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Dimethyl sulfone

  • Product Name: Dimethyl sulfone
  • CasNo: 67-71-0
  • Purity:
  • Appearance: colourless crystals

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CasNo: 67-71-0

Molecular Formula: C2H6O2S

Appearance: colourless crystals

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  • Molecular Formula:C2H6O2S
  • Molecular Weight:94.1344
  • Appearance/Colour:colourless crystals 
  • Vapor Pressure:0.0573mmHg at 25°C 
  • Melting Point:107-109 °C(lit.) 
  • Refractive Index:1.4775 - 1.4790 
  • Boiling Point:240.9 °C at 760 mmHg 
  • PKA:28(at 25℃) 
  • Flash Point:132.7 °C 
  • PSA:42.52000 
  • Density:1.139 g/cm3 
  • LogP:0.74160 

Dimethyl sulfone(Cas 67-71-0) Usage

Purification methods

Using different purification methods, the products contained different impurities. in the finished product is different purification methods are also different. In general, it is decolored by active carbon, demineralized by ion exchange, and then recrystallized the solvent, dried by vacuum. After that, it is sieved and added an antistatic agent and a slip agent, in order to meet the export requirements. There is no national or ministerial standards. Currently, the countries in the world continue to enforce corporate standards or contract specifications.

chemical synthesis

Dimethyl sulfone is obtained by oxidizing methyl sulfone using nitric acid as oxidation. Methyl sulfone was oxidized at 140-145 ℃ by nitric oxide. After completion of the reaction, It was cooled and filtered to give white needles crude. Then vacuum distillation, collecting 138-145 ℃ (98.42kPa) distillate products which are the finished goods.

Synthesis Reference(s)

Journal of the American Chemical Society, 91, p. 3992, 1969 DOI: 10.1021/ja01042a075

Purification Methods

Crystallise the sulfone from water. Dry it over P2O5. [Beilstein 1 IV 1279.]

description

Dimethyl Sulfone (MSM) is an organic sulfur-containing compound that occurs naturally in a variety of fruits, vegetables, grains, and animals including humans. a white, odorless, slightly bitter-tasting crystalline substance containing 34-percent elemental sulfur, MSM is a normal oxidative metabolite product of dimethyl sulfoxide (DMSO). Cow’s milk is the most abundant source of MSM, containing approximately 3.3 parts per million (ppm). Other foods containing MSM are coffee (1.6 ppm), tomatoes (trace to 0.86 ppm), tea (0.3 ppm), Swiss chard (0.05-0.18 ppm), beer (0.18 ppm), corn (up to 0.11 ppm), and alfalfa (0.07 ppm).MSM has been isolated from plants such as Equisetum arvense, also known as horsetail. Dimethyl Sulfone has the ability to enhance the body to produce insulin, while it can promote carbohydrate metabolism. It is essential for the synthesis of human collagen. It can not only promote wound healing, but also contribute for metabolic and neurological health requirement of vitamin B and vitamin C, biotin synthesis and activation, so it is known as "naturally beautiful carbon material". Dimethyl Sulfone exists in human skin, hair, nails, bones, muscles and various organs. Once people who are lack of it will get health disorders or diseases. It is the main substance for people to maintain the balance of biological sulfur. It has therapeutic value and healthcare function for people. It is an essential drug for human survial and health protection.

application

Dimethyl sulfone can eliminate the virus, enhance blood circulation, soften tissue, relieve pain, strengthen sinews and bones, calm the spirit, enhance physical strength, maintain skin, make beauty salons, treat the arthritis, oral ulcers, asthma and constipation, dredge the blood vessels, Clear gastrointestinal toxins. Dimethyl sulfone can be used as food and feed additives to supplement the organic sulfur nutrients for humans, pets and livestock. For external use, it can make the skin smooth, supple muscles, and reduce pigmentation. Recently, it surges in the amount as the cosmetic additives. In medicine, it has a good analgesic, it can promote wound healing and others. Dimethyl sulfone is a good penetrant in medicines production.

Chemical properties

white needle-like crystals. Melting point 109 ℃, boiling point 238 ℃, relative density 1.1702 (110/0 ℃), refractive index 1.4226, flash point 143 ℃. Soluble in water, ethanol, benzene, methanol and acetone, slightly soluble in ether and chloroform. Stink.

InChI:InChI=1/C2H6O2S/c1-5(2,3)4/h1-2H3

67-71-0 Relevant articles

Kinetics and mechanism of oxidation of dimethyl sulphoxide by mono- and di-substituted N,N-dichlorobenzenesulphonamides in aqueous acetic acid

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In an effort to introduce N,N-dichloroar...

Kinetics and mechanism of oxidation of dimethyl sulfoxide with benzoyl peroxide in superbasic media

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, p. 885 - 889 (2004)

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, p. 574 - 575 (1998)

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Synthesis method of sulfone compound

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Paragraph 0025-0029, (2020/01/25)

The invention discloses a synthesis meth...

