Tripitramine
Chemical compound
| Tripitramine | |
|---|---|
| INN | |
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| CAS Number | 91-66-7 |
| PubChem | 7045 |
| DrugBank | |
| ChemSpider | 6780 |
| KEGG | |
Tripitramine is a chemical compound that belongs to the class of aromatic amines. It is primarily used in research settings and has applications in various chemical processes. The compound is known for its role as a precursor in the synthesis of other chemical substances.
Chemical Structure and Properties
Tripitramine is characterized by its IUPAC name, N,N,N′,N′-Tetramethyl-1,4-benzenediamine. The molecular formula is C10H16N2, and it has a molar mass of 164.25 g/mol. The structure consists of a benzene ring substituted with two dimethylamino groups at the para positions.
The compound is a solid at room temperature and is typically synthesized through the methylation of p-phenylenediamine. It is soluble in organic solvents and exhibits typical properties of aromatic amines, such as basicity and the ability to form hydrogen bonds.
Applications
Tripitramine is used in various synthetic applications. It serves as an intermediate in the production of dyes, polymers, and other complex organic compounds. Its ability to donate electrons makes it useful in redox reactions and as a stabilizer in certain chemical processes.
In research, tripitramine is often employed in studies involving electron transfer and catalysis. Its properties make it a valuable tool in understanding the mechanisms of these reactions.
Safety and Handling
As with many chemical compounds, proper safety precautions should be taken when handling tripitramine. It should be stored in a cool, dry place, away from sources of ignition. Personal protective equipment such as gloves and goggles should be worn to prevent skin and eye contact.
Tripitramine can be hazardous if ingested or inhaled, and it may cause irritation to the skin and respiratory tract. In case of exposure, it is important to seek medical attention and follow appropriate first aid measures.
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Contributors: Prab R. Tumpati, MD