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2-Amino-5-Bromo-4-Methyl-3-Nitropyridine

    • Product Name 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine
    • Alias 5-Bromo-4-methyl-3-nitro-2-pyridinamine
    • Einecs 629-606-6
    • 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

    474810

    Product Name 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine
    Cas Number None Assigned
    Molecular Formula C6H6BrN3O2
    Molecular Weight 232.04 g/mol
    Appearance Yellow to brown solid
    Solubility Slightly soluble in common organic solvents
    Smiles CC1=CN=C(C(=C1Br)[N+](=O)[O-])N
    Inchi InChI=1S/C6H6BrN3O2/c1-3-2-10-6(8)4(7)5(3)9(11)12/h2H,1H3,(H2,8,10)
    Purity Typically >= 95%
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine is supplied in a sealed amber glass vial with a screw cap.
    Shipping **Shipping Description:** 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine is shipped in secure, sealed containers, compliant with chemical safety regulations. The package is clearly labeled with hazard and handling instructions, and protected against moisture, light, and physical damage. Shipments are routed via certified carriers suitable for hazardous laboratory chemicals, with a detailed safety data sheet included.
    Storage Store 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Keep the chemical tightly sealed in a clearly labeled, chemical-resistant container. Protect from moisture and direct sunlight. Handle using appropriate personal protective equipment and follow all relevant safety procedures.
    Application of 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine

    Applications of 2-Amino-5-Bromo-4-Methyl-3-Nitropyridine in Industrial Manufacturing

    2-Amino-5-Bromo-4-Methyl-3-Nitropyridine serves as a key intermediate in multiple regulated industries, enabling downstream manufacturers to construct advanced molecules across pharmaceutical, agrochemical, and specialty dye sectors. Below, we outline core industrial scenarios where this raw material directly contributes to the creation of high-value, compliance-driven finished products.

    1. Active Pharmaceutical Ingredient (API) Synthesis — Pyridine-Based Drug Development

    This material provides a crucial building block for the development of pyridine-derived drug candidates, especially within anti-infective and central nervous system (CNS) pharmaceutical programs. Research labs and contract manufacturers incorporate the compound’s functional groups to anchor halogenated and methylated motifs into new chemical entities, using its aminopyridine core to refine pharmacokinetic and pharmacodynamic profiles in lead optimization campaigns.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters: Residual Solvents, Elemental Impurities
    • 21 CFR Part 210/211: cGMP for Finished Pharmaceuticals
    • EDQM Guidelines for Intermediates in Drug Substances

    Typical usage ratio

    • Batch-level addition ranges from 0.8% to 4% (w/w), controlled by target molecule design and the number of synthetic steps; chemists adjust input based on expected yield, limiting intermediate overuse where purification costs rise.

    Downstream process integration

    • Material is introduced during early-stage heterocyclic core formation or as a halogen source in late-stage coupling reactions, integrally feeding into Buchwald or Suzuki cross-coupling units, and amidation protocols under anhydrous conditions.

    Final product types

    • Small molecule APIs for anti-bacterial, anti-viral, or CNS-related indications (e.g., kinase inhibitors or neuromodulators)
    • Advanced pharmaceutical intermediates for further combination into fixed-dose or combination therapies

    2. Crop Protection Agents — Pyridine-Derived Agrochemical Synthesis

    Multinational and regional agrochemical formulators rely on this nitropyridine intermediate to build pre-emergent and selective pesticides. Its electron-withdrawing and nucleophilic features enable the stepwise synthesis of protected pyridine scaffolds, which act as crucial pharmacophores in modern insecticides, fungicides, and herbicides for regulatory markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for Agrochemical Manufacturing Quality Systems
    • European Regulation (EC) No 1107/2009 for Plant Protection Product Authorizations
    • US EPA PRIA Standards for Chemical Intermediates

    Typical usage ratio

    • 0.3% to 2.5% (w/w), determined by active substance loading and downstream protection groups; usage typically peaks in multi-step syntheses to maximize conversion rate and minimize wasteful by-products.

