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178837

Sigma-Aldrich

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

97%

Sinónimos:

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

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About This Item

Fórmula lineal:
(CH3)3Si(CH2)3SO3Na
Número de CAS:
2039-96-5
Peso molecular:
218.32
Beilstein:
4035923
Número CE:
218-031-5
Número MDL:
MFCD00007537
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
24850773
NACRES:
NA.22

Ensayo

97%

Formulario

solid

mp

~165 °C (dec.) (lit.)

grupo funcional

sulfonic acid

cadena SMILES

[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

Clave InChI

HWEXKRHYVOGVDA-UHFFFAOYSA-M

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Descripción general

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.

Aplicación

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.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000147201
0000358536
0000358535
0000340964
MKCW6450

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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
Nicole D Wagner et al.
Environmental toxicology and chemistry, 37(9), 2448-2457 (2018-06-20)
Anthropogenic activity is increasing the presence of contaminants that enter waterways through wastewater effluent and urban and/or agricultural runoff, generally in complex mixtures. Depending on the mode of action of the individual contaminant within the mixture, toxicity can occur due
Douglas V Laurents et al.
The Journal of biological chemistry, 280(5), 3675-3685 (2004-11-24)
The Alzheimer's Abeta40 peptide forms soluble oligomers that are extremely potent neurotoxins and strongly impede synapses function. In this study the formation and structure of the large, soluble, neurotoxic Abeta40 oligomer called "beta-ball" were characterized by two-dimensional NMR, circular dichroism
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
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