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Catalog Number:
05704
CAS Number:
214750-74-0
Nα-Fmoc-Nδ-allyloxycarbonyl-D-ornithine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Orn(Aloc)-OH
Documents
$60.40 /250MG
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Product Information

Na-Fmoc-Nd-allyloxycarbonyl-D-ornithine is a versatile 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 allows for the incorporation of the allyloxycarbonyl group, enhancing its reactivity and compatibility in various coupling reactions. Researchers and industry professionals appreciate its role in the development of bioactive peptides, particularly in the fields of pharmaceuticals and biotechnology, where precise modifications are crucial for achieving desired biological activities.

This compound is particularly beneficial in solid-phase peptide synthesis (SPPS), where it facilitates the assembly of complex peptide chains with high purity and yield. Its stability under standard reaction conditions and ease of deprotection make it an ideal choice for chemists looking to streamline their synthesis processes. Additionally, Na-Fmoc-Nd-allyloxycarbonyl-D-ornithine can be employed in the design of peptide-based therapeutics, offering potential applications in targeted drug delivery and the development of novel therapeutic agents.

Synonyms
Fmoc-D-Orn(Aloc)-OH
CAS Number
214750-74-0
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O6
Molecular Weight
438.5
MDL Number
MFCD00798638
PubChem ID
3525953
Melting Point
99 - 120 °C
Appearance
White powder
Optical Rotation
[a]D20 = 8.5 ± 1 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Orn(Aloc)-OH
CAS Number
214750-74-0
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O6
Molecular Weight
438.5
MDL Number
MFCD00798638
PubChem ID
3525953
Melting Point
99 - 120 °C
Appearance
White powder
Optical Rotation
[a]D20 = 8.5 ± 1 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-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 the development of custom peptides for pharmaceuticals and research applications.
  • Drug Development: It plays a crucial role in the design of peptide-based drugs, offering advantages in specificity and efficacy compared to traditional small-molecule drugs.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Protein Engineering: It aids in the modification of proteins, enabling the creation of novel protein variants with improved properties for industrial and therapeutic applications.
  • Research in Cancer Therapy: This chemical is being explored for its potential in targeted cancer therapies, providing a means to deliver drugs directly to cancer cells while minimizing side effects.

Citations