2,2'-Bipyridine-5,5'-dicarboxylic acid

    • Product Name: 2,2'-Bipyridine-5,5'-dicarboxylic acid
    • Chemical Name (IUPAC): 5,5'-dicarboxy-[2,2'-bipyridine]
    • CAS No.: 30652-11-0
    • Chemical Formula: C12H8N2O4
    • 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

    726732

    Product Name 2,2'-Bipyridine-5,5'-dicarboxylic acid
    Cas Number 4766-35-6
    Molecular Formula C12H8N2O4
    Molecular Weight 244.20 g/mol
    Appearance Off-white to light yellow powder
    Melting Point Greater than 300°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Chemical Structure Contains two pyridine rings joined at the 2-position, each substituted with a carboxylic acid group at the 5-position
    Synonyms 5,5'-Dicarboxy-2,2'-bipyridine
    Smiles C1=CC(=NC=C1C2=NC=CC(=C2)C(=O)O)C(=O)O

    As an accredited 2,2'-Bipyridine-5,5'-dicarboxylic acid 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-5,5'-dicarboxylic acid is packaged in a 5-gram amber glass bottle with a tamper-evident seal.
    Container Loading (20′ FCL) 20′ FCL typically accommodates about 10–12 metric tons of 2,2′-Bipyridine-5,5′-dicarboxylic acid, securely packed in drums or bags.
    Shipping 2,2'-Bipyridine-5,5'-dicarboxylic acid is typically shipped in tightly sealed containers, protected from moisture and light. It is classified as a non-hazardous material for transport, but should be handled with care. Ensure the packaging prevents leaks or spills and complies with applicable shipping regulations for chemicals. Store at room temperature upon arrival.
    Storage 2,2'-Bipyridine-5,5'-dicarboxylic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Follow standard laboratory practices, including appropriate labeling and secure shelving, ensuring access is restricted to trained personnel. Store at room temperature unless otherwise specified by the supplier.
    Shelf Life 2,2'-Bipyridine-5,5'-dicarboxylic acid is stable for at least 2 years when stored in a cool, dry place.
    Application of 2,2'-Bipyridine-5,5'-dicarboxylic acid

    Purity 98%: 2,2'-Bipyridine-5,5'-dicarboxylic acid with purity 98% is used in transition metal complex synthesis, where it ensures high ligand coordination efficiency.

    Melting Point 315°C: 2,2'-Bipyridine-5,5'-dicarboxylic acid with a melting point of 315°C is used in high-temperature catalysis, where it maintains structural integrity during thermal processes.

    Particle Size <10 μm: 2,2'-Bipyridine-5,5'-dicarboxylic acid with particle size less than 10 μm is used in catalyst support materials, where it achieves homogeneous dispersion in reaction media.

    Stability Temperature 200°C: 2,2'-Bipyridine-5,5'-dicarboxylic acid with a stability temperature of 200°C is used in organic semiconductor fabrication, where it provides thermal endurance during device processing.

    Molecular Weight 258.18 g/mol: 2,2'-Bipyridine-5,5'-dicarboxylic acid with molecular weight 258.18 g/mol is used in coordination polymer construction, where it produces predictable and reproducible material architectures.

    Water Solubility 2 mg/mL: 2,2'-Bipyridine-5,5'-dicarboxylic acid with water solubility of 2 mg/mL is used in homogeneous aqueous-phase metal catalysis, where it promotes efficient catalyst dissolution and performance.

    UV Absorption λmax 320 nm: 2,2'-Bipyridine-5,5'-dicarboxylic acid with UV absorption at λmax 320 nm is used in photochemical sensor development, where it enables sensitive detection of metal ions.

    Crystallinity >95%: 2,2'-Bipyridine-5,5'-dicarboxylic acid with crystallinity above 95% is used in MOF (metal-organic framework) synthesis, where it enhances framework order and porosity.

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    Certification & Compliance
    More Introduction

    2,2'-Bipyridine-5,5'-dicarboxylic Acid: Field Notes on Precision Chemistry from the Factory Floor

    Behind the Beaker: Why This Molecule Gets Our Attention

    Every so often, a compound nudges its way to the front lines in a chemical plant. 2,2'-Bipyridine-5,5'-dicarboxylic acid, known in some labs by its structural acronym BPYDC, stands out for a reason. Over the years, we’ve come to appreciate the distinct role this molecule plays in ligand chemistry and advanced material synthesis. With two pyridine rings stitched together by a carbon bond and capped by carboxylic acid groups at the 5 and 5' positions, BPYDC offers real utility where both coordination strength and tunable reactivity are needed.

    On our production line, workers measure each batch of BPYDC from reactor to drum by hand and eye. We know that this solid presents as an off-white powder when it's pure – and we’ve learned to spot the faint gray tinge signaling a batch meant for rerun. We focus on the purity above 99%, confirmed by HPLC and NMR. Some chemists want up-to-the-second GC-MS trace data, especially those building high-purity metal-organic frameworks. We pull random samples from every lot to check for trace iron and other transition metals, since a slip in reagent quality can turn a bright, crystalline sample into a dull, contaminated relic.

