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87920

Supelco

Tetramethylsilane

analytical standard, for NMR spectroscopy, ACS reagent

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Linear Formula:
Si(CH3)4
CAS Number:
Molecular Weight:
88.22
Beilstein/REAXYS Number:
1696908
EC Number:
MDL number:
UNSPSC Code:
12142201
PubChem Substance ID:
NACRES:
NA.24

grade

ACS reagent
analytical standard
for NMR spectroscopy

Quality Level

vapor pressure

11.66 psi ( 20 °C)

assay

≥99.5% (GC)

form

liquid

autoignition temp.

842 °F

refractive index

n20/D 1.358 (lit.)
n20/D 1.359

bp

26-28 °C (lit.)

mp

−99 °C (lit.)

density

0.648 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-8°C

SMILES string

C[Si](C)(C)C

InChI

1S/C4H12Si/c1-5(2,3)4/h1-4H3

InChI key

CZDYPVPMEAXLPK-UHFFFAOYSA-N

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General description

Tetramethylsilane has been recommended by the International Union of Pure and Applied Chemistry (IUPAC) as a universal reference for all nuclides. It is commonly used as a reference standard in nuclear magnetic resonance (NMR) for measuring proton chemical shifts and the temperature dependence of the 1H chemical shift of TMS in solvents such as chloroform, methanol, and dimethylsulfoxide is studied.

Application

Tetramethylsilane may be used as an internal standard for the quantitative analysis of medicinal plant extracts and herbal products using the quantitative NMR (qNMR) method. It may also be used as an internal standard to investigate peroxide-based chemical systems for the crosslinking reactions carried on isotactic polypropylene using FT-IR spectrometry and proton nuclear magnetic resonance (1H NMR) techniques.

pictograms

Flame

signalword

Danger

hcodes

pcodes

Hazard Classifications

Flam. Liq. 1

wgk_germany

WGK 3

flash_point_f

-16.6 °F

flash_point_c

-27 °C

ppe

Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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Sigma-Aldrich

431915

Chloroform-d

Temperature dependence of the 1H chemical shift of tetramethylsilane in chloroform, methanol, and dimethylsulfoxide
Hoffman ER, et al.
Journal of Magnetic Resonance, 176(1), 87-98 (2005)
Monitoring the chemical crosslinking of propylene polymers through rheology
Romani F, et al.
Polymer, 43(4), 1115-1131 (2002)
Siddheshwar K Chauthe et al.
Phytochemical analysis : PCA, 23(6), 689-696 (2012-06-19)
Quantitative analysis and standardisation of plant extracts or herbal products is a tedious process requiring time-consuming sample preparation and analytical method development for the resolution of analyte peaks from the complex natural extract. Quantitative analysis by HPLC requires a pure
Roy E Hoffman
Journal of magnetic resonance (San Diego, Calif. : 1997), 163(2), 325-331 (2003-08-14)
The chemical shift of TMS is commonly assumed to be zero. However, it varies by over 1 ppm for 1H and 4 ppm for 13C and shows a correlation with the physical properties of the solvent. Using the commonly accepted
Thierry Rohmer et al.
The journal of physical chemistry. A, 115(42), 11696-11714 (2011-08-19)
The open-chain tetrapyrrole compound bilirubin was investigated in chloroform and dimethyl sulfoxide solutions by liquid-state NMR and as solid by (1)H, (13)C, and (15)N magic-angle spinning (MAS) solid-state NMR spectroscopy. Density functional theory (DFT) calculations were performed to interpret the

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