|
HS Code |
938823 |
| Chemical Name | 3-(Ethylaminomethyl)pyridine |
| Molecular Formula | C8H12N2 |
| Molecular Weight | 136.19 g/mol |
| Cas Number | 1603-40-3 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 238-239 °C |
| Density | 1.01 g/cm³ |
| Refractive Index | 1.539 |
| Solubility | Miscible with water and most organic solvents |
| Flash Point | 107 °C |
| Smiles | CCNCC1=CN=CC=C1 |
As an accredited 3-(Ethylaminomethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-(Ethylaminomethyl)pyridine, 100g is supplied in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL loads 3-(Ethylaminomethyl)pyridine in securely sealed drums or IBCs, typically 14–16 metric tons per container, ensuring safe transit. |
| Shipping | 3-(Ethylaminomethyl)pyridine should be shipped in secure, leak-proof containers, clearly labeled according to chemical safety regulations. It must be protected from heat, moisture, and incompatible substances. Ship in compliance with local, national, and international hazardous material transport guidelines, with appropriate documentation, using reliable carriers specializing in chemical shipments. |
| Storage | 3-(Ethylaminomethyl)pyridine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature, avoiding excessive heat and moisture. Ensure proper labeling, use secondary containment to prevent spills, and restrict access to authorized personnel while following all safety precautions and local regulatory requirements. |
| Shelf Life | **Shelf Life:** 3-(Ethylaminomethyl)pyridine typically has a shelf life of 2 years when stored tightly sealed, dry, and protected from light. |
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Purity 98%: 3-(Ethylaminomethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and consistency. Melting point 74°C: 3-(Ethylaminomethyl)pyridine with a melting point of 74°C is applied in catalyst formulation, where it provides stable phase behavior under operational conditions. Molecular weight 150.22 g/mol: 3-(Ethylaminomethyl)pyridine with a molecular weight of 150.22 g/mol is used in agrochemical development, where precise stoichiometry enhances reaction efficiency. Low water content ≤0.5%: 3-(Ethylaminomethyl)pyridine with low water content (≤0.5%) is utilized in electronics materials synthesis, where it prevents hydrolysis and increases product reliability. Stability temperature up to 120°C: 3-(Ethylaminomethyl)pyridine stable up to 120°C is employed in industrial coatings, where thermal resistance supports long-term performance. Colorless liquid: 3-(Ethylaminomethyl)pyridine as a colorless liquid is used in analytical reagent preparation, where visual clarity allows for precise solution handling. |
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3-(Ethylaminomethyl)pyridine stands out as a valuable intermediate in a world increasingly focused on specialization and efficiency. In my time working alongside research scientists and industry professionals, I’ve seen how often this compound forms a key piece in countless synthesis puzzles. As the industry adapts to modern manufacturing challenges—sustainability, quality assurance, and supply chain complexity—having an intermediate like this offers more than just a chemical name. It delivers reliability bred from consistent performance and trusted chemical integrity.
This compound falls into the aminomethylpyridine family, distinguished by a subtle, yet fundamental, structural difference: the presence of an ethylamino group attached to the methylpyridine core. That extra ethyl chain, small as it may be, changes its reactivity profile when compared to similar chemicals such as 3-(methylaminomethyl)pyridine or unsubstituted aminomethylpyridines. As a result, chemists gravitate toward it not out of habit, but because its attributes offer real-world advantages—namely, an ability to bridge functional groups for more targeted active ingredient production.
Several years back, I worked on a project requiring an intermediate that could hold up under repeated kinetic trials. Many commercial sources struggled to hit the right purity profile for 3-(Ethylaminomethyl)pyridine. The right lot, sourced from a dedicated supplier, helped us sidestep impurity-driven side reactions. On the bench, in viscous batch reactors, and even on the QC line, the product retained its signature: a clear or pale yellow liquid, not easily mistaken for others, with a boiling point and density within narrow, published ranges. These small but precise windows allow process chemists to optimize flow chemistry setups or batch scale-up runs.
The material often comes with established trace analysis—LC, GC, and NMR datasets—though the most confident users confirm identity and purity with their own in-house systems. Batch-to-batch consistency underpins repeatable synthesis, whether you're scaling anti-infective drug intermediates or gearing up for small molecule crop protection agents.
