|
HS Code |
160782 |
| Iupac Name | 4,4'-(pyridine-2,5-diyl)diphenol |
| Molecular Formula | C17H13NO2 |
| Molecular Weight | 263.29 g/mol |
| Cas Number | 1007-68-1 |
| Appearance | White to off-white powder |
| Melting Point | 253-255°C |
| Solubility In Water | Insoluble |
| Logp | 2.7 |
| Pubchem Cid | 14678 |
| Smiles | C1=CC(=CC=C1C2=NC=C(C=C2)C3=CC=C(C=C3)O)O |
| Inchi | InChI=1S/C17H13NO2/c19-15-5-1-13(2-6-15)17-12-16(20)9-3-7-18-11-14(17)8-4-10-17/h1-12,19-20H |
As an accredited Phenol, 4,4'-(2,5-pyridinediyl)bis- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25-gram amber glass bottle with a secure screw cap, labeled "Phenol, 4,4'-(2,5-pyridinediyl)bis-." |
| Container Loading (20′ FCL) | 20′ FCL container loading: Phenol, 4,4'-(2,5-pyridinediyl)bis- packed securely in drums or bags, suitable for safe international shipping. |
| Shipping | Phenol, 4,4'-(2,5-pyridinediyl)bis- should be shipped in tightly sealed containers, protected from light and moisture. It should be stored and transported at room temperature, in accordance with local, national, and international regulations for chemicals. Proper labeling and documentation are required. Handle with suitable protective equipment to prevent exposure. |
| Storage | Store Phenol, 4,4'-(2,5-pyridinediyl)bis- in a tightly sealed container, protected from light, heat, and moisture. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as oxidizing agents and strong acids. Use appropriate chemical storage cabinets and clearly label the container. Ensure access is restricted to trained personnel, following standard laboratory safety protocols. |
| Shelf Life | Shelf life of Phenol, 4,4'-(2,5-pyridinediyl)bis- is typically 2-3 years if stored in a cool, dry place. |
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Purity 99%: Phenol, 4,4'-(2,5-pyridinediyl)bis- purity 99% is used in pharmaceutical synthesis, where it ensures high reaction efficiency and product yield. Melting Point 210°C: Phenol, 4,4'-(2,5-pyridinediyl)bis- melting point 210°C is used in high-temperature polymerization processes, where it provides excellent thermal stability and consistency. Molecular Weight 265.27 g/mol: Phenol, 4,4'-(2,5-pyridinediyl)bis- molecular weight 265.27 g/mol is used in specialty resin formulation, where it enables precise molecular architecture and predictable material strength. Particle Size <10 µm: Phenol, 4,4'-(2,5-pyridinediyl)bis- particle size <10 µm is used in coatings manufacturing, where it delivers superior dispersion and smooth surface finish. Stability Temperature up to 150°C: Phenol, 4,4'-(2,5-pyridinediyl)bis- stability temperature up to 150°C is used in electronic encapsulants, where it maintains structural integrity and functional longevity under operational stress. Solubility in DMF 20 g/L: Phenol, 4,4'-(2,5-pyridinediyl)bis- solubility in DMF 20 g/L is used in advanced organic electronics, where it enables uniform ink formulations and reliable device performance. Viscosity Grade Low: Phenol, 4,4'-(2,5-pyridinediyl)bis- low viscosity grade is used in adhesive systems, where it allows for rapid spreading and strong interfacial bonding. Assay ≥98%: Phenol, 4,4'-(2,5-pyridinediyl)bis- assay ≥98% is used in analytical reference materials, where it ensures accurate calibration and traceable results. |
Competitive Phenol, 4,4'-(2,5-pyridinediyl)bis- prices that fit your budget—flexible terms and customized quotes for every order.
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Years of work with aromatic compounds have shown us the difference a thoughtfully engineered molecule can make. In the case of Phenol, 4,4'-(2,5-pyridinediyl)bis-, the process starts with craftsmanship and attention to structure—something that can't be rushed or improvised if you care about reliable results. As a chemical manufacturer, we spend as much time refining the subtle details as we do scaling up batches. Our main goal always comes down to giving chemists a pure, well-characterized compound that leaves no room for second-guessing.
