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HS Code |
735263 |
| Chemicalname | 6-(Hydroxymethyl)pyridine-2-carboxamide |
| Molecularformula | C7H8N2O2 |
| Molecularweight | 152.15 g/mol |
| Casnumber | 27331-97-7 |
| Appearance | White to off-white solid |
| Meltingpoint | 170-174°C |
| Solubility | Soluble in water and dimethyl sulfoxide (DMSO) |
| Pka | Approximately 10.1 (hydroxymethyl group) |
| Smiles | C1=CC(=NC(=C1)C(=O)N)CO |
| Inchi | InChI=1S/C7H8N2O2/c8-7(11)6-3-1-2-5(4-10)9-6/h1-3,10H,4H2,(H2,8,11) |
| Synonyms | 6-Hydroxymethyl-2-pyridinecarboxamide |
As an accredited 6-(Hydroxymethyl)pyridine-2-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White powder supplied in a sealed amber glass bottle, 25 grams, labeled with chemical name, CAS number, and safety information. |
| Container Loading (20′ FCL) | 20′ FCL can load about 12-14MT of 6-(Hydroxymethyl)pyridine-2-carboxamide, packed in 25kg fiber drums with pallets. |
| Shipping | 6-(Hydroxymethyl)pyridine-2-carboxamide is shipped in tightly sealed containers to prevent moisture absorption and contamination. Standard packaging follows regulations for non-hazardous chemicals, ensuring safe transport. The product is clearly labeled and accompanied by a safety data sheet (SDS). Shipping is via ground or air, depending on destination and customer requirements. |
| Storage | Store 6-(Hydroxymethyl)pyridine-2-carboxamide in a tightly sealed container, protected from moisture and light. Keep at room temperature or as specified in the material safety data sheet (typically 2-8°C). Ensure good ventilation in the storage area and keep away from incompatible substances such as strong oxidizers and acids. Clearly label the container and restrict access to authorized personnel. |
| Shelf Life | Shelf life: Store at 2–8°C, tightly sealed. Stable for at least 2 years under recommended conditions, protected from moisture and light. |
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Purity 99%: 6-(Hydroxymethyl)pyridine-2-carboxamide with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity reactions. Melting point 162°C: 6-(Hydroxymethyl)pyridine-2-carboxamide with a melting point of 162°C is utilized in solid-state formulation processes, where thermal stability and processability are enhanced. Molecular weight 152.15 g/mol: 6-(Hydroxymethyl)pyridine-2-carboxamide at 152.15 g/mol is applied in fine chemical manufacturing, where precise molecular mass supports accurate dosage formulations. Particle size <50 μm: 6-(Hydroxymethyl)pyridine-2-carboxamide with particle size less than 50 μm is employed in high-surface-area catalysis, where reaction rates and active site exposure are optimized. Stability at 25°C: 6-(Hydroxymethyl)pyridine-2-carboxamide stable at 25°C is used in ambient storage applications, where it maintains consistent activity over extended periods. Aqueous solubility 30 mg/mL: 6-(Hydroxymethyl)pyridine-2-carboxamide with aqueous solubility of 30 mg/mL is used in injectable formulation development, where it enables effective drug delivery. UV Absorbance λmax 280 nm: 6-(Hydroxymethyl)pyridine-2-carboxamide with a UV absorbance maximum at 280 nm is applied in analytical reference standards, where detection sensitivity is increased. Residual solvent <0.1%: 6-(Hydroxymethyl)pyridine-2-carboxamide with residual solvent content below 0.1% is used in regulated substance production, where compliance with safety standards is achieved. |
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At our facility, we handle batches of chemicals every day. Among the candidates that keep finding a place in specialized research and practical applications, 6-(Hydroxymethyl)pyridine-2-carboxamide stands out for its stability, clean reactivity, and straightforward synthesis process. The molecule features a pyridine ring connected to an amide and a hydroxymethyl group, giving it a distinct profile compared to other pyridine derivatives.
What gives this compound a unique identity is not just the structure. The incorporation of a hydroxymethyl group at the 6-position and an amide at the 2-position makes it a versatile intermediate. In our day-to-day operations, we notice how shelf-stability plays a large role in its popularity, especially when compared to more oxidation-prone or moisture-sensitive pyridines. Our chemists prefer handling this compound over several others simply because it handles extended storage, minor fluctuations in temperature, and repeated sampling better.
We produce 6-(Hydroxymethyl)pyridine-2-carboxamide as a white to off-white solid, generally processed in lots between 10 and 200 kilograms, depending on client demand. The melting range consistently lies between 108°C and 112°C, a narrow span that reflects our careful purification routines. Purity—measured by HPLC—does not dip below 99%, a benchmark we committed to after receiving feedback from formulation labs struggling with less consistent sources. Minute quantities of moisture do not trigger rapid degradation, and the compound’s solubility in methanol and DMSO matches lab expectations, saving researchers from adjusting standard procedures.
