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Catalog Number:
22672
CAS Number:
557756-85-1
Acide Fmoc-15-amino-4,7,10,13-tétraoxapentadécanoïque
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-NH-(PEG) 3- COOH
Documents
$65.40 /100 mg
Taille
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Product Information

Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis. Its tetraoxapentadecanoic structure allows for increased flexibility and functionality in the design of complex peptides, facilitating the development of therapeutic agents and research tools in biochemistry and molecular biology.

Researchers and industry professionals benefit from the compound's ability to streamline the synthesis of peptides with specific sequences and modifications. Its application extends to the creation of peptide-based drugs, biomaterials, and diagnostic agents, showcasing its versatility in various fields, including pharmaceuticals and biotechnology. The unique properties of Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid position it as a valuable asset in advancing peptide chemistry and enhancing the efficacy of therapeutic compounds.

Synonyms
Fmoc-NH-(PEG) 3- COOH
CAS Number
557756-85-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C 26 H 338
Molecular Weight
487.55
MDL Number
MFCD06656472
PubChem ID
2756186
Appearance
Huile jaune ou sirop incolore
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-NH-(PEG) 3- COOH
CAS Number
557756-85-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C 26 H 338
Molecular Weight
487.55
MDL Number
MFCD06656472
PubChem ID
2756186
Appearance
Huile jaune ou sirop incolore
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The chemical can be employed in bioconjugation techniques, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Material Science: Its properties are leveraged in developing advanced materials, such as hydrogels, which are used in tissue engineering and regenerative medicine.
  • Analytical Chemistry: This compound is useful in the analytical characterization of peptides, aiding researchers in understanding peptide behavior and interactions in biological systems.

Citations