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Catalog Number:
11800
CAS Number:
402497-81-8
Ac-Phe(4-NH2-OH
Purity:
≥ 98% (HPLC)
Synonym(s):
Ac-4-amino-L-phenylalanine, Acetyl-p-amino-L-Phe-OH, (S-Ac-2-amino-3-(4-aminophenyl)propionic acid
Documents
$86.23 /250MG
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Product Information

Ac-Phe(4-NH2)-OH, also known as Acetyl-4-aminophenylalanine, is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This amino acid derivative features an acetyl group that enhances its solubility and stability, making it an ideal choice for peptide synthesis and drug formulation. Its unique structure allows for specific interactions in biological systems, which is particularly beneficial in the development of targeted therapies and drug delivery systems. Researchers often leverage Ac-Phe(4-NH2)-OH in studies related to protein engineering and enzyme activity, as it can serve as a building block for modified peptides that exhibit improved biological activity or stability.

In addition to its applications in research, Ac-Phe(4-NH2)-OH is also valuable in the synthesis of novel compounds for therapeutic use, including potential treatments for various diseases. Its ability to mimic natural amino acids while providing enhanced properties makes it a preferred choice among chemists and biochemists. With its broad range of applications and significant benefits, Ac-Phe(4-NH2)-OH stands out as a crucial compound for advancing scientific research and pharmaceutical development.

Synonyms
Ac-4-amino-L-phenylalanine, Acetyl-p-amino-L-Phe-OH, (S-Ac-2-amino-3-(4-aminophenyl)propionic acid
CAS Number
402497-81-8
Purity
≥ 98% (HPLC)
Molecular Formula
C11H14N2O3
Molecular Weight
222.22
MDL Number
MFCD03788154
PubChem ID
21838874
Appearance
Pale brown powder
Optical Rotation
[a]D25 = + 56 ± 2 º (c=0.24 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Ac-4-amino-L-phenylalanine, Acetyl-p-amino-L-Phe-OH, (S-Ac-2-amino-3-(4-aminophenyl)propionic acid
CAS Number
402497-81-8
Purity
≥ 98% (HPLC)
Molecular Formula
C11H14N2O3
Molecular Weight
222.22
MDL Number
MFCD03788154
PubChem ID
21838874
Appearance
Pale brown powder
Optical Rotation
[a]D25 = + 56 ± 2 º (c=0.24 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ac-Phe(4-NH2)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require specific amino acid sequences for therapeutic applications.
  • Drug Development: It is used in the development of novel pharmaceuticals, especially in creating compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: Ac-Phe(4-NH2)-OH is employed in bioconjugation processes, allowing researchers to attach drugs or imaging agents to biomolecules, improving their delivery and effectiveness.
  • Research in Cancer Therapeutics: This chemical plays a role in studies aimed at developing targeted cancer therapies, where its structural properties can influence the interaction with cancer cells.
  • Protein Engineering: It is utilized in protein engineering to modify protein structures, which can lead to enhanced stability and activity in various biotechnological applications.

Citations