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2'-Iodoacetophenone

    • Product Name 2'-Iodoacetophenone
    • Alias 2-Iodophenyl methyl ketone
    • Einecs 219-040-8
    • 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
    VTB
    Specifications

    HS Code

    809696

    Iupac Name 1-(2-iodophenyl)ethan-1-one
    Cas Number 4563-63-1
    Molecular Formula C8H7IO
    Molar Mass 246.05 g/mol
    Appearance White to off-white solid
    Melting Point 46-50°C
    Boiling Point 150-152°C at 12 mmHg
    Density 1.67 g/cm³
    Smiles CC(=O)C1=CC=CC=C1I
    Solubility In Water Low
    Refractive Index 1.650 (predicted)
    Pubchem Cid 68178

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

    Packing & Storage
    Packing A 5-gram amber glass bottle, tightly sealed, labeled "2'-Iodoacetophenone" with hazard warnings and CAS number for laboratory use.
    Shipping 2'-Iodoacetophenone is typically shipped in secure, tightly sealed containers to prevent leakage or contamination. It is protected from light and moisture and often packed with cushioning material. Shipping complies with relevant regulations for hazardous chemicals, including correct labeling, documentation, and temperature control if required. Handle only by trained personnel.
    Storage 2'-Iodoacetophenone should be stored in a tightly sealed container, protected from light and moisture. Keep the container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid extreme temperatures. Ensure proper chemical labeling, and follow local regulations and institutional safety protocols for hazardous chemicals.
    Application of 2'-Iodoacetophenone

    Applications of 2'-Iodoacetophenone in Industrial Manufacturing

    2'-Iodoacetophenone serves as a critical intermediate in several chemical manufacturing sectors, supporting specialized synthesis with strict adherence to industry protocols and customer quality requirements. Below you will find a breakdown of practical industrial application segments our clients deploy, with details on compliance, ratios, processing, and target end-use.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers employ 2'-Iodoacetophenone as a halogenated building block in the synthesis of targeted active pharmaceutical ingredient (API) scaffolds, especially for complex heterocyclic molecules and kinase inhibitor development. Synthesis routes integrate this material during the arylation and subsequent functionalization stage, requiring full traceability and compliance according to industry standards. Controlled reaction environments, precise stoichiometry, documentation for GMP certification, and analytical validation for residuals are essential.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP/EP Impurity Protocols
    • 21 CFR Part 210/211
    • Ph. Eur. Monograph References for Building Blocks

    Typical usage ratio

    • 0.95–1.2 molar equivalents per transformation step, adjusted based on target molecule structure and reactivity

    Downstream process integration

    • Halogenated aromatic coupling steps in multi-stage synthetic route
    • Direct addition to batch reactors with controlled temperature and inert atmosphere

    Final product types

    • Small-molecule kinase inhibitors
    • Pyridine- and imidazole-derived APIs
    • Specialty oncology drug intermediates

    2. Agrochemical Active Ingredient Synthesis

    Major agrochemical companies use 2'-Iodoacetophenone for introducing iodine substituents during the early-stage synthesis of fungicides and herbicides. The compound integrates into proprietary processes such as Suzuki-Miyaura cross-coupling and further oxidation/hydrolysis steps. All workflows must observe REACH registration for safe chemical handling, and manufacturers require batch traceability in accordance with ISO procedures and local agriculture chemical regulation.

    Industry compliance standards

    • REACH Regulation (EC No 1907/2006)
    • ISO 9001:2015 certified QC process
    • FAO/WHO Guidelines for Pesticide Specifications
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 10–20% by weight in active ingredient precursor formulation, adjusted by end-use molecule reactivity

    Downstream process integration

    • Entry at the aromatic halogenation stage for aryl-aryl bond formation
    • Used in coupling reactions preceding oxidation or cyclization step

    Final product types

    • Triazole-class fungicide intermediates
    • Selective herbicide scaffolds
    • Regulatory-approved pesticide actives

    3. Specialty Dye and Pigment Manufacturing

    Colorants and pigment manufacturers utilize 2'-Iodoacetophenone to introduce functional iodine into aromatic rings, allowing fine-tuned absorption properties in specialty dyes, including those for security inks and high-stability coatings. GMP coloring agents require accurate formulation and compliance with chemical purity standards, and customers typically demand full batch characterization for trace element content.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toy Colorants
    • ISO 18314-1:2015 Analytical Color Measurement
    • REACH Annex XVII for Pigment Substances
    • Customer-specific purity specifications

    Typical usage ratio

    • 5–12% by weight in coupling reactions, variable by desired color strength and final chromophore structure

    Downstream process integration

    • Aromatic iodination step before azo or anthraquinone dye assembly
    • Reaction in solvent-based batch reactors under controlled conditions

    Final product types

    • Security printing dyes
    • Long-lasting architectural pigments
    • Optically active specialty inks

    4. Fine Chemical Synthesis for Organic Electronics

    Producers in the organic electronics domain integrate 2'-Iodoacetophenone as a key monomer precursor for synthesizing high-performance organic semiconductors and OLED intermediates. The compound is incorporated in surface functionalization and cross-coupling processes to modulate the electronic character of polymer backbones. Electro-optical material synthesis must conform to RoHS and proprietary electronics chemistry guidelines, with all process waste strictly managed as per WEEE and ISO 14001 protocols.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics
    • ISO 14001 Environmental Management
    • Supplier electronic materials restrictions
    • TSE/EHS requirements for specialty chemicals

    Typical usage ratio

    • 0.8–1.5 molar equivalents per coupling reaction, tuned per electronic performance target

    Downstream process integration

    • Monomer synthesis via halogen-metal exchange methods
    • Implemented in staged coupling and functionalization for polymer chain construction

    Final product types

    • OLED emitter and host molecules
    • Semiconducting polymer intermediates
    • Sensor substrate coatings

    5. Advanced Materials for Photoinitiators

    Manufacturers of specialty photoinitiators use 2'-Iodoacetophenone to chemically modify acetophenone skeletons, improving UV absorption and free-radical reactivity in UV-curable coatings and inks. Selection criteria include controlled substitution and high-purity requirements. Production lines comply with industrial coatings safety norms and analytical specifications for purity, and documentation supports downstream RoHS and environmental controls.

    Industry compliance standards

    • ISO 19007:2015 Photoinitiator Analysis
    • RoHS and SVHC substance exclusion
    • ASTM E2271 Photochemical Process QC
    • Customer-specific optical absorption specs

    Typical usage ratio

    • 3–8% by weight in upstream acetophenone functionalization reactions, optimized by UV absorption profile targets

    Downstream process integration

    • Used in batch functionalization prior to condensation or alkylation steps
    • Quality control verification for photoactivity and purity at each stage

    Final product types

    • High reactivity photoinitiators
    • UV-curable ink additives
    • Specialty 3D printing resin initiators
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    Certification & Compliance