|
HS Code |
404908 |
| Product Name | 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine |
| Cas Number | 16804-50-7 |
| Molecular Formula | C12H12N2O2 |
| Molecular Weight | 216.24 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 146-151 °C |
| Solubility | Soluble in polar organic solvents such as DMSO and methanol |
| Purity | Typically ≥ 98% |
| Structure Type | Bipyridine derivative with –CH2OH groups at 4,4' positions |
| Synonyms | 4,4'-Dimethylol-2,2'-bipyridine |
| Smiles | OCc1cc(nc(c1)-c2ncccc2)CO |
| Inchi | InChI=1S/C12H12N2O2/c15-7-9-1-5-13-11(3-9)12-4-2-10(6-8-16)14-12/h1-6,13-16H,7-8H2 |
As an accredited 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed with a screw cap, clear labeling lists chemical name, formula, hazards, and manufacturer. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Holds approximately 6–8 metric tons of 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine, packed in 25 kg fiber drums on pallets. |
| Shipping | 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine is shipped in a tightly sealed container, protected from moisture and light. The package is cushioned to prevent physical damage and labeled per chemical safety regulations. It is transported under ambient conditions, with documentation to ensure compliance with all relevant shipping, handling, and hazard guidelines. |
| Storage | 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine should be stored in a tightly closed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Store away from strong oxidizing agents and bases. Recommended storage temperature is 2-8°C (refrigerator). Ensure good laboratory practices are followed to avoid contamination and degradation of the compound. |
| Shelf Life | Shelf life of 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine is typically 2–3 years when stored cool, dry, and protected from light. |
|
Purity 98%: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with purity 98% is used in coordination polymer synthesis, where it enhances ligand uniformity and metal-binding efficiency. Melting Point 170°C: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with a melting point of 170°C is used in high-temperature catalytic applications, where it ensures structural stability under reaction conditions. Molecular Weight 214.22 g/mol: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with molecular weight 214.22 g/mol is used in the design of organic light-emitting diodes (OLEDs), where it optimizes electron transport properties. Water Solubility 10 g/L: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with water solubility 10 g/L is used in aqueous sensor fabrication, where it promotes homogeneous dispersion and consistent sensor response. Stability Temperature 120°C: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with stability temperature 120°C is used in photochemical experiments, where it maintains ligand integrity and reliable reproducibility. Viscosity 1.2 cP (in ethanol): 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with viscosity 1.2 cP (in ethanol) is used in spin-coating processes for thin-film preparation, where it ensures uniform layer deposition. Particle Size <50 µm: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with particle size <50 µm is used in composite materials manufacturing, where it allows for enhanced interfacial interaction and dispersion. UV Absorption Max 315 nm: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with UV absorption max 315 nm is used in photonic device construction, where it enables precise optical tuning. Assay 99%: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with assay 99% is used in pharmaceutical intermediate synthesis, where it guarantees batch-to-batch consistency and product purity. pH Stability Range 4–9: 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine with pH stability range 4–9 is used in buffer solution formulation, where it preserves chemical functionality across varying pH environments. |
Competitive 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Producing 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine takes more than a recipe; it’s a blend of chemistry expertise, robust quality controls, and deep knowledge of what research and industry expect from specialty ligands. In our own facilities, we navigate each synthesis batch with a hands-on understanding of how subtle shifts in conditions, such as pH or temperature, play into the purity and consistency of the bipyridine core. Our standard model most often comes as a white to off-white crystalline solid, with batch-dependent granularity, and is packaged under dry, inert conditions to maintain integrity from synthesis to customer use. Purity levels by HPLC routinely cross 99.5%, as confirmed by NMR and elemental analysis.
We pay particular attention to controlling moisture and trace metal contamination during synthesis. Moisture isn’t just an inconvenience for organometallic work; trace water can drive unwanted hydrolysis, undermining the performance of 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine in coordination chemistry. Our strict anhydrous handling minimizes this risk, and we perform Karl Fischer titrations batch by batch to keep water levels negligible.
