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5-Chloro-2,4-Difluorobenzonitrile

    • Product Name 5-Chloro-2,4-Difluorobenzonitrile
    • Alias 5-Chloro-2,4-difluorobenzene-1-carbonitrile
    • Einecs 843-716-4
    • 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

    187001

    Chemical Name 5-Chloro-2,4-Difluorobenzonitrile
    Cas Number 143782-23-4
    Molecular Formula C7H2ClF2N
    Molecular Weight 173.55
    Appearance White to off-white solid
    Boiling Point 251 °C (estimated)
    Melting Point 53-55 °C
    Density 1.43 g/cm3 (estimated)
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=C(C=C(C(=C1F)Cl)F)C#N
    Inchi InChI=1S/C7H2ClF2N/c8-5-1-6(9)4(3-11)2-7(5)10
    Refractive Index 1.542 (estimated)
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Synonyms 2,4-Difluoro-5-chlorobenzonitrile

    As an accredited 5-Chloro-2,4-Difluorobenzonitrile 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, tightly sealed, with a white label displaying "5-Chloro-2,4-Difluorobenzonitrile" and handling precautions.
    Shipping 5-Chloro-2,4-Difluorobenzonitrile is shipped in sealed, chemical-resistant containers, protected from moisture and light. It is handled in accordance with hazardous material regulations, including labeling and documentation. During shipping, it should be kept upright and secured to prevent leaks or spills, and transported by certified carriers trained in hazardous goods.
    Storage 5-Chloro-2,4-Difluorobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents and moisture. Ensure the storage area is free from ignition sources. Protect from direct sunlight and keep away from heat. Use appropriate chemical safety labels and restrict access to trained personnel only.
    Application of 5-Chloro-2,4-Difluorobenzonitrile

    Applications of 5-Chloro-2,4-Difluorobenzonitrile in Industrial Manufacturing

    5-Chloro-2,4-difluorobenzonitrile serves as a critical intermediate in advanced industrial synthesis. As a manufacturer, we supply this raw material to key production sectors, supporting precise formulation, integration, and compliance within various specialized fields. Below are practical examples of downstream utilization in real-world industries.

    1. Agrochemical Active Ingredient Synthesis

    Leading crop protection manufacturers use this compound in the synthesis pathway for particular herbicide and fungicide actives. The aromatic nitrile structure provides an essential building block during key coupling or substitution steps, typically as an intermediate that undergoes further halogenation or amination. Accurate control of impurity levels ensures compliance and downstream molecule integrity.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Good Laboratory Practice (GLP) for active ingredient development
    • ISO 9001:2015 for chemical manufacturing quality management
    • REACH Annex VII–X substance registration

    Typical usage ratio

    • 20–40% of the total mass during precursor stage in multi-step herbicide synthesis, ratio adjusted according to required batch scale and end-molecule yield

    Downstream process integration

    • Added in initial coupling or halogen-exchange reactors before stepwise transformation to target agrochemical active

    Final product types

    • Phenoxycarboxylic acid herbicides
    • Triazine-based fungicides
    • Commercial weed control formulations

    2. Pharmaceutical Intermediate for API Synthesis

    Generic and specialty pharmaceutical firms employ this compound as an early-stage intermediate to construct benzene-based pharmacophores. Stringent pharmaceutical standards dictate pre-processing with advanced purification, and all transformation steps undergo in-house QC to ensure minimal carryover of residual halide or nitrile. Process chemists validate the specifications for each incoming batch to comply with regulatory submission.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF Monographs for intermediates
    • EDQM CEP/COS procedures for nominated intermediates
    • 21 CFR Part 211 (Current GMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 5–20% based on overall synthetic batch mass, depending on specific API molecular scaffold required

    Downstream process integration

    • Reacted in aniline substitution, Grignard reactions, or amidation steps to build advanced pharmaceutical intermediates

    Final product types

    • Chlorinated benzamide APIs
    • Anti-inflammatory agents
    • Precursors for oncology and CNS treatment molecules

    3. Specialty Polymer Modifier Production

    Producers of high-performance fluorinated polymers incorporate this raw material in the synthesis of fluoropolymer modifiers and fluorinated resin intermediates. The unique halogen/nitrile substitution pattern supports advanced monomer design, imparting chemical and thermal resistance to final copolymers. Technical teams optimize input level to balance process reactivity and desired final material properties.

    Industry compliance standards

    • ISO 9001:2015 (QMS for polymer manufacturers)
    • ASTM D5203 for fluoropolymer derivatives
    • RoHS Directive (EU) 2011/65/EU for restricted substances
    • REACH Pre-registration for polymer intermediates

    Typical usage ratio

    • 10–35% as part of the reaction mass in fluorinated monomer or oligomer synthesis; adjusted for polymer chain length and incorporation efficiency

    Downstream process integration

    • Charged in monomer feed or functionalized in chain-extension reactions, prior to co-polymerization with other fluorinated or aromatic blocks

    Final product types

    • Specialty fluororesins
    • UV-resistant fluoropolymer coatings
    • High-durability fluoropolymer films

    4. Electronic Chemical Intermediate for OLEDs

    Advanced materials manufacturers utilize this compound in the scale-up of intermediates for organic electronic device fabrication, particularly in the production of emitter hosts and electron-transport layers for OLED displays. Purity and trace halogen content are closely monitored, as electronic performance often relies on reducing trace metal or ionic contaminants to sub-ppm levels.

    Industry compliance standards

    • IEC 62474 for material declaration in electronic devices
    • IPC-4101 for base materials in electronics
    • JEDEC JESD720 for low-halogen requirements
    • Sony SS-00259 Green Partner environmental requirements

    Typical usage ratio

    • 3–15% of the precursor blend for organic semiconducting molecules; adjusted based on purity levels and device specifications

    Downstream process integration

    • Introduced in the functional group introduction phase for organic light-emitting host and transport material build-out

    Final product types

    • Organic emitter hosts
    • Electron transport layer materials for OLED displays
    • Intermediate compounds for advanced flat-panel displays

    5. Fine Chemical Synthesis for Dyestuffs

    Manufacturers in the colorant sector use this raw material within multi-step synthesis for select specialty dyes and pigments where specific aromatic substitution is required. The chemical framework enables production of high-purity dye intermediates, enhancing chromophore stability and performance for demanding applications in textiles and specialty coatings.

    Industry compliance standards

    • OEKO-TEX Standard 100 (product class I–IV)
    • ZDHC Manufacturing Restricted Substances List
    • ISO 9001 for production traceability
    • EN 71-3 migration limits for toy finishes (when relevant)

    Typical usage ratio

    • 10–25% of the total batch during dye precursor synthesis; refined based on chromophore formation and batch yield targets

    Downstream process integration

    • Utilized during diazotization or coupling steps in high-purity colorant synthesis, prior to further sulfonation or metallization

    Final product types

    • Specialty disperse dyes
    • High-stability pigment intermediates
    • Colorants for technical textile applications
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