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HS Code |
417572 |
| Chemical Name | 2-Amino-3-Ethyl-6-Methylpyridine |
| Molecular Formula | C8H12N2 |
| Molar Mass | 136.19 g/mol |
| Cas Number | 6290-10-4 |
| Appearance | Colorless to pale yellow liquid |
| Density | 0.985 g/cm3 |
| Boiling Point | 210-213 °C |
| Solubility In Water | Slightly soluble |
| Flash Point | 93 °C |
| Refractive Index | 1.537 (at 20 °C) |
| Smiles | CCc1c(C)nc(N)cc1 |
| Inchi | InChI=1S/C8H12N2/c1-3-7-6(2)4-5-10-8(7)9/h4-5H,3,9H2,1-2H3 |
As an accredited 2-Amino-3-Ethyl-6-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, labeled "2-Amino-3-Ethyl-6-Methylpyridine, 100g," includes hazard symbols and safety information. |
| Shipping | **Shipping for 2-Amino-3-Ethyl-6-Methylpyridine:** This chemical should be shipped in tightly sealed containers under standard conditions. Protect from moisture, heat, and direct sunlight during transit. Ensure compliance with regional chemical transport regulations. Handle with appropriate labeling and safety documentation. Avoid shipping with incompatible substances or strong oxidizers to prevent hazardous reactions. |
| Storage | Store 2-Amino-3-Ethyl-6-Methylpyridine in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Label the container appropriately and keep it away from food, drink, and animal feed. Use secondary containment to prevent accidental spillage. |
Applications of 2-Amino-3-Ethyl-6-Methylpyridine in Industrial ManufacturingAs a specialized manufacturer of 2-Amino-3-Ethyl-6-Methylpyridine, we provide technical-grade material serving industrial synthesis routes for advanced intermediates. Below, we present verified downstream application fields based on real-world formulation protocols and compliance systems across the pharmaceutical and agrochemical industries. Each scenario details established usage standards, dosage principles, manufacturing points of addition, and the types of end products processed by our international partners. 1. API Intermediate Synthesis: Third-Generation Cephalosporin AntibioticsOur pyridine derivative serves as a building block in the fine chemical phase of active pharmaceutical ingredient (API) manufacturing, particularly for third-generation cephalosporin antibiotics production. Integrators use it for constructing the 7-ACA nucleus substituents, with strict traceability and impurity control specified by regulatory agencies. The purity grade and impurity profile critically determine downstream fermentation and product batch reproducibility, especially under current GMP guidelines. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate: Pyridine-Based Herbicide SynthesisKey agrochemical manufacturers rely on our material for the synthesis of specialty pyridine herbicides that target post-emergence grasses and broadleaf weeds. Its ethyl- and methyl-substituted architecture provides a precursor scaffold for downstream chlorination and ring functionalization. Product stewardship emphasizes compliance with international pesticide regulations and rigorous batch-to-batch physical property inspection. Industry compliance standards
Typical usage ratio
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Final product types
3. Fine Chemical Intermediate: Dye and Pigment ManufacturingThe compound acts as a targeted intermediate for synthesizing specialty azo and anthraquinone dyes used in textile coloration, inks, and coatings. Its electron-rich pyridine ring modulates chromophore properties, and its alkyl substitution patterns lead to high-yield coupling reactions. Quality assurance requires close control of color index, residual solvent, and byproduct profiles in accordance with end-use colorant standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Pharmaceutical Intermediate: Antiviral Drug Precursor2-Amino-3-Ethyl-6-Methylpyridine is incorporated as a precursor for certain antiviral nucleoside analogues, enabling high-selectivity transformations in the nucleoside modification process. Pharmaceutical processors value its low residual catalyst content, supporting compliance with active ingredient monographs and pharmaceutical GMP traceability protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
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At the manufacturing facility where we produce 2-Amino-3-Ethyl-6-Methylpyridine, people and machinery work in tandem around the clock. This isn’t just about shipping another drum of fine chemical—our operation brings together decades of industry experience, technical discipline, and a tight feedback loop with customers who need their intermediates to function, not just exist. Anyone who has handled this molecule in a lab or a large-scale reactor knows that specifics matter—a lot. You can’t downplay the subtle interactions with solvents, or the influence of trace impurities on downstream synthesis. Every stage of our process, from raw material vetting to final quality release, revolves around ensuring 2-Amino-3-Ethyl-6-Methylpyridine reaches customers ready to perform in synthesis pipelines without surprise deviations.
