|
HS Code |
538126 |
| Chemical Name | 6-methylpyridine-2-carbaldehyde |
| Cas Number | 5507-44-8 |
| Molecular Formula | C7H7NO |
| Molecular Weight | 121.14 |
| Appearance | colorless to pale yellow liquid |
| Melting Point | -17°C |
| Boiling Point | 213-214°C |
| Density | 1.121 g/cm3 |
| Smiles | CC1=NC(=CC=C1)C=O |
| Flash Point | 90°C |
| Solubility | soluble in organic solvents, slightly soluble in water |
| Iupac Name | 6-methylpyridine-2-carbaldehyde |
As an accredited 6-methylpyridine-2-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, with secure screw cap and tamper-evident seal; labeled with product name, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 6-methylpyridine-2-carbaldehyde is securely packed in sealed drums, stacked efficiently, maximizing container space safely. |
| Shipping | 6-Methylpyridine-2-carbaldehyde should be shipped in tightly sealed containers, protected from light and moisture. Transport in accordance with local and international regulations for hazardous chemicals, ensuring proper labeling and documentation. Store upright, in a cool, well-ventilated area, and use secondary containment to prevent leaks during transit. Handle with appropriate personal protective equipment. |
| Storage | 6-Methylpyridine-2-carbaldehyde should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store in a corrosive-resistant container with a resistant inner liner. Ensure storage is in accordance with local regulations and labeled appropriately to prevent accidental misuse or exposure. |
| Shelf Life | **Shelf Life:** 6-Methylpyridine-2-carbaldehyde is stable under recommended storage conditions; store tightly closed, protected from light and moisture, for several years. |
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Purity 99%: 6-methylpyridine-2-carbaldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Boiling Point 208°C: 6-methylpyridine-2-carbaldehyde with a boiling point of 208°C is used in organic reaction setups, where precise temperature control increases reaction selectivity. Molecular Weight 121.14 g/mol: 6-methylpyridine-2-carbaldehyde with molecular weight 121.14 g/mol is used in fine chemical production, where accurate stoichiometry enables consistent batch reproducibility. Melting Point 17°C: 6-methylpyridine-2-carbaldehyde with a melting point of 17°C is used in automated liquid handling systems, where its low melting point allows seamless material transfer. Light Sensitivity: 6-methylpyridine-2-carbaldehyde with high light stability is used in photochemical studies, where product integrity is maintained during exposure to illumination. Density 1.09 g/cm³: 6-methylpyridine-2-carbaldehyde with density 1.09 g/cm³ is used in liquid-liquid extraction methods, where phase separation efficiency is improved. Aldehyde Content ≥98%: 6-methylpyridine-2-carbaldehyde with aldehyde content ≥98% is used in agrochemical synthesis, where high functional group concentration promotes optimal reactivity. Stability Temperature up to 50°C: 6-methylpyridine-2-carbaldehyde with stability temperature up to 50°C is used in controlled storage environments, where chemical degradation is minimized. Low Water Content ≤0.5%: 6-methylpyridine-2-carbaldehyde with water content ≤0.5% is used in anhydrous reaction processes, where side reactions from moisture are effectively prevented. Refractive Index n20/D 1.530: 6-methylpyridine-2-carbaldehyde with a refractive index of 1.530 is used in analytical calibration standards, where measurement accuracy is enhanced. |
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In synthetic chemistry, some molecules stand out for their practical usefulness and resilience during challenging reactions. 6-Methylpyridine-2-carbaldehyde proves itself here, delivering a particular kind of versatility that lab workers and production chemists appreciate every day. The compound’s structure—a methyl group on the sixth position and an aldehyde on the second carbon of the pyridine ring—gives it a set of reactivity options that simpler aldehydes or basic pyridines just can’t match. Its molecular formula is C7H7NO, and it often appears as a colorless to pale yellow liquid. That color may seem like a trivial detail until you’ve tried to pick out the right fraction during a tricky distillation, and the visual cue lets you move on to the next step instead of wasting more time.
Whether you're preparing ligands for catalysis, exploring heterocyclic drug scaffolds, or looking for a precursor in agricultural chemistry, the right building blocks save hassle and time. In solid and liquid phases, this compound gives reliable performance across a range of temperatures for both academic and industrial environments. Its boiling point hovers around the expected mark for similar pyridines, making purification mostly uncomplicated. Unexpected impurities can still ruin purity, but careful suppliers provide high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) profiles so users can check quality before use.
For those of us who spend late nights overseeing glassware, 6-methylpyridine-2-carbaldehyde offers more than just a peculiar name—it serves as a gateway reagent. Its formyl group opens up access to Schiff bases and other imines through straightforward condensation with amines, a feature quite handy for both academic labs and pilot plant processes. Since the aldehyde sits right next to the ring nitrogen, it can direct nucleophilic addition with more precision than its positionally-isomeric cousins. Functionalization of the neighboring methyl group adds further routes, expanding the toolbox for constructing pharmaceuticals, agrochemicals, and specialty ligands.
