|
HS Code |
290285 |
| Productname | 6-Amino-3-cyano-2-methylpyridine |
| Chemicalformula | C7H7N3 |
| Casnumber | 24522-31-2 |
| Molecularweight | 133.15 g/mol |
| Purity | 97% |
| Appearance | Off-white to yellow solid |
| Meltingpoint | 123-127°C |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Storagetemperature | 2-8°C |
| Smiles | CC1=NC=C(C#N)C(=C1)N |
| Inchi | InChI=1S/C7H7N3/c1-5-2-6(4-8)3-7(9)10-5/h2-3H,1H3,(H2,9,10) |
As an accredited 6-Amino-3-cyano-2-methylpyridine 97% factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed 25-gram amber glass bottle, clearly labeled with "6-Amino-3-cyano-2-methylpyridine 97%" and safety information. |
| Container Loading (20′ FCL) | 20′ FCL container loading: 6-Amino-3-cyano-2-methylpyridine 97% securely packed in drums or bags, ensuring safe and efficient transport. |
| Shipping | 6-Amino-3-cyano-2-methylpyridine 97% is shipped in tightly sealed containers to protect from moisture and light. Standard shipping involves hazard labeling and documentation according to regulations. The chemical is packed securely with cushioning material to prevent breakage during transit, and typically shipped via ground or air freight, depending on destination and urgency. |
| Storage | 6-Amino-3-cyano-2-methylpyridine (97%) should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and acids. Protect from direct sunlight and moisture. Store at room temperature, and ensure proper labeling. Follow all relevant safety guidelines and local regulations for handling and storage of laboratory chemicals. |
| Shelf Life | 6-Amino-3-cyano-2-methylpyridine 97% typically has a shelf life of 2-3 years when stored in a cool, dry place. |
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Purity 97%: 6-Amino-3-cyano-2-methylpyridine 97% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal byproduct formation. Melting Point 130-132°C: 6-Amino-3-cyano-2-methylpyridine 97% is used in solid-phase reagent preparation, where controlled melting point allows precise heat processing. Molecular Weight 135.15 g/mol: 6-Amino-3-cyano-2-methylpyridine 97% is used in ligand development for metal complexes, where defined molecular weight facilitates stoichiometric calculations. Stability Temperature up to 80°C: 6-Amino-3-cyano-2-methylpyridine 97% is used in high-throughput screening assays, where stability at elevated temperatures prevents degradation. Particle Size ≤ 50 μm: 6-Amino-3-cyano-2-methylpyridine 97% is used in fine chemical formulation, where small particle size enhances dissolution rate. Solubility in DMSO: 6-Amino-3-cyano-2-methylpyridine 97% is used in bioactive compound discovery, where DMSO solubility supports diverse assay compatibility. UV Absorbance (λmax 300 nm): 6-Amino-3-cyano-2-methylpyridine 97% is used in analytical method development, where strong UV absorbance aids sensitive spectroscopic detection. Low Residual Solvent (<0.1%): 6-Amino-3-cyano-2-methylpyridine 97% is used in agrochemical synthesis, where low solvent content prevents formulation instability. |
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Scientists and formulators searching for a solid foundation in their synthetic routes often turn their attention toward reliable heterocyclic compounds. 6-Amino-3-cyano-2-methylpyridine, available at a purity of 97%, gives the confidence needed for progress in laboratory and industrial applications. With its distinct structure and consistent performance, this compound keeps standing out in an ever-evolving landscape.
The structure of 6-Amino-3-cyano-2-methylpyridine speaks volumes. Containing both an amino and a cyano group on a methyl-substituted pyridine ring, it brings together nucleophilic and electrophilic sites in a single molecule. This particular arrangement translates to versatility. Synthetic chemists have found that this blend of reactivity takes the guesswork out of building more complex molecules, especially within pharmaceutical research.
Purity counts just as much as ingenuity. A 97% grade supplies enough assurance for sophisticated synthesis, screening, and scale-up. Many standard lab reagents fall short in purity, complicating analysis or introducing background noise. Here, trace impurities remain low enough to minimize unwanted side reactions or degradation, giving researchers space to focus on innovation rather than cleanup.
Experience in early-stage drug discovery shows the value of building blocks that perform as promised. I’ve watched synthetic chemists reach for 6-Amino-3-cyano-2-methylpyridine as a trusted starting point to design novel heterocycles. The way this molecule accepts or donates groups makes it a practical intermediate for crafting pyridyl derivatives, which can serve as essential scaffolds in medicinal chemistry.
