|
HS Code |
383818 |
| Chemicalname | 2-Amino-4-methylpyridine |
| Casnumber | 695-98-7 |
| Molecularformula | C6H8N2 |
| Molecularweight | 108.14 |
| Appearance | Light yellow to brown solid |
| Meltingpoint | 115-119°C |
| Boilingpoint | 251°C |
| Density | 1.113 g/cm3 |
| Solubilityinwater | Slightly soluble |
| Pka | 6.68 (for the amino group) |
| Flashpoint | 126°C |
| Synonyms | 4-Methyl-2-aminopyridine |
| Smiles | Cc1ccnc(N)c1 |
| Inchi | InChI=1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8) |
| Refractiveindex | 1.588 |
As an accredited 2-Amino-4-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Amino-4-methylpyridine, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | 2-Amino-4-methylpyridine is typically loaded in a 20′ FCL with securely sealed drums, ensuring safe, moisture-free, and stable transport. |
| Shipping | 2-Amino-4-methylpyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. Packages comply with chemical transport regulations, clearly labeled with hazard warnings if applicable. Standard shipping includes cushioning materials to prevent breakage, and temperature control may be used to ensure product stability during transit. Refer to MSDS for detailed handling instructions. |
| Storage | 2-Amino-4-methylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Properly label the storage area and use secondary containment to prevent accidental spills or leaks. Follow all relevant safety guidelines. |
| Shelf Life | 2-Amino-4-methylpyridine typically has a shelf life of 2-3 years when stored tightly sealed in a cool, dry place. |
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Purity 99%: 2-Amino-4-methylpyridine with high purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures minimal contamination and high yield of active compounds. Melting Point 61-65°C: 2-Amino-4-methylpyridine with a melting point of 61-65°C is used in organic synthesis reactions, where it allows for precise thermal processing and consistent reaction conditions. Molecular Weight 108.14 g/mol: 2-Amino-4-methylpyridine of molecular weight 108.14 g/mol is used in heterocyclic compound manufacturing, where it provides accurate stoichiometric calculations for efficient formulations. Particle Size < 100 µm: 2-Amino-4-methylpyridine with particle size less than 100 µm is used in fine chemical production, where it enhances dissolution rates and promotes homogeneous mixing. Stability Temperature up to 120°C: 2-Amino-4-methylpyridine stable up to 120°C is used in catalyst preparation, where it maintains chemical integrity under elevated reaction temperatures. Water Solubility 52 g/L at 20°C: 2-Amino-4-methylpyridine with water solubility of 52 g/L at 20°C is used in aqueous solution formulations, where it enables high-concentration preparations for efficient delivery. Low Moisture Content < 0.5%: 2-Amino-4-methylpyridine with low moisture content below 0.5% is used in electronic chemical manufacturing, where it prevents unwanted hydrolysis and maintains product stability. High Chemical Stability: 2-Amino-4-methylpyridine with high chemical stability is used in agrochemical synthesis, where it allows storage and transport without significant degradation. |
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In the landscape of specialty chemicals, 2-Amino-4-methylpyridine stands out thanks to its practical advantages and its straightforward chemistry. Chemists working in pharmaceutical, agrochemical, or fine chemical labs often need reliable compounds that bring predictable results. This molecule—a pyridine ring with a methyl at the 4-position and an amino at the 2-position—offers that kind of reliability for various synthetic goals.
Those who spend their days with glassware and stirring rods know just how much small structural tweaks can transform reactivity. Methylation at pyridine’s 4-position doesn’t just change the look of the molecule; it adds a degree of selectivity in catalytic processes or coupling reactions. The amine function opens up a range of possibilities for derivatization, making this compound a useful intermediate for chemists shaping complex molecules.
Most chemists working with 2-Amino-4-methylpyridine count on a consistent melting point just over 80°C, pointing to dependable purity batch to batch. It presents as a pale solid, and its modest solubility in water means it’s well suited for extraction-phase techniques and nonaqueous organic reactions. People familiar with pyridine derivatives often appreciate how the combination of amino and methyl groups here plays into reactions—they steer the molecule toward selective alkylations, reductive aminations, and other transformations that might frustrate efforts with plain pyridine or less substituted cousins.
Standing in front of a shelf filled with heterocycles, the experienced chemist picks 2-Amino-4-methylpyridine not because it’s new, but because it’s proven. Compared to 2-aminopyridine, its methyl group changes the electronic properties, thus altering how it behaves under certain catalytic conditions. This difference can mean cleaner reactions or greater selectivity—a clear win in fast-paced research or manufacturing. On the other hand, 4-methylpyridine won’t give the same reactivity, since it’s missing the amine’s capabilities for nucleophilic attack or coordination to metals.
