To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

DSS (NMR standard)

From Wikipedia, the free encyclopedia

DSS (NMR standard)
Names
Preferred IUPAC name
Sodium 3-(trimethylsilyl)propane-1-sulfonate
Other names
3-trimethylsilyl-1-propanesulfonate, sodium salt; 2,2-Dimethyl-2-silapentane-5-sulfonate sodium salt; DSS sodium salt(trimethylsilyl)-1-propanesulfonate
Identifiers
3D model (JSmol)
Abbreviations DSS
ChemSpider
EC Number
  • 218-031-5
  • 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
    Key: HWEXKRHYVOGVDA-UHFFFAOYSA-M
  • C[Si](C)(C)CCCS(=O)(=O)[O-].[Na+]
Properties
C6H15NaO3SSi
Molar mass 218.32 g·mol−1
Appearance White solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Sodium trimethylsilylpropanesulfonate (DSS) is the organosilicon compound with the formula (CH3)3SiCH2CH2CH2SO3Na+. It is the sodium salt of trimethylsilylpropanesulfonic acid. A white, water-soluble solid, it is used as a chemical shift standard for proton NMR spectroscopy of aqueous solutions.[1] The chemical shift, specifically the signal for the trimethylsilyl group, is relatively insensitive to pH.[2]

The proton spectrum of DSS also exhibits resonances at 2.91 ppm (m), 1.75 ppm (m), and 0.63 ppm (m) at an intensity of 22% of the reference resonance at 0 ppm.

YouTube Encyclopedic

  • 1/3
    Views:
    1 903
    4 108
    354
  • Why tetramethylsilane (TMS) is used as the reference standard in NMR?
  • Lecture 2: NMR-based Metabolomics
  • Lec. No. 9; The Unit of Chemical Shift and TMS in NMR spectroscopy

Transcription

Alternatives

Sodium trimethylsilyl propionate (TSP) is a related compound used as an NMR standard. It uses a carboxylic acid instead of the sulfonic acid found in DSS to confer water solubility. As a weak acid, TSP is more sensitive to changes in pH.

4,4-Dimethyl-4-silapentane-1-ammonium trifluoroacetate (DSA) has also been proposed as an alternative, to overcome certain drawbacks of DSS.[3]

References

  1. ^ Harris, Robin K.; Becker, Edwin D.; Cabral De Menezes, Sonia M.; Granger, Pierre; Hoffman, Roy E.; Zilm, Kurt W. (2008). "Further Conventions for NMR Shielding and Chemical Shifts (IUPAC Recommendations 2008)". Pure and Applied Chemistry. 80 (2): 59–84. Bibcode:2008JMagR.191..340.. doi:10.1351/pac200880010059.
  2. ^ De Marco, Antonio (1977). "pH Dependence of Internal References". Journal of Magnetic Resonance. 26 (3): 527–528. Bibcode:1977JMagR..26..527D. doi:10.1016/0022-2364(77)90104-4.
  3. ^ Nowick, James S.; Khakshoor, Omid; Hashemzadeh, Mehrnoosh; Brower, Justin O. (2003). "DSA: A New Internal Standard for NMR Studies in Aqueous Solution". Org. Lett. 5 (19): 3511–3513. doi:10.1021/ol035347w. PMID 12967312.
This page was last edited on 20 June 2022, at 08:17
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.