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Methyl 5-Chloro-2-Methoxybenzoate

    • Product Name Methyl 5-Chloro-2-Methoxybenzoate
    • Alias Methyl 5-chloro-o-anisate
    • Einecs EINECS 606-276-4
    • 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

    770182

    Iupac Name Methyl 5-chloro-2-methoxybenzoate
    Molecular Formula C9H9ClO3
    Molecular Weight 200.62
    Cas Number 38050-02-9
    Appearance White to off-white solid
    Melting Point 61-64°C
    Boiling Point 276°C
    Density 1.31 g/cm3
    Solubility Soluble in organic solvents like ethanol, methanol, and dichloromethane
    Smiles COC1=CC(=CC=C1C(=O)OC)Cl
    Purity Typically ≥98%
    Refractive Index 1.539 (predicted)
    Flash Point 123°C
    Storage Temperature Store at 2-8°C

    As an accredited Methyl 5-Chloro-2-Methoxybenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25g amber glass bottle with a secure screw cap, labeled with product name, quantity, and hazard symbols.
    Shipping Methyl 5-Chloro-2-Methoxybenzoate is typically shipped in tightly sealed containers, protected from light and moisture. It should be handled and transported according to standard regulations for chemicals. Ensure packaging is secure to prevent leaks, and include proper labeling and documentation in compliance with local, national, and international shipping guidelines.
    Storage **Methyl 5-chloro-2-methoxybenzoate** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. The storage area should be protected from moisture and direct sunlight. Proper labeling and safety precautions, including use of gloves and goggles when handling, are recommended.
    Application of Methyl 5-Chloro-2-Methoxybenzoate

    Applications of Methyl 5-Chloro-2-Methoxybenzoate in Industrial Manufacturing

    Methyl 5-Chloro-2-Methoxybenzoate is a highly specialized intermediate widely used by downstream manufacturers for the synthesis of advanced pharmaceutical actives, pesticide compounds, functional dyestuffs, and agrochemical ingredients. Below, we delineate the primary application domains where this compound offers focused value through stringent compliance, precise formulation integration, and targeted end product development.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug Synthesis

    This compound frequently serves as a building block for the preparation of certain non-steroidal anti-inflammatory drugs (NSAIDs), especially in the research and commercial production of chlorinated aromatic APIs. Manufacturers incorporate it during the initial steps of targeted ester or acid construction to assure molecular precision, batch purity, and regulatory traceability.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph requirements for starting materials
    • Ph. Eur. 5.10 on Impurities
    • 21 CFR Part 210/211 for finished dosage processing traceability

    Typical usage ratio

    • 10–25% w/w relative to total input for targeted pathway reactions, adjusted according to API synthetic yield.

    Downstream process integration

    • Loaded during the initial esterification or substitution stages—most commonly as the main chloro-aromatic source in multi-step batch reactors, preceding hydrolysis, amidation, or further chlorination.

    Final product types

    • API intermediates for NSAIDs (e.g., mefenamic acid derivatives, chlorinated benzoic acid-based pharmaceuticals)
    • Active molecule scaffolds for clinical trials

    2. Agrochemical Intermediate in Herbicide Synthesis

    Downstream agrochemical producers utilize this compound as a key aromatic ester precursor in the creation of selective post-emergence herbicides. Its structural attributes facilitate targeted etherification and chlorination reactions central to producing high-purity, high-potency active ingredients in crop protection formulations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Food and Agriculture Organization specifications for technical grade agrochemicals
    • Regulation (EC) No 1907/2006 (REACH) for EU market entry
    • GB 2763-2023 (China MRL standards for pesticides)

    Typical usage ratio

    • 8–15% w/w relative to total herbicidal intermediate mass; final content depends on active load required in the synthesis route.

    Downstream process integration

    • Charged at the coupling or condensation stage; reacts with open-chain alkyl halides or amines to form chlorinated heterocycles, followed by downstream hydrolysis and salt formation.

    Final product types

    • Technical grade herbicide intermediates
    • Commercial post-emergence herbicide actives (e.g., chloro-aryl-based selective herbicides)

    3. Dye Intermediate for Chlorinated Benzene-based Pigment Manufacture

    In the colorants industry, manufacturers integrate this material as a controlled-source aromatic ester, primarily for the development of specific chlorinated azo dyes and pigments offering enhanced light fastness and unique color profiles for plastics and inks. Its precise substitution pattern is essential for maintaining hue consistency and minimizing byproduct formation in successive diazotization steps.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile colorants
    • EN 71-3 Toy Safety standards for coloring materials
    • ISO 9001:2015 for process and batch quality tracking
    • REACH SVHC restrictions for aromatic amines

    Typical usage ratio

    • 4–10% w/w in pigment synthesis batches, modified on the basis of targeted shade intensity and required tinctorial strength.

    Downstream process integration

    • Introduced during the initial ester condensation or nucleophilic aromatic substitution step prior to azo coupling, ensuring strict molar ratios for uniform chromophore development.

    Final product types

    • Chlorinated azo dye intermediates
    • High-performance organic pigments for plastics, coatings, and specialty inks

    4. Precursor in Synthesis of Veterinary Pharmaceutical Compounds

    This compound supports veterinary drug manufacturers aiming to produce advanced benzoate-based active intermediates, especially where halogen-and-methoxy-substitution confers targeted metabolic clearance and pharmacokinetic profiles for livestock medications. Producers leverage its purity profile and reactivity to control subsequent amidation or hydrolysis output.

    Industry compliance standards

    • VICH GL24: Good Manufacturing Practice for Active Pharmaceutical Ingredients for Veterinary Medicinal Products
    • USP Veterinary Medicine General Chapters
    • Chinese Pharmacopoeia (2020) requirements for starting materials
    • EudraLex Volume 4 GMP for veterinary active substances

    Typical usage ratio

    • 12–18% w/w, tailored based on the target intermediate’s theoretical yield and required assay per validated veterinary drug synthesis process.

    Downstream process integration

    • Employed at the N-alkylation or amidation step as a base structure for further benzoic acid derivative extension in batch or continuous flow reactors.

    Final product types

    • Veterinary pharmaceutical intermediates for livestock medication synthesis
    • Halogenated benzoate-based active compounds for animal health applications

    5. Intermediate for Fine Chemical Synthesis in UV-Absorber Additives

    Advanced additive manufacturers incorporate this material as a controlled-reactivity precursor in the creation of substituted benzotriazole or benzophenone UV-absorbers for high-transparency applications. Its defined chemical structure allows predictable transesterification or cyclization, crucial for achieving stringent performance and migration resistance in UV stabilizer production.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics and plastics
    • FDA 21 CFR 175.300 for indirect food additives (coating applications)
    • EN 14582: Determination of halogens in materials for UV-absorber safety
    • ISO 9001:2015 for production process management

    Typical usage ratio

    • 6–12% w/w as an intermediate step in transesterification or cyclization processes, balanced according to required UV-absorber assay and end-use formulation strength.

    Downstream process integration

    • Added at the cyclization or ester-interchange stage; undergoes high-purity condensation or nucleophilic addition with triazole/phenol building blocks to finalize the UV-absorber core.

    Final product types

    • Benzotriazole-based UV-absorber additives
    • High-performance benzophenone photostabilizers for polymers, films, and coatings
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