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13676-91-0

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13676-91-0 Usage

Description

1,8-Bis(phenylthio)-9,10-anthracenedione is an organic compound with the molecular formula C28H16O2S2. It is characterized by its red light yellow color and has a melting point of 315°C. 1,8-Bis(phenylthio)-9,10-anthracenedione exhibits stable properties, with no significant changes observed when exposed to water, 5% sodium carbonate, or 5% hydrochloric acid. It has a light fastness rating of ISO 8, indicating its resistance to fading under the Carbon arc lamp.

Uses

Used in Dye Industry:
1,8-Bis(phenylthio)-9,10-anthracenedione is used as a dyestuff for its red light yellow color. Its stability in various conditions makes it suitable for use in the dye industry to produce colorfast products.
Used in Chemical Research:
Due to its unique chemical structure and properties, 1,8-Bis(phenylthio)-9,10-anthracenedione can be used as a research compound in the field of organic chemistry. It may be utilized in the development of new synthetic methods, the study of reaction mechanisms, or the investigation of its potential applications in various chemical processes.
Used in Photochemical Applications:
The light fastness rating of 1,8-Bis(phenylthio)-9,10-anthracenedione suggests that it may have potential applications in photochemical processes where resistance to light-induced degradation is required. This could include uses in the development of light-sensitive materials or in the study of photochemical reactions.
Used in Material Science:
The heat-resistant nature of 1,8-Bis(phenylthio)-9,10-anthracenedione, with a melting point of 315°C, indicates that it may be useful in material science applications where high-temperature stability is required. This could include the development of new high-temperature materials or the study of thermal properties in various applications.

Preparation

1,8-Dichloroanthracene-9,10-dione and Benzenethiol (2 Moore) condensation.

Flammability and Explosibility

Notclassified

Standard

Light Fastness

Melting point

Stable

ISO

8(Carbon arc lamp)

Check Digit Verification of cas no

The CAS Registry Mumber 13676-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13676-91:
(7*1)+(6*3)+(5*6)+(4*7)+(3*6)+(2*9)+(1*1)=120
120 % 10 = 0
So 13676-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H12O2S2/c23-21-15-7-1-5-13(17-9-3-11-25-17)19(15)22(24)20-14(6-2-8-16(20)21)18-10-4-12-26-18/h1-12H

13676-91-0SDS

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 1,8-Bis(phenylthio)-9,10-anthracenedione

1.2 Other means of identification

Product number -
Other names C.I.Solvent Yellow 163

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:13676-91-0 SDS

13676-91-0Downstream Products

13676-91-0Relevant articles and documents

Method for producing solvent yellow 163 dye

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Paragraph 0026, (2018/10/27)

The invention relates to a method for producing a solvent yellow 163 dye. The method comprises (a) adding an organic solvent, chlorobenzene, a hydrosulfiding reagent and an auxiliary agent into a reaction vessel, stirring to dissolve materials to obtain a first mixture, and then heating the first mixture to 100-150 DEG C until the reaction end point, (b) cooling the product to 40 to 50 DEG C, directly adding 1, 8-dinitroguanidine into the product, and carrying out stirring for a reaction until the end point, (c) cooling the product to 20 to 35 DEG C and carrying out suction filtration to obtain filter cake and a filtrate, and (d) washing and soaking the filter cake through a separation solvent, mixing the soaking solution and the filtrate, carrying out distillation recovery, washing the filter cake through hot water until pH of 7 and carrying out drying. The method solves the problem of the logistics and storage costs caused by the difficulty in purchasing thiophenols due to environmental protection. The thiophenol intermediate is prepared through a one-bath method so that the normal production is ensured. The method greatly reduces the production cost by about 30-40% and has goodeconomic benefits.

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