Skip to Content
Merck
CN

358959

Sodium 1-propanesulfonate monohydrate

99%

Synonym(s):

1-Propanesulfonic acid sodium salt monohydrate

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
CH3CH2CH2SO3Na · H2O
CAS Number:
304672-01-3
Molecular Weight:
164.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24862040
MDL number:
MFCD00167033
Beilstein/REAXYS Number:
3714817
Assay:
99%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Sodium 1-propanesulfonate monohydrate, 99%

InChI

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

SMILES string

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

InChI key

QBQVXXQXZXDEHE-UHFFFAOYSA-M

assay

99%

mp

250 °C (dec.) (lit.)

solubility

water: soluble 10%, clear, colorless

functional group

sulfonic acid

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD4431
0001450497
1450497V
BCBB3373V
BCBB3369V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service