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Catalog Number:
06319
CAS Number:
201473-83-8
Nα,γ-Bis-Fmoc-L-2,4-diaminobutyric acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Dab(Fmoc)-OH
Documents
$75.49 /250MG
Pack Size Availability Price
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Product Information

Na,g-Bis-Fmoc-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features two Fmoc (9-fluorenylmethoxycarbonyl) groups, which provide stability and facilitate the selective deprotection necessary for the synthesis of complex peptides. Its unique structure allows for efficient incorporation into peptide chains, making it an essential building block in the design of bioactive molecules and therapeutic agents. Researchers appreciate its ability to enhance solubility and improve the overall yield of peptide synthesis, particularly in the development of peptide-based drugs and vaccines.

In addition to its applications in pharmaceutical research, Na,g-Bis-Fmoc-L-2,4-diaminobutyric acid is also valuable in the fields of biochemistry and molecular biology. It can be employed in the synthesis of peptide ligands for receptor studies, as well as in the preparation of peptide-based probes for various biological assays. Its robust properties and ease of use make it a preferred choice for professionals seeking reliable and efficient solutions in peptide chemistry.

Synonyms
Fmoc-L-Dab(Fmoc)-OH
CAS Number
201473-83-8
Purity
≥ 99% (HPLC)
Molecular Formula
C34H30N2O6
Molecular Weight
562.5
MDL Number
MFCD00237004
PubChem ID
68662008
Melting Point
187 - 191 °C
Appearance
Solid
Optical Rotation
[a]20D = -15 ± 1 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dab(Fmoc)-OH
CAS Number
201473-83-8
Purity
≥ 99% (HPLC)
Molecular Formula
C34H30N2O6
Molecular Weight
562.5
MDL Number
MFCD00237004
PubChem ID
68662008
Melting Point
187 - 191 °C
Appearance
Solid
Optical Rotation
[a]20D = -15 ± 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,g-Bis-Fmoc-L-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in solid-phase peptide synthesis, enabling the formation of complex peptides with high purity and yield.
  • Drug Development: It plays a significant role in the development of pharmaceutical compounds, particularly in designing peptide-based drugs that target specific biological pathways.
  • Bioconjugation: The Fmoc protecting group allows for selective reactions in bioconjugation processes, facilitating the attachment of peptides to various biomolecules for therapeutic applications.
  • Research in Cancer Therapy: Researchers utilize this compound to explore novel peptide sequences that can inhibit cancer cell growth, contributing to advancements in targeted cancer therapies.
  • Protein Engineering: It is employed in the modification of proteins to enhance their stability and functionality, which is essential in various biotechnological applications.

Citations