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3'-Iodo-4'-Methoxyacetophenone

    • Product Name 3'-Iodo-4'-Methoxyacetophenone
    • Alias IMAP
    • Einecs 810-029-7
    • 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

    740542

    Chemical Name 3'-Iodo-4'-Methoxyacetophenone
    Molecular Formula C9H9IO2
    Molecular Weight 276.07 g/mol
    Cas Number 137838-63-4
    Appearance Off-white to light yellow solid
    Melting Point 50-54 °C
    Boiling Point No data available (likely decomposes)
    Solubility Soluble in organic solvents (e.g., DMSO, chloroform)
    Density No data available
    Purity Typically ≥98%
    Smiles CC(=O)C1=CC(=C(C=C1)I)OC
    Inchikey OWOMYCCGWOKDBA-UHFFFAOYSA-N

    As an accredited 3'-Iodo-4'-Methoxyacetophenone 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 with a screw cap, labeled clearly with "3'-Iodo-4'-Methoxyacetophenone, CAS 6944-08-5, For Research Use Only."
    Shipping 3'-Iodo-4'-Methoxyacetophenone is shipped in secure, airtight containers compliant with chemical safety regulations. Packaging is designed to prevent moisture, light, and contamination exposure. During transit, labeling includes hazard and handling information. Shipping is strictly via licensed carriers with documentation, in accordance with national and international regulations for hazardous chemicals.
    Storage 3'-Iodo-4'-Methoxyacetophenone should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and avoid exposure to heat. Store at room temperature unless otherwise specified by the manufacturer’s guidelines or safety datasheet.
    Application of 3'-Iodo-4'-Methoxyacetophenone

    Applications of 3'-Iodo-4'-Methoxyacetophenone in Industrial Manufacturing

    3'-Iodo-4'-Methoxyacetophenone serves as a crucial intermediate in multiple fine chemical and pharmaceutical synthesis routes. Our facility supplies this compound with high purity to ensure consistent downstream performance across demanding industrial sectors. Below, we detail core application sectors with crucial process and compliance insights.

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

    In API manufacturing, 3'-Iodo-4'-Methoxyacetophenone acts as a starting reagent in the construction of complex heterocyclic and aromatic frameworks. Customers use it particularly in the synthesis of anti-cancer and anti-viral drug candidates, incorporating its iodo functionality through Suzuki or Buchwald–Hartwig coupling reactions. Batch traceability, impurity profiling, and regulatory documentation hold significant importance in this segment, along with validated GMP processes and secure material handling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USFDA 21 CFR Part 211 (for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) process-related impurity limits
    • DMF support for audit trail and regulatory filings

    Typical usage ratio

    • 5–18% molar ratio relative to main building block, adjusted based on target API scaffold

    Downstream process integration

    • Loaded in initial coupling or functionalization stage of multi-step synthesis under inert atmosphere; managed under strict in-process control to assure reagent purity and prevent side product formation.

    Final product types

    • Targeted kinase inhibitors
    • Antineoplastic drug intermediates
    • Antiviral pharmaceutical bases
    • Research-grade small molecule libraries

    2. Advanced Agrochemical Synthesis

    Leading agrochemical manufacturers incorporate this iodo-methoxy acetophenone as a key functionalized precursor during the synthesis of modern fungicides and herbicides, particularly for molecules targeting complex resistance mechanisms. Quality requirements focus on batch reproducibility, minimal by-product levels, and precise delivery schedules to support campaign-based plant operations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Annex IX and X (intermediate use registration and handling)
    • ISO 9001:2015 certified quality management system
    • OECD guidelines for the testing of chemicals (eco-tox assessment phase)

    Typical usage ratio

    • 8–24% by weight in target intermediate batch, modified according to route and downstream crop specificity requirements

    Downstream process integration

    • Enters at nucleophilic aromatic substitution or C–C cross-coupling stage; controls residue content via real-time HPLC and GC-MS analysis at production scale.

    Final product types

    • Systemic triazole fungicides
    • Pyridine-based herbicides
    • Selective pre-emergent formulations
    • New-generation resistance-breaking crop protectants

    3. Specialty Dye and Pigment Intermediate

    Producers of high-performance dyes and analytical pigments rely on this compound for the selective introduction of iodo and methoxy functional groups into aromatic dye scaffolds. Strict color specification, purity, and analytical profile drive acceptance. Custom solutions may require tracker samples and specification sheets before each production lot.

    Industry compliance standards

    • EN 71-3 migration standards (for colorants used in toys and textiles)
    • ISO 9001 process and documentation requirements
    • REACH registration and substance restriction guidelines
    • OEKO-TEX Standard 100 (if applied in textile dyeing chains)

    Typical usage ratio

    • 10–35% in intermediate condensation mixtures, with batch size adjusted to match downstream color intensity targets and substrate type

    Downstream process integration

    • Feeds into diazotization, azo-coupling or aromatic alkylation stage—precursor additions tracked to verify shade and lightfastness in finished pigments.

    Final product types

    • Analytical-grade azo dyes
    • Organic pigments for high-spec plastics
    • Electronic material colorants for displays
    • Specialized textile printing dyes

    4. Building Block for Material Science and Organic Electronics

    R&D centers and manufacturers engaged in organic electronics employ this raw material to construct custom aryl and heterocyclic motifs found in OLEDs and liquid crystal arrays. Chain-of-custody and impurity profile control prove critical, while the electronic grade variant undergoes extra filtration and dry-room packing.

    Industry compliance standards

    • RoHS Directive (for electronics sector chemicals)
    • TSCA compliance for U.S. electronics applications
    • JEITA guidelines for organic electronic materials
    • ISO 14644 cleanroom compatibility (for ultra-high purity grades)

    Typical usage ratio

    • 4–12% by mole in aromatic electrophilic substitution or coupling mixtures, depending on the final structure requirements and targeted film properties

    Downstream process integration

    • Introduced in metal-catalyzed cross-coupling or cyclization step; purity verified by LC-MS prior to solid-phase purification or film casting on preparatory lines.

    Final product types

    • OLED display component precursors
    • Advanced liquid crystal materials
    • Functionalized polymers for sensor films
    • Molecular building blocks for flexible circuit substrates
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