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Catalog Number:
04994
CAS Number:
147290-11-7
Nα-Fmoc-Nδ-allyloxycarbonyl-L-ornithine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Orn(Aloc)-OH
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Product Information

Na-Fmoc-Nd-allyloxycarbonyl-L-ornithine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an ideal choice for solid-phase peptide synthesis. The allyloxycarbonyl group enhances its reactivity, allowing for selective modifications that are essential in the design of bioactive peptides. Researchers and industry professionals utilize this compound in the development of therapeutics, particularly in the fields of oncology and immunology, where precise peptide structures are critical for efficacy.

The unique properties of Na-Fmoc-Nd-allyloxycarbonyl-L-ornithine enable it to serve as a building block for complex peptide sequences, facilitating the exploration of novel drug candidates. Its compatibility with various coupling reagents and its ability to undergo further functionalization make it a valuable tool in medicinal chemistry. By incorporating this compound into their workflows, researchers can streamline the synthesis of peptides with enhanced biological activity and specificity, ultimately contributing to advancements in drug discovery and development.

Synonyms
Fmoc-L-Orn(Aloc)-OH
CAS Number
147290-11-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O6
Molecular Weight
438.5
MDL Number
MFCD00798637
PubChem ID
3525953
Melting Point
106 - 118 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -8.5 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Orn(Aloc)-OH
CAS Number
147290-11-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O6
Molecular Weight
438.5
MDL Number
MFCD00798637
PubChem ID
3525953
Melting Point
106 - 118 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -8.5 ± 2 º (C=1 in DMF)
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-allyloxycarbonyl-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 peptide structures with high purity.
  • Drug Development: Its unique functional groups make it valuable in the development of novel pharmaceuticals, especially in creating targeted therapies that require specific amino acid sequences.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and drug delivery systems.
  • Research in Protein Engineering: It plays a significant role in protein engineering, aiding researchers in modifying proteins to enhance their stability and functionality, which is essential in various biotechnological applications.
  • Cosmetic Formulations: The compound finds applications in cosmetic chemistry, particularly in formulations aimed at skin rejuvenation, where its properties can enhance the delivery of active ingredients.

Citations