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Catalog Number:
15079
CAS Number:
172089-14-4
Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-TTDS, N-(Fmoc-13-amino-4,7,10-trioxa-13-tridecayl)-succinamic acid
Documents
$55.40 /250MG
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Product Information

Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure incorporates multiple ether linkages, enhancing solubility and stability, making it an excellent choice for researchers focused on developing complex peptide-based therapeutics.

In practical applications, Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is particularly valuable in the synthesis of bioactive peptides and in the formulation of drug delivery systems. Its ability to facilitate the formation of stable peptide bonds while providing a robust protective group allows for efficient and streamlined synthesis processes. Researchers in medicinal chemistry and biochemistry can leverage this compound to enhance the efficacy of their peptide-based projects, ultimately contributing to advancements in therapeutic solutions.

Synonyms
Fmoc-TTDS, N-(Fmoc-13-amino-4,7,10-trioxa-13-tridecayl)-succinamic acid
CAS Number
172089-14-4
Purity
≥ 98% (HPLC)
Molecular Formula
C29H38N2O8
Molecular Weight
542.63
MDL Number
MFCD05663769
PubChem ID
17040159
Appearance
White powder
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-TTDS, N-(Fmoc-13-amino-4,7,10-trioxa-13-tridecayl)-succinamic acid
CAS Number
172089-14-4
Purity
≥ 98% (HPLC)
Molecular Formula
C29H38N2O8
Molecular Weight
542.63
MDL Number
MFCD05663769
PubChem ID
17040159
Appearance
White powder
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of drug candidates, particularly in creating compounds that require specific solubility and stability profiles, enhancing bioavailability in medicinal chemistry.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules like proteins and antibodies to therapeutic agents, improving targeted delivery systems in cancer therapy.
  • Polymer Chemistry: It finds applications in the development of functionalized polymers, which can be utilized in drug delivery systems and smart materials, offering tailored properties for specific applications.
  • Analytical Chemistry: The compound is employed in analytical methods for the detection and quantification of biomolecules, providing researchers with reliable tools for studying complex biological systems.

Citations