|
HS Code |
858035 |
| Name | 2-Amino-3-methylpyridine |
| Cas Number | 13360-65-1 |
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.14 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 76-79 °C |
| Boiling Point | 255 °C |
| Density | 1.10 g/cm³ |
| Solubility In Water | Moderately soluble |
| Flash Point | 110 °C |
| Pka | 6.57 (for amino group) |
| Refractive Index | 1.595 |
| Purity | Typically ≥98% |
As an accredited 2-Amino-3-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-3-methylpyridine is supplied in a 100g amber glass bottle, featuring a screw cap and clear safety labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 16 metric tons net, packed in 200 kg HDPE drums, securely palletized for safe international shipment. |
| Shipping | 2-Amino-3-methylpyridine is shipped in tightly sealed containers, compliant with chemical safety regulations. It is packed to prevent leaks and protected from moisture and incompatible substances. Appropriate hazard labeling and documentation are included. Shipping follows guidelines for transporting hazardous chemicals to ensure safe handling during transit and delivery. |
| Storage | 2-Amino-3-methylpyridine should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from light and moisture. Use in a designated chemical storage cabinet if available. Proper labeling and secondary containment are recommended to prevent spills and accidental exposure. |
| Shelf Life | 2-Amino-3-methylpyridine typically has a shelf life of 2–3 years when stored tightly sealed, away from light and moisture. |
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Purity 99%: 2-Amino-3-methylpyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity final products. Melting Point 106°C: 2-Amino-3-methylpyridine with a melting point of 106°C is used in heterocyclic compound manufacture, where it provides thermal stability during reaction processing. Molecular Weight 108.14 g/mol: 2-Amino-3-methylpyridine with molecular weight 108.14 g/mol is used in catalyst design for organic synthesis, where precise stoichiometry leads to reproducible catalytic activity. Particle Size <20 μm: 2-Amino-3-methylpyridine with particle size less than 20 μm is used in fine chemical formulation, where rapid dissolution and uniform dispersion are achieved. Stability Temperature up to 150°C: 2-Amino-3-methylpyridine stable up to 150°C is used in high-temperature reaction environments, where chemical integrity is maintained throughout processing. |
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Ask a roomful of chemists about analytical tools, and you'll get a dozen different answers about what's essential in their lab. Sprinkle in questions about building blocks for complex molecules, and talk often pivots to the much-lauded world of heterocycles. Somewhere in between, you’ll find 2-Amino-3-methylpyridine. It might not have the flashiest name in the business, nor does it carry the dramatic tales of more notorious lab chemicals, but it plays a steady, reliable, nearly invisible role in pushing scientific discovery forward.
During my own years in pharmaceutical research, I saw how often projects quietly relied on this molecule. It never gets a press release, but 2-Amino-3-methylpyridine frequently forms key pieces of much bigger puzzles. Its versatility outpaces expectations for a modest six-membered ring decorated with an amino and a methyl group.
2-Amino-3-methylpyridine stands out because of its ring structure: you've got a pyridine backbone—a nitrogen in a six-ring carbon chain. Toss in an amino group at the second carbon and a methyl on the third, and you arrive at a layout that both simplifies and supercharges chemical transformations. That kind of structure offers opportunities for selective reactions, not only because chemists know exactly where the functional groups sit, but because the electronic properties of the molecule steer those reactions in predictable and reliable ways.
From a user’s perspective, this predictability matters. In organic synthesis, confidence in a starting material saves weeks or even months, which adds up over the course of long, complicated projects. You don’t want to second-guess your reagents, and 2-Amino-3-methylpyridine has built a track record for consistency in both academic and industrial settings.
What does someone reaching for this substance in their supply cabinet actually care about? Here’s where performance and practicality merge. High-purity 2-Amino-3-methylpyridine usually appears as an off-white to pale yellow solid. The melting point tends to fall comfortably within a range (often cited as about 85-89°C), which lets you avoid surprises on the hotplate. Most labs store it at room temperature without headaches about rapid degradation. Solubility in common organic solvents like ethanol or acetone means fewer struggles with bottlenecking reactions.
