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Catalog Number:
33473
CAS Number:
2250433-79-3
Spermine (N 3 HH N 3 ·2 TsOH
Purity:
99 - 100 % (dosage par titrage)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
Antibiotic
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$141.41 /25 mg
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Product Information

Spermine(N3HHN3)·2TsOH is a versatile compound recognized for its unique properties and applications in various fields, particularly in biochemistry and pharmaceuticals. This compound, a derivative of spermine, features two tosyl groups that enhance its reactivity and solubility, making it an excellent candidate for use in drug development and molecular biology research. Its azidopropyl groups allow for click chemistry applications, facilitating the synthesis of complex molecules and enabling researchers to explore novel therapeutic pathways.

In addition to its utility in synthetic chemistry, Spermine(N3HHN3)·2TsOH has shown promise in the development of targeted drug delivery systems, where its ability to form stable complexes with biomolecules can be leveraged to improve the efficacy of therapeutic agents. Researchers in the fields of cancer therapy and gene delivery are particularly interested in this compound due to its potential to enhance cellular uptake and bioavailability of drugs. With its unique structural features and functional versatility, Spermine(N3HHN3)·2TsOH stands out as a valuable tool for advancing scientific research and innovation.

Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
2250433-79-3
Purity
99 - 100 % (dosage par titrage)
Molecular Formula
C 10 H 22 N 8 ·2C 7 H 8 O 3 S
Molecular Weight
598.7
PubChem ID
137946956
Melting Point
109 - 113 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
2250433-79-3
Purity
99 - 100 % (dosage par titrage)
Molecular Formula
C 10 H 22 N 8 ·2C 7 H 8 O 3 S
Molecular Weight
598.7
PubChem ID
137946956
Melting Point
109 - 113 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Oui
DEA-regulated
Non
Warnings
-
Applications

Spermine(N3HHN3)·2TsOH is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a vital tool in studying cellular processes, particularly in understanding polyamine metabolism and its role in cell growth and differentiation.
  • Drug Development: It is employed in the synthesis of novel pharmaceuticals, especially in the development of targeted therapies for cancer, due to its ability to interact with cellular pathways.
  • Gene Delivery Systems: Researchers use this compound to enhance the efficiency of gene delivery vectors, improving the transfection rates in gene therapy applications.
  • Material Science: The chemical is explored for its potential in creating advanced materials, such as hydrogels, which have applications in drug delivery and tissue engineering.
  • Diagnostics: It is also investigated for use in diagnostic assays, where its unique properties can help in the detection of specific biomarkers in clinical samples.

Citations