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Catalog Number:
03728
CAS Number:
201046-59-5
N α,δ - Bis - Fmoc-L-ornithine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Orn(Fmoc)-OH
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$45.47 /1G
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Product Information

Dérivé utile pour la synthèse de peptides ramifiés.

Synonyms
Fmoc-L-Orn(Fmoc)-OH
CAS Number
201046-59-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C35H32N2O6
Molecular Weight
576.7
MDL Number
MFCD00153362
PubChem ID
13783706
Melting Point
141-148 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[α] D 20 = -3 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-L-Orn(Fmoc)-OH
CAS Number
201046-59-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C35H32N2O6
Molecular Weight
576.7
MDL Number
MFCD00153362
PubChem ID
13783706
Melting Point
141-148 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[α] D 20 = -3 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na,d-Bis-Fmoc-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 the development of therapeutic proteins and vaccines.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for creating novel drug candidates, especially those targeting specific biological pathways.
  • Bioconjugation: Researchers use it to facilitate bioconjugation processes, enhancing the delivery of drugs or imaging agents to specific cells or tissues.
  • Research in Cancer Therapy: The compound is explored in cancer research for its potential to create targeted therapies that minimize side effects while maximizing efficacy.
  • Protein Engineering: It is applied in the field of protein engineering to modify protein structures, improving their stability and function for various applications.

Citations