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HS Code |
687459 |
| Cas Number | 104-29-6 |
| Molecular Formula | C7H10N2 |
| Molecular Weight | 122.17 g/mol |
| Iupac Name | 2-amino-4-ethylpyridine |
| Appearance | Yellow to brown solid |
| Melting Point | 43-46°C |
| Boiling Point | 245-248°C |
| Density | 1.06 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 4-Ethyl-2-pyridinamine |
As an accredited 2-Amino-4-Ethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-4-Ethylpyridine is packaged in a 25g amber glass bottle with a tamper-evident screw cap and detailed labeling. |
| Shipping | 2-Amino-4-Ethylpyridine is shipped in tightly sealed containers, protected from moisture and light. It should be handled in accordance with standard chemical shipping regulations, including proper labeling and documentation. The compound is transported as a hazardous material and must comply with relevant international and local safety and transportation guidelines. |
| Storage | 2-Amino-4-ethylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect the chemical from moisture and direct sunlight. Store at room temperature or as directed by the manufacturer, and ensure appropriate labeling and access controls to prevent unauthorized handling. |
Applications of 2-Amino-4-Ethylpyridine in Industrial ManufacturingOur facility produces 2-Amino-4-Ethylpyridine for use in advanced synthesis processes across several distinct sectors. Below, we detail actual downstream fields and practical application aspects based on direct manufacturer collaboration and technical data. 1. Active Pharmaceutical Ingredient (API) Intermediate for Anti-Inflammatory DrugsPharma formulators use 2-Amino-4-Ethylpyridine as a reaction intermediate during multi-step synthesis of selected nonsteroidal anti-inflammatory drug (NSAID) molecules. It enters amidation and subsequent cyclization steps, providing a robust platform for consistent batch yields. Integrated QA includes in-process HPLC monitoring to control impurity profiles and regulatory documentation for traceability, meeting the requirements of regulated drug substance manufacturing. Strict solvent residue limits and specification-driven lot release ensure suitability for subsequent conversion to finished dosages or out-licensing as API powder. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Fungicide PrecursorsChemical crop protection producers utilize this pyridine derivative as a key building block in producing certain selective herbicides and fungicides. It reacts with specific halogenated compounds under controlled pH to achieve functionalised pyridine scaffolds. Downstream blending involves stringent residue control and consistency monitoring by GC-MS. Our technical support extends to adjusting input concentration according to required product activity data and season-specific formulation needs. Manufacturers using our material focus on process safety, precise batch monitoring, and compatibility checks with co-formulants. Industry compliance standards
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3. Dye and Pigment Manufacturing: Azo Dye Synthesis ComponentSpecialty dye manufacturers adopt 2-Amino-4-Ethylpyridine for its capacity to generate stable colorant intermediates, especially for high-purity azo dye production. The compound introduces specific functional groups through diazotization and further coupling with aromatic compounds. Routine QA requires colorimetric analysis and TLC tracking to confirm conversion and intensity profiles. The controlled feed enables consistent tone and minimizing byproducts. Our customers integrate this raw material at the primary amination stage prior to final chromophore assembly and blending. Industry compliance standards
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4. Flavor and Fragrance IntermediateProducers of synthetic fragrances and flavor molecules use this compound as an intermediate for manufacturing specific pyrazine derivatives, valued for their characteristic nutty and roasted notes. The process includes selective alkylation followed by controlled condensation to promote aroma yield. QC departments run GC and olfactory panel analyses for each batch. Formulators adapt the input ratio based on the intended end-use, batch size, and blend matrix, maintaining food-grade specifications and allergen control in compliance with international regulations for flavor ingredients. Industry compliance standards
Typical usage ratio
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For years, our facility has specialized in making pyridine derivatives, taking pride in the way every batch of 2-Amino-4-Ethylpyridine leaves our reactors. The substance, also known by its model AE42, owes its value to its distinct molecular backbone—a pyridine ring bearing both an amino group and an ethyl chain. This unique shape unlocks uses across pharma and in fine chemical syntheses where purity and reactivity drive outcomes. We’ve invested continually in raw material sourcing and process controls, so customers receive a consistent, high-assay product batch after batch.
2-Amino-4-Ethylpyridine’s structure sets it apart from plain pyridine or other aminopyridines. That ethyl chain at the fourth position, combined with the amino placement, gives both a different solubility profile and often milder odor. These substitutions impact how it reacts—with a more targeted nucleophilicity than unsubstituted aminopyridines, this building block enables manufacturers to steer synthesis along more reliable pathways, cutting down on side products and improving yields. Our R&D team knows from hands-on experience that not every reaction calls for the “strongest” amine base: sometimes fine-tuning the reactivity smooths out the path to the desired intermediate, making downstream purification much less of a headache.
