4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID, identified by its CAS number 393-06-6, stands as a pivotal chemical compound in various synthesis pathways. This versatile chemical intermediate is highly valued for its unique structural characteristics, particularly the trifluoromethyl group, which imparts specific chemical and physical properties essential for advanced applications. Its importance spans across several high-tech industries, making it a subject of continuous interest for researchers and developers worldwide. As a key building block, 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID plays a critical role in the creation of complex molecules, offering distinct advantages in terms of reactivity and stability.

The chemical formula for 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID is C8H6F3NO2, with a molecular weight of approximately 205.13 g/mol. It typically presents as an off-white crystalline powder, though variations from white to orange or green powder to crystal form have been noted. This compound exhibits a melting point in the range of 183-186℃, with some reports indicating 185-187°C, showcasing its thermal stability. Its predicted boiling point is around 318.8±42.0 °C, and a predicted density of 1.489±0.06 g/cm3 further defines its physical characteristics. For optimal preservation, 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID should be stored in a dark place under an inert atmosphere at room temperature, ensuring its purity, which is typically supplied at 97% or higher, reaching up to 99% for high-grade applications. It is known to be soluble in Methanol, facilitating its use in various chemical reactions.

Primarily, 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID finds significant application as a pharmaceutical intermediate. Its distinctive trifluoromethyl and amino benzoic acid functionalities make it an indispensable precursor for synthesizing a wide array of active pharmaceutical ingredients (APIs) and other complex organic compounds. Beyond pharmaceuticals, it serves as a valuable reagent in advanced organic synthesis, contributing to the development of novel chemicals with enhanced properties. Researchers in academic and industrial laboratories utilize this compound for various chemical reactions, including those in the fields of agrochemicals, specialty chemicals, and material science, where its unique structure can introduce desired characteristics into final products. It is important to note that this product is typically supplied for research and industrial use only, not intended for diagnostic or therapeutic use in humans or animals.

Handling 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID requires adherence to strict safety protocols due to its hazardous properties. It is classified under GHS hazard statements as toxic if swallowed (H301), and it causes skin irritation (H315), serious eye irritation (H319), and may cause respiratory irritation (H335). Precautionary measures include avoiding breathing dust/fume/gas/mist/vapors/spray (P261), washing thoroughly after handling (P264b), and wearing protective gloves/eye protection/face protection (P280). In case of exposure, immediate medical attention is advised. Proper storage in a well-ventilated area and maintaining an inert atmosphere are crucial to ensure safe handling and preserve the integrity of the compound. Comprehensive Safety Data Sheets (SDS) should always be consulted prior to use to ensure all necessary safety precautions are taken.

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In conclusion, 4-AMINO-2-TRIFLUOROMETHYLBENZOIC ACID (CAS: 393-06-6) remains a vital chemical intermediate, indispensable for innovation across various scientific and industrial sectors. Its precise chemical properties and broad applicability underscore its value in modern chemistry. For those seeking a reputable source, our commitment to providing superior chemical products ensures that your projects can proceed with confidence, supported by high-quality materials delivered efficiently.