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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:
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

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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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
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
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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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