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Catalog Number:
31993
CAS Number:
1926163-90-7
Fmoc-β-azido-Aib-OH·BHA·OH
Purity:
≥ 99% (ensayo por titulación, HPLC)
Synonym(s):
Fmoc-β-azido-α-Me-Ala-OH·BHA
Antibiotic
Documents
$125.00 /25 mg
Tamaño
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Product Information

Fmoc-b-azido-Aib-OH·BHA·OH is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique azido group, which enhances its reactivity and allows for various modifications, making it an essential tool for researchers in the fields of medicinal chemistry and biochemistry. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group facilitates the selective deprotection of amino acids during peptide assembly, ensuring high purity and yield in synthetic processes.

In practical applications, Fmoc-b-azido-Aib-OH·BHA·OH is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions. Its ability to introduce azide functionalities opens avenues for click chemistry, enabling the formation of stable conjugates with biomolecules. This compound is ideal for researchers looking to explore innovative drug delivery systems or develop novel therapeutic agents. With its unique properties and broad applicability, Fmoc-b-azido-Aib-OH·BHA·OH stands out as a crucial reagent in modern chemical research.

Synonyms
Fmoc-β-azido-α-Me-Ala-OH·BHA
CAS Number
1926163-90-7
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4 · C13H13N
Molecular Weight
549.63
MDL Number
MFCD30748656
Appearance
Polvo blanco
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
Fmoc-β-azido-α-Me-Ala-OH·BHA
CAS Number
1926163-90-7
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C19H18N4O4 · C13H13N
Molecular Weight
549.63
MDL Number
MFCD30748656
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-Aib-OH·BHA·OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS). Its azido group allows for further modifications, making it versatile for creating complex peptide structures.
  • Drug Development: In pharmaceutical research, it serves as a precursor for developing new drugs, especially in the field of targeted therapies. Its ability to facilitate the introduction of functional groups enhances drug efficacy.
  • Bioconjugation: The azido group is useful in click chemistry, enabling the attachment of biomolecules to surfaces or other compounds. This application is crucial in creating targeted delivery systems in biotechnology.
  • Material Science: It can be incorporated into polymer matrices to create materials with specific properties, such as enhanced biocompatibility or tailored mechanical strength, which are important in developing medical devices.
  • Research in Chemical Biology: The compound is used in studies involving protein labeling and tracking, aiding researchers in understanding protein interactions and functions in various biological processes.

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