Some research groups use this compound to build advanced coordination complexes, exploring metal-organic frameworks that trap gases or catalyze harsh transformations. The combination of the heterocyclic nitrogen and the aldehyde acts almost like a molecular hand—strong enough to guide reactivity, gentle enough to preserve selectivity. Its balance makes it a reliable intermediate during the tricky, multistep routes common in natural product synthesis or fine-tuning of physical properties in scent and flavor molecules. For chemical educators, it introduces students to the subtle effects of electronic structure on reactivity, blending hands-on learning with real-world applications.
Some might ask, “What sets this apart from other pyridine carbaldehydes?” The answer goes deeper than just the additional methyl group. That methyl, hanging at the six-position, acts as a shield and a trigger. It blocks unwanted side reactions that can make cleaning up a product difficult. At the same time, it tweaks the electron balance in the molecule, letting chemists steer the outcome of a reaction with lower risk of forming byproducts or tars.
Contrasted with 2-pyridinecarboxaldehyde, the methyl version shows less reactivity toward oxidation and sometimes offers more robust handling in air or with moisture present. Many in the profession remember frustrating afternoons wrestling with more sensitive aldehydes, where a slight humidity shift ruined a whole batch. 6-Methylpyridine-2-carbaldehyde doesn’t solve every one of those problems, but it tends to forgive minor slips in technique. Its physical stability means you spend less time double-checking the conditions and more time moving the project forward.
Any chemical with an aldehyde group deserves respect in the lab. Sensible handling practices—secure storage, chemical-resistant gloves, and good ventilation—cut down risk. From experience, this molecule won’t fill the workbench with harsh odor like old-school benzaldehyde, but its volatility means inhalation remains a concern at larger scales. Reliable suppliers include up-to-date safety information, which keeps procedures consistent and reduces anxiety for newer lab staff.
Most teams store it in amber vials, kept far from oxidants and sources of ignition. The methylpyridine odors quickly mark an area, serving as a good reminder to minimize splashes and take care with syringes or pipettes. Washing spills right away with suitable solvents—often ethanol or acetone—works for most mishaps. Environmental impact, always a concern, rests mainly on local disposal guidelines, and smaller users rarely encounter major compliance hurdles as long as they keep track of waste streams.
A trustworthy source keeps projects on track. In the past, dealing with off-color, poorly sealed, or impure aldehydes from questionable suppliers sent research spiraling into repeat purifications and null data. Verified chemical providers now offer certificates of analysis, and these reports, confirmed by independent third-party labs, add confidence to expectations and planning. For mission-critical syntheses in pharma, or grant-funded academic work where every dollar gets counted, that reliability means less lost time troubleshooting.
Transparency helps as well. Clear records of batch numbers, analytical data, and open communication about supply chain issues make it far easier for users to trace problems back to their source. Suppliers with long histories of compliance and rigorous quality tracking, audited by international bodies, support the credibility of science as a whole. Since 6-methylpyridine-2-carbaldehyde is used both for experimental research and commercial production, that trust runs both ways: product developers rely on accurate materials, and customers expect the data to back up marketing and claims.
For those of us who work with trace-level impurities, the purity of 6-methylpyridine-2-carbaldehyde can make or break an experiment. Even a few tenths of a percent off specification may steer a reaction in a totally different direction. Solid analytical techniques—such as gas chromatography, HPLC, and NMR—confirm the identity and purity, minimizing guesswork. Some years back, a collaborator shared how a failed batch led them down a week-long search for a source of contamination, only to find an out-of-spec aldehyde. After switching to a better provider, yields shot up, and side reactions disappeared. Many researchers would say that sort of reliability is always worth a small premium.
Commercial manufacturing environments feel these benefits even more strongly. Modern process chemistry runs on consistency: matching regulatory filings, batch records, and internal audits. Purity sets the stage for repeatable and scalable processes. Companies producing flavors, advanced polymers, or catalysts feel competitive pressure to streamline operations, so reducing variables at the early building-block stage pays off down the line. I’ve seen production teams calculate losses from single contaminants, and the right supplies closed those expensive gaps.
Chemical innovation sometimes starts with small details—the placement of a methyl group, the orientation of an aldehyde. Over the last few decades, 6-methylpyridine-2-carbaldehyde has bridged fields: from pharmaceutical leads and targeted agrochemicals to materials used in new devices. In one recent study, researchers leveraged its ring structure as a launchpad for photoactive compounds that help visualize cellular processes. The Mickey Mouse simplicity of its formula hides a world of non-obvious applications, made possible by those subtle reactivity shifts.
As new fields like chemical biology and advanced materials demand more specialized reagents, the ready availability of well-characterized intermediates allows researchers to move fast. The old days of months-long waits for critical building blocks slow down patent filings and product launches. Now, researchers select from stock, tweak the target molecule, and walk into the lab ready to test an idea. That agility drives faster innovation, making cutting-edge therapies and products available sooner to those who count on them.
