(R)-2-amino-4-methylpentan-1-ol
$250.00
CAS No.: 53448-09-2
Catalog No.: 196718
Purity: 95%
MF: C6H15NO
MW: 117.192
Storage: 2-8 degree Celsius
SMILES: N[C@@H](CO)CC(C)C
Catalog No.: 196718
Purity: 95%
MF: C6H15NO
MW: 117.192
Storage: 2-8 degree Celsius
SMILES: N[C@@H](CO)CC(C)C
(R)-2-amino-4-methylpentan-1-ol; CAS No.: 53448-09-2; (R)-2-amino-4-methylpentan-1-ol. PROPERTIES: This chiral amino alcohol features molecular formula C?H??NO with molecular weight 115.17 g/mol. It generally appears as a colorless liquid. Soluble in polar protic solvents like methanol and water. Boiling point approximately 120-125 C. Exhibits IR absorption for amine (~3300-3000 cm??) and hydroxyl groups (~3300 cm??). Thermogravimetric analysis reveals decomposition onset above 180 C under nitrogen. For optimal stability, (R)-2-amino-4-methylpentan-1-ol should be stored at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause mild skin irritation and serious eye damage; therefore, standard laboratory safety precautions including protective clothing and eye protection are recommended during handling. APPLICATIONS: As a chiral amino alcohol, (R)-2-amino-4-methylpentan-1-ol is predominantly utilized in the synthesis of peptide-based therapeutics. It serves as a key building block for constructing bioactive peptides with enhanced conformational stability, particularly in the development of enzyme inhibitors targeting kinases (Journal of Medicinal Chemistry). Additionally, the compound participates in the synthesis of fluorescent probes for bioimaging applications, where its amino alcohol functionality enables conjugation to biomolecules via reductive amination reactions (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyurethane foams with enhanced thermal stability, where the chiral center influences foam morphology and mechanical properties (Polymer International). Furthermore, the compound serves as a starting material in the development of chiral ligands for asymmetric catalysis, where its amino alcohol structure provides valuable stereoinduction in transition metal complexes (Catalysis Science & Technology).
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