We operate our synthesis lines under tightly maintained conditions. Feedstocks go through a multi-stage quality check before any chemistry even starts. Temperatures, pressures, and reaction times suit the specific structure of 2-Amino-4-Ethylpyridine, allowing us to control not just product purity, but also particle size and moisture levels if customers require a certain format. Years back, when we adjusted our drying step, we saw a drop in clumping and graininess, leading directly to faster solubilization in customer reactors. This level of nuance comes only from making the compound at scale, solving the real issues that bulk buyers face on their end.
Each bulk lot runs through HPLC and GC checks, while UV-vis data confirms the minimal presence of known byproducts, such as 4-Ethylpyridine or 2-Aminopyridine. Moisture analyses, often overlooked by traders, have saved several clients from headaches with anhydrous or highly sensitive reactions. This hands-on approach means our product keeps tight limits on water and eliminates high-boiling impurities that can gum up downstream glassware and process lines.
Most buyers turn to 2-Amino-4-Ethylpyridine seeking high-value intermediates or pharmaceutical ingredients. Its reactivity appeals to those building complex heterocycles or scaffold modifications for medicinal chemistry projects, with the amino group acting as a powerful nucleophile under controlled conditions. Our bulk customers in the pharma sector keep reporting improved overall conversion and cleaner separations, compared with what they see from the more reactive, but less predictable, 2-Aminopyridine. That ethyl side chain not only changes solubility in various solvents but often blocks side reactions that eat up starting material. In contract manufacturing, time is money—it’s frustrating to trace a byproduct’s origin back to low-quality feedstock.
Agrochemical groups also value this compound for tweaking lead structures or designing new activity profiles, often needing modifications at the 2 or 4 positions of the pyridine ring. The mild odor and manageable vapor pressure simplify handling, reducing off-gassing incidents in large-scale setups. During pilot production runs, several customers mentioned that easier handling lets teams reduce the number of air changes or filtration changes in production rooms. Safety gains come with fewer headaches for the crew monitoring the line.
Compare the performance of 2-Amino-4-Ethylpyridine to products like 2-Aminopyridine or 4-Aminopyridine. Those classic amines offer broad applicability but often lead to sloppy byproducts during acylation or alkylation steps, especially under aggressive conditions. The ethyl group at the 4 position subtly dampens reactivity, steering reactions away from undesired positions on the ring, which both increases product selectivity and reduces the need for repeated extractions or distillations. The downstream waste load decreases, saving costs in solvent recovery and waste processing.
When production chemists face pressure to simplify downstream steps, getting the initial coupling reaction controlled remains essential. After introducing our material to a multi-step pharmaceutical route, one customer reported an extra 7% yield boost at the penultimate stage. Less time spent purifying means faster project turnaround—which matters when a patent clock is ticking or a regulatory submission is targeted. These real, practical gains stem from the predictable behavior of the well-made molecule, not some theoretical purity number. We’ve seen advanced syntheses with several ring modifications rely specifically on the ethyl group, both for steric steering and for easier purification. In the hands of an experienced chemist, these nuanced differences aren’t small—they’re the difference between a process that works on paper and one that delivers in the plant.
On our floors, 2-Amino-4-Ethylpyridine takes the form of a free-flowing crystalline solid, with very low tendency toward caking under controlled humidity. We manage production controls to minimize the build-up of dust, which not only supports safer working conditions but also improves downstream consistency for customers. We learned early that batch-to-batch consistency in melting point and color directly tracks with reaction outcome. Working directly with end users to tailor heating ramp rates and mixing times, we’ve optimized our solidification and packaging protocols.
Bags and drums used for shipping see special lining to prevent any interaction with interior surfaces, keeping the product dry and clean through transport. Over the years, we switched from multi-layer paper bags to HDPE drums for majority of overseas shipping—a change driven by live feedback from large-scale clients in both North America and East Asia. Fewer packaging failures means lost material, but also fewer incidents of airborne exposure for anyone opening a new package at the customer site. Local supply partners know to store material away from direct sunlight and moisture, but our product’s lower volatility and mild scent keep warehouse safety requirements manageable without specialized ventilation.
Several years back, we dealt with a batch delay after a steam line malfunction caused partial hydrolysis of a reactor charge. Trace impurities climbed above our release threshold as a result. Rather than ship subpar material or keep customers in the dark, we flagged every affected load, moved production to a parallel line, and doubled the downstream QC checks for affected orders. Communicating early, directly, and with real-time facts kept projects on track, proving that crystal structure and analytical data mean little if trust fails. With each challenge, our technical team develops new process tweaks that plug back into the next batch run, so mistakes seldom repeat. Industry relies on this hard-earned responsiveness, not just numbers on a data sheet.
