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Methyl 2-Fluorobenzoate

    • Product Name Methyl 2-Fluorobenzoate
    • Alias methyl-2-fluorobenzoate
    • Einecs 238-586-9
    • 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

    123355

    Productname Methyl 2-Fluorobenzoate
    Casnumber 446-35-5
    Molecularformula C8H7FO2
    Molecularweight 154.14
    Appearance Colorless to pale yellow liquid
    Boilingpoint 206-208°C
    Meltingpoint -1°C
    Density 1.187 g/mL at 25°C
    Purity Typically >98%
    Refractiveindex 1.514
    Canonicalsmiles COC(=O)C1=CC=CC=C1F
    Synonyms 2-Fluorobenzoic acid methyl ester

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

    Packing & Storage
    Packing Methyl 2-Fluorobenzoate, 100g, is packaged in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling.
    Shipping Methyl 2-Fluorobenzoate is shipped in tightly sealed containers to prevent leakage and exposure. It is transported as a hazardous chemical, following relevant regulations. The packaging protects against breakage, moisture, and contamination. Proper labeling and documentation, including hazard identification, are included to ensure safe handling during transit and upon delivery.
    Storage Methyl 2-Fluorobenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure that the storage area is equipped with appropriate fire suppression systems and that containers are properly labeled to prevent any accidental misuse or exposure.
    Application of Methyl 2-Fluorobenzoate

    Applications of Methyl 2-Fluorobenzoate in Industrial Manufacturing

    Methyl 2-Fluorobenzoate serves as a crucial intermediate across multiple industrial chemical manufacturing sectors. The following application overview outlines real-world usage scenarios, process roles, compliance frameworks, and integration details observed in global production settings.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    In pharmaceutical manufacturing, Methyl 2-Fluorobenzoate acts as a precursor for fluorinated aromatic compounds, especially within the synthesis of anti-inflammatory, anti-tumor, and central nervous system drug molecules. It enters complex reaction sequences such as nucleophilic aromatic substitution, amidation, or hydrolysis, serving as the fluorinated benzoic acid source for higher-value active pharmaceutical ingredient (API) assembly. Process engineers control feed rates and reactions using validated batch records to ensure batch-wise traceability and meet regulatory inspection requirements. Functionally, its use lowers synthetic steps where specific fluorination patterns are essential for regulatory-submitted formulations. Teams maintain strict segregation and cleaning protocols to minimize cross-contamination in GMP facilities.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP; 21 CFR 210/211, FDA)
    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • EDQM CEP/Ph. Eur. raw material requirements
    • Chinese Pharmacopoeia (ChP) reference for controlled substances

    Typical usage ratio

    • Commonly used at 0.5–2.5 molar equivalents relative to main coupling substrates. Chemists adjust based on process yield optimization and impurity control, verified through in-process HPLC assays.

    Downstream process integration

    • Charge into glass-lined or stainless reactors as a primary aromatic precursor during stage 1–2 of multistep API synthesis, typically after intermediate purification and prior to amide coupling or ring closure reactions.

    Final product types

    • Non-steroidal anti-inflammatory APIs (e.g., fluorinated analogues)
    • Pyridine-based CNS medicines
    • Oncology therapy intermediates
    • Specialty fluoroaromatic pharmaceuticals under patented and generic portfolios

    2. Agrochemical and Herbicide Compound Synthesis

    Agricultural chemistry manufacturers use Methyl 2-Fluorobenzoate as a fundamental building block for select herbicide and crop protection agents containing fluorinated benzene moieties. The ester structure is conducive to further transformations, such as chlorination, coupling, and oxidation, producing versatile scaffolds for active substances. Formulation R&D chooses this molecule for streamlined access to high-purity fluorinated acids via ester hydrolysis, which is critical to achieve consistent biological activity and field stability for regulated agrochemicals. Quality assurance teams perform residue and impurity profiling to align with destination market pesticide approval guidelines.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • OECD Test Guidelines for Chemicals: Physicochemical/Residue Standards
    • EPA Pesticide Registration Technical Data Requirements (40 CFR 158)
    • EU Regulation (EC) No 1107/2009 on the placing of plant protection products on the market

    Typical usage ratio

    • Applied in 1.0–1.6 molar equivalents per batch for core coupling or hydrolysis steps. Can be increased to 2.0 equivalents in process routes aiming for ester-to-acid conversion with minimal by-product.

    Downstream process integration

    • Direct charge to reaction vessel post solvent charging, proceeding to alkaline hydrolysis or acyl chloride formation for further condensation steps in active ingredient assembly.