    Downstream process integration

    • Actively used during ring elaboration and halogenation in pre-final steps or included as a brominated intermediary in multi-purpose reactors ahead of downstream sulfur-based or nitro-group substitutions.

    Final product types

    • Active ingredients for insecticide and herbicide formulations
    • Fungicidal additive intermediates for protective crop coatings
    • Stabilized seed treatments incorporating pyridine motifs

    3. Specialty Dyes and Pigments — Precursors for High-Performance Colorants

    Leading specialty dye manufacturers incorporate this aminopyridine derivative into the synthesis of advanced pigment markers with brominated or nitro functionalities, achieving specific lightfastness and solvent resistance. It features predominantly in the design of disperse and reactive dyes, serving as a critical intermediate for building dye bases used in technically demanding application spaces such as polyester fiber coloration and specialty printing inks.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for reactive dye intermediates in textiles)
    • REACH Annex XVII Restrictions (EC No 1907/2006)
    • ZDHC MRSL (Manufacturing Restricted Substances List v3.1)
    • ISO 9001:2015 (Colorant and Dye Quality Management)

    Typical usage ratio

    • Ranges from 1.2% to 3.8% (w/w) within pigment-batch syntheses, tuned to final chromophore yield and target molar extinction coefficients during product development and quality control validation.

    Downstream process integration

    • Reactant is introduced in nucleophilic substitution phases, primarily during azo-coupling or cyclization steps that impart thermal stability and color intensity to disperse dye backbones.

    Final product types

    • Disperse dyes for synthetic fiber applications (polyester, acetate)
    • Reactive dyes for digital printing on textiles
    • Specialty pigment concentrates for technical ink formulations

    4. Electronic Chemical Synthesis — Functional Heterocycle Additives for OLED Materials

    This pyridine intermediate enters the workflow of functional organic electronics manufacturing, particularly as a structural precursor for small-molecule hosts and transport materials in organic light-emitting diodes (OLEDs). The electron-rich aminopyridine moiety delivers unique photophysical tuning, aiding downstream partners who target high-brightness and long-lifetime emissive layers in advanced display and lighting devices.

    Industry compliance standards

    • RoHS 3 (Directive (EU) 2015/863) for hazardous substance control
    • IEC 62321-7-1: Determination of bromine content in electronic devices
    • ISO 14001:2015 for Environmental Management
    • IECQ QC 080000: Hazardous Substance Process Management

    Typical usage ratio

    • 0.5% to 2.1% (w/w) in formulation runs, depending on target device emissive profile and molecular layer thickness; adjusted in pilot batches to align with end-of-line quality metrics such as luminance and lifespan.

    Downstream process integration

    • Added to solution-phase or vacuum deposition processes during the final synthesis of emitter or host molecules, downstream of initial heterocycle functionalization and prior to purification via column chromatography or sublimation.

    Final product types

    • Blue and green OLED emitter molecules for advanced display panels
    • Charge-transport intermediate layers in high-contrast lighting modules

    5. Analytical Reference Standards — Certified Reference Material Preparation

    Accredited laboratories and diagnostic kit developers source this highly pure intermediate to synthesize reference standards for pharmaceutical, environmental, and forensic analysis. The compound’s well-defined molecular structure offers unique retention times and target validation parameters in liquid chromatography–mass spectrometry (LC-MS) and HPLC testing.

    Industry compliance standards

    • ISO 17034:2016 (General Requirements for the Competence of Reference Material Producers)
    • ISO/IEC 17025:2017 (Testing and Calibration Laboratories)
    • Pharmaceutical Reference Standard Preparation Protocols (USP, EP, BP)

    Typical usage ratio

    • Reference material standards typically use 99.5%+ purity compound, with batch-level tip-in from 0.01% to 0.2% (w/w) depending on concentration of the analytical standard being prepared.

    Downstream process integration

    • Pulled from high-purity production lots, this compound enters as the principal analyte or as a comparator for calibration blend preparations prior to lyophilization or ampoule filling processes.

    Final product types

    • Certified pharmaceutical reference substances (CRS)
    • LC-MS and HPLC analytical standards used in pharmaceutical quality control and environmental monitoring labs
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