Manufacturing this molecule involves single-pot reactions designed to reduce byproduct formation. We rely on in-house catalyst recovery and recrystallization to get the best yield without unacceptable environmental load or worker exposure risk. After trials with less direct synthetic routes, we adopted this protocol because it reduces both remediation cycle costs and batch-to-batch variability. We have kept documentation from early runs on file, and process refinements are based as much on operator suggestions as on process engineering theory.
Our clients in pharmaceuticals and advanced materials synthesis look to this compound as more than a building block. The hydroxymethyl group offers a handle for downstream functionalization. We get requests from peptide synthesis groups interested in pyridine-modified backbones. Others exploit the amide group’s stability for introducing the molecule into co-polymer frameworks, where thermal and chemical stability matter just as much as reactivity.
Unlike pyridine-2-carboxamide, which lacks the extra reactivity of the hydroxymethyl tail, this molecule finds broader uptake in advanced ligands and catalyst supports. For chemists seeking a platform amenable to mild oxidation or for conjugation with biologically active species, it just makes sense to use this more feature-rich structure. Organic light-emitting diode (OLED) projects sometimes draw on nucleophilic modification possibilities provided by the hydroxymethyl. Here, the compound slots in well, offering access to custom electron-withdrawing or donating groups, which shift device emission characteristics.
Beyond that, some agricultural chemistry groups source the compound for its role in building more elaborate, photo-stable actives. Synthesis teams looking to tweak UV absorption profiles take advantage of the dual-functionality, while others focus on basic heterocycle extension using the intact pyridine core. In all these fields, what sets our product apart comes down to repeatability, impurity profile, and logistical support we offer during unexpected project twists.
Inside the production line, we note the difference between this and other similar materials. Some pyridine carboxamides show unpredictable clumping after weeks on the shelf, demanding extra steps before automated dispensing. That interrupts workflow for compounding teams trying to keep momentum. Our 6-(Hydroxymethyl)pyridine-2-carboxamide, by contrast, maintains powder flow characteristics. Even minor details—a tendency to absorb less ambient moisture, less static buildup—mean fewer jams and material losses.
From our angle, another important difference lies in the downstream waste stream. Many nitrogen heterocycles leave persistent degradation products that complicate effluent treatment. This compound, after a controlled breakdown, presents fewer regulatory headaches. We see this confirmed in feedback from clients working under tighter environmental rules, who come back to us for transparency about test results and compliance records.
With regard to reactivity, the molecule responds predictably under common functionalization conditions—borohydride reductions, alkylations, and amide coupling reactions all behave by the book. Other pyridines we've handled tend toward radical side reactions or the formation of tars under comparable temperature regimes. Chemists on both development and manufacturing sides mention fewer headaches with machine cleaning and recovery, and that is not trivial when moving from the bench to multi-ton production.
Day in, day out, our lot records keep track of every variable—operator ID, temperature logs, incoming raw materials. Traceability is not only a regulatory checkbox. Over the years, we have encountered unexpected analytical results in outside labs, and these records allowed us to troubleshoot and adjust the process in close to real time. For example, a few years back, a batch destined for a photochemical synthesis project showed a slight discoloration. Diving into the archived logs, we found a minor temperature deviation at a crucial synthesis step, and rapidly recalibrated process controls, passing along the insights to affected clients who then avoided similar setbacks.
Strong relationships with raw material suppliers also allow us to update specification sheets based on evolving analytical technology. We switched to higher purity 2-pyridinecarboxamide intermediates in response to customer requests, and we publish updated impurity profiles for all new campaigns. Lab groups appreciate this transparency in their own documentation and compliance routines.
Operating a plant with strict timelines and shifting client priorities presents challenges. One recurring hiccup comes from supply chain volatility, especially for basic pyridine building blocks. Our procurement team deals with this by working with a pool of suppliers and conducting secondary verification for every lot. When other producers struggled with shortages in recent years, we rerouted sourcing, ran extra quality analysis on substitute lots, and flagged any out-of-specification materials before they could enter the reactor.
Temperature and humidity swings in storage warehouses created another set of headaches early on. Rather than invest in costly, energy-hungry climate controls, we tested different packaging formats. Multi-layer, low-permeability liners now protect shipments, preventing moisture-dependent clumping and reducing the chances of downstream processing delays. Our warehouse crew documents all packaging changes with the same rigor as production steps, making sure every box that leaves our facility stands up to cross-border transit and unpredictable warehouse conditions.
Transport restrictions for nitrogen-containing organics add another layer of complexity. We have built relationships with vetted freight companies that understand the handling requirements, which saves customers time and uncertainty with customs checks or rejections. Over time, our logistics workflow has matured through both trial and feedback from partners who received product in less-than-optimal condition or packaging. We revise shipping protocols annually to reflect these lessons.
