55517
Methanesulfonic acid concentrate
0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
Synonym(s):
Methanesulfonic acid solution
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About This Item
Linear Formula:
CH3SO3H
CAS Number:
Molecular Weight:
96.11
UNSPSC Code:
12161700
NACRES:
NB.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1446024
Product Name
Methanesulfonic acid concentrate, 0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
SMILES string
CS(O)(=O)=O
InChI key
AFVFQIVMOAPDHO-UHFFFAOYSA-N
InChI
1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)
concentration
0.1 M CH3SO3H in water (0.1N)
technique(s)
ion chromatography: suitable
Quality Level
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Application
- Design of a new nanocomposite based on Keggin-type [ZnW(12)O(40)](6-) anionic cluster anchored on NiZn(2)O(4) ceramics: Explores the synthesis of advanced materials using Methanesulfonic acid, contributing to developments in energy storage and catalysis technology (Rezvani et al., 2024).
- Nanosuspensions in ophthalmology: Overcoming challenges and enhancing drug delivery for eye diseases: Discusses the role of Methanesulfonic acid in the formulation of nanosuspensions, enhancing therapeutic efficiency in ophthalmologic applications (Fathi-Karkan et al., 2024).
- Building Flame-Retardant Polymer Electrolytes via Microcapsule Technology for Stable Lithium Batteries: Methanesulfonic acid may be utilized in the synthesis of flame-retardant materials for safer lithium battery technologies, addressing critical needs in electronic manufacturing (Zhang et al., 2024).
- Catalysts for C-N coupling in urea electrosynthesis under ambient conditions from carbon dioxide and nitrogenous species: Highlights the application of Methanesulfonic acid in developing catalysts for green chemistry processes, particularly in the efficient synthesis of urea from environmentally benign sources (Yang et al., 2024).
General description
This eluent concentrate for ion chromatography is determined by potentiometric titration. Content and expiry date can be found on the certificate.
Other Notes
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Preparation Note
Prepared with methanesulfonic acid and high purity water (18.2 MΩ, 0.2 μm filtered)
Storage Class
12 - Non Combustible Liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Chris Twelves et al.
Breast cancer research and treatment, 148(3), 553-561 (2014-11-09)
Data from two phase 3 studies of eribulin were pooled in analyses initially requested by the European Medicines Agency to assess whether specific patient subgroups, previously treated with an anthracycline and a taxane, benefited from eribulin. Study 305/EMBRACE included women
Claudio Pettinari et al.
Inorganic chemistry, 50(21), 11173-11183 (2011-10-18)
Five new silver(I) complexes of formulas [Ag(Tpms)] (1), [Ag(Tpms)(PPh(3))] (2), [Ag(Tpms)(PCy(3))] (3), [Ag(PTA)][BF(4)] (4), and [Ag(Tpms)(PTA)] (5) {Tpms = tris(pyrazol-1-yl)methanesulfonate, PPh(3) = triphenylphosphane, PCy(3) = tricyclohexylphosphane, PTA = 1,3,5-triaza-7-phosphaadamantane} have been synthesized and fully characterized by elemental analyses, (1)H, (13)C
Cassandra J Gaston et al.
Environmental science & technology, 44(5), 1566-1572 (2010-02-04)
Dimethyl sulfide (DMS), produced by oceanic phytoplankton, is oxidized to form methanesulfonic acid (MSA) and sulfate, which influence particle chemistry and hygroscopicity. Unlike sulfate, MSA has no known anthropogenic source making it a useful tracer for ocean-derived biogenic sulfur. Despite
Renata Solarska et al.
Nanoscale, 4(5), 1553-1556 (2012-02-01)
Nanostructuring of semiconductor films offers the potential means for producing photoelectrodes with improved minority charge carrier collection. Crucial to the effective operation of the photoelectrode is also the choice of a suitable electrolyte. The behaviour of the nanostructured WO(3) photoanodes
Norio Murai et al.
Organic letters, 14(11), 2818-2821 (2012-05-18)
A one-pot primary aminomethylation of aryl halides, triflates, mesylates, and tosylates via Suzuki-Miyaura cross-coupling reactions with sodium phthalimidomethyltrifluoroborate followed by deamidation with ethylenediamine is reported.
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