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Catalog Number:
15043
CAS Number:
331763-51-0
Fmoc-(R)-4-amino-5-methylhexanoic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-γ-L-valine
Documents
$79.22 /100MG
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Product Information

Fmoc-(R)-4-amino-5-methylhexanoic acid 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 structure allows for efficient incorporation into peptide chains, making it an invaluable tool for researchers in the fields of biochemistry and medicinal chemistry. The (R) configuration enhances its applicability in creating biologically active peptides, which are crucial in pharmaceutical research and development.

This compound is particularly beneficial in solid-phase peptide synthesis (SPPS), where it facilitates the formation of complex peptide sequences with high purity and yield. Its stability under various reaction conditions and compatibility with other reagents make it a preferred choice among professionals. Additionally, Fmoc-(R)-4-amino-5-methylhexanoic acid can be employed in the synthesis of peptide-based therapeutics, contributing to advancements in targeted drug delivery systems and therapeutic agents. Its practical applications and unique properties position it as a key component in modern peptide chemistry.

Synonyms
Fmoc-γ-L-valine
CAS Number
331763-51-0
Purity
≥ 97% (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD02094563
PubChem ID
73358295
Melting Point
124-130 °C
Appearance
Amorphous white powder
Optical Rotation
[a] = +4 to +6º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-γ-L-valine
CAS Number
331763-51-0
Purity
≥ 97% (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD02094563
PubChem ID
73358295
Melting Point
124-130 °C
Appearance
Amorphous white powder
Optical Rotation
[a] = +4 to +6º (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

Fmoc-(R)-4-amino-5-methylhexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), enabling the creation of complex peptides with high purity.
  • Drug Development: Its unique structure allows for the development of novel pharmaceuticals, especially in the field of peptide-based drugs, enhancing therapeutic efficacy.
  • Bioconjugation: The Fmoc protecting group facilitates selective reactions, making it useful in bioconjugation processes for attaching biomolecules to surfaces or other molecules in drug delivery systems.
  • Research in Neuroscience: This compound is utilized in studies related to neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Custom Synthesis Services: Its demand in the custom synthesis market allows researchers to obtain tailored compounds for specific applications, addressing unique research needs efficiently.

Citations