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HS Code |
106651 |
| Productname | 3-Methoxy-2,4,5-Trifluorobenzoic Acid |
| Casnumber | 886762-98-7 |
| Molecularformula | C8H5F3O3 |
| Molecularweight | 206.12 |
| Appearance | White to off-white solid |
| Meltingpoint | 107-112°C |
| Solubility | Soluble in organic solvents like DMSO, methanol |
| Purity | Typically ≥97% |
| Smiles | COC1=C(C=C(C(=C1F)C(=O)O)F)F |
| Inchi | InChI=1S/C8H5F3O3/c1-14-5-2-4(10)7(8(12)13)6(11)3-5/h2-3H,1H3,(H,12,13) |
| Synonyms | 3-Methoxy-2,4,5-trifluorobenzoic acid |
As an accredited 3-Methoxy-2,4,5-Trifluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3-Methoxy-2,4,5-Trifluorobenzoic Acid, securely sealed, labeled with hazard and identification information. |
| Shipping | **Shipping Description:** 3-Methoxy-2,4,5-Trifluorobenzoic Acid is shipped in tightly sealed, chemically compatible containers to prevent moisture and contamination. The package is clearly labeled with product and hazard information, and is transported according to local, national, and international regulations for chemicals, including all safety and environmental guidelines. |
| Storage | 3-Methoxy-2,4,5-trifluorobenzoic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably in a designated corrosive or chemical storage cabinet. Ensure it is properly labeled, and segregate it from incompatible substances such as strong oxidizers and bases. |
Applications of 3-Methoxy-2,4,5-Trifluorobenzoic Acid in Industrial Manufacturing3-Methoxy-2,4,5-Trifluorobenzoic Acid functions as a specialized aromatic intermediate in multiple advanced chemical manufacturing sectors. As the original producer, we supply this compound to qualified manufacturers spanning pharmaceutical, agrochemical, electronics, and specialty polymer markets, consistently supporting precise formulation, process reliability, and regulatory compliance throughout demanding downstream processes. 1. Pharmaceutical Active Ingredient SynthesisOur material finds targeted use as a key building block in active pharmaceutical ingredient (API) synthesis for innovative oral and injectable drugs. It introduces multiple electron-withdrawing fluorine substituents into molecular scaffolds, enabling improved bioavailability, stability, and metabolic profile of drug candidates. In these reactions, this benzoic acid derivative undergoes acylation, amidation, and halogen-lithiation to yield intermediates for anti-inflammatory, antiviral, and CNS acting molecules, in accordance with the latest GMP and pharmacopeial requirements for process impurities and residual solvents. Industry compliance standards
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2. Agrochemical Herbicide and Fungicide Intermediate ProductionLeading agrochemical synthesis utilizes this material to introduce highly stable fluorine-bearing motifs into new-generation herbicide and fungicide actives. Its distinct substitution pattern supports synthesis of carboxamide and oxadiazole-type intermediates with strong crop selectivity and weather resistance. Formulators select and dose this acid according to downstream cyclization and acylation reaction efficiencies, considering EU REACH and global pesticide MRL residue expectations. Industry compliance standards
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3. Liquid Crystal Display (LCD) Intermediate ManufactureSpecialty electronics manufacturers employ this molecule for synthesis of key mesogenic intermediates in high-performance liquid crystal materials. The tri-fluorinated system imparts high dielectric anisotropy and chemical durability to commercial display films. Integration into these proprietary routes adheres to specific electronics-sector protocols on ultra-trace metal and halide impurity control, with batchwise addition based on precise phase transition requirements for the targeted nematic mixtures. Industry compliance standards
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4. Fluorinated Polymer ManufacturingThe specialty polymer sector incorporates this acid as a functional monomer precursor for engineering polymers requiring precise control of chemical resistance and mechanical properties. Through direct copolymerization or pre-condensation with diols and diamines, processors achieve highly-defined molecular weights and controlled distribution of fluorinated units. Manufacturers comply with exhaustive regulatory and customer-specific analytical protocols for extractables and leachables, with dosing set to meet proprietary film or resin performance targets. Industry compliance standards
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