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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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About This Item

Linear Formula:
(CH3)3Si(CH2)3SO3Na
CAS Number:
Molecular Weight:
218.32
Beilstein:
4035923
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

~165 °C (dec.) (lit.)

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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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 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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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
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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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