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Catalog Number:
06172
CAS Number:
14173-41-2
DL-4-Iodophénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
DL-Phe(4-I)-OH, p -Iodo-DL-phénylalanine, Acide 2-amino-3-(4-iodophényl)propionique
Documents
$51.18 /1G
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Product Information

DL-4-Iodophenylalanine is a versatile amino acid derivative that plays a significant role in biochemical research and pharmaceutical applications. This compound is recognized for its unique ability to serve as a building block in the synthesis of various peptides and proteins, particularly in studies involving protein structure and function. Its iodine substitution enhances the compound's properties, making it a valuable tool for researchers exploring the interactions of proteins in biological systems.

In addition to its applications in peptide synthesis, DL-4-Iodophenylalanine is also utilized in the development of radiolabeled compounds for imaging and therapeutic purposes in medical research. Its incorporation into biomolecules can facilitate the study of receptor-ligand interactions and metabolic pathways, providing insights that are crucial for drug development and disease understanding. With its distinctive features, DL-4-Iodophenylalanine stands out as an essential compound for professionals in the fields of biochemistry and medicinal chemistry, offering both practical applications and the potential for innovative research breakthroughs.

Synonyms
DL-Phe(4-I)-OH, p -Iodo-DL-phénylalanine, Acide 2-amino-3-(4-iodophényl)propionique
CAS Number
14173-41-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H10INO2
Molecular Weight
291.1
MDL Number
MFCD00063066
PubChem ID
5152312
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
DL-Phe(4-I)-OH, p -Iodo-DL-phénylalanine, Acide 2-amino-3-(4-iodophényl)propionique
CAS Number
14173-41-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H10INO2
Molecular Weight
291.1
MDL Number
MFCD00063066
PubChem ID
5152312
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

DL-4-Iodophenylalanine is widely utilized in research focused on:

  • Protein Engineering: This compound serves as a useful tool for incorporating iodine into proteins, allowing researchers to study protein structure and function through techniques like X-ray crystallography.
  • Radiopharmaceutical Development: Its iodine content makes it valuable in developing radiolabeled compounds for imaging and therapeutic applications in nuclear medicine.
  • Neuroscience Research: Used as a precursor in the synthesis of neurotransmitter analogs, it helps in studying neurotransmitter systems and their role in various neurological disorders.
  • Biochemical Assays: The compound can be employed in assays to investigate enzyme activity and interactions, providing insights into metabolic pathways and disease mechanisms.
  • Drug Design: Its unique properties enable the design of novel therapeutic agents, particularly in oncology, where iodine's radiological properties can be exploited for targeted therapies.

Citations