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Catalog Number:
32570
CAS Number:
1926163-00-9
Fmoc-D-Asp(OtBu)-(Hmb)Gly-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Asp(OtBu)-N-(2-hydroxy-4-méthoxy-bzl)-Gly-OH
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$134.70 /100 mg
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Product Information

Fmoc-D-Asp(OtBu)-(Hmb)Gly-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is characterized by its unique protective groups, which facilitate the selective modification of amino acids during solid-phase peptide synthesis. Its structure allows for enhanced stability and solubility, making it an ideal choice for researchers looking to create complex peptides with improved bioactivity.

In the pharmaceutical industry, Fmoc-D-Asp(OtBu)-(Hmb)Gly-OH is particularly valuable for the synthesis of peptide-based therapeutics, where precision and efficiency are paramount. Its application extends to the development of targeted drug delivery systems and the design of novel biomaterials. Researchers appreciate its ability to streamline the synthesis process while maintaining high yields and purity, which is essential for advancing drug discovery and development. With its robust performance and versatility, this compound stands out as a preferred choice for professionals in the fields of biochemistry and medicinal chemistry.

Synonyms
Fmoc-D-Asp(OtBu)-N-(2-hydroxy-4-méthoxy-bzl)-Gly-OH
CAS Number
1926163-00-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C33H36N2O9
Molecular Weight
604.67
MDL Number
MFCD08458577
PubChem ID
4712616
Appearance
Poudre blanche
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Fmoc-D-Asp(OtBu)-N-(2-hydroxy-4-méthoxy-bzl)-Gly-OH
CAS Number
1926163-00-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C33H36N2O9
Molecular Weight
604.67
MDL Number
MFCD08458577
PubChem ID
4712616
Appearance
Poudre blanche
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-D-Asp(OtBu)-(Hmb)Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: It is used in the design of peptide-based therapeutics, particularly in developing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical's unique functional groups facilitate bioconjugation processes, enabling the attachment of peptides to various biomolecules for targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in synthesizing neuropeptides, which are crucial for studying neurological functions and developing treatments for neurodegenerative diseases.
  • Protein Engineering: This compound aids in the modification of proteins, allowing scientists to study structure-function relationships and improve protein stability and activity.

Citations