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2,2,2-TRIFLUOROETHYLAMINE CAS:753-90-2

2,2,2-Trifluoroethylamine (TFEA) is a notable chemical compound recognized for its unique molecular structure and diverse applications across various industries. With the chemical formula CF3CH2NH2, TFEA consists of a trifluoromethyl group (-CF3) attached to an amino group (-NH2). This compound is synthesized through the reaction of trifluoroacetaldehyde with ammonia or via reductive amination of trifluoroacetonitrile, resulting in a volatile, colorless liquid with a distinctive ammonia-like odor. TFEA is valued for its role as a building block in organic synthesis, pharmaceutical chemistry, and as a precursor in the production of specialized chemicals and materials requiring enhanced stability and functionality.


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Application and Effect:

2,2,2-Trifluoroethylamine (TFEA) is characterized by its molecular structure, featuring a trifluoromethyl group (-CF3) linked to an amino group (-NH2). This combination results in a volatile, colorless liquid with a boiling point around 56°C and a pungent odor resembling ammonia. TFEA exhibits moderate solubility in water and good solubility in polar organic solvents, contributing to its versatility in various chemical processes. Its chemical stability under mild conditions makes it suitable for applications requiring inertness and compatibility with sensitive chemical environments. Uses Organic Synthesis: TFEA serves as a versatile building block in organic synthesis, particularly in the pharmaceutical industry for introducing trifluoromethyl groups into drug molecules. This modification often enhances biological activity, metabolic stability, and membrane permeability of pharmaceutical compounds, making TFEA crucial in drug discovery and development. Catalysis: TFEA and its derivatives act as catalysts in numerous chemical transformations, including asymmetric synthesis and amidation reactions. As a catalyst precursor, TFEA enhances reaction efficiency and selectivity, supporting its application in fine chemical manufacturing and academic research. Specialty Chemicals: TFEA is utilized in the production of specialty chemicals such as surfactants, agrochemicals, and materials requiring enhanced chemical stability and hydrophobic characteristics. Its ability to impart unique properties to end products makes it valuable in formulations where performance enhancement is critical. Synthesis TFEA can be synthesized through several methods, including the reaction of trifluoroacetaldehyde with ammonia or the reductive amination of trifluoroacetonitrile. The former method involves condensing trifluoroacetaldehyde with ammonia under controlled conditions to yield TFEA. Alternatively, reductive amination of trifluoroacetonitrile with hydrogen and ammonia provides another pathway to synthesize TFEA. Purification techniques such as distillation or solvent extraction are employed to obtain TFEA in high purity suitable for industrial applications. In summary, 2,2,2-trifluoroethylamine is a versatile compound essential in organic synthesis, catalysis, and the production of specialty chemicals. Its unique chemical properties, including volatility, stability, and solubility characteristics, contribute to its widespread use across various industrial sectors, supporting advancements in pharmaceuticals, fine chemicals, and materials science.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C2H4F3N
Assay 99%
Appearance white powder
CAS No.  753-90-2
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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