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2-Amino-3-Nitro-4-Picoline

    • Product Name 2-Amino-3-Nitro-4-Picoline
    • Alias 2-Amino-6-methyl-3-nitropyridine
    • Einecs 629-685-6
    • 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
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    Specifications

    HS Code

    345713

    Chemical Name 2-Amino-3-Nitro-4-Picoline
    Molecular Formula C6H7N3O2
    Molecular Weight 153.14 g/mol
    Cas Number 22483-10-3
    Appearance Yellow to orange solid
    Melting Point 110-115°C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Storage Temperature Store at room temperature
    Synonyms 2-Amino-3-nitro-4-methylpyridine
    Smiles CC1=NC=C(C(=C1)N)[N+](=O)[O-]
    Inchi InChI=1S/C6H7N3O2/c1-4-2-3-5(7)6(8)9(4)10/h2-3H,7H2,1H3

    As an accredited 2-Amino-3-Nitro-4-Picoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, sealed cap, labeled “2-Amino-3-Nitro-4-Picoline, 100g,” hazard pictograms, batch number, and handling instructions.
    Shipping 2-Amino-3-Nitro-4-Picoline should be shipped in tightly sealed containers, away from incompatible materials, under cool and dry conditions. Ensure appropriate labeling for chemical hazards. Transport must comply with local, national, and international regulations for hazardous substances, using suitable protective packaging to prevent leaks, contamination, or exposure during transit.
    Storage 2-Amino-3-Nitro-4-Picoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, moisture, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Label the container clearly and store it in a designated chemical storage cabinet. Handle with suitable protective equipment to prevent exposure.
    Application of 2-Amino-3-Nitro-4-Picoline

    Applications of 2-Amino-3-Nitro-4-Picoline in Industrial Manufacturing

    As an established producer of 2-Amino-3-Nitro-4-Picoline, we supply this compound to multiple high-value manufacturing sectors. Below we provide structured references for its main downstream industrial applications, including detailed usage guidance, compliance requirements, integration stages, and typical end products.

    1. Synthesis of Agrochemical Intermediates

    Many agrochemical manufacturers use 2-Amino-3-Nitro-4-Picoline as a starting material for heterocyclic building blocks in the synthesis of broad-spectrum pesticides and herbicides. Its electron-rich structure promotes efficient coupling during key condensation steps, particularly in the creation of pyridine-based active components. Control of impurity profiles remains critical to meet downstream residue limits for food crop safety.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Technical Materials
    • ISO 9001:2015 Quality Management System
    • REACH Annex VII–X, substance registers and safety data requirements
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products

    Typical usage ratio

    • 10–18% weight basis in precursor blend, adjusted based on active group yield and downstream impurity controls

    Downstream process integration

    • Charged into the primary condensation reaction stage with chlorinated aromatics under controlled pH
    • Used in closed-loop systems to limit operator exposure during high-temperature coupling
    • Intermediate isolation prior to final active or salt formation
    • Continuous feeding for multi-ton batch operations

    Final product types

    • Pyridine-based herbicides (e.g., picoline derived)
    • Insecticidal metabolites
    • Fungicidal pre-cursors for crop protection
    • Seed treatment compounds

    2. API Intermediate for Pyridine-containing Pharmaceuticals

    Pharmaceutical groups rely on this raw material for constructing key fragments in active pharmaceutical ingredient (API) synthesis, most notably within antimicrobial and anti-inflammatory drugs. Our strict QC manages trace nitro and halide content below pharmacopeial thresholds to enable safe downstream conversions. Customers favor this input for high-yield amidation and cyclization reactions that demand precise impurity control.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP Monographs pertaining to API-grade intermediates
    • FDA 21 CFR Part 211: cGMP for finished pharmaceuticals
    • ISO 17025 analytical method validation for release testing

    Typical usage ratio

    • 12–23% of reaction mass, depending on targeted API framework and conversion efficiency

    Downstream process integration

    • Initial amination or cyclization in the first synthesis stage
    • Feeding into closed or semi-continuous reactors with real-time HPLC monitoring
    • Intermediary isolation for downstream derivatization, such as nitration or acylation
    • Involvement in catalytic hydrogenation for subsequent API development

    Final product types

    • Pyridine ring-based anti-infectives
    • Anti-tuberculosis pharmaceutical APIs
    • Pyridopyrimidine intermediates for CNS drug synthesis
    • Specialty analgesic and anti-inflammatory agents

    3. Colorants and Pigment Manufacturing

    Colorant producers employ 2-Amino-3-Nitro-4-Picoline chiefly in the formulation of specialty azo and phthalocyanine pigments. Its distinct substitution pattern enables efficient diazotization and subsequent coupling, delivering both solvent and light stability essential for ink, plastic, and coating applications. Tight upstream control of moisture and trace metal contaminants is critical due to the high sensitivity of pigment crystal formation.

    Industry compliance standards

    • ISO 1248 Pigments—Specifications and test methods
    • REACH Annex XIV for Restricted Substances (colorant safety)
    • EN 71-3 Safety of Toys—Migration of Certain Elements (for pigments used in child products)
    • AP(89)1 for food contact colorants

    Typical usage ratio

    • 2–7% by mass in pigment precursor blends; varies with required chromatic intensity and shade specificity

    Downstream process integration

    • Charging to the diazotization reactor
    • Pre-neutralization and staged addition for color shade consistency
    • In-line blending with coupling components for batch and continuous pigment synthesis
    • Filtration and drying precede final pigment stabilization

    Final product types

    • Azo and phthalocyanine colorants for plastics
    • Industrial textile, fiber, and paper dyes
    • High-performance printing inks
    • Special effect pigments in automotive coatings

    4. Electronic Chemical Intermediates

    Producers of semiconductor and LCD materials source 2-Amino-3-Nitro-4-Picoline for the creation of heteroaromatic compounds used in organic electronic layers. This molecule’s nitrogen content and substitution pattern promote charge transport and facilitate precise alignment in oligomer synthesis. Stringent control during purification and packaging prevents ionic and particulate contamination which is critical for downstream electronic performance and cleanroom compatibility.

    Industry compliance standards

    • SEMI C59 standard for ultrahigh purity (UHP) chemicals
    • ISO 14644 for cleanroom and associated environments
    • RoHS 2 (2011/65/EU) restriction compliance for consumer electronics
    • IEC 62474 substance declaration requirements

    Typical usage ratio

    • 0.3–2% in precursor feed, depending on device structure and batch scale

    Downstream process integration

    • Dosed into oligomerization or polymerization stages under inert gas blanketing
    • Filtered with sub-micron membranes before use in high-vacuum coating equipment
    • Wet-chemically purified and transported in UHP-certified packaging
    • Integrated into solution-based or vapor-deposition processes for thin film formation

    Final product types

    • Organic semiconductor layers in OLED displays
    • P-type and N-type materials for thin-film transistors
    • Conductive intermediates for printed electronics
    • Charge-transport compounds in solar panels
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