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Catalog Number:
31954
CAS Number:
1998701-26-0
Nα-Fmoc-Nδ-trityl-L-Ornithine
Purity:
≥ 99.9% (Chiral HPLC)
Synonym(s):
Fmoc-L-Orn(Trt)-OH, (S-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-5-(tritylamino)pentanoicacid
Documents
$65.40 /100MG
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Product Information

Na-Fmoc-Nd-trityl-L-Ornithine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis process. Its trityl group enhances stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Na-Fmoc-Nd-trityl-L-Ornithine is particularly valuable in the production of bioactive peptides, which have applications in pharmaceuticals, biotechnology, and materials science.

This compound's unique structure allows for efficient coupling reactions, enabling the creation of peptides with high purity and yield. Its compatibility with various coupling reagents and solvents further enhances its utility in laboratory settings. Researchers and industry professionals can leverage Na-Fmoc-Nd-trityl-L-Ornithine to streamline their workflows in peptide synthesis, ultimately leading to innovative solutions in drug discovery and development.

Synonyms
Fmoc-L-Orn(Trt)-OH, (S-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-5-(tritylamino)pentanoicacid
CAS Number
1998701-26-0
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C39H36N2O4
Molecular Weight
596.71
MDL Number
MFCD30478737
PubChem ID
138114618
Melting Point
140-142 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = + 11 ± 2° (C=1 in THF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Orn(Trt)-OH, (S-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-5-(tritylamino)pentanoicacid
CAS Number
1998701-26-0
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C39H36N2O4
Molecular Weight
596.71
MDL Number
MFCD30478737
PubChem ID
138114618
Melting Point
140-142 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = + 11 ± 2° (C=1 in THF)
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-trityl-L-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, allowing for the creation of complex and functional peptides.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, providing researchers with the ability to modify peptide structures for enhanced efficacy and stability.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, aiding in the exploration of their roles in neurological functions and potential treatments for neurological disorders.
  • Custom Synthesis Services: Many laboratories offer custom synthesis services for this compound, catering to specific research needs and providing tailored solutions for scientists in academia and industry.

Citations