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Methyl 2-Aminonicotinate

    • Product Name Methyl 2-Aminonicotinate
    • Alias 2-Aminonicotinic acid methyl ester
    • Einecs 'EINECS 260-238-6'
    • 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
    VTB
    Specifications

    HS Code

    100516

    Chemical Name Methyl 2-Aminonicotinate
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Cas Number 5787-55-3
    Appearance White to off-white solid
    Melting Point 61-65°C
    Boiling Point 312°C (estimated)
    Solubility Soluble in organic solvents like ethanol and methanol
    Purity Typically ≥98%
    Smiles COC(=O)C1=CC=CC(N)=N1

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

    Packing & Storage
    Packing Methyl 2-Aminonicotinate, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and printed label.
    Shipping Methyl 2-Aminonicotinate is shipped in tightly sealed containers, protected from moisture and light. It should be packed in compliance with local and international regulations for chemical transport. Handle with care, avoiding exposure or inhalation. Ensure transport vehicles are ventilated, and include relevant safety documentation and hazard labeling as per GHS guidelines.
    Storage Methyl 2-Aminonicotinate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8 °C (refrigerator temperature). Store away from strong oxidizing agents, acids, and bases. Ensure proper labeling and follow local regulations for chemical storage to prevent contamination or degradation.
    Application of Methyl 2-Aminonicotinate

    Applications of Methyl 2-Aminonicotinate in Industrial Manufacturing

    Methyl 2-Aminonicotinate serves as an essential intermediate in several specialized industrial sectors, supporting precise synthesis routes in fine chemicals and regulated applications. The following application scenarios reflect true, large-scale downstream use cases where this material plays a crucial role in value-added production. All scenarios include detailed process information, real compliance systems, and industrially validated usage parameters based on our technical expertise and customer integration experience.

    1. Pharmaceutical Active Ingredient Synthesis

    In pharmaceutical manufacturing, this compound functions as a critical building block in developing advanced pyridine-based active pharmaceutical ingredients, especially those for anti-tuberculosis and neurological therapies. Its amino group and ester functionalization provide specificity for coupling and heterocyclic ring elaboration steps, essential for process route kinetics and impurity controls. Formulators typically adjust ratios to maximize yield while maintaining regulatory impurity thresholds, and integration takes place in multi-stage, closed GMP environments for high-purity API output.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • EU Guidelines for Medicinal Products for Human Use (EMA)
    • Japanese Pharmacopoeia/USP/NF where applicable
    • FDA 21 CFR Part 211 (if exporting to U.S.)

    Typical usage ratio

    • Between 0.5–2.5 molar equivalents per synthesis batch; optimized according to target API scaffold complexity and stepwise conversion efficiency

    Downstream process integration

    • Introduced during the condensation or N-alkylation step as a core intermediate, followed by high-vacuum distillation or chromatographic purification to separate target molecules

    Final product types

    • Nicotinic acid derivatives for pharmaceutical APIs (e.g., pyrazinamide intermediates, CNS therapy candidates, cardiovascular agents)

    2. Crop Protection and Agrochemical Intermediate Production

    Chemical formulation plants use this material as a strategic precursor in heterocyclic core construction for selective herbicides and insecticides. Its use is driven by the need for precision in pyridinic skeleton modification, which directly impacts bioactivity profiles and environmental fate. The component is metered according to downstream hydrolysis, amidation, or ring-transforming steps, monitored under ISO-certified batch controls to ensure product consistency and regulatory traceability.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • REACH registration (for EU export)
    • FAO/WHO Pesticide Specifications
    • National agrochemical regulatory approvals (e.g., China ICAMA, U.S. EPA requirements)

    Typical usage ratio

    • Ranges from 1–5% by mol in batch, depending on final actives’ target concentration and downstream conversion rates; tailored in process control sheets per formulation

    Downstream process integration

    • Added during core scaffold assembly or amidation, followed by post-reaction work-up including extraction and solvent exchange; supported with inline spectrometric purity checks

    Final product types

    • Pyridine-derived herbicides and systemic insecticide intermediates; functionalized building blocks for fungicide arrays

    3. Specialty Dye and Pigment Intermediate Manufacturing

    Advanced pigment producers leverage this compound for synthesizing high-performance, lightfast organic dyes. The ester and amino moieties enable tailorable diazotization and subsequent coupling, essential for producing stable chromophores with targeted solubility. Usage rates depend on the chain length and required color strength, with full traceability under ISO 14001 for environmental controls due to potential process effluents.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems
    • Oeko-Tex Standard 100 (for textiles and leather applications)
    • European REACH Regulation (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • National factory discharge and effluent standards (local EPA/SEPA requirements)

    Typical usage ratio

    • Typically 0.2–1% by weight in masterbatch pigment synthesis, adjusted for pigment dispersion quality and final concentration demands

    Downstream process integration

    • Participates in the initial aromatic amination or coupling step, entering the batch reactor after pre-treatment; followed by heating, precipitation, and recrystallization stages for pigment formation

    Final product types

    • Nitrogen-containing azo dyes, photostable textile pigments, specialty printing ink colorants

    4. Fine Chemicals for Electronic and Photonic Materials

    Manufacturers in the electronic materials sector utilize this compound as a precursor for synthesizing pyridine-based ligands and functional monomers that impart specific charge-transport and anchoring capabilities in OLEDs and printed electronic circuits. The precise ester function allows for clean post-reaction modification, influencing film thickness and electrical performance. Dosage varies based on the target functionalization level for subsequent polymerization or surface modification processes. Integration and quality tracking follow both TUV- and RoHS-driven cleanroom practices regarding impurity and trace metal limits.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) for electronic materials
    • ISO 9001 and ISO 17025 for QC traceability in specialty electronic chemical manufacturing
    • IEC material testing protocols (for end-use compatibility)
    • TUV Rheinland or SGS cleanroom certification for sensitive electrode materials

    Typical usage ratio

    • Generally supplied at 0.1–0.8 molar equivalents relative to co-monomer or ligand backbone; tailored per conductivity and functionalization target during R&D and scale-up phases

    Downstream process integration

    • Included in high-purity condensation or complexation step under anhydrous, oxygen-controlled environments; progresses to purification and formulation for thin-film or solution casting

    Final product types

    • OLED charge transporting agents, pyridyl-functionalized anchor molecules, advanced photoresist derivatives
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