Z-D-Orn-OH, also known as Z-D-ornithine, is a synthetic amino acid derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group of D-ornithine. This compound is typically used in peptide synthesis and research due to its ability to serve as a building block for the formation of peptides. The Z group protects the amino functionality, allowing for selective reactions at other sites on the molecule. Z-D-Orn-OH is generally soluble in polar solvents, which facilitates its use in various chemical reactions. Its structure includes a primary amine and a carboxylic acid functional group, making it an amino acid. The D-configuration indicates that it is a non-natural isomer, which can be important in studies of biological activity and interactions. As with many amino acid derivatives, Z-D-Orn-OH may exhibit specific biological properties, making it of interest in pharmacological and biochemical research. Proper handling and storage conditions are essential to maintain its stability and reactivity.

Z-D-Orn-OH

112229-51-3: Z-D-Orn-OH, also known as Z-D-ornithine, is a synthetic amino acid derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group of D-ornithine. This compound is typically used in peptide synthesis and research due to its ability to serve as a building block for the formation of peptides. The Z group protects the amino functionality, allowing for selective reactions at other sites on the molecule. Z-D-Orn-OH is generally soluble in polar solvents, which facilitates its use in various chemical reactions. Its structure includes a primary amine and a carboxylic acid functional group, making it an amino acid. The D-configuration indicates that it is a non-natural isomer, which can be important in studies of biological activity and interactions. As with many amino acid derivatives, Z-D-Orn-OH may exhibit specific biological properties, making it of interest in pharmacological and biochemical research. Proper handling and storage conditions are essential to maintain its stability and reactivity.

CAS 112229-51-3

Z-D-Orn-OH

(R)-5-Amino-2-(((benzyloxy)carbonyl)amino)pentanoic acid

Ref: IN-DA008Z0Y

(R)-5-Amino-2-(((benzyloxy)carbonyl)amino)pentanoic acid

Ref: 54-OR1052518

(R)-5-Amino-2-(((benzyloxy)carbonyl)amino)pentanoic acid

Ref: 10-F325720