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4-Iodoanisole

    • Product Name 4-Iodoanisole
    • Alias p-Iodoanisole
    • Einecs 226-939-8
    • 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

    544023

    Name 4-Iodoanisole
    Chemical Formula C7H7IO
    Molecular Weight 234.04 g/mol
    Cas Number 637-89-8
    Appearance White to off-white crystalline powder
    Melting Point 56-59 °C
    Boiling Point 265 °C
    Density 1.74 g/cm3
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms p-Iodoanisole, 1-Iodo-4-methoxybenzene
    Pubchem Cid 12136
    Smiles COC1=CC=C(C=C1)I

    As an accredited 4-Iodoanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Iodoanisole is packaged in a 25-gram amber glass bottle, sealed securely, and labeled with hazard symbols and handling instructions.
    Shipping 4-Iodoanisole is shipped in tightly sealed containers to ensure stability and prevent contamination. It is classified as a hazardous material and should be handled with care, in compliance with local regulations. The package is clearly labeled, protected from direct sunlight, extreme temperatures, moisture, and physical damage during transport.
    Storage 4-Iodoanisole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from light and moisture. Proper chemical storage cabinets, specifically those designated for organic chemicals, are recommended to ensure safety and preserve the compound’s stability.
    Application of 4-Iodoanisole

    Applications of 4-Iodoanisole in Industrial Manufacturing

    As a dedicated manufacturer specializing in halogenated aromatic intermediates, we supply 4-Iodoanisole to a select group of high-value downstream industries where its chemical properties are essential for specific reaction steps or advanced synthesis. Below, we outline core industrial applications, highlighting each sector’s compliance standards, usage ratios, integration methods, and typical finished products.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers depend on this specialty compound as a key building block in the synthesis of several active pharmaceutical ingredients, particularly for introducing an iodo or methoxy moiety in advanced-stage molecules. This intermediate plays a crucial role during palladium-catalyzed cross-coupling reactions such as Suzuki–Miyaura and Sonogashira, supporting the formation of aryl–aryl and aryl–alkyne bonds tailored to target drugs. Controlled material specification and batch-to-batch reproducibility meet stringent regulatory and quality expectations for use in drug intermediate manufacturing plants.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – ICH Q7
    • USP, EP, JP (where applicable for intermediates)
    • FDA 21 CFR Part 211 for API manufacturing environments
    • Relevant EU REACH chemical safety assessment

    Typical usage ratio

    • Ranges from 0.18 to 0.35 molar equivalents, calculated based on the targeted coupling yields and desired molecular substitutions; adjustment depends on downstream product batch size and reaction stoichiometry.

    Downstream process integration

    • Used as a coupling substrate directly after the completion of core ring construction in the multistep synthetic sequence; dissolved in anhydrous solvents prior to introduction to the catalytic reactor, usually under inert atmosphere.

    Final product types

    • Advanced pharmaceutical intermediates for anti-cancer drugs
    • Targeted kinase inhibitor scaffolds
    • Intermediate compounds for CNS or cardiovascular APIs

    2. Agrochemical Active Ingredient Manufacturing

    Specialty crop protection companies employ this aromatic iodo derivative in the synthesis of select fungicides and herbicides, where electron-rich aromatic rings with iodo substituents enable fine-tuned biological activity. The molecule’s stability and reactivity suit regulated agricultural chemical processes, supporting highly specific halogenation or O-demethylation steps during the late-stage assembly of bioactive compounds.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001:2015 Quality Management System
    • Good Laboratory Practice (GLP, OECD Principles)
    • National agrochemical manufacturing regulations (e.g., China ICAMA, US EPA registrant guidelines)

    Typical usage ratio

    • Generally 3–8% by weight of the reaction charge, optimized per specific agrochemical molecular target and overall yield targets; adjusted based on process redevelopment for active ingredient innovation or substitution pathways.

    Downstream process integration

    • Introduced during the final halogenation or ring functionalization of the synthetic route, frequently processed under temperature-controlled and pressure-regulated systems to ensure purity of bioactive ingredient prototypes.

