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2320-38-9

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2320-38-9 Usage

Description

2',4',5',7'-tetrachlorofluorescein is a synthetic organic compound that exhibits blue fluorescence under UV light and changes to pink when exposed to visible light. It is insoluble in water but soluble in a 10% sodium hydroxide solution. 2',4',5',7'-tetrachlorofluorescein has a stable melting point and is characterized by its poor light fastness and heat resistance.

Uses

Used in Research and Diagnostic Applications:
2',4',5',7'-tetrachlorofluorescein is used as a fluorescent marker in various research and diagnostic applications due to its unique optical properties. It can be used to label biological molecules, such as proteins or nucleic acids, allowing for their detection and tracking under specific light conditions.
Used in Environmental Testing:
2',4',5',7'-tetrachlorofluorescein is used as an indicator in environmental testing to measure water quality and pollution levels. Its fluorescence properties make it an effective tool for detecting the presence of contaminants in water samples.
Used in Chemical Synthesis:
2',4',5',7'-tetrachlorofluorescein can be used as a starting material or intermediate in the synthesis of other fluorescent dyes and compounds. Its unique chemical structure allows for further modification and functionalization to create new molecules with specific properties and applications.
Used in Quality Control:
2',4',5',7'-tetrachlorofluorescein can be used in quality control processes to test the effectiveness of various chemicals, such as sodium carbonate and hydrochloric acid, in their ability to dissolve or react with the compound. This information can be useful in determining the suitability of these chemicals for specific industrial applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2',4',5',7'-tetrachlorofluorescein is used as a reference standard for the development and validation of analytical methods. Its unique properties make it an ideal candidate for assessing the performance of chromatographic and spectroscopic techniques used in the analysis of pharmaceutical products.
Used in Analytical Chemistry:
2',4',5',7'-tetrachlorofluorescein is used as a reference material in analytical chemistry to calibrate and validate instruments used for fluorescence measurements. Its stable melting point and known optical properties make it a reliable standard for ensuring the accuracy and precision of these instruments.

Preparation

2,4-Dichlororesorcinol (2 Moore) and Phthalic anhydride (1 Moore) condensation, with Sodium hydroxide extraction segregating out 2 ‘, 4 ‘, 5 ‘, 7 ‘- tetrachlorofluorescein?(melting point of 296 ~ 305 ℃), then use Hydrochloric acid acidification.

Standard

Light Fastness

Melting point

Stable

ISO

Poor

Check Digit Verification of cas no

The CAS Registry Mumber 2320-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2320-38:
(6*2)+(5*3)+(4*2)+(3*0)+(2*3)+(1*8)=49
49 % 10 = 9
So 2320-38-9 is a valid CAS Registry Number.

2320-38-9SDS

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 2',4',5',7'-tetrachloro-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one

1.2 Other means of identification

Product number -
Other names 2',4',5',7'-Tetrachlorofluorescein

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:2320-38-9 SDS

2320-38-9Downstream Products

2320-38-9Relevant articles and documents

PROCESS FOR SYNTHESIZING HALOGENATED DERIVATIVES OF FLUORESCEIN FOR USE IN THE PRODUCTION OF NON-VOLATILE MEMORY DEVICES

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Page/Page column 7-8, (2008/06/13)

A process performs solid phase synthesis of halogenated derivatives of fluorescein, and includes reacting fluorescein with a halide MX, wherein M is an alkali metal and X is a halogen, and Oxone? (2 KHSO5.KHSO4.K2SO4), at a temperature higher than or equal to 150° C. A structure uses a halogenated derivative of fluorescein selected from the group consisting of 2′,4′,5′-trichlorofluorescein, 2′,4′,5′,7′-tetrachlorofluorescein, 4′,5′-diiodofluorescein diacetate and 2′,4′,5′-triiodofluorescein as electro-bistable material in a non-volatile memory device.

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