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4253-99-0

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4253-99-0 Usage

Description

DI-N-AMYL SULFOXIDE, with the molecular formula C10H23OS, is a versatile chemical compound that exhibits a broad solubility in both organic and inorganic solvents. This makes it a valuable asset in various industries, including pharmaceuticals and industrial applications. Its potential medicinal properties, such as anti-inflammatory and antioxidant effects, further enhance its appeal for the development of new drugs.

Uses

Used in Pharmaceutical Industry:
DI-N-AMYL SULFOXIDE is used as a solvent for the development of new drugs due to its wide range of solubility in different solvents. Its potential medicinal properties, including anti-inflammatory and antioxidant effects, make it a promising candidate for the creation of innovative pharmaceutical formulations.
Used in Industrial Applications:
In the industrial sector, DI-N-AMYL SULFOXIDE is utilized as a solvent for various processes. Its versatility in solubility allows it to be employed in a range of applications, making it a valuable component in the development and manufacturing of different products.

Check Digit Verification of cas no

The CAS Registry Mumber 4253-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4253-99:
(6*4)+(5*2)+(4*5)+(3*3)+(2*9)+(1*9)=90
90 % 10 = 0
So 4253-99-0 is a valid CAS Registry Number.

4253-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pentylsulfonylpentane

1.2 Other means of identification

Product number -
Other names DI-n-AMYL SULFOXIDE

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:4253-99-0 SDS

4253-99-0Downstream Products

4253-99-0Relevant articles and documents

A novel binuclear iron(III)-salicylaldazine complex; synthesis, X-ray structure and catalytic activity in sulfide oxidation

Akbari, Ali,Amini, Mojtaba,Bagherzadeh, Mojtaba,Ellern, Arkady,Mesbahi, Elnaz,Woo, L. Keith

, (2020/04/08)

A novel binuclear iron(III)-salicylaldazine complex has been synthesized and characterized by various techniques such as IR and UV–Vis spectroscopy and X-ray crystallography. The catalytic oxidation of sulfides in the presence of the aforementioned complex was explored at room temperature using urea hydrogen peroxide (UHP) as an oxidant. Effects of different reaction conditions consisting catalyst and oxidant amount, solvent effect and reaction time on the catalytic activity and selectivity in the reaction of methylphenylsulfide oxidation has been surveyed. Perfect selectivity toward sulfoxide was achieved after 15 min in CH3CN by choice of a properly optimized reaction condition.

Kinetics and Mechanism of Oxidation of Dipentyl and Diphenyl Sulphoxides with Nitric Acid in Acetic Acid-Water Medium

Bhatta, D.,Behera, S. M.,Mohanty, S. R.

, p. 776 - 777 (2007/10/02)

The title reaction shows first order dependence each in and and the active oxidant species is found to be HNO3.The reaction involves an electron transfer from the sulphoxide to the oxidant resulting in the formation of a radical cation in the rate-determining step, which gives rise to a dication in a fast step followed by hydrolysis and deprotonation to form the sulphone.

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