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Catalog Number:
47457
CAS Number:
1858255-08-9
Succinimidyl 6-[[7-( N , N -Diméthylaminosulfonyl)-2,1,3-benzoxadiazol-4-yl]amino]hexanoate
Purity:
≥ 98 % (HPLC)
Synonym(s):
4-( N , N -Diméthylaminosulfonyl)-7-[5-(succinimidyloxycarbonyl)pentylamino]-2,1,3-benzoxadiazole, DBD-C6-NHS
Documents
$494.40 /100 mg
Taille
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Informations sur le produit

Succinimidyl 6-[[7-(N,N-Dimethylaminosulfonyl)-2,1,3-benzoxadiazol-4-yl]amino]hexanoate is a versatile compound widely utilized in bioconjugation and labeling applications. This compound features a unique structure that allows for effective conjugation with biomolecules, making it an excellent choice for researchers in the fields of biochemistry and molecular biology. Its sulfonamide group enhances solubility and stability, while the benzoxadiazole moiety provides strong fluorescence, enabling sensitive detection in various assays.

This compound is particularly beneficial in the development of fluorescent probes and labels for imaging studies, as well as in the synthesis of targeted drug delivery systems. Its ability to form stable conjugates with proteins and nucleic acids opens up possibilities for applications in diagnostics, therapeutic development, and cellular imaging. Researchers can leverage its properties to enhance the specificity and sensitivity of their assays, making it a valuable addition to any laboratory focused on advanced biochemical research.

Numéro CAS 
1858255-08-9
Formule moléculaire
C18H23N5O7S
Poids moléculaire 
453.47
Point de fusion 
137 - 141 °C
Rotation optique 
[a]20/D = -125 à -145 ° (C=2 dans le méthanol)
Informations générales
Numéro CAS 
1858255-08-9
Formule moléculaire
C18H23N5O7S
Poids moléculaire 
453.47
Point de fusion 
137 - 141 °C
Rotation optique 
[a]20/D = -125 à -145 ° (C=2 dans le méthanol)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Succinimidyl 6-[[7-(N,N-Dimethylaminosulfonyl)-2,1,3-benzoxadiazol-4-yl]amino]hexanoate is widely utilized in research focused on:

  • Fluorescent Labeling: This compound is used to label biomolecules, such as proteins and nucleic acids, allowing researchers to visualize and track these molecules in various biological processes.
  • Drug Development: Its unique structure aids in the design of targeted drug delivery systems, enhancing the efficacy of therapeutic agents by ensuring they reach their intended targets in the body.
  • Diagnostics: Employed in the development of diagnostic assays, this chemical helps in the detection of specific biomolecules, improving the accuracy and reliability of medical tests.
  • Bioconjugation: It facilitates the conjugation of drugs or imaging agents to antibodies, enabling the creation of more effective and precise treatments for diseases like cancer.
  • Research in Cellular Biology: The compound is valuable in studying cellular processes, as it can be used to tag and monitor cellular components, providing insights into cell function and behavior.

Citations