What is the Bis(methylthio)methane?

Bis(methylthio)methane is Clear colourless to pale yellow liquid, while it's Molecular Formula is C3H8S2. Clear colourless to pale yellow liquid Bis(methylthio)methane is used in method for reducing odor in room in remodeling work by removing causative substances.

What is the CAS number for Bis(methylthio)methane?

The CAS number of Bis(methylthio)methane is 1618-26-4.

What is Bis(methylthio)methane (1618-26-4) used for?

Bis(methylthio)methane, also known as bis(methylthiomethyl) disulfide, is an organic compound with the chemical formula C3H8S2. It is a clear, colorless to pale yellow liquid at room temperature and is characterized by a mustard-like odor. Bis(methylthio)methane has been reported to be found in various natural sources such as Camembert and Gruyere cheeses, milk, fish oil, cooked and canned beef, shitake mushroom, truffle, prawn, and lobster.InChI:InChI=1/C3H8S2/c1-4-3-5-2/h3H2,1-2H3

What is the Bis(methylthio)methane?

Bis(methylthio)methane is Clear colourless to pale yellow liquid, while it's Molecular Formula is C3H8S2. Clear colourless to pale yellow liquid Bis(methylthio)methane is used in method for reducing odor in room in remodeling work by removing causative substances.

What is the CAS number for Bis(methylthio)methane?

The CAS number of Bis(methylthio)methane is 1618-26-4.

What is Bis(methylthio)methane (1618-26-4) used for?

Bis(methylthio)methane, also known as bis(methylthiomethyl) disulfide, is an organic compound with the chemical formula C3H8S2. It is a clear, colorless to pale yellow liquid at room temperature and is characterized by a mustard-like odor. Bis(methylthio)methane has been reported to be found in various natural sources such as Camembert and Gruyere cheeses, milk, fish oil, cooked and canned beef, shitake mushroom, truffle, prawn, and lobster.InChI:InChI=1/C3H8S2/c1-4-3-5-2/h3H2,1-2H3

Detailed introduction

China cas 1618-26-4 manufacturer wholesale Bis(methylthio)methane at affordable price

Molecular Formula:C3H8S2
Molecular Weight:108.229
Appearance/Colour:Clear colourless to pale yellow liquid
Vapor Pressure:5.71mmHg at 25°C
Melting Point:-20.5ºC
Refractive Index:n20/D 1.53(lit.)
Boiling Point:146.999 °C at 760 mmHg
Flash Point:43.889 °C
PSA：50.60000
Density:1.021 g/cm³
LogP:1.66990

Bis(methylthio)methane(Cas 1618-26-4) Usage

Flammability and Explosibility	Notclassified
Purification Methods	Work in an efficient fume cupboard as the substance may contain traces (or more) of methylmercaptan which has a very bad odour. Dissolve the mercaptal in Et2O, shake it with aqueous alkalis then dry it over anhydrous K2CO3, filter and distil it over K2CO3 under a stream of N2. If the odour is very strong, then allow all gas efluents to bubble through 5% aqueous NaOH solution which is then treated with dilute KMnO4 in order to oxidise MeSH to odourless products. UV: max 238 nm (log 2.73) [Fehnel & Carmack J Am Chem Soc 71 90 1949, Fehér & Vogelbruch Chem Ber 91 996 1958, B.hme & Marz Chem Ber 74 1672 1941]. Oxidation with aqueous KMnO4 yields bis-(methylsulfonyl)methane which has m 142-143o [Fiecchi et al. Tetrahedron Lett 1681 1967]. [Beilstein 1 IV 3088.]
General Description	The liquid structure of bis(methylthio)methane at room temperature was studied by the bonding and non-bonding interatomic potential functions (FMP-RMC) simulation.

InChI:InChI=1/C3H8S2/c1-4-3-5-2/h3H2,1-2H3

1618-26-4 Relevant articles

Stereoelectronic Effects in the Gas Phase. 2. Negative Ion Reactions of 1,3-Dithianes and 1,3-Dithiane 1-Oxides

Fisher, Cindy L.,Kahn, Scott D.,Hehre, Warren J.,Caserio, Marjorie C.

