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 | Please contact Customer Service for Availability | 443,00 kr. |
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)
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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1 of 1
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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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
Eric D Nacsa et al.
Organic letters, 15(1), 38-41 (2012-12-15)
The cyclopropenone catalyzed nucleophilic substitution of alcohols by methanesulfonate ion with inversion of configuration is described. This work provides an alternative to the Mitsunobu reaction that avoids the use of azodicarboxylates and generation of hydrazine and phosphine oxide byproducts. This
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
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?
1 answer-
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