We’ve watched the market bounce around for years, seeing new traders pop up and vanish, but veterans know that reliability comes only from hands-on control over actual production lines. Our model covers the entire journey of 2-Amino-3-Ethyl-6-Methylpyridine on-site. The specifications we adhere to aren’t a patchwork of third-party standards—they are born from repeated lab scrutiny, process scale-ups, and real feedback whenever a chemist somewhere faces a clog or yield drop in their downstream step. That means robust batch verification, close monitoring of purity (typically 98% minimum by HPLC, with trace isomer and solvent content tightly tracked), and a no-shortcuts approach to packaging and storage.
From a manufacturer’s chair, numbers on a spec sheet take on new life. The difference between 96% and 99% isn’t academic—just ask anyone troubleshooting side reactions in complex heterocycle syntheses or scaling a pharmaceutical intermediate. We focus on delivering a crystalline or fine powder form, pale yellow to light brown, with moisture levels kept below 0.5%. In practice, batches consistently hit under 0.2% moisture, even after extended transit. Any sight of caking or off-spec color triggers a full re-examination. Some competitors blend lots to mask substandard product; we segregate and reprocess any batch falling short. Our certificates don’t just come from routine checks, but from reproducible, transparent analysis, run in-house rather than farmed out.
Most of our clients use 2-Amino-3-Ethyl-6-Methylpyridine as a building block for pharmaceutical and agrochemical synthesis. This compound serves as a backbone in the assembly of a wide array of active ingredients, especially where unique electron-donating and structural properties are required from the pyridine ring. It stands apart from generic pyridines by the specific pattern of electron-rich and sterically-influenced groups—ethyl and methyl—in defined positions. These groups promote desirable reactivity, making subsequent coupling, amide formation, or cyclization steps both more selective and more predictable. Across years of supplying kilo to multi-ton quantities, we’ve heard from formulation leads struggling with competitor samples that gummed up columns or led to ambiguous spectral peaks during process validation. Our batches stand up to repeated analytical cross-checks and behave consistently in multi-step syntheses.
One recurring question from process engineers touches on temperature sensitivity, stability in storage, and risk of degradation. Decades working with this compound reveal a broad stability window under dry, sealed conditions; degradation paths often trace back to preventable storage mishaps or poor packaging. By using tight-seal laminated liners or HDPE barrels with desiccant pouches, the risk of hydrolysis and airborne contamination drops dramatically. Operators at our plant routinely monitor for anything outside spec, which builds customer trust—no surprises when batches sit idle in customs or during seasonal transit delays. Freight teams also receive hands-on training on handling this and similar compounds, strengthening the supply chain beyond paperwork and logistics emails.
You can buy chemicals from countless places, but direct sourcing from the manufacturer saves time and eliminates doubt. Distributor and reseller inventories turn over slowly, and spot buys often saddle customers with unknown storage histories or mixed-origin material. As manufacturers, we track every step, from the molecular structure all the way to tamper-evident seals. If a pharmacist or synthetic chemist picks up a sample, that traceability matters—a contaminant at the ppm level can throw off bioactivity screens or even land your process batch in the reject pile. The structure:
2-Amino-3-Ethyl-6-Methylpyridine features an amino group at the second position, ethyl at the third, and methyl at the sixth, each influencing regioselectivity and reactivity in the hands of practical synthetic chemists. Some buyers ask whether cheaper isomers or alternate substitutions can ‘do the job’—hard-won production feedback says otherwise. A mismatch in even one position often leads to wasted cycles and lost yields further downstream.
It’s easy to lump lateral pyridine derivatives together, but the fine details shape outcomes.
Other methyl-ethyl pyridines or amino-pyridines might carry groups at alternate positions, but changing just one position radically alters the way coupling reagents or catalysts interact. Unintended isomers won’t mimic the target’s polarity, making them less reactive or introducing byproducts you just can’t filter away. In our plant, reaction vessels and purification systems are adjusted for the precise boiling point and solubility curve of our product—66.11 °C melting point, precise TLC/Rf behavior, and a reliable spot in NMR or MS runs. Working hands-on has shown that ignoring such specifics makes a mess in any scale-up or regulatory validation.
Another key variation relates to odor and volatility. Some rival pyridine derivatives are notorious for strong, persistent smells—our compound, when sealed and handled correctly, remains unobtrusive, so facilities can avoid cross-odor contamination. Many process engineers appreciate this when running semi-batch or continuous flow steps where even trace emissions can trigger alarms or require frequent scrubber replacement.
We get calls from R&D labs reporting unusually clean chromatograms, smooth solubilization in target solvents, and high yield recovery on pilot batches run with our material. Scale-up teams value transparency: we provide not only a Certificate of Analysis but also retain reference samples from every production run, available for retrospective testing. When one pharmaceutical partner ran into an unexpected crystallization issue, joint troubleshooting traced the cause not to our 2-Amino-3-Ethyl-6-Methylpyridine but to a minor solvent switch further up their process—a relief for both sides, and a reflection of the open dialogue built on traceability.