    Applications Built on Experience

    BPYDC is not just another bipyridine. This molecule grabs the attention of synthesis groups aiming to control metal-ligand interactions with extra precision. Its dual carboxylic functionality sets it apart from simpler bipyridine analogs. When ligating to metals, these carboxylic acid arms reach out and form robust chelates, helping to engineer coordination polymers, MOFs, and supramolecular assemblies with defined geometry. At our facility, we’ve seen research shifts: years ago, BPYDC mostly left our warehouse for academic groups mapping out crystal structures. Lately, orders trace back to teams ramping up pilot lines in battery materials and gas adsorption technologies.

    Some applications demand tough performance; not just a theoretical ligand, but a reproducible reagent. Every winter, clients race for crystalline BPYDC samples that insert predictably into newly designed frameworks. Some compete for a small window of funding with tight timelines, and quality issues cost them more than just materials – they cost time, reputations, and grant cycles. We field direct phone calls every production week, not from intermediary traders, but from postdocs at the bench who’ve spent three days re-running syntheses because an off-brand source introduced unwanted impurities. We’ve traced back issues to unreacted starting materials, clipped bipyridine rings, or subtle isomer mixtures. From every misstep, we adjust our own process, asking the plant shift leader to stretch out the last hydrogenation step, or to swap in a more robust purification run before letting anything near the packing room.

    Where BPYDC Shines: Material Synthesis and Beyond

    Across the last decade, this compound’s main calling card lies in the world of MOFs. The push for cleaner energy and smarter molecular separations has driven new demands for frameworks that show more reliable selectivity, higher uptake capacity, and improved cycling stability. BPYDC’s two carboxylic acids offer multiple binding sites with metals like zinc, copper, or lanthanides – the keys to locking down the desired crystal lattice.

    Our manufacturing process evolved as these requirements sharpened. Early on, we realized that just churning out the minimum purity and calling it ‘reagent grade’ opened the door to variable results downstream. So, we keep tight controls on residual solvents and potential side products, since even a small contaminant can sabotage the slow, intricate growth of MOF crystals. Analytical teams at our plant carry out solid-state NMR, FTIR, and elemental analysis on every batch before it ships. We hear from advanced material labs that even slight deviations impact pore geometry or thermal stability.

    Similar chemistry undergirds progress in electrocatalysis. BPYDC complexes offer symmetry and rigidity useful for anchoring catalytically active metals. During one of our rare supplier visits, a customer in Europe shared an application using our BPYDC as the backbone for coordination cages, where electron transfer and catalytic turnover rates matter. They depend on the predictable carboxy-pyridine units to template a single-site metal active center, making sure each cycle of catalysis runs without friction or defect. Their confidence in the raw material flows from batch-to-batch reproducibility – not just a line in a spec sheet, but a hard-won product from process chemists who fix problems before they leave the building.

    What Sets It Apart from Other Bipyridines

    Plenty of fine bipyridine derivatives crowd the market, each bringing unique strengths. But BPYDC’s defining trait comes down to those two carboxyl groups at the 5 and 5' positions. Compare this with standard 2,2'-bipyridine or its 4,4'-dicarboxylic analogs, and you notice a difference in how these groups direct chelation and framework propagation. Some compounds like 4,4'-dicarboxy-2,2'-bipyridine align the acid groups linearly across from each other; BPYDC bends them nearby, opening up other geometries, which in turn influence pore size and flexibility in finished MOFs.

    From our manufacturing side, the challenge lies in steering isomer formation and avoiding incomplete oxidation. We learned this lesson years ago when shipments received at a customer site failed to yield the desired MOF phase, traced back to a blend of 5,5' and 4,4' isomers. Since then, stricter chromatographic and crystallization controls allow us to deliver batches with isomeric purity higher than industry norms. The synthesis routes for BPYDC are less forgiving than some related derivatives; it demands more careful choice of starting materials and aches for a balance between oxidizing strength and ring stability.

    The difference becomes clear once these molecules enter practical syntheses. Chemists using unsubstituted bipyridine often try to engineer new reactivity by swapping in functional group handles post-synthetically. By offering BPYDC, we let customers start from a template already bearing well-positioned carboxylic acids, leading to less downstream modification, greater site-specificity, and more predictable performance. This matters in industries scaling up solid-state devices or targeting pharmaceutical intermediates where reproducibility and process streamlining shave weeks off development time.

    Scaling from Lab to Plant: Lessons in Reproducibility

    In real terms, bringing BPYDC to scale means more than increasing volume – it requires understanding every reaction parameter’s downstream impact. We’ve seen semi-scale reactors build up side reactions unseen at bench scale, and even seemingly minor temperature fluctuations swing the final purity by several tenths of a percent. Our control engineers now set stricter cooling profiles for the oxidation phase and demand real-time analytics fed by inline probes. The result is not just a number on a COA, but a measurable uptick in crystal yields and lower batch-to-batch variance reported from those developing next-generation crystalline materials.

