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3,3,5,5-Tetramethyl-1,2,4-trithiolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38348-31-1

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38348-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38348-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,4 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38348-31:
(7*3)+(6*8)+(5*3)+(4*4)+(3*8)+(2*3)+(1*1)=131
131 % 10 = 1
So 38348-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12S3/c1-5(2)7-6(3,4)9-8-5/h1-4H3

38348-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5,5-tetramethyl-1,2,4-trithiolane

1.2 Other means of identification

Product number -
Other names tetramethyl-[1,2,4]trithiolane

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:38348-31-1 SDS

38348-31-1Downstream Products

38348-31-1Relevant academic research and scientific papers

Studies on the low-temp oxidation of coal containing organic sulfur and the corresponding model compounds

Zhang, Lanjun,Li, Zenghua,Li, Jinhu,Zhou, Yinbo,Yang, Yongliang,Tang, Yibo,McPhee, Derek J.

, p. 22241 - 22256 (2016/01/25)

This paper selects two typical compounds containing organic sulfur as model compounds. Then, by analyzing the chromatograms of gaseous low-temp oxidation products and GC/MS of the extractable matter of the oxidation residue, we summarizing the mechanism of low-temp sulfur model compound oxidation. The results show that between 30 °C to 80 °C, the interaction between diphenyl sulfide and oxygen is mainly one of physical adsorption. After 80 °C, chemical adsorption and chemical reactions begin. The main reaction mechanism in the low-temp oxidation of the model compound diphenyl sulfide is diphenyl sulfide generates diphenyl sulfoxide, and then this sulfoxide is further oxidized to diphenyl sulphone. A small amount of free radicals is generated in the process. The model compound cysteine behaves differently from diphenyl sulfide. The main reaction low-temp oxidation mechanism involves the thiol being oxidized into a disulphide and finally evolving to sulfonic acid, along with SO2 being released at 130 °C and also a small amount of free radicals. We also conducted an experiment on coal from Xingcheng using X-ray photoelectron spectroscopy (XPS). The results show that the major forms of organic sulfur in the original coal sample are thiophene and sulfone. Therefore, it can be inferred that there is none or little mercaptan and thiophenol in the original coal. After low-temp oxidation, the form of organic sulfur changes. The sulfide sulfur is oxidized to the sulfoxide, and then the sulfoxide is further oxidized to a sulfone, and these steps can be easily carried out under experimental conditions. What's more, the results illustrate that oxidation promotes sulfur element enrichment on the surface of coal.

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