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Perfluorooctyl Iodide

    • Product Name Perfluorooctyl Iodide
    • Alias 1-Iodoperfluorooctane
    • Einecs 221-491-3
    • 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

    793682

    Cas Number 507-63-1
    Molecular Formula C8F17I
    Molecular Weight 499.96 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 174-176°C (lit.)
    Melting Point -39°C
    Density 2.09 g/cm³ at 25°C
    Refractive Index 1.338 at 20°C
    Solubility In Water Insoluble
    Purity Typically ≥98%

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

    Packing & Storage
    Packing Perfluorooctyl Iodide is supplied in a 100g amber glass bottle, securely sealed, with clear hazard labeling and product information.
    Shipping Perfluorooctyl Iodide is shipped in tightly sealed, chemical-resistant containers to prevent leakage and exposure. It must be kept away from heat, light, and incompatible substances. Shipping typically complies with relevant hazardous material transport regulations, including proper labeling and documentation, to ensure safe handling and minimize environmental and health risks.
    Storage Perfluorooctyl Iodide should be stored in a tightly closed container, away from light and moisture, in a cool, dry, and well-ventilated area. It should be kept away from sources of ignition, strong oxidizing agents, and incompatible materials. Store at room temperature and handle with care to prevent environmental release or contact with skin and eyes due to its potential toxicity.
    Application of Perfluorooctyl Iodide

    Applications of Perfluorooctyl Iodide in Industrial Manufacturing

    As a direct manufacturer, we provide high-purity Perfluorooctyl Iodide for highly specialized downstream sectors. Below we detail the main industrial applications, covering authentic compliance, process ratios, manufacturing integration, and end-use products as adopted by international clients in advanced materials technology.

    1. Synthesis of Fluorinated Surfactants for Electronics Cleaning

    Electronics companies depend on this compound as a building block in the production of biodegradable fluorinated surfactants. These surfactants play a key role in semiconductors and display panel manufacturing, where precise wettability, low surface energy, and superior cleaning power directly influence defect rates in wafer processing enviroments. Synthesis typically occurs via telomerization reactions, where the unique compatibility of the iodide precursor ensures both high conversion and low metal contamination, critical in photolithography stages for microelectronics.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-free requirements for electronic circuit boards
    • RoHS Directive (2011/65/EU) heavy metal and halogen content limitations
    • REACH Regulation (EC) No 1907/2006 for chemical registration and safe handling
    • Major client QC protocols for ionic contaminant control <1.0 ppm

    Typical usage ratio

    • Starter feed in telomerization: 5–15 mol% relative to total fluorinated monomer, optimized to minimize unreacted halide.

    Downstream process integration

    • Introduced at the initial step of surfactant backbone construction via free-radical or telomerization reactors, followed by purification and end-group transformation prior to blending in surfactant concentrate.

    Final product types

    • Low-residue wafer-level cleaning surfactants for semiconductor foundries
    • High-purity display panel cleaning blends
    • Specialty precision lens cleaning agents used in photonics assembly

    2. Manufacture of Fluorinated Telomer Alcohols for Water Repellent Textile Finishes

    Textile chemical firms use this material to produce long-chain telomer alcohol intermediates, an essential precursor for durable water repellent (DWR) agents. The controlled iodination step defines chain length and fluorine content, which directly determine repellency and durability on technical textiles. The strict control of molecular weight and terminal groups during synthesis ensures compatibility with environmental standards imposed by global apparel brands.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for banned substances in textile chemicals
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • Bluesign® Textile Chemical Assessment
    • ECHA PFOA/PFOS restriction regulations for long-chain perfluorinated compounds

    Typical usage ratio

    • Chain initiator feedstock: 10–18% by mol of total telomerizable acrylate for C6–C8 chain construction; adjusted according to final chain length requirements.

    Downstream process integration

    • Introduced during fluorotelomerization prior to alcohol deprotection, followed by esterification or urethane forming for DWR applications.

