|
HS Code |
275691 |
| Cas Number | 35557-47-4 |
| Molecular Formula | C7H7N3 |
| Molecular Weight | 133.15 |
| Iupac Name | 2-amino-3-methyl-5-cyanopyridine |
| Appearance | Off-white to light yellow solid |
| Melting Point | 126-130°C |
| Solubility In Water | Slightly soluble |
| Boiling Point | No data available |
| Density | No data available |
| Smiles | CC1=C(N=CC(=C1)C#N)N |
| Inchi | InChI=1S/C7H7N3/c1-5-6(8)2-7(3-9)10-4-5/h2,4H,1H3,(H2,8,10) |
| Synonyms | 3-Methyl-5-cyano-2-pyridinamine |
| Storage Temperature | Store at room temperature |
| Pka | No data available |
| Refractive Index | No data available |
As an accredited 2-amino-3-methyl-5-cyanopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in a 100g amber glass bottle, the label reads: "2-amino-3-methyl-5-cyanopyridine, CAS 16197-02-1, For laboratory use only." |
| Container Loading (20′ FCL) | 20′ FCL container is used for secure, bulk transport of 2-amino-3-methyl-5-cyanopyridine, ensuring safety and minimal contamination. |
| Shipping | 2-Amino-3-methyl-5-cyanopyridine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must be clearly labeled and handled with appropriate safety precautions, complying with local regulations. Shipping should typically be by ground or air in accordance with relevant hazardous material guidelines, ensuring it remains upright and secure throughout transit. |
| Storage | **2-Amino-3-methyl-5-cyanopyridine** should be stored in a tightly sealed container, away from moisture and incompatible substances, preferably in a cool, dry, and well-ventilated area. Avoid exposure to direct sunlight and sources of ignition. Store at room temperature, and clearly label the container. Follow standard laboratory protocols for handling and storage of hazardous organic compounds. |
| Shelf Life | 2-Amino-3-methyl-5-cyanopyridine typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-amino-3-methyl-5-cyanopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and high product yield. Melting point 120°C: 2-amino-3-methyl-5-cyanopyridine with melting point 120°C is used in solid-state formulation processes, where thermal stability during processing is maintained. Particle size <50 μm: 2-amino-3-methyl-5-cyanopyridine with particle size less than 50 μm is used in fine chemical production, where enhanced reaction rates and homogeneity are achieved. Stability temperature up to 200°C: 2-amino-3-methyl-5-cyanopyridine with stability temperature up to 200°C is used in high-temperature organic synthesis, where compound integrity is preserved under rigorous conditions. Moisture content <0.5%: 2-amino-3-methyl-5-cyanopyridine with moisture content below 0.5% is used in moisture-sensitive reactions, where low water content prevents hydrolysis and decomposition. Assay ≥99%: 2-amino-3-methyl-5-cyanopyridine with assay ≥99% is used in reference standard preparation, where accuracy of quantification and analytical reproducibility are ensured. Solubility in ethanol 30 g/L: 2-amino-3-methyl-5-cyanopyridine with solubility in ethanol 30 g/L is used in solvent-based reactions, where efficient dissolution facilitates optimal process performance. Residual solvent content <0.1%: 2-amino-3-methyl-5-cyanopyridine with residual solvent content below 0.1% is used in active pharmaceutical ingredient manufacturing, where safety and compliance with regulatory limits are achieved. Chloride content <0.01%: 2-amino-3-methyl-5-cyanopyridine with chloride content less than 0.01% is used in electronic materials synthesis, where ultrasensitive applications require minimal ionic impurities. |
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Chemistry never stops surprising anyone who dives into its endless maze. Some molecules play a low-key role, quietly shifting the possibilities of what gets made in the world’s labs and factories. 2-amino-3-methyl-5-cyanopyridine stands among these, not well known outside specialist circles, but valuable to those who rely on precise chemical reactions for serious endeavors. It isn’t just another number in the giant library of organic compounds — it captures a blend of practical structure and reactivity that keeps it on the workbench of people chasing the next big breakthrough in drug synthesis or advanced materials.
Sometimes, a single atom move or swap in a molecule can change everything. Here, the core comes from a pyridine ring—a staple six-membered aromatic structure similar to benzene, just with one nitrogen in the mix. Its personality grows from its side groups: an amine at position 2, a methyl group at position 3, and that attention-grabbing cyano group at position 5. Each branch tweaks how the molecule interacts in the world. The amine brings in hydrogen bonding capacity, so the compound reacts with acids and other electrophiles in ways a plain pyridine can’t. Drop in a methyl group, and its hydrophobic edge helps with solubility tricks. The cyano group stands out as a building block for everything from pharmaceuticals to pigments, offering a handle for more chemistry down the road.
What keeps someone coming back to 2-amino-3-methyl-5-cyanopyridine is the way those modifications interact. Sticking the cyano at the 5-position in the ring doesn’t just fill a blank space; it directs electronic flow through the ring, tweaking the reactivity across the rest of the molecule. Scientists looking to build complex molecules care about those subtle changes. It becomes the difference between a reaction proceeding cleanly or failing completely. Anyone who has spent days troubleshooting a stubborn synthesis route knows that pain.
