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

Este material se utiliza en conjugados de anticuerpos y fármacos como un socio de reacción SPAAC superior en comparación con H-Phe(4-N3). Puede servir como un indicador vibracional de entornos proteicos locales después de la incorporación genética a las proteínas.

Synonyms
H-Phe(4-CH2-N3)-OH · HCl, Clorhidrato de p -azidometil-L-fenilalanina
CAS Number
1446772-80-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H12N4O2 · HCl
Molecular Weight
256.7
MDL Number
MFCD31560135
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -13 ± 2 ° (C=1 en agua)
Conditions
Conservar entre 2 y 8 °C.
Warnings
0
General Information
Synonyms
H-Phe(4-CH2-N3)-OH · HCl, Clorhidrato de p -azidometil-L-fenilalanina
CAS Number
1446772-80-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H12N4O2 · HCl
Molecular Weight
256.7
MDL Number
MFCD31560135
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -13 ± 2 ° (C=1 en agua)
Conditions
Conservar entre 2 y 8 °C.
Warnings
0
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
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.

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