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Catalog Number:
30547
Ácido 2R , 3S- (Fmoc-amino)-3-azidobutírico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Abu( 3S- N3)-OH
Documents
$312.77 /100 mg
Tamaño
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Product Information

The compound (2R,3S)-(Fmoc-amino)-3-azidobutyric acid is a versatile building block in peptide synthesis and drug development. This compound features an azide functional group, which is particularly valuable in click chemistry, allowing for efficient conjugation reactions. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group provides stability during synthesis, making it an ideal choice for researchers looking to create complex peptide structures. The unique combination of the azide and Fmoc functionalities enables the development of novel therapeutics, including targeted drug delivery systems and bioconjugates.

In addition to its applications in pharmaceutical research, (2R,3S)-(Fmoc-amino)-3-azidobutyric acid can be utilized in the development of biomaterials and diagnostic tools. Its ability to participate in bioorthogonal reactions opens up possibilities for innovative applications in the fields of molecular biology and materials science. Researchers can leverage this compound to create customized molecules with specific functionalities, enhancing the efficacy and targeting of therapeutic agents.

Synonyms
Fmoc-D-Abu( 3S- N3)-OH
Purity
≥ 99 % (HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD23380092
Melting Point
142-148 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +7,8 ± 1º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Abu( 3S- N3)-OH
Purity
≥ 99 % (HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD23380092
Melting Point
142-148 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +7,8 ± 1º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2R,3S)-(Fmoc-amino)-3-azidobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Click Chemistry: Its azide functional group enables efficient click chemistry reactions, facilitating the attachment of various biomolecules, which is crucial in bioconjugation applications.
  • Drug Development: By modifying the structure of this compound, researchers can explore new therapeutic agents, particularly in the fields of oncology and infectious diseases.
  • Biomaterials: The compound can be incorporated into polymeric materials for biomedical applications, such as drug delivery systems, enhancing the efficacy of treatments.
  • Fluorescent Probes: It can be used to develop fluorescent probes for imaging studies, aiding in the visualization of cellular processes and disease mechanisms.

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