Subtle shifts in production climate—like high summer humidity—prompt us to retest stored batches for water content or sign out extra desiccant for containers. We’ve caught small upticks in byproduct profiles early enough to rework material before it leaves the building, protecting customer campaigns from unexpected surprises. That vigilance fuels strong word-of-mouth within the tight-knit fine chemical industry, where buyers talk shop and trade war stories about problem materials that torpedoed entire months of lab work. We work to ensure our molecule does its job with no drama.
As more customers take their routes from the kilo scale into commercial reactors, process variables shift. Small losses or inefficiencies magnify into major cost drivers. Over years of on-site visits and joint process reviews, we’ve watched customer teams fine-tune their solvent regimes and work-up steps, guided by the consistent properties of our material. In one project, a pharmaceutical manufacturer swapped a column chromatography step for a single, low-temperature crystallization—all enabled by the minimal impurity load in our 2-Amino-4-Ethylpyridine. This reduced both solvent waste and labor hours by more than 20%, leading directly to lower per-kilo costs of their active compound.
Similar experiences come up in agrochemical synthesis, where clients push for new actives that demand solid yet flexible chemistries. Starting with a pure, well-characterized 2-Amino-4-Ethylpyridine gives them the confidence to explore new functionalizations or late-stage derivatizations, without the constant headaches of adjusting for missing mass or mystery spots on the NMR. We keep our analytical methods broad, so we catch any drift in side product profiles before they hit customer reactors. Lessons learned from our floors—about thermal stability, storage, and solvent compatibility—filter back through technical bulletins and troubleshooting calls, giving process chemists real grounding for their next run.
Meeting high-purity standards is more than a paperwork exercise. From an operator’s view, safe handling and predictable product behavior reduce the real risks, not just the perceived ones. With regulations tightening on both workplace exposure and downstream residuals, we keep a running dialogue with compliance teams worldwide, sharing the latest batch analyses and supporting data. Our material meets established global thresholds for contaminants and known hazardous impurities, let alone exceeding in-house targets for purity. Yet this is only effective when paired with staff training—whether it’s safe charging procedures, fresh filter change logs, or accurate record keeping in the blending room.
Feedback loops between production, QC, and customer QA teams keep us sharp. Issues get flagged quickly, logged, and solutions developed before reoccurrence. We send out updated documentation as manufacturing regulations evolve, because failing an audit or slowing down a partner’s compliance review is not an option. Customers trust that questions about trace levels or process contaminants elicit quick, data-backed answers rather than runarounds. In this sector, a company’s reputation rides not just on what’s made, but how it’s documented and supported in the field.
Beyond the molecules, relationships carry the work from laboratory to market. Chemists across the globe bring new projects and process tweaks to us for input, seeking out hard-earned advice on troubleshooting or route optimization. Our technical service lines run on real stories, not just numbers—like the time a process engineer in South America needed our insight to prevent emulsions when switching work-up solvents, or when a pharmaceutical startup needed guidance picking the right storage drums for high-humidity regions. These moments drive our process improvements and keep us searching for new ways to minimize headaches for everyone down the line.
We invest heavily in new process automation and analytical upgrades not for show, but because they matter day-to-day. Faster batch release, tighter impurity profiling, and real-time data tracking come out of our own shop floors, shaped by the demands and crises we’ve seen firsthand. Working through pandemic-driven shortages, we retooled part of our line to prioritize consistent quality over pure quantity, ensuring that our mainstay pharma partners could rely on continuity in both product and service.
We approach every production run of 2-Amino-4-Ethylpyridine as a learning opportunity. New project launches or chemical route changes at customer sites bring a fresh perspective on the kind of consistency and responsiveness that matters most. As we refine analytical techniques, trial novel reaction controls, and implement smarter data systems, we collect new insights into what separates a “good batch” from a “great batch.” These lessons flow directly into the hands of the next chemist or process engineer taking our material to scale, closing the loop from raw material to finished product and back to quality improvement.
We see demand for 2-Amino-4-Ethylpyridine expanding as pharma and agrochemical sectors stretch for more complex targets, safer intermediates, and cleaner reactions. The drive within the industry toward “greener,” higher-yield, and safer chemistry fits cleanly with the properties of this molecule—reactive enough for versatility but less prone to hazardous volatility and unwanted side products compared to less substituted aminopyridines. At every stage, our approach rests on evidence, transparency, and the knowledge that each new batch contributes to solutions shaped both by lab science and the lived experience of modern manufacturing.
Drawing on a decades-long focus on aminopyridines, we continue improving robustness, documentation, and service—with a core commitment to helping customers turn their best chemistry into reliable, real-world progress. Every advancement we make loops back to where it matters: cleaner synthesis, safer processing, and stronger trust between supplier and end user. This, above all, has taught us why the difference between a generic grade and a purpose-made batch isn’t found just in a purity percentage, but in the unstated confidence it brings to every chemist counting on the next step to work exactly as planned.