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Ethyl 2-Iodobenzoate

    • Product Name Ethyl 2-Iodobenzoate
    • Alias 2-Iodobenzoic acid ethyl ester
    • Einecs 241-289-2
    • 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

    827591

    Cas Number 2867-74-9
    Molecular Formula C9H9IO2
    Molecular Weight 276.07 g/mol
    Iupac Name Ethyl 2-iodobenzoate
    Appearance Colorless to pale yellow liquid
    Boiling Point 124-126°C at 10 mmHg
    Density 1.662 g/cm3 at 25°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractive Index 1.592 at 20°C
    Smiles CCOC(=O)C1=CC=CC=C1I
    Inchi InChI=1S/C9H9IO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6H,2H2,1H3

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

    Packing & Storage
    Packing Ethyl 2-Iodobenzoate is supplied in a 25g amber glass bottle, sealed, with tamper-proof cap and clear hazard labeling.
    Shipping Ethyl 2-Iodobenzoate is shipped in tightly sealed, chemically resistant containers to prevent leaks or contamination. It is transported in compliance with relevant hazardous materials regulations, ensuring protection from light, moisture, and physical damage. Proper labeling and documentation accompany each shipment for safe handling and regulatory conformity during transit.
    Storage Ethyl 2-iodobenzoate should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat, and incompatible materials such as strong oxidizers. Store at room temperature and avoid moisture exposure. Properly label the container and handle using appropriate personal protective equipment to avoid contact and contamination.
    Application of Ethyl 2-Iodobenzoate

    Applications of Ethyl 2-Iodobenzoate in Industrial Manufacturing

    As a manufacturer specializing in high-purity halogenated aromatic intermediates, we supply Ethyl 2-Iodobenzoate for well-established industrial sectors where stringent compliance, controlled formulation, and reliable batch traceability are mandatory. Below, we outline the precise downstream application scenarios, technical integration details, and typical compliance environments for this material in real industrial settings.

    1. Pharmaceutical Intermediate Synthesis (Active Pharmaceutical Ingredient Intermediate)

    Ethyl 2-Iodobenzoate serves as a key building block in fine organic synthesis, particularly for producing iodinated pharmaceutical intermediates where the iodine atom acts as a handle for further functionalization. Integrated early in multi-step syntheses, it enables downstream customization for non-steroidal anti-inflammatory agents and advanced heterocyclic APIs. Procurement teams source this intermediate for exclusive routes where metal-catalyzed cross-coupling reactions must meet international regulatory expectations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) monographs for synthetic intermediates
    • Chinese Pharmacopoeia, as applicable to intermediate controls

    Typical usage ratio

    • Ranges from 0.15 to 0.4 molar equivalents per synthesis batch, depending on target molecule yield requirements and presence of side groups in subsequent coupling steps.

    Downstream process integration

    • Integrated during the initial halogenated aromatic activation phase; used as a substrate in palladium-catalyzed Suzuki and Sonogashira coupling reactions for constructing core frameworks of APIs.

    Final product types

    • Advanced pharmaceutical intermediates (e.g., precursors for NSAIDs, anti-infective agents)
    • Fully functionalized heterocycles
    • Regulatory-submitted API candidates
    • Small-molecule compound libraries for drug screening

    2. Agrochemical Active Discovery and Intermediate Production

    Downstream agrochemical companies incorporate Ethyl 2-Iodobenzoate as an aromatic iodine source to develop crop protection actives requiring selective iodination. R&D centers and pilot plants use its reactivity profile to assemble target scaffolds in fungicides, herbicides, and pre-emergent chemistries where halogen migration enhances molecule persistence or bioactivity. Manufacturers secure controlled lots and document all input traceability for regulatory registration dossiers.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • China GB 4839-2009 Pesticide Registration Product Standard
    • ISO 9001 for raw material traceability in agrochemicals
    • REACH Annex XI intermediate substance protocols

    Typical usage ratio

    • 0.1–0.3 molar equivalents per batch, adjusted seasonally based on agronomist-driven bioequivalence studies and targeted impurity thresholds.

    Downstream process integration

    • Fed as a halogen donor in the initial arylation stages and followed by oxidation, coupling, or hydrolysis steps to complete the core agrochemical structure.

    Final product types

    • Crop-specific fungicide intermediates
    • Herbicide molecule scaffolds with iodine substitution
    • Pre-emergent seed treatment chemistries
    • Developmental actives under regulatory evaluation

    3. Specialty Material and Polymer Modifier Manufacturing

    Producers of custom polymers or high-value specialty materials employ Ethyl 2-Iodobenzoate during the design of halogen-containing aromatic monomers. The compound delivers precise iodine incorporation for downstream cross-linkable polymer backbones, where selective substitution supports optical, electrical, or barrier property enhancement. Production planning teams reference compliance matrices and batch QC logs to satisfy advanced application requirements in coatings and engineered resins.

    Industry compliance standards

    • ISO 9001 Quality Management for engineered polymers
    • RoHS Directive (2011/65/EU) assessments for final polymer additives
    • REACH Registration for monomers and intermediates
    • ASTM D3010 for halogen content in specialty bulk polymers

    Typical usage ratio

    • 1–5% by weight in formulation of halogenated monomers, tailored according to required level of iodine in the polymer chain and downstream process compatibility.

    Downstream process integration

    • Reacted with base polymers in polycondensation or step-growth processes; typically activated via nucleophilic aromatic substitution or metal-catalyzed coupling before extrusion or molding.

    Final product types

    • Halogenated engineering plastics for electronics
    • Polymeric coating additives with customized halogen profile
    • Advanced optoelectronic material components
    • Custom resin blends for high-barrier films

    4. Fine & Performance Chemical Synthesis (Aromatic Iodination Source)

    Manufacturers in the fine chemicals sector integrate Ethyl 2-Iodobenzoate into customized syntheses requiring controlled aromatic iodination. The compound provides consistent iodine introduction to support creation of reagents, catalysts, and specialty small molecules for photonic, flavor, and colorant applications. Process engineers prioritize documented source certification and lot-to-lot analytical reproducibility to ensure high downstream reliability.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for quality and environmental compliance in batch synthesis
    • REACH registration for standalone intermediates
    • CQC GB/T 19001 for Chinese chemical manufacturers
    • Good Laboratory Practice (GLP) audit guidelines for specialty chemical routes

    Typical usage ratio

    • 0.05–0.3 molar equivalents, based on desired halogen density in the target structure and monitored by in-line analytics during the synthesis step.

    Downstream process integration

    • Introduced during phenyl iodination or as a coupling partner in metal-catalyzed aromatic ring extension reactions; batch controls implemented before isolation of downstream fine chemicals.

    Final product types

    • Aromatic iodinated reagents for laboratory use
    • Photoinitiator precursor molecules
    • Colorant and dye intermediate scaffolds
    • Specialty organic catalysts and ligands
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