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2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile

    • Product Name 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile
    • Alias 2-Chloro-6-(4-fluorophenyl)nicotinonitrile
    • Einecs 826-220-5
    • 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

    668591

    Productname 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile
    Casnumber 1072955-26-8
    Molecularformula C12H6ClFN2
    Molecularweight 232.64
    Appearance Off-white to pale yellow solid
    Meltingpoint 106-110°C
    Solubility Slightly soluble in organic solvents
    Purity Typically >98%
    Chemicalclass Nicotinonitrile derivative
    Smiles C1=CC(=CC=C1)C2=NC(=C(C=N2)Cl)C#N
    Storageconditions Store at room temperature, keep container tightly closed, protect from light

    As an accredited 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 50 grams of 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile, sealed in an amber glass bottle with tamper-evident cap.
    Shipping 2-Chloro-6-(4-Fluorophenyl)nicotinonitrile is shipped securely in sealed, chemical-resistant containers to prevent contamination and ensure safety. It is transported according to relevant chemical shipping regulations, with appropriate labeling and documentation. Handling and storage follow safety guidelines, keeping the product away from heat, moisture, and incompatible substances during transit.
    Storage Store **2-Chloro-6-(4-Fluorophenyl)nicotinonitrile** in a tightly sealed container, away from moisture, light, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Clearly label the container and use secondary containment to prevent spills. Follow all relevant safety protocols and local regulations when handling and storing this compound.
    Application of 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile

    Applications of 2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile in Industrial Manufacturing

    2-Chloro-6-(4-Fluorophenyl)Nicotinonitrile serves as a key intermediate in several highly regulated industrial synthesis chains. Our manufacturing expertise ensures high material consistency, supporting downstream customers in sectors that require strict formulation controls, advanced process integration, and compliance with international standards. See the following key application fields and detailed use cases in B2B industrial production.

    1. Agrochemical Active Ingredient Synthesis

    Many global agrochemical producers rely on this compound to build advanced heterocyclic scaffolds for selective herbicides and crop protection agents, particularly high-performance pyridine derivatives. Formulation teams use it in key cross-coupling or nucleophilic substitution steps. Direct inclusion in multistep batch reactors ensures high purity and yield, minimizing side-product formation right from early kilo-lab synthesis to full industrial scale. Exact grade and material consistency support companies fulfilling crop protection data dossiers for regulated markets.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Ingredients
    • US EPA pesticide registration guidance (40 CFR Part 158)
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 Total Quality Management for agrochemical actives

    Typical usage ratio

    • 5–18% by weight in multistep agrochemical synthesis intermediates, adjusted based on the target active and process technology

    Downstream process integration

    • Charged directly as a limiting reagent in Buchwald–Hartwig amination, Suzuki coupling, or nucleophilic aromatic substitution
    • Processed under controlled temperature and inert atmosphere in jacketed reactors
    • Incorporated with in-process QC (HPLC, GC) checkpoints for impurity profile control

    Final product types

    • Selective pre- and post-emergent herbicides
    • Nicotinamide-based fungicidal intermediates
    • Pyridine-derived insecticidal scaffolds for further downstream derivatization
    • Ready-to-formulate technical-grade actives for finished crop protection blends

    2. Pharmaceutical Intermediate Manufacturing

    Bulk API manufacturers and contract development organizations (CDMOs) use this material to access fluorinated pyridine building blocks. Its structure supports synthesis routes for kinase inhibitors and small molecule APIs under strict GMP regimes. The compound's reactivity allows for customized derivatization at the 4-fluorophenyl and cyanide positions, essential for routes where late-stage functionalization increases yield and process safety. QC-controlled supply ensures consistent spectral and impurity profiles compatible with regulatory submissions.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals – relevant to intermediates impacting final product quality)
    • European Pharmacopoeia General Monographs (CEP procedures for API pathway registration)
    • Japanese Pharmaceutical Excipients/Registered Drug Master File (when applicable)

    Typical usage ratio

    • Varies from 2–10% within total synthesis mass balance of API process, based on target molecule complexity and coupling step efficiency

    Downstream process integration

    • Introduced in the late-stage synthesis step or as a heterocyclic precursor in process route
    • Handled under GMP cleanroom procedures for intermediates that impact impurity profile and ultimate registration
    • Real-time analytical monitoring (LC-MS, NMR) ensures batch uniformity and documentation for regulatory dossiers