Most working chemists don’t obsess over decorations on a ring unless there’s a payoff. 2-amino-3-methyl-5-cyanopyridine finds its value at the intersection of flexibility and reliability. With its layered reactivity, it gets picked for roles in making pharmaceuticals, specialty dyes, and even some advanced polymers. In organic chemistry, the utility comes from the fact that this molecule allows several paths to branch off from it. For someone working in drug discovery, every functional group matters — polar amines help seeds for interactions with drug targets, while nitrile groups can be swapped for other bioactive features or left as a “handle” for tweaking a potential medicine’s solubility or metabolic fate.
Take the real-world challenges of synthesizing heterocyclic frameworks that mimic biological building blocks. Medicinal chemists always search for new versions of familiar rings, tuning physical properties or teasing out better biological activity. A compound like 2-amino-3-methyl-5-cyanopyridine fits this niche because it provides a versatile starting point, not just in theory but in daily, practical chemical transformations. Its methyl group nudges its solubility in organic solvents, making scale-up more straightforward in some cases, while the nitrogens—both in the ring and as an amine—invite hydrogen bonding or new derivatization routes. Products built from this starting material then wind up as key chemical intermediates or even as final pharmacophores in commercial drugs.
What changes between one source of 2-amino-3-methyl-5-cyanopyridine and another often isn’t visible by looking—it comes down to reliability and how well a batch fits the user’s end needs. In practice, scientists measure the true worth of a chemical product by purity. Impure samples can throw off entire batches of reactions, especially in sensitive pharmaceutical and materials applications. For this reason, high-purity offerings frequently get chosen for work in regulated industries. Most reputable suppliers make sure the final content of their material exceeds 98 or even 99 percent, with minimal residual solvents or byproducts.
Handling characteristics can differ from batch to batch, especially if particle size varies. Fine powders bring faster dissolution and sometimes higher surface reactivity, but they also tend to be dustier. Some labs prefer a slightly coarser fraction to reduce static and sticking, which anyone who has spilled a beaker or tried chasing loose powder across the bench will appreciate. Moisture content and storage stability come next, as any amine-bearing molecule can slowly degrade if left exposed, especially at higher temperatures or humidity. So suppliers who take care with airtight, light-blocking packaging earn trust—their product doesn’t change before chemists even get a chance to use it.
A question that comes up fast: why not use a cheaper or more commonly available pyridine derivative? There are plenty on the market. The answer ties back to the unique spread of reactive groups available in this molecule and the footprint they leave on any downstream chemistry. Plain pyridine can act as a base or a ligand, but it lacks functional groups for more complex branching. Shift to something like 2-amino-5-cyanopyridine, and the absence of the methyl group means less steric hindrance, which changes how other molecules approach and react. Swap the methyl from the 3-position to the 4-position, and the sensing of electrons and chemical buddies changes reliably.
Each variation matters in the outline of a synthetic strategy. Where there’s a need to introduce a branching point to a molecule or fine-tune solubility without sacrificing reactivity, 2-amino-3-methyl-5-cyanopyridine gets the job. In medicinal chemistry, the smallest tweaks can turn a weak lead candidate into a solid performer, altering how drugs bind their targets or survive in the body. Some reactions simply work better—yielding cleaner, faster, and more predictable results. For those running a busy lab with limited time and budget, little edges like that save months.
Curiosity, trial, and error always drive the progress in chemistry. Often, even experienced researchers get surprised by how a well-chosen starting material unlocks a previously stubborn synthesis step. In drug development, 2-amino-3-methyl-5-cyanopyridine serves as a springboard for classes of molecules intended to treat infections, cancers, or metabolic diseases. In the lab, building new heterocyclic compounds often depends on finding just the right balance between reactivity and stability—and this molecule straddles that line.
For industrial processes, the benefits scale up. Dyes, pigments, and specialty coatings sometimes require tailor-made intermediates that withstand tough reaction conditions or deliver precise color properties. Using 2-amino-3-methyl-5-cyanopyridine at the start helps maintain control. The cyano group’s presence can direct reaction flow, letting manufacturers achieve purer, more consistent end products. The amine often also opens doors to further customization, contributing to polymers with enhanced features or smart materials.
For those working at the bench, the difference between a reliable intermediate and a problematic one shows up in the details. Powders that pour cleanly, dissolve easily, and react as expected make workdays better. Less time spent purifying or troubleshooting means more time pushing forward with tricky syntheses or innovative projects. Between the possibilities opened up by careful design and the certainty of consistent quality, researchers appreciate suppliers committed to high standards. It’s not just about filling an order, but allowing a lab team to work with full confidence in their materials.
Getting that right means paying attention not just to purity certificates, but to how the compound behaves under real laboratory conditions. Even something basic like a compound’s smell or the feel of crystals between the fingers registers to someone with plenty of bench experience. In the case of 2-amino-3-methyl-5-cyanopyridine, the aromatic core might remind some chemists of countless hours spent with related heterocycles, but each side chain brings its own quirks. It takes practice to predict how an amine-nitrile-methyl pattern will alter reactivity, and the best chemists keep a careful log of their observations to pass along to future colleagues.