Within analytical chemistry, using a reliable product often means fewer headaches during high-performance liquid chromatography or mass spectrometry runs. Enough downstream purification gets avoided simply through picking a source of high purity. The 97% mark on this compound isn’t just a number; it’s a detail that saves hours and cuts operational risk.
The combination of methyl, amino, and cyano groups opens up countless synthetic pathways. From one angle, the amino group at the 6-position attracts acylation or alkylation. Elsewhere, the cyano group offers a strong handle for nucleophilic attack or reduction, giving rise to amines, carboxylic acids, or other valuable moieties.
People familiar with heterocycle chemistry recognize that subtle electronic effects change reactivity. Here, the electron-withdrawing cyano and electron-donating methyl round out the aromatic ring’s character, customizing its performance with each use. Whether targeting kinase inhibitors, anti-inflammatory leads, or even new materials, this compound fits a broad set of tasks without needing elaborate activation or protective steps.
Not every pyridine derivative behaves the same. Close relatives, such as simple 2-methylpyridine or 3-cyanopyridine, lack the combined flexibility that comes with both amino and cyano functionalities present. The extra handle from the amino group lets medicinal chemists craft analogs with more complexity; meanwhile, the cyano offers a rapid entry to carboxamides and carboxylic acids, crucial in developing prodrugs or bioisosteres.
Comparing with basic 2-aminopyridine or 3-aminopyridine, one notices the missing options for further modification. Without the cyano, potential for ring expansion or functional group interconversion drops off. The 6-Amino-3-cyano-2-methylpyridine molecule delivers a wider toolkit for addressing multiple targets at once.
Bringing new drugs from idea to shelf calls for shortcuts. Directly synthesizing a potential active from a robust intermediate speeds development and slices through regulatory hurdles. Chemists have leaned on scaffolds like this because one building block can serve as a pivot point for dozens of analogues. In crowded intellectual property spaces, that really counts.
Considering patent filings and medicinal chemistry papers, structures rooted in methylated, aminated, and cyanated pyridines keep showing up across kinase, GPCR, and anti-infective drug classes. A reliable source of 6-Amino-3-cyano-2-methylpyridine with high purity cuts the resource drain spent on raw material quality verification, which often dominates early-stage research.
Working in a pharmaceutical research group, I’ve seen how such a compound becomes more than a raw material, but a workhorse. Multiple project teams can share a single drum and each access the diversified transformation routes—amide formation, reductive amination, or C–N coupling. Having a dependable supply reduces downtime and keeps programs on faster timelines.
Chemical catalogs brim with pyridine derivatives, each offering a sliver of utility. What often sets 6-Amino-3-cyano-2-methylpyridine apart isn’t just its multifunctional nature but its compatibility with a wide range of reagents and conditions. Some molecules degrade, decarboxylate, or hydrolyze under mild conditions—this one tends toward resilience in a broad pH window.
On a practical note, a 97% purity level makes it easier to plan and scale reactions, as each batch brings less variability. Compared to more dilute or contaminated options, fewer resources go into analytical requalification or reaction recalibration. Other commonly used aminopyridines can drag along colored impurities or low-level solvents; this grade avoids those pitfalls, which matters for late-stage development, or process validation.
Many alternatives claim versatility but often introduce their own hurdles, either in the form of stability issues, or a tendency to react at less convenient sites. The unique substitution pattern in this compound keeps the sites of reaction predictable, preventing ambiguous side products.
Working closely with multi-functional pyridine derivatives across several labs, issues with shelf life and storage occasionally pop up. Hygroscopicity, or the tendency to absorb moisture from the air, creates headaches for bulk storage. This compound generally keeps its form without caking or rapid decomposition, meaning fewer losses due to spoilage.
Handling fine powders in a lab environment involves trade-offs between exposure and containment. The solid form of 6-Amino-3-cyano-2-methylpyridine flows more freely and avoids excessive dust. In programs focusing on green chemistry, the lower hazard rating compared to some halogenated intermediates supports safer and more sustainable process development.
Industrial chemists working toward pilot-plant synthesis see substantial value in intermediates that don’t require constant adjustment. Reproducibility under high-throughput or continuous flow conditions defines success. The consistent analytical profile of 6-Amino-3-cyano-2-methylpyridine 97% allows engineers to maintain streamlined processes and reproducible output.
