(S)-()-2-Aminobutanamide hydrochloride
≥97%
- Product Code: 113885
Alias:
L-2-aminobutanamide hydrochloride
CAS:
7682-20-4
| Molecular Weight: | 138.6 g./mol | Molecular Formula: | C₄H₁₀N₂OHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00136565 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. It is often employed in the development of medications that require precise stereochemistry to ensure efficacy and safety. Additionally, it serves as a building block in organic synthesis, contributing to the creation of complex molecules with potential therapeutic applications. Researchers also use it in studies focusing on the structure-activity relationships of chiral compounds, aiding in the design of more effective drugs.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $17.44 |
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| 25.000 | 10-20 days | $49.42 |
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| 100.000 | 10-20 days | $128.74 |
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| 500.000 | 10-20 days | $414.04 |
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(S)-()-2-Aminobutanamide hydrochloride
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. It is often employed in the development of medications that require precise stereochemistry to ensure efficacy and safety. Additionally, it serves as a building block in organic synthesis, contributing to the creation of complex molecules with potential therapeutic applications. Researchers also use it in studies focusing on the structure-activity relationships of chiral compounds, aiding in the design of more effective drugs.
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