(S)-2-Aminobutyramide-d3 Hydrochloride
AR
- Product Code: 91386
CAS:
1217605-54-3
| Molecular Weight: | 141.61 g./mol | Molecular Formula: | C₄H₈D₃ClN₂O |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
(S)-2-Aminobutyramide-d3 Hydrochloride is primarily utilized in research and development within the pharmaceutical industry. It serves as a labeled compound in metabolic studies, enabling scientists to track and analyze the pathways and mechanisms of drug metabolism with high precision. The deuterium labeling allows for the use of advanced analytical techniques such as mass spectrometry and NMR spectroscopy, providing detailed insights into the pharmacokinetics and pharmacodynamics of new drug candidates. This compound is particularly valuable in the study of amino acid derivatives and their role in therapeutic agents, helping to optimize drug efficacy and safety profiles. Additionally, it is employed in the synthesis of isotopically labeled analogs for use in clinical trials, ensuring accurate and reliable data collection. Its application extends to the investigation of neurological disorders, where it aids in understanding the biochemical processes involved in disease progression and the development of targeted treatments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $1,599.59 |
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(S)-2-Aminobutyramide-d3 Hydrochloride
(S)-2-Aminobutyramide-d3 Hydrochloride is primarily utilized in research and development within the pharmaceutical industry. It serves as a labeled compound in metabolic studies, enabling scientists to track and analyze the pathways and mechanisms of drug metabolism with high precision. The deuterium labeling allows for the use of advanced analytical techniques such as mass spectrometry and NMR spectroscopy, providing detailed insights into the pharmacokinetics and pharmacodynamics of new drug candidates. This compound is particularly valuable in the study of amino acid derivatives and their role in therapeutic agents, helping to optimize drug efficacy and safety profiles. Additionally, it is employed in the synthesis of isotopically labeled analogs for use in clinical trials, ensuring accurate and reliable data collection. Its application extends to the investigation of neurological disorders, where it aids in understanding the biochemical processes involved in disease progression and the development of targeted treatments.
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