    Final product types

    • Selective herbicides (fluorinated aromatic actives)
    • Pre-emergence weed control agents
    • Systemic fungicide intermediates
    • Crop protection compound intermediates for regulatory submission

    3. Fine Chemical Building Block for Liquid Crystal Monomer Synthesis

    The electronic materials industry integrates Methyl 2-Fluorobenzoate as a strategic intermediate for the development of liquid crystal materials deployed in display panels and advanced optical devices. It provides essential fluorinated aromatic units, improving the molecule’s dielectric anisotropy and photo-stability crucial for high-performance LCD and OLED applications. Process chemists perform transesterification, halogen exchange, or Grignard reactions to tailor-make monomers with tightly controlled purity and functionalization required by end-user customers. Production batches adhere to strict analytical protocols to certify absence of metal and halogen contamination at ppb levels, directly impacting display quality and lifespan.

    Industry compliance standards

    • JIS C6267 (Japanese Industrial Standards for liquid crystal materials)
    • IEC 61249-2-51 (Halogen Free Material Standard for Electronic Industries)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances Directive)
    • ISO 9001:2015 Certified Quality Management Systems

    Typical usage ratio

    • 0.75–1.3 molar equivalents, dependent on the number of functionalization cycles required for the target mesogenic monomer, as determined by customer formulation specs.

    Downstream process integration

    • Integrated during early-stage monomer functionalization and continues through fluorination or ester exchange stages, prior to purification and final blending for liquid crystal formulation.

    Final product types

    • Liquid crystal monomers for TFT LCD panels
    • Intermediate oligomers for OLED displays
    • Photoalignment material precursors
    • Polymerizable specialty mesogens for advanced photonic applications

    4. Specialty Polymer and Performance Chemical Intermediate

    Producers of high-value specialty polymers select Methyl 2-Fluorobenzoate for introducing fluorinated aromatic side groups during polyester or polyamide synthesis. Its use enhances polymer weatherability, solvent resistance, and dielectric properties, meeting the requirements in sectors such as automotive coatings, wire insulation, and membrane materials. Technicians implement controlled polymerization or copolymerization, ensuring precise incorporation at targeted repeat units. Downstream quality labs verify fluorine integration using NMR and FTIR analysis. Waste reduction protocols and process ventilation address occupational and environmental safety mandated by regional industrial safety agencies.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • UL 94 (Flammability Standard for Plastics)
    • ASTM D638, D882 (Mechanical properties for plastics/films)
    • ISO 14001:2015 Environmental Management Systems

    Typical usage ratio

    • 5–12% by monomer weight for copolymerization, adjusted based on mechanical and thermal property targets established during pilot batch validation.

    Downstream process integration

    • Incorporated directly into prepolymer reaction mixtures prior to catalyst activation. May also serve as a capping agent for molecular weight control in continuous reaction setups.

    Final product types

    • High-performance fluorinated polyesters for optical fiber coatings
    • Modified polyamides for automotive electrical connectors
    • Dielectric layer materials for flexible electronic substrates
    • Weather-resistant architectural coatings

    5. Aroma Intermediate for Fine Fragrance and Flavor Chemical Synthesis

    The aroma chemicals sector employs Methyl 2-Fluorobenzoate in the synthesis of fine fragrance and flavor molecules, utilizing its stability and distinctive aromatic note. It experiences further esterification, reduction, or condensation to deliver nuanced fragrance accords favored by the perfumery and flavor formulations industries. Precision in sourcing and analytical QC is critical due to IFRA guidelines on purity and residual solvents. Blenders test the material in organoleptic panels to verify desired olfactory attributes before release into compounding centers. Process engineers monitor waste solvent recovery to align with sustainability targets as required by end-customer brands.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Regulation (EC) No 1334/2008 (Flavorings and certain food ingredients regulation)
    • FEMA GRAS (Generally Recognized as Safe) as set by US Flavor and Extract Manufacturers Association
    • ISO 9235 (Essential oils and aromatic raw materials)

    Typical usage ratio

    • Used at 0.3–1.0% in aroma chemical batches, with precise dosing based on target scent intensity and matrix compatibility of end products.

    Downstream process integration

    • Added during blending or pre-reaction stages in batch reactors, followed by post-modification or further ester preparation for targeted sensorial effects.

    Final product types

    • Fine fragrance base notes
    • Flavoring esters for beverages and confections
    • Specialty aroma compounds for oral care goods
    • Functional fragrance additives for home and fabric care
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