(S)-()-DBD-Py-NCS [=(S)-()-4-(N,N-Dimethylaminosulfonyl)-7-(3-isothiocyanatopyrrolidin-1-yl)-2,1,3-benzoxadiazole]
≥98%
- Product Code: 93710
CAS:
163927-32-0
Molecular Weight: | 353.42 g./mol | Molecular Formula: | C₁₃H₁₅N₅O₃S₂ |
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EC Number: | MDL Number: | MFCD00671494 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
The chemical is widely used as a fluorescent derivatization reagent for the analysis of chiral amines and amino acids in high-performance liquid chromatography (HPLC). It reacts selectively with primary and secondary amines to form stable thiourea derivatives, which can be detected with high sensitivity due to their strong fluorescence. This property makes it particularly useful in the field of pharmaceutical analysis, where it helps in the quantification and enantiomeric separation of chiral drugs. Additionally, it is applied in biological research for labeling and detecting amino compounds in complex matrices, such as biological fluids and tissue samples. Its chiral selectivity ensures accurate identification and measurement of enantiomers, which is crucial for understanding their biological activity and pharmacokinetics.
Product Specification:
Test | Specification |
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APPEARANCE | Light yellow to Brown powder to crystal |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $690.71 |
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(S)-()-DBD-Py-NCS [=(S)-()-4-(N,N-Dimethylaminosulfonyl)-7-(3-isothiocyanatopyrrolidin-1-yl)-2,1,3-benzoxadiazole]
The chemical is widely used as a fluorescent derivatization reagent for the analysis of chiral amines and amino acids in high-performance liquid chromatography (HPLC). It reacts selectively with primary and secondary amines to form stable thiourea derivatives, which can be detected with high sensitivity due to their strong fluorescence. This property makes it particularly useful in the field of pharmaceutical analysis, where it helps in the quantification and enantiomeric separation of chiral drugs. Additionally, it is applied in biological research for labeling and detecting amino compounds in complex matrices, such as biological fluids and tissue samples. Its chiral selectivity ensures accurate identification and measurement of enantiomers, which is crucial for understanding their biological activity and pharmacokinetics.
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