|
HS Code |
371004 |
| Chemical Name | Pyridine-2-aldoxime methochloride |
| Cas Number | 2751-68-0 |
| Molecular Formula | C6H9ClN2O |
| Molecular Weight | 176.60 |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 220-225°C (decomposes) |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Synonyms | 2-Pyridinealdoxime methochloride |
| Application | Reactivator of cholinesterase, used as an antidote for organophosphate poisoning |
As an accredited Pyridine-2-aldoxime methochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyridine-2-aldoxime methochloride is supplied in a 25g amber glass bottle with a secure screw cap and detailed labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 6 MT with 25kg fiber drums, lined with double polythene bags, securely palletized for Pyridine-2-aldoxime methochloride. |
| Shipping | Pyridine-2-aldoxime methochloride should be shipped in tightly sealed containers, protected from moisture and light, and stored at room temperature. The packaging must be compatible with chemical regulations for hazardous materials. Proper labeling and documentation are required for safe transport, following local and international shipping guidelines for chemicals. |
| Storage | **Pyridine-2-aldoxime methochloride** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, moisture, and direct sunlight. Keep the chemical separate from incompatible substances such as strong oxidizers and acids. Properly label the container and keep it in a designated corrosive storage cabinet to minimize risk. Store at room temperature. |
| Shelf Life | Pyridine-2-aldoxime methochloride typically has a shelf life of 2-3 years when stored in a cool, dry, and sealed container. |
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Purity 98%: Pyridine-2-aldoxime methochloride of 98% purity is used in pharmaceutical synthesis, where it ensures high-yield intermediate formation. Melting Point 230°C: Pyridine-2-aldoxime methochloride with a melting point of 230°C is used in chemical reagent preparation, where it provides stability during thermal processing. Particle Size <75 µm: Pyridine-2-aldoxime methochloride with particle size below 75 µm is used in laboratory-scale research, where it enables rapid dissolution and homogeneous reaction mixtures. Moisture Content <0.5%: Pyridine-2-aldoxime methochloride with less than 0.5% moisture content is used in analytical chemistry, where it prevents unwanted hydrolysis in sample preparation. Stability up to 60°C: Pyridine-2-aldoxime methochloride stable up to 60°C is used in storage and transport of chemical stocks, where it reduces decomposition risk and preserves product integrity. Assay ≥99%: Pyridine-2-aldoxime methochloride with assay greater than or equal to 99% is used in manufacturing of antidote formulations, where it guarantees batch-to-batch consistency. Solubility in Water >10 g/L: Pyridine-2-aldoxime methochloride with water solubility above 10 g/L is used in injectable solution development, where it facilitates convenient dosing and administration. |
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Starting out in a working lab, one quickly learns that not all reagents are created equal. Reagents form the backbone of accurate research, and the smallest details can mean the difference between success and frustration. Pyridine-2-aldoxime methochloride has emerged as a popular choice in many research settings, favored for its stability and consistent performance as a key organic building block and analytical reagent.
This compound, often selected for its reliable structure—C6H7N2ClO—stands out when purity is a top concern. Its crystalline appearance and moisture sensitivity tell me that proper storage isn’t just a suggestion; it’s the difference between years of use or starting over. You’ll often find this reagent stored in tightly sealed containers, shielded from humidity and direct light, much like a favorite tool put carefully back in its box after every job.
Many reagents in the pyridine family deliver on certain tasks, but pyridine-2-aldoxime methochloride offers unique advantages for those navigating organic synthesis or intricate analytical work. Its position as a salt (methochloride) version offers improved solubility in common laboratory solvents and a reliable release of the oxime functional group under defined conditions. This makes it useful both as a reactant and as a tool for capturing, transforming, or detecting other molecular targets.
In my experience, specificity often guides chemists toward one reagent over another. The structure of pyridine-2-aldoxime methochloride gives it an edge where nucleophilic substitution or chelation is required. That makes it a common choice for coordination chemistry experiments or for scavenging certain metal ions in solution. Some may reach for alternatives like the free base or other oxime derivatives, but stability and shelf life tend to keep this methochloride form in regular use.
