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Catalog Number:
47703
CAS Number:
446847-81-0
Na-Fmoc-Ng-Boc-Ng-methyl-L-2,4-diaminobutanoic acid
Purity:
≥ 99.7% (Chiral HPLC)
Synonym(s):
Fmoc-L-Dab(Boc,Me)-OH
Documents
$215.00 /25MG
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Product Information

Na-Fmoc-Nb-Boc-Nb-methyl-L-2,3-diaminobutanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features protective groups that enhance its stability and reactivity, making it an ideal choice for researchers focused on synthesizing complex peptides. Its unique structure allows for selective deprotection, facilitating the stepwise assembly of peptides with high fidelity. The Fmoc and Boc groups provide robust protection during synthesis, ensuring that the amino acid remains intact until the desired stage of the reaction.

This compound is particularly valuable in the pharmaceutical industry, where it can be employed in the development of peptide-based therapeutics. Its application extends to the creation of biologically active compounds, including potential drug candidates for various diseases. Researchers appreciate its ease of use and compatibility with standard peptide coupling methods, which streamline the synthesis process. With its favorable properties, Na-Fmoc-Nb-Boc-Nb-methyl-L-2,3-diaminobutanoic acid stands out as a crucial tool for advancing peptide chemistry and drug discovery.

Synonyms
Fmoc-L-Dab(Boc,Me)-OH
CAS Number
446847-81-0
Purity
≥ 99.7% (Chiral HPLC)
Molecular Formula
C25H30N2O6
Molecular Weight
454.5
MDL Number
MFCD32666077
Melting Point
142 - 158 °C
Appearance
White powder
Optical Rotation
[a]D20 = -13.5 to -16.5 °(C=1 in DMF)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-L-Dab(Boc,Me)-OH
CAS Number
446847-81-0
Purity
≥ 99.7% (Chiral HPLC)
Molecular Formula
C25H30N2O6
Molecular Weight
454.5
MDL Number
MFCD32666077
Melting Point
142 - 158 °C
Appearance
White powder
Optical Rotation
[a]D20 = -13.5 to -16.5 °(C=1 in DMF)
Conditions
Store at 2 - 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-Nb-Boc-Nb-methyl-L-2,3-diaminobutanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological activities.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing new drugs, particularly those targeting specific receptors or enzymes, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of therapeutic agents.
  • Research in Cancer Therapy: It is being explored in cancer research for its potential to create targeted therapies that can selectively attack cancer cells while sparing healthy tissue.
  • Protein Engineering: This chemical aids in the modification of proteins to enhance their stability and functionality, which is essential in various biotechnological applications.

Citations