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Atomfair 3-Tyrosine, DL- DL-m-Tyr C9H11NO3

Description 3-Tyrosine, DL- (CAS No. 32140-49-1) is a high-purity non-natural amino acid derivative with the molecular formula C9H11NO3and IUPAC name 2-amino-3-(3-hydroxyphenyl)propanoic acid. This racemic mixture of D- and L-enantiomers is a key intermediate in biochemical research, particularly in studies of tyrosine metabolism, enzyme inhibition, and neurotransmitter synthesis. Our product is synthesized under strict quality control to ensure ??95% purity (HPLC), with comprehensive analytical data including1H NMR,13C NMR, and mass spectrometry available upon request. Supplied as a white to off-white crystalline powder, it is packaged under inert atmosphere to ensure stability and shipped with a certificate of analysis. Ideal for neuroscientific…

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Description

Description

3-Tyrosine, DL- (CAS No. 32140-49-1) is a high-purity non-natural amino acid derivative with the molecular formula C9H11NO3 and IUPAC name 2-amino-3-(3-hydroxyphenyl)propanoic acid. This racemic mixture of D- and L-enantiomers is a key intermediate in biochemical research, particularly in studies of tyrosine metabolism, enzyme inhibition, and neurotransmitter synthesis. Our product is synthesized under strict quality control to ensure ??95% purity (HPLC), with comprehensive analytical data including 1H NMR, 13C NMR, and mass spectrometry available upon request. Supplied as a white to off-white crystalline powder, it is packaged under inert atmosphere to ensure stability and shipped with a certificate of analysis. Ideal for neuroscientific research, medicinal chemistry, and as a building block for peptidomimetics.

  • CAS No: 32140-49-1
  • Molecular Formula: C9H11NO3
  • Molecular Weight: 181.19
  • Exact Mass: 181.07389321
  • Monoisotopic Mass: 181.07389321
  • IUPAC Name: 2-amino-3-(3-hydroxyphenyl)propanoic acid
  • SMILES: C1=CC(=CC(=C1)O)CC(C(=O)O)N
  • Synonyms: DL-m-Tyrosine, 775-06-4, m-Tyrosine, DL-, D,L-Metatyrosine, 3-tyrosine dl-

Application

DL-m-Tyrosine serves as a valuable tool compound for studying aromatic amino acid decarboxylase activity and dopamine biosynthesis pathways. Researchers utilize this meta-substituted tyrosine analog to investigate substrate specificity in tyrosine hydroxylase and phenylalanine hydroxylase enzymes. The compound finds particular utility in creating modified peptides with altered receptor binding properties and in metabolic studies of alternative tyrosine degradation routes.

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