6,7-Dihydroxycoumarin-3-carboxylic Acid

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Reagent Code: #174341
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CAS Number 84738-35-2

science Other reagents with same CAS 84738-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.15 g/mol
Formula C₁₀H₆O₆
badge Registry Numbers
MDL Number MFCD18450959
thermostat Physical Properties
Melting Point 270°C(dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a fluorescent probe in biochemical assays due to its strong fluorescence properties, particularly in detecting metal ions such as aluminum and iron in environmental and biological samples. Its hydroxyl and carboxylic acid groups enable chelation with metal ions, making it valuable in sensor development. Also investigated for its antioxidant activity in pharmaceutical research, where it serves as a scaffold for designing compounds with radical-scavenging effects. Applied in studies related to oxidative stress due to its ability to interact with reactive oxygen species.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,000.00
inventory 1g
10-20 days ฿6,060.00

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6,7-Dihydroxycoumarin-3-carboxylic Acid
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Used as a fluorescent probe in biochemical assays due to its strong fluorescence properties, particularly in detecting metal ions such as aluminum and iron in environmental and biological samples. Its hydroxyl and carboxylic acid groups enable chelation with metal ions, making it valuable in sensor development. Also investigated for its antioxidant activity in pharmaceutical research, where it serves as a scaffold for designing compounds with radical-scavenging effects. Applied in studies related to oxid

Used as a fluorescent probe in biochemical assays due to its strong fluorescence properties, particularly in detecting metal ions such as aluminum and iron in environmental and biological samples. Its hydroxyl and carboxylic acid groups enable chelation with metal ions, making it valuable in sensor development. Also investigated for its antioxidant activity in pharmaceutical research, where it serves as a scaffold for designing compounds with radical-scavenging effects. Applied in studies related to oxidative stress due to its ability to interact with reactive oxygen species.

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