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HS Code |
332752 |
| Chemicalname | 2-Methyl-5-Amino Pyridine |
| Casnumber | 1603-40-3 |
| Molecularformula | C6H8N2 |
| Molecularweight | 108.14 g/mol |
| Appearance | Light yellow to brown crystalline powder |
| Boilingpoint | 249-251°C |
| Meltingpoint | 53-56°C |
| Solubility | Soluble in water and organic solvents |
| Density | 1.12 g/cm³ |
| Purity | >98% |
| Storageconditions | Store in a cool, dry place away from direct sunlight |
| Synonyms | 5-Amino-2-methylpyridine, 2-Methylpyridin-5-amine |
| Flashpoint | 110°C |
| Ecnumber | 216-464-1 |
As an accredited 2-Methyl-5-Amino Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 100 grams of 2-Methyl-5-Amino Pyridine; labeled with hazard symbols, batch number, and handling instructions. |
| Container Loading (20′ FCL) | For 2-Methyl-5-Amino Pyridine, a 20′ FCL typically loads securely packaged drums or bags, maximizing space and ensuring safe transit. |
| Shipping | 2-Methyl-5-Amino Pyridine is shipped in tightly sealed containers under dry, cool conditions to prevent moisture absorption and degradation. Proper labeling and documentation ensure compliance with safety regulations. Packaging follows hazardous material guidelines, with cushioning to avoid breakage or leakage during transit. Personnel handling shipment must wear appropriate protective equipment. |
| Storage | 2-Methyl-5-Amino Pyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, incompatible substances, and direct sunlight. It is recommended to keep it away from strong oxidizing agents and acids. Use proper labeling and ensure access to spill containment measures and appropriate personal protective equipment when handling. |
| Shelf Life | 2-Methyl-5-Amino Pyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and well-sealed container. |
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Purity 99%: 2-Methyl-5-Amino Pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yield and minimal impurities in final products. Melting Point 99-102°C: 2-Methyl-5-Amino Pyridine with a melting point of 99-102°C is used in agrochemical formulations, where precise melting behavior facilitates efficient processing and incorporation. Molecular Weight 108.14 g/mol: 2-Methyl-5-Amino Pyridine at a molecular weight of 108.14 g/mol is used in dye manufacturing, where the defined mass allows for accurate stoichiometric calculations in colorant production. Stability Temperature up to 120°C: 2-Methyl-5-Amino Pyridine with stability up to 120°C is used in chemical catalyst research, where thermal stability enables consistent catalytic performance during high-temperature reactions. Particle Size <100 µm: 2-Methyl-5-Amino Pyridine with particle size less than 100 µm is used in specialty coatings, where fine particle distribution improves coating uniformity and surface finish. Assay ≥98%: 2-Methyl-5-Amino Pyridine with an assay of at least 98% is used in laboratory synthesis protocols, where reliable assay concentration supports reproducible experimental outcomes. Solubility in Ethanol: 2-Methyl-5-Amino Pyridine with solubility in ethanol is used in formulation sciences, where efficient solubility enables homogeneous mixture preparation for downstream processes. Moisture Content <0.5%: 2-Methyl-5-Amino Pyridine with moisture content below 0.5% is used in electronics material development, where low moisture enhances shelf life and prevents hydrolytic degradation. pH (1% Solution) 6.0-7.0: 2-Methyl-5-Amino Pyridine at pH 6.0-7.0 in a 1% solution is used in analytical chemistry applications, where neutral pH minimizes interference in sensitive assays. Storage Condition (Ambient, Dry): 2-Methyl-5-Amino Pyridine requiring ambient, dry storage condition is used in chemical inventory management, where proper storage maintains chemical integrity and stability over time. |
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Stepping into any chemicals lab or production line, you come across countless reagents, intermediates, and active ingredients. Every single one plays a role, but the fine distinctions often matter most. Take 2-Methyl-5-Amino Pyridine. It’s more than just another building block. This compound isn’t one most people outside pharmaceutical or fine chemical circles have heard about, but in the right hands, it helps unlock complex chemistry that makes a real difference. For those who navigate organic synthesis, breaking down what this compound brings to the table—beyond the data sheet—proves worthwhile.
2-Methyl-5-Amino Pyridine, often referred to as MAP or by its CAS number, stands out with its own structure: a six-membered aromatic ring with one nitrogen atom, a methyl group at the second position, and an amino group at the fifth. This arrangement influences its electronic and steric behavior and, as a result, the way it reacts. The standard product appears as an off-white to pale brown crystalline powder. Chemists who have worked hands-on with samples know to look for solid, free-flowing material free from any caking or obvious contamination.
