2-((4-Aminobenzoyl)amino)ethanesulfonic acid, commonly referred to as a sulfonic acid derivative, is characterized by its unique functional groups, including an amino group and a sulfonic acid group. This compound typically exhibits good solubility in water due to the presence of the sulfonic acid moiety, which enhances its ionic character. The presence of the amino group allows for potential interactions with biological systems, making it of interest in biochemical applications. It is often utilized as a buffering agent in various biochemical assays and can play a role in stabilizing pH levels in solutions. The molecular structure suggests that it may participate in hydrogen bonding, contributing to its solubility and reactivity. Additionally, the compound's ability to form complexes with metal ions or other biomolecules can be leveraged in research and industrial applications. Overall, its properties make it a valuable compound in both laboratory and industrial settings, particularly in the fields of biochemistry and analytical chemistry.

2-((4-aminobenzoyl)amino)ethanesulfonic acid

860707-78-4: 2-((4-Aminobenzoyl)amino)ethanesulfonic acid, commonly referred to as a sulfonic acid derivative, is characterized by its unique functional groups, including an amino group and a sulfonic acid group. This compound typically exhibits good solubility in water due to the presence of the sulfonic acid moiety, which enhances its ionic character. The presence of the amino group allows for potential interactions with biological systems, making it of interest in biochemical applications. It is often utilized as a buffering agent in various biochemical assays and can play a role in stabilizing pH levels in solutions. The molecular structure suggests that it may participate in hydrogen bonding, contributing to its solubility and reactivity. Additionally, the compound's ability to form complexes with metal ions or other biomolecules can be leveraged in research and industrial applications. Overall, its properties make it a valuable compound in both laboratory and industrial settings, particularly in the fields of biochemistry and analytical chemistry.

CAS 860707-78-4

2-((4-aminobenzoyl)amino)ethanesulfonic acid

2-(4-Aminobenzamido)ethanesulfonic acid

Ref: IN-DA01DOQ6