CAS 5188-07-8
:Sodium methanethiolate
Description:
Sodium methanethiolate, with the CAS number 5188-07-8, is an organosulfur compound that serves as a sodium salt of methanethiol. It is typically encountered as a white to off-white solid, which is highly soluble in water due to the presence of the sodium ion. This compound is characterized by its strong nucleophilic properties, making it useful in various organic synthesis reactions, particularly in the formation of thioethers and other sulfur-containing compounds. Sodium methanethiolate is also known for its ability to act as a reducing agent and can participate in reactions involving electrophiles. It has a distinct, pungent odor reminiscent of rotten cabbage, which is characteristic of methanethiol. Safety precautions are necessary when handling this compound, as it can be irritating to the skin, eyes, and respiratory system. Additionally, it should be stored in a cool, dry place, away from incompatible substances, to maintain its stability and reactivity.
Formula:CH4S·Na
InChI:InChI=1S/CH4S.Na/c1-2;/h2H,1H3;
InChI key:InChIKey=XHXXWWGGXFUMAJ-UHFFFAOYSA-N
SMILES:CS.[Na]
Synonyms:- (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
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Found 11 products.
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:<p>Sodium methanethiolate</p>Formula:·CH3S·NaPurity:≥95%Color and Shape: white to off-white crystalline powderMolecular weight:70.08929g/molSodium thiomethoxide
CAS:Formula:CH3NaSColor and Shape:White to yellow or brown powder or crystalsMolecular weight:70.09Sodium thiomethoxide solution
CAS:<p>Sodium thiomethoxide solution</p>Purity:≥95%Color and Shape:LiquidMolecular weight:70.08929g/molSodium Methanethiolate (~20% in Water)
CAS:Controlled Product<p>Applications 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.<br> E0<br>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),<br></p>Formula:CH3S·NaColor and Shape:ColourlessMolecular weight:70.09Sodium Methanethiolate (95%)
CAS:Controlled ProductFormula:CH3S·NaPurity:95%Color and Shape:NeatMolecular weight:70.09Sodium methanethiolate
CAS:<p>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.</p>Formula:CH3NaSPurity:Min. 95%Color and Shape:White PowderMolecular weight:70.09 g/mol3-Methyl-2-buten-1-thiol Preparation Kit
CAS:<p>Stability Readily Oxidized<br>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.<br>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),<br></p>Formula:MixtureVisitourWebsiteColor and Shape:Colourless To YellowMolecular weight:Mixture - Visit our WebsiteSodium methanethiolate - 15% aqueous solution
CAS:<p>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.</p>Formula:CH3NaSPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:70.09 g/molSodium Methanethiolate-13C
CAS:Controlled Product<p>Applications Sodium Methanethiolate-13C, is the labeled analogue of Sodium Methanethiolate (S644805), used as a nucleophile in organic synthesis. Sodium methanethiolate is also being used as a reagent to synthesize thiol-based suberoylanilide hydroxamic acid (SAHA) analogues, compounds that act as potent histone deacetylase inhibitors.<br>References Bergman, A. & Wachtmeister, Chemosphere, 7, 949 (1978); Suzuki, T.,et al.: Bioorg. Med. Chem. Lett., 14, 3313 (2004)<br></p>Formula:CH3NaSPurity:>90%Color and Shape:NeatMolecular weight:71.082





