N-(2-Aminoethyl)carbamic acid, also known as carbamic acid, 2-aminoethyl derivative, is an organic compound characterized by its amine and carbamate functional groups. It appears as a white crystalline solid or a colorless liquid, depending on its form and purity. This compound is soluble in water due to its polar nature, which is attributed to the presence of both amino and carbamate groups. It has a relatively low molecular weight and exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including those involving nucleophilic substitution. N-(2-Aminoethyl)carbamic acid is of interest in biochemical applications, particularly in the study of enzyme mechanisms and as a potential intermediate in the synthesis of pharmaceuticals. Its stability can be influenced by pH and temperature, making it important to handle under controlled conditions to prevent degradation. Safety precautions should be observed, as it may pose health risks upon exposure. Overall, this compound serves as a valuable building block in organic synthesis and medicinal chemistry.

N-(2-Aminoethyl)carbamic acid

109-58-0: N-(2-Aminoethyl)carbamic acid, also known as carbamic acid, 2-aminoethyl derivative, is an organic compound characterized by its amine and carbamate functional groups. It appears as a white crystalline solid or a colorless liquid, depending on its form and purity. This compound is soluble in water due to its polar nature, which is attributed to the presence of both amino and carbamate groups. It has a relatively low molecular weight and exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including those involving nucleophilic substitution. N-(2-Aminoethyl)carbamic acid is of interest in biochemical applications, particularly in the study of enzyme mechanisms and as a potential intermediate in the synthesis of pharmaceuticals. Its stability can be influenced by pH and temperature, making it important to handle under controlled conditions to prevent degradation. Safety precautions should be observed, as it may pose health risks upon exposure. Overall, this compound serves as a valuable building block in organic synthesis and medicinal chemistry.

CAS 109-58-0

N-(2-Aminoethyl)carbamic acid

Azacitidine Impurity 41

Ref: 4Z-A-8150

Azacitidine Impurity 41

Ref: ST-EA-CP-A35043