    Final product types

    • Kinase inhibitor drug substances (e.g., antineoplastic agents)
    • Pyridinyl-fluorinated intermediates for pharmaceutical specialties
    • Advanced intermediates for Central Nervous System (CNS) small molecules
    • Custom fluorinated analogs supplied for clinical trial candidate synthesis

    3. Custom Electronic Chemical Synthesis

    Producers in the electronics industry integrate this compound as a precursor for high-purity functional molecules needed in OLED displays, organic semiconductors, and specialty fluorinated dielectrics. The precise electronic nature of the 4-fluorophenyl and nicotinonitrile motifs enables companies to create materials with tailored electrical, optical, and solubility properties. Controlled formulation and trace impurity management are critical since downstream applications demand exceptional batch consistency and certification for trace metals and organic contamination.

    Industry compliance standards

    • SEMI C93 Specification for Electronic Chemicals
    • ISO 9001:2015 (Certification for electronic materials)
    • RoHS (2011/65/EU) restricting hazardous substances (post-processing compliance)
    • Customer-specific trace impurity requirements (ppb/ppm levels)

    Typical usage ratio

    • 1–5% by mass in precursor blends for downstream organic electronic materials

    Downstream process integration

    • Charged as a nucleophile or electrophile in condensation or cross-coupling reactions during precursor synthesis
    • Tested for photo and thermal stability pre-integration in display or microelectronic materials manufacture
    • Material purity is validated with ICP-MS or GPC methods prior to scale-up in thin-film or device production

    Final product types

    • Electroluminescent emitter precursors for OLEDs
    • Electron transport layer additives for display backplanes
    • Specialty pyridine-fluorinated resins used in advanced IC packaging
    • High-dielectric materials for organic TFTs and MEMS devices

    4. Specialty Polymer and Performance Resin Modification

    Advanced polymer manufacturers use this compound to introduce rigidity and tailored polarity into engineering plastics, coatings resins, and thermoset pre-polymers. The aromatic nitrile and fluorophenyl functionalities offer improved solvent resistance, flame retardance, and processability in high-performance formulation blending. We supply production lots with controlled particle size and low residual moisture, directly supporting extrusion, compounding, and reactive extrusion lines where process reproducibility is critical for demanding automotive, electronics, and specialty packaging applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (substance registration for polymers and monomer use)
    • ISO 14001:2015 Environmental Management for chemical processors
    • UL 94 Flame Classification for plastics (relevant for modified polymer evaluation)
    • Customer specification for extractables and leachables (especially in automotive/electronics supply chain)

    Typical usage ratio

    • Typically 0.2–2.5% by weight in polymer or resin formulation, depending on target mechanical and thermal property profile

    Downstream process integration

    • Fed as a dry blend or pre-dissolved masterbatch into melt compounding or reactive extrusion process
    • Mixed under nitrogen with polycondensation or copolymerization agents at elevated temperatures
    • Spectral QC (FTIR, DSC, GPC) benchmarks composition and integration consistency

    Final product types

    • Pyridine-modified high-performance engineering plastics
    • UV- and solvent-resistant electronic encapsulation resins
    • Fluorinated specialty coatings for industrial tools and equipment parts
    • Automotive and aerospace grade composite panels/pellets with enhanced flame resistance

    5. Research and Analytical Reference Standard Production

    Certified reference material laboratories and chemical R&D centers use our high-purity production lots as reference compounds for quantitative method development in analytical chemistry and trace impurity analysis. Traceable batches feature spectral matching and impurity profiling, supporting calibration of analytical methods for regulatory and industrial QC. Proper documentation and batch release certificates guarantee traceability and comparability across global multi-site R&D and QA programs.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO/IEC 17025:2017 (Testing and calibration laboratory accreditation)
    • Traceable certification per NIST or equivalent national standards
    • Customer-specific certificate of analysis for purity and identity

    Typical usage ratio

    • Used directly at 50–500 mg per analytical batch; diluted in acetonitrile, methanol, or DMSO for calibration curves

    Downstream process integration

    • Weighing and dissolving for standard preparations in HPLC, GC-MS, or LC-MS applications
    • Integration into proficiency testing and reference database validation
    • Direct use as process control standard in API and agrochemical plant laboratories

    Final product types

    • Calibration standards for quantitative analytical methods
    • Quality control reference materials for industrial and pharmaceutical labs
    • Spectral match standards for identity testing across global laboratory networks
    • Proficiency testing kits for certified analytical laboratories
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