(S)-3-Amino-2-methylpropanoic acid

≥95%

  • Product Code: 38432
  CAS:    4249-19-8
Molecular Weight: 103.12 g./mol Molecular Formula: C₄H₉NO₂
EC Number: MDL Number: MFCD07372875
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, protected from light, stored in an inert gas
Product Description: (S)-3-Amino-2-methylpropanoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for developing medications with specific biological activities. It is often employed in the creation of beta-lactam antibiotics, where its stereochemistry plays a critical role in enhancing the efficacy and reducing side effects of the final product. Additionally, this compound is used in peptide synthesis, contributing to the development of therapeutic peptides and peptidomimetics. Its application extends to research settings, where it serves as a building block for studying enzyme mechanisms and designing enzyme inhibitors.
Product Specification:
Test Specification
APPEARANCE white to off white powder
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿4,750.00
+
-
0.250 10-20 days ฿6,650.00
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-
1.000 10-20 days ฿9,280.00
+
-
(S)-3-Amino-2-methylpropanoic acid
(S)-3-Amino-2-methylpropanoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for developing medications with specific biological activities. It is often employed in the creation of beta-lactam antibiotics, where its stereochemistry plays a critical role in enhancing the efficacy and reducing side effects of the final product. Additionally, this compound is used in peptide synthesis, contributing to the development of therapeutic peptides and peptidomimetics. Its application extends to research settings, where it serves as a building block for studying enzyme mechanisms and designing enzyme inhibitors.
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