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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 | 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. |
Applications of Methyl 2-Fluorobenzoate in Industrial ManufacturingMethyl 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 SynthesisIn 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
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2. Agrochemical and Herbicide Compound SynthesisAgricultural 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
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3. Fine Chemical Building Block for Liquid Crystal Monomer SynthesisThe 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
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4. Specialty Polymer and Performance Chemical IntermediateProducers 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
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5. Aroma Intermediate for Fine Fragrance and Flavor Chemical SynthesisThe 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
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