CAS 5188-07-8
:Sodium methanethiolate
- (Methylsulfanyl)sodium
- Metanotiolato De Sodio
- Methanethiol, sodium salt (1:1)
- Methanethiolate de sodium
- Methyl mercaptan sodium salt
- Methylthiosodium
- Natriummethanthiolat
- Sodium Methanethiolate
- Sodium methanesulfenate
- Sodium methyl mercaptan
- Sodium methyl mercaptide
- Sodium methyl sulfide
- Sodium methylmercaptide
- Sodium methylthiolate
- Sodium thiomethoxide
- Sodium thiomethylate
- Sodium, (methylthio)-
- Thiomethoxide, Sodium
- See more synonyms
- Lower prices
- Higher prices
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Methyl Mercaptan Sodium Salt (ca. 15% in Water)
CAS:Formula:CH3NaSColor and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:70.08Sodium methanethiolate
CAS:Sodium methanethiolateFormula:·CH3S·NaPurity:≥95%Color and Shape:Beige SolidMolecular weight:70.08929Sodium thiomethoxide solution
CAS:Sodium thiomethoxide solutionFormula:·CH3S·NaPurity:≥95%Color and Shape:LiquidMolecular weight:70.08929Sodium thiomethoxide
CAS:Formula:CH3NaSColor and Shape:White to yellow or brown powder or crystalsMolecular weight:70.09Sodium Methanethiolate (~20% in Water)
CAS:Controlled ProductApplications Strong nucleophile used for the synthesis of methyl aryl sulfides from halo-arenes. Alkanethiolates are efficient reagents for SN2 dealkylation of esters and aryl ethers.
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References Le Brazidec, J., et al.: J. Med. Chem., 47, 3865 (2004), Grem, J., et al.: J. Clin. Oncol., 23, 1885 (2005), Levason, W., et al.: Dalton Trans, 439 (2007),Formula:CH3S·NaColor and Shape:Single SolutionMolecular weight:70.09Sodium Methanethiolate (95%)
CAS:Controlled ProductFormula:CH3S·NaPurity:95%Color and Shape:NeatMolecular weight:70.09Sodium methanethiolate
CAS:Methanethiol is a compound that occurs naturally in the environment. It is used as a fungicide, insecticide and herbicide. Methanethiol inhibits the growth of microorganisms by binding to metal ions on the surface of cells. This prevents DNA replication and protein synthesis, leading to cell death. Methanethiol also has anti-inflammatory properties which may be due to its ability to inhibit adenosine A1 receptor activity in humans.
Formula:CH3NaSPurity:Min. 95%Color and Shape:White PowderMolecular weight:70.09 g/mol3-Methyl-2-buten-1-thiol Preparation Kit
CAS:Stability Readily Oxidized
Applications A volatile aroma compound. We will provide a detailed procedure for the preparation of the thiol from the thiolacetate with spectral data upon request.
References Majcher, M., et al.: J. Agric. Food Chem., 55, 5754 (2007), Akiyama, M., et al.: Food Sci. Technol. Res., 15, 233 (2009), Breme, K., et al.: J. Agric. Food Chem., 57, 8572 (2009),Formula:MixtureColor and Shape:Colourless To YellowMolecular weight:MixtureSodium methanethiolate - 15% aqueous solution
CAS:Sodium methanethiolate is an antimicrobial agent that is a white, crystalline solid. It reacts with trifluoroacetic acid and water to produce the active form of sodium trifluoroacetate. The reaction mechanism is likely due to the formation of a bicyclic heterocycle that has been shown to be effective against a number of bacteria. Sodium methanethiolate has been used for the treatment of infectious diseases, such as respiratory infections and skin infections, as well as autoimmune diseases and cardiovascular disorders. The oxidation catalyst in this compound may also have physiological effects on the body's cells and tissues.Formula:CH3NaSPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:70.09 g/mol





