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2-Amino-3-Methoxybenzoic Acid

    • Product Name 2-Amino-3-Methoxybenzoic Acid
    • Alias Anthranilic acid, 3-methoxy-
    • Einecs 219-029-4
    • 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

    145210

    Iupac Name 2-Amino-3-methoxybenzoic acid
    Molecular Formula C8H9NO3
    Molecular Weight 167.16 g/mol
    Cas Number 616-10-6
    Appearance Off-white to beige solid
    Melting Point 163-166 °C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 3-Methoxyanthranilic acid; o-Amino-m-anisic acid
    Smiles COC1=C(C=CC(=C1)C(=O)O)N
    Inchi InChI=1S/C8H9NO3/c1-12-6-3-2-5(8(11)10)4-7(6)9/h2-4H,9H2,1H3,(H,10,11)
    Pka Approx. 3.9 (carboxylic acid)
    Storage Conditions Store at room temperature, away from moisture and light

    As an accredited 2-Amino-3-Methoxybenzoic 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, sealed with a screw cap, labeled "2-Amino-3-Methoxybenzoic Acid," includes hazard and purity information.
    Shipping 2-Amino-3-Methoxybenzoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packages are clearly labeled with hazard and handling information and transported according to applicable regulations for non-hazardous laboratory chemicals, ensuring safe delivery. Proper documentation accompanies each shipment for traceability and compliance purposes.
    Storage 2-Amino-3-methoxybenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from moisture, heat, and direct sunlight. Use appropriate personal protective equipment when handling, and label storage containers clearly to avoid accidental misuse or contamination.
    Application of 2-Amino-3-Methoxybenzoic Acid

    Applications of 2-Amino-3-Methoxybenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 2-Amino-3-Methoxybenzoic Acid, we supply this intermediate to specialized downstream sectors requiring consistency in material quality and regulatory traceability. Below, we outline its principal industrial applications, highlighting compliance requirements, formulation concentrations, process roles, and end product categories for each segment.

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

    In the pharmaceutical sector, this compound serves as a key intermediate during the synthesis of certain APIs, especially in the preparation of non-steroidal anti-inflammatory drugs and specific benzoxazole or benzothiazole derivatives. Our customers use it at defined stages in multi-step reaction cascades, where purity and trace metal content directly influence the safety and value of the resulting medical compounds. Such processes require traceability and batch reproducibility, with downstream documentation for regulatory dossiers and pre-registration of production batches tied to Good Manufacturing Practice (GMP) frameworks.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for relevant APIs
    • U.S. FDA 21 CFR Part 211 – Current GMP for Finished Pharmaceuticals
    • ISO 9001 – Quality Management Systems

    Typical usage ratio

    • Used in molar ratios of 0.5:1 to 2:1 with key condensing agents depending on target molecule route
    • Precise concentration based on stoichiometric requirements, adjusted for impurity limits specific to API impurity profiles

    Downstream process integration

    • Introduced following initial aromatic amination and prior to cyclization or acylation stage
    • Purified as a key intermediate and subjected to further transformations including methylation, sulfonation, or amide bond formation

    Final product types

    • Benzoxazole class APIs for analgesic preparations
    • Benzothiazole-based drugs for neurological indications
    • Anti-inflammatory drug intermediates

    2. Dye and Pigment Synthesis Building Block

    Dye manufacturers incorporate our material in the synthesis of azo and anthraquinone dyes, specifically for applications requiring tailored electronic properties and solubility. Its methoxy and amino functionalities allow for highly specific coupling reactions, impacting tone, fastness, and chromatic purity in textile and specialty pigment production. Large-scale downstream use aligns with both chemical process safety and environmental standards, given heightened scrutiny on aromatic intermediates.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 – Registration, Evaluation, Authorization, and Restriction of Chemicals
    • OEKO-TEX Standard 100 – For harmful substances in textiles
    • ISO 9001 – Quality Management for batch consistency
    • ZDHC MRSL v3.1 – Manufacture Restricted Substances List for dyes and pigments

    Typical usage ratio

    • Added at 5–15% by mass relative to the total aromatic amine content in coupling reactions
    • Adjusted between 7–12% for high-purity reactive dye production, depending on target chromophore structure

    Downstream process integration

    • Acts as a coupling component in diazotization or condensation stages
    • Processed prior to final sulfonation or metal complexation steps

    Final product types

    • Disperse dyes for synthetic fiber coloring
    • Mordant dyes for wool and silk
    • Fluorescent pigments for plastics and coatings

    3. Agrochemical Intermediates for Selective Herbicide Synthesis

    Manufacturers of crop protection agents utilize this material in synthesis routes for heterocyclic-based selective herbicides. Its reactivity profile enables formation of target ring structures vital for bioactivity, supporting the production of actives compliant with regional pesticide residue and environmental fate requirements. Integrated use in multi-step agrochemical syntheses ensures traceable input streams for regulatory review and sustainability audits.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • ISO 17025 – Laboratory Accreditation for residue analysis
    • European Union Regulation (EU) 1107/2009 for Plant Protection Products
    • EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)

    Typical usage ratio

    • Utilized between 3–8% in initial alkylation and cyclization steps, relative to total precursor batch
    • Adjusted lower or higher (2–10%) based on desired yield of specific heterocycle or active constituent

    Downstream process integration

    • Fed into amidation or alkylation reactor following precursor preparation
    • Acts as nucleophile or electrophile depending on synthetic path

    Final product types

    • Selective herbicide actives for broadleaf and grass weeds
    • Growth regulator intermediates
    • Precursors for fungicidal agents

    4. Specialty Chemical Synthesis—Photoresist Materials

    Producers of advanced materials for microelectronics integrate our product as an intermediate for fabricating aromatic ester and amide groups within photoresist polymers. The balance of electron-donating and withdrawing substituents suits pattern resolution and sensitivity requirements in semiconductor lithography. Strict control over base purity and trace organic analytes ensures photoresist resins meet defect density and etch resistance targets set by wafer fabs.

    Industry compliance standards

    • SEMI C15 – Specifications for Photoresist Materials
    • ISO 14644 – Cleanroom and Controlled Environment Standards
    • IATF 16949 – Quality Management for Automotive Electronics
    • RoHS Directive 2011/65/EU for electronic chemicals

    Typical usage ratio

    • Integrated at 1–4% by weight in photoresist polymer precursor blends
    • Adjusted according to molecular weight target and developer compatibility for resists

    Downstream process integration

    • Condensed or esterified in resist resin monomer formations
    • Added just prior to final resin polymerization and compounded with photoactive components

    Final product types

    • Positive and negative tone photoresists for semiconductor fabrication
    • Anti-reflective coating intermediates for photolithography
    • Specialty polymer additives for circuit board manufacturing
    Free Quote

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