Labs ask for chemical purities above 98 percent— sometimes up to 99 percent—for demanding research or large-scale production. Water content and heavy metal traces must remain low to avoid throwing off yields and risking equipment corrosion. When dealing with pyridines like 2-Methyl-5-Amino Pyridine, careful attention also goes to melting point (somewhere in the 80-90°C range is common), solubility (readily soluble in organic solvents, much less so in water), and the appearance of the powder. Not every batch stays the same, so consistent supply chains and trustworthy provenance matter.
One overlooked aspect involves the small-scale batch technologies used to make these pyridines. Old processes might use outdated reagents or leave behind hard-to-separate byproducts. Newer, cleaner methods—sometimes catalyzed by palladium or copper—can minimize impurities, giving greater peace of mind to downstream users. No single pathway is perfect, but reputable suppliers share third-party analytical data, letting chemists compare quality instead of flying blind.
The value of this compound doesn’t rest on giant market volumes or household-name recognition. It remains a specialty intermediate, essential for making other molecules that end up in medicines, dyes, and specialty polymers. It stands out for its reactivity profile; the amino group brings nucleophilicity, while the methyl at the 2-position changes the game by introducing a slight steric shield and shifting electron density. This dual impact helps chemists create connections and ring substitutions that plain 5-aminopyridine or even plain methylpyridines can’t easily manage.
Sitting face-to-face with a synthetic puzzle—say, a medicinal chemist wanting a pyridine ring decorated in just the right way—2-Methyl-5-Amino Pyridine gives more flexibility. The methyl group directs reactivity so that selective functionalization can happen at destinations otherwise prone to overreaction or unwanted cross-linking. The amino group participates in coupling reactions, amide bond formation, diazotization, or ring closure. In one research project, our team needed to introduce a diazo functionality in the 5-position while blocking ortho reactivity: MAP offered the best solution where alternatives either didn’t work or caused more headaches down the road.
Pharmaceutical players often search for ways to assemble active pharmaceutical ingredients faster and with fewer steps. Here, 2-Methyl-5-Amino Pyridine can act as a starting piece for blockbuster drugs or as an intermediate for antibiotics, antivirals, and anti-cancer compounds. Its unique substitution pattern enables efficient linking to moieties like sulfonamides, carboxylic acids, or reactive esters. With regulatory scrutiny ramping up, every production run counts. Using a well-characterized input like this one means less guesswork, smoother audits, and more consistent API performance.
It’s not limited to pharma. The pigment and dye industry uses pyridine derivatives for their color-brightening power and lightfastness. In that context, 2-Methyl-5-Amino Pyridine’s structure offers a combination of reactivity and stability, helping create new shades or boost performance in existing formulations. Material science researchers have picked up these compounds for making tailored polymers and resins with improved thermal stability or UV resistance. Time and again, the results depend on small tweaks in structure—a methyl here, an amino there—that set the product apart from the crowd.
Raw numbers only tell half the story. Two samples with the same nominal purity can yield wildly different results. Micro-impurities, residual solvents, or batch-to-batch variation put a wrench in reproducibility. My own experience tracking failed syntheses more than once traced the issue to differences in feedstock reagents. In the case of 2-Methyl-5-Amino Pyridine, a supplier able to guarantee transparent sourcing, fully documented analytical profiles, and robust logistics makes a real difference. Especially in pharma, downstream risk from out-of-spec products can exceed the cost of the raw material by orders of magnitude in lost time, regulatory delays, and missed opportunities.
Transparency around possible contaminants, residual metals, or even certificate of analysis (COA) authenticity stands as part of modern good manufacturing practice. Today’s buyers expect much more than a label and a sticker price. Some years ago, our procurement team ran into a batch of pyridine derivative from an unknown overseas factory—cheaper on paper, but plagued with high background on GC-MS analysis and inconsistent melting points. Fixing the damage cost more than double the original savings. “Buy cheap, pay twice” holds doubly true for specialty inputs like this.
Stacking 2-Methyl-5-Amino Pyridine up against its close relatives highlights differences that impact real-world projects. Plain 5-aminopyridine offers a similar nucleophilic group, but lacks the methyl’s subtle electronic effect. That shift might not sound dramatic, but the way reactions proceed—rates, selectivity, yields—can move enough to warrant switching intermediates. In some cases, methyl-substituted pyridines like 2-methylpyridine lack sufficient functionality to grab onto other groups or introduce the right complexity. It’s in this Goldilocks position, with one methyl and one amino group, that MAP carves out its own territory.
