• Dimethyl sulphoxide

Dimethyl sulphoxide

  • CasNo:67-68-5
  • Purity:99%

Product Details;

CasNo: 67-68-5

Molecular Formula: C2H6OS

Appearance: colorless liquid

67-68-5 Wholesale Price Powder Safe Transportation

  • Molecular Formula:C2H6OS
  • Molecular Weight:78.135
  • Appearance/Colour:colorless liquid 
  • Melting Point:18.4 °C 
  • Refractive Index:n20/D 1.479(lit.)  
  • Boiling Point:189 °C at 760 mmHg 
  • Flash Point:85 °C 
  • PSA:36.28000 
  • Density:1.1 g/cm3 
  • LogP:0.86040 

Dimethyl sulphoxide(Cas 67-68-5) Usage

 

 

History and Use

Dimethyl Sulfoxide (DMSO) has a long history of use as a polar solvent and active pharmaceutical ingredient. It is widely used for its excellent solvent properties.

Chemical Structure and Decomposition

DMSO can decompose autocatalytically, with the chemical structure and function of the autocatalyst still under debate.
Thermal decomposition of DMSO produces several organic and inorganic acids, with DMSO acting as both an oxidizer and a reactant in their formation.
The presence of acids generated in situ serves as autocatalysts for the thermal decomposition of DMSO.

Environmental Friendliness and Safety

DMSO is considered more environmentally friendly and harmless to the human body compared to N, N-dimethylformamide (DMF). It is classified as class 3 (nontoxic) by regulatory authorities like the United States Food and Drug Administration (FDA) and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH).

Applications

DMSO is widely used as a nonaqueous solvent, particularly in the life sciences, where it serves as a vehicle for hydrophobic compounds and as a cryoprotectant for cell storage. Its high complexation ability and solubility make it suitable for various applications, including in perovskite solutions.

Toxicity and Effects on Cells

Despite its widespread use, DMSO is somewhat toxic and can affect cell behaviors in various ways.
Mechanistically, DMSO binds to proteins in the cytoplasm or nucleus, disrupting their functions and potentially leading to apoptosis.
While indispensable, DMSO is not without its drawbacks and should be used with caution in biological applications.

General Description

Dimethyl sulfoxide (DMSO) is a highly polar and aprotic organic compound that is a colorless and odorless liquid. It is commonly used as a powerful solvent and has a wide range of applications in industrial, pharmaceutical and laboratory settings. DMSO is known for its ability to easily penetrate biological membranes and can be used as a vehicle for drug delivery. It is also used in the preservation of stem cells and tissues, as well as in cryopreservation due to its ability to prevent ice crystal formation. Additionally, DMSO has anti-inflammatory and analgesic properties, making it a popular choice for topical pain relief and anti-inflammatory treatments. However, it is important to handle DMSO with caution as it can easily absorb through the skin and can carry other substances into the body.

InChI:InChI=1/C2H6OS/c1-4(2)3/h1-2H3

67-68-5 Relevant articles

-

Addison,Sheldon

, p. 2705,2708 (1956)

-

Synthesis and reactivity of two new trichloromethyl substituted dihydroisoquinoline-derived oxaziridines

Aydi, Rihab,Kammoun, Majed

, p. 134 - 144 (2016)

N-Alkyl oxaziridines may be used as reag...

Magnetic nanoparticles supported Cu2+ and Ce3+ complexes: toward the chemical and electrochemical oxidation of alcohol and sulfide derivatives

Tamoradi, Taiebeh,Navaee, Aso,Salimi, Abdollah,Mousavi, Seyedeh Masoumeh,Ghadermazi, Mohammad,Veisi, Hojat

, p. 4517 - 4530 (2019)

Abstract: Heterogeneous catalysts are mo...

Ozone and oxygen atom reactions with dimethylsulfide and methanethiol in argon matrices

Tevault, D. E.,Mowery, R. L.,Smardzewski, R. R.

, p. 4480 - 4487 (1981)

Ground state oxygen atoms, generated by ...

Kinetics and mechanism of the oxidation of dimethyl sulfide by hydroperoxides in aqueous medium: Study on the potential contribution of liquid-phase oxidation of dimethyl sulfide in the atmosphere

Amels, Peter,Elias, Horst,Wannowius, Klaus-Juergen

, p. 2537 - 2544 (1997)

Conventional and multi-wavelength stoppe...

THE CHEMISTRY OF 3-TRIFLUOROMETHYL-PERFLUORO-AZA-2-BUTENE AND THE SYNTHESIS OF A NEW OXAZIRIDINE: 3,3-BISTRIFLUOROMETHYL-2-TRIFLUOROMETHYLOXAZIRIDINE

Bragante, Letanzio,Desmarteau, Darryl D.

