7-(4-Carboxyphenyl)quinoline-3-carboxylic acid

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Reagent Code: #129909
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CAS Number 1891085-32-7

science Other reagents with same CAS 1891085-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.27 g/mol
Formula C₁₇H₁₁NO₄
thermostat Physical Properties
Boiling Point 551.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.415±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a fluorescent probe in biochemical and analytical applications due to its strong emission properties. It serves as a key component in sensors for detecting metal ions, especially in environmental and biological samples. Its carboxylic acid groups allow easy conjugation to biomolecules, making it useful in labeling peptides, proteins, and nucleic acids for imaging and detection. Also employed in the development of optoelectronic devices and dye-sensitized solar cells because of its stable photoluminescence and electron-accepting characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,690.00
inventory 1g
10-20 days ฿18,070.00

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7-(4-Carboxyphenyl)quinoline-3-carboxylic acid
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Used as a fluorescent probe in biochemical and analytical applications due to its strong emission properties. It serves as a key component in sensors for detecting metal ions, especially in environmental and biological samples. Its carboxylic acid groups allow easy conjugation to biomolecules, making it useful in labeling peptides, proteins, and nucleic acids for imaging and detection. Also employed in the development of optoelectronic devices and dye-sensitized solar cells because of its stable photolum

Used as a fluorescent probe in biochemical and analytical applications due to its strong emission properties. It serves as a key component in sensors for detecting metal ions, especially in environmental and biological samples. Its carboxylic acid groups allow easy conjugation to biomolecules, making it useful in labeling peptides, proteins, and nucleic acids for imaging and detection. Also employed in the development of optoelectronic devices and dye-sensitized solar cells because of its stable photoluminescence and electron-accepting characteristics.

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