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178837

Sigma-Aldrich

3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt

97%

Synonym(s):

2,2-Dimethyl-2-silapentane-5-sulfonate sodium salt, DSS sodium salt, Sodium 3-(trimethylsilyl)-1-propanesulfonate

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1 G
$183.00
5 G
$473.00

$183.00

Estimated to ship onApril 28, 2025

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1 G
$183.00
5 G
$473.00

About This Item

Linear Formula:
(CH3)3Si(CH2)3SO3Na
CAS Number:
2039-96-5
Molecular Weight:
218.32
Beilstein/REAXYS Number:
4035923
EC Number:
218-031-5
MDL number:
MFCD00007537
UNSPSC Code:
12352100
PubChem Substance ID:
24850773
NACRES:
NA.22

$183.00

Estimated to ship onApril 28, 2025

Request a Bulk Order

Quality Level

100

assay

97%

form

solid

mp

~165 °C (dec.) (lit.)

functional group

sulfonic acid

SMILES string

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

InChI

1S/C6H16O3SSi.Na/c1-11(2,3)6-4-5-10(7,8)9;/h4-6H2,1-3H3,(H,7,8,9);/q;+1/p-1

InChI key

HWEXKRHYVOGVDA-UHFFFAOYSA-M

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General description

3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt, also known as DSS sodium salt, is commonly used as an internal standard for referencing chemical shifts and scaling the intensity of all ¹H-NMR spectroscopy signals. [1]

Application

3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt can be used as a reagent to synthesize polyamine block-copolymers. It can also be used as an internal standard in 1H NMR spectroscopy for the measurement of chemical shifts.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000147201
0000358535
0000358536
MKCW6450
0000147201

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Radha Sharma et al.
Journal of pharmaceutical and biomedical analysis, 49(4), 1092-1096 (2009-03-21)
A rapid selective and accurate quantitative (1)H NMR method was developed for the simultaneous analysis of obidoxime chloride and atropine sulfate, the active components in parenteral injection devices (PID) used for the emergency treatment of poisoning by toxic organophosphates. The
Nicole D Wagner et al.
Environmental toxicology and chemistry, 36(4), 938-946 (2016-08-31)
The use of consumer products and pharmaceuticals that act as contaminants entering waterways through runoff and wastewater effluents alters aquatic ecosystem health. Traditional toxicological endpoints may underestimate the toxicity of contaminants, as lethal concentrations are often orders of magnitude higher
Ingrid Dijkgraaf et al.
Organic & biomolecular chemistry, 5(6), 935-944 (2007-03-07)
This report describes the design and synthesis of a series of alpha(V)beta(3) integrin-directed monomeric, dimeric and tetrameric cyclo[Arg-Gly-Asp-d-Phe-Lys] dendrimers using "click chemistry". It was found that the unprotected N-epsilon-azido derivative of cyclo[Arg-Gly-Asp-d-Phe-Lys] underwent a highly chemoselective conjugation to amino acid-based
J F Clark et al.
Biochimica et biophysica acta, 1014(3), 235-238 (1989-12-14)
3-(Trimethylsilyl)propanesulfonic acid (TMSPS) is used as a water-soluble NMR frequency marker. It has its major resonance at 0.00 ppm relative to trimethylsilane, and smaller resonances at 0.62, 1.77 and 2.85 ppm. Its toxicity was tested by exposing contracted porcine carotid
Jerome Kretzschmar et al.
Inorganic chemistry, 59(7), 4244-4254 (2020-03-10)
The interactions between glutathione disulfide, GSSG, the redox partner and dimer of the intracellular detoxification agent glutathione, GSH, and hexavalent uranium, U(VI), were extensively studied by solution NMR (in D2O), complemented by time-resolved laser-induced fluorescence and IR spectroscopies. As expected
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