People who design synthesis routes for pharmaceutical intermediates usually can’t afford delays from poorly characterized side reactions. That’s where smart structure selection shines. In a field where regulatory scrutiny and production scale-up matter, using a compound like 2-Amino-4-methylpyridine cuts down on surprises. The amine and methyl group, placed just so, help skip unnecessary protection/deprotection steps and offer a direct handle for building up molecular complexity.
Many years at the bench have taught me that textbooks only get you halfway. Real-world results depend on nuances such as how easily a compound handles purification, how stable it feels to air and light, and whether suppliers can deliver consistent product. With 2-Amino-4-methylpyridine, colleagues and I have noticed how its balance between hydrophilicity and hydrophobicity makes solvent choice more forgiving. We’ve run Suzuki couplings and amide formations where its amine group played well with a variety of activating agents, avoiding sticky byproducts or decomposition that can so often halt a project.
In teaching settings, students regularly see just how subtle changes—like a methyl group—dictate the outcome of what seem like ‘textbook’ reactions. With this compound, yields climb, pure fractions appear more quickly, and the workflow simply goes smoother. That brings peace of mind in environments where every hour at the bench translates to real project progress or cost control in industry.
Across pharmaceutical firms, the trend in recent years has come to favor intermediates with both specificity and reliability. 2-Amino-4-methylpyridine fits that bill. Medicinal chemists use it to access pyridine-based scaffolds—structures found in drugs aimed at everything from neurological disorders to anti-cancer therapies. Industrial chemists, working at the kilogram scale, value how its chemical stability reduces concerns over shipment or long-term storage.
Agrochemical companies also gravitate toward heterocycles, since minor tweaks in a molecule’s shape can create new modes of biological action. Here, 2-Amino-4-methylpyridine offers a foundation for tailored pesticides or herbicides, putting scientists a step ahead in regulatory compliance. That translates to a more agile approach to product registration and market approval.
Manufacturers dealing with daily production headaches recognize 2-Amino-4-methylpyridine for its lack of volatility and ease of handling. Unlike some low-molecular-weight amines, it poses less risk for inhalation exposure, providing relief for those running fume hoods every day. Purity control stays straightforward, with clear HPLC and NMR signatures, so QC labs save time without sacrificing diligence.
Growing attention to green chemistry and workplace safety has changed how facilities view basic building blocks. Compounds like 2-Amino-4-methylpyridine offer compatibility with less hazardous solvents and milder reaction conditions, which in turn help companies meet both emissions standards and staff health targets. Compared to more volatile pyridines or halogenated derivatives, risks associated with flammability and chronic exposure noticeably drop. This uptick in workplace satisfaction shouldn’t go unrecognized, as any health and safety professional will tell you.
Though any compound with an amine group deserves care, experienced safety officers note that routine procedures—wearing gloves, using fume extraction, and labeling containers—cover most daily risks. Waste disposal for pyridine derivatives remains a point of focus, but established protocols and regular staff training keep surprises rare.
Quality matters at every level, from research vials up to drums for scale-up. 2-Amino-4-methylpyridine typically arrives as a free-flowing powder, packaged to prevent moisture intrusion. Analytical chemists appreciate how its signals in NMR appear sharp and definitive, giving confidence that what’s in the bottle matches the label. Those in charge of procurement tend to stick with sources that document trace impurities or residual solvents. Several labs I’ve worked in no longer tolerate vague COAs—clarity in each shipment’s specs creates smoother handoffs across the team.
Pyridine chemistry offers a forest of possibilities, but only a few options deliver repeated success both at the bench and on the production line. For example, unsubstituted aminopyridine comes up in classic reactions but runs into solubility challenges and sometimes introduces competing side products. Other substituted pyridines might fare better under certain conditions, but the pairing of amino and methyl groups in 2-Amino-4-methylpyridine changes how catalysts or bases activate it. That leads to higher selectivity and fewer clean-up steps downstream.
Researchers tasked with developing new active pharmaceutical ingredients often evaluate dozens of heterocyclic cores. 2-Amino-4-methylpyridine wins favor here because its physical properties simplify downstream purification: it behaves predictably in chromatography and resists oxidation under ambient conditions. This stability means it can be stored longer without worrying about decomposition.
In fast-paced industrial settings, losing a day to impure intermediates or hard-to-remove byproducts triggers budget overruns and missed deadlines. Every reliability boost in a key intermediate like this one echoes across supply chains and project calendars. I’ve seen scale-ups falter using less stable analogs—losing active amine content to air oxidation or finding that a slightly different ring substitution blocks a crucial reaction downstream. These details, learned through years of hands-on work, make all the difference.
Anyone using 2-Amino-4-methylpyridine relies on predictable performance in the face of real-world variables: changing solvents, metal catalysts with batch-to-batch quirks, or process upsets in continuous production. The truth is, not every process will go smoothly out of the gate. Sometimes, recrystallization parameters call for adjustment as humidity or temperature fluctuates. Those who plan for these minor disruptions by running parallel trials and monitoring reaction progress enjoy a smoother scale-up.
