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Catalog Number:
16179
CAS Number:
851392-68-2
Nα-Fmoc-Nγ-(4-methyltrityl)-L-2,4-diaminobutyric acid Solvate with MTBE
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Dab(Mtt)-OH
Documents
$79.22 /250MG
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Product Information

Na-Fmoc-Ng-(4-methyltrityl)-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative is particularly valuable in the field of medicinal chemistry, where it serves as a building block for the synthesis of complex peptides and proteins. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group and a 4-methyltrityl moiety, enhances its stability and solubility, making it an ideal choice for researchers aiming to develop novel therapeutics.

In addition to its applications in peptide synthesis, this compound is also employed in the study of enzyme interactions and protein folding, providing insights into biological processes. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid chain makes it a preferred choice for chemists and biochemists alike. With its robust properties and practical applications, Na-Fmoc-Ng-(4-methyltrityl)-L-2,4-diaminobutyric acid stands out as a key reagent in advancing research and development in pharmaceutical sciences.

Synonyms
Fmoc-L-Dab(Mtt)-OH
CAS Number
851392-68-2
Purity
≥ 99% (HPLC)
Molecular Formula
C39H36N2O4
Molecular Weight
596.7
MDL Number
MFCD02094096
PubChem ID
53395250
Melting Point
> 107 °C (dec.)
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = -5.4 ± 1º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Dab(Mtt)-OH
CAS Number
851392-68-2
Purity
≥ 99% (HPLC)
Molecular Formula
C39H36N2O4
Molecular Weight
596.7
MDL Number
MFCD02094096
PubChem ID
53395250
Melting Point
> 107 °C (dec.)
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = -5.4 ± 1º (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-Ng-(4-methyltrityl)-L-2,4-diaminobutyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of novel therapeutic peptides, contributing to the development of targeted treatments in areas such as cancer and metabolic disorders.
  • Bioconjugation: The compound aids in the conjugation of peptides to various biomolecules, enhancing the efficacy and specificity of drug delivery systems.
  • Research in Neuroscience: It plays a role in synthesizing neuropeptides, which are critical for understanding neurological functions and developing treatments for neurodegenerative diseases.
  • Analytical Chemistry: This chemical is employed in the development of analytical methods for characterizing complex peptide mixtures, improving the accuracy of biochemical assays.

Citations