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Catalog Number:
31994
CAS Number:
1926163-91-8
Fmoc-β-azido-D-Aib-OH·BHA
Purity:
≥ 99% (ensayo por titulación, HPLC)
Synonym(s):
Fmoc-β-azido-α-Me-D-Ala-OH·BHA
Antibiotic
Documents
$121.28 /25 mg
Tamaño
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Product Information

Fmoc-b-azido-D-Aib-OH·BHA is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique azido group, which enhances its utility in click chemistry, allowing for efficient conjugation reactions. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group provides stability during synthesis, making it an ideal choice for researchers focused on developing complex peptides and biomolecules. Its application extends to the fields of medicinal chemistry and bioconjugation, where it can facilitate the creation of targeted therapeutics and diagnostic agents.

Researchers and industry professionals will appreciate the compound's versatility in various applications, including the development of peptide-based drugs and the synthesis of novel materials. The azido functionality allows for straightforward incorporation into diverse chemical environments, enabling the exploration of new therapeutic avenues. With its robust properties and ease of use, Fmoc-b-azido-D-Aib-OH·BHA stands out as a valuable tool for advancing research in peptide chemistry and drug discovery.

Synonyms
Fmoc-β-azido-α-Me-D-Ala-OH·BHA
CAS Number
1926163-91-8
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4 · C13H13N
Molecular Weight
549.63
MDL Number
MFCD30748657
Appearance
Polvo blanco
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
Fmoc-β-azido-α-Me-D-Ala-OH·BHA
CAS Number
1926163-91-8
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4 · C13H13N
Molecular Weight
549.63
MDL Number
MFCD30748657
Appearance
Polvo blanco
Conditions
Conservar a ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
DEA-regulated
No
Warnings
-
Applications

Fmoc-b-azido-D-Aib-OH·BHA 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 modified peptides that can enhance biological activity or stability.
  • Drug Development: Its azido group allows for click chemistry applications, facilitating the attachment of drug candidates to targeting moieties, which can improve the efficacy of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes to link biomolecules, such as proteins and antibodies, to other molecules, enhancing their functionality for diagnostic and therapeutic purposes.
  • Material Science: In polymer chemistry, it can be employed to create functionalized polymers that have specific properties, making it valuable in the development of advanced materials.
  • Research in Chemical Biology: This compound is instrumental in studying protein interactions and modifications, aiding researchers in understanding complex biological systems and pathways.

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