7-(Diethylamino)coumarin-3-carboxylic Acid | CAS 50995-74-9

Name: 7-(Diethylamino)coumarin-3-carboxylic Acid
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog Number	F05-0017
Category	Coumarin
Molecular Formula	C14H15NO4
Molecular Weight	261.28

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Product Introduction

This fluorescent coumarin compound offers bright blue emission and strong conjugation ability for biolabeling applications. Buy fluorescent dyes online to develop custom fluorescent probes for live-cell and biochemical imaging.

Chemical Information
Product Specification
Application

Synonyms	7-(diethylamino)-2-oxo-1-benzopyran-3-carboxylic acid; 7-(diethylamino)-2-oxochromene-3-carboxylic acid
Purity	> 98 %
IUPAC Name	7-(diethylamino)-2-oxochromene-3-carboxylic acid
Canonical SMILES	CCN(CC)C1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)O
InChI	InChI=1S/C14H15NO4/c1-3-15(4-2)10-6-5-9-7-11(13(16)17)14(18)19-12(9)8-10/h5-8H,3-4H2,1-2H3,(H,16,17)
InChIKey	WHCPTFFIERCDSB-UHFFFAOYSA-N
Density	1.317 g/cm³
Appearance	Solid
Boiling Point	464.7 °C at 760 mmHg
Melting Point	229 °C
MDL Number	MFCD00068721
LogP	2.33740

Excitation	430-440 nm
Emission	470-480 nm
Condition To Avoid	Light Sensitive,Moisture Sensitive
Store Under Inert Gas	Store under inert gas

7-(Diethylamino)coumarin-3-carboxylic Acid, a versatile fluorescent dye, renowned for its myriad applications in biological and chemical research. Here are four key applications:

Fluorescent Labeling: Widely utilized for labeling biomolecules such as proteins, nucleic acids, and lipids, 7-(Diethylamino)coumarin-3-carboxylic Acid shines in experimental setups. Its intense fluorescence facilitates the visualization and tracking of these molecules across diverse scenarios, playing a pivotal role in live-cell imaging, flow cytometry, and other fluorescence-based assays.

Biosensing: A game-changer in biosensor technology, this compound seamlessly detects a wide array of analytes, from ions to small organic molecules. The fluorescent properties of 7-(Diethylamino)coumarin-3-carboxylic Acid undergo a transformative shift upon binding to specific targets, enabling ultra-sensitive and highly targeted detection. These biosensors find utility in realms like medical diagnostics, environmental monitoring, and food safety assessments, showcasing their far-reaching impact.

Enzyme Assays: At the forefront of enzyme analysis, 7-(Diethylamino)coumarin-3-carboxylic Acid serves as a pivotal component in monitoring enzymatic activities. When linked to substrates, its fluorescent dye is released upon enzymatic cleavage, enabling precise quantitative measurement. This crucial application fuels investigations in enzyme kinetics, screening for enzyme inhibitors, and other intricate biochemical analyses, shedding light on the intricacies of enzymatic processes.

Chemical Probes: Researchers wield 7-(Diethylamino)coumarin-3-carboxylic Acid as a potent chemical probe to delve into diverse chemical landscapes and reactions. Its fluorescence dynamics exhibit sensitivity to factors like pH and polarity, making it a valuable tool for exploring chemical processes, designing drug delivery systems, and innovating novel materials, opening new horizons in chemical research.