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Catalog Number:
05510
CAS Number:
137524-82-4
Nα,δ-Bis-Boc-D-ornithine
Purity:
≥ 99%
Synonym(s):
Boc-D-Orn(Boc)-OH
Documents
$89.13 /1G
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Product Information

Na,d-Bis-Boc-D-ornithine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical development. This compound is particularly valued for its protective Boc (tert-butyloxycarbonyl) groups, which facilitate the selective modification of amino acids during the synthesis of complex peptides. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers and professionals in the fields of medicinal chemistry and biochemistry.

In practical applications, Na,d-Bis-Boc-D-ornithine is commonly utilized in the development of peptide-based therapeutics, where it serves as a building block for various bioactive compounds. Its ability to improve the yield and purity of synthesized peptides makes it a preferred choice in both academic and industrial laboratories. Additionally, its compatibility with various coupling reagents and conditions further enhances its utility in peptide synthesis, paving the way for innovative drug design and development.

Synonyms
Boc-D-Orn(Boc)-OH
CAS Number
137524-82-4
Purity
≥ 99%
Molecular Formula
C15H28N2O6
Molecular Weight
332.4
MDL Number
MFCD00151881
PubChem ID
11099624
Melting Point
117-123 °C
Optical Rotation
[α]D20 = +5 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Orn(Boc)-OH
CAS Number
137524-82-4
Purity
≥ 99%
Molecular Formula
C15H28N2O6
Molecular Weight
332.4
MDL Number
MFCD00151881
PubChem ID
11099624
Melting Point
117-123 °C
Optical Rotation
[α]D20 = +5 ± 2º (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,d-Bis-Boc-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 therapeutic agents. Its protective Boc (tert-butyloxycarbonyl) groups allow for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates targeting various diseases. The compound's structural properties facilitate the design of molecules with improved bioavailability and efficacy.
  • Bioconjugation: Na,d-Bis-Boc-D-ornithine is employed in bioconjugation processes, linking biomolecules to therapeutic agents. This application is crucial in developing targeted therapies, particularly in cancer treatment.
  • Research in Neuroscience: The compound is utilized in studies exploring neuropeptides and their roles in neurological functions. Its ability to mimic natural amino acids makes it valuable for understanding peptide interactions in the nervous system.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis of this compound, catering to specific research needs. This flexibility allows researchers to obtain tailored compounds for their unique applications, enhancing experimental outcomes.

Citations