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HS Code |
449656 |
| Cas Number | 586-80-5 |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 g/mol |
| Iupac Name | pyridin-4-ylmethanol |
| Synonyms | 4-Pyridylmethanol, 4-Hydroxymethylpyridine |
| Appearance | White to off-white solid |
| Melting Point | 54-58°C |
| Boiling Point | 265°C |
| Solubility In Water | Soluble |
| Density | 1.14 g/cm³ |
| Smiles | C1=CC(=NC=C1)CO |
| Inchi | InChI=1S/C6H7NO/c8-5-6-1-3-7-4-2-6/h1-4,8H,5H2 |
As an accredited Pyridine-4-carbinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyridine-4-carbinol is supplied in a 25g amber glass bottle with a tamper-evident cap and chemical hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine-4-carbinol: Typically 12-14 metric tons, securely packed in drums or IBCs, following safety regulations. |
| Shipping | Pyridine-4-carbinol is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent leaks and contamination. It is transported as a stable, non-hazardous chemical under normal conditions, but should be stored away from heat and incompatible substances. Standard labeling and documentation ensure safe and compliant handling during transit. |
| Storage | Pyridine-4-carbinol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. Keep it separate from strong oxidizing agents and acids. Store in a corrosion-resistant container with a resistant inner liner. Proper labeling and secure shelving are recommended to prevent accidental spillage or mixing. |
| Shelf Life | Pyridine-4-carbinol typically has a shelf life of 2 years when stored in a cool, dry place, tightly sealed. |
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Purity 99%: Pyridine-4-carbinol Purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures low impurity levels and consistent drug yield. Melting Point 64°C: Pyridine-4-carbinol Melting Point 64°C is used in fine chemical formulation processes, where predictable melting behavior facilitates precise temperature control during manufacturing. Molecular Weight 123.14 g/mol: Pyridine-4-carbinol Molecular Weight 123.14 g/mol is used in organic reaction scaling, where accurate stoichiometric calculations enhance reaction efficiency and product output. Stability Temperature up to 120°C: Pyridine-4-carbinol Stability Temperature up to 120°C is used in high-temperature catalytic reactions, where thermal stability maintains compound integrity and minimizes degradation. Low Water Content (<0.2%): Pyridine-4-carbinol Low Water Content (<0.2%) is used in moisture-sensitive synthesis, where reduced hydrolysis risk improves yield and product quality. Particle Size <50 µm: Pyridine-4-carbinol Particle Size <50 µm is used in solid dispersion techniques, where fine particles enhance dissolution rate and uniform blending. Refractive Index 1.528: Pyridine-4-carbinol Refractive Index 1.528 is used in analytical calibration standards, where precise optical properties enable accurate spectroscopic analysis. UV Absorbance at 280 nm: Pyridine-4-carbinol UV Absorbance at 280 nm is used in quality control assays, where reliable absorbance facilitates sensitive detection and quantification. Assay (HPLC) ≥98%: Pyridine-4-carbinol Assay (HPLC) ≥98% is used in research reagent preparation, where high assay values confirm suitability for reproducible experimental workflows. Residual Solvent <500 ppm: Pyridine-4-carbinol Residual Solvent <500 ppm is used in active pharmaceutical ingredient development, where low solvent content ensures regulatory compliance and product safety. |
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Working in the lab or running production lines, I’ve learned something important: details matter. Every molecule on my bench or in my workflow can make my job easier or turn a routine day upside down. Pyridine-4-carbinol has become one of those chemicals I pay attention to, not just because it's common, but because it delivers where it counts. Its reliability and features set it apart when searching for a useful pyridine derivative.
Pyridine-4-carbinol brings a distinct structure to the table. I’ve worked with plenty of pyridines—some more suited for solvent use, some specially made for synthesis of fine chemicals. Pyridine-4-carbinol, with its hydroxymethyl group at the para position, introduces a balance between polarity and reactivity. I remember the first time I took a closer look at its performance in heterocyclic chemistry; it delivered stable results where classic pyridine or other position isomers failed to keep side reactions under control. Its model, recognized as 4-pyridinemethanol, isn’t just chemistry on paper—it’s tangible to anyone who's handled reactions that call for both activation and selectivity.
