methyl 2-aminopyridine-3-carboxylate

    • Product Name: methyl 2-aminopyridine-3-carboxylate
    • Chemical Name (IUPAC): methyl 2-aminopyridine-3-carboxylate
    • CAS No.: 57500-67-1
    • Chemical Formula: C7H8N2O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    449813

    Chemical Name methyl 2-aminopyridine-3-carboxylate
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Cas Number 53135-33-8
    Appearance Light yellow to brown solid
    Melting Point 96-100°C
    Boiling Point No data available
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, away from moisture and light
    Smiles COC(=O)C1=C(N=CC=C1)N
    Inchi InChI=1S/C7H8N2O2/c1-11-7(10)5-3-2-4-9-6(5)8/h2-4H,1H3,(H2,8,9)
    Synonyms Methyl 2-amino-3-pyridinecarboxylate
    Pka No data available
    Density No data available

    As an accredited methyl 2-aminopyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of methyl 2-aminopyridine-3-carboxylate, with tamper-evident seal and hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed 16000 kg methyl 2-aminopyridine-3-carboxylate in 25 kg drums, ensuring safe transport.
    Shipping Ship methyl 2-aminopyridine-3-carboxylate in tightly sealed, chemically resistant containers. Protect from light, moisture, and incompatible substances during transit. Follow standard hazardous material regulations, including appropriate labeling and documentation. Store upright, at controlled room temperature. Handle with personal protective equipment (PPE) as specified in the material safety data sheet (MSDS).
    Storage Methyl 2-aminopyridine-3-carboxylate should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Store in a cool, dry, and well-ventilated area, ideally at room temperature. Avoid excessive heat and direct sunlight. Proper labeling and secure placement are essential to prevent accidental exposure or contamination.
    Shelf Life Methyl 2-aminopyridine-3-carboxylate has a typical shelf life of 2–3 years when stored in a cool, dry, airtight container.
    Application of methyl 2-aminopyridine-3-carboxylate

    Purity 98%: Methyl 2-aminopyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where high-purity ensures optimal yield of target compounds.

    Particle size <50 µm: Methyl 2-aminopyridine-3-carboxylate with particle size <50 µm is used in fine chemical manufacturing, where improved surface area enhances reactivity and dissolution rate.

    Melting point 158-160°C: Methyl 2-aminopyridine-3-carboxylate with melting point 158-160°C is used in organic synthesis processes, where stable phase transition supports controlled reaction conditions.

    Stability up to 120°C: Methyl 2-aminopyridine-3-carboxylate with stability up to 120°C is used in heat-sensitive formulations, where chemical integrity is maintained during processing.

    Molecular weight 166.16 g/mol: Methyl 2-aminopyridine-3-carboxylate with molecular weight 166.16 g/mol is used in drug design, where predictable stoichiometric calculations facilitate accurate formulation development.

    Water content ≤0.5%: Methyl 2-aminopyridine-3-carboxylate with water content ≤0.5% is used in moisture-sensitive reactions, where minimized hydrolysis risk ensures product consistency.

    HPLC assay ≥99%: Methyl 2-aminopyridine-3-carboxylate with HPLC assay ≥99% is used in analytical chemistry, where high assay results support stringent quality control requirements.

    Residual solvents <200 ppm: Methyl 2-aminopyridine-3-carboxylate with residual solvents <200 ppm is used in GMP-compliant production, where minimized impurities meet regulatory standards.

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    Certification & Compliance
    More Introduction

    Methyl 2-aminopyridine-3-carboxylate: Reliable Synthesis, Practical Application

    Our Hands-On Approach in Manufacturing

    Every batch of methyl 2-aminopyridine-3-carboxylate that leaves our facility reflects the direct involvement of our team at each step. We work from raw material selection to finished packing, avoiding shortcuts and improvisation. Our production process stands on proven chemistry and decades of collective experience. Our reactors run under constant supervision, and we monitor temperature, reaction time, and purity checkpoints at every stage. As a chemical manufacturer, we've found that a committed eye for detail pays off in the consistency and reliability of our methyl 2-aminopyridine-3-carboxylate.

    Key Characteristics and Specifications

    Pure methyl 2-aminopyridine-3-carboxylate emerges as a crystalline powder, free from noticeable impurities when processed with care. By maintaining rigorous control during crystallization and drying, we reliably achieve high assay results—consistently over 98% by HPLC in our most recent runs. Moisture content remains low thanks to controlled atmosphere packaging inside our facility.

    Typical lot data often reveals a melting point centering around 120°C as verified through repeated internal checks, with little batch-to-batch deviation. Impurities such as methyl 2-pyridinecarboxylate or isomeric byproducts stay well below 0.5%, as confirmed by our in-house LC analysis. We base these numbers on our own manufacturing records and not just the limits listed on commodity data sheets.