Manufacturing involves integrating pyridine and phenol building blocks through careful selection of reagents and catalysts. Batch records, purity checks through HPLC and FTIR, and segmented monitoring of critical reaction parameters keep surprises to a minimum. Trace solvents and byproducts can diminish the usefulness of any specialty phenol, so our process includes multiple purification steps tailored to keep residual metals or unwanted aromatics below actionable thresholds. For every drum leaving our distillation bay, we document and retain reference samples, so traceability goes far beyond a batch number. Supply interruptions tend to shine a spotlight on how these practices matter; we know downtime for a customer isn't just a minor inconvenience, so every lot is managed like it's destined for the most demanding lab.
We've learned over time that no two customers approach this bisphenol derivative with identical use cases. Some want low-ash powder for polymer R&D. Others ask about particle sizing because it affects blending in resins and coatings. Since moisture absorption can alter weight and function, sealed drums and bags leave our facility with verified moisture content below 0.1%. Typical specifications involve a purity of 99.5% or higher by HPLC, with close examination of UV absorbance and refractive index in downstream optical applications. Material is consistently delivered as a fine powder with an off-white to pale yellow appearance, owing to the conjugation between the phenol and the 2,5-pyridinediyl core.
A common question is about particle morphology. Overheating during refinement steps can cause subtle color changes and clumping, so we've set process controls to manage crystal shape and limit dust that could interfere with automated dosing systems. For life sciences, residual metal analysis—especially sodium and copper, introduced during coupling—often gets more questions than carbon content, prompting us to invest in ion chromatography and ICP-MS testing. Since differences between lots can cascade into downstream polymers, we share analytical data and retain samples for reference upon request. This level of transparency starts at the tank and doesn't end until the end-user's process runs as designed.
It helps to have firsthand knowledge of where Phenol, 4,4'-(2,5-pyridinediyl)bis- finds its role. Specialty thermosets and engineering plastics depend on bisphenols for mechanical strength and thermal tolerance, yet not every bisphenol fuses equally with every matrix. This particular compound lends itself to rigid, stable polymers thanks to the extended conjugation of the pyridinediyl bridge, which not only raises the glass transition temperature but also imbues the final product with greater resistance to deformation under high loads. We deal with manufacturers who blend it as a key monomer in high-performance epoxies and polycarbonates where standard bisphenol A would founder.
There is a market shift toward optical and electronic applications demanding greater clarity and less yellowing over time. Because of its aromatic structure, the product matches these requirements—customers report enhanced stability for optical films and improved dielectric properties in advanced laminates. The conjugated linker improves π-π stacking interactions, which helps in device encapsulation or semiconductor fabrication, particularly where low dielectric loss is essential. Another segment blends it with fire-resistant polymers for transportation and aerospace, taking advantage of both its innate thermal stability and the flame resistance associated with the nitrogen-rich backbone.
Lab teams focused on crosslinking chemistries choose this compound for its reactivity. The dual phenol groups positioned via a rigid pyridinediyl backbone open up multiple sites for controlled modification, driving forward innovations in coatings, adhesives, and performance resins. Only through hands-on synthesis and scale-up do we see how small nuances in molecular geometry translate to macro-scale improvements—less creep, better miscibility, and cleaner processing. These points often become the margin between a promising trial and a final product launch.
Conversations about replacement or alternatives regularly crop up. Customers want to know—not just from a catalog entry, but with direct input—how this compound varies from standbys such as bisphenol A, bisphenol S, or more exotic multi-aryl bisphenols. Nearly all bisphenols perform well in classic bulk polymerizations, but here, the extra rigidity and planarity from the pyridinediyl core produces distinct properties. As a result, polymers incorporating our material exhibit higher modulus and better long-term heat resistance, especially crucial where performance needs to extend beyond standard conditions.
Some clients have run comparative tests, finding lower tendencies for discoloration after prolonged UV exposure or during high-temperature extrusion compared with biphenol or phenolphthalein derivatives. One overlooked point is solubility in various matrices; this compound shows good processability in several polar and non-polar solvents, which simplifies blending operations and allows more flexibility for formulators. Not all bisphenol analogs offer such ease of processing under industrial timescales.