In terms of specifications, reputable suppliers keep the purity above 98%, often exceeding 99% after careful distillation and chromatography. Moisture content stays controlled—important for condensation reactions or redox steps. The formula, C6H7NO, and molecular weight of 109.13 g/mol, put it within easy reach for calculations and upscaling. These numbers don’t mean much until you see how this purity actually matters in real-life runs, especially when unwanted byproducts can throw entire synthetic campaigns off track.
Colleagues often ask why this compound gets picked over regular pyridinol or non-pyridine alcohols. In pharmaceutical development, our teams depend on molecules that act predictably, particularly when forming complex bonds or introducing heterocyclic cores without risking over-oxidation. Once, I needed a precursor that could endure mild oxidation but break down easily under nucleophilic attack. Choosing Pyridine-4-carbinol over 2- or 3-pyridinemethanol made a dramatic difference. The para position and reduced steric hindrance gave much smoother product isolation.
Synthetic organic departments count on it for scalable reactions. The hydroxymethyl group opens the door for transformations—forming aldehydes, alkylating other aromatic systems, and serving in heterocycle ring expansions or contractions. Anyone scaling up has seen how a small tweak in structure can improve downstream stability, storage, and purification. Pyridine-4-carbinol often allows for cleaner separation, especially in medium-pressure chromatographic setups, cutting down solvent use and time.
Experience tells me that inconsistent batches can spell disaster. Once I ran an imine synthesis where a competitor’s pyridinemethanol led to unpredictable residue and a drop in overall yield. Switching to a higher-grade Pyridine-4-carbinol fixed both the yield and the reproducibility, proving that not all so-called equivalents really compare in practice. Precision in aromatic substitution reactions became much more achievable. Labs running spectral analysis routinely report sharper NMR and clean mass spectra with this material, speeding up publication and patent work by eliminating the guesswork of impurity origin.
In medicinal chemistry, being sure about what goes into a reaction means being sure about what comes out. Pyridine-4-carbinol has played a hand in leading molecules targeting cardiovascular and neurological conditions. Synthetic routes that start here often avoid the tangled web of protecting group strategies. In agrochemistry, it acts as a valuable intermediate—solid enough to withstand prolonged storage yet not so inert that synthesis becomes a slog.
Back on the manufacturing floor, the same qualities help process engineers. I met a process chemist who shared that switching intermediates mid-process nearly derailed a critical production run. Pyridine-4-carbinol kept them on schedule by integrating seamlessly with the facility’s existing purification steps. Daily, I see how small choices in raw material selection ripple outwards, affecting the ease of regulatory submissions and the cost-effectiveness of each kilogram produced.
The science behind the bottle doesn’t stop at chemistry. Reputable sources test beyond minimum standards, screening for heavy metals and trace solvents. Analytical methods—NMR, GC-MS, and titrations—confirm the absence of problematic contaminants, which is something I’ve appreciated when supporting toxicological studies. Regulatory documentation often accompanies the shipment, including safety data that matches international requirements for shipping and storage. In my experience, batches kept dry and sealed remain stable for over a year, which lowers waste and purchasing frequency for cash-strapped research budgets.
Working with any pyridine derivative means respecting its basic toxicity. Pyridine-4-carbinol, while less volatile than the parent base, requires proper gloves and ventilation—typical for aromatic amines and their relatives. I’ve seen that good training and adherence to material safety protocols mean incidents are rare and manageable, contributing to a safer workspace for everyone on the team.
It’s tempting to lump all pyridine-based alcohols together. Still, I’ve run side-by-side tests with 2-pyridinemethanol and 3-pyridinemethanol. The differences pop up in both reactivity and handling. The 4-carbinol stands out with greater solubility in polar and moderately polar solvents. While some benzylic alcohols share similar properties, few offer the unique combination of pyridine nitrogen for coordination and the flexibility of a terminal methylol group.
Teams working in coordination chemistry often dive right in with Pyridine-4-carbinol when constructing metal-organic frameworks. The para substitution allows for multi-point ligation, which is rarely as straightforward with ortho or meta analogs. Where electronic effects need finetuning, I’ve watched as researchers stick with this isomer to limit unpredictability—especially important in academic studies where reproducibility makes or breaks advancement.
