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HS Code |
653323 |
| Product Name | 4'-Chloro-2'-Fluoroacetanilide |
| Molecular Formula | C8H7ClFNO |
| Cas Number | 86404-64-8 |
| Appearance | White to off-white solid |
| Melting Point | 108-112°C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC(=O)NC1=CC(=C(C=C1)Cl)F |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | N-(4-chloro-2-fluorophenyl)acetamide |
| Hazard Statements | Irritant to skin, eyes, and respiratory system |
As an accredited 4'-Chloro-2'-Fluoroacetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A sealed amber glass bottle containing 100 grams of 4'-Chloro-2'-Fluoroacetanilide, labeled with chemical details and safety information. |
| Shipping | The shipping of 4'-Chloro-2'-Fluoroacetanilide complies with standard chemical transport regulations. The substance is securely packaged in sealed containers, clearly labeled, and protected from moisture, heat, and direct sunlight. Appropriate documentation and safety data sheets accompany the shipment to ensure safe handling and regulatory compliance during transit. |
| Storage | 4'-Chloro-2'-Fluoroacetanilide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and avoid exposure to moisture. Use secondary containment and restrict access to trained personnel only. |
Applications of 4'-Chloro-2'-Fluoroacetanilide in Industrial ManufacturingAs an industrial chemical producer with years of experience in aromatic intermediates, we supply 4'-Chloro-2'-Fluoroacetanilide to specialized sectors strictly based on verified downstream applications. Its selectivity, halogen substitution, and chemical stability allow integration into several advanced synthesis routes. Below are the principal industrial manufacturing scenarios where this compound demonstrates clear performance and regulatory fit. 1. Synthesis of Agrochemical Active IngredientsKey agrochemical formulators incorporate 4'-Chloro-2'-Fluoroacetanilide as an intermediate in the production of specific phenoxyalkanoic acid herbicides and substituted aniline-based crop protection agents. Its precise halogen pattern enables controlled aromatic substitution, supporting the synthesis of molecules for high-selectivity weed management. Production plants employ this compound during the pre-coupling or amidation stages to yield actives with integrity and compliance for agricultural standards. Industry compliance standards
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2. Pharmaceutical Intermediate for Antipyretic and Analgesic AgentsIn API manufacturing, pharmaceutical companies utilize 4'-Chloro-2'-Fluoroacetanilide as a key stage intermediate in the preparation of next-generation N-acylarylamine analgesics. Its structure enables targeted substitution to build up paracetamol-like molecules with improved halogen-modified pharmacological profiles. Manufacturers value its reproducible reactivity and high purity output critical for successive acetylation and dehalogenation steps under GMP-controlled environments. Industry compliance standards
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3. Dye Intermediate for Specialty PigmentsThe specialty dye sector employs 4'-Chloro-2'-Fluoroacetanilide as a diazo or coupling partner during the synthesis of functionalized monoazo and anthraquinone pigments. Its dual halogenation supports specific chromophore tuning and fastness performance demanded in automotive coatings, industrial plastics coloration, and high-performance printing inks. Downstream pigment manufacturers optimize its use for batch-to-batch chromatic control and improved dispersibility profiles. Industry compliance standards
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4. Intermediate for Fluorinated Fine ChemicalsChemical manufacturers leverage 4'-Chloro-2'-Fluoroacetanilide as a precursor for synthesizing fluorine-containing aromatic building blocks. Owing to the robust halogen placement, it aids in the stepwise generation of advanced intermediates tailored for electronic, polymer, and material science applications. Process teams implement it for nucleophilic aromatic substitution and controlled hydrolysis, facilitating the construction of custom molecules for modern functional materials sectors. Industry compliance standards
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