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HS Code |
353898 |
| Iupac Name | methyl 2-(aminomethyl)pyridine-4-carboxylate |
| Molecular Formula | C8H10N2O2 |
| Molecular Weight | 166.18 g/mol |
| Cas Number | 84122-94-9 |
| Appearance | white to off-white solid |
| Melting Point | 90-93°C |
| Solubility In Water | Partially soluble |
| Smiles | COC(=O)c1cc(ncc1)CN |
| Inchi | InChI=1S/C8H10N2O2/c1-12-8(11)6-2-3-10-7(4-6)5-9/h2-4H,5,9H2,1H3 |
As an accredited 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester is supplied in a sealed amber glass bottle. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester involves secure, sealed drum or bag packaging. |
| Shipping | **Shipping Description:** 4-Pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester is shipped in tightly sealed, chemical-resistant containers under ambient conditions. The packaging ensures protection from moisture and light. All shipments comply with relevant regulations for chemical transport, including labeling for laboratory use. Accompanying documents detail safety, handling, and emergency procedures. |
| Storage | Store 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and follow all relevant chemical storage regulations. Use appropriate containment to avoid leaks, and handle with suitable personal protective equipment. |
| Shelf Life | **Shelf Life:** Store 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester tightly sealed at 2-8°C; typically stable for 2 years. |
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Purity 98%: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reduced impurity levels. Molecular weight 166.18 g/mol: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester at a molecular weight of 166.18 g/mol is applied in medicinal chemistry research, where precise molecular mass supports accurate compound modification studies. Melting point 93°C: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with a melting point of 93°C is utilized in solid formulation processes, where thermal stability enhances safe handling and storage. Solubility in methanol: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with high solubility in methanol is used in analytical sample preparation, where improved dissolution facilitates accurate quantification. Stability at 25°C: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester demonstrating stability at 25°C is applied in chemical library storage, where prolonged shelf-life is achieved. Particle size <10 µm: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with particle size below 10 µm is used in fine chemical formulations, where uniform dispersion enhances formulation homogeneity. Viscosity 1.2 cP: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester at viscosity 1.2 cP is used in liquid-phase synthesis protocols, where low viscosity promotes efficient mixing and reaction rates. Moisture content <0.5%: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with moisture content below 0.5% is used in peptide coupling reactions, where reduced hydrolysis risk improves coupling efficiency. Optical purity >99%: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with optical purity above 99% is applied in chiral drug development, where enantiomeric excess enhances target specificity. pH stability 4–8: 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester with pH stability between 4 and 8 is used in buffer solution preparations, where reliable performance under variable conditions is critical. |
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We have spent years navigating the intricacies of fine chemical manufacturing, and each product brings a unique set of challenges and opportunities. Among the specialty pyridine derivatives we produce, 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester stands out for its clean reaction profile and reliable handling. Many of our clients in pharmaceuticals, crop protection, and material science rely on this molecule to bridge key steps in their synthesis pipelines. The blend of a methyl ester and aminomethyl substituent on the pyridine ring opens multiple routes in downstream chemistry, giving formulators the flexibility to design targeted molecules without the hassle of extensive protecting group strategies.
In our experience, the quality of this ester hinges on maintaining strict temperature controls during the synthesis, especially during amination. Trace impurities from incomplete esterification or over-alkylation can undermine yields and scale-up efficiency for the end user. Through years of optimizing batch and continuous processes, we've learned to tune solvents and reagents for minimal byproduct formation, leading to a reproducible product.
Customers often ask about batch-to-batch consistency. We run gas chromatography and NMR analyses for every lot. Our process delivers a typical assay above 99%, and water content stays low, often below 0.3%, essential in preventing hydrolysis—especially during storage or transport across humid climates. We keep heavy metal impurities far below accepted industry thresholds. Such vigilance means users spend less time troubleshooting and more time developing their own value-added compounds.
Pyridine rings offer metabolic stability as well as coordination sites for catalysts or metals. Attaching an aminomethyl group at the 2-position amplifies its reactivity: the group activates the ring towards selective functionalization, while the methyl ester serves as an efficient point of attachment for further chain elongation or amidation. This dual functionality—rare in off-the-shelf intermediates—gives chemists the chance to design modular synthetic routes rather than relying on lengthy, inefficient builds from base materials.
Pharmaceutical researchers appreciate that this intermediate avoids side reactions that can occur with unprotected amines or free acids. The methyl ester group poses fewer handling hazards and is easier to remove or convert than bulkier esters, shortening downstream workflows. Agrochemical developers also mention how the well-behaved reactivity profile, combined with straightforward purification, accelerates candidate library assembly during early discovery cycles.
Compared to its close relatives, such as the ethyl or tert-butyl esters, the methyl ester variant balances reactivity and volatility. Ethyl esters hydrolyze a bit slower but bring higher boiling points, complicating removal under vacuum for some downstream users. Tert-butyl esters resist cleavage longer but introduce more steric hindrance, often dragging out amidation or transesterification sequences. In contrast, our methyl ester enables reliable transformations under mild conditions without excessive energy input or risk of decomposition.
Within our product family, we also offer related pyridine derivatives with substitutions at different positions or with protected amines. Over years of feedback from R&D partners and custom synthesis teams, chemists find the 2-(aminomethyl) group on the 4-carboxylic acid skeleton balances both nucleophilic and electrophilic reactivity. This lets customers tune reaction rates during screening assays, minimizing the risk of runaway reactions or side pathway formation.
Handling any aminomethyl-pyridine involves both chemical and regulatory considerations. During early days of scaling production, we encountered runaway exotherms during methyl esterification if temperature ramps ran uncontrolled. By investing in automated monitoring and rapid quench systems, we now manage process safety at every turn. We source raw materials with full traceability, screening for nitrosamine and other unwanted byproducts—all in line with the evolving landscape of pharmaceutical regulations.