The pharmaceutical world in particular has gravitated toward heterocyclic aldehydes as lead compounds in medicinal chemistry campaigns. The nitrogen in the pyridine ring influences binding affinities in proteins, sometimes unlocking pathways that aliphatic or benzene-based aldehydes miss entirely. Adding a methyl group tweaks the fit, tuning the strength and selectivity in drug candidates. Librarians, analysts, and researchers recognize the value of starting with a reliable, customizable base structure, one robust enough to endure high-throughput screening and downstream modification.
Sustainability in chemical manufacturing isn’t just a buzzword; it shapes regulatory approvals and consumer trust. Building blocks like 6-methylpyridine-2-carbaldehyde matter here too. Suppliers aware of their environmental impact offer documentation on manufacturing footprints, energy use, and waste handling. Some have transitioned to more efficient synthetic routes, cutting carbon emissions or switching to greener solvents without sacrificing quality. Using intermediates whose upstream production is auditable increases confidence, especially for companies navigating ever-tightening regulations.
At the research bench, waste mitigation matters as much as it does for multi-ton operations. Chemists sometimes redesign routes just to use intermediates that sidestep heavy metals or reduce persistent byproducts. 6-Methylpyridine-2-carbaldehyde, because of its stability and solubility profile, helps keep waste streams focused and easier to treat. Improvements in supply chain transparency also reassure both researchers and public agencies that best practices are followed throughout procurement and use.
From the earliest days in lab training, most chemists carry strong memories of particular reagents—maybe a stubborn reaction that finally worked after months of optimization, or a project that ground to a halt because the starting material couldn’t be sourced. Talking with others in the field, I’ve heard similar stories involving this aldehyde: its arrival often marks the turning point for otherwise stalled projects. Its reliability, coupled with the underlying flexibility of pyridine chemistry, gives researchers confidence to push ahead with ambitious syntheses.
Some colleagues report that specific modifications made possible with 6-methylpyridine-2-carbaldehyde led to granted patents or key advances in materials science. By comparison, less versatile scaffolds limited experimental design or forced circuitous workarounds. Especially in environments where both time and materials are limited, the ability to depend on a reagent cuts frustration and boosts engagement. Students, too, find the hands-on lessons stick longer when small molecular nuances lead to big effects—turning textbook concepts into real, publishable data.
Costs always play a role in selection, but paying for quality up front can save far more down the line. Less expensive sources sometimes turn out to be false economies, dragging down project timelines or increasing purification cycles. Premium providers justify their higher prices by delivering consistent physical properties, more detailed analysis, and robust logistics. Packaging designed for both laboratory and bulk quantities allows everyone from academic research groups to commercial engineers to get what they need without overspending.
Accessibility matters too. Supply shortages, geopolitical interference, or weak supply chains can cripple even the best-planned efforts. Providers able to maintain stocks in multiple regions, offer flexible shipping, and guarantee traceable production inspire greater trust. Global demand for heterocyclic building blocks keeps growing, and producers able to meet volume while respecting local regulations help ensure researchers can focus on discovery and development, not procurement headaches.
Chemistry never offers a guarantee, but some challenges show up more often than others. Batch-to-batch inconsistency frustrates those trying to scale up: rigorous supplier vetting and regular quality control can address most of these worries. For labs working with older glassware or improvised setups, small changes in purity or solvent compatibility sometimes derail reactions. Working with compounds like 6-methylpyridine-2-carbaldehyde that come with full analytical documentation minimizes troubleshooting and lets chemists compare results with collaborators more directly.
Another challenge: regulatory compliance. Changing requirements for trace impurities or handling make recordkeeping and traceability more important. Providers that offer robust, accessible data management systems become valuable partners, not just raw material vendors. Training staff in safe handling reduces incidents and builds organizational knowledge. Peer-to-peer learning, through seminars or shared documentation, strengthens lab reliability over time.
Finally, sustainability pressures won’t decrease. Selecting intermediates that fit with green protocols—whether through less hazardous synthesis routes, reduced waste output, or easier downstream treatment—saves both regulatory headaches and ethical concerns. Community efforts, such as shared solvent recovery or best-practices roundtables, offer ways to solve problems together, building toward more sustainable research without sacrificing ambition or creativity.
The story of this compound intertwines with the broader narrative of modern chemistry. Practical steps—a methyl group here, a documentation upgrade there—mean real progress for bench scientists, engineers, and innovators across fields. It’s easy to overlook details in the push for results, but selecting high-quality, thoughtfully sourced intermediates sets the tone for projects that meet both technical and ethical standards. While solutions for all future challenges aren’t yet in hand, smart choices about building blocks like 6-methylpyridine-2-carbaldehyde prepare chemical teams for what comes next. The cumulative impact, from better yields to more sustainable practices, reflects not just smarter chemistry but a more responsible approach to scientific and commercial progress.