|
HS Code |
490843 |
| Iupac Name | pyridine-2,6-diyldimethanol |
| Molecular Formula | C7H9NO2 |
| Molar Mass | 139.15 g/mol |
| Cas Number | 1193-79-9 |
| Appearance | white to off-white crystalline powder |
| Melting Point | 134-136°C |
| Solubility In Water | Moderately soluble |
| Density | 1.24 g/cm3 (approximate) |
| Structure | Pyridine ring substituted at positions 2 and 6 with hydroxymethyl groups |
| Smiles | C1=CC(=NC(=C1)CO)CO |
| Inchi | InChI=1S/C7H9NO2/c9-3-6-1-2-7(4-10)8-5-6/h1-2,5,9-10H,3-4H2 |
| Synonyms | 2,6-Bis(hydroxymethyl)pyridine |
| Logp | -0.02 (estimated) |
As an accredited pyridine-2,6-diyldimethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of pyridine-2,6-diyldimethanol is provided in a sealed amber glass bottle with a tamper-evident screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine-2,6-diyldimethanol typically involves 10-12 metric tons, securely packed in drums or IBCs. |
| Shipping | Pyridine-2,6-diyldimethanol should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must comply with local and international regulations, typically as a non-hazardous or low-hazard chemical. Standard packaging involves robust bottles cushioned against breakage, with clear labeling and documentation for safe handling, transport, and storage conditions. |
| Storage | Pyridine-2,6-diyldimethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Use proper chemical storage cabinets, and label all containers clearly. Ensure safety showers and eyewash stations are accessible in the storage area. |
| Shelf Life | Pyridine-2,6-diyldimethanol typically has a shelf life of 2–3 years when stored in a cool, dry, and airtight container. |
|
Purity 99%: Pyridine-2,6-diyldimethanol with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side product formation. Molecular weight 139.15 g/mol: Pyridine-2,6-diyldimethanol with molecular weight 139.15 g/mol is used in heterocyclic compound manufacturing, where precise molecular weight enables accurate reagent dosing. Melting point 128°C: Pyridine-2,6-diyldimethanol with melting point 128°C is used in organic synthesis processes, where thermal stability facilitates controlled reaction temperatures. Water solubility 10 g/L: Pyridine-2,6-diyldimethanol with water solubility 10 g/L is used in aqueous polymer formulations, where good solubility supports homogeneous mixing. Stability temperature up to 150°C: Pyridine-2,6-diyldimethanol with stability temperature up to 150°C is used in high-temperature resin modification, where thermal resistance allows persistent performance under process conditions. Particle size <75 µm: Pyridine-2,6-diyldimethanol with particle size below 75 µm is used in fine chemical production, where small particle size enhances reaction kinetics. Viscosity 25 mPa·s (at 25°C): Pyridine-2,6-diyldimethanol with viscosity 25 mPa·s at 25°C is used in liquid formulation blending, where suitable viscosity improves processability and uniform dispersion. |
Competitive pyridine-2,6-diyldimethanol 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@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Stepping into any lab, you quickly realize that chemical building blocks shape industries far beyond the beakers. Pyridine-2,6-diyldimethanol stands out for its ability to connect molecular complexity with day-to-day utility. This compound, part of the pyridine family, features two alcohol groups ringing the 2 and 6 positions on its aromatic core. It sounds technical, but spend any time synthesizing specialty polymers or crafting pharmaceutical intermediates, and this structure’s usefulness shows up fast. The dual alcohol groups open up pathways that straight-chain diols or simpler pyridines just don’t offer. Whenever I talk with colleagues in materials chemistry, they point out that molecules like this didn’t get enough attention just ten years ago. Now formulas for coatings, adhesives, and even some medical agents often rely on such multi-functional compounds.
It helps to take a closer look at what makes pyridine-2,6-diyldimethanol unique. In a market crowded with glycols, simple diols, and pyridine derivatives with single modifications, this compound pulls its weight by providing a well-balanced reactivity. The pyridine ring’s nitrogen atom engages in both hydrogen bonding and metal coordination, while each alcohol group lends itself to forming esters, ethers, or even moving further to produce active pharmaceutical ingredients (APIs). Compare it to 2-methylpyridine or plain ethylene glycol—which work fine for basic formulations—pyridine-2,6-diyldimethanol delivers both aromatic stability and the flexibility of branching chemistries. Its molecular structure steers syntheses towards more targeted end-products, whether that’s a step in crafting a new drug or prepping a specialty resin.
In the chemical world, even a minor impurity throws a wrench into the gears. A lesson I learned running pilot batches: purity isn’t just a technical specification, it turns into real-world differences downstream. High-grade pyridine-2,6-diyldimethanol typically appears as a white to slightly off-white crystalline powder, reflecting careful synthesis and purification. With a melting point that supports manageable storage, and robust solubility in solvents like ethanol and DMSO, users find it more adaptable in both research labs and production environments than some lower-grade, mixed-content alternatives. Custom projects—be it crafting UV-curable polymers, engineering new photoinitiators, or developing antimicrobial agents—depend on this predictability.
