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Catalog Number:
16733
CAS Number:
361161-57-1
Fmoc-(2S,3S)-3-amino-2-hydroxy-5-methylhexanoic acid
Purity:
≥ 95% (HPLC)
Documents
$93.14 /25MG
Pack Size Availability Price
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Product Information

Fmoc-(2S,3S)-3-amino-2-hydroxy-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 crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of both a hydroxyl and a methyl group, enhances its solubility and reactivity, making it an ideal candidate for various applications in medicinal chemistry and biochemistry. Researchers often leverage this compound in the development of bioactive peptides and pharmaceuticals, where precise control over amino acid sequences is essential.

In addition to its role in peptide synthesis, Fmoc-(2S,3S)-3-amino-2-hydroxy-5-methylhexanoic acid is also valuable in the study of protein interactions and enzyme activity. Its ability to form stable linkages with other molecules allows for the exploration of complex biological systems, providing insights into therapeutic targets and mechanisms of action. With its favorable properties and broad applicability, this compound stands out as a key tool for researchers aiming to innovate in the fields of drug discovery and development.

CAS Number
361161-57-1
Purity
≥ 95% (HPLC)
Molecular Formula
C22H25NO5
Molecular Weight
277.36
MDL Number
MFCD04974449
PubChem ID
53398432
Appearance
White powder
Optical Rotation
[a]D25 = -11 ± 1 º (C=1, in DMF) or D25 = -17 ± 1 º (C=1, in MeOH)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
361161-57-1
Purity
≥ 95% (HPLC)
Molecular Formula
C22H25NO5
Molecular Weight
277.36
MDL Number
MFCD04974449
PubChem ID
53398432
Appearance
White powder
Optical Rotation
[a]D25 = -11 ± 1 º (C=1, in DMF) or D25 = -17 ± 1 º (C=1, 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

Fmoc-(2S,3S)-3-amino-2-hydroxy-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, allowing for the creation of complex peptides with high purity.
  • Drug Development: It is employed in the pharmaceutical industry for the development of new drugs, especially those targeting specific biological pathways, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: Its application in neuroscience research helps in studying neuropeptides, contributing to a better understanding of neurological disorders and potential treatments.
  • Protein Engineering: This compound aids in the modification of proteins, improving their stability and functionality, which is essential for various biotechnological applications.

Citations