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2-Chloroquinoxaline

    • Product Name 2-Chloroquinoxaline
    • Alias 2-Chloroquinoxaline
    • Einecs 219-333-5
    • 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
    VTB
    Specifications

    HS Code

    794131

    Cas Number 3440-14-6
    Molecular Formula C8H5ClN2
    Molecular Weight 164.59
    Iupac Name 2-chloroquinoxaline
    Appearance Pale yellow to light brown crystalline powder
    Melting Point 128-132°C
    Boiling Point 325.3°C at 760 mmHg
    Density 1.35 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 150.2°C
    Smiles C1=CC=C2C(=C1)N=CC=N2Cl
    Refractive Index 1.710

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

    Packing & Storage
    Packing Amber glass bottle, 25 g, with tamper-evident seal; labeled with hazard symbols, chemical name, CAS number, and handling instructions.
    Shipping 2-Chloroquinoxaline is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. The package is clearly labeled with hazard information, and handled according to chemical safety regulations. Transportation complies with local and international guidelines for hazardous chemicals, using secure containers to prevent leakage or contamination during transit.
    Storage 2-Chloroquinoxaline should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep it protected from light and moisture. Clearly label the container and keep it away from direct sunlight. Always follow standard laboratory safety protocols and local regulations when storing this chemical.
    Application of 2-Chloroquinoxaline

    Applications of 2-Chloroquinoxaline in Industrial Manufacturing

    2-Chloroquinoxaline serves as a specialized intermediate in advanced chemical manufacturing. This compound plays a critical role for various industrial sectors, where its chemical structure enables targeted synthesis and complex end product development. Our facility supplies consistent quality and verified purity for downstream integration.

    1. Pharmaceutical Intermediates for Kinase Inhibitor Synthesis

    Pharmaceutical manufacturers utilize 2-Chloroquinoxaline as a core scaffold for the synthesis of heterocyclic kinase inhibitors, especially in targeted anti-cancer drug development. The specific halogenation at the quinoxaline ring allows precise nucleophilic substitution and further derivatization. Synthesis protocols demand tight control of the reaction environment to ensure selective modification and high final yield, with close adherence to registration batch reproducibility. Formulations often employ this intermediate in the assembly of complex quinoxaline-based molecules under GMP-compliant conditions, supporting the launch of new molecular entities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EMA Guidelines on process validation
    • Chinese Pharmacopoeia quality requirements for intermediates

    Typical usage ratio

    • 0.95 to 1.15 molar equivalents, adjusted by downstream chain length and desired substitution pattern
    • Exact quantity tailored per target intermediate yield based on validated route

    Downstream process integration

    • Introduced in nucleophilic aromatic substitution (SNAr) stages
    • Requires careful solvent selection (e.g., DMF, DMSO) and control of reaction temperature 80-120°C
    • Isolated intermediates pass HPLC purity analysis and structure confirmation (NMR)

    Final product types

    • Kinase inhibitor APIs for oncology
    • Advanced research intermediates for small-molecule drugs
    • Targeted therapeutics for clinical trials
    • IMP reference standards

    2. Agrochemical Synthesis: Fungicide and Herbicide Intermediates

    Major agrochemical plants employ 2-Chloroquinoxaline in the multi-step synthesis of systemic fungicides and selective herbicides. Its chlorinated aromatic structure enables the creation of bioactive molecules that impact plant-pathogen interactions. Downstream processes rely on clean substitution chemistry, often under inert gas, to ensure residue thresholds and product performance comply with current agricultural safety regulations. Production schedules coordinate with seasonal demand and field efficacy trials, with each batch validated for active content and residual solvents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO JMPR)
    • REACH Regulation EC/1907/2006
    • ISO 17025 Analytical Testing Accreditation
    • China Pesticide Registration Guidelines (ICAMA)

    Typical usage ratio

    • 80-120 g per kg synthesis lot, depending on route and final molecule design
    • Adjusted by activity profile and downstream formulation needs

    Downstream process integration

    • Used in the initial halogenated heterocycle synthesis
    • Participates in coupling and cyclization reactions under nitrogen or argon
    • Purification via crystallization and column chromatography for residue control