    Particle size in our standard product suits workflow in both bench-top and larger-scale applications. For customers working with microreactors or requiring special size fractions, we offer adjustable sieve protocols during the final processing.

    We ship methyl 2-aminopyridine-3-carboxylate in sealed, inert-lined containers directly from our production line. Over the years, feedback from customers in pharmaceuticals, agrochemicals, and fine chemicals has helped us fine-tune both our formulation and how we handle material flow to match expectations for ease of weighing and dissolution.

    Performance in Synthesis

    We watch closely how our methyl 2-aminopyridine-3-carboxylate performs in actual laboratory and pilot environments. Research chemists regularly return with reports about consistent reactivity, and we’ve run our own parallel tests to confirm strong amide coupling efficiency in small molecule API synthesis. For broad applications like heterocycle building blocks, our experience shows the product holds up well under heating and varied pH. We’ve had occasions to scale up amidation routes ourselves, and our data confirms that purity at each stage directly improves product conversion downstream.

    One product batch often sees use in multi-step processes where deviations in quality or physical properties can disrupt yield. Through careful control and continuous dialogue with end-users, we identify points where trace impurities could cause issues in reactions—such as incomplete couplings or formation of colored by-products during cyclization. We use that information to further improve our internal filtration and polishing steps.

    It’s not uncommon for outside labs to compare our material head-to-head with other manufacturers. We remain motivated by this scrutiny, and routinely submit samples for third-party verification when users request additional confirmation of purity, solubility, or melting range.

    Differences from Other Pyridine Derivatives

    We have manufactured and tested several amino pyridine derivatives in our facility, including the 3-amino, 4-amino, and unsubstituted methyl pyridine carboxylates. From side-by-side comparative synthesis trials, it’s clear that the 2-amino group in our product increases its value for coupling reactions, especially in fields looking for site-selective modification. In peptide synthesis, chemists report that nucleophilicity and orientation differ significantly compared to the 4-amino isomer, allowing better control over substitution patterns. For customers working with organometallic ligands, small tweaks in substitution heavily influence catalyst formation—something we’ve explored with collaborators.

    Other methyl pyridine carboxylate products we see on the market often arrive with broader impurity profiles. Through feedback networks with pharmaceutical process teams, we have found that seemingly minor differences in starting material quality can reveal themselves at later synthetic stages. For example, higher levels of trace nitro compounds or isomeric impurities often lead to longer purification times. We prioritize purification even when batch yields drop a few percent as a result.

    Compared to unprotected amino-pyridine carboxylic acids, our methyl ester variant demonstrates greater solubility in organic solvents. This property enables easier integration into DMF, DCM, and acetonitrile-based reactions. Our team ran direct dissolution trials in collaboration with pharma customers to confirm this, which helped support process modifications that reduce wasted solvent and shorten mixing times.

    A short note on shelf life: we've tracked stability here for several years, and when our product is stored under normal indoor conditions, it retains specification for a minimum of two years without significant loss of assay or color change. Free acids in related products degrade more rapidly, requiring cooler storage and faster use. Methyl ester forms continue to show resilience in bulk packaging and end-user laboratories.

    Applications We See Most Often

    Because we manufacture and follow the path of our methyl 2-aminopyridine-3-carboxylate into downstream projects, we recognize which segments benefit from it most. The compound frequently appears as a key intermediate in small molecule pharmaceuticals, especially those containing fused N-heterocyclic systems such as pyrazolo[1,5-a]pyrimidines and pyrido[2,3-d]pyrimidines. We support several projects where our product enters kinase inhibitor programs or custom pesticide R&D. Based on direct collaboration with research customers, we know that specific substitution at the 2-amino position enables unique SAR (structure–activity relationship) exploration.

    Agrochemical customers routinely use the methyl group as a handle for subsequent hydrolysis, taking advantage of the easy conversion to free acid under mild base conditions. Our process chemists have ourselves run hydrolysis experiments to confirm mild conditions suffice, which helps conserve more sensitive functional groups downstream.

    We also deliver to advanced material and dye chemistry groups. These groups value the combination of amine and ester functionalities in a single scaffold for constructing novel ligands and polymer backbone fragments. They’ve sent feedback that our compound offers a good bridge between easily manipulated building blocks and chemically robust frameworks.

    Direct Experience with User Challenges

    Handling concerns often arise from users unfamiliar with pyridine derivatives, especially regarding odor and volatilization. Our process includes several odor abatement measures and packaging protocols because we’ve noticed that even trace residues of the starting pyridine base can cause strong olfactory responses during product transfer. We routinely improve venting and sealing procedures based on these observations.

