Framework and Its Utility

    The structure of 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine stands out due to its carefully positioned bulky tert-butyl groups adjacent to the imine functionalities. This orientation plays a role in restricting rotational freedom and enhancing the stability of coordination complexes. We see this structural attribute manifest in real-world experiments, where researchers report excellent selectivity and yield using metal-ligand complexes based on our ligand.

    Our customers, especially those developing olefin polymerization catalysts, rely on this ligand to fine-tune their catalytic systems. The electronic properties favor certain metal centers, supporting activities that more basic aromatic Schiff bases cannot achieve. Through countless feedback cycles and collaborative testing, our product maintains a consistent track record for batch uniformity and trace impurity control, directly supporting downstream catalytic performance.

    Specifications Shaped by Industry Demands

    On the shop floor, we work closely with our chemists to monitor the crystal form, color, melting point, and solubility. The ligand typically presents as a pale-yellow crystalline powder, signifying high purity, and dissolves in common organic solvents crucial for catalyst preparation. We maintain a precise specification, ensuring that every shipment supports the reproducibility necessary for both exploratory research and scale-up operations.

    Routine use in our partner laboratories often involves the formation of nickel, iron, or cobalt complexes. These complexes garner attention for their application in alkene polymerizations and C–C bond-forming reactions. The ligand’s bulky groups minimize dimer formation, leading to greater catalyst efficiency. We hear from our industrial partners that this feature allows them to push process parameters further, controlling polymer molecular weight and branching—benefits less accessible with leaner, less protected ligand systems.

    Setting Ourselves Apart from Competing Ligands

    In the ligand landscape, the importance of steric protection cannot be overlooked. The unique tert-butylphenyl groups at the imine positions offer both electronic and spatial control around the metal center, addressing shortcomings seen in simpler analogues such as unsubstituted bis(imino)pyridine ligands. By increasing the size and electron-donating capacity at key sites, our ligand can shield the central metal from undesired side reactions. We’ve observed this time and again in customer reports and in our own R&D applications.

    Competitor products often fail to achieve the same level of purity or batch consistency, either due to less advanced purification or reliance on non-integrated production. Our integrated process minimizes residual metal content and tightly regulates moisture ingress. This commitment to upstream and downstream control translates to lower batch-to-batch variability, a concern regularly echoed by scientists and engineers scaling reactions from milligram to kilogram scales.

    Field Performance: Lessons From Real Catalysis

    Years spent supporting research groups and process chemists bring us firsthand stories of how critical ligands like ours shape performance. In late-transition-metal-catalyzed polymerization, the ability to manipulate the ligand sphere around the active center dictates the microstructure of the resultant polymer. Field reports describe reproducibly higher activity and molecular weight control in polymerizations using our 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine derived complexes over those relying on plain pyridine or less substituted imines.

    We watch as the landscape shifts from conventional phosphine and all-aryl systems toward imine functionalized platforms due to growing health, safety, and sustainability requirements. Our ligand routes typically avoid hazardous intermediates, reducing potential for halogenated waste streams, which has become a growing concern across the specialty chemical sector. End users increasingly want traceability and minimal environmental footprint, both in their catalyst components and in the final polymer products.

    Challenges Faced and Solutions Built

    Pyridine-based ligands featuring bulky substituents often demand careful handling during both synthesis and application. We encountered material stability issues early in product development, particularly with respect to air and moisture sensitivity during complex formation. By redesigning packaging and modifying drying protocols, we lengthened in-use shelf life and facilitated easier handling for customers operating in conventional laboratory atmospheres.

    Shipping to distant industrial sites introduced challenges related to temperature fluctuations and vibration. Our logistics group stepped in with new containment strategies to maintain product quality without driving up costs for customers. Through direct dialogue with users in various climates, we built a system that delivers the same high-purity ligand, irrespective of geographic or transport hurdles.

    The Evolution of Olefin Polymerization Catalysts

    Working with polymer producers, our technical team observed the push away from traditional catalysts toward those built on late-transition-metal centers paired with designer ligands. Many shift toward bis(imino)pyridine analogues for sharper control over molecular properties, a trend visible across both academic literature and patent filings. With a structure that resists undesired chain transfer and offers thermal stability in demanding processes, 2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine regularly wins out over older ligand systems.

    Our multi-stage quality checks and robust continuous feedback loop with end users foster trust—a crucial ingredient in long-term supply partnerships. When academic research groups share results using our ligand, they often mention high reproducibility and the lack of challenging byproducts. This supports their publication goals and smooths the path to industrial adoption.

    Advantages Versus Less Substituted Ligands

    Direct conversations with catalytic chemists highlight frustration with ligand systems where insufficient steric bulk leads to adventitious dimerization or activation pathways that reduce productivity. The tert-butylphenyl substituents in our design address these concerns head-on, reducing intermolecular interactions and stabilizing the desired monomeric complexes. In our experience, this small design alteration increases the functional window of the resulting catalysts.

    Pure bis(imino)pyridine ligands tend to display multiple closely spaced NMR signals due to isomerism and fluxionality, making complex distribution challenging to interpret. Our tert-butyl-protected variant exhibits cleaner spectra and easier integration during spectroscopic quality control. These tractable analytical features speed up troubleshooting and method development, which paid off in our scale-up trials where quick decisions carry real cost implications.

    Impact on Synthesis: Smooth Pathways for Active Catalyst Formation

    Many catalysts built from this ligand form rapidly from straightforward mixing steps, increasing operational safety and reducing waste. From hands-on experience, we see shorter reaction times and fewer purification steps after complexation due to the tailored nature of the ligand’s reactivity profile. Teams developing process-amenable catalysts often comment on the minimization of side-product formation, attributed to the steric and electronic characteristics built into our product.

    We calibrate ligand quality to anticipate the most widely used transition metals, such as iron and nickel. Routine use cases include the formation of active catalyst complexes for the production of polyethylene with well-defined architectures. The ability of our ligand to suppress chain transfer and branching events, as demonstrated in side-by-side catalyst trials, consistently produces higher-quality polymer without the need for constant process tuning.

    Prioritizing Sustainable Chemistry

    Growing focus on green chemistry principles influenced our process design from the earliest development stages. We repeatedly optimized solvent choice and reaction conditions to minimize hazardous wastes and energy usage. The final synthetic route relies on scalable, low-footprint transformations, and our solvent recovery rates exceed industry averages. Company-wide, we prioritize closed-loop systems and regular audits to track material use, supporting broader corporate sustainability goals.

    We support customers running large-volume programs with advice on recyclability and end-of-life disposal of catalyst residues. This dialogue often leads to custom packaging or supply-chain innovations, tailored to the downstream recovery of precious metals or reduction of auxiliary chemicals. In this way, our product not only meets technical needs but fits within the growing regulatory and ethical requirements around specialty chemical sourcing and waste minimization.

    Focusing on What Matters Most: Reliability and Partnership

    All our long-term users value transparency around quality and technical performance. We invest heavily in ongoing analytical verification, from high-resolution NMR to advanced chromatographic fingerprinting. Fast response to customer inquiries and direct access to our technical teams set us apart in a field often marked by delayed feedback or generic troubleshooting. Our support doesn’t stop at shipment; we welcome process feedback and integrate real-world insights into our continuous product improvement cycles.

    We maintain a library of successful field applications, built from user feedback and internal R&D. Insights gathered from these projects enable us to preempt many common process pitfalls before they arise for new customers. Problems—whether solubility limits, stability under scale-up, or compatibility with co-catalyst systems—find workable solutions through partnership, not one-off transactions.

    Looking to the Future with Confidence

    As demand grows for precision polymer architectures and robust, sustainable catalysis, we remain committed to refining both product and process. Experience tells us that performance depends on more than molecular formula; every aspect, from raw material source to process controls, shapes the final result. Ongoing investments in lab automation, analytical equipment, and process optimization keep our production ahead of shifting regulatory, economic, and environmental trends.

    Collaborative research projects with academic partners sharpen our understanding of ligand–metal interactions and guide future improvements. Many recent breakthroughs in controlled radical and chain-transfer polymerization drew directly from data generated using our ligand. These advances now filter back into new product features, expanded application notes, and comprehensive technical support for users navigating increasingly complex synthesis challenges.

    Conclusion: More than Just a Chemical, a Foundation for Progress

    2,6-Bis[1-[2-(tert-butylphenyl)imino]ethyl]pyridine continues to power advances in polymer chemistry and catalyst science, enabling more precise, selective, and sustainable chemical processes. Every gram reflects not only advanced synthesis but a shared commitment to user success, safety, and ongoing improvement.

    By focusing on direct feedback and responsible, consistent manufacturing, we offer a product that helps users meet new technical challenges with confidence. With every order, we build on years of hands-on chemical manufacturing experience, driving both innovation and reliability for those pushing the boundaries of what specialty ligands can achieve.