(R)-(-)-2-Amino-3-methylbutane

98%,ee 97%

  • Product Code: 71672
  Alias:    (R)-(-)-3-methyl-2-butylamine ;(R)-(−)-2-amino-3-methylbutane
  CAS:    34701-33-2
Molecular Weight: 87.16 g./mol Molecular Formula: C₅H₁₃N
EC Number: MDL Number: MFCD01075731
Melting Point: Boiling Point: 85-87°C
Density: 0.75 g/mL at 20 °C(lit.) Storage Condition: Room temperature, sealed, inert gas atmosphere
Product Description: (R)-(-)-2-Amino-3-methylbutane finds its primary application in the field of organic synthesis, where it serves as a chiral building block. It is particularly valuable in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. The compound is used to synthesize active pharmaceutical ingredients (APIs) with specific stereochemistry, ensuring the desired biological activity and efficacy. Additionally, it is employed in the preparation of fine chemicals and intermediates for agrochemicals, contributing to the creation of pesticides and herbicides with enhanced performance. Its role in asymmetric synthesis also extends to the development of flavors and fragrances, where precise stereochemistry is essential for achieving the intended sensory properties.
Product Specification:
Test Specification
APPEARANCE colorless liquid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €733.42
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(R)-(-)-2-Amino-3-methylbutane
(R)-(-)-2-Amino-3-methylbutane finds its primary application in the field of organic synthesis, where it serves as a chiral building block. It is particularly valuable in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. The compound is used to synthesize active pharmaceutical ingredients (APIs) with specific stereochemistry, ensuring the desired biological activity and efficacy. Additionally, it is employed in the preparation of fine chemicals and intermediates for agrochemicals, contributing to the creation of pesticides and herbicides with enhanced performance. Its role in asymmetric synthesis also extends to the development of flavors and fragrances, where precise stereochemistry is essential for achieving the intended sensory properties.
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