I’ve seen this compound show up everywhere from big pharma’s high-throughput research teams to specialty materials startups aiming to disrupt traditional supply chains. Its primary use lies as a versatile building block for pharmaceutical and agrochemical research. Academics favor it for medicinal chemistry projects where introducing an ethylaminomethyl moiety opens new SAR (structure-activity relationship) possibilities.
Over the years, I've watched formulation scientists turn to it when developing intermediates used in novel active pharmaceutical ingredients (APIs). Its balanced electronic properties can help modulate solubility or tune reactivity for custom synthesis projects. In my experience, when the assignment calls for greater selectivity and less off-target reactivity, 3-(Ethylaminomethyl)pyridine often earns a place in the reaction scheme.
There’s a reason process chemists in the agrochemicals sector keep this chemical on hand: it reacts smoothly in Mannich-type transformations or in coupling protocols for constructing more complex bioactive molecules. Whether the aim is to introduce greater diversity into compound libraries or to optimize lead compounds for patented applications, the compound proves its worth.
It can be tempting to overlook the subtle differences among aminomethylpyridines. That can be a costly mistake. Take, for example, 3-(methylaminomethyl)pyridine: the absence of the ethyl group shortens the chain, which impacts both the physicochemical properties and metabolic fate in drug-like molecules. During a collaboration with a process development team, we tested both versions in multistep syntheses aiming to modify the pharmacokinetics of a series of analogs. Only the ethyl derivative gave us the right blend of reactivity and downstream compatibility.
Another moment I remember well: a project manager asked why we couldn’t simply substitute another pyridine-based intermediate. Beyond the textbook answer on electronic effects, the truth lay in practical experience—yield drops, side-product headaches, downstream filtration woes. Using 3-(Ethylaminomethyl)pyridine cut our workup steps and let us achieve a cleaner separation profile at scale. That’s not a matter of theory, but of lived lab reality.
I’ve learned—sometimes the hard way—just how much headaches a batch with out-of-spec impurities can cause. Purity isn’t just a line on a data sheet. It means fewer regulatory questions, more confident downstream operations, and lower risk of process deviation. Trustworthy suppliers offer not just COA paperwork but a record of stability data across shipments.
For pharmaceutical use, consistency rises above most other concerns. Each lot’s profile ties directly to batch records and regulatory filings. Regulatory auditors zero in on trace contaminants, and internal QA teams review every retention sample for minute changes. A solid supply of 3-(Ethylaminomethyl)pyridine—one where transparency and batch reproducibility define the relationship—lets organizations focus on innovation, not last-minute troubleshooting.
All chemicals carry some responsibility. My early days in the lab taught me that even a minor deviation in storage or handling can cascade into larger issues. 3-(Ethylaminomethyl)pyridine deserves practical respect: it gets stored in a cool, dry place, kept sealed until use, and handled using established PPE. Controlling humidity protects against hydrolysis, which could impact yield or purity.
Safe working routines, built on both training and common sense, go a long way. I’ve always advocated for double-checking labels and managing inventory actively—rotation, timely ordering, and tight record-keeping. No team wants to discover mid-run that a stock bottle has deteriorated or been contaminated.
In today’s research ecosystem, transparency builds both trust and credibility. I have looked for suppliers willing to provide detailed data—full NMR traces, recent HPLC chromatograms, updated SDS files. Long gone are the days when a vague batch number on a rusty tin sufficed. Chemists, QA managers, and procurement officers rely on that transparency as part of broader risk mitigation.
I’ve found that organizations which invest in supply chain visibility and quality partnerships save time and money down the line. Whether that means custom packaging to prevent cross-contamination or flexible batch sizing to fit pilot project timelines, transparent use of 3-(Ethylaminomethyl)pyridine ties directly to smoother operations.
Regulations don’t stand still. What passed muster a decade ago likely won’t today, as both chemical safety and environmental standards push manufacturers to do better. I’ve seen this in action during site audits and regulatory reviews: authorities expect traceability, robust documentation, and a demonstrated commitment to reducing hazardous byproducts.
Reputable suppliers respond by offering detailed impurity profiles and updating documentation as regulations evolve. End-users who stay current with these changes reduce the risk of imported batches being seized, delayed, or triggering red flags. I encourage procurement teams to review supplier certifications and ensure that the product matches not just intended use, but also current global guidelines.