Pyridine-2-aldoxime methochloride factors into a range of research and industrial workflows. One of its standout roles comes in toxicology. Here, researchers use it to regenerate acetylcholinesterase, an enzyme disabled by organophosphate poisoning. The practical point: in medical or emergency settings where rapid enzyme reactivation is life-saving, dependable reagents matter more than abstract chemistry. Its mechanism—nucleophilic attack that cleaves phosphate and reactivates the enzyme—forms a cornerstone in antidote research and has practical consequences for public safety.
Outside toxicology, this compound helps build complex coordination compounds in analytical laboratories. In my time analyzing transition metal ions, I’ve seen reactions with pyridine-2-aldoxime methochloride unravel tangled mixtures, letting spectroscopists zero in on target species. It chelates metals, pulling them out and stabilizing them for further study. Choosing the methochloride salt over less soluble forms can clarify results and cut down on time spent filtering and prepping samples.
The reputation of pyridine-2-aldoxime methochloride doesn’t rest only on textbook chemistry; it’s proven itself in actual research settings. It supports nucleophilic substitution reactions with reliable yields, and the presence of the methochloride counterion gives the molecule robust solubility, easing workups and product isolation. In organic synthesis, that predictability helps streamline steps, avoiding the trial-and-error that drains time and spirits in a busy lab.
Few things slow a project more than contamination or inconsistent purity. Producers of pyridine-2-aldoxime methochloride recognize that high-purity lots are, at this point, an expectation, not a luxury. Reputable suppliers offer material with purity well above 98%, reducing interference that could skew reaction outcomes. From my experience running reproducibility tests, a single outlier batch can force an entire investigation back to step one, so quality sourcing is non-negotiable. The best suppliers commit to consistent crystalline texture and clear labeling, making everyday handling safer and more efficient.
Anyone who’s felt the sting of wasted time on an uncooperative reagent will understand why the right form matters. Other oxime derivatives exist—like pyridine-4-aldoxime and related free bases or salts—but few offer the same blend of solubility and controlled reactivity. The methochloride version resists moisture better during storage, and dissolves promptly in methanol or water. In troubleshooting troublesome reactions, I’ve sometimes changed to the methochloride form and watched once-sluggish reactions click into gear, delivering the expected yield.
Where speed, precision, and reactivity count, this compound steps up compared to alternatives like lower-purity salts or less stable free bases. Chemists often point to operational simplicity—fewer purification steps, less time lost troubleshooting, and cleaner product isolations. It’s a lesson picked up the hard way: relying on a consistent, proven chemical lets you think more about your research question and less about unpredictable setbacks. I have heard colleagues echo the sentiment that getting reliable results begins with investing in quality reagents—this one earns a spot near the top of the list.
For scientists interested in metal ion analysis, pyridine-2-aldoxime methochloride finds regular use as a chelating agent. Its structure encourages the formation of strong, selective complexes with a range of transition metals, such as copper, cobalt, and nickel. This attribute proves vital in colorimetric determinations and advanced spectroscopy. I’ve seen this compound enable accurate readings in atomic absorption and UV-visible analysis, especially when separating closely related ions in environmental and biological samples.
It’s also valued for the unique properties that oxime ligands bring to coordination chemistry. Compared to other chelators, compounds built around pyridine-2-aldoxime methochloride can display sharper, more defined signals across measurement platforms. Researchers working toward new catalysts or material science functions frequently draw from this molecular toolkit, building complexes that would be almost impossible with simpler ligands.
Talking with practicing chemists and process engineers, there’s a common thread: proper handling protects the life and purity of pyridine-2-aldoxime methochloride as much as careful synthesis does. The compound’s moisture sensitivity calls for dry storage and rapid closing after each use. I’ve found that double-sealed containers kept in a desiccator can make a real difference, preserving the crystalline appearance for months, even years. Direct contact should always be avoided, as with most laboratory chemicals, and gloves and eyewear are standard parts of the equation.
Simple steps—prompt cleanup, tight seals, labeling with opening dates—reduce waste and lower the risk of degradation over time. In undergrad labs, I saw peers handle reagents carelessly, only for the entire stock to degrade within weeks. Experienced hands know that passive storage won’t do: active attention preserves not just the reagent, but the results downstream. Less product lost to spoilage means more funds for the actual research, and fewer surprises during crucial runs.
