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3-Iodobenzonitrile

    • Product Name 3-Iodobenzonitrile
    • Alias m-Iodobenzonitrile
    • Einecs 210-996-7
    • 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

    229211

    Chemical Name 3-Iodobenzonitrile
    Cas Number 618-51-9
    Molecular Formula C7H4IN
    Molecular Weight 229.02 g/mol
    Appearance White to off-white solid
    Melting Point 74-78°C
    Boiling Point 256°C
    Density 1.79 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=CC(=C1)I)C#N
    Inchi InChI=1S/C7H4IN/c8-6-2-1-3-7(4-6)5-9
    Refractive Index 1.661 (predicted)

    As an accredited 3-Iodobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Iodobenzonitrile is supplied in a 25g amber glass bottle, tightly sealed, labeled with product details, and hazard information.
    Shipping 3-Iodobenzonitrile is typically shipped in tightly sealed containers to prevent moisture ingress and contamination. It should be packed according to hazardous material regulations, using appropriate labeling and documentation. The shipment is transported in compliance with local and international chemical safety guidelines, ensuring the container is protected from physical damage, heat, and direct sunlight.
    Storage 3-Iodobenzonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. The storage area should be clearly labeled and access limited to trained personnel, with appropriate spill containment and fire safety equipment available.
    Application of 3-Iodobenzonitrile

    Applications of 3-Iodobenzonitrile in Industrial Manufacturing

    As a direct manufacturer of 3-Iodobenzonitrile, we supply this specialty intermediate to diverse sectors requiring traceable origin, tightly controlled batch synthesis, and technical support for route development or scale-up. Below, we outline major industrial application fields, each with their specific compliance, formulation ratios, process steps, and end uses as established in the global market.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Major pharmaceutical manufacturers select 3-Iodobenzonitrile for building key molecular frameworks in heterocyclic and aromatic API syntheses, such as tyrosine kinase inhibitors and other oncology products. When constructing advanced intermediates, chemists value the nitrile and iodine functions for selective substitution and coupling reactions under GMP environments. Process chemistries frequently use this molecule during late-stage route transformation or as a nucleophilic partner in palladium-catalyzed cross-coupling reactions, ensuring structural precision and stringent impurity profiling necessary for finished drug approval.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (U.S. FDA cGMP)
    • EU GMP Part II for APIs
    • Ph. Eur., JP, or USP related reference standards by API route

    Typical usage ratio

    • Varies by synthetic route: typically 1.0–1.3 molar equivalents relative to target intermediate
    • Adjustment based on coupling yield, impurity control, and downstream stoichiometry requirements

    Downstream process integration

    • Introduced at the coupling or functionalization stage in multi-step organometallic syntheses
    • Employed in nitrile group transformations or C–N/C–C bond-forming sequences
    • Often followed by hydrogenation, hydrolysis, or further derivatization steps

    Final product types

    • Targeted anticancer drug molecules
    • Aromatic amine or carboxamide APIs
    • Advanced pharmaceutical building blocks intended for further synthetic elaboration

    2. Agrochemical Synthesis: Herbicides and Fungicides

    Manufacturers in the crop protection sector employ 3-Iodobenzonitrile for synthesizing selective aromatic intermediates needed in post-emergence herbicides and systemic fungicides. Its ortho-substituted benzonitrile scaffold allows for functionalization via metal-catalyzed cross-coupling or nucleophilic aromatic substitution, enabling creation of high-value active substances for both open-field and greenhouse applications. Production runs often follow seasonal campaigns in compliance with agrichemical registration specifications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC 1907/2006) for raw material registration
    • ISO 23195:2012 for agrochemical product traceability
    • National agrochemical certification and residue guidelines (EPA, Chinese ICAMA)

    Typical usage ratio

    • Applied at 0.8–1.5 weight equivalents in batch synthesis depending on product class and desired conversion rate
    • Ratio tailored to crop protection molecule structure and downstream scale

    Downstream process integration

    • Used after halogen exchange or in direct coupling to generate diaryl ether herbicide skeletons
    • Engaged in cyanation, diazotization, or alkylation steps during pre-formulation synthesis

    Final product types

    • Fungicidal actives for seed treatment
    • Selective herbicide actives for broadleaf weed control
    • Agrochemical intermediates for further formulation

    3. Electronic Chemicals: Liquid Crystal Display Material Synthesis

    In the production of specialty liquid crystals used for TFT and OLED display manufacturing, 3-Iodobenzonitrile serves as a critical halogenated aromatic building block for tuning polarity, birefringence, and phase stability of display alignment layers. Display material formulating companies incorporate this component in custom synthesis of cyanobiphenyl or polycyanoaromatic compounds under strict EHS and impurity control for high-resolution panel markets.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (lead-, mercury-, and halogen-content limits)
    • IEC 62474 Declarable Substance List for electronic materials
    • ISO 9001:2015 Quality Management for specialty chemical manufacturing
    • Toyota, LCD panel makers’ internal supplier standards

    Typical usage ratio

    • 0.5–1.2 molar equivalents according to final liquid crystal compound design
    • Ratio adjusted for coupling efficiency and downstream product performance

    Downstream process integration

    • Introduced in the aryl-aryl coupling or cyanation phase of liquid crystal precursor synthesis
    • Employed in continuous flow or multi-ton batch operations with stringent dryness and light controls

    Final product types

    • Nemantic and smectic liquid crystals for thin-film transistor displays
    • Specialty polycyano compounds for advanced display applications
    • Alignment layer additives for panel uniformity

    4. Dye and Pigment Intermediate Manufacture

    Producers of high-performance dyes and pigments utilize 3-Iodobenzonitrile for constructing benzene-derived chromophore intermediates. This raw material enables precise halogenation and cyanation in rigid application processes, facilitating manufacture of lightfast, solvent-resistant pigments and specialty dyes for textile, plastic, and ink printing markets. Its reactivity profile ensures efficient conversion with tight control over side products and heavy metal content, in line with end user QC protocols.

    Industry compliance standards

    • ISO 9001:2015 for pigment and dye manufacturing traceability
    • Oeko-Tex Standard 100 for textile dye safety
    • REACH Annex XVII restrictions for aromatic amines and heavy metals
    • EN 71-3 migration limits (pigments for toy and children’s product applications)

    Typical usage ratio

    • 1.0–1.2 weight equivalents in aromatic coupling, substitutions, or ring modification reactions
    • Ratio modified for required chromophore depth and application substrate

    Downstream process integration

    • Fed into azo-coupling or halide exchange steps in pigment base synthesis
    • Used as an intermediate for dye molecules where lightfastness or color strength needs enhancement
    • Processed in solvent or water-based batch reactors with in-line QC for aldehyde and cyanide residues

    Final product types

    • High-purity dyes for polyester, cotton, and polyamide fibers
    • Organic pigments for automotive, industrial, and packaging inks
    • Colorant intermediates in plastics and synthetic resins
    Free Quote

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