Unlike more sensitive amines, this one also doesn’t throw off noxious clouds under normal handling. Sometimes the strongest praise for a chemical is that it doesn’t cause unnecessary trouble. From the shelf to the scale to the flask, it delivers on repeat performance with minimal fuss. You won’t find yourself wasting time trying to coax it into solution or worrying about special storage.
People often talk about chemistry as if it floats above the world, a realm only for academics. 2-Amino-3-methylpyridine says otherwise. In pharma development, it acts as a solid partner in the synthesis of pyridine-based drugs. Drop it into a medicinal chemistry workflow and you unlock routes to key intermediates for antihistamines, antibiotics, and even newer experimental treatments.
Moving beyond medicine, agrochemical research banks on this molecule’s unassuming utility. Certain fungicides and plant growth regulators trace their roots back to substituted pyridines. Subtle tweaks at the amino or methyl position frequently change biological activity, so having a reliable scaffold tops the wish list for chemists hunting for better yields or safer compounds.
In specialty chemicals, 2-Amino-3-methylpyridine steps in as a building block for dyes or ligands used in material science. Even if end users never hear its name, value ripples out through coatings, electronic materials, or optical brighteners. It never yells for attention, but quietly enables innovation.
It’s easy to lump aromatic amines together, staring at formulae that blur into each other. Here’s the catch: tiny differences can have big consequences in the real world. Swap the methyl position to another carbon, or move the amino up the ring, and you shift steric hindrance or electronic influence. Such fine control translates into sharper selectivity in advanced synthesis. That edge matters for producing single-target drugs or minimizing side products.
You can’t overlook how 2-Amino-3-methylpyridine stacks up against its siblings like 2-Aminopyridine or 3-Aminopyridine. Lose or move the methyl group, and reactivity patterns shift. These subtle changes open or close doors in downstream chemistry, sometimes making progress possible, other times bottlenecking entire projects. That’s not a lesson out of theory books—development teams learn it the hard way if the wrong isomer clogs up synthesis or wrecks a biological assay.
From my own experience, selecting the right methylpyridine isomer often meant the difference between a reaction going like clockwork or devolving into a mess of tars and intractable byproducts. With 2-Amino-3-methylpyridine, you see fewer surprises, more clean conversions, and far less frustration at the bench.
In research settings, purity rarely stays a theoretical concern. Impurities skew results, gum up purification steps, or introduce unknowns into sensitive tests. Quality control for 2-Amino-3-methylpyridine sits at the top of mind, especially because its applications can lead to human therapeutics. Labs sourcing material with high assay results and minimal trace solvents find that experiments flow more smoothly, saving both time and headaches.
Documented provenance and regular batch testing add levels of security. You don’t want to lose weeks of screening because a reagent didn’t meet expected standards. In the best setups, labs build trust with reputable suppliers who share certificates of analysis and encourage transparency.
Even the safest-seeming aromatic amines deserve smart handling. While 2-Amino-3-methylpyridine doesn’t jump off a shelf as a notorious hazard, it still qualifies as a chemical worth respecting. You want gloves, goggles, and fume hoods as part of normal procedure. Repeated exposure, even at low levels, can create problems you don’t want down the line. In the places I’ve worked, a little mindfulness meant no unnecessary trips to the on-site medical staff.
Disposal protocols matter, too. No need to cut corners just because a chemical flies under the radar. Responsible collection and disposal protect not just workers, but the environment that supports every branch of science. I’ve seen more than one up-and-coming chemist internalize this, learning that small acts of care now pay off over lifetimes.
Accessibility takes on practical weight with research tools. A reagent as useful as 2-Amino-3-methylpyridine shouldn't be hard to source or wildly unpredictable in availability. In my early years juggling tight project timelines, nothing grated more than hearing the words “back-ordered” on a bottle needed for this week’s experiment. Robust chemical supply chains mean fewer stops and starts, smoother research trajectories, and ultimately faster answers for people waiting at the end of the discovery pipeline.