67-71-0 Process route

5-phenyl-1,3-dithiane 1,1,3,3-tetraoxide
111012-66-9

5-phenyl-1,3-dithiane 1,1,3,3-tetraoxide

dimethylsulfone
67-71-0

dimethylsulfone

bis(methylsulfonyl)methane
1750-62-5

bis(methylsulfonyl)methane

benzaldehyde
100-52-7

benzaldehyde

acetophenone
98-86-2

acetophenone

Conditions
Conditions Yield
With sodium hydroxide; at 100 ℃; for 8h; Product distribution;
52 % Turnov.
11 % Turnov.
dimethylsulfide
75-18-3

dimethylsulfide

dimethylsulfone
67-71-0

dimethylsulfone

dimethyl sulfoxide
67-68-5,8070-53-9

dimethyl sulfoxide

Conditions
Conditions Yield
With C30H24N2O7W; dihydrogen peroxide; In dichloromethane; water; for 1h; Reflux;
6%
94%
With dihydrogen peroxide; In ethanol; hexane; water; at 60 ℃; for 0.0833333h;
92%
6%
With dihydrogen peroxide; In water; at 30 - 35 ℃; for 24h; Sealed tube; Green chemistry;
68%
62%
With 3-hydroperoxy-3-methyl-1-phenylindolin-2-one; In dichloromethane; for 2h; Heating;
24%
49%
With 1,1,4,4-Tetramethyl-2,3-dioxa-1,4-disilacyclohexane; In Petroleum ether; at 50 ℃; for 12h;
19%
15%
With tert.-butylhydroperoxide; aluminum tri-tert-butoxide; In benzene;
17%
With oxaziridinium salt 1; In [D3]acetonitrile; at 20 ℃;
3 % Spectr.
94 % Spectr.
With 3,3-bistrifluoromethyl-2-trifluoromethyl-oxaziridine; In chloroform-d1; trichlorofluoromethane; at -30 ℃; for 0.333333h;
0.4 % Spectr.
75 % Spectr.
With bis-[(trifluoroacetoxy)iodo]benzene; In chloroform; at 20 ℃; for 12h;
15 % Spectr.
45 % Spectr.
With dihydrogen peroxide; methyltrioxorhenium(VII); In chloroform-d1; at 20 ℃; for 24h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
 
With ozone; In solid matrix; at -263.2 ℃; Mechanism; Irradiation; also methanethiol;
 
With dihydrogen peroxide; methyltrioxorhenium(VII); In chloroform-d1; at 20 ℃; for 24h; Product distribution; reactions of derivatives under var. conditions;
 
With dihydrogen peroxide; In water; at 19.9 ℃; Product distribution; Mechanism; Kinetics; other reagents, pH dependence;
 
With oxaziridinium salt 1; In [D3]acetonitrile; at 20 ℃; for 1.5h;
10 % Spectr.
90 % Spectr.
With dihydrogen peroxide; Further Variations:; Temperatures; molar ratio; Product distribution;
 
With cis-VI(6,6'-Cl2bpy)2O2>; In acetonitrile; at 20 ℃; for 0.5h;
68 % Chromat.
9 % Chromat.
With dihydrogen peroxide; at 5 ℃; for 0.166667h; Further Variations:; Temperatures; Product distribution;
 
With nitric acid; In acetonitrile; at 20 ℃; for 15h; chemoselective reaction;
 
With dihydrogen peroxide; In methanol; at 20 ℃; for 0.25h; chemoselective reaction;
 
With dihydrogen peroxide; In acetonitrile; at 20 ℃; for 0.5h;
 
With C38H26N6NiS2(2+)*2NO3(1-); dihydrogen peroxide; In water; acetonitrile; at 20 ℃;
 
With 3-chloro-benzenecarboperoxoic acid; In chloroform-d1;
 
With (η5-C5H5)Mo(CO)3C2Ph; dihydrogen peroxide; In acetonitrile; at 20 ℃; for 2h; Inert atmosphere; Schlenk technique;
 
With dihydrogen peroxide; In acetonitrile; at 20 ℃; for 1h; Catalytic behavior;
 
With ozone; In acetone; at 60 ℃; for 2h; under 3750.38 Torr; Solvent; Pressure; Temperature; Reagent/catalyst;
 
With bismuth oxybromide; oxygen; In acetonitrile; for 12h; under 750.075 Torr; Irradiation;
 
With dihydrogen peroxide; In methanol; at 30 ℃; for 600h; under 1125.11 Torr; Reagent/catalyst; Solvent; Temperature; Molecular sieve;
 
With dihydrogen peroxide; [Ni0.5(1-vinylimidazole)2]3[Ni0.5(1-vinylimidazole)H2O][V4O12]*H2O; In ethanol; water; at 45 ℃; for 4h;
 
With water; dihydrogen peroxide; C16H17MoN3O6; In ethanol;
 

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