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Catalog Number:
37065
CAS Number:
1373763-34-8
Nα -Fmoc- Nβ -Boc-diethylene triamine succinamic acid
Purity:
≥ 98% (HPLC, TLC)
Synonym(s):
Fmoc-DETA(Boc)-Suc-OH
Documents
$70.00 /100MG
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Product Information

Na -Fmoc- Nb -Boc-diethylene triamine succinamic acid is a versatile compound widely used in peptide synthesis and drug development. This compound features protective groups that enhance its stability and reactivity, making it an ideal choice for researchers working on complex organic syntheses. Its unique structure allows for selective reactions, facilitating the formation of intricate peptide chains essential in pharmaceuticals and biochemistry.

In addition to its role in peptide synthesis, this compound is also valuable in the development of targeted drug delivery systems, where its functional groups can be modified to improve solubility and bioavailability. Researchers appreciate its ability to streamline the synthesis process, reducing the time and resources needed to produce high-quality peptides. With its robust applications in medicinal chemistry and bioconjugation, Na -Fmoc- Nb -Boc-diethylene triamine succinamic acid stands out as a crucial tool for advancing scientific research and innovation.

Synonyms
Fmoc-DETA(Boc)-Suc-OH
CAS Number
1373763-34-8
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C28H35N3O7
Molecular Weight
525.6
MDL Number
MFCD31380733
PubChem ID
57414016
Appearance
White powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-DETA(Boc)-Suc-OH
CAS Number
1373763-34-8
Purity
≥ 98% (HPLC, TLC)
Molecular Formula
C28H35N3O7
Molecular Weight
525.6
MDL Number
MFCD31380733
PubChem ID
57414016
Appearance
White powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na -Fmoc- Nb -Boc-diethylene triamine succinamic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing researchers to selectively modify amino acids without affecting others. This is crucial for creating complex peptides with specific functions.
  • Drug Development: Its structure aids in the design of new pharmaceuticals, particularly in developing targeted drug delivery systems. The ability to modify the compound enhances the efficacy and specificity of drug formulations.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules for therapeutic applications. This is particularly useful in creating antibody-drug conjugates that improve treatment outcomes in cancer therapy.
  • Research in Biochemistry: It is employed in various biochemical assays to study enzyme activity and protein interactions, providing insights into cellular processes and disease mechanisms.
  • Material Science: The compound can be integrated into polymer systems, enhancing their properties for applications in coatings and adhesives, thus improving durability and performance in industrial settings.

Citations