Potassium methanesulfonate - CAS 2386-56-3

Catalog:	BB018215
Product Name:	Potassium methanesulfonate
CAS:	2386-56-3
Synonyms:	potassium;methanesulfonate

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	potassium;methanesulfonate
Description:	Potassium methanesulfonate (CAS# 2386-56-3) is used in preparation method of Fatty Acyl glycinate surfactant.
Molecular Weight:	134.20
Molecular Formula:	CH3KO3S
Canonical SMILES:	CS(=O)(=O)[O-].[K+]
InChI:	InChI=1S/CH4O3S.K/c1-5(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1
InChI Key:	XWIJIXWOZCRYEL-UHFFFAOYSA-M
Boiling Point:	167 ℃ at 10 mmHg
Melting Point:	20 ℃
Purity:	95 %
Solubility:	Soluble in water.
Appearance:	White powder
MDL:	MFCD00070544
LogP:	0.24220

Publication Number	Title	Priority Date
CN-113270581-A	Potassium ion battery electrode material and preparation method and application thereof	20210423
CN-113072045-A	Negative electrode active material, preparation method thereof, negative electrode material, negative electrode and potassium ion battery	20210326
CN-113045272-A	Green environment-friendly concrete and preparation method thereof	20210323
CN-112779518-A	High-luminous-intensity film, preparation method and application thereof	20201217
CN-112151795-A	Positive electrode active material, positive electrode, and secondary battery	20200907

PMID	Publication Date	Title	Journal
22801556	20120828	1H-1,2,4-Triazole as solvent for imidazolium methanesulfonate	Physical chemistry chemical physics : PCCP
22799458	20120803	Synthesis of aryl ethers via a sulfonyl transfer reaction	Organic letters
22124336	20120801	Evaluation of dibutyrylchitin as new excipient for sustained drug release	Drug development and industrial pharmacy
22591586	20120601	One-pot primary aminomethylation of aryl and heteroaryl halides with sodium phthalimidomethyltrifluoroborate	Organic letters
22342146	20120315	One pot synthesis and anticancer activity of dimeric phloroglucinols	Bioorganic & medicinal chemistry letters

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Related Functional Groups

Sulfur Compounds

[123-43-3]
Sulfoacetic acid
[2006276-82-8]
[3-(N,N-Dimethylsulfamoyl)phenyl]methanesulfonyl Chloride
[1866059-82-6]
1,1,2,2-Tetrafluoro-3-methylsulfonylpropane
[85-47-2]
1-Naphthalenesulfonic acid
[42729-26-0]
3-(Trifluoromethylthio)phenyl isothiocyanate
[15863-41-9]
4-(Methylthio)phenyl isothiocyanate

GHS Hazard Statement:	H315 (97.62%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	96.5
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	2
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	133.94399661
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	133.94399661
Rotatable Bond Count:	0
Topological Polar Surface Area:	65.6 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0