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Methyl 3-Amino-2-Methylbenzoate

    • Product Name Methyl 3-Amino-2-Methylbenzoate
    • Alias Methyl 3-amino-o-toluate
    • Einecs 629-715-8
    • 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
    VTB
    Specifications

    HS Code

    349272

    Name Methyl 3-Amino-2-Methylbenzoate
    Cas Number 7497-06-1
    Molecular Formula C9H11NO2
    Molecular Weight 165.19 g/mol
    Appearance Light yellow to brown solid
    Melting Point 54-58°C
    Boiling Point 311.3°C at 760 mmHg
    Density 1.18 g/cm3
    Smiles CC1=C(C=CC(=C1)N)C(=O)OC
    Synonyms 3-Amino-2-methylbenzoic acid methyl ester
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Purity Typically ≥ 98%

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, tightly sealed with screw cap, labeled with product name, CAS number, hazard symbols, and manufacturer details.
    Shipping Methyl 3-Amino-2-Methylbenzoate is shipped in tightly sealed containers to prevent leakage or contamination. It should be stored and transported in a cool, dry place, away from incompatible substances. All packaging complies with chemical safety and regulatory standards. Handle with care, using appropriate protective equipment during loading and unloading.
    Storage Methyl 3-Amino-2-Methylbenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. It should be kept at room temperature, protected from moisture, and clearly labeled. Handle with appropriate personal protective equipment to prevent inhalation, ingestion, or skin contact.
    Application of Methyl 3-Amino-2-Methylbenzoate

    Applications of Methyl 3-Amino-2-Methylbenzoate in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply Methyl 3-Amino-2-Methylbenzoate to established downstream partners active in advanced material synthesis, pharmaceuticals, specialty dye manufacturing, and agrochemical intermediate production. Below we outline the specific commercial applications, detailed compliance frameworks, process integration points, formulation ratios, and the typical finished products manufactured using our material.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical formulation specialists utilize Methyl 3-Amino-2-Methylbenzoate as a key building block in the synthesis of certain API intermediates, particularly for non-steroidal anti-inflammatory drugs (NSAIDs) and selective serotonin reuptake inhibitors (SSRIs). It enters multi-step synthesis routes, serving as an aromatic amino ester precursor where amination and further derivatization are required at precise locations on the benzoate ring. Drug manufacturers adhere closely to pharmacopeial standards and regulatory documentation for safety, traceability, and impurity profiling during scale-up and validation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs as applicable to intermediates
    • 21 CFR Part 210/211 US cGMP requirements
    • ISO 9001 Quality Management Systems (for upstream supplier auditing)

    Typical usage ratio

    • 5–15% w/w relative to total reaction mass in intermediate synthesis; final ratio set by stoichiometry and yield optimization in validation trials

    Downstream process integration

    • Introduced after initial aromatic ring activation, typically as one of the critical starting materials for esterification or amidation sequences; timed addition ensures control of reaction kinetics and downstream purity

    Final product types

    • Key intermediates for NSAIDs (e.g., mefenamic acid derivatives)
    • Intermediates for SSRIs and other API molecule frameworks
    • Custom aromatic amino ester building blocks for clinical trial compounds

    2. Specialty Dye & Pigment Manufacture

    Manufacturers in the dye and pigment industry adopt Methyl 3-Amino-2-Methylbenzoate to synthesize tailored azo and anthraquinone dyes, which require aromatic amino functional groups for high chromatic purity and stability. The chemical’s defined substitution pattern improves tinctorial strength and colorfastness in textile, leather, and paper applications. Precise input ratios and staging help meet high-purity requirements and minimize residual byproducts during scale-up for commercial production.

    Industry compliance standards

    • OEKO-TEX® Standard 100: Textile dye safety compliance
    • EU REACH Regulation (EC 1907/2006) for chemical safety and registration
    • ZDHC MRSL for restricted substance management
    • ISO 14001: Environmental Management Certification

    Typical usage ratio

    • 2–10% of the starting dye batch mass, adjustable based on target chromatic intensity and coupling reagent efficiency

    Downstream process integration

    • Enters the diazotization or coupling stage in batch reactors; precise addition critical for achieving color uniformity and reproducibility across batches

    Final product types

    • Azo dyes for cotton and cellulose fabrics
    • Anthraquinone pigments for industrial and artist paints
    • Disperse dyes for polyester fiber applications

    3. Fluorescent Brightener Intermediate Production

    In the production of optical brighteners, Methyl 3-Amino-2-Methylbenzoate functions as a fundamental aromatic amino ester component for constructing stilbene and coumarin derivatives. These intermediates enable high fluorescence intensity required for paper, detergent, and textile applications. Its selective reactivity ensures batch-to-batch reproducibility critical for downstream brightener performance and compliance with international quality benchmarks.

    Industry compliance standards

    • EU Regulation (EC) No 648/2004 on detergents (Annex VII: labeling of optical brighteners)
    • FDA 21 CFR 73.2995 (when used in food contact paper applications, subject to purity and migration criteria)
    • ISO 9001/QC protocols for dye intermediates
    • China GB/T 6682 for analytical reagent requirements in paper industry use

    Typical usage ratio

    • 8–20% by weight as a core precursor in the brightener intermediate’s condensation and alkylation stages, proportion adjusted for fluorescence output targets

    Downstream process integration

    • Charged during initial condensation reactions with cyanuric chloride or stilbene cores; reaction completion and byproduct control monitored using in-line fluorescence spectrometry

    Final product types

    • Optical brightener intermediates for detergent formulation
    • Fluorescent paper whitening agents
    • Textile finishing brighteners

    4. Agrochemical Synthesis Intermediate

    Commercial agrochemical producers integrate Methyl 3-Amino-2-Methylbenzoate into synthesis routes for herbicide and fungicide intermediates, where aromatic amino esters offer enhanced reactivity and selectivity during cyclization and acylation steps. Use of this molecule supports efficient process flows and traceable impurity management in compliance with agrochemical regulatory frameworks.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticides
    • EU Regulation (EC) No 1107/2009 for plant protection product approval
    • ISO 17025 testing standards for QC labs
    • China Registration Standards for Pesticides (GB 4839 and GB/T 1600 series)

    Typical usage ratio

    • 5–12% of the precursor input, with dosing levels set during process engineering based on molecular yield and target selectivity

    Downstream process integration

    • Incorporated after initial halogenation or nitration when forming cyclic imide or anilide scaffolds central to active ingredient synthesis; kinetic profiles adjusted with process analytical controls

    Final product types

    • Key intermediates for herbicidal active ingredients
    • Fungicide precursor compounds
    • Synthesis blocks for selective plant growth regulators
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