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Catalog Number:
05022
CAS Number:
205528-30-9
Fmoc-3-(4'-pyridyl)-D-alanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Ala(4'-pyridyl)-OH, Fmoc-β-(4'-pyridyl)-D-Ala-OH
Documents
$85.00 /1G
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Product Information

Fmoc-3-(4'-pyridyl)-D-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique pyridyl side chain enhances its utility in various applications, particularly in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and ease of use in solid-phase peptide synthesis, making it an ideal choice for those looking to create complex peptide structures with precision.

In addition to its role in peptide synthesis, Fmoc-3-(4'-pyridyl)-D-alanine has shown potential in the development of targeted therapies and drug delivery systems. Its ability to form stable interactions with biological targets allows for the exploration of novel therapeutic agents. This compound is particularly relevant in the fields of medicinal chemistry and biochemistry, where it can be employed to study protein interactions and enzyme activity. With its favorable properties and applications, Fmoc-3-(4'-pyridyl)-D-alanine stands out as a valuable tool for researchers and industry professionals alike.

Synonyms
Fmoc-D-Ala(4'-pyridyl)-OH, Fmoc-β-(4'-pyridyl)-D-Ala-OH
CAS Number
205528-30-9
Purity
≥ 98% (HPLC)
Molecular Formula
C23H20N2O4
Molecular Weight
388.4
MDL Number
MFCD00672567
PubChem ID
3882867
Melting Point
190 - 210 °C
Appearance
White powder
Optical Rotation
[a]D20 = +46 ±2 °(C=1 in DMF)
Conditions
Store at 0 - 8 °
General Information
Synonyms
Fmoc-D-Ala(4'-pyridyl)-OH, Fmoc-β-(4'-pyridyl)-D-Ala-OH
CAS Number
205528-30-9
Purity
≥ 98% (HPLC)
Molecular Formula
C23H20N2O4
Molecular Weight
388.4
MDL Number
MFCD00672567
PubChem ID
3882867
Melting Point
190 - 210 °C
Appearance
White powder
Optical Rotation
[a]D20 = +46 ±2 °(C=1 in DMF)
Conditions
Store at 0 - 8 °
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-3-(4'-pyridyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it a valuable building block in the design of novel pharmaceuticals, particularly in targeting specific receptors due to its pyridine moiety.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems and improving the efficacy of therapeutic agents.
  • Research in Neuroscience: Its derivatives are explored for their potential role in modulating neurotransmitter systems, which can lead to advancements in treatments for neurological disorders.
  • Analytical Chemistry: Fmoc-3-(4'-pyridyl)-D-alanine is utilized in various analytical techniques, such as HPLC, for the separation and quantification of peptides and proteins in complex mixtures.

Citations