In my own projects, collaboration between chemists and production engineers always improves outcomes. A clear handover—sharing data on melting points, spectral signatures, and impurity thresholds—reduces risk for both sides. Teams that include both lab scientists and process operators speed up development cycles. Chemists may find it useful to document the solubility and stability of 2-Amino-4-methylpyridine in solvents they actually use, rather than relying only on literature values or supplier data. These real-world notes often lead to nuanced tweaks in process design, trimming costs and reducing material waste.
Some facilities switch suppliers due to changes in price or logistics. Before swapping, it’s wise to run side-by-side trials using samples from both sources, comparing not just stated purity but also byproduct profiles. Supplies that seem similar can show up as clear differences on analytical runs, especially at a larger scale. Investing time in preliminary comparisons reduces costly troubleshooting down the line.
Those of us who work with chemicals year in and year out know that fine-tuning reactions never ends. Even a reliable intermediate like 2-Amino-4-methylpyridine benefits from constant scrutiny. Many teams now maintain ‘living’ process dossiers—updating protocols as fresh data arrives, so every discovery feeds back into production. This culture of transparency and documentation strengthens quality across the board.
Open forums, where chemists share both their successes and hard lessons from the bench, play a role in improving outcomes. Industry events and collaboration networks help connect users of 2-Amino-4-methylpyridine, driving new approaches for controlling exotherms, isolating products, or improving yields. Working together, users often identify subtle trends—like a new solvent blend improving batch purity or a change in catalyst source nudging yields slightly higher.
Sometimes, project leaders develop relationships with suppliers beyond transactional purchasing. By giving feedback on batch characteristics—aroma, color, or impurity levels—they encourage suppliers to tighten their own quality controls. This feedback loop results in better supply reliability and lowers the chance of last-minute surprises just before a big campaign.
What sets effective chemical supply apart is a blend of technical expertise, real-world pragmatism, and an open channel for feedback. In my experience, organizations who commit to cross-disciplinary training—pairing synthetic chemists with analytical specialists and process engineers—get the most out of intermediates like 2-Amino-4-methylpyridine. Teams who know how to adjust column conditions or troubleshoot solubility jumps can pivot quickly if something changes in their supply chain.
On the research side, students and newcomers pick up skills faster when mentors point out not just ‘what works’ but ‘why it works.’ For example, talking through how the methyl at position four and the amine at position two affect reaction rates makes it easier to anticipate issues, rather than react to them late. That translates into smarter workflows and less wasted material.
Specialty chemical intermediates such as 2-Amino-4-methylpyridine don’t usually grab headlines, but their impact runs deep. Countless new medicines, crop protection agents, and dyes trace their family trees back to a choice made at the early synthesis stage. The right heterocycle, used as a building block, helps researchers push the boundaries of what’s possible in drug discovery and beyond.
The push for sustainability further underscores the value of intermediates that tolerate greener solvents or milder conditions. Across projects I’ve observed, teams working with robust compounds cut down both hazardous waste and utility consumption—a win for both the budget and the environment. While regulatory pressures may get the attention, daily working conditions for staff improve too: less time spent fighting unpredictable byproducts frees up hours for more creative and productive work.
A dependable product, used for many years in many labs, is more than just a chemical. It represents the cumulative work of everyone in the supply chain—from those refining the synthetic route, to quality assurance staff checking each batch, to logistics planners ensuring fast, safe shipping. That human effort shows up in the bottle and in every successful reaction it fuels.
From the perspective of a chemist who has run reactions with dozens of pyridine derivatives, 2-Amino-4-methylpyridine stands out for a clear set of reasons. Its unique pairing of amino and methyl groups unlocks selectivity and efficiency that’s tough to match with bare pyridine or other substitutions. It’s easier to work with—less odor, less volatility, and a physical form that lends itself to measured scooping or weighing. At the analytical bench, results remain clear and consistent, a welcome change from some less stable analogs.
Scaling up work with this compound doesn’t bring hidden issues. Rather, it fits naturally in the stepwise build-up of pharmaceuticals, crop protectants, and performance materials. Years of use in research, teaching, and production have cemented its reputation as a ‘go-to’ intermediate—one that helps projects run smoothly from the lab to the plant.
For teams considering adding 2-Amino-4-methylpyridine to their workflow, gathering data upfront always pays off. Run small-scale test reactions, document reactivity with your exact catalysts, and compare analytical outputs to published data or supplier info. Communicate early with both internal teams and external suppliers—it builds both efficiency and trust. Finally, treat each experiment as a source of feedback: unexpected results aren’t just setbacks, but stepping stones toward more robust methods.
In sum, years of hands-on chemistry have shown me that dependable building blocks make all the difference in both project success and staff morale. 2-Amino-4-methylpyridine is one of those compounds that delivers—balancing reactivity, stability, and usability for the modern scientist in search of progress.