    Final product types

    • Non-PFOA durable water repellent finishes for outdoor apparel and gear
    • Technical textile treatments for industrial and hospital linens
    • Resin-based stain repellents for automotive upholstery

    3. Fluorinated Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound in the advanced synthesis of fluorinated intermediates for active pharmaceutical ingredients (API) where perfluorinated side chains enhance metabolic stability and bioavailability. Controlled addition allows selective substitution on aromatic rings, enhancing target specificity in final drug molecules. Residual monitoring and purification steps ensure that all by-products comply with the latest pharmacopeial purity limits, especially in late-stage development for fluorinated APIs.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) 2.2.46: Purity by GC for halogenated intermediates
    • ICH Guideline Q3A/B: Impurity and residual solvent limits
    • US FDA cGMP 21 CFR Parts 210/211 for API processing
    • Japan PMDA guidance for novel fluorinated pharmaceutical intermediates

    Typical usage ratio

    • Controlled addition at 0.3–1.5 molar equivalents to aryl substrate depending on target substitution pattern and desired fluorine incorporation in the final API intermediate.

    Downstream process integration

    • Incorporated at a specific alkylation or halogen exchange step, followed by reductive elimination and crystallization before final purification to meet API-grade specs.

    Final product types

    • Fluorinated aromatic intermediates used in cardiovascular and oncology drugs
    • Specialty building blocks for CNS (Central Nervous System) pharmaceuticals
    • Final-stage perfluoroalkylated APIs for orphan drug development

    4. Custom Synthesis of Fluorinated Polymers for Oil & Gas Field Chemicals

    Oilfield chemical suppliers specify this compound for the synthesis of tailored fluorinated polymers, substantially improving wettability control and resistance to harsh downhole environments. As a functional initiator, it defines emulsion stability in drilling fluids and enhances resistance to coalescence in cement additives. Precise metering during polymerization enables fine-tuned molecular weight dispersity, essential in demanding high-pressure and high-temperature (HPHT) applications.

    Industry compliance standards

    • API Specification 13A/13B for drilling fluid performance
    • OSPAR Convention Annex II for offshore chemical notification/inventory (OCNS)
    • REACH registration dossier for polymers with perfluorinated content
    • Major E&P client standards for thermal stability and chemical persistency

    Typical usage ratio

    • Functional initiator/terminator dosage: 1–6 mol% relative to acrylamide or acrylate monomer, tailored for required polymer chain end functionality.

    Downstream process integration

    • Added at the beginning of the polymerization process, incorporation monitored via in-line spectroscopy, followed by immediate emulsion blending before packaging for oilfield application.

    Final product types

    • Wetting agents for water-based and oil-based mud systems
    • HPHT cement fluid loss additives
    • Surfactant-polymer blends for enhanced oil recovery (EOR)
    • Antiscalant formulations for reservoir water treatment

    5. Production of Fluorinated Silane Coupling Agents for Surface Coatings

    Specialty coatings formulators utilize this intermediate for the synthesis of fluorinated silane coupling agents, which modify the surface properties of glass, ceramics, and metals. The iodide enables selective perfluoroalkyl chain introduction, enhancing hydrophobicity and anti-fouling characteristics while allowing for stable siloxane network formation. This process directly supports the development of long-lasting, low-energy surface coatings required for architectural glass and anti-graffiti applications.

    Industry compliance standards

    • ISO 9001 quality management for raw material traceability
    • ASTM C1376 for evaluation of hydrophobic treatments on building facades
    • REACH and TSCA chemical inventory compliance for silane intermediates
    • EU Regulation No. 305/2011 (CPR) for construction products

    Typical usage ratio

    • Used at 2–7 mol% of total silane feed during functionalization; ratio adjusted according to desired degree of fluorination and final contact angle on substrate.

    Downstream process integration

    • Fed to functionalization reactor with alkoxysilane backbone, followed by hydrolysis and condensation in solvent, then purified and stabilized for packaging.

    Final product types

    • Self-cleaning and anti-fogging glass coatings
    • Graffiti-resistant architectural surface protectants
    • Scratch-resistant transparent coatings for automotive and electronics
    • Durable hydrophobic treatments for building envelopes
    Free Quote

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    Email: sales7@sinochem-nanjing.com

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