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1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one, commonly known as fluorescein, is a fluorescent dye with a xanthenone core and multiple functional groups such as hydroxyl and methoxy groups. These functional groups contribute to its fluorescent properties, making it a valuable compound in various scientific and industrial applications.

15222-53-4

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15222-53-4 Usage

Uses

Used in Scientific Research:
1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one is used as a fluorescent tracer for staining cells and tissues in microscopic examination, allowing for the visualization and analysis of biological structures.
Used in Chemical Testing:
Fluorescein is employed in chemical testing as a fluorescent indicator, helping to detect and measure the presence of specific substances.
Used in Dye Production:
1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one is used as a key component in the production of various colored dyes, contributing to their vibrant hues and properties.
Used in Food Industry:
Fluorescein is used as a coloring agent in the food industry, providing bright and attractive colors to various food products.
Used in Cosmetics Industry:
In the cosmetics industry, 1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one is used as a coloring agent, adding vibrant shades to various cosmetic products while maintaining their safety and quality.
Overall, 1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one, or fluorescein, is a versatile and indispensable tool in scientific, industrial, and consumer applications due to its unique fluorescent properties and wide range of uses.

Check Digit Verification of cas no

The CAS Registry Mumber 15222-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15222-53:
(7*1)+(6*5)+(5*2)+(4*2)+(3*2)+(2*5)+(1*3)=74
74 % 10 = 4
So 15222-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O5/c1-8-4-9(19-2)6-12-14(8)16(18)15-11(17)5-10(20-3)7-13(15)21-12/h4-7,17H,1-3H3

15222-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name lichexanthone

1.2 Other means of identification

Product number -
Other names Lichexanthone

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:15222-53-4 SDS

15222-53-4Relevant academic research and scientific papers

Depsidone Synthesis. Part 21. A New Synthesis of Grisa-2',5'-diene-3,4'-diones

Sargent, Melvyn V.

, p. 403 - 411 (2007/10/02)

Treatment of suitably substituted methyl 2-phenoxybenzoates with titanium(IV) chloride and dry hydrogen chloride afforded grisa-2',5'-diene-3,4'-diones in high yield.The structures of these compounds followed from their thermal stability, their methanolysis to methyl 2-(4-hydroxyphenoxy)benzoates, and their reductive cleavage to 2,4'-dihydrobenzophenones.Treatment of the benzophenones with base gave xanthones.An attempt to synthesize dehydrogriseofulvin (1) by this method failed.

Synthesis of Grisa-2',5'-dien-3,4'-diones by Intramolecular ipso-Substitution

Sargent, Melvyn

, p. 285 (2007/10/02)

Appropriately substituted o-phenoxybenzoic esters on treatment with dry hydrogen chloride and titanium(IV) chloride in dichloromethane yield grisa-2',5'-dien-3,4'-diones by intramolecular ipso-substitution.

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