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2-Chloro-6-Fluorobenzonitrile

    • Product Name 2-Chloro-6-Fluorobenzonitrile
    • Alias 2-Chloro-6-fluorobenzenecarbonitrile
    • Einecs 619-021-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    834599

    Chemical Name 2-Chloro-6-Fluorobenzonitrile
    Cas Number 13361-32-5
    Molecular Formula C7H3ClFN
    Molecular Weight 155.56
    Appearance White to light yellow powder
    Boiling Point 230-232°C
    Melting Point 31-34°C
    Density 1.34 g/cm³
    Solubility Slightly soluble in water
    Pubchem Cid 151445
    Smiles C1=CC(=NC(=C1Cl)F)C#N
    Inchi InChI=1S/C7H3ClFN/c8-6-2-1-3-7(9)5(6)4-10
    Refractive Index 1.547
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Synonyms 2-Chloro-6-fluorobenzenecarbonitrile

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

    Packing & Storage
    Packing A 100g amber glass bottle, sealed with a screw cap, labeled "2-Chloro-6-Fluorobenzonitrile," featuring hazard symbols and batch information.
    Shipping 2-Chloro-6-Fluorobenzonitrile is typically shipped in tightly sealed containers to prevent leaks and contamination. It should be handled as a hazardous material, following all relevant local, national, and international regulations. Proper labeling, protective packaging, and documentation are required during transportation to ensure safety and regulatory compliance.
    Storage 2-Chloro-6-Fluorobenzonitrile should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep it away from heat and direct sunlight. Ensure proper labeling, and use corrosion-resistant storage materials. Store in accordance with local and national regulations for hazardous chemicals.
    Application of 2-Chloro-6-Fluorobenzonitrile

    Applications of 2-Chloro-6-Fluorobenzonitrile in Industrial Manufacturing

    2-Chloro-6-Fluorobenzonitrile is an industrial intermediate with critical roles in several downstream specialty chemical fields. As an original manufacturer, we have supplied this raw material to high-precision fine chemical sectors worldwide. Below are established application scenarios validated by practical usage in the fields of agrochemical active ingredients, pharmaceutical building blocks, pigment intermediates, and advanced materials manufacturing.

    1. Agrochemical Active Ingredient Synthesis

    Producers of selective herbicides and fungicides deploy this raw material as a key aromatic building block, particularly in the synthesis of pyridine and pyrimidine-based actives. The compound enters the reaction scheme at the arylation stage, facilitating downstream chlorination, amination, or condensation steps. Customers typically use this intermediate for molecules requiring electron-withdrawing substituents for target weed or pest selectivity, and process parameters hinge on reaction scale and desired purity of the active ingredient.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (EC 1907/2006) Compliance for agro intermediates
    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • Specific crop residue tolerance levels per EU Regulation (EC) No 396/2005

    Typical usage ratio

    • 0.8–1.3 molar equivalents per batch depending on molecular target and reaction route
    • Adjusted for by-product minimization and yield optimization per process validation results

    Downstream process integration

    • Added after initial base-catalyzed halide exchange as the aromatic core
    • Participates in nucleophilic aromatic substitution followed by cyclization or coupling reactions
    • Serves as a feedstock in continuous or batch agitation reactors under controlled temperature

    Final product types

    • Triazole herbicide active ingredients
    • Strobilurin and pyridine-based fungicides
    • Precursor molecules for selective insecticide agents

    2. Pharmaceutical Intermediate for API Synthesis

    This compound forms part of multistep synthetic pathways for pharmaceutical active ingredients, notably for drugs containing substituted benzene and pyridine rings. Customers in the pharmaceutical sector introduce 2-Chloro-6-Fluorobenzonitrile as a locked aromatic synthon before halogen exchange, alkylation, or amidation stages to build complex API scaffolds. Such usage demands high analytical purity for GMP compliance and effective batch-to-batch reproducibility.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • Ph. Eur., USP, and JP monograph compliance for starting/intermediate materials
    • EU EudraLex Volume 4 GMP guidelines

    Typical usage ratio

    • Stoichiometric dosing at 0.95–1.10 equivalents per intermediate formed
    • Adjusted during scale-up for impurity profile and intermediate stability

    Downstream process integration

    • Introduced after initial Grignard/formylation and before substitution or reduction stages
    • Diverse reaction environments including high-pressure hydrogenations and anodic oxidations
    • Critical input in both pilot and commercial-scale API manufacturing under validated protocols

    Final product types

    • Oncology drug intermediates with fused ring structures
    • Antiviral agents built on heterocyclic benzene cores
    • Antihypertensive and CNS drug scaffolds

    3. Pigment and Specialty Dye Intermediate

    Manufacturers in the colorant industry harness this raw material as a precursor for high-performance azo and anthraquinone pigments, particularly those requiring fluoro-chloro aromaticity for enhanced weatherability and lightfastness. It is incorporated during diazotization or coupling steps, often serving as a substituent source for specialty pigment molecules offering superior brightness tolerance to heat and light exposure.

    Industry compliance standards

    • DIN EN 71-3 (Safety of toys—Migration of certain elements, Europe)
    • REACH (EC 1907/2006) regulatory dossier for coloring agents
    • OEKO-TEX® Standard 100 for textile pigments
    • BfR IX (Plastics Colourants in Food Packaging, Germany)

    Typical usage ratio

    • 0.5–1.5% of weight in pigment blend formulations depending on shade and end-application
    • Precision titration based on batch color consistency testing

    Downstream process integration

    • Introduced in early-stage diazo coupling or condensing reactions with phenol derivatives
    • In situ application during wet cake filtration and solvent switching phases
    • Adjusted in microreactor systems for fine-tuning color index results

    Final product types

    • High-performance yellow and red pigments for industrial coatings
    • Textile and plastics dyes with improved UV resistance
    • Printing ink color bases requiring solvent durability

    4. Advanced Materials and Polymer Additives

    This intermediate enables the construction of specialty polymers and engineered plastics through copolymerization or functionalization steps where halogenated aromatics are essential for flame retardancy, chemical resistance, or refractive index modification. Downstream manufacturers integrate this compound into backbone modification procedures or as a monomer for crosslinking applications in electronics, optical films, and specialty engineering plastics.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics Materials)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 environmental management requirements in polymer production
    • ASTM D2863 (Limiting Oxygen Index of Plastics)

    Typical usage ratio

    • 250–800 ppm in specialty polymer batches for performance optimization
    • Increased loading for flame-retarded grades, decreased in clear applications

    Downstream process integration

    • Blended into monomer mix pre-polymerization via in-line dosing systems
    • Grafted onto polymer chains in post-polymerization functionalization reactors
    • Monitored with spectrophotometric and chromatographic batch controls

    Final product types

    • Flame-retardant engineering thermoplastics
    • Optical grade polyimide films with tailored refractivity
    • High-resistance cable insulation compounds
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