(S)-()-2-Aminobutanamide hydrochloride
Analytical reference substance, ≥99%
- Product Code: 113891
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:
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of chiral drugs. It is particularly valuable in the production of medications targeting neurological disorders due to its structural properties. Additionally, it plays a role in the development of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Its application extends to biochemical studies where it aids in understanding enzyme interactions and metabolic pathways.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 99-100 |
| Specific Rotation [A]20/D(C=1, H2O) | 23 Degree Celsius-25 Degree Celsius |
| Appearance | White To Tan Powder, Crystals And/Or Chunks |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $38.21 |
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(S)-()-2-Aminobutanamide hydrochloride
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of chiral drugs. It is particularly valuable in the production of medications targeting neurological disorders due to its structural properties. Additionally, it plays a role in the development of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Its application extends to biochemical studies where it aids in understanding enzyme interactions and metabolic pathways.
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