    Final product types

    • Precursor for select triazole fungicides
    • Pyridine and phenyl ether herbicidal intermediates
    • Regulated active substances for field trials and commercialization

    3. OLED Material Precursor Synthesis

    4-Iodoanisole serves as a precision intermediate within the optoelectronic industry for constructing high-performance organic light-emitting diode (OLED) materials. Its clean reactivity profile ensures minimal side-product formation during C–C or C–N coupling, which is critical in fabricating stable emitter and transport layers. OLED material manufacturers integrate this raw material into semiconductor-grade cleanrooms, enforcing rigorous analytical protocols to ensure the purity required for thin-film device performance.

    Industry compliance standards

    • Cleanroom manufacturing ISO 14644-1 (Class 6 or better)
    • RoHS 2 (2011/65/EU) for electronic material restrictions
    • REACH SVHC compliance
    • Quality conformance: JEITA (Japan Electronics and Information Technology Industries Association) technical guides

    Typical usage ratio

    • Varies from 1–5 mol% of total aromatic intermediate blend; usage determined by emissive molecule design and the desired balance of hole/electron mobility within the device structure.

    Downstream process integration

    • Added during the cross-coupling stage for emitter/host layer formation, immediately prior to purification steps such as column chromatography and vacuum sublimation, to ensure strict control over optical and electrical characteristics.

    Final product types

    • Blue and green OLED emitter molecules
    • Hole-transport and electron-transport materials for displays
    • Organic semiconductors for flexible screens

    4. Liquid Crystal Intermediate Production

    Manufacturers in the advanced liquid crystal sector utilize this compound as a functionalized aromatic starting material to tailor mesogenic cores during the synthesis of specialty liquid crystalline mixtures. The methoxy and iodine substitutions enable precise tuning of phase transition behavior, directly impacting alignment and optical properties crucial for high-performance display technologies.

    Industry compliance standards

    • IEC 61249-2-43 (Materials for printed boards – Fire hazard testing)
    • ISO 9001:2015 for Quality Management in high-purity chemical manufacturing
    • RoHS & REACH regulatory frameworks for LC mixture components
    • Quality specifications set by prominent display panel OEMs

    Typical usage ratio

    • 0.5–2 mol% as a component within the mesogen precursor blend; proportion tailored for target birefringence, clearing temperature, and viscosity of the resulting LC mixture.

    Downstream process integration

    • Integrated via esterification or etherification reactions following core aromatic substrate preparation; commonly enters the process prior to custom blending and panel-specific formulation.

    Final product types

    • Liquid crystal host compounds for TFT-LCD panels
    • Custom LC mixtures for advanced display subassemblies
    • High-performance nematic or smectic LC domain controllers

    5. Advanced Dye and Pigment Intermediates

    Producers of functional dyes, particularly for electronics or specialty printing, incorporate this iodoaryl ether as a strategic precursor for extended conjugation and controlled chromophore assembly. It participates in regioselective C–H activation and substitution steps, affording unique colors and fastness properties without introducing impurity profiles that compromise end-use application integrity.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for eco-friendly colorants
    • EN 71-3 (Migration of certain elements, for pigments in toys/consumer goods)
    • REACH Annex XVII for dye and pigment manufacturing chemicals
    • ISO 18451-1:2019 for pigment and dye product identification

    Typical usage ratio

    • 2–6 mol% of aromatic precursor input depending on target chromophore length and electronics of the desired colorant; adjusted according to specific fastness and application properties required by customers.

    Downstream process integration

    • Introduced in early- or mid-stage synthesis, enabling palladium-catalyzed coupling or direct arylation for pigment molecule core construction; followed by purification, filtration, and micronization prior to downstream blending.

    Final product types

    • Organic pigments for inkjet and laser printing
    • Specialty dyes for OLED and display technologies
    • Electronic-grade colorants for sensor and smart card applications
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    Email: admin@sinochem-nanjing.com

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