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Catalog Number:
06292
CAS Number:
80445-78-9
Nα-Boc-D-2,4-diaminobutyric acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-Dab-OH
Documents
$58.39 /250MG
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Product Information

Na-Boc-D-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected amino acid derivative features a Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for the synthesis of complex peptides and biologically active molecules. Researchers appreciate its role in facilitating the construction of peptide chains, particularly in the development of therapeutic agents and drug candidates.

With its unique structural properties, Na-Boc-D-2,4-diaminobutyric acid serves as a valuable building block in the synthesis of various bioactive compounds, including those used in cancer research and other therapeutic applications. Its ability to provide functional groups that can be easily modified allows for the creation of diverse molecular architectures. This compound stands out in the field of medicinal chemistry due to its efficiency in streamlining synthetic pathways, ultimately accelerating the drug discovery process.

Synonyms
Boc-D-Dab-OH
CAS Number
80445-78-9
Purity
≥ 99% (HPLC)
Molecular Formula
C9H18N2O4
Molecular Weight
218.2
MDL Number
MFCD00798622
PubChem ID
14291852
Melting Point
201 - 205 °C
Appearance
White crystalline powder
Optical Rotation
[a]20D = -17 ± 2 ° (C=0.5 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Dab-OH
CAS Number
80445-78-9
Purity
≥ 99% (HPLC)
Molecular Formula
C9H18N2O4
Molecular Weight
218.2
MDL Number
MFCD00798622
PubChem ID
14291852
Melting Point
201 - 205 °C
Appearance
White crystalline powder
Optical Rotation
[a]20D = -17 ± 2 ° (C=0.5 in MeOH)
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-Boc-D-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are vital in drug development and biological research.
  • Bioconjugation: Its protective Boc group allows for selective reactions, making it useful in attaching biomolecules to surfaces or other compounds in bioconjugation applications.
  • Drug Development: Researchers leverage its unique structure to design and optimize new therapeutic agents, particularly in the field of oncology and neurology.
  • Protein Engineering: It aids in the modification of proteins to enhance their stability and functionality, which is crucial for developing effective biopharmaceuticals.
  • Research on Amino Acid Analogues: The compound is instrumental in studying amino acid analogues, helping scientists understand metabolic pathways and enzyme functions.

Citations