Diethylaminopyridine (DEAP) is an organic compound characterized by its pyridine ring substituted with diethylamino groups. It is typically a colorless to pale yellow liquid with a distinctive amine-like odor. DEAP is known for its role as a nucleophilic catalyst in various organic reactions, particularly in acylation and amidation processes, enhancing reaction rates and selectivity. The compound is soluble in organic solvents such as dichloromethane and ethanol, but it is less soluble in water due to its hydrophobic nature. With a molecular formula of C12H16N2 and a molecular weight of approximately 188.27 g/mol, DEAP exhibits basic properties, making it a useful reagent in synthetic organic chemistry. It is important to handle this substance with care, as it can be irritating to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment, are recommended when working with this chemical.

Diethylaminopyridine; 97%

36075-06-6: 2-Diethylaminopyridine, N,N-diethylpyridin-2-amine

2-DIETHYLAMINOPYRIDINE

N,N-Diethylpyridin-2-amine

2-Diethylaminopyridine

2-Diethylaminopyridine is a chloride that has anticancer activity. It is a functional group of aromatic hydrocarbons, which are organic compounds containing carbon and hydrogen in the form of an aromatic ring. 2-Diethylaminopyridine is used as a precursor for the synthesis of n-oxide and as a pharmaceutical preparation. This molecule is also used as an optical property to detect copper complex. The methoxy groups on the 2-diethylaminopyridine molecule make it soluble in organic solvents such as chloroform or dichloromethane.

CAS 36075-06-6: Diethylaminopyridine; 97%

2-DIETHYLAMINOPYRIDINE

Ref: 10-F538665

N,N-Diethylpyridin-2-amine

Ref: IN-DA003H5G

2-Diethylaminopyridine

Ref: 54-OR922656

2-Diethylaminopyridine

Ref: 3B-D1681

2-Diethylaminopyridine

Ref: 3D-LBA07506