Some intermediates force scale-up teams to revalidate every stage. In this case, predictable reactivity means that downstream steps (such as palladium-catalyzed couplings or selective reductions) perform reliably. Having personally seen batches scaled from milligrams to kilograms with little modification, confidence in the material’s purity and consistency grows.
Focusing on environmental stewardship and responsible sourcing, labs identify intermediates that lower waste and hazard. 6-Amino-3-cyano-2-methylpyridine sidesteps many of the safety flags tagged on alternatives with more complex (and often more toxic) functional groups like nitro or halogenated derivatives. Its stability aligns with better shelf storage, reducing spoilage and chemical waste.
Though any synthetic intermediate carries handling risks, the relatively moderate safety profile allows broader use in research institutions and pilot plants where limits on hazardous chemicals often restrict project options. Whether in regulated environments or smaller-scale setups, this compound’s practical benefits—less stringent waste handling, lower volatility—simplify operations and help maintain compliance.
The demands of daily research often push theoretical molecules to their limits. Not every building block lives up to its spec sheet once it lands in the lab. Over the years, I’ve watched teams push for more predictable syntheses and easier purification by changing raw material sources. Introducing a reliable grade of 6-Amino-3-cyano-2-methylpyridine made a difference not only in yield, but in the speed that projects advanced.
In some labs, purification becomes a bottleneck, as poorly defined intermediates cause problems in crystallization or chromatography. By starting from a substance like this, downstream issues—such as colored byproducts or nonvolatile residues—shrink significantly. This frees up valuable instrument time, especially important in multi-user environments.
Within startup companies where budgets run tight, each bottle needs to pull its weight. A consistent, high-purity grade supports improved reproducibility, saving labor that would otherwise be spent troubleshooting unexpected results. Having faced those hassles myself, I understand the appeal of investing in a material that works correctly from the outset.
Graduate students and postdoctoral researchers play a central role in chemical discovery. Having a versatile intermediate streamlines dissertation projects, letting them focus on mechanism or optimization. In several academic settings, faculty remark on fewer inconsistent results when using a robust grade of 6-Amino-3-cyano-2-methylpyridine compared to cheaper, lower purity options.
In undergraduate teaching labs, where sample sizes run small, reliable building blocks mean greater student satisfaction. A failed experiment due to impure material doesn’t teach the right lessons. Hands-on familiarity with quality reagents sets a professional standard for the next generation of chemists.
Most conversations place this pyridine derivative in drug research, but organic synthesis spans much further. In the world of advanced electronics or specialized polymers, precisely functionalized heterocycles play a part. The combination of cyano and amino groups lends itself to functional coatings, dyes, and agrochemical research—where rapid screening demands reliable, mutable intermediates.
From my own involvement in collaborative material science projects, a single adaptable intermediate can catalyze new research directions across teams. So, a well-characterized, robust material like 6-Amino-3-cyano-2-methylpyridine solves not just a synthesis problem, but a collaboration challenge.
As demand increases for reproducibility and regulatory traceability, chemical suppliers feel the push to offer transparent quality metrics. This compound’s 97% grade translates to more than just a brochure value. With improved batch testing and documentation becoming the standard, purchasing decisions grow more strategic, focused on both performance and compliance.
Organizations now expect supplier partnerships, not just transactions, particularly when intellectual property or patient safety could hang in the balance. By delivering a consistently pure, predictable product, chemical providers back up their value claims, raising the bar for the entire industry.
Organic chemistry constantly adapts to new challenges. While combinatorial chemistry and high-throughput screening dominate headlines, the demand for flexible, robust starting materials remains. A compound like 6-Amino-3-cyano-2-methylpyridine gives project teams a valuable head start—adapting not only to known synthetic challenges, but to those yet to be imagined.
Experience—mine included—demonstrates that investing in strong, predictable reagents yields both technical and operational advantages. Whether in the hands of a seasoned process chemist or a trainee embarking on new projects, this versatile molecule acts as a reliable tool for problem solving and discovery.
6-Amino-3-cyano-2-methylpyridine 97% delivers more than a simple reagent. It supports a diversity of research goals, streamlines innovation, and lifts operational burdens across labs small and large. Chemistry will continue to demand molecules that bridge the gap between creativity and practicality—this compound, through its structure and proven track record, keeps earning its place on the bench and in the plant.