318183
Methyl sulfate sodium salt
Synonym(s):
Monomethyl ester sulfuric acid sodium salt, Sodium methyl sulfate
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About This Item
Linear Formula:
CH3OSO3Na
CAS Number:
Molecular Weight:
134.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
powder
Quality Level
impurities
<3% methanol
<5% water
mp
210 °C (lit.)
SMILES string
[Na+].COS([O-])(=O)=O
InChI
1S/CH4O4S.Na/c1-5-6(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1
InChI key
DZXBHDRHRFLQCJ-UHFFFAOYSA-M
Application
Methyl sulfate sodium salt can be used to synthesize:
- Methylsulfate anion based 1,3,4-trialkyl-1,2,3-triazolium ionic liquids for use in Morita–Baylis–Hillman reaction.
- Anisole by reacting with phenol.
- Hydroxyanilino quinolines for use as RET kinase inhibitors.
Reactant or reagent involved in:
- Studying lamellar structure formation in hybrid nanomaterials created by miniemulsion
- EPR studies of radical ions radiolytically generated from ionic liquids, used as a reference
- Micellular studies specifically the rate-retarding effects on hydrolysis of substituted 1-benzoyl-1,2,4-triazoles and self-assembly / microstructure of mixed micelles
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of anisole from phenol and sodium methyl sulfate, a byproduct from synthesis of medicine intermediates
Guoping W, et al.
Petrochemical Technology, 45(11), 1337-1337 (2016)
Dean Kirson et al.
The Journal of pharmacology and experimental therapeutics, 364(1), 70-76 (2017-11-10)
The amino acid taurine is an endogenous ligand acting on glycine receptors (GlyRs), which is released by astrocytes in many brain regions, such as the nucleus accumbens and prefrontal cortex. Taurine is a partial agonist with an efficacy significantly lower
Catherine Cook Kaczorowski et al.
The Journal of physiology, 578(Pt 3), 799-818 (2006-12-02)
CA1 pyramidal neurons from animals that have acquired hippocampal tasks show increased neuronal excitability, as evidenced by a reduction in the postburst afterhyperpolarization (AHP). Studies of AHP plasticity require stable long-term recordings, which are affected by the intracellular solutions potassium
M A Sallam et al.
Carbohydrate research, 330(1), 53-63 (2001-02-24)
Dehydration of 4-(D-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole with 20% methanolic sulfuric acid afforded the anomeric pairs of nucleosides, 4-(alpha-D-lyxopyranosyl)-2-phenyl-2H-1,2,3-triazole (major component) and its beta-anomer, as well as 4-(alpha-D-lyxofuranosyl)-2H-1,2,3-triazole and its beta-anomer. The four anomeric C-nucleosides were separated by chromatography, and their structure and anomeric
J Lännergren et al.
The Journal of physiology, 526 Pt 3, 597-611 (2000-08-02)
Isolated, living muscle fibres from either Xenopus or mouse were observed in a confocal microscope and t-tubules were visualized with sulforhodamine B. Observations were made before and after fatiguing stimulation. In addition, experiments were performed on fibres observed in an
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