| Weight | 112.106 g/mol |
|---|---|
| Formula | CH4O4S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Methyl sulfate (75-93-4, 77-78-1)
sodium methyl sulfate · monomethyl sulfate · methyl sulfate, sodium salt
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- Pregnenolone sulfate: a positive allosteric modulator at the N-methyl-D-aspartate receptor. (Molecular Pharmacology, 1991)
- Efficient, halide free synthesis of new, low cost ionic liquids: 1,3-dialkylimidazolium salts containing methyl- and ethyl-sulfate anions (Green Chemistry, 2002)
- Pregnenolone sulfate potentiation of N-methyl-D-aspartate receptor channels in hippocampal neurons. (Molecular Pharmacology, 1993)
- Physical Properties of 1-Butyl-3-methylimidazolium Methyl Sulfate as a Function of Temperature (Journal of Chemical & Engineering Data, 2007)
- Pharmacology of the Urotensin-II Receptor Antagonist Palosuran (ACT-058362; 1-[2-(4-Benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea Sulfate Salt): First Demonstration of a Pathophysiological Role of the Urotensin System (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Preparation, characterization, and photocatalytic activity of sulfate-modified titania for degradation of methyl orange under visible light (Journal of Colloid and Interface Science, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - sodium methyl sulfate
- monomethyl sulfate
- methyl sulfate, sodium salt
- methyl sulfate, potassium salt
- methyl sulfate, ammonium salt
-
SMILESCOS(=O)(=O)O
-
InChIKeyJZMJDSHXVKJFKW-UHFFFAOYSA-N
- Pubchem - Methyl sulfate
- Wikipedia - methyl sulfate
Methyl bisulfate is a chemical compound with the molecular formula CH4O4S. This compound is the mono-methyl ester of sulfuric acid. The significance of methyl bisulfate is that it is an intermediate in the hydrolysis of the important reagent dimethyl sulfate, (CH3)2SO4: (CH3)2SO4 + H2O (CH3)HSO4 + CH3OH Methyl bisulfate is an acid: (CH3)HSO4 (CH3)SO4 + H+ Methyl bisulfate came into the public view in 1993 with the discovery that certain mercury compounds catalyze the conversion of methane to methylbisulfate in good yields with excellent selectivity in concentrated sulfuric acid.
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