Sustainability also matters. Customers increasingly ask about waste streams and energy consumption. We have engineered our manufacturing line for solvent recovery and recirculation, reclaiming upwards of 80% of process solvents and minimizing emissions. Our operators work with closed transfer systems to reduce fugitive dusts and vapors, keeping the workplace safe and the environmental footprint small.
Our daily reality teaches us that specifications alone don't guarantee performance. Several pharmaceutical partners have shifted from buying off-the-shelf intermediates from traders or resellers to sourcing directly from us as the original manufacturer. The reason is clear: transparency. We maintain real-time records of process parameters, and we routinely share process validation data during audits. Trust is built on a willingness to answer tough questions—not just sending over a certificate.
Volume flexibility is another concern most resellers cannot match. We build from kilograms for custom library work up to multi-metric ton lots for scalable drug synthesis. Transition between scales stays smooth, as our plant layout gives direct access to pilot and production vessels without cross-contamination. Even when weather or logistics throw in curveballs such as transport delays or port bottlenecks, our direct supply chain means clients avoid the months-long waits typical for some imported intermediates.
No production line runs perfectly forever. About four years ago, we encountered an unexpected impurity during a scale-up campaign—a stubborn spot on LC that eluded our standard isolation techniques. Our technical team dug into the process chemistry, partnering with both academia and downstream users, finally pinning the culprit as a minor overalkylated side product. Once identified, we traced the root cause to a reagent impurity, updated our supplier QA protocol, and the blip never returned.
These learning moments shape how we monitor and respond. Feedback from customers drives our Kaizen improvement approach. Some have suggested alternative packaging that reduces atmospheric moisture uptake. In response, we trialed upgraded tamper-resistant drums with inert liners, pushing down product degradation across long supply routes. We never view complaints or requests as problems; rather, they're the fuel for continuing to raise the bar.
A decade ago, the primary buyers for our pyridinecarboxylic acid methyl esters clustered in major pharma hubs in the US and Europe. Times have changed. Today, demand rises fastest from contract research organizations in Asia and fast-moving specialty chemical houses in South America and Africa. We support these partners by navigating compliance and shipping barriers, including REACH registration in Europe and other export requirements. Instead of supplying a generic intermediate, we serve as an extension of the customer’s technical arm, ready to offer both quality product and synthesis troubleshooting.
Our logistics teams have ironed out the complexities of export licensing and multi-modal transport. Temperature-controlled storage and real-time tracking prevent temperature spikes and shipping delays from damaging sensitive lots. Since many government contracts and pharmaceutical tenders require transparent documentation, we provide complete product histories, including change control records and audit trails, setting us apart from less-direct supply chains.
Real innovation rarely happens in isolation. Newly patented compounds entering the development pipeline often draw from common intermediates such as 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester. Our technical staff meets regularly with clients’ lab teams to discuss reactivity trends, purification tips, and reaction optimization. One client encountered difficulty removing a side product during amide coupling; working together, we adjusted their reaction conditions and suggested an updated purification solvent, reducing workup time and solvent usage by nearly half.
Sometimes, research partners pose unexpected synthesis requests—such as isotope labeling for reaction tracing studies or ultra-pure material for spectroscopic analysis. Because we retain full control of our plant and process records, we can modify synthesis pathways or adapt impurity profiles with minimal lead time. By coupling raw chemistry expertise with operational agility, we help shorten time-to-market for breakthrough compounds.
Many chemists who’ve experienced delays or surprises with intermediates from brokers remark on the difference with a direct manufacturing source. No more waiting for answers to routine questions like, “How fresh is this lot?” or “Can you provide spectral data for our QA release?” Each batch in our system tracks analytic results, from melting point to infrared spectra, all available prior to shipment.
During process transfer or technical dispatch, sometimes a client discovers a workflow change or purification hitch. Immediate, detailed feedback from our team—often including staff who developed the original process—unblocks problems quickly. We can dispatch extra samples or alternative packaging in days, not weeks. This hands-on model builds deeper connections as chemists move new ideas from bench to plant.
Looking back across the years, it’s clear that intermediates like this methyl ester play outsize roles in pharmaceutical scale-up and agrochemical innovation. The short supply chain, paired with proven technology, gives formulators confidence as regulatory standards tighten and cost pressures intensify. Unlike many generic intermediates sourced from brokers or non-specialists, material from our plant arrives with both the analytic records and user support needed for real-world production.
The blend of functional groups on this molecule creates possibilities across drug, dye, and catalyst research. Our own teams use it internally in catalyst design programs, exploring ligand effects and constructing new chelation motifs for next-generation metal complexes. This provides a constant feedback loop to our manufacturing group—each new derivative or use case offering ideas for tweaking process parameters, improving yield, or broadening reactivity.
The global chemical supply chain remains fragile. Natural disasters, policy shifts, and raw material shortages test even the most robust sourcing plans. Direct relationships between manufacturers and users buffer these shocks. As regulatory landscapes evolve—with new restrictions on impurities, process documentation, and hazardous substances—direct oversight and transparency become ever more crucial.
Our ongoing commitment: invest in process automation, reinforce compliance, and continue active dialogue with partners in R&D and manufacturing. Each kilogram we ship reflects the lessons learned from thousands of batches and dozens of customer collaborations. The spirit of innovation and reliability shapes everything we do, from raw material selection to final analytical sign-off. For chemists and formulators turning to 4-pyridinecarboxylic acid, 2-(aminomethyl)-, methyl ester, that experience translates to fewer surprises, more robust synthon transformation, and real support at every stage.