Comparing to alcohols lacking a pyridine ring—like benzyl alcohol—Pyridine-4-carbinol offers nitrogen’s lone pair for more complex binding or catalysis. In projects seeking specific hydrogen bond networks or tuning catalyst solubility, these subtle molecular differences have sharpened the focus of many grant applications and thesis projects. In direct trial, it shortens optimization timelines, making the product especially valued in deadline-driven environments.
Every chemist has stories about projects that got stuck until the right piece of the puzzle arrived. For me, it was a multi-step project targeting cross-coupling reactions. I found Pyridine-4-carbinol responded much better in Suzuki and Heck setups than older, analogous alcohols. The clean functionalization led to better yields, less column time, and repeatable success in small molecule discovery. This molecule’s robust tolerance to various conditions opened up routes that shortened syntheses by several steps—saving weeks in pharmaceutical pipelines.
Catalyst researchers explore its coordination chemistry and reactivity as templates for new ligands. In my own runs, the para configuration allowed me to build larger libraries of ligands without reworking purification every time. The alcohol group provides a meaningful handle for introducing chirality or building hybrid organic-inorganic complexes. Rather than fighting with side products, I found that Pyridine-4-carbinol’s selectivity sped up design and testing of new catalytic cycles.
Even products I trust deserve scrutiny from batch to batch. Laboratories and factories alike point out the pitfalls of supply disruptions or fluctuating purity. The best Pyridine-4-carbinol on the market comes from manufacturers who have invested in process quality and traceability, giving peace of mind about what’s in the drum or bottle. Reliable quality assurance sets minds at ease when planning critical syntheses or tech transfers.
Scalability always sits just around the corner in any research success. In discussions with process chemists, I’ve seen Pyridine-4-carbinol move from gram-scale to pilot-plant runs without unexpected side products or sudden changes in physical handling properties. Good batches keep melting points tight and limit color changes, both of which matter during crystallization and downstream processing.
Environmental questions land on my desk even in pure research. Pyridine derivatives, including Pyridine-4-carbinol, are certainly not benign, but careful solvent choice and responsible waste management make a positive difference. Water solubility supports some greener workup methods over strictly organic extractions. The molecule’s ability to engage in both aerobic and controlled anaerobic oxidation pathways opens up chances for less harsh oxidants and reagents, which matters to anyone balancing regulatory and sustainability goals.
Despite its strengths, Pyridine-4-carbinol could see broader adoption through clearer packaging information and better digital access to analytical data. Purchasing teams and researchers both benefit from transparent supply-chain practices. I’d appreciate more suppliers providing downloadable certificates of analysis and tracking tools for compliance. Newer distribution models already move this way—combining traceability, rapid shipping, and robust documentation.
Education remains crucial. I've seen young researchers confuse the different isomers or select products that seem similar, only to find that reactivity varies widely with even subtle changes. Direct, practical instruction—emphasizing not just reaction pathways but also firsthand experience with handling, storage, and troubleshooting—would help maintain safety records and research integrity.
Interest in green chemistry keeps pushing scientists to rethink familiar molecules. I notice more teams experimenting with biocatalytic transformations and renewable feedstocks for specialty pyridines. Pyridine-4-carbinol finds itself at the center of some of these efforts, thanks to its compatibility with both classic and modern synthetic routes. In collaborative projects with material scientists, its functionality in electrochemical and photo-initiated processes continues to expand its reputation and appeal.
Regulation and supply chain transparency only continue to grow in importance. As the world reevaluates which specialty chemicals deserve priority in global commerce, Pyridine-4-carbinol stands a good chance of remaining a reliable choice. Its track record supports smooth certifications and approval processes across several countries. In regions striving to hold suppliers to high environmental and safety standards, reliable documentation and ongoing scrutiny will reinforce confidence in this molecule for years to come.
Looking back on a decade of working with complex molecules, few have made as smooth and consistent an impression as Pyridine-4-carbinol. Its versatility suits the needs of research teams and scale-up engineers alike. It brings more than pure chemical interest—there’s an everyday value to knowing I can rely on a batch, plan for months of inventory, and trust it through the twists of regulatory scrutiny and peer review.
For organizations seeking robustness at every stage of research and production, Pyridine-4-carbinol stands out as a smart, reliable building block. Each advance in technology, safety, and supply chain transparency only increases its relevance. As science keeps evolving, having well-understood, trustworthy molecules on hand remains critical to progress, innovation, and safety. Pyridine-4-carbinol, in my experience, fits that bill.