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Catalog Number:
15169
CAS Number:
168135-77-1
N α -Fmoc- O - di - tert -butyl-malonyl-L-tyrosine
Purity:
≥ 95 % (CCM)
Synonym(s):
Fmoc-L-Tyr (malonyl-di-OtBu) -OH
Documents
$325.09 /25 mg
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Product Information

Na-Fmoc-O-di-tert-butyl-malonyl-L-tyrosine is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative is particularly valuable for researchers focusing on the design of peptide-based therapeutics, as it facilitates the introduction of specific functionalities while maintaining stability during synthesis. Its unique structure, featuring the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for complex peptide sequences.

In addition to its role in peptide synthesis, Na-Fmoc-O-di-tert-butyl-malonyl-L-tyrosine is also employed in the development of novel biomaterials and drug delivery systems. Its ability to form stable conjugates enhances the efficacy of therapeutic agents, making it a crucial component in the formulation of targeted therapies. Researchers and industry professionals can leverage this compound to streamline their workflows and improve the performance of their products, ultimately leading to advancements in pharmaceutical and biotechnological applications.

Synonyms
Fmoc-L-Tyr (malonyl-di-OtBu) -OH
CAS Number
168135-77-1
Purity
≥ 95 % (CCM)
Molecular Formula
C 35 H 399
Molecular Weight
617.7
MDL Number
MFCD00672344
PubChem ID
72759487
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-L-Tyr (malonyl-di-OtBu) -OH
CAS Number
168135-77-1
Purity
≥ 95 % (CCM)
Molecular Formula
C 35 H 399
Molecular Weight
617.7
MDL Number
MFCD00672344
PubChem ID
72759487
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na-Fmoc-O-di-tert-butyl-malonyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS). Its protective groups allow for selective reactions, enhancing the efficiency of creating complex peptide structures.
  • Drug Development: In pharmaceutical research, it is used to develop novel therapeutic peptides. The ability to modify the structure helps in optimizing drug properties, such as stability and bioavailability, which are crucial for effective treatments.
  • Bioconjugation: The compound plays a role in bioconjugation processes, where it can be attached to biomolecules for targeted drug delivery. This application is particularly beneficial in cancer therapy, where precision is vital.
  • Research in Neuroscience: It is utilized in the study of neuropeptides, which are important for understanding various neurological functions and disorders. This can lead to breakthroughs in treatments for conditions like depression and anxiety.
  • Material Science: The compound is also explored in the development of new materials, such as hydrogels, which can be used in drug delivery systems. Its unique properties allow for controlled release, improving therapeutic outcomes.

Citations