, p. 7379 - 7387 (1989)

Reactions of gaseous anions (methoxide, ...

Transformation of dimethyl Sulfoxide into bis(methylsulfanyl)methane

Zaraiskii,Zaraiskaya,Velichko,Anikeeva

, p. 1728 - 1729 (2007)

-

Haszeldine,R.N. et al.

, p. 249 - 250 (1972)

Formation of Dithioacetals by Treatment of Sulfoxides Carrying α-Hydrogens with Magnesium Amides

Kobayashi, Kazuhiro,Kawakita, Masataka,Mannami, Tohru,Morikawa, Osamu,Konishi, Hisatoshi

, p. 1551 - 1554 (1994)

Sulfoxides carrying α-hydrogens were all...

Static and dynamic structures of pentacarbonyl-chromium(0) and -tungsten(0) complexes of dithioether ligands I. Symmetrical dithioether complexes and X-ray crystal structure of

Abel, Edward W.,Orrell, Keith G.,Rahoo, Haji,Sik, Vladimir,Mazid, Mohammed A.,Hursthouse, Michael B.

, p. 191 - 199 (1992)

The complexes (M=Cr, R=Et, iPr, t-Bu; M...

Effect of Zinc Oxide on the Thermal Decomposition of Dimethyl Sulfoxide

Chen, Liping,Chen, Wanghua,Guo, Zichao,Li, Huabo,Weng, Shichun,Wu, Wenqian

, (2022/03/14)

Dimethyl sulfoxide (DMSO) is widely used...

Photocatalytic Deoxygenation of Sulfoxides Using Visible Light: Mechanistic Investigations and Synthetic Applications

Clarke, Aimee K.,Parkin, Alison,Rossi-Ashton, James A.,Taylor, Richard J. K.,Unsworth, William P.

, p. 5814 - 5820 (2020/07/21)

The photocatalytic deoxygenation of sulf...

Nickel phosphide nanoalloy catalyst for the selective deoxygenation of sulfoxides to sulfides under ambient H2pressure

Fujita, Shu,Mitsudome, Takato,Mizugaki, Tomoo,Yamaguchi, Sho,Yamasaki, Jun,Yamazoe, Seiji

supporting information, p. 8827 - 8833 (2020/11/23)

Exploring novel catalysis by less common...

Rh-Catalyzed Hydrogenation of CO2 to Formic Acid in DMSO-based Reaction Media: Solved and Unsolved Challenges for Process Development

Jens, Christian M.,Scott, Martin,Liebergesell, Bastian,Westhues, Christian G.,Sch?fer, Pascal,Franciò, Giancarlo,Leonhard, Kai,Leitner, Walter,Bardow, André

supporting information, p. 307 - 316 (2018/11/10)

Process concepts have been conceived and...

1618-26-4 Process route

: 925-90-6
ethylmagnesium bromide

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

: 75-18-3
dimethylsulfide

: 624-89-5
Ethyl methyl sulfide

: 3877-15-4
1-(methylthio)-propane

: 4110-50-3
ethyl propyl sulfide

: 1618-26-4
2,4-dithiapentane

Conditions

Conditions	Yield
With magnesium bromide; In diethyl ether; at 36 ℃; for 5h; Product distribution; other reagent, reagents ratios;	13 % Chromat. 4 % Chromat. 8 % Chromat. 1 % Chromat. 11 % Chromat.

: 624-92-0
Dimethyldisulphide

: 2949-92-0,31761-75-8
methanethiosulfonic acid S-methyl ester

: 5756-24-1
dimethyl tetrasulfide

: 1618-26-4
2,4-dithiapentane

: 3658-80-8
dimethyltrisulfane

: 42474-44-2
2,3,5-trithiahexane

: 103439-78-7
2,3,5,6-tetrathiaheptane