(S)-3-Amino-5-methylhexanoic acid
97%
- Product Code: 54246
CAS:
22818-43-5
| Molecular Weight: | 145.20 g./mol | Molecular Formula: | C₇H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01076258 | |
| Melting Point: | Boiling Point: | 249.1°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
(S)-3-Amino-5-methylhexanoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. Additionally, it serves as a building block in the development of peptide-based therapeutics, where its unique properties enhance the stability and efficacy of the final product. The compound is also explored in research for its potential role in modulating metabolic pathways, contributing to studies on metabolic diseases and enzyme inhibition.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £56.99 |
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| 0.250 | 10-20 days | £92.28 |
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| 1.000 | 10-20 days | £232.96 |
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(S)-3-Amino-5-methylhexanoic acid
(S)-3-Amino-5-methylhexanoic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular disorders. Additionally, it serves as a building block in the development of peptide-based therapeutics, where its unique properties enhance the stability and efficacy of the final product. The compound is also explored in research for its potential role in modulating metabolic pathways, contributing to studies on metabolic diseases and enzyme inhibition.
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