With solid partnerships among distributors and chemical producers, most labs can count on having this compound on hand. Bulk packaging options help scale up from milligram screens to kilogram batches without a hitch. Careful attention to shelf life and storage, from supplier warehouse to lab shelf, rounds out the circle of reliability. Everyone in the chain benefits when promises made on a spec sheet show up, bottle after bottle, in the real world.
Today’s drug and material pipelines grow longer and more complex by the year. Predictable, reliable reagents like 2-Amino-3-methylpyridine serve as quiet heroes in this arms race against disease and technological stagnation. While innovation often grabs headlines, the true story includes every workhorse molecule that streamlines discovery under the radar.
In a world that prizes green chemistry and efficiency, small molecules with robust safety profiles and low waste footprints make a difference. More research groups now factor in the ease of purification and downstream impact when making procurement decisions. That mindset, tuned toward both cost and conscience, promises a future where science doesn’t just work fast, it works clean. 2-Amino-3-methylpyridine shines in these settings because its straightforward use history encourages good lab practice and informed purchasing.
In the big picture, moving research from bench to bedside needs both bright ideas and steady hands. Substances like 2-Amino-3-methylpyridine form the backbone, allowing bold leaps without derailing daily progress. Regulatory bodies and funding agencies now ask deeper questions about starting materials, scrutinizing documentation and supply chains for everything downstream. Transparency and traceability, built around trusted molecules, become non-negotiables.
Students coming up through STEM programs benefit by learning early how reliability at the chemical level ripples outward into the reproducibility of results. Years ago, I worked alongside teams that drilled these lessons into every study design—no amount of brilliant thinking could rescue a failed project tied to an unreliable chemical supply. Investment in both people and products underpins real progress, not just for isolated labs but for society as a whole. Reliable reagents make academic and industrial research safer, bolder, and more honest.
Every scientist carries stories about breakthrough moments born from surprising places. Reagents like 2-Amino-3-methylpyridine don’t often star in those tales, but ask about the behind-the-scenes, and you realize their quiet ubiquity. They free up cognitive space for creativity. Instead of worrying about whether an amine will throw a reaction sideways, you can focus on exploring new pathways, chasing tough targets, or answering big questions that may shape entire fields.
It’s easy to overlook the “boring” chemicals until they’re missing, contaminated, or out of stock. Consistency over years builds reputations—of labs, companies, and the very molecules they rely on. Honest, transparent sourcing, straightforward safety guidance, and ongoing testing ensure that trust is earned, not assumed.
For anyone navigating the world of chemical research, the lesson is clear: don’t cut corners on building blocks. Choose reliable suppliers with a documented commitment to quality. Watch for signs of mishandling, such as clumping or odd discoloration, and ask questions if any batch doesn’t meet the mark. Chemists and procurement teams do well to involve each other early in project planning to avoid unnecessary holdups.
Shared experience counts, too. Peer networks often flag good or bad sources long before industry news catches up. Don’t hesitate to check forums, professional societies, or old colleagues for insights about how different suppliers perform over time. In the past, a quick phone call to a peer saved projects on more than one occasion, keeping research on track and costs under control.
With science moving into ever more ambitious territory, access to well-characterized, trustworthy compounds becomes part of the shared groundwork for global progress. Whether for advancing medicine, agriculture, or new materials, making smart choices about reagents like 2-Amino-3-methylpyridine lays the foundation for results that stand up to scrutiny and drive meaningful change. Small decisions about individual chemicals ripple out through whole systems, from the bench to the world at large.
So while 2-Amino-3-methylpyridine may not make the covers of chemistry journals, it underpins the steady, real work of innovation. Its continued presence supports not only professional standards—accuracy, safety, responsibility—but also collective growth. Every experiment that starts from a solid base like this gains a better shot at success, for teams and for the world waiting just beyond the walls of the lab.