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HS Code |
652944 |
| Chemical Name | 2-Aminoisonicotinic Acid |
| Cas Number | 5345-47-1 |
| Molecular Formula | C6H6N2O2 |
| Molecular Weight | 138.13 |
| Appearance | Off-white to light brown solid |
| Melting Point | 261-263°C |
| Solubility In Water | Slightly soluble |
| Density | 1.486 g/cm3 |
| Pubchem Id | 11656 |
As an accredited 2-Aminoisonicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 2-Aminoisonicotinic Acid is sealed in an amber glass bottle with a secure screw cap and safety labeling. |
| Shipping | 2-Aminoisonicotinic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically packaged according to hazardous material regulations, with clear labeling for safe handling. Transportation is conducted under controlled conditions, avoiding direct sunlight and extreme temperatures to maintain product integrity and comply with safety standards. |
| Storage | 2-Aminoisonicotinic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid excessive heat to prevent decomposition. Clearly label the container and ensure only trained personnel handle and access the chemical. |
Applications of 2-Aminoisonicotinic Acid in Industrial Manufacturing2-Aminoisonicotinic Acid serves as a critical intermediate across multiple industrial segments, with each downstream application demanding strict adherence to process, formulation, and regulatory controls. As a raw material manufacturer, we partner directly with end-use industries to ensure stable supply tailored to their specific requirements. The following sections detail genuine application scenarios in pharmaceutical synthesis, agrochemical intermediates, organic electronics, and specialized pigment manufacturing. 1. Pharmaceutical API Intermediate: Anti-Tuberculosis and Anti-Viral AgentsPharmaceutical producers utilize 2-Aminoisonicotinic Acid for the synthesis of advanced intermediates in anti-tuberculosis medication and select antiviral APIs. This material enters multistep synthetic routes where amination and subsequent derivatization yield core heterocyclic scaffolds found in pyrazinamide analogs and related quinoline derivatives. Downstream synthesis integrates our product in condensation or chloroamination steps under carefully controlled reaction conditions, supporting end products registered under regulated markets. Industry compliance standards
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2. Agrochemical Intermediate: Synthesis of Systemic FungicidesFormulators of modern systemic fungicides depend on 2-Aminoisonicotinic Acid during the multi-step creation of active ingredients in pyridine carboxamide and isonicotinic-based agrochemicals. The compound forms key building blocks in the manufacture of fungicidal agents designed for high selectivity and low toxicity. Commercial scale-up requires strict analytical verification of input quality to ensure reproducible yields and minimal impurity carryover into technical-grade actives, meeting international agrochemical registration file demands. Industry compliance standards
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3. Organic Electronics: Precursor for Electroluminescent MaterialsSpecialty electronic materials manufacturers employ 2-Aminoisonicotinic Acid as a key precursor in synthesizing functional dyes and charge transport molecules for organic electroluminescent devices. The unique substitution pattern facilitates the formation of stable conjugated frameworks crucial for optoelectronic applications. Downstream synthesis includes Suzuki-Miyaura coupling and amide coupling reactions, producing materials incorporated into thin films and OLED prototypes with tightly controlled purity and batch reproducibility demands. Industry compliance standards
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4. Specialty Pigment Manufacturing: High-Performance ColorantsProducers of advanced pigments utilize 2-Aminoisonicotinic Acid in syntheses where nitrogen-rich aromatic rings impart enhanced lightfastness and chromatic stability to specialty colorants. The compound is involved in diazotization or coupling reactions with phenolic or aromatic amines, forming pigments for plastics, inks, and coatings. Batch consistency, freedom from inorganic contaminants, and low moisture content are vital, as pigment performance depends closely on the purity and precise stoichiometry of the precursor materials. Industry compliance standards
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