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N-(2-hydroxyethyl)-Naphthalimide | 5450-40-8
| Catalog Number | A16-0018 |
| Category | Other Cell Fluorescent Probes |
| Molecular Formula | C14H11NO3 |
| Molecular Weight | 241.2 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| A16-0018 | -- | $-- |
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Product Introduction
N-(2-hydroxyethyl)-Naphthalimide is a fluorescent probe for detecting nucleic acids and their precursors, which quench the fluorescence of N-(2-hydroxyethyl)-naphthalimide.
Chemical Information |
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|---|---|
| Synonyms | N-(2-hydroxyethyl)-1,8-Naphthalimide; 2-(2-hydroxyethyl)-1H-benz[de]isoquinoline-1,3(2H)-dione |
| Purity | ≥95% |
| Canonical SMILES | C1=CC2=C3C(=C1)C(=O)N(C(=O)C3=CC=C2)CCO |
| InChI | InChI=1S/C14H11NO3/c16-8-7-15-13(17)10-5-1-3-9-4-2-6-11(12(9)10)14(15)18/h1-6,16H,7-8H2 |
| InChI Key | XKPZHSCHHBRGLY-UHFFFAOYSA-N |
| Appearance | Solid Powder |
- Product Specification
- Application
| Excitation | 330-333, 344-347 nm |
| Emission | 366-378 nm |
| Storage | Store at -20°C |
N-(2-hydroxyethyl)-Naphthalimide, a versatile fluorescent compound, finds applications across scientific research and industry. Here are four key applications of N-(2-hydroxyethyl)-Naphthalimide:
Fluorescent Probes: Embraced as a radiant fluorescent probe, N-(2-hydroxyethyl)-Naphthalimide plays a pivotal role in biological imaging and analytical chemistry realms. Its robust fluorescence characteristics enable the visualization and tracking of intricate cellular structures and biomolecules. Researchers leverage its prowess to examine dynamic processes within live cells, encompassing protein localization and cell signaling intricacies.
Environmental Sensing: Unveiling its potential in environmental sensing, this compound becomes a cornerstone in fabricating sensors for detecting noxious environmental residues and chemicals. Emitting fluorescence upon encountering specific analytes, it becomes a linchpin in water quality monitoring and the identification of hazardous substances. These sensors facilitate real-time monitoring endeavors, bolstering environmental conservation initiatives.
Material Science: Entwined with material science innovations, N-(2-hydroxyethyl)-Naphthalimide emerges as a catalyst in propelling optoelectronic devices and luminescent materials forward. Its integration into polymers and nanomaterials births components vital for light-emitting diodes (LEDs) and other photonics applications. Capitalizing on its distinctive properties, it elevates the performance and functionality of these avant-garde materials.
Chemical Assays: Stepping into the realm of chemical assays, this compound assumes a pivotal role as a vital reagent essential for quantifying diverse biochemical substances. In enzymatic reactions, N-(2-hydroxyethyl)-Naphthalimide takes on the mantle of a substrate, setting forth a fluorescent signal upon transformation. Its presence proves indispensable in high-throughput screening initiatives and diagnostic applications demanding swift and sensitive detection methodologies.
Applications of Fluorescent Probes & Dyes
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