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Methyl 4-Aminopyridine-3-Carboxylate

    • Product Name Methyl 4-Aminopyridine-3-Carboxylate
    • Alias 4-Amino-3-pyridinecarboxylic acid methyl ester
    • Einecs EINECS 619-354-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    354657

    Chemical Name Methyl 4-Aminopyridine-3-Carboxylate
    Cas Number 30724-41-7
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15
    Appearance Off-white to light yellow solid
    Melting Point 98-102°C
    Solubility Soluble in organic solvents such as methanol and DMSO
    Smiles COC(=O)C1=CN=CC(=C1)N
    Inchi InChI=1S/C7H8N2O2/c1-11-7(10)6-5(8)2-3-9-4-6/h2-4H,1H3,(H2,8,9)
    Purity Typically ≥98%
    Storage Store at 2-8°C, in a dry place
    Synonyms Methyl 4-amino-3-pyridinecarboxylate

    As an accredited Methyl 4-Aminopyridine-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of Methyl 4-Aminopyridine-3-Carboxylate is supplied in a sealed amber glass bottle with a printed safety and content label.
    Shipping Methyl 4-Aminopyridine-3-Carboxylate is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is typically transported at ambient temperature unless otherwise specified. It complies with safety regulations, including appropriate labeling and documentation. Handle with care, using protective equipment during transit and storage. Not regulated as hazardous for transport unless noted.
    Storage Methyl 4-Aminopyridine-3-Carboxylate should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Protect from moisture and incompatible substances such as strong oxidizing agents. Store at room temperature or as recommended by the manufacturer. Ensure proper labeling and access is restricted to trained personnel.
    Application of Methyl 4-Aminopyridine-3-Carboxylate

    Applications of Methyl 4-Aminopyridine-3-Carboxylate in Industrial Manufacturing

    Methyl 4-Aminopyridine-3-Carboxylate is a specialty pyridine heterocyclic intermediate with precise value in the downstream synthesis of advanced pharmaceutical actives, agricultural chemicals, and custom fine chemical derivatives. As the original manufacturer, we support clients requiring this molecule for regulated synthesis pipelines, stringent batch traceability, and high-conversion processes. Below are its core industrial application areas recognized by leading sector standards and actual B2B formulation practices.

    1. Pharmaceutical Intermediates for API Synthesis

    Branded and generic drug manufacturers use this pyridine derivative as a selective precursor for constructing key molecular frameworks within central nervous system (CNS) agents, antimuscarinic actives, and certain anti-infectives. Its precise reactivity allows controlled derivatization at the 3- and 4- positions for high-value small-molecule APIs. Production sites require consistent purity and traceability for qualification into GMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)
    • EMA Guidelines on the Manufacture of the Finished Dosage Form (EU GMP Annex 1 & 8)
    • Relevant monographs in USP–NF and Ph. Eur. (if classified as a starting material or specified impurity)

    Typical usage ratio

    • 0.8–5 mol% relative to downstream target intermediate; adjustment depends on step yield and required phenyl/alkyl substitution.

    Downstream process integration

    • Introduced in coupling, cyclization, or amidation reaction steps—typically as a nucleophilic or amination substrate under inert conditions prior to final purification, in multi-step synthesis for specialty APIs.

    Final product types

    • Central nervous system (CNS) active ingredients (e.g., muscle relaxants, antiemetics)
    • Intermediate scaffolds for further functionalization in small-molecule APIs
    • Branded and generic bulk drug substances
    • High-value investigational or orphan drug actives

    2. Crop Protection Actives and Intermediates

    Research-driven agrochemical manufacturers employ this material as a structurally defined pyridine backbone, vital for synthesis of custom herbicides, fungicides, and select insecticides. Specialized functional group modifications enable precise binding in the design of target-specific crop protection agents, thanks to its aromatic amine and ester moieties facilitating further transformations.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides (JMPS)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • China National Standard GB 22223—Production and Approval of Pesticide Intermediates

    Typical usage ratio

    • 1.5–6% by weight of the precursor batch, depending on the step in the synthetic cycle and purity of downstream crop protection intermediates.

    Downstream process integration

    • Used at the second or third synthetic step to introduce aminopyridine functionalities before ester hydrolysis, chlorination, or amidation, depending on the mode-of-action design of the final pesticide active.

    Final product types

    • Herbicide intermediates (pyridine-based pre-emergent agents)
    • Fungicide building blocks with targeted aromatic backbones
    • Specialty insecticide cores for seed treatments or foliar applications
    • Registered technical pesticide concentrates

    3. Specialty Fine Chemical Synthesis

    Custom synthesis laboratories and industrial chemical producers utilize this pyridine ester in the preparative routes for advanced heterocyclics, colorants, and functional monomers. Its substitution sites allow efficient construction of libraries for electronic materials and performance additives demanded by high-tech sectors. Close control of process impurities is critical for downstream use.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Internal QC as per American Chemical Society (ACS) Reagent Grade requirements (when used as a reference or precursor)
    • National and regional chemical safety protocols (OSHA PSM and EU SEVESO III where applicable)
    • Custom specification sheets based on B2B supplier agreements

    Typical usage ratio

    • 0.3–3% weight basis in preparative or pilot scale, adjusted for target reaction completeness and minimization of side reaction profiles.

    Downstream process integration

    • Added during the nucleophilic aromatic substitution or amidation stages in closed-batch or continuous-feed reactors; precise timing minimizes hazardous intermediates for safety and batch yield optimization.

    Final product types

    • Functional monomers for specialty polymer applications
    • Niche dyestuff intermediates and custom pigments
    • Electronic material intermediates for optoelectronic coatings
    • High-purity research molecules for structure-activity studies

    4. Active Pharmaceutical Research and Custom Synthesis

    Contract research organizations (CROs) and academic laboratories select this material for medicinal chemistry platforms, where the aminopyridine scaffold expedites SAR (structure–activity relationship) screening in the early-stage design of bioactive agents. The robust chemical identity ensures reproducible outcomes for IP-protected discovery pipelines and phase I manufacturing supply.

    Industry compliance standards

    • Good Laboratory Practice (GLP) as per OECD or FDA 21 CFR Part 58
    • USP <795> for compounding and laboratory quality control
    • IUPAC and ACS purity guidelines for reagent qualification
    • ISO/IEC 17025 for laboratory analytical method validation

    Typical usage ratio

    • Varies from 0.1–2 mmol in screening libraries, or as specified by synthetic design; scales to 15–25 g per batch for preclinical candidate supply.

    Downstream process integration

    • Dosed in combinatorial or parallel synthesis set-ups at the stage of precursor condensation or ring-closure; handled under fully documented traceability for experimental reproducibility and intellectual property tracking.

    Final product types

    • Small-molecule lead compounds for patenting and licensing
    • Bioactive analogs for drug discovery projects
    • Intermediates for new chemical entities (NCEs) in preclinical studies
    • Lab-scale SAR libraries for screening and assay development
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