, p. 181 - 197 (1991)

Some reactions of (CF3)2C=NCF3 1 (3-trif...

Thermal analysis, phase transitions and molecular reorientations in [Fe(OS(CH3)2)6](ClO4)2

Szostak, El?bieta,Migda?-Mikuli, Anna

, p. 1151 - 1158 (2017)

Thermogravimetric analysis connected wit...

Fast oxidation of organic sulfides by hydrogen peroxide by in situ generated peroxynitrous acid

Vayssie, Stephane,Elias, Horst

, p. 2088 - 2090 (1998)

-

Selective oxidation of alcohols and sulfides: Via O2using a Co(ii) salen complex catalyst immobilized on KCC-1: Synthesis and kinetic study

Allahresani, Ali,Hemmat, Kaveh,Naghdi, Elaheh,Nasseri, Mohammad Ali

, p. 37974 - 37981 (2020)

The aim of this study was to immobilize ...

Chemoselective methyltrioxorhenium(VII)-catalyzed sulfoxidations with hydrogen peroxide

Adam, Waldemar,Mitchell, Catherine M.,Saha-Moeller, Chantu R.

, p. 13121 - 13124 (1994)

The selective oxidation of sulfides to s...

Synthesis of a Novel μ-Oxo Binuclear Copper(II) Complex Ligated by Hydrotris(3,5-dimethyl-1-pyrazolyl)borate

Kitajima, Nobumasa,Koda, Takayuki,Moro-Oka, Yoshihiko

, p. 347 - 350 (1988)

A novel μ-oxo binuclear copper(II) compl...

Copper based on diaminonaphthalene-coated magnetic nanoparticles as robust catalysts for catalytic oxidation reactions and C-S cross-coupling reactions

Yarmohammadi, Nasrin,Ghadermazi, Mohammad,Mozafari, Roya

, p. 9366 - 9380 (2021/03/16)

In this work, the immobilization of copp...

Synthesis and Characterization of Magnetic Functionalized Ni and Cu Nano Catalysts and Their Application in Oxidation, Oxidative Coupling and Various Multi-Component Reactions

Hajjami, Maryam,Sheikhaei, Shiva,Gholamian, Fatemeh,Yousofvand, Zakieh

, p. 2420 - 2435 (2021/01/04)

Abstract: Two magnetic nano catalysts of...

l-Arginine complex of copper on modified core–shell magnetic nanoparticles as reusable and organic–inorganic hybrid nanocatalyst for the chemoselective oxidation of organosulfur compounds

Nikoorazm, Mohsen,Moradi, Parisa,Noori, Nourolah,Azadi, Gouhar

, p. 467 - 478 (2020/09/01)

In this paper, we report the fabrication...

Trialkylammonium salt degradation: Implications for methylation and cross-coupling

Assante, Michele,Baillie, Sharon E.,Juba, Vanessa,Leach, Andrew G.,McKinney, David,Reid, Marc,Washington, Jack B.,Yan, Chunhui

, p. 6949 - 6963 (2021/06/02)

Trialkylammonium (most notably N,N,N-tri...

67-68-5 Process route

water
7732-18-5

water

bromo-dimethyl sulfonium ; nitrate

bromo-dimethyl sulfonium ; nitrate

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

nitric acid
7697-37-2,78989-43-2

nitric acid

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

dimethyl sulfoxide

Conditions
Conditions Yield
 
 
dimethylbromosulphonium bromide
50450-21-0

dimethylbromosulphonium bromide

Benzaldoxime
932-90-1

Benzaldoxime

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

dimethyl sulfoxide

benzonitrile
100-47-0

benzonitrile

Conditions
Conditions Yield
In acetonitrile; at 20 ℃; for 5.5h;
94%

67-68-5 Upstream products

  • 75-18-3
    75-18-3

    dimethylsulfide

  • 1774-47-6
    1774-47-6

    trimethylsulfoxonium iodide

  • 13904-95-5
    13904-95-5

    S,S-dimethylsulfodiimide

  • 42429-63-0
    42429-63-0

    3,4-dihydroisoquinoline 1,2-oxide

67-68-5 Downstream products

  • 16437-69-7
    16437-69-7

    (methylthio)methyl acetate

  • 19207-88-6
    19207-88-6

    benzoyloxy-methylsulfanyl-methane

  • 603-54-3
    603-54-3

    N,N-diphenylurea

  • 102-07-8
    102-07-8

    bis(diphenyl)urea

Inquiry

Name:
*CompanyName:
*Email:
*Requirements:
*Code:
Submit