Raw material quality remains a constant challenge. Any fluctuation in a precursor source can snowball into off-spec material—not acceptable on our lines. In response, we built supplier relationships spanning years, sometimes decades, with quarterly audits and shared improvement plans. Our in-house GC and HPLC analysis keeps things in check, and we make it a policy to requalify every new lot before it enters main production.
Environmental responsibility factors in from the outset. We minimize waste effluent by reprocessing solvent streams, treating wash water, and carefully managing offcuts from batch filtration. Years ago, routine batch washing generated uncomfortable volumes of pyridine-laden rinse; now, recovery units reclaim both solvent and product, with refined distillation equipment slashing losses to under 1%. Lessons learned here often ripple through later product launches, keeping regulatory compliance cost-effective and in step with global ESG trends.
Real product support isn’t about boilerplate emails or out-of-date safety data sheets. When customers discover an anomaly—maybe a shift in reactivity, or an odd trace impurity picked up by LC-MS—we invite them to compare results with our retained material and full batch records. Open collaboration shortens troubleshooting, saves valuable man-hours, and solidifies working relationships that outlast market trends and price cycles.
Pharma buyers want more than just ‘pyridine intermediate, meets X standard.’ They need assurance that scale-up from 250 mL to 2000 L won’t introduce variables that wipe out yield or compromise regulatory review. Our production records document every variable, from agitation speed to drying time, with supporting spectral and chromatographic data. Have a regulatory filing to close? We can trace every step, no matter when the batch shipped.
Clients developing new pharmaceuticals, crop protection agents, or specialty resins count on consistent reactivity. Over the years, our QC teams honed protocols to target not only peak purity, but also batch-to-batch homogeneity. Tweaks in crystallization temperature or solvent choice may seem small, but in our world, these define the difference between a clean reaction and an unpredictable one. The industry moves fast—people can’t afford downtime tracking unknowns.
A recent collaboration with a materials startup required rigorous screening for trace residuals—less than 10 ppm on certain byproducts—before their downstream polymerization would pass internal QA. By coupling targeted re-crystallization with micro-scale analytics, we delivered the cleanest batch on record for their application, allowing them to meet their launch deadline without revisiting process variables. Experiences like this highlight the value of manufacturer-to-user communication: the right details, at the right time, help unlock new applications.
While our production volumes have expanded to serve customers across North America, Europe, and Southeast Asia, core team members retain the same hands-on approach that marked our earliest days. Whether tuning reactor feed rates or optimizing packing to minimize vibration in long-haul shipments, our staff train and retrain on the specifics of 2-Amino-3-Ethyl-6-Methylpyridine because the job requires care at every stage. It doesn’t matter if a package lands in a biotech incubator in Boston or an ag chem pilot plant in the Rhône valley—all receive the same batch documentation, storage instructions, and hotline access to our team for quick problem-solving.
Custom packaging requests, whether for smaller R&D quantities or drum-scale commitments, are handled by staff with a practical grasp of lab and plant realities. In one instance, extra secondary containment and vacuum-sealed liners prevented a costly recall when customs inspections ran longer than expected—anticipating potential hiccups shows that a manufacturer’s job goes well beyond the shop floor.
Our longest-standing customers often cite fewer headaches and increased confidence when using our material—because they know what’s inside the container, who made it, and where it came from. R&D teams can plan synthetic routes around known reactivity. Scale-up managers avoid process drift or messy rework. Even regulatory associates appreciate the clarity that accompanies a fully traceable, consistently produced intermediate.
Anyone who’s driven a tech transfer project can tell stories of obscure impurities complicating validation for months. By sticking to a consistent process with transparent change control and full batch trace, we help eliminate those project delays. The technical staff who oversee our reactors, dryers, and filling stations have solved more than a few troubleshooting crises for downstream users, simply by pulling historical batch data or running targeted re-analysis.
Novel applications keep emerging as researchers and process teams explore ways to modify and harness pyridine derivatives. With access to our analytic labs and technical archives, co-development projects gain speed—a few recent collaborations have resulted in more stable, better-performing intermediates by modifying not just purity targets, but also particle size range or solubility profiles at source. We rarely chase the lowest price per kilo; rather, we focus on value per batch, knowing that a reliable manufacturing partner adds more to a project’s success rate than a small cost saving up front.
Anyone can quote catalog specs, but hands-on experience in manufacturing brings a deeper understanding of what those specs mean in the real world. Paying close attention to the nuances of 2-Amino-3-Ethyl-6-Methylpyridine manufacturing keeps batches reliable, processes predictable, and customer relationships secure. Our team takes pride in sending out product that arrives exactly as expected—never with unwelcome surprises, always with technical support just a call away. Whether your interest lies in R&D, large-scale production, or regulatory support, you find value not just in our intermediate itself, but in the proven methods and transparency behind every unit we produce.