    Inconsistencies in moisture uptake once troubled our early production, leading to clumping and weighing difficulty in some customer labs. In response, we altered drying times and updated our storage drums to include layered desiccant treatments. Ongoing water content monitoring with Karl Fischer titration ensures repeatable performance on delivery.

    Shipping outside our home region highlighted another issue: regulatory patchwork can slow movement if documentation is incomplete or ambiguous. We have a dedicated compliance team who track customs requirements and routinely run mock submissions covering REACH or regional equivalents to keep paperwork correct and timely. Years spent bridging regulatory gaps mean our product moves from our facility to customers with fewer supply chain surprises.

    The most impactful improvements to our workflow often come from less predictable feedback—such as noticing how packaging design affects powder transfer, or learning that slight changes in powder density improve automated dosing. We incorporate these lessons rapidly, realizing that as a direct manufacturer, such tweaks can make the difference between a good experience and a frustrating one on the user’s end.

    Technical teams from partner companies sometimes request deeper access to our batch records or even tour our facility. We remain open to these visits and data-sharing after appropriate review. These exchanges foster direct trust and allow us to demonstrate, with physical records and on-the-ground presence, the quality systems that support each shipment.

    The Role of Consistency and Transparency

    Consistency is often missing from intermediates purchased off the global market. We regularly receive samples from new customers along with requests to match or improve on color, purity, or reactivity profiles seen in competitors’ batches. We welcome this scrutiny—realizing someone, somewhere, will actually perform the comparison. We invite these challenges. Open communication about origin, synthetic route, and batch level data builds a relationship that supports ongoing supply rather than a transactional, one-time purchase.

    Full disclosure builds trust. We keep detailed records for each batch, including chromatograms, titration graphs, and trace impurity logs. Customers often ask for atypical documentation, such as method validation for specific applications or historical lot data. We treat these requests as routine rather than exceptional and update our archives as standard practice.

    Unexpected challenges have sometimes exposed weaknesses in our internal training or workflow. Based on customer incident reports, we regularly re-examine practices in raw material inspection, operator training, or cleaning protocols between campaigns. Cycles of self-assessment and engagement with users let us spot issues before they reach process-critical stages for customers.

    Environmental and Safety Practices

    We have integrated several on-site measures addressing the environmental profile of pyridine derivatives. Waste streams containing methyl 2-aminopyridine-3-carboxylate or any of its precursors undergo monitored neutralization and carbon filtration. Our solvent recovery units extract and reuse over 60% of the organic solvent input from major processes—verified by internal yearly audits. This practical approach both reduces cost and addresses concerns sustainable procurement teams raise.

    A focus on plant operator safety stays central to our process. Pyridine derivatives have a long history of concern for skin and mucous membrane exposure. We require closed transfers, proper labeling, and engineering controls at all points of manufacture. Our in-house training emphasizes hands-on PPE use and spill response. Customers occasionally ask for safety protocol sharing, and we provide detailed SOPs tailored to their in-house environments since we know no two labs face exactly the same hazards.

    While we maintain compliance with all regional safety and environmental guidelines, our experience suggests direct engagement—at both management and floor-operation levels—prevents lapses. A steady record of low incident rates demonstrates the payoff from ongoing investment in process safety and environmental controls.

    Continuous Improvement and Direct Dialogue

    As with any specialized intermediate, methyl 2-aminopyridine-3-carboxylate benefits from an iterative approach to improvement. Every quality complaint, every unexpected reaction outcome traced to a minor contaminant, becomes a learning opportunity. Open conversations with end-users pinpoint features most valued—sometimes solubility under non-standard conditions, sometimes exacting control of polymorphic form.

    Transparency in manufacturing lets us track not just chemical data, but reasons behind each adjustment. We find, for example, that including customer application data—such as solvent systems in use for new kinase inhibitor scaffolds or specific temperature ramps in dye formation—helps us refine both process and specification with visible quality improvements.

    On several occasions, customers working in confidential research have connected with our technical team to develop custom variants. Making adjustments to ester length, amine position, or even trace-level impurity tolerances helps accelerate their projects, and our flexible manufacturing setup enables quick adaptation without compromising on control.

    Contributing Valuable Materials to Research and Industry

    Our production of methyl 2-aminopyridine-3-carboxylate combines strict technical standards and responsiveness to the real-world needs of chemical developers. Each kilogram produced not only supports a named reaction or target molecule but also feeds a larger ecosystem of investigation and discovery in fine chemical manufacturing. We take pride in the role our team plays, knowing that as direct manufacturers, our product often forms the backbone of progress in both new drug substances and advanced materials.

    It remains a source of satisfaction to know that what we deliver has passed not just regulatory and specification checks, but also meets the nuanced, hands-on standards of users who perform the demanding work of chemical innovation. Every challenge reported, every adjustment made, reflects our ongoing partnership with those who transform base building blocks into something greater.