    The benefit reaches into more industrial domains: BPYDC-based linkers pop up in adsorption columns for separating CO2 from flue gas, or in sensors where stable, functionalized ligands deliver predictable signal strength. The cost of failure in these niches isn’t just academic – it threatens the reliability of entire pilot processes struggling to reach commercialization.

    We pay attention to storage and transit. Improper humidity control invites degradation over time, producing tarry residues that never show up on shipping manifests but show up fast in the lab as irreproducible reactions. By tracking humidity and packaging every kilo under inert atmosphere, we minimize that risk before a shipment rides out the door. Packaging teams double-seal sensitive consignments headed to more humid regions, and we’ve set up relationships with specialty couriers who get the urgency of cold-chain and dry-ship logistics. Years ago, before these steps, we saw customer complaints crop up about decomposition due to week-long customs delays. Each bit of learning shaped how we box, label, and monitor batches today.

    Supporting Chemists and Engineers: Field Feedback Drives Quality

    Feedback from those at the bench matters. We run periodic surveys and reach out to researchers using our BPYDC in new catalytic or separation applications. Many mention how their yield and reproducibility increase with reliably high-purity samples; some even credit successful funding applications to trouble-free pilot runs built on solid material. More practically, several groups found that with our BPYDC batches, fewer purification steps were needed, cutting down on solvent use and saving both effort and environmental impact.

    Environmental performance weighs heavily on many customers' minds as green chemistry picks up speed. Our synthetic process limits the use of chlorinated solvents and recycles aqueous washes, shrinking our overall waste load. Regular process audits help shave emissions and solvent residues from historical levels. Most of the environmental improvements trace back to field complaints – once, after a partner flagged solvent odors in warehousing, we reengineered the drying step. Now, offgassing falls well within safe, measurable limits, benefiting both the end-user and our plant teams.

    Roadblocks and Workarounds: What’s Hard, What’s Possible

    Every production season uncovers new wrinkles. BPYDC’s reactivity and sensitivity to process variables make it more challenging compared to some easier-to-handle ligands. Earlier bottlenecks stemmed from scaling up the critical oxidation phase where pyridine rings acquire the right configuration. We saw that slight changes in precursor quality led to hard-to-remove side products.

    Instead of writing off failed reactions as inevitable loss, our plant teams experimented with in-process sampling and reaction monitoring. By tweaking reagent addition rates and fine-tuning crystallization times, we reduced the frequency of failed batches. Each failed barrel, though expensive, forced our process chemists to think more like bench researchers, not just plant operators. The leap from gram-scale glassware to ton-scale reactors brought with it new risks—in particular, occluded solvents in product drums and slow, creeping color changes that show up only after a few weeks’ storage.

    Over the years, we improved process robustness by documenting every successful workaround and feeding it into our digital batching systems. Software now flags drift in key metrics, prompting closer scrutiny before problems compound. Instead of just relying on a fixed recipe, we adapt in real time, aiming to hit critical quality targets every time.

    Looking Forward: Trends Shaping the Future Use of BPYDC

    BPYDC’s star continues to rise as more teams chase next-level materials. The global push for sustainable energy storage, smart sensing, and selective molecular separations means material scientists prize compounds like BPYDC for the architectural flexibility they grant. Research leaders now pursue MOFs built for hydrogen storage, CO2 capture, and rare-earth separations – all demanding predictable, high-functionality linkers.

    Upcoming regulatory demands focus attention on purity and trace contaminant control. Advanced battery and electronic manufacturers scrutinize every upstream input for metals like iron, copper, or nickel that might drift in during precursor handling. We adapted by introducing higher-level trace metals analysis, drawing on ICP-MS data and sharing it directly with development partners so their own processes stay in regulatory bounds.

    There’s also growing attention on lifecycle management. We field more questions about end-of-life material streams and reprocessing spent MOFs for components. Our teams work alongside R&D partners exploring scalable depolymerization or ligand recovery approaches, looking to make chemical usage less of a linear journey and more a closed loop. In several pilot projects, we supply tailored BPYDC samples designed for enhanced re-solubility, easing the recovery of spent ligands from solid-state matrices.

    Conclusions Scrawled on the Loading Dock

    Years of manufacturing BPYDC taught us that supplying a high-touch, function-driven compound is never rote. Each batch is the sum of many lessons – missteps in handling, process tweaks, real-world feedback from frustrated or delighted chemists. The push to meet new analytical targets and the race to deliver reproducible, field-proven batches shape every improvement back in our facility. As the uses of BPYDC continue to evolve – from core ligand chemistry to specialized roles in energy, catalysis, and sensing – the importance of quality, reliability, and deep process knowledge only grows. Our plant floor won’t see the end products, but we live every day with the cause-and-effect that those end products depend on: chemistry that works, scales, and leads to something better.