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2-(4-Nitrophenyl)Pyridine

    • Product Name 2-(4-Nitrophenyl)Pyridine
    • Alias 4-Nitrophenyl-2-pyridine
    • Einecs 249-846-5
    • 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

    715623

    Chemical Name 2-(4-Nitrophenyl)Pyridine
    Molecular Formula C11H8N2O2
    Molecular Weight 200.20 g/mol
    Cas Number 21574-26-7
    Appearance Yellow solid
    Melting Point 159-163 °C
    Solubility Slightly soluble in organic solvents
    Smiles c1ccnc(c1)c2ccc(cc2)[N+](=O)[O-]
    Iupac Name 2-(4-nitrophenyl)pyridine
    Pubchem Cid 24901255

    As an accredited 2-(4-Nitrophenyl)Pyridine 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 2-(4-Nitrophenyl)Pyridine; labeled with chemical name, hazard symbols, and lot number.
    Shipping 2-(4-Nitrophenyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical and must comply with international regulations for the transport of dangerous goods. Appropriate safety labeling, cushioning, and documentation are included during shipment to ensure safe delivery and regulatory compliance.
    Storage 2-(4-Nitrophenyl)pyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and reducing agents. Protect from light and moisture. Label the container clearly, and handle using appropriate personal protective equipment to prevent exposure and contamination.
    Application of 2-(4-Nitrophenyl)Pyridine

    Applications of 2-(4-Nitrophenyl)Pyridine in Industrial Manufacturing

    2-(4-Nitrophenyl)Pyridine serves as a critical intermediate in fine chemical manufacturing. Our facility supplies this compound for advanced synthesis processes in key industrial sectors. Each application scenario demonstrates specific pathways, regulated standards, and formulation practices, supporting downstream manufacturers in complex production lines.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Our product is widely adopted by pharmaceutical companies to synthesize pyridine-based APIs, particularly in the production of kinase inhibitors and anti-inflammatory agents. The compound typically functions as a functionalized scaffold in multi-step organic synthesis, contributing nitro and pyridyl groups that enable structural modifications and biological activity required for drug candidates. Pharmaceutical manufacturers integrate this raw material under controlled conditions, emphasizing trace impurity control and process validation throughout API synthesis chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP <823> Chapter for Radiopharmaceuticals (where relevant)
    • EDQM CEP (Certificate of Suitability of Monographs of the European Pharmacopoeia)
    • 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Used at 0.5%–3% by molar equivalence in advanced synthetic steps, with adjustment based on the specific synthetic route and targeted yield efficiency.

    Downstream process integration

    • Added during the intermediate coupling stage of heterocyclic synthesis.
    • Integrated into batch reactors equipped for high-purity condensation and substitution reactions.
    • Processed under inert atmosphere to avoid reduction of the nitro group.

    Final product types

    • Small molecule kinase inhibitors
    • Anti-inflammatory agents
    • Compounds for clinical trial supply
    • Generic pyridine-based pharmaceuticals

    2. Agrochemical Intermediate for Crop Protection Compound Manufacturing

    Leading agrochemical producers rely on this compound as a key intermediate in the synthesis of selective herbicides and pesticide actives that feature a nitrophenyl-pyridine moiety. Consistent quality and batch reproducibility are required to meet regulatory approvals during technical-grade synthesis, particularly due to heightened scrutiny around trace nitroaromatic residues in the formulated end products destined for agricultural use.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems Certification
    • EPA Pesticide Registration Standards (40 CFR Parts 150–189)

    Typical usage ratio

    • Utilized in the range of 1%–4% of total formulation mass, depending on target active loading and base structure modification needs.

    Downstream process integration

    • Introduced during the formation of pyridine-derived ring structures in technical concentrate manufacturing.
    • Engaged in catalytic coupling reactions with various amines, producing targeted agrochemical actives.
    • Monitored closely throughout post-reaction purification to ensure removal of residual nitro intermediates.

    Final product types

    • Selective herbicide actives for cereals and broadleaf crops
    • Nitrophenyl-based pesticide concentrates
    • Pre-emergence weed control agents
    • Registered crop protection brands

    3. OLED and Electronics Material Precursor

    Manufacturers in the organic electronics sector utilize 2-(4-nitrophenyl)pyridine for fabricating advanced organic light-emitting diode (OLED) charge transport molecules. The compound’s structure enables the construction of pyridine-containing ligands used to build phosphorescent emitters. Downstream integration focuses on batch consistency and ultra-high purity during the synthesis of organic semiconductors, as trace impurities impact device performance such as brightness and operational lifespan.

    Industry compliance standards

    • JEITA EM-201 Semiconductor Materials Inspection Guidelines
    • RoHS Directive 2011/65/EU (for heavy metals and restricted compounds)
    • IEC 62474 Material Declaration for Products of and for the Electrotechnical Industry
    • Internal ISO 14644-1 Certified Cleanroom Protocols

    Typical usage ratio

    • Employed at 0.2%–1.5% relative to total mass of ligand synthesis step, adjusted per photophysical yield analysis and efficiency benchmarks.

    Downstream process integration

    • Fed into ligand coupling reactions for iridium complexes.
    • Used in bench-scale and semi-batch reactors aligned with moisture- and light-sensitive processing parameters.
    • Purified through chromatographic separation before device fabrication.

    Final product types

    • Blue and green phosphorescent OLED materials
    • Organic semiconducting ligands
    • Small molecule emitters for display panels
    • Mobile device and TV panel components

    4. Specialty Dye and Pigment Synthesis

    Producers of specialty dyes select this material for synthesizing high-heat stable colorants based on nitroaromatic-pyridine motifs. Its controlled reactivity enables production of pigments used in coatings, plastics, and fiber coloration. Downstream processors emphasize strict handling protocols to prevent contamination and ensure the photostability and colorfastness of the resulting pigment dispersions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for Textile Dye Safety
    • EN 71-3 Safety of Toys – Migration of Certain Elements (for pigment in toys/coatings)
    • ISO 1248:2006 for Pigments and Extenders
    • EU REACH Annex XVII (restrictions on aromatic amines/nitro compounds)

    Typical usage ratio

    • Applied within 1%–6% of total pigment synthesis batch, variation determined by chromatographic purity targets and substrate compatibility.

    Downstream process integration

    • Incorporated during diazotization and coupling stages of dye synthesis.
    • Engages as a nitrogen source for complex pigment backbone construction.
    • Processed in closed reactor systems with continuous color value (C.I.) monitoring.

    Final product types

    • Nitroaromatic-based powder pigments
    • Heat-stable specialty dyes for technical textiles
    • Masterbatch colorants for plastics industry
    • UV-resistant coatings for industrial flooring
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