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Catalog Number:
30532
CAS Number:
131669-42-6
(2S,3S)-(Fmoc-amino)-3-azidobutyric acid
Purity:
≥ 99% (HPLC, TLC)
Synonym(s):
Fmoc-L-Abu(3S-N3)-OH
Antibiotic
Documents
$98.10 /100MG
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Product Information

(2S,3S)-(Fmoc-amino)-3-azidobutyric acid is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This amino acid derivative features an azido group, which enhances its reactivity and makes it an ideal candidate for click chemistry applications. Researchers often leverage its unique properties for the development of peptide-based therapeutics and bioconjugation strategies. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield.

In addition to its applications in peptide synthesis, (2S,3S)-(Fmoc-amino)-3-azidobutyric acid is also valuable in the creation of functionalized materials and drug delivery systems. Its ability to participate in various coupling reactions opens up new avenues for the design of innovative biomaterials. This compound stands out for its stability and ease of handling, making it a preferred choice for researchers looking to explore new frontiers in chemical biology and materials science.

Synonyms
Fmoc-L-Abu(3S-N3)-OH
CAS Number
131669-42-6
Purity
≥ 99% (HPLC, TLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363164
PubChem ID
14683492
Melting Point
151 - 152 ?C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 13 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Abu(3S-N3)-OH
CAS Number
131669-42-6
Purity
≥ 99% (HPLC, TLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363164
PubChem ID
14683492
Melting Point
151 - 152 ?C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 13 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

(2S,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, particularly in the development of novel therapeutic agents. Its unique azido group allows for further modifications, enhancing the versatility of peptide design.
  • Click Chemistry: The azido functional group enables applications in click chemistry, facilitating the efficient and selective coupling of biomolecules. This is particularly useful in drug discovery and bioconjugation processes.
  • Biotechnology: In the field of biotechnology, it is used to create modified proteins and enzymes, improving their stability and activity. This can lead to more effective biocatalysts for industrial processes.
  • Drug Development: Researchers leverage this compound in the development of new drugs, particularly in targeting specific diseases. Its ability to incorporate into larger molecular frameworks makes it valuable in medicinal chemistry.
  • Diagnostic Applications: The compound can be utilized in the development of diagnostic tools, such as imaging agents or biosensors, due to its reactive azido group that can be linked to various detection systems.

Citations