2,2'-Bipyridine-4,4'-diyldimethanol

    • Product Name: 2,2'-Bipyridine-4,4'-diyldimethanol
    • Chemical Name (IUPAC): 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine
    • CAS No.: 87132-16-1
    • Chemical Formula: C12H12N2O2
    • 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

    717986

    Cas Number 109239-92-5
    Molecular Formula C12H12N2O2
    Molecular Weight 216.24 g/mol
    Iupac Name 2,2'-Bipyridine-4,4'-diyldimethanol
    Appearance White to off-white powder
    Melting Point 122-125 °C
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Boiling Point Decomposes before boiling
    Storage Temperature 2-8 °C
    Smiles OCc1cc(ncc1)-c2cc(ncc2)CO
    Inchi InChI=1S/C12H12N2O2/c15-7-9-1-3-13-11(5-9)12-6-10(8-16)4-2-14-12/h1-6,15-16H,7-8H2

    As an accredited 2,2'-Bipyridine-4,4'-diyldimethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,2'-Bipyridine-4,4'-diyldimethanol (1 gram) is packaged in a sealed amber glass vial, labeled with product and safety information.
    Container Loading (20′ FCL) 20′ FCL container loaded with securely packaged 2,2'-Bipyridine-4,4'-diyldimethanol, ensuring stability, safety, and compliance with transport regulations.
    Shipping 2,2'-Bipyridine-4,4'-diyldimethanol is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported under cool, dry conditions, with appropriate labeling as a laboratory chemical. Handle in compliance with relevant regulations for chemical transport and storage, ensuring safety during transit.
    Storage Store *2,2'-Bipyridine-4,4'-diyldimethanol* in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Label the container clearly and avoid prolonged exposure to air. Ensure proper laboratory safety measures are in place to prevent contamination or accidental release.
    Shelf Life 2,2'-Bipyridine-4,4'-diyldimethanol typically has a shelf life of 2–3 years when stored in a cool, dry, and dark place.
    Application of 2,2'-Bipyridine-4,4'-diyldimethanol

    Purity 98%: 2,2'-Bipyridine-4,4'-diyldimethanol with 98% purity is used in homogeneous catalysis synthesis, where high chemical selectivity is achieved.

    Melting Point 150°C: 2,2'-Bipyridine-4,4'-diyldimethanol with a melting point of 150°C is used in ligand design for coordination chemistry, where thermal stability ensures consistent complexation.

    Molecular Weight 214.22 g/mol: 2,2'-Bipyridine-4,4'-diyldimethanol of 214.22 g/mol is used in research-scale metal ion sensing, where defined mass allows accurate stoichiometric calculations.

    Particle Size <10 μm: 2,2'-Bipyridine-4,4'-diyldimethanol with particle size below 10 μm is used in high-performance thin film deposition, where uniform particle distribution enhances film homogeneity.

    Solubility in Methanol: 2,2'-Bipyridine-4,4'-diyldimethanol with high solubility in methanol is used in photochemical studies, where solution processing increases reaction efficiency.

    Stability up to 120°C: 2,2'-Bipyridine-4,4'-diyldimethanol stable up to 120°C is used in thermal polymerization protocols, where decomposition is minimized.

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    Certification & Compliance
    More Introduction

    2,2'-Bipyridine-4,4'-diyldimethanol: Reaching New Standards in Ligand Chemistry

    After years of hands-on experience in the synthesis and scaling of custom pyridine ligands, we know every nuance that pushes a bipyridine derivative from the lab bench to real-world applications. 2,2'-Bipyridine-4,4'-diyldimethanol stands out for chemists who need reliability over long campaigns, not just textbook purity on paper. Here at our manufacturing site, we maintain oversight through every batch, starting from the initial sourcing of precursor materials. Only full transparency about the raw inputs and stepwise fidelity in process control lets us consistently deliver material meeting strict specifications.

    Model and Specifications Built Around Real-World Needs

    We produce 2,2'-Bipyridine-4,4'-diyldimethanol in the most-used research and industrial model: bis(4-hydroxymethyl)-2,2'-bipyridine. Each lot matches our internal benchmarks for purity (typically >99% by HPLC) and water content (low ppm levels confirmed by Karl Fischer). The product arrives as a pale powder, easy to dissolve in polar solvents like methanol or DMSO without leaving residue. Every drum passes through identity checks—NMR, IR, and MS—so you see exactly what you expect, batch after batch. We stick very closely to drying times and avoid unnecessary exposure to moisture, which we’ve noticed in the past can lead to subtle but frustrating product inconsistency.

    From long shifts on manufacturing floors and troubleshooting issues with other ligands, we know high purity guarantees only part of the story. Physical handling matters. No one wants to spend a chunk of a workday laboriously breaking up a lumpy or sticky solid. We adjusted our crystallization and drying steps years ago to keep our product free-flowing. If the powder compacts inside storage drums, shipping disasters happen, so we intervene quickly to correct granule size before release.