Run-of-the-mill pyridines used in agrochemicals or simple dye intermediates often don’t ask for such a specific substitution pattern. They serve as solvents, catalysts, or less challenging linkers. By contrast, applications needing highly selectivity, such as receptor modulators or targeted enzyme inhibitors, get a real edge with this compound. Planning a multi-step route to a chiral pharmaceutical or a custom dye, limiting side-products saves time and waste. Anyone who’s ever spent a week laboring through column purifications and NMR checks because of unwanted isomers can appreciate a building block that tilts the outcome toward the product you actually want.
Working with amine-substituted aromatics always calls for respect and planning. 2-Methyl-5-Amino Pyridine brings a low odor compared to some pyridines, but proper ventilation and gloves remain basic rules. Modern labs track environmental impact, seeking to minimize both exposure and downstream waste, particularly because pyridine rings can persist in water and soil if improperly handled. Safe transportation and storage—cool, dry, with minimal exposure to strong oxidizers—cut down on risks that escalate during scale-up or in busy warehouse conditions.
Regulatory frameworks around pyridine derivatives are strict, with compliance standards enforced across North America, Europe, and Asia-Pacific. Reach registration in Europe and EPA oversight in the U.S. both demand tight documentation—everything from route of synthesis to impurity profiles and shelf-life stability. Manufacturers that support transparent hazard communication and easy access to up-to-date safety information keep their customers ahead of regulatory headaches.
Breakthroughs in chemistry depend on every piece coming together. As a research chemist, I’ve seen how switching just one intermediate for a slightly different one can determine whether a reaction stalls out or sails through. For those designing next-generation APIs, energetic materials, or tailor-made dyes, 2-Methyl-5-Amino Pyridine unlocks possibilities that more generic reagents cannot. Its combination of reactivity, selectivity, and adaptability remains unmatched in certain contexts, especially for late-stage functional group introductions or challenging heterocycle chemistry.
Research teams working on novel pharmaceuticals gravitate toward scaffolds that allow quick tuning of biological properties without endless rounds of re-synthesis. A methyl group at the 2-position gives just enough bulk and electron release to shift binding properties, drug logP, or metabolic stability. On a personal note, it’s rewarding to see a carefully chosen intermediate save dozens of hours—and weeks of setback—down the line by smoothing the path to patentable endpoints.
Market volatility often flies under the radar for specialty chemicals like this. Sudden spikes in demand, caused by a wave of new patents or an uptick in custom manufacturing, can leave downstream users scrambling for reliable inventory. Building resilient supply chains means partnering with suppliers who don’t cut corners and who know how to forecast future needs in step with changing regulations and scientific trends. The last thing any R&D team wants is to halt a promising lead optimization campaign waiting on backordered intermediates.
Volatile input costs—especially for starting materials derived from petroleum or rare metals—can ripple through to pricing and delivery reliability. In my experience, vertical integration or long-term contracts produce more stable results, but not every buyer can command such arrangements. Open dialogue and frank sharing of analytical results and typical lead times protect both small startups and global producers from unwelcome surprises.
Increasing focus on sustainability drives real change in the specialty chemicals sector. As green chemistry moves from buzzword to business norm, even a pyridine derivative like 2-Methyl-5-Amino Pyridine sees scrutiny. Large-scale users ask about the carbon footprint of synthesis, energy use, and the fate of waste streams. Companies that document lifecycle analysis, avoid hazardous reagents, or certify renewable energy use for their processes create more value—not only for their customers, but for the environment as well.
For anyone preparing for audits under GMP or ISO standards, chain-of-custody data, validated batch records, and clear documentation on environmental and labor practices matter more than ever. Firsthand, I’ve watched customers move contracts away from suppliers who couldn’t meet evolving sustainability metrics, even after years of reliable performance. In markets that innovate quickly and change regulations regularly, adaptability in production sets leaders apart from followers.
2-Methyl-5-Amino Pyridine shows how a carefully chosen reagent can tip the scales for major breakthroughs in medicine, industry, and research. Reliable, high-purity MAP stands as a linchpin for many synthetic campaigns that need specific selectivity and efficiency. Its success depends not just on laboratory performance, but on transparency, traceability, and alignment with modern regulatory and sustainability standards. Chemists and procurement experts alike know that investing in quality, sustainability, and trust pays dividends—from bench-top discovery to commercial-scale production. The smallest differences in molecular structure and supply chain honesty trickle up to outcomes with broad impact. In specialty chemistry, as in so many other fields, details add up.