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Catalog Number:
47694
CAS Number:
1446772-80-0
Chlorhydrate de 4-azidométhyl-L-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
H-Phe(4-CH2-N3)-OH · HCl, Chlorhydrate de p -azidométhyl-L-phénylalanine
Documents
$105.00 /25 mg
Taille
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Product Information

Ce matériau est utilisé dans les conjugués anticorps-médicaments comme partenaire de réaction SPAAC supérieur à H-Phe(4-N3). Il peut servir de rapporteur vibrationnel des environnements protéiques locaux après incorporation génétique dans les protéines.

Synonyms
H-Phe(4-CH2-N3)-OH · HCl, Chlorhydrate de p -azidométhyl-L-phénylalanine
CAS Number
1446772-80-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H12N4O2 · HCl
Molecular Weight
256.7
MDL Number
MFCD31560135
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -13 ± 2 ° (C = 1 dans l'eau)
Conditions
Conserver entre 2 et 8 °C
Warnings
0
General Information
Synonyms
H-Phe(4-CH2-N3)-OH · HCl, Chlorhydrate de p -azidométhyl-L-phénylalanine
CAS Number
1446772-80-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H12N4O2 · HCl
Molecular Weight
256.7
MDL Number
MFCD31560135
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -13 ± 2 ° (C = 1 dans l'eau)
Conditions
Conserver entre 2 et 8 °C
Warnings
0
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
0
Applications

4-Azidomethyl-L-phenylalanine hydrochloride is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile building block for bioconjugation, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Protein Labeling: It is used in the labeling of proteins for visualization in various assays, aiding in the study of protein interactions and functions.
  • Drug Development: The compound plays a significant role in the development of novel therapeutics, particularly in creating targeted treatments that can improve efficacy and reduce side effects.
  • Click Chemistry: Its azide functional group is ideal for click chemistry applications, facilitating the rapid and selective formation of chemical bonds, which is essential in creating complex molecular structures.
  • Research in Neuroscience: This chemical is utilized in neuroscience studies to investigate the role of specific amino acids in neuronal signaling and behavior, contributing to advancements in understanding brain function.

Citations