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Sigma-Aldrich

Sodium 1-propanesulfonate monohydrate

99%

Synonym(s):

1-Propanesulfonic acid sodium salt monohydrate

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About This Item

Linear Formula:
CH3CH2CH2SO3Na · H2O
CAS Number:
304672-01-3
Molecular Weight:
164.16
Beilstein:
3714817
MDL number:
MFCD00167033
UNSPSC Code:
12352100
PubChem Substance ID:
24862040
NACRES:
NA.22

Assay

99%

mp

250 °C (dec.) (lit.)

solubility

water: soluble 10%, clear, colorless

SMILES string

O.[Na+].CCCS([O-])(=O)=O

InChI

1S/C3H8O3S.Na.H2O/c1-2-3-7(4,5)6;;/h2-3H2,1H3,(H,4,5,6);;1H2/q;+1;/p-1

InChI key

QBQVXXQXZXDEHE-UHFFFAOYSA-M

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General description

Sodium 1-propanesulfonate monohydrate is sulfonate-containing compound. Multicollision dissociation threshold (MCDT) values for the dissociation of the anion dopant from lacto-N-difucohexaoses I for sodium 1-propanesulfonate monohydrate (1-propanesulfonic acid sodium salt monohydrate) has been evaluated.

Application

Sodium 1-propanesulfonate monohydrate (1-Propanesulfonic acid sodium salt monohydrate) is suitable for use in a study to investigate the reaction between active methyl-coenzyme M reductase (MCR) and the potent inhibitor, 3-bromopropanesulfonate by UV-visible and EPR spectroscopy and by steady-state and rapid kinetics.

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A W Wong et al.
Analytical chemistry, 72(7), 1419-1425 (2000-04-14)
Alkylsulfonates are examined as anion dopants for the matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS) of neutral oligosaccharides. The anion dopants allow neutral oligosaccharides to be examined in the same mixture as acidic oligosaccharides. The alkylsulfonate dopants interact strongly with the oligosaccharide
Ryan C Kunz et al.
The Journal of biological chemistry, 281(45), 34663-34676 (2006-09-13)
Methyl-coenzyme M reductase (MCR) catalyzes the final step of methanogenesis in which coenzyme B and methyl-coenzyme M are converted to methane and the heterodisulfide, CoMS-SCoB. MCR also appears to initiate anaerobic methane oxidation (reverse methanogenesis). At the active site of
Kevin G Schmitt et al.
Physical chemistry chemical physics : PCCP, 21(30), 16838-16847 (2019-07-25)
We evaluate the effect of chain length for a series of alkyl sulfonic acid additives on Cu electrodeposition by using a combination of electrochemical and Raman spectroscopic methods. Rotating disk linear sweep voltammetry revealed the influence of these additives on

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