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Catalog Number:
23142
CAS Number:
441052-82-0
4-(4-azidofenil)butirato de succinimidilo
Purity:
≥ 99% (RMN)
Synonym(s):
SAPB
Antibiotic
Documents
$93.14 /25 mg
Tamaño
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Product Information

Succinimidyl 4-(4-azidophenyl)butyrate is a versatile chemical compound widely utilized in bioconjugation and labeling applications. This compound features a unique azide functional group, making it an excellent choice for click chemistry, particularly in the development of bioconjugates for drug delivery systems and targeted therapies. Its ability to form stable linkages with biomolecules such as proteins and nucleic acids enhances its relevance in the fields of molecular biology and biochemistry. Researchers appreciate its ease of use and efficiency in facilitating the attachment of various probes, which is crucial for imaging and therapeutic applications.

In addition to its role in bioconjugation, Succinimidyl 4-(4-azidophenyl)butyrate is also employed in the synthesis of novel materials and in the development of biosensors. Its unique properties allow for the creation of advanced diagnostic tools that can detect specific biomolecules with high sensitivity. The compound's stability and reactivity make it a valuable asset in both academic research and industrial applications, providing significant advantages over similar compounds in terms of specificity and ease of handling.

Synonyms
SAPB
CAS Number
441052-82-0
Purity
≥ 99% (RMN)
Molecular Formula
C14H14N4O4
Molecular Weight
302.29
MDL Number
MFCD09952663
PubChem ID
9879446
Appearance
Sólido microcristalino de color canela
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
SAPB
CAS Number
441052-82-0
Purity
≥ 99% (RMN)
Molecular Formula
C14H14N4O4
Molecular Weight
302.29
MDL Number
MFCD09952663
PubChem ID
9879446
Appearance
Sólido microcristalino de color canela
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
DEA-regulated
No
Warnings
-
Applications

Succinimidyl 4-(4-azidophenyl)butyrate is widely utilized in research focused on:

  • Bioconjugation: This compound is commonly used to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies and diagnostics.
  • Drug Delivery Systems: It plays a crucial role in creating advanced drug delivery systems, allowing for the controlled release of therapeutic agents, which improves treatment efficacy and reduces side effects.
  • Imaging Techniques: The azide group enables the use of click chemistry for labeling in imaging applications, making it easier to visualize biological processes in real-time.
  • Protein Modification: Researchers utilize this compound to modify proteins for various applications, including the study of protein interactions and the development of novel therapeutic proteins.
  • Material Science: It is also applied in the synthesis of functionalized materials, enhancing the properties of polymers and nanomaterials for use in electronics and sensors.

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