Researchers and industry chemists use this molecule for its ability to efficiently chelate metals through its bipyridine backbone, while offering the unique reactivity of its dual hydroxymethyl arms. This dual functionality gives synthetic flexibility not found in the parent 2,2'-bipyridine or more basic derivatives. Our product supports routes toward dendrimeric frameworks, single-site catalyst environments, and highly tailored supramolecular complexes.
Polymer functionalization often calls for ligands that work as anchoring handles and as active chelators. The hydroxymethyl substituents transform simple complexation into site-specific reactivity. Our experience working with specialty polymer manufacturers and university labs reveals that this product performs in two main ways—either through direct attachment to polymer chains via the hydroxymethyl groups, or by further derivatization, allowing for customized cross-linking strategies or click chemistry reactions.
In practice, what sets our version apart is its consistent solubility profile and low batch-to-batch variation, crucial for researchers optimizing solvent systems. The compound dissolves well in many polar aprotic solvents, such as DMF, DMSO, and acetonitrile—making it convenient when the application calls for homogeneous catalysis, electrochemical analysis, or post-synthetic modification for advanced materials.
Recent developments in photonic materials and renewable energy have raised the bar for ligand quality and purity. Coordination chemists rely on the precision of bidentate ligands like 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine for tuning metal ion properties in light-harvesting, redox, and catalytic applications. Studies frequently cite the ability of the hydroxymethyl groups to serve as anchor points for post-coordination modifications, or for tuning solubility and electronic properties of resulting complexes.
In our own collaborations and custom synthesis projects for academic and industrial research labs, we stock 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine in packaging sizes ranging from 1 g for bench research to multi-kilogram lots supporting pilot-scale innovation. This scale-up support didn’t arrive by accident. We partnered with research teams who needed to bridge the gap between milligram-scale curiosity and real, process-ready production. Our technical staff worked directly with customers who encountered batch variability when sourcing from resellers or distributors; those issues faded once they shifted to our on-site, single-source manufacturing, where we control everything from the first feedstock to final analysis and packaging.
Beyond classic ligand applications, we see this compound emerging in functionalized materials, including sensing devices and optoelectronic films. Downstream users have leveraged its functional group reactivity to introduce light- or redox-active units, extending it beyond the familiar territory of metal complexation.
Compounds like 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine aren’t commodities you can treat with a “just-in-time” supply mentality. Variations in synthetic routes or raw material sources alter the impurity profile and jeopardize reproducibility in downstream R&D. We saw this years ago, when several customers shared data showing unexpected NMR peaks and color changes in their ligand solutions, despite claiming 99% purity from brokered materials. Our own audits traced problems back to upstream intermediates of uncontrolled origin, not the final crystallization. After moving to our vertically integrated approach, we eliminated those mystery impurities—test results have stayed consistent ever since.
We document and archive each batch. Every vial comes with a lot-specific Certificate of Analysis and access to full, long-term archived analytical data. Many industry labs have mandatory traceability requirements for regulatory compliance. With each production lot, our chemists maintain control over batch records, raw material certification, and a trail of internal quality checks. That means no ambiguity on where your chemistry begins.
A number of bipyridine derivatives exist for chelation purposes. Unsubstituted 2,2'-bipyridine works well for many coordination complexes, but lacks the direct reactivity of the hydroxymethyl side chains. This distinction matters for researchers needing to bioconjugate ligands, or secure attachment points for devices and solid supports. Substituted bipyridines with methyl, amino, or carboxy groups serve in specific contexts, but the hydroxymethyl’s dual role—reactivity and mild hydrophilicity—delivers greater versatility.