    Final product types

    • Fungicide actives like quinoxaline derivatives
    • Herbicide technical grade products
    • Crop-protection formulated products
    • Field trial samples for new registrations

    3. Dye and Pigment Manufacturing: Heterocyclic Colorant Precursors

    Industrial dye producers integrate 2-Chloroquinoxaline as a key heterocyclic building block for the synthesis of specialty pigments. Its unique aromatic structure enables the production of nitrogen-containing colorants with high lightfastness and solvent resistance. Typical synthesis involves electrophilic substitution and subsequent coupling steps to build extended chromophore systems. Quality control protocols require strict batch-traceability to ensure colorimetric consistency and compliance with restricted substance legislation.

    Industry compliance standards

    • EN 71-3 Safety of Toys (colorant limits for pigments)
    • GHS Classification, Labeling & Packaging (CLP) Regulation
    • OEKO-TEX Standard 100 (applicability for textiles)
    • REACH Annex XVII (restricted colorant substances)

    Typical usage ratio

    • 3-6% of total bicolorant batch, varying based on desired tone intensity and solvent compatibility
    • Adjustment by downstream dye molecule complexity requirements

    Downstream process integration

    • Added as base heterocycle in initial pigment precursor condensation stage
    • Mixed with auxiliary diazo compounds at tightly controlled pH
    • Following synthesis, pigment filtered and milled for particle size

    Final product types

    • Specialty dyes for plastics and synthetic fibers
    • High-performance pigments for coatings
    • Reactive colorants for inkjet printing
    • Light-stable architectural colorants

    4. Material Science R&D: Advanced Polymer Additive Development

    Research facilities and polymer manufacturers utilize 2-Chloroquinoxaline as a monomer unit in the fabrication of conductive and photoactive polymers. Its aromatic core and reactive chlorine substituent enable controlled copolymerization and functional material design. Pilot plant protocols stipulate precise dosing and reaction time to control molecular weight distribution and preserve functional group availability for subsequent crosslinking or performance tuning. The additive supports research into novel materials for electronics, sensors, and specialty coatings, with scale-up guided by progressive QC milestones.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in R&D
    • IEC 60695-11-10 for flame retardancy (where relevant)
    • RoHS Directive 2011/65/EU (hazardous substances, for electronics)
    • ASTM D638 for polymer film tensile properties

    Typical usage ratio

    • 2-8 mol% in copolymer blends, adjusted by desired thermal and optical properties
    • Optimization based on lab-scale pilot feedback

    Downstream process integration

    • Introduced during pre-polymerization stage as a functionalized monomer
    • Polymerization under controlled temperature and inert atmosphere
    • Processed further to form films, coatings, or composite resins

    Final product types

    • Conductive polymer films for electronic devices
    • Photoresponsive coatings
    • Innovative research composites
    • Next-generation sensor substrates

    5. Specialty Fine Chemical Synthesis: Custom Heterocyclic Building Blocks

    Custom synthesis providers and fine chemical manufacturers select 2-Chloroquinoxaline as a versatile precursor for contract research and tailored molecular assembly. Its defined halogen position offers a starting point for elaborating multiple derivatives through cross-coupling and metal-catalyzed processes. Production batches require careful stoichiometric planning and purification to meet the diverse demands of R&D partners in the pharmaceutical, agrochemical, and electronics sectors. Full documentation and impurity profiles accompany each lot for seamless integration into proprietary projects.

    Industry compliance standards

    • ISO 9001 quality system
    • REACH compliant supply chain disclosure
    • Custom synthesis per client NDA and intellectual property protection
    • Batch record retention for traceability (21 CFR Part 211.180)

    Typical usage ratio

    • 0.5-2.0 equivalents, customized for each route based on step and reactivity map
    • Fine-tuned per final molecular objective and scale (from grams to kilograms)

    Downstream process integration

    • Introduced in Suzuki, Buchwald-Hartwig, or other cross-coupling reactions
    • Participates in directed lithiation or SNAr for responsive moieties
    • Purified by column chromatography and preparative HPLC

    Final product types

    • Advanced research compounds
    • Custom intermediates for molecule libraries
    • Reference materials for analytical standards
    • Fine chemical motifs for patent portfolios
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