1021902-10-2

Basic information

• Product Name: 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE
• Synonyms: MITO RED;RHODAMINE B 4-METHYLUMBELLIFERYL ESTER CHLORIDE;3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE;Rhodamine B 4-methylumbelliferyl ester chloride, 3,6-Bis(diethylamino)-9-[2-(4-methylcoumarin-7-yloxycarbonyl)phenyl]xanthylium chloride
• CAS NO: 1021902-10-2
• Molecular Formula: C38H37ClN2O5
• Molecular Weight: 637.16
• Mol File: 1021902-10-2.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE(1021902-10-2)
• EPA Substance Registry System: 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE(1021902-10-2)

Safety Data

• WGK Germany: 3
• F: 10-21
• Hazardous Substances Data: 1021902-10-2(Hazardous Substances Data)

Usage

Description

3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE is a complex organic compound with a unique molecular structure. It is characterized by its xanthylium cation, which is derived from xanthene and features a chlorine atom as a counterion. The molecule also contains two diethylamino groups at the 3 and 6 positions, as well as a substituted phenyl group at the 9 position, which is connected to a 4-methylcoumarin-7-yloxycarbonyl moiety. 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE is likely to have interesting photophysical and chemical properties due to its structure, making it potentially useful in various applications.

Uses

Used in Fluorescent Dyes:
3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE is used as a fluorescent dye for its ability to emit light upon excitation. The compound's unique structure, which includes a xanthene core and a coumarin-7-yloxycarbonyl group, may contribute to its fluorescence properties, making it suitable for use in various analytical and diagnostic applications.
Used in Cell Membrane Staining:
In the field of cell biology, 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE can be used as a cell membrane staining agent. Its interaction with the cell membrane may depend on the membrane potential, allowing for selective staining and visualization of specific cellular components.
Used in Analytical Chemistry:
The compound's fluorescence properties can also be exploited in analytical chemistry for the detection and quantification of various substances. By designing assays that involve the binding of the target analyte to the compound, it may be possible to develop sensitive and selective methods for detecting specific molecules in complex samples.
Used in Photodynamic Therapy:
Due to its potential to absorb light and generate reactive species, 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE may be used in photodynamic therapy (PDT) for the treatment of various diseases, including cancer. The compound could be administered to patients, and upon illumination with light of a specific wavelength, it could generate reactive oxygen species (ROS) that can cause damage to diseased cells, leading to their destruction.
Used in the Pharmaceutical Industry:
The unique structure of 3,6-BIS(DIETHYLAMINO)-9-[2-(4-METHYLCOUMARIN-7-YLOXYCARBONYL)PHENYL]XANTHYLIUM CHLORIDE may also make it a candidate for the development of new drugs. Its potential applications in the pharmaceutical industry could include the treatment of various diseases, such as cancer, by targeting specific cellular pathways or by acting as a photosensitizer in PDT.