The pace of scientific progress relies on intermediates that perform without surprises. 3-(Ethylaminomethyl)pyridine, as I’ve experienced, offers predictability. It lets R&D teams spend their critical hours on new chemistry—exploring analogs, optimizing leads, scaling up—to keep their projects moving forward.
One team I worked with used the compound as a handle to click extra pieces onto complex scaffolds, rapidly expanding their library of test candidates. Others adopted it as a more lipophilic variant, giving better membrane penetration in assay systems. The compound’s performance wasn’t theoretical; data-backed successes kept it in regular use.
Every product faces rough patches—price fluctuations, raw material shortages, even geopolitical hurdles. Not long ago, when logistical bottlenecks disrupted availability, our lab sat at a standstill. The solution didn’t come from wishful thinking. We dug into alternate sources, carefully validated the new supply, and set up parallel qualification rounds. Cross-referencing trace impurity fingerprints let us maintain consistency in our analytical records.
That experience reinforced the value of building robust relationships with suppliers willing to communicate about stock levels, lead times, and testing parameters. Teams benefit when they ask pointed questions, request reference spectra, and keep open files on supplier verification. Leaning into these best practices pays dividends in project uptime and data quality.
While the core applications lie in pharma and agrochemicals, emerging areas push the boundaries of 3-(Ethylaminomethyl)pyridine’s utility. Materials science groups value its functional group for post-synthetic modifications. Biotech startups explore its role in fine-tuning molecular probes or ligands for diagnostic platforms.
As a science writer and industry observer, I appreciate how pragmatic innovation turns once-specialist intermediates into common tools. This compound’s journey from bench curiosity to industry staple reflects real-world demand for both reliability and adaptability.
Sometimes, a lack of practical knowledge holds back adoption. Newer team members, fresh from university, often haven’t handled intermediates outside the well-controlled university stockroom. Onboarding programs matter—a good supplier doesn’t just deliver product but supports education on correct usage, troubleshooting, and routine analysis.
In several industry workshops, having hands-on presentations helped bridge textbook knowledge and industrial know-how. People learned to pay attention to storage stability, to run quick qualitative checks before scaling up, and to lean on QC data as a decision aid. Making these resources more widely available, whether online or through in-person sessions, can push the envelope on efficiency and safety.
The world keeps asking tough questions about sustainability. 3-(Ethylaminomethyl)pyridine, like most fine chemicals, comes with an environmental footprint—solvent choice, reaction energy, and waste management all factor in. Responsible teams look beyond price tags and purity. I’ve seen purchasing managers probe for waste minimization strategies, green chemistry credentials, or supplier commitments to responsible disposal.
Continuous process improvement sometimes shifts the picture. Enabling recycling of byproducts or improving process yields can change the economics and environmental impact. Sharing insights across organizations—even across supply chains—unlocks collective action on these tough problems. If every link in the chain, from synthesis to packaging, leans into better stewardship, the industry as a whole benefits.
The chemical industry thrives on predictability paired with innovation. I expect 3-(Ethylaminomethyl)pyridine’s role as a flexible intermediate to expand, especially as pharmaceutical and agricultural research becomes more demanding. Real-world supply shocks or market shifts can test any intermediate’s value, and the teams that prepare by fostering deep supplier relationships and investing in robust analytical protocols will weather these storms best.
Software-driven inventory management, tighter traceability, and ongoing supplier evaluation remain important trends. Whether you’re overseeing an academic startup or a global pharma firm, investing in better visibility over your fine chemical supply lines pays off. Lessons learned from real-world disruptions reinforce the need for diversified sourcing while staying rooted in rigorous scientific analysis.
Having spent years talking to production chemists, regulatory specialists, and R&D managers, I’ve learned that a good intermediate is more than just a specification on a brochure. It becomes part of how teams solve real problems—whether that’s tracking down impurity sources, improving process efficiency, or meeting the tough expectations of health authorities.
3-(Ethylaminomethyl)pyridine lives up to this role. Its adaptability, paired with trusted sourcing and consistent quality, supports the long-term success of scientific projects. Teams that take a practical, fact-driven approach to handling, storage, and regulatory compliance can leverage its benefits and minimize unexpected challenges.
Experience convinced me that no single compound guarantees success or failure. What counts is the careful attention to process, partners, and data. 3-(Ethylaminomethyl)pyridine delivers not because of its name, but because the people who rely on it care about getting things right—batch after batch, project after project, from discovery to finished product.