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TCI

CAS 2018-61-3

N-Acetyl-L-phenylalanine TCI A1541

N-Acetyl-L-phenylalanine TCI A1541

Chemical Identity

Other names
Ac-Phe-OH
CAS No.
2018-61-3
PubChem
CID 74839·SID 87562989
Formula
C11H13NO3
Molecular weight
207.23 g/mol
Purity
>99.0%(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2S)-2-acetamido-3-phenylpropanoic acid
SMILES
CC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O
InChIKey
CBQJSKKFNMDLON-JTQLQIEISA-N
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N-Acetyl-L-phenylalanine is a chemical compound widely used in laboratory experiments across chemical and biochemical fields. It serves as a crucial component in peptide synthesis, playing a significant role in the development of pharmaceuticals and organic chemicals. This compound is essential for research involving protein structure and metabolism, particularly within the domain of chemical biology. Its stability and controlled reactivity make it a popular choice among researchers for various experimental applications.

The compound’s molecular structure features an acetylated amine group and a phenylalanine moiety, which are key to its chemical behavior. It is non-polar and dissolves well in organic solvents such as ethyl acetate and acetone, making it ideal for synthesis reactions and laboratory testing. These properties ensure its versatility in different experimental setups. Additionally, its low toxicity at normal dosages enhances its safety profile, allowing for broader use in research environments.

In Indonesian laboratories, N-Acetyl-L-phenylalanine is commonly utilized in chemical biology, pharmaceutical, and biotechnology research. It is an integral part of experiments aimed at understanding molecular interactions, drug development, and biochemical processes. Its availability and reliability make it a standard material in academic and industrial research settings.

TCI brochures (PDF)

  • Peptide Synthesis: N-Acetyl-L-phenylalanine is a key building block in the synthesis of peptides, supporting the creation of complex molecular structures used in drug development.
  • Protein Structure Analysis: Its role in mimicking amino acid residues makes it valuable for studying protein folding and conformational changes.
  • Organic Chemistry Reactions: The compound’s solubility in organic solvents facilitates its use in various synthetic pathways and reaction mechanisms.
  • Metabolic Research: It is used to investigate metabolic pathways and enzyme activity in biochemical systems.
  • Drug Development: Its involvement in peptide-based therapeutics makes it relevant for pharmaceutical research and compound screening.

Brand TCI
CAS number 2018-61-3
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid powder
Storage Store in a cool, dry place away from moisture and direct sunlight

N-Acetyl-L-phenylalanine should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its non-polar nature, it is advisable to use glass or plastic containers that are resistant to organic solvents. Avoid storing it near heat sources or in areas with high humidity. General laboratory precautions include wearing appropriate personal protective equipment when handling the compound to ensure safety during experiments. Proper labeling of containers is essential for safe handling and to prevent accidental misuse.

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