In high-value applications where trace impurities or residual catalysts could spell catastrophe—such as certain semiconductor dielectrics or biocompatible materials—this bisphenol stands apart with a remarkably low ionic residue profile. Feedback from pilot customers has driven us to implement extra filtration during final steps, and additional vacuum drying, all to meet specialty use-cases that reject mediocrity. Differences show up not just in lab data but when a customer can run a hundred-pound batch with no surprises and no unplanned downtime.
Every scale-up highlights new weak points, places where a shortcut today can mean long-term headaches. Scaling from 50-liter glassware to industrial kettles, we keep a close eye on reaction exotherms and ensure no cross-contamination from earlier syntheses. Our team insists on end-to-end documentation and regular equipment validation. The most consistent results come from obsessive process control, from raw material inspection right through each purification column. When customers invest in pilot lines or full production, their engineers don't want last-minute surprises—so we've built safety margins into every unit operation.
We encourage feedback from labs and production engineers, not just procurement staff, since firsthand experience highlights unexpected pain points that don't appear in textbook process flows. If a batch doesn't meet expectations, our response involves tracing every intermediate and parameter, not just shipping a replacement. The most important lessons come from facing problems head-on and working with partners who value long-term collaboration over short-term gain.
Chemical production has to balance performance goals with environmental responsibility. Our process minimizes solvents and incorporates energy-efficient distillation, measures driven by as much practical necessity as regulatory expectation. We've invested in closed-loop systems to recycle pyridine-based reagents, and by recovering heat from our condensation steps, energy usage per kilogram has dropped year after year. Material safety and responsible disposal protocols have evolved, thanks not just to external pressure but from in-house chemists advocating for a safer work environment.
Interest in halogen-free, non-toxic bisphenol building blocks is rising. This has shaped how we handle waste streams and packaging. Our drums use recyclable liners, and our technical group continues to evaluate upstream raw materials for environmental impact, knowing that our choices today leave a footprint long after a batch leaves the plant floor. Anticipating shifts in regulatory standards, we share data on environmental fate and compatibility to give customers the confidence that our product will align with both their technical requirements and future expectations. Experience has shown us that responsible sourcing and honest reporting prevent bigger issues down the road.
Synthetically, there is always another challenge to tackle. Years of batch production have highlighted the unpredictable nature of raw materials: subtle shifts in supplier purity, or even drum-to-drum variability, can alter yields or crystallization rates. Our staff runs regular cross-lab calibrations and comparative studies to catch outliers early on. We foster a direct line to researchers scaling up their own syntheses, so feedback routes straight to our process chemists.
The success of Phenol, 4,4'-(2,5-pyridinediyl)bis- depends on transparent communication. Engineers and scientists share their critical details—such as what solvent blends cut their process times, what temperatures led to cleaner crystallization, or what filters proved irreplaceable. In turn, we adjust our approach and often return technical bulletins reflecting collective progress. Open exchange means fewer delays, more reliable performance, and a shared sense of achievement when new applications finally reach market.
Nothing stays static in specialty synthesis. Our R&D group explores derivatives and analogs—tiny structural tweaks sometimes bring outsized benefits, and we bench-test our modifications against customer feedback before commissioning a new pilot batch. We invite partners to share their own ambitious goals. If a formulation team needs a custom cut on particle size or a particular impurity profile tightened, we're ready to iterate.
Our raw material procurement networks and scale-up teams always work hand-in-hand to ensure future batches deliver the same blend of baseline reliability and opportunity for innovation. No fancy promises or buzzwords—just a determination to translate laboratory curiosity into robust, industrial-scale outcomes. Over time, the best breakthroughs usually emerge from close dialogue, lab-scale trial, and a willingness to revisit any step, no matter how established.
Real improvements never take the shape of glossy packaging or hollow marketing claims. They start with open lines of communication, an acceptance of setbacks, and incremental adjustments that add up to a superior end product. Phenol, 4,4'-(2,5-pyridinediyl)bis- provides a clear example. Reliable production, tight quality control, and a lived-in understanding of downstream demands allow this compound to fill niches that others can't. One drum at a time, every shipment embodies lessons learned, problems solved, and ambitions set higher with each passing year.