5-Bromo-3-indoxyl nonanoate is a chemical compound characterized by its structure, which includes a bromine atom and an indoxyl moiety linked to a nonanoate chain. This compound is typically used in biochemical applications, particularly as a substrate in enzyme assays, due to its ability to produce a colored product upon enzymatic cleavage. The presence of the bromine atom enhances its reactivity and specificity in various chemical reactions. The nonanoate portion contributes to its lipophilicity, allowing it to interact effectively with biological membranes. In terms of solubility, it is generally soluble in organic solvents but may have limited solubility in water, which is a common trait for many indoxyl derivatives. Safety data for this compound should be consulted, as it may pose hazards typical of brominated organic compounds. Overall, 5-bromo-3-indoxyl nonanoate serves as a valuable tool in molecular biology and biochemistry for studying enzyme activity and other biochemical processes.

5-BROMO-3-INDOXYL NONANOATE

133950-70-6: Rarechem Ah Bs 0021, Blue-Nonanoate, Lapis(Tm)-Nonanoate, 5-Bromo-3-Indolyl Nonanoate, 5-bromo-1H-indol-3-yl nonanoate

5-Bromo-3-indolyl nonanoate (BIN) is a chromogenic enzyme substrate often used for the detection of esterase activity. It is hydrolyzed by esterase to produce a blue product, which can be detected visually or by spectrophotometry. BIN is particularly useful for the detection of esterase activity in bacteria and fungi, and can be used to differentiate between different types of organisms based on their esterase activity patterns

5-Bromo-3-indolyl nonanoate

Chromogenic substrate for esterase with C9 activity yielding a lapis colored precipitate upon cleavage.

CAS 133950-70-6: 5-BROMO-3-INDOXYL NONANOATE

5-Bromo-3-indolyl nonanoate

Ref: 3D-EB04036

5-Bromo-3-indolyl nonanoate

Ref: 7W-GE4104

5-Bromo-3-indolyl nonanoate

Ref: 54-BIB1409

5-Bromo-3-indoxyl nonanoate

Ref: 3D-B-8910