(S)-()-DBD-APy [=(S)-()-4-(N,N-Dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole]
98%
- Product Code: 93712
CAS:
143112-50-9
| Molecular Weight: | 311.36 g./mol | Molecular Formula: | C₁₂H₁₇N₅O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191378 | |
| Melting Point: | 130°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a fluorescent derivatization reagent in analytical chemistry. It is particularly effective for the sensitive detection and quantification of carboxylic acids, amino acids, and other compounds in biological and environmental samples. Its application is crucial in high-performance liquid chromatography (HPLC) for enhancing the fluorescence of analytes, enabling precise and accurate measurements. Additionally, it is employed in proteomics and metabolomics studies to label and identify biomolecules, aiding in the understanding of complex biological processes. Its chiral nature also makes it valuable in enantiomeric separation and analysis, ensuring high specificity in detecting optically active compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Yellow to Orange powder to crystal |
| PURITY | 97.5-100 |
| Specific rotation a20DC1 CH3CN | 3.0-+7.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $73.97 |
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(S)-()-DBD-APy [=(S)-()-4-(N,N-Dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole]
This chemical is widely used as a fluorescent derivatization reagent in analytical chemistry. It is particularly effective for the sensitive detection and quantification of carboxylic acids, amino acids, and other compounds in biological and environmental samples. Its application is crucial in high-performance liquid chromatography (HPLC) for enhancing the fluorescence of analytes, enabling precise and accurate measurements. Additionally, it is employed in proteomics and metabolomics studies to label and identify biomolecules, aiding in the understanding of complex biological processes. Its chiral nature also makes it valuable in enantiomeric separation and analysis, ensuring high specificity in detecting optically active compounds.
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