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Catalog Number:
03731
CAS Number:
198545-20-9
Nα-Fmoc-Nδ-methyltrityl-D-Ornithine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-D-Orn(Mtt)-OH
Documents
$95.60 /250MG
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Product Information

Na-Fmoc-Nd-methyltrityl-D-Ornithine is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, which includes a methyltrityl group, enhances its stability and solubility, making it an ideal choice for researchers focused on complex peptide sequences.

In practical applications, Na-Fmoc-Nd-methyltrityl-D-Ornithine is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics, including those targeting cancer and metabolic disorders. Its ability to facilitate the formation of stable peptide bonds allows for the efficient synthesis of high-purity peptides, which are crucial for biological assays and drug formulation. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, ensuring high yields and purity in their projects.

Synonyms
Fmoc-D-Orn(Mtt)-OH
CAS Number
198545-20-9
Purity
≥ 99% (HPLC)
Molecular Formula
C40H38N2O4
Molecular Weight
610.8
MDL Number
MFCD00797879
PubChem ID
75210723
Melting Point
128 - 142 °C (Lit.)
Appearance
White to off-white crystals
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Orn(Mtt)-OH
CAS Number
198545-20-9
Purity
≥ 99% (HPLC)
Molecular Formula
C40H38N2O4
Molecular Weight
610.8
MDL Number
MFCD00797879
PubChem ID
75210723
Melting Point
128 - 142 °C (Lit.)
Appearance
White to off-white crystals
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nd-methyltrityl-D-Ornithine 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. Its protective groups facilitate the stepwise addition of amino acids, ensuring high purity and yield.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. The ability to modify its structure allows researchers to design compounds with specific biological activities, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is employed in bioconjugation techniques, linking peptides to other biomolecules such as antibodies or enzymes. This application is crucial in developing targeted drug delivery systems.
  • Research in Cancer Therapy: It has potential applications in cancer research, where modified peptides can be used to target cancer cells specifically, improving treatment outcomes while minimizing side effects.
  • Protein Engineering: The compound is valuable in protein engineering, allowing scientists to create novel proteins with enhanced properties for various applications, including diagnostics and therapeutics.

Citations