Running side-by-side comparisons, I’ve found that switching from simple diols to pyridine-2,6-diyldimethanol can trim reaction steps and reduce side-reactions that waste time and materials. Anyone scaling processes appreciates time saved and less cleaning after fouled reactions. Talking to folks at specialty manufacturers, purity matters even more if the product enters regulated industries, like pharmaceuticals or medical devices. Analytical reports back this up: high-performance liquid chromatography (HPLC) and NMR analyses consistently show tighter quality control with pyridine-2,6-diyldimethanol sourced from established suppliers.
Pyridine-2,6-diyldimethanol lands right at the intersection of versatility and specificity. In pharmaceuticals, chemists value its ability to open new synthetic routes, especially for drugs that demand both aromatic stability and modifiable side chains. Its two alcohol groups can each be protected or activated in sequence, revealing or hiding reactivity as needed for complex, step-wise syntheses.
In my own experience with medicinal chemistry workflows, swapping a linear diol for pyridine-2,6-diyldimethanol paves the way for etherification reactions that give cleaner, more selective products. It helps control regioselectivity because the pyridine ring’s electronic structure influences reactivity at each alcohol site. In polymer chemistry, the molecule works well as a cross-linker, building up three-dimensional networks in hydrogels and specialty adhesives. This contrasts with simple 1,4-butanediol or diethylene glycol, which bring flexibility but less control over reactivity and less chemical resistance after curing.
Colleagues working on fine chemicals have shared that pyridine-2,6-diyldimethanol often outshines both mono-substituted pyridines and simple diols when the goal is to introduce multiple functional handles onto a single aromatic system. That ability speeds up timelines and makes troubleshooting a bit less painful. Been there myself—when a late-stage intermediate stalls in the process, having a building block that tolerates a variety of reaction conditions can save the whole project.
Responsible use always plays a part in handling specialty chemicals. Pyridine-2,6-diyldimethanol, like many compounds in its family, calls for the usual precautions in processing and storage—gloves, safety glasses, and controlled environments keep everyone safe. Most modern labs and production plants have best practice guidelines in place, but it pays to reinforce basic safety culture. Over the years, I’ve seen safety shortcuts lead to headaches down the line; no shortcut ever truly saves time in the long run. While toxicological profiles put pyridine-2,6-diyldimethanol in a less-hazardous bracket compared to some pyridine analogues, vigilance makes all the difference, especially in scale-up or multi-step syntheses.
Waste management also sets apart responsible suppliers. The reality is that specialty chemicals, no matter how benign, generate residues. Partnering with suppliers who take environmental stewardship seriously helps everyone in the chain—operators, communities, regulatory agencies.
Larger producers have begun implementing closed-loop production cycles and developing safer solvent systems, all while keeping product quality high. I’ve served on project teams where greener solvent choices and better containment have slashed waste disposal costs and improved team morale. These upstream improvements translate to better outcomes—and fewer headaches—on the end-user side.
In talking through options with chemists and purchasers, the conversation always circles back to the trade-off between cost, availability, and downstream performance. Basic diols—think ethylene glycol or propylene glycol—serve well for mass applications, but they lack the aromatic backbone and specific nitrogen interactions that drive specialized syntheses. Mono-substituted pyridines offer some reactivity, but usually fall short in side-chain modification and overall process flexibility.
Other 2,6-disubstituted pyridine derivatives do exist. Compounds bearing amine or halide groups at those same positions rarely provide the same clean reactivity or easy handling found with two primary alcohols. And if you ever tried to swap in a similar bifunctional molecule with wider availability, you’ll have seen purity suffer and end-product profiles drift outside of specification—especially in pharmaceutical or specialty polymer settings.
This is the value everyone in research and production circles talks about: pyridine-2,6-diyldimethanol offers real chemistry that translates to more predictable processes and tighter quality outcomes. It closes gaps that appear in formulations built from simpler starting materials. The measurable difference surfaces in fewer failed batches, more robust formulations, and less scrambling to tweak reaction conditions.
Access plays a crucial role in moving the field forward. Decades ago, sourcing pyridine-2,6-diyldimethanol took patience and favored well-connected labs over small teams. That’s changed with advances in global logistics and information sharing—now even smaller ventures or academic labs can secure reliable batches at reasonable prices. This shift has prompted waves of innovation, as researchers in emerging markets or interdisciplinary projects bring new eyes to old problems.
Reaching out through conferences and online networks, I’ve noticed more collaborative problem-solving across industries. Synthetic chemists, material scientists, and regulatory experts compare notes, swap protocols, and share lessons from both success and failure. The result is a growing collective knowledge base. Pyridine-2,6-diyldimethanol now gets featured in peer-reviewed papers, industry white papers, and supply chain audits, which boosts transparency and supports smart purchasing decisions.
As this knowledge broadens, more users seize opportunities to refine their syntheses. This widens the compound’s reach—from narrow applications in advanced R&D to larger-scale roles in green chemistry and sustainable materials science.
