3-Aminophthalimide
≥97%
- Product Code: 69523
CAS:
2518-24-3
Molecular Weight: | 162.15 g./mol | Molecular Formula: | C₈H₆N₂O₂ |
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EC Number: | MDL Number: | MFCD00041853 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
3-Aminophthalimide is widely used in the field of analytical chemistry as a fluorescent probe due to its strong emission properties. It is particularly valuable in studying protein interactions and conformational changes, as it can be incorporated into peptides or proteins to monitor their behavior under various conditions. In material science, it serves as a key intermediate in the synthesis of advanced polymers and dyes, contributing to the development of high-performance materials with specific optical properties. Additionally, it is employed in organic synthesis to create complex molecules, including pharmaceuticals, where its amino group facilitates the formation of bonds with other functional groups. Its versatility makes it a crucial component in research and industrial applications.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow Solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $25.83 |
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5.000 | 10-20 days | $65.75 |
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25.000 | 10-20 days | $296.81 |
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3-Aminophthalimide
3-Aminophthalimide is widely used in the field of analytical chemistry as a fluorescent probe due to its strong emission properties. It is particularly valuable in studying protein interactions and conformational changes, as it can be incorporated into peptides or proteins to monitor their behavior under various conditions. In material science, it serves as a key intermediate in the synthesis of advanced polymers and dyes, contributing to the development of high-performance materials with specific optical properties. Additionally, it is employed in organic synthesis to create complex molecules, including pharmaceuticals, where its amino group facilitates the formation of bonds with other functional groups. Its versatility makes it a crucial component in research and industrial applications.
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