Those who spend long hours in chemical analysis understand the subtle impact that a salt’s solubility or sensitivity can have on results. More hygroscopic variants tend to absorb atmospheric water rapidly, which alters concentrations and can spoil carefully prepared solutions. Free base versions, on the other hand, often struggle with lower stability and can introduce structural changes during long-term storage. Pyridine-2-aldoxime methochloride strikes a practical balance: it stays stable under reasonable handling, offers reliable solubility, and delivers predictable reactivity that many chemists have come to trust.
From my perspective, the value proposition is simple: fewer hiccups, smoother workflows. The alternative—experimenting with less stable or mixed-purity lots—can appeal for specific niche reactions but rarely matches the broad practical application of this salt. Efforts to substitute with lower-cost options often backfire, with time lost to trouble-shooting inconsistent results or purifying lower-grade products. In a field where time and reproducibility matter, a stable benchmark chemical frees up resources for actual scientific discovery.
One area where the significance of pyridine-2-aldoxime methochloride stands out is in medical antidote development, particularly against organophosphate poisoning. This compound has supported in-depth research into nerve agent deactivation, enabling scientists to test rapid interventions and optimize drug designs. The science here is far from abstract: each improvement translates to stronger, more accessible treatments, saving lives in moments where timing can be everything.
In controlled studies, researchers found that the oxime group’s strong nucleophilicity is critical for cleaving enzyme-inhibitor bonds, reactivating crucial biological functions. Pyridine-2-aldoxime methochloride, in particular, balances reactivity with patient safety, avoiding runaway toxicity or side reactions that can hamper clinical trials. Medical chemistry teams value this reliability, as even one unpredictable reagent can send a development program off-track.
Despite its practical strengths, there are still areas for improvement. The methochloride form, while stable, remains moisture sensitive and requires disciplined storage, which isn’t always possible in field conditions or under rapid deployment scenarios. Research teams have begun exploring alternative packaging, such as single-use vials or stabilized bulk containers, to address this issue.
Supply chain reliability also matters, especially in emergency stockpiles or ongoing clinical research. Teams sourcing the compound regularly should check for clear, consistent batch documentation, including purity testing and traceability. This often means paying a premium for proven suppliers, but the trade-off is fewer research stoppages and minimal wasted effort.
As the focus on sustainability grows, the chemical industry’s expectations shift. Researchers and manufacturers evaluating pyridine-2-aldoxime methochloride increasingly look to greener synthesis methods. Advances in catalytic production and reduced-waste purification, if adopted widely, can make this essential reagent even more viable as a modern laboratory staple. Academic institutions and commercial labs alike have begun to request transparency about energy inputs and byproduct management, reflecting a broader move toward responsible chemical production.
From my experience working with green chemistry teams, progress often starts with simple changes—switching to renewable solvents, minimizing water use, and collaborating directly with producers to fine-tune specifications. These conversations pay off not just for compliance, but for the long-term reliability of the scientific supply chain.
The divide between optimal and mediocre results often comes down to day-to-day lab habits. Reliable reagents like pyridine-2-aldoxime methochloride reward a culture of careful measurement, batch-to-batch tracking, and openness about process tweaks. I’ve seen projects turn around quickly after a once-struggling team instituted routine checks: standardizing storage, sharing notes on solvent compatibility, and flagging outlier data right away. These habits spread naturally when team leads model them, and the impact on morale and research quality is both immediate and lasting.
Education also matters. Training early-career chemists on the why, not just the how, of careful reagent handling turns a basic protocol into a critical skill. Lab seminars, quick checklists by the storage shelf, and peer teaching speed up the learning curve and help avoid common mishaps—such as condensation buildup or accidental light exposure—that can diminish the utility of any aldehyde oxime derivative.
In the world of chemistry, lab-scale and industrial researchers alike make trade-offs between cost, convenience, and reliability. Pyridine-2-aldoxime methochloride earns its place through a practical blend of stability, functional specificity, and ease of use. Its role in both routine analytical work and life-saving antidote research makes it more than just another chemical on the shelf. Teams that focus on careful handling, consistent sourcing, and process transparency get the most out of every gram—saving time, reducing waste, and supporting real progress in science and medicine.
Trustworthy reagents will always form the backbone of sound research, and it’s often small changes—sourcing high-purity lots, tightening storage protocols, demanding more sustainable production—that drive big improvements. Experienced chemists never underestimate the importance of these choices, knowing that the pursuit of reliable and impactful science begins long before a reaction flask hits the hotplate.