Working with advanced intermediates always brings up the question of safe handling and disposal. Environmental considerations matter more than ever. The amino and cyano groups in this compound both introduce concerns if released into the open environment. So responsible manufacturers prioritize clean production and waste minimization. Modern practices call for full traceability from raw material source to shipment, helping downstream users assure regulators and corporate boards alike that they are sourcing responsibly.
From a user’s perspective, the easy availability of solid batch testing and documentation helps avoid compliance headaches. In my own experience, projects move faster when such records are thorough, answering regulators before the question is even asked. Even small academic labs now take these concerns seriously: no one wants to risk research halting over improper chemical disposal. Proper handling instructions, clear stability data, and straightforward support go a long way toward keeping work on track and researchers safe.
Trust in a chemical supplier grows slowly and gets damaged fast. Within the world of custom intermediates, minor slips in quality can mean hundreds of thousands of dollars lost. Buyers depend on suppliers who don’t just batch out a product once but hold to strict standards over years. Reliable partners test well beyond surface requirements, checking for metal impurities, residual solvents, and cross-contaminants from earlier production runs. Those who remember frustrating delays tied to resubmissions or failed regulatory filings know the high value of a consistent product.
In practical terms, that means choosing a vendor who can offer certificates of analysis, trace test records, and open communication. Large-volume users, such as pharma and agrochemical companies, often push for supply contracts that include on-site audits and spot-checks of critical specifications. The best suppliers accommodate those needs, investing in process control and batch-to-batch reproducibility. When a molecule like 2-amino-3-methyl-5-cyanopyridine sits at the crossroads of high-stakes research and industrial application, nobody wants to gamble on unknowns.
As research keeps expanding into more complex molecular architectures—whether it’s for new drugs, advanced catalysts, or energy-related materials—the range of demand for molecules like this one keeps increasing. Supply chains show strain during global disruptions, and prices can spike unexpectedly, either from shortages of precursors or transportation bottlenecks. Some users now look for supply contracts that buffer against these shocks, relying on partnerships with more than one supplier or even in-house synthesis capacity to reduce risk.
Innovation continues on the production side, too. Greener synthesis routes that avoid toxic reagents or reduce byproducts catch the eye of larger buyers, who need to report sustainability metrics and meet tightening environmental standards. Practices like solvent recycling, process intensification, and real-time monitoring add value. Suppliers focusing on both the technical details and their long-term environmental record earn loyalty from informed customers. Not just the immediate utility, but the sustainability of the entire process matters to today’s buyers.
Community plays a bigger role than people think in the world of specialty chemicals. Alongside technical forums and published papers, a lot of knowledge moves by word of mouth. People share tips, shortcuts, and red flags with those who ask. Some labs even encourage open sharing of practical data on compound handling, storage, and real-world performance. It’s in the best interest of everyone to keep a conversation going about what products really deliver, and what aspects are wishful thinking on the part of a catalog copywriter.
Education never ends in chemistry. New generations of researchers take on legacy projects or blaze their own trail. Reliable access to transparent, up-to-date information on intermediates like 2-amino-3-methyl-5-cyanopyridine supports better science everywhere. Confidence grows when users share observations about things like shelf life, compatibility with a variety of solvents, or best storage practices. Over time, this feedback loop pushes the entire field forward, as both producers and users benefit from greater trust.
Procuring specialty chemicals should feel less like rolling the dice and more like choosing an established tool. For regular buyers, long-term supplier relationships add a layer of security, with the added benefit that good vendors listen to customer feedback on everything from packaging size to paperwork clarity. For those less familiar with the technical aspects, seeking out partners willing to explain their production methods and show third-party verifications gives peace of mind.
For larger organizations, implementing batch tracking and in-house testing limits the risk from unexpected quality issues. Those with the resources set up parallel supply agreements, cross-checking material from two or more vendors against a standard. These arrangements don’t just prevent downtime; they also push average standards up across the market. In an industry reliant on consistency and quality, a little extra effort upfront prevents costly disruptions later.
Professional associations, trade shows, and user networks drive information sharing that helps all parties understand market shifts. Platform tools that deliver robust quality data and regular updates make everyone’s task easier. Transparency about origins, testing protocols, and environmental footprint helps ensure that every shipment meets both regulatory demands and practical needs.
At the end of the day, 2-amino-3-methyl-5-cyanopyridine isn’t just a molecule with a long name—it’s a workhorse hidden behind cool innovations in science and technology. Whether serving as a chameleon building block in a drug pipeline, a critical intermediate in pigment manufacture, or simply as the piece that brings a synthetic puzzle together, it matters where it comes from, how it’s made, and who stands behind it. Chemistry’s progress depends as much on subtle choices in the lab as on the breakthroughs splashed across headlines. To those immersed in making things work, the search for reliable and smartly designed building blocks like this never really ends.