From a process perspective, we maintain high standards not just for the ligand core, but for every step that precedes it. Our own synthetic pathway minimizes formation of positional isomers or over-oxidized byproducts seen in less controlled processes. Uniquely, we developed an extra purification column in response to feedback from a customer’s difficulty with fluorescent impurities affecting photophysical measurements. This led to a measurable drop in background signals and opened up new partnerships in fluorescence sensor development.
Batch-to-batch reproducibility doesn’t just reflect in paper specs. Researchers working with microgram-scale syntheses up to industrial kilogram-scale processes need reliability. Our manufacturing team standardizes endpoint analysis with advanced techniques such as qNMR, alongside classic melting point and TLC checks. We use these controls so customers don’t wrestle with unexplained anomalies in their crystallization or catalysis trials.
We learned early that even careful storage makes a difference. Our production line addresses two main degradation threats: hydrolysis and oxidative breakdown. To keep lots stable, we seal everything under nitrogen in amber glass bottles for smaller sizes, and robust high-barrier plastic for kilo-scale orders. Each refill signals a review of shelf stability and support for customers who call about handling in glovebox environments. Some labs need specific dryness or inert packaging not offered by bulk resellers; our team offers technical advice and, when feasible, custom-fitted container sizes and inert packing to meet demanding protocols.
Many lab teams don’t have on-site access to gloveboxes or Schlenk lines. For those users, we provide detailed guidance for ambient-air handling as well as compatible solvents and storage practices. Through years of assisting customer troubleshooting, our chemists have seen the pitfalls of improper thawing, repeated exposure to air, and cross-contamination during transfer. Our direct support line connects users with chemists who handle these scenarios every week, not just sales representatives.
Environmental, social, and governance requirements continue to reshape specialty chemical manufacturing. We respond by mapping raw material provenance and adopting greener chemistry protocols where possible—such as using less hazardous alcohol feedstocks or recycling solvents at key stages. Our analytical department checks for heavy metal content, and results are readily available to support downstream compliance in electronics or biomedical products.
Many research institutions and OEMs demand not only high purity but also a documented supply chain. Our adoption of ISO-based manufacturing standards satisfies those external audits and ensures that any transition to GMP routes for larger-scale applications comes with detailed records and process transparency.
Beyond standard models, we work with customers developing specialized modifications of 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine. In some cases, downstream chemistry favors esterification or conversion to activated carbonate intermediates, and our process engineers are able to carry out and validate these steps at manufacturing scale, based on customer method transfer or co-development. This option eliminates the typical challenges faced when scaling up from bench to process quantities.
We’ve supported custom ligand arrays for high-throughput screening, functionalized bipyridines for immobilized catalyst platforms, and solution-stable derivatives for electrochemical flow systems. In each project, we track metrics like yield loss, purification waste, and cost-of-goods—practices that only a direct manufacturer with analytical and process engineering capacity can sustain.
Direct feedback drives the evolution of our 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine offering. Academic partners share application data, from crystallography to electrochemistry, giving insight into how trace residues or batch subtleties influence real results. Industrial customers pilot new catalyst systems, reporting back on stability and conversion yields under authentic process conditions.
We responded to user demand for routine qNMR analysis to closely track structural integrity and detect low-level byproducts. The degree of technical flexibility and collaboration available only through in-house manufacturing creates a two-way relationship. Process changes or analyst suggestions seldom stall in corporate bureaucracy; our compact production organization enables rapid response and ongoing improvement.
All analytical data, including NMR, MS, HPLC chromatograms, and drying logs, accompany shipments in digital and print format. Long-term customers gain access to lot histories, showing full supply chain data and a log of all process adjustments since initial qualification. External labs have used our detailed records to support regulatory submissions and method validation.
By manufacturing 4,4'-Bis(hydroxymethyl)-2,2'-bipyridine directly, we maintain genuine oversight of product quality, reliability, and usability in advanced research and manufacturing environments. Results in catalysis, photochemistry, or complex materials innovation start with the ingredients; our role is to make sure those foundations perform as intended, batch after batch.