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Atomfair Z-DL-Asp-OH Z-DL-Asp-OH C12H13NO6

Description Z-DL-Asp-OH (N-Carbobenzoxy-DL-aspartic Acid) is a high-purity, synthetic amino acid derivative widely used in peptide synthesis and biochemical research. With the molecular formula C12H13NO6and CAS number 141091-37-4 , this compound is characterized by its carbobenzoxy (Cbz or Z) protecting group, which enhances stability during synthetic processes. The DL-racemic mixture ensures versatility in chiral studies and asymmetric synthesis applications. Ideal for researchers, this product is rigorously tested for purity (>98% by HPLC) and is supplied as a white crystalline powder with excellent solubility in organic solvents like DMF and DMSO. Store under inert conditions at 2-8??C to maintain optimal stability.

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Description

Description

Z-DL-Asp-OH (N-Carbobenzoxy-DL-aspartic Acid) is a high-purity, synthetic amino acid derivative widely used in peptide synthesis and biochemical research. With the molecular formula C12H13NO6 and CAS number 141091-37-4, this compound is characterized by its carbobenzoxy (Cbz or Z) protecting group, which enhances stability during synthetic processes. The DL-racemic mixture ensures versatility in chiral studies and asymmetric synthesis applications. Ideal for researchers, this product is rigorously tested for purity (>98% by HPLC) and is supplied as a white crystalline powder with excellent solubility in organic solvents like DMF and DMSO. Store under inert conditions at 2-8??C to maintain optimal stability.

  • CAS No: 141091-37-4
  • Molecular Formula: C12H13NO6
  • Molecular Weight: 267.23
  • Exact Mass: 267.07428713
  • Monoisotopic Mass: 267.07428713
  • IUPAC Name: 2-(phenylmethoxycarbonylamino)butanedioic acid
  • SMILES: C1=CC=C(C=C1)COC(=O)NC(CC(=O)O)C(=O)O
  • Synonyms: Z-DL-Asp-OH, 4515-21-3, N-Carbobenzoxy-DL-aspartic Acid, Z-D-aspartic acid, Z-DL-aspartic acid

Application

Z-DL-Asp-OH is a key intermediate in solid-phase peptide synthesis (SPPS), where its carbobenzoxy group protects the amine functionality during coupling reactions. It is also employed in the study of enzyme-substrate interactions, particularly in aspartic acid-based proteases. Researchers utilize this compound to investigate racemic crystallization and chiral resolution techniques in pharmaceutical development.

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