Unfortunately, stability timeframe data for opened bottles is not available.
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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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 L | Available to ship TODAYfromMILWAUKEE | $58.00 |
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
Concentration:
0.1 M CH3SO3H in water (0.1N)
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Quality Level
concentration
0.1 M CH3SO3H in water (0.1N)
technique(s)
ion chromatography: suitable
SMILES string
CS(O)(=O)=O
InChI
1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)
InChI key
AFVFQIVMOAPDHO-UHFFFAOYSA-N
General description
This eluent concentrate for ion chromatography is determined by potentiometric titration. Content and expiry date can be found on the certificate.
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).
Preparation Note
Prepared with methanesulfonic acid and high purity water (18.2 MΩ, 0.2 μm filtered)
Other Notes
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This Item | |||
|---|---|---|---|
| concentration 0.1 M CH3SO3H in water (0.1N) | concentration 70 wt. % in H2O | concentration 4 M (with 0.2% (w/v) tryptamine) | concentration - |
| Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level 100 |
| technique(s) ion chromatography: suitable | technique(s) - | technique(s) - | technique(s) HPLC: suitable |
Storage Class
12 - Non Combustible Liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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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
Neal W Sach et al.
Organic letters, 14(15), 3886-3889 (2012-07-18)
A general synthesis of aryl ethers from primary and secondary alcohols and aryl mesylates is presented. The reaction proceeds via a sulfonyl-transfer mechanism. In this paper, we compare the sulfonyl transfer reaction to Mitsunobu ether formation. The reaction can be
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 36564-250MG | 04061831825855 |
| 55517-1L | 04061832582528 |
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For storing and handling it is mentioned that "This eluent concentrate solution shall be stored between 5°C and 30°C. In order to avoid evaporation the bottle should be tightly closed prior to use". After the bottle is opened, how long it can be used?
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