On the client side, we field a steady stream of technical queries about the suitability of 6-(Hydroxymethyl)pyridine-2-carboxamide for applications ranging from click chemistry to diagnostic kit assembly. We actively share our hands-on experience, noting subtle behavioral traits the molecule shows during multi-step reactions, or under specific analytical techniques such as mass spectrometry or NMR. Open dialogue between manufacturing chemists and R&D partners has prevented many failed reactions, or costly scalings-up of unworkable procedures.
Safe handling forms the cornerstone of reliable operations. Our floor technicians receive regular updates on trending concerns in chemical safety, especially since the amide function in this molecule can react under certain conditions to release minor amounts of ammonia or generate reactive esters. We have built mitigation steps into batch documentation and routinely audit these at every stage. Safety drills and small batch scale-ups catch most practical pitfalls before any risk arises downstream.
Waste minimization receives equal attention. The reaction vessels, resin beds, and solvents used in making 6-(Hydroxymethyl)pyridine-2-carboxamide cycle through standardized cleaning and recovery steps. Runoff and solvent residues head to in-house treatment before shipment to waste management partners. Several years ago, we upgraded filtration and recycling capacity in response to both local regulation and voluntary environmental goals. The results show up in both cost reductions and lowered incident reports, not just in compliance paperwork.
The ongoing transition to greener chemistry prompts us to experiment with new reagents and less hazardous catalysts. We work with process engineers and pilot reactors to limit the need for nitrogen stripping or excess cooling. Open book policy on these experiments encourages buy-in from our staff—some of the best suggestions for minor process tweaks come from technicians proposing alternative equipment arrangements, rather than from outside consultants or trend reports.
Science moves quickly, and today’s specialty chemical buyers span the globe. We routinely collaborate with both established pharmaceutical majors and upstart contract research organizations on several continents. Meeting varying national regulatory standards—be it in documentation, shipment labeling, or inspection protocols—requires more than ticking boxes. Rather, direct feedback from partner QA teams helps us evolve the way we prepare certificates of analysis and update compliance data. For example, we added a UV-vis scan as a routine test parameter after several academic groups reported that the compound’s absorption profile affected downstream applications in photochemical synthesis.
Continual communication with different industries has shaped the way we categorize and store lots of 6-(Hydroxymethyl)pyridine-2-carboxamide. Academic collaborations occasionally demand small, ultra-pure batches, while manufacturing customers need consistent supply at larger scale, even amid market volatility. To address both, we established a two-tier production system, dedicating separate reactors to minimize cross-contamination and ease access to tailored lot sizes. Our experience shows that proactive engagement, rather than a reactive approach, drives satisfaction across a diverse client base.
In over a decade synthesizing 6-(Hydroxymethyl)pyridine-2-carboxamide, one lesson keeps resurfacing: real chemical manufacturing thrives on adaptation, not rigid adherence to “how it’s always been done.” Working directly with this compound through hundreds of campaigns, we’ve witnessed how open data sharing, day-to-day process refinement, and hands-on involvement at every level lead to improvements both small and transformative.
For researchers selecting materials, our advice is simple. Consider not just the published purity or spec sheet, but also the track record of product support and communication from the makers. Problems in the lab or on the factory floor often stem from minor variations in impurity profiles or inconsistent packaging. Manufacturers who prioritize traceability and rigorous quality control help minimize those risks, leading to less downtime and fewer wasted resources.
For fellow makers, we recommend ongoing dialogue with end-users—not just sales teams or procurement, but the actual chemists and engineers working with the product. Their insight often uncovers subtle process improvements or reveals emerging requirements the lab cannot foresee on its own. We have changed drying, milling, and storage protocols in response to specifics relayed from partners facing unique environmental or regulatory constraints. Maintaining this feedback loop translates into a better product for everyone involved.
Demand for more precise and reliable heterocyclic intermediates continues to grow as research into novel pharmaceuticals, materials, and diagnostics accelerates. Through persistent quality audits, process upgrades, and hands-on troubleshooting, we aim to ensure that every shipment of 6-(Hydroxymethyl)pyridine-2-carboxamide matches the most stringent user needs. This approach helps researchers and production chemists meet tight project timelines and innovate with confidence.
On the horizon, new applications are emerging. Clients working in flow chemistry have begun experimenting with the compound in continuous processing, citing its manageable safety profile and straightforward purification steps. Others probe its role in producing more complex macrocycles or as a linker for targeted conjugation. We stay ready to adapt, to adjust production parameters, and to engage in joint R&D projects, bringing practical insights from the manufacturing floor directly to research benches and pilot plants around the world.
We look forward to sharing experience-backed solutions—whether it’s about tackling bottlenecks, keeping raw material quality high, or ensuring compliance with shifting global standards. In our shop, the journey with 6-(Hydroxymethyl)pyridine-2-carboxamide revolved not only around chemistry, but around the daily challenges, adjustments, and collaborations that keep science progressing and supply chains moving.