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2-(6-hydroxy-2,4,5,7-tetraiodo-3-oxo-3H-xanthen-9-yl)benzoic acid is a complex organic compound with the molecular formula C20H7I4O5. It is a derivative of xanthene, a heterocyclic aromatic compound, and features a benzoic acid group attached to the xanthene core. The molecule is characterized by the presence of four iodine atoms, which contribute to its unique properties. This chemical is known for its strong absorbance in the visible light spectrum, particularly in the blue and green regions, which makes it useful in applications such as dyes and pigments. Its chemical structure also endows it with potential applications in the field of fluorescence, where it can be used as a marker or indicator in various analytical techniques. The compound's specific properties and applications are closely related to its molecular structure and the presence of the iodine atoms, which influence its electronic and optical characteristics.

548-25-4

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548-25-4 Usage

Complex organic compound

The compound has a complex structure composed of multiple elements and functional groups.

Xanthene core

The central structure of the compound is a xanthene, which is an organic compound containing a fused ring of four carbon atoms.

Benzoic acid side chain

The compound has a side chain of benzoic acid, which is a simple aromatic acid.

Fluorescent dye

The compound exhibits fluorescent properties, meaning it can absorb light at one wavelength and emit light at a longer wavelength.

pH indicator

The compound can be used to indicate changes in pH levels, as it changes color in response to changes in the acidity or basicity of a solution.

Biological stain

The compound can be used to stain biological samples, such as cells or tissues, to make them more visible under a microscope.

Multiple iodine atoms

The compound contains four iodine atoms, which contribute to its distinctive fluorescent properties.

Hydroxyl group

The compound has a hydroxyl (-OH) functional group, which provides reactivity and allows the compound to interact with other molecules.

Ketone functional group

The compound has a ketone (C=O) functional group, which provides solubility in different solvents and contributes to its reactivity.

Diverse applications

The compound has a wide range of applications in chemical and biological research, including as a pH indicator, biological stain, and fluorescent probe.

Versatility

The compound's unique properties make it a valuable tool in various scientific disciplines, including chemistry, biology, and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 548-25-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 548-25:
(5*5)+(4*4)+(3*8)+(2*2)+(1*5)=74
74 % 10 = 4
So 548-25-4 is a valid CAS Registry Number.

548-25-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name erythrosin

1.2 Other means of identification

Product number -
Other names FD and C Red No. 4

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:548-25-4 SDS

548-25-4Downstream Products

548-25-4Relevant academic research and scientific papers

Rose Bengal analogs and vesicular glutamate transporters (VGLUTs)

Pietrancosta, Nicolas,Kessler, Albane,Favre-Besse, Franck-Cyril,Triballeau, Nicolas,Quentin, Thomas,Giros, Bruno,Mestikawy, Salah El,Acher, Francine C.

experimental part, p. 6922 - 6933 (2010/10/19)

Vesicular glutamate transporters (VGLUTs) allow the loading of presynaptic glutamate vesicles and thus play a critical role in glutamatergic synaptic transmission. Rose Bengal (RB) is the most potent known VGLUT inhibitor (K i 25 nM); therefore we designed, synthesized and tested in brain preparations, a series of analogs based on this scaffold. We showed that among the two tautomers of RB, the carboxylic and not the lactonic form is active against VGLUTs and generated a pharmacophore model to determine the minimal structure requirements. We also tested RB specificity in other neurotransmitter uptake systems. RB proved to potently inhibit VMAT (Ki 64 nM) but weakly VACHT (Ki >9.7 μM) and may be a useful tool in glutamate/acetylcholine co-transmission studies.

Reaction of Alcohols and Amines with Diacetyldihydrofluorescein (DADF): Conversion into Erythrosine-Derivatives on TLC-Plates by Ammonia and Iodine Vapors

Sharma, Padam N.,Brossi, Arnold

, p. 301 - 304 (2007/10/02)

Reaction of deacetylcolchicine (2) and colchifoline (3) with diacetyldihydrofluorescein (1, DADF) afforded the corresponding amide and ester derivatives, converted on TLC-plates after exposure to ammonia and iodine vapors into red colored pigments.This re

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