(S)-()-2-Aminobutanamide hydrochloride
99.0%
- Product Code: 113893
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, this compound serves as a key intermediate in the synthesis of various chiral drugs. Its role is crucial in the development of medications targeting neurological disorders, where enantiomeric purity is essential for efficacy and safety. Additionally, it finds application in the production of active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to interact effectively with biological targets. In medicinal chemistry, it is employed to create analogs and derivatives for screening potential therapeutic agents, particularly in the realm of central nervous system (CNS) diseases. Its utility extends to academic laboratories, where it aids in studying stereoselective reactions and chiral synthesis pathways.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 99-100 |
| Purity (Titration By AgNO3) | 99-100.5 |
| Specific Rotation [A]20/D(C=1, H2O) | 23-25 |
| 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 |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿850.00 |
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| 25.000 | 10-20 days | ฿1,990.00 |
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| 100.000 | 10-20 days | ฿5,000.00 |
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| 500.000 | 10-20 days | ฿17,900.00 |
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(S)-()-2-Aminobutanamide hydrochloride
Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various chiral drugs. Its role is crucial in the development of medications targeting neurological disorders, where enantiomeric purity is essential for efficacy and safety. Additionally, it finds application in the production of active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to interact effectively with biological targets. In medicinal chemistry, it is employed to create analogs and derivatives for screening potential therapeutic agents, particularly in the realm of central nervous system (CNS) diseases. Its utility extends to academic laboratories, where it aids in studying stereoselective reactions and chiral synthesis pathways.
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| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
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