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HS Code |
201788 |
| Compound Name | 4-(4-Fluorobenzoyl)butyric acid |
| Chemical Formula | C11H11FO3 |
| Molecular Weight | 210.20 g/mol |
| Cas Number | 83432-60-8 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Melting Point | 78-82°C |
| Boiling Point | No data available |
| Solubility | Soluble in DMSO, methanol, and ethanol |
| Storage Conditions | Store at room temperature, away from light and moisture |
| Inchi Key | XQRFHESHNLHPNP-UHFFFAOYSA-N |
| Smiles | C1=CC(=CC=C1C(=O)CCCC(=O)O)F |
As an accredited 4-(4-Fluorobenzoyl)Butyric Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 25g amber glass bottle with a secure screw cap, labeled clearly with chemical name and hazard warnings. |
| Shipping | **Shipping Description:** 4-(4-Fluorobenzoyl)butyric acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. Packages include clear hazard labeling and are handled in accordance with relevant chemical safety regulations. Transport is conducted via ground or air, with appropriate documentation, to ensure safe and compliant delivery. |
| Storage | 4-(4-Fluorobenzoyl)butyric acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid sources of ignition and incompatible materials such as strong oxidizers. Label the container clearly and ensure access is restricted to trained personnel. Use appropriate personal protective equipment when handling. |
Applications of 4-(4-Fluorobenzoyl)Butyric Acid in Industrial ManufacturingAs a direct manufacturer with extensive experience in advanced aromatic acid intermediates, we provide 4-(4-Fluorobenzoyl)butyric acid for several downstream sectors. This material supports regulated syntheses across pharmaceuticals, agrochemicals, specialty polymers, and fine chemical intermediates, where precision and regulatory alignment guide every production stage. 1. Pharmaceutical API SynthesisPharmaceutical manufacturers use this raw material as a benzoyl moiety donor in the synthesis of specific active pharmaceutical ingredients, particularly in the development of anti-inflammatory and central nervous system (CNS) agents. Its fluorinated aromatic structure grants metabolic stability and improved pharmacokinetics. Process engineers directly introduce this intermediate into the acylation or condensation stages to construct advanced building blocks. Quality assurance teams employ stringent batch traceability to satisfy GMP and registration needs throughout the chain. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisAgrochemical producers utilize this building block for synthesizing selective herbicide and plant growth regulator candidates, leveraging the fluoroaromatic functionality for increased bioactivity and environmental stability. Formulators precisely dose and activate this intermediate during active ingredient construction, commonly incorporating halogen management protocols and yield optimization steps. Continuous analytics ensure batch compliance and trace impurity elimination. Industry compliance standards
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3. Specialty Polymer ModificationPolymer manufacturers incorporate this specialty acid during functional monomer synthesis to build fluorinated polymer chains with controlled hydrophobicity, chemical resistance, and mechanical properties. Material scientists add this intermediate to improve adhesion and solvent resistance of engineered plastics used in demanding industrial environments. All input batches undergo chemical identity testing and end-use performance simulation to verify property distribution across the polymer matrix. Industry compliance standards
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4. Fine Chemical Intermediate for Advanced SynthesisFine chemical producers implement this benzoyl acid in multi-stage syntheses, especially where a para-fluorophenyl group is necessary for downstream reactivity or to impart electronic effects in final molecules. Chemists typically handle precise reaction monitoring and purification to enable reliable scale-up. All lots receive full traceability, and analytical teams document impurity profiles to support specialty chemical applications or additional contract manufacturing. Industry compliance standards
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