    Applications: Real Process Experience Matters

    Most of our customers request 2,2'-Bipyridine-4,4'-diyldimethanol for ligand-based catalysis, especially when bidentate chelation with a secondary functional handle is required. The methanol substitutions at the 4,4' positions are not just molecular window dressing—they open up conjugation options and surface anchoring strategies that plain bipyridines can’t support. We’ve seen labs use this ligand to immobilize metal catalysts on silica, craft molecular wires for electronic research, and develop new photophysical probes.

    In scale-up, this compound works well for constructing solid-supported complexes or tuning electronic properties through derivatization. Its structural configuration lets researchers perform targeted functionalizations for diverse metal-catalyzed reactions. Teams exploring electroluminescence or designing hypertension sensors see clear advantages in the dual alcohol functionality—it stays reactive and expands the modification playbook. We think the real testament lies in how chemists keep coming back for multi-kilogram orders: the production runs remain smooth, and the subsequent complexation reactions flow predictably.

    What Sets 2,2'-Bipyridine-4,4'-diyldimethanol Apart?

    Working with dozens of pyridine derivatives, we have a direct sense of the challenges chemists run into during development. Compared with simple bipyridine, the dihydroxymethyl modification unlocks more straightforward crosslinking and covalent attachment reactions. Older variants like 4,4'-dimethyl-2,2'-bipyridine lack the polarity and nucleophilicity necessary for certain synthesis schemes. Customers running ligand exchange in aqueous or mixed media repeatedly point out enhanced solubility using our dimethanol version, sidestepping some solvation headaches.

    Standard 2,2'-bipyridine remains a staple in classic coordination chemistry, but in multidisciplinary research, scientists want that extra flexibility. The presence of two primary alcohol groups in 2,2'-Bipyridine-4,4'-diyldimethanol supports modification through alkylation, esterification, or coupling with PEG chains. We’ve fielded requests from protein labeling groups who report that only the dimethanol variant supports stable linker formation under their target conditions. In previous jobs, I recall the frustration when a straightforward methylated ligand would not support direct conjugation—the extra steps needed for functionalization just ate up time and added costs.

    Lessons Learned from Decades of Handling Pyridine Ligands

    Every manufacturing campaign highlights the careful balance needed between product stability and reactivity. We have seen oxygen-sensitive metals destabilize if exposed to trace residual formaldehyde from improperly neutralized dimethanol bipyridines. Rigorous vacuum drying solves this, but only if the manufacturer oversees protocol details—relying on standard batch sheets rarely works. Several years ago, we updated our analytical suite to cross-check for micro-level organic impurities and didn’t look back: feedback from complex-building labs dropped complaints about interference or off-color complexes.

    Fielding technical calls, we’re often asked about alternative products, especially 4,4'-dichloro or 4,4'-diamino bipyridine. These function in many of the same coordination complexes, but we see lower chemical flexibility in post-synthesis modification. Our dimethanol product bridges the gap between unreactive parent bipyridines and extensively modified “designer” ligands. For many labs, scaling up synthesis means avoiding extra purification or tedious conversions—here, the dimethanol variant saves days of labor and extra solvents.

    Supporting Modern Research, Not Just Bulk Chemistry

    Over the last decade, much of the innovation in bipyridine chemistry has shifted toward cross-disciplinary projects blending catalysis, materials science, bioconjugation, and sensing. Our team supports growing demand from academic and industrial researchers who need ligands with reliable reaction handles.

    Supply chains have changed dramatically since our founding: international logistics can introduce temperature swings and handling inconsistencies that far-off resellers never even see. By controlling packaging and storage protocols ourselves, we block out a source of frustration: the end-user gets the same material, batch after batch, with no surprises at the bottom of a jar or drum. Minimizing clumping and protecting against moisture ingress pays dividends for everyone, especially for large-scale or automated workflows.

    Some customers need guidance adapting protocols written for classic bipyridine derivatives. In practice, most substitution reactions or catalyst preparations proceed similarly or more efficiently with the dimethanol ligand, assuming water and temperature-sensitive steps are managed properly. We keep clear records of all manufacturing parameters. If an adjustment or clarification is needed, our technical staff can dig back through batch histories and suggest refinements so a synthesis bottleneck doesn’t derail an entire development project. Most chemists we support don’t just want a high-purity chemical—they want predictable, explainable results that accelerate research rather than hold it back.

    Practical Solutions for Persistent Challenges

    Our experience shows that comfort and trust in a reagent come not purely from the datasheet but from what it does—or doesn’t—do when it’s on the bench. No one wants a “finicky” ligand, and we have worked methodically to eliminate those negative surprises. Only hands-on oversight and accumulated process refinements deliver a product that is chemically unambiguous and physically easy to use for its full shelf life.

    Years ago, we dealt with repeated clumping complaints from beta testers using resins and chromatographic beds preloaded with the ligand. We adapted packaging and added small in-line drying steps, dropping complaints about low solubility to nearly zero. Direct feedback shapes our manufacturing modifications: a suggestion from a team developing supported catalysts led us to gently adjust the particle size distribution, which in turn ended filter clogging across multiple sites. These incremental changes add up, and the ultimate benefit flows to clusters of researchers who depend on small operational improvements to prove their science out at scale.

