3-Isopropyl-d7-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide
GC
- Product Code: 64577
CAS:
131842-77-8
| Molecular Weight: | 247.32 g./mol | Molecular Formula: | C₁₀D₇H₅N₂O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953755 | |
| Melting Point: | 131-134°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used extensively in research and development, particularly in the field of analytical chemistry, this compound serves as a deuterated internal standard. Its primary application is in mass spectrometry, where it aids in the accurate quantification of non-deuterated analogs in complex biological matrices. The deuterium labeling enhances the precision of measurements by providing a distinct mass difference, which is crucial for reliable detection and analysis. This makes it invaluable in pharmacokinetic studies, metabolic profiling, and environmental monitoring, ensuring high sensitivity and specificity in trace analysis. Additionally, it is employed in the synthesis of labeled compounds for mechanistic studies in organic chemistry, helping to elucidate reaction pathways and intermediates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $1,937.72 |
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3-Isopropyl-d7-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide
Used extensively in research and development, particularly in the field of analytical chemistry, this compound serves as a deuterated internal standard. Its primary application is in mass spectrometry, where it aids in the accurate quantification of non-deuterated analogs in complex biological matrices. The deuterium labeling enhances the precision of measurements by providing a distinct mass difference, which is crucial for reliable detection and analysis. This makes it invaluable in pharmacokinetic studies, metabolic profiling, and environmental monitoring, ensuring high sensitivity and specificity in trace analysis. Additionally, it is employed in the synthesis of labeled compounds for mechanistic studies in organic chemistry, helping to elucidate reaction pathways and intermediates.
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