Supply chain transparency remains one of the biggest hurdles. Just because a product label reads “pyridine-2,6-diyldimethanol” doesn’t always guarantee high purity or ethical sourcing. Some suppliers take shortcuts or offer mixed purity grades that jeopardize downstream results. I once fielded calls from a production engineer frustrated after a contaminant derailed a whole pilot batch—turns out the issue traced back to inconsistent supply chain paperwork.
What works? Reliable documentation, routine third-party analysis, and ongoing dialogue with suppliers. Groups that take extra steps to certify traceability—including origin, batch records, and environmental compliance—stand apart. This sort of diligence gets the attention of both regulatory agencies and end-users. It’s not just about ticking boxes; robust supply chain management saves money, reputation, and time in the long run.
Stepping into the future, I would urge both buyers and producers to favor suppliers that put quality and transparency front and center. Working with partners who support third-party audits and value openness delivers real advantages, especially once scaling up becomes a priority.
Progress in chemistry and related industries traces back to foundational materials. Pyridine-2,6-diyldimethanol provides one such foundation. Its dual functional groups, bolstered by the aromatic pyridine core, open the door to new classes of pharmaceuticals, polymers, and specialty coatings. I’ve watched projects that might have hit dead ends instead pivot and push ahead, thanks to the right choice of intermediates.
Think about high-performance adhesives engineered to withstand extremes of heat, cold, or chemical exposure—engineers credit new cross-linkers for these advances. Many times, compounds like pyridine-2,6-diyldimethanol step in as crucial linkers, providing durability and resistance that older formulations can’t match. Pharmaceutical teams use its structure as a launchpad for custom modifications—tailoring bioactivity, solubility, and metabolic stability in new drug candidates.
Students and emerging professionals should keep an eye on these flexible molecules. Mastering both basic handling and the nuances of advanced functionalization puts young chemists in a good position to solve tomorrow’s problems. As more training modules and open-access research focus on these next-generation building blocks, the pathway to smarter, faster problem solving gets a bit clearer.
More buyers now value suppliers who demonstrate responsible stewardship. Greener solvents, renewable raw materials, and safe waste handling are not just sales pitches; they have tangible impact on both cost and reputation. Looking back, product recalls or supply interruptions often link back to overlooked environmental or safety practices. The shift in attitudes—where sustainability and performance intertwine—increases demand for suppliers who build clean processes into every shipment.
I’ve witnessed small steps pay off: substituting safer reagents, tweaking purification steps to cut down on energy use, and improving packaging to minimize plastic waste. Reverse logistics—where empties are recovered and reused—cuts costs and reduces landfill strain. These measures, embedded throughout the production and delivery pipeline, win over regulatory agencies and foster long-term partnerships.
With growing attention to circular economy principles, compounds like pyridine-2,6-diyldimethanol will play an even larger role. As industries demand less waste, lower emissions, and smarter life-cycle management, users and producers alike stand to benefit from chemistry that supports both profitability and environmental goals.
Trust builds over repeated positive outcomes. Buyers expect accurate documentation, consistent quality, and honest communication about production limits or unexpected delays. Users should also take time to vet suppliers beyond price tags—checking audit reports, reading user feedback, and verifying batch analyses against accepted standards. Small efforts early can save big headaches further down the road.
Open feedback loops push the market to improve. By sharing batch results, reporting problems transparently, and participating in voluntary certifications, labs and factories help raise the community’s baseline. I’ve seen firsthand how feedback from a single plant can prompt suppliers to tighten controls and even publish updated specs. This reciprocal relationship between end-users and producers forms the backbone of responsible supply chains.
Training and ongoing education lend another edge. Bringing teams up to speed on new protocols, process controls, and safety improvements keeps operations efficient and compliant. I often advise new hires: never hesitate to ask about handling, storage, or disposal—and be skeptical of shortcuts. A strong culture of continuous improvement beats any single piece of equipment or software.
Looking toward the future, compounds like pyridine-2,6-diyldimethanol will drive innovation across sectors. As researchers and manufacturers continue to break new ground—from advanced biodegradable plastics to targeted therapeutic agents—having access to flexible, reliable chemical building blocks becomes ever more critical. Industry trends already show a shift toward specialty intermediates with well-documented performance benefits. Familiar faces in research and procurement circles talk about reducing time to market, cutting waste, and opening new product categories—all tracing back to the types of building blocks they trust.
For start-ups working at the intersection of chemistry and technology, making the right sourcing decisions at the outset impacts everything downstream. Pyridine-2,6-diyldimethanol won’t always be the cheapest choice, but its return on investment often shows up in faster development, fewer process headaches, and better scalability. Open communication across the supply chain—from bench chemists to logistics coordinators—builds in resilience and responsiveness.
I’d urge existing producers to continue investing in analytical technologies, sustainable production, and open technical support. End-users, on the other hand, should prioritize transparency, feedback, and continual evaluation of protocols. In these ways, everyone who touches the pyridine-2,6-diyldimethanol pipeline—whether in formulation labs, environmental teams, or procurement offices—plays a part in shaping a more innovative, reliable, and responsible chemical industry.