    Supply reliability remains a persistent stressor in research-driven sectors. Spikes and delays hurt both timeframes and confidence. Instead of strictly just-in-time production, we maintain buffer stocks tied to forecasted demand, so large or urgent orders don’t force customers into costly procurement scrambles. During periods of heavy demand, such as grant season or contract cycles, our customers avoid line stoppages or interrupted synthesis because we plan forward with raw material suppliers and maintain batch overlap capacity.

    From the Factory Floor to Your Laboratory: Knowledge Baked Into Every Batch

    We thrive on the details. Each lot of 2,2'-Bipyridine-4,4'-diyldimethanol reflects practical improvements learned from hundreds of real use cases. Our process engineers work alongside PhD chemists and bench technicians to anticipate where the next production kink or analytical hurdle might spring up—not just for ourselves, but for the end-users relying on our compound to support advanced projects. Some of the best product suggestions have come from end-users troubleshooting a stubborn synthesis. Their insights drive tweaks to crystallization time, solvent ratios, or packaging adjustments that feed right back into the next manufacturing cycle.

    Direct engagement with university researchers, process development teams, and start-ups lets us see new applications as soon as they’re being formulated or tested. Whether it’s a new electrocatalytic process or innovative surface-functionalized polymers, 2,2'-Bipyridine-4,4'-diyldimethanol gives real advantages by blending chemical reliability with a straightforward platform for targeted derivatization.

    Every bottle represents accumulated expertise: from high-purity, free-flowing powder to guaranteed batch consistency, we minimize operational risk so scientists can amplify their creative potential. Whether creating a new optoelectronic material, developing a bioactive conjugate, or seeking a robust bidentate ligand for process catalysis, this product earns its place in complex synthetic campaigns. Keeping every step inside our factory, from reaction to finishing, gives customers full transparency and product confidence, batch after batch. We see this as not just supplying a compound, but providing a tool that knits together reliability, innovation, and operational efficiency for the modern lab.

    Industry-Driven Improvements

    Working as the original manufacturer and not just a distributor, we keep large-scale process capabilities under our own quality systems. Over time, we redesigned synthesis routes to trim unnecessary purification steps, protect reactive groups, and improve yields—a direct response to feedback from scale-up chemists dealing with classic bottlenecks in bipyridine derivatization. By choosing supply partners based on full traceability and contaminant profiles, we shield our end-users from unexpected variability that can creep in with spot-market resellers.

    Quality isn’t defined only by data on a certificate of analysis. It shows itself through hands-on bench tests, pilot projects, and continued compatibility with downstream processes. Dusty, impure, or unstable bipyridine ligands stall projects or lead to non-reproducible data. In contrast, supplying a well-characterized, high-yielding dimethanol bipyridine gives teams confidence to plan, execute, and publish without hedging bets on each new batch. Our QC and technical support deal with the real questions: solubility outliers, compatibility with emerging catalysts, or troubleshooting compositional analyses—practical touchpoints, not just checklists.

    Trusted by Bench Chemists and Process Developers

    We serve a broad cross-section of the research landscape. Analytical teams reach for our 2,2'-Bipyridine-4,4'-diyldimethanol for its crisp, unambiguous NMR and MS signatures—vital for characterizing metal complexes or confirming new synthetic intermediates. Synthetic chemists value predictable behavior in building functionalized bipyridine motifs: the dual hydroxymethyl groups provide reactive sites for further diversification or enable straightforward immobilization on supports.

    Our direct sourcing, batch-to-batch control, and process feedback loops keep quality high and surprises low. Years of tight collaboration with downstream users means we anticipate the pain points that can derail even well-planned workflows. Whether scaling up a new photophysical probe or executing ligand platform screens for homogeneous catalysis, our product scales from gram-vial research to drum-level campaigns without loss of fidelity or performance.

    Commitment to Transparent, Responsible Manufacturing

    We track every input and adjustment, providing confidence not only in chemical identity but also in supply consistency and regulatory conformance. Our internal framework aligns tightly with updated safety guidance and sustainability goals, limiting waste and avoiding hazardous byproduct formation wherever we can. The entire process, from raw material intake to shippable powder, stays traceable and verifiable. Instead of hiding the realities of chemical production, we actively share our improvements with partners and customers who demand not just product, but methods and outcomes they can count on.

    Direct control of every production phase means you don’t have to worry about middleman substitutions, unpredictable lead times, or unexpected formulation changes. Each lot reflects an ongoing learning process guided by customer input, buttressed by our own continuous improvement cycle. This deep integration supports not just current needs, but also new challenges in the years ahead as research pivots, regulations shift, or fresh innovation demands arise.

    Using 2,2'-Bipyridine-4,4'-diyldimethanol from an experienced manufacturer brings more than basic material quality. It’s the outcome of sustained collaboration, technical expertise, and responsiveness born out of working shoulder-to-shoulder with the labs and factories that define global progress in chemicals and materials science. For workhorse ligands that bridge pure research and scalable industrial processes, these details make all the difference.