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Catalog Number:
37061
CAS Number:
934502-72-4
Ácido ( S )-3-(Fmoc-amino)-4-azidobutírico
Purity:
≥ 99% (ensayo por titulación, HPLC)
Synonym(s):
Fmoc-L-Dbu( N3 )-OH
Documents
$72.31 /100 mg
Tamaño
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Product Information

(S)-3-(Fmoc-amino)-4-azidobutyric acid is a versatile compound widely utilized in the fields of medicinal chemistry and bioconjugation. This amino acid derivative features an azido group, making it an ideal candidate for click chemistry applications, particularly in the synthesis of complex biomolecules. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide synthesis, facilitating the development of peptide-based therapeutics and research tools. Researchers appreciate its stability and compatibility with various coupling reactions, which enhances its utility in the design of novel drug candidates.

In addition to its role in peptide synthesis, (S)-3-(Fmoc-amino)-4-azidobutyric acid can be employed in the development of targeted delivery systems and imaging agents due to its unique functional groups. The azido moiety enables selective labeling and conjugation to biomolecules, providing a powerful tool for studying biological processes and disease mechanisms. Its applications extend to the creation of bioconjugates for diagnostics and therapeutics, making it a valuable asset for researchers and industry professionals looking to innovate in drug development and molecular biology.

Synonyms
Fmoc-L-Dbu( N3 )-OH
CAS Number
934502-72-4
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363163
PubChem ID
130147183
Melting Point
136 - 139 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -7 ± 1 ° (C=1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Fmoc-L-Dbu( N3 )-OH
CAS Number
934502-72-4
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD21363163
PubChem ID
130147183
Melting Point
136 - 139 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -7 ± 1 ° (C=1 en DMF)
Conditions
Conservar entre 2 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

(S)-3-(Fmoc-amino)-4-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 custom sequences for various applications in drug development and biotechnology.
  • Click Chemistry: Its azide functional group enables efficient click chemistry reactions, facilitating the attachment of biomolecules or labels, which is crucial in fields like bioconjugation and molecular imaging.
  • Drug Development: The compound's ability to modify drug candidates enhances their efficacy and selectivity, making it valuable in pharmaceutical research aimed at developing targeted therapies.
  • Biomaterials: It is used in the creation of functionalized polymers and hydrogels, which are important in tissue engineering and regenerative medicine, providing scaffolds for cell growth and differentiation.
  • Diagnostics: The compound's properties allow for the development of novel diagnostic tools, particularly in the detection of diseases through targeted delivery of imaging agents or therapeutic compounds.

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