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2-Iodo-3-Methylbenzoic Acid

    • Product Name 2-Iodo-3-Methylbenzoic Acid
    • Alias 2-Iodo-m-toluic acid
    • Einecs 253-125-1
    • 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

    737228

    Product Name 2-Iodo-3-Methylbenzoic Acid
    Cas Number 57311-83-4
    Molecular Formula C8H7IO2
    Molecular Weight 262.05 g/mol
    Appearance White to off-white solid
    Melting Point 168-171 °C
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Structural Formula IC6H3(CH3)COOH
    Smiles CC1=C(C=CC(=C1)C(=O)O)I
    Inchi InChI=1S/C8H7IO2/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4H,1H3,(H,10,11)
    Storage Temperature Store at 2-8 °C

    As an accredited 2-Iodo-3-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled “2-Iodo-3-Methylbenzoic Acid, 98% min, CAS 6937-34-4.”
    Shipping 2-Iodo-3-Methylbenzoic Acid is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical and should be handled with appropriate safety precautions. Shipping complies with all relevant regulations, including labeling and documentation, to ensure safe transport. Store in a cool, dry environment upon arrival.
    Storage 2-Iodo-3-methylbenzoic acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Store separately from strong oxidizing agents and acids. Avoid moisture and exposure to incompatible materials. Clearly label the container and ensure only trained personnel handle the chemical, following standard laboratory safety protocols.
    Application of 2-Iodo-3-Methylbenzoic Acid

    Applications of 2-Iodo-3-Methylbenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 2-Iodo-3-Methylbenzoic Acid, we support value chains requiring high-purity halogenated benzoic acids for advanced synthesis. Below are critical downstream routes in which our material plays a key role, covering specific industry standards, recommended process ratios, integration points, and the nature of finished goods.

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

    Pharmaceutical formulation developers utilize 2-Iodo-3-Methylbenzoic Acid as a halogenated aromatic building block, most notably in Suzuki coupling and amidation processes. These reactions support the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) and other complex molecules. The compound's iodine substitution enables selective late-stage functionalization, which enhances molecular diversity in advanced intermediates for regulatory-compliant manufacturing pipelines.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) guidelines
    • US FDA 21 CFR Part 210/211 for API lines
    • ISO 9001:2015 for supplier approval

    Typical usage ratio

    • 0.2 to 0.8 molar equivalents per synthesis stage, fine-tuned according to yield optimization and process scale

    Downstream process integration

    • Entry at aromatic halogen exchange or direct C–C coupling stage in anhydrous conditions
    • Follows rigorous QC in-house before batch release to reactor loading

    Final product types

    • API intermediates such as substituted benzoic acid moieties
    • Central core scaffolds for specialty pharmaceuticals
    • Building blocks for contract API development
    • Chemical standards and reference compounds

    2. Custom Synthesis of Agrochemical Intermediates

    Process scale producers in the crop protection segment rely on the iodo-functional moiety for creating novel fungicide, herbicide, and pesticide backbones. 2-Iodo-3-Methylbenzoic Acid serves as a coupling precursor or modification substrate in C-H activation reactions under inert atmospheres, significantly supporting SAR exploration in lead compound projects.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius agrochemical guidelines
    • China National Standard GB/T 1600 for pesticide intermediates
    • REACH (EC No. 1907/2006) substance registration standards
    • ISO 17025 accredited lab testing for purity and residue

    Typical usage ratio

    • 5–15% of total substrate mass per transformation; adjusted per synthetic route and crop use restriction

    Downstream process integration

    • Dosed during early-stage aromatic modification and halogen incorporation
    • Subject to solvent extraction and LC-MS purity verification in pilot runs

    Final product types

    • Key intermediates for triazole and strobilurin fungicides
    • Pyridine and pyrimidine derivatives for herbicide actives
    • In-process control compounds for agrochemical QC
    • Stock solutions for structure-activity relationship (SAR) studies

    3. Raw Material in Electronic Chemicals for Specialty Polymers

    Manufacturers in microelectronics chemical supply teams use 2-Iodo-3-Methylbenzoic Acid as a halogenation agent or intermediate for custom function monomers. The compound enables precise placement of iodo groups in monomer synthesis, required for conjugated polymers and advanced liquid crystal alignments. Its unique structure supports electronics-grade resin and advanced display material formulation, particularly targeting anti-static and dielectric modification.

    Industry compliance standards

    • SEMI C94/SEMI C96 chemical purity protocols
    • IEC 62474 for hazardous materials in electronic devices
    • RoHS 3 compliance for downstream safety
    • Material purity specification ≥99.0% traceable by GC-MS

    Typical usage ratio

    • 0.05–0.2 functional group equivalents per mole of polymer backbone, set by chain length and degree of substitution

    Downstream process integration

    • Introduced during step-growth or chain-growth polymerization with controlled thermal cycling
    • Monitored in-line with real-time FTIR or NMR to validate iodo retention

    Final product types

    • Specialty polyimides for flexible electronics
    • Functional polymers for OLED/LC display films
    • Dielectric resins and anti-static films
    • Polymerizable liquid crystal monomers

    4. Starting Material for Specialty Fine Chemicals

    Producers of halogenated specialties and high-purity fine chemicals depend on 2-Iodo-3-Methylbenzoic Acid for downstream conversion into pyridyl, biphenyl, or phenolic derivatives. It reacts under palladium-catalyzed cross-coupling conditions and other directed ortho-metalation steps, yielding specialty molecules for use in diagnostics, fragrance chemistry, and analytical standards.

    Industry compliance standards

    • ISO 9001:2015 for chemical production traceability
    • Harmonized System (HS) classification for customs declaration
    • Purity and identity per ACS analytical reagent specifications
    • Full compliance with local Hazard Communication Standards (HCS)

    Typical usage ratio

    • 0.5–1.5 equivalents per target molecule, subject to stoichiometric requirements of specific coupling schemes

    Downstream process integration

    • Charged during Suzuki, Heck, and Sonogashira coupling workflows
    • Isolated via preparative HPLC for end-use refinement

    Final product types

    • High-purity biphenyls for analytical laboratories
    • Pyridine-based ligands for catalysis kits
    • Fragrance molecule precursors
    • Research reagents and calibration standards
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