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358959

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

functional group

sulfonic acid

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD4431
